A paucity of literature exists linking acute extremity compartment syndrome associated with cocaine or olanzapine overdose. LJ, a 38-year male, was initially seen at an outside hospital for acute encephalopathy and left lower extremity swelling shortly after cocaine and suspected olanzapine overdose. On presentation, totalcreatinine kinase levels were >1000 units/liter but quickly rose to 23,000 units/liter after 12 hours. He was transferred to a tertiary care center for surgical evaluation. Upon the exam, it was quickly determined that he had compartment syndrome and he was urgently taken to the operating room for a four-compartment lower extremity fasciotomy. Acute compartment syndrome is a limb threatening condition generally diagnosed clinically. Cocaine, a potent vasoconstrictor, is widely reported to cause rhabdomyolysis from ischemia of skeletal muscle tissue and direct toxicity to myocytes resulting in leakage of creatinine kinase. Other complications including cardiovascular, respiratory, neurological, and gastrointestinal disturbances have also been well documented. Olanzapine, an atypical antipsychotic, has also been reported to cause rhabdomyolysis. However, myositis with lower extremity compartment syndrome is a rare occurrence and requires quick diagnosis and aggressive treatment in order to achieve limb salvage. The potential causality of compartment syndrome from either cocaine, olanzapine, or both will be examined in this case report.
Drug induced focal myositis with subsequent compartment syndrome is a rare phenomenon. A limited number of case reports linking drugs to extremity compartment syndrome exist [1,2]. Statins have a well-known side effect of myopathy potentially leading to rhabdomyolysis [
A 38-year-old male was brought to an outside hospital emergency department by Emergency Medical Servicesafter being found unresponsive slumped against a wall with vomitus around him. No seizure activity was witnessed. Medical history abstracted from his spouse included a psychiatric disorder and depression. No surgical history was obtained. He had no known drug allergies. His wife denied any tobacco or alcohol use by her husband but admitted he used cocaine recently. His medications included Olanzapine for bi-polar disorder and unspecified anti-hypertensives.
He was given a total of 4 mg of naloxone by EMS with no significant response. Initial reported GlascowComa Score was 3 with no signs of trauma. Hispupils were constricted but equal and reactive. Trachea was midline with clear breath sounds bilaterally. Heart sounds were normal with a soft, systolic murmur appreciated. His abdomen was non-tender, non-distended. Exam was significant for a swollen and tender left lower extremity with no erythema (
He was transferred to a large, urban level I trauma center for further management. Upon arrival, clinical exam revealed signs and symptoms of compartment syndrome. His lower extremity compartments were tight and painful to palpation. He grimaced in discomfort with passive motion of the extremity. Distal pulses were intact. Initial laboratory data revealed a creatinine kinase of 38,156 units/liter with urine positive for myoglobin. Aggressive intravenous hydration with crystalloid solution and a bicarbonate drip for renal protection were started. LJ was quickly taken to the operating room where a four compartment fasciotomy was performed revealing bulging but viable muscles (Figures 2 and 3). His post operative recovery was uneventful. The patient was transferred to the surgical intensive care unit after the operation. He returned to the OR 2 days later for delayed closure of his lateral wound. His medial wound underwent a staged closure with the first and second (final) procedures on post operative days 6 and 9, respectively. He was discharged in good condition on post operative day 10.
Cocaine is a common drug throughout the United States and across the world. It is second only to alcohol as the most used and abused drug. In 2009, the Drug Abuse Warning Network (DAWN) reported approximately 4.6 million emergency department visits pertaining to drug use. Of these, cocaine was attributed to around 420,000 visits or 137.7 visits per 100,000 [
As an amphetamine, cocaine exerts its vascular and cardiac effects by modifying the sympathetic nervous system. It also has neurological effects. Cocaine has three primary sympathomimetic mechanisms of action. It inhibits cathecholamine reuptake at sympathetic nerve terminals, increases sensitivity of adrenergic nerve endings to norepinephrine, and blocks sodium and potassium channels [
Cocaine induced muscle damage and rhabomyolysis has been widely reported, with a Pub Med search of “co-
caine + rhabdomyolysis” revealing more than 50 articles. The mechanism of toxicity is multifactorial, likely involving intense vasoconstriction leading to ischemic damage and direct muscle toxicity. Cardiac, versus skeletal, muscle toxicity from cocaine abuse is better studied. Mechanisms for cardiotoxicity and arrhythmia generation that have been described include the blocking K+ channels, increase in L-type Ca2+ channel current, and inhibition Na+ influx during depolarization [
Olanzapine (Zyprexa) belongs in the class of atypical antipsychotics which exert their effects by modulating and having high affinity for 5-HT (serotonin) receptors. They have less affinity for D1 and D2 receptors, thus decreasing the incidence of extrapyramidal symptoms [
Compartmentsyndrome is defined as an elevation of the interstitial pressure in a closed fascialcompartment that results in microvascular compromise [
While both olanzapine and cocaine have been shown to cause muscle damage and rhabdomyolysis in isolated cases, compartment syndrome resulting from an overdose of either has only reported for one specific instance of cocaine abuse. Rhabdomyolysis resulting in compartment syndrome is also particularly rare. The authors theorize that combination of two muscle damaging drugs, olanzapine and cocaine, caused LJ’s compartment syndrome. It was unlikely to be caused by positional damage because of the short time course of presentation. As such, it is important for clinicians to review a patient’s medications when faced with a similar situation. While ultimately resulting in the same treatment, it is important to recognize the increased risk of combinations of muscle damaging drugs and to counsel patients on the signs and symptoms of compartment syndrome. Regardless of the mechanism, quick clinical diagnosis and treatment of extremity compartment syndrome is essential for limb salvage.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.