Complex Combined Thoracic/liver Transplant: A Seven Year Experience
Liver and Pancreas Transplant, UCLA, Los Angeles, CA.
Meeting: 2018 American Transplant Congress
Abstract number: 73
Keywords: Biopsy, Heart transplant patients, Liver transplantation
Session Information
Session Name: Concurrent Session: Liver: Recipient Selection
Session Type: Concurrent Session
Date: Sunday, June 3, 2018
Session Time: 2:30pm-4:00pm
Presentation Time: 3:30pm-3:42pm
Location: Room 6C
Background: While rare, combined Thoracic/Liver transplants are employed with increasing frequency. Consistent data regarding the technical conduct, patient selection and outcomes in this highly complex group is lacking.
Methods: Patients with end stage cardiac/pulmonary and liver disease who underwent heart-liver (HL) or lung-liver (LL) transplantation were evaluated. Transplants were performed sequentially (thoracic-first approach.) Liver pre-operative pathology were reviewed. (12 consecutive patients, 3 LL and 9 HL tx , 2010-2017, retrospective, single center)
Organs Transplanted | Indication for transplant | Pre-OLT liver biopsy |
LL | + hTERc mutation w/ IPF/portal fibrosis | Nodular Regenerative Hyperplasia (NRH) |
LL | +hTERc mutation NOS with UIF/hepatic venous obstruction/HPS | Cirr |
LL | Cystic fibrosis | Cirr |
HL | Amyloidosis | n/a |
HL | Ischemic cardiomyopathy/cardiac cirrhosis (CC) | Cirr |
HL | ETOH cirr/cardiomyopathy | n/a |
HL | Familial Hypercholesterolemia | n/a |
HL | Tricuspid atresia/failed Fontan/CC | Cirr |
HL | Tricuspid atresia/failed Fontan/CC | Bridging fibr with NRH |
HL | double outlet right ventricle (DORV), transposition of the great arteries (TGA), mitral atresia | NRH/incomplete cirr |
HL | DORV, TGA, pulmonic stenosis | Cirr |
HL | Dextrocardia, single ventricle, right AV valve atresia, subaortic stenosis | Cirr |
Results: Age was 34.8±13.8 years. Median MELD was 12.5 (range 8-40). 56% of HL were secondary to congenital cardiac defects. Median patient follow up was 17 months (range 8-90). Patient survival was 100%. Graft survival was 96%. One graft failure from HAT required re-do liver tx on POD 22. 9 patients had pre-tx liver biopsy (8 with cirr/bridging fibr.) Amongst LL recipients there was one case of ACR (liver and lung). For HL, 3 patients had ≥ 1 episode of ACR (33%), 2 developed AMR (22%) in the heart. One patient had ACR in the liver allograft (11%)
Conclusions: Thoracic/Liver tx have excellent short-term graft and patient survival. Congenital heart disease with cardiac failure and cirrhosis represents a growing indication for HL tx. hTERc mutations is an emerging etiology for LL tx. Establishing the degree of pre-transplant liver disease is crucial to prevent inappropriate allocation of these life-saving organs.
CITATION INFORMATION: Presser N., DiNorcia J., Agopian V., Yersiz H., Farmer D., Busuttil R., Kaldas F. Complex Combined Thoracic/liver Transplant: A Seven Year Experience Am J Transplant. 2017;17 (suppl 3).
To cite this abstract in AMA style:
Presser N, DiNorcia J, Agopian V, Yersiz H, Farmer D, Busuttil R, Kaldas F. Complex Combined Thoracic/liver Transplant: A Seven Year Experience [abstract]. https://atcmeetingabstracts.com/abstract/complex-combined-thoracic-liver-transplant-a-seven-year-experience/. Accessed November 21, 2024.« Back to 2018 American Transplant Congress