Multicenter Emergency Department Validation of the Canadian Syncope Risk Score.


Journal

JAMA internal medicine
ISSN: 2168-6114
Titre abrégé: JAMA Intern Med
Pays: United States
ID NLM: 101589534

Informations de publication

Date de publication:
01 05 2020
Historique:
pubmed: 24 3 2020
medline: 21 1 2021
entrez: 24 3 2020
Statut: ppublish

Résumé

The management of patients with syncope in the emergency department (ED) is challenging because no robust risk tool available has been recommended for clinical use. To validate the Canadian Syncope Risk Score (CSRS) in a new cohort of patients with syncope to determine its ability to predict 30-day serious outcomes not evident during index ED evaluation. This prospective multicenter cohort study conducted at 9 EDs across Canada included patients 16 years and older who presented to EDs within 24 hours of syncope. Patients were enrolled from March 2014 to April 2018. Baseline characteristics, CSRS predictors, and 30-day adjudicated serious outcomes, including arrhythmic (arrhythmias, interventions for arrhythmia, or unknown cause of death) and nonarrhythmic (myocardial infarction, structural heart disease, pulmonary embolism, or hemorrhage) serious outcomes, were collected. Calibration and discrimination characteristics for CSRS validation were calculated. A total of 3819 patients were included (mean [SD] age 53.9 [22.8] years; 2088 [54.7%] female), of whom 139 (3.6%) experienced 30-day serious outcomes, including 13 patients (0.3%) who died. In the validation cohort, there were no differences between the predicted and observed risk, the calibration slope was 1.0, and the area under the receiver operating characteristic curve was 0.91 (95% CI, 0.88-0.93). The empirical probability of a 30-day serious outcome during validation was 3.64% (95% CI, 3.09%-4.28%) compared with the model-predicted probability of 3.17% (95% CI, 2.66%-3.77%; P = .26). The proportion of patients with 30-day serious outcomes increased from 3 of 1631 (0.3%) in the very-low-risk group to 40 of 78 (51.3%) in the very-high-risk group (Cochran-Armitage trend test P < .001). There was a similar significant increase in the serious outcome subtypes with increasing CSRS risk category. None of the very-low-risk and low-risk patients died or experienced ventricular arrhythmia. At a threshold score of -1 (2145 of 3819 patients), the CSRS sensitivity and specificity were 97.8% (95% CI, 93.8%-99.6%) and 44.3% (95% CI, 42.7%-45.9%), respectively. The CSRS was successfully validated and its use is recommended to guide ED management of patients when serious causes are not identified during index ED evaluation. Very-low-risk and low-risk patients can generally be discharged, while brief hospitalization can be considered for high-risk patients. We believe CSRS implementation has the potential to improve patient safety and health care efficiency.

Identifiants

pubmed: 32202605
pii: 2763181
doi: 10.1001/jamainternmed.2020.0288
pmc: PMC7091474
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

737-744

Subventions

Organisme : CIHR
Pays : Canada

Commentaires et corrections

Type : CommentIn

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Auteurs

Venkatesh Thiruganasambandamoorthy (V)

Department of Emergency Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital Research Institute, Ottawa Hospital, Ottawa, Ontario, Canada.
University of Ottawa School of Epidemiology and Public Health, Ottawa, Ontario, Canada.

Marco L A Sivilotti (MLA)

Department of Emergency Medicine, Queen's University, Kingston, Ontario, Canada.
Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario, Canada.

Natalie Le Sage (N)

Department of Family Medicine and Emergency Medicine, Laval University, Quebec City, Quebec, Canada.
CHU de Québec - Université Laval Research Center, Quebec City, Quebec, Canada.

Justin W Yan (JW)

Division of Emergency Medicine, Western University, London, Ontario, Canada.

Paul Huang (P)

Department of Emergency Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Mona Hegdekar (M)

Department of Emergency Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

Eric Mercier (E)

Department of Family Medicine and Emergency Medicine, Laval University, Quebec City, Quebec, Canada.
CHU de Québec - Université Laval Research Center, Quebec City, Quebec, Canada.

Muhammad Mukarram (M)

Ottawa Hospital Research Institute, Ottawa Hospital, Ottawa, Ontario, Canada.

Marie-Joe Nemnom (MJ)

Ottawa Hospital Research Institute, Ottawa Hospital, Ottawa, Ontario, Canada.

Andrew D McRae (AD)

Department of Emergency Medicine, University of Calgary, Calgary, Alberta, Canada.
Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.

Brian H Rowe (BH)

Department of Emergency Medicine, University of Alberta, Edmonton, Alberta, Canada.
School of Public Health, University of Alberta, Edmonton, Alberta, Canada.

Ian G Stiell (IG)

Department of Emergency Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Ottawa Hospital Research Institute, Ottawa Hospital, Ottawa, Ontario, Canada.
University of Ottawa School of Epidemiology and Public Health, Ottawa, Ontario, Canada.

George A Wells (GA)

University of Ottawa School of Epidemiology and Public Health, Ottawa, Ontario, Canada.

Andrew D Krahn (AD)

Division of Cardiology, University of British Columbia, Vancouver, British Columbia, Canada.

Monica Taljaard (M)

Ottawa Hospital Research Institute, Ottawa Hospital, Ottawa, Ontario, Canada.
University of Ottawa School of Epidemiology and Public Health, Ottawa, Ontario, Canada.

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