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1.
Eur J Public Health ; 23(4): 642-7, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23132874

RESUMO

BACKGROUND: Increased migration volume and different Hepatitis B prevalence between immigration and emigration countries have changed the Hepatitis B virus (HBV) epidemiology considerably in Northern and North-Western European migrants-receiving countries. Due to the difference in migration status monitoring, the HBV infection data on migrants are not easily comparable among those countries. The study aims were: to compare the migration status indicators used by the national surveillance system in six Northern and North-Western European countries (the Netherlands, Germany, Finland, Denmark, Sweden and the UK); to determine the impact of the migration status on HBV infection by comparing the available data on prevalence and transmission routes of Hepatitis B in the migration and the general population in the six countries; to recommend sensible indicators and pertinent measures for HBV infection surveillance and control in the region. METHODS: Literature review, statistical data analysis on migration and HBV infection in the six countries; expert interviews to identify migration status indicators used in national surveillance systems. RESULTS: Evident differences were found between the migration and the general population in Hepatitis B prevalence and transmission routes in the six countries. Migration status is monitored differently in six surveillance systems; immigrants from high/intermediate Hepatitis B endemic countries constitute a substantial proportion of HBsAg(+) and chronic cases in all six countries. CONCLUSIONS: International migration has an obvious impact on Hepatitis B prevalence in the six countries. It is important to include common migration status indicators and to collect comparable data for HBV infection surveillance in different notification systems.


Assuntos
Vírus da Hepatite B/patogenicidade , Hepatite B/epidemiologia , Hepatite B/transmissão , Comparação Transcultural , Dinamarca/epidemiologia , Emigrantes e Imigrantes , Finlândia/epidemiologia , Alemanha/epidemiologia , Hepatite B/virologia , Humanos , Imunização/tendências , Países Baixos/epidemiologia , Prevalência , Suécia/epidemiologia , Suécia/etnologia , Reino Unido/epidemiologia
2.
Cancer Nurs ; 34(5): 410-6, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21242767

RESUMO

BACKGROUND: Malnutrition is prevalent among patients within certain cancer types. There is lack of universal standard of care for nutrition screening and a lack of agreement on an operational definition and on validity of malnutrition indicators. OBJECTIVE: In a secondary data analysis, we investigated prevalence of malnutrition diagnosis with 3 classification methods using data from medical records of a National Cancer Institute-designated comprehensive cancer center. METHODS: Records of 227 patients hospitalized during 1998 with head and neck, gastrointestinal, or lung cancer were reviewed for malnutrition based on 3 methods: (1) physician-diagnosed malnutrition-related International Classification of Diseases, Ninth Revision codes; (2) in-hospital nutritional assessment summaries conducted by registered dietitians; and (3) body mass indexes (BMIs). For patients with multiple admissions, only data from the first hospitalization were included. RESULTS: Prevalence of malnutrition diagnosis ranged from 8.8% based on BMI to approximately 26% of all cases based on dietitian assessment. κ coefficients between any methods indicated a weak (κ = 0.23, BMI and dietitians; and κ = 0.28, dietitians and physicians)-to-fair strength of agreement (κ = 0.38, BMI and physicians). CONCLUSIONS: Available methods to identify patients with malnutrition in a National Cancer Institute-designated comprehensive cancer center resulted in varied prevalence of malnutrition diagnosis. A universal standard of care for nutrition screening that uses validated tools is needed. IMPLICATIONS FOR PRACTICE: The Joint Commission on the Accreditation of Healthcare Organizations requires nutritional screening of patients within 24 hours of admission. For this purpose, implementation of a validated tool that can be used by various healthcare practitioners, including nurses, needs to be considered.


Assuntos
Índice de Massa Corporal , Classificação Internacional de Doenças , Desnutrição/epidemiologia , Programas de Rastreamento/métodos , Neoplasias/complicações , Avaliação Nutricional , Feminino , Neoplasias Gastrointestinais/complicações , Neoplasias de Cabeça e Pescoço/complicações , Humanos , Neoplasias Pulmonares/complicações , Masculino , Desnutrição/diagnóstico , National Cancer Institute (U.S.) , Prevalência , Reprodutibilidade dos Testes , Estudos Retrospectivos , Estados Unidos/epidemiologia
3.
Pflege ; 19(5): 303-7, 2006 Oct.
Artigo em Alemão | MEDLINE | ID: mdl-17051516

RESUMO

In Germany a minimal quota of 50% professionally qualified nursing personnel is statutory for the care of nursing home inhabitants. The influence of this quota on the quality outcome of nursing care is controversially discussed. The study investigated the question, whether there is an association between the proportion of qualified personnel and the incidence of pressure ulcers in nursing homes. A historical cohort study was performed. Incidence data were taken from a routine survey on pressure ulcers. Nursing homes participating in this survey were asked for information about their proportion of qualified personnel and some additional factors that could possibly influence the incidence of bedsores. Included nursing home inhabitants (n = 2813) were divided into three groups according to whether they have been cared for with a low (< 50%), medium (50-60%) or high (> or = 60%) proportion of qualified personnel. Multivariate logistic regression models were calculated. Comparing medium to low proportion of qualified personnel, an odds ratio of 1.5 (p = 0.455), comparing high to low proportion, an odds ratio of 0.8 (p = 0.703) and comparing high to medium proportion, an odds ratio of 0.54 (p = 0,09) was calculated. The study question can not be answered by the contradictory results.


Assuntos
Casas de Saúde/normas , Recursos Humanos de Enfermagem/normas , Úlcera por Pressão/epidemiologia , Idoso , Alemanha/epidemiologia , Instituição de Longa Permanência para Idosos/normas , Humanos , Incidência , Pessoa de Meia-Idade , Análise Multivariada , Garantia da Qualidade dos Cuidados de Saúde , Análise de Regressão
4.
Onkologie ; 28(12): 647-50, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16330888

RESUMO

BACKGROUND: We investigated the combination of docetaxel and cisplatin as first-line chemotherapy in patients with metastatic esophageal cancer. PATIENTS AND METHODS: 16 chemotherapy-naïve patients with distant metastases were included in the study (15 male, 1 female; median age: 58.5 years (range 37-69); median ECOG performance status: 1). 11 patients (69%) had esophageal cancer, and 5 patients (31%) had cancer of the gastroesophageal junction. Patients received docetaxel 75 mg/m2 and cisplatin 80 mg/m2 on day 1 every 3 weeks. A total of 55 chemotherapy cycles was administered. The median number of cycles was 3 (range 1-6). RESULTS: The overall response rate was 31.3%. 4 out of 10 patients (40%) with squamous cell carcinoma and 1 out of 5 patients (20%) with adenocarcinoma responded to chemotherapy. The median overall survival was 29.6 weeks, and the median progression-free survival was 18.6 weeks. Hematological and non-hematological toxicities were moderate (neutropenia WHO grade III/IV: 42.9%, alopecia grade II/III: 64.3%, nausea/vomiting grade II/III: 57.2%, neurotoxicity grade II: 14.3%). CONCLUSION: The combination of docetaxel and cisplatin is an active regimen with moderate toxicity in the treatment of patients with metastatic esophageal cancer. This pilot study demonstrates the feasibility of a combination treatment containing a taxane and cisplatin in metastatic esophageal cancer.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/administração & dosagem , Cisplatino/administração & dosagem , Neoplasias Esofágicas/tratamento farmacológico , Neoplasias Esofágicas/epidemiologia , Taxoides/administração & dosagem , Adulto , Idoso , Docetaxel , Feminino , Alemanha/epidemiologia , Humanos , Metástase Linfática , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Prevalência , Resultado do Tratamento
5.
Lung Cancer ; 36(3): 303-7, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12009242

RESUMO

The aim of this pilot study was to evaluate the activity and toxicity of docetaxel plus carboplatin as second-line treatment in patients with metastatic non-small cell lung cancer (NSCLC). Patients received docetaxel 75 mg/m(2) followed by carboplatin AUC 5 on day 1 every 3 weeks in an out-patient setting. Twenty-six patients were enrolled; 23 patients were diagnosed stage IV disease and three patients had a IIIB disease with malignant pleural effusion. The median interval from first to second-line treatment was 3.5 months (range 1-13). Patients received a total of 101 cycles with a median number of four cycles per patient (range 1-6). Five patients achieved a partial remission (19.23%; 95% confidence interval (CI) 6.55-39.35%), 11 had stable disease (42.31%) and ten progressed (38.46%) after initiation of second-line therapy. Median survival was 243 days (95% CI 182-336 days), the median progression-free survival was 118 days (95% CI 89-170 days), and the 1-year survival rate was 25.98% (95% CI 6.33-45.63%). Moderate haematological and mild nonhaematological toxicities were observed. No treatment-related death occurred. In conclusion, docetaxel plus carboplatin as second-line regimen has a reasonable activity with good tolerance and encouraging survival data.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Carcinoma Pulmonar de Células não Pequenas/tratamento farmacológico , Neoplasias Pulmonares/tratamento farmacológico , Paclitaxel/análogos & derivados , Taxoides , Adulto , Idoso , Carboplatina/administração & dosagem , Progressão da Doença , Intervalo Livre de Doença , Docetaxel , Feminino , Humanos , Infusões Intravenosas , Masculino , Pessoa de Meia-Idade , Paclitaxel/administração & dosagem , Projetos Piloto , Taxa de Sobrevida , Resultado do Tratamento
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