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
{"title":"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","authors":"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","doi":"10.1177/23971983231209809","DOIUrl":null,"url":null,"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.","PeriodicalId":506053,"journal":{"name":"Journal of Scleroderma and Related Disorders","volume":"55 15","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"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\",\"doi\":\"10.1177/23971983231209809\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":506053,\"journal\":{\"name\":\"Journal of Scleroderma and Related Disorders\",\"volume\":\"55 15\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Scleroderma and Related Disorders\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/23971983231209809\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Scleroderma and Related Disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/23971983231209809","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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
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.