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Treatment for beta-blocker poisoning: a systematic review
Joe-Anthony Rotella1,2, Shaun L Greene1,3, Zeff Koutsogiannis1,2
1Victorian Poisons Information Centre, Austin Health, Victoria, Australia.
Beta-blocker poisoning can be fatal. Treatments like catecholamines, vasopressors, high-dose insulin, and ECMO show promise for survival and improved hemodynamics, though evidence quality is low.
Area of Science:
- Toxicology
- Cardiology
- Emergency Medicine
Background:
- Beta-adrenoreceptor antagonist (beta-blocker) poisoning is a frequent overdose scenario associated with significant morbidity and mortality.
- Effective treatment strategies are crucial for managing patients experiencing beta-blocker toxicity.
Purpose of the Study:
- To systematically evaluate the efficacy of various treatments for beta-adrenoreceptor antagonist poisoning.
- To identify interventions associated with improved survival and hemodynamic parameters in beta-blocker overdose.
Main Methods:
- Comprehensive literature searches were conducted across MEDLINE, Embase, and CENTRAL databases up to November 2019.
- Two reviewers screened over 15,000 citations, selecting 141 articles for analysis.
- Primary outcomes assessed included mortality and improvement in hemodynamic parameters.
Main Results:
- High risk of bias was noted across all interventions evaluated.
- Catecholamines, vasopressors, high-dose insulin euglycemic therapy, and veno-arterial extracorporeal membrane oxygenation were associated with reduced mortality.
- Hemodynamic improvements were observed with catecholamines, vasopressin, and high-dose insulin therapy, though evidence quality is low.
Conclusions:
- While evidence quality is low, catecholamines, vasopressors, high-dose insulin, and VA-ECMO appear beneficial in beta-blocker poisoning.
- A graduated treatment approach is recommended, starting with fluids and vasopressors/inotropes, followed by insulin, and then VA-ECMO for refractory cases.
- Further high-quality research is needed to establish definitive treatment guidelines.
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