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Hydroxychloroquine with azithromycin in patients hospitalized for mild and moderate COVID-19
Lamback, Elisa Baranski; Oliveira, Monica Amorim de; Haddad, Andrea Ferreira; Vieira, André Filipe Marcondes; Ferreira Neto, Armando Leão; Maia, Taciana da Silva; Chrisman, Juliana de Rezende; Spineti, Pedro Pimenta de Mello; Mattos, Marco Antonio de; Costa, Eduardo.
  • Lamback, Elisa Baranski; Hospital Unimed Rio. Rio de Janeiro. BR
  • Oliveira, Monica Amorim de; Hospital Unimed Rio. Rio de Janeiro. BR
  • Haddad, Andrea Ferreira; Hospital Unimed Rio. Rio de Janeiro. BR
  • Vieira, André Filipe Marcondes; Hospital Unimed Rio. Rio de Janeiro. BR
  • Ferreira Neto, Armando Leão; Hospital Unimed Rio. Rio de Janeiro. BR
  • Maia, Taciana da Silva; Universidade do Estado do Rio de Janeiro. Rio de Janeiro. BR
  • Chrisman, Juliana de Rezende; Instituto Unimed-Rio. Rio de Janeiro. BR
  • Spineti, Pedro Pimenta de Mello; Hospital Unimed Rio. Rio de Janeiro. BR
  • Mattos, Marco Antonio de; Hospital Unimed Rio. Rio de Janeiro. BR
  • Costa, Eduardo; Universidade do Estado do Rio de Janeiro. Rio de Janeiro. BR
Braz. j. infect. dis ; 25(2): 101549, 2021. tab
Article Dans Anglais | LILACS | ID: biblio-1278580
ABSTRACT
ABSTRACT

Objectives:

To assess the efficacy of hydroxychloroquine in combination with azithromycin in terms of clinical and biochemical outcomes in adult patients with COVID-19 hospitalized for acute respiratory distress syndrome (ARDS), and to describe the occurrence of adverse events.

Method:

Retrospective comparative study, based in a quaternary private hospital in Rio de Janeiro, Brazil, involving 193 adult patients hospitalized for mild and moderate COVID-19 related ARSD, analyzing treatment efficacy based on clinical and biochemical outcomes.

Results:

The active group comprised 101 (52.3%) patients using hydroxychloroquine associated with azithromycin and the control group 92 (47.7%) patients who did not take these medications. Median age was 59 (47-70) in the active group and 65 (47−77) in the control group (p < 0.05). Patients in the control group had greater extent of pulmonary involvement on baseline chest CT scans (p < 0.05). All other baseline variables (BMI, comorbidities, previous use of medications and biochemical assessments) were similar between groups. In the medication group, 25% (25 out of 101) were admitted to the ICU, compared to 21% (19 out of 92) in the control group (p > 0.05). No difference in mortality, duration of non-invasive oxygen use or duration of hospitalization was seen between groups. The therapeutic regimen was well tolerated, with only eight (7.9%) patients presenting gastrointestinal symptoms and eight (7.9%) patients withdrawn treatment due to QTc prolongation.

Conclusions:

Patients treated with hydroxychloroquine combined with azithromycin and the control group had similar clinical outcomes. This therapeutic regimen was considered ineffective in hospitalized patients with mild to moderate COVID-19 related ARDS and was associated with few non-severe adverse events.
Sujets)


Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: COVID-19 / Hydroxychloroquine Type d'étude: Étude observationnelle / Facteurs de risque Limites du sujet: Adulte / Humains Pays comme sujet: Amérique du Sud / Brésil langue: Anglais Texte intégral: Braz. j. infect. dis Thème du journal: Maladies transmissibles Année: 2021 Type: Article Pays d'affiliation: Brésil Institution/Pays d'affiliation: Hospital Unimed Rio/BR / Instituto Unimed-Rio/BR / Universidade do Estado do Rio de Janeiro/BR

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: COVID-19 / Hydroxychloroquine Type d'étude: Étude observationnelle / Facteurs de risque Limites du sujet: Adulte / Humains Pays comme sujet: Amérique du Sud / Brésil langue: Anglais Texte intégral: Braz. j. infect. dis Thème du journal: Maladies transmissibles Année: 2021 Type: Article Pays d'affiliation: Brésil Institution/Pays d'affiliation: Hospital Unimed Rio/BR / Instituto Unimed-Rio/BR / Universidade do Estado do Rio de Janeiro/BR