# Dilemmas and Challenges in the Anesthetic Management of Liver Transplantation for Transthyretin Amyloidosis in the Asian Context: A Case Report

**Authors:** Jacklyn Yek, Steffi Chan, Sook Muay Tay, Selene Tan

PMC · DOI: 10.7759/cureus.82784 · Cureus · 2025-04-22

## TL;DR

This paper discusses the challenges of anesthetic management during liver transplantation for a rare amyloidosis variant in an Asian patient, highlighting the lack of data and difficult decisions.

## Contribution

The paper presents a case report highlighting anesthetic dilemmas in liver transplantation for non-Val30Met TTR amyloidosis in Asia, where data is limited.

## Key findings

- Liver transplantation outcomes for non-Val30Met TTR amyloidosis in Asian patients are unpredictable due to genetic heterogeneity and disease progression.
- Anesthetic management of TTR amyloidosis patients requires difficult decisions due to limited data, as demonstrated by the use of verapamil for tachyarrhythmias.
- Access to disease-modifying therapies and high costs influence liver transplant decisions for TTR amyloidosis in Asia.

## Abstract

Transthyretin (TTR) amyloidosis is a progressive, debilitating, and eventually fatal disease that is under-recognized and underdiagnosed in Asian patients. Liver transplantation is performed in patients with hereditary transthyretin amyloidosis to remove the source of abnormal transthyretin production to slow disease progression. There is uncertainty about the risk-benefit ratio due to the less favourable five-year survival of liver transplantation for Asian patients with non-Val30Met transthyretin amyloidosis, as the heterogeneity of non-Val30Met mutations and the potential for disease progression despite transplantation can make transplant outcomes unpredictable. Additionally, limited access and the prohibitive costs of disease-modifying therapies may influence the decision-making process with regard to liver transplantation.

We present a case of a 57-year-old male with Ala117Ser TTR amyloidosis and clinical manifestations of polyneuropathy, cardiac amyloidosis, and autonomic neuropathy. He received a living-related liver transplant. We describe the dilemmas and challenges in the anesthetic planning and management of this patient. Along with limited scientific data on liver transplantation for non-Val30Met TTR amyloidosis patients, we faced challenges in the management of intraoperative tachyarrhythmias, which eventually necessitated the use of a relatively contraindicated drug, verapamil, to achieve rate control. The lack of specific data meant that we had to base some decisions on practical wisdom.

## Linked entities

- **Genes:** TTR (transthyretin) [NCBI Gene 7276]
- **Chemicals:** verapamil (PubChem CID 2520)
- **Diseases:** polyneuropathy (MONDO:0001824), autonomic neuropathy (MONDO:0001300)

## Full-text entities

- **Genes:** TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}
- **Diseases:** amyloidosis (MESH:D000686), polyneuropathy (MESH:D011115), autonomic neuropathy (MESH:D009422), tachyarrhythmias (MESH:D013610), Transthyretin (TTR) amyloidosis (MESH:C567782)
- **Chemicals:** verapamil (MESH:D014700)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Val30Met, Ala117Ser

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12097723/full.md

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Source: https://tomesphere.com/paper/PMC12097723