TY - JOUR
T1 - Clinical outcomes of TAVI or SAVR in men and women with aortic stenosis at intermediate operative risk
T2 - A post hoc analysis of the randomised SURTAVI trial
AU - Van Mieghem, Nicolas M.
AU - Reardon, Michael J.
AU - Yakubov, Steven J.
AU - Heiser, John
AU - Merhi, William
AU - Windecker, Stephan
AU - Makkar, Raj
AU - Cheng, Wen
AU - Robbins, Mark
AU - Fail, Peter
AU - Feinberg, Edgar
AU - Stoler, Robert C.
AU - Hebeler, Robert
AU - Serruys, Patrick W.
AU - Popma, Jeffrey J.
N1 - Funding Information:
N. Van Mieghem has received research grants from Boston Scientific, Medtronic, Edwards Lifesciences, and Abbott Vascular. M. Reardon has received fees from Medtronic for providing educational services. S. Yakubov has received institutional research grants from Boston Scientific and Medtronic. S. Windecker has received institutional research grants from Abbott, Medtronic, Boston Scientific, Edwards Lifesciences, and Terumo. R. Makkar has received research grants from Edwards Lifesciences and St. Jude Medical, and personal fees from Abbott Vascular, Cordis, and Medtronic. P.W. Serruys has received grant support and fees from Medtronic, Philips, and ReCor Medical. J. Popma is an employee of (and reports other from) Medtronic. The other authors have no conflicts of interest to declare.
Funding Information:
This work was supported by Medtronic, plc (Minneapolis, MN, USA).
Publisher Copyright:
© Europa Digital & Publishing 2020.
PY - 2020/11/20
Y1 - 2020/11/20
N2 - AIMS: In patients with aortic stenosis randomised to transcatheter aortic valve implantation (TAVI) or surgical aortic valve replacement (SAVR), sex-specific differences in complication rates are unclear in intermediate-risk patients. The purpose of this analysis was to identify sex-specific differences in outcome for patients at intermediate surgical risk randomised to TAVI or SAVR in the international Surgical Replacement and Transcatheter Aortic Valve Implantation (SURTAVI) trial.METHODS AND RESULTS: A total of 1,660 intermediate-risk patients underwent TAVI with a supra-annular, self-expanding bioprosthesis or SAVR. The population was stratified by sex and treatment modality (female TAVI=366, male TAVI=498, female SAVR=358, male SAVR=438). The primary endpoint was a composite of all-cause mortality or disabling stroke at two years. Compared to males, females had a smaller body surface area, a higher Society of Thoracic Surgeons score (4.7±1.6% vs 4.3±1.6%, p<0.01) and were more frail. Men required more concomitant revascularisation (23% vs 16%). All-cause mortality or disabling stroke at two years was similar between TAVI and SAVR for females (10.2% vs 10.5%, p=0.90) and males (14.5% vs 14.4%, p=0.99); the difference between females and males was 10.2% vs 14.5%, for TAVI (p=0.08) and 10.5% vs 14.4%, SAVR (p=0.13). Functional status improvement was more pronounced after TAVI in females than in males.CONCLUSIONS: Aortic valve replacement, either by surgical or transcatheter approach, appears similarly effective and safe for males and females at intermediate surgical risk. Functional status appears to improve most in females after TAVI.CLINICAL TRIAL REGISTRATION: http://clinicaltrials.gov NCT01586910.
AB - AIMS: In patients with aortic stenosis randomised to transcatheter aortic valve implantation (TAVI) or surgical aortic valve replacement (SAVR), sex-specific differences in complication rates are unclear in intermediate-risk patients. The purpose of this analysis was to identify sex-specific differences in outcome for patients at intermediate surgical risk randomised to TAVI or SAVR in the international Surgical Replacement and Transcatheter Aortic Valve Implantation (SURTAVI) trial.METHODS AND RESULTS: A total of 1,660 intermediate-risk patients underwent TAVI with a supra-annular, self-expanding bioprosthesis or SAVR. The population was stratified by sex and treatment modality (female TAVI=366, male TAVI=498, female SAVR=358, male SAVR=438). The primary endpoint was a composite of all-cause mortality or disabling stroke at two years. Compared to males, females had a smaller body surface area, a higher Society of Thoracic Surgeons score (4.7±1.6% vs 4.3±1.6%, p<0.01) and were more frail. Men required more concomitant revascularisation (23% vs 16%). All-cause mortality or disabling stroke at two years was similar between TAVI and SAVR for females (10.2% vs 10.5%, p=0.90) and males (14.5% vs 14.4%, p=0.99); the difference between females and males was 10.2% vs 14.5%, for TAVI (p=0.08) and 10.5% vs 14.4%, SAVR (p=0.13). Functional status improvement was more pronounced after TAVI in females than in males.CONCLUSIONS: Aortic valve replacement, either by surgical or transcatheter approach, appears similarly effective and safe for males and females at intermediate surgical risk. Functional status appears to improve most in females after TAVI.CLINICAL TRIAL REGISTRATION: http://clinicaltrials.gov NCT01586910.
KW - Aortic stenosis
KW - Gender issues
KW - TAVI
KW - Heart Valve Prosthesis Implantation
KW - Humans
KW - Risk Factors
KW - Aortic Valve Stenosis/surgery
KW - Female
KW - Male
KW - Transcatheter Aortic Valve Replacement/adverse effects
KW - Treatment Outcome
KW - Aortic Valve/diagnostic imaging
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UR - http://www.scopus.com/inward/citedby.url?scp=85096814390&partnerID=8YFLogxK
U2 - 10.4244/EIJ-D-20-00303
DO - 10.4244/EIJ-D-20-00303
M3 - Article
C2 - 32715995
AN - SCOPUS:85096814390
SN - 1774-024X
VL - 16
SP - 833
EP - 841
JO - EuroIntervention
JF - EuroIntervention
IS - 10
ER -