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1.
BMC Public Health ; 20(1): 724, 2020 May 19.
Artigo em Inglês | MEDLINE | ID: mdl-32429879

RESUMO

BACKGROUND: Globally only 79% of adults living with HIV (human immunodeficiency virus) know their status and men in sub-Saharan Africa are considered a particularly hard-to-reach population for HIV testing. Home-based HIV couple testing during the antenatal period is a safe and effective method that has been used to test male partners of pregnant women. The goal of this qualitative study was to identify elements that made couple testing successful and describe important characteristics of this home-based intervention from couples' perspectives. METHODS: Couples who received scheduled home-based couple testing during pregnancy in Kisumu, Kenya, were purposively sampled based on HIV status from January to May 2015. An interviewer administered all of the in-depth interviews and two coders were directly involved in the data analysis and reconciled codes several times in the process. RESULTS: Twenty-one couples were enrolled: 9 concordant HIV-negative couples, 8 HIV discordant couples, 3 HIV concordant HIV-positive couples, and 1 whose concordance status was unknown. Median age at the time of home-based couple testing was 24 and 28 years for women and men, respectively. Median relationship duration was 3 years and couples had a median of two pregnancies. The major themes that emerged were that home-based couple testing 1) removed the female burden of requesting couple testing, 2) overcame logistical barriers associated with clinic-based testing, 3) encouraged participants to overcome their fear of testing and disclosure, 4) provided privacy in the home, and 5) provided quality time with the health advisors. Importantly, some women appreciated individual testing at the clinic before couple testing and some couples preferred skilled, anonymous health advisors delivering the intervention rather than known community health workers. CONCLUSIONS: The results of this qualitative study suggest that home-based couple testing during pregnancy overcame many of the barriers that limit men's access to and uptake of clinic-based testing. It encouraged participants to overcome their fear of testing and disclosure through a setting that afforded privacy and quality time with skilled health advisors. These qualitative results may help design effective partner and couple HIV testing programs in the antenatal setting and alongside or within other assisted partner notification services. TRIAL REGISTRATION: Clinicaltrials.gov registry: NCT01784783. Registered prospectively on June 15, 2012.


Assuntos
Infecções por HIV/diagnóstico , Homens/psicologia , Gestantes/psicologia , Testes Sorológicos/psicologia , Parceiros Sexuais/psicologia , Adulto , Busca de Comunicante/métodos , Revelação , Feminino , Infecções por HIV/psicologia , Acessibilidade aos Serviços de Saúde/estatística & dados numéricos , Serviços de Assistência Domiciliar/estatística & dados numéricos , Humanos , Quênia , Masculino , Programas de Rastreamento/métodos , Programas de Rastreamento/psicologia , Testes para Triagem do Soro Materno/métodos , Testes para Triagem do Soro Materno/psicologia , Motivação , Gravidez , Pesquisa Qualitativa , Testes Sorológicos/métodos , Adulto Jovem
2.
Prenat Diagn ; 40(10): 1265-1271, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32441820

RESUMO

OBJECTIVE: Advances in prenatal genetics place additional challenges as patients must receive information about a growing array of screening and testing options. This raises concerns about how to achieve a shared decision-making process that prepares patients to make an informed decision about their choices about prenatal genetic screening and testing options, calling for a reconsideration of how healthcare providers approach the first prenatal visit. METHODS: We conducted interviews with 40 pregnant women to identify components of decision-making regarding prenatal genetic screens and tests at this visit. Analysis was approached using grounded theory. RESULTS: Participants brought distinct notions of risk to the visit, including skewed perceptions of baseline risk for a fetal genetic condition and the implications of screening and testing. Participants were very concerned about financial considerations associated with these options, ranking out-of-pocket costs on par with medical considerations. Participants noted diverging priorities at the first visit from those of their healthcare provider, leading to barriers to shared decision-making regarding screening and testing during this visit. CONCLUSION: Research is needed to determine how to restructure the initiation of prenatal care in a way that best positions patients to make informed decisions about prenatal genetic screens and tests.


Assuntos
Tomada de Decisões , Testes Genéticos , Cuidado Pré-Natal , Adulto , Atitude Frente a Saúde , Ácidos Nucleicos Livres/análise , Ácidos Nucleicos Livres/sangue , Feminino , Testes Genéticos/economia , Testes Genéticos/métodos , Testes Genéticos/normas , Humanos , Programas de Rastreamento/economia , Programas de Rastreamento/organização & administração , Programas de Rastreamento/psicologia , Programas de Rastreamento/normas , Testes para Triagem do Soro Materno/economia , Testes para Triagem do Soro Materno/psicologia , Testes para Triagem do Soro Materno/normas , Visita a Consultório Médico/economia , Participação do Paciente/psicologia , Participação do Paciente/estatística & dados numéricos , Percepção , Gravidez , Cuidado Pré-Natal/economia , Cuidado Pré-Natal/organização & administração , Cuidado Pré-Natal/psicologia , Cuidado Pré-Natal/normas , Diagnóstico Pré-Natal/economia , Diagnóstico Pré-Natal/métodos , Diagnóstico Pré-Natal/psicologia , Diagnóstico Pré-Natal/normas , Medição de Risco , Estados Unidos
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