DOCSLIB.ORG

Large Scale Implementation of a Medicines Reconciliation Care Bundle in NHS GGC GP Practices

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Large Scale Implementation of a Medicines Reconciliation Care Bundle in NHS GGC GP Practices Downloaded from http://qir.bmj.com/ on November 10, 2016 - Published by group.bmj.com Open Access BMJ Quality Improvement Programme Large scale implementation of a medicines reconciliation care bundle in NHS GGC GP practices Rachel Bruce To cite: Bruce R. Large scale ABSTRACT The Scottish Patient Safety Programme implementation of a Medicines reconciliation (MR) is an essential process (SPSP) is a unique national initiative that medicines reconciliation care for patient safety, promoting safer use of medicines aims to improve the safety and reliability of bundle in NHS GGC GP with effective communication at the interface, practices. BMJ Quality healthcare and reduce harm, whenever care Improvement Reports particularly when patients are admitted and discharged is delivered. One of the aims within SPSP is from hospital. Much of the work on MR has been 2016;5:u212988.w6116. to reduce the number of adverse events focussed in secondary care, however, the principles are doi:10.1136/bmjquality. causing avoidable harm to patients through u212988.w6116 equally important in primary care. The aim of the work was to test the Scottish Patient Safety in Primary Care safer use of medicines. Medicines reconcili- (SPSP-PC) MR care bundle and consider scale up and ation (MR) has been a focus of the Acute spread across all NHS Greater Glasgow and Clyde Adult Scottish Patient Safety Programme for Received 9 August 2016 fi Revised 22 September 2016 (NHS GGC) GP practices. Care bundles are a quality several years. It was identi ed nationally that Published Online First improvement tool which can drive improvement by MR is also a key feature in primary care and 31 October 2016 standardising processes to deliver optimum care. Pilot a focus on the MR process in both acute and work and testing began with 5 GP practices in 2011 primary care has safety benefits for both and and was spread to over 200 practices by 2015/16. A most importantly, patients. Safer medicines care bundle compliance process measure was management across the interface is a core measured monthly, with practices sampling 10 patients programme work stream to encourage devel- per month. Practices could view their run charts in real time and identify which measures resulted in “non- opment and implementation of reliable safe compliance” and PDSA cycles were promoted to test systems for reconciling medicines in GP prac- and implement improvements. Data was collated at tices following discharge from hospital. A NHS GGC level with an aim of 95% compliance with robust standardised approach to MR in GP the care bundle by March 2016. MR care bundle practice on discharge should improve the GP compliance started at 40% (5 practices reporting) in prescribing record and therefore the 2011 with final data in March 2016 demonstrating Emergency Care Summary (ECS) that is 92% compliance (192 practices reporting). A sustained extracted from GP systems and used as the “ ” reliability of 92-93% across >200 practices has been basis for MR on admission to hospital. Local observed since January 2015. In conclusion, the data identified that this was only correct bundle was implemented by 97% of NHS GGC GP around 50% of the time. There was a practices and resulted in process improvements. national care bundle in development for MR which had been piloted in another Health Board but not been adopted or tested in PROBLEM NHS GGC GP practices. Practices acknowl- Scotland has a population of approximately edged that MR is an important area of 5.3 million and healthcare is provided by the patient safety but none could demonstrate National Health Service and delivered across they had a standard process in place. To 14 territorial health boards. NHS Greater determine if there was a problem five prac- Glasgow and Clyde (NHS GGC) is the largest tices agreed to participate in a pilot project health board providing care to a population to test and measure the MR care bundle.1 of ~1.2 million and has ~135,000 emergency Run chart data and practice visits identified admissions per year. There are currently 242 that their processes were not as robust as GP practices across NHS GGC with a primary they had anticipated and they were not stan- NHS GGC, Scotland care prescribing budget of ~£242 million. dardised across the whole practice team. The Correspondence to 101 million prescription items are dispensed main aim of the project was to develop, test Rachel Bruce annually and 59% of over 70 year olds and implement at scale an MR care bundle [email protected] receive 5 or more medicines. focussing on process reliability which was Bruce R. BMJ Quality Improvement Reports 2016;5:u212988.w6116. doi:10.1136/bmjquality.u212988.w6116 1 Downloaded from http://qir.bmj.com/ on November 10, 2016 - Published by group.bmj.com Open Access defined as 95% compliance with the MR care bundle in improvement work was to test a recognised SPSP care general practice across participating NHS GGC GP prac- bundle at small scale for consideration of implementa- tices by March 2016. Secondary aims to indicate tion and spread across a large organisation. Following improved outcomes were defined as an improvement in testing, large scale implementation and spread was the accuracy of ECS on admission and a reduction in carried out in 2013, with 242 GP practices in NHS GGC readmissions within 30 days for patients aged over 65. participating. This is the largest scale MR programme in GP practice and was the first of it’s kind in Scotland in terms of measurement and spread. BACKGROUND Taking a medicine is the most common intervention BASELINE MEASUREMENT patients use to improve their health. Older people and At the outset of the project it was not possible to deter- those with long term conditions often take multiple mine how well MR was done as this data was not rou- medicines (polypharmacy) to treat and manage their ill- tinely collected as part of routine general practice. nesses. Evidence shows that there is a greater risk of Practices anecdotally felt they had good processes in error and potential harm from medicines when patients place but had no robust measurement strategy to move between care settings, resulting in 30-70% of support this. The SPSP PC MR care bundle sought to patients having an error or unintentional change in address this. their medication when their care is transferred.2 Five practices initially applied the care bundle to all Incidents of avoidable harm to patients can result in their discharges and randomly sampled ten patients per unnecessary readmissions, with an estimated 72% of month for compliance with the care bundle over 12 adverse events after discharge due to medications3 and months - this provided baseline results. Sampling was 38% of readmissions considered to be medicines related done by identifying all patients who had been dis- (61% of these preventable).4 Apart from the clear charged that month and randomly selecting 10. From patient safety risks there are also implications for profes- this the pilot practices could see month on month their sionals with 19.3% of GP negligence claims relating to results and it was aggregated up to give a collated overall prescribing and medication (3.8% of which were due to picture for all 5 practices. The 12 month baseline data supplying incorrect or inappropriate medication).5 and median value of 64% can be seen in supplementary Medicines reconciliation is an essential component of file “MR compliance baseline data”. patient safety promoting safer use of medicines with Individual practice visits were carried out to determine effective communication when patients move between if they felt the process was beneficial, establish what they care settings and is particularly important when patients had learned and what improvements they had made are admitted and discharged from hospital. There is evi- using PDSA. Consensus was sought in whether it was dence that this process does not happen reliably67with worthwhile to scale up and spread. local audits conducted in NHSGG&C reporting just over half of patients admitted in one hospital had one or more of their usual medicines unintentionally omitted DESIGN from their prescription chart.8 60% of patients had Run chart data and practice feedback (including PDSA medication discrepancies on discharge, specifically relat- cycles) demonstrated there was room for improvement ing to medicines that had been started and/or stopped and using the established SPSP PC national MR care during the admission.910 bundle was an efficient way to measure MR process reli- A robust reliable process for carrying out timely medi- ability. Practices reported it was an effective QI tool to cines reconciliation in general practice post hospital dis- improve MR in the practice and it would be appropriate charge ensures the GP prescribing record is current and to consider for NHS GGC roll out. A wider stakeholder accurate. This in turn improves the accuracy of the consultation took place with SPSP programme leads, Emergency Care Summary (ECS). The ECS is a clinical directors, the local medical committee (LMC) summary of basic important information about a patient and the pharmacy and prescribing support unit (PPSU) including a list of current medication which is extracted to explore and agree options for spread. The anticipated from the GP systems twice a day. The ECS is often used problems at this stage were around potential funding for as a source of information used to carry out medicines the work and GP acceptability for this care bundle to reconciliation on admission to hospital. Inaccurate or improve MR processes. As the care bundle was a recog- incomplete medicines reconciliation in primary care will nised national intervention tool and had tested positively result in an inaccurate GP prescribing record and there- in a small number of practices, the final care bundle fore a flawed ECS for any medicines reconciliation on design was not changed, and after multiple stakeholder admission with the potential for medication errors, agreement it was planned to offer this out as an optional patient harm and readmission.
Load more

Recommended publications
  • Medication Reconciliation: Barriers and Facilitators from the Perspectives of Resident Physicians and Pharmacists
    ORIGINAL RESEARCH Medication Reconciliation: Barriers and Facilitators from the Perspectives of Resident Physicians and Pharmacists Kenneth S. Boockvar, MD, MS1,2,3, Susan L. Santos, PhD4,5, Andre Kushniruk, PhD6, Christopher Johnson, PhD7,8, Jonathan R. Nebeker, MD9 1Geriatrics Research, Education, and Clinical Center, James J. Peters Veterans Affairs Medical Center, Bronx, New York; 2Department of Geriatrics and Palliative Medicine, Mount Sinai School of Medicine, New York, New York; 3Jewish Home Lifecare, New York, New York; 4VA New Jersey Health Care System, East Orange, New Jersey; 5Department of Health Education and Behavioral Science, University of Medicine and Dentistry of New Jersey, New Brunswick, New Jersey; 6School of Health Information Science, University of Victoria, Victoria, British Columbia, Canada; 7Department of Health Policy and Management, Texas A&M Health Science Center, College Station, Texas; 8VA South Central Mental Illness Research, Education, and Clinical Center, and Houston Center for Quality of Care and Utilization Studies, Michael E. Debakey VA Medical Center, Houston, Texas; 9VA Geriatrics Research, Education, and Clinical Center, and University of Utah, Salt Lake City, Utah BACKGROUND: Medication reconciliation can prevent barriers and facilitators. Interviews were recorded and medication errors and harm when patients transition analyzed using social science methods for analyzing between hospital and other care settings. Though a Joint qualitative data. Commission hospital Patient Safety Goal since 2006, RESULTS: Participants agreed that a central goal of organizations continue to have difficulty implementing the medication reconciliation is to prevent prescribing errors, process. but disagreed about whether it achieves this goal. OBJECTIVE: To determine factors that influence performance Computerization facilitated the task, but participants said of medication reconciliation in a hospital setting with a that computers and patients can be unreliable sources of computerized medication reconciliation tool.
    [Show full text]
  • Wales Multidisciplinary Medicines Reconciliation Policy
    All Wales Multidisciplinary Medicines Reconciliation Policy June 2017 This document has been prepared by the Quality and Patient Safety Delivery Group of the All Wales Chief Pharmacists Group, with support from the All Wales Prescribing Advisory Group (AWPAG) and the All Wales Therapeutics and Toxicology Centre (AWTTC), and has subsequently been endorsed by the All Wales Medicines Strategy Group (AWMSG). Please direct any queries to AWTTC: All Wales Therapeutics and Toxicology Centre University Hospital Llandough Penlan Road Llandough Vale of Glamorgan CF64 2XX [email protected] 029 2071 6900 This document should be cited as: All Wales Medicines Strategy Group, All Wales Multidisciplinary Medicines Reconciliation Policy. June 2017. All Wales Multidisciplinary Medicines Reconciliation Policy CONTENTS 1.0 INTRODUCTION ................................................................................................ 2 2.0 PURPOSE .......................................................................................................... 2 3.0 SCOPE ............................................................................................................... 2 4.0 ROLES AND RESPONSIBILITIES ...................................................................... 3 5.0 MEDICINES RECONCILIATION PROCESS....................................................... 4 6.0 REFERENCES ................................................................................................... 5 APPENDIX 1: GOOD PRACTICE GUIDE WHEN TAKING A MEDICATION HISTORY FROM A
    [Show full text]
  • Medicines Reconciliation Protocol
    Medicines Reconciliation Protocol Version 2 RATIFYING COMMITTEE Drugs and Therapeutics Group DATE RATIFIED May 2021 NEXT REVIEW DATE May 2024 EXECUTIVE SPONSOR Chief Medical Officer POLICY AUTHORS Principal Pharmacists Deputy Chief Pharmacist Specialist Pharmacy Technicians Executive Summary: • This protocol outlines the requirements and process relating to medicines reconciliation within the Trust. • Includes staffing skill mix, information sources to be used and documentation standards. • Identifies specific areas and medicines to be given further consideration. If you require this document in an alternative format, i.e. easy read, large text, audio, Braille or a community language please contact the pharmacy team on 01243 623349 (Text Relay calls welcome) CONTENTS Page 1. Introduction 3 2. Scope 3 3. Definition 3 4. Duties and responsibilities 4-5 5. Medicines reconciliation process 6-9 6. Standards 11 7. Training 11 8. Monitoring compliance 11 Appendix 1 Medicines reconciliation template 12 Appendix 2 Medicines reconciliation flowchart 13 Appendix 3 Summary Care Record (SCR) process 14 Appendix 4 Summary Care Record (SCR) flowchart 15 Page 2 of 14 1. Introduction 1.1. Medicines reconciliation (MR) is the process by which medicines prescribed for patients on admission, corresponds to the medicines they were taking before admission, unless there is clear clinical justification for changing or discontinuing a medicine. 1.2. Historically, medicines reconciliation was performed by junior doctors on admission as part of the clerking process. In 2007, NICE and NPSA issued joint guidance highlighting the risks associated with medication prescribed on admission, with an unintentional error rate of 30-70% reported. POMH-UK shows that the Trust’s doctors undertake a drug history in 84% of patients but only find 4% discrepancies in those patients.
    [Show full text]
  • Medicines Reconciliation in Hospital
    Medicines Reconciliation In Hospital Author(s) Dr A MacLaren on behalf of NHSGG&C Medicines Reconciliation Oversight Group Responsible Dr D Stewart, Lead Director for Acute Medical Services Director(s) Prof. Norman Lannigan, Head of Pharmacy & Prescribing Support Unit Approved by Acute Division Clinical Governance Forum Date Approved March 2015 Date of Review March 2018 1 1. Introduction Medicines are the most common intervention in the NHS and their safe use requires collective and collaborative effort between the multidisciplinary team and patients. Medicines reconciliation is a key step to ensuring that patients are prescribed the correct medicines, in the correct doses appropriate to their current clinical presentation and that avoidable harm from medicines is reduced. Accurate, timely medicines reconciliation on admission to, and discharge from, hospital is an integral part of clinical care and takes time to complete. The Scottish Government Chief Medical Officer letter (SGHD/CMO(2013)18)1 sets out the national definition, goals, measures and best practice for medicines reconciliation as part of the Scottish Patient Safety Programme. NHSGG&C is required to implement this guidance and demonstrate compliance through monitoring. 2. Aims of Policy The policy aims to describe: • how medicines reconciliation is undertaken and documented within NHSGG&C • the roles and responsibilities of staff associated with the process • monitoring and reporting arrangements regarding policy compliance 3. Scope This policy applies to all clinical areas within the hospital environment which admit and discharge in- patients and to all NHSGG&C employees working within these areas. 4. Responsibilities Management and the multidisciplinary clinical team have a collective responsibility to ensure medicines reconciliation is reliably completed for each patient.
    [Show full text]
  • Methodology Report Medication Reconciliation on Admission
    Methodology Report Medication Reconciliation on Admission Version 1.1 Current as of : August 16, 2017 IPF Outcome and Process Measure Development and Maintenance Project PREPARED FOR THE CENTERS FOR MEDICARE & MEDICAID SERVICES (CMS) BY HEALTH SERVICES ADVISORY GROUP, INC. (HSAG) Almut G. Winterstein, RPh, PhD, FISPE1,2 Xinyue Liu, Ph.D1 Nakyung Jeon, MPH, PhD1 Marie C. Hall, RN Megan Keenan, MPH Patti McKay, BA Ben Staley, PharmD, BCPS1,3 Kimberly Smuk, BS, RHIA Brianne Stanback, PhD Kristen Turner, MS Suzanne Wright, MS Tsu-Hsuan “Sherry” Yang, PharmD Regina Bussing, MD, MS4 Kyle Campbell, PharmD ACKNOWLEDGEMENTS The Measure Developer would like to thank the members of the Medication Reconciliation Workgroup and the Inpatient Psychiatric Facility Measure Development and Maintenance Technical Expert Panels (TEP) from 2015- 2016 and 2016-2017, who provided important insight and feedback during measure development and testing. MEDICATION RECONCILIATION WORKGROUP Workgroup Members from the TEP Kathleen Delaney, PhD, PMH-NP, RN Jonathan Delman, PhD, JD, MPH Irene Ortiz, MD, MSW Elvira Ryan, MBA, BSN, RN Lisa Shea, MD Workgroup Members from the University of Florida Regina Bussing, MD Michael Shapiro, MD Ben Staley, PharmD, BCPS Gigi Lipori, MBA Carl Henricksen, MS Xinyue Liu, Ph.D Nakyung Jeon, MPH, PhD Almut Winterstein, RPh, PhD, FISPE 1 Department of Pharmaceutical Outcomes and Policy, University of Florida 2 Department of Epidemiology, University of Florida 3 Department of Pharmacy, UF Health Shands Hospital 4 Department of Psychiatry,
    [Show full text]
  • Implementation Guide. Assuring Medication Accuracy at Transitions
    The High 5s Project Medication Reconciliation Implementation Guide Page 1 of 78 Implementation Guide Assuring Medication Accuracy at Transitions in Care Attribution Statement This work was carried out as part of the High 5s Project set up by the World Health Organization in 2007 and coordinated globally by the WHO Collaborating Centre for Patient Safety, The Joint Commission in the United States of America, with the participation of the following Lead Technical Agencies including: Australian Commission on Safety and Quality in Health Care, Australia; Canadian Patient Safety Institute, Canada and the Institute for Safe Medication Practices Canada, Canada; National Authority for Health- HAS, France, with CEPPRAL (Coordination pour L’ Evaluation des pratiques professionnelles en santé en Rhône-Alpes), France, OMEDIT Aquitaine (Observatoire du Medicament, Dispositifs medicaux et Innovation Therapeutique), France (from 2012- 2015) and EVALOR (EVAluation LORraine), France (from 2009-2011); German Agency for Quality in Medicine, Germany and the German Coalition for Patient Safety, Germany; CBO Dutch Institute for Healthcare Improvement, the Netherlands; Singapore Ministry of Health, Singapore; Trinidad and Tobago Ministry of Health, Trinidad & Tobago; Former National Patient Safety Agency, United Kingdom of Great Britain and Northern Ireland; and the Agency for Healthcare Research and Quality, USA. This work is a part of the High 5s Project which has been supported by the Agency for Healthcare Research and Quality, USA, WHO, and the Commonwealth
    [Show full text]
  • Medication Safety in Transitions of Care
    Medication Safety in Transitions of Care Technical Report Medication Safety in Transitions of Care Technical Report WHO/UHC/SDS/2019.9 © World Health Organization 2019 Some rights reserved. This work is available under the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 IGO licence (CC BY-NC-SA 3.0 IGO; https://creativecommons.org/licenses/by-nc-sa/3.0/igo). Under the terms of this licence, you may copy, redistribute and adapt the work for non-commercial purposes, provided the work is appropriately cited, as indicated below. In any use of this work, there should be no suggestion that WHO endorses any specific organization, products or services. The use of the WHO logo is not permitted. If you adapt the work, then you must license your work under the same or equivalent Creative Commons licence. If you create a translation of this work, you should add the following disclaimer along with the suggested citation: “This translation was not created by the World Health Organization (WHO). WHO is not responsible for the content or accuracy of this translation. The original English edition shall be the binding and authentic edition”. Any mediation relating to disputes arising under the licence shall be conducted in accordance with the mediation rules of the World Intellectual Property Organization (http://www.wipo.int/amc/en/mediation/rules). Suggested citation. Medication Safety in Transitions of Care. Geneva: World Health Organization; 2019 (WHO/UHC/SDS/2019.9). Licence: CC BY-NC-SA 3.0 IGO. Cataloguing-in-Publication (CIP) data. CIP data are available at http://apps.who.int/iris.
    [Show full text]
  • Optimising Medicine Reconciliation at the Healthcare Interface Final Version
    Optimising Medicine Reconciliation at the Healthcare Interface Eman A. Hammad Submitted for the degree of Doctor of Philosophy University of East Anglia School of Pharmacy Submitted in June 2013 This copy of the thesis has been supplied on condition that anyone who consults it is understood to recognise that its copyright rests with the author and that use of any information derived there from must be in accordance with current UK Copyright Law. In addition, any quotation or extract must include full attribution. © 2013 Abstract Optimising medicine reconciliation at the healthcare interface By Eman A. Hammad BSc MSc Keywords: Medicine/ medication reconciliation, care transition, pharmacist service, discharge communication, medication discrepancies, health interface Background: Medicine reconciliation (MR) is the process of obtaining and maintaining an accurate, detailed list of all medicines taken by a patient and using this list anywhere within the health care system to ensure that the patient receives the correct medicines. This thesis aimed to design an MR intervention and develop a strategy for its evaluation. Methods: A health Trust-wide evaluation of the quality of discharge information relative to national guidance for the minimum dataset of information transfer was undertaken to identify the areas of sub-optimal practice. A systematic review informed the content and design of a pharmacy led medicines reconciliation service. A pilot randomised controlled trial was conducted to provide an early indication of the intervention’s costs and effects and to inform the design of a definitive trial. Results: A review of 3,444 discharge summaries in one primary care trust found that 80% had at least one medication discrepancy.
    [Show full text]
  • Principles of Good Practice in Medication Reconciliation
    Guidance for health and social care providers Principles of good practice in medication reconciliation May 2014 Guidance for Health and Social Care Providers: Principles of good practice in medication reconciliation (GHSP1) Health Information and Quality Authority About the Health Information and Quality Authority The Health Information and Quality Authority (HIQA) is the independent Authority established to drive high quality and safe care for people using our health and social care services. HIQA’s role is to promote sustainable improvements, safeguard people using health and social care services, support informed decisions on how services are delivered, and promote person-centred care for the benefit of the public. The Authority’s mandate to date extends across the quality and safety of the public, private (within its social care function) and voluntary sectors. Reporting to the Minister for Health and the Minister for Children and Youth Affairs, the Health Information and Quality Authority has statutory responsibility for: . Setting Standards for Health and Social Services – Developing person- centred standards, based on evidence and best international practice, for those health and social care services in Ireland that by law are required to be regulated by the Authority. Supporting Improvement – Supporting health and social care services to implement standards by providing education in quality improvement tools and methodologies. Social Services Inspectorate – Registering and inspecting residential centres for dependent people and inspecting children detention schools, foster care services and child protection services. Monitoring Healthcare Quality and Safety – Monitoring the quality and safety of health and personal social care services and investigating as necessary serious concerns about the health and welfare of people who use these services.
    [Show full text]
  • Medicines Optimisation: Helping Patients to Make the Most of Medicines
    Medicines Optimisation: Helping patients to make the most of medicines Good practice guidance for healthcare professionals in England May 2013 Endorsed by Foreword The NHS Constitution establishes the principles and values of the NHS in England. It sets out rights to which patients, public and staff are entitled, and pledges which the NHS is committed to achieve, together with responsibilities, which the public, patients and staff owe to one another to ensure that the NHS operates fairly and effectively. Set in this context, the evidence base, which clearly demonstrates there is much to be done to help patients, public and society more broadly get best outcomes from medicines, is concerning. From patients receiving insufficient information about their medicines to too many hospital admissions caused by the adverse effects of medicines which could have been prevented, professionals and patients need to work much closer together to improve the quality of medicines use. This important document represents a collaboration between patients and the health professionals that care for them. It sets out four simple but important principles of “medicines optimisation” that could revolutionise medicines use and outcomes: aim to understand the patient’s experience, evidence based choice of medicines, ensure medicines use is as safe as possible, make medicines optimisation part of routine practice. We would encourage everyone to adopt these principles whether prescribing, dispensing, administering or taking medicines. Given that medicines remain the most common therapeutic intervention in healthcare, and colleagues in research and the broad pharmaceutical industry have worked hard to discover and develop safe and effective medicines, we must all work even harder together to ensure that individual patients and society gets as much value out of that effort as possible, and resources are used wisely and effectively.
    [Show full text]
  • The Role of the Nurse in the Management of Medicines During Transitional Care: a Systematic Review
    Journal of Multidisciplinary Healthcare Dovepress open access to scientific and medical research Open Access Full Text Article REVIEW The Role of the Nurse in the Management of Medicines During Transitional Care: A Systematic Review This article was published in the following Dove Press journal: Journal of Multidisciplinary Healthcare Abbas Mardani 1 Purpose: To synthesise knowledge and to explore the role of the nurse in medicines Pauline Griffiths 2 management during transitional care. Mojtaba Vaismoradi 3 Methods: An integrative systematic review was conducted. Electronic databases such as PubMed [including Medline], Web of Knowledge, Scopus, and Cinahl from January 2010 to 1Nursing Care Research Center, School of Nursing and Midwifery, Iran University April 2020 were searched. Original qualitative and quantitative studies written in English that of Medical Sciences, Tehran, Iran; focused on the role of the nurse in medicines management during transitional care, which 2 Department of Nursing, College of included movement between short-term, long-term, and community healthcare settings were Human and Health Sciences, Swansea University, Swansea, Wales, UK; 3Faculty included. of Nursing and Health Sciences, Nord Results: The search process led to the retrieval of 10 studies, which were published in University, Bodø, Norway English from 2014 to 2020. They focused on the role of the nurse in patients' medicines management during transitional care in various healthcare settings. Given variations in the aims and methods of selected studies, the review findings were presented narratively utilizing three categories developed by the authors. In the first category as ‘medication reconciliation process’ the nurse participated in obtaining medication history, performing medication review, identifying medication discrepancies, joint medication reconciliation and adjustment.
    [Show full text]
  • Economic Value of Pharmacist-Led Medication Reconciliation for Reducing Medication Errors After Hospital Discharge
    MANAGERIAL Economic Value of Pharmacist-Led Medication Reconciliation for Reducing Medication Errors After Hospital Discharge Mehdi Najafzadeh, PhD; Jeffrey L. Schnipper, MD, MPH; William H. Shrank, MD, MSHS; Steven Kymes, PhD; Troyen A. Brennan, MD, JD, MPH; and Niteesh K. Choudhry, MD, PhD isruptions to, and changes in, a patient’s outpatient medica- tion regimen occur frequently during hospitalization. This ABSTRACT D often results in discrepancies between drugs prescribed at dis- charge and the medications outpatient providers believe that patients OBJECTIVES: Medication discrepancies at the time of hospital discharge are common and can harm patients. should be on.1 Although the majority of such discrepancies do not have Medication reconciliation by pharmacists has been shown clinically important effects, their consequences can be profound. These to prevent such discrepancies and the adverse drug events events are defined as preventable adverse drug events (ADEs) because (ADEs) that can result from them. Our objective was to estimate the economic value of nontargeted and targeted they are caused by medication discrepancies that could have been medication reconciliation conducted by pharmacists and avoided. It is estimated that 2.4% to 4.1% of all hospital admissions are pharmacy technicians at hospital discharge versus usual care. directly related to ADEs, and up to 69% of those ADEs are preventable.2-5 STUDY DESIGN: Discrete-event simulation model. There are other circumstances in which the presence of a medication discrepancy has not yet resulted in an ADE, but may still be costly and/ METHODS: We developed a discrete-event simulation model to prospectively model the incidence of drug-related or may expose patients to the risks of additional testing or monitoring.6 events from a hospital payer’s perspective.
    [Show full text]