Incidence of Allergic Drug Eruption due to Cotrimoxazole in HIV-Positive Individuals with CD4 ≤200 Cells/ul.

IF 2.2 Q3 INFECTIOUS DISEASES
Irene Rosali, Putu Siska Virgayanti, Della Sabrina Marta, Emon Winardi Danudirgo, Sisca Hadinata
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Abstract

Allergic drug eruptions (ADE) remain a challenge in people living with HIV (PLWH), requiring more studies to guide clinical approaches. While cotrimoxazole is widely used as prophylaxis in PLWH, relationship between client characteristics toward the occurrence of cotrimoxazole ADEs is still poorly understood.A retrospective cohort study followed PLWH initiated with antiretroviral therapy (ART) in St. Carolus Hospital between January 2009 to December 2021. ADE occurrence due to cotrimoxazole were tested for significance using Pearson's Chi-square and Fisher's Exact Test (significant outcome measured as p < 0.05) against CD4 levels at very low (0-100 cells/ul) and low (101-200 cells/ul) groups, comorbidities, and retention status.Cotrimoxazole-related ADEs occurred in 258 (14%) of 1789 subjects with CD4 levels ≤200 cells/ul. Comorbidities of Hepatitis B, Hepatitis C, and M. tuberculosis infections were found in 11, 4, and 95 subjects respectively. 151 (59%) of ADE group had very low CD4 levels (p value > 0.05). No significant difference was found in ADE incidence between age groups, genders, CD4 levels, comorbidities, and ART retention.Cotrimoxazole-induced ADE is unrelated to CD4 levels, and ART retention was not affected. ADE severity ranges from mild to serious manifestations, and close monitoring is crucial to ensure ADEs are treated ART are well-maintained.

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CD4≤200 Cells/ul hiv阳性患者复方新诺明致过敏性药疹的发生率
过敏性药物疹(ADE)仍然是HIV感染者(PLWH)面临的一个挑战,需要更多的研究来指导临床方法。虽然复方新诺明被广泛用于PLWH预防,但患者特征与复方新诺明不良反应发生之间的关系尚不清楚。2009年1月至2021年12月,在圣卡洛勒斯医院进行了一项回顾性队列研究,追踪了在抗逆转录病毒治疗(ART)下开始的PLWH。采用Pearson's卡方检验和Fisher's精确检验检验复方新诺明所致ADE发生率的显著性(p > 0.05)。在年龄组、性别、CD4水平、合并症和ART保留率之间,ADE发生率无显著差异。复方新诺唑诱导的ADE与CD4水平无关,ART保留率不受影响。不良反应的严重程度从轻微到严重不等,密切监测对于确保不良反应得到治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
43
审稿时长
13 weeks
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