Mario Henrique Mendes de Mattos Meine
Universidade Federal do Rio Grande do Sul
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Transplantation proceedings | 2015
Mario Henrique Mendes de Mattos Meine; Ian Leipnitz; Maria Lucia Zanotelli; Eduardo Schlindwein; Guillermo Kiss; J. Martini; A. de Medeiros Fleck; M. Mucenic; A. de Mello Brandão; Claudio Augusto Marroni; G.P. Craco Cantisani
The effectiveness of liver preservation solutions remains in evidence. Cold ischemia time, steatosis, expanded criterion donors, operational cost, and survival represent important roles in its success. In a prospective cohort study between August 2009 and April 2014, 178 patients were allocated into an Institut Georges Lopez - 1 (IGL-1) solution group (63.5%) or histidine-tryptophan-ketoglutarate (HTK) group (36.5%). There were no differences among recipients characteristics including age, skin color, gender, Model for End-stage Liver Disease score, acute rejection, cholestasis, and reperfusion syndrome incidences. Also, donors, age average, skin color, donor risk index, time in intensive care unit, hemodynamic variables, infections, and steatosis incidences were similar. The average cold ischemia time was 494 minutes in the IGL-1 group and 489 minutes in the HTK group (P = .77). Alanine aminotransferase and aspartate aminotransferase serum levels on the first postoperative day were 707 and 1185 mg/dL, respectively, with IGL-1 and 1298 and 2291 mg/dL, respectively, with HTK (P = .016) and similar at day 15 (P > .88). The incidence of delayed graft function was 4.5% with IGL-1 and 4.6% with HTK (P = .90). The incidence primary nonfunction was 2.7% with IGL-1 and 3.1% with HTK (P = .71). The incidence of perioperative death was 11.5% with IGL-1 and 13.8% with HTK (P = .94). The survival in 30 months was 86% in IGL-1 group and 82% in HTK group (P = .66). Both preservation solutions are efficient to liver transplantations with deceased donors. Major prospective trials are necessary to evaluate each preservation solutions particularities. The preservation solution availability in each transplantation center must guide its use at the present moment.
Acta Cirurgica Brasileira | 2006
Tomáz de Jesus Maria Grezzana Filho; Carlos Otavio Corso; Maria Lucia Zanotelli; Claudio Augusto Marroni; Ajacio Bandeira de Mello Brandao; Eduardo Schlindwein; Ian Leipnitz; Mario Henrique Mendes de Mattos Meine; Alfeu de Medeiros Fleck; Ricardo Hoppen; Guillermo Kiss; Guido Cantisani
PURPOSE The oxidative stress is an important mechanism responsible for dysfunction after orthotopic liver transplantation (OLT). Glutathione (GSH) low levels after cold storage render the grafts vulnerable to reperfusion injury. Aim of this study was to evaluate GSH and oxidized glutathione (GSSG) liver concentrations, the hepatocellular injury and function in optimal and suboptimal grafts after human OLT. METHODS Liver biopsies were taken in 33 patients before the implant and two hours after reperfusion, allowing determination of GSH, GSSG and oxidative stress ratio (GSH/GSSG). Serum transaminases, prothrombin activity (PT) and factor V were measured to evaluate injury and function respectively. Histopathological injury was analyzed by an index of five parameters. RESULTS There was a decrease in GSH (p<0.01) after reperfusion (0.323 +/- 0.062 ìmol/g to 0.095 +/- 0.01 ìmol/g and 0.371 +/- 0.052 ìmol/g to 0.183 +/- 0.046 ìmol/g) in suboptimal and optimal groups, respectively. An increase of GSSG (p<0.05) occurred after reperfusion (0.172 +/- 0.038 ìmol/g to 0.278 +/- 0.077 ìmol/g and 0.229 +/- 0.048 ìmol/g to 0.356 +/- 0.105 ìmol/g) in suboptimal and optimal groups, respectively. A decrease (p<0.01) occurred in the GSH/GSSG ratio after reperfusion (2.23 +/- 0.31 to 0.482 +/- 0.042 and 2.47 +/- 0.32 to 0.593 +/- 0.068) in suboptimal and optimal groups, respectively. Histopathological injury scores were higher (p<0.05) in the suboptimal group than in optimal (6.46 +/- 0.4 vs. 5.39 +/- 1.1) and showed correlation with PT and factor V in the optimal group (p<0.05). Multivariate analysis pointed steatosis as an independent risk factor to histopathological injury (p<0.05). CONCLUSION There was a significant GSH depletion and GSSG formation after cold storage and reperfusion due to a similar oxidative stress in optimal and suboptimal grafts, but these levels were not related to graft viability.
World Journal of Gastroenterology | 2018
Claudio Augusto Marroni; Alfeu de Medeiros Fleck; Sabrina Alves Fernandes; Lucas Homercher Galant; Marcos Mucenic; Mario Henrique Mendes de Mattos Meine; Guilherme Mariante-Neto; Ajacio Bandeira de Mello Brandao
Alcohol consumption accounts for 3.8% of annual global mortality worldwide, and the majority of these deaths are due to alcoholic liver disease (ALD), mainly alcoholic cirrhosis. ALD is one of the most common indications for liver transplantation (LT). However, it remains a complicated topic on both medical and ethical grounds, as it is seen by many as a “self-inflicted disease”. One of the strongest ethical arguments against LT for ALD is the probability of relapse. However, ALD remains a common indication for LT worldwide. For a patient to be placed on an LT waiting list, 6 mo of abstinence must have been achieved for most LT centers. However, this “6-mo rule” is an arbitrary threshold and has never been shown to affect survival, sobriety, or other outcomes. Recent studies have shown similar survival rates among individuals who undergo LT for ALD and those who undergo LT for other chronic causes of end-stage liver disease. There are specific factors that should be addressed when evaluating LT patients with ALD because these patients commonly have a high prevalence of multisystem alcohol-related changes. Risk factors for relapse include the presence of anxiety or depressive disorders, short pre-LT duration of sobriety, and lack of social support. Identification of risk factors and strengthening of the social support system may decrease relapse among these patients. Family counseling for LT candidates is highly encouraged to prevent alcohol consumption relapse. Relapse has been associated with unique histopathological changes, graft damage, graft loss, and even decreased survival in some studies. Research has demonstrated the importance of a multidisciplinary evaluation of LT candidates. Complete abstinence should be attempted to overcome addiction issues and to allow spontaneous liver recovery. Abstinence is the cornerstone of ALD therapy. Psychotherapies, including 12-step facilitation therapy, cognitive-behavioral therapy, and motivational enhancement therapy, help support abstinence. Nutritional therapy helps to reverse muscle wasting, weight loss, vitamin deficiencies, and trace element deficiencies associated with ALD. For muscular recovery, supervised physical activity has been shown to lead to a gain in muscle mass and improvement of functional activity. Early LT for acute alcoholic hepatitis has been the subject of recent clinical studies, with encouraging results in highly selected patients. The survival rates after LT for ALD are comparable to those of patients who underwent LT for other indications. Patients that undergo LT for ALD and survive over 5 years have a higher risk of cardiorespiratory disease, cerebrovascular events, and de novo malignancy.
Transplantation Proceedings | 2006
Mario Henrique Mendes de Mattos Meine; Maria Lucia Zanotelli; J. Neumann; Guillermo Kiss; T. de Jesus Grezzana; Ian Leipnitz; Eduardo Schlindwein; Alfeu de Medeiros Fleck; Ana L. M. Gleisner; A. de Mello Brandão; Claudio Augusto Marroni; Guido Cantisani
Rev. AMRIGS | 2006
Tomáz Jesus Maria Grezzana; Mario Henrique Mendes de Mattos Meine; Eduardo Schlindwein; Lenine Cunha; Claudio Galleano Zettler; Carlos Otavio Corso
Transplantation Proceedings | 2018
M. Mucenic; A. Bandeira de Mello Brandao; Claudio Augusto Marroni; A. Medeiros Fleck; Maria Lucia Zanotelli; Guillermo Kiss; Mario Henrique Mendes de Mattos Meine; Ian Leipnitz; E. Soares Schlindwein; J. Martini; Ane Micheli Costabeber; F.K.F. Sacco; G.P. Cracco Cantisani
Archive | 2005
Douglas Alano Simonetto; Alex Schwengber; Anderson Ricardo Caldas Nunes; Maria Lucia Zanotelli; Guido Cantisani; Carlos Thadeu Schmidt Cerski; Ajacio Bandeira de Mello Brandao; Guilhermo Kiss; Alfeu de Medeiros Fleck Júnior; Ian Leipnitz; Mario Henrique Mendes de Mattos Meine
Archive | 2005
Leonardo Leiria de Moura da Silva; Nadima Vieira Toscani; Christina Garcia da Silva Fraga; Alex Schwengber; Carlos Thadeu Schmidt Cerski; Alfeu de Medeiros Fleck Júnior; Guilhermo Kiss; Tomáz de Jesus Maria Grezzana Filho; Mario Henrique Mendes de Mattos Meine; Ian Leipnitz; Eduardo Schlindwein; Maria Lucia Zanotelli; Ajacio Bandeira de Mello Brandao; Guido Pio Gracco Cantisani; Claudio Augusto Marroni
Archive | 2005
Anderson Ricardo Caldas Nunes; Christina Garcia da Silva Fraga; Leonardo Leiria de Moura da Silva; Alfeu de Medeiros Fleck Júnior; Guillermo Kiss; Thomaz Grezzana Filho; Mario Henrique Mendes de Mattos Meine; Ian Leipnitz; Eduardo Schlindwein; Maria Lucia Zanotelli; Ajacio Bandeira de Mello Brandao; Guido Cantisani; Douglas Alano Simonetto
Archive | 2004
Alex Schwengber; Claudio Augusto Marroni; Christina Garcia da Silva Fraga; Leonardo Leiria de Moura da Silva; Felipe S. Paz; Alfeu de Medeiros Fleck Júnior; Guilhermo Kiss; Tomáz de Jesus Maria Grezzana Filho; Mario Henrique Mendes de Mattos Meine; Ian Leipnitz; Eduardo Schlindwein; Maria Lucia Zanotelli; Ajacio Bandeira de Mello Brandao; Guido Pio Gracco Cantisani
Collaboration
Dive into the Mario Henrique Mendes de Mattos Meine's collaboration.
Universidade Federal de Ciências da Saúde de Porto Alegre
View shared research outputsAjacio Bandeira de Mello Brandao
Universidade Federal do Rio Grande do Sul
View shared research outputsTomáz de Jesus Maria Grezzana Filho
Universidade Federal do Rio Grande do Sul
View shared research outputsLeonardo Leiria de Moura da Silva
Universidade Federal de Ciências da Saúde de Porto Alegre
View shared research outputs