Peyronie病的未来概念和治疗方法

IF 0.8 4区 医学 Q4 PHARMACOLOGY & PHARMACY
E. Choi, D. Schneider, P. Xu, F. El-Khatib, F. Yafi
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引用次数: 0

摘要

胶原酶溶组织梭菌(Clostridium histolyticum, CCh)是美国食品和药物管理局(fda)批准的唯一用于治疗佩罗尼氏病(PD)的药物。然而,它的批准范围以及在国际上的使用受到限制。本综述讨论了自FDA首次批准CCh以来,CCh在急性和非典型PD中扩大使用的证据,以及新的非手术治疗选择。PubMed数据库在2013年1月至2020年5月期间发表的英文摘要中使用关键词Peyronie病,治疗和治疗进行了全面审查。共有90篇独特的文章被发现与PD的保守治疗有关。在剔除冗余文章后,39篇论文被全面审查并纳入本研究,代表2807例PD患者。专家意见在确定的治疗方法出现之前,结合不同的治疗方式可能是解决每位患者独特问题的最可行的选择。此外,现有文献的质量参差不齐。有必要系统地定义疾病过程,并确定治疗基准,以最大限度地提高患者的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Future concepts and therapy approaches for Peyronie’s disease
ABSTRACT Introduction Collagenase Clostridium histolyticum (CCh) is the only drug approved by the US Food and Drug Administration for the treatment of Peyronie’s Disease (PD). However, it is limited in its scope of approval as well as its access for use internationally. Areas covered This review discusses the evidence on the expanded use of CCh for acute and atypical PD as well as novel, non-surgical treatment options that have been investigated since the FDA first approved of CCh. The PubMed database was thoroughly reviewed in the English-language for abstracts published between January 2013 to May 2020 using the keywords Peyronie’s disease, treatments, and therapy. A total of 90 unique articles were found to be relevant to the conservative management of PD. After excluding redundant articles, 39 manuscripts were given full review and included in this study, representing 2,807 patients with PD. Expert opinion Until definitive treatment becomes available, combinations of differing modalities may be the most viable option in addressing the unique concerns for each patient. Furthermore, the literature available varies widely in quality. There is a need for systematic definitions of the disease process as well as identifying treatment benchmarks that would maximize the patient quality of life.
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来源期刊
Expert Opinion on Orphan Drugs
Expert Opinion on Orphan Drugs PHARMACOLOGY & PHARMACY-
CiteScore
2.30
自引率
0.00%
发文量
8
期刊介绍: Expert Opinion on Orphan Drugs is an international, peer-reviewed journal that covers all aspects of R&D on rare diseases and orphan drugs.
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