治疗经验丰富的艾滋病病毒感染者的眼部受累。

Mihaela Cobaschi, Carmen Mihaela Dorobăț, Victor Daniel Dorobăț, Isabela Ioana Loghin, Mioara-Laura Macovei, Adrian Marinescu, Victoria Aramă
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引用次数: 0

摘要

导言:尽管抗逆转录病毒疗法(ART)药物取得了进步,但人类免疫缺陷病毒(HIV)感染者和有治疗经验的患者的眼部受累仍是一个重大问题。艾滋病病毒感染者预期寿命的延长改变了艾滋病病毒相关眼部疾病的范围,从轻微问题到严重视力损害或失明不等。因此,了解这些并发症对于提供全面的医疗护理和提高生活质量至关重要。由于治疗方案、药物毒性、免疫重建和机会性感染的复杂性,接受多种抗逆转录病毒疗法的艾滋病患者可能会出现各种眼部疾病。最值得考虑的是:巨细胞病毒(CMV)视网膜炎、免疫恢复性葡萄膜炎(IRU)、角膜结膜炎(干眼症)和艾滋病相关神经视网膜疾病。材料和方法:对 2013 年 1 月 1 日至 2023 年 12 月 31 日期间感染艾滋病毒/艾滋病的患者进行了回顾性临床调查。研究包括 62 名 18 岁以上的患者,他们通过酶联免疫吸附试验(ELISA)检测出 HIV 阳性,并经免疫印迹(WB)证实,同时还评估了 HIV 血浆病毒载量(VL)和 CD4+ T 细胞计数(CD4)。收集的数据包括人口统计学、病理病史、临床特征、血液检测、机会性感染评估、患者分期、抗逆转录病毒疗法的启动以及疾病预后。研究结果研究发现,大多数患者的年龄在 30-39 岁之间(占 59.7%),其中男性占 59.7%,女性占 40.3%。大多数患者已感染艾滋病毒 10-19 年(35.5%)。46.8%的患者最初的 CD4 细胞计数小于 200 cells/mm3,研究完成后这一比例下降到 19.3%。尽管进行了抗逆转录病毒疗法,但 CMV 视网膜炎的发病率仍从最初的 46.8% 降至 35.5%。其他疾病包括眼弓形虫病(3.22%)、结核相关性葡萄膜炎(1.6%)、角膜结膜炎(19.3%)和艾滋病视网膜病变(29%)。值得注意的是,62.1%的巨细胞病毒视网膜炎患者视力明显下降。口服缬更昔洛韦对影响多个部位的 CMV 患者有益,对 CMV 视网膜炎的诱导和维持治疗均有效。结论治疗艾滋病病毒感染者的眼部并发症需要采用多学科方法,定期进行眼科评估、及时治疗感染并持续监测抗逆转录病毒疗法的效果。早期发现和干预对于保护视力和改善预后至关重要。该研究强调了即使在病毒抑制后仍需持续监测的重要性。缩写:HIV = 人类免疫缺陷病毒,ART = 抗逆转录病毒疗法,CMV = 巨细胞病毒,IRU = 免疫恢复性葡萄膜炎,ELISA = 酶联免疫吸附试验,WB = 免疫印迹,VL = 病毒载量,CD4 = CD4+ T 细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ocular involvement in highly treatment-experienced patients with HIV.

Introduction: Ocular involvement in human immunodeficiency virus (HIV) infected and treatment-experienced patients is a significant concern, despite the advancements in antiretroviral therapy (ART) medication. The extended life expectancy of HIV patients has altered the spectrum of HIV-associated ocular diseases, ranging from minor issues to severe vision impairment or blindness. Therefore, understanding these complications becomes crucial in providing comprehensive medical care and quality of life improvement. HIV patients on multiple ARTs can experience various ocular disorders due to the complexity of their treatment regimens, drug toxicities, immune reconstitution, and opportunistic infections. Most worthy to consider are: cytomegalovirus (CMV) retinitis, immune recovery uveitis (IRU), keratoconjunctivitis sicca (dry eye syndrome), and HIV-associated neuroretinal disorders. Materials and methods: A retrospective clinical investigation was conducted on HIV/AIDS-infected patients from January 1, 2013, to December 31, 2023. The study included 62 patients over 18 years, who tested HIV-positive via enzyme-linked immunosorbent assay (ELISA) and confirmed by Western blot (WB), with assessments of HIV plasma viral load (VL) and CD4+ T cell counts (CD4). Data collected included demographics, pathological histories, clinical characteristics, blood tests, assessments for opportunistic infections, patient staging, antiretroviral therapy initiation, and disease prognosis. Results: The study found that of most patients, 37 were aged 30-39 (59.7%), with 59.7% males and 40.3% females. Most had been living with HIV for 10-19 years (35.5%). Initial CD4 counts were < 200 cells/mm3 in 46.8% of patients, which improved to 19.3% when the study was done. CMV retinitis prevalence decreased from 46.8% initially to 35.5% despite ART. Other conditions included ocular toxoplasmosis (3.22%), tuberculosis-related uveitis (1,6%), keratoconjunctivitis sicca (19.3%), and HIV retinopathy (29%). Notably, 62.1% of CMV retinitis patients experienced significant visual acuity reduction. Oral valganciclovir was beneficial for patients with CMV disease affecting multiple sites and effective for both induction and maintenance therapy of CMV retinitis. Conclusions: Managing ocular complications in HIV-experienced patients requires a multidisciplinary approach with regular ophthalmologic evaluations, prompt treatment of infections, and continuous monitoring of ART effectiveness. Early detection and intervention are crucial for preserving vision and improving outcomes. The study highlighted the importance of constant monitoring even after viral suppression. Abbreviations: HIV = Human immunodeficiency virus, ART = antiretroviral therapy, CMV = cytomegalovirus, IRU = immune recovery uveitis, ELISA = enzyme-linked immunosorbent assay, WB = Western Blot, VL = viral load, CD4 = CD4+ T cells.

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