Pediatric combined liver–kidney transplantation. Issue 5 (October 2015)
- Record Type:
- Journal Article
- Title:
- Pediatric combined liver–kidney transplantation. Issue 5 (October 2015)
- Main Title:
- Pediatric combined liver–kidney transplantation
- Authors:
- Bacchetta, Justine
Mekahli, Djalila
Rivet, Christine
Demède, Delphine
Leclerc, Anne-Laure - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Purpose of review</title> <p>The experience of combined liver–kidney transplantation (CLKT) is limited in pediatric populations. This strategy is, however, required in specific diseases such as metabolic diseases (namely primary hyperoxaluria type one and methylmalonic acidemia), autosomal recessive polycystic kidney disease, miscellaneous ciliopathies and atypical hemolytic uremic syndrome.</p> </sec> <sec> <title>Recent findings</title> <p>Different series and registry studies have confirmed the feasibility of pediatric CLKT with encouraging results in the long term, even in the youngest and smallest patients, provided that highly trained multidisciplinary teams are involved in this global management. As such, the long-term outcomes after CLKT are currently comparable to that of isolated liver or kidney transplantations, even though the immediate postoperative period remains challenging.</p> </sec> <sec> <title>Summary</title> <p>Some questions remain nevertheless unanswered, such as the respective place of combined versus sequential liver–kidney transplantation, especially in primary hyperoxaluria and autosomal recessive polycystic kidney disease. The aim of this review was therefore to provide a 2015 update on pediatric CLKT. In the future, international collaborative studies and registries may help to improve our knowledge of this rare and still highly challenging technique.</p> </sec><abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Purpose of review</title> <p>The experience of combined liver–kidney transplantation (CLKT) is limited in pediatric populations. This strategy is, however, required in specific diseases such as metabolic diseases (namely primary hyperoxaluria type one and methylmalonic acidemia), autosomal recessive polycystic kidney disease, miscellaneous ciliopathies and atypical hemolytic uremic syndrome.</p> </sec> <sec> <title>Recent findings</title> <p>Different series and registry studies have confirmed the feasibility of pediatric CLKT with encouraging results in the long term, even in the youngest and smallest patients, provided that highly trained multidisciplinary teams are involved in this global management. As such, the long-term outcomes after CLKT are currently comparable to that of isolated liver or kidney transplantations, even though the immediate postoperative period remains challenging.</p> </sec> <sec> <title>Summary</title> <p>Some questions remain nevertheless unanswered, such as the respective place of combined versus sequential liver–kidney transplantation, especially in primary hyperoxaluria and autosomal recessive polycystic kidney disease. The aim of this review was therefore to provide a 2015 update on pediatric CLKT. In the future, international collaborative studies and registries may help to improve our knowledge of this rare and still highly challenging technique.</p> </sec> </abstract> … (more)
- Is Part Of:
- Current opinion in organ transplantation. Volume 20:Issue 5(2015:Oct.)
- Journal:
- Current opinion in organ transplantation
- Issue:
- Volume 20:Issue 5(2015:Oct.)
- Issue Display:
- Volume 20, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 20
- Issue:
- 5
- Issue Sort Value:
- 2015-0020-0005-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-10
- Subjects:
- Transplantation of organs, tissues, etc -- Periodicals
Immunosuppression -- Periodicals
Transplantation immunology -- Periodicals
617.954 - Journal URLs:
- http://journals.lww.com/co-transplantation/pages/default.aspx ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/MOT.0000000000000225 ↗
- Languages:
- English
- ISSNs:
- 1087-2418
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.776520
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3778.xml