Abstract

BackgroundObtaining patients’ views of their health and outcomes of interventions utilising patient-reported outcome measures (PROMs) is a well-established method, but there is still uncertainty about the impact of PROMs on services and patient care. Studies are now needed of alternative ways of implementing PROMs. This paper describes a case study of the introduction of a new PROM to assess musculoskeletal (MSK) problems, known as the Musculoskeletal Health Questionnaire (MSK-HQ).MethodsFollowing an invitation from the Arthritis Research UK (ARUK), 11 groups and organisations agreed to become ‘partners’ in piloting the MSK-HQ. Twenty-nine interviews and a focus group were carried out with key informants from the partners. Interviews were supplemented with some documentary evidence of partners’ meetings. Data were coded and analysed with NVivo software V.10. Analysis was carried out via a framework method.ResultsParticipants reported positive evidence that the MSK-HQ is feasible and practical for use in patient care with content that helped health professionals identify and address patients’ main presenting problems. Although mediated and reported through health professionals’ judgments, the questionnaire was also seen as very relevant and acceptable to a wide spectrum of patients.There was also broad support for the view that whilst the MSK-HQ is relevant to individual patient care, it could also, when aggregated, reflect the experiences of patients as a group and be used as evidence for third parties concerned with the provision and commissioning of services.The main difficulties revealed by the case study were in the form of logistics and sustainability. It was recognised that electronic systems would be more effective for administration and data processing but they were not feasible to develop and implement within reasonable timelines and available budgets. A sustainable approach to using the PROM required significant long-term commitment of budget, a coherent system, and active support from diverse organisations.ConclusionsThe current study supports the view that a bottom-up approach is a promising method to generate PROM-related insights that are relevant to patients and health professionals. The partnership approach to developing and using PROMs may have wider relevance and potential as a model of implementation.

Highlights

  • Obtaining patients’ views of their health and outcomes of interventions utilising patient-reported outcome measures (PROMs) is a well-established method, but there is still uncertainty about the impact of PROMs on services and patient care

  • There is growing uncertainty about the overall impact of the PROM programme on the quality of services and about optimal methods of implementing PROM programmes [4]. Evidence from this programme and related initiatives suggests that if health professionals are insufficiently engaged at the outset, and are unclear about the meaning and value of information from PROMs, this may reduce the potential impact of this new form of evidence about outcomes [4, 5]

  • This paper describes a case study of the introduction of a new PROM to assess musculoskeletal (MSK) problems, known as the Musculoskeletal Health Questionnaire (MSK-HQ) [8]

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Summary

Introduction

Obtaining patients’ views of their health and outcomes of interventions utilising patient-reported outcome measures (PROMs) is a well-established method, but there is still uncertainty about the impact of PROMs on services and patient care. One of the most ambitious programmes to introduce PROMs was carried out in the National Health Service (NHS) in the form of a centrally coordinated and nationally mandated initiative to monitor patients undergoing selected elective surgical procedures (hip and knee replacement, hernia and varicose vein surgery) with a view to providing aggregate-level evidence of the performance of services [3]. It has produced a wealth of information about needs, outcomes and surgical performance in relation to the four procedures selected. Evidence from this programme and related initiatives suggests that if health professionals are insufficiently engaged at the outset, and are unclear about the meaning and value of information from PROMs, this may reduce the potential impact of this new form of evidence about outcomes [4, 5]

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