Výskyt agranulocytózy po tyreostaticích v kohortě pacientů s Gravesovou nemocí léčených radioaktivním jodem 131I v průběhu 14 let
[The occurrence of agranulocytosis due to antithyroid drugs in a cohort of patients with Graves disease treated with radioactive iodine 131I during 14 years]
Language Czech Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25382005
PII: 50186
- MeSH
- Agranulocytosis chemically induced MeSH
- Adult MeSH
- Graves Disease complications drug therapy radiotherapy MeSH
- Carbimazole administration & dosage adverse effects MeSH
- Middle Aged MeSH
- Humans MeSH
- Methimazole administration & dosage adverse effects MeSH
- Propylthiouracil administration & dosage adverse effects MeSH
- Iodine Radioisotopes * MeSH
- Retrospective Studies MeSH
- Aged MeSH
- Antithyroid Agents administration & dosage adverse effects MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Carbimazole MeSH
- Methimazole MeSH
- Propylthiouracil MeSH
- Iodine Radioisotopes * MeSH
- Antithyroid Agents MeSH
INTRODUCTION: Agranulocytosis is a serious complication of antithyroid drugs (ATD) treatment of thyrotoxicosis. The aim of our work was to assess the occurrence of agranulocytosis in Graves disease (GD) patients admitted for radioactive iodine 131I (RAI) treatment to our thyroid unit. PATIENTS AND METHODS: We analyzed retrospectively a cohort of 603 GD patients (500 women and 103 men; mean age 51.5 ± 12.7 years) who received RAI between 1999 and 2012. Of them, 327 (54 %) patients were originally treated with carbimazole (CBZ), 215 (36 %) with methimazole (MMI) and 61 (10 %) with propylthiouracil (PTU). RESULTS: Agranulocytosis due to ATD was the cause of RAI treatment in 7 patients of 603. All of them were women (mean age 48.7 years; range 23-78). In 4 patients, agranulocytosis occurred on MMI treatment, and in 3 patients on CBZ. After recalculation of CBZ to the equipotent dose of MMI, the mean ATD dose was 22.4 mg MMI/day (range 9-40). No agranulocytosis due to PTU was found in our cohort. The time from beginning ATD treatment to agranulocytosis was 20-41 days. In 5 patients there was a development of fever, while in 2 patients the complication was diagnosed from routine blood count. The mean duration of agranulocytosis was 5.9 days (range 4-8). CONCLUSION: Agranulocytosis incidence in our cohort of patients was 1.2 %, while in most reports the prevalence ranged from 0.2 to 0.5 %. In all patients, agranulocytosis occurred early, and in one third it was asymptomatic when found. The aim of our report is to bring attention to a relatively rare, but potentially serious, complication of ATD treatment.