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EuroPCR 2011 research highlights:
A slideshow presentation
EuroPCR 2011 Research Highlights
                    EuroPCR 2011 took place in Paris, France, from May 17 through May 20,
                    2011. The conference was attended by 12 567 people.

                    Key trials/topics presented at the conference include:

                    RECLOSE 2-ACS: Poor clopidogrel responders with ACS face twofold
                    risk of cardiac death
                    DISCOVER FLOW: Adding function to CTA with "noninvasive FFR" ups
                    accuracy, may cut procedures
                    TAVI spotlight swings to risks of paravalvular leaks
                    Renal denervation: Wider role for procedure considered, amid calls for
                    more studies
                    BASE-ACS: Could a bare-metal stent be "noninferior" to a leading DES?
                    SOURCE: New numbers from registry bolster PARTNER results in real
                    world
                    DES meta-analysis: Less stent thrombosis with biodegradable vs
                    permanent polymers
                    SCAAR registry: Transradial PCI cuts mortality in STEMI


                    View our complete EuroPCR coverage here.
RECLOSE 2 ACS
                Responsiveness to Clopidogrel and Stent-Related Events
                in Acute Coronary Syndromes

                Results: ACS patients identified as being "poor
                responders" to a 600-mg loading dose of clopidogrel face
                a twofold risk of cardiac death in the next few years,
                results from the RECLOSE 2 ACS study show. Of note,
                however, doubling the maintenance dose of clopidogrel
                or shifting patients to ticlopidine did not appear to
                mitigate this risk over time.

                "This will allow us to narrow the focus of where we're going
                to be using the more potent agents, because clopidogrel
                still has a role," said Dr Dominick Angiolillo (University of
                Florida College of Medicine, Jacksonville)."Even in ACS
                patients, there are patients who respond to clopidogrel and
                do well."

                See: Poor clopidogrel responders with ACS face twofold
                risk of cardiac death: RECLOSE 2 ACS
DISCOVER FLOW
                                                             Results: As arguments over the necessity of stent procedures
                                                             and imaging tests approach a fever pitch, a new computer
                                                             modeling system that can add functional information to standard
                                                             coronary computed-tomography (CT) angiography may once
                                                             again shake up the world of diagnostic imaging and clinical
                                                             decision making. According to study investigators, the new
                                                             technique, dubbed noninvasive fractional flow reserve (FFRCT),
                                                             can dramatically improve the diagnostic accuracy of CT imaging
                                                             without the need for an invasive test, adenosine, or additional
                                                             radiation exposure.




"This noninvasive 'all-in-one' technology may reduce unnecessary invasive coronary angiography and revascularization
procedures," said Dr Bon-Kwon Koo (Seoul National University Hospital, Korea). "Because this model starts with just
conventional CT imaging, there are no [additional] radiation, imaging procedures, or medication. Any CT images, taken
from any lab, can be transferred to this novel technology."

See: Adding function to CTA with "noninvasive FFR" ups accuracy, may cut procedures: DISCOVER FLOW
TAVI Spotlight
                                                            Summary: Paravalvular leaks are extremely rare in surgical aortic-valve
                                                            replacement--seen in just 1.5% to 2% of cases. But as experts observed at
                                                            EuroPCR 2011, mild paravalvular leaks are relatively common in
                                                            transcatheter aortic-valve implantation (TAVI). New data presented at the
                                                            conference suggest that more severe paravalvular aortic regurgitation (AR)
                                                            is a key reason for prosthetic valve dysfunction.




"Our primary focus initially was actually on device success and procedural success, so people were focusing on implanting
the devices in the correct position and without perivascular complications--the focus was not so much on aortic
regurgitation or residual regurgitation," said Dr Peter Wenaweser (Bern University Hospital, Switzerland). "Now we are
quite happy about all the device success and the hemodynamic performance as well, so now . . . we are now trying to get a
better understanding of how we can further improve this technology."

See: TAVI spotlight swings to risks of paravalvular leaks
Renal denervation
                                                               Summary: Interventional cardiologists gathered at EuroPCR
                                                               2011 mulled the potential new applications for renal
                                                               denervation--the centerpiece of the "live case" presentation that
                                                               kicked off this year's meeting--even as they admitted that the
                                                               very limited data supporting the procedure in resistant
                                                               hypertension need to be replicated in larger studies. The
                                                               speculation on future uses comes as longer-term data from the
                                                               Symplicity HTN-1 pilot study are published in the May 2011
                                                               issue of Hypertension.




"We have relatively limited numbers of patients who have been included in the trials, yet the potential size of the population who
could benefit is huge," session chair Dr William Wijns (Cardiovascular Center Aalst, Belgium) observed. "Should this mismatch
be addressed by larger trials?"

See: Wider role for renal denervation considered, amid calls for more studies
BASE-ACS
           Comparison of Bio-Active-Stent to the Everolimus-Eluting Stent
           in Acute Coronary Syndrome

           Results: BASE-ACS, presented during the late-breaking clinical-
           trials session at EuroPCR 2011, showed the Titan-2 BAS
           (Hexacath) bare-metal stent to have nearly identical rates of
           major adverse cardiovascular events (MACE) as the market-
           leading Xience V (Abbott Vascular) at 12 months, in ACS
           patients.

           "The present study suggests that a stent coated with titanium
           nitride-oxide represents a safe and effective alternative to
           Xience V everolimus-eluting stents in ACS patients," concluded
           Dr Pasi Karjalainen (Heart Center, Satakunta Hospital, Pori,
           Finland).

           See: BASE-ACS: Could a bare-metal stent be "noninferior" to a
           leading DES?
SOURCE Registry

                                                                              Results: New numbers from the SOURCE registry,
                                                                              which tracks patients treated with the Sapien valve
                                                                              (Edwards) by either the transapical or transfemoral
                                                                              route, suggest that the groundbreaking randomized
                                                                              controlled PARTNER trial results are more or less in
                                                                              keeping with outcomes seen in "real-world" practice
                                                                              outside the US. One-year survival for the entire
                                                                              cohort (over 23,000 patients) was 76.5%, climbing to
                                                                              80.1% in the transfemoral group and dipping to
                                                                              74.2% in the transapical group.

The registry gives "very good information . . . in real-world terms, in all [the types of] patients coming for this kind of treatment,"
said Dr Olaf Wendler (Kings College Hospital, London, UK) . "On the other hand, it's not covering all implantations of the
Sapien valves, and it's not covering all the implantations with other devices. In the end, there are no better data than these, but
they cover only one part of the TAVI experience at the moment."

See: New SOURCE numbers bolster PARTNER results in real world
DES meta-analysis:
Biodegradable vs permanent polymers
                             Results: A new meta-analysis with three-year data is offering
                             the first solid proof that drug-eluting stents (DES) with
                             bioerodable polymers are associated with less stent thrombosis
                             and better clinical outcomes than stents with permanent
                             polymers.

                             "The issue to date has been that because late adverse events
                             are very rare, we need large numbers of patients so we can
                             detect any differences," said Dr Robert Byrne (Deutsches
                             Herzzentrum, Munich, Germany. "I think this is probably the first
                             time that we've detected a clear signal toward reduced clinical
                             events. It may be that these differences only start to emerge or
                             we can only tease them out after three years, and earlier time
                             points aren't really showing the benefit of these platforms."

                             See: Less stent thrombosis with biodegradable vs permanent
                             polymers: Meta-analysis
SCAAR Registry

                 Results: Use of radial PCI in the treatment of STEMI
                 patients in Sweden is associated with a 22% reduction in
                 mortality and lower rates of bleeding and
                 rehospitalizations, a new retrospective analysis of the
                 SCAAR registry suggests.

                 "While the study supports the feasibility and safety of
                 radial for STEMI, it does not contribute to [the question
                 of] the comparison with transfemoral, due to case
                 selection, time-sensitive anticoagulation regimens, and
                 crossover," said Dr Ron Waksman (Washington
                 Hospital, Washington, DC). "Operators should continue
                 to perform PCI with the access that they feel comfortable
                 with, and there is not sufficient evidence from this study
                 to switch to radial from femoral."

                 See: SCAAR registry: Transradial PCI cuts mortality in
                 STEMI
For more information
                       EuroPCR

                       EuroPCR 2011 coverage on theheart.org

                       EuroPCR 2011 coverage on Medscape
Credits and disclosures
                      Editor-in-Chief/Journalist:
                      Shelley Wood
                      Managing Editor, heartwire
                      Kelowna, BC
                      Disclosure: Shelley Wood has disclosed no relevant financial relationships.

                      Contributor:
                      Steven Rourke
                      Manager, Editorial Programming
                      theheart.org
                      Montreal, QC
                      Disclosure: Steven Rourke has disclosed no relevant financial relationships.
More slideshows
                  HRS 2011 research highlights

                  ACC 2011 research highlights

                  AHA 2010 research highlights: A slideshow
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                  TCT 2010 research highlights: A slideshow
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EuroPCR 2011 research highlights: A slideshow presentation

  • 1. EuroPCR 2011 research highlights: A slideshow presentation
  • 2. EuroPCR 2011 Research Highlights EuroPCR 2011 took place in Paris, France, from May 17 through May 20, 2011. The conference was attended by 12 567 people. Key trials/topics presented at the conference include: RECLOSE 2-ACS: Poor clopidogrel responders with ACS face twofold risk of cardiac death DISCOVER FLOW: Adding function to CTA with "noninvasive FFR" ups accuracy, may cut procedures TAVI spotlight swings to risks of paravalvular leaks Renal denervation: Wider role for procedure considered, amid calls for more studies BASE-ACS: Could a bare-metal stent be "noninferior" to a leading DES? SOURCE: New numbers from registry bolster PARTNER results in real world DES meta-analysis: Less stent thrombosis with biodegradable vs permanent polymers SCAAR registry: Transradial PCI cuts mortality in STEMI View our complete EuroPCR coverage here.
  • 3. RECLOSE 2 ACS Responsiveness to Clopidogrel and Stent-Related Events in Acute Coronary Syndromes Results: ACS patients identified as being "poor responders" to a 600-mg loading dose of clopidogrel face a twofold risk of cardiac death in the next few years, results from the RECLOSE 2 ACS study show. Of note, however, doubling the maintenance dose of clopidogrel or shifting patients to ticlopidine did not appear to mitigate this risk over time. "This will allow us to narrow the focus of where we're going to be using the more potent agents, because clopidogrel still has a role," said Dr Dominick Angiolillo (University of Florida College of Medicine, Jacksonville)."Even in ACS patients, there are patients who respond to clopidogrel and do well." See: Poor clopidogrel responders with ACS face twofold risk of cardiac death: RECLOSE 2 ACS
  • 4. DISCOVER FLOW Results: As arguments over the necessity of stent procedures and imaging tests approach a fever pitch, a new computer modeling system that can add functional information to standard coronary computed-tomography (CT) angiography may once again shake up the world of diagnostic imaging and clinical decision making. According to study investigators, the new technique, dubbed noninvasive fractional flow reserve (FFRCT), can dramatically improve the diagnostic accuracy of CT imaging without the need for an invasive test, adenosine, or additional radiation exposure. "This noninvasive 'all-in-one' technology may reduce unnecessary invasive coronary angiography and revascularization procedures," said Dr Bon-Kwon Koo (Seoul National University Hospital, Korea). "Because this model starts with just conventional CT imaging, there are no [additional] radiation, imaging procedures, or medication. Any CT images, taken from any lab, can be transferred to this novel technology." See: Adding function to CTA with "noninvasive FFR" ups accuracy, may cut procedures: DISCOVER FLOW
  • 5. TAVI Spotlight Summary: Paravalvular leaks are extremely rare in surgical aortic-valve replacement--seen in just 1.5% to 2% of cases. But as experts observed at EuroPCR 2011, mild paravalvular leaks are relatively common in transcatheter aortic-valve implantation (TAVI). New data presented at the conference suggest that more severe paravalvular aortic regurgitation (AR) is a key reason for prosthetic valve dysfunction. "Our primary focus initially was actually on device success and procedural success, so people were focusing on implanting the devices in the correct position and without perivascular complications--the focus was not so much on aortic regurgitation or residual regurgitation," said Dr Peter Wenaweser (Bern University Hospital, Switzerland). "Now we are quite happy about all the device success and the hemodynamic performance as well, so now . . . we are now trying to get a better understanding of how we can further improve this technology." See: TAVI spotlight swings to risks of paravalvular leaks
  • 6. Renal denervation Summary: Interventional cardiologists gathered at EuroPCR 2011 mulled the potential new applications for renal denervation--the centerpiece of the "live case" presentation that kicked off this year's meeting--even as they admitted that the very limited data supporting the procedure in resistant hypertension need to be replicated in larger studies. The speculation on future uses comes as longer-term data from the Symplicity HTN-1 pilot study are published in the May 2011 issue of Hypertension. "We have relatively limited numbers of patients who have been included in the trials, yet the potential size of the population who could benefit is huge," session chair Dr William Wijns (Cardiovascular Center Aalst, Belgium) observed. "Should this mismatch be addressed by larger trials?" See: Wider role for renal denervation considered, amid calls for more studies
  • 7. BASE-ACS Comparison of Bio-Active-Stent to the Everolimus-Eluting Stent in Acute Coronary Syndrome Results: BASE-ACS, presented during the late-breaking clinical- trials session at EuroPCR 2011, showed the Titan-2 BAS (Hexacath) bare-metal stent to have nearly identical rates of major adverse cardiovascular events (MACE) as the market- leading Xience V (Abbott Vascular) at 12 months, in ACS patients. "The present study suggests that a stent coated with titanium nitride-oxide represents a safe and effective alternative to Xience V everolimus-eluting stents in ACS patients," concluded Dr Pasi Karjalainen (Heart Center, Satakunta Hospital, Pori, Finland). See: BASE-ACS: Could a bare-metal stent be "noninferior" to a leading DES?
  • 8. SOURCE Registry Results: New numbers from the SOURCE registry, which tracks patients treated with the Sapien valve (Edwards) by either the transapical or transfemoral route, suggest that the groundbreaking randomized controlled PARTNER trial results are more or less in keeping with outcomes seen in "real-world" practice outside the US. One-year survival for the entire cohort (over 23,000 patients) was 76.5%, climbing to 80.1% in the transfemoral group and dipping to 74.2% in the transapical group. The registry gives "very good information . . . in real-world terms, in all [the types of] patients coming for this kind of treatment," said Dr Olaf Wendler (Kings College Hospital, London, UK) . "On the other hand, it's not covering all implantations of the Sapien valves, and it's not covering all the implantations with other devices. In the end, there are no better data than these, but they cover only one part of the TAVI experience at the moment." See: New SOURCE numbers bolster PARTNER results in real world
  • 9. DES meta-analysis: Biodegradable vs permanent polymers Results: A new meta-analysis with three-year data is offering the first solid proof that drug-eluting stents (DES) with bioerodable polymers are associated with less stent thrombosis and better clinical outcomes than stents with permanent polymers. "The issue to date has been that because late adverse events are very rare, we need large numbers of patients so we can detect any differences," said Dr Robert Byrne (Deutsches Herzzentrum, Munich, Germany. "I think this is probably the first time that we've detected a clear signal toward reduced clinical events. It may be that these differences only start to emerge or we can only tease them out after three years, and earlier time points aren't really showing the benefit of these platforms." See: Less stent thrombosis with biodegradable vs permanent polymers: Meta-analysis
  • 10. SCAAR Registry Results: Use of radial PCI in the treatment of STEMI patients in Sweden is associated with a 22% reduction in mortality and lower rates of bleeding and rehospitalizations, a new retrospective analysis of the SCAAR registry suggests. "While the study supports the feasibility and safety of radial for STEMI, it does not contribute to [the question of] the comparison with transfemoral, due to case selection, time-sensitive anticoagulation regimens, and crossover," said Dr Ron Waksman (Washington Hospital, Washington, DC). "Operators should continue to perform PCI with the access that they feel comfortable with, and there is not sufficient evidence from this study to switch to radial from femoral." See: SCAAR registry: Transradial PCI cuts mortality in STEMI
  • 11. For more information EuroPCR EuroPCR 2011 coverage on theheart.org EuroPCR 2011 coverage on Medscape
  • 12. Credits and disclosures Editor-in-Chief/Journalist: Shelley Wood Managing Editor, heartwire Kelowna, BC Disclosure: Shelley Wood has disclosed no relevant financial relationships. Contributor: Steven Rourke Manager, Editorial Programming theheart.org Montreal, QC Disclosure: Steven Rourke has disclosed no relevant financial relationships.
  • 13. More slideshows HRS 2011 research highlights ACC 2011 research highlights AHA 2010 research highlights: A slideshow presentation TCT 2010 research highlights: A slideshow presentation
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