N-Methyl-3,4-methylendioxymethamphetamine (MDMA)-related coagulopathy and rhabdomyolysis: A case series and literature review.
3,4‐methylenedioxymethylamphetamine
coagulopathy
critical care
rhabdomyolysis
serotonin syndrome
Journal
Research and practice in thrombosis and haemostasis
ISSN: 2475-0379
Titre abrégé: Res Pract Thromb Haemost
Pays: United States
ID NLM: 101703775
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
received:
30
12
2019
revised:
03
04
2020
accepted:
10
04
2020
entrez:
21
7
2020
pubmed:
21
7
2020
medline:
21
7
2020
Statut:
epublish
Résumé
Coagulation changes, thrombosis, and hemorrhage have been described in patients following N-methyl-3,4-methylenedioxymethylamphetamine (MDMA) intoxication who subsequently developed serotonin syndrome and rhabdomyolysis. The clinical features and mechanism of this remain poorly described. We describe 5 sequential cases admitted to critical care due to severe recreational MDMA toxicity where coagulopathy occurred, and discuss key clinical issues. All patients presented with hyperpyrexia then developed subsequent rhabdomyolysis accompanied by a coagulopathy within 24 hours of presentation. This included a severe thrombocytopenia, prolonged coagulation times, grossly elevated D-dimer levels, and hypofibrogenemia. Multiorgan dysfunction was seen in all patients, including stroke in one patient and major hemorrhage in another. In 2 cases, low-dose low-molecular-weight heparin was used early after presentation, with no significant bleeding complications. Blood products usage was high but variable between the patients with lower use in those who received low-molecular-weight heparin early. Other treatments included intravascular therapeutic cooling, renal replacement therapy with large filter pores and cyprohepatidine. Current evidence suggests that in this group, rhabdomyolysis with subsequent myosin release may be a profound activator of coagulation leading to disseminated intravascular coagulation. Myosin-activated coagulation seems a potential cause of MDMA-related coagulopathy in the setting of rhabdomyolysis and serotonin syndrome. Further studies are needed to validate this and explore the use of low-molecular-weight heparin to reduce the clinical effects of this coagulopathy.
Identifiants
pubmed: 32685891
doi: 10.1002/rth2.12360
pii: S2475-0379(22)02034-9
pmc: PMC7354411
doi:
Types de publication
Case Reports
Langues
eng
Pagination
829-834Informations de copyright
© 2020 The Authors. Research and Practice in Thrombosis and Haemostasis by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH).
Références
Clin Chim Acta. 2001 Apr;306(1-2):27-33
pubmed: 11282091
Blood. 2016 Oct 6;128(14):1870-1878
pubmed: 27421960
Nephron Clin Pract. 2012;121(3-4):c159-64
pubmed: 23327834
Crit Care Med. 1996 Jul;24(7):1173-8
pubmed: 8674331
JBR-BTR. 2014 Jan-Feb;97(1):42-3
pubmed: 24765773
Ann Rheum Dis. 2016 Jan;75(1):110-6
pubmed: 25193998
J Appl Physiol (1985). 2015 May 15;118(10):1207-20
pubmed: 25814640
JAMA. 1987 Aug 14;258(6):780-1
pubmed: 2886672
J R Soc Med. 1991 Jun;84(6):371
pubmed: 1676424
J Neurol Sci. 2012 Dec 15;323(1-2):257-60
pubmed: 22998806
Ther Clin Risk Manag. 2018 Jan 23;14:157-165
pubmed: 29416342
Arch Neurol. 1995 Dec;52(12):1210-4
pubmed: 7492296
Ann Intern Med. 1970 Jul;73(1):81-5
pubmed: 5433281
NDT Plus. 2010 Oct;3(5):459-60
pubmed: 25984053
Lancet. 1992 Aug 15;340(8816):384-7
pubmed: 1353554
Lancet. 1992 Mar 14;339(8794):677-8
pubmed: 1347361
J Biol Chem. 2019 Oct 11;294(41):15176-15181
pubmed: 31481465
Hum Exp Toxicol. 1999 Feb;18(2):119-25
pubmed: 10100025
Clin Res Hepatol Gastroenterol. 2017 Feb;41(1):e12-e13
pubmed: 27459877
Eur Heart J Cardiovasc Imaging. 2016 Oct;17(10):1187
pubmed: 27325808
Am J Case Rep. 2017 Oct 04;18:1058-1065
pubmed: 28974669
Case Rep Crit Care. 2011;2011:951719
pubmed: 24826326