The efficacy of a single-dose anakinra injection during disease attack in pediatric familial Mediterranean fever.

IF 3.2 3区 医学 Q2 RHEUMATOLOGY
Rheumatology International Pub Date : 2024-11-01 Epub Date: 2023-06-06 DOI:10.1007/s00296-023-05351-0
Sinem Oral Cebeci, Mehmet Yildiz, Aybuke Gunalp, Memnune Nur Cebi, Berivan Kilinc, Eymen Pinar, Elif Kilic Konte, Esma Aslan, Fatih Haslak, Amra Adrovic, Sezgin Sahin, Kenan Barut, Ozgur Kasapcopur
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引用次数: 0

Abstract

The aim of this retrospective study is to evaluate the efficacy of a single-dose anakinra during familial Mediterranean fever (FMF) attacks and its effect on the duration, severity, and frequency of attacks. The patients with FMF who had disease episode and received a single-dose anakinra during disease episode between December 2020 and May 2022 were included. Demographic characteristics, MEFV gene variants detected, concomitant medical conditions, demographics of recent and previous episodes, laboratory findings and length of hospital stay were recorded. A retrospective analysis of medical records revealed 79 attacks from 68 patients who met inclusion criteria. The patients had a median age of 13 (2.5-25) years. All patients reported that the average duration of their previous episodes lasted longer than 24 h. When the recovery time of attacks after subcutaneous anakinra application at the disease attack was examined, it was observed that 4 attacks (5.1%) ended in 10 min; 10 attacks (12.7%) in 10-30 min; 29 attacks (36.7%) in 30-60 min; 28 attacks (35.4%) in 1-4 h; 4 attacks (5.1%) in 24 h; and 4 attacks (5.1%) ended in more than 24 h. There was no patient who did not recover from their attack after a single dose of anakinra. Although the efficacy of a single-dose anakinra administration during FMF attacks in children needs to be confirmed by prospective studies, our results suggest that use of a single-dose anakinra during FMF attacks is effective in reduction of severity and duration of disease attacks.

在小儿家族性地中海热疾病发作期间注射单剂量 Anakinra 的疗效。
这项回顾性研究旨在评估家族性地中海热(FMF)发作期间单剂量阿纳金拉的疗效及其对发作持续时间、严重程度和频率的影响。研究纳入了2020年12月至2022年5月期间发病并在发病期间接受单剂量阿纳金拉治疗的FMF患者。研究人员记录了患者的人口统计学特征、检测到的MEFV基因变异、并发症、最近和以前发作的人口统计学特征、实验室检查结果和住院时间。通过对病历进行回顾性分析,发现符合纳入标准的 68 名患者中有 79 人发病。患者的中位年龄为 13(2.5-25)岁。所有患者都报告说,他们之前发作的平均持续时间超过了 24 小时。在对发作时皮下注射 anakinra 后的恢复时间进行检查时发现,4 次发作(5.没有患者在单次使用阿纳金拉后发作仍未痊愈。尽管在儿童FMF发作期间服用单剂量阿纳金拉的疗效还需要通过前瞻性研究来证实,但我们的研究结果表明,在FMF发作期间使用单剂量阿纳金拉能有效降低疾病发作的严重程度并缩短持续时间。
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来源期刊
Rheumatology International
Rheumatology International 医学-风湿病学
CiteScore
7.30
自引率
5.00%
发文量
191
审稿时长
16. months
期刊介绍: RHEUMATOLOGY INTERNATIONAL is an independent journal reflecting world-wide progress in the research, diagnosis and treatment of the various rheumatic diseases. It is designed to serve researchers and clinicians in the field of rheumatology. RHEUMATOLOGY INTERNATIONAL will cover all modern trends in clinical research as well as in the management of rheumatic diseases. Special emphasis will be given to public health issues related to rheumatic diseases, applying rheumatology research to clinical practice, epidemiology of rheumatic diseases, diagnostic tests for rheumatic diseases, patient reported outcomes (PROs) in rheumatology and evidence on education of rheumatology. Contributions to these topics will appear in the form of original publications, short communications, editorials, and reviews. "Letters to the editor" will be welcome as an enhancement to discussion. Basic science research, including in vitro or animal studies, is discouraged to submit, as we will only review studies on humans with an epidemological or clinical perspective. Case reports without a proper review of the literatura (Case-based Reviews) will not be published. Every effort will be made to ensure speed of publication while maintaining a high standard of contents and production. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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