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1.
J Clin Oncol ; 26(35): 5671-8, 2008 Dec 10.
Artigo em Inglês | MEDLINE | ID: mdl-19001333

RESUMO

PURPOSE: To compare prospectively and retrospectively defined benchmarks for the quality of end-of-life care, including a novel indicator for the use of opiate analgesia. METHODS: Linked claims and cancer registry data from 1994 to 2003 for New Jersey and Pennsylvania were used to examine prospective and retrospective benchmarks for seniors with breast, colorectal, lung, or prostate cancer who participated in state pharmaceutical benefit programs. RESULTS: Use of opiates, particularly long-acting opiates, was low in both the prospective and retrospective cohorts (9.1% and 10.1%, respectively), which supported the underuse of palliative care at the end-of-life. Although hospice was used more commonly in the retrospective versus prospective cohort, admission to hospice within 3 days of death was similar in both cohorts (28.8% v 26.4%), as was the rate of death in an acute care hospital. Retrospective and prospective measures identified similar physician and hospital patterns of end-of-life care. In multivariate models, a visit with an oncologist was positively associated with the use of chemotherapy, opiates, and hospice. Patients who were cared for by oncologists in small group practices were more likely to receive chemotherapy (retrospective only) and less likely to receive hospice (both) than those in large groups. Compared with patients who were cared for in teaching hospitals, those in other hospitals were more likely to receive chemotherapy (both) and to have toxicity (prospective) but were less likely to receive opiates (both) and hospice (retrospective). CONCLUSION: Retrospective and prospective measures, including a new measure of the use of opiate analgesia, identify some similar physician and hospital patterns of end-of-life care.


Assuntos
Analgésicos Opioides/uso terapêutico , Pesquisa sobre Serviços de Saúde , Neoplasias/terapia , Cuidados Paliativos , Padrões de Prática Médica , Indicadores de Qualidade em Assistência à Saúde , Qualidade de Vida , Idoso , Idoso de 80 Anos ou mais , Antineoplásicos/uso terapêutico , Benchmarking , Uso de Medicamentos , Feminino , Hospitais para Doentes Terminais/estatística & dados numéricos , Hospitalização/estatística & dados numéricos , Humanos , Seguro de Serviços Farmacêuticos , Masculino , Oncologia/estatística & dados numéricos , Medicare , Neoplasias/mortalidade , New Jersey , Cuidados Paliativos/estatística & dados numéricos , Pennsylvania , Padrões de Prática Médica/estatística & dados numéricos , Estudos Prospectivos , Indicadores de Qualidade em Assistência à Saúde/estatística & dados numéricos , Sistema de Registros , Estudos Retrospectivos , Resultado do Tratamento , Estados Unidos
3.
J Assoc Nurses AIDS Care ; 14(5 Suppl): 80S-86S, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-14571562

RESUMO

A large percentage of HIV-infected patients are coinfected with hepatitis C virus (HCV). Current treatment available for HCV combines interferon and ribavirin therapy for 6 months or longer. Interferon is associated with numerous neuropsychiatric side effects including depression, cognitive impairment, anxiety, and irritability. The potential for developing depression is particularly concerning with coinfection because the incidence of depression is higher in the HIV-seropositive population than in the general population. This article discusses the mechanism and prevalence of interferon-induced depression and the debate regarding appropriateness of treatment in certain segments of the HIV population. The role of antidepressants as both treatment and a prophylaxis against interferon-related depression is reviewed. Nurses have a critical role in the care of HIV/HCV coinfected patients who are undergoing treatment with interferon and ribavirin. They both assess for treatment readiness prior to initiation and provide close monitoring for the development of neuropsychiatric disturbances while on therapy.


Assuntos
Antivirais/efeitos adversos , Depressão/induzido quimicamente , Infecções por HIV/enfermagem , Hepatite C/enfermagem , Interferons/efeitos adversos , Antivirais/administração & dosagem , Infecções por HIV/complicações , Infecções por HIV/tratamento farmacológico , Hepatite C/complicações , Hepatite C/tratamento farmacológico , Humanos , Interferons/administração & dosagem , Avaliação em Enfermagem/métodos
4.
Clin Infect Dis ; 36(12): 1602-5, 2003 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-12802762

RESUMO

We screened 651 human immunodeficiency virus (HIV)-1-infected subjects for hepatitis B surface antigen (HBsAg) and antibody to hepatitis B surface antigen (anti-HBs). Of a total of 387 subjects who tested negative for both HBsAg and anti-HBs, 142 underwent further testing for isolated presence of antibody to hepatitis B core antigen (anti-HBc). Of these 142 subjects, 60 (42%) tested positive for anti-HBc (isolated anti-HBc). Individuals coinfected with HIV-1 and hepatitis C virus (HCV) were more likely to have isolated anti-HBc than were subjects with HIV-1 alone (80% vs. 16%, respectively). Our findings suggest that individuals with HIV-1/HCV coinfection for whom there is no serological evidence for hepatitis B virus when screened with HBsAg and anti-HBs will be positive for anti-HBc in >75% of cases. A screening strategy that tests only for HBsAg and anti-HBs in HIV-1-infected patients will miss a large number of individuals with isolated anti-HBc.


Assuntos
Infecções por HIV/complicações , Anticorpos Anti-Hepatite B/isolamento & purificação , Antígenos do Núcleo do Vírus da Hepatite B/isolamento & purificação , Vírus da Hepatite B/isolamento & purificação , Hepatite B/complicações , Adulto , Infecções por HIV/imunologia , HIV-1 , Hepatite B/virologia , Humanos
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