Zhu Lei, Qi Bo-Xiang, Fang Dai-Hua, Qi Gong-Jian, Gao Kun, Hu Bao-Li
Department of Intensive Care Unit, Xuzhou Children's Hospital, Xuzhou, Jiangsu 221006, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2017 Jan;19(1):44-48. doi: 10.7499/j.issn.1008-8830.2017.01.006.
To study the clinical effect and mechanism of action of esmolol in the treatment of severe hand, foot, and mouth disease (HFMD).
A prospective randomized controlled trial was performed. A total of 102 children with severe HFMD were enrolled in the study and were randomly divided into conventional treatment and esmolol treatment groups (n=51 each). The children in the conventional treatment group were given conventional treatment according to the guidelines for the diagnosis and treatment of HFMD. Those in the esmolol treatment group were given esmolol in addition to the conventional treatment. The heart rate (HR), systolic blood pressure (SBP), and respiratory rate (RR) were continuously monitored for all children. Blood samples were collected from all children before treatment and 1, 3, and 5 days after treatment to measure the levels of norepinephrine (NE), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and nuclear factor-kappa B (NF-κB) p65 in mononuclear cells. Serum levels of myocardial enzymes and N-terminal pro-brain natriuretic peptide (NT-proBNP) were measured before treatment and after 5 days of treatment.
There were no significant differences in HR, SBP, RR, NE, TNF-α, IL-6, NF-κB p65, serum myocardial enzymes, and NT-proBNP before treatment between the conventional treatment and esmolol treatment groups. Both groups had significant reductions in these parameters at each time point (P<0.05). Compared with the conventional treatment group, the esmolol treatment group had significant improvements in the above parameters after 1 and 3 days of treatment (P<0.05). After 5 days of treatment, the esmolol treatment group had significant improvements in serum levels of myocardial enzymes and NT-proBNP compared with the conventional treatment group (P<0.05).
Early application of esmolol can effectively stabilize the vital signs of the children with severe HFMD. Its mechanism of action may be related to reducing serum catecholamine concentration, alleviating myocardial damage, improving cardiac function, and reducing inflammatory response.
研究艾司洛尔治疗重症手足口病(HFMD)的临床疗效及作用机制。
进行一项前瞻性随机对照试验。共纳入102例重症手足口病患儿,随机分为常规治疗组和艾司洛尔治疗组(每组n = 51)。常规治疗组患儿按照手足口病诊疗指南给予常规治疗。艾司洛尔治疗组患儿在常规治疗基础上给予艾司洛尔。持续监测所有患儿的心率(HR)、收缩压(SBP)和呼吸频率(RR)。在治疗前及治疗后1、3、5天采集所有患儿的血样,检测单核细胞中去甲肾上腺素(NE)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和核因子-κB(NF-κB)p65的水平。在治疗前及治疗5天后检测血清心肌酶和N末端脑钠肽前体(NT-proBNP)水平。
常规治疗组和艾司洛尔治疗组治疗前在HR、SBP、RR、NE、TNF-α、IL-6、NF-κB p65、血清心肌酶和NT-proBNP方面无显著差异。两组在各时间点这些参数均有显著降低(P<0.05)。与常规治疗组相比,艾司洛尔治疗组在治疗1天和3天后上述参数有显著改善(P<0.05)。治疗5天后,艾司洛尔治疗组血清心肌酶和NT-proBNP水平与常规治疗组相比有显著改善(P<0.05)。
早期应用艾司洛尔可有效稳定重症手足口病患儿的生命体征。其作用机制可能与降低血清儿茶酚胺浓度、减轻心肌损伤、改善心功能及减轻炎症反应有关。