RESUMO
AIM: To evaluate the prevalence of organ system disorders and describe healthcare utilization among adults with spina bifida at a regional clinic. METHOD: This study was a structured chart review using the Rochester Health Status Survey-IV. 65 males, 57 females aged 16 to 59 years were seen at the Spina Bifida Center of Central New York between January 2007 and December 2008 (annual hospitalization rate was 15 out of 100). RESULTS: Hospitalizations and acute outpatient visits were associated with having shunted hydrocephalus, whereas visits to the emergency department were associated with having a decubitus ulcer. Logistic regression models revealed that older adults made proportionately fewer visits to primary care providers than younger adults (odds ratio 0.919; p=0.02). Yet for every 1-year increase in age, the odds of being hospitalized increased by 5% (odds ratio 1.051; p=0.03). INTERPRETATION: Adults with spina bifida have multiple organ-system disorders. They have greater difficulty accessing services, and utilize emergency and inpatient healthcare at higher rates than the general population. In the future, adults with spina bifida will require access to more medical care and preventive services if they are to have optimal health, well-being, and functioning.
Assuntos
Atenção à Saúde/estatística & dados numéricos , Nível de Saúde , Disrafismo Espinal/fisiopatologia , Disrafismo Espinal/terapia , Adolescente , Adulto , Derivações do Líquido Cefalorraquidiano/métodos , Transtornos Cognitivos/etiologia , Atenção à Saúde/métodos , Feminino , Inquéritos Epidemiológicos , Hospitalização , Humanos , Hidrocefalia/etiologia , Hidrocefalia/cirurgia , Masculino , Pessoa de Meia-Idade , Prevalência , Fatores Sexuais , Disrafismo Espinal/epidemiologia , Adulto JovemRESUMO
The number of older adults with intellectual and developmental disabilities (IDD) has increased rapidly in the United States as part of the general "graying"of the country. This has presented challenges in maintaining the quality of life and health for these individuals in later years. Issues including diagnostic overshadowing (the tendency to overlook symptoms of mental or physical illness as causes for decline), lack of knowledge about aging in adults with IDD, and health care disparities are discussed in this article along with recommendations for clinicians to help them meet this growing challenge.
Assuntos
Envelhecimento/psicologia , Deficiências do Desenvolvimento/enfermagem , Deficiência Intelectual/enfermagem , Barreiras de Comunicação , Comorbidade , Comportamento Cooperativo , Estudos Transversais , Atenção à Saúde , Deficiências do Desenvolvimento/epidemiologia , Deficiências do Desenvolvimento/psicologia , Erros de Diagnóstico , Feminino , Disparidades em Assistência à Saúde/estatística & dados numéricos , Humanos , Hiperopia/enfermagem , Hiperopia/psicologia , Deficiência Intelectual/epidemiologia , Deficiência Intelectual/psicologia , Comunicação Interdisciplinar , Pessoa de Meia-Idade , Diagnóstico de Enfermagem , Defesa do Paciente , Dinâmica Populacional , Qualidade de Vida/psicologia , Encaminhamento e ConsultaRESUMO
Similar to the general population, adults with intellectual and developmental disabilities (IDD) are living into their 70s and beyond. Health care disparities have been well-documented for this vulnerable and underserved population. Social workers are often responsible for assessment, coordination of care, and negotiation of needed services for people with IDD. This article explores the challenges facing social workers in meeting the growing health and social needs of aging adults with IDD and their families. Trends in social work practice and gaps in education are discussed as they relate to addressing and reducing current health disparities.
Assuntos
Deficiências do Desenvolvimento , Disparidades nos Níveis de Saúde , Deficiência Intelectual , Serviço Social , Idoso , Continuidade da Assistência ao Paciente , Necessidades e Demandas de Serviços de Saúde , Humanos , Pessoa de Meia-Idade , Serviço Social/educação , Serviço Social/métodos , Serviço Social/organização & administração , Estados UnidosRESUMO
BACKGROUND: Health literacy is an important predictor of healthcare outcomes, but research on this topic has largely been absent from the emergency medicine literature. OBJECTIVE: We measured the prevalence of health literacy in parents or guardians of pediatric patients seen in the emergency department (ED). METHODS: This was an observational study conducted in a Midwestern urban, university-based, tertiary, Level 1 trauma center ED with 33,000 visits/year. Using convenience sampling during a three-month period, English-speaking parents or guardians of pediatric patients (< 19 yrs.) were asked to complete the short version of the Test of Functional Health Literacy for Adults (s-TOFHLA). Parents/guardians were excluded if they had uncorrected visual impairment, required an interpreter, had altered mental status, or if the patients they accompanied were the subjects of a medical or trauma activation. RESULTS: Of the 188 parents or guardians approached, six did not consent or withdrew, one was excluded, leaving 181 (96.3%) in the study. Of these, 19 (10.5%) had either "marginal" or "inadequate" health literacy, while 162 (89.5%, 95% CI: 84.1%, 93.6%) had "adequate" health literacy. CONCLUSION: A large majority (89.5%) of English-speaking parents or guardians of pediatric patients evaluated in the ED have adequate health literacy. This data may prompt ED professionals to adjust their communication styles in the evaluation of children. Future multi-center studies are needed to confirm the findings in this pilot study.