Critical Care Department, Hospital de Clínicas de Porto Alegre, Universidade La Salle, Porto Alegre, Brazil.
Critical Care Department, Hospital Nossa Senhora da Conceição, Porto Alegre, Porto Alegre, Brazil.
PLoS One. 2020 Sep 21;15(9):e0239452. doi: 10.1371/journal.pone.0239452. eCollection 2020.
Highly active antiretroviral therapy (HAART) has reduced HIV-related morbidity and mortality at all stages of infection and reduced transmission of HIV. Currently, the immediate start of HAART is recommended for all HIV patients, regardless of the CD4 count. There are several concerns, however, about starting treatment in critically ill patients. Unpredictable absorption of medication by the gastrointestinal tract, drug toxicity, drug interactions, limited reserve to tolerate the dysfunction of other organs resulting from hypersensitivity to drugs or immune reconstitution syndrome, and the possibility that subtherapeutic levels of drug may lead to viral resistance are the main concerns. The objective of our study was to compare the early onset (up to 5 days) with late onset (after discharge from the ICU) of HAART in HIV-infected patients admitted to the ICU.
This was a randomized, open-label clinical trial enrolling HIV-infected patients admitted to the ICU of a public hospital in southern Brazil. Patients randomized to the intervention group had to start treatment with HAART within 5 days of ICU admission. For patients in the control group, treatment should begin after discharge from the ICU. The patients were followed up to determine mortality in the ICU, in the hospital and at 6 months. The primary outcome was hospital mortality. The secondary outcome was mortality at 6 months.
The calculated sample size was 344 patients. Unfortunately, we decided to discontinue the study due to a progressively slower recruitment rate. A total of 115 patients were randomized. The majority of admissions were for AIDS-defining illnesses and low CD4. The main cause of admission was respiratory failure. Regarding the early and late study groups, there was no difference in hospital (66.7% and 63.8%, p = 0.75) or 6-month (68.4% and 79.2%, p = 0.20) mortality. After multivariate analysis, the only independent predictors of in-hospital mortality were shock and dialysis during the ICU stay. For the mortality outcome at 6 months, the independent variables were shock and dialysis during the ICU stay and tuberculosis at ICU admission.
Although the early termination of the study precludes definitive conclusions being made, early HAART administration for HIV-infected patients admitted to the ICU compared to late administration did not show benefit in hospital mortality or 6-month mortality. ClinicalTrials.gov, NCT01455688. Registered 20 October 2011, https://clinicaltrials.gov/show/NCT01455688.
高效抗逆转录病毒疗法(HAART)降低了所有感染阶段的 HIV 相关发病率和死亡率,并降低了 HIV 的传播。目前,建议所有 HIV 患者立即开始 HAART,无论 CD4 计数如何。然而,对于危重症患者开始治疗存在一些担忧。胃肠道吸收药物的情况不可预测、药物毒性、药物相互作用、对药物过敏或免疫重建综合征引起的其他器官功能障碍的耐受性有限,以及药物可能未达到治疗水平导致病毒耐药性的可能性是主要关注点。我们的研究目的是比较 ICU 收治的 HIV 感染患者早期(5 天内)和晚期(ICU 出院后)开始 HAART 的效果。
这是一项在巴西南部一家公立医院 ICU 收治的 HIV 感染患者中进行的随机、开放标签临床试验。随机分配到干预组的患者必须在 ICU 入院后 5 天内开始 HAART 治疗。对于对照组患者,治疗应在 ICU 出院后开始。患者接受随访,以确定 ICU 内、医院内和 6 个月时的死亡率。主要结局是 ICU 内死亡率。次要结局是 6 个月时的死亡率。
计算的样本量为 344 例患者。不幸的是,由于招募率逐渐下降,我们决定停止研究。共随机分配了 115 例患者。大多数入院是为了治疗 AIDS 定义的疾病和低 CD4。主要入院原因是呼吸衰竭。关于早期和晚期研究组,医院内死亡率无差异(66.7%和 63.8%,p=0.75)或 6 个月死亡率(68.4%和 79.2%,p=0.20)。多变量分析后,ICU 期间休克和透析是 ICU 内死亡率的唯一独立预测因素。对于 6 个月时的死亡率,独立变量是 ICU 期间休克和透析以及 ICU 入院时结核病。
尽管研究提前终止,无法得出明确结论,但与晚期开始相比,早期开始对 ICU 收治的 HIV 感染患者进行 HAART 治疗并未降低医院内死亡率或 6 个月死亡率。ClinicalTrials.gov,NCT01455688。2011 年 10 月 20 日注册,https://clinicaltrials.gov/show/NCT01455688。