Following the Patient
Every year, more than 35 million patients walk through the doors of hospitals and clinics with questions about their health and about their care. Questions range from medication dosing to treatment expectations to paying the bill. Every question is equally important to patients, and to those who love them. At the DCRI, finding answers to those questions is a commitment we’re making through our Health Services Research efforts. Because a significant part of improving outcomes is improving what patients know.
- BRISC—Behavioral Research Intervention Science Center
- Comparative Effectiveness Studies
- Disease Registries
- Evidence Synthesis
- Health Economics
- Health Policy Hub
- Patient-Reported Outcomes
- Pragmatic Health Systems Research
- Preference Evaluation Research (PrefER) Group
- Quality Improvement
Our Research is Focused on Three Critical Areas
Assessing Population Health
Who are the patients and what are their experiences?
- Pharmaco-epidemiology
- Population studies
- Quality of care
- Existing registries
Researching Clinical Care and Outcomes
Are patients getting the right treatment, at the right time, for the right outcomes?
- Clinical effectiveness research (CER)
- Drug and device safety
- Mobile health
- Medical decision making
- Informed health decisions
- Patient-reported outcomes
Changing Care
How do we fundamentally change
clinical practice?
- Quality improvement
- Shared decision making
- Decision modeling
- Health economics
- Health policy
- DCRI Education
- Evidence synthesis
DCRI Health Services Research by the Numbers
Our commitment is evidenced by the number of resources we can access to find the answers that will improve patient care.
- 10 million+ patients in outcomes studies
- 3,000+ publications in the past 10 years
- Millions of patients enrolled in DCRI-created registries
- 50+ clinical and statistical faculty
- 150+ full-time employees