Abstract
Background/Objectives
In the context of an aging surgical population, appropriate anesthetic induction dose adjustments for the older adult remain poorly defined. In the present study, we describe the prevalence of excess induction agent dose in reference to US Food and Drug Administration (FDA) guidance and seek to investigate the possible association of such excess dose with postinduction hypotension and postoperative acute kidney injury (AKI).
Study Design
A retrospective observational study was conducted in a large tertiary teaching hospital in accordance with our a priori analytic protocol as registered on ClinicalTrials.gov (NCT03699696). For inclusion, patients had to be 65 years or older and to have received general anesthesia with propofol induction for gynecologic oncology surgery between December 1, 2014 and July 8, 2018. Descriptive variables of the patients, machine-captured perioperative vital signs, induction anesthetic, and vasopressor/inotrope administrations were recorded.
Main Outcome Measures
A total of 541 female patients met inclusion criteria. The mean (standard deviation) age of the cohort was 72.20 (5.93) years. Regarding the primary outcome, 65.43% (354 patients, 95% confidence interval 61.2–69.4) of the cohort received more than the FDA recommended 1–1.5 mg/kg induction dose for patients of advanced age undergoing general anesthesia.
Results
The percentage of patients receiving doses in excess of the FDA guidance remained substantial across all age groups, but decreased progressively with increasing 5-year age intervals (from 74% among those aged 65–69 years to 44% among those aged > 80 years). Excess propofol dose in the present cohort was not associated with our a priori definition of postinduction hypotension. Regarding AKI, among the 30 patients suffering this outcome, it occurred less often in patients who received higher propofol doses (4.1% [9/217] vs. 15.3% [21/138], p < 0.001), a result that may have been confounded by differential rates of missingness.
Conclusions
Older adults commonly receive propofol induction doses in excess of the FDA guidance. The immediate hemodynamic effects of these doses on postinduction hypotension were not seen in the present cohort, suggesting that propofol dose adjustments may serve as a marker of physicians’ judgments as to the frailty of patients. The relevance of the AKI association is difficult to interpret due to the non-differential missingness of AKI data between the two groups.
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Dr. Schonberger holds an equity stake in Johnson & Johnson, a publicly traded, diversified manufacturer of healthcare products. The remaining authors, Eric Y. Chen, George Michel, Bin Zhou, Feng Dai, and Shamsuddin Akhtar, declare that they have no conflict of interest.
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This work was supported in part by grant R01 AG059607 from the National Institute on Aging, as well as CTSA Grant Number UL1RR024139 from the National Center for Research Resources and the National Center for Advancing Translational Science, components of the NIH.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
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Chen, E.Y., Michel, G., Zhou, B. et al. An Analysis of Anesthesia Induction Dosing in Female Older Adults. Drugs Aging 37, 435–446 (2020). https://doi.org/10.1007/s40266-020-00760-3
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DOI: https://doi.org/10.1007/s40266-020-00760-3