{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,26]],"date-time":"2026-09-26T13:33:19Z","timestamp":1790429599171,"version":"4.1.0"},"reference-count":20,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"8","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["Circ: Cardiovascular Imaging"],"published-print":{"date-parts":[[2021,8]]},"abstract":"<jats:sec>\n            <jats:title>Background:<\/jats:title>\n            <jats:p>\n              Severe prosthesis-patient mismatch (PPM) is diagnosed by an indexed effective orifice area &lt;0.65 cm\n              <jats:sup>2<\/jats:sup>\n              \/m\n              <jats:sup>2<\/jats:sup>\n              , which is derived from stroke volume index. We examined the impact of flow, determined by stroke volume index, on severe PPM following transcatheter aortic valve replacement (TAVR) and surgical aortic valve replacement (SAVR).\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Methods:<\/jats:title>\n            <jats:p>We included SAVR patients from the PARTNER 2A trial (Placement of Aortic Transcatheter Valve 2A) and TAVR patients from the PARTNER 2 S3i (Placement of Aortic Transcatheter Valve 2 S3i) registry. The primary end point was the separate analysis of all-cause death, cardiac death, and rehospitalization at 5 years. Following TAVR and SAVR, we compared the primary end points between severe versus no-severe PPM in all patients, in low flow (LF), and in normal flow. Multivariable analysis was performed to determine variables associated with the end points.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Results:<\/jats:title>\n            <jats:p>\n              Nine hundred fifty-four TAVR and 726 SAVR patients with PPM and flow data were included. Severe PPM following TAVR was significantly lower compared with SAVR in all patients (9% versus 28%,\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              &lt;0.0001), in normal flow (5% versus 8%,\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              =0.04), and in LF (20% versus 42%,\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              &lt;0.0001). Severe PPM was associated with rehospitalization following TAVR (odds ratio, 1.52 [95% CI, 1.01\u20132.29],\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              =0.0456) and SAVR (odds ratio, 1.51 [95% CI, 1.06\u20132.16],\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              =0.0237). Severe PPM in LF was independently associated with cardiac death following TAVR (odds ratio, 1.85 [95% CI, 1.06\u20133.23],\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              =0.0308). Following SAVR, severe PPM in LF and low ejection fraction was associated with increased cardiac death (35.26% versus 12.51%,\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              =0.01) and rehospitalization (37.59% versus 15.46%,\n              <jats:italic toggle=\"yes\">P<\/jats:italic>\n              =0.006) compared with severe PPM in LF and preserved ejection fraction, respectively. Severe PPM in normal flow was not associated with clinical outcomes despite higher gradients and smaller valves compared with severe PPM in LF.\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Conclusions:<\/jats:title>\n            <jats:p>Severe PPM is more common following SAVR compared with TAVR. Regardless of the implanted valve size or gradient, severe PPM impacts mortality only in patients with LF following TAVR and LF and low ejection fraction following SAVR. Severe PPM in normal flow is not associated with poor outcomes.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec>\n            <jats:title>Registration:<\/jats:title>\n            <jats:p>\n              URL:\n              <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/www.clinicaltrials.gov\">https:\/\/www.clinicaltrials.gov<\/jats:ext-link>\n              ; Unique identifiers: NCT01314313 and NCT02687035.\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/circimaging.120.012364","type":"journal-article","created":{"date-parts":[[2021,8,13]],"date-time":"2021-08-13T05:00:17Z","timestamp":1628830817000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":33,"title":["Impact of Flow on Prosthesis-Patient Mismatch Following Transcatheter and Surgical Aortic Valve Replacement"],"prefix":"10.1161","volume":"14","clinical-trial-number":[{"clinical-trial-number":"nct02687035","registry":"10.18810\/clinical-trials-gov"},{"clinical-trial-number":"nct01314313","registry":"10.18810\/clinical-trials-gov"}],"author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7316-4247","authenticated-orcid":true,"given":"Amr E.","family":"Abbas","sequence":"first","affiliation":[{"name":"Department of Internal Medicine. Oakland University William Beaumont School of Medicine, Auburn Hills, MI (A.E.A.)."},{"name":"Department of Cardiovascular Medicine. Beaumont Hospital Royal Oak, MI (A.E.A.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9629-5864","authenticated-orcid":true,"given":"Julien","family":"Ternacle","sequence":"additional","affiliation":[{"name":"Institut Universitaire de cardiologie et de Pneumologie de Qu\u00e9bec- Universit\u00e9 Laval\/Qu\u00e9bec Heart and Lung Institute, Laval University, Canada (J.T., P.P.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3607-279X","authenticated-orcid":true,"given":"Philippe","family":"Pibarot","sequence":"additional","affiliation":[{"name":"Institut Universitaire de cardiologie et de Pneumologie de Qu\u00e9bec- Universit\u00e9 Laval\/Qu\u00e9bec Heart and Lung Institute, Laval University, Canada (J.T., P.P.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ke","family":"Xu","sequence":"additional","affiliation":[{"name":"Edwards Lifesciences, Irvine, CA (K.X., E.R.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0430-3020","authenticated-orcid":true,"given":"Maria","family":"Alu","sequence":"additional","affiliation":[{"name":"Department of Cardiovascular Medicine, Columbia University Medical Center\/NewYork-Presbyterian Hospital (M.A., R.T.H., M.L.)."},{"name":"Cardiovascular Research Foundation, New York, NY (M.A., R.T.H., M.L.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Erin","family":"Rogers","sequence":"additional","affiliation":[{"name":"Edwards Lifesciences, Irvine, CA (K.X., E.R.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1342-9191","authenticated-orcid":true,"given":"Rebecca T.","family":"Hahn","sequence":"additional","affiliation":[{"name":"Department of Cardiovascular Medicine, Columbia University Medical Center\/NewYork-Presbyterian Hospital (M.A., R.T.H., M.L.)."},{"name":"Cardiovascular Research Foundation, New York, NY (M.A., R.T.H., M.L.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Martin","family":"Leon","sequence":"additional","affiliation":[{"name":"Department of Cardiovascular Medicine, Columbia University Medical Center\/NewYork-Presbyterian Hospital (M.A., R.T.H., M.L.)."},{"name":"Cardiovascular Research Foundation, New York, NY (M.A., R.T.H., M.L.)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vinod H.","family":"Thourani","sequence":"additional","affiliation":[{"name":"Department of Cardiovascular Surgery, Marcus Valve Center, Piedmont Heart Institute, Atlanta, GA 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