Kumar Sumir, Dhillon Simranjeet Singh, Brar B K, Singh Amarbir
All authors are with the Department of Dermatology, Venereology, and Leprology at Guru Gobind Singh Medical College and Hospital in Faridkot, Punjab, India.
J Clin Aesthet Dermatol. 2021 Mar;14(3):38-41. Epub 2021 Mar 1.
Urticaria affects 0.5 to 1 percent of the population at any given time. Treatments include nonsedative antihistamines, autologous serum therapy, and injected histaglobulin. This study sought to compare the therapeutic efficacy and safety of injected histaglobulin with autologous serum therapy in chronic urticaria. This was a hospital-based prospective study performed in the Department of Dermatology, Venereology, and Leprology at Guru Gobind Singh Medical College and Hospital in Faridkot, India. A total of 96 patients with chronic idiopathic urticaria were enrolled after applying inclusion and exclusion criteria and were divided into two groups of 48 patients each using an envelope method. Autologous serum skin tests were performed in each patient irrespective of their group assignment. Group A then received injected histaglobulin and Group B received autologous serum therapy (AST). Patient were evaluated using the Urticaria Activity Score (UAS) every week for six weeks, with follow-up conducted at three and six weeks after the completion of treatment. The Chronic Urticaria Quality of Life questionnaire was used to assess the quality of life of the study participants. Out of the 96 initially enrolled patients, 62 completed the six weeks of treatment and two follow-up visits. Twenty patients dropped out due to remission and 14 patients left the study for other reasons. Reductions in UAS values occurred in both the groups by the end of follow-up but were more significant in Group A. Improvement in quality of life scores was also greater in Group A. Recurrence occurred in both groups after treatment cessation but was less common in Group A. Both treatments were validated for treating chronic urticaria; however, injected histaglobulin showed statistically more consequential results than AST.
在任何给定时间,荨麻疹影响着0.5%至1%的人口。治疗方法包括非镇静性抗组胺药、自体血清疗法和注射组胺球蛋白。本研究旨在比较注射组胺球蛋白与自体血清疗法治疗慢性荨麻疹的疗效和安全性。这是一项在印度法里德科特古鲁·戈宾德·辛格医学院和医院皮肤科、性病科和麻风病科进行的基于医院的前瞻性研究。在应用纳入和排除标准后,共招募了96例慢性特发性荨麻疹患者,并采用信封法将其分为两组,每组48例。无论患者属于哪一组,均对其进行自体血清皮肤试验。然后,A组接受注射组胺球蛋白,B组接受自体血清疗法(AST)。每周使用荨麻疹活动评分(UAS)对患者进行评估,为期六周,并在治疗结束后三周和六周进行随访。使用慢性荨麻疹生活质量问卷评估研究参与者的生活质量。在最初招募的96例患者中,62例完成了六周的治疗和两次随访。20例患者因病情缓解退出,14例患者因其他原因离开研究。随访结束时,两组的UAS值均有所下降,但A组下降更为显著。A组的生活质量评分改善也更大。治疗停止后,两组均出现复发,但A组复发较少见。两种治疗方法均被证实可治疗慢性荨麻疹;然而,注射组胺球蛋白在统计学上比AST显示出更显著的效果。