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首页> 外文期刊>Medicine. >Rhabdomyolysis: an evaluation of 475 hospitalized patients.
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Rhabdomyolysis: an evaluation of 475 hospitalized patients.

机译:横纹肌溶解症:对475名住院患者的评估。

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摘要

Rhabdomyolysis is a common and potentially lethal clinical syndrome that results from acute muscle fiber necrosis with leakage of muscle constituents into blood. Myoglobinuria is the most significant consequence, leading to acute renal failure (ARF) in 15%-33% of patients with rhabdomyolysis. Rhabdomyolysis occurs from inherited diseases, toxins, muscle compression or overexertion, or inflammatory processes, among other disorders. In some cases, no cause is found.We describe 475 patients from the Johns Hopkins Hospital inpatient records between January 1993 and December 2001 for the following discharge diagnosis codes: myoglobinuria, rhabdomyolysis, myopathy, toxic myopathy, malignant hyperthermia, neuroleptic malignant syndrome, and polymyositis. Of 1362 patients, 475 patients with an acute neuromuscular illness with serum creatine kinase (CK) more than 5 times the upper limit of normal (>975 IU/L) were included. Patients with recent myocardial infarction or stroke were excluded. The etiology was assigned by chart review. For all, the highest values of serum CK, serum creatinine and urine myoglobin, hemoglobin, and red blood cells were recorded. Forty-one patients had muscle biopsy within at least 2 months from the onset of rhabdomyolysis.Of the 475 patients, 151 were female and 324 were male (median age, 47 yr; range, 4-95 yr). Exogenous toxins were the most common cause of rhabdomyolysis, with illicit drugs, alcohol, and prescribed drugs responsible for 46%. Among the medical drugs, antipsychotics, statins, zidovudine, colchicine, selective serotonin reuptake inhibitors, and lithium were the most frequently involved. In 60% of all cases, multiple factors were present. In 11% of all cases, rhabdomyolysis was recurrent. Underlying myopathy or muscle metabolic defects were responsible for 10% of cases, in which there was a high percentage of recurrence, only 1 etiologic factor, and a low incidence of ARF. In 7%, no cause was found. ARF was present in 218 (46%) patients, and 16 died (3.4%). A linear correlation was found between CK and creatinine and between multiple factors and ARF, but there was no correlation between ARF and death or between multiple factors and death. Urine myoglobin detected by dipstick/ultrafiltration was positive in only 19%.Toxins are the most frequent cause of rhabdomyolysis, but in most cases more than 1 etiologic factor was present. Patients using illicit drugs or on prescribed polytherapy are at risk for rhabdomyolysis. The absence of urine myoglobin, by qualitative assay, does not exclude rhabdomyolysis. With appropriate care, death is rare.
机译:横纹肌溶解症是一种常见的且可能致命的临床综合征,由急性肌肉纤维坏死和肌肉成分渗入血液引起。肌红蛋白尿是最重要的结果,在15%-33%的横纹肌溶解患者中导致急性肾衰竭(ARF)。横纹肌溶解症是由遗传性疾病,毒素,肌肉压迫或过度劳累或炎症过程以及其他疾病引起的。在某些情况下,没有发现原因。我们描述了1993年1月至2001年12月间约翰霍普金斯医院住院记录的475名患者,其出院诊断代码为:肌红蛋白尿,横纹肌溶解症,肌病,中毒性肌病,恶性高热,神经安定性恶性综合症和多发性肌炎。在1362名患者中,纳入了475例急性神经肌肉疾病患者的血清肌酸激酶(CK)超过正常上限(> 975 IU / L)的5倍以上。排除近期有心肌梗塞或中风的患者。病因通过图表检查确定。总体而言,记录了最高的血清CK,血清肌酐和尿肌红蛋白,血红蛋白和红细胞值。横纹肌溶解症发作后至少2个月内有41例患者进行了肌肉活检.475例患者中,女性151例,男性324例(中位年龄47岁;范围4-95岁)。外源性毒素是横纹肌溶解的最常见原因,其中非法药物,酒精和处方药占46%。在药物中,抗精神病药,他汀类药物,齐多夫定,秋水仙碱,选择性5-羟色胺再摄取抑制剂和锂含量最高。在所有病例的60%中,存在多种因素。在所有病例中,有11%复发横纹肌溶解。潜在的肌病或肌肉代谢缺陷占10%的病例,其中复发率高,病因仅1种,ARF的发生率低。在7%中,未找到原因。 ARF存在于218名(46%)患者中,并且16例死亡(3.4%)。 CK与肌酐之间,多因素与ARF之间存在线性关系,但ARF与死亡之间或多因素与死亡之间没有线性关系。试纸/超滤检出的尿肌红蛋白仅19%呈阳性。毒素是横纹肌溶解的最常见原因,但在大多数情况下,存在超过一种病因。使用非法药物或采用处方综合疗法的患者有横纹肌溶解的风险。通过定性测定,尿肌红蛋白的缺乏并不排除横纹肌溶解。有了适当的照顾,死亡是罕见的。

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