31-08-2013 t/m 4-09-2013 ESC Congres 2013 Amsterdam (NH)

Auteur Topic: 31-08-2013 t/m 4-09-2013 ESC Congres 2013 Amsterdam (NH)  (gelezen 26869 keer)

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Reactie #60 Gepost op: 2 september 2013, 10:05:51


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Reactie #61 Gepost op: 2 september 2013, 11:27:59
Prof. David Hasdai FESC / Prof. Steen Dalby Kristensen FESC

ESC TV 2013 - Village 3: Become a part of the ischaemia congress programme


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Reactie #62 Gepost op: 2 september 2013, 12:04:28
In this 3 minute video interview conducted at the ESC conference, Prof. Juan Carlos Plana introduces the joint US/EU statement on imaging evaluation of cardiovascular complications of radiotherapy.

Interview with Prof. Juan Carlos Plana - ESC 2013: Statement on CV risk following radiotherapy


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Reactie #63 Gepost op: 2 september 2013, 12:08:29
In this 3 minute video interview conducted at the ESC conference, Associate Prof. Koen Nieman discusses the utility of Computer Tomography (CT) scanning in patients with valvular heart disease.

Interview with Dr Koen Nieman - ESC 2013: Computer tomography scanning


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Reactie #64 Gepost op: 2 september 2013, 12:11:51
Prof. Richard Underwood discusses the changed landscape of risk assessment before non-cardiac surgery, at the ESC conference in Amsterdam.

Interview with Prof. Richard Underwood - ESC 2013: Perioperative beta-blockade


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Reactie #65 Gepost op: 2 september 2013, 12:22:02
In this 5 minute video interview conducted at the ESC conference, Prof. Antonio Coca outlines key recommendations on hypertension from the European Society of Hypertension and the European Society of Cardiology.

Interview with Prof. Antonio Coca - ESC 2013: New 2013 guidelines for hypertension


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Reactie #66 Gepost op: 2 september 2013, 12:33:53
Citaat
AMSTERDAM | Mon Sep 2, 2013 5:53am EDT
(Reuters) - Diabetes pills known as DPP-4 therapies got a mixed safety report on Monday as studies showed they did not raise the risk of heart attacks but might be linked to heart failure, where the heart fails to pump blood adequately.

"It is a little bit concerning," said Dr. Christopher Grainger of Duke University Medical Center, who was not involved in the research. "I'm sure the FDA (U.S. Food and Drug Administration) will want to know more about it."

http://www.reuters.com/article/2013/09/02/us-heart-diabetes-idUSBRE98103I20130902


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Reactie #67 Gepost op: 2 september 2013, 12:47:52
Amsterdam, The Netherlands – Monday 2 september 2013: Transcatheter aortic valve implantation (TAVI) is feasible in patients with bicuspid aortic valve, according to research presented at ESC Congress 2013 today by Dr Timm Bauer from Germany. The findings open up a new treatment possibility in patients with BV, which has been considered a contraindication for TAVI.

Bicuspid aortic valve (BV) is the most common congenital valvular abnormality, occurring in 1-2% of the general population. Two of the aortic valvular leaflets fuse during development resulting in a valve that is bicuspid instead of the normal tricuspid configuration. BV is associated with increased mechanical stress which predisposes to calcification and development of aortic stenosis which narrows the opening of the aortic valve.

Dr Bauer said: “TAVI is used to treat elderly high risk patients with severe aortic stenosis. Despite previous assumptions the frequency of BV is quite high even among elderly patients with symptomatic aortic stenosis.”

But he added: “BV has been considered a relative contraindication to TAVI. One of the main reasons is the presumed risk for relevant aortic regurgitation, where blood leaks back through the aortic valve during ventricular diastole. However, case reports and small case series have suggested that TAVI can be successfully performed with acceptable clinical outcomes in high risk patients with BV.”

The study prospectively enrolled 1,424 patients with severe aortic stenosis undergoing TAVI into the German TAVI-Registry between January 2009 and June 2010. For the present analysis patients with valve-in-valve procedures were excluded and those with BV (n=38, 2.7%) were compared to those with tricuspid aortic valve (TV) (n=1,357, 97.3%). Patient characteristics did not markedly differ and procedural success was very high in both groups.

The researchers found a higher rate of relevant aortic regurgitation (≥ grade 2) after TAVI among patients with BV (BV=25%, TV=14.7%; p=0.05) (see figure), whereas pacemakers were more often implanted in patients with TV (BV=16.7%, TV=35.4%; p=0.02). Dr Bauer said: “The higher rate of aortic regurgitation in BV patients was expected and is still acceptable because it did not lead to higher mortality. However, substantial improvements in the field of device technology and imaging have to be made to perform TAVI in a safer and more effective way in BV-patients.”

He added: “The difference between groups in the need for a pacemaker can be partly explained by the higher implantation rate of Sapien EdwardsTM prosthesis. Maybe anatomic differences in the aortic root or left ventricular outflow tract of BV play a role, too.”

The 30-day mortality was similar in both cohorts (BV=10.5%, TV=10.8%). In a Cox proportional regression analysis after adjustment for several risk factors BV was not associated with higher 1-year mortality (hazard ratio=0.64, 95% confidence interval [CI]=0.29-1.41). Dr Bauer said: “Both 30-day and 1-year mortality were not elevated in BV patients compared to patients with TV. We can therefore conclude that TAVI gave a satisfactory clinical outcome in BV patients despite their higher rate of relevant aortic regurgitation.”

He concluded: “As the nature of our study is exploratory and the number of BV patients is quite low, the findings should be interpreted cautiously. However, our study opens up a new treatment possibility for selected high risk patients with BV, who until now have received medical treatment only or conventional valve surgery. TAVI has the potential to be a safe alternative in these patients, but more studies are needed to support these findings.”



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Reactie #68 Gepost op: 2 september 2013, 12:49:50
Amsterdam, The Netherlands – Monday 2 September 2013: TAVI is a safe alternative to redo cardiac surgery for failing bioprosthetic valves, according to research presented at the ESC Congress today by Dr Spyridon Katsanos from The Netherlands. The findings suggest that transcatheter aortic valve implantation (TAVI) is a treatment alternative for inoperable elderly patients and high risk patients with failing bioprostheses.

Use of bioprosthetic heart valves has dramatically increased (from 18% in 1991 to 59% in 2003), mainly in older patients with comorbidities. This is due to the increased risk of bleeding complications associated with lifelong use of anticoagulation for mechanical prostheses.

But structural valve deterioration is one the main complications associated with bioprosthetic heart valves. In large registries including more than 300 000 patients undergoing aortic valve replacement the reoperation rate for patients receiving a bioprosthesis was 3.1% at 11-13 years of follow-up compared with 2.3% reoperation rate for recipients of an aortic mechanical prosthesis.1

Dr Katsanos said: “Reoperation for failed bioprostheses, also called redo cardiac surgery, is associated with increased rates of mortality and morbidity. Less invasive treatments have emerged such as transcatheter valve-in-valve implantation, a type of TAVI operation which is a safe therapeutic option for patients with failed bioprostheses and contraindications for surgery. But until now there has not been a direct comparison of survival between high risk patients treated with either reoperation or a TAVI operation.”

The current study assessed the prognosis of patients with failed bioprosthetic aortic and mitral valves and high predicted operative risk who underwent transcatheter valve-in-valve intervention with the Edwards Sapien (23 or 26 mm) valve. They were compared with a historical cohort of patients who underwent elective redo cardiac surgery for failing mitral and aortic prostheses and failing mitral valve annuloplasty.

The TAVI group (age 80±2 years, 25% men) included 12 patients with failing aortic bioprostheses, 2 with failing mitral bioprostheses and 2 with failed mitral valve annuloplasty. The redo cardiac surgery group (age 70±1 years, 50% men) had 15 patients with failing aortic bioprostheses and 1 with failing mitral bioprostheses. The reason for valve dysfunction was stenosis in 11 patients, regurgitation in 14 patients and mixed pathology in 7 patients. Patients with endocarditis were excluded. Both groups had similar operative risk, New York Heart Association functional class, and left ventricular ejection fraction.

After a median follow up of 21 (range 7-44) months, 10 (30%) patients died. As shown in the figure, 3-year survival did not differ between patients treated with transcatheter valve-in-valve implantation and those treated with redo cardiac surgery (log-rank p=0.939).

Dr Katsanos said: “We have shown for the first time that the long term survival of high risk patients with failing bioprostheses treated with transcatheter valve-in-valve implantation is comparable to high risk patients treated with redo cardiac surgery.”

He concluded: “Transcatheter valve-in-valve implantation is a minimally invasive procedure performed through transfemoral or transapical approach under fluoroscopic guidance and does not require sternotomy and cardiopulmonary bypass. Elderly patients deemed not operable and also high risk patients with failing bioprostheses may have a treatment alternative to redo cardiac surgery.”




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Reactie #69 Gepost op: 2 september 2013, 12:51:49
Amsterdam, The Netherlands – Monday 2 September 2013: Women are 25% less likely to die one year after TAVI than men, according to research presented at the ESC Congress today by Dr Mohammad Sherif from Germany. The findings suggest that TAVI might be the preferred treatment option for elderly women with symptomatic severe aortic stenosis.

Dr Sherif said: “Earlier studies on the impact of gender on outcome after transcatheter aortic valve implantation (TAVI) have had conflicting results. A Canadian study reported in 641 consecutive patients that female sex is associated with a better long-term and short-term survival after TAVI.1 An Italian study of 305 high risk patients found no gender differences in composite safety and efficacy endpoints at 30 days and one year after TAVI.”

The current analysis examined gender differences in outcomes for 1432 consecutive patients from 27 centers who were enrolled in the German TAVI registry between January 2009 and June 2010. Women comprised 57.8% of the cohort. At baseline the average age of women was 83 years vs 80 years for men. Women had aortic valve gradients at baseline of 52 mmHg vs 45 mmHg for men (severe aortic stenosis is defined as gradients exceeding 40 mmHg).

At baseline men had more prior myocardial infarction (22% vs 11.5%, p<0.001); more extensive coronary artery disease (36% vs 16%, p<0.001); more history of open-heart surgery (33% vs 14%, p<0.001); more peripheral vascular disease (37% vs 26%, p<0.001); and more COPD (28% vs 21%, p<0.001).

During the TAVI procedure, 25.2% of women had vascular complications (including iliac artery dissection, and bleeding from the puncture site requiring blood transfusion) compared to 17.2% of men (p<0.001).

At 30 days follow-up mortality was 7.6% for women versus 8.6% for men (p=0.55); however by one year the all cause mortality was 17.3% for women vs 23.6% for men (p<0.01). Dr Sherif said: “Our results show that mortality at 30 days was the nearly same for women and men. Women’s higher survival rate at one year could be explained by their longer life expectancy and lower rates of comorbidity in comparison to men.”

The investigators did a multivariate analysis to adjust for the effect of differences between women and men in demographic, procedural, and clinical variables on one year mortality. Figure 1 shows women’s survival advantage at 12 months. Even after adjustment, female gender was an independent predictor for one-year survival after TAVI with a hazard ratio of 0.75.

Dr Sherif said: “This means that women are 25% less likely to die after TAVI than men.

Dr Sherif said: “Lower levels of fibrosis in women might explain the more rapid reversal of myocardial hypertrophy after correction of aortic stenosis and might partially explain the better outcome in women compared with men.3 This might account for the time delay in the female advantage, since the reversal process takes longer than 30 days.”

He added: “As a limitation for registry data, these data are observational, and therefore can only be considered to be hypothesis generating rather than causative.”

Dr Sherif concluded: “Future work should focus on the effect of sex differences in outcomes for intermediate risk patients undergoing TAVI, and provide longer-term follow up for high-risk patients.”