Evidence map›Paper›PMID 36875169›Full record

ArticleJournal of geriatric cardiology : JGC2023

Predicting short-term adverse outcomes in the geriatric population presenting with syncope: a comparison of existing syncope rules and beyond.

Suud A Kiradoh, Timothy E Craven, Maria O Rangel, Lillian M Nosow, Erfan Zarrinkhoo, Suma Menon, Parag A Chevli, Tareq M Islam, Luqman A Thazhatuveetil-Kunhahamed

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Article in Journal of geriatric cardiology : JGC, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Suud A KiradohDepartment of Internal Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.
Timothy E CravenBiostatistics, Epidemiology, Research, and Design (BERD), Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.
Maria O RangelDepartment of Cardiology, Atrium Health Wake Forest Baptist Medical Center, USA.
Lillian M NosowDepartment of Internal Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.
Erfan ZarrinkhooDepartment of Internal Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.
Suma MenonDepartment of Internal Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.
Parag A ChevliDepartment of Internal Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.
Tareq M IslamDepartment of Internal Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.
Luqman A Thazhatuveetil-KunhahamedDepartment of Internal Medicine, Atrium Health Wake Forest Baptist Medical Center, Winston-Salem, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSyncope at age 65+ is associated with increased mortality, irrespective of cause. Syncope rules were designed to aid in risk-stratification but were only validated in the general adult population. Our objective was to determine if they can be applied to a geriatric population in predicting short-term adverse outcomes.

methodsIn this single-center retrospective study, we evaluated 350 patients aged 65+ presenting with syncope. Exclusion criteria included confirmed non-syncope, active medical condition, drug or alcohol-related syncope. Patients were stratified into high or low risk based on Canadian Syncope Risk Score (CSRS), Evaluation of Guidelines in Syncope Study (EGSYS), San Francisco Syncope Rule (SFSR), and Risk Stratification of Syncope in the Emergency Department (ROSE). Composite adverse outcomes at 48-hour and 30-day included all-cause mortality, major adverse cardiac and cerebrovascular events (MACCE), return emergency department visit, hospitalization, or medical intervention. We assessed each score's ability to predict the outcomes using logistic-regression and compared performances using receiver-operator curves. Multivariate analyses were performed to study the associations between recorded parameters and outcomes.

resultsCSRS outperformed with AUC of 0.732 (95% CI: 0.653-0.812) and 0.749 (95% CI: 0.688-0.809) for 48-h and 30-day outcomes, respectively. Sensitivities for CSRS, EGSYS, SFSR, and ROSE for 48-hour outcomes were 48%, 65%, 42% and 19%; and for 30-day outcomes were 72%, 65%, 30% and 55%, respectively. Atrial fibrillation/flutter on EKG, congestive heart failure, antiarrhythmics, systolic blood-pressure < 90 at triage, and associated chest pain highly correlated with 48-h outcomes. An EKG abnormality, heart disease history, severe pulmonary hypertension, BNP > 300, vasovagal predisposition, and antidepressants highly correlated with 30-day outcomes.

conclusionsPerformance and accuracy of four prominent syncope rules were suboptimal in identifying high-risk geriatric patients with short-term adverse outcomes. We identified some significant clinical and laboratory information that may play a role in predicting short-term adverse events in a geriatric cohort.

Identifiers

PMID36875169
PMCPMC9975484

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