McCampbell Lillian E, Zaino Mallory L, Ranpariya Manas, Patel Tejesh, Feldman Steven R
University of Tennessee Health Science Center, Memphis, TN, USA.
Center for Dermatology Research, Department of Dermatology, Wake Forest School of Medicine, Winston-Salem, NC, USA.
J Cutan Med Surg. 2023 Nov;27(6):641-645. doi: 10.1177/12034754231211797. Epub 2023 Nov 21.
Prurigo nodularis (PN) is a debilitating inflammatory skin disease characterized by red to violaceous pruritic lesions. The goal of therapy is to break the scratch-itch cycle. Treatment varies and often requires a multimodal approach to target both immune and neural mediated aspects of disease.
To review the efficacy of systemic treatment used to treat PN.
A systematic search of keywords and Medical Subject Headings was performed in Ovid MEDLINE, Embase, Scopus, and ClinicalTrials.gov. The first 200 results of an abbreviated search in Google Scholar were also included. PRISMA guidelines were followed and the review was registered on PROSPERO (CRD42023412012). GRADE criteria were used to assess articles for quality of evidence.
The search resulted in 1153 articles; 382 were duplicates, 643 were irrelevant, 19 were not retrieved, 21 were abstract only, and 88 are included in this review. There were 24 studies on dupilumab, 16 on thalidomide, 8 on cyclosporin, 7 on methotrexate, 3 each on lenalidomide and aprepitant, 2 each on alitretinoin, apremilast, baricitinib, gabapentin, intravenous (IV) immunoglobulins, pregabalin, tofacitinib, and 1 each on amitriptyline, azathioprine, butorphanol, isoquercitin, IV dexamethasone-cyclophosphamide/ oral cyclophosphamide, ketotifen, metronidazole, montelukast, nalbuphine, nemolizumab, serolopitant, tacrolimus, and herose derma zima capsule.
Dupilumab reduces pruritus and appearance of lesions and is associated with the fewest number of side effects. Thalidomide and pregabalin are also effective, but their long-term use is limited by muscle and nerve pain. Janus Kinase inhibitors may be beneficial, but large population studies are lacking.
结节性痒疹(PN)是一种使人衰弱的炎症性皮肤病,其特征为红色至紫罗兰色的瘙痒性皮损。治疗的目标是打破搔抓-瘙痒循环。治疗方法各异,通常需要采用多模式方法来针对疾病的免疫和神经介导方面。
综述用于治疗PN的全身治疗的疗效。
在Ovid MEDLINE、Embase、Scopus和ClinicalTrials.gov中对关键词和医学主题词进行了系统检索。还纳入了谷歌学术简略检索的前200个结果。遵循PRISMA指南,并在PROSPERO(CRD42023412012)上注册了该综述。采用GRADE标准评估文章的证据质量。
检索结果为1153篇文章;382篇为重复文章,643篇不相关,19篇未检索到,21篇仅有摘要,88篇纳入本综述。关于度普利尤单抗的研究有24项,沙利度胺16项,环孢素8项,甲氨蝶呤7项,来那度胺和阿瑞匹坦各3项,阿利维A酸、阿普斯特、巴瑞替尼、加巴喷丁、静脉注射免疫球蛋白、普瑞巴林、托法替布各2项,阿米替林、硫唑嘌呤、布托啡诺、异槲皮苷、静脉注射地塞米松-环磷酰胺/口服环磷酰胺、酮替芬、甲硝唑、孟鲁司特、纳布啡、奈莫利单抗、塞洛匹坦、他克莫司以及赫罗斯皮肤紫麻胶囊各1项。
度普利尤单抗可减轻瘙痒和皮损外观,且副作用最少。沙利度胺和普瑞巴林也有效,但它们的长期使用受到肌肉和神经疼痛的限制。Janus激酶抑制剂可能有益,但缺乏大型人群研究。