Evidence map›Paper›PMID 36948542›Full record

ArticleBMJ quality & safety2023

What works in medication reconciliation: an on-treatment and site analysis of the MARQUIS2 study.

Jeffrey L Schnipper, Harry Reyes Nieva, Catherine Yoon, Meghan Mallouk, Amanda S Mixon, Stephanie Rennke, Eugene S Chu, Stephanie K Mueller, G Randy Smith, Mark V Williams and 15 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in BMJ quality & safety, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Observational
  5. Observational
  6. Article
  7. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 13 institutions in 1 country.

Jeffrey L SchnipperDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA jschnipper@bwh.harvard.edu.ORCID 0000-0001-7072-0781
Harry Reyes NievaDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.ORCID 0000-0001-7774-2561
Catherine YoonDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
Meghan MalloukCenter for Quality Improvement, Society of Hospital Medicine, Philadelphia, Pennsylvania, USA.
Amanda S MixonCenter for Clinical Quality and Implementation Research, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Stephanie RennkeUCSF Health and Department of Medicine, Division of Hospital Medicine, University of California San Francisco Medical Center, San Francisco, California, USA.
Eugene S ChuParkland Health and Hospital System and Hospital Medicine Service, Department of Internal Medicine, University of Texas Southwestern School of Medicine, Dallas, Texas, USA.
Stephanie K MuellerDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
G Randy SmithDivision of Hospital Medicine, Northwestern University Feinberg School of Medicine and Northwestern Memorial Hospital, Chicago, Illinois, USA.ORCID 0000-0002-1296-4881
Mark V WilliamsDivision of Hospital Medicine, Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA.
Tosha B WetterneckDepartment 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.
Jason SteinSection of Hospital Medicine, Emory University Hospital and 1Unit, Atlanta, Georgia, USA.
Anuj K DalalDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.ORCID 0000-0003-1431-2972
Stephanie LabonvilleDepartment of Pharmacy, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Anirudh SridharanDepartment of Medicine, Howard County General Hospital, Columbia, Maryland, USA.
Deonni P StolldorfGeriatric Research, Education, and Clinical Center, Tennessee Valley Healthcare System, Nashville, Tennessee, USA.ORCID 0000-0002-1352-5397
Endel John OravDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
Marcus GreshamDivision of General Internal Medicine and Primary Care, Brigham and Women's Hospital Department of Medicine, Boston, Massachusetts, USA.
Jenna GoldsteinCenter for Quality Improvement, Society of Hospital Medicine, Philadelphia, Pennsylvania, USA.
Sara PlattCenter for Quality Improvement, Society of Hospital Medicine, Philadelphia, Pennsylvania, USA.
Christopher Tugbéh NyenpanCenter for Quality Improvement, Society of Hospital Medicine, Philadelphia, Pennsylvania, USA.
Eric HowellDivision of Hospital Medicine, Johns Hopkins Bayview Medical Center, Baltimore, Maryland, USA.
Sunil KripalaniCenter for Clinical Quality and Implementation Research, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID 0000-0002-4214-7129
MARQUIS2 Site Leaders for the MARQUIS2 Study Group
MARQUIS2 Site Leaders
Brigham and Women's Hospital · USSociety of Critical Care Medicine · USEmory University Hospital · USHoward County General Hospital · USJohns Hopkins University · USNorthwestern University · USParkland Health & Hospital System · USSaint Louis University Hospital · USUniversity of California San Francisco Medical Center · USUniversity of Wisconsin–Madison · USVanderbilt University · USVanderbilt University Medical Center · USVA Tennessee Valley Healthcare System · US

Funding

Implementation of a Medication Reconciliation Toolkit to Improve Patient SafetyR18HS023757 · AHRQ · BRIGHAM AND WOMEN'S HOSPITAL · PI SCHNIPPER, JEFFREY LAWRENCE · 2015 to 2017
$1.5M
AHRQ HHS R18 HS023757
6 · The paper itself

Abstract

backgroundThe 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.

methodsThis 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.

resultsAmong 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.

Indexed as

HospitalizationMedication ReconciliationHospitalsHumansPatient DischargePatient TransferPharmacistsmedication reconciliationmedication safetypharmacistsquality improvement

Identifiers

PMID36948542
PMCPMC11046420
OpenAlexW4353057815

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.