19 research outputs found
Thrombotic Obstruction of Mechanical Prosthetic Valve in Mitral Position The Old “X-Ray” Fights the New 3-Dimensional Transesophageal Echocardiography
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Reduction in Recurrent Cardiovascular Events with Prasugrel Compared with Clopidogrel in Patients with Acute Coronary Syndromes from the TRITON-TIMI 38 Trial
Aims: In the TRITON-TIMI 38 trial, greater platelet inhibition with prasugrel reduced the first occurrence of the primary endpoint (cardiovascular death, MI, or stroke) compared with clopidogrel in patients with an acute coronary syndrome (ACS) undergoing planned percutaneous coronary intervention. We hypothesized that prasugrel would reduce not only first events but also recurrent primary endpoint events and therefore total events compared with clopidogrel. Methods and results: Poisson regression analysis was performed to compare the number of occurrences of the primary endpoint between prasugrel and clopidogrel in TRITON-TIMI 38. Landmark analytic methods were used to evaluate the risk of a recurrent primary endpoint event following an initial non-fatal endpoint event. Among patients with an initial non-fatal event, second events were significantly reduced with prasugrel compared to clopidogrel (10.8 vs. 15.4%, HR 0.65, 95% CI 0.46–0.92; P = 0.016), as was CV death following the non-fatal event (3.7 vs. 7.1%, HR 0.46, 95% CI 0.25–0.82; P = 0.008). Overall there was a reduction of 195 total primary efficacy events with prasugrel vs. clopidogrel (rate ratio 0.79, 95% CI 0.71–0.87; P < 0.001). Recurrent bleeding events occurred infrequently (TIMI major non-CABG bleeds: four with prasugrel and two with clopidogrel). Study drug discontinuation was frequent following the initial major bleeding event (42% of patients discontinued study drug). Conclusion: While standard statistical analytic techniques for clinical trials censor patients who experience a component of the primary composite endpoint, total cardiovascular events remain important to both patients and clinicians. Prasugrel, a more potent anti-platelet agent, reduced both first and subsequent cardiovascular events compared with clopidogrel in patients with ACS
Right Ventricular Strain and Dyssynchrony Assessment in Arrhythmogenic Right Ventricular Cardiomyopathy: Cardiac Magnetic Resonance Feature-Tracking Study
BACKGROUND:
Analysis of right ventricular (RV) regional dysfunction by cardiac magnetic resonance (CMR) imaging in arrhythmogenic RV cardiomyopathy (ARVC) may be inadequate because of the complex contraction pattern of the RV. Aim of this study was to determine the use of RV strain and dyssynchrony assessment in ARVC using feature-tracking CMR analysis.
METHODS AND RESULTS:
Thirty-two consecutive patients with ARVC referred to CMR imaging were included. Thirty-two patients with idiopathic RV outflow tract arrhythmias and 32 control subjects, matched for age and sex to the ARVC group, were included for comparison purpose. CMR imaging was performed to assess biventricular function; feature-tracking analysis was applied to the cine CMR images to assess regional and global longitudinal, circumferential, and radial RV strains and RV dyssynchrony (defined as the SD of the time-to-peak strain of the RV segments). RV global longitudinal strain (-17\ub15% versus -26\ub16% versus -29\ub16%; P-23.2%, SD of the time-to-peak RV longitudinal strain >113.1 ms, and SD of the time-to-peak RV circumferential strain >177.1 ms allowed correct identification of 88%, 75%, and 63% of ARVC patients with no or only minor CMR criteria for ARVC diagnosis.
CONCLUSIONS:
Strain analysis by feature-tracking CMR helps to objectively quantify global and regional RV dysfunction and RV dyssynchrony in patients with ARVC and provides incremental value over conventional cine CMR imaging
Evaluation of in-stent restenosis in the APPROACH trial (assessment on the prevention of progression by Rosiglitazone on atherosclerosis in diabetes patients with cardiovascular history)
To determine (1) the medium-term effect of rosiglitazone and glipizide on intra-stent neointima hyperplasia, (2) restenosis pattern as assessed by intra-vascular ultrasound (IVUS) and quantitative coronary angiography (QCA) in patients with T2DM and coronary artery disease. A total of 462 patients with T2DM were randomized to rosiglitazone or glipizide for up to 18 months in the APPROACH trial, and had evaluable baseline and follow-up IVUS examinations. There was no significant difference in the size of plaque behind stent between the rosiglitazone and glipizide groups at 18 months among those treated with a bare metal stent (−5.6 mm3 vs. 1.9 mm3; P = 0.61) or with a drug-eluting stent (12.1 mm3 vs. 5.5 mm3; P = 0.09). Similarly, there was no significant difference in percentage intimal hyperplasia volume between the rosiglitazone and glipizide groups at 18 months among those treated with a bare metal stent (24.1% vs. 19.8%; P = 0.38) or with a drug-eluting stent (9.8% vs. 8.3%; P = 0.57). QCA data (intra-stent late loss, intra-stent diameter stenosis or binary restenosis) were not different between the rosiglitazone and glipizide groups. This study suggests that both rosiglitazone and glipizide have a similar effect on neointimal growth at medium term follow-up, a finding that warrants investigation in dedicated randomized trials
Effects of Anacetrapib in Patients with Atherosclerotic Vascular Disease
BACKGROUND:
Patients with atherosclerotic vascular disease remain at high risk for cardiovascular events despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels. The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels. However, trials of other CETP inhibitors have shown neutral or adverse effects on cardiovascular outcomes.
METHODS:
We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with atherosclerotic vascular disease who were receiving intensive atorvastatin therapy and who had a mean LDL cholesterol level of 61 mg per deciliter (1.58 mmol per liter), a mean non-HDL cholesterol level of 92 mg per deciliter (2.38 mmol per liter), and a mean HDL cholesterol level of 40 mg per deciliter (1.03 mmol per liter). The patients were assigned to receive either 100 mg of anacetrapib once daily (15,225 patients) or matching placebo (15,224 patients). The primary outcome was the first major coronary event, a composite of coronary death, myocardial infarction, or coronary revascularization.
RESULTS:
During the median follow-up period of 4.1 years, the primary outcome occurred in significantly fewer patients in the anacetrapib group than in the placebo group (1640 of 15,225 patients [10.8%] vs. 1803 of 15,224 patients [11.8%]; rate ratio, 0.91; 95% confidence interval, 0.85 to 0.97; P=0.004). The relative difference in risk was similar across multiple prespecified subgroups. At the trial midpoint, the mean level of HDL cholesterol was higher by 43 mg per deciliter (1.12 mmol per liter) in the anacetrapib group than in the placebo group (a relative difference of 104%), and the mean level of non-HDL cholesterol was lower by 17 mg per deciliter (0.44 mmol per liter), a relative difference of -18%. There were no significant between-group differences in the risk of death, cancer, or other serious adverse events.
CONCLUSIONS:
Among patients with atherosclerotic vascular disease who were receiving intensive statin therapy, the use of anacetrapib resulted in a lower incidence of major coronary events than the use of placebo. (Funded by Merck and others; Current Controlled Trials number, ISRCTN48678192 ; ClinicalTrials.gov number, NCT01252953 ; and EudraCT number, 2010-023467-18 .)
Uncommon cause of ST-segment elevation in V1-V3: incremental value of cardiac magnetic resonance imaging
Although ST-segment elevation in precordial leads is a
characteristic of anterior left ventricular infarction (LVI), it
may also be observed in patients with proximal right coronary
occlusion. An isolated right ventricular infarction
(RVI) accounts for only 3 % of all myocardial infarctions
(MI) [1]; in these cases, the ST-segment elevation in the
precordial leads V1\u2013V3 also may occur in the absence of
inferior electrocardiographic changes [2], whereas the
combination of RVI with inferior LVI suppresses ST-segment
elevation in the precordial leads and yields an STsegment
elevation in leads DII, DIII, and aVF [3].
Although certain electrocardiographic features have been
suggested to help differentiate ST-segment elevation secondary
to isolated RVI from LVI [3], it may be impossible
to make a differential diagnosis on the basis of electrocardiography
alone because these features are not pathognomonic.
Furthermore, when a patient is admitted for
typical chest pain, slight ST-segment elevation in leads
V1\u2013V3 and significant increase of cardiac troponin but
with normal coronary main vessels at the coronary angiography,
the diagnosis of a RVI is challenging; taking into
account the multiple causes of myocardial injury and
treatment consequences, there is great clinical need to
clarify the underlying reason for cardiac troponin release.
Although some studies report that echocardiography is a
valuable clinical tool for the evaluation of global RV
function [4], geometric assumptions in modeling the
complex RV shape restricts the ability of this technique in
accurate and precise quantification of RV function; furthermore,
RV function assessment can be difficult in
patients with poor acoustic window or when minor alterations
of RV function are present.
Cardiac magnetic resonance (CMR) provides a comprehensive,
multifaceted view of the heart and can be
useful to characterize an infarct site and size accurately [5].
CMR in this particular setting can confirm the presence of
a minor RVI and aid to exclude other potential causes of
troponin rise with normal coronary main vessels at the coronary
angiography, such as embolic myocardial infarction or
myocarditis [6]. Acute MI treatment [7\u201310] and traditional
predictors of long-term mortality after acute MI are well
characterized [11\u201314] but with introduction of CMR, new
predictors of cardiovascular events are emerging [15, 16] and
the evaluation of RV function using CMR can improve risk
stratification and potentially refine patient management after
MI [17]. Moreover, the extent of myocardial scar characterized
by CMR is significantly associated with the occurrence
of spontaneous ventricular arrhythmias [18].
There have been few reports of anterior ST-segment
elevation caused by isolated RVI due to right ventricle
branch occlusion [19\u201321]. Occlusion of the conus branch
has been described essentially as a complication of coronary
angioplasty or during cardiac surgery [19\u201321]. Only
one report described a spontaneous RVI with culprit lesion
in the conus branch [22]. Assessment of isolated RVI due
to a critical stenosis of the conus branch by magnetic resonance
is never been reported