دورية أكاديمية

Development of the individualised Comparative Effectiveness of Models Optimizing Patient Safety and Resident Education (iCOMPARE) trial: a protocol summary of a national cluster-randomised trial of resident duty hour policies in internal medicine

التفاصيل البيبلوغرافية
العنوان: Development of the individualised Comparative Effectiveness of Models Optimizing Patient Safety and Resident Education (iCOMPARE) trial: a protocol summary of a national cluster-randomised trial of resident duty hour policies in internal medicine
المؤلفون: Shea, Judy A, Silber, Jeffrey H, Desai, Sanjay V, Dinges, David F, Bellini, Lisa M, Tonascia, James, Sternberg, Alice L, Small, Dylan S, Shade, David M, Katz, Joel Thorp, Basner, Mathias, Chaiyachati, Krisda H, Even-Shoshan, Orit, Bates, David Westfall, Volpp, Kevin G, Asch, David A, the iCOMPARE Research Group
بيانات النشر: BMJ Publishing Group Ltd
سنة النشر: 2018
المجموعة: HighWire Press (Stanford University)
مصطلحات موضوعية: Protocol
الوصف: Introduction Medical trainees’ duty hours have received attention globally; restrictions in Europe, New Zealand and some Canadian provinces are much lower than the 80 hours per week enforced in USA. In USA, resident duty hours have been implemented without evidence simultaneously reflecting competing concerns about patient safety and physician education. The objective is to prospectively evaluate the implications of alternative resident duty hour rules for patient safety, trainee education and intern sleep and alertness. Methods and analysis 63 US internal medicine training programmes were randomly assigned 1:1 to the 2011 Accreditation Council for Graduate Medical Education resident duty hour rules or to rules more flexible in intern shift length and number of hours off between shifts for academic year 2015–2016. The primary outcome is calculated for each programme as the difference in 30-day mortality rate among Medicare beneficiaries with any of several prespecified principal diagnoses in the intervention year minus 30-day mortality in the preintervention year among Medicare beneficiaries with any of several prespecified principal diagnoses. Additional safety outcomes include readmission rates, prolonged length of stay and costs. Measures derived from trainees’ and faculty responses to surveys and from time-motion studies of interns compare the educational experiences of residents. Measures derived from wrist actigraphy, subjective ratings and psychomotor vigilance testing compare the sleep and alertness of interns. Differences between duty hour groups in outcomes will be assessed by intention-to-treat analyses. Ethics and dissemination The University of Pennsylvania Institutional Review Board (IRB) approved the protocol and served as the IRB of record for 40 programmes that agreed to sign an Institutional Affiliation Agreement. Twenty-three programmes opted for a local review process. Trial registration number NCT02274818 ; Pre-results.
نوع الوثيقة: text
وصف الملف: text/html
اللغة: English
العلاقة: http://bmjopen.bmj.com/cgi/content/short/8/9/e021711Test; http://dx.doi.org/10.1136/bmjopen-2018-021711Test
DOI: 10.1136/bmjopen-2018-021711
الإتاحة: https://doi.org/10.1136/bmjopen-2018-021711Test
http://bmjopen.bmj.com/cgi/content/short/8/9/e021711Test
حقوق: Copyright (C) 2018, British Medical Journal Publishing Group
رقم الانضمام: edsbas.17517AAD
قاعدة البيانات: BASE