Reducing door-to-needle times in stroke thrombolysis to 13 min through protocol revision and simulation training: a quality improvement project in a Norwegian stroke centre.


Journal

BMJ quality & safety
ISSN: 2044-5423
Titre abrégé: BMJ Qual Saf
Pays: England
ID NLM: 101546984

Informations de publication

Date de publication:
11 2019
Historique:
received: 18 11 2018
revised: 02 06 2019
accepted: 06 06 2019
pubmed: 1 7 2019
medline: 10 6 2020
entrez: 1 7 2019
Statut: ppublish

Résumé

In eligible patients with acute ischaemic stroke, rapid revascularisation is crucial for good outcome. At our treatment centre, we had achieved and sustained a median door-to-needle time of under 30 min. We hypothesised that further improvement could be achieved through implementing a revised treatment protocol and in situ simulation-based team training sessions. This report describes a quality improvement project aiming to reduce door-to-needle times in stroke thrombolysis. All members of the acute stroke treatment team were surveyed to tailor the interventions to local conditions. Through a review of responses and available literature, the improvement team suggested changes to streamline the protocol and designed in situ simulation-based team training sessions. Implementation of interventions started in February 2017. We completed 14 simulation sessions from February to June 2017 and an additional 12 sessions from November 2017 to March 2018. Applying Kirkpatrick's four-level training evaluation model, participant reactions, clinical behaviour and patient outcomes were measured. Statistical process control charts were used to demonstrate changes in treatment times and patient outcomes. A total of 650 consecutive patients, including a 3-year baseline, treated with intravenous thrombolysis were assessed. Median door to needle times were significantly reduced from 27 to 13 min and remained consistent after 13 months. Risk-adjusted cumulative sum charts indicate a reduced proportion of patients deceased or bedridden after 90 days. There was no significant change in balancing measures (stroke mimics, fatal intracranial haemorrhage and prehospital times). Implementing a revised treatment protocol in combination with in situ simulation-based team training sessions for stroke thrombolysis was followed by a considerable reduction in door-to-needle times and improved patient outcomes. Additional work is needed to assess sustainability and generalisability of the interventions.

Sections du résumé

BACKGROUND
In eligible patients with acute ischaemic stroke, rapid revascularisation is crucial for good outcome. At our treatment centre, we had achieved and sustained a median door-to-needle time of under 30 min. We hypothesised that further improvement could be achieved through implementing a revised treatment protocol and in situ simulation-based team training sessions. This report describes a quality improvement project aiming to reduce door-to-needle times in stroke thrombolysis.
METHODS
All members of the acute stroke treatment team were surveyed to tailor the interventions to local conditions. Through a review of responses and available literature, the improvement team suggested changes to streamline the protocol and designed in situ simulation-based team training sessions. Implementation of interventions started in February 2017. We completed 14 simulation sessions from February to June 2017 and an additional 12 sessions from November 2017 to March 2018. Applying Kirkpatrick's four-level training evaluation model, participant reactions, clinical behaviour and patient outcomes were measured. Statistical process control charts were used to demonstrate changes in treatment times and patient outcomes.
RESULTS
A total of 650 consecutive patients, including a 3-year baseline, treated with intravenous thrombolysis were assessed. Median door to needle times were significantly reduced from 27 to 13 min and remained consistent after 13 months. Risk-adjusted cumulative sum charts indicate a reduced proportion of patients deceased or bedridden after 90 days. There was no significant change in balancing measures (stroke mimics, fatal intracranial haemorrhage and prehospital times).
CONCLUSIONS
Implementing a revised treatment protocol in combination with in situ simulation-based team training sessions for stroke thrombolysis was followed by a considerable reduction in door-to-needle times and improved patient outcomes. Additional work is needed to assess sustainability and generalisability of the interventions.

Identifiants

pubmed: 31256015
pii: bmjqs-2018-009117
doi: 10.1136/bmjqs-2018-009117
doi:

Types de publication

Journal Article

Langues

eng

Pagination

939-948

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: SCA is a research fellow funded by a Safer Healthcare Grant (University Research Fund). MG has a consulting agreement with Mentice, the remaining authors report no disclosures.

Auteurs

Soffien Chadli Ajmi (SC)

Department of Neurology, Stavanger University Hospital, Stavanger, Norway soffiena@yahoo.com.
Department of Quality and Health Technology, University of Stavanger, Stavanger, Norway.

Rajiv Advani (R)

Department of Neurology, Stroke Unit, Oslo University Hospital, Oslo, Norway.

Lars Fjetland (L)

Department of Radiology, Stavanger University Hospital, Stavanger, Norway.

Kathinka Dehli Kurz (KD)

Department of Radiology, Stavanger University Hospital, Stavanger, Norway.
Department of Mathematics and Physics, University of Stavanger, Stavanger, Norway.

Thomas Lindner (T)

Department of Anesthesiology and Intensive Care, Stavanger University Hospital, Stavanger, Norway.
Research, The Regional Centre for Emergency Medical Research and Development, Stavanger, Norway.

Sigrunn Anna Qvindesland (SA)

Research, Stavanger Acute Medicine Foundation for Education and Research, Stavanger, Norway.

Hege Ersdal (H)

Department of Quality and Health Technology, University of Stavanger, Stavanger, Norway.
Department of Anesthesiology and Intensive Care, Stavanger University Hospital, Stavanger, Norway.

Mayank Goyal (M)

Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.

Jan Terje Kvaløy (JT)

Department of Mathematics and Physics, University of Stavanger, Stavanger, Norway.
Department of Research, University of Stavanger, Stavanger, Norway.

Martin Kurz (M)

Department of Neurology, Stavanger University Hospital, Stavanger, Norway.
Department of Clinical Medicine, University of Bergen, Bergen, Norway.

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