Sedative Dose for Rapid Sequence Intubation and Postintubation Hypotension: Is There an Association? - 20/09/23
Abstract |
Study objective |
For patients with hemodynamic instability undergoing rapid sequence intubation, experts recommend reducing the sedative medication dose to minimize the risk of further hemodynamic deterioration. Scant data support this practice for etomidate and ketamine. We sought to determine if the dose of etomidate or ketamine was independently associated with postintubation hypotension.
Methods |
We analyzed data from the National Emergency Airway Registry from January 2016 to December 2018. Patients aged 14 years or older were included if the first intubation attempt was facilitated with etomidate or ketamine. We used multivariable modeling to determine whether drug dose in milligrams per kilogram of patient weight was independently associated with postintubation hypotension (systolic blood pressure < 100 mm Hg).
Results |
We analyzed 12,175 intubation encounters facilitated by etomidate and 1,849 facilitated by ketamine. The median drug doses were 0.28 mg/kg (interquartile range [IQR] 0.22 mg/kg to 0.32 mg/kg) for etomidate and 1.33 mg/kg (IQR 1 mg/kg to 1.8 mg/kg) for ketamine. Postintubation hypotension occurred in 1,976 patients (16.2%) who received etomidate and in 537 patients (29.0%) who received ketamine. In multivariable models, neither the etomidate dose (adjusted odds ratio [aOR] 0.95, 95% confidence interval [CI] 0.90 to 1.01) nor ketamine dose (aOR 0.97, 95% CI 0.81 to 1.17) was associated with postintubation hypotension. Results were similar in sensitivity analyses excluding patients with preintubation hypotension and including only patients intubated for shock.
Conclusion |
In this large registry of patients intubated after receiving either etomidate or ketamine, we observed no association between the weight-based sedative dose and postintubation hypotension.
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Please see page 418 for the Editor’s Capsule Summary of this article. |
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Supervising editor: Steven M. Green, MD, MD, MPP. Specific detailed information about possible conflict of interest for individual editors is available at editors. |
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Author contributions: BD, ST, MP, RR, and CAB conceived and designed the study. BD performed the data analysis. BD drafted the initial manuscript and made final editorial decisions; all authors contributed substantially to its revision. CAB is the registry’s principal investigator. BD takes responsibility for the study as a whole. |
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Data sharing statement: The complete dataset and data dictionary are available for centers that participated in data collection, with a valid data use agreement, upon request to Andrea Fantegrossi at afantegrossi@partners.org. |
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All authors attest to meeting the four ICMJE.org authorship criteria: (1) Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; AND (2) Drafting the work or revising it critically for important intellectual content; AND (3) Final approval of the version to be published; AND (4) Agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. |
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Funding and support: By Annals’ policy, all authors are required to disclose any and all commercial, financial, and other relationships in any way related to the subject of this article as per ICMJE conflict of interest guidelines (see www.icmje.org). The authors have stated that no such relationships exist. |
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Previous presentation: Presented at the annual meeting for the Society of Academic Emergency Medicine, May 2023, Austin, TX. |
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Continuing Medical Education exam for this article is available at ACEPeCME/. |
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Vol 82 - N° 4
P. 417-424 - octobre 2023 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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