静脉注射奈利膦酸钠治疗 1 型复杂性区域疼痛综合征 (CRPS) 患者的良性发展:单中心真实体验。

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Pharmaceuticals Pub Date : 2024-11-08 DOI:10.3390/ph17111500
Jacopo Ciaffi, Gianluca Festuccia, Claudio Ripamonti, Luana Mancarella, Veronica Brusi, Federica Pignatti, Lucia Lisi, Lisa Berti, Piero Ruscitti, Cesare Faldini, Francesco Ursini
{"title":"静脉注射奈利膦酸钠治疗 1 型复杂性区域疼痛综合征 (CRPS) 患者的良性发展:单中心真实体验。","authors":"Jacopo Ciaffi, Gianluca Festuccia, Claudio Ripamonti, Luana Mancarella, Veronica Brusi, Federica Pignatti, Lucia Lisi, Lisa Berti, Piero Ruscitti, Cesare Faldini, Francesco Ursini","doi":"10.3390/ph17111500","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the long-term effects of intravenous neridronate treatment in patients with complex regional pain syndrome type 1 (CRPS) in a real-life setting.</p><p><strong>Methods: </strong>We conducted a retrospective study on consecutive CRPS patients treated at our hospital from February 2018 to July 2023. All were treated within three months of the onset of CRPS symptoms. The Patient-Reported Outcomes Measurement Information System 29-Item Health Profile (PROMIS-29) version 2.1 was administered. The main outcome of interest was the evolution of the PROMIS-29 scores from baseline to the last follow-up visit. Patients were categorized as \"complete responders\" or \"non-complete responders\". The association of clinical and demographic variables with a complete response was analyzed using chi-square tests and univariate logistic regression.</p><p><strong>Results: </strong>Thirty-six patients were included, with a median follow-up time of 4.8 years. A significant improvement was noted in the mean numerical pain rating scale (from 6.4 ± 1.9 to 3.1 ± 2.4, <i>p</i> < 0.001), as well as across all PROMIS-29 domains. Physical function improved from 34.2 ± 4.9 to 49.2 ± 9.9, <i>p</i> < 0.001; anxiety from 58.0 ± 6.7 to 49.6 ± 6.9, <i>p</i> < 0.001; depression from 55.3 ± 6.3 to 47.7 ± 6.6, <i>p</i> < 0.001; fatigue from 55.7 ± 7.7 to 50.9 ± 8.7, <i>p</i> < 0.001; sleep disturbance from 53.8 ± 6.8 to 51.3 ± 6.6, <i>p</i> = 0.034; social roles and activities from 41.8 ± 5.2 to 51.8 ± 8.9, <i>p</i> < 0.001; and pain interference from 64.1 ± 5.9 to 52.4 ± 9.9, <i>p</i> < 0.001. The likelihood of achieving a complete response was associated with the male sex, foot or ankle injuries (compared to hand and wrist injuries), and a younger age. No association was found with the type of inciting event or with the body mass index.</p><p><strong>Conclusions: </strong>Our real-life data indicate that early treatment with neridronate leads to substantial benefits in patients affected by CRPS type 1. The strongest responses are seen in young patients, males, and those with lower limb involvement.</p>","PeriodicalId":20198,"journal":{"name":"Pharmaceuticals","volume":"17 11","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Benign Evolution of Complex Regional Pain Syndrome (CRPS) Type 1 in Patients Treated with Intravenous Neridronate: A Single-Center Real-Life Experience.\",\"authors\":\"Jacopo Ciaffi, Gianluca Festuccia, Claudio Ripamonti, Luana Mancarella, Veronica Brusi, Federica Pignatti, Lucia Lisi, Lisa Berti, Piero Ruscitti, Cesare Faldini, Francesco Ursini\",\"doi\":\"10.3390/ph17111500\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To investigate the long-term effects of intravenous neridronate treatment in patients with complex regional pain syndrome type 1 (CRPS) in a real-life setting.</p><p><strong>Methods: </strong>We conducted a retrospective study on consecutive CRPS patients treated at our hospital from February 2018 to July 2023. All were treated within three months of the onset of CRPS symptoms. The Patient-Reported Outcomes Measurement Information System 29-Item Health Profile (PROMIS-29) version 2.1 was administered. The main outcome of interest was the evolution of the PROMIS-29 scores from baseline to the last follow-up visit. Patients were categorized as \\\"complete responders\\\" or \\\"non-complete responders\\\". The association of clinical and demographic variables with a complete response was analyzed using chi-square tests and univariate logistic regression.</p><p><strong>Results: </strong>Thirty-six patients were included, with a median follow-up time of 4.8 years. A significant improvement was noted in the mean numerical pain rating scale (from 6.4 ± 1.9 to 3.1 ± 2.4, <i>p</i> < 0.001), as well as across all PROMIS-29 domains. Physical function improved from 34.2 ± 4.9 to 49.2 ± 9.9, <i>p</i> < 0.001; anxiety from 58.0 ± 6.7 to 49.6 ± 6.9, <i>p</i> < 0.001; depression from 55.3 ± 6.3 to 47.7 ± 6.6, <i>p</i> < 0.001; fatigue from 55.7 ± 7.7 to 50.9 ± 8.7, <i>p</i> < 0.001; sleep disturbance from 53.8 ± 6.8 to 51.3 ± 6.6, <i>p</i> = 0.034; social roles and activities from 41.8 ± 5.2 to 51.8 ± 8.9, <i>p</i> < 0.001; and pain interference from 64.1 ± 5.9 to 52.4 ± 9.9, <i>p</i> < 0.001. The likelihood of achieving a complete response was associated with the male sex, foot or ankle injuries (compared to hand and wrist injuries), and a younger age. No association was found with the type of inciting event or with the body mass index.</p><p><strong>Conclusions: </strong>Our real-life data indicate that early treatment with neridronate leads to substantial benefits in patients affected by CRPS type 1. The strongest responses are seen in young patients, males, and those with lower limb involvement.</p>\",\"PeriodicalId\":20198,\"journal\":{\"name\":\"Pharmaceuticals\",\"volume\":\"17 11\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-11-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pharmaceuticals\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3390/ph17111500\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceuticals","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/ph17111500","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

摘要

目的在真实环境中研究静脉注射奈利膦酸钠治疗1型复杂区域疼痛综合征(CRPS)患者的长期效果:我们对 2018 年 2 月至 2023 年 7 月在我院接受治疗的连续 CRPS 患者进行了回顾性研究。所有患者均在出现 CRPS 症状后三个月内接受治疗。采用了患者报告结果测量信息系统 29 项健康档案(PROMIS-29)2.1 版。主要研究结果是PROMIS-29评分从基线到最后一次随访的变化情况。患者被分为 "完全应答者 "和 "非完全应答者"。采用卡方检验和单变量逻辑回归分析了临床和人口统计学变量与完全应答的关系:共纳入 36 名患者,中位随访时间为 4.8 年。平均疼痛评分量表(从 6.4 ± 1.9 降至 3.1 ± 2.4,p < 0.001)以及 PROMIS-29 的所有领域均有明显改善。身体功能从 34.2 ± 4.9 改善到 49.2 ± 9.9,p < 0.001;焦虑从 58.0 ± 6.7 改善到 49.6 ± 6.9,p < 0.001;抑郁从 55.3 ± 6.3 改善到 47.7 ± 6.6,p < 0.001;疲劳从 55.7 ± 7.7 改善到 50.9 ± 8.7,p < 0.001;睡眠障碍从(53.8 ± 6.8)降至(51.3 ± 6.6),p = 0.034;社会角色和活动从(41.8 ± 5.2)降至(51.8 ± 8.9),p < 0.001;疼痛干扰从(64.1 ± 5.9)降至(52.4 ± 9.9),p < 0.001。获得完全应答的可能性与男性、足部或踝部损伤(与手部和腕部损伤相比)以及年龄较小有关。与诱发事件的类型或体重指数没有关联:我们的实际数据表明,使用奈利膦酸钠进行早期治疗可为1型CRPS患者带来很大益处。年轻患者、男性和下肢受累者的反应最为强烈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benign Evolution of Complex Regional Pain Syndrome (CRPS) Type 1 in Patients Treated with Intravenous Neridronate: A Single-Center Real-Life Experience.

Objective: To investigate the long-term effects of intravenous neridronate treatment in patients with complex regional pain syndrome type 1 (CRPS) in a real-life setting.

Methods: We conducted a retrospective study on consecutive CRPS patients treated at our hospital from February 2018 to July 2023. All were treated within three months of the onset of CRPS symptoms. The Patient-Reported Outcomes Measurement Information System 29-Item Health Profile (PROMIS-29) version 2.1 was administered. The main outcome of interest was the evolution of the PROMIS-29 scores from baseline to the last follow-up visit. Patients were categorized as "complete responders" or "non-complete responders". The association of clinical and demographic variables with a complete response was analyzed using chi-square tests and univariate logistic regression.

Results: Thirty-six patients were included, with a median follow-up time of 4.8 years. A significant improvement was noted in the mean numerical pain rating scale (from 6.4 ± 1.9 to 3.1 ± 2.4, p < 0.001), as well as across all PROMIS-29 domains. Physical function improved from 34.2 ± 4.9 to 49.2 ± 9.9, p < 0.001; anxiety from 58.0 ± 6.7 to 49.6 ± 6.9, p < 0.001; depression from 55.3 ± 6.3 to 47.7 ± 6.6, p < 0.001; fatigue from 55.7 ± 7.7 to 50.9 ± 8.7, p < 0.001; sleep disturbance from 53.8 ± 6.8 to 51.3 ± 6.6, p = 0.034; social roles and activities from 41.8 ± 5.2 to 51.8 ± 8.9, p < 0.001; and pain interference from 64.1 ± 5.9 to 52.4 ± 9.9, p < 0.001. The likelihood of achieving a complete response was associated with the male sex, foot or ankle injuries (compared to hand and wrist injuries), and a younger age. No association was found with the type of inciting event or with the body mass index.

Conclusions: Our real-life data indicate that early treatment with neridronate leads to substantial benefits in patients affected by CRPS type 1. The strongest responses are seen in young patients, males, and those with lower limb involvement.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信