The metabolic and renal effects of adrenaline and milrinone in patients with myocardial dysfunction after coronary artery bypass grafting

被引:30
作者
Heringlake, Matthias [1 ]
Wernerus, Marit
Gruenefeld, Julia
Klaus, Stephan
Heinze, Hermann
Bechtel, Matthias
Bahlmann, Ludger
Poeling, Jochen
Schoen, Julika
机构
[1] Univ Lubeck, Dept Anesthesiol, D-23538 Lubeck, Germany
[2] Herz Jesu Krankenhaus Munster Hiltrup, Dept Anesthesiol, D-48165 Munster, Germany
[3] Univ Lubeck, Dept Cardiac Surg, D-23538 Lubeck, Germany
[4] Krankenhaus Weser Egge, Dept Anesthesiol, D-37671 Hoxter, Germany
[5] Schuchtermann Klin, Dept Cardiac Surg, D-49214 Bad Rothenfelde, Germany
来源
CRITICAL CARE | 2007年 / 11卷 / 02期
关键词
D O I
10.1186/cc5904
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction Myocardial dysfunction necessitating inotropic support is a typical complication after on-pump cardiac surgery. This prospective, randomized pilot study analyzes the metabolic and renal effects of the inotropes adrenaline and milrinone in patients needing inotropic support after coronary artery bypass grafting ( CABG). Methods During an 18-month period, 251 patients were screened for low cardiac output upon intensive care unit ( ICU) admission after elective, isolated CABG surgery. Patients presenting with a cardiac index ( CI) of less than 2.2 liters/minute per square meter upon ICU admission - despite adequate mean arterial ( titrated with noradrenaline or sodium nitroprusside) and filling pressures - were randomly assigned to 14-hour treatment with adrenaline ( n = 7) or milrinone ( n = 11) to achieve a CI of greater than 3.0 liters/minute per square meter. Twenty patients not needing inotropes served as controls. Hemodynamics, plasma lactate, pyruvate, glucose, acid-base status, insulin requirements, the urinary excretion of alpha-1-microglobuline, and creatinine clearance were determined during the treatment period, and cystatin-C levels were determined up to 48 hours after surgery ( follow-up period). Results After two to four hours after ICU admission, the target CI was achieved in both intervention groups and maintained during the observation period. Plasma lactate, pyruvate, the lactate/pyruvate ratio, plasma glucose, and insulin doses were higher ( p < 0.05) in the adrenaline-treated patients than during milrinone or control conditions. The urinary excretion of alpha-1-microglobuline was higher in the adrenaline than in the control group 6 to 14 hours after admission ( p < 0.05). No between-group differences were observed in creatinine clearance, whereas plasma cystatin-C levels were significantly higher in the adrenaline than in the milrinone or the control group after 48 hours ( p < 0.05). Conclusion This suggests that the use of adrenaline for the treatment of postoperative myocardial dysfunction - in contrast to treatment with the PDE-III inhibitor milrinone - is associated with unwarranted metabolic and renal effects.
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