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What works in medication reconciliation: an on-treatment and site analysis of the MARQUIS2 study.
Schnipper, Jeffrey L; Reyes Nieva, Harry; Yoon, Catherine; Mallouk, Meghan; Mixon, Amanda S; Rennke, Stephanie; Chu, Eugene S; Mueller, Stephanie K; Smith, G Randy; Williams, Mark V; Wetterneck, Tosha B; Stein, Jason; Dalal, Anuj K; Labonville, Stephanie; Sridharan, Anirudh; Stolldorf, Deonni P; Orav, Endel John; Gresham, Marcus; Goldstein, Jenna; Platt, Sara; Nyenpan, Christopher Tugbéh; Howell, Eric; Kripalani, Sunil.
Afiliación
  • Schnipper JL; Division of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA jschnipper@bwh.harvard.edu.
  • Reyes Nieva H; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
  • Yoon C; Hospital Medicine Unit, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
  • Mallouk M; Division of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
  • Mixon AS; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
  • Rennke S; Division of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
  • Chu ES; Center for Quality Improvement, Society of Hospital Medicine, Philadelphia, Pennsylvania, USA.
  • Mueller SK; Center for Clinical Quality and Implementation Research, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Smith GR; Geriatric Research, Education, and Clinical Center, Tennessee Valley Healthcare System, Nashville, Tennessee, USA.
  • Williams MV; Section of Hospital Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Wetterneck TB; UCSF Health and Department of Medicine, Division of Hospital Medicine, University of California San Francisco Medical Center, San Francisco, California, USA.
  • Stein J; Parkland Health and Hospital System and Hospital Medicine Service, Department of Internal Medicine, University of Texas Southwestern School of Medicine, Dallas, Texas, USA.
  • Dalal AK; Division of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
  • Labonville S; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
  • Sridharan A; Hospital Medicine Unit, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
  • Stolldorf DP; Division of Hospital Medicine, Northwestern University Feinberg School of Medicine and Northwestern Memorial Hospital, Chicago, Illinois, USA.
  • Orav EJ; Division of Hospital Medicine, Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA.
  • Gresham M; Department of Medicine, Center for Quality and Productivity Improvement, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison College of Engineering, Madison, Wisconsin, USA.
  • Goldstein J; Section of Hospital Medicine, Emory University Hospital and 1Unit, Atlanta, Georgia, USA.
  • Platt S; Division of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
  • Nyenpan CT; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
  • Howell E; Hospital Medicine Unit, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
  • Kripalani S; Department of Pharmacy, Brigham and Women's Hospital, Boston, Massachusetts, USA.
BMJ Qual Saf ; 32(8): 457-469, 2023 08.
Article en En | MEDLINE | ID: mdl-36948542
BACKGROUND: The second Multicenter Medication Reconciliation Quality Improvement Study demonstrated a marked reduction in medication discrepancies per patient. The aim of the current analysis was to determine the association of patient exposure to each system-level intervention and receipt of each patient-level intervention on these results. METHODS: This study was conducted at 17 North American Hospitals, the study period was 18 months per site, and sites typically adopted interventions after 2-5 months of preintervention data collection. We conducted an on-treatment analysis (ie, an evaluation of outcomes based on patient exposure) of system-level interventions, both at the category level and at the individual component level, based on monthly surveys of implementation site leads at each site (response rate 65%). We then conducted a similar analysis of patient-level interventions, as determined by study pharmacist review of documented activities in the medical record. We analysed the association of each intervention on the adjusted number of medication discrepancies per patient in admission and discharge orders, based on a random sample of up to 22 patients per month per site, using mixed-effects Poisson regression with hospital site as a random effect. We then used a generalised linear mixed-effects model (GLMM) decision tree to determine which patient-level interventions explained the most variance in discrepancy rates. RESULTS: Among 4947 patients, patient exposure to seven of the eight system-level component categories was associated with modest but significant reductions in discrepancy rates (adjusted rate ratios (ARR) 0.75-0.97), as were 15 of the 17 individual system-level intervention components, including hiring, reallocating and training personnel to take a best possible medication history (BPMH) and training personnel to perform discharge medication reconciliation and patient counselling. Receipt of five of seven patient-level interventions was independently associated with large reductions in discrepancy rates, including receipt of a BPMH in the emergency department (ED) by a trained clinician (ARR 0.40, 95% CI 0.37 to 0.43), admission medication reconciliation by a trained clinician (ARR 0.57, 95% CI 0.50 to 0.64) and discharge medication reconciliation by a trained clinician (ARR 0.64, 95% CI 0.57 to 0.73). In GLMM decision tree analyses, patients who received both a BPMH in the ED and discharge medication reconciliation by a trained clinician experienced the lowest discrepancy rates (0.08 per medication per patient). CONCLUSION AND RELEVANCE: Patient-level interventions most associated with reductions in discrepancies were receipt of a BPMH of admitted patients in the ED and admission and discharge medication reconciliation by a trained clinician. System-level interventions were associated with modest reduction in discrepancies for the average patient but are likely important to support patient-level interventions and may reach more patients. These findings can be used to help hospitals and health systems prioritise interventions to improve medication safety during care transitions.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Conciliación de Medicamentos / Hospitalización Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: BMJ Qual Saf Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Conciliación de Medicamentos / Hospitalización Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: BMJ Qual Saf Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos