[Considerations concerning the perioperative use of metamizole].

Überlegungen zum perioperativen Einsatz von Metamizol.

Journal

Der Anaesthesist
ISSN: 1432-055X
Titre abrégé: Anaesthesist
Pays: Germany
ID NLM: 0370525

Informations de publication

Date de publication:
08 2019
Historique:
pubmed: 23 8 2019
medline: 28 10 2020
entrez: 23 8 2019
Statut: ppublish

Résumé

The non-opioid analgesic metamizole (dipyrone) is approved for the treatment of severe pain and is often used in the perioperative period. As it can cause agranulocytosis, a severe adverse event, its perioperative administration is controversially discussed. Is there enough evidence for a high risk of metamizol-induced agranulocytosis (MIA)? What are the consequences of its perioperative use with respect to the risk profiles of alternative analgesics? Rapid review of the literature on the risk of MIA and adverse effects of non-opioid analgesics. The incidence of MIA is estimated to be one case per million inhabitants per year. The risk seems low compared to other drugs associated with a risk of agranulocytosis, such as antithyroid drugs and ticlopidine. The risk profile of metamizole concerning hepatotoxicity, nephrotoxicity, bleeding and cardiovascular adverse effects is favorable compared to other non-opioid analgesics. None of the non-opioid analgesics are licensed to be administered intraoperatively. The perioperative use of metamizole is possible after a thorough evaluation of the indications as it provides good analgesia with a generally favorable side effect profile and is administered intravenously. The risk of agranulocytosis is small but needs to be mentioned during patient informed consent in order to optimize early recognition. Intraoperative administration aims at reducing the expected severe postoperative pain. A documentation and justification for the evaluation of the indications are recommended.

Sections du résumé

BACKGROUND
The non-opioid analgesic metamizole (dipyrone) is approved for the treatment of severe pain and is often used in the perioperative period. As it can cause agranulocytosis, a severe adverse event, its perioperative administration is controversially discussed.
OBJECTIVE
Is there enough evidence for a high risk of metamizol-induced agranulocytosis (MIA)? What are the consequences of its perioperative use with respect to the risk profiles of alternative analgesics?
MATERIAL AND METHODS
Rapid review of the literature on the risk of MIA and adverse effects of non-opioid analgesics.
RESULTS
The incidence of MIA is estimated to be one case per million inhabitants per year. The risk seems low compared to other drugs associated with a risk of agranulocytosis, such as antithyroid drugs and ticlopidine. The risk profile of metamizole concerning hepatotoxicity, nephrotoxicity, bleeding and cardiovascular adverse effects is favorable compared to other non-opioid analgesics. None of the non-opioid analgesics are licensed to be administered intraoperatively.
CONCLUSION
The perioperative use of metamizole is possible after a thorough evaluation of the indications as it provides good analgesia with a generally favorable side effect profile and is administered intravenously. The risk of agranulocytosis is small but needs to be mentioned during patient informed consent in order to optimize early recognition. Intraoperative administration aims at reducing the expected severe postoperative pain. A documentation and justification for the evaluation of the indications are recommended.

Identifiants

pubmed: 31435718
doi: 10.1007/s00101-019-00637-0
pii: 10.1007/s00101-019-00637-0
doi:

Substances chimiques

Analgesics, Non-Narcotic 0
Dipyrone 6429L0L52Y

Types de publication

Journal Article Review

Langues

ger

Sous-ensembles de citation

IM

Pagination

530-537

Références

J Clin Epidemiol. 1998 Dec;51(12):1357-65
pubmed: 10086830
Int J Clin Pharmacol Ther. 1999 Apr;37(4):168-74
pubmed: 10235419
Lancet. 1999 Jun 12;353(9169):2051-8
pubmed: 10376632
Br J Surg. 1999 Dec;86(12):1528-31
pubmed: 10594500
Anesthesiology. 2000 Oct;93(4):1123-33
pubmed: 11020770
BMJ. 2000 Dec 16;321(7275):1493
pubmed: 11118174
Am J Surg. 2002 Jun;183(6):630-41
pubmed: 12095591
Eur J Clin Pharmacol. 2002 Jul;58(4):265-74
pubmed: 12136373
Rev Esp Anestesiol Reanim. 2002 Oct;49(8):391-6
pubmed: 12455318
Cochrane Database Syst Rev. 2002;(4):CD003867
pubmed: 12519613
Pharmacoepidemiol Drug Saf. 2003 Apr-May;12(3):195-202
pubmed: 12733472
Digestion. 2003;67(3):138-45
pubmed: 12853725
Anaesthesist. 2004 Mar;53(3):263-80
pubmed: 15021958
Eur J Clin Pharmacol. 2005 Jan;60(11):821-9
pubmed: 15580488
Anesthesiol Clin North Am. 2005 Mar;23(1):21-36
pubmed: 15763409
Arch Intern Med. 2005 Apr 25;165(8):869-74
pubmed: 15851637
FASEB J. 2007 Aug;21(10):2343-51
pubmed: 17435173
Cochrane Database Syst Rev. 2008 Oct 08;(4):CD004602
pubmed: 18843665
J Am Geriatr Soc. 2009 Jan;57(1):1-10
pubmed: 19054187
Cochrane Database Syst Rev. 2009 Apr 15;(2):CD004771
pubmed: 19370610
Eur J Anaesthesiol. 2011 Feb;28(2):125-32
pubmed: 20890207
Thromb Haemost. 2013 May;109(5):825-33
pubmed: 23238666
Basic Clin Pharmacol Toxicol. 2015 Mar;116(3):257-63
pubmed: 25154757
Schmerz. 2014 Dec;28(6):584-90
pubmed: 25199942
Eur J Clin Pharmacol. 2015 Feb;71(2):219-27
pubmed: 25378038
Eur J Pain. 2015 Aug;19(7):953-65
pubmed: 25429980
PLoS One. 2015 Apr 13;10(4):e0122918
pubmed: 25875821
Eur J Anaesthesiol. 2015 Oct;32(10):725-34
pubmed: 26241763
Cochrane Database Syst Rev. 2015 Sep 28;(9):CD008659
pubmed: 26414123
Cochrane Database Syst Rev. 2016 Apr 20;4:CD011421
pubmed: 27096578
Cochrane Database Syst Rev. 2016 May 23;(5):CD007126
pubmed: 27213715
J Clin Transl Hepatol. 2016 Jun 28;4(2):131-42
pubmed: 27350943
J Clin Pharm Ther. 2016 Oct;41(5):459-77
pubmed: 27422768
Schmerz. 2017 Feb;31(1):5-13
pubmed: 27766404
QJM. 2017 Jan 9;:null
pubmed: 28069912
Cochrane Database Syst Rev. 2017 May 25;5:CD007355
pubmed: 28540716
J Hepatol. 2017 Dec;67(6):1324-1331
pubmed: 28734939
J Pain Res. 2017 Sep 25;10:2287-2298
pubmed: 29026331
Fundam Clin Pharmacol. 2019 Apr;33(2):134-147
pubmed: 30383903
JAMA. 1986 Oct 3;256(13):1749-57
pubmed: 3747087
Intensive Care Med. 1996 Oct;22(10):1043-7
pubmed: 8923067
Chirurg. 1997 Aug;68(8):806-10
pubmed: 9377992

Auteurs

R Sittl (R)

Interdisziplinäre Schmerzambulanz, Klinik für Anaesthesiologie, Klinikum der Ludwig-Maximilians-Universität München, Pettenkoferstr. 8a, 80336, München, Deutschland.

P Bäumler (P)

Interdisziplinäre Schmerzambulanz, Klinik für Anaesthesiologie, Klinikum der Ludwig-Maximilians-Universität München, Pettenkoferstr. 8a, 80336, München, Deutschland.

A-M Stumvoll (AM)

Interdisziplinäre Schmerzambulanz, Klinik für Anaesthesiologie, Klinikum der Ludwig-Maximilians-Universität München, Pettenkoferstr. 8a, 80336, München, Deutschland.

D Irnich (D)

Interdisziplinäre Schmerzambulanz, Klinik für Anaesthesiologie, Klinikum der Ludwig-Maximilians-Universität München, Pettenkoferstr. 8a, 80336, München, Deutschland. dominik.irnich@med.uni-muenchen.de.

B Zwißler (B)

Klinik für Anaesthesiologie, Klinikum der Ludwig-Maximilians-Universität München, Marchioninistr. 15, 81377, München, Deutschland.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH