Metamizole-induced agranulocytosis (MIA): a mini review

Abstract Metamizole is an analgesic, antipyretic, and spasmolytic drug in Germany only approved for the treatment of severe pain or high fever that does not respond to other measures. In recent years, an increased use has been described among both adults and children, often against the approved indi...

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Main Authors: Markos K. Tomidis Chatzimanouil, Ines Goppelt, Yvonne Zeissig, Ulrich J. Sachs, Martin W. Laass
Format: Article
Language:English
Published: SpringerOpen 2023-08-01
Series:Molecular and Cellular Pediatrics
Subjects:
Online Access:https://doi.org/10.1186/s40348-023-00160-8
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author Markos K. Tomidis Chatzimanouil
Ines Goppelt
Yvonne Zeissig
Ulrich J. Sachs
Martin W. Laass
author_facet Markos K. Tomidis Chatzimanouil
Ines Goppelt
Yvonne Zeissig
Ulrich J. Sachs
Martin W. Laass
author_sort Markos K. Tomidis Chatzimanouil
collection DOAJ
description Abstract Metamizole is an analgesic, antipyretic, and spasmolytic drug in Germany only approved for the treatment of severe pain or high fever that does not respond to other measures. In recent years, an increased use has been described among both adults and children, often against the approved indication. The most important side effect of metamizole is the development of agranulocytosis (neutrophil count < 500/µL). Incidence of metamizole-induced agranulocytosis (MIA) ranges depending on the study from 0.96 cases per million per year to 1:1602 per patient and metamizole prescription. The risk of agranulocytosis in children remains unclear, but is probably lower than in adults. Female gender and older age are associated with higher incidence, reflecting prescription distribution. MIA is dose-independent and risk seems to increase with duration of intake. In patients with past exposure, re-exposure may lead to rapid onset. MIA is believed to be induced either through immunologic or toxic mechanisms. MIA presents with fever, sore throat, fatigue, and mucosal inflammation, up to ulceration. Even in the case of suspected MIA, treatment with metamizole should be immediately paused and an examination of the blood cell count is required. In case of local or systemic infections, empirical therapy with broad-spectrum antibiotics should be administered. G-CSF therapy should be limited to patients with poor prognostic factors. The patient should be monitored closely until the neutrophil count returns to normal. Re-exposure to metamizole must be avoided.
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spelling doaj.art-6dc9b22e935f43c0928d663c551567362023-11-20T09:41:59ZengSpringerOpenMolecular and Cellular Pediatrics2194-77912023-08-011011710.1186/s40348-023-00160-8Metamizole-induced agranulocytosis (MIA): a mini reviewMarkos K. Tomidis Chatzimanouil0Ines Goppelt1Yvonne Zeissig2Ulrich J. Sachs3Martin W. Laass4Department of Pediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität DresdenDepartment of Pediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität DresdenDepartment of Pediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität DresdenInstitute for Clinical Immunology, Transfusion Medicine, and Haemostasis, Justus Liebig University GiessenDepartment of Pediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität DresdenAbstract Metamizole is an analgesic, antipyretic, and spasmolytic drug in Germany only approved for the treatment of severe pain or high fever that does not respond to other measures. In recent years, an increased use has been described among both adults and children, often against the approved indication. The most important side effect of metamizole is the development of agranulocytosis (neutrophil count < 500/µL). Incidence of metamizole-induced agranulocytosis (MIA) ranges depending on the study from 0.96 cases per million per year to 1:1602 per patient and metamizole prescription. The risk of agranulocytosis in children remains unclear, but is probably lower than in adults. Female gender and older age are associated with higher incidence, reflecting prescription distribution. MIA is dose-independent and risk seems to increase with duration of intake. In patients with past exposure, re-exposure may lead to rapid onset. MIA is believed to be induced either through immunologic or toxic mechanisms. MIA presents with fever, sore throat, fatigue, and mucosal inflammation, up to ulceration. Even in the case of suspected MIA, treatment with metamizole should be immediately paused and an examination of the blood cell count is required. In case of local or systemic infections, empirical therapy with broad-spectrum antibiotics should be administered. G-CSF therapy should be limited to patients with poor prognostic factors. The patient should be monitored closely until the neutrophil count returns to normal. Re-exposure to metamizole must be avoided.https://doi.org/10.1186/s40348-023-00160-8Metamizole-induced agranulocytosisMetamizoleAgranulocytosisAnalgesicsAntibodies against granulocytes
spellingShingle Markos K. Tomidis Chatzimanouil
Ines Goppelt
Yvonne Zeissig
Ulrich J. Sachs
Martin W. Laass
Metamizole-induced agranulocytosis (MIA): a mini review
Molecular and Cellular Pediatrics
Metamizole-induced agranulocytosis
Metamizole
Agranulocytosis
Analgesics
Antibodies against granulocytes
title Metamizole-induced agranulocytosis (MIA): a mini review
title_full Metamizole-induced agranulocytosis (MIA): a mini review
title_fullStr Metamizole-induced agranulocytosis (MIA): a mini review
title_full_unstemmed Metamizole-induced agranulocytosis (MIA): a mini review
title_short Metamizole-induced agranulocytosis (MIA): a mini review
title_sort metamizole induced agranulocytosis mia a mini review
topic Metamizole-induced agranulocytosis
Metamizole
Agranulocytosis
Analgesics
Antibodies against granulocytes
url https://doi.org/10.1186/s40348-023-00160-8
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