Effect of Intravenous Acetaminophen on Postoperative Hypoxemia After Abdominal Surgery: The FACTOR Randomized Clinical Trial
- Alparslan Turan 1,2, Hani Essber 2, Wael Saasouh 2, Karen Hovsepyan 2, Natalya Makarova 2,3, Sabry Ayad 1,4, Barak Cohen 1,5, Kurt Ruetzler 1,2, Loran Mounir Soliman 2, Kamal Maheshwari 1,2, Dongsheng Yang 2,3, Edward J Mascha 2,3, Wael Ali Sakr Esa 2, Herman Kessler 6, Conor P Delaney 6, Daniel I Sessler 1,
- Alparslan Turan 1,2, Hani Essber 2, Wael Saasouh 2
- 1Department of Outcomes Research, Cleveland Clinic, Cleveland, Ohio.
- 2Department of General Anesthesiology, Cleveland Clinic, Cleveland, Ohio.
- 3Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.
- 4Department of Regional Anesthesia, Anesthesiology Institute, Cleveland Clinic, Cleveland, Ohio.
- 5Division of Anesthesiology, Intensive Care, and Pain Management, Tel Aviv Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
- 6Department of Colorectal Surgery, Cleveland Clinic, Cleveland, Ohio.
- 0Department of Outcomes Research, Cleveland Clinic, Cleveland, Ohio.
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View abstract on PubMed
Summary
This summary is machine-generated.Postoperative hypoxemia was not significantly reduced by intravenous acetaminophen compared to placebo in abdominal surgery patients. This study does not support its use for decreasing hypoxemia duration.
Area Of Science
- Anesthesiology
- Critical Care Medicine
- Surgical Outcomes
Background
- Opioid-induced ventilatory depression and hypoxemia are common postoperative complications.
- Nonopioid analgesics may reduce opioid consumption and subsequent hypoxemia.
Purpose Of The Study
- To test if intravenous acetaminophen reduces the duration of hypoxemia compared to placebo in postoperative patients.
- To evaluate the impact of acetaminophen on opioid consumption and pain.
Main Methods
- A randomized, placebo-controlled, double-blind trial involving 570 patients undergoing abdominal surgery.
- Patients received intravenous acetaminophen (1g) or placebo every 6 hours for 48 hours postoperatively.
- Primary outcome was the total duration of hypoxemia (SpO2 <90%) over 48 hours.
Main Results
- The median duration of hypoxemia was not significantly different between the acetaminophen and placebo groups (0.7 vs 1.1 minutes/hour, P=.29).
- No significant differences were observed in secondary outcomes, including opioid consumption, pain scores, nausea, vomiting, and sedation.
- Mean pain scores were similar (4.2 vs 4.4) and opioid use was not significantly reduced.
Conclusions
- Postoperative intravenous acetaminophen did not significantly reduce the duration of hypoxemia in patients undergoing abdominal surgery.
- The findings do not support the use of intravenous acetaminophen for the specific purpose of reducing postoperative hypoxemia.
- Further research may be needed to explore alternative strategies for managing postoperative hypoxemia.
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