Abstract

ABSTRACTBackground: The systems-based management of laboratory test ordering and results handling is a known source of error in primary care settings worldwide. The consequences are wide-ranging for patients (e.g. avoidable harm or poor care experience), general practitioners (e.g. delayed clinical decision making and potential medico-legal implications) and the primary care organization (e.g. increased allocation of resources to problem-solve and dealing with complaints). Guidance is required to assist care teams to minimize associated risks and improve patient safety.Objective: To identify, develop and build expert consensus on ‘good practice’ guidance statements to inform the implementation of safe systems for ordering laboratory tests and managing results in European primary care settings.Methods: Mixed methods studies were undertaken in the UK and Ireland, and the findings were triangulated to develop ‘good practice’ statements. Expert consensus was then sought on the findings at the wider European level via a Delphi group meeting during 2013.Results: We based consensus on 10 safety domains and developed 77 related ‘good practice’ statements (≥ 80% agreement levels) judged to be essential to creating safety and minimizing risks in laboratory test ordering and subsequent results handling systems in international primary care.Conclusion: Guidance was developed for improving patient safety in this important area of primary care practice. We need to consider how this guidance can be made accessible to frontline care teams, utilized by clinical educators and improvement advisers, implemented by decision makers and evaluated to determine acceptability, feasibility and impacts on patient safety.

Highlights

  • The reliability of formal ordering and tracking systems to oversee the management of laboratory test requests and subsequent results handling is problematic and a known source of error in primary care settings worldwide [1,2,3,4]

  • The final international meeting led to consensus on 10 generic safety domains and the inclusion of 77 ‘good practice’ statements that were judged by experts to be relevant to creating patient safety and minimizing risks in laboratory test ordering and subsequent results handling systems in European primary care settings (Table 1)

  • Application of the content validity index (CVI) exercise led to full agreement by the expert group on retaining the 10 safety domains identified in the initial consensus building development work undertaken in the UK and Ireland contexts

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Summary

Introduction

The reliability of formal ordering and tracking systems to oversee the management of laboratory test requests and subsequent results handling is problematic and a known source of error in primary care settings worldwide [1,2,3,4]. For patients and their relatives this may have multiple consequences in terms of contributing to avoidable harm and unnecessary distress, sub-optimal clinical management of illness and delayed treatments (Box 1), poor experience with care, miscommunication of test (Received 21 June 2013; revised 2 February 2015; accepted 10 March 2015) ISSN 1381-4788 print/ISSN 1751-1402 online ß 2015 The Author(s). Results: We based consensus on 10 safety domains and developed 77 related ‘good practice’ statements (Ն 80% agreement levels) judged to be essential to creating safety and minimizing risks in laboratory test ordering and subsequent results handling systems in international primary care

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