Effect of Intravenous Acetaminophen on Postoperative Hypoxemia After Abdominal Surgery

医学 麻醉 低氧血症 四分位间距 安慰剂 对乙酰氨基酚 镇静 随机对照试验 外科 恶心 术后恶心呕吐 病理 替代医学
作者
Alparslan Turan,Hani Essber,Wael Saasouh,Karen Hovsepyan,Natalya Makarova,Sabry Ayad,Barak Cohen,Kurt Ruetzler,Loran Mounir Soliman,Kamal Maheshwari,Dongsheng Yang,Edward J. Mascha,Wael Ali Sakr Esa,Herman Kessler,Conor P. Delaney,Daniel I. Sessler
出处
期刊:JAMA [American Medical Association]
卷期号:324 (4): 350-350 被引量:29
标识
DOI:10.1001/jama.2020.10009
摘要

Importance

Opioid-induced ventilatory depression and hypoxemia is common, severe, and often unrecognized in postoperative patients. To the extent that nonopioid analgesics reduce opioid consumption, they may decrease postoperative hypoxemia.

Objective

To test the hypothesis that duration of hypoxemia is less in patients given intravenous acetaminophen than those given placebo.

Design, Setting, and Participants

Randomized, placebo-controlled, double-blind trial conducted at 2 US academic hospitals among 570 patients who were undergoing abdominal surgery, enrolled from February 2015 through October 2018 and followed up until February 2019.

Interventions

Participants were randomized to receive either intravenous acetaminophen, 1 g (n = 289), or normal saline placebo (n = 291) starting at the beginning of surgery and repeated every 6 hours until 48 postoperative hours or hospital discharge, whichever occurred first.

Main Outcomes and Measures

The primary outcome was the total duration of hypoxemia (hemoglobin oxygen saturation [Spo2] <90%) per hour, with oxygen saturation measured continuously for 48 postoperative hours. Secondary outcomes were postoperative opioid consumption, pain (0- 10-point scale; 0: no pain; 10: the most pain imaginable), nausea and vomiting, sedation, minimal alveolar concentration of volatile anesthetic, fatigue, active time, and respiratory function.

Results

Among 580 patients randomized (mean age, 49 years; 48% women), 570 (98%) completed the trial. The primary outcome, median duration with Spo2of less than 90%, was 0.7 (interquartile range [IQR], 0.1-5.1) minutes per hour among patients in the acetaminophen group and 1.1 (IQR, 0.1-6.6) minutes per hour among patients in the placebo group (P = .29), with an estimated median difference of −0.04 (95% CI,−0.18 to 0.11) minutes per hour. None of the 8 secondary end points differed significantly between the acetaminophen and placebo groups. Mean pain scores within initial 48 postoperative hours were 4.2 (SD, 1.8) in the acetaminophen group and 4.4 (SD, 1.8) in the placebo group (difference, −0.28; 95% CI, –0.71 to 0.15); median opioid use in morphine equivalents was 50 mg (IQR, 18-122 mg) and 58 mg (IQR, 24-151 mg) , respectively, with a ratio of geometric means of 0.86 (95% CI, 0.61-1.21).

Conclusions and Relevance

Among patients who underwent abdominal surgery, use of postoperative intravenous acetaminophen, compared with placebo, did not significantly reduce the duration of postoperative hypoxemia over 48 hours. The study findings do not support the use of intravenous acetaminophen for this purpose.

Trial Registration

ClinicalTrials.gov Identifier:NCT02156154
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