Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial

Bibliographic Details
Main Author: Boniatti, Márcio Manozzo
Publication Date: 2020
Other Authors: Pellegrini, José Augusto Santos, Marques, Leonardo da Silva, John, Josiane França, Marin, Luiz Gustavo, Maito, Lina Rosa Dal Moro, Lisboa, Thiago Costa, Damiani, Lucas Petri, Falci, Diego Rodrigues
Format: Article
Language: eng
Source: Repositório Institucional da UFRGS
Download full: http://hdl.handle.net/10183/255553
Summary: Background: 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. Methods: 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. Results: 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. Conclusions: 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.
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spelling Boniatti, Márcio ManozzoPellegrini, José Augusto SantosMarques, Leonardo da SilvaJohn, Josiane FrançaMarin, Luiz GustavoMaito, Lina Rosa Dal MoroLisboa, Thiago CostaDamiani, Lucas PetriFalci, Diego Rodrigues2023-03-10T03:26:58Z20201932-6203http://hdl.handle.net/10183/255553001160451Background: 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. Methods: 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. Results: 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. Conclusions: 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.application/pdfengPloS one. San Francisco, CA. Vol. 15, no. 9 (Sept. 2020), e0239452, 11 p.HIVTerapia antirretroviral de alta atividadeIntervenção médica precoceEarly antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trialEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001160451.pdf.txt001160451.pdf.txtExtracted Texttext/plain40303http://www.lume.ufrgs.br/bitstream/10183/255553/2/001160451.pdf.txt9c6467ff7815aa855e4483889697e738MD52ORIGINAL001160451.pdfTexto completo (inglês)application/pdf1030040http://www.lume.ufrgs.br/bitstream/10183/255553/1/001160451.pdf12f182cd0bc48bf79ec1f94ad11b0fd5MD5110183/2555532023-09-24 03:40:05.227352oai:www.lume.ufrgs.br:10183/255553Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-09-24T06:40:05Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
title Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
spellingShingle Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
Boniatti, Márcio Manozzo
HIV
Terapia antirretroviral de alta atividade
Intervenção médica precoce
title_short Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
title_full Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
title_fullStr Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
title_full_unstemmed Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
title_sort Early antiretroviral therapy for HIV-infected patients admitted to an intensive care unit (EARTH-ICU) : a randomized clinical trial
author Boniatti, Márcio Manozzo
author_facet Boniatti, Márcio Manozzo
Pellegrini, José Augusto Santos
Marques, Leonardo da Silva
John, Josiane França
Marin, Luiz Gustavo
Maito, Lina Rosa Dal Moro
Lisboa, Thiago Costa
Damiani, Lucas Petri
Falci, Diego Rodrigues
author_role author
author2 Pellegrini, José Augusto Santos
Marques, Leonardo da Silva
John, Josiane França
Marin, Luiz Gustavo
Maito, Lina Rosa Dal Moro
Lisboa, Thiago Costa
Damiani, Lucas Petri
Falci, Diego Rodrigues
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Boniatti, Márcio Manozzo
Pellegrini, José Augusto Santos
Marques, Leonardo da Silva
John, Josiane França
Marin, Luiz Gustavo
Maito, Lina Rosa Dal Moro
Lisboa, Thiago Costa
Damiani, Lucas Petri
Falci, Diego Rodrigues
dc.subject.por.fl_str_mv HIV
Terapia antirretroviral de alta atividade
Intervenção médica precoce
topic HIV
Terapia antirretroviral de alta atividade
Intervenção médica precoce
description Background: 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. Methods: 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. Results: 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. Conclusions: 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.
publishDate 2020
dc.date.issued.fl_str_mv 2020
dc.date.accessioned.fl_str_mv 2023-03-10T03:26:58Z
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dc.relation.ispartof.pt_BR.fl_str_mv PloS one. San Francisco, CA. Vol. 15, no. 9 (Sept. 2020), e0239452, 11 p.
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