The Copenhagen Triage Algorithm is non-inferior to a traditional triage algorithm: A cluster-randomized study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 01 02 2018
accepted: 19 01 2019
entrez: 5 2 2019
pubmed: 5 2 2019
medline: 7 11 2019
Statut: epublish

Résumé

Triage systems with limited room for clinical judgment are used by emergency departments (EDs) worldwide. The Copenhagen Triage Algorithm (CTA) is a simplified triage system with a clinical assessment. The trial was a non-inferiority, two-center cluster-randomized crossover study where CTA was compared to a local adaptation of Adaptive Process Triage (ADAPT). CTA involves initial categorization based on vital signs with a final modification based on clinical assessment by an ED nurse. We used 30-day mortality with a non-inferiority margin at 0.5%. Predictive performance was compared using Receiver Operator Characteristics. We included 45,347 patient visits, 23,158 (51%) and 22,189 (49%) were triaged with CTA and ADAPT respectively with a 30-day mortality of 3.42% and 3.43% (P = 0.996) a difference of 0.01% (95% CI: -0.34 to 0.33), which met the non-inferiority criteria. Mortality at 48 hours was 0.62% vs. 0.71%, (P = 0.26) and 6.38% vs. 6.61%, (P = 0.32) at 90 days for CTA and ADAPT. CTA triaged at significantly lower urgency level (P<0.001) and was superior in predicting 30-day mortality, Area under the curve: 0.67 (95% CI 0.65-0.69) compared to 0.64 for ADAPT (95% CI 0.62-0.66) (P = 0.03). There were no significant differences in rate of admission to the intensive care unit, length of stay, waiting time nor rate of readmission within 30 or 90 days. A novel triage system based on vital signs and a clinical assessment by an ED nurse was non-inferior to a traditional triage algorithm by short term mortality, and superior in predicting 30-day mortality. Clinicaltrials.gov NCT02698319.

Identifiants

pubmed: 30716123
doi: 10.1371/journal.pone.0211769
pii: PONE-D-18-02656
pmc: PMC6361446
doi:

Banques de données

ClinicalTrials.gov
['NCT02698319']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0211769

Déclaration de conflit d'intérêts

Dr. Torp-Pedersen reports grants and personal fees from Bayer, grants from Biotronic, outside the submitted work.

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Auteurs

Rasmus Bo Hasselbalch (RB)

Department of Cardiology, Herlev-Gentofte Hospital, Copenhagen, Denmark.

Mia Pries-Heje (M)

Department of Cardiology, Herlev-Gentofte Hospital, Copenhagen, Denmark.

Martin Schultz (M)

Department of Cardiology, Herlev-Gentofte Hospital, Copenhagen, Denmark.

Louis Lind Plesner (LL)

Department of Cardiology, Herlev-Gentofte Hospital, Copenhagen, Denmark.

Lisbet Ravn (L)

Department of Emergency Medicine, Herlev-Gentofte Hospital, Copenhagen, Denmark.

Morten Lind (M)

Department of Emergency Medicine, Herlev-Gentofte Hospital, Copenhagen, Denmark.

Rasmus Greibe (R)

Department of Cardiology, Bispebjerg Hospital, Copenhagen, Denmark.

Birgitte Nybo Jensen (BN)

Department of Emergency Medicine, Bispebjerg Hospital, Copenhagen, Denmark.

Thomas Høi-Hansen (T)

Department of Cardiology, Herlev-Gentofte Hospital, Copenhagen, Denmark.

Nicholas Carlson (N)

Department of Cardiology, Gentofte Hospital, Copenhagen, Denmark.
The Danish Heart Foundation, Copenhagen, Denmark.

Christian Torp-Pedersen (C)

Department of Health, Science and Technology, Aalborg University and Department of Cardiology and Epidemiology/Biostatistics, Aalborg University Hospital, Aalborg, Denmark.

Lars S Rasmussen (LS)

Department of Anaesthesia, Center of Head and Orthopaedics, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Kasper Iversen (K)

Department of Cardiology, Herlev-Gentofte Hospital, Copenhagen, Denmark.
Department of Emergency Medicine, Herlev-Gentofte Hospital, Copenhagen, Denmark.

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