Table 4.
Outcome analysis
Non-OLS (n = 130) | OLS (n = 130) | Unadjusted relative risk (95% CI) | P value | Adjusted relative risk (95% CI)a | P valuea | |
Primary outcomeb | ||||||
Major postoperative pulmonary and extrapulmonary complications | 43 (33.1) | 24 (18.5) | 0.46 (0.26 to 0.81) | 0.010 | 0.46 (0.26 to 0.82) | 0.009 |
Secondary and post hoc outcomes | ||||||
Complications within 7 days | ||||||
Major pulmonary complications | 41 (31.5) | 24 (18.5) | 0.49 (0.28 to 0.88) | 0.022 | 0.49 (0.28 to 0.88) | 0.016 |
Major extrapulmonary complications | 6 (4.6) | 2 (1.5) | 0.32 (0.06 to 1.63) | 0.281 | 0.32 (0.06 to 1.63) | 0.171 |
Acute respiratory failure | 39 (30.0) | 24 (18.5) | 0.53 (0.30 to 0.94) | 0.042 | 0.53 (0.30 to 0.94) | 0.031 |
Modified acute respiratory failurec,f | 30 (23.1) | 17 (13.1) | 0.50 (0.26 to 0.96) | 0.052 | 0.50 (0.26 to 0.96) | 0.038 |
Suspected pneumoniag | 16 (12.3) | 3 (2.3) | 0.17 (0.05 to 0.59) | 0.003 | 0.18 (0.05 to 0.62) | 0.007 |
Sustained hypoxaemia | 24 (18.5) | 15 (11.5) | 0.58 (0.29 to 1.16) | 0.164 | 0.58 (0.29 to 1.16) | 0.121 |
Severe respiratory failured,f | 0 (0.0) | 0 (0.0) | 1.000 | |||
All defined major PPCs in one patientf | 11 (8.5) | 3 (2.3) | 0.26 (0.07 to 0.94) | 0.051 | 0.26 (0.07 to 0.98) | 0.047 |
Sepsis | 6 (4.6) | 2 (1.5) | 0.32 (0.06 to 1.63) | 0.281 | 0.32 (0.06 to 1.63) | 0.171 |
Severe sepsis | 0 (0.0) | 0 (0.0) | 1.000 | |||
Septic shock | 0 (0.0) | 0 (0.0) | 1.000 | |||
SIRS | 36 (27.7) | 30 (23.1) | 0.78 (0.48 to 1.37) | 0.476 | 0.79 (0.44 to 1.41) | 0.420 |
Acute myocardial infarction | 0 (0.0) | 0 (0.0) | 1.000 | |||
Intra-abdominal abscess or anastomotic leakage | 5 (3.8) | 2 (1.5) | 0.39 (0.07 to 2.05) | 0.447 | 0.39 (0.07 to 2.05) | 0.267 |
Death within 30 days | 0 (0.0) | 0 (0.0) | 1.000 | |||
Admission to the ICU within 30 days | 0 (0.0) | 1 (0.8) | 1.01 (0.99 to 1.02) | 1.000 | ||
Postoperative hospital stay (days) | 9 [8 to 13] | 10 [8 to 12] | 0.943 | |||
Modified postoperative hospital staye,f | 9 [8 to 10] | 8 [7 to 9] | 0.130 | |||
Intra-operative complications (n = 140) | ||||||
Pneumothorax | 0 (0.0) | 0 (0.0) | 1.000 | |||
Rescue therapy for desaturation | 0 (0.0) | 0 (0.0) | 1.000 | |||
Potentially harmful hypotension | 6 (4.3) | 21 (15.0) | 3.94 (1.54 to 10.09) | 0.004 | 3.32 (1.27 to 8.66) | 0.014 |
Need for vasopressors | 12 (8.6) | 35 (25.0) | 3.56 (1.76 to 7.19) | <0.001 | 2.98 (1.45 to 6.13) | 0.003 |
Data are number (%) or median [IQR] as appropriate. Ten patients in each group were excluded from the study. All postoperative complications were defined according to consensus criteria (see the main text or the Supplementary Appendix). ICU, intensive care unit; OLS, open-lung strategy; PPCs, postoperative pulmonary complications; SIRS, systemic inflammatory response syndrome.
Adjustment was performed for preoperative risk index for PPCs, duration of mechanical ventilation, ASA physical status, abnormalities on chest radiography (and/or having COPD) and intra-operative red blood cells transfusion (and/or intra-operative blood loss ≥300 ml, and/or preoperative haemoglobin <8 g dl−1).
The primary outcome was a composite of major pulmonary complications (acute respiratory failure, suspected pneumonia and sustained hypoxaemia) and extrapulmonary complications (sepsis, severe sepsis, septic shock and death from any cause), defined as positive if any component occurred within the first 7 days after surgery.
Met the criterion of acute respiratory failure in twice follow-up or acute respiratory failure with sustained hypoxaemia.
Experienced an invasive or noninvasive ventilator therapy, or PaO2 less than 60 mmHg or SpO2 less than 90% when administering oxygen via a nasal catheter at 3 l min−1 or more.
On the basis of the final analysis population (130 patients per group), this analysis excluded the patients who had none of the primary outcome events but had a postoperative hospital stay more than 10 days.
Post hoc outcomes.
All of these patients had a postoperative chest X-ray except for three in the non-OLS group.