Bio

Clinical Focus


  • Obstetrics and Gynecology
  • Gynecology
  • Cervical Cancer Prevention
  • Abortion
  • Advanced Contraception
  • Family Planning Services
  • Family Planning Training

Academic Appointments


Administrative Appointments


  • Chief The Stanford Gynecology Service, Department of Obstetrics and Gynecology (2011 - Present)
  • Director, Stanford Program for International Reproductive Education and Services (SPIRES) (2008 - Present)
  • Director, Family Planning Services and Research, Department of Obstetrics and Gynecology (2007 - Present)
  • Director, Ambulatory Care, Department of Obstetrics and Gynecology (2007 - Present)

Honors & Awards


  • Faculty Teaching Award in Gynecology, Stanford University Department of Obstetrics and Gynecology (June, 2008)
  • Kenneth J Ryan Leadership Award, Physicians for Reproductive Choice and Health (May, 2008)
  • Michael Burnhill Award, Association of Reproductive Health Professionals (2007)
  • Golden Apple Faculty Teaching Award, Michael Reese Hospital and Medical Center (1987)
  • Helena Rubenstein Award, University of the Health Sciences/Chicago Medical School (1977)

Professional Education


  • Internship:Michael Reese Hospital and Medical Center (1978) IL
  • Residency:Michael Reese Hospital and Medical Center (1982) IL
  • Board Certification: Obstetrics and Gynecology, American Board of Obstetrics and Gynecology (1985)
  • Fellowship:UCLA Health Sciences (1984) CA
  • Medical Education:University of Health Services/Chicago Medical School (1977) IL

Community and International Work


  • Post Partum IUD Services in Zambia, Lusaka

    Topic

    Family Planning

    Partnering Organization(s)

    Society for Family Health (Zambia) and Population Services International

    Populations Served

    Women of reproductive age in Zambia

    Location

    International

    Ongoing Project

    Yes

    Opportunities for Student Involvement

    No

  • Cervical Cancer Prevention in Etiopia, Ethiopia

    Partnering Organization(s)

    CDC, Pathfinder International, Government of Ethiopia

    Populations Served

    Women of Ethiopia

    Location

    US

    Ongoing Project

    Yes

    Opportunities for Student Involvement

    No

Research & Scholarship

Current Research and Scholarly Interests


Improving Access to Family Planning Services in Low Resource Settings:

Through a collaboration with Population Services International, the Stanford Program for International Reproductive Education and Services (SPIRES) provides technical direction in a program designed to improve access to and uptake of family planning, particularly Long Acting Reversible Contraception (LARC) such as IUDs and implants, in 14 developing countries globally. The first year saw insertion of over 280,000 IUDs.

Clinical Trials


  • Value of Mifepristone in Cervical Preparation Prior to Dilation and Evacuation 19-24 Weeks Not Recruiting

    A common practice for preparation for surgical abortion after 19 weeks gestation is the placement of multiple sets of osmostic dilators 1-2 days prior to the procedure. The investigators aim to study the addition of mifepristone as an adjunct to cervical dilation prior to abortion between 19-24 weeks gestation, and its potential to minimize the number of painful procedures and time in clinic (or away from work/home) that multiple sets of dilators can require. The investigators hypothesize that one set of dilators with mifepristone will result in similar procedure times and decreased "total" time as two sets of dilators.

    Stanford is currently not accepting patients for this trial.

    View full details

  • Exploring the Role of At-home Semi-Quantitative Pregnancy Tests for Medical Abortion Follow-up Recruiting

    This study will examine the feasibility, acceptability and usability of a semi-quantitative urine pregnancy test (dBest One Step hCG Panel Test Kit) for at-home follow-up after early medical abortion using mifepristone+misoprostol. The study seeks to: 1. Assess the feasibility of using this test in lieu of standard one-week clinic-based follow up for determination of complete abortion status as part of normal service delivery. In Mexico, follow up will be in two weeks, as is standard care in that . 2. To determine if women using this test at home understand how to use it and can correctly interpret the results; is it practical. 3. Assess women's and provider's acceptability of using at-home pregnancy tests in lieu of clinic-based follow up for confirmation of complete medical abortion in the future.

    View full details

  • Exploring Semi-Quantitative Pregnancy Tests and Their Impact on Reproductive Health Service Provision Not Recruiting

    This study will examine the feasibility, practicality, utility and usability of a semi-quantitative urine pregnancy test (dBest One Step hCG Panel Test Kit) recently approved by the food and drug administration (FDA) for both Professional (physician office) and over-the-counter (consumer) use. The study seeks to: 1. Assess the correlation of this pregnancy test results with serum values (as distinct from urine) hCG. 2. Assess whether or not time of day of urine collection has any impact on the outcome of the dBest test. 3. Assess user comprehension of the pregnancy test, especially assessment of the result.

    Stanford is currently not accepting patients for this trial. For more information, please contact Kelsey Lynd, (650) 721 - 1237.

    View full details

Teaching

Publications

Journal Articles


  • Factors Influencing Women's Decision to Seek Antenatal Care in the ANDES of Peru MATERNAL AND CHILD HEALTH JOURNAL Ayala, L. S., Blumenthal, P. D., Sarnquist, C. C. 2013; 17 (6): 1112-1118

    Abstract

    This qualitative study aimed to assess factors influencing pregnant women's decision to seek or avoid antenatal care (ANC) in the Andes of Peru. Open-ended, semi-structured interviews were conducted with 24 women utilizing ANC (+) and 10 women avoiding ANC (-). Interviews were translated to English from Quechua and Spanish, transcribed, and analyzed using grounded theory. Factors influencing ANC- women included: expecting criticism for having additional children; long ANC wait time and inconvenient hours of operation; and masculine gender of health workers. For ANC+ women, motivating factors included: maximizing positive health outcomes; past negative maternity experiences; pressure from family members; and avoidance of rumored fines or fees associated with ANC non-attendance and in-hospital deliveries, respectively. Both ANC+ and ANC- women were fearful and embarrassed about possible criticism for having additional children and the gender of the health workers, yet they weighed these factors differently. To better understand how rural women make decisions about ANC attendance, it is important to consider the value they place on the factors influencing their decision, and their emotional assessment of such issues.

    View details for DOI 10.1007/s10995-012-1113-9

    View details for Web of Science ID 000321785300017

    View details for PubMedID 22956365

  • Feasibility of community-based careHPV for cervical cancer prevention in rural Thailand. Journal of lower genital tract disease Trope, L. A., Chumworathayi, B., Blumenthal, P. D. 2013; 17 (3): 315-319

    Abstract

    OBJECTIVE: This study aimed to assess the safety, acceptability and feasibility of primary human papillomavirus (HPV) testing for cervical cancer prevention at the community level in a low-resource setting. MATERIALS AND METHODS: After training a technician to run specimens on the careHPV unit, the study team traveled to a different village each day in rural Roi-et Province, Thailand. Women were tested for HPV using self-swab, followed by careHPV testing. Those with positive result were assessed immediately by visual inspection with acetic acid. Women positive for HPV and visual inspection with acetic acid were offered cryotherapy. Safety was determined by monitoring adverse events. Exit surveys assessed acceptability and feasibility. Feasibility was also assessed by measuring testing and triage throughputs. RESULTS: Technician training required 2.5 days to achieve competency. A total of 431 women were screened in 14 days, with an average of 31 women screened daily. No adverse events were reported. Women deemed the program overwhelmingly acceptable: 90.5% reported that they would take the self-swab again, 71.3% preferred the self-swab to a clinician swab. The program was also feasible: 99.8% of eligible women agreed to testing, 94.8% returned for same-day follow-up, and women only spent 30 to 50 minutes of their total time with the program from screening to results. CONCLUSIONS: Cervical cancer prevention programs based on self-swab HPV testing could be safe, acceptable, feasible, and effective at the community level in low-resource settings.

    View details for DOI 10.1097/LGT.0b013e31826b7b70

    View details for PubMedID 23422644

  • Simplified medical abortion using a semi-quantitative pregnancy test for home-based follow-up. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics Lynd, K., Blum, J., Ngoc, N. T., Shochet, T., Blumenthal, P. D., Winikoff, B. 2013; 121 (2): 144-148

    Abstract

    To simplify follow-up after medical abortion by examining whether women could use a semi-quantitative pregnancy test at home to screen for ongoing pregnancy.Three hundred women seeking medical abortion at a tertiary hospital in Vietnam participated in the study. Participants used a semi-quantitative pregnancy test at the hospital to estimate baseline human chorionic gonadotropin (hCG) levels and administered another test at home 2 weeks later for comparison. Women interpreted the test result at home and then returned to hospital for follow-up care. At this visit, self-assessment was verified. To assess further the feasibility of the test as a follow-up tool in service delivery, 200 additional women completed a user comprehension survey.The tests identified all 11 ongoing pregnancies among study participants (100% sensitivity; 89.7% specificity). Women reported that the test was easy to use (255/292 [87.3%]) and that provider instructions helped them to use the test (291/292 [99.7%]).Semi-quantitative pregnancy tests offer high sensitivity and negative predictive value. If user instructions can be further simplified, the tests could be used in lieu of transvaginal ultrasound and/or serum hCG at clinic-based follow-up or by women themselves for home-based follow-up. Clinical trials.gov:NCT01150279.

    View details for DOI 10.1016/j.ijgo.2012.11.022

    View details for PubMedID 23477704

  • Revitalizing long-acting reversible contraceptives in settings with high unmet need: a multicountry experience matching demand creation and service delivery CONTRACEPTION Blumenthal, P. D., Shah, N. M., Jain, K., Saunders, A., Clemente, C., Lucas, B., Jafa, K., Eber, M. 2013; 87 (2): 170-175

    Abstract

    Contraception in many developing countries is characterized by high unmet need, irregular access, low utilization and presumed demand for long-acting reversible contraceptives (LARCs).A 13-country initiative focused on increasing consumer demand and high quality services for intrauterine devices (IUDs) began in 2009. Services were provided through (a) private sector-franchised or affiliated clinics; (b) providers seconded to the public sector and (c) special "event" days. Client intake data are used to compare the profile of IUD acceptors with IUD users from representative national datasets of select countries, as well as examine trends in IUD uptake.During 2009-2010, 575,601 IUDs were inserted across the 13 countries. Compared to national IUD users, users in this project were slightly younger and less educated. Among IUD acceptors, 24% used no modern method at the time of IUD initiation, and 28% reported injectable use in the three previous months.Convenient, quality, affordable services with demand creation can result in significant uptake of LARCs in settings with low use.

    View details for DOI 10.1016/j.contraception.2012.10.002

    View details for Web of Science ID 000313929000010

    View details for PubMedID 23153895

  • Mifepristone-misoprostol dosing interval and effect on induction abortion times: a systematic review. Obstetrics and gynecology Shaw, K. A., Topp, N. J., Shaw, J. G., Blumenthal, P. D. 2013; 121 (6): 1335-47

    Abstract

    To examine the effect of the interval between mifepristone and misoprostol administration on induction time (first misoprostol dose to abortion), total procedure time (mifepristone administration to abortion), and safety and efficacy in second-trimester induction abortion (13-24 weeks).We searched MEDLINE (1966-2012), ClinicalTrials.gov, POPLINE, and the Cochrane Controlled Trials Register using search terms for second trimester, abortion, misoprostol, and mifepristone and reviewed reference lists of published reports.Our search revealed 138 articles of which 29 met inclusion criteria: 20 randomized controlled trials and nine observational studies. Studies were included if, in any study arm, mifepristone and misoprostol were used for medical abortion in the second trimester.Two authors independently reviewed the articles and abstracted the data using standardized data abstraction templates to summarize data. Discrepancies were resolved by consensus. Three studies directly compared a 1-day to 2-day mifepristone-misoprostol interval; they showed small differences in median induction times (weighted average 7.3 hours, range 7-8.5 for a 1-day interval; weighted average 6.8 hours, range 6.3-7.2 for a 2-day interval) and no significant difference in percent expelled by 12 hours or 24 hours. When all randomized studies using mifepristone and misoprostol were pooled by comparable mifepristone-misoprostol interval and misoprostol dose, induction times (first misoprostol dose to expulsion) were only 1-2 hours longer for a 12- to 24-hour interval compared with a 36-48-hour interval, whereas total abortion times (mifepristone to expulsion) were at least 18 hours longer in the 36- to 48-hour group. Induction times varied by misoprostol dosing, with 400-microgram misoprostol protocols resulting in shorter induction times than 200-microgram protocols.Shortening the mifepristone-misoprostol interval, thereby reducing total abortion time, does not compromise the safety or efficacy of second-trimester medication abortion and may be used to accommodate patient or health care provider preference.

    View details for PubMedID 23812471

  • Efficacy, safety, acceptability and affordability of cryotherapy: a review of current literature. Minerva ginecologica McClung, E. C., Blumenthal, P. D. 2012; 64 (2): 149-171

    Abstract

    As a result of widespread screening and treatment programs, the incidence of cervical cancer has decreased by as much as 75% in the developed world. Commonly used treatment modalities for precancerous lesions include cone biopsy, the Loop Electrosurgical Excision Procedure (LEEP), laser ablation and cryotherapy. In recent years LEEP has replaced cryotherapy as a commonly provided outpatient procedure in many places; however increased awareness of the burden of cervical cancer in the developing world and increased awareness of long term consequences of LEEP ? such as cervical insufficiency ? have renewed interest in cryotherapy. We reviewed current literature addressing the technique, efficacy, safety and acceptability of cryotherapy, as well as special topics such as cost effectiveness, HIV, and low resource settings. Among studies we reviewed, cure rates ranged from 56.8-96.6% among prospective controlled trials and from 70-95.5% among observational studies. Cryotherapy has very low complication rates and serious complications requiring medical intervention or affecting future reproductive outcomes are extremely rare. Side effects including vaginal discharge and cramping are temporary, generally self-limited, and well tolerated after anticipatory patient counseling. When surveyed, women find cryotherapy highly acceptable. Compared to other treatment modalities, cryotherapy is very affordable and feasible to integrate into cervical cancer screening and treatment programs.

    View details for PubMedID 22481625

  • Cost-effectiveness and quality of life associated with heavy menstrual bleeding among women using the levonorgestrel-releasing intrauterine system INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Blumenthal, P. D., Dawson, L., Hurskainen, R. 2011; 112 (3): 171-178

    Abstract

    To review the literature for economic and health-related quality of life outcomes data associated with the use of the levonorgestrel-releasing intrauterine system (LNG-IUS) in the management of heavy menstrual bleeding.We searched the MEDLINE and EMBASE databases simultaneously using the Ovid interface to review the literature in a systematic manner for economic and health-related quality of life outcomes data associated with the use of the LNG-IUS in women with heavy menstrual bleeding. Articles were then selected for further review based on the relevance of their titles and/or abstracts. We identified 17 articles for inclusion in this review.Treating heavy menstrual bleeding with the LNG-IUS was found to be cost-effective in various countries and settings. Moreover, irrespective of the measuring instrument used, health-related quality-of-life outcomes were found to be improved to a degree similar to that achieved with endometrial ablation or hysterectomy. In some cases, the LNG-IUS appeared to be more effective and less costly than the surgical options.The LNG-IUS is a cost-effective treatment option for heavy menstrual bleeding when pharmacologic treatment is indicated.

    View details for DOI 10.1016/j.ijgo.2010.08.025

    View details for Web of Science ID 000288294400006

    View details for PubMedID 21269626

  • Strategies to prevent unintended pregnancy: increasing use of long-acting reversible contraception HUMAN REPRODUCTION UPDATE Blumenthal, P. D., Voedisch, A., Gemzell-Danielsson, K. 2011; 17 (1): 121-137

    Abstract

    Despite increasing contraceptive availability, unintended pregnancy remains a global problem, representing as many as 30% of all known pregnancies. Various strategies have been proposed to reverse this disturbing trend, especially increased use of long-acting reversible contraceptive (LARC) methods. In this review we aim to discuss the role of LARC methods and importance of contraceptive counseling in reducing unintended pregnancy rates.References/resources cited were identified based on searches of medical literature (MEDLINE, 1990-2009), bibliographies of relevant publications and the Internet.LARC methods-copper intrauterine devices (IUDs), progestogen-releasing intrauterine system and injectable and implantable contraceptives-are safe and effective contraceptive options (unintended pregnancy rates with typical versus perfect use: 0.05-3.0 versus 0.05-0.6%) that are appropriate for a wide range of women seeking to limit or space childbearing. Despite their safety and efficacy records, these methods remain underutilized; injectable and implantable methods are used by an estimated 3.4% and intrauterine methods by 15.5% of women worldwide. LARC methods require no daily or coital adherence and avoid the adverse events and health risks of estrogen-containing contraceptives. The copper IUD and progestin-only injections and implants have been shown to be more cost-effective than more commonly used methods, such as condoms and the pill (5-year savings: $13,373-$14,122, LARC; $12,239, condoms; $12,879, pill). Women who are considering use of LARC methods should receive comprehensive contraceptive counseling, as women who receive counseling before use demonstrate higher rates of after-use method satisfaction, continuation and acceptance than those who do not.

    View details for DOI 10.1093/humupd/dmq026

    View details for Web of Science ID 000285415400011

    View details for PubMedID 20634208

  • Frequency of Cervical Cancer and Breast Cancer Screening in HIV-Infected Women in a County-Based HIV Clinic in the Western United States JOURNAL OF WOMENS HEALTH Rahangdale, L., Sarnquist, C., Yavari, A., Blumenthal, P., Israelski, D. 2010; 19 (4): 709-712

    Abstract

    Women's primary-care services are frequently dispensed to HIV-infected women through HIV specialty clinics. Our objective was to evaluate cervical cancer and breast cancer screening practices in a county-based HIV clinic in San Mateo, California.This was a retrospective cohort study of medical records of HIV-infected women obtaining HIV care at this site.Between January 1, 2002 and December 31, 2006, 69 women were documented to have at least 12 months of medical care at the clinic. Median followup time was 51 months. Over 253 person-years of followup, there were 656 pap smears performed per 1,000 person-years; 77.9% of women had at least one Pap smear during the study time period. A total of 59.5% (47/79) of normal pap smears had a followup pap smear within 18 months; 62.0% of abnormal pap smears had a followup pap smear within 12 months. A CD4 count of less than 200 cells/mm(3) was associated with not receiving a pap smear in multivariable analysis. Mammogram screening was performed on 64.7% of women aged 40 or older.Based on the results of this study, the majority of HIV-infected women at this clinic received cervical and breast cancer screening at some point during their care. Only two-thirds of abnormal pap smear results had followup pap smear screening within a year. With the increased risk of cervical cancer in HIV-infected women, efforts should be made to promote cervical cancer screening, particularly in high-risk women.

    View details for DOI 10.1089/jwh.2009.1412

    View details for Web of Science ID 000277030400009

    View details for PubMedID 20201703

  • Preventing Cervical Cancer Stakeholder Attitudes Toward CareHPV-Focused Screening Programs in Roi-et Province, Thailand INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER Trope, L. A., Chumworathayi, B., Blumenthal, P. D. 2009; 19 (8): 1432-1438

    Abstract

    To assess which of the 5 CareHPV-inclusive protocols stakeholders in Roi-et Province, Thailand found (1) most preferable and (2) most beneficial to the overall goal of reducing cervical cancer.Five CareHPV-inclusive cancer prevention approaches were presented to a convenience sample of colposcopists, trainers, health care providers, district medical directors, and district health officers. Participants ranked their preference for each plan (A-E) compared with the current screening protocol and also the perceived comparative benefit of the plans. Plans differed in whether every patient was screened using both the human papillomavirus (HPV) test and visual inspection with acetic acid (VIA) or only HPV-positive women were screened with VIA; in clinician versus self-swab and in hospital/clinic-based or village-based screening.Overall, participants supported an innovative plan in which women would be screened in their homes and villages using the self-swab version of the CareHPV DNA test, and only those who screened positive for HPV are screened with VIA. When results were stratified by provider type (physician vs nonphysician) and/or practice concentration (hospital-oriented vs field-oriented), preference and perceived benefit for the plans differed significantly with physician/hospital-oriented participants and are more likely to be skeptical of the self-swab version of the CareHPV test.Providers in Thailand recognize the potential value of a rapid HPV test as part of a cervical cancer prevention program and, overall, support a patient-administered self-swab followed by visual confirmation and treatment as the most practical CareHPV-inclusive approach largely because of the likely increase in coverage. Future studies will further define the clinical benefits and limitations of this test.

    View details for DOI 10.1111/IGC.0b013e3181a83dd0

    View details for Web of Science ID 000272035900026

    View details for PubMedID 20009903

  • Rates of Serious Infection after Medical Abortion NEW ENGLAND JOURNAL OF MEDICINE Kapp, N., Winikoff, B., Blumenthal, P. D. 2009; 361 (15): 1511-1512

    View details for Web of Science ID 000270540000027

    View details for PubMedID 19812412

  • The levonorgestrel-releasing intrauterine system: Safety, efficacy, and patient acceptability. Therapeutics and clinical risk management Beatty, M. N., Blumenthal, P. D. 2009; 5 (3): 561-574

    Abstract

    The levonorgestrel-releasing intrauterine system (LNG-IUS) is a safe, effective and acceptable form of contraception used by over 150 million women worldwide. It also has a variety of noncontraceptive benefits including treatment for menorrhagia, endometriosis, and endometrial hyperplasia. The LNG-IUS has also been used in combination with estrogen for hormone replacement therapy and as an alternative to hysterectomy. Overall, the system is very well tolerated and patient satisfaction is quite high when proper education regarding possible side effects is provided. However, despite all of the obvious benefits of the LNG-IUS, utilization rates remain quite low in the developed countries, especially in the United States. This is thought to be largely secondary to the persistent negative impressions from the Dalkon Shield intrauterine experience in the 1970s. This history continues to negatively influence the opinions of both patients and health care providers with regards to intrauterine devices. Providers should resolve to educate themselves and their patients on the current indications and uses for this device, as it, and intrauterine contraception in general, remains a largely underutilized approach to a variety of women's health issues.

    View details for PubMedID 19707273

  • Hormonal contraception OBSTETRICS AND GYNECOLOGY Blumenthal, P. D., Edelman, A. 2008; 112 (3): 670-684

    Abstract

    Hormonal contraceptives have been a part of clinical practice for more than 40 years, and family planning programs, based largely on contraceptive provision, are regarded as one of the most successful public health interventions of the 20th century. Thus, discussion of family planning issues and contraceptive considerations has become an integral component of women's health care and one of the benchmarks of the traditional annual well-women visit. In terms of cost-effectiveness, prevention of unplanned pregnancies through contraceptive use has repeatedly been shown to be a highly cost-effective use of health care dollars. Options for effective hormonal contraception have expanded tremendously and include a variety of delivery options, including the pills both in traditional 21/7 format, and more recently in a 24/4 format, as well as a vaginal ring, a skin patch, implants, and the hormonally medicated intrauterine device. Importantly, the overall risks associated with hormonal contraceptives have been reduced as compared with older formulations, even for women with medical conditions. Many modern hormonal contraceptives also offer valuable noncontraceptive benefits. To help clinical decision making, a number of evidence-based guides have been published, and the American College of Obstetricians and Gynecologists has recently updated their practice bulletin on contraception use in women with medical conditions. In general, clinical protocols for provision of hormonal contraceptives have been streamlined, and unnecessary practices, tests, and procedures are identified and discouraged. In this review, we will summarize both technical and programmatic aspects of hormonal contraceptive use, and methods are discussed in order of efficacy from highest to lowest.

    View details for Web of Science ID 000259179100024

    View details for PubMedID 18757668

  • Tolerability and clinical safety of Implanon (R) EUROPEAN JOURNAL OF CONTRACEPTION AND REPRODUCTIVE HEALTH CARE Blumenthal, P. D., Gemzell-Danielsson, K., Marintcheva-Petrova, M. 2008; 13: 29-36

    Abstract

    To evaluate the tolerability and clinical safety of the subdermal, long-acting hormonal contraceptive Implanon.This integrated safety analysis included 11 international studies concerning Implanon (68 mg etonogestrel) of which 10 had a duration of at least two years. Assessments included reports of adverse events (AEs), reasons and rates of discontinuation, insertion/removal complications, and the condition of the implant site. Metabolic and coagulation parameters are briefly discussed to fully describe the clinical safety profile.In total 942 women were exposed to Implanon for 24,679 cycles over the course of one to five years. The overall discontinuation rate was 32.7%; the most frequently reported reasons for discontinuation were adverse events (13.9%), bleeding irregularities (10.4%), and planning pregnancy (4.1%). The most commonly reported drug-related AE was headache (15.3%); however, headache was reported in only 1.6% of women as a reason for discontinuation. Insertion and removal times for Implanon were short with few complications, none of which were major. From earlier studies it is known that treatment with Implanon has little effect on metabolic and coagulation parameters.Implanon is a well-tolerated and safe method of long-acting hormonal contraception for women.

    View details for DOI 10.1080/13625180801960012

    View details for Web of Science ID 000257896200004

    View details for PubMedID 18330815

  • A systematic review evaluating health-related quality of life, work impairment, and health-care costs and utilization in abnormal uterine bleeding VALUE IN HEALTH Liu, Z., Doan, Q. V., Blumenthal, P., Dubois, R. 2007; 10 (3): 183-194

    Abstract

    Abnormal uterine bleeding (AUB) impacts women's health-related quality of life (HRQoL) and puts a heavy economic burden on society. To date, this burden has not been systematically studied. We conducted a systematic review of the medical literature to evaluate the impact of AUB on HRQoL and to quantify the economic burden of AUB from a societal perspective.We searched the PubMed and Cochrane databases, and article bibliographies for the period up to July 2005. Teams of two reviewers independently abstracted data from studies that reported outcomes of interest: prevalence, HRQoL, work impairment, and health-care utilization and costs associated with AUB.The search yielded 1009 English-language articles. Ninety-eight studies (including randomized controlled trials, observational studies, and reviews) that met the inclusion and exclusion criteria underwent a full-text review. The prevalence of AUB among women of reproductive age ranged from 10% to 30%. The HRQoL scores from the 36-item Short-Form Health Survey Questionnaire (SF-36) suggested that women with AUB have HRQoL below the 25th percentile of that for the general female population within a similar age range. The conservatively estimated annual direct and indirect economic costs of AUB were approximately $1 billion and $12 billion, respectively. These figures do not account for intangible costs and productivity loss due to presenteeism.The burden of AUB needs further and more thorough investigation. Additional research should prospectively evaluate the impact of AUB and the value of treatment provided to help guide future health resource allocation and clinical decision-making.

    View details for DOI 10.1111/j.1524-4733.2007.00168.x

    View details for Web of Science ID 000246714800002

    View details for PubMedID 17532811

  • Cervical cancer prevention: safety, acceptability, and feasibility of a single-visit approach in Accra, Ghana AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY Blumenthal, P. D., Gaffikin, L., Deganus, S., Lewis, R., Emerson, M., Adadevoh, S. 2007; 196 (4)

    Abstract

    The purpose of this study was to assess the safety and acceptability of a single-visit approach to cervical cancer prevention combining visual inspection of the cervix with acetic acid wash (VIA) and cryotherapy.The study was observational. Nine clinicians were trained in VIA and cryotherapy. Over 18 months 3665 women were VIA-tested. If positive and eligible, cryotherapy was offered immediately. Treated women were followed-up at 3 months and 1 year.The test-positive rate was 13.2%. Of those eligible, 70.2% and 21% received immediate or delayed treatment, respectively. No major complications were recorded, and 5.6% presented for a perceived problem post-cryotherapy. Among those treated over 90% expressed satisfaction with their experience, and 96% had an indentifiable squamo-columnar junction. Only 2.6% (6/232) were test positive, 1-year posttreatment.A single-visit approach using VIA and cryotherapy proved to be safe, acceptable, and feasible in an urban African setting.

    View details for DOI 10.1016/j.ajog.2006.12.031

    View details for Web of Science ID 000245747600053

    View details for PubMedID 17403438

  • Family planning: a cornerstone for public health and sustainable development. MedGenMed : Medscape general medicine Blumenthal, P. D., Gaffikin, L. 2007; 9 (4): 16-?

    View details for PubMedID 18311366

  • The supreme court and the Partial-Birth Abortion Ban Act of 2003: a political procedure replaces woman-centered care. MedGenMed : Medscape general medicine Blumenthal, P. D., Winikoff, B. 2007; 9 (2): 52-?

    View details for PubMedID 17955106

  • Cost-effectiveness of treatments for dysfunctional uterine bleeding in women who need contraception CONTRACEPTION Blumenthal, P. D., Trussell, J., Singh, R. H., Guo, A., Borenstein, J., Dubois, R. W., Liu, Z. 2006; 74 (3): 249-258

    Abstract

    This study aims to compare the cost-effectiveness of oral contraceptives (OCs), the levonorgestrel-releasing intrauterine system (LNG-IUS) and surgical management in treating dysfunctional uterine bleeding (DUB) in women not desiring additional children.A Markov model was constructed from the perspective of the health services payers for a 5-year period. Treatment costs, DUB treatment success rates and contraception success rates were obtained through a literature review.In women not responding to an initial trial of OCs, surgical management was more effective than the LNG-IUS (95.5% vs. 92%) but at higher cost (US$4853 vs. US$2796 per woman). Among responders to OCs, continuing treatment with the LNG-IUS instead of OCs was more effective (92% vs. 90.4%) and less expensive (US$2796 vs. US$4711). For women naïve to medical therapy, the LNG-IUS and OCs had similar effectiveness, but cost for the LNG-IUS was lower (US$2796 vs. US$4895). In all scenarios, surgery followed if medical therapy failed; rates of primary method failure were 62.5% with OCs and 34% with the LNG-IUS at 12 months.Treatment strategies employing the LNG-IUS are the most cost-effective in managing DUB, regardless of whether a woman has previously tried OC therapy.

    View details for DOI 10.1016/j.contraception.2006.03.024

    View details for Web of Science ID 000240085500010

    View details for PubMedID 16904420

  • Letter from Madagascar OBSTETRICS AND GYNECOLOGY Blumenthal, P. D. 2006; 108 (3): 684-686

    View details for Web of Science ID 000246769000029

    View details for PubMedID 16946231

  • Introduction of the dilation and evacuation procedure for second-trimester abortion in Vietnam using manual vacuum aspiration and buccal misoprostol CONTRACEPTION Castleman, L. D., Oanh, K. T., Hyman, A. G., Thuy, L. T., Blumenthal, P. D. 2006; 74 (3): 272-276

    Abstract

    The dilation and evacuation (D&E) procedure was modified for use in a low-resource setting where access to electric vacuum aspiration is limited.In this demonstration project, buccal misoprostol is used for cervical preparation, followed by evacuation using manual vacuum aspiration (MVA) and forceps. Senior physicians at the Hanoi Obstetrics and Gynecology Hospital were trained in D&E and subsequently conducted 439 D&E procedures.The primary outcomes were efficacy and safety. Secondary outcome measures include efficacy of buccal misoprostol for cervical preparation prior to D&E and the feasibility of MVA for use in the D&E procedure.Successful abortion took place in 100% of the cases. Three major complications occurred. This procedure may be appropriate in other low-resource settings lacking safe, effective abortion services in the second trimester.

    View details for DOI 10.1016/j.contraception.2006.03.021

    View details for Web of Science ID 000240085500013

    View details for PubMedID 16904423

  • Mortality associated with mifepristone-misoprostol medical abortion. MedGenMed : Medscape general medicine Creinin, M., Blumenthal, P., Shulman, L. 2006; 8 (2): 26-?

    View details for PubMedID 16926765

  • Postpartum contraception: the New Mexico Pregnancy Risk Assessment Monitoring System CONTRACEPTION DePineres, T., Blumenthal, P. D., Diener-West, M. 2005; 72 (6): 422-425

    Abstract

    To examine factors associated with postpartum contraception, including the relationship between ethnicity and postpartum contraceptive use.We used data from the New Mexico Pregnancy Risk Assessment Monitoring System, which monitors selected maternal events occurring before, during and after pregnancy.Our findings in 4096 women revealed that women who are aged >or=35 years, unmarried and lacking a postpartum visit have increased risk of no postpartum contraception. The odds of postpartum contraception were over three times greater in women with a postpartum visit [adjusted odds ratio (OR)=3.06, 95% confidence interval (CI): 2.17-4.31) and over 50% greater in married women (adjusted OR=1.57, 95% CI: 1.16-2.11). Hispanic women were more likely than were Native Americans to use postpartum contraception (OR=1.25, 95% CI: 0.95-1.64).Focused contraception counseling, especially in the postpartum setting, is important to help ensure the well-being of women and children.

    View details for DOI 10.1016/j.contraception.2005.05.022

    View details for Web of Science ID 000233979100005

    View details for PubMedID 16307963

  • Cervical cancer prevention - Making programs more appropriate and pragmatic JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION Blumenthal, P. D., Gaffikin, L. 2005; 294 (17): 2225-2228

    View details for Web of Science ID 000232957700027

    View details for PubMedID 16264166

  • Digital camera assessment for detection of cervical intraepithelial neoplasia in rural El Salvador INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Cremer, M., Jamshidi, R. M., Muderspach, L., Tsao-Wei, D., Felix, J. C., Blumenthal, P. D. 2005; 91 (1): 42-46

    Abstract

    To explore the feasibility of digital photography for primary cervical cancer screening in a low-resource setting in El Salvador.Three independent examiners performed Pap test, visual inspection, digital camera assessment and colposcopy on each subject.Lesions were detected in 99 of 504 patients (20%) by visual inspection, 72/504 (14%) by DART and 90/504 (18%) by colposcopic impression. Seven of 504 patients (1.3%) had CIN on histology. Pap detected 2 of 7 subjects (29% sensitivity) (C.I. 4%, 56%), visual inspection detected 5 of 7 (71% sensitivity, C.I. 34%, 95%), digital assessment detected 6 of 7 (86% sensitivity C. I. 45%, 99%), and colposcopic impression detected 5 of 7 (71% sensitivity, C.I. 34%, 95%).This small pilot trial demonstrates the potential value and feasibility of performing digital camera assessment of the reproductive tract on women in a developing country setting.

    View details for DOI 10.1016/j.ijgo.2005.05.015

    View details for Web of Science ID 000232315400008

    View details for PubMedID 16043183

  • Hormonal management of abnormal uterine bleeding CLINICAL OBSTETRICS AND GYNECOLOGY Singh, R. H., Blumenthal, P. 2005; 48 (2): 337-352

    View details for Web of Science ID 000231531600008

    View details for PubMedID 15805791

  • Training for cervical cancer prevention programs in low-resource settings: Focus on visual inspection with acetic acid and cryotherapy INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Blumenthal, P. D., Lauterbach, M., SELLORS, J. W., Sankaranarayanan, R. 2005; 89: S30-S37

    Abstract

    The modern approach to cervical cancer prevention, characterized by use of cytology and multiple visits for diagnosis and treatment, has frequently proven challenging and unworkable in low-resource settings. Because of this, the Alliance for Cervical Cancer Prevention (ACCP) has made it a priority to investigate and assess alternative approaches, particularly the use of visual screening methods, such as visual inspection with acetic acid (VIA) and visual inspection with Lugol's iodine (VILI), for precancer and cancer detection and the use of cryotherapy as a precancer treatment method. As a result of ACCP experience in providing training to nurses and doctors in these techniques, it is now widely agreed that training should be competency based, combining both didactic and hands-on approaches, and should be done in a clinical setting that resembles the service-delivery conditions at the program site. This article reviews ACCP experiences and perceptions about the essentials of training in visual inspection and cryotherapy and presents some lessons learned with regard to training in these techniques in low-resource settings.

    View details for DOI 10.1016/j.ijgo.2005.01.012

    View details for Web of Science ID 000229977000005

    View details for PubMedID 15823264

  • Multicenter trial of a simplified mifepristone medical abortion regimen OBSTETRICS AND GYNECOLOGY Shannon, C. S., Winikoff, B., Hausknecht, R., Schaff, E., Blumenthal, P. D., Oyer, D., Sankey, H., Wolff, J., Goldberg, R. 2005; 105 (2): 345-351

    Abstract

    To provide evidence regarding the safety, efficacy, and acceptability of 200 mg mifepristone followed by home administration of 400 mug oral misoprostolThe 376 women enrolled in this prospective, open-label, multicenter trial were administered mifepristone in the clinic and were given 2 tablets of 200 mug misoprostol to swallow at home 48 hours later. On day 15, women returned to the clinic for a gynecologic examination. Success was defined as a complete termination without surgical intervention or additional misoprostol by day 21. All participants completed an exit interview before discharge from the studyOf the women enrolled, 58.8% had gestations of between 43 and 49 days, 54.7% had had a previous abortion, and 76% had had a previous pregnancy. Of the 354 women included in the efficacy analysis, 324 (91.5%) had a successful termination. The most common adverse effects reported by patients were pain or cramps (93.2%) and nausea (66.6%), followed by weakness (54.7%), headache (46.2%), and dizziness (44.4%). Overall acceptability of the regimen was high, with 63.3% of women reporting that it was very satisfactory and an additional 23% reporting that it was satisfactoryA regimen of 200 mg mifepristone followed in 48 hours by home administration of 400 mug oral misoprostol is effective, associated with rare severe adverse effects or adverse events, and acceptable for women seeking medical abortion of pregnancies of up to 49 days duration as compared with the regimen currently approved by the Food and Drug Administration.III.

    View details for DOI 10.1097/01.AOG.0000152003.94320.59

    View details for Web of Science ID 000226700600021

    View details for PubMedID 15684163

  • A consensus regimen for early abortion with misoprostol INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Philip, N. M., Winikoff, B., Moore, K., Blumenthal, P. 2004; 87 (3): 281-283

    View details for DOI 10.1016/j.ijgo.2004.08.018

    View details for Web of Science ID 000225515800018

    View details for PubMedID 15548409

  • Digital assessment of the reproductive tract (DART) JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES Jamshidi, R., Blumenthal, P. 2004; 37: S171-S173

    Abstract

    As the AIDS epidemic grows through heterosexual transmission, the development of women-controlled methods for defence against sexually transmitted infections and HIV, such as vaginally applied microbicides, is increasingly important. As part of the evaluation of the safety of all new topical microbicides, an evaluation of the cervix and vagina for any physical or mechanical effects of a potential agent is imperative. Traditionally, colposcopy has been used for such an evaluation. We introduce the concept of using a digital camera to assess the reproductive tract as a practical and effective means for studying the effects of microbicides on the vaginal and cervical epithelium. As much research on microbicides will be undertaken in areas with limited resources, digital assessment of the reproductive tract offers the advantage of portability, ease of use, durability, and accessibility. In addition, it allows digital data storage that can be used to review images, allow quality control, and provide an effective means to compare changes over time.

    View details for Web of Science ID 000224829100007

    View details for PubMedID 16419268

  • Sensitive methods to detect epithelial disruption: tests for microhemorrhage in cervicovaginal lavages JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES Moench, T., Mehrazar, K., Cone, R., Blumenthal, P. 2004; 37: S194-S200

    Abstract

    The toxic effects of topical microbicides might include epithelial disruption, and if sufficiently severe, may cause visible bleeding. We have developed two sensitive methods to detect hemorrhage far below the visual detection threshold: an enzyme-linked immunosorbent assay for human hemoglobin and a method for staining and enumerating red blood cells by fluorescent microscopy. We have applied these methods to cervicovaginal and introital lavages, and found them to be sensitive and quantitative over a broad range. Comparing the new techniques with a standard heme-detection assay (Hemastix) we found them to be more sensitive, more objective, more fully quantitative, and more likely to be indicative of recent events. In pilot studies we found that the red blood cell and hemoglobin concentrations in samples taken in the luteal phase of the menstrual cycle are low, but still within the detection range of the new assays, providing a quantifiable baseline from which increases in blood from epithelial disruption can be detected and quantified. We propose that these new methods may be used for the safety assessment of microbicides by detecting and quantifying microhemorrhage in cervicovaginal secretions before and after exposure to microbicide.

    View details for Web of Science ID 000224829100011

    View details for PubMedID 16419272

  • Hormonal contraceptive use, cervical ectopy, and the acquisition of cervical infections SEXUALLY TRANSMITTED DISEASES Morrison, C. S., Bright, P., Wong, E. L., Kwok, C., Yacobson, I., Gaydos, C. A., Tucker, H. T., Blumenthal, P. D. 2004; 31 (9): 561-567

    Abstract

    Several previous studies have suggested that hormonal contraception could be associated with increased risk of cervical infections. However, few high-quality prospective studies have examined this relationship.The goal of this study was to measure the effect of oral contraceptives (OC) and depot-medroxyprogesterone acetate (DMPA) on the acquisition of cervical chlamydial and gonococcal infections.Women attending 2 reproductive health centers in Baltimore, MD, were enrolled into a prospective cohort study. Participants were 15 to 45 years and were initiating OCs or DMPA or not using hormonal contraception. Interviews, physical examinations, and testing for incident cervical infections were conducted at 3, 6, and 12 months.The analysis included 819 women. Most were single (77%) and nulliparous (75%); 43% were black. Median age was 22 years. During the study, 45 women acquired a chlamydial or gonococcal infection (6.2 per 100 women-years). DMPA use (hazard ratio [HR], 3.6; 95% confidence interval [CI], 1.6-8.5), but not OC use (HR, 1.5; 95% CI, 0.6-3.5), was significantly associated with increased acquisition of cervical infections after adjusting for other risk factors. Cervical ectopy was not an important mediator of cervical infection risk.DMPA use, but not OC use, appeared to be significantly associated with increased acquisition of cervical chlamydial and gonococcal infections.

    View details for DOI 10.1097/01.olq.0000137904.56037.70

    View details for Web of Science ID 000223754600009

    View details for PubMedID 15480119

  • Are partners available for post-abortion contraceptive counseling? A pilot study in a Baltimore City clinic CONTRACEPTION Beenhakker, B., Becker, S., Hires, S., Di Targiana, N. M., Blumenthal, P., Huggins, G. 2004; 69 (5): 419-423

    Abstract

    About half of the 1.2 million abortions each year in the United States are repeat abortions. While most abortion providers counsel women about contraception, one reason for the high repeat rate could be failure to take into account the social context of the women--in particular, the male partner. To assess whether there might be a window of opportunity for a contraceptive intervention that includes the male partner at the time of the abortion, we undertook a pilot study at an urban abortion clinic to examine the role of the male partner among women receiving abortions. Between May 2001 and August 2002, two questionnaires were administered to 109 women receiving abortions in a Baltimore City clinic. On the procedure day, women were more likely to be accompanied by a male partner upon arrival (30%) or when leaving (34%) than by any other individual. The majority of women receiving abortions reported that their partners played positive decision-making and support roles throughout the abortion process. A significant proportion of couples could be available for contraceptive counseling following an abortion, providing rationale for couples' post-abortion contraceptive counseling for women whose partners are already actively and positively involved in the abortion process. Such an intervention may help to reduce repeat abortions.

    View details for DOI 10.1016/j.contraception.2003.12.013

    View details for Web of Science ID 000221176000013

    View details for PubMedID 15105066

  • Oral contraceptives and cervical cancer: critique of a recent review CONTRACEPTION Miller, K., Blumenthal, P., Blanchard, K. 2004; 69 (5): 347-351

    Abstract

    A recent review article by Smith et al. in The Lancet purports to find a causal relationship between long-term use of oral contraceptives (OCs) and cervical cancer. While we endorse the search for such a relationship, we felt it important to critically examine Smith et al.'s review process and, as a result, we have questions about the validity of their conclusions. In our view, the findings of published articles as presented by Smith et al. do not confirm a causal connection between long-term use of OCs and cervical cancer. Our goal is not to conduct another formal review of the evidence, but to evaluate whether Smith et al. have met the burden of proof for establishing a causal relationship. Given the importance of OCs to women the world over, we urge reproductive health professionals to consider this issue carefully before accepting that a causal relationship exists.

    View details for DOI 10.1016/j.contraception.2003.12.012

    View details for Web of Science ID 000221176000002

    View details for PubMedID 15105055

  • Manual vacuum aspiration for second-trimester pregnancy termination INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Todd, C. S., Soler, M. E., Castleman, L., Rogers, M. K., Blumenthal, P. D. 2003; 83 (1): 5-9

    Abstract

    To compare manual and electric vacuum aspiration for surgical abortions between 14 and 18 weeks of pregnancy.A consecutive case series of pregnant women presenting to Johns Hopkins Bayview Medical Center for abortion. There were 73 women in the manual vacuum aspiration group and 37 women in the electric vacuum aspiration group. Dilatation and evacuation was performed using manual or electric vacuum aspiration according to protocol. Procedure time was assessed with the t-test.In all cases, abortion was performed with initial vacuum. Group sizes were sufficient to detect a 20% difference in mean procedure time with 80% power (calculated with two separate S.D.s for procedure time). There was no significant difference in procedure time between the two groups.Manual vacuum aspiration can be safely and effectively used in second-trimester abortion procedures and should be more widely investigated for this purpose.

    View details for DOI 10.1016/S0020-7292(03)00304-7

    View details for Web of Science ID 000185867100001

    View details for PubMedID 14511866

  • Performance of visual inspection with acetic acid for cervical cancer screening: A qualitative summary of evidence to date OBSTETRICAL & GYNECOLOGICAL SURVEY Gaffikin, L., Lauterbach, M., Blumenthal, P. D. 2003; 58 (8): 543-550

    Abstract

    Developing countries often lack the necessary resources to use the Papanicolaou (Pap) smear as a screening tool for cervical abnormalities. Because the burden of cervical cancer is highest in such low-resource settings, alternative techniques have been sought. Recently, interest in visual inspection with acetic acid (VIA) has increased. Numerous studies have been conducted on its accuracy and its ability to detect cervical lesions when compared with other techniques, both conventional and nonconventional. This review summarizes key findings from the literature to provide researchers and policymakers with an up-to-date summary on VIA. PubMed was used to identify relevant journal articles published between 1982 and 2002. Key words were cervical cancer screening, visual inspection, VIA (visual inspection with acetic acid), DVI (direct visual inspection), AAT (acetic acid test), and cervicoscopy. Studies were eligible for review only if they involved analysis of primary VIA data (ie, not review articles); studies involving magnification devices were excluded. Fifteen studies were reviewed in total; key results were extracted and a summary analysis was performed for sensitivity and specificity parameters. When reported, sensitivity ranged between 66% and 96% and specificity between 64% and 98%. Authors comparing VIA with cytology noted that the overall usefulness of VIA compares favorably with that of the Pap test. The reported findings reviewed here suggest that VIA has the potential to be a cervical cancer screening tool, especially in low resource settings.Obstetricians & Gynecologists, Family Physicians.After completion of this article, the reader will be able to describe how visual inspection of the cervix for cervical cancer screening (VIA) is performed, to summarize the current literature on VIA, and to list potential advantages of VIA.

    View details for Web of Science ID 000184485800002

    View details for PubMedID 12886165

  • The federal ban on so-called "partial-birth abortion" is a dangerous intrusion into medical practice. MedGenMed : Medscape general medicine Blumenthal, P. D. 2003; 5 (2): 37-?

    View details for PubMedID 14603136

  • Safety, acceptability, and feasibility of a single-visit approach to cervical-cancer prevention in rural Thailand: a demonstration project LANCET Gaffikin, L., Blumenthal, P. D., Emerson, M., Limpaphayom, K., LUMBIGANON, P., Ringers, P., Srisupundit, S., Warakamin, S., Lewis, R., Chumworathayee, B., Kanavacharakul, S. 2003; 361 (9360): 814-820

    Abstract

    To increase screening and treatment coverage, innovative approaches to cervical-cancer prevention are being investigated in rural Thailand. We assessed the value of a single-visit approach combining visual inspection of the cervix with acetic acid wash (VIA) and cryotherapy.12 trained nurses provided services in mobile (village health centre-based) and static (hospital-based) teams in four districts of Roi-et Province, Thailand. Over 7 months, 5999 women were tested by VIA. If they tested positive, after counselling about the benefits, potential risks, and probable side-effects they were offered cryotherapy. Data measuring safety, acceptability, feasibility, and effort to implement the programme were gathered.The VIA test-positive rate was 13.3% (798/5999), and 98.5% (609/618) of those eligible accepted immediate treatment. Overall, 756 women received cryotherapy, 629 (83.2%) of whom returned for their first follow-up visit. No major complications were recorded, and 33 (4.4%) of those treated returned for a perceived problem. Only 17 (2.2%) of the treated women needed clinical management other than reassurance about side-effects. Both VIA and cryotherapy were highly acceptable to the patients (over 95% expressed satisfaction with their experience). At their 1-year visit, the squamocolumnar junction was visible to the nurses, and the VIA test-negative rate was 94.3%.A single-visit approach with VIA and cryotherapy seems to be safe, acceptable, and feasible in rural Thailand, and is a potentially efficient method of cervical-cancer prevention in such settings.

    View details for Web of Science ID 000181466600009

    View details for PubMedID 12642047

  • Similarities in women's perceptions and acceptability of manual vacuum aspiration and electric vacuum aspiration for first trimester abortion CONTRACEPTION Bird, S. T., Harvey, S. M., Beckman, L. J., Nichols, M. D., Rogers, K., Blumenthal, P. D. 2003; 67 (3): 207-212

    Abstract

    This paper examines women's acceptability of and experiences with manual vacuum aspiration (MVA) as compared with electric vacuum aspiration (EVA) for first trimester abortion. Women requesting pregnancy terminations were randomly assigned to either MVA (n = 64) or EVA (n = 63). Participants completed questionnaires before and after their abortions and approximately 2-4 weeks later. We observed some differences by group in participants' ratings of the importance of method characteristics and in their perceptions of their abortion methods after their abortions. The two groups did not, however, differ in their reports of pain, anxiety or bleeding or in the acceptability of their method.

    View details for DOI 10.1016/S0010-7824(02)00484-5

    View details for Web of Science ID 000181536700006

    View details for PubMedID 12618255

  • More on science and politics SCIENCE Bass, G. D., Blumenthal, P. D., Corfman, P., Darney, P. D., Gonsalves, G., Levin, A. A., Trussell, J., Shields, W. C. 2003; 299 (5611): 1313-1313

    View details for Web of Science ID 000181192300019

    View details for PubMedID 12610277

  • Risk factors as the basis for triage in low-resource cervical cancer screening programs INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Gaffikin, L., Ahmed, S., Chen, Y. Q., McGrath, J. M., Blumenthal, P. D. 2003; 80 (1): 41-47

    Abstract

    Several studies have shown impressive sensitivity and specificity of visual inspection using acetic acid wash (VIA) in detecting cervical dysplasia. This study examines how risk-factor based triage, using clinical history-taking to limit the testing to those at highest risk of disease, improves the clinical utility of VIA.The study population included 2206 woman aged 25-56 from peri-urban primary care clinics in Zimbabwe. Three risk factors variables [age, lifetime number of sexual partners and history of a sexually transmitted infection (STI)] were selected as the basis for computer-simulated patient triage. Criteria for selecting risk factors were biological relevance, programmatic feasibility, historical evidence in the scientific literature as a risk factor for cervical cancer and a significant (P<0.05) predictor of dysplasia in this study population. Predictive values for VIA were calculated on subgroups of women with combinations of the three risk factors and then compared with the predictive value of VIA calculated on the full study population.The positive predictive value (PPV) among women with all three risk factors (30.2%) was 1.6 times higher than that of all study women and 4.5 times higher than women with none of the three risk factors (4.1%). Additionally, the PPV was slightly (30%) higher than that obtained from computer-simulated serial testing using VIA as the primary test followed by HPV testing (27.4%).Clinical history-taking could provide the basis for patient triage to increase the clinical utility of VIA. Such an approach could also serve to prioritize who gets tested first in low-resource countries with high disease prevalence that are struggling to strengthen national cervical cancer prevention programs.

    View details for Web of Science ID 000180638700010

    View details for PubMedID 12527459

  • A revolution in cervical screening BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY Blumenthal, P. D., Gaffikin, L., McInstosh, N. 2002; 109 (12): 1417-1418

    View details for Web of Science ID 000180063100025

    View details for PubMedID 12504988

  • Costs and benefits of different strategies to screen for cervical cancer in less-developed countries JOURNAL OF THE NATIONAL CANCER INSTITUTE Mandelblatt, J. S., Lawrence, W. F., Gaffikin, L., Limpahayom, K. K., LUMBIGANON, P., Warakamin, S., KING, J., Yi, B., Ringers, P., Blumenthal, P. D. 2002; 94 (19): 1469-1483

    Abstract

    About 80% of cervical cancers occur in less-developed countries. This disproportionate burden of cervical cancer in such countries is due mainly to the lack of well-organized screening programs. Several cervical cancer screening strategies have been proposed as more cost-effective than cytology screening. We compared the costs and benefits of different strategies and their effectiveness in saving lives in a less-developed country.We used a population-based simulation model to evaluate the incremental societal costs and benefits in Thailand of seven screening techniques, including visual inspection of the cervix after applying acetic acid (VIA), human papillomavirus (HPV) testing, Pap smear, and combinations of screening tests, and examined the discounted costs per year of life saved (LYS).Compared with no (i.e., not well-organized) screening, all strategies saved lives, at costs ranging from 121 US dollars to 6720 US dollars per LYS, and reduced mortality, by up to 58%. Comparing each strategy with the next least expensive alternative, VIA performed at 5-year intervals in women of ages 35-55 with immediate treatment if abnormalities are found was the least expensive option and saved the greatest number of lives, with a cost of 517 US dollars per LYS. HPV screening resulted in similar costs and benefits, if the test cost is 5 US dollars and if 90% of women undergo follow-up after an abnormal screen. Cytology (Pap smear) was a reasonable alternative if sensitivity exceeds 80% and if 90% of women undergo follow-up. Compared with no screening, use of a combination of Pap smear and HPV testing at 5-year intervals in women of ages 20-70 could achieve greater than 90% reduction in cervical cancer mortality at a cost of 1683 US dollars per LYS, and VIA could achieve 83% reduction at 524 US dollars per LYS.Well-organized screening programs can reduce cervical cancer mortality in less-developed countries at low costs. These cost-effectiveness data can enhance decision-making about optimal policies for a given setting.

    View details for Web of Science ID 000178289300013

    View details for PubMedID 12359856

  • Buccal misoprostol as cervical preparation for second trimester pregnancy termination CONTRACEPTION Todd, C. S., Soler, M., Castleman, L., Rogers, M. K., Blumenthal, P. D. 2002; 65 (6): 415-418

    Abstract

    The objective of the study was to assess the efficacy of cervical preparation with misoprostol or laminaria suction abortion up to 18 weeks gestation. The study was conducted among a consecutive case series of patients presenting for dilatation and evacuation at a single center. Cervical preparation was effected by either 600 mg buccal misoprostol (n = 32) or laminaria (n = 78). Dilatation and evacuation was then performed using vacuum aspiration, with fetal parts or placenta removed as necessary with appropriate forceps. The principle outcome of interest was procedure time. Complete abortion was effected in 100% of the cases. In all cases, the cervix was adequately prepared to allow either the introduction of a size 14-mm suction cannula or was easily dilated to this diameter. Group size was sufficient for detection of a 20% difference in mean procedure time with 80% power (calculated with two separate standard deviations for procedure time). Procedure times were not significantly different when misoprostol was used compared to laminaria for cervical preparation. It is concluded that the use of misoprostol to provide cervical preparation in second trimester abortion procedures appeared effective and offers an alternative to laminaria. Buccal misoprostol should be more widely investigated for this purpose.

    View details for Web of Science ID 000177296200007

    View details for PubMedID 12127640

  • Edward J. Haupt (1936-2001). History of psychology Blumenthal, P. E., Blumenthal, A. L. 2002; 5 (2): 207-209

    View details for PubMedID 12096763

  • Assessment of the cervix after acetic acid wash: Inter-rater agreement using photographs OBSTETRICS AND GYNECOLOGY Sellors, J. W., Jeronimo, J., Sankaranarayanan, R., Wright, T. C., Howard, M., Blumenthal, P. D. 2002; 99 (4): 635-640

    Abstract

    To estimate the inter-rater agreement on the assessment of cervical photographs after acetic acid wash, using visual inspection with acetic acid categories.Three raters individually assessed 144 photographs as negative, positive, or suspicious for cancer. The inter-rater agreement was analyzed using the unweighted and weighted kappa coefficient. To explore the reasons for concordancy and discordancy, photographs were compared on histologic evidence of cervical intraepithelial neoplasia and on testing for oncogenic types of human papillomavirus.Overall raw agreement among the three raters was 66.7% (96 of 144) with a kappa of 0.57 (95% confidence interval 0.48, 0.66). Pair-wise agreement using unweighted and weighted kappa was moderate to substantial: 0.54-0.60 and 0.56-0.63, respectively. There was concordance on negative in 25.7% (37 of 144) and on positive or suspicious for cancer in 41.0% (59 of 144). Cervical intraepithelial neoplasia II or III was not present on biopsy if photographs were concordant-negative, and the human papillomavirus test was less likely to be positive (relative risk 0.3; 95% confidence interval 0.2, 0.6) in concordant-negatives compared with concordant-positives, including suspicious for cancer. Cervical intraepithelial neoplasia II or III was more common in photographs that were concordant-positive, including suspicious for cancer, compared with discordants (relative risk 3.4, 95% confidence interval 1.5, 7.6).Based on photographs of the cervix taken after acetic acid wash, the level of agreement among raters using visual inspection with acetic acid categories was moderate to substantial, consistent with other commonly used tests.

    View details for Web of Science ID 000174635200024

    View details for PubMedID 12039126

  • Mifepristone at one year: a forward look back. Medscape women's health Burke, A. E., Moore, K., Blumenthal, P. D. 2002; 7 (2): 1-?

    View details for PubMedID 12142857

  • Reflections on the WHI findings: Avoiding a pill scare and taking sensible steps forward MEDSCAPE WOMENS HEALTH Blumenthal, P. D. 2002; 7 (4)

    View details for Web of Science ID 000178613900003

    View details for PubMedID 12466738

  • Successful use of oral contraceptives SEMINARS IN REPRODUCTIVE MEDICINE Burke, A. E., Blumenthal, P. D. 2001; 19 (4): 313-321

    Abstract

    Typical failure rates for oral contraceptives remain much higher than ideal failure rates. Patients can cite the pill's perceived risks more readily than its benefits, and many women use oral contraceptives inconsistently or discontinue them entirely without a medical reason. Successful use of oral contraceptives mandates that we rethink our roles as providers. Medical barriers, such as mandatory pelvic examinations, impede clients' access to services and require reevaluation. Efforts must also focus on thorough, individualized counseling. Because compliance poses difficulties for many women and noncompliance results in reduced efficacy, counseling must address content points relevant to proper, consistent use. Additionally, as unexpected side effects often cause frustration and method discontinuation, counseling should anticipate their occurrence. Adolescents present additional challenges. However, with careful attention to concerns relevant to teenage women and consideration of obstacles to compliance, oral contraceptives can indeed be used successfully in this group. Regardless of age, all clients should receive information regarding emergency contraception, and instructions for pill use should be individualized to meet the needs of each patient.

    View details for Web of Science ID 000172704700005

    View details for PubMedID 11727173

  • Innovative approaches to cervical cancer prevention MEDSCAPE WOMENS HEALTH Blumenthal, P. D., Ringers, P., McIntosh, N., Gaffikin, L. 2001; 6 (6)

    View details for Web of Science ID 000173122800002

    View details for PubMedID 11965215

  • Computerized planimetry versus clinical assessment for the measurement of cervical ectopia AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY Morrison, C. S., Bright, P., Blumenthal, P. D., Yacobson, I., Kwok, C., Zdenek, S., Pan, Z. Y. 2001; 184 (6): 1170-1176

    Abstract

    As part of a study to assess the role of cervical ectopia in the acquisition of cervical infections, we determined the reliability of cervical ectopia measurements made by computer planimetry and by clinical (visual) assessment.We conducted pelvic examinations of 1004 women seeking contraceptive services at two health centers in Baltimore. After application of acetic acid, clinicians estimated the relative area of ectopia by visual inspection and took cervical photographs. Two independent raters measured the absolute and relative areas of ectopia from the digitized images by means of an analytic software program. Agreement levels between raters, between multiple readings by the same rater, and between the two measurement methods were quantified by means of the intraclass correlation coefficient and weighted kappa.Intrarater agreement was excellent for computer planimetry measurements of the absolute (intraclass correlation coefficient, 0.97) and relative (intraclass correlation coefficient, 0.89) areas of ectopia. Interrater agreement was also high for computer planimetry measurements of the absolute (intraclass correlation coefficient, 0.83) and relative (intraclass correlation coefficient, 0.85) areas of ectopia. Agreement levels were moderate between clinician assessment and computer planimetry measurements of the relative area of ectopia (kappa = 0.48), but agreement was better when clinical assessment was limited to observations by a single, experienced clinician.Measurement of cervical ectopia by computer planimetry was highly reliable and appears appropriate for assessment of the role of ectopia in the acquisition of cervical infections. Clinical assessment of cervical ectopia may be used when computer planimetry is not available.

    View details for Web of Science ID 000168758300032

    View details for PubMedID 11349184

  • The Filshie clip for laparoscopic adnexal surgery. JSLS : Journal of the Society of Laparoendoscopic Surgeons / Society of Laparoendoscopic Surgeons Garcia, F. A., Barker, B., Myloyde, T., Blumenthal, P., Huggins, G. R. 2001; 5 (2): 179-181

    Abstract

    Gynecologic endoscopic procedures are increasingly common and require the ability to control large vascular structures.The Filshie clip is a silicone-lined, titanium occlusive device, originally designed and Food and Drug Administration (FDA) approved for surgical contraception. This device also has the potential for occluding vascular structures during laparoscopic surgery.We describe a salpingectomy, an excision of bilateral hydrosalpinges, and a salpingo-oopherectomy. We performed all procedures laparoscopically using this device as the primary modality for assuring hemostasis.The Filshie clip is a useful and economical device for assuring hemostasis during gynecologic endoscopic surgery.

    View details for PubMedID 11394433

  • Human embryonic germ cell derivatives express a broad range of developmentally distinct markers and proliferate extensively in vitro PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA Shamblott, M. J., Axelman, J., Littlefield, J. W., Blumenthal, P. D., Huggins, G. R., Cui, Y., Cheng, L. Z., Gearhart, J. D. 2001; 98 (1): 113-118

    Abstract

    Human pluripotent stem cells (hPSCs) have been derived from the inner cell mass cells of blastocysts (embryonic stem cells) and primordial germ cells of the developing gonadal ridge (embryonic germ cells). Like their mouse counterparts, hPSCs can be maintained in culture in an undifferentiated state and, upon differentiation, generate a wide variety of cell types. Embryoid body (EB) formation is a requisite step in the process of in vitro differentiation of these stem cells and has been used to derive neurons and glia, vascular endothelium, hematopoietic cells, cardiomyocytes, and glucose-responsive insulin-producing cells from mouse PSCs. EBs generated from human embryonic germ cell cultures have also been found to contain a wide variety of cell types, including neural cells, vascular endothelium, muscle cells, and endodermal derivatives. Here, we report the isolation and culture of cells from human EBs as well as a characterization of their gene expression during growth in several different culture environments. These heterogeneous cell cultures are capable of robust and long-term [>70 population doublings (PD)] proliferation in culture, have normal karyotypes, and can be cryopreserved, clonally isolated, and stably transfected. Cell cultures and clonal lines retain a broad pattern of gene expression including simultaneous expression of markers normally associated with cells of neural, vascular/hematopoietic, muscle, and endoderm lineages. The growth and expression characteristics of these EB-derived cells suggest that they are relatively uncommitted precursor or progenitor cells. EB-derived cells may be suited to studies of human cell differentiation and may play a role in future transplantation therapies.

    View details for Web of Science ID 000166222600025

    View details for PubMedID 11134532

  • Visual inspection of the cervix as a primary low-cost means of screening cervical cancer SEXUAL AND REPRODUCTIVE HEALTH, VOL II Gaffikin, L., Blumenthal, P. 2001: 399-408
  • Adjunctive testing for cervical cancer in low resource settings with visual inspection, HPV, and the Pap smear INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Blumenthal, P. D., Gaffikin, L., Chirenje, Z. M., McGrath, J., Womack, S., Shah, K. 2001; 72 (1): 47-53

    Abstract

    To test whether the performance of visual inspection using acetic acid (VIA) could be improved through adjunctive testing and to determine whether the combination of visual inspection of the cervix and HPV testing could prove useful for identifying those at highest risk of cervical precancer.Between October 1995 and August 1997, 2199 women willing to be screened for cervical cancer in peri-urban clinics in Harare, Zimbabwe received VIA, Pap smear and HPV as screening tests. The presence or absence of (pre)cancer was confirmed via colposcopy with biopsy as indicated for >97% of all women. Computerized simulations of sequential testing scenarios provided estimates of the joint (net) test qualities of different paired combinations of the three tests and allowed for comparisons with the individual test qualities.Using HGSIL/CIN II-III as the reference threshold of disease, the net sensitivity and specificity of VIA and HPV when used sequentially were 63.6 and 81.9%, respectively, compared to 43.3 and 91%, respectively, when Pap smears were followed by HPV testing. VIA followed by the Pap smear yielded a net sensitivity of 37.5% and net specificity of 94.3%.For programs with limited resources but with the capacity for HPV testing, sequential testing involving the use of VIA followed by HPV could yield fewer false positives than the use of VIA alone at a cost of relatively few additional false negatives.

    View details for Web of Science ID 000166468300008

    View details for PubMedID 11146077

  • The Filshie clip in nonsterilization gynecologic laparoscopy OBSTETRICS AND GYNECOLOGY Garcia, F. A., Barker, B., Myloyde, T., Blumenthal, P. 2000; 96 (5): 848-848

    View details for Web of Science ID 000090130000029

    View details for PubMedID 11094240

  • New technologies in cervical cancer precursor detection CURRENT OPINION IN ONCOLOGY Soler, M. E., Blumenthal, P. D. 2000; 12 (5): 460-465

    Abstract

    The current literature reflects three routes toward improving cervical cancer screening. The first is to improve the test qualities of cytology-based screening. The use of liquid-based cytology and computerized analysis of Papanicolaou tests are examples of attempts at this approach. Secondly, through various combinations of parallel or sequential tests, either the sensitivity or the specificity of a given test could be improved depending on the tests chosen and the order in which they were performed (eg, Papanicolaou test followed by human papillomavirus [HPV] or vice versa). Several excellent studies have been published this year on the use of HPV DNA testing as a primary screening modality and as an adjunct to the triage of mildly abnormal cytologic findings. The recent literature also reflects increasing interest in visual inspection of the cervix and self-collected samples for HPV testing as an equally effective and viable alternative to cytology in low-resource settings. A third possibility is to make use of advances in digital and spectroscopic techniques. In these cost-conscious times, a significant number of articles address the cost-effectiveness of these technologies and the real value of cervical cancer screening. This article reviews the current literature concerning both the advent of new cervical cancer screening technologies and the rediscovery of old ones.

    View details for Web of Science ID 000169265000013

    View details for PubMedID 10975554

  • The approval of mifepristone (RU486) in the United States: What's wrong with this picture? Medscape women's health Blumenthal, P., Johnson, J., Stewart, F. 2000; 5 (4): E7-?

    View details for PubMedID 11109052

  • HPV-based cervical cancer screening in a population at high risk for HIV infection INTERNATIONAL JOURNAL OF CANCER Womack, S. D., Chirenje, Z. M., Gaffikin, L., Blumenthal, P. D., McGrath, J. A., Chipato, T., Ngwalle, S., Munjoma, M., Shah, K. V. 2000; 85 (2): 206-210

    Abstract

    We determined the utility of an assay for 13 cancer-associated HPV types in primary cervical cancer screening of Zimbabwe women at high risk of HIV infection. HIV antibody status was determined by ELISA of oral mucosal specimens, and HPV DNA in the genital tract was identified by hybridization of cervical scrapes with probe B of Hybrid Capture II. Among the 466 women investigated, the prevalence of HPV, low-grade squamous intraepithelial lesions (LGSIL) and high-grade SIL (HGSIL) were 47.2%, 13.9% and 12%. Fifty-three and one-half percent of the women were HIV-seropositive. As compared with HIV-seronegative women, HIV-infected women had a greater than 2-fold HPV prevalence (64.3% vs. 27.6%), a greater than 7-fold amount of HPV DNA (RLU of 82.6 vs. 10.7) in HPV(+) women assessed as normal on the reference standard, and a nearly 3-fold greater HGSIL prevalence (17.3% vs. 5.9%). The strong link between HGSIL and HPV DNA positivity was seen in both HIV-infected and HIV-seronegative women. The amount of HPV DNA increased with disease severity in both HIV-seronegative and HIV-infected women. The sensitivity and specificity of the HPV test for HGSIL were, respectively, 90.7% (95% confidence limit 77.9-97.4%) and 41.3% (34.5-48.3%) in HIV-infected women and 61.5% (31.6-86.1%) and 74.5% (68.0-80.3%), respectively, in HIV(-) women. The usefulness of the HPV test as a screening test for cervical cancer in areas of high HPV prevalence will depend upon local health resource availability, disease priorities and policies regarding clinical case management.

    View details for Web of Science ID 000084589400010

    View details for PubMedID 10629079

  • The "boom and bust phenomenon": The hopes, dreams, and broken promises of the contraceptive revolution CONTRACEPTION Boonstra, H., Duran, V., Gamble, V. N., Blumenthal, P., Dominguez, L., Pies, C. 2000; 61 (1): 9-25

    Abstract

    The "boom and bust phenomenon" is a pattern that has emerged in the development, introduction, and delivery of a number of significant new contraceptive products in the United States. When a new contraceptive product is introduced with great promise and publicity, it usually experiences a "boom" during which sales, demand, and expectations are high. This boom is often followed by a "bust" phase during which a product does not live up to expectations, initial excitement falls off, and a drop in sales and use ensues. The boom and bust phenomenon goes to the heart of what some have referred to as the failed promise of the contraception revolution by creating obstacles to significant expansion of contraceptive choice in the United States. Case studies of oral contraceptives, intrauterine devices, and Norplant(R) are used to illustrate the boom and bust phenomenon and the effect it has had in shaping the direction of advances in contraceptive technology.

    View details for Web of Science ID 000086370900003

    View details for PubMedID 10745065

  • Cervical cancer screening in developing countries. Primary care update for Ob/Gyns Soler, M. E., Gaffikin, L., Blumenthal, P. D. 2000; 7 (3): 118-123

    Abstract

    In developing countries, cervical cancer remains a clinical problem of public health proportions. Eighty percent of the approximately 400,000 new cases of cervical cancer each year occur in such settings. Primarily as a result of the introduction and success of screening programs, cervical cancer rates in developed countries have dropped remarkably. However, in most developing countries, screening programs are virtually nonexistent. Reasons for this relate primarily to lack of public awareness and the fact that screening via cytology is an untenable proposition for mass screening in such low-resource settings. Matching the resources available to provide cervical cancer screening in such settings requires alternative means of providing testing and treatment. Recent evidence indicates that, depending on local conditions and locally-made decisions, visual inspection of the cervix with acetic acid wash, coupled with a benign form of therapy, such as cryotherapy, could hold promise as a means of testing and treatment. By adapting resource-appropriate technologies and building local consensus regarding clinically driven public health approaches that are safe and feasible, the challenge of reducing the mortality from cervical cancer in developing countries can yet be met.

    View details for PubMedID 10840215

  • Evaluation of a human papillomavirus assay in cervical screening in Zimbabwe BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY Womack, S. D., Chirenje, Z. M., Blumenthal, P. D., Gaffikin, L., McGrath, J. A., Chipato, T., Ngwalle, E., Shah, K. V. 2000; 107 (1): 33-38

    Abstract

    To determine the utility of an assay for high risk genital human papillomavirus (HPV) in cervical screening in Zimbabwe, Africa.Cross-sectional study.Harare, Zimbabwe.Zimbabwe women (n = 2,140), 25 to 55 years old, recruited in clinics in Chitungwiza and Greater Harare.Genital specimens were assessed for HPV, using the HPV DNA test Hybrid Capture II (probe B). Further assessment of the women was conducted using colposcopy and biopsy as indicated. High grade squamous intraepithelial lesions were diagnosed in 215 women. Colposcopy and/or biopsy showed low grade lesions in 346 women.The overall prevalences were: 42 x 7% for HPV, 10% for high grade squamous intraepithelial lesions and 16% for low grade lesions. Prevalence for HPV decreased significantly with increase in age (P for trend < 0 x 0001) and increased significantly with increasing disease severity, from 35% in normal women, to 53% in women with low grade lesions and 81% in women with high grade lesions (P for trend < 0 x 001). In specimens positive for HPV, the amount was 14-fold higher in women with high grade lesions compared with normal women. In screening for high grade lesions the assay for HPV had a sensitivity of 81% (CI 75%-86%); sensitivity for low grade lesions was 64% (CI 60%-68%). Specificity was 62% (CI 59%-64%) for high grade lesions and 65% (CI 62%-67%) for low grade lesions. The positive predictive value was 19% (CI 17%-22%) for high grade lesions and 39% (CI 36%-42%) for low grade lesions.For high grade squamous intraepithelial lesions the sensitivity of the Hybrid Capture II HPV DNA test was high, but the specificity was relatively low. The test may therefore be most useful in conjunction with other screening tests.

    View details for Web of Science ID 000084833900008

    View details for PubMedID 10645859

  • Timing of onset of contraceptive effectiveness in Norplant (R) implant users II - Effect on the ovarian function in the first cycle of use CONTRACEPTION Brache, V., Blumenthal, P. D., Alvarez, F., DUNSON, T. R., Cochon, L., Faundes, A. 1999; 59 (4): 245-251

    Abstract

    The objective of this study was to time the onset of contraceptive effectiveness in Norplant implant users, when the capsules were inserted beyond the first 7 days of the cycle, based on the immediate effect on the ovarian activity. A total of 42 healthy women requesting Norplant implant contraception were enrolled at clinics in Santo Domingo, Dominican Republic, and in Baltimore, Maryland. Implants were inserted on days 8-13 of the menstrual cycle. Blood samples for estradiol (E2), progesterone (P), luteinizing hormone (LH) (in a subset of 12 women), and levonogestrel (LNG) assay, were taken at 0 h and at 6, 12, 24, 72, and 168 h postinsertion. Ovulation, as defined by P > 2.5 ng/mL, occurred in 40% of subjects. A short lasting, frequently blunted, LH peak occurred within 12 h postinsertion, in all these subjects. The remaining subjects had anovulatory cycles with two distinct E2 profiles: continuously increasing E2 levels to a high mean of 414.3 pg/mL (28%), or no sustained increase in E2 (32%). Most cycles (86%) in which Norplant was inserted with high E2 levels (> 175 pg/mL) were ovulatory, whereas none were ovulatory with low E2 (< 100 pg/mL) at insertion. Based on the endocrine effects of Norplant implant insertion in the midadvanced follicular phase, in which ovulation will either occur within 48 h of insertion or will be impaired, additional contraceptive protection is necessary only for 3 days.

    View details for Web of Science ID 000081928500006

    View details for PubMedID 10457869

  • Visual inspection with acetic acid for cervical-cancer screening: test qualities in a primary-care setting LANCET Gaffikin, L., Blumenthal, P. D., McGrath, J., Chirenje, Z. M., Sanghvi, H., Chipato, T., Makunike, R., Kasule, J., Ngwalle, E., Rusakaniko, S. 1999; 353 (9156): 869-873
  • Derivation of pluripotent stem cells horn cultured human primordial germ cells PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA Shamblott, M. J., Axelman, J., Wang, S. P., Bugg, E. M., Littlefield, J. W., Donovan, P. J., Blumenthal, P. D., Huggins, G. R., Gearhart, J. D. 1998; 95 (23): 13726-13731

    Abstract

    Human pluripotent stem cells would be invaluable for in vitro studies of aspects of human embryogenesis. With the goal of establishing pluripotent stem cell lines, gonadal ridges and mesenteries containing primordial germ cells (PGCs, 5-9 weeks postfertilization) were cultured on mouse STO fibroblast feeder layers in the presence of human recombinant leukemia inhibitory factor, human recombinant basic fibroblast growth factor, and forskolin. Initially, single PGCs in culture were visualized by alkaline phosphatase activity staining. Over a period of 7-21 days, PGCs gave rise to large multicellular colonies resembling those of mouse pluripotent stem cells termed embryonic stem and embryonic germ (EG) cells. Throughout the culture period most cells within the colonies continued to be alkaline phosphatase-positive and tested positive against a panel of five immunological markers (SSEA-1, SSEA-3, SSEA-4, TRA-1-60, and TRA-1-81) that have been used routinely to characterize embryonic stem and EG cells. The cultured cells have been continuously passaged and found to be karyotypically normal and stable. Both XX and XY cell cultures have been obtained. Immunohistochemical analysis of embryoid bodies collected from these cultures revealed a wide variety of differentiated cell types, including derivatives of all three embryonic germ layers. Based on their origin and demonstrated properties, these human PGC-derived cultures meet the criteria for pluripotent stem cells and most closely resemble EG cells.

    View details for Web of Science ID 000076997000067

    View details for PubMedID 9811868

  • Developments in contraception: A comprehensive review of desogen (R) (Desogestrel and ethinyl estradiol) CONTRACEPTION Lammers, P., Blumenthal, P. D., Huggins, G. R. 1998; 57 (5): 1S-27S

    View details for Web of Science ID 000074916300001

    View details for PubMedID 9673846

  • Provider attitudes toward IUD provision in Zimbabwe: perception of HIV risk and training implications ADVANCES IN CONTRACEPTION Gaffikin, L., Phiri, A., McGrath, J., Zinanga, A., Blumenthal, P. D. 1998; 14 (1): 27-39

    Abstract

    This study was conducted to assess providers' attitudes toward the provision of long-term methods of contraception, in particular the IUD, and provider concerns about human immunodeficiency virus (HIV) in the context of family planning (FP) services. The data were collected using self-administered structured questionnaires. Between 65% and 80% of the public and private providers thought that the IUD is a good contraceptive method for Zimbabwean women. In addition, the majority of these two provider groups felt that neither the IUD nor tubal sterilization (TL) posed much risk of HIV infection to the client. A significant number of providers (especially the public nurses), however, thought that the provision of TL put the provider at high risk of HIV infection and a significant proportion of public nurses were also concerned about provider risk associated with providing IUD and injectables. To address such concerns, future training interventions should emphasize appropriate infection prevention practices associated with surgical FP method provision. Nurses, in particular, should be informed about the magnitude of risk associated with FP service provision and ways to protect themselves. Logistic activities also need to be strengthened so that legitimate concerns among providers regarding lack of adequate infection prevention supplies (e.g. gloves) in the field can be addressed.

    View details for Web of Science ID 000072865200003

    View details for PubMedID 9587006

  • Timing of onset of contraceptive effectiveness in norplant implant users. Part I. Changes in cervical mucus FERTILITY AND STERILITY DUNSON, T. R., Blumenthal, P. D., Alvarez, F., Brache, V., Cochon, L., Dalberth, B., Glover, L., Remsburg, R., Vu, K., Katz, D. 1998; 69 (2): 258-266

    Abstract

    To provide scientific data regarding the changes in cervical mucus within the first hours to days after Norplant implant insertion and to estimate when the cervical mucus is hostile enough to suggest a contraceptive effect.Multicenter, clinical descriptive study.Family planning clinics.Forty-two women who were between days 8 and 13 of their menstrual cycle and who had requested Norplant implants were admitted to the study.Cervical mucus and blood samples were obtained.Cervical mucus scores, sperm penetration distances, and serum levels of progesterone, estradiol, and levonorgestrel.The median cervical mucus score observed at baseline was 6 ("fair"), indicating that the mucus was already somewhat hostile before insertion of the Norplant implants. The median scores declined to 5 at 12 and 24 hours and continued to decrease through day 7 to 2 ("poor"), a score that is judged as hostile to sperm penetration. Overall, 73% of all subjects had a poor cervical mucus score by 3 days after insertion; at 7 days after insertion, 90% exhibited poor mucus and none had a good score. There was a substantial drop in the overall median distance traveled by the vanguard sperm after 12 hours for each cervical mucus score grouping. The distance traveled decreased rapidly between 12 and 24 hours to < 0.5 cm in subjects with fair and poor mucus, and by day 3, 91% of the subjects exhibited poor sperm penetration.On the basis of our findings, deterioration of the quality of the cervical mucus and sperm penetration is evident by 24 hours after insertion, although not to a level that would suggest adequate protection until 72 hours after insertion. Therefore, we are confident in recommending that backup methods of contraception (e.g, condoms) need not be used for more than 3 days after insertion, even when the implants are inserted close to ovulation. These findings provide policy makers, clinic managers, and clinicians with important information about how they can improve client access to Norplant implants.

    View details for Web of Science ID 000072202700015

    View details for PubMedID 9496339

  • Ulnar nerve injury associated with removal of norplant implants CONTRACEPTION Smith, J. M., Conwit, R. A., Blumenthal, P. D. 1998; 57 (2): 99-101

    Abstract

    Improperly placed Norplant implants pose a risk to neurovascular structures at the time of removal. Appropriate attention to insertion and removal should minimize the chance of injury. However, when injuries do occur, a logical and systematic approach to evaluation of the injury can help predict the outcome and establish a plan of care for the patient.

    View details for Web of Science ID 000073470900006

    View details for PubMedID 9589836

  • Training for Norplant implant removal: Assessment of learning curves and competency OBSTETRICS AND GYNECOLOGY Blumenthal, P. D., Gaffikin, L., Affandi, B., Bongiovanni, A., McGrath, J., GLEW, G. 1997; 89 (2): 174-178

    Abstract

    To determine the learning curves and rapidity with which clinicians become competent in implant removal using two Norplant removal techniques.Twenty-four physicians, none of whom were experienced in the use of Norplant implants, were randomly assigned to learn either the "U" removal technique or the standard technique. The physicians in the two groups received identical training in all other respects. Each physician then performed ten supervised removals. Removal times, procedure problem rates, and the number of procedures performed by the clinicians before they were judged "competent" were assessed for both groups.Data from 240 removals were analyzed. Mean removal times were 38% faster in the "U" group than in the standard group. None of the "U" group procedures took longer than 20 minutes, compared with 11% of removals in the standard group (P < .001). The mean number of cases required before the provider consistently performed all steps adequately was significantly (P < .02) higher in the standard group (5.8 cases) than in the "U" group (3.9 cases).Using competency-based training methods, the "U" removal technique was learned easily by inexperienced clinicians. It appears to offer significant improvements in speed and achievement of proficiency over the standard technique recommended by the manufacturer. Large-scale programs should consider using competency-based training and the "U" technique as the removal method of choice when providing training in implant removal.

    View details for Web of Science ID A1997WE57600004

    View details for PubMedID 9015016

  • Lea's Shield(R): A study of the safety and efficacy of a new vaginal barrier contraceptive used with and without spermicide CONTRACEPTION Mauck, C., Glover, L. H., Miller, E., Allen, S., Archer, D. F., Blumenthal, P., Rosenzweig, B. A., Dominik, R., STURGEN, K., Cooper, J., Fingerhut, F., Peacock, L., Gabelnick, H. L. 1996; 53 (6): 329-335

    Abstract

    The purpose of this study was to evaluate the safety, efficacy and acceptability of Lea's Shield, a new vaginal contraceptive barrier device, when used with either spermicidal or non-spermicidal lubricant. One-hundred-eighty-five (185) women enrolled at six centers. Half were randomized to use the device with spermicide and half with a non-spermicidal lubricant. To be eligible, volunteers had to be 18-40 years old (inclusive), in good health with regular menses, sexually active in an ongoing relationship and at risk for pregnancy, and willing to use Lea's Shield as their sole means of contraception for six months. Participants were seen at admission, one week, one month, three months and six months. Gross cumulative life table rates were calculated for pregnancy and others reasons for discontinuation. Adverse experiences and responses to an acceptability questionnaire were evaluated. One-hundred-eighty-two (182) volunteers contributed data to the analysis of safety and 146 to that of contraceptive efficacy. The unadjusted six-month life table pregnancy rate was 8.7 per 100 women for spermicide users and 12.9 for non-spermicide users (p = 0.287). After controlling for age, center, and frequent prior use of barrier methods, the adjusted six-month life table pregnancy rate was 5.6 for spermicide users and 9.3 for non-spermicide users (p = 0.086), indicating that use of spermicide lowered pregnancy rates, although not significantly, during typical use. For purposes of comparison, it is important to note that this study differed from the cap/diaphragm and sponge/ diaphragm studies in that a high percentage (84%) of volunteers were parous. For reasons that are unclear, pregnancy rates among parous women using barrier contraceptives tend to be higher than among nulliparous women. Indeed, in this study there were no pregnancies among nulliparous users of Lea's Shield. Standardization of parity of this study population on those of the cap/diaphragm and sponge/diaphragm studies suggests that unadjusted pregnancy rates for this device would have been considerably lower (2.2 and 2.9 per 100 users of spermicide and non-spermicide, respectively) had the study been done using the populations of earlier studies. Since no directly comparative study has been done, these figures provide a tentative estimate of the relative efficacy of Lea's Shield compared with the sponge, cap, and diaphragm. There were no serious adverse experiences attributed to the use of Lea's Shield. Acceptability was very good. Seventy-five percent (75%) of women responded to an end-of-study questionnaire; 87% of these reported that they would recommend Lea's Shield to a friend. Lea's Shield is a new vaginal contraceptive that does not require clinician fitting. Pregnancy rates in this study compare favorably with other studies of barrier contraceptive methods including the cervical cap, diaphragm, and sponge, even though this study was done with greater rigor and with a greater percentage of parous women than previous barrier studies. Lea's Shield appears to be safe and very acceptable to study volunteers.

    View details for Web of Science ID A1996UP78600002

    View details for PubMedID 8773419

  • Usefulness of a clinical scoring system to anticipate difficulty of Norplant removal ADVANCES IN CONTRACEPTION Blumenthal, P. D., Remsburg, R. E., GLEW, G., McGrath, J. A., Gaffikin, L. 1995; 11 (4): 345-352

    Abstract

    Removal of contraceptive implants (e.g. Norplant) is an issue affecting its worldwide acceptability. Reports of difficult, painful removals have resulted in lawsuits and reduced demand. To improve quality of care, we developed a scoring system to anticipate difficult removals. We report on the usefulness of such a system and present client perspectives about the removal experience.A 9-point scoring system based on the visibility, arrangement, and position (VAP) of Norplant capsules was used to assess the anticipated difficulty of removal in 53 consecutive patients. The VAP score was then correlated with removal time and related parameters.Mean removal time was 14.74 min (range 4.75-47). In 20% of patients, the VAP score indicated a potentially difficult removal and the VAP score correlated significantly with removal time (r = 0.3, p = 0.05). Patients expected removal to be moderately difficult (mean visual analog score 4.7 out of a possible 10), but after removal they rated the actual removal experience as relatively easy (mean score 2.6/10). Before the removal, only 48% of patients said they would recommend Norplant to a friend but after removal, 70% said they would do so.A scoring system such as the VAP score can help identify potentially difficult removals so that an experienced remover can be present at the time of removal or an appropriate referral made. However, the VAP score cannot predict variables such as the density of the subcutaneous fibrous tissue "envelope". Although patient anxiety concerning removal may be high, the presence of a competent remover and an easy removal experience reduces this anxiety and encourages patients to be more positive about this method. The value of having properly trained, competent personnel available to perform removals cannot be over-emphasized.

    View details for Web of Science ID A1995TV47900009

    View details for PubMedID 8659320

  • LAPAROSCOPIC STERILIZATION IN THE SUPINE POSITION USING THE RAMATHIBODI UTERINE MANIPULATOR FERTILITY AND STERILITY Blumenthal, P. D. 1995; 64 (1): 204-207

    Abstract

    To investigate the usefulness of the Ramathibodi uterine manipulator (AMZURA Enterprises, Freeport, NY) in performing laparoscopic sterilization procedures in the supine position under local anesthesia.Descriptive prospective study.Ambulatory surgical unit of university-affiliated hospital.Women presenting for elective sterilization and weighing < 110 kg.The Ramathibodi uterine manipulator was used to provide uterine manipulation in 85 cases of laparoscopic sterilization, all performed in the supine position as local anesthesia-sedation sterilization operations. Because such procedures are becoming more common worldwide, we propose the acronym "LASSO" (Local Anesthesia-Sedation Sterilization Operation) for this class of operations. Although commonly used in minilaparotomy procedures, use of this uterine manipulation device in laparoscopic procedures has not been published previously.Successful tubal occlusion.Among the 85 cases reported here there were no failures to manipulate the uterus successfully, to identify the tubes, and to occlude them.The simplicity of the Ramathibodi uterine manipulator provided several advantages over other means of uterine manipulation, notably [1] constant easy-to-learn maneuvers, [2] no tenaculum or balloon requirement, [3] the procedure could be performed in the supine position, and [4] there are no working parts, screws, or springs that could be lost or broken by operating room staff. Our experience with this device leads us to recommend it to colleagues as an inexpensive, safe, and effective alternative to currently available instruments for providing uterine elevation during laparoscopic sterilization procedures.

    View details for Web of Science ID A1995RD42100038

    View details for PubMedID 7789563

  • CONTRACEPTIVE OUTCOMES AMONG POSTPARTUM AND POST-ABORTAL ADOLESCENTS CONTRACEPTION Blumenthal, P. D., Wilson, L. E., Remsburg, R. E., Cullins, V. E., Huggins, G. R. 1994; 50 (5): 451-460

    Abstract

    Between January 1992 and January 1993, there were 280 teens (ages 13-18) who either delivered a baby or terminated a pregnancy at Johns Hopkins Bayview Medical Center. Of these, 92 chose to contracept with Norplant implants, and 188 chose another method including "no" method. In July 1993, telephone interviews were conducted with 37 of those who chose Norplant implants and 41 of the non-Norplant implants users. After 1 year, 47% of oral contraceptive (COC) users had discontinued the method compared to only 16% of Norplant implants users (P < 0.03). Reasons for discontinuation centered on side effects for both groups but with some COC and condom users, discontinuing use due to "forgetfulness" or failure (pregnancy). Among the COC group (which was the most common choice after Norplant implant), 25% of the adolescents had experienced a subsequent unplanned pregnancy compared to 0% of the Norplant implant group (P < 0.01). Norplant implants were clearly an acceptable and effective contraceptive for these post-partum and post-abortal teens, who articulated a high motivation to avoid a subsequent unplanned pregnancy. However, it is clearly not the only method teens will choose to use, and more attention must be paid to adequate counseling of those choosing another method.

    View details for Web of Science ID A1994PR67100006

    View details for PubMedID 7859454

  • RECOVERY FROM OUTPATIENT LAPAROSCOPIC TUBAL-LIGATION IS NOT IMPROVED BY PREOPERATIVE ADMINISTRATION OF KETOROLAC OR IBUPROFEN ANESTHESIA AND ANALGESIA Higgins, M. S., GIVOGRE, J. L., Marco, A. P., Blumenthal, P. D., Furman, W. R. 1994; 79 (2): 274-280

    Abstract

    The analgesic efficacy of a single dose of ketorolac or ibuprofen given preoperatively was assessed in healthy outpatients undergoing general anesthesia for laparoscopic tubal ligation. Fifty patients were randomized to receive either ketorolac 60 mg intravenously (i.v.), ibuprofen 800 mg orally, or placebo in a double-blind manner. Anesthesia was induced with fentanyl 2 micrograms/kg, thiopental 5 mg/kg, and either vecuronium 0.1 mg/kg or succinylcholine 1.5 mg/kg i.v. and was maintained with nitrous oxide 67% in oxygen and isoflurane. Patients were assessed at 15-min intervals in the postanesthesia care unit (PACU) and treated for pain with i.v. morphine by protocol. Patients were evaluated for pain, analgesic requirements, side effects, and recovery times. After discharge, patients completed questionnaires to assess pain, analgesic use, and side effects 6 and 24 h postoperatively. Parenteral morphine was required in 80% of patients in the control group, and 73% of patients in both treatment groups, and the difference was not statistically significant. The dose of parenteral morphine required in the PACU was not different between the control (7 +/- 1.2 mg), ibuprofen (5.7 +/- 1.4 mg), and ketorolac (6.1 +/- 1.4 mg) groups. There was no difference between groups in terms of pain visual analog scale (VAS) scores, fatigue VAS scores, recovery times, or the incidence of postoperative nausea and vomiting. The preoperative administration of either parenteral ketorolac or oral ibuprofen did not decrease postoperative pain or side effects when compared to placebo in this outpatient population.

    View details for Web of Science ID A1994NZ33700012

    View details for PubMedID 7639363

  • A TIME AND COST-ANALYSIS OF THE MANAGEMENT OF INCOMPLETE ABORTION WITH MANUAL VACUUM ASPIRATION INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS Blumenthal, P. D., Remsburg, R. E. 1994; 45 (3): 261-267

    Abstract

    Traditionally, management of incomplete abortion involves use of D&C or suction curettage in the operating room. Such management is costly and time-consuming. In order to potentially save time and money, we studied the use of manual vacuum aspiration curettage (MVAC) for the management of this problem.Data on hospital charges and times (e.g. waiting time, procedure time) were obtained for all cases of incomplete abortion presenting to hospital between January 1990 and July 1992. Between January 1990 and July 1991, all cases were managed traditionally. After July 1991, all cases were managed using MVAC in either the emergency room or the labor ward.Compared to the use of electrical suction equipment in the operating theatre, MVAC procedures resulted in significant savings in terms of both waiting times and costs. Waiting time was reduced by 52% and procedure time was reduced from a mean of 33 min to 19 min (P < 0.01). Total hospital costs were reduced by 41% (P < 0.01).Use of manual vacuum aspiration curettage in the management of incomplete abortion can reduce hospital costs and save time for both patients and clinicians.

    View details for Web of Science ID A1994NT19000009

    View details for PubMedID 7926246

  • COMPARISON OF ADOLESCENT AND ADULT EXPERIENCES WITH NORPLANT LEVONORGESTREL CONTRACEPTIVE IMPLANTS OBSTETRICS AND GYNECOLOGY Cullins, V. E., Remsburg, R. E., Blumenthal, P. D., Huggins, G. R. 1994; 83 (6): 1026-1032

    Abstract

    To compare acceptability, tolerance of side effects, and continuation rates among adolescent and adult Norplant accepters.An 18-month observational study was conducted of 136 adolescents and 542 adults who received Norplant at the Francis Scott Key Medical Center in Baltimore, Maryland. Data were collected from the following: a self-administered history form completed at the preinsertion visit, a self-administered follow-up form completed at routine follow-up visits, problem-visit chart review, and telephone contact for patients noncompliant with follow-up appointments.The adolescents ranged in age from 13-18 years (mean 16.4), and adults ranged in age from 19-46 (mean 24.7). The mean parity among teenagers was 1.4; among adults, 3.2. Thirty-nine percent of teenagers and 64% of adults had had one or more therapeutic abortions. Forty percent of adolescents and 47% of adults reported at least one contraceptive failure in the past. Both adolescent and adult Norplant accepters made few telephone calls or problem visits because of complaints or side effects. Compliance with routine annual follow-up was poor for adolescents (24 of 136, 18%) and adults (72 of 542, 13%). Follow-up of noncompliant patients revealed low rates of implant removal. Fifteen adolescents (11%) and 60 adults (11%) had Norplant removed. The most common reasons for removal included irregular bleeding, weight gain, headaches, and desire for pregnancy.Implant acceptability, continuation, and tolerance of side effects were high and comparable among adolescent and adult accepters. Initial implant users were primarily adolescents or adults who had experienced problems with other forms of reversible contraception. Adherence to scheduled follow-up appointments was poor, regardless of age.

    View details for Web of Science ID A1994NN17400025

    View details for PubMedID 8190418

  • PRELIMINARY EXPERIENCE WITH NORPLANT(R) IN AN INNER-CITY POPULATION CONTRACEPTION Cullins, V. E., Blumenthal, P. D., Remsburg, R. E., Huggins, G. R. 1993; 47 (2): 193-203

    Abstract

    Norplant, the five-year subdermal contraceptive system, is the first implantable contraceptive method approved for general use in the United States. We describe the preliminary experiences of 246 U.S. women who accepted Norplant between April, 1991 and September, 1991. Norplant was well accepted among this diverse general population. Intensive counselling about side effects, especially menstrual changes, is crucial for patient satisfaction. Although 48% of acceptors experienced menstrual cycle changes and 70% experienced at least one side effect, phone calls and unscheduled visits for problems were infrequent. Adequate counselling about side effects obviates the need for a routine follow-up visit one month after insertion.

    View details for Web of Science ID A1993KM47300007

    View details for PubMedID 8449019

  • ABORTION - EPIDEMIOLOGY, SAFETY, AND TECHNIQUE CURRENT OPINION IN OBSTETRICS & GYNECOLOGY Blumenthal, P. D. 1992; 4 (4): 506-512

    Abstract

    In 1991, the abortion literature was characterized by articles relating to 1) epidemiologic issues in abortion care, 2) advances in knowledge and experience with medical abortifacients such as mifepristone (RU 486), and 3) cervical ripening prior to abortion with the use of both mifepristone and prostaglandins. Technical methods of achieving termination of pregnancy continue to be similar in the United States, the United Kingdom, and Europe, although induction-abortion times are generally slower in Europe than in the United States. Surgically, dilatation and evacuation procedures continue to be more common in the United States than in other countries. The effectiveness of mifepristone is undisputed, and the recommended dose for early first-trimester termination is being compared with lower dose alternative regimens. There is additional evidence that at least in the short term, the negative psychological sequelae of abortion are infrequent and are inconsequential as a public health issue.

    View details for Web of Science ID A1992JG69900003

    View details for PubMedID 1504270

  • ABORTION CURRENT OPINION IN OBSTETRICS & GYNECOLOGY Blumenthal, P. D. 1991; 3 (4): 496-500

    Abstract

    In 1990 abortion literature was characterized by articles relating to 1) the safety of surgical abortion procedures, 2) advances in knowledge and experience with medical abortifacients such as mifepristone (RU 486), and 3) reviews of psychologic and ethical considerations. Although technical methods differ greatly between countries and continents, there is increasing similarity between termination protocols in the United States, the United Kingdom, and Europe. The advent of mifepristone will make this even more so. Surgically, although dilatation and evacuation procedures are far more common in the United States than in other countries, the literature reflects a fine-tuning of analysis and technique, with safety the major consideration. Knowledge about the effectiveness of mifepristone continues to grow, and the effective dose for early first-trimester termination appears established. There is increasing evidence that at least in the short term, the negative psychologic sequelae of abortion are infrequent and are inconsequential as a public health issue.

    View details for Web of Science ID A1991GA55800007

    View details for PubMedID 1878507

  • NONPHARMACEUTICAL RIPENING OF THE UNFAVORABLE CERVIX AND INDUCTION OF LABOR BY A NOVEL DOUBLE BALLOON DEVICE OBSTETRICS AND GYNECOLOGY Blumenthal, P. D., Gaffikin, L. 1991; 77 (6): 967-968

    View details for Web of Science ID A1991FN40100048

    View details for PubMedID 2030880

  • LETTER FROM AFRICA OBSTETRICS AND GYNECOLOGY Blumenthal, P. D. 1990; 76 (1): 147-148

    Abstract

    A day in obstetric-gynecologic practice in Kenya involves uterine rupture and other conditions resulting from inadequate care and facilities for labor, as well as infected abortions. Technology and equipment taken for granted in America either don't exist or don't work. Although practice is primitive in many ways, some of the concerns of doctors are the same as in developed countries.

    View details for Web of Science ID A1990DK68300032

    View details for PubMedID 2359560

  • RANDOMIZED TRIAL OF DILAPAN AND LAMINARIA AS CERVICAL RIPENING AGENTS BEFORE INDUCTION OF LABOR OBSTETRICS AND GYNECOLOGY Blumenthal, P. D., Ramanauskas, R. 1990; 75 (3): 365-368

    Abstract

    A randomized trial was conducted to evaluate the comparative effectiveness of Dilapan cervical dilators and Laminaria japonicum as cervical ripening agents before induction of labor at term. Patients with Bishop scores of 4 or less and a fetal or maternal indication for induction at 34 or more weeks' gestation were eligible for the study. The outcome variables of interest were Bishop score upon removal of the devices, number of devices used, induction-to-delivery time, and induction-to-complete dilatation time. In the Dilapan group, an average of 4.3 devices per patient was used, compared with 9.7 devices in the laminaria group (P less than .01). Among patients who eventually achieved complete dilatation, the mean (+/- SD) time for the Dilapan group was 10.8 +/- 6.1 hours, compared with 14.7 +/- 9.2 hours with laminaria. For women undergoing induction of labor at term with an unripe cervix, Dilapan appeared to be a preferable alternative to Laminaria japonicum because its use may result in a shorter induction-to-delivery interval with fewer devices required to obtain significant cervical ripening.

    View details for Web of Science ID A1990CQ07400013

    View details for PubMedID 2406658

  • COMPARISON OF THE NIPPLE STIMULATION AND EXOGENOUS OXYTOCIN CONTRACTION STRESS TESTS - A RANDOMIZED, PROSPECTIVE-STUDY JOURNAL OF REPRODUCTIVE MEDICINE Rosenzweig, B. A., Levy, J. S., SCHIPIOUR, P., Blumenthal, P. D. 1989; 34 (12): 950-954

    Abstract

    In a prospective, randomized trial, 103 women underwent a total of 203 antenatal stress tests. One hundred four nipple stimulation contraction stress tests (BSTs) and 99 oxytocin challenge tests (OCTs) were performed. The patient populations were similar for the two groups. Uterine hyperstimulation with abnormal fetal heart rate patterns occurred with 2.9% and 1% of the BSTs and OCTs, respectively. The failure rate for the BST group was 22%. Maternal age and weight, parity and gestational age were not associated with test failure. Only one patient failed more than one BST, but she did not fail every such test. When test time (time from initiation to completion of the test) was compared between the two groups, a significant difference was found when the BST was successful. However, when test time in the total BST group (successful and unsuccessful BSTs followed by an OCT was compared to that in the OCT group, no difference could be found. Though an OCT following an unsuccessful BST took longer to perform than did a primary OCT, the difference was not statistically significant. It appears that BST test failure may relate more to the technique of nipple stimulation used than to intrinsic patient factors.

    View details for Web of Science ID A1989CG74000004

    View details for PubMedID 2695647

  • PROSPECTIVE COMPARISON OF DILAPAN AND LAMINARIA FOR PRETREATMENT OF THE CERVIX IN 2ND-TRIMESTER INDUCTION ABORTION OBSTETRICS AND GYNECOLOGY Blumenthal, P. D. 1988; 72 (2): 243-246

    Abstract

    Fifty-four women presenting for second-trimester induction abortion received either Dilapan synthetic dilators or laminaria for pretreatment of the cervix before induction abortion using intra-amniotic prostaglandin (PG) F2 alpha. The two groups were similar with respect to age, parity, previous abortion, and gestational age. Neither group experienced any unusual complications. The same protocol for intraamniotic PGF2 alpha (40 mg) was used in all patients except for three with histories of asthma, in whom PGE2 vaginal suppositories (20 mg) were used as the induction agent. For the Dilapan group, an average of three devices was used, compared with an average of six in the laminaria group. The mean (+/- SEM) induction-abortion time for Dilapan patients was 10.9 +/- 1.3 hours, compared with 16.1 +/- 1.4 hours in the laminaria group, a statistically significant difference (P less than .05). When nulliparous women were examined separately, the mean times were 11.0 +/- 1.7 for Dilapan and 16.5 +/- 1.6 for laminaria, a medically relevant and statistically significant difference (P less than .05). Dilapan appears to be an effective alternative to laminaria that results in shorter induction-abortion intervals.

    View details for Web of Science ID A1988P381400022

    View details for PubMedID 3292981

  • THE PROPHYLACTIC EFFECT OF DOXYCYCLINE ON POSTOPERATIVE INFECTION-RATE AFTER 1ST-TRIMESTER ABORTION OBSTETRICS AND GYNECOLOGY Blumenthal, P. D., Rosenzweig, B. A. 1988; 72 (1): 146-146

    View details for Web of Science ID A1988P035900034

    View details for PubMedID 3380506

  • PROBLEM VISITS TO A FAMILY-PLANNING CLINIC JOURNAL OF REPRODUCTIVE MEDICINE Blumenthal, P. D., Jacobson, J., Gaffikin, L. 1988; 33 (1): 58-62

    Abstract

    In order to obtain information necessary for optimum delivery of services, data were collected on the nature of the services provided at a family planing clinic. Clinic visits were divided into initial, annual, routine, problem, supply, educational and unknown. An analysis of the "problem" visits was undertaken to assess various epidemiologic aspects of such visits and to identify areas of clinic efficiency that could be improved. Problem visits were defined as any visits for which the patient had a presenting complaint. Age, level of education, method of contraception and parity were statistically associated with problem visits. When compared to Pill users, diaphragm users, intrauterine device users and non-users had a higher-than-expected number of problem visits. Less educated women and teenagers had a lower-than-expected number of problem visits when compared to more educated and older women. Socioeconomic status and problem visits were not statistically associated. Problem visits required more time, utilized more medical services and resulted in more referrals to the gynecology clinic than did other visit types. As a result of this analysis, we have increased our educational efforts for patients at high risk of problem visits and have instituted a special problem-oriented family planning clinic in which a full complement of house staff and ancillary personnel are available. This arrangement makes the uncomplicated family planning clinic run more smoothly and efficiently and obviates the need for time-consuming and cost-ineffective referrals.

    View details for Web of Science ID A1988L778900014

    View details for PubMedID 3351808

  • COMPARISON OF UTERINE ACTIVITY INDUCED BY NIPPLE STIMULATION AND OXYTOCIN OBSTETRICS AND GYNECOLOGY Levy, J., Rosenzweig, B., Blumenthal, P. 1987; 70 (3): 430-431

    View details for Web of Science ID A1987J669700037

    View details for PubMedID 3627596

  • COMPARISON OF URINARY HUMAN FOLLICLE-STIMULATING-HORMONE AND HUMAN MENOPAUSAL GONADOTROPINS FOR OVARIAN STIMULATION IN AN INVITRO FERTILIZATION PROGRAM FERTILITY AND STERILITY Scoccia, B., Blumenthal, P., Wagner, C., Prins, G., Scommegna, A., Marut, E. L. 1987; 48 (3): 446-449

    Abstract

    This report compares the effects of human menopausal gonadotropin (hMG) and purified urinary human follicle-stimulating hormone (hFSH) protocols in patients with irreparable tubal disease as the sole indication for in vitro fertilization-embryo transfer (IVF-ET). The hFSH protocol was associated with significantly more uniform folliculogenesis and more effective steroidogenesis than the one using hMG. In addition, the hFSH protocol showed a trend toward more oocytes per laparoscopy and more embryos per transfer than the hMG group, although the difference was not statistically significant. More oocytes in the hMG group were classified as immature when compared with the hFSH group (P less than 0.05). Pregnancy rates in both groups were not significantly different. An allergic drug reaction that occurred in one patient on the hFSH protocol is the first such reaction reported with hFSH in the literature. The hFSH protocol is associated with a trend toward parameters that correlate with improved success rates in the IVF-ET program.

    View details for Web of Science ID A1987K012300015

    View details for PubMedID 3114011

  • ETHNICITY AND HIP FRACTURE AMERICAN JOURNAL OF PUBLIC HEALTH Blumenthal, P. D., MARUT, E., Gaffikin, L. 1987; 77 (3): 369-369

    View details for Web of Science ID A1987G091400026

    View details for PubMedID 3812850

  • AMNIOINFUSION FOR FETAL DISTRESS AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY Levy, J., Rosenzweig, B., Blumenthal, P. D. 1986; 155 (6): 1361-1361

    View details for Web of Science ID A1986F194500046

    View details for PubMedID 3789047

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