Extended-time of noninvasive positive pressure ventilation improves tissue perfusion after coronary artery bypass surgery: a randomized clinical trial
Rev. bras. cir. cardiovasc; 33 (3), 2018
Publication year: 2018
Abstract Objective:
To compare the effects of extended- versus short-time noninvasive positive pressure ventilation on pulmonary function, tissue perfusion, and clinical outcomes in the early postoperative period following coronary artery bypass surgery in patients with preserved left ventricular function.Methods:
Patients were randomized into two groups according to noninvasive positive pressure ventilation intensity: short-time noninvasive positive pressure ventilation n=20 (S-NPPV) and extended-time noninvasive positive pressure ventilation n=21 (E-NPPV). S-NPPV was applied for 60 minutes during immediate postoperative period and 10 minutes, twice daily, from postoperative days 1-5. E-NPPV was performed for at least six hours during immediate postoperative period and 60 minutes, twice daily, from postoperative days 1-5. As a primary outcome, tissue perfusion was determined by central venous oxygen saturation and blood lactate level measured after anesthetic induction, immediately after extubation and following noninvasive positive pressure ventilation protocols. As a secondary outcome, pulmonary function tests were performed preoperatively and in the postoperative days 1, 3, and 5; clinical outcomes were recorded.Results:
Significant drop in blood lactate levels and an improvement in central venous oxygen saturation values in the E-NPPV group were observed when compared with S-NPPV group after study protocol (P<0.01). The E-NPPV group presented higher preservation of postoperative pulmonary function as well as lower incidence of respiratory events and shorter postoperative hospital stay (P<0.05).Conclusion:
Prophylactic E-NPPV administered in the early postoperative period of coronary artery bypass surgery resulted in greater improvements in tissue perfusion, pulmonary function and clinical outcomes than S-NPPV, in patients with preserved left ventricular function.Trial Registration:
Brazilian Registry of Clinical trial - RBR7sqj78 - http://www.ensaiosclinicos.gov.br
Análisis de Varianza, Puente de Arteria Coronaria/efectos adversos, Puente de Arteria Coronaria/métodos, Volumen Espiratorio Forzado, Ácido Láctico/sangre, Tiempo de Internación, Enfermedades Pulmonares/sangre, Enfermedades Pulmonares/etiología, Enfermedades Pulmonares/prevención & control, Ventilación no Invasiva/métodos, Oxígeno/sangre, Respiración con Presión Positiva/métodos, Complicaciones Posoperatorias/sangre, Complicaciones Posoperatorias/prevención & control, Factores de Riesgo, Estadísticas no Paramétricas, Factores de Tiempo, Resultado del Tratamiento, Capacidad Vital