Chaney 2000.
Methods | RCT with parallel groups Institutional review board approval and informed consents obtained Site: Loyola University Medical Center Setting: university hospital Dates of data collection: unspecified |
|
Participants | 25 participants scheduled for elective coronary artery bypass graft surgery and early tracheal extubation Exclusion criteria: previous lung surgery or who required preoperative mechanical ventilation |
|
Interventions |
Treatment group: tidal volume 6 mL/kg; FiO2 1.0; respiratory rate 16 breaths/min; and
PEEP 5, after tracheal intubation (n = 12) Control group: tidal volume 12 mL/kg; respiratory rate 8 breaths/min; FiO2 1.0; and PEEP 5 cmH2O, after tracheal intubation (n = 13) In both groups, the inspiratory/expiratory ratio was 1:3, and the inspiratory flow was adjusted so that the calculated tidal volume was delivered during the entire inspiratory cycle (creating the lowest peak airway pressure). Each mode of ventilation (conventional or protective) was used during the entire intraoperative period and during the first hour after arrival in the ICU. After 1 hour following ICU arrival (and after last data collection time), all participants received mechanical ventilation parameters of respiratory rate 10 breaths/min; tidal volume 8 mL/kg; FiO2 1.0 and PEEP 15, and were weaned from mechanical ventilation according to the normal ICU protocol. Criteria for extubation in the ICU at this institution included an appropriate sensorium, normothermia, haemodynamic stability, adequate pulmonary function (PaO2 > 60 mmHg with a FiO2 0.4), adequate urine output and minimal chest tube output. |
|
Outcomes |
Relevant to this review
Others
|
|
Notes | Funding: supported by Loyola University Medical Center, Department of Anesthesiology, Research Fund Declaration of interest: none mentioned Postoperative complications and treatments were recorded daily until hospital discharge Volume per body weight: method used to determine body weight unspecified |
|
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Quote: "each patient was randomized to one of two groups by a random numbers table." |
Allocation concealment (selection bias) | Unclear risk | Quote: "before arriving in the operating room"; no other details. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Not mentioned |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not mentioned |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No loss to follow‐up |
Selective reporting (reporting bias) | Low risk | All results reported |
Other bias | Low risk | Groups well balanced |