Internal Medicine and Endocrinology, Endocrine Research Center of Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, P.O. Box: 19395-4763, Tehran, Islamic Republic of Iran.
Internal Medicine and Endocrinology, Endocrine Research Center, Institute of Endocrinology and Metabolism, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran.
J Endocrinol Invest. 2019 Nov;42(11):1273-1283. doi: 10.1007/s40618-019-01054-1. Epub 2019 May 27.
Continued low-dose MMI treatment for longer than 12-18 months may be considered in patients not in remission. However, ATDs are not free from adverse effects. We undertook a systematic review to clarify safety of long-term ATD treatment. Medline and the Cochrane Library for trials published between 1950 and Nov 2018 were systematically searched. We included original studies containing data for long-term (> 18 months) ATD treatment. Two reviewers independently extracted data from included trials and any disagreement was adjudicated by consensus. Of 615 related articles found, 12 fulfilled the criteria. Six articles had data for adults, five for non-adults and one article had data for both groups. The sample sizes ranged between 20 and 249 individuals, and the mean duration of ATD treatment ranged between 2.1 and 14.2 years. Considering all data from 1660 patients treated with ATD for a mean duration of 5.8 years (around 10,000 patient-years), major complications occurred only in 14 patients: 7 severe agranulocytosis, 5 severe liver damage, one ANCA-associated glomerulonephritis and one vasculitis with small cutaneous ulcerations. Minor complications rates were between 2 and 36%, while more complications were in higher doses and in the children. The most reported AE was cutaneous reaction; the other adverse events were elevated liver enzymes, leukocytopenia, arthritis, arthralgia, myalgia, thrombocytopenia, fever, nausea and oral aphthous. Long-term ATD treatment is safe, especially in low dose and in adults, indicating that it should be considered as an earnest alternative treatment for GD.
对于未缓解的患者,可考虑继续低剂量 MMI 治疗 12-18 个月以上。然而,ATD 并非没有不良反应。我们进行了一项系统评价,以明确长期 ATD 治疗的安全性。系统检索了 1950 年至 2018 年 11 月发表的 Medline 和 Cochrane 图书馆的试验。我们纳入了包含长期(>18 个月)ATD 治疗数据的原始研究。两名评审员独立提取纳入试验的数据,如果存在分歧,则通过共识进行裁决。在 615 篇相关文章中,有 12 篇符合标准。其中 6 篇文章的数据来自成人,5 篇来自非成人,1 篇文章的数据来自成人和非成人。样本量范围为 20 至 249 人,ATD 治疗的平均持续时间范围为 2.1 至 14.2 年。考虑到 1660 名患者接受 ATD 治疗的平均时间为 5.8 年(约 10000 患者年)的数据,主要并发症仅发生在 14 名患者中:7 例严重粒细胞缺乏症、5 例严重肝损伤、1 例抗中性粒细胞胞浆抗体相关性肾小球肾炎和 1 例伴有小皮肤溃疡的血管炎。小并发症的发生率在 2%至 36%之间,而更高剂量和儿童中并发症更多。最常报告的 AE 是皮肤反应;其他不良事件包括肝酶升高、白细胞减少症、关节炎、关节痛、肌痛、血小板减少症、发热、恶心和口腔阿弗他溃疡。长期 ATD 治疗是安全的,尤其是在低剂量和成人中,这表明它应被视为 GD 的一种替代治疗选择。