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伊洛前列素在真实世界经验中的系统性硬化症中的安全性。

The safety of iloprost in systemic sclerosis in a real-life experience.

机构信息

Department of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence and Division of Rheumatology AOUC, Florence, Italy.

Internal Medicine Unit 3, Careggi University Hospital Florence, Florence, Italy.

出版信息

Clin Rheumatol. 2018 May;37(5):1249-1255. doi: 10.1007/s10067-018-4043-0. Epub 2018 Feb 22.

Abstract

Iloprost (ILO) is employed intravenously for the treatment of severe Raynaud phenomenon (RP) and digital ulcers (DU) in systemic sclerosis (SSc). The aim of this study was to evaluate the safety and tolerability of the intravenous treatment with ILO in different phases of SSc. Eighty-one consecutive non-selected SSc patients, all on nifedipine, with moderate RP, treated with ILO infusion, were retrospectively evaluated. Patients were sub classified according to the edematous or fibrotic/atrophic cutaneous phase of the disease. ILO was infused with a progressive increase of the dosage up to the achievement of patient's tolerance, 1 day/week. In cases of slower infusion regimen due to adverse events (AE) at the beginning of the administration, patients received a lower dose of the drug (not possible to quantify precisely the final cumulative dosage). 16/81 SSc patients presented digital edema, 5 developed diarrhea, and 9 developed transient hypotension during the infusion at 20 ml/h that ameliorated when the drug was withdrawn. Moreover, 10/16 edematous patients experienced significant and painful digital swelling, unlike patients in the fibrotic group (p < 0.0001); 11/16 patients reported flushing and 7/16 headache, always controlled with dose tapering below 10 ml/h. In the atrophic/fibrotic phase patients (65/81), 10 developed diarrhea and 24 hypotension at infusion rate of 20 ml/h that led to temporary withdrawal of the drug. When ILO was restarted and kept below 10 ml/h, no side effects were experienced. 23/65 patients experienced flushing and 8/65 headache, all controlled with infusion reduction below 10 ml/h. In these patients, adverse events were significantly less frequent than in the edematous group (p = 0.023 and p = 0.008, respectively). Our data suggest that calcium channel blockers should be transitorily stopped while using ILO and that a pre-treatment approach might reduce or control adverse events. In patients with digital edema, ILO infusion should be carefully employed after the evaluation of patient's drug tolerance.

摘要

依前列醇(ILO)用于静脉内治疗严重的雷诺现象(RP)和系统性硬化症(SSc)中的手指溃疡(DU)。本研究的目的是评估静脉内使用 ILO 在 SSc 不同阶段的安全性和耐受性。对 81 例连续非选择性 SSc 患者进行回顾性评估,所有患者均接受硝苯地平治疗,有中度 RP,接受 ILO 输注治疗。根据疾病的水肿或纤维化/萎缩性皮肤阶段对患者进行亚分类。ILO 以逐渐增加剂量的方式输注,直至达到患者的耐受程度,每周 1 天。在开始给药时由于不良反应(AE)而输注速度较慢的情况下,患者接受较低剂量的药物(无法精确量化最终累积剂量)。81 例 SSc 患者中有 16 例出现手指水肿,5 例出现腹泻,9 例在以 20ml/h 输注时出现短暂低血压,停药后缓解。此外,16 例水肿患者中有 10 例出现显著且疼痛的手指肿胀,与纤维化组患者不同(p<0.0001);11 例患者报告出现潮红,7 例患者报告头痛,均通过将剂量减少至 10ml/h 以下得到控制。在萎缩/纤维化阶段的患者(65/81)中,10 例患者在以 20ml/h 输注时出现腹泻,24 例患者出现低血压,导致药物暂时停药。当 ILO 重新开始并保持在 10ml/h 以下时,未出现不良反应。23 例患者出现潮红,8 例患者出现头痛,所有患者均通过将输注量减少至 10ml/h 以下得到控制。与水肿组相比,这些患者的不良反应发生率显著降低(p=0.023 和 p=0.008)。我们的数据表明,在使用 ILO 时应暂时停用钙通道阻滞剂,并且预处理方法可能会减少或控制不良反应。在手指水肿患者中,在评估患者的药物耐受性后,应谨慎使用 ILO 输注。

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