Track 7: TAVR Flashcards
Prevalance of AS
4% in ages 70-79
10% in ages 80-89
Generally speaking, based on age, what are the recommendations for aortic bioprosthesis versus mechanical?
< 50 yo: Mechanical
50-70 yo: shared decision making, either reasonable
(perhaps if under 55 mechanical better choice)
> 70(65) yo: biologic prosthesis
Typical longevity for biologic prostheses?
10-15 years
* less in younger patients and those with smaller aortic annulus size
* Higher rate of reoperation
* Degradation d/t immune mediated response
Outline some of the pros and cons of mechanical prostheses
Con:
- Lifelong anticoagulation
- Risk of hemorrhage (15% increased absolute of bleeding over 15 years, 1% per year)
- Risk of thromboembolism (5% increased absolute risk of stroke over 15 years)
Pros:
- Durability ~30+ years
Pt between 50-70(65) yo
Name some factors that would make mechanical valve preferable
Prosthetic valve preferable?
Mechanical:
- Able/willing to take A/C
- Low bleeding risk
- Good longevity
- Normal lifestyle
- High risk 2nd operation
Prosthetic:
- Unable/unwilling to take A/C
- High bleeding risk
- Limited longevity
- Extreme sports activity
- Poor compliance
Key findings with TAVR in intermediate risk patients
- TAVR was noninferior to surgery with respect to 2 year outcomes of death and stroke
- Transfemoral outcomes were superior to SAVR
- Hemodynamic profile more favorable but paravalvular leak and pacemaker requirement were more common compared to SAVR
- Major bleeding, kidney injury, and AF less common with TAVR
What 2 associated risk were more common in TAVR than SAVR with intermediate risk patients?
Which associated risk were less common with TAVR?
- Paravalvular leak (AR)
- Pacemaker requirement
+ new LBBB
Major bleeding, kidney injury, AF
Name the 2 trials to evaluate TAVR in low surgical risk populations
PARTNER 3 Trial (less incidence AF, shorter hospitalization, lower death, lower stroke) *TAVR now approved in low risk patients
Corevalve Evolut Low-Risk Trial
New LBBB risk TAVR verus SAVR
Higher in TAVR
2 major TAVR valves
Edwards Sapien
Self expanding Core
Mayo clinic conduction management post TAVR
Normal QRS duration
No transient HAVB
PR <240 ms
Next day dismissal without monitoring if no further ECG changes
Mayo clinic conduction management post TAVR
New LBBB + PR <240 ms and QRS <150 ms
Isolated PR ≥240 ms
Isolated RBBB (PR <200 ms and no LAFB or LPFB)
Monitor 24-48 hours, then ambulatory 30 day ECG monitoring if no further ECG changes
Mayo clinic conduction management post TAVR
Transient HAVB
New LBBB + PR ≥240 ms
New LBBB + QRS ≥150 ms with 1st degree AVB or incalculable PR
RBBB + 1st degree AVB
RBBB + LAFB or LPFB
Permanent PM implant
OR
Prolong inpatient monitoring with temporary PM > 48 hours
Mayo clinic conduction management post TAVR
Transient HAVB
New LBBB + PR ≥240 ms
New LBBB + QRS ≥150 ms with 1st degree AVB or incalculable PR
RBBB + 1st degree AVB
RBBB + LAFB or LPFB
Permanent PM implant
OR
Prolong inpatient monitoring with temporary PM > 48 hours
Name some of the populations in which TAVR is still being studied
(ongoing questions)
- Bicuspid AV
- Prosthetic valve degeneration (valve in valve)
- AR
What are some of the limiting factors to TAVR in bicuspid valve?
***RCT have not been done in this population
- Valve may be asymmetrically expanded
- Underexpansion
Risk of PM after TAVR is closely related to
baseline conduction
Every patient with valve prosthesis (even if on warfarin with mechanical valve) should also be on:
*unless contraindication exists or high bleed risk
ASA 75-100 mg/day
Class I
Aortic position, bileaflet/M-H, no risk factors. INR goal?
Everything else, INR goal?
2.5
3.0
Antithrombotics for bioprosthesis
SAVR
TAVR
SAVR
First 3 months: warfarin, INR 2.5
After 3 months: ASA alone (unless other indication for OAC)
TAVR
First 3 months: ASA + Clopidogrel vs warfarin
After 3 months: ASA alone (unless other indication for OAC)
Periprocedural OAC in mechanical prosthesis
- Most patients have only slight risk off OAC for a few days
- Low risk (aortic, bileaflet or tilting disc, no risk factors): No bridging needed
- High risk (everything else): Bridging (UFH in inpatient)
*In order from highest risk to lowest thrombosis risk
Tricuspid > Mitral > Aortic
Ball in cage >Tilting disc > Bileaflet
Other risk: AF, prior thrombosis, hypercoaguability, low EF