Laboratory Studies
- If a patient gives a clear history of MDMA ingestion with mild symptoms and is hemodynamically stable, no laboratory studies are indicated.
- If the history is absent and/or questionable or if the patient exhibits signs of moderate-to-severe toxicity, appropriate laboratory studies include the following:
- Obtain a CBC count to exclude infection as a cause of fever and altered mental status.
- Measure electrolyte levels and pay particular attention to sodium and renal function.
- A bedside glucose determination is always indicated in patients with altered mental status.
- Obtain liver function tests (LFTs), prothrombin time, and/or activated partial thromboplastin time. Patients manifesting significant or prolonged hyperthermia require evaluation of hepatic and coagulation studies to exclude DIC.
- Perform pregnancy tests in women of childbearing age.
- A creatine kinase measurement is helpful to exclude rhabdomyolysis.
- Dipstick urinalysis findings can be positive for myoglobinuria.
- The urine toxicology screen fails to detect MDMA unless large doses have been ingested. It is nonspecific, and positive test findings only indicate presence of an amphetamine drug class. Confirmation by means of gas chromatography and/or mass spectrometry is strongly recommended when test findings are positive for amphetamines.
- Patients complaining of chest pain should undergo electrocardiographic testing and monitoring. Include cardiac enzymes in laboratory studies for chest pain secondary to suspected ischemia.
- In addition to the tests listed above, laboratory studies for altered mental status may include serum osmolality, alcohol, and ketones.
- Send cultures of blood and urine for testing if signs of infection and fever are present. Consider lumbar puncture to exclude meningitis.
Imaging Studies
- Patients demonstrating only mild symptoms without any hemodynamic instability do not require imaging studies. Observation and supportive care is recommended.
- Obtain a chest radiograph in patients complaining of chest pain, demonstrating low oxygen saturations, or experiencing respiratory distress.
- Patients presenting with a seizure or prolonged mental status changes despite initial resuscitation should undergo cranial CT scan. Metabolic causes such as hyponatremia should be found quickly and corrected cautiously.
Other Tests
- Patients complaining of chest pain should undergo electrocardiographic testing and monitoring.
Procedures
- Patients complaining of persistent headache may require a head CT and a lumbar puncture to rule out a subarachnoid hemorrhage.
Carvalho M, Pontes H, Remiao F, Bastos ML, Carvalho F. Mechanisms underlying the hepatotoxic effects of ecstasy. Curr Pharm Biotechnol. Aug 2010;11(5):476-95. [Medline].
National Institute on Drug Abuse. MDMA (Ecstasy) Research Report Series. Electronic Version] http://nida.nih.gov/Research Reports/MDMA/. March 2006;[Full Text].
Drug Abuse Warning Network (DAWN) Reports 2005. [Electronic Version]. Retrieved June 8, 2008 from http://dawninfo.samhsa.gov/.
Cuomo MJ, Dyment PG, Gammino VM. Increasing use of "Ecstasy" (MDMA) and other hallucinogens on a college campus. J Am Coll Health. May 1994;42(6):271-4. [Medline].
O'Shea E, Escobedo I, Orio L, et al. Elevation of ambient room temperature has differential effects on MDMA-induced 5-HT and dopamine release in striatum and nucleus accumbens of rats. Neuropsychopharmacology. Jul 2005;30(7):1312-23. [Medline].
Galineau L, Belzung C, Kodas E, Bodard S, Guilloteau D, Chalon S. Prenatal 3,4-methylenedioxymethamphetamine (ecstasy) exposure induces long-term alterations in the dopaminergic and serotonergic functions in the rat. Brain Res Dev Brain Res. Feb 8 2005;154(2):165-76. [Medline].
Grunau BE, Wiens MO, Brubacher JR. Dantrolene in the treatment of MDMA-related hyperpyrexia: a systematic review. CJEM. Sep 2010;12(5):435-42. [Medline].
McElhatton PR, Bateman DN, Evans C, Pughe KR, Thomas SH. Congenital anomalies after prenatal ecstasy exposure. Lancet. Oct 23 1999;354(9188):1441-2. [Medline].
Ames D, Wirshing WC. Ecstasy, the serotonin syndrome, and neuroleptic malignant syndrome--a possible link?. JAMA. Feb 17 1993;269(7):869-70. [Medline].
Andreu V, Mas A, Bruguera M, et al. Ecstasy: a common cause of severe acute hepatotoxicity. J Hepatol. Sep 1998;29(3):394-7. [Medline].
Burgess C, O'Donohoe A, Gill M. Agony and ecstasy: a review of MDMA effects and toxicity. Eur Psychiatry. Aug 2000;15(5):287-94. [Medline].
Christophersen AS. Amphetamine designer drugs - an overview and epidemiology. Toxicol Lett. Mar 15 2000;112-113:127-31. [Medline].
Cloud J. The lure of ecstasy. Time. Jun 5 2000;155(23):62-8. [Medline].
Cunningham M. Ecstasy-induced rhabdomyolysis and its role in the development of acute renal failure. Intensive Crit Care Nurs. Aug 1997;13(4):216-23. [Medline].
Fahal IH, Sallomi DF, Yaqoob M, Bell GM. Acute renal failure after ecstasy. BMJ. Jul 4 1992;305(6844):29. [Medline].
Freudenmann RW, Oxler F, Bernschneider-Reif S. The origin of MDMA (ecstasy) revisited: the true story reconstructed from the original documents. Addiction. Sep 2006;101(9):1241-5. [Medline].
Green AR, Cross AJ, Goodwin GM. Review of the pharmacology and clinical pharmacology of 3,4-methylenedioxymethamphetamine (MDMA or "Ecstasy"). Psychopharmacology (Berl). Jun 1995;119(3):247-60. [Medline].
Henry JA, Fallon JK, Kicman AT, Hutt AJ, Cowan DA, Forsling M. Low-dose MDMA ("ecstasy") induces vasopressin secretion. Lancet. Jun 13 1998;351(9118):1784. [Medline].
Holden R, Jackson MA. Near-fatal hyponatraemic coma due to vasopressin over-secretion after "ecstasy" (3,4-MDMA). Lancet. Apr 13 1996;347(9007):1052. [Medline].
Joseph M. Ecstasy - Its History and Lore. Carlton Books; 2000:1-96.
Lai TI, Hwang JJ, Fang CC, Chen WJ. Methylene 3, 4 dioxymethamphetamine-induced acute myocardial infarction. Ann Emerg Med. Dec 2003;42(6):759-62. [Medline].
Maxwell DL, Polkey MI, Henry JA. Hyponatraemia and catatonic stupor after taking "ecstasy". BMJ. Nov 27 1993;307(6916):1399. [Medline].
McCann UD, Eligulashvili V, Ricaurte GA. (+/-)3,4-Methylenedioxymethamphetamine ('Ecstasy')-induced serotonin neurotoxicity: clinical studies. Neuropsychobiology. 2000;42(1):11-6. [Medline].
Office of Applied Studies. The Substance Abuse and Mental Health Services Administration (SAMHSA). Drug Abuse Warning Network. 2003.
Randall T. 'Rave' scene, ecstasy use, leap atlantic. JAMA. Sep 23-30 1992;268(12):1506. [Medline].
Reneman L, Booij J, Schmand B, van den Brink W, Gunning B. Memory disturbances in "Ecstasy" users are correlated with an altered brain serotonin neurotransmission. Psychopharmacology (Berl). Feb 2000;148(3):322-4. [Medline].
Ricaurte GA, Martello AL, Katz JL, Martello MB. Lasting effects of (+-)-3,4-methylenedioxymethamphetamine (MDMA) on central serotonergic neurons in nonhuman primates: neurochemical observations. J Pharmacol Exp Ther. May 1992;261(2):616-22. [Medline].
Saadat KS, O'shea E, Colado MI, Elliott JM, Green AR. The role of 5-HT in the impairment of thermoregulation observed in rats administered MDMA ('ecstasy') when housed at high ambient temperature. Psychopharmacology (Berl). Jun 2005;179(4):884-90. [Medline].
Schwartz RH, Miller NS. MDMA (ecstasy) and the rave: a review. Pediatrics. Oct 1997;100(4):705-8. [Medline].
Sporer KA. The serotonin syndrome. Implicated drugs, pathophysiology and management. Drug Saf. Aug 1995;13(2):94-104. [Medline].
Steele TD, McCann UD, Ricaurte GA. 3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy"): pharmacology and toxicology in animals and humans. Addiction. May 1994;89(5):539-51. [Medline].
Weir E. Raves: a review of the culture, the drugs and the prevention of harm. CMAJ. Jun 27 2000;162(13):1843-8. [Medline].

