The delay between the indication and the embodiment of the procedure decrease the effectiveness of percutaneous aortic valve replacement

Original title: Impact of wait times on the effectiveness of transcatheter aortic-valve replacement (TAVR) in severe aortic valve disease: a discrete event simulation model. Reference: Wijeysundera HC et al. Can J Cardiol. 2014; Epub ahead of print.

Once patients are accepted for percutaneous aortic valve replacement (TAVR), the higher the expected for the valve, the greater the risk of dying by peri-procedure or within a year.

In the PARTNER A study that used the Edwards Sapien balloon expandable valve a mathematical model to simulate the death risk was applied, according to the time elapsed (from 10 days to 180 days) while completing diagnostic studies to accept it as TAVR candidate and the time at which the procedure was performed. The daily risk of dying both peri-procedure or within one year post implant, increased progressively with longer waiting time, showing a difference of up to 27% between the longest and shortest waiting time for inoperable patients (10 day waiting time 1.9% risk, 60 days 10.7%, and 180 days 28.9%) and up to 20% of difference in high-risk patients (10 days 2.2% risk, 60 days 8.1% and 180 days 22.4%).

In contrast to this, waiting time and death risk were relatively stable for those who received medical treatment or surgery, respectively. In the inoperable cohort, most patients receiving TAVR (99.2%) had lower mortality than those receiving medical treatment beyond what they had to wait for the procedure. In the high-risk cohort, when the waiting time exceeded 60 days, patients receiving TAVR showed higher mortality than those receiving surgery. With longer waits for 180 days, non-inferiority between TAVR and proven surgery in PARTNER A study missed almost half of the patients.

Conclusion

Modest increases in waiting time to percutaneous aortic valve replacement have a significant impact on mortality in the inoperable cohort as well as in the high-risk cohort.

Editorial comment

The findings of this study are particularly important for those patients who might be candidates for surgery so as to TVAR, since the loss of time could tip the balance in favour of surgery. 

SOLACI.ORG

More articles by this author

Long Term Results of the International Chimney Registry

The International Chimney Registry was an observational study aimed at assessing the use of chimney stenting during TAVR either to predict or treat coronary...

CANNULATE TAVR extended study: Impact of Commissural and Coronary Alignment in Coronary Cannulation Following TAVR with Evolut Fx

The new valve Evolut FX has shown better commissural alignment vs. its predecessor Evolut Pro+. Prior studies have already shown commissure alignment facilitates post...

TRISCEND II: Transcatheter Replacement vs. Medical Treatment for Tricuspid Regurgitation

The EVOQUE device is designed with an intra-annular sealing system that provides excellent anatomical compatibility and an adaptable shape. It is currently available in...

J-Valve for Chronic AR: 30-Day Outcomes of Transfemoral Valve J-Valve in Chronic Aortic Regurgitation

Chronic aortic regurgitation (AR) poses a significant challenge as far as transcatheter alternatives go due to the absence of calcification and a suitable anchoring...

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Related Articles

SOLACI Sessionsspot_img

Recent Articles

Long Term Results of the International Chimney Registry

The International Chimney Registry was an observational study aimed at assessing the use of chimney stenting during TAVR either to predict or treat coronary...

CANNULATE TAVR extended study: Impact of Commissural and Coronary Alignment in Coronary Cannulation Following TAVR with Evolut Fx

The new valve Evolut FX has shown better commissural alignment vs. its predecessor Evolut Pro+. Prior studies have already shown commissure alignment facilitates post...

TRISCEND II: Transcatheter Replacement vs. Medical Treatment for Tricuspid Regurgitation

The EVOQUE device is designed with an intra-annular sealing system that provides excellent anatomical compatibility and an adaptable shape. It is currently available in...