Impact of MitraClip™ therapy on secondary mitral valve surgery in patients at high surgical risk

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Impact of MitraClip™ therapy on secondary mitral valve surgery in patients at high surgical risk. / Conradi, Lenard; Treede, Hendrik; Franzen, Olaf; Seiffert, Moritz; Baldus, Stephan; Schirmer, Johannes; Meinertz, Thomas; Reichenspurner, Hermann.

In: EUR J CARDIO-THORAC, Vol. 40, No. 6, 12.2011, p. 1521-1526.

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@article{f92da38cf5c14500a81c51d275dd112e,
title = "Impact of MitraClip{\texttrademark} therapy on secondary mitral valve surgery in patients at high surgical risk",
abstract = "OBJECTIVE: Conventional or minimally invasive surgical mitral valve repair (MVR) is the gold-standard treatment for severe mitral regurgitation (MR) of any etiology. Given its good safety profile, trans-catheter MVR with the MitraClip{\texttrademark} device is used increasingly for high-risk or inoperable patients. We report our experience with failed MitraClip{\texttrademark} therapy and its impact on subsequent surgical strategies, such as the feasibility of MVR in high-risk patients.METHODS: During a follow-up of 344 ± 227 days from the first 215 consecutive patients treated with the MitraClip{\texttrademark} device, six patients required surgical re-intervention due to failed repair (n = 3) or recurrent severe MR (n = 3) at 35.8 ± 47.7 (range 0-117) days after trans-catheter MVR. Feasibility of secondary surgical MVR was assessed with regard to prior clip therapy.RESULTS: In three patients, secondary surgical MVR was successfully performed following the surgical strategy deemed optimal before trans-catheter treatment. Injury of the mitral leaflets caused by prior clip treatment was present in three other patients and influenced the surgical strategy toward more complex surgical techniques in one case and MV replacement in two others. One patient died 6 days after MV replacement. All other patients are alive with adequate valve function at the latest follow-up of 12.4 ± 7.4 months (range 4-22).CONCLUSIONS: Secondary surgical MVR was feasible in some patients after prior clip treatment, but led to valve replacement in others. At present, patient selection criteria for trans-catheter MVR should not be expanded toward more healthy patients, as primary trans-catheter MVR may complicate secondary surgery in certain cases and may even preclude reconstructive valve surgery.",
keywords = "Aged, Feasibility Studies, Female, Follow-Up Studies, Heart Valve Prosthesis Implantation, Humans, Male, Middle Aged, Minimally Invasive Surgical Procedures/instrumentation, Mitral Valve/surgery, Mitral Valve Insufficiency/surgery, Prostheses and Implants, Prosthesis Failure, Recurrence, Reoperation/methods",
author = "Lenard Conradi and Hendrik Treede and Olaf Franzen and Moritz Seiffert and Stephan Baldus and Johannes Schirmer and Thomas Meinertz and Hermann Reichenspurner",
note = "Copyright {\textcopyright} 2011 European Association for Cardio-Thoracic Surgery. Published by Elsevier B.V. All rights reserved.",
year = "2011",
month = dec,
doi = "10.1016/j.ejcts.2011.03.007",
language = "English",
volume = "40",
pages = "1521--1526",
journal = "EUR J CARDIO-THORAC",
issn = "1010-7940",
publisher = "Elsevier",
number = "6",

}

RIS

TY - JOUR

T1 - Impact of MitraClip™ therapy on secondary mitral valve surgery in patients at high surgical risk

AU - Conradi, Lenard

AU - Treede, Hendrik

AU - Franzen, Olaf

AU - Seiffert, Moritz

AU - Baldus, Stephan

AU - Schirmer, Johannes

AU - Meinertz, Thomas

AU - Reichenspurner, Hermann

N1 - Copyright © 2011 European Association for Cardio-Thoracic Surgery. Published by Elsevier B.V. All rights reserved.

PY - 2011/12

Y1 - 2011/12

N2 - OBJECTIVE: Conventional or minimally invasive surgical mitral valve repair (MVR) is the gold-standard treatment for severe mitral regurgitation (MR) of any etiology. Given its good safety profile, trans-catheter MVR with the MitraClip™ device is used increasingly for high-risk or inoperable patients. We report our experience with failed MitraClip™ therapy and its impact on subsequent surgical strategies, such as the feasibility of MVR in high-risk patients.METHODS: During a follow-up of 344 ± 227 days from the first 215 consecutive patients treated with the MitraClip™ device, six patients required surgical re-intervention due to failed repair (n = 3) or recurrent severe MR (n = 3) at 35.8 ± 47.7 (range 0-117) days after trans-catheter MVR. Feasibility of secondary surgical MVR was assessed with regard to prior clip therapy.RESULTS: In three patients, secondary surgical MVR was successfully performed following the surgical strategy deemed optimal before trans-catheter treatment. Injury of the mitral leaflets caused by prior clip treatment was present in three other patients and influenced the surgical strategy toward more complex surgical techniques in one case and MV replacement in two others. One patient died 6 days after MV replacement. All other patients are alive with adequate valve function at the latest follow-up of 12.4 ± 7.4 months (range 4-22).CONCLUSIONS: Secondary surgical MVR was feasible in some patients after prior clip treatment, but led to valve replacement in others. At present, patient selection criteria for trans-catheter MVR should not be expanded toward more healthy patients, as primary trans-catheter MVR may complicate secondary surgery in certain cases and may even preclude reconstructive valve surgery.

AB - OBJECTIVE: Conventional or minimally invasive surgical mitral valve repair (MVR) is the gold-standard treatment for severe mitral regurgitation (MR) of any etiology. Given its good safety profile, trans-catheter MVR with the MitraClip™ device is used increasingly for high-risk or inoperable patients. We report our experience with failed MitraClip™ therapy and its impact on subsequent surgical strategies, such as the feasibility of MVR in high-risk patients.METHODS: During a follow-up of 344 ± 227 days from the first 215 consecutive patients treated with the MitraClip™ device, six patients required surgical re-intervention due to failed repair (n = 3) or recurrent severe MR (n = 3) at 35.8 ± 47.7 (range 0-117) days after trans-catheter MVR. Feasibility of secondary surgical MVR was assessed with regard to prior clip therapy.RESULTS: In three patients, secondary surgical MVR was successfully performed following the surgical strategy deemed optimal before trans-catheter treatment. Injury of the mitral leaflets caused by prior clip treatment was present in three other patients and influenced the surgical strategy toward more complex surgical techniques in one case and MV replacement in two others. One patient died 6 days after MV replacement. All other patients are alive with adequate valve function at the latest follow-up of 12.4 ± 7.4 months (range 4-22).CONCLUSIONS: Secondary surgical MVR was feasible in some patients after prior clip treatment, but led to valve replacement in others. At present, patient selection criteria for trans-catheter MVR should not be expanded toward more healthy patients, as primary trans-catheter MVR may complicate secondary surgery in certain cases and may even preclude reconstructive valve surgery.

KW - Aged

KW - Feasibility Studies

KW - Female

KW - Follow-Up Studies

KW - Heart Valve Prosthesis Implantation

KW - Humans

KW - Male

KW - Middle Aged

KW - Minimally Invasive Surgical Procedures/instrumentation

KW - Mitral Valve/surgery

KW - Mitral Valve Insufficiency/surgery

KW - Prostheses and Implants

KW - Prosthesis Failure

KW - Recurrence

KW - Reoperation/methods

U2 - 10.1016/j.ejcts.2011.03.007

DO - 10.1016/j.ejcts.2011.03.007

M3 - SCORING: Journal article

C2 - 21497508

VL - 40

SP - 1521

EP - 1526

JO - EUR J CARDIO-THORAC

JF - EUR J CARDIO-THORAC

SN - 1010-7940

IS - 6

ER -