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1.
J Hum Hypertens ; 25(12): 705-10, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21451570

ABSTRACT

High dietary salt is a major contributor to increased blood pressure, the leading risk for death worldwide. In several countries, national programmes to reduce dietary salt have been implemented with leadership and involvement of hypertension experts. Other hypertension experts may be interested in assisting or leading a national programme to reduce dietary salt, however, may not have the experience or training to do so. The article is based on the experiences of three hypertension experts who have led the development of national dietary salt reduction programmes in the United Kingdom, Australia and Canada. The article advises developing leadership and a coalition, conducting a nation-specific environmental scan of facilitators and barriers, estimating the national health and financial costs of high dietary salt and the benefits of reducing salt intake, obtaining core documents to provide the scientific rational for the programme, developing a policy statement to outline the required actions to be undertaken, engaging government and industry, using media to gain public support, overcoming industry supported opposition and sustaining the effort long term. Resources and potential sources for international collaboration are provided as well as caveats for developing the programme within the specific nations' context and overall effort to improve health. Developing and leading a national salt reduction programme is a major commitment, however, reducing dietary salt is estimated to be one of the most effective strategies to improve a nation's health.


Subject(s)
Diet, Sodium-Restricted/trends , Hypertension/prevention & control , National Health Programs/trends , Australia , Canada , Humans , Sodium Chloride, Dietary , United Kingdom
2.
Diabetologia ; 52(11): 2288-98, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19655124

ABSTRACT

AIMS/HYPOTHESIS: Improved glucose control in type 2 diabetes is known to reduce the risk of microvascular events. There is, however, continuing uncertainty about its impact on macrovascular disease. The aim of these analyses was to generate more precise estimates of the effects of more-intensive, compared with less-intensive, glucose control on the risk of major cardiovascular events amongst patients with type 2 diabetes. METHODS: A prospectively planned group-level meta-analysis in which characteristics of trials to be included, outcomes of interest, analyses and subgroup definitions were all pre-specified. RESULTS: A total of 27,049 participants and 2,370 major vascular events contributed to the meta-analyses. Allocation to more-intensive, compared with less-intensive, glucose control reduced the risk of major cardiovascular events by 9% (HR 0.91, 95% CI 0.84-0.99), primarily because of a 15% reduced risk of myocardial infarction (HR 0.85, 95% CI 0.76-0.94). Mortality was not decreased, with non-significant HRs of 1.04 for all-cause mortality (95% CI 0.90-1.20) and 1.10 for cardiovascular death (95% CI 0.84-1.42). Intensively treated participants had significantly more major hypoglycaemic events (HR 2.48, 95% CI 1.91-3.21). Exploratory subgroup analyses suggested the possibility of a differential effect for major cardiovascular events in participants with and without macrovascular disease (HR 1.00, 95% CI 0.89-1.13, vs HR 0.84, 95% CI 0.74-0.94, respectively; interaction p = 0.04). CONCLUSIONS/INTERPRETATION: Targeting more-intensive glucose lowering modestly reduced major macrovascular events and increased major hypoglycaemia over 4.4 years in persons with type 2 diabetes. The analyses suggest that glucose-lowering regimens should be tailored to the individual.


Subject(s)
Blood Glucose/analysis , Diabetes Mellitus, Type 2/physiopathology , Diabetic Angiopathies/prevention & control , Blood Glucose/metabolism , Blood Pressure , Cholesterol/blood , Clinical Trials as Topic , Diabetes Mellitus, Type 2/blood , Fasting , Follow-Up Studies , Glycated Hemoglobin/analysis , Homeostasis , Humans , Patient Compliance , Patient Selection , Risk Reduction Behavior , Treatment Outcome
3.
J Epidemiol Community Health ; 63(5): 379-85, 2009 May.
Article in English | MEDLINE | ID: mdl-19179368

ABSTRACT

BACKGROUND: Coronary heart disease (CHD) risk estimation tools are a simple means of identifying those at high risk in a community and hence a potentially cost-effective strategy for CHD prevention in resource-poor countries. Since India has few local data upon which to develop such a tool de novo, in this study a Framingham risk equation has been recalibrated to estimate CHD risks in a population from rural India and the sensitivity of the method to information resources examined. Recent surveys of this population have found high levels of cardiovascular risk factors, particularly metabolic risk factors and a high proportion of mortality due to cardiovascular diseases. METHODS: The proportion of a rural Indian population at high risk of CHD using three risk estimation equations was estimated. The first a published version of the Framingham risk equation, the second a recalibrated equation using local mortality surveillance data and local risk factor data, and the third a recalibrated equation using national mortality data and local risk factor data. RESULTS: The mean 10-year probability of CHD for adults >30 years was 10.4% (9.6% to 11.1%) for men and 5.3% (4.9% to 5.7%) for women using the Framingham equation; 10.7% (9.9% to 11.5%) for men and 4.2% (3.9% to 4.5%) for women using the local recalibration; and 18.9% (17.7% to 20.1%) for men and 8.2% (7.6% to 8.8%) for women using the national recalibration. CONCLUSION: These findings indicate that in India, equations recalibrated to summary national data are unlikely to be relevant to all regions of India and demonstrate the importance of local data collection to enable development of relevant CHD risk tools.


Subject(s)
Cardiovascular Diseases/epidemiology , Adult , Age Distribution , Aged , Cardiovascular Diseases/etiology , Epidemiologic Methods , Female , Humans , India/epidemiology , Male , Middle Aged , Rural Health/statistics & numerical data , Sex Distribution , Sex Factors
4.
Inj Prev ; 14(4): 232-7, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18676781

ABSTRACT

BACKGROUND: Little is known about the burden or causes of injury in rural villages in India. OBJECTIVE: To examine injury-related mortality and morbidity in villages in the state of Andhra Pradesh, India. METHODS: A verbal-autopsy-based mortality surveillance study was used to collect mortality data on all ages from residents in 45 villages in 2003-2004. In early 2005, a morbidity survey in adults was carried out using stratified random sampling in 20 villages. Participants were asked about injuries sustained in the preceding 12 months. Both fatal and non-fatal injuries were coded using classification methods derived from ICD-10. RESULTS: Response rates for the mortality surveillance and morbidity survey were 98% and 81%, respectively. Injury was the second leading cause of death for all ages, responsible for 13% (95% CI 11% to 15%) of all deaths. The leading causes of fatal injury were self-harm (36%), falls (20%), and road traffic crashes (13%). Non-fatal injury was reported by 6.7% of survey participants, with the leading causes of injury being falls (38%), road traffic crashes (25%), and mechanical forces (16.1%). Falls were more common in women, with most (72.3%) attributable to slipping and tripping. Road traffic injuries were sustained mainly by men and were primarily the result of motorcycle crashes (48.8%). DISCUSSION: Injury is an important contributor to disease burden in rural India. The leading causes of injury-falls, road traffic crashes, and suicides-are all preventable. It is important that effective interventions are developed and implemented to minimize the impact of injury in this region.


Subject(s)
Rural Health/statistics & numerical data , Wounds and Injuries/epidemiology , Accidental Falls/statistics & numerical data , Accidents, Traffic/statistics & numerical data , Adolescent , Adult , Age Distribution , Aged , Child , Child, Preschool , Epidemiologic Methods , Female , Humans , India/epidemiology , Infant , Infant, Newborn , Male , Middle Aged , Motorcycles , Self-Injurious Behavior/mortality , Wounds and Injuries/etiology , Young Adult
5.
Acta Orthop Scand ; 71(2): 122-8, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10852316

ABSTRACT

We performed a systematic survey of randomized trials to determine the effects of perioperative NSAIDs on the occurrence of heterotopic bone formation, gastrointestinal side-effects and long-term clinical outcomes after major hip surgery. 13 trials involving 4,129 individuals were identified. Overall, in 12 small trials of medium-to-high-dose regimens, there was a 57% reduction (95% confidence interval 51%-63%) in the risk of heterotopic bone formation. The results of one large trial of low-dose aspirin differed markedly (2% reduction (95% CI 12% reduction to 15% increase)). The NSAID regimens studied had no definite effect on gastrointestinal complications, and data about the effects of NSAIDs on pain and function were too few, and too incompletely reported, to draw conclusions about their effects on these outcomes. Routine prophylaxis against heterotopic bone formation with NSAIDs may be a useful adjuvant therapy for patients undergoing major hip surgery, but the overall balance of risks and benefits requires assessment in a large-scale randomized trial.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arthroplasty, Replacement, Hip/adverse effects , Ossification, Heterotopic/etiology , Ossification, Heterotopic/prevention & control , Randomized Controlled Trials as Topic , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Chemotherapy, Adjuvant , Gastrointestinal Diseases/chemically induced , Humans , Incidence , Ossification, Heterotopic/diagnostic imaging , Pain, Postoperative/prevention & control , Radiography , Regression Analysis , Research Design , Risk Factors , Treatment Outcome
6.
Acta Orthop Scand ; 71(2): 129-34, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10852317

ABSTRACT

2,649 patients scheduled for elective total hip replacement were recruited to the Heterotopic Bone Formation Sub-study of the Pulmonary Embolism Prevention Trial. Heterotopic bone formation was determined by radiographic examination and associated late postoperative outcomes were assessed by telephone interview. Heterotopic bone formation was observed in 627 (31%) of 2,048 radiographic examinations. There was no detectable effect of low-dose aspirin on the risks of heterotopic bone formation (RR 0.98; 95% CI 0.85-1.12), late postoperative pain (RR 1.10; 95%CI 0.91-1.35) or late postoperative impaired function (RR 1.03; 95% CI 0.94-1.12). The balance of benefits and risks of low-dose aspirin is determined by its effects on vascular events and bleeding, since it has no major effects on heterotopic bone formation or associated clinical outcomes.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arthroplasty, Replacement, Hip/adverse effects , Aspirin/therapeutic use , Ossification, Heterotopic/etiology , Ossification, Heterotopic/prevention & control , Activities of Daily Living , Aged , Arthroplasty, Replacement, Hip/psychology , Double-Blind Method , Female , Humans , Male , Ossification, Heterotopic/classification , Ossification, Heterotopic/diagnostic imaging , Pain, Postoperative/prevention & control , Patient Compliance , Radiography , Risk Factors , Severity of Illness Index , Treatment Outcome
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