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2.
Ann Allergy Asthma Immunol ; 115(1): 10-6.e1, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26123420

RESUMO

BACKGROUND: Despite the significant burden of childhood asthma, little is known about prevention-oriented management before and after hospitalizations for asthma exacerbation. OBJECTIVE: To investigate the proportion and characteristics of children admitted to the intensive care unit (ICU) for asthma exacerbation and the frequency of guideline-recommended outpatient management before and after the hospitalization. METHODS: A 14-center medical record review study of children aged 2 to 17 years hospitalized for asthma exacerbation during 2012-2013. Primary outcome was admission to the ICU; secondary outcomes were 2 preventive factors: inhaled corticosteroid (ICS) use and evaluation by asthma specialists in the pre- and posthospitalization periods. RESULTS: Among 385 children hospitalized for asthma, 130 (34%) were admitted to the ICU. Risk factors for ICU admission were female sex, having public insurance, a marker of chronic asthma severity (ICS use), and no prior evaluation by an asthma specialist. Among children with ICU admission, guideline-recommended outpatient management was suboptimal (eg, 65% were taking ICSs at the time of index hospitalization, and 19% had evidence of a prior evaluation by specialist). At hospital discharge, among children with ICU admission who had not previously used controller medications, 85% were prescribed ICSs. Furthermore, 62% of all children with ICU admission were referred to an asthma specialist during the 3-month posthospitalization period. CONCLUSION: In this multicenter study of US children hospitalized with asthma exacerbation, one-third of children were admitted to the ICU. In this high-risk group, we observed suboptimal pre- and posthospitalization asthma care. These findings underscore the importance of continued efforts to improve prevention-oriented asthma care at all clinical encounters.


Assuntos
Antiasmáticos/uso terapêutico , Asma/tratamento farmacológico , Fidelidade a Diretrizes , Guias de Prática Clínica como Assunto , Adolescente , Alergia e Imunologia , Criança , Pré-Escolar , Gerenciamento Clínico , Feminino , Humanos , Imunoglobulina E/análise , Pacientes Internados/estatística & dados numéricos , Seguro Saúde/estatística & dados numéricos , Unidades de Terapia Intensiva , Tempo de Internação/estatística & dados numéricos , Masculino , Encaminhamento e Consulta , Estudos Retrospectivos , Índice de Gravidade de Doença , Distribuição por Sexo , Estados Unidos
3.
Clin J Am Soc Nephrol ; 10(2): 260-8, 2015 Feb 06.
Artigo em Inglês | MEDLINE | ID: mdl-25614492

RESUMO

BACKGROUND AND OBJECTIVES: Survival, symptom burden, and quality of life (QOL) are uncertain for elderly patients with advanced CKD managed without dialysis. We examined these outcomes in patients managed with renal supportive care without dialysis (RSC-NFD) and those planned for or commencing dialysis. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: In this prospective observational study, symptoms were measured using the Memorial Symptom Assessment Scale and the Palliative care Outcomes Scale - Symptoms (renal) inventory and QOL was measured using the Short Form-36 survey. This study comprised 273 predialysis patients who had usual nephrology care and 122 nondialysis pathway patients who also attended a renal supportive care clinic adding the skills of a palliative medicine team. A further 72 patients commenced dialysis during this period without attending either clinic. RESULTS: Nondialysis patients were older than the predialysis group (82 versus 67 years; P<0.001) but had similar eGFR at the first clinic visit (16 ml/min per 1.73 m(2); P=0.92). Of the predialysis patients, 92 (34%) commenced dialysis. Compared with the RSC-NFD group, the death rate was lower in the predialysis group who did not require dialysis (hazard ratio, 0.23; 95% confidence interval, 0.12 to 0.41] and in those requiring dialysis (0.30; 0.13 to 0.67) but not in dialysis patients who had not attended the predialysis clinic (0.60; 0.35 to 1.03). Median survival in RSC-NFD patients was 16 (interquartile range, 9, 37) months and 32% survived >12 months after eGFR fell below 10 ml/min per 1.73 m(2). For the whole group, age, serum albumin, and eGFR <15 ml/min per 1.73 m(2) were associated with poorer survival. Of the nondialysis patients, 57% had stable or improved symptoms over 12 months and 58% had stable or improved QOL. CONCLUSIONS: Elderly patients who choose not to have dialysis as part of shared decision making survive a median of 16 months and about one-third survive 12 months past a time when dialysis might have otherwise been indicated. Utilizing the skills of palliative medicine helps provide reasonable symptom control and QOL without dialysis.


Assuntos
Envelhecimento/psicologia , Conhecimentos, Atitudes e Prática em Saúde , Pacientes/psicologia , Qualidade de Vida , Diálise Renal/psicologia , Insuficiência Renal Crônica/terapia , Recusa do Paciente ao Tratamento , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Comportamento de Escolha , Efeitos Psicossociais da Doença , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , New South Wales/epidemiologia , Cuidados Paliativos , Participação do Paciente , Prognóstico , Modelos de Riscos Proporcionais , Estudos Prospectivos , Diálise Renal/efeitos adversos , Insuficiência Renal Crônica/complicações , Insuficiência Renal Crônica/diagnóstico , Insuficiência Renal Crônica/mortalidade , Insuficiência Renal Crônica/psicologia , Fatores de Risco , Inquéritos e Questionários , Fatores de Tempo
5.
Mil Med ; 176(7 Suppl): 35-40, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21916328

RESUMO

This article makes the case that current Agent Orange compensation policy for Vietnam War veterans is based neither wholly upon scientific findings about Agent Orange health effects nor on pure public health policy considerations. Rather, it is the logical culmination of decades of experience among policy makers and public health scientists trying to establish clear-cut, equitable, and scientifically defensible compensation policy in the face of limited relevant science and poor or nonexistent exposure data-all within the broader context of Veterans Affairs disability compensation policies, and a deep-seated commitment to support the men and women who served their country during the Vietnam War. Finally, attempts to update current policy will benefit from an understanding of this background.


Assuntos
Ácido 2,4,5-Triclorofenoxiacético/efeitos adversos , Ácido 2,4-Diclorofenoxiacético/efeitos adversos , Desfolhantes Químicos/efeitos adversos , Política de Saúde , Exposição Ocupacional/efeitos adversos , Dibenzodioxinas Policloradas/efeitos adversos , Ajuda a Veteranos de Guerra com Deficiência/legislação & jurisprudência , Agente Laranja , Compensação e Reparação/legislação & jurisprudência , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Militares/legislação & jurisprudência , National Academy of Sciences, U.S. , Ciência , Estados Unidos , Guerra do Vietnã
7.
Blood Press ; 14(3): 133-8, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16036492

RESUMO

The characterization of blood pressure in treatment trials assessing the benefits of blood pressure lowering regimens is a critical factor for the appropriate interpretation of study results. With numerous operators involved in the measurement of blood pressure in many thousands of patients being screened for entry into clinical trials, it is essential that operators follow pre-defined measurement protocols involving multiple measurements and standardized techniques. Blood pressure measurement protocols have been developed by international societies and emphasize the importance of appropriate choice of cuff size, identification of Korotkoff sounds, and digit preference. Training of operators and auditing of blood pressure measurement may assist in reducing the operator-related errors in measurement. This paper describes the quality control activities adopted for the screening stage of the 2nd Australian National Blood Pressure Study (ANBP2). ANBP2 is cardiovascular outcome trial of the treatment of hypertension in the elderly that was conducted entirely in general practices in Australia. A total of 54 288 subjects were screened; 3688 previously untreated subjects were identified as having blood pressure >140/90 mmHg at the initial screening visit, 898 (24%) were not eligible for study entry after two further visits due to the elevated reading not being sustained. For both systolic and diastolic blood pressure recording, observed digit preference fell within 7 percentage points of the expected frequency. Protocol adherence, in terms of the required minimum blood pressure difference between the last two successive recordings, was 99.8%. These data suggest that adherence to blood pressure recording protocols and elimination of digit preferences can be achieved through appropriate training programs and quality control activities in large multi-centre community-based trials in general practice. Repeated blood pressure measurement prior to initial diagnosis and study entry is essential to appropriately characterize hypertension in these elderly patients.


Assuntos
Determinação da Pressão Arterial/normas , Monitorização Ambulatorial da Pressão Arterial/métodos , Hipertensão/diagnóstico , Programas de Rastreamento/normas , Garantia da Qualidade dos Cuidados de Saúde/normas , Idoso , Idoso de 80 Anos ou mais , Austrália , Determinação da Pressão Arterial/métodos , Monitorização Ambulatorial da Pressão Arterial/estatística & dados numéricos , Educação/organização & administração , Feminino , Fidelidade a Diretrizes , Humanos , Hipertensão/terapia , Masculino , Programas de Rastreamento/métodos , Auditoria Médica , Estudos Multicêntricos como Assunto/normas , Ensaios Clínicos Controlados Aleatórios como Assunto/normas , Projetos de Pesquisa
8.
Am J Ind Med ; 46(5): 432-45, 2004 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15490471

RESUMO

BACKGROUND: Hospitals distant from the immediate site of an incident involving a hazardous materials (HAZMATs) release which could include chemical warfare agents, must develop emergency response plans (ERPs) to protect healthcare professionals if they receive potentially contaminated victims. The ERP must address OSHA, EPA, and JCAHO requirements. METHODS: The VHA convened groups to develop a hazard and exposure assessment, identify actions for compliance with existing regulatory standards, and review site and operational planning issues. Exposure modeling results were used to derive relationships between operational parameters (time and distance from sites/sources) and potential exposure for healthcare workers. RESULTS: According to exposure modeling, level C personal protective equipment is adequate to protect hospital staff distant from the chemical release site. Decontamination runoff and contaminated clothing should also be controlled to limit exposure. CONCLUSIONS: Development and coordination of ERPs must include the local emergency planning committee, with clear assignment of tasks, locations, and training in order to prevent exposures to healthcare workers.


Assuntos
Guerra Química , Planejamento em Desastres/métodos , Substâncias Perigosas , Hospitais/normas , Capacitação em Serviço , Saúde Ocupacional , Equipamentos de Proteção , Descontaminação/métodos , Planejamento em Desastres/legislação & jurisprudência , Planejamento em Desastres/normas , Ambiente Controlado , Humanos , Método de Monte Carlo , Estados Unidos
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