Postoperative Pulmonary Complications in the ENIGMA II Trial: APost HocAnalysis

Author:

Peyton Philip J.1ORCID,Liskaser Grace2,Ho Alexander3,Marsh Harry4,Etherington Christopher5,Torlot Frederick6,Desai Manisha7,Perrett George8,Chee Brian9,Leslie Kate10,Myles Paul S.11

Affiliation:

1. 1Department of Anaesthesia, Austin Health, Heidelberg, Victoria, Australia; and the Department of Critical Care, Melbourne Medical School, University of Melbourne, Melbourne, Victoria, Australia.

2. 2Department of Anaesthesia, Austin Health, Heidelberg, Victoria, Australia.

3. 3Department of Anaesthesia, Austin Health, Heidelberg, Victoria, Australia.

4. 4Department of Anaesthesia, Austin Health, Heidelberg, Victoria, Australia.

5. 5Department of Anaesthesia, Barwon Health, Geelong, Victoria, Australia.

6. 6Department of Anaesthesia, Royal Perth Hospital, Perth, Western Australia, Australia.

7. 7Department of Anaesthesia, Fremantle Hospital, Fremantle, Western Australia, Australia.

8. 8Department of Anaesthesia, Westmead Hospital, Sydney, New South Wales, Australia.

9. 9Department of Anaesthesia, Austin Health, Heidelberg, Victoria, Australia.

10. 10Department of Critical Care, Melbourne Medical School, University of Melbourne, Melbourne, Victoria, Australia; the Royal Melbourne Hospital, Parkville, Victoria, Australia; and Monash University, Melbourne, Victoria, Australia.

11. 11Department of Anaesthesia and Perioperative Medicine, The Alfred, Melbourne, Victoria, Australia; and Monash University, Melbourne, Victoria, Australia.

Abstract

BackgroundNitrous oxide promotes absorption atelectasis in poorly ventilated lung segments at high inspired concentrations. The Evaluation of Nitrous oxide In the Gas Mixture for Anesthesia (ENIGMA) trial found a higher incidence of postoperative pulmonary complications and wound sepsis with nitrous oxide anesthesia in major surgery compared to a fraction of inspired oxygen of 0.8 without nitrous oxide. The larger ENIGMA II trial randomized patients to nitrous oxide or air at a fraction of inspired oxygen of 0.3 but found no effect on wound infection or sepsis. However, postoperative pulmonary complications were not measured. In the current study, post hoc data were collected to determine whether atelectasis and pneumonia incidences were higher with nitrous oxide in patients who were recruited to the Australian cohort of ENIGMA II.MethodsDigital health records of patients who participated in the trial at 10 Australian hospitals were examined blinded to trial treatment allocation. The primary endpoint was the incidence of atelectasis, defined as lung atelectasis or collapse reported on chest radiology. Pneumonia, as a secondary endpoint, required a diagnostic chest radiology report with fever, leukocytosis, or positive sputum culture. Comparison of the nitrous oxide and nitrous oxide–free groups was done according to intention to treat using chi-square tests.ResultsData from 2,328 randomized patients were included in the final data set. The two treatment groups were similar in surgical type and duration, risk factors, and perioperative management recorded for ENIGMA II. There was a 19.3% lower incidence of atelectasis with nitrous oxide (171 of 1,169 [14.6%] vs. 210 of 1,159 [18.1%]; odds ratio, 0.77; 95% CI, 0.62 to 0.97; P = 0.023). There was no difference in pneumonia incidence (60 of 1,169 [5.1%] vs. 52 of 1159 [4.5%]; odds ratio, 1.15; 95% CI, 0.77 to 1.72; P = 0.467) or combined pulmonary complications (odds ratio, 0.84; 95% CI, 0.69 to 1.03; P = 0.093).ConclusionsIn contrast to the earlier ENIGMA trial, nitrous oxide anesthesia in the ENIGMA II trial was associated with a lower incidence of lung atelectasis, but not pneumonia, after major surgery.Editor’s PerspectiveWhat We Already Know about This TopicWhat This Article Tells Us That Is New

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

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