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6th October 2008 @ 3:01pm |
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Volume 12, Number 4, July-August 2005HOT Br J Cardiol 2005;12:249-253. EDITORIALWhat’s in a name? From anticoagulation clinics to thrombosis management centres Br J Cardiol 2005;12:255-256. HOT This article describes the diagnosis, classification and management of atrial fibrillation (AF) in primary care. It looks at its increasing incidence, its risk factors, and the identification and classification of this common arrhythmia. The routine investigations for AF and its treatment, including drug therapy and cardioversion, are also discussed. Finally, with AF being a major risk factor for stroke, strategies to prevent thromboembolism are considered. Br J Cardiol 2005;12:308-311. HOT Treatments for heart failure include digoxin, angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, aldosterone antagonists and beta blockers. Beta blockers have been contra-indicated until fairly recently, with recognition of the role of the sympathetic nervous system in chronic progression of heart damage. Br J Cardiol 2005;12:313-317. HOT Atherosclerotic cardiovascular disease (CVD) is common in patients with diabetes, and antiplatelet therapy has been the cornerstone of preventative therapy for many years. The majority of the evidence for the use of aspirin in patients with diabetes comes from subgroup analysis of major secondary prevention trials. Secondary prevention data from the Antiplatelet Trialist’s Collaboration meta-analysis suggests that the benefit derived from aspirin is similar in diabetic and non-diabetic populations. In the general population, data from primary prevention studies have shown the benefit of aspirin in terms of cardiovascular mortality, but there is little evidence to suggest that aspirin is beneficial in terms of total or cardiovascular mortality for primary prevention in a diabetic population. Clopidogrel may have advantages over aspirin and combined therapy may be superior for certain types of coronary artery disease and stroke, although this is offset by an increased risk of haemorrhage in the latter setting. The use of aspirin in the prevention of CVD in patients with diabetes should therefore be focused on those with a history of vascular events or aggressively treated hypertension. Br J Cardiol 2005;12:275-282. REVIEWMilk, heart disease and obesity: an examination of the evidence Milk drinking causes a rise in serum cholesterol level and it is therefore assumed that this will increase vascular disease risk. At the same time, a reduction in blood pressure by milk is largely ignored. An overview of large, long-term cohort studies gives no evidence of an increase, but rather, a significant reduction in vascular disease risk in subjects with a high milk intake relative to those who report drinking little or no milk. Br J Cardiol 2005;12:283-290. HOT The efficacy and tolerability of two candesartan treatment regimens were evaluated in 578 severely hypertensive patients already receiving a diuretic plus an angiotensin-converting enzyme (ACE) inhibitor, a calcium channel blocker (CCB) or a beta blocker. Existing treatments were standardised during a two-week run-in period. Patients with uncontrolled blood pressure (diastolic blood pressure [DBP] > 90 mmHg) were randomly switched to a regimen comprising candesartan 16 mg plus hydrochlorothiazide (HCT) 12.5 mg once daily for four weeks (switch regimen, n=291), or had candesartan 8 mg once daily added to their existing treatment (add-on regimen, n=287). After four weeks’ treatment, mean sitting DBP was reduced from baseline by 11.2 mmHg (SD 11.2) and 13.9 mmHg (SD 11.5) in the switch and add-on treatment groups, respectively. Mean sitting SBP was decreased by 15.3 mmHg (SD 18.7) and 20.7 mmHg (SD 20.3), respectively. During an additional four weeks’ treatment, ‘switch’ non-responders had their doses of study medications doubled, resulting in a further reduction of 5.4 mmHg (SD 9.8) DBP and 5.9 mmHg (SD 14.9) SBP. Both treatment regimens were well tolerated. Thus, in patients with severe hypertension, adding candesartan to a standard-dose two-drug combination, or switching from a pre-existing two-drug, standard-dose combination to high-dose candesartan plus HCT enables enhanced BP control, with superiority of the three- over the two-drug combination. Br J Cardiol 2005;12:291-297. REVIEWCardiac patients’ concerns and desire for information: a case for unmet needs Tailoring healthcare provision to fulfil patients' needs is a principal objective of health services. Data on needs are sparse, especially in patients with coronary heart disease, who tend to have a high mortality rate, who often require admission to hospital and have an impaired health-related quality of life. A novel questionnaire was administered concomitantly with generic and specific quality of life tools in a cross-sectional study of a random sample of patients (n=242) aged 31–93 years (median 71 years) admitted with suspected acute coronary syndromes. Br J Cardiol 2005;12:298-301. REVIEWProfile of documented medical history of chest pain: a multicentre audit of 1,226 consecutive patients with validated acute MI This study set out to evaluate the completeness of medical records of chest pain. A planned, multicentre, structured abstraction of data from case-notes was made at 20 adjacent acute hospitals in Yorkshire on 1,226 consecutive patients presenting with chest pain and validated myocardial infarction (MI). The hospital records included those collected by ambulance crews, accident and emergency staff, and admitting medical teams. The main outcome measure was completeness of medical records with regard to 10 commonly advocated descriptors of chest pain. Br J Cardiol 2005;12:302-305. REVIEWNew analysis of LIFE trial shows reduction of new-onset atrial fibrillation with losartan A new analysis of the LIFE study has shown that losartan can reduce new-onset atrial fibrillation in hypertensive patients with left ventricular hypertrophy. General practitioner Brian Crichton summarises this new analysis and explains how losartan might achieve these effects. Br J Cardiol 2005;12:268-269. CASE REPORTTranexamic acid and acute myocardial infarction The plasminogen activator inhibitors have an important therapeutic role in controlling bleeding in patients with congenital and acquired coagulation disorders. They are being increasingly used in patients with blood loss and to prevent bleeding. However, these antifibrinolytic agents can also facilitate the development of thrombosis. We report a patient with severe gastrointestinal bleeding who developed acute myocardial infarction following the administration of the antifibrinolytic agent, tranexamic acid. Br J Cardiol 2005;12:306-307. AICAre drug-eluting stents living up to the hype?
Br J Cardiol 2005;12:AIC42-AIC44. HOT The National Institute for Clinical Excellence (NICE) stent appraisal (2003) defined criteria for the use of drug-eluting stents (DES) on the basis of lesion length, vessel diameter and the absence of recent myocardial infarction or intra-luminal thrombus. The appraisal suggested that as many as one third of all stents may need to be DES. Br J Cardiol 2005;12:AIC45-AIC48. AICDiabetic revascularisation by coronary angioplasty: is one stent better than another? As confidence in the use of drug-eluting stents (DES) increases, they are being used in patients with progressively more complex disease. Diabetes is still an independent risk factor for restenosis along with lesion length and reference vessel diameter. Br J Cardiol 2005;12:AIC49-AIC53. HOT The objective of this study was to assess the feasibility and impact of providing a primary percutaneous coronary intervention (PCI) programme for ST elevation myocardial infarction (STEMI) in a district general hospital (DGH) in the UK. Br J Cardiol 2005;12:AIC56-AIC59. AICSub-intimal dissection guided by retrograde angiography to recanalise a chronic coronary artery occlusion Br J Cardiol 2005;12:AIC61. AICOral treatments for pulmonary arterial hypertension The management of pulmonary arterial hypertension (PAH) has changed dramatically over the last decade. Where once the physician had only limited tools to combat this devastating condition, recent randomised controlled trials have shown that there are now treatments that both prolong the rate of progression and improve survival. The ‘gold standard’ of treatment, due to its beneficial effect on survival, is epoprostenol, a prostacyclin analogue. However, there are a number of problems with the prostacyclin analogues, mainly centred on their administration and cost, which led to their use only in severely ill patients. A better understanding of the pathophysiology of PAH has led to a number of other pharmacological targets, namely antagonism of endothelin (ET) receptors and increasing local levels of nitric oxide (NO) via inhibition of phosphodiesterase 5. Br J Cardiol 2005;12:AIC62-AIC67. |