Target Trial Emulation Meta-Analysis of Benzodiazepines For Out-of-Hospital Status Epilepticus in Adults

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Autori principali: Alromaihi, Mona Abdullrahman, Alalwani, Yazan J., Almazrui, Manal Mudhhi, Alzahrani, Layan Bandar, Alzahrani, Abdulaziz A., Alotaibi, Alwaleed, Harun, Shahad Tariq, Alhadlah, Dena Nasser, Alshehri, Arwa Ali, Alrommani, Naif Abdullah, Barabea, Mohammed Salem, Alharbi, Ethar Ghazi, Azzam, Ahmed Y.
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Lingua:inglese
Pubblicazione: Zenodo 2026
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author Alromaihi, Mona Abdullrahman
Alalwani, Yazan J.
Almazrui, Manal Mudhhi
Alzahrani, Layan Bandar
Alzahrani, Abdulaziz A.
Alotaibi, Alwaleed
Harun, Shahad Tariq
Alhadlah, Dena Nasser
Alshehri, Arwa Ali
Alrommani, Naif Abdullah
Barabea, Mohammed Salem
Alharbi, Ethar Ghazi
Azzam, Ahmed Y.
author_facet Alromaihi, Mona Abdullrahman
Alalwani, Yazan J.
Almazrui, Manal Mudhhi
Alzahrani, Layan Bandar
Alzahrani, Abdulaziz A.
Alotaibi, Alwaleed
Harun, Shahad Tariq
Alhadlah, Dena Nasser
Alshehri, Arwa Ali
Alrommani, Naif Abdullah
Barabea, Mohammed Salem
Alharbi, Ethar Ghazi
Azzam, Ahmed Y.
contents <p><strong>Introduction:</strong> Benzodiazepines represent the first-line management for status epilepticus; however, heterogeneity in study designs has resulted in conflicting efficacy estimates. We aimed to conduct a target trial emulation meta-analysis to quantify design-induced bias and estimate the efficacy of benzodiazepines for adults in out-of-hospital settings under an ideal double-blind randomized controlled trial (RCT) setting.</p><p><strong>Methods:</strong> Following PRISMA 2020 guidelines, we searched PubMed, Scopus, Web of Science, Cochrane Library, and Google Scholar up to November 25, 2025. Studies evaluating benzodiazepines for status epilepticus in adults were included. The T3-Meta framework was utilized to model design features as bias covariates, with the target trial effect (θ*) representing seizure cessation rates under ideal RCT conditions. Network meta-analysis was used to evaluate comparative effectiveness.</p><p><strong>Results:</strong> Fourteen studies (2,803 adult patients) were included. Traditional random-effects pooling demonstrated a seizure cessation rate of 68.8% (95% confidence interval [CI]: 63.2–74.0%, I²=82.0%). Target trial analysis revealed significant open-label bias (β=0.757, odds ratio [OR]=2.13, P=0.048), with the bias-adjusted θ* of 64.9% (95% CI: 53.9–74.6%, I²=41.5%). Design features explained 49.4% of the between-study heterogeneity. Network meta-analysis demonstrated midazolam superiority over lorazepam (OR=1.60, P=0.001) and diazepam (OR=2.21, P=0.002). Midazolam achieved the highest P-Score (96.2%), followed by lorazepam (50.9%) and diazepam (2.9%).</p><p><strong>Conclusions:</strong> Traditional meta-analysis was found to overestimate benzodiazepine efficacy by 3.9 percentage points due to open-label design bias. Intramuscular midazolam demonstrated superior effectiveness compared to intravenous lorazepam and diazepam for status epilepticus in adults.</p>
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spellingShingle Target Trial Emulation Meta-Analysis of Benzodiazepines For Out-of-Hospital Status Epilepticus in Adults
Alromaihi, Mona Abdullrahman
Alalwani, Yazan J.
Almazrui, Manal Mudhhi
Alzahrani, Layan Bandar
Alzahrani, Abdulaziz A.
Alotaibi, Alwaleed
Harun, Shahad Tariq
Alhadlah, Dena Nasser
Alshehri, Arwa Ali
Alrommani, Naif Abdullah
Barabea, Mohammed Salem
Alharbi, Ethar Ghazi
Azzam, Ahmed Y.
Benzodiazepines
Status Epilepticus
Target Trial Emulation
Meta-Analysis
Midazolam
Lorazepam
Diazepam
Prehospital
Seizure
<p><strong>Introduction:</strong> Benzodiazepines represent the first-line management for status epilepticus; however, heterogeneity in study designs has resulted in conflicting efficacy estimates. We aimed to conduct a target trial emulation meta-analysis to quantify design-induced bias and estimate the efficacy of benzodiazepines for adults in out-of-hospital settings under an ideal double-blind randomized controlled trial (RCT) setting.</p><p><strong>Methods:</strong> Following PRISMA 2020 guidelines, we searched PubMed, Scopus, Web of Science, Cochrane Library, and Google Scholar up to November 25, 2025. Studies evaluating benzodiazepines for status epilepticus in adults were included. The T3-Meta framework was utilized to model design features as bias covariates, with the target trial effect (θ*) representing seizure cessation rates under ideal RCT conditions. Network meta-analysis was used to evaluate comparative effectiveness.</p><p><strong>Results:</strong> Fourteen studies (2,803 adult patients) were included. Traditional random-effects pooling demonstrated a seizure cessation rate of 68.8% (95% confidence interval [CI]: 63.2–74.0%, I²=82.0%). Target trial analysis revealed significant open-label bias (β=0.757, odds ratio [OR]=2.13, P=0.048), with the bias-adjusted θ* of 64.9% (95% CI: 53.9–74.6%, I²=41.5%). Design features explained 49.4% of the between-study heterogeneity. Network meta-analysis demonstrated midazolam superiority over lorazepam (OR=1.60, P=0.001) and diazepam (OR=2.21, P=0.002). Midazolam achieved the highest P-Score (96.2%), followed by lorazepam (50.9%) and diazepam (2.9%).</p><p><strong>Conclusions:</strong> Traditional meta-analysis was found to overestimate benzodiazepine efficacy by 3.9 percentage points due to open-label design bias. Intramuscular midazolam demonstrated superior effectiveness compared to intravenous lorazepam and diazepam for status epilepticus in adults.</p>
title Target Trial Emulation Meta-Analysis of Benzodiazepines For Out-of-Hospital Status Epilepticus in Adults
topic Benzodiazepines
Status Epilepticus
Target Trial Emulation
Meta-Analysis
Midazolam
Lorazepam
Diazepam
Prehospital
Seizure
url https://doi.org/10.5281/zenodo.19398234