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1.
AIDS Care ; 31(sup1): 1-9, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31189333

RESUMO

Low perceived social support (SS) negatively impacts health outcomes. We developed a measure of perceived SS for use in HIV care. We sought and categorized legacy items, selecting strongest items within categories. We elicited SS concepts from patients in English/Spanish, coded transcripts to match item pool content, and developed new items for salient unrepresented content. In focus groups, patients prioritized highly-matched items. We conducted cognitive interviews on high-priority items, and validity testing on final items against two legacy measures. From interviews (n = 32), we matched the following concepts: sense of belonging/inclusion; communication; emotional support; feeling accepted by others as a person; companionship; and practical support. We identified a new concept: support from friends/family in remaining healthy. Focus groups (n = 23) prioritized emotional support, communication, and support to remain healthy. Cognitive interviews (n = 30) found items were well-understood. The final 8-item measure performed well with patients (n = 708), with good construct validity. We used an Item Response Theory program to create a 3-item Short Form version of the measure, which captures 96% of patients indicating low social support. We developed the Multifactoral Assessment of Perceived Social Support (MAPSS) and Short Form (MAPSS-SF); brief, clinically relevant, sufficiently unidimensional measures of SS for use in HIV care.


Assuntos
Infecções por HIV/psicologia , Medidas de Resultados Relatados pelo Paciente , Pacientes/psicologia , Psicometria/métodos , Qualidade de Vida/psicologia , Apoio Social , Inquéritos e Questionários/normas , Adulto , Feminino , Grupos Focais , Infecções por HIV/diagnóstico , Nível de Saúde , Humanos , Relações Interpessoais , Masculino , Pessoa de Meia-Idade , Psicometria/instrumentação
2.
J Assoc Nurses AIDS Care ; 32(1): 29-36, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-32541195

RESUMO

ABSTRACT: Although the number of older people living with HIV (PLWH) is growing, prior research has focused on older PLWH as care recipients and psychosocial factors (e.g., stigma, social support) associated with their HIV care. Literature on HIV caregiving mainly focuses on family members providing care to PLWH or children of parents with HIV. There is a gap in the literature in terms of older PLWH's roles as caregivers to their family members. Thanks to combination antiretrovirals that help PLWH live longer and have healthier lives, many older PLWH now find themselves in a position to provide care to family members. To help older PLWH age successfully, it is important to understand their role as caregivers while they juggle responsibilities with their own health care needs. This article elucidates this gap in the literature on older PLWH who are caregivers and provides direction for a research agenda and potential clinical implications.


Assuntos
Envelhecimento , Fármacos Anti-HIV/uso terapêutico , Terapia Antirretroviral de Alta Atividade , Cuidadores/psicologia , Família/psicologia , Infecções por HIV/tratamento farmacológico , Adulto , Idoso , Idoso de 80 Anos ou mais , Infecções por HIV/psicologia , Humanos , Pessoa de Meia-Idade , Estigma Social , Apoio Social , Fatores Socioeconômicos
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