1. Patient Safety Outcomes under Flexible and Standard Resident Duty-Hour Rules
- Author
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Mathias Basner, Richard N. Ross, Joel T. Katz, Kevin G. Volpp, James Tonascia, David A. Asch, Jeffrey H. Silber, Orit Even-Shoshan, Alice L. Sternberg, Lauren L. Hochman, Judy A. Shea, David M. Shade, Lisa M. Bellini, Sanjay V. Desai, David F. Dinges, Alexander S. Hill, and Dylan S. Small
- Subjects
medicine.medical_specialty ,Urology ,media_common.quotation_subject ,MEDLINE ,Workload ,Hospital mortality ,030204 cardiovascular system & hematology ,Affect (psychology) ,Article ,law.invention ,03 medical and health sciences ,Patient safety ,0302 clinical medicine ,Randomized controlled trial ,law ,Humans ,Medicine ,030212 general & internal medicine ,Duty ,media_common ,business.industry ,Internship and Residency ,General Medicine ,medicine.disease ,Equivalence Trial ,Multicenter study ,Emergency medicine ,Medical emergency ,Patient Safety ,business - Abstract
BACKGROUND: Concern persists that extended shifts in medical residency programs may adversely affect patient safety. METHODS: We conducted a cluster-randomized noninferiority trial in 63 internal-medicine residency programs during the 2015–2016 academic year. Programs underwent randomization to a group with standard duty hours, as adopted by the Accreditation Council for Graduate Medical Education (ACGME) in July 2011, or to a group with more flexible duty-hour rules that did not specify limits on shift length or mandatory time off between shifts. The primary outcome for each program was the change in unadjusted 30-day mortality from the pretrial year to the trial year, as ascertained from Medicare claims. We hypothesized that the change in 30-day mortality in the flexible programs would not be worse than the change in the standard programs (difference-in-difference analysis) by more than 1 percentage point (noninferiority margin). Secondary outcomes were changes in five other patient safety measures and risk-adjusted outcomes for all measures. RESULTS: The change in 30-day mortality (primary outcome) among the patients in the flexible programs (12.5% in the trial year vs. 12.6% in the pretrial year) was noninferior to that in the standard programs (12.2% in the trial year vs. 12.7% in the pretrial year). The test for noninferiority was significant (P = 0.03), with an estimate of the upper limit of the one-sided 95% confidence interval (0.93%) for a between-group difference in the change in mortality that was less than the prespecified noninferiority margin of 1 percentage point. Differences in changes between the flexible programs and the standard programs in the unadjusted rate of readmission at 7 days, patient safety indicators, and Medicare payments were also below 1 percentage point; the noninferiority criterion was not met for 30-day readmissions or prolonged length of hospital stay. Risk-adjusted measures generally showed similar findings. CONCLUSIONS: Allowing program directors flexibility in adjusting duty-hour schedules for trainees did not adversely affect 30-day mortality or several other measured outcomes of patient safety. (Funded by the National Heart, Lung, and Blood Institute and Accreditation Council for Graduate Medical Education; iCOMPARE ClinicalTrials.gov number, NCT02274818.)
- Published
- 2019