Stanford population-health sciences to add director, research opportunities

The center, under the directorship of Mark Cullen, will offer universitywide research funding, education and access to insurance claims and medical records databases.

Mark Cullen will oversee the Stanford Center for Population Health Sciences.
Norbert von der Groeben

Mark Cullen, MD, cut his teeth on large population data sets in 1997, when he partnered with Alcoa, America’s largest aluminum producer, to research ways to improve its employees’ health. Back then, it took his Yale University-based team five years to create data bridges between the company’s hundreds of thousands of fragmented health, employment, injury and environmental records.

“Our goal was to understand factors that undermine worker health, then to develop prevention and treatment strategies,” said Cullen. “This research led to groundbreaking occupational health reforms, including environmental controls and new strategies to reduce injury and illness. It was eye-opening to discover that other aspects of work and life — not just toxins and bad behavior — conspire to produce positive and negative outcomes. When I witnessed how multidisciplinary teams could unlock knowledge hidden within population data, I was hooked.”

Now Cullen, professor of medicine and chief of the Division of General Medical Disciplines at Stanford, is bringing his experience and enthusiasm to the Stanford Center for Population Health Sciences as its first director.

“Backed by Stanford’s research and computational engines, the Center for Population Health Sciences is poised to harness the power of big data to improve health here and around the world,” said Lloyd Minor, MD, dean of the School of Medicine. “Mark Cullen is the right person to bring together clinicians and researchers in social, biologic and data sciences to meet these challenges.”

The population health science mission

Launched in 2012 by Spectrum, the Stanford Center for Clinical and Translational Research and Education, the center’s mission is to use population-level evidence to improve bedside care and the overall health of society. 

This evidence can come from a variety of sources — electronic medical records, genomic sequences, biospecimen repositories, insurance records, wearable sensors and social and environmental data. The challenge is to create methods to deliver this information to researchers and care providers in relevant and privacy-protected formats.

“This isn’t rocket science, but there were no financial incentives to develop these tools until the Accountable Care Act came along,” said Cullen.

The 2010 Patient Protection and Affordable Care Act includes cost-reduction and quality-improvement incentives that health-care institutions can take advantage of through the wise use of population-health data. There are incentives for hospitals that show improved outcomes for heart failure, pneumonia and surgery. And there are incentives for clinicians and hospitals to set up accountable care organizations to lower annual per-capita growth on health spending and improve health for large populations.

Population-health scientists can be instrumental in creating the tools to more effectively and efficiently help institutions take advantage of these quality-focused incentives, said Cullen.

We want to add intelligence to medical records in the same way that smartphone navigation apps have added real-time traffic alerts and alternate routes.

During the last year, Lorene Nelson, PhD, associate professor of health research and policy and the center’s associate director, helped lay the foundation for the center, engaging more than 200 faculty members in a series of meetings and symposia. With the assistance of Spectrum staff, she also organized a distinguished lecture series to bring new ideas to the Stanford community, launched a website and Twitter feed to foster collaborations, and expanded the pilot grant program.

To date, the center has awarded 26 project teams with grant awards ranging from $20,000 to $50,000. Funded by Spectrum’s Clinical and Translational Science Award from the National Institutes of Health and by Stanford Health Care, many of these projects are focused on developing a “learning health system,” in which clinical data can be linked to external information relevant to patient health, such as neighborhood locations and environmental conditions. Representative projects include:

  • Design of an electronic clinical-decision support system to improve emergency care for children.
  • Development of a personalized medicine practice using genomic data.
  • Methodologies for using Google Street View to assess neighborhoods for population health research.

“Today’s electronic medical records are like MapQuest a decade ago — they provide a snapshot of a chart without much added value,” said Cullen. “We want to add intelligence to medical records in the same way that smartphone navigation apps have added real-time traffic alerts and alternate routes. For example, when an asthmatic child comes to the emergency department, a physician’s dashboard might include information on air quality, viral outbreaks in the patient’s neighborhood and the child’s vaccination record.”

Access to new data and study populations

To better support the efforts of population-health scientists, the center is working on providing centralized access to a variety of U.S. and international health databases. Stanford population scientists say they are particularly excited about the pending acquisition of several large insurance-claims data sets from public and private insurers.

“To understand the complex financial, social and regional incentives that drive health-care delivery in the United States, researchers need easier access to detailed information on what types of services patients are using, where they are accessing these services and how much they cost,” said Kate Bundorf, MBA, MPH, PhD, associate professor of health research and policy. “Developing a large repository of insurance claims will enable Stanford researchers to examine these types of questions.”

Researchers need easier access to detailed information on what types of services patients are using, where they are accessing these services and how much they cost.

The center plans to make these data sets available at very low cost to Stanford trainees and investigators at every level. But even more important, center staff will provide technical support to help users get access to the data needed to answer their research questions. Other data sets the center hopes to make available over time include those from the Google X Baseline Study and Indepth Network.

The Google study is a five-year pilot study in which daily health information is being collected from healthy people in Southern California via a Google-designed web portal and with biometrics devices, such as glucose-measuring contact lenses and activity-measuring accelerometers. The study’s objective is to provide researchers with a comprehensive picture of human health and the transition to disease. Collaborators include the Stanford School of Medicine and Duke University School of Medicine. Baseline studies have just begun.

Indepth Network is a coalition of health and demographic surveillance systems in 23 low- and middle-income countries in Africa and Asia. Negotiations are underway to enable Stanford researchers to initiate collaborative studies on geographically defined groups under regular surveillance by local scientific teams.

In addition to large data sets, the center is developing easier access to clinical, volunteer and demographically segmented study populations. As with the databases, center staff will work with investigators to identify and facilitate connections with population groups that could be of importance to their research.

Nationwide clinical data access

Population-health researchers can also look forward to enhancements to STRIDE, the Stanford Translational Research Integrated Data Environment, a comprehensive warehouse of de-identified clinical notes, diagnoses and prescriptions for nearly 2 million patients treated since 1994 at Stanford Hospital & Clinics, now called Stanford Health Care, and Lucile Packard Children’s Hospital Stanford.

The center is poised to take the next step in becoming the hub for research and educational activities related to population health across the university.

Michael Halaas, chief information officer for the School of Medicine, has led the effort, initiated by Spectrum and other member institutions in the CTSA consortium, to connect STRIDE to a nationwide, scalable informatics framework called i2b2. When this project is complete, Stanford researchers will be able to access anonymized clinical data from participating health-care systems around the country for research and clinical trial recruitment.

The i2b2 framework is based on the Research Patient Data Registry developed at Massachusetts General Hospital. It has a number of advantages, including extensive testing by the Boston-based Partners Health System and Harvard faculty; an easily understood database schema; release under an open-source license; an organized user group for sharing information and applications; and the capacity to share translational research data with collaborators across other i2b2 institutions.

“I couldn’t be more pleased with the tremendous progress that all the faculty who have worked on this initiative have made over the last two years,” said Harry Greenberg, MD, senior associate dean of research for the medical school and director of Spectrum. “With the appointment of Mark Cullen, the center is poised to take the next step in becoming the hub for research and educational activities related to population health across the university. Perhaps most exciting to me, with all the marvelous talent we have at Stanford, we will be able to provide much-needed guidance to investigators, clinicians and policymakers concerning the very difficult task of drawing accurate inferential conclusions from the great wealth of new data now available at our fingertips. This data has the potential to improve the health and well-being of local, national and even global populations.”

The Stanford Center for Population Health Sciences is supported by Spectrum, which is funded by the National Center for Advancing Translational Sciences at the NIH; Stanford Health Care; the dean’s office; and various clinical departments. Under the umbrella of Stanford’s Biomedical Data Science Initiative, this funding aims to help fuel transformations in human health and scientific discovery by fostering innovative collaborations among medical researchers, computer scientists, statisticians and physicians.


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