The impact of ketamine on emergency rapid sequence intubation: a systematic review and meta-analysis.

Ketamine compared with other sedatives during rapid sequence intubation (RSI) in critically ill patients shows no significant difference in in-hospital mortality, physiological function, or adverse events. A systematic review and meta-analysis of 15 studies (5 randomized controlled trials and 10 cohort studies) involving 16,807 participants found no overall mortality benefit (odds ratio 0.90, 95% confidence interval 0.72 to 1.12). Low-quality evidence suggests ketamine may reduce mortality within the first seven days of hospitalization (odds ratio 0.42, 95% confidence interval 0.19 to 0.93) but may also prolong intensive care unit stay (mean difference -0.71 days free of ICU at day 28, 95% confidence interval -1.38 to -0.05).

Study at a glance

Abstract

Rapid sequence intubation (RSI) is a crucial step in the resuscitation process for critically ill patients, and the judicious use of sedative drugs during RSI significantly influences the clinical outcomes of patients. Ketamine is a commonly used anesthetic sedative; however, its impact on the mortality of patients undergoing RSI has yielded inconsistent findings. Therefore, we conducted a systematic review and meta-analysis investigating ketamine's role in RSI to provide insights into selecting appropriate sedatives for critically ill patients. In this systematic review and meta-analysis, we conducted a systematic search on MEDLINE (PubMed), Embase, and Cochrane Central Register of Controlled Trials, without restricting to randomized controlled trials (RCTs) or cohort studies. The search was performed from inception until Dec 12, 2023, with no language restrictions. All studies comparing the use of sedatives, including ketamine, and documenting in-hospital mortality were included in this study. A total of 991 studies were identified, out of which 15 studies (5 RCTs and 10 cohort studies) involving 16,807 participants fulfilled the inclusion criteria. No significant impact on in-hospital mortality was observed with the use of ketamine compared to other drugs during RSI (OR 0.90, 95%CI 0.72 to 1.12). Low-quality evidence suggested that ketamine might reduce mortality within the first seven days of hospitalization (OR 0.42, 95%CI 0.19 to 0.93), but it may also have a potential effect on prolonging ICU-free days at day 28 (MD -0.71, 95%CI -1.38 to -0.05). There were no significant differences in the results of the other RSI-related outcomes, such as physiological function and adverse events. Based on existing studies, ketamine showed no significant difference compared to other sedatives in terms of in-hospital mortality, physiological impact, and side effects following RSI. However, it may reduce mortality within 7 days while probably prolong the length of stay in the ICU. CRD42023478020.