Position & Affiliation:
Education:
-
BS Biology, 1985, Stanford
University
-
MD, 1990, Stanford
University School of Medicine
-
Primary Care Internal Medicine Residency, Massachussetts
General Hospital, 1990-1993
-
Fellow, Ambulatory
Care Practice and Research, Palo Alto VA Health Care System,
1993-1996
-
PhD, 1998, Medical
Informatics, Stanford University
Awards:
Research Interests:
-
Informatics for clinical research
-
Clinical trial registration and publication into
structured knowledge bases (trial banks)
-
Decision support systems for evidence-based practice
-
Economics of health information technology
My broad research objective is to define and build
foundational informatics systems for clinical trial research and
reporting that will enable a new generation of
clinical decision support systems for evidence-based practice.
My work has four major inter-related parts:
-
Understanding the
information needs of rigorous evidence-based reasoning.
Randomized
clinical trials (RCTs) are one of the least biased and most
valuable sources of evidence for improving clinical care. To better
understand
how RCT evidence is appraised and combined, I
have conducted meta-analyses of RCTs using hierarchical Bayes and
meta-regression methods. I also defined the first formal
definition of the gap between evidence and practice, and proposed a
new measure (the Number Not Prevented, NNP) to quantify it (SMDM Best
Paper by a Young
Investigator, 2004). This work contributes to detailing the nature of
computer-based
decision support that is required to promote best practices in
evidence-based medicine.
-
Developing new informatics for clinical research.
Informatics is the use of computation to understand and manage
complexity. The
complexity of clinical research is rapidly exploding with the advent of
translational methods and opportunities. My lab focuses on clinical
trial informatics in the broader context of clinical and translational
research. My Trial Bank
Project continues to define the fundamental informatics
science of trial banks:
computable knowledge bases of clinical trials that will enable more
powerful decision support for evidence-based practice and trial quality
assessment. Trial banks contain all the trial
information needed for systematic reviewing and evidence-based
reasoning
(i.e., the trial’s design, execution, and summary results). We are
integrating trial banks with the Electronic
Primary Care Research Network, a national computing infrastructure
for distributed primary care
research. We are also driving the development of fundamental
technologies for biomedical knowledge management through our
participation as a Driving Biological
Project of the National Center for
Biomedical Ontology.
-
Promoting universal trial
registration and trial reporting into computable "trial banks." Several
recent cases of companies withholding negative clinical trial results
have galvanized the movement towards universal trial registration
and results reporting. As the founding Project Coordinator of the World
Health Organization's International
Clinical Trials Registry Platform project from 2005-6, I advance
the science, policy, and informatics of a global system for
clinical trial registration and reporting.
Through the Trial Bank
Project, we are working with research funders, major medical
journals, and trial registers to explore fundamental research issues in
capturing and reporting trials through trial-bank reporting, in which
randomized trials are published as both a journal article and as an
entry into a trial bank. Complementing our research in the Trial Bank
Project is Global Trial Bank,
an AMIA project that is developing an operational implementation of the
trial bank concept.
-
Understanding the
socio-technical and economic barriers to use of health information
technologies. Despite their much ballyhooed promise, electronic
medical records (EHRs) and CDSSs are not widely used. I have been
investigating with Robert Miller the organizational and economic
factors
contributing to this limited uptake. In addition, we have defined a
comprehensive taxonomy of CDSS design and usage for understanding
heterogeneity among CDSSs.
These projects contribute to a greater understanding of
both
the technical and non-technical challenges of providing computer-based
decision support for clinical research and for closing proof to
practice gaps.
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