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1.
Int J Tuberc Lung Dis ; 17(12): 1581-6, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24200272

RESUMO

OBJECTIVES: To evaluate the population-based impact of a comprehensive intervention to strengthen tuberculosis (TB) control in Rocinha, the largest urban slum in Rio de Janeiro, Brazil. DESIGN: In July 2003, 40 lay persons were hired and trained as community health workers to supervise treatment, implement educational activities and establish a supportive social network for anti-tuberculosis treatment. Between July 2005 and June 2008, a door-to-door active case finding campaign was conducted. Data were obtained from the Brazilian National Reporting System, which collects information from the TB notification form for every reported case. RESULTS: Between January 2001 and December 2008, 2623 TB cases were reported, 852 before and 1771 after the start of the program. Following the intervention, treatment success rates increased (67.6% vs. 83.2%, P < 0.001) and default rates dropped (17.8% vs. 5.5%, P < 0.001). Compared to the pre-intervention period, the TB case rate declined by an average of 39 cases per 100,000 population per 6 months (P = 0.003) in the post-intervention period, although this may have been due to secular trends already in place at the start of the intervention. Case rates declined from 591/100,000 in 2001 to 496/100,000 in 2008. CONCLUSION: With proper planning and effective community involvement, a successful intervention can lead to high cure rates and may contribute to a decrease in TB notification rates.


Assuntos
Antituberculosos/uso terapêutico , Serviços de Saúde Comunitária , Terapia Diretamente Observada , Áreas de Pobreza , Tuberculose/tratamento farmacológico , Serviços Urbanos de Saúde , Populações Vulneráveis , Adolescente , Adulto , Brasil/epidemiologia , Serviços de Saúde Comunitária/organização & administração , Agentes Comunitários de Saúde , Notificação de Doenças , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Incidência , Masculino , Objetivos Organizacionais , Educação de Pacientes como Assunto , Avaliação de Programas e Projetos de Saúde , Apoio Social , Fatores de Tempo , Resultado do Tratamento , Tuberculose/diagnóstico , Tuberculose/epidemiologia , Tuberculose/transmissão , Serviços Urbanos de Saúde/organização & administração , Adulto Jovem
2.
J Dent Res ; 92(6): 512-7, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23589387

RESUMO

The Xylitol for Adult Caries Trial was a three-year, double-blind, multi-center, randomized clinical trial that evaluated the effectiveness of xylitol vs. placebo lozenges in the prevention of dental caries in caries-active adults. The purpose of this secondary analysis was to investigate whether xylitol lozenges had a differential effect on cumulative caries increments on different tooth surfaces. Participants (ages 21-80 yrs) with at least one follow-up visit (n = 620) were examined at baseline, 12, 24, and 33 months. Negative binomial and zero-inflated negative binomial regression models were used to estimate incidence rate ratios (IRR) for xylitol's differential effect on cumulative caries increments on root and coronal surfaces and, among coronal surfaces, on smooth (buccal and lingual), occlusal, and proximal surfaces. Participants in the xylitol arm developed 40% fewer root caries lesions (0.23 D2FS/year) than those in the placebo arm (0.38 D2FS/year; IRR = 0.60; 95% CI [0.44, 0.81]; p < .001). There was no statistically significant difference between xylitol and control participants in the incidence of smooth-surface caries (p = .100), occlusal-surface caries (p = .408), or proximal-surface caries (p = .159). Among these caries-active adults, xylitol appears to have a caries-preventive effect on root surfaces (ClinicalTrials.gov NCT00393055).


Assuntos
Cariostáticos/uso terapêutico , Cárie Dentária/prevenção & controle , Xilitol/uso terapêutico , Adulto , Idoso , Idoso de 80 Anos ou mais , Cariostáticos/administração & dosagem , Índice CPO , Suscetibilidade à Cárie Dentária , Método Duplo-Cego , Feminino , Fluoretos/uso terapêutico , Fluoretos Tópicos/uso terapêutico , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Placebos , Cárie Radicular/prevenção & controle , Comprimidos , Coroa do Dente/patologia , Escovação Dentária , Cremes Dentais/uso terapêutico , Resultado do Tratamento , Xilitol/administração & dosagem , Adulto Jovem
3.
Int J Tuberc Lung Dis ; 16(10): 1405-11, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22863565

RESUMO

BACKGROUND: The presence of restrictive lung disease has classically required the measure of total lung capacity to document 'true' restriction, which has limited its detection in large population-based studies. METHODS: We used spirometric data to classify people with restricted spirometry (forced expiratory volume in 1 second [FEV(1)]/forced vital capacity ≥ 0.70 and FEV(1) < 80% predicted) in the Burden of Lung Disease (BOLD) Study and determined the relation between this finding and demographic factors and the presence of chronic diseases, including diabetes mellitus, hypertension and cardiovascular disease. RESULTS: Overall, we found that 11.7% of men (546/4664) and 16.4% of women (836/5098) had restricted spirometry. Prevalence varied widely by site, from a low of 4.2% among males in Sydney, Australia, to a high of 48.7% among females in Manila, The Philippines. Compared to people with normal lung function, those with restricted spirometry had a higher prevalence of diabetes (12.2% vs. 4.6%), heart disease (15.0% vs. 7.7%) and hypertension (38.8% vs. 22.8%). CONCLUSIONS: Restricted spirometry is a common finding in population studies. Additional research is needed to better define and describe the mechanisms that lead to restricted spirometry and potential interventions.


Assuntos
Pneumopatias/diagnóstico , Capacidade Pulmonar Total , Capacidade Vital , Doença Crônica , Estudos de Viabilidade , Feminino , Volume Expiratório Forçado , Saúde Global , Humanos , Pneumopatias/epidemiologia , Pneumopatias/fisiopatologia , Masculino , Prevalência , Reprodutibilidade dos Testes , Espirometria/métodos
4.
J Dent Res ; 91(2): 150-5, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22156917

RESUMO

The Prevention of Adult Caries Study, an NIDCR-funded multicenter, double-blind, randomized clinical trial, enrolled 983 adults (aged 18-80 yrs) at high risk for developing caries (20 or more intact teeth and 2 or more lesions at screening) to test the efficacy of a chlorhexidine diacetate 10% weight per volume (w/v) dental coating (CHX). We excluded participants for whom the study treatment was contraindicated or whose health might affect outcomes or ability to complete the study. Participants were randomly assigned to receive either the CHX coating (n = 490) or a placebo control (n = 493). Coatings were applied weekly for 4 weeks and a fifth time 6 months later. The primary outcome (total net D(1-2)FS increment) was the sum of weighted counts of changes in tooth surface status over 13 months. We observed no significant difference between the two treatment arms in either the intention-to-treat or per-protocol analyses. Analysis of 3 protocol-specified secondary outcomes produced similar findings. This trial failed to find that 10% (w/v) chlorhexidine diacetate coating was superior to placebo coating for the prevention of new caries (Clinicaltrials.gov registration number NCT00357877).


Assuntos
Anti-Infecciosos Locais/administração & dosagem , Clorexidina/administração & dosagem , Cárie Dentária/prevenção & controle , Administração Tópica , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Coroas , Índice CPO , Cárie Dentária/classificação , Suscetibilidade à Cárie Dentária/efeitos dos fármacos , Esmalte Dentário/efeitos dos fármacos , Esmalte Dentário/patologia , Restauração Dentária Permanente , Dentina/efeitos dos fármacos , Dentina/patologia , Progressão da Doença , Método Duplo-Cego , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Placebos , Cárie Radicular/prevenção & controle , Perda de Dente/classificação , Raiz Dentária/efeitos dos fármacos , Raiz Dentária/patologia , Resultado do Tratamento , Adulto Jovem
5.
Respir Med ; 105(10): 1507-15, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21549584

RESUMO

OBJECTIVE: to determine the ability of participants in the Burden of Obstructive Lung Disease (BOLD) study to meet quality goals for spirometry test session quality and to assess factors contributing to good quality. METHODS: Following 2 days of centralized training, spirometry was performed pre- and post-bronchodilator (BD) at 14 international sites, in random population-based samples of persons aged ≥40 years, following a standardized protocol. The quality of each test session was evaluated by the spirometer software and an expert reading center. Descriptive statistics were calculated for key maneuver acceptability variables. A logistic regression model identified the predictors of acceptable quality test sessions. RESULTS: About 96% of test sessions met our quality goals for a low back-extrapolated volume (BEV), time to peak flow (PEFT), and end-of-test volume (EOTV). The mean forced expiratory time (FET) was 10.4 s. Ninety percent of the maneuvers with the highest FVC had a forced expiratory time (FET) > 6.8 s. About 90% of test sessions had FEV(1) and FVC which were repeatable within 150 mL. Test quality was slightly better for post-BD test sessions when compared to pre-BD. Independent predictors of adequate test quality included female sex, younger age, higher education, lack of dyspnea, higher pre-BD FEV(1), less BD responsiveness, and study site. CONCLUSIONS: Quality goals for spirometry tests were met about 90% of the time in these population-based samples of adults from several countries.


Assuntos
Fluxo Expiratório Forçado , Doença Pulmonar Obstrutiva Crônica/fisiopatologia , Garantia da Qualidade dos Cuidados de Saúde/normas , Espirometria/normas , Adulto , Idoso , Feminino , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Pico do Fluxo Expiratório , Controle de Qualidade , Inquéritos e Questionários
6.
Eur Respir J ; 35(1): 132-7, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19574323

RESUMO

Obstructive sleep apnoea syndrome (OSAS) often coexists in patients with chronic obstructive pulmonary disease (COPD). The present prospective cohort study tested the effect of OSAS treatment with continuous positive airway pressure (CPAP) on the survival of hypoxaemic COPD patients. It was hypothesised that CPAP treatment would be associated with higher survival in patients with moderate-to-severe OSAS and hypoxaemic COPD receiving long-term oxygen therapy (LTOT). Prospective study participants attended two outpatient advanced lung disease LTOT clinics in São Paulo, Brazil, between January 1996 and July 2006. Of 603 hypoxaemic COPD patients receiving LTOT, 95 were diagnosed with moderate-to-severe OSAS. Of this OSAS group, 61 (64%) patients accepted and were adherent to CPAP treatment, and 34 did not accept or were not adherent and were considered not treated. The 5-yr survival estimate was 71% (95% confidence interval 53-83%) and 26% (12-43%) in the CPAP-treated and nontreated groups, respectively (p<0.01). After adjusting for several confounders, patients treated with CPAP showed a significantly lower risk of death (hazard ratio of death versus nontreated 0.19 (0.08-0.48)). The present study found that CPAP treatment was associated with higher survival in patients with moderate-to-severe OSAS and hypoxaemic COPD receiving LTOT.


Assuntos
Pressão Positiva Contínua nas Vias Aéreas , Hipóxia/mortalidade , Hipóxia/terapia , Oxigenoterapia , Doença Pulmonar Obstrutiva Crônica/mortalidade , Doença Pulmonar Obstrutiva Crônica/terapia , Síndromes da Apneia do Sono/mortalidade , Síndromes da Apneia do Sono/terapia , Idoso , Feminino , Humanos , Hipóxia/complicações , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Doença Pulmonar Obstrutiva Crônica/complicações , Índice de Gravidade de Doença , Síndromes da Apneia do Sono/complicações , Taxa de Sobrevida
7.
Int J Tuberc Lung Dis ; 13(8): 1023-8, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19723384

RESUMO

BACKGROUND: The association of tobacco smoke with the prevalence of asthma and rhinitis has not been well-characterized in adolescents. METHODS: As part of the International Study of Asthma and Allergies in Childhood (ISAAC), we conducted a cross-sectional survey of 3000 adolescents aged 13-14 years in northern Argentina. Data included questions about asthma and rhinitis symptoms and about parental and personal smoking. Logistic regression and Pearson chi(2) statistics were used to estimate these associations. RESULTS: Over 13% of respondents described themselves as current smokers, and half indicated that at least one parent smoked at home. Active smoking was associated with both asthma (OR 1.83, 95%CI 1.42-2.35) and rhinitis (OR 1.61, 95%CI 1.33-1.92) in unadjusted analysis. These associations persisted after adjusting for parental smoking status, mother's educational level and sex. Boys were significantly less likely than girls to report current asthma or rhinitis. CONCLUSIONS: Active and passive smoking are both risk factors for asthma and rhinitis in adolescents. Assuming that some children with asthma never started smoking due to symptoms, then the true risk could be higher than reported here. These results reinforce the need to develop better strategies for primary and secondary prevention of tobacco exposure in children.


Assuntos
Asma/epidemiologia , Rinite/epidemiologia , Fumar/epidemiologia , Adolescente , Argentina/epidemiologia , Estudos Transversais , Feminino , Humanos , Modelos Logísticos , Masculino , Prevalência , Prevenção Primária , Fatores de Risco , Prevenção do Hábito de Fumar , Poluição por Fumaça de Tabaco/estatística & dados numéricos
8.
Eur Respir J ; 34(3): 588-97, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19460786

RESUMO

Published guidelines recommend spirometry to accurately diagnose chronic obstructive pulmonary disease (COPD). However, even spirometry-based COPD prevalence estimates can vary widely. We compared properties of several spirometry-based COPD definitions using data from the international Burden of Obstructive Lung Disease (BOLD)study. 14 sites recruited population-based samples of adults aged > or =40 yrs. Procedures included standardised questionnaires and post-bronchodilator spirometry. 10,001 individuals provided usable data. Use of the lower limit of normal (LLN) forced expiratory volume in 1 s (FEV(1)) to forced vital capacity (FVC) ratio reduced the age-related increases in COPD prevalence that are seen among healthy never-smokers when using the fixed ratio criterion (FEV(1)/FVC <0.7) recommended by the Global Initiative for Chronic Obstructive Lung Disease. The added requirement of an FEV(1) either <80% predicted or below the LLN further reduced age-related increases and also led to the least site-to-site variability in prevalence estimates after adjusting for potential confounders. Use of the FEV(1)/FEV(6) ratio in place of the FEV(1)/FVC yielded similar prevalence estimates. Use of the FEV(1)/FVC

Assuntos
Volume Expiratório Forçado , Doença Pulmonar Obstrutiva Crônica/diagnóstico , Doença Pulmonar Obstrutiva Crônica/fisiopatologia , Espirometria , Capacidade Vital , Adulto , Idoso , Estudos de Coortes , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Guias de Prática Clínica como Assunto , Valor Preditivo dos Testes , Prevalência , Doença Pulmonar Obstrutiva Crônica/epidemiologia , Reprodutibilidade dos Testes , Estudos Retrospectivos , Inquéritos e Questionários
9.
Int J Tuberc Lung Dis ; 13(3): 387-93, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19275802

RESUMO

BACKGROUND: Chronic obstructive pulmonary disease (COPD) is underdiagnosed. One barrier to diagnosis is the limited availability of spirometry testing, but in adults at risk for COPD, a normal pre-bronchodilator (pre-BD) peak expiratory flow (PEF) may rule out clinically significant COPD. OBJECTIVE: To identify post-BD airway obstruction using data from 13 708 individuals aged >or=40 years from the PLATINO and BOLD studies. METHODS: We evaluated different cut-off points of pre-BD. The PEF was obtained from a diagnostic-quality spirometer (not a mechanical PEF meter). At least one of the following COPD risk factors was present in 77% of the subjects: chronic respiratory symptoms; exposure to tobacco smoke, biomass smoke or dust in the workplace; or a previous diagnosis of asthma, COPD, emphysema or chronic bronchitis. RESULTS: Although the positive predictive value was low as expected, a pre-BD PEF of >or=70% predicted effectively ruled out Stages III and IV COPD of the Global Initiative for Chronic Obstructive Lung Disease. Among those with at least one risk factor, only 12% would require confirmatory spirometry using this criterion. CONCLUSIONS: Adding PEF measurement to a screening questionnaire may rule out severe to very severe COPD without the need for pre- and post-BD spirometry testing. Confirmation is needed from a study using inexpensive PEF meters or pocket spirometers with a staged screening protocol.


Assuntos
Pico do Fluxo Expiratório , Doença Pulmonar Obstrutiva Crônica/diagnóstico , Espirometria , Idoso , Obstrução das Vias Respiratórias/tratamento farmacológico , Broncodilatadores/uso terapêutico , Feminino , Volume Expiratório Forçado , Humanos , Masculino , Pessoa de Meia-Idade , Doença Pulmonar Obstrutiva Crônica/tratamento farmacológico , Sensibilidade e Especificidade , Espirometria/estatística & dados numéricos
10.
Int J Tuberc Lung Dis ; 12(7): 703-8, 2008 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-18544191

RESUMO

SETTING: Burden of Obstructive Lung Disease (BOLD) Initiative sites worldwide. OBJECTIVE: To measure the prevalence of chronic obstructive pulmonary disease (COPD) and its risk factors, investigate variation in prevalence across countries and develop standardized methods that can be used in industrialized and developing countries. DESIGN: Non-institutionalized adults aged > or =40 years were recruited using population-based sampling plans. Each site targeted a minimum of 600 participants (300 women, 300 men), who filled out questionnaires and performed spirometry before and after administration of 200 mug salbutamol using standardized methods. Random effects meta-analysis models were used to estimate pooled prevalence estimates and risk factor effects and to test for heterogeneity across sites and sex. RESULTS: Data published from 12 sites (n = 8775) showed that the estimated population prevalence of COPD (Global Initiative for Chronic Obstructive Lung Disease [GOLD] Stage II and higher) was 10.1 +/- SE = 4.8% overall (11.8 +/- 7.9% for men and 8.5 +/- 5.8% for women). Prevalence increased with age and pack-years of smoking, but other less understood risk factors, such as biomass heating and cooking exposures, occupational exposures and tuberculosis, also contribute to the location-specific variations in disease prevalence that BOLD is finding. CONCLUSION: BOLD has estimated the social and economic burden of COPD in 12 countries to date. BOLD and the Proyecto Latinoamericano de Investigación en Obstrucción Pulmonar (the PLATINO study) are developing a growing database of COPD prevalence. Cigarette smoking and age are the most important COPD risk factors, but other risk factors should also be explored.


Assuntos
Efeitos Psicossociais da Doença , Países Desenvolvidos/estatística & dados numéricos , Países em Desenvolvimento/estatística & dados numéricos , Doença Pulmonar Obstrutiva Crônica/epidemiologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Doença Pulmonar Obstrutiva Crônica/diagnóstico , Fatores de Risco , Espirometria
11.
Osteoporos Int ; 19(11): 1527-40, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18373049

RESUMO

UNLABELLED: This study used in-depth interviews and focus groups to evaluate osteoporosis care after a fracture. Patients (eligible women aged 67 who sustained a clinical fracture(s)), clinicians, and staff stated that an outreach program facilitated osteoporosis care management, but more-tailored education and support and increased participation of orthopedic specialists appear necessary. INTRODUCTION: Osteoporosis treatment reduces fracture risk, but screening and treatment are underutilized, even after a fracture has occurred. This study evaluated key stakeholder perspectives about the care of osteoporosis after a fracture. METHODS: Participants were from a nonprofit health maintenance organization in the United States: eligible women members aged 67 or older who sustained a clinical fracture(s) (n = 10), quality and other health care managers (n = 20), primary care providers (n = 9), and orthopedic clinicians and staff (n = 28); total n = 67. In-depth interviews and focus groups elicited participant perspectives on an outreach program to patients and clinicians and other facilitators and barriers to care. Interviews and focus group sessions were transcribed and content-analyzed. RESULTS: Patients, clinicians, and staff stated that outreach facilitated osteoporosis care management, but important patient barriers remained. Patient knowledge gaps and fatalism were common. Providers stated that management needed to begin earlier, and longer-term patient support was necessary to address adherence. Orthopedic clinicians and staff expressed lack of confidence in their osteoporosis management but willingness to encourage treatment. CONCLUSIONS: Although an outreach program assisted with the management of osteoporosis after a fracture, more-tailored education and support and increased participation of orthopedic specialists appear necessary to maximize osteoporosis management.


Assuntos
Fraturas Ósseas/etiologia , Osteoporose Pós-Menopausa/tratamento farmacológico , Qualidade da Assistência à Saúde , Idoso , Densidade Óssea , Conservadores da Densidade Óssea/uso terapêutico , Atenção à Saúde/normas , Feminino , Grupos Focais , Fraturas Ósseas/prevenção & controle , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Entrevistas como Assunto , Osteoporose Pós-Menopausa/complicações , Atenção Primária à Saúde/normas , Avaliação de Programas e Projetos de Saúde , Estados Unidos
12.
Thorax ; 61(6): 503-6, 2006 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16517579

RESUMO

BACKGROUND: Bronchiolitis obliterans (BO) is an uncommon and severe form of chronic obstructive lung disease in children that results from an insult to the lower respiratory tract. METHODS: A case-control study of children under the age of 3 years was performed in 109 cases and 99 controls to determine risk factors for the development of BO. Participants were evaluated by immunofluorescence viral tests, pulmonary function tests, and questions to assess tobacco and other exposures. RESULTS: Bronchiolitis due to adenovirus (odds ratio (OR) 49, 95% confidence interval (CI) 12 to 199) and the need for mechanical ventilation (OR 11, 95% CI 2.6 to 45) were strongly and independently associated with an increased risk for BO. Factors not associated with post-infectious BO included age of the child, sex, and environmental tobacco exposure (either in utero or during infancy). CONCLUSIONS: Adenovirus infection and need for mechanical ventilation are significant risk factors for developing BO in children. Further research is needed to determine why these risk factors are so strong and how they may contribute to the development of the disease.


Assuntos
Infecções por Adenoviridae , Bronquiolite Obliterante/virologia , Bronquiolite Obliterante/diagnóstico por imagem , Bronquiolite Obliterante/terapia , Pré-Escolar , Feminino , Hospitalização , Humanos , Lactente , Recém-Nascido , Masculino , Radiografia , Análise de Regressão , Respiração Artificial , Testes de Função Respiratória , Fatores de Risco
13.
Clin Exp Allergy ; 35(11): 1466-72, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16297144

RESUMO

BACKGROUND: The composition of the intestinal flora in young children, if unfavourable, may increase the susceptibility to allergic disorders. Beneficial intestinal microbes originate from the maternal vaginal tract and thus are more likely to be transferred during vaginal births than during Caesarean sections (C-sections). OBJECTIVE: To determine whether children born by C-section have a different risk of allergic disorders compared with those delivered vaginally. We also tested the hypothesis that the risk of allergic disorders is highest for children born after 'repeat C-sections'. METHODS: A retrospective cohort study of 8,953 children aged 3-10 years. Children diagnosed with allergic rhinoconjunctivitis (AR), asthma, atopic dermatitis (AD), or food allergies were identified from the Kaiser Permanente Northwest Region electronic records. The children's sex, birth weight, birth order, postnatal exposure to antibiotics as well as the mothers' age, ethnicity, education, marital status, smoking status during pregnancy, and use of asthma or hayfever medications were identified through the mothers' medical records or through the Oregon Birth Registry. RESULTS: The risk of being diagnosed with AR was significantly higher in the children born by C-section than in those delivered vaginally: adjusted odds ratio (OR)=1.37%, 95% confidence interval (CI)=1.14-1.63. Delivery by C-section was also associated with the subsequent diagnosis of asthma (OR=1.24%, 95% CI=1.01-1.53); this association was gender specific, with a positive association restricted to girls (OR for asthma in girls: OR=1.53%, 95% CI=1.11-2.10; in boys: OR=1.08%, 95% CI=0.81-1.43). There was no significant association between mode of delivery and AD. If children born in a 'repeat C-section' were considered separately the risk of being diagnosed with AR increased further (OR=1.78%, 95% CI=1.34-2.37). The same increase was noted for asthma in girls (OR=1.83%, 95% CI=1.13-2.97) but not in boys. CONCLUSION: Caesarean sections may be associated with an increased risk of developing AR in childhood.


Assuntos
Cesárea/efeitos adversos , Hipersensibilidade/imunologia , Anti-Infecciosos/uso terapêutico , Asma/etnologia , Asma/imunologia , Ordem de Nascimento , Criança , Pré-Escolar , Conjuntivite Alérgica/etnologia , Conjuntivite Alérgica/imunologia , Dermatite Atópica/etnologia , Dermatite Atópica/imunologia , Feminino , Hipersensibilidade Alimentar/etnologia , Hipersensibilidade Alimentar/imunologia , Humanos , Hipersensibilidade/etnologia , Masculino , Idade Materna , Gravidez , Medicamentos para o Sistema Respiratório/uso terapêutico , Estudos Retrospectivos , Rinite Alérgica Perene/etnologia , Rinite Alérgica Perene/imunologia , Fatores de Risco , Fatores Sexuais
14.
J Hum Hypertens ; 19(1): 21-31, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15385946

RESUMO

Recommendations for control of high blood pressure (BP) emphasize lifestyle modification, including weight loss, reduced sodium intake, increased physical activity, and limited alcohol consumption. The Dietary Approaches to Stop Hypertension (DASH) dietary pattern also lowers BP. The PREMIER randomized trial tested multicomponent lifestyle interventions on BP in demographic and clinical subgroups. Participants with above-optimal BP through stage 1 hypertension were randomized to an Advice Only group or one of two behavioural interventions that implement established recommendations (Est) or established recommendations plus DASH diet (Est plus DASH). The primary outcome was change in systolic BP at 6 months. The study population was 810 individuals with an average age of 50 years, 62% women, 34% African American (AA), 95% overweight/obese, and 38% hypertensive. Participants in all the three groups made lifestyle changes. Mean net reductions in systolic (S) BP in the Est intervention were 1.2 mmHg in AA women, 6.0 in AA men, 4.5 in non-AA women, and 4.2 in non-AA men. The mean effects of the Est Plus DASH intervention were 2.1, 4.6, 4.2, and 5.7 mmHg in the four race-sex subgroups, respectively. BP changes were consistently greater in hypertensives than in nonhypertensives, although interaction tests were nonsignificant. The Est intervention caused statistically significant BP reductions in individuals over and under age 50. The Est Plus DASH intervention lowered BP in both age groups, and significantly more so in older individuals. In conclusion, diverse groups of people can adopt multiple lifestyle changes that can lead to improved BP control and reduced CVD risk.


Assuntos
Dieta Hipossódica , Aconselhamento Diretivo , Hipertensão/terapia , Estilo de Vida , Educação de Pacientes como Assunto , Adulto , Negro ou Afro-Americano , Fatores Etários , Feminino , Comportamentos Relacionados com a Saúde , Humanos , Masculino , Pessoa de Meia-Idade , Fatores Sexuais , Redução de Peso
15.
J Hum Hypertens ; 19(1): 77-82, 2005 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15361888

RESUMO

Ambulatory blood pressure monitoring (ABPM) is commonly used in clinical trials. Yet, its ability to detect blood pressure (BP) change in comparison to multiple office-based measurements has received limited attention. We recorded ambulatory and five daily pairs of random zero (RZ) BPs pre- and post-intervention on 321 adult participants in the multicentre Dietary Approaches to Stop Hypertension trial. Treatment effect estimates measured by ambulatory monitoring were similar to those measured by RZ and did not differ significantly for waking vs 24-h ambulatory measurements. For systolic BP, the standard deviations of change in mean 24-h ambulatory BP (8.0 mmHg among hypertensives and 6.0 mmHg among nonhypertensives) were comparable to or lower than the corresponding standard deviations of change in RZ-BP based on five daily readings (8.9 and 5.9 mmHg). The standard deviations of change for mean waking ambulatory BP (8.7 and 6.7 mmHg) were comparable to those obtained using three to four daily RZ readings. Results for diastolic BP were qualitatively similar. Ambulatory monitoring was more efficient (ie, a smaller sample size could detect a given BP change) than three to four sets of daily RZ readings and required fewer clinic visits. The average of 33 ambulatory BP readings during the waking hours had an efficiency comparable to that from the mean of four daily pairs of RZ-BPs. Participants readily accepted the ABPM devices, and their use requires less staff training. ABPM provides a useful alternative to RZ-BP measurements in clinical trials.


Assuntos
Monitorização Ambulatorial da Pressão Arterial , Hipertensão/fisiopatologia , Visita a Consultório Médico , Adulto , Ritmo Circadiano/fisiologia , Protocolos Clínicos , Feminino , Humanos , Hipertensão/dietoterapia , Masculino , Reprodutibilidade dos Testes , Estudos Retrospectivos
17.
Respir Med ; 97(2): 134-42, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12587963

RESUMO

We aimed to investigate whether dietary vitamin C intake, an important antioxidant, is inversely related to self-reported respiratory symptoms in young adults of a community. A random sample of 4300 subjects, aged 20-44 years, living in Bergen, Norway, received a postal questionnaire on respiratory symptoms; 80% responded. Vitamin C intake (mg per week) was estimated from a food-frequency questionnaire asking how often the subject, during the last year, had consumed units of orange juice, oranges, potatoes, carrots and tomatoes. Significant differences in the intake of vitamin C were observed across smoking categories with current smokers having the lowest intake, while there was no variation by gender, age or occupational dust exposure. Dietary vitamin C intake was in univariate analyses inversely related to "morning cough", "chronic cough", "wheeze" and "wheeze ever". After adjusting for gender, age, body mass index, "occupational exposure" pack-years as well as having and stratified on smoking habits in multiple logistic regression analyses, the relationship between dietary vitamin C intake and "cough" and "wheeze" tended to be associated to smoking. The odds ratio (OR) for "morning cough" was 0.68 (95% CI: 0.35-0.95), "chronic cough" OR 0.69 (95% CI: 0.47-1.04) and "wheeze ever" OR 0.75 (95% CI: 0.56-1.01) in current-smokers with dietary vitamin C intake in the upper (> or =395 mg/ week) vs. the lower (<209 mg/week) tertile. The OR for "wheeze" was 0.56 (95% CI: 0.35-0.88) in ex-smokers. The magnitude ofthese effects remained after excluding subjects with supplementary vitamin C intake (n=199) from the statistical analyses. Among young Norwegian adults, having a low prevalence of asthma and high prevalences of smoking-related respiratory symptoms, dietary vitamin C intake may act as an antioxidant and thereby reduce cough and wheeze in smokers having high oxidant stress.


Assuntos
Antioxidantes/administração & dosagem , Ácido Ascórbico/administração & dosagem , Tosse/epidemiologia , Dieta , Sons Respiratórios/etiologia , Fumar/epidemiologia , Adulto , Estudos Transversais , Feminino , Humanos , Masculino , Noruega/epidemiologia , Razão de Chances , Análise de Regressão
18.
Eur Respir J ; 20(5): 1117-22, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12449163

RESUMO

The Global Initiative for Chronic Obstructive Lung Disease (GOLD) has defined stage I chronic obstructive pulmonary disease (COPD) as forced expiratory volume in one second/forced vital capacity (FEV1/FVC)% <70% and a FEV1% predicted of >80%. Stage 2 has been defined as FEV1/FVC <70% and a FEV1% pred of <80%. The authors examined the extent of COPD misdiagnosis using this definition in healthy, never-smoker, asymptomatic adults aged >70 yrs in Bergen, Norway. A respiratory questionnaire was mailed to a random sample of 2,871 persons aged >70 yrs. In a random, well-defined subgroup of 208 never-smoker respondents with no current respiratory disease and significant dyspnoea or heart disease/hypertension complicated with dyspnoea, 71 were able to perform an acceptable spirometry. Approximately 35% of these healthy, elderly never-smokers had an FEV1/FVC% of <70% and would be classified as having at least a stage 1 COPD. This percentage increased with age and in those aged >80 yrs approximately 50% would be classified as having COPD and approximately one-third would have an FEV1 of <80% pred (stage 2 COPD). The estimated 5th percentile of FEV1 was consistently <80% pred. The Global Initiative for Chronic Obstructive Lung Disease criteria will probably lead to a significant degree of over-diagnosis of chronic obstructive pulmonary disease in those aged >70 yrs. The criteria used to define the various stages of chronic obstructive pulmonary disease need to be age-specific.


Assuntos
Doença Pulmonar Obstrutiva Crônica/diagnóstico , Idoso , Idoso de 80 Anos ou mais , Erros de Diagnóstico , Feminino , Volume Expiratório Forçado , Humanos , Masculino , Doença Pulmonar Obstrutiva Crônica/fisiopatologia , Valores de Referência , Fumar , Espirometria , Capacidade Vital
19.
Ann Epidemiol ; 12(5): 295-302, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12062915

RESUMO

PURPOSE: To evaluate patterns of lung function in healthy, working Chinese men and women in different geographic areas of the People's Republic of China (PRC). METHODS: We conducted lung function tests on 2926 asymptomatic, never smoking Chinese men and women aged 35-56 years residing in or around Beijing and Guangzhou. Within each of these locations, separate urban and rural samples were recruited. RESULTS: Age and height adjusted lung function was greater in Beijing than in Guangzhou, and within each city for residents of rural vs. urban areas. Among women, estimated rates of lung aging were greater in Beijing than in Guangzhou, and in urban vs. rural areas. Both FEV(1) and FVC exhibited a curvilinear association with body mass index. CONCLUSIONS: Lung function data from this largely working cohort exhibited marked geographic and urban-rural differences in this never smoking, adult Chinese cohort. Such variation is not uncommon and may reflect differences in body size, diet, and environmental and occupational exposures across these different settings. Caution should be used in applying published reference equations to populations from different parts of the PRC.


Assuntos
Pulmão/fisiologia , Exposição Ocupacional , Adulto , Fatores Etários , Constituição Corporal , China/epidemiologia , Estudos de Coortes , Dieta , Feminino , Geografia , Humanos , Masculino , Pessoa de Meia-Idade , Valores de Referência , Testes de Função Respiratória , População Rural , Fatores Sexuais , População Urbana
20.
Ann Intern Med ; 135(12): 1019-28, 2001 Dec 18.
Artigo em Inglês | MEDLINE | ID: mdl-11747380

RESUMO

BACKGROUND: Initial findings from the Dietary Approaches to Stop Hypertension (DASH)-Sodium Trial demonstrated that reduction of sodium intake in two different diets decreased blood pressure in participants with and without hypertension. OBJECTIVE: To determine effects on blood pressure of reduced sodium intake and the DASH diet in additional subgroups. DESIGN: Randomized feeding study. SETTING: Four clinical centers and a coordinating center. PARTICIPANTS: 412 adults with untreated systolic blood pressure of 120 to 160 mm Hg and diastolic blood pressure of 80 to 95 mm Hg. INTERVENTION: Participants followed the DASH diet or a control (typical U.S.) diet for three consecutive 30-day feeding periods, during which sodium intake (50, 100, and 150 mmol/d at 2100 kcal) varied according to a randomly assigned sequence. Body weight was maintained. MEASUREMENTS: Systolic and diastolic blood pressure. RESULTS: In all subgroups, the DASH diet and reduced sodium intake were each associated with significant decreases in blood pressure; these two factors combined produced the greatest reductions. Among nonhypertensive participants who received the control diet, lower (vs. higher) sodium intake decreased blood pressure by 7.0/3.8 mm Hg in those older than 45 years of age (P < 0.001) and by 3.7/1.5 mm Hg in those 45 years of age or younger (P < 0.05). CONCLUSION: The DASH diet plus reduced sodium intake is recommended to control blood pressure in diverse subgroups.


Assuntos
Pressão Sanguínea/fisiologia , Dieta Hipossódica , Hipertensão/prevenção & controle , Adulto , Fatores Etários , Etnicidade , Feminino , Humanos , Hipertensão/etnologia , Hipertensão/fisiopatologia , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Análise de Regressão , Fatores Sexuais
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