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      Feasibility of transnasal endoscopy in screening for esophageal and gastric varices in patients with chronic liver disease

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          Abstract

          Background and study aims

           Screening for esophageal and gastric varices is indicated for patients with portal hypertension or cirrhosis. Typically, conventional endoscopy is used; however, the need for sedation increases the costs and risks, especially in cirrhotic patients. Use of transnasal endoscopy with an ultrathin endoscope enables study of the upper gastrointestinal tract without the need for sedation. The objective of this study is to evaluate the feasibility of transnasal endoscopy in screening for esophageal and gastric varices in patients with chronic liver disease.

          Patients and methods 

          This was a prospective study in which transnasal endoscopy was carried out in patients with cirrhosis or portal hypertension who had indications for screening of esophageal and gastric varices. The following variables were evaluated: demographical data, duration of procedure, patient tolerance and acceptance, adverse events (AEs), endoscopic findings and interobserver agreement related to portal hypertension alterations ( kappa index).

          Results 

          A total of 50 patients entered the study. The most common cause of liver disease was chronic viral hepatitis (66 %). Among the cirrhotic patients, most of the patients were Child-Pugh A (74 %). In 5 patients (10 %), nasal intubation was not possible. Two patients (4 %) experienced minor epistaxis. Tolerance was excellent or good in 92 % according with a visual analogic scale. In 16 patients (32 %), esophageal varices were detected and in 2 patients (4 %) gastric varices were detected. The mean duration of the procedure was 7 minutes.

          Conclusions 

          Transnasal endoscopy is feasible, effective and well tolerated for screening of esophageal and gastric varices in patients with chronic liver disease. It can be performed in outpatient clinics safely and without the use of sedation.

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          Most cited references30

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          Pharmacological treatment of portal hypertension: an evidence-based approach.

          Continuing advances in the knowledge of the pathophysiology of portal hypertension result in the progressive expansion of the spectrum of drugs with a potential role for clinical practice, with objectives that now tend to include the prevention of the enlargement or even the development of esophageal varices. This systematic review summarizes the evidence of efficacy of drug therapy for portal hypertension and draws recommendations for clinical practice. Although there is not yet enough evidence to support the treatment for the prevention of the development or enlargement of varices, nonselective beta-blockers are the first-choice therapy to prevent the first bleeding in patients with medium or large-sized varices and rebleeding in patients surviving a bleeding episode. The clinical role of isosorbide-5-mononitrate either alone or in association with beta-blockers still remains unsettled. Vasoactive drugs are generally effective and safe in controlling acute variceal bleeding, although the evidence is not equivalent for each of them.
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            The course of patients after variceal hemorrhage.

            We analyzed the clinical course of 85 consecutive, endoscopically verified variceal bleeders. Most patients were alcoholics with advanced stages of hepatic dysfunction. Bleeding was major in all, and medical mortality was 42% at 6 wk. Factors affecting mortality and factors not affecting survival, such as age and comorbid conditions, were identified. Sixty percent of early deaths and 40% of late deaths were attributable to bleeding. Approximately one-third of patients experienced rebleeding within 6 wk, and one-third of survivors experienced subsequent bleeds. In these patients significant improvement with observation was often anticipated, but could not be verified. The majority of deaths associated with variceal bleeding occur soon after the bleeding episode. Those who survive the hospitalization for bleeding may not fare worse than others of similar hepatic functional reserve but who have not experienced bleeding. We demonstrated that statistically significantly different survival curves could be obtained from the same population by changing the zero time for calculating survival. For example, a 1-yr survival rate of 34% for all medically treated patients could be raised to 52% by eliminating from consideration those who failed to survive 2 wk. The long-term survival course of those surviving greater than 2 wk was not statistically significantly different from published series of unselected cirrhotics without bleeding. Variceal bleeding is a common accompaniment of advanced liver disease. We propose that any substantial improvement in long-term survival must improve survival for the early period. If controlled trials are to be done, patients should be matched for hepatic functional reserve and identical zero time for calculating survival must be used.
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              Prevalence and risk factors of non-alcoholic fatty liver disease in potential living liver donors in Korea: a review of 589 consecutive liver biopsies in a single center.

              The aim of the study was to evaluate the prevalence and risk factors of biopsy-proven non-alcoholic fatty liver disease (NAFLD) in potential living liver donors and to evaluate the efficacy of imaging techniques for the detection of steatosis in donors. We reviewed the results of liver biopsy, ultrasonography (USG) and computed tomography (CT) and biochemical data performed in 589 consecutive potential liver donors as a pretransplantation work up from July 2004 to September 2005 at Asan Medical Centre. Of 589 participants, 408 (69.3%) were men, with a mean age of 31.1+/-9.5 years. NAFLD (5% steatosis in biopsy) was diagnosed in 303 (51.4%); >30% steatosis in 61 (10.4%) and non-alcoholic steatohepatitis in 13 (2.2%). The independent risk factors for >30% steatosis were age over 30 (OR=2.223; p=0.014), obesity (OR=5.320; p 30% steatosis was 92.3% and 64.1%, and positive predictive value was only 34.5% and 45.1%, respectively. NAFLD was highly prevalent in potential living liver donors. The independent risk factors for significant steatosis were older age, obesity and hypertriglyceridemia. USG and CT had limitations in detecting significant steatosis in liver donors.
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                Author and article information

                Journal
                Endosc Int Open
                Endosc Int Open
                10.1055/s-00025476
                Endoscopy International Open
                © Georg Thieme Verlag KG (Stuttgart · New York )
                2364-3722
                2196-9736
                July 2017
                06 July 2017
                : 5
                : 7
                : E646-E651
                Affiliations
                Hospital das Clínicas, Federal University of Mimas Gerais, Alfa Institute of Gastroenterology, Belo Horizonte, Minas Gerais, Brazil
                Author notes
                Corresponding author Anderson Antônio de Faria Universidad Federal de Minas Gerais – Medicine Avenida Professor Alfredo Balena 100. Santa Efigenia Instituto Alfa de Gatroenterologia Belo Horizonte Belo Horizonte Minas Gerais31270-901 Brazil+3409-9408 andersonpita@ 123456yahoo.com.br
                Article
                10.1055/s-0043-107781
                5500113
                a4380231-8247-4ca1-9a3a-d096a542351a
                © Thieme Medical Publishers
                History
                : 23 October 2016
                : 24 March 2017
                Categories
                Original article

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