Evidence map›Paper›PMID 42866079›Full record

ArticleFrontiers in veterinary science2026

Hematologic follow-up of metamizole-associated Heinz body anemia in dogs.

Cathrina Richter, Vera Geisen, Jelena Palić, René Dörfelt

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Cathrina RichterLMU Small Animal Clinic, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universität in Munich, Munich, Germany.
Vera GeisenLMU Small Animal Clinic, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universität in Munich, Munich, Germany.
Jelena PalićDivision of IDEXX Laboratories, Vet Med Labor GmbH, Kornwestheim, Germany.
René DörfeltLMU Small Animal Clinic, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universität in Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Heinz body (HB) anemia is uncommon in dogs. Metamizole is described as a potential trigger in isolated cases. Aim of the study: The present study describes the course of metamizole-associated HB anemia in dogs with the development of hematocrit, HBs, and eccentrocytes. In addition, the correlation between HBs, eccentrocytes, hematocrit, and reticulocytes is investigated. Materials and methods: In this prospective observational study, 25 dogs with metamizole-associated HB anemia were included. Hematologic examinations and blood smear evaluations for quantification of HBs and eccentrocytes (stained with brilliant cresyl blue and modified Wright's stain) were performed on day 0 and at the control intervals 1-3, 4-6, 7-13, and 14-20 days after discontinuation of metamizole and initiation of antioxidant treatment. Known alternative causes of oxidative erythrocyte damage were excluded. Data were analyzed using Kruskal-Wallis test, Friedman test, and Spearman correlation. Results: HB anemia was detected a median of 10 days after initiation of metamizole (median cumulative dose 720 mg/kg). On day 0, HB percentage did not correlate with metamizole dose or hematocrit. The eccentrocyte count did not correlate with metamizole dose, hematocrit, or reticulocyte count. However, a moderate to strong correlation was identified between HB percentage and reticulocyte count ( Conclusion: In dogs with concurrent disease, metamizole administration may be associated with clinically relevant erythrocyte oxidative damage. Discontinuation of metamizole and initiation of antioxidant therapy were followed by a decrease in HBs and recovery of hematocrit. The use of metamizole in multimorbid dogs should be carefully considered and accompanied by regular hematology controls.

Indexed as

dipyronedrug-associated hematotoxicityeccentrocyteserythrocytehemolysisoxidative stress

Identifiers

PMID42866079
PMCPMC13656853

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