Schmittinger Christian A, Dünser Martin W, Haller Maria, Ulmer Hanno, Luckner Günter, Torgersen Christian, Jochberger Stefan, Hasibeder Walter R
Department of Anaesthesiology and Critical Care Medicine, Innsbruck Medical University, Anichstrasse 35, 6020 Innsbruck, Austria.
Crit Care. 2008;12(4):R99. doi: 10.1186/cc6976. Epub 2008 Aug 4.
The multifactorial etiology of septic cardiomyopathy is not fully elucidated. Recently, high catecholamine levels have been suggested to contribute to impaired myocardial function.
This retrospective analysis summarizes our preliminary clinical experience with the combined use of milrinone and enteral metoprolol therapy in 40 patients with septic shock and cardiac depression. Patients with other causes of shock or cardiac failure, patients with beta-blocker therapy initiated more than 48 hours after shock onset, and patients with pre-existent decompensated congestive heart failure were excluded. In all study patients, beta blockers were initiated only after stabilization of cardiovascular function (17.7 +/- 15.5 hours after shock onset or intensive care unit admission) in order to decrease the heart rate to less than 95 beats per minute (bpm). Hemodynamic data and laboratory parameters were extracted from medical charts and documented before and 6, 12, 24, 48, 72, and 96 hours after the first metoprolol dosage. Adverse cardiovascular events were documented. Descriptive statistical methods and a linear mixed-effects model were used for statistical analysis.
Heart rate control (65 to 95 bpm) was achieved in 97.5% of patients (n = 39) within 12.2 +/- 12.4 hours. Heart rate, central venous pressure, and norepinephrine, arginine vasopressin, and milrinone dosages decreased (all P < 0.001). Cardiac index and cardiac power index remained unchanged whereas stroke volume index increased (P = 0.002). In two patients (5%), metoprolol was discontinued because of asymptomatic bradycardia. Norepinephrine and milrinone dosages were increased in nine (22.5%) and six (15%) patients, respectively. pH increased (P < 0.001) whereas arterial lactate (P < 0.001), serum C-reactive protein (P = 0.001), and creatinine (P = 0.02) levels decreased during the observation period. Twenty-eight-day mortality was 33%.
Low doses of enteral metoprolol in combination with phosphodiesterase inhibitors are feasible in patients with septic shock and cardiac depression but no overt heart failure. Future prospective controlled trials on the use of beta blockers for septic cardiomyopathy and their influence on proinflammatory cytokines are warranted.
脓毒症性心肌病的多因素病因尚未完全阐明。最近,有人提出高儿茶酚胺水平会导致心肌功能受损。
这项回顾性分析总结了我们对40例脓毒症休克合并心功能抑制患者联合使用米力农和肠内美托洛尔治疗的初步临床经验。排除其他休克或心力衰竭病因的患者、休克发作后48小时以上开始使用β受体阻滞剂治疗的患者以及已有失代偿性充血性心力衰竭的患者。在所有研究患者中,仅在心血管功能稳定后(休克发作或入住重症监护病房后17.7±15.5小时)才开始使用β受体阻滞剂,以使心率降至每分钟95次以下。从病历中提取血流动力学数据和实验室参数,并记录首次使用美托洛尔前以及用药后6、12、24、48、72和96小时的数据。记录不良心血管事件。采用描述性统计方法和线性混合效应模型进行统计分析。
97.5%的患者(n = 39)在12.2±12.4小时内实现了心率控制(65至95次/分钟)。心率、中心静脉压以及去甲肾上腺素、精氨酸加压素和米力农的用量均降低(均P < 0.001)。心脏指数和心脏功率指数保持不变,而每搏量指数增加(P = 0.002)。两名患者(5%)因无症状性心动过缓停用美托洛尔。分别有9例(22.5%)和6例(15%)患者增加了去甲肾上腺素和米力农的用量。在观察期内,pH值升高(P < 0.001),而动脉血乳酸(P < 0.001)、血清C反应蛋白(P = 0.001)和肌酐(P = 0.02)水平降低。28天死亡率为33%。
低剂量肠内美托洛尔联合磷酸二酯酶抑制剂对脓毒症休克合并心功能抑制但无明显心力衰竭的患者是可行的。未来有必要针对脓毒症性心肌病使用β受体阻滞剂及其对促炎细胞因子的影响进行前瞻性对照试验。