Literature DB >> 29397971

Aortic valve replacement in patients with amyloidosis.

Amit P Java1, Kevin L Greason2, Angela Dispenzieri3, Martha Grogan4, Katherine S King5, Joseph J Maleszewski6, Richard C Daly1, Mackram F Eleid4, Alberto Pochettino1, Hartzell V Schaff1.   

Abstract

BACKGROUND: Outcome data on aortic valve replacement in patients with amyloidosis are limited. To address this issue, we reviewed our experience of patients with amyloidosis who underwent aortic valve replacement.
METHODS: We retrospectively reviewed the records of 16 patients with amyloidosis who underwent aortic valve replacement between May 2000 and February 2017.
RESULTS: The cohort comprised 11 males (69%) and 5 females (31%). The median patient age was 76 years (interquartile range [IQR], 71-82 years), and Society of Thoracic Surgeons predicted rate of mortality was 5.0% (IQR, 2.4%-8.7%). Amyloidosis type was immunoglobulin light chain in 6 patients (38%), age-related in 6 (38%), and localized in 4 (25%). The operation was surgical aortic valve replacement in 11 patients (69%) and balloon-expandable transfemoral transcatheter aortic valve insertion in the other 5. There was no procedure-related stroke, need for new-onset dialysis or pacemaker, or death within 30 days of surgery. The median length of hospital stay was 1 day (IQR, 1-2 days) in the transcatheter valve insertion group and 6 days (IQR, 6-8 days) in the surgical group (P = .002). Follow-up was available for all patients at a median of 1.9 years (IQR, 1.2-4.8 years). During the follow-up period, there were 4 deaths, all occurring >1 year after surgery.
CONCLUSIONS: Aortic valve replacement can be performed with low risk of operative morbidity and mortality in patients with amyloidosis. Transcatheter valve insertion has the advantage of reduced hospital length of stay. The 1-year survival is excellent.
Copyright © 2017 The American Association for Thoracic Surgery. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  amyloid, amyloidosis; aortic valve; aortic valve stenosis; cardiac amyloid; cardiac amyloidosis; surgical aortic valve replacement; transcatheter aortic valve insertion; transcatheter aortic valve replacement

Mesh:

Year:  2017        PMID: 29397971     DOI: 10.1016/j.jtcvs.2017.12.048

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  3 in total

1.  Coexistence of aortic valve stenosis and cardiac amyloidosis: echocardiographic and clinical significance.

Authors:  Gergely Peskó; Zsigmond Jenei; Gergely Varga; Astrid Apor; Hajnalka Vágó; Sándor Czibor; Zoltán Prohászka; Tamás Masszi; Zoltán Pozsonyi
Journal:  Cardiovasc Ultrasound       Date:  2019-12-26       Impact factor: 2.062

2.  Red Flags, Prognostic Impact, and Management of Patients With Cardiac Amyloidosis and Aortic Valve Stenosis: A Systematic Review and Meta-Analysis.

Authors:  Veronika A Myasoedova; Maddalena Conte; Vincenza Valerio; Donato Moschetta; Ilaria Massaiu; Laura Petraglia; Dario Leosco; Paolo Poggio; Valentina Parisi
Journal:  Front Med (Lausanne)       Date:  2022-03-09

3.  Transthyretin Cardiac Amyloidosis and Aortic Stenosis: Connection and Therapeutic Implications.

Authors:  Jorge Penalver; Maxwell Ambrosino; Hee D Jeon; Akanksha Agrawal; Napatt Kanjanahattakij; Marie Pitteloud; Jessica Stempel; Aman Amanullah
Journal:  Curr Cardiol Rev       Date:  2020
  3 in total

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