Dexamethasone for Cardiac Surgery: A Practice Preference-Randomized Consent Comparative Effectiveness Trial

被引:6
作者
Myles, Paul S. [1 ,2 ]
Dieleman, Jan M. [3 ]
Munting, Karin E. [4 ]
Forbes, Andrew [5 ]
Martin, Catherine A. [5 ]
Smith, Julian A. [6 ,7 ]
Mcgiffin, David [8 ]
Verheijen, Lieke P. J. [4 ]
Wallace, Sophie [1 ,2 ]
DECS II Investigators
ANZCA Clinical Trials Network
机构
[1] Alfred Hosp, Dept Anaesthesiol & Perioperat Med, Commercial Rd, Melbourne, Vic 3004, Australia
[2] Monash Univ, Melbourne, Australia
[3] Western Sydney Univ, Westmead Hosp, Dept Anaesthesia, Penrith, Australia
[4] Univ Med Ctr, Dept Anaesthesia, Utrecht, Netherlands
[5] Monash Univ, Sch Publ Hlth & Prevent Med, Biostat Unit, Melbourne, Australia
[6] Monash Univ, Sch Clin Sci, Dept Cardiothorac Surg, Monash Hlth, Clayton, Australia
[7] Monash Univ, Sch Clin Sci, Dept Surg, Monash Hlth, Clayton, Australia
[8] Alfred Hosp, Dept Cardiothorac Surg, Melbourne, Australia
关键词
CARDIOPULMONARY BYPASS; CLINICAL-TRIALS; DOUBLE-BLIND; CREDIBILITY;
D O I
10.1097/ALN.0000000000005127
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BackgroundHigh-dose corticosteroids have been used to attenuate the inflammatory response to cardiac surgery and cardiopulmonary bypass, but patient outcome benefits remain unclear. The primary aim was to determine whether using dexamethasone was superior to not using dexamethasone to increase the number of home days in the first 30 days after cardiac surgery. The secondary aim was to evaluate efficiency, value, and impact of the novel trial design. MethodsThis pragmatic, international trial incorporating a prerandomized consent design favoring local practice enrolled patients undergoing cardiac surgery across seven hospitals in Australia and The Netherlands. Patients were randomly assigned to dexamethasone 1 mg/kg or not (control). The primary outcome was the number of days alive and at home up to 30 days after surgery ("home days"). Secondary outcomes included prolonged mechanical ventilation (more than 48 h), sepsis, renal failure, myocardial infarction, stroke, and death. ResultsOf 2,562 patients assessed for eligibility, 1,951 were randomized (median age, 63 yr; 80% male). The median number of home days was 23.0 (interquartile range, 20.1 to 24.1) in the no dexamethasone group and 23.1 (interquartile range, 20.1 to 24.6) in the dexamethasone group (median difference, 0.1; 95% CI, -0.3 to 0.5; P = 0.66). The rates of prolonged mechanical ventilation (risk ratio, 0.72; 95% CI, 0.48 to 1.08), sepsis (risk ratio, 1.02; 95% CI, 0.57 to 1.82), renal failure (risk ratio, 0.94; 95% CI, 0.80 to 1.12), myocardial infarction (risk ratio, 1.20; 95% CI, 0.30 to 4.82), stroke (risk ratio, 1.06; 95% CI, 0.54 to 2.08), and death (risk ratio, 0.72; 95% CI, 0.22 to 2.35) were comparable between groups (all P > 0.10). Dexamethasone reduced intensive care unit stay (median, 29 h; interquartile range, 22 to 50 h vs. median, 43 h; interquartile range, 24 to 72 h; P = 0.004). The authors' novel trial design was highly efficient (89.3% enrollment). ConclusionsAmong patients undergoing cardiac surgery, high-dose dexamethasone decreased intensive care unit stay but did not increase the number of home days after surgery.
引用
收藏
页码:859 / 869
页数:11
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