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Efficacy of early treatment with hydroxychloroquine in people with mild to moderate COVID-19: a systematic review and meta-analysis.
Hernandez, Adrian V; Ingemi, John; Sherman, Michael; Pasupuleti, Vinay; Barboza, Joshuan J; Piscoya, Alejandro; Roman, Yuani M; White, C Michael.
  • Hernandez AV; Department of Pharmacy Practice, University of Connecticut School of Pharmacy, Storrs, CT, USA.
  • Ingemi J; Unidad de Revisiones Sistemáticas y Meta-análisis (URSIGET), Vicerrectorado de Investigación, Universidad San Ignacio de Loyola (USIL), Lima, Peru.
  • Sherman M; Department of Pharmacy Practice, University of Connecticut School of Pharmacy, Storrs, CT, USA.
  • Pasupuleti V; Department of Pharmacy Practice, University of Connecticut School of Pharmacy, Storrs, CT, USA.
  • Barboza JJ; Department of Research, Cello Health, Yardley, PA, USA.
  • Piscoya A; Unidad de Revisiones Sistemáticas y Meta-análisis (URSIGET), Vicerrectorado de Investigación, Universidad San Ignacio de Loyola (USIL), Lima, Peru.
  • Roman YM; Unidad de Revisiones Sistemáticas y Meta-análisis (URSIGET), Vicerrectorado de Investigación, Universidad San Ignacio de Loyola (USIL), Lima, Peru.
  • White CM; Department of Pharmacy Practice, University of Connecticut School of Pharmacy, Storrs, CT, USA.
Arch Med Sci ; 18(4): 939-948, 2022.
Article in English | MEDLINE | ID: covidwho-1911939
ABSTRACT

Introduction:

No early treatment intervention for COVID-19 has proven effective to date. We systematically reviewed the efficacy of hydroxychloroquine as early treatment for COVID-19. Material and

methods:

Randomized controlled trials (RCTs) evaluating hydroxychloroquine for early treatment of COVID-19 were searched in five engines and preprint websites until September 14, 2021. Primary outcomes were hospitalization and all-cause mortality. Secondary outcomes included COVID-19 symptom resolution, viral clearance, and adverse events. Inverse variance random-effects meta-analyses were performed and quality of evidence (QoE) per outcome was assessed with GRADE methods.

Results:

Five RCTs (n = 1848) were included. The comparator was placebo in four RCTs and usual care in one RCT. The RCTs used hydroxychloroquine total doses between 1,600 and 4,400 mg and had follow-up times between 14 and 90 days. Compared to the controls, early treatment with hydroxychloroquine did not reduce hospitalizations (RR = 0.80, 95% CI 0.47-1.36, I 2 = 2%, 5 RCTs, low QoE), all-cause mortality (RR = 0.77, 95% CI 0.16-3.68, I 2 = 0%, 5 RCTs, very low QoE), symptom resolution (RR = 0.94, 95% CI 0.77-1.16, I 2 = 71%, 3 RCTs, low QoE) or viral clearance at 14 days (RR = 1.02, 95% CI 0.82-1.27, I 2 = 65%, 2 RCTs, low QoE). There was a larger non-significant increase of adverse events with hydroxychloroquine vs. controls (RR = 2.17, 95% CI 0.86-5.45, I 2 = 92%, 5 RCTs, very low QoE).

Conclusions:

Hydroxychloroquine was not efficacious as early treatment for COVID-19 infections in RCTs with low to very low quality of evidence for all outcomes. More RCTs are needed to elucidate the efficacy of hydroxychloroquine as early treatment intervention.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Language: English Journal: Arch Med Sci Year: 2022 Document Type: Article Affiliation country: Aoms

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Prognostic study / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Language: English Journal: Arch Med Sci Year: 2022 Document Type: Article Affiliation country: Aoms