In vivo tissue reaction within the outflow conduit in patients supported by HeartWare HVAD.


Journal

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
ISSN: 1879-1336
Titre abrégé: Cardiovasc Pathol
Pays: United States
ID NLM: 9212060

Informations de publication

Date de publication:
Historique:
received: 01 08 2019
revised: 23 09 2019
accepted: 24 09 2019
pubmed: 25 11 2019
medline: 26 3 2020
entrez: 25 11 2019
Statut: ppublish

Résumé

The frequency, extent, and nature of tissue ingrowth within the continuous-flow left ventricular assist device (cf-LVAD) outflow conduit has not been systematically assessed. We sought to characterize conduit histopathology at explantation in a cohort of patients with HeartWare ventricular assist device (HVAD) and assess the effect on pump performance. Patients undergoing routine histopathological assessment of a HeartWare HVAD removed at transplantation or autopsy were assessed. Outflow conduits were examined macroscopically, and visible tissue was sectioned for microscopic evaluation. In patients who had undergone prior contrast-enhanced computerized tomography (CT) with HVAD in situ, the outflow conduit was measured at the aortic anastomosis and 5 cm proximal to the anastomosis, in the axial and sagittal planes. All patients had their pump flow, flow pulsatility, current, and speed determined from log files examined at 1, 3, 6, 9, and 12 months after LVAD implantation. Twenty-five consecutive patients were assessed (24 LVAD, 1 biventricular assist device (BiVAD)). Of the 26 outflow grafts assessed, there was evidence of tissue ingrowth reaction in 24 (92%) grafts. The most common site was the distal anastomosis (18/24, 75%), with the graft body involved in 14 of 24 (58%) grafts. Microscopic evaluation revealed acute inflammatory infiltrate in 4 of 24 grafts (17%), chronic inflammatory infiltrate in 14 of 24 (58%), neointima formation in 18 of 24 (75%) and fibrosis in 18 of 24 (75%) grafts. The median depth of tissue was 1 mm (range, 0-2 mm). The mean conduit diameter was 9.5 ± 0.6 mm at the aortic anastomosis compared with 11.1 ± 0.5 mm 5 cm proximal to the anastomosis (p < 0.0001). In patients with unchanged pump speed one month after implantation, analysis of log files revealed a significant (5.8 ± 8.6%) decrease in pump flow (4.65 ± 0.86 vs 4.38 ± 0.92 L/min, p = 0.01) and flow pulsatility (5.00 ± 1.10 vs 4.16 ± 1.05 L/min, p = 0.006). There is evidence of tissue formation within the HVAD outflow conduit in the vast majority of patients, most commonly located at the aortic anastomosis. This is associated with significantly decreased pump flow over time.

Identifiants

pubmed: 31760240
pii: S1054-8807(19)30321-7
doi: 10.1016/j.carpath.2019.107156
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107156

Informations de copyright

Crown Copyright © 2019. Published by Elsevier Inc. All rights reserved.

Auteurs

P Jain (P)

Cardiology Department, St Vincent's Hospital, Sydney, Australia; University of New South Wales, Sydney, Australia.

D Robson (D)

Cardiology Department, St Vincent's Hospital, Sydney, Australia.

S Shehab (S)

Victor Chang Cardiac Research Institute, Sydney, Australia.

K Muthiah (K)

Cardiology Department, St Vincent's Hospital, Sydney, Australia; Victor Chang Cardiac Research Institute, Sydney, Australia.

P Jansz (P)

Cardiology Department, St Vincent's Hospital, Sydney, Australia.

M R Qiu (MR)

Anatomical Pathology Department, St Vincent's Hospital, Sydney, Australia.

W Barrett (W)

Anatomical Pathology Department, St Vincent's Hospital, Sydney, Australia.

V Sivasubramaniam (V)

Anatomical Pathology Department, St Vincent's Hospital, Sydney, Australia.

N Kumaradevan (N)

Anatomical Pathology Department, St Vincent's Hospital, Sydney, Australia.

P S Macdonald (PS)

Cardiology Department, St Vincent's Hospital, Sydney, Australia; University of New South Wales, Sydney, Australia; Victor Chang Cardiac Research Institute, Sydney, Australia.

C S Hayward (CS)

Cardiology Department, St Vincent's Hospital, Sydney, Australia; University of New South Wales, Sydney, Australia; Victor Chang Cardiac Research Institute, Sydney, Australia. Electronic address: cshayward@stvincents.com.au.

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