Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
4th Department of Internal Medicine and HIV/ID Unit, ATTIKON University General Hospital, Athens, Greece.
Euro Surveill. 2024 Nov;29(48). doi: 10.2807/1560-7917.ES.2024.29.48.2400138.
BackgroundLate HIV diagnosis (CD4+ T-cell count < 350 cells/μL, or with an AIDS-defining event) remains a persistent challenge in Greece, indicating potential missed opportunities (MOs) for earlier testing.AimTo determine the frequency of HIV indicator conditions (ICs) preceding diagnosis and to quantify MOs for earlier testing at a nationwide level in Greece.MethodsThis multicentre retrospective study analysed data on 823 antiretroviral therapy-naive adults (≥ 18 years) diagnosed with HIV during 2019-21. Medical records were reviewed to identify pre-diagnosis healthcare contacts (HCCs) and ICs justifying HIV testing. Univariable and multivariable logistic regression identified factors associated with ≥ 1 MO. A Bayesian model estimated the time from seroconversion to diagnosis.ResultsAmong 517 participants with HCC data, 249 had ≥ 1 HCC. Of these, 59.0% (147/249) were late presenters. These cases had 365 HCCs, and 191 (52.3%) were MOs for testing. The most common ICs were sexually transmitted infections (39.8%; 76/191) and fever (11.0%; 21/191). Non-Greek origin was associated with lower odds of experiencing ≥ 1 MO (adjusted odds ratio: 0.48; 95% CI: 0.22─1.02), while higher education increased odds of MOs for early HIV diagnosis. Median time from seroconversion to diagnosis was 3.2 years for the full sample and 3.7 years for those with HCC, with about half of the latter reporting MOs post-estimated seroconversion. Recognising MOs would have potentially spared approximately 1 year of delay in diagnosis.ConclusionMOs for earlier HIV diagnosis were prevalent in Greece. Leveraging IC-guided testing and addressing barriers could support earlier diagnosis and treatment, limiting adverse health outcomes and preventing transmission.
在希腊,CD4+T 细胞计数<350 个/μL 或出现艾滋病定义性事件的晚期 HIV 诊断仍然是一个持续存在的挑战,这表明存在潜在的检测机会错失(MO)。
在全国范围内确定希腊 HIV 诊断前 HIV 指标情况(IC)的频率,并量化更早进行检测的 MO。
这项多中心回顾性研究分析了 2019 年至 2021 年期间诊断为 HIV 的 823 名初治抗逆转录病毒治疗成年人(≥18 岁)的数据。回顾医疗记录以确定诊断前的医疗保健接触(HCC)和证明 HIV 检测合理的 IC。单变量和多变量逻辑回归确定了与≥1 MO 相关的因素。贝叶斯模型估计了从血清转换到诊断的时间。
在 517 名有 HCC 数据的参与者中,249 名有≥1 HCC。其中,59.0%(147/249)为晚期就诊者。这些病例有 365 次 HCC,其中 191 次(52.3%)是检测的 MO。最常见的 IC 是性传播感染(39.8%;76/191)和发热(11.0%;21/191)。非希腊血统与经历≥1 MO 的可能性较低相关(调整后的优势比:0.48;95%可信区间:0.22-1.02),而较高的教育程度增加了早期 HIV 诊断的 MO 可能性。从血清转换到诊断的中位时间为全样本的 3.2 年和 HCC 的 3.7 年,后者中约有一半报告在估计的血清转换后出现 MO。认识到 MO 将有可能使诊断延迟大约 1 年。
在希腊,HIV 诊断前的 MO 很常见。利用 IC 指导的检测和解决障碍可以支持更早的诊断和治疗,从而限制不良健康结果和预防传播。