Cause of death analysis and temporal trends in survival after liver transplantation for transthyretin familial amyloid polyneuropathy. (2nd October 2018)
- Record Type:
- Journal Article
- Title:
- Cause of death analysis and temporal trends in survival after liver transplantation for transthyretin familial amyloid polyneuropathy. (2nd October 2018)
- Main Title:
- Cause of death analysis and temporal trends in survival after liver transplantation for transthyretin familial amyloid polyneuropathy
- Authors:
- Algalarrondo, Vincent
Antonini, Teresa
Théaudin, Marie
Chemla, Denis
Benmalek, Anouar
Castaing, Denis
Cauquil, Cécile
Rouzet, François
Mika, Delphine
Duong, Eric
Dinanian, Sylvie
Eliahou, Ludivine
Le Guludec, Dominique
Samuel, Didier
Adams, David
Slama, Michel S. - Abstract:
- Abstract: Background: Hereditary transthyretin amyloidosis (ATTR) is a multisystemic disease involving mainly the peripheral nervous system and the heart. Liver transplantation (LT) is the reference treatment for ATTR neuropathy and preoperative detection of high risk patients is crucial. We aimed to document the causes of death of ATTR patients after LT, their temporal trends, and to evaluate whether the available preoperative tools that predict the risk of death after LT for hereditary ATTR amyloidosis matched with these trends. Methods: A retrospective longitudinal cohort study was performed on 215 consecutive ATTR patients who underwent LT between January 1993 and January 2011. Each patient's death cause and timing were classified. Results: Over a median follow up of 5.9 years, 84 patients died. The rate of death was higher in the first year following LT than thereafter (13.0 vs. 4.3 ± 1.8%/year; p = .004). Cardiac events ranked as the leading cause of death (C: 38%), followed by infections (I: 24%), graft complications (G: 17%), end stage amyloidosis, stroke and others (ASO: 7% each). Deaths due to graft complications and infections (GI) occurred earlier than those due to end stage amyloidosis and stroke. Death prediction was less accurate for GI-related mortality than for other causes, which blunted the accuracy of the early-term risk prediction scores. Conclusions In ATTR amyloidosis, cardiac events were the leading cause of death after liver transplantation. CloseAbstract: Background: Hereditary transthyretin amyloidosis (ATTR) is a multisystemic disease involving mainly the peripheral nervous system and the heart. Liver transplantation (LT) is the reference treatment for ATTR neuropathy and preoperative detection of high risk patients is crucial. We aimed to document the causes of death of ATTR patients after LT, their temporal trends, and to evaluate whether the available preoperative tools that predict the risk of death after LT for hereditary ATTR amyloidosis matched with these trends. Methods: A retrospective longitudinal cohort study was performed on 215 consecutive ATTR patients who underwent LT between January 1993 and January 2011. Each patient's death cause and timing were classified. Results: Over a median follow up of 5.9 years, 84 patients died. The rate of death was higher in the first year following LT than thereafter (13.0 vs. 4.3 ± 1.8%/year; p = .004). Cardiac events ranked as the leading cause of death (C: 38%), followed by infections (I: 24%), graft complications (G: 17%), end stage amyloidosis, stroke and others (ASO: 7% each). Deaths due to graft complications and infections (GI) occurred earlier than those due to end stage amyloidosis and stroke. Death prediction was less accurate for GI-related mortality than for other causes, which blunted the accuracy of the early-term risk prediction scores. Conclusions In ATTR amyloidosis, cardiac events were the leading cause of death after liver transplantation. Close preoperative evaluation allowed for accurate mid-term prediction of mortality, but the high rate of graft complications and infections blunted the early-term risk prediction. … (more)
- Is Part Of:
- Amyloid. Volume 25:Number 4(2018)
- Journal:
- Amyloid
- Issue:
- Volume 25:Number 4(2018)
- Issue Display:
- Volume 25, Issue 4 (2018)
- Year:
- 2018
- Volume:
- 25
- Issue:
- 4
- Issue Sort Value:
- 2018-0025-0004-0000
- Page Start:
- 253
- Page End:
- 260
- Publication Date:
- 2018-10-02
- Subjects:
- Hereditary transthyretin amyloidosis -- liver transplantation -- prognosis -- survival
Amyloidosis -- Periodicals
616.3995 - Journal URLs:
- http://informahealthcare.com/loi/amy ↗
http://informahealthcare.com ↗ - DOI:
- 10.1080/13506129.2018.1550061 ↗
- Languages:
- English
- ISSNs:
- 1350-6129
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0859.841173
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20375.xml