• Sao Paulo Med J · Jan 2014

    Randomized Controlled Trial

    Continuous positive airway pressure (CPAP) after lung resection: a randomized clinical trial.

    • Lígia dos Santos Roceto, Fernanda Diório Masi Galhardo, Ivete Alonso Bredda Saad, and Ivan Felizardo Contrera Toro.
    • Clinical Hospital, School of Medical Sciences, Universidade Estadual de Campinas, CampinasSão Paulo, Brazil.
    • Sao Paulo Med J. 2014 Jan 1; 132 (1): 414741-7.

    Context And ObjectiveNoninvasive mechanical ventilation during the postoperative period (PO) following lung resection can restore residual functional capacity, improve oxygenation and spare the inspiratory muscles. The objective of this study was to assess the efficacy of continuous positive airway pressure (CPAP) associated with physiotherapy, compared with physiotherapy alone after lung resection.Design And SettingOpen randomized clinical trial conducted in the clinical hospital of Universidade Estadual de Campinas.MethodSessions were held in the immediate postoperative period (POi) and on the first and second postoperative days (PO1 and PO2), and the patients were reassessed on the discharge day. CPAP was applied for two hours and the pressure adjustment was set between 7 and 8.5 cmH2O. The oxygenation index (OI), Borg scale, pain scale and presence of thoracic drains and air losses were evaluated.ResultsThere was a significant increase in the OI in the CPAP group in the POi compared to the Chest Physiotherapy (CP) group, P = 0.024. In the CP group the OI was significantly lower on PO1 (P = 0,042), than CPAP group. The air losses were significantly greater in the CPAP group in the POi and on PO1 (P = 0.001, P = 0.028), but there was no significant difference between the groups on PO2 and PO3. There was a statistically significant difference between the groups regarding the Borg scale in the POi (P < 0.001), but there were no statistically significant differences between the groups regarding the pain score.ConclusionCPAP after lung resection is safe and improves oxygenation, without increasing the air losses through the drains.Clinical Trial RegistrationNCT01285648.

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