March 2004 Br J Cardiol 2004;11:144-7
Christodoulos Stefanadis
One of the main targets of current research in cardiology is a diagnostic modality able not only to identify vulnerable atherosclerotic lesions but also to monitor the effects of therapeutic interventions on plaque composition. Most of the currently available techniques identify luminal diameter or stenosis, wall thickness or plaque volume, but are not capable of recognising vulnerable plaques that are prone to rupture. Thermography is a new technique which provides insight into the local inflammatory process within the atherosclerotic plaque. In this review we will present in detail the developments and the clinical implications of thermography in the human arterial system.
March 2004 Br J Cardiol 2004;11:138-43
ohn HB Scarpello
The prevalence of type 2 diabetes is set to double over the next 25 years, leading to substantial morbidity and mortality, particularly from macrovascular diabetic complications. Pre-diabetic dysglycaemia, characterised by impaired glucose tolerance (IGT) and/or impaired fasting glucose (IFG), is associated with an increased risk of developing both type 2 diabetes and cardiovascular disease. IGT and IFG appear well before type 2 diabetes is diagnosed, thereby presenting an opportunity for intervention to reduce the future burden of diabetes and cardiovascular disease. Intensive lifestyle interventions are effective in preventing or delaying diabetes but are difficult to sustain long term. Intervention trials with pharmacological agents, e.g. the Diabetes Prevention Program (DPP) with metformin, and the STOP-NIDDM study with acarbose, have demonstrated significant decreases in the risk of progression to type 2 diabetes in populations with IGT. Moreover, preliminary evidence with these agents supports a possible beneficial effect on cardiovascular outcomes.
March 2004 Br J Cardiol 2004;11:129-36
Christopher J Packard
Recent trials have broadened the evidence base for statin use. It has now been documented that these drugs are effective agents not only in the general at-risk population, but also in the primary and secondary prevention of coronary heart disease in type 2 diabetics and in the elderly. The Heart Protection Study demonstrated the benefits of statin therapy in diabetics free of vascular disease, regardless of initial low-density lipoprotein (LDL) cholesterol level. Age is no longer a barrier to treatment, as revealed in the Prospective Study of Pravastatin in the Elderly at Risk, a trial which found that even a relatively brief period of statin therapy in elderly patients can result in a 19% reduction in the risk of a coronary event.
Statins have the ability to lower the plasma concentration of all apoB-containing lipoproteins. This may help explain their clinical efficacy in diabetics who generally have unremarkable LDL-cholesterol levels. Most currently available statins are also able to induce a modest (5% to 10%) rise in high-density lipoprotein cholesterol, an effect that appears distinct from LDL lowering. This broadens their use to subjects with a variety of problems such as the metabolic syndrome and insulin resistance.
The success of large-scale trials in coronary heart disease contrasts with the abundant evidence of under-treatment, even in high-risk groups. Thus the greatest need, at present, is to close the gap between the principles and practice of coronary disease prevention.
March 2004 Br J Cardiol 2004;11:123-27
Anthony H Barnett
Treatment to reduce blood pressure is effective in preventing and slowing the progression of the vascular complications of diabetes. Recent studies have suggested that use of antihypertensives that inhibit the renin-angiotensin system may have particular benefit in patients with type 2 diabetes in terms of cardiovascular and renal protection. Present practice is to use angiotensin-converting enzyme (ACE) inhibitors as first-line agents, with angiotensin II receptor antagonists (AIIAs) as back-up drugs in the event of side effects or intolerance. The findings of recent trials with AIIAs, however, suggest that they are an equivalent class of drugs to the ACE inhibitors from the point of view of renal profile and that their better side-effect profile could also make them suitable first-line drugs for patients with microalbuminuria and overt nephropathy.
March 2004 Br J Cardiol 2004;11:112-7
Bryan Williams, Neil Poulter
The British Hypertension Society (BHS) has recently published its latest guidance for the management of hypertension, BHS-IV.1,2 This article summarises these recommendations and discusses the main features of the new guidance.
March 2004 Br J Cardiol (Acute Interv Cardiol) 2004;11:AIC 9–AIC 13
Ghada W Mikhail, Flavio Airoldi, Antonio Colombo
Percutaneous treatment of bifurcation coronary lesions is less successful than treatment of non-bifurcation lesions, with a higher incidence of side branch occlusion and restenosis.
The ‘crush technique’ was developed to ensure complete coverage of the ostium of the side branch, where restenosis frequently occurs. Drug-eluting stents are deployed in both side and main branches. The main branch stent crushes the side branch stent against the wall of the main vessel. The ‘reversed crush’ is used when the side branch result is unsatisfactory following stenting of the main branch, or when a 6F guiding catheter is needed.
The ‘skirt technique’ was designed to treat pseudobifurcation lesions (lesions in the main branch which are immediately proximal to a bifurcation). It involves sandwiching two balloons in one stent.
Preliminary results using the crush technique in 35 patients show angiographic success in all lesions.
January 2004 Br J Cardiol 2004;11:75-9
Huw Williams, Elizabeth Morrison, Debra Elliott
Echocardiography remains the ‘gold standard’ for the objective assessment of left ventricular systolic function. Even with the high prevalence of left ventricular systolic dysfunction, echocardiography is not universally available within UK primary care, despite the fact that the condition is predominantly managed within this arena.
We describe a service within one Primary Care Trust, where general practitioners and nurses refer patients who are suspected of having, or who are at high risk of developing heart failure, for a clinical assessment and an echocardiogram. Following this, a treatment plan is formulated and those with systolic dysfunction are followed up by a heart failure nurse. She ensures that the treatment regimen is adhered to and that the correct physiological and biochemical monitoring takes place.
In our study we found that of those referred, only 33% had evidence of left ventricular systolic dysfunction, with 62% showing normal function. Of those patients with left ventricular systolic dysfunction, 86% required a significant change in their medication. Three months after the assessment, using the ‘Minnesota Living with Heart Failure Questionnaire’, considerable improvement was noted in the quality of life of patients with left ventricular systolic dysfunction. This paper suggests that there is considerable scope for improvement in the management of chronic heart failure.
January 2004 Br J Cardiol 2004;11:71-4
Philip H Evans, Manjo Luthra, Christine Pike, Alison Round, Maurice Salzmann
The secondary prevention of coronary heart disease (CHD) is a recognised priority for primary care and is a fundamental part of the published National Service Framework (NSF). The majority of patients receive statins to reduce their total cholesterol (TC) and low-density lipoprotein chol-esterol (LDL-C) levels. The NSF set out targets for both TC and LDL-C. This study was designed to investigate the applicability of these targets in a real-life setting. One hundred and ten patients aged under 75 with established CHD were screened and their lipids measured. Eighty (73%) were on a statin. Mean TC was 6.3 mmol/L before treatment and 4.8 mmol/L after. Of these 80 patients, 46 (58%) had a TC below 5.0 mmol/L. Only 39% of patients met the stricter criterion of less than 5.0 mmol/L and a 25% fall in TC. No patient whose pre-treatment TC was below 5.0 mmol/L had reached a 25% reduction as well. The use of a threshold and a percentage may be potentially confusing to GPs and reduce the implementation of these targets.
January 2004 Br J Cardiol 2004;11:69-70
F Runa Ali, Andrew J Hails, Bernard Yung
In patients presenting with persistent hoarseness due to left recurrent laryngeal nerve (LRLN) palsy and an abnormal left hilum on chest radiographs, a major cause is bronchogenic carcinoma. We describe two cases presenting with such a combination of symptoms and signs in whom a diagnosis of bronchogenic carcinoma was suspected. In each case, the LRLN palsy was in fact due to direct compression of the nerve by an aortic aneurysm.
January 2004 Br J Cardiol 2004;11:65-8
Johannes A Kragten, Gilbert Wagener
The ACTION (A Coronary disease Trial Investigating Outcome with Nifedipine GITS) study is the largest ever performed randomised trial of an anti-anginal drug in patients with chronic stable angina. Its aim is to assess the effect of nifedipine GITS 60 mg versus placebo on standard therapy for coronary artery disease on event-free survival; its composite end point includes death from any cause, acute myocardial infarction, hospitalisation for overt heart failure, emergency coronary angiography, disabling stroke and procedures for peripheral revascularisation.
ACTION is one in a series of trials assessing drug effects in chronic stable coronary artery disease. The IONA (Impact Of Nicorandil in Angina) and EUROPA (EURopean trial On reduction of cardiac events with Perindopril in stable coronary artery disease) studies demonstrated that the K-ATP channel activator nicorandil and the angiotensin-converting enzyme inhibitor perindopril reduced the primary composite end point for cardiac events by 17% and 20%, respectively.
Nifedipine GITS is an effective antihypertensive and anti-anginal drug. In the INSIGHT trial, nifedipine GITS 30/60 mg demonstrated comparable outcomes to a diuretic combination therapy with significant effects on intermediate end points. ENCORE I (Evaluation of Nifedipine and Cerivastatin on Recovery of coronary Endothelial function) demonstrated that nifedipine GITS 30/60 mg positively affected the pathophysiology of coronary artery disease. We therefore anticipate that nifedipine will affect blood pressure, anginal symptoms and resulting complications, and the coronary atherosclerotic process in those patients randomised to receive this agent in the ACTION study.
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