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横纹肌溶解症在儿科急诊的临床表现。

Clinical spectrum of rhabdomyolysis presented to pediatric emergency department.

机构信息

Department of Pediatrics, Taichung Tzuchi Hospital, the Buddhist Medical Foundation, Taichung, Taiwan.

出版信息

BMC Pediatr. 2013 Sep 3;13:134. doi: 10.1186/1471-2431-13-134.

Abstract

BACKGROUND

Rhabdomyolysis is a potentially life-threatening syndrome that can develop from a variety of causes. The aim of the work is to analyze the clinical spectrum and to evaluate the prevalence of various etiologies in children, who present to the emergency department (ED) with rhabdomyolysis.

METHODS

During a 6-year study period, we retrospectively analyzed the medical charts of patients, aged 18 years or younger, with a definite diagnosis of rhabdomyolysis and serum creatinine phosphokinase (CK) levels greater than 1000IU/L. We analyzed the clinical spectrum and evaluated the potential risk factors of acute renal failure (ARF).

RESULTS

Thirty-seven patients (mean age = 10.2 ± 5.5 years), including 26 males and 11 females, were enrolled in the study. Two of the most common presented symptoms in these 37 patients were muscle pain and muscle weakness (83.8% and 73%, respectively). Dark urine was reported in only 5.4% of the patients. The leading cause of rhabdomyolysis in the 0- to 9-year age group was presumed infection, and the leading cause in the 10- to 18-year age group was trauma and exercise. The incidence of ARF associated with rhabdomyolysis was 8.1 % and no child needed for renal replacement therapy (RRT). We did not identify any reliable predictors of ARF or need for RRT.

CONCLUSIONS

The classic triad of symptoms of rhabdomyolysis includes myalgia, weakness and dark urine are not always presented in children. The cause of rhabdomyolysis in younger age is different from that of teenager group. However, the prognosis of rhabdomyolysis was good with appropriate management.

摘要

背景

横纹肌溶解症是一种潜在危及生命的综合征,可由多种原因引起。本研究的目的是分析其临床特征,并评估各种病因在儿童中出现横纹肌溶解症的患病率。

方法

在 6 年的研究期间,我们回顾性分析了年龄在 18 岁以下,血清肌酸磷酸激酶(CK)水平大于 1000IU/L,明确诊断为横纹肌溶解症且病历资料完整的患者。我们分析了临床特征,并评估了急性肾功能衰竭(ARF)的潜在危险因素。

结果

37 例患者(平均年龄 10.2±5.5 岁,男 26 例,女 11 例)纳入研究。37 例患者中最常见的两种表现是肌肉疼痛和肌肉无力(83.8%和 73%)。仅有 5.4%的患者出现茶色尿。0-9 岁年龄组横纹肌溶解症的主要原因是感染,10-18 岁年龄组的主要原因是创伤和运动。横纹肌溶解症相关 ARF 的发生率为 8.1%,没有患儿需要肾脏替代治疗(RRT)。我们没有发现 ARF 或需要 RRT 的任何可靠预测因素。

结论

横纹肌溶解症的经典三联征包括肌痛、无力和茶色尿,在儿童中并非总是同时出现。较小年龄的横纹肌溶解症病因与青少年组不同。然而,横纹肌溶解症的预后良好,经适当治疗后可缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf1/3766249/6b596a8b6e3c/1471-2431-13-134-1.jpg

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