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Opportunities for improving the efficiency of paediatric HIV treatment programmes.
Revill, Paul A; Walker, Simon; Mabugu, Travor; Nathoo, Kusum J; Mugyenyi, Peter; Kekitinwa, Adeodata; Munderi, Paula; Bwakura-Dangarembizi, Mutsawashe; Musiime, Victor; Bakeera-Kitaka, Sabrina; Nahirya-Ntege, Patricia; Walker, A Sarah; Sculpher, Mark J; Gibb, Diana M.
Afiliação
  • Revill PA; aCentre for Health Economics, University of York, York, UK bClinical Research Centre, University of Zimbabwe cUniversity of Zimbabwe, College of Health Sciences, Harare, Zimbabwe dJoint Clinical Research Centre, Kampala ePaediatric Infectious Diseases Clinic/Baylor - Uganda, Mulago Hospital, Mulago fMedical Research Council/Uganda Research Unit on AIDS, Uganda Virus Research Institute, Entebbe, Uganda gMedical Research Council (MRC) Clinical Trials Unit at University College London, London, UK.
AIDS ; 29(2): 201-10, 2015 Jan 14.
Article em En | MEDLINE | ID: mdl-25396263
ABSTRACT

OBJECTIVES:

To conduct two economic analyses addressing whether to routinely monitor HIV-infected children on antiretroviral therapy (ART) clinically or with laboratory tests; continue or stop cotrimoxazole prophylaxis when children become stabilized on ART. DESIGN AND

METHODS:

The ARROW randomized trial investigated alternative strategies to deliver paediatric ART and cotrimoxazole prophylaxis in 1206 Ugandan/Zimbabwean children. Incremental cost-effectiveness and value of implementation analyses were undertaken. Scenario analyses investigated whether laboratory monitoring (CD4 tests for efficacy monitoring; haematology/biochemistry for toxicity) could be tailored and targeted to be delivered cost-effectively. Cotrimoxazole use was examined in malaria-endemic and non-endemic settings.

RESULTS:

Using all trial data, clinical monitoring delivered similar health outcomes to routine laboratory monitoring, but at a reduced cost, so was cost-effective. Continuing cotrimoxazole improved health outcomes at reduced costs. Restricting routine CD4 monitoring to after 52 weeks following ART initiation and removing toxicity testing was associated with an incremental cost-effectiveness ratio of $6084 per quality-adjusted life-year (QALY) across all age groups, but was much lower for older children (12+ years at initiation; incremental cost-effectiveness ratio = $769/QALY). Committing resources to improve cotrimoxazole implementation appears cost-effective. A healthcare system that could pay $600/QALY should be willing to spend up to $12.0 per patient-year to ensure continued provision of cotrimoxazole.

CONCLUSION:

Clinically driven monitoring of ART is cost-effective in most circumstances. Routine laboratory monitoring is generally not cost-effective at current prices, except possibly CD4 testing amongst adolescents initiating ART. Committing resources to ensure continued provision of cotrimoxazole in health facilities is more likely to represent an efficient use of resources.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Infecções por HIV / Combinação Trimetoprima e Sulfametoxazol / Custos de Cuidados de Saúde Tipo de estudo: Clinical_trials Aspecto: Implementation_research / Patient_preference Limite: Child / Child, preschool / Female / Humans / Male País/Região como assunto: Africa Idioma: En Revista: AIDS Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 / 3_ND Base de dados: MEDLINE Assunto principal: Infecções por HIV / Combinação Trimetoprima e Sulfametoxazol / Custos de Cuidados de Saúde Tipo de estudo: Clinical_trials Aspecto: Implementation_research / Patient_preference Limite: Child / Child, preschool / Female / Humans / Male País/Região como assunto: Africa Idioma: En Revista: AIDS Ano de publicação: 2015 Tipo de documento: Article