Literature DB >> 34988145

Editorial: reducing blood loss in liver transplantation-the impact of surgical technique.

Marcos V Perini1,2, Vijayaragavan Muralidharan1,2.   

Abstract

Entities:  

Year:  2021        PMID: 34988145      PMCID: PMC8667100          DOI: 10.21037/atm-2021-13

Source DB:  PubMed          Journal:  Ann Transl Med        ISSN: 2305-5839


× No keyword cloud information.
Liver transplantation is the standard of care for end stage liver disease, fulminant liver failure and selected liver malignancies. It is performed world-wide with acceptable morbidity and mortality. There are many parallels between transplantation surgery and abdominal oncological surgery ranging from pre-operative work up, imaging, peri-operative management and post-operative recovery, with advances in each translating to the other. Peri-operative blood transfusion and in particular, massive blood transfusion, has been shown to be associated with increased morbidity (1), mortality (2), worse oncological outcomes (3), survival (4,5) and a significant health economic cost (6). Many initiatives have been investigated and applied to minimize this precious resource in various clinical settings. These include pre-operative correction of anaemia and iron deficiency, auto-transfusion, donor blood usage (7), perioperative management of coagulopathy, advanced anaesthetic techniques including low CVP anaesthesia, objective intra-operative monitoring of coagulopathy (8), the intra operative use of topical haemostatic agents and the operative use of energy devices (1,9,10). In liver transplantation, surgeons have to face the added challenge of clinical or sub-clinical portal hypertension. This burden begins at the skin incision (caput medusae, recanalized paraumbilical vein) through porta hepatis dissection (porta hepatis varices, peri-choledochal vessels) and the retroperitoneal and para-caval regions where further portosystemic shunts are usually present. The vessels that form collaterals or varices tend to be anatomically thinner, more friable and have raised venous pressure within them, increasing the risk of inadvertent injury and bleeding during surgery. Obtaining haemostasis may involve surgical ligatures, stapling devices, energy sealant devices or monopolar cautery. Liver transplantation is undertaken by highly skilled, clinically experienced and technically proficient teams whose meticulous surgical technique contribute significantly to the reduction in operative and post-operative blood loss. Surgeons would make a clinical judgement to mentally classify a vessel to be treated to be low, moderate or high-risk vessel. This decision is likely to be biased by the size of the vessel, vessel wall quality, amount of tissue around it, vicinity with a major vascular structure and difficulty in access before the vessel is treated or in the event of failure after the treatment. When dealing with portal hypertension and abnormal collateral vessels, in which the vein wall tends to be thinner and more friable, surgeons tend to avoid taking risks, even more in the setting of a long and exhaustive operation. Vessels with low risk of bleeding, in the interest of time, tend to be treated with monopolar or even bipolar cautery. Medium risk vessels are often treated by a sealant device or by surgical ligation. High-risk vessels are usually treated with surgical ties, sutures or staplers. Therefore, the interplay between monopolar, sealant device and surgical ligation is likely to be unique in each individual operation making it hard to assess objectively the relative efficiency of each technique. In this issue, Lee et al., objectively analyzed the use of a sealant device (LigaSureTM) versus a monopolar cautery during the recipient operation (hepatectomy and after vascular reconstruction) in the liver transplant setting in a major HPB and Liver Transplant center is South Korea (11). From a pool of 187 patients having liver transplant in 15 months, 118 had the hepatectomy performed with monopolar and 69 with LigaSureTM, showing that the most common energy device used in the author’s centre is the monopolar cautery (63.1%). The authors used a propensity score matching analysis controlling 14 variables. They were able to compare 138 patients, with 69 in each group. There was no difference regarding intra-operative blood loss and blood transfusion, however there was significantly higher rates of postoperative bleeding (measured by re-operation) in the monopolar cautery group (18.8%) when compared to the LigaSureTM group (4.35%). The authors also found less infective complications rates in the LigaSureTM group. However, the outcomes variable (infective complication) is not clearly defined in the methodology (intra-abdominal infection, surgical site infection, lung or catheter related infection). One could speculate that the source of bleeding requiring re-operation and potential source of subsequent infective complications were the smaller vessels routinely ablated by monopolar cautery. This would support the hypothesis that the regular use of sealant energy devices on these small vessels may be the reason for the better outcome. The medium and larger vessels would be expected to be routinely sealed by energy device, surgical ligatures or stapling devices. This is particularly relevant when clamping the portal vein at the time of liver explantation, when there is an increase in the portal pressure which could lead to bleeding in areas previous sealed by the LigaSure or the monopolar cautery and the former may provide better seal. This study published by Lee et al., has shown that simple expediency of using a sealant energy device in areas where monopolar cautery is used, may have a significant effect on post-operative bleeding, return to theatre and infective complications. Other studies addressing the use of sealant devices in liver transplantation have shown they have the potential to save hospital costs, reduce surgical time and decrease blood loss. Moreover, it has been suggested that it may also reduce staff exposure to sharp instruments (10,12). Results from a prospective trial are, however, still pending (9). Additional areas of interest would be the impact of temporary portocaval shunts (in temporary decompressing the portal venous pressure until the cirrhotic liver is removed and the new graft re-anastomosed), use of topical haemostatic agents, the use of a haemostatic pause after revascularization and details of infective complications. While a prospective study would confirm these findings, this study strengthens the concept that a multi-modal approach is important to minimizing perioperative blood loss, even more in situations where high blood loss is expected such as liver transplantation surgery. The article’s supplementary files as
  12 in total

1.  Perioperative Fresh Red Blood Cell Transfusion May Negatively Affect Recipient Survival After Liver Transplantation.

Authors:  Sangbin Han; Ji Hye Kwon; Sun Hee Jung; Ji Young Seo; Yong Jun Jo; Jin Sung Jang; Seung Min Yeon; Sin Ho Jung; Justin Sangwook Ko; Mi Sook Gwak; Duck Cho; Hee Jeong Son; Gaab Soo Kim
Journal:  Ann Surg       Date:  2018-02       Impact factor: 12.969

2.  Blood transfusion requirement during liver transplantation is an important risk factor for mortality.

Authors:  Abbas Rana; Henrik Petrowsky; Johnny C Hong; Vatche G Agopian; Fady M Kaldas; Douglas Farmer; Hasan Yersiz; Jonathan R Hiatt; Ronald W Busuttil
Journal:  J Am Coll Surg       Date:  2013-03-09       Impact factor: 6.113

Review 3.  Massive haemorrhage in liver transplantation: Consequences, prediction and management.

Authors:  Stuart Cleland; Carlos Corredor; Jia Jia Ye; Coimbatore Srinivas; Stuart A McCluskey
Journal:  World J Transplant       Date:  2016-06-24

4.  Comparison of harmonic scalpel versus conventional knot tying for transection of short hepatic veins at liver transplantation: prospective randomized study.

Authors:  A Olmez; K Karabulut; C Aydin; C Kayaalp; S Yilmaz
Journal:  Transplant Proc       Date:  2012 Jul-Aug       Impact factor: 1.066

5.  Efficiency of the LigaSure vessel sealing system for recipient hepatectomy in liver transplantation.

Authors:  J C Lamattina; M Hosseini; S A Fayek; B Philosophe; R N Barth
Journal:  Transplant Proc       Date:  2013-06       Impact factor: 1.066

6.  Intraoperative red blood cell transfusion in liver transplantation: influence on patient outcome, prediction of requirements, and measures to reduce them.

Authors:  Emilio Ramos; Antonia Dalmau; Antonio Sabate; Carmen Lama; Laura Llado; Juan Figueras; Eduardo Jaurrieta
Journal:  Liver Transpl       Date:  2003-12       Impact factor: 5.799

7.  SEALIVE: the use of technical vessel-sealing devices for recipient hepatectomy in liver transplantation: study protocol for a randomized controlled trial.

Authors:  Philipp Houben; Elias Khajeh; Ulf Hinz; Phillip Knebel; Markus K Diener; Arianeb Mehrabi
Journal:  Trials       Date:  2018-07-16       Impact factor: 2.279

8.  Perioperative blood transfusion decreases long-term survival in pediatric living donor liver transplantation.

Authors:  Karina Gordon; Estela Regina Ramos Figueira; Joel Avancini Rocha-Filho; Luiz Antonio Mondadori; Eduardo Henrique Giroud Joaquim; Joao Seda-Neto; Eduardo Antunes da Fonseca; Renata Pereira Sustovitch Pugliese; Agustin Moscoso Vintimilla; Jose Otavio Costa Auler; Maria Jose Carvalho Carmona; Luiz Augusto Carneiro D'Alburquerque
Journal:  World J Gastroenterol       Date:  2021-03-28       Impact factor: 5.742

9.  LigaSure versus monopolar cautery for recipient hepatectomy in liver transplantation: a propensity score-matched analysis.

Authors:  Jeong-Moo Lee; Kwangpyo Hong; Eui Soo Han; Sanggyun Suh; Suyoung Hong; Suk Kyun Hong; YoungRok Choi; Nam-Joon Yi; Kwang-Woong Lee; Kyung-Suk Suh
Journal:  Ann Transl Med       Date:  2021-07

10.  The effect of perioperative packed red blood cells transfusion on patient outcomes after liver transplant for hepatocellular carcinoma.

Authors:  Hala Muaddi; Phillipe Abreu; Tommy Ivanics; Marco Claasen; Peter Yoon; Andre Gorgen; David Al-Adra; Adam Badenoch; Stuart McCluskey; Anand Ghanekar; Trevor Reichman; Gonzalo Sapisochin
Journal:  HPB (Oxford)       Date:  2021-07-05       Impact factor: 3.647

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.