Köppel C
Reanimationszentrum/Drug Information Center, Universitätsklinikum Rudolf Virchow, Standort Charlottenburg Freie Universität Berlin, West Germany.
Med Toxicol Adverse Drug Exp. 1989 Mar-Apr;4(2):108-26. doi: 10.1007/BF03259907.
Striated musculature is considered unusually tolerant to all kinds of injuries, and rhabdomyolysis associated with drug overdose or chronic drug intake is a rare event. This may be because striated musculature, in contrast to other tissues such as liver and kidney, shows little affinity for most drugs. Several different types of drug-induced rhabdomyolysis may be distinguished, and the clinical features of the condition may vary widely, from moderate myalgia to involvement of groups of muscles to involvement of the total skeletal musculature. In clinically asymptomatic rhabdomyolysis, early diagnosis is only made if routine laboratory tests include determination of serum creatine kinase. Determination of myoglobin in serum and urine is more sensitive and allows earlier diagnosis of muscle necrosis. Myoglobinaemia may lead to toxin-induced tubular necrosis, and impairment of renal function or even acute renal failure. About 10% of all cases of acute renal failure are due to rhabdomyolysis. Fulminant rhabdomyolysis may be associated with excessive hyperkalaemia and hypocalcaemia which may induce further life-threatening complications. Therefore, early diagnosis of rhabdomyolysis is most important for prevention of its potentially life-threatening sequelae. Therapy of rhabdomyolysis consists of supportive and specific measures. Early diagnosis may help to prevent life-threatening sequelae like acute renal failure, electrolyte imbalance and shock. Withdrawal of the incriminated drug or detoxification in drug overdose should be followed by supportive measures including infusion therapy and correction of dehydration and electrolyte imbalances. Forced diuresis with sodium bicarbonate may protect the kidney function from acidosis and precipitation of myoglobin in tubules. Elimination of myoglobin from plasma may be enhanced by plasmapheresis. In patients with acute renal failure, haemodialysis is necessary. In malignant hyperthermia, immediate infusion of dantrolene sodium is required. This drug also seems to have a beneficial effect in neuroleptic malignant syndrome. The repair mechanisms of striated musculature function extremely well. The prognosis of muscular atrophy after the acute stage of rhabdomyolysis is excellent. The same is true for the prognosis of acute renal failure. However, the extent of complications or survival of the acute stage of rhabdomyolysis strongly depend on early diagnosis and start of adequate therapy.
横纹肌组织被认为对各种损伤具有异常的耐受性,与药物过量或长期药物摄入相关的横纹肌溶解是一种罕见事件。这可能是因为与肝脏和肾脏等其他组织相比,横纹肌组织对大多数药物的亲和力较低。可以区分几种不同类型的药物性横纹肌溶解,该病症的临床特征可能差异很大,从中度肌痛到肌群受累再到整个骨骼肌组织受累。在临床无症状的横纹肌溶解中,只有当常规实验室检查包括血清肌酸激酶测定时才能做出早期诊断。血清和尿液中肌红蛋白的测定更敏感,能够更早诊断肌肉坏死。肌红蛋白血症可能导致毒素诱导的肾小管坏死以及肾功能损害甚至急性肾衰竭。所有急性肾衰竭病例中约10% 是由横纹肌溶解引起的。暴发性横纹肌溶解可能与严重的高钾血症和低钙血症相关,这可能引发进一步危及生命的并发症。因此,横纹肌溶解的早期诊断对于预防其潜在的危及生命的后遗症最为重要。横纹肌溶解的治疗包括支持性措施和特异性措施。早期诊断有助于预防危及生命的后遗症,如急性肾衰竭、电解质失衡和休克。停用相关药物或对药物过量进行解毒后,应采取支持性措施,包括输液治疗以及纠正脱水和电解质失衡。用碳酸氢钠进行强制利尿可保护肾功能免受酸中毒和肌红蛋白在肾小管中沉淀的影响。血浆置换可增强血浆中肌红蛋白的清除。对于急性肾衰竭患者,血液透析是必要的。在恶性高热中,需要立即输注丹曲林钠。这种药物似乎对神经阻滞剂恶性综合征也有有益作用。横纹肌组织的修复机制功能良好。横纹肌溶解急性期后肌肉萎缩的预后极佳。急性肾衰竭的预后也是如此。然而,横纹肌溶解急性期并发症的程度或存活率在很大程度上取决于早期诊断和适当治疗的开始。