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4.
Liver Int ; 42(5): 1121-1131, 2022 05.
Article in English | MEDLINE | ID: mdl-35220668

ABSTRACT

BACKGROUND & AIMS: limited evidence is available to guide hepatologists regarding endoscopic surveillance of oesophageal varices (EV) in Hepatitis C Virus (HCV)-positive cirrhotic patients achieving a sustained virologic response. To address these issues, we conducted a long-term prospective study on 427 HCV-positive cirrhotic patients successfully treated by Direct Antiviral Agents (DAAs). METHODS: Patients were divided into two groups according to their baseline Baveno VI status: Group 1 (92, 21.5%, favourable Baveno VI status) and Group 2 (335, 78.5%, unfavourable Baveno VI status). Each patient underwent baseline endoscopy and was endoscopically monitored for a median follow-up of 65.2 months according to Baveno VI recommendations. RESULTS: About 4.3% of Group 1 patients showed baseline EV compared with 30.1% of Group 2 patients (p < .0001). No patients belonging to Group 1 without baseline EV developed EV at follow-up endoscopy compared with 6.5% in Group 2 patients (p = .02); 69/107 (64.5%) patients with baseline EV showed small varices. During the endoscopic follow-up, EV disappeared/improved in 36 (33.6%), were stable in 39 (36.4%) and worsened in 32 (29.9%) patients, all belonging to Group 2 (p = .001). Improvement in Baveno VI status was observed in 118/335 (35.2%, p < .0001) of Group 2 patients and among those without pre-therapy EV, none developed EV throughout the follow-up. CONCLUSIONS: HCV-positive cirrhotic patients cured by DAAs showing baseline favourable Baveno VI status and no worsening during follow-up can safely avoid endoscopic screening and surveillance. Patients having unfavourable Baveno VI status without baseline EV who improve their status may suspend further endoscopic surveillance.


Subject(s)
Elasticity Imaging Techniques , Esophageal and Gastric Varices , Hepatitis C, Chronic , Antiviral Agents/therapeutic use , Endoscopy, Gastrointestinal , Esophageal and Gastric Varices/etiology , Hepatitis C, Chronic/complications , Hepatitis C, Chronic/drug therapy , Humans , Liver Cirrhosis , Prospective Studies
5.
Minerva Gastroenterol (Torino) ; 68(2): 121-132, 2022 Jun.
Article in English | MEDLINE | ID: mdl-33793163

ABSTRACT

As the clinical applications of endoscopic retrograde cholangiopancreatography (ERCP) and endoscopic ultrasound (EUS) take more and more root in everyday practice and these endoscopic procedures become increasingly more complex and interventional with a higher chance for complications, the demand for expert biliopancreatic endoscopists continues to increase. In response to this growing need, specific postgraduate fellowships have been developed, however the standardization of training programs and the assessment of the achieved competence still remains an open debate. ERCP and EUS competency often requires training beyond the scope of a standard GI fellowship program, which lasts at least 1-2 years, and there are some differences in the way to face the issues of advanced biliopancreatic endoscopy training between Europe, America and the Asian regions. Today there is no role for the self-teaching of ERCP and EUS through trial and error without supervision and, in the near future, it is necessary to critically revise current training guidelines, to establish a standardized curriculum for advanced biliopancreatic endoscopists and to implement universally validated skill assessment tools, able to ensure constant and targeted feedback to trainees.


Subject(s)
Cholangiopancreatography, Endoscopic Retrograde , Clinical Competence , Endoscopy, Gastrointestinal , Endosonography , Fellowships and Scholarships
6.
Eur J Gastroenterol Hepatol ; 33(11): 1414-1419, 2021 11 01.
Article in English | MEDLINE | ID: mdl-32925507

ABSTRACT

INTRODUCTION: Gastric antral vascular ectasia is a significant cause of gastrointestinal bleeding in patients with cirrhosis. AIM: To assess safety/efficacy and cost/advantages of radiofrequency ablation for the treatment of gastric antral vascular ectasia in patients with cirrhosis. MATERIALS AND METHODS: Patients with cirrhosis and severe gastric antral vascular ectasia who underwent radiofrequency ablation were enrolled. Clinical data, gastric antral vascular ectasia grade, and gastric antral vascular ectasia-related hospitalizations were collected. Primary outcome was defined as the absence of transfusion over the 6 months after radiofrequency. An economic analysis was performed in the same period. RESULTS: Forty patients (50% Child B) were enrolled (80% refractory to argon plasma coagulation). Gastric antral vascular ectasia eradication was obtained in all patients and 65% of these patients achieved primary outcome. After radiofrequency, mean number of red blood cells transfusions dropped (from 25 to 0.9, P < 0.0001), with a parallel increase in hemoglobin (from 8 to 10.5 g/dL, P < 0.0001). No major complication occurred and liver function remained stable in all patients. The cost-analysis demonstrated a profound reduction of health care cost (from € 536.084 to € 189.044 in the 6 months before vs. after radiofrequency, respectively). These results were confirmed in the subgroup analysis in patients refractory to argon plasma coagulation. CONCLUSIONS: Radiofrequency ablation is safe and effective for the treatment of gastric antral vascular ectasia in patients with cirrhosis, including those refractory to argon plasma coagulation. Although the cost of single radiofrequency ablation is relatively high, the cost-analysis demonstrated considerable saving.


Subject(s)
Gastric Antral Vascular Ectasia , Radiofrequency Ablation , Argon Plasma Coagulation , Gastric Antral Vascular Ectasia/complications , Gastric Antral Vascular Ectasia/diagnosis , Gastric Antral Vascular Ectasia/surgery , Gastrointestinal Hemorrhage/etiology , Gastrointestinal Hemorrhage/surgery , Humans , Liver Cirrhosis/complications , Radiofrequency Ablation/adverse effects
7.
Dig Liver Dis ; 47(1): 45-9, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25464898

ABSTRACT

BACKGROUND: Managing antiplatelet and anticoagulant drugs before endoscopy may be challenging. AIMS: To assess whether the pre-endoscopic management of antiplatelet/anticoagulant drugs is adherent to current guidelines and the influence of patients' characteristics, referring physician's specialty, type of endoscopic procedure and therapeutic regimen on adherence. METHODS: Two hundred and twenty patients taking aspirin, thienopyridines or warfarin and scheduled for upper endoscopy (± biopsies), variceal band ligation, colonoscopy (± biopsies or polypectomy), were prospectively analyzed. RESULTS: In 109 patients (49.5%) the management of antiplatelet/anticoagulant drugs was thoroughly compliant with guidelines. Neither demographic characteristics, nor in/outpatient status, nor type of endoscopic procedure, nor physician's specialty influenced the adherence but the therapeutic regimen had a significant impact (p < 0.0001) as compliance was less likely in patients on warfarin. Unwarranted drugs withholding was more frequent before colonoscopy than upper endoscopy (p = 0.0001). Warfarin was stopped longer than recommended more frequently than aspirin (p = 0.009). The International Normalized Ratio was properly checked before endoscopy in 47.7% of patients. Among the 55 patients who withheld warfarin, the decision about bridging to low molecular weight heparin was appropriate in 21 (38.2%). CONCLUSIONS: Compliance with guidelines is low especially in the management of warfarin, both among gastroenterologists and other physicians.


Subject(s)
Anticoagulants/therapeutic use , Endoscopy, Gastrointestinal/methods , Guideline Adherence/statistics & numerical data , Platelet Aggregation Inhibitors/therapeutic use , Practice Guidelines as Topic , Preoperative Care/methods , Aged , Aged, 80 and over , Aspirin/therapeutic use , Biopsy , Cohort Studies , Colonic Polyps/surgery , Colonoscopy/methods , Colonoscopy/standards , Endoscopy, Digestive System/methods , Endoscopy, Digestive System/standards , Endoscopy, Gastrointestinal/standards , Esophageal and Gastric Varices/surgery , Female , Gastroenterology/statistics & numerical data , Humans , Ligation , Male , Middle Aged , Practice Patterns, Physicians'/statistics & numerical data , Preoperative Care/standards , Prospective Studies , Thienopyridines/therapeutic use , Warfarin/therapeutic use
8.
Dig Liver Dis ; 42(6): 441-5, 2010 Jun.
Article in English | MEDLINE | ID: mdl-19643684

ABSTRACT

AIM: We evaluated the etiology and risk factors for transient and persistently elevated aspartate and/or alanine aminotransferase levels in virus-free blood donors. INCLUSION CRITERIA: HBsAg/HBV-DNA and anti-HCV/HCV-RNA negative blood donors with elevated aspartate aminotransferase and/or alanine aminotransferase, observed in 5 blood transfusion centres in Italy from 2004 to 2005. Aspartate aminotransferase/alanine aminotransferase levels were measured at entry and every 2 months during a period of 6 months. RESULTS: 291 individuals were evaluated (144 with persistent and 147 with transient abnormal aminotransferases). High body mass index was the most frequent (75.5%) etiological factor and was more common in the persistent elevated levels group, compared to the transient elevated levels group (82.0% vs 65.3%; p<0.01). Excessive alcohol intake (>2 units/day) was reported in 23.6%, with no differences between the two groups. Instead, recent use of medication or paint exposure were most frequently associated with transient elevated levels than persistent elevated levels (61.6% vs 23.3% for drugs and 13.7% vs 4.3% for paint, p<0.001). Considering the participants with transient elevated levels as controls, the multivariate analysis showed that high body mass index was the only independent predictor of persistent elevated aminotransferase levels (OR=5.3; 95%CI=1.88-13.42 for those with body mass index>29.9). CONCLUSIONS: In virus-free blood donors, excessive body mass index is the most frequent etiological factor of abnormal aminotransferases and it is the sole risk factor associated with persistently elevated aminotransferases.


Subject(s)
Alanine Transaminase/blood , Aspartate Aminotransferases/blood , Blood Donors , Blood Transfusion/methods , Disease Transmission, Infectious/prevention & control , Hepatitis B, Chronic/enzymology , Hepatitis C, Chronic/enzymology , Adult , Body Mass Index , Female , Follow-Up Studies , Hepacivirus/genetics , Hepacivirus/immunology , Hepatitis B Surface Antigens/analysis , Hepatitis B virus/genetics , Hepatitis B virus/immunology , Hepatitis B, Chronic/transmission , Hepatitis B, Chronic/virology , Hepatitis C Antibodies/analysis , Hepatitis C, Chronic/transmission , Hepatitis C, Chronic/virology , Humans , Male , RNA, Viral/analysis , Retrospective Studies , Risk Factors
10.
Ann Intern Med ; 142(11): 903-9, 2005 Jun 07.
Article in English | MEDLINE | ID: mdl-15941697

ABSTRACT

BACKGROUND: The potential role of digestive endoscopy as a mode for transmission of hepatitis C virus (HCV) is controversial. OBJECTIVE: To evaluate the role of digestive endoscopy in transmitting HCV by comparing the incidence of HCV infection in a cohort of patients undergoing endoscopy and in a cohort of blood donors. DESIGN: Prospective cohort study. SETTING: 3 endoscopic units and 2 blood banks in northwestern Italy. PATIENTS: The potentially exposed cohort consisted of 9188 outpatients consecutively recruited from 3 endoscopic units. Of 9008 patients negative for antibody to HCV (anti-HCV), 8260 (92%) were retested for anti-HCV 6 months after endoscopy. The unexposed cohort consisted of 51,230 healthy, anti-HCV-negative persons who donated blood at 2 blood banks in the same area and during the same time period; 38,280 of them (75%) were tested again for anti-HCV 6 to 48 months after the first blood donation (95,317 person-years of observation). MEASUREMENTS: Differences in the anti-HCV seroconversion rate between the exposed cohort (patients undergoing endoscopy) and the unexposed cohort (blood donors). Seroconversion was evaluated by a third-generation enzyme immunoassay for anti-HCV; persons positive for anti-HCV were tested for HCV RNA by polymerase chain reaction. RESULTS: All 8260 persons undergoing endoscopy remained negative for anti-HCV 6 months after the procedure (risk per 1000 persons, 0 [95% CI, 0 to 0.465]); in particular, none of the 912 patients who underwent endoscopy with the same instrument previously used on HCV carriers showed anti-HCV seroconversion (risk per 1000 persons, 0 [CI, 0 to 4.195]). Four blood donors became positive for anti-HCV and HCV RNA (mean follow-up, 2.49 years; 0.042 case per 1000 person-years [CI, 0.011 to 0.107 case per 1000 person-years]); each had undergone minor surgery before the second test. LIMITATIONS: In the endoscopy cohort, 8.3% of patients were lost to follow-up. CONCLUSIONS: These findings support the hypothesis that properly performed digestive endoscopy is not a major risk factor for the transmission of HCV.


Subject(s)
Endoscopy, Gastrointestinal/standards , Hepatitis C/transmission , Adult , Ambulatory Care/standards , Blood Donors , Female , Follow-Up Studies , Hepatitis C/epidemiology , Hepatitis C Antibodies/blood , Humans , Incidence , Infection Control/standards , Italy/epidemiology , Male , Middle Aged , Prospective Studies , RNA, Viral/blood , Risk Factors
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