Practice pattern for the use of intravenous iloprost for the treatment of peripheral vasculopathy in systemic sclerosis: A case–control study from the Italian national multicenter “SPRING” (Systemic Sclerosis Progression InvestiGation) Registry

V. Riccieri, G. Pellegrino, E. Cipolletta, D. Giuggioli, G. Bajocchi, S. Bellando-Randone, L. Dagna, G. Zanframundo, Rosario Foti, F. Cacciapaglia, G. Cuomo, A. Ariani, E. Rosato, G. Lepri, F. Girelli, E. Zanatta, S. Bosello, I. Cavazzana, F. Ingegnoli, M. De Santis, G. Murdaca, G. Abignano, N. Romeo, A. Della Rossa, Maurizio Caminiti, A. Iuliano, G. Ciano, L. Beretta, G. Bagnato, E. Lubrano, I. de Andres, A. Giollo, M. Saracco, C. Agnes, F. Lumetti, A. Spinella, Luca Magnani, C. Campochiaro, G. de Luca, V. Codullo, E. Visalli, C. Di Vico, A. Gigante, F. Saccon, Maria Grazia Lazzaroni, F. Franceschini, E. Generali, G. Mennillo, S. Barsotti, G. Pagano Mariano, Francesca Calabrese, F. Furini, Licia Vultaggio, S. Parisi, C. Peroni, Gerolamo Bianchi, Fabrizio Conti, Franco Cozzi, Salvatore D'Angelo, Andrea Doria, E. Fusaro, M. Govoni, S. Guiducci, F. Iannone, C. Salvarani, G. Sebastiani, C. Ferri, M. Matucci-Cerinic, R. De Angelis
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Abstract

Intravenous iloprost has been widely used for the treatment of systemic sclerosis peripheral vasculopathy. No agreement has been found on the regimen and the dosage of intravenous iloprost in different scleroderma subset conditions. This study aimed to evaluate the modalities of intravenous iloprost administration within a large cohort of systemic sclerosis patients from the SPRING Registry and to identify any associated clinical-demographic, instrumental or therapeutic data. Data of systemic sclerosis patients treated with intravenous iloprost for at least 1 year (case group) were retrospectively analyzed, including different timing and duration of intravenous iloprost session, and compared with those of untreated patients (control group). Out of 1895 analyzed patients, 937 (49%) received intravenous iloprost treatment, while 958 (51%) were assigned to the control group. Among cases, about 70% were treated every 4 weeks, 24% with an interval of more than 4 weeks, and only 6% of less than 4 weeks. Most patients receiving the treatment every 4 weeks, or less, underwent infusion cycle for 1 day only, while if it was scheduled with an interval of more than 4 weeks, a total number of 5 consecutive days of infusions was the preferred regimen. The comparison between the two groups revealed that patients treated with intravenous iloprost had a higher frequency of DUs (p < 0.001), pitting scars (p < 0.001), diffuse cutaneous involvement (p < 0.001), interstitial lung disease (p < 0.002), as well as higher rates of anti-topoisomerase I, “ late” scleroderma pattern at nailfold videocapillaroscopy. These findings were confirmed by multivariate analysis. Our data provide a picture on the Italian use of intravenous iloprost among systemic sclerosis patients and showed that it was usually employed in patients with a more aggressive spectrum of the disease. The disparity of intravenous iloprost treatment strategies in the different centers suggests the need of a rational therapeutical approach based on the clinical characteristics of different patients’ subsets.
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使用静脉注射伊洛前列素治疗系统性硬化症外周血管病变的实践模式:意大利国家多中心 "SPRING"(系统性硬化症进展调查)登记处的病例对照研究
静脉注射伊洛前列素被广泛用于治疗系统性硬化症外周血管病变。在不同的硬皮病亚型中,静脉注射伊洛前列素的方案和剂量尚未达成一致。本研究旨在评估来自 SPRING 登记处的一大批系统性硬化症患者静脉注射伊洛前列素的方式,并确定任何相关的临床-人口学、器械或治疗数据。研究人员回顾性分析了接受静脉注射伊洛前列素治疗至少一年的系统性硬化症患者(病例组)的数据,包括静脉注射伊洛前列素的不同时间和持续时间,并与未接受治疗的患者(对照组)的数据进行了比较。在分析的 1895 例患者中,937 例(49%)接受了静脉注射伊洛前列素治疗,958 例(51%)被分配到对照组。在病例中,约 70% 的患者每 4 周接受一次治疗,24% 的患者间隔超过 4 周,只有 6% 的患者间隔少于 4 周。大多数患者每 4 周或更短时间接受一次治疗,输液周期仅为 1 天,而如果治疗间隔超过 4 周,则首选连续输液 5 天的治疗方案。两组患者的比较结果显示,接受静脉注射伊洛前列素治疗的患者出现 DUs(p < 0.001)、点状疤痕(p < 0.001)、弥漫性皮肤受累(p < 0.001)、间质性肺病(p < 0.002)的频率更高,而且甲襞视频硬皮镜检查中出现抗拓扑异构酶 I、"晚期 "硬皮病模式的比例更高。多变量分析证实了这些发现。我们的数据提供了意大利系统性硬化症患者静脉注射伊洛前列素的情况,并显示该药物通常用于病情较重的患者。不同中心在静脉注射伊洛前列素治疗策略上的差异表明,需要根据不同患者的临床特征采取合理的治疗方法。
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