瑞典一项以全国登记为基础的队列研究中,按艾滋病病毒感染状况和非典-CoV-2 疫苗接种状况分列的 COVID-19 住院风险(前奥美康时代和后奥美康时代)。

Isabela Killander Möller, Pontus Hedberg, Philippe Wagner, Hannes Lindahl, Sofia Nyström, Lisa Blixt, Sandra Eketorp Sylvan, Åsa Nilsdotter-Augustinsson, Anders Österborg, Mats Fredrikson, Lotta Hansson, Fredrik Kahn, Pär Sparén, Magnus Gisslén, Pontus Nauclér, Peter Bergman, Soo Aleman, Christina Carlander
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引用次数: 0

摘要

背景:在 Omicron 时代,缺乏有关 COVID-19 在艾滋病毒感染者(PLHIV)中的结果的数据,特别是与疫苗接种情况有关的数据:这项基于登记的全国性研究纳入了 2021 年 1 月至 2023 年 2 月期间所有 SARS-CoV-2 PCR 检测呈阳性的 18 岁以上瑞典居民。我们根据 SARS-CoV-2 疫苗接种情况(0-1 剂、2 剂和≥3 剂)和 HIV 感染情况,估算了 COVID-19 住院率和严重 COVID-19(入住 ICU 和 90 天死亡率)的调整赔率比 (adjOR)。然后按 "奥米克龙 "前、公共检测期间的 "奥米克龙 "和公共检测后的 "奥米克龙 "时间段进行分类分析:结果:共纳入了 1348 名艾滋病毒感染者和 1 669 389 名未感染艾滋病毒者(PWoH)。艾滋病病毒感染者年龄较大,多为移民(65% 对 22%),男性(59% 对 46%)。在艾滋病毒感染者中,96% 正在接受抗逆转录病毒治疗,94% 病毒得到抑制。在控制了人口统计学、感染日历月、合并症和收入的情况下,COVID-19住院治疗的AdjORs与HIV感染状况相似。在 Omicron 检测和公共检测期间,PLHIV 比 PWoH 更有可能住院(adjOR 2.3,95% CI 1.1-4.2),但在公共检测之后则没有这种可能性。与接种 2 剂疫苗的公共卫生人员相比,PLHIV 感染严重 COVID-19 的几率要高出三倍(adjOR 3.2,95% CI 1.3-6.9),但接种≥3 剂疫苗时则不会出现这种情况(adjOR 0.7,95% CI 0.2-1.6)。在未接种疫苗的艾滋病毒感染者中,流动人口和低基底CD4+ T细胞与较高的住院几率有关:这项全国性研究包括了大部分治疗良好的艾滋病毒感染者,它强调了在艾滋病毒感染者中接种加强剂量疫苗以有效预防严重 COVID-19 的重要性。关键点:在调整了包括合并症和社会经济状况在内的已知风险因素后,无论 SARS-CoV-2 疫苗接种情况如何(0-1 剂、2 剂、≥3 剂),艾滋病毒感染者与非艾滋病毒感染者相比,COVID-19 住院几率并不高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of COVID-19 hospitalisation by HIV-status and SARS-CoV-2 vaccination status during pre- and post-Omicron era in a national register-based cohort study in Sweden.

Background: Data on the outcomes of COVID-19 in people living with HIV (PLHIV), specifically in relation to vaccination status, are lacking during the Omicron era.

Methods: This nationwide registry-based study included all resident in Sweden ≥18 years with a positive SARS-CoV-2 PCR test during January 2021-February 2023. We estimated adjusted odds ratios (adjOR) for COVID-19 hospitalisation and severe COVID-19 (ICU admission and 90-day mortality), categorised by SARS-CoV-2 vaccination status (0-1, 2, and ≥3 doses), and HIV-status. Analyses were then categorised by time periods of pre-Omicron, Omicron during public testing, and Omicron after public testing.

Results: 1348 PLHIV and 1 669 389 people without HIV (PWoH) were included. PLHIV were older, more migrant (65 vs. 22%) and male (59 vs. 46%). Of PLHIV, 96% were on antiretroviral treatment and 94% virally suppressed. AdjORs of COVID-19 hospitalisation were similar irrespective of HIV-status, controlled for demographics, calendar month of infection, comorbidities, and income. PLHIV were more likely to be hospitalised than PWoH during Omicron and public testing (adjOR 2.3, 95% CI 1.1-4.2), but not after public testing. The odds of severe COVID-19 were three times higher in PLHIV compared to PWoH vaccinated with 2 doses (adjOR 3.2, 95% CI 1.3-6.9), but not when vaccinated with ≥3 doses (adjOR 0.7, 95% CI 0.2-1.6). Migrant and low nadir CD4+ T-cells were associated with higher odds of hospitalisation in unvaccinated PLHIV.

Conclusions: This nationwide study, including mostly well-treated PLHIV, highlights the importance of vaccination with booster dose/s for effective protection against severe COVID-19 in PLHIV.KEY POINTPeople living with HIV compared to people without HIV did not have higher odds of COVID-19 hospitalisation irrespective of SARS-CoV-2 vaccination status (0-1 dose, 2 doses, ≥3 doses) when adjusting for known risk factors including comorbidities and socioeconomic status.

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