-
Something wrong with this record ?
Heterogeneity of Bile Duct Management in the Development of Ischemic Cholangiopathy After Liver Transplantation: Results of a European Liver and Intestine Transplant Association Survey
N. Meurisse, D. Monbaliu, G. Berlakovich, P. Muiesan, M. Oliverius, R. Adam, J. Pirenne,
Language English Country United States
Document type Journal Article
- MeSH
- Cholangitis etiology MeSH
- Ischemia etiology MeSH
- Humans MeSH
- Tissue and Organ Harvesting adverse effects methods MeSH
- Perfusion adverse effects methods MeSH
- Postoperative Complications etiology MeSH
- Graft Survival MeSH
- Surveys and Questionnaires MeSH
- Reperfusion adverse effects methods MeSH
- Liver Transplantation adverse effects MeSH
- Organ Preservation adverse effects methods MeSH
- Bile Ducts blood supply transplantation MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Europe MeSH
BACKGROUND: Surgical factors and direct cytotoxicity of bile salts on cholangiocytes may play a role in the development of ischemic cholangiopathy (IC) after liver transplantation (LTx). There is no validated consensus on how to protect the bile ducts during procurement, static preservation, and LTx. Meanwhile, IC remains the most troublesome complication after LTx. AIM: To characterize bile duct management techniques during the LTx process among European transplant centers in cases of donation after brain death (DBD) and circulatory death (DCD). METHOD: An European Liver and Intestine Transplant Association-European Liver Transplant Registry web survey designed to conceal respondents' personal information was sent to surgeons procuring and/or transplanting livers in Europe. RESULTS: Sixty-five percent of responses came from large transplant centers (>50 procurements/y). In 8% of DBDs and 14% of DCDs the bile duct is not rinsed. In 46% of DBDs and 52% of DCDs surgeons prefer to remove the gallbladder after graft reperfusion. Protocols concerning preservation solutions (nature, pressure, volume) are extremely heterogeneous. In 54% of DBDs and 61% of DCDs an arterial back table pressure perfusion is performed. Steroids (20%-10%), heparin (72%-60%), prostacyclin (3%-7%), and fibrinolytics (4%-11%) are used as donor-protective interventions in DBD and DCD cases, respectively. In 2% of DBD and 6% of DCD cases a hepatic artery reperfusion is performed first. In 4% of DBD and 6% of DCD cases, fibrinolytics are administered through the hepatic artery during the bench and/or implantation. CONCLUSION: This European web survey shows for the first time the heterogeneity in the management of bile ducts during procurement, preservation, and transplantation in Europe. In the context of sharing more marginal liver grafts, an expert meeting must be organized to formulate guidelines to be applied to protect liver grafts against IC.
APHP Hospital Paul Brousse Inserm U985 University Paris Sud Paris France
Department of Abdominal Transplant Surgery University Hospitals Leuven KU Leuven Leuven Belgium
Division of Transplantation Department of Surgery Medical University of Vienna Vienna Austria
Liver Unit University of Birmingham Birmingham United Kingdom
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19044666
- 003
- CZ-PrNML
- 005
- 20200120103542.0
- 007
- ta
- 008
- 200109s2019 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.transproceed.2019.04.018 $2 doi
- 035 __
- $a (PubMed)31301856
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Meurisse, Nicolas $u Department of Abdominal Transplant Surgery, University of Liege Academic Hospital, ULg CHU, Liege, Belgium; Department of Abdominal Transplant Surgery, University Hospitals Leuven, KU Leuven, Leuven, Belgium.
- 245 10
- $a Heterogeneity of Bile Duct Management in the Development of Ischemic Cholangiopathy After Liver Transplantation: Results of a European Liver and Intestine Transplant Association Survey / $c N. Meurisse, D. Monbaliu, G. Berlakovich, P. Muiesan, M. Oliverius, R. Adam, J. Pirenne,
- 520 9_
- $a BACKGROUND: Surgical factors and direct cytotoxicity of bile salts on cholangiocytes may play a role in the development of ischemic cholangiopathy (IC) after liver transplantation (LTx). There is no validated consensus on how to protect the bile ducts during procurement, static preservation, and LTx. Meanwhile, IC remains the most troublesome complication after LTx. AIM: To characterize bile duct management techniques during the LTx process among European transplant centers in cases of donation after brain death (DBD) and circulatory death (DCD). METHOD: An European Liver and Intestine Transplant Association-European Liver Transplant Registry web survey designed to conceal respondents' personal information was sent to surgeons procuring and/or transplanting livers in Europe. RESULTS: Sixty-five percent of responses came from large transplant centers (>50 procurements/y). In 8% of DBDs and 14% of DCDs the bile duct is not rinsed. In 46% of DBDs and 52% of DCDs surgeons prefer to remove the gallbladder after graft reperfusion. Protocols concerning preservation solutions (nature, pressure, volume) are extremely heterogeneous. In 54% of DBDs and 61% of DCDs an arterial back table pressure perfusion is performed. Steroids (20%-10%), heparin (72%-60%), prostacyclin (3%-7%), and fibrinolytics (4%-11%) are used as donor-protective interventions in DBD and DCD cases, respectively. In 2% of DBD and 6% of DCD cases a hepatic artery reperfusion is performed first. In 4% of DBD and 6% of DCD cases, fibrinolytics are administered through the hepatic artery during the bench and/or implantation. CONCLUSION: This European web survey shows for the first time the heterogeneity in the management of bile ducts during procurement, preservation, and transplantation in Europe. In the context of sharing more marginal liver grafts, an expert meeting must be organized to formulate guidelines to be applied to protect liver grafts against IC.
- 650 _2
- $a žlučové cesty $x krevní zásobení $x transplantace $7 D001652
- 650 _2
- $a cholangitida $x etiologie $7 D002761
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a přežívání štěpu $7 D006085
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a ischemie $x etiologie $7 D007511
- 650 _2
- $a transplantace jater $x škodlivé účinky $7 D016031
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a uchovávání orgánů $x škodlivé účinky $x metody $7 D009926
- 650 _2
- $a perfuze $x škodlivé účinky $x metody $7 D010477
- 650 _2
- $a pooperační komplikace $x etiologie $7 D011183
- 650 _2
- $a reperfuze $x škodlivé účinky $x metody $7 D015424
- 650 _2
- $a průzkumy a dotazníky $7 D011795
- 650 _2
- $a odběr tkání a orgánů $x škodlivé účinky $x metody $7 D020858
- 651 _2
- $a Evropa $7 D005060
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Monbaliu, Diethard $u Department of Abdominal Transplant Surgery, University Hospitals Leuven, KU Leuven, Leuven, Belgium.
- 700 1_
- $a Berlakovich, Gabriela $u Division of Transplantation, Department of Surgery, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Muiesan, Paolo $u Liver Unit, University of Birmingham, Birmingham, United Kingdom.
- 700 1_
- $a Oliverius, Martin $u Department of Surgery of the 3rd Faculty of Medicine Charles University and Kralovske Vinohrady Hospital, Prague, Czech Republic.
- 700 1_
- $a Adam, René $u APHP Hospital Paul Brousse, Inserm U985, University Paris Sud, Paris, France.
- 700 1_
- $a Pirenne, Jacques $u Department of Abdominal Transplant Surgery, University Hospitals Leuven, KU Leuven, Leuven, Belgium. Electronic address: jacques.pirenne@uzleuven.be.
- 773 0_
- $w MED00004556 $t Transplantation proceedings $x 1873-2623 $g Roč. 51, č. 6 (2019), s. 1926-1933
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31301856 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20200109 $b ABA008
- 991 __
- $a 20200120103918 $b ABA008
- 999 __
- $a ok $b bmc $g 1482935 $s 1083339
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 51 $c 6 $d 1926-1933 $e 20190710 $i 1873-2623 $m Transplantation proceedings $n Transplant Proc $x MED00004556
- LZP __
- $a Pubmed-20200109