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1.
AMIA Annu Symp Proc ; 2018: 932-941, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30815136

RESUMO

With an increasingly elderly population, families are finding it increasingly challenging to coordinate care for their older family members. This paper reports on the findings of InfoSAGE, an online private social network that has tools for communication and care coordination for elders and their families. The InfoSAGE system has 257 registered users; 52 of these opted into an in-depth longitudinal study. A descriptive analysis of these early participants, the online family networks, and barriers to participation that were encountered are presented.


Assuntos
Cuidadores , Família , Redes Sociais Online , Apoio Social , Interface Usuário-Computador , Idoso , Idoso de 80 Anos ou mais , Comunicação , Feminino , Humanos , Internet/estatística & dados numéricos , Estudos Longitudinais , Masculino , Massachusetts
2.
J Am Heart Assoc ; 6(9)2017 Sep 22.
Artigo em Inglês | MEDLINE | ID: mdl-28939708

RESUMO

BACKGROUND: Implantable cardioverter-defibrillators (ICDs) are commonly implanted in older patients, including those with multiple comorbidities. There are few prospective studies assessing the clinical course and end-of-life circumstances for these patients. METHODS AND RESULTS: We prospectively followed 51 patients with ICDs for up to 18 months to longitudinally assess in terms of (1) advance care planning, (2) health status, (3) healthcare utilization, and (4) end-of-life circumstances through quarterly phone interviews and electronic medical record review. The mean age was 71.1±8.3, 74.5% were men, and 19.6% were non-white. Congestive heart failure was predominant (82.4%), as was chronic kidney disease (92%). At baseline, a total of 12% of subjects met criteria for major depression, and 78.4% met criteria for mild cognitive impairment. From this initial study cohort, 76% survived to 18 months and completed all follow-up interviews, 18% died, and 19% withdrew or were lost to follow-up. Though living will completion and healthcare proxy assignment were common (cumulative outcome at 18 months 88% and 98%, respectively), discussions of prognosis were uncommon (baseline, 9.8%; by 18 months, 22.7%), as were conversations regarding ICD deactivation (baseline, 15.7%; by 18 months, 25.5%). Five decedents with available data received shocks in the days immediately prior to death, including 3 of whom ultimately had their ICDs deactivated prior to death. CONCLUSIONS: We demonstrated the feasibility of prospective enrollment and follow-up of older, vulnerable ICD patients. Early findings suggest a high burden of cognitive and psychological impairment, poor communication with providers, and frequent shocks at the end of life. These findings will inform the design of a larger cohort study designed to further explore the experiences of living and dying with an ICD in this important patient population.


Assuntos
Tomada de Decisão Clínica , Desfibriladores Implantáveis , Cardioversão Elétrica/instrumentação , Insuficiência Cardíaca/terapia , Planejamento de Assistência ao Paciente , Pessoalidade , Assistência Terminal , Idoso , Boston/epidemiologia , Cognição , Comorbidade , Cardioversão Elétrica/efeitos adversos , Cardioversão Elétrica/mortalidade , Registros Eletrônicos de Saúde , Estudos de Viabilidade , Feminino , Avaliação Geriátrica , Pesquisa sobre Serviços de Saúde , Nível de Saúde , Insuficiência Cardíaca/mortalidade , Insuficiência Cardíaca/fisiopatologia , Insuficiência Cardíaca/psicologia , Humanos , Entrevistas como Assunto , Estudos Longitudinais , Masculino , Saúde Mental , Pessoa de Meia-Idade , Projetos Piloto , Estudos Prospectivos , Qualidade de Vida , Direito a Morrer , Fatores de Risco , Telefone , Fatores de Tempo , Resultado do Tratamento
3.
Stud Health Technol Inform ; 234: 280-285, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28186055

RESUMO

Aging creates new information and communication needs for families who are helping to coordinate care for frail parents. To identify how information and communication needs evolve with the aging process, we created a living laboratory of families, supported by an online private social network with tools for care coordination. Site registrants are invite to participate in a more in-depth survey-based longitudinal study. In year one, we assessed the feasibility of an online living laboratory. During this first year, 155 individuals registered on InfoSAGE, and 26% opted into the more in-depth longitudinal study. The survey response rate for those in the study was 61%. We present here a descriptive analysis of our early participants and networks, as well as barriers to participation that the study team encountered.


Assuntos
Comunicação , Atenção à Saúde , Internet , Idoso , Humanos , Estudos Longitudinais , Pais , Inquéritos e Questionários
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