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Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy

Objectives: Evaluation of the outcome and experience in 2 years of management of portal hypertensive gastropathy (PHG) by argon plasma coagulation (APC) in a cohort of Egyptian cirrhotic patients. Methods: This study was conducted over a 2-year period from January 2011 to February 2013. Upper gastro...

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Autores principales: Hanafy, Amr Shaaban, El Hawary, Amr Talaat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: © Georg Thieme Verlag KG 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063638/
https://www.ncbi.nlm.nih.gov/pubmed/27747278
http://dx.doi.org/10.1055/s-0042-114979
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author Hanafy, Amr Shaaban
El Hawary, Amr Talaat
author_facet Hanafy, Amr Shaaban
El Hawary, Amr Talaat
author_sort Hanafy, Amr Shaaban
collection PubMed
description Objectives: Evaluation of the outcome and experience in 2 years of management of portal hypertensive gastropathy (PHG) by argon plasma coagulation (APC) in a cohort of Egyptian cirrhotic patients. Methods: This study was conducted over a 2-year period from January 2011 to February 2013. Upper gastrointestinal endoscopy was performed to evaluate the degree and site of PHG. APC was applied to areas with mucosal vascular lesions. Results: In total, 200 cirrhotic patients were enrolled; 12 patients were excluded due to death (n = 6) caused by hepatic encephalopathy (n = 3), hepatorenal syndrome (n = 2), or chronic lymphatic leukemia (n = 1), or did not complete the treatment sessions (n = 6), so 188 patients completed the study. PHG was mainly fundic in 73 patients (38.8 %), corporeal in 66 patients (35.1 %), and pangastric in 49 patients (26.1 %) (P = 0.026). Patients were exposed to APC and received proton pump inhibitors together with propranolol at a dose sufficient to reduce the heart rate by 25 % or down to 55 beats/min. The mean (± standard deviation) number of sessions was 1.65 ± 0.8; six patients needed four sessions (3.2 %), 19 patients needed three sessions (10.1 %), 74 patients needed two sessions (39.4 %), and 89 patients needed one session (47.3 %). Patients with fundic and corporeal PHG required the lowest number of sessions (P = 0.000). Patients were followed up every 2 months for up to 1 year; the end point was a complete response with improved anemia and blood transfusion requirement which was achieved after one session in 89 patients (75.4 %), two sessions in 24 patients (20.3 %) and three sessions in five patients (4.3 %). A complete response was more prevalent in patients with corporeal and fundic PHG (P = 0.04). Conclusions: After 2 years’ experience in managing PHG, we found that a combination of APC and non-selective beta blockers was highly efficacious and safe in controlling bleeding from PHG. In addition, APC alone is rapid, and effective in the control of PHG induced bleeding, especially when beta blockers are contraindicated.
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spelling pubmed-50636382016-10-14 Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy Hanafy, Amr Shaaban El Hawary, Amr Talaat Endosc Int Open Objectives: Evaluation of the outcome and experience in 2 years of management of portal hypertensive gastropathy (PHG) by argon plasma coagulation (APC) in a cohort of Egyptian cirrhotic patients. Methods: This study was conducted over a 2-year period from January 2011 to February 2013. Upper gastrointestinal endoscopy was performed to evaluate the degree and site of PHG. APC was applied to areas with mucosal vascular lesions. Results: In total, 200 cirrhotic patients were enrolled; 12 patients were excluded due to death (n = 6) caused by hepatic encephalopathy (n = 3), hepatorenal syndrome (n = 2), or chronic lymphatic leukemia (n = 1), or did not complete the treatment sessions (n = 6), so 188 patients completed the study. PHG was mainly fundic in 73 patients (38.8 %), corporeal in 66 patients (35.1 %), and pangastric in 49 patients (26.1 %) (P = 0.026). Patients were exposed to APC and received proton pump inhibitors together with propranolol at a dose sufficient to reduce the heart rate by 25 % or down to 55 beats/min. The mean (± standard deviation) number of sessions was 1.65 ± 0.8; six patients needed four sessions (3.2 %), 19 patients needed three sessions (10.1 %), 74 patients needed two sessions (39.4 %), and 89 patients needed one session (47.3 %). Patients with fundic and corporeal PHG required the lowest number of sessions (P = 0.000). Patients were followed up every 2 months for up to 1 year; the end point was a complete response with improved anemia and blood transfusion requirement which was achieved after one session in 89 patients (75.4 %), two sessions in 24 patients (20.3 %) and three sessions in five patients (4.3 %). A complete response was more prevalent in patients with corporeal and fundic PHG (P = 0.04). Conclusions: After 2 years’ experience in managing PHG, we found that a combination of APC and non-selective beta blockers was highly efficacious and safe in controlling bleeding from PHG. In addition, APC alone is rapid, and effective in the control of PHG induced bleeding, especially when beta blockers are contraindicated. © Georg Thieme Verlag KG 2016-10 2016-10-06 /pmc/articles/PMC5063638/ /pubmed/27747278 http://dx.doi.org/10.1055/s-0042-114979 Text en © Thieme Medical Publishers
spellingShingle Hanafy, Amr Shaaban
El Hawary, Amr Talaat
Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy
title Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy
title_full Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy
title_fullStr Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy
title_full_unstemmed Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy
title_short Efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy
title_sort efficacy of argon plasma coagulation in the management of portal hypertensive gastropathy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063638/
https://www.ncbi.nlm.nih.gov/pubmed/27747278
http://dx.doi.org/10.1055/s-0042-114979
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