Journal of clinical anesthesia · 2026
Postoperative residual neuromuscular blockade and hypoventilation after rocuronium and sugammadex or neostigmine for kidney transplantation: A randomized clinical trial.
СтатьяРандомизированное исследованиеСравнительное исследованиеПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Stewart Erin, Kaizer Alexander, Fioravanti Jesse, Russell Nicole, Hendrickse Adrian, Adams Megan, Pshak Thomas, Fernandez-Bustamante Ana
Аннотация
BACKGROUND: Inadequate neuromuscular blockade (NMB) reversal can cause residual NMB (RNMB) and hypoventilation, but the incidence after sugammadex or neostigmine for kidney transplantation is unknown. We compared hypoventilation for up to three days after neostigmine or sugammadex for kidney transplantation, adjusting for RNMB, opioids, and other confounders.
METHODS: This single-center double-blind trial randomized adults undergoing renal transplantation with rocuronium-based NMB and reversal with neostigmine at train-of-four count (TOFC) ≥ 2 or sugammadex at post-tetanic count PTC ≥ 1 following institutional practices. We identified postoperative quantitative TOF ratio (TOFR) < 0.9 events, and ≥ 1-min-long hypoventilation episodes (minute ventilation <40% of predicted for each patient) using continuous non-invasive bioimpedance ventilation monitoring in the post-anesthesia care unit (PACU) (primary outcome) and ward for up to three days. Logistic regression compared the incidence of hypoventilation, adjusting for TOFR<0.9, opioids, and other factors. We also analyzed patient-reported dyspnea scores, outcomes, and hospital resources utilization for two postoperative weeks.
RESULTS: The intention-to-treat analysis included 84 patients: 52(62%) males, age 49(15) years. 42(50%) patients received sugammadex or neostigmine. Sugammadex patients had similar TOFR<0.9 events, normalized to patient's baseline, in PACU (40% vs. 60%, p = 0.127) and the ward (17% vs. 26%, p = 0.425). Hypoventilation incidence was similar in PACU (sugammadex 55% vs. neostigmine 58%, p = 1.000) and the ward (69% vs. 67%, p = 1.000) before or after adjusting for RNMB, opioids received, and other covariates.
CONCLUSIONS: Sugammadex was non-inferior to neostigmine on the incidence of RNMB and hypoventilation, even after adjusting for RNMB, opioids, and other covariates, in PACU and up to three days after kidney transplantation.
TRIAL REGISTRATION: ClinicalTrial.govNCT03923556https://clinicaltrials.gov/ct2/show/NCT03923556.
METHODS: This single-center double-blind trial randomized adults undergoing renal transplantation with rocuronium-based NMB and reversal with neostigmine at train-of-four count (TOFC) ≥ 2 or sugammadex at post-tetanic count PTC ≥ 1 following institutional practices. We identified postoperative quantitative TOF ratio (TOFR) < 0.9 events, and ≥ 1-min-long hypoventilation episodes (minute ventilation <40% of predicted for each patient) using continuous non-invasive bioimpedance ventilation monitoring in the post-anesthesia care unit (PACU) (primary outcome) and ward for up to three days. Logistic regression compared the incidence of hypoventilation, adjusting for TOFR<0.9, opioids, and other factors. We also analyzed patient-reported dyspnea scores, outcomes, and hospital resources utilization for two postoperative weeks.
RESULTS: The intention-to-treat analysis included 84 patients: 52(62%) males, age 49(15) years. 42(50%) patients received sugammadex or neostigmine. Sugammadex patients had similar TOFR<0.9 events, normalized to patient's baseline, in PACU (40% vs. 60%, p = 0.127) and the ward (17% vs. 26%, p = 0.425). Hypoventilation incidence was similar in PACU (sugammadex 55% vs. neostigmine 58%, p = 1.000) and the ward (69% vs. 67%, p = 1.000) before or after adjusting for RNMB, opioids received, and other covariates.
CONCLUSIONS: Sugammadex was non-inferior to neostigmine on the incidence of RNMB and hypoventilation, even after adjusting for RNMB, opioids, and other covariates, in PACU and up to three days after kidney transplantation.
TRIAL REGISTRATION: ClinicalTrial.govNCT03923556https://clinicaltrials.gov/ct2/show/NCT03923556.