Lung-Protective Ventilation Strategies for Relief from Ventilator-Associated Lung Injury in Patients Undergoing Craniotomy: A Bicenter Randomized, Parallel, and Controlled Trial.
Chaoliang TangJuan LiShao-Qing LeiBo ZhaoZhetao ZhangWenting HuangSi ShiXiaoqing ChaiChaoshi NiuZhong-Yuan XiaPublished in: Oxidative medicine and cellular longevity (2017)
Current evidence indicates that conventional mechanical ventilation often leads to lung inflammatory response and oxidative stress, while lung-protective ventilation (LPV) minimizes the risk of ventilator-associated lung injury (VALI). This study evaluated the effects of LPV on relief of pulmonary injury, inflammatory response, and oxidative stress among patients undergoing craniotomy. Sixty patients undergoing craniotomy received either conventional mechanical (12 mL/kg tidal volume [VT] and 0 cm H2O positive end-expiratory pressure [PEEP]; CV group) or protective lung (6 mL/kg VT and 10 cm H2O PEEP; PV group) ventilation. Hemodynamic variables, lung function indexes, and inflammatory and oxidative stress markers were assessed. The PV group exhibited greater dynamic lung compliance and lower respiratory index than the CV group during surgery (P < 0.05). The PV group exhibited higher plasma interleukin- (IL-) 10 levels and lower plasma malondialdehyde and nitric oxide and bronchoalveolar lavage fluid, IL-6, IL-8, tumor necrosis factor-α, IL-10, malondialdehyde, nitric oxide, and superoxide dismutase levels (P < 0.05) than the CV group. There were no significant differences in hemodynamic variables, blood loss, liquid input, urine output, or duration of mechanical ventilation between the two groups (P > 0.05). Patients receiving LPV during craniotomy exhibited low perioperative inflammatory response, oxidative stress, and VALI.
Keyphrases
- mechanical ventilation
- oxidative stress
- inflammatory response
- patients undergoing
- acute respiratory distress syndrome
- nitric oxide
- respiratory failure
- intensive care unit
- lung function
- lipopolysaccharide induced
- dna damage
- diabetic rats
- induced apoptosis
- ischemia reperfusion injury
- lps induced
- chronic obstructive pulmonary disease
- open label
- minimally invasive
- hydrogen peroxide
- double blind
- cystic fibrosis
- rheumatoid arthritis
- randomized controlled trial
- pulmonary hypertension
- toll like receptor
- percutaneous coronary intervention
- coronary artery bypass
- heat shock
- phase ii