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Intravenous vs intraosseous adrenaline administration in cardiac arrest: A protocol for systematic review and
Wei Zhang1,2, Yi Liu1,2, Jing Yu2
1Department of Emergency Medicine, Laboratory of Emergency Medicine, West China Hospital, and Disaster Medical Center.
Insights
This study compares intravenous versus intraosseous adrenaline administration for cardiac arrest. It aims to determine the optimal delivery method for improving resuscitation outcomes and patient survival.
Area of Science:
- Emergency Medicine
- Cardiology
- Clinical Research
Background:
- Cardiac arrest necessitates prompt intervention, with adrenaline being a critical resuscitation drug.
- Current adrenaline delivery methods include intraosseous infusion and intravenous access, but their comparative effectiveness is unclear.
- This study addresses the need for evidence-based guidance on optimal adrenaline administration routes in cardiac arrest.
Purpose of the Study:
- To synthesize evidence comparing intravenous versus intraosseous adrenaline administration in cardiac arrest.
- To identify the most effective route for adrenaline delivery to improve patient outcomes.
- To inform clinical decision-making in the management of cardiac arrest.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs).
- Searches of major databases including PubMed, EMBASE, and Cochrane Library.
- Assessment of bias risk using Cochrane's tool and certainty of evidence with GRADE approach.
Main Results:
- Primary outcome: prehospital restoration of spontaneous circulation (ROSC).
- Secondary outcomes: survival, favorable and poor neurological outcomes at discharge and follow-up.
- Meta-analysis will be conducted using fixed or random effects models based on heterogeneity.
Conclusions:
- This protocol will establish the optimal epinephrine delivery method for cardiac arrest management.
- Findings will guide clinicians in making informed decisions regarding adrenaline administration.
- Evidence synthesis will enhance resuscitation protocols and patient care.
Introduction:
Cardiac arrest refers to the sudden termination of cardiac ejection function due to various causes. Adrenaline is an important component of resuscitation among individuals experiencing cardiac arrest. The adrenaline delivery method chiefly involved intraosseous infusion and intravenous access. However, the impact of different adrenaline delivery methods on cardiac arrest has been unclear in previous research. Thus, the present study aimed to synthesize the available evidence regarding intravenous vs intraosseous adrenaline administration in cardiac arrest.
Methods And Analysis:
We will search PubMed, EMBASE, Cochrane Library, Wanfang, and China National Knowledge Infrastructure. As per the inclusion criteria, randomized controlled trials (RCTs) on adrenaline administration in cardiac arrest were selected. The primary outcome was prehospital restoration of spontaneous circulation (ROSC); the secondary endpoints were survival, favorable neurological outcome at discharge, and poor neurological outcome at ≥3 mon.We plan to use the Cochrane Collaboration's tool for assessing the bias risk for RCTs. The Grading of Recommendations Assessment, Development and Evaluation approach will grade the certainty of the evidence for all the outcome measures across studies. RevMan 5.3.5 will be used for meta-analysis. If the heterogeneity tests show slight or no statistical heterogeneity, the fixed effects model will be used, in other cases, the random effect model will be used for data synthesis.
Results And Conclusion:
This protocol will determine which epinephrine delivery method is the optimal in the management of cardiac arrest. Our findings will help clinicians and health professionals in making accurate clinical decisions about adrenaline administrations in cardiac arrest.
Ethics And Dissemination:
Ethical approval was not required because this study was planned as a secondary analysis. The results will be disseminated in peer-reviewed publications, journals, and academic.
Inplasy Registration Number:
INPLASY202090100 (DOI:10.37766/inplasy2020.9.0100).
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