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A meta-analysis comparing 48-week treatment outcomes of single and multi-tablet antiretroviral regimens for the treatment of people living with HIV.
Clay, Patrick G; Yuet, Wei C; Moecklinghoff, Christiane H; Duchesne, Inge; Tronczynski, Krzysztof L; Shah, Sandip; Shao, Dong.
Afiliação
  • Clay PG; University of North Texas System College of Pharmacy, 3500 Camp Bowie Blvd, Fort Worth, TX, 76107, USA. Patrick.Clay@unthsc.edu.
  • Yuet WC; University of North Texas System College of Pharmacy, 3500 Camp Bowie Blvd, Fort Worth, TX, 76107, USA.
  • Moecklinghoff CH; Jannsen-Cilag GmbH, Johnson & Johnson Platz 1, 41470, Neuss, Germany.
  • Duchesne I; Janssen EMEA, Turnhoutseweg 30, 2340, Beerse, Belgium.
  • Tronczynski KL; Janssen-Cilag Polska Sp. Z o.o, Ilzecka 24, 02-135, Warsaw, Poland.
  • Shah S; Market Access Solutions, LLC, 575 NJ-28, Raritan, NJ, 08869, USA.
  • Shao D; Market Access Solutions, LLC, 575 NJ-28, Raritan, NJ, 08869, USA.
AIDS Res Ther ; 15(1): 17, 2018 10 30.
Article em En | MEDLINE | ID: mdl-30373620
ABSTRACT

OBJECTIVES:

To compare outcomes with single tablet regimens (STR) versus multi-tablet regimens (MTR) for human immunodeficiency virus (HIV) treatment using published data.

DESIGN:

Systematic review and random-effects meta-analysis of literature on approved and investigational HIV regimens.

METHODS:

The research followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Single or un-blinded studies reporting a direct comparison between STR and MTR were eligible for the meta-analysis. Double-blinded studies were excluded due to lack of difference in pill burden between cohorts. The key outcomes of interest included adherence rates/proportion meeting target, efficacy, safety/tolerability, non-clinical and economic outcomes.

RESULTS:

After screening 63 full-text articles and posters, 14 studies were eligible for the meta-analysis. The analysis showed that patients taking STR had improved outcomes over those taking MTR. Patients were significantly more adherent regardless of daily dosing frequency (odds ratio [OR] 1.96, p < 0.001) and were more likely to achieve virological suppression (relative risk [RR] 1.05, p = 0.002). There was a trend toward a lower discontinuation risk in the STR cohort, together with reported higher therapy satisfaction, better symptom control, improved health status, reduced healthcare resource utilization and demonstrated cost-effectiveness compared to MTR. There were no differences in CD4 cell count increase (at 48 weeks) or safety outcomes.

CONCLUSIONS:

The findings of this study confirm previously reported preliminary findings of the advantages of STR over MTR for HIV treatment in adherence, therapy continuation, viral suppression, tolerability, quality of life improvement, cost-effectiveness and healthcare resource utilization.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Fármacos Anti-HIV Tipo de estudo: Etiology_studies / Guideline / Systematic_reviews Limite: Humans Idioma: En Revista: AIDS Res Ther Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Fármacos Anti-HIV Tipo de estudo: Etiology_studies / Guideline / Systematic_reviews Limite: Humans Idioma: En Revista: AIDS Res Ther Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos