Article Text
Abstract
Objective To assess the diagnostic accuracy of peripheral capillary oxygen saturation (SpO2) while breathing room air for 5 min (the ‘Air-Test’) in detecting postoperative atelectasis.
Design Prospective cohort study. Diagnostic accuracy was assessed by measuring the agreement between the index test and the reference standard CT scan images.
Setting Postanaesthetic care unit in a tertiary hospital in Spain.
Participants Three hundred and fifty patients from 12 January to 7 February 2015; 170 patients scheduled for surgery under general anaesthesia who were admitted into the postsurgical unit were included.
Intervention The Air-Test was performed in conscious extubated patients after a 30 min stabilisation period during which they received supplemental oxygen therapy via a venturi mask. The Air-Test was defined as positive when SpO2 was ≤96% and negative when SpO2 was ≥97%. Arterial blood gases were measured in all patients at the end of the Air-Test. In the subsequent 25 min, the presence of atelectasis was evaluated by performing a CT scan in 59 randomly selected patients.
Main outcome measures The primary study outcome was assessment of the accuracy of the Air-Test for detecting postoperative atelectasis compared with the reference standard. The secondary outcome was the incidence of positive Air-Test results.
Results The Air-Test diagnosed postoperative atelectasis with an area under the receiver operating characteristic curve of 0.90 (95% CI 0.82 to 0.98) with a sensitivity of 82.6% and a specificity of 87.8%. The presence of atelectasis was confirmed by CT scans in all patients (30/30) with positive and in 5 patients (17%) with negative Air-Test results. Based on the Air-Test, postoperative atelectasis was present in 36% of the patients (62 out of 170).
Conclusion The Air-Test may represent an accurate, simple, inexpensive and non-invasive method for diagnosing postoperative atelectasis.
Trial Registration NCT02650037.
- postoperative
- atelectasis
- oxygenation
- SpO2
- adult anaesthesia
- adult intensive & critical care
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Footnotes
Contributors CF and FJB had full access to all data and are responsible for the integrity and the accuracy of the data analysis. Study design: CF, CR, JR, GT, FSS and FJB. Acquisition and analysis of data: CF, CR, JR, RD, GT, MS, PV, AV, FS, AJ, JuC, JN, CP, NP, CR, JR, JV and FJB. Interpretation of data: CF, GT and JaC. Drafting of the manuscript: CF, JV and FJB. Critical revision of the manuscript for intellectual content: CF, GT, FSS, JaC, JV and FJB.
Funding This research received no specific grants from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests All the authors have completed the ICMJE uniform disclosure form atwww.icmje.org/coi_disclosure.pdf and declare they received/have: no support from any organisation for the submitted work; no financial relationships.
Ethics approval The study was approved by the Local Ethics Committee for Clinical Research in accordance with the Declaration of Helsinki (Chairperson: Dr Antonio Peláez), and registered on 28 December 2015 at
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement Additional unpublished data are available by request to the lead author.