Rhabdomyolysis causes

Rhabdomyolysis Microchapters
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Venkata Sivakrishna Kumar Pulivarthi M.B.B.S [2]

Overview

Injuries leading to rhabdomyolysis can be due to mechanical, physical, and chemical causes.

Causes

Causes by Pathophysiology

Rhadomyolysis

Traumatic or Muscle Compression

Non - Traumatic

Non-Traumatic Exertional

Non-Traumatic Non-Exertional

Non - Traumatic Exertional Rhadomyolysis in a Normal Muscle

Non - Traumatic Exertional Rhadomyolysis in an Abnormal Muscle

❑ Crush injury ❑ Coma ❑ Post ictal state ❑ Post - Operative Surgical trauma ❑ Electrical Injury ❑ Compartment Syndrome ❑ Immobilizaion

❑ Exertional Heat Stroke ❑ Sickle cell trait ❑ Hyperkinetic States Such as * Grand mal Seizures * Delirium tremens * Psychotic agitation * Amphetamine Overdose

❑ Metabolic myopathies ❑ Mitochondrial myopathies ❑ Malignant hyperthermia ❑ Neuroleptic malignant syndrome

❑ Drugs and toxins ❑ Infections ❑ Electrolyte abnormalities ❑ Endocrinopathies ❑ Inflammatory myopathies ❑ Miscellaneous

Non-Traumatic Exertional Rhabdomyolysis in an Abnormal Muscle
Metabolic myopathies	Mitochondrial myopathies	Malignant hyperthermia	Neuroleptic malignant syndrome
Disorders of glycogenolysis Myophosphorylase deficiency Phosphorylase kinase deficiency Disorders of glycolysis Phosphofructokinase deficiency Phosphoglycerate kinase deficiency Phosphoglycerate mutase deficiency Lactate dehydrogenase deficiency Disorders of lipid metabolism Carnitine palmitoyltransferase deficiency Carnitine deficiency Short-chain acyl-coenzyme A dehydrogenase deficiency Long-chain acyl-CoA dehydrogenase deficiency Lipin-1 deficiency Disorders of purine metabolism Myoadenylate deaminase deficiency Other defects Malignant hyperthermia susceptibility caused by RYR1 gene mutations Alpha-methylacyl-CoA racemase (AMACR) deficiency Brody myopathy (Calcium adenosine triphosphatase deficiency)	Isolated myopathy Chronic Progressive External Ophthalmoplegia Kearns-Sayre syndrome Severe encephalomyopathy of infancy or childhood Barth syndrome GRACILE syndrome Leigh's disease Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) Myoclonic epilepsy with ragged red fibers (MERRF)	Volatile anesthetic agent Halothane Isoflurane Sevoflurane Desflurane Depolarising Neuro-Muscular Blocker Succinylcholine	Neuroleptics Aripiprazole Asenapine maleate Chlorpromazine Clozapine Fluphenazine Haloperidol Iloperidone Loxapine Olanzapine Paliperidone Perphenazine Prochlorperazine Quetiapine Risperidone Thioridazine Thiothixene Trifluoperazine Ziprasidone Antiemetic agents Domperidone Droperidol Metoclopramide Prochlorperazine Promethazine Anti Parkison drug withdrawl L-dopa Bromocriptine Cabergoline

Infections	Electrolyte abnormalities	Endocrinopathies	Inflammatory myopathies	Miscellaneous
Viral infections Adenovirus Coxsackievirus Cytomegalovirus Echovirus Epstein-Barr Herpes simplex Human immunodeficiency virus Influenza A and B Parainfluenza Bacterial infections Bacterial pyomyositis Coxiella burnetii(Q fever) E. coli Ehrlichiosis Falciparum malaria Legionella Leptospirosis Mycoplasma pneumoniae Salmonella Staphylococcal infection Streptococcus Tularemia	Hypokalemia Hypophosphatemia	Hypothyroidism Diabetic ketoacidosis Non-ketotic hyperglycemia	Dermatomyositis Polymyositis	Alcoholism Baclofen withdrawl Capillary leak syndrome Status asthmaticus