Complexity and involvement as implementation challenges: results from a process analysis.

Guideline adherence Implementation Multifaceted approach Patient safety Perioperative care Stepped-wedge design

Journal

BMC health services research
ISSN: 1472-6963
Titre abrégé: BMC Health Serv Res
Pays: England
ID NLM: 101088677

Informations de publication

Date de publication:
23 Oct 2021
Historique:
received: 08 02 2021
accepted: 21 09 2021
entrez: 24 10 2021
pubmed: 25 10 2021
medline: 27 10 2021
Statut: epublish

Résumé

The study objective was to analyse the implementation challenges experienced in carrying out the IMPROVE programme. This programme was designed to implement checklist-related improvement initiatives based on the national perioperative guidelines using a stepped-wedge trial design. A process analysis was carried out to investigate the involvement in the implementation activities. An involvement rating measure was developed to express the extent to which the implementation programme was carried out in the hospitals. This measure reflects the number of IMPROVE-implementation activities executed and the estimated participation in these activities in all nine participating hospitals. These data were compared with prospectively collected field notes. Considerable variation between the hospitals was found with involvement ratings ranging from 0 to 6 (mean per measurement = 1.83 on a scale of 0-11). Major implementation challenges were respectively the study design (fixed design, time planning, long duration, repeated measurements, and data availability); the selection process of hospitals, departments and key contact person(s) (inadequately covering the entire perioperative team and stand-alone surgeons); the implementation programme (programme size and scope, tailoring, multicentre, lack of mandate, co-interventions by the Inspectorate, local intervention initiatives, intervention fatigue); and competitive events such as hospital mergers or the introduction of new IT systems, all reducing involvement. The process analysis approach helped to explain the limited and delayed execution of the IMPROVE-implementation programme. This turned out to be very heterogeneous between hospitals, with variation in the number and content of implementation activities carried out. The identified implementation challenges reflect a high complexity with regard to the implementation programme, study design and setting. The involvement of the target professionals was put under pressure by many factors. We mostly encountered challenges, but at the same time we provide solutions for addressing them. A less complex implementation programme, a less fixed study design, a better thought-out selection of contact persons, as well as more commitment of the hospital management and surgeons would likely have contributed to better implementation results. Dutch Trial Registry: NTR3568 , retrospectively registered on 2 August 2012.

Sections du résumé

BACKGROUND BACKGROUND
The study objective was to analyse the implementation challenges experienced in carrying out the IMPROVE programme. This programme was designed to implement checklist-related improvement initiatives based on the national perioperative guidelines using a stepped-wedge trial design. A process analysis was carried out to investigate the involvement in the implementation activities.
METHODS METHODS
An involvement rating measure was developed to express the extent to which the implementation programme was carried out in the hospitals. This measure reflects the number of IMPROVE-implementation activities executed and the estimated participation in these activities in all nine participating hospitals. These data were compared with prospectively collected field notes.
RESULTS RESULTS
Considerable variation between the hospitals was found with involvement ratings ranging from 0 to 6 (mean per measurement = 1.83 on a scale of 0-11). Major implementation challenges were respectively the study design (fixed design, time planning, long duration, repeated measurements, and data availability); the selection process of hospitals, departments and key contact person(s) (inadequately covering the entire perioperative team and stand-alone surgeons); the implementation programme (programme size and scope, tailoring, multicentre, lack of mandate, co-interventions by the Inspectorate, local intervention initiatives, intervention fatigue); and competitive events such as hospital mergers or the introduction of new IT systems, all reducing involvement.
CONCLUSIONS CONCLUSIONS
The process analysis approach helped to explain the limited and delayed execution of the IMPROVE-implementation programme. This turned out to be very heterogeneous between hospitals, with variation in the number and content of implementation activities carried out. The identified implementation challenges reflect a high complexity with regard to the implementation programme, study design and setting. The involvement of the target professionals was put under pressure by many factors. We mostly encountered challenges, but at the same time we provide solutions for addressing them. A less complex implementation programme, a less fixed study design, a better thought-out selection of contact persons, as well as more commitment of the hospital management and surgeons would likely have contributed to better implementation results.
TRIAL REGISTRATION BACKGROUND
Dutch Trial Registry: NTR3568 , retrospectively registered on 2 August 2012.

Identifiants

pubmed: 34688287
doi: 10.1186/s12913-021-07090-z
pii: 10.1186/s12913-021-07090-z
pmc: PMC8542304
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1149

Informations de copyright

© 2021. The Author(s).

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Auteurs

Yvette Emond (Y)

Scientific Center for Quality of Healthcare (IQ healthcare), Radboud Institute for Health Sciences (RIHS), Radboud university medical center, PO Box 9101, 114 IQ healthcare, 6500 HB, Nijmegen, The Netherlands. Yvette.Emond@radboudumc.nl.
Department of Anesthesiology, Pain and Palliative Care, Radboud university medical center, Nijmegen, The Netherlands. Yvette.Emond@radboudumc.nl.

André Wolff (A)

Department of Anesthesiology, Pain Center, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Gerrit Bloo (G)

Scientific Center for Quality of Healthcare (IQ healthcare), Radboud Institute for Health Sciences (RIHS), Radboud university medical center, PO Box 9101, 114 IQ healthcare, 6500 HB, Nijmegen, The Netherlands.
Department of Anesthesiology, Pain and Palliative Care, Radboud university medical center, Nijmegen, The Netherlands.

Johan Damen (J)

Department of Anesthesiology, Pain and Palliative Care, Radboud university medical center, Nijmegen, The Netherlands.

Gert Westert (G)

Scientific Center for Quality of Healthcare (IQ healthcare), Radboud Institute for Health Sciences (RIHS), Radboud university medical center, PO Box 9101, 114 IQ healthcare, 6500 HB, Nijmegen, The Netherlands.

Hub Wollersheim (H)

Scientific Center for Quality of Healthcare (IQ healthcare), Radboud Institute for Health Sciences (RIHS), Radboud university medical center, PO Box 9101, 114 IQ healthcare, 6500 HB, Nijmegen, The Netherlands.

Hiske Calsbeek (H)

Scientific Center for Quality of Healthcare (IQ healthcare), Radboud Institute for Health Sciences (RIHS), Radboud university medical center, PO Box 9101, 114 IQ healthcare, 6500 HB, Nijmegen, The Netherlands.

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