44 results on '"Dionigi E"'
Search Results
2. Comparison of three therapeutic regimens for genotype-3 hepatitis C virus infection in a large real-life multicentre cohort
- Author
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Soria, A, Fava, M, Bernasconi, D, Lapadula, G, Colella, E, Valsecchi, M, Migliorino, G, D'Ambrosio, R, Landonio, S, Schiavini, M, Spinetti, A, Carriero, C, Degasperi, E, Cologni, G, Gatti, F, Vigano, P, Hasson, H, Uberti-Foppa, C, Pasulo, L, Baiguera, C, Rossotti, R, Vinci, M, Puoti, M, Giorgini, A, Menzaghi, B, Lombardi, A, Pan, A, Aghemo, A, Grossi, P, Boldizzoni, R, Colombo, S, Vigano, M, Rumi, M, Del Poggio, P, Valenti, L, Giglio, O, De Bona, A, d'Arminio Monforte, A, Colombo, A, Spinelli, O, Pigozzi, M, Molteni, C, Bonfanti, P, Terreni, N, Perini, P, Capretti, A, Bella, D, Liani, C, Polo, S, Aimo, G, Pagnucco, L, Bhoori, S, Centenaro, R, Graffeo, M, Ciaccio, A, Dionigi, E, Lazzaroni, S, Carderi, I, Di Marco, M, Rizzardini, G, Noventa, F, Lampertico, P, Fagiuoli, S, Soria A., Fava M., Bernasconi D. P., Lapadula G., Colella E., Valsecchi M. G., Migliorino G. M., D'Ambrosio R., Landonio S., Schiavini M., Spinetti A., Carriero C., Degasperi E., Cologni G., Gatti F., Vigano P., Hasson H., Uberti-Foppa C., Pasulo L., Baiguera C., Rossotti R., Vinci M., Puoti M., Giorgini A., Menzaghi B., Lombardi A., Pan A., Aghemo A., Grossi P. A., Boldizzoni R., Colombo S., Vigano M., Rumi M. G., Del Poggio P., Valenti L., Giglio O., De Bona A., d'Arminio Monforte A., Colombo A., Spinelli O., Pigozzi M. G., Molteni C., Bonfanti P., Terreni N., Perini P., Capretti A., Bella D., Liani C., Polo S., Aimo G., Pagnucco L., Bhoori S., Centenaro R., Graffeo M., Ciaccio A., Dionigi E., Lazzaroni S., Carderi I., Di Marco M., Rizzardini G., Noventa F., Lampertico P., Fagiuoli S., Soria, A, Fava, M, Bernasconi, D, Lapadula, G, Colella, E, Valsecchi, M, Migliorino, G, D'Ambrosio, R, Landonio, S, Schiavini, M, Spinetti, A, Carriero, C, Degasperi, E, Cologni, G, Gatti, F, Vigano, P, Hasson, H, Uberti-Foppa, C, Pasulo, L, Baiguera, C, Rossotti, R, Vinci, M, Puoti, M, Giorgini, A, Menzaghi, B, Lombardi, A, Pan, A, Aghemo, A, Grossi, P, Boldizzoni, R, Colombo, S, Vigano, M, Rumi, M, Del Poggio, P, Valenti, L, Giglio, O, De Bona, A, d'Arminio Monforte, A, Colombo, A, Spinelli, O, Pigozzi, M, Molteni, C, Bonfanti, P, Terreni, N, Perini, P, Capretti, A, Bella, D, Liani, C, Polo, S, Aimo, G, Pagnucco, L, Bhoori, S, Centenaro, R, Graffeo, M, Ciaccio, A, Dionigi, E, Lazzaroni, S, Carderi, I, Di Marco, M, Rizzardini, G, Noventa, F, Lampertico, P, Fagiuoli, S, Soria A., Fava M., Bernasconi D. P., Lapadula G., Colella E., Valsecchi M. G., Migliorino G. M., D'Ambrosio R., Landonio S., Schiavini M., Spinetti A., Carriero C., Degasperi E., Cologni G., Gatti F., Vigano P., Hasson H., Uberti-Foppa C., Pasulo L., Baiguera C., Rossotti R., Vinci M., Puoti M., Giorgini A., Menzaghi B., Lombardi A., Pan A., Aghemo A., Grossi P. A., Boldizzoni R., Colombo S., Vigano M., Rumi M. G., Del Poggio P., Valenti L., Giglio O., De Bona A., d'Arminio Monforte A., Colombo A., Spinelli O., Pigozzi M. G., Molteni C., Bonfanti P., Terreni N., Perini P., Capretti A., Bella D., Liani C., Polo S., Aimo G., Pagnucco L., Bhoori S., Centenaro R., Graffeo M., Ciaccio A., Dionigi E., Lazzaroni S., Carderi I., Di Marco M., Rizzardini G., Noventa F., Lampertico P., and Fagiuoli S.
- Abstract
Background & Aims: In the direct-acting antiviral era, treatment of genotype-3 HCV (HCV-GT3) is still challenging. Real-life comparisons between recommended regimens, sofosbuvir (SOF)+daclatasvir (DAC), SOF/velpatasvir (VEL), glecaprevir/pibrentasvir (GLE/PIB), are scarce. We aimed at filling this data gap. Methods: Sustained virological response 12 weeks after treatment completion (SVR12) was assessed for all HCV-GT3 patients consecutively treated within the Lombardia web-based Navigatore HCV-Network; differences in SVR12 across regimens were evaluated by logistic regression. Results: Of the 2082 subjects with HCV-GT3, 1544 were evaluable for comparisons between regimens: SOF + DAC (1023, 66.2%), SOF/VEL (369, 23.9%), GLE/PIB (152, 9.8%). Patients treated with former regimens were more frequently male, cirrhotic, HIV-positive, pretreated, used ribavirin in their regimen, and had lower baseline HCV-RNA. SVR12 was similar across groups: 94.8% in SOF + DAC, 97.6% in SOF/VEL, 96.7% in GLE/PIB (P =.065). At univariate analysis, SVR12 was associated with female gender (97.9% vs 94.8%, P =.007) and lower median pretreatment Log10HCV-RNA (5.87 vs 6.20, P =.001). At multivariate logistic regression analysis, treatment with SOF/VEL was associated with a higher likelihood of SVR12 than SOF + DAC, but only in the absence of ribavirin (98% vs 90.3%). Female gender and lower pretreatment HCV-RNA were independently associated with SVR12. Conclusions: In a large real-life setting of HCV-GT3-infected patients with a high proportion of cirrhosis, the success rate was remarkable. The slight advantage of SOF/VEL on SOF + DAC was significant only without ribavirin. The current prescription shift towards novel regimens (ie SOF/VEL and GLE/PIB) in easier-to-treat patients allows ribavirin-free and shorter schedules without mining SVR12 in this <> genotype.
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- 2020
3. Renal safety in 3264 HCV patients treated with DAA-based regimens: Results from a large Italian real-life study
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D'Ambrosio, R, Pasulo, L, Giorgini, A, Spinetti, A, Messina, E, Fanetti, I, Puoti, M, Aghemo, A, Vigano, P, Vinci, M, Menzaghi, B, Lombardi, A, Pan, A, Pigozzi, M, Grossi, P, Lazzaroni, S, Spinelli, O, Invernizzi, P, Maggiolo, F, Terreni, N, Monforte, A, Poggio, P, Taddei, M, Colombo, S, Pozzoni, P, Molteni, C, Brocchieri, A, Bhoori, S, Buscarini, E, Centenaro, R, Mendeni, M, Colombo, A, Di Marco, M, Dionigi, E, Bella, D, Borghi, M, Zuin, M, Zaltron, S, Noventa, F, Annalisa, D, Lampertico, P, Fagiuoli, S, D'Ambrosio R., Pasulo L., Giorgini A., Spinetti A., Messina E., Fanetti I., Puoti M., Aghemo A., Vigano P., Vinci M., Menzaghi B., Lombardi A., Pan A., Pigozzi M. G., Grossi P., Lazzaroni S., Spinelli O., Invernizzi P., Maggiolo F., Terreni N., Monforte A. D., Poggio P. D., Taddei M. T., Colombo S., Pozzoni P., Molteni C., Brocchieri A., Bhoori S., Buscarini E., Centenaro R., Mendeni M., Colombo A. E., Di Marco M., Dionigi E., Bella D., Borghi M., Zuin M., Zaltron S., Noventa F., Annalisa D. S., Lampertico P., Fagiuoli S., D'Ambrosio, R, Pasulo, L, Giorgini, A, Spinetti, A, Messina, E, Fanetti, I, Puoti, M, Aghemo, A, Vigano, P, Vinci, M, Menzaghi, B, Lombardi, A, Pan, A, Pigozzi, M, Grossi, P, Lazzaroni, S, Spinelli, O, Invernizzi, P, Maggiolo, F, Terreni, N, Monforte, A, Poggio, P, Taddei, M, Colombo, S, Pozzoni, P, Molteni, C, Brocchieri, A, Bhoori, S, Buscarini, E, Centenaro, R, Mendeni, M, Colombo, A, Di Marco, M, Dionigi, E, Bella, D, Borghi, M, Zuin, M, Zaltron, S, Noventa, F, Annalisa, D, Lampertico, P, Fagiuoli, S, D'Ambrosio R., Pasulo L., Giorgini A., Spinetti A., Messina E., Fanetti I., Puoti M., Aghemo A., Vigano P., Vinci M., Menzaghi B., Lombardi A., Pan A., Pigozzi M. G., Grossi P., Lazzaroni S., Spinelli O., Invernizzi P., Maggiolo F., Terreni N., Monforte A. D., Poggio P. D., Taddei M. T., Colombo S., Pozzoni P., Molteni C., Brocchieri A., Bhoori S., Buscarini E., Centenaro R., Mendeni M., Colombo A. E., Di Marco M., Dionigi E., Bella D., Borghi M., Zuin M., Zaltron S., Noventa F., Annalisa D. S., Lampertico P., and Fagiuoli S.
- Abstract
Background: Sofosbuvir (SOF)-based regimens have been associated with renal function worsening in HCV patients with estimated glomerular filtration rate (eGFR) ≤ 45 ml/min, but further investigations are lacking. Aim: To assess renal safety in a large cohort of DAA-treated HCV patients with any chronic kidney disease (CKD). Methods: All HCV patients treated with DAA in Lombardy (December 2014–November 2017) with available kidney function tests during and off-treatment were included. Results: Among 3264 patients [65% males, 67% cirrhotics, eGFR 88 (9–264) ml/min], CKD stage was 3 in 9.5% and 4/5 in 0.7%. 79% and 73% patients received SOF and RBV, respectively. During DAA, eGFR declined in CKD-1 (p < 0.0001) and CKD-2 (p = 0.0002) patients, with corresponding rates of CKD stage reduction of 25% and 8%. Conversely, eGFR improved in lower CKD stages (p < 0.0001 in CKD-3a, p = 0.0007 in CKD-3b, p = 0.024 in CKD-4/5), with 33–45% rates of CKD improvement. Changes in eGFR and CKD distribution persisted at SVR. Baseline independent predictors of CKD worsening at EOT and SVR were age (p < 0.0001), higher baseline CKD stages (p < 0.0001) and AH (p = 0.010 and p < 0.0001, respectively). Conclusions: During DAA, eGFR significantly declined in patients with preserved renal function and improved in those with lower CKD stages, without reverting upon drug discontinuation.
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- 2020
4. Scheda n. 34 Maestro dei Compianti, Compianto sul corpo di Cristo
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Renzo Dionigi e Filippo Maria Ferro, Salsi, Claudio Antonio Marco, Salsi, Claudio, Renzo Dionigi e Filippo Maria Ferro, Salsi, Claudio Antonio Marco, and Salsi, Claudio
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- 2020
5. OP05 The impact of comorbidities on outcome of patients assessed for liver transplantation, waiting list mortality and post liver transplantation survival using the Charlson comorbidity index
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Al-Freah, M A B, Dionigi, E, Blackmore, L, Johnston, E, Zubir, A, Foxton, M, Bernal, W, Auzinger, G, Rela, M, Heaton, N D, OʼGrady, J G, Heneghan, M A, and Wendon, J A
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- 2011
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6. Clinical patterns of hepatocellular carcinoma in nonalcoholic fatty liver disease: A multicenter prospective study
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Piscaglia, Fabio, Svegliati Baroni, Gianluca, Barchetti, Andrea, Pecorelli, Anna, Marinelli, Sara, Tiribelli, Claudio, Bellentani, Stefano, Bernardi M, Biselli M, Bernardi M, Biselli M, Caraceni P, Domenicali M, Garuti F, Gramenzi A, Lenzi B, Magalotti D, Cescon M, Ravaioli M, Del Poggio P, Olmi S, Rapaccini GL, Balsamo C, Di Nolfo MA, Vavassori E, Alberti A, Benvegnù L, Gatta A, Giacomin A, Vanin V, Pozzan C, Maddalo G, Giampalma E, Cappelli A, Golfieri R, Mosconi C, Renzulli M, Roselli P, Dell'Isola S, Ialungo AM, Risso D, Marenco S, Sammito G, Bruzzone L, Bosco G, Grieco A, Pompili M, Rinninella E, Siciliano M, Chiaramonte M, Guarino M, Cammà C, Maida M, Costantino A, Barcellona MR, Schiadà L, Gemini S, Lanzi A, Stefanini GF, Dall'Aglio AC, Cappa FM, Suzzi A, Mussetto A, Treossi O, Missale G, Porro E, Mismas V, Vivaldi C, Bolondi L, Zoli M, Granito A, Malagotti D, Tovoli F, Trevisani F, Venerandi L, Brandi G, Cucchetti A, Bugianesi E, Vanni E, Mezzabotta L, Cabibbo G, Petta S, Fracanzani A, Fargion S, Marra F, Fani B, Biasini E, Sacco R, CAPORASO, NICOLA, Colombo M, D'Ambrosio R, Crocè LS, Patti R, Giannini EG, Loria P, Lonardo A, Baldelli E, Miele L, Farinati F, Borzio M, Dionigi E, Soardo G, Caturelli E, Ciccarese F, Virdone R, Affronti A, Foschi FG, Borzio F., MORISCO, FILOMENA, Piscaglia, Fabio, Svegliati Baroni, Gianluca, Barchetti, Andrea, Pecorelli, Anna, Marinelli, Sara, Tiribelli, Claudio, Bellentani, Stefano, Bernardi M, Biselli M, Bernardi, M, Biselli, M, Caraceni, P, Domenicali, M, Garuti, F, Gramenzi, A, Lenzi, B, Magalotti, D, Cescon, M, Ravaioli, M, Del Poggio, P, Olmi, S, Rapaccini, Gl, Balsamo, C, Di Nolfo, Ma, Vavassori, E, Alberti, A, Benvegnù, L, Gatta, A, Giacomin, A, Vanin, V, Pozzan, C, Maddalo, G, Giampalma, E, Cappelli, A, Golfieri, R, Mosconi, C, Renzulli, M, Roselli, P, Dell'Isola, S, Ialungo, Am, Risso, D, Marenco, S, Sammito, G, Bruzzone, L, Bosco, G, Grieco, A, Pompili, M, Rinninella, E, Siciliano, M, Chiaramonte, M, Guarino, M, Cammà, C, Maida, M, Costantino, A, Barcellona, Mr, Schiadà, L, Gemini, S, Lanzi, A, Stefanini, Gf, Dall'Aglio, Ac, Cappa, Fm, Suzzi, A, Mussetto, A, Treossi, O, Missale, G, Porro, E, Mismas, V, Vivaldi, C, Bolondi, L, Zoli, M, Granito, A, Malagotti, D, Tovoli, F, Trevisani, F, Venerandi, L, Brandi, G, Cucchetti, A, Bugianesi, E, Vanni, E, Mezzabotta, L, Cabibbo, G, Petta, S, Fracanzani, A, Fargion, S, Marra, F, Fani, B, Biasini, E, Sacco, R, Morisco, Filomena, Caporaso, Nicola, Colombo, M, D'Ambrosio, R, Crocè, L, Patti, R, Giannini, Eg, Loria, P, Lonardo, A, Baldelli, E, Miele, L, Farinati, F, Borzio, M, Dionigi, E, Soardo, G, Caturelli, E, Ciccarese, F, Virdone, R, Affronti, A, Foschi, Fg, Borzio, F., Fabio Piscagliaxxx, Gianluca Svegliati-Baroni, Andrea Barchetti, Anna Pecorellixxx, Sara Marinellixxx, Claudio Tiribelli, and, Stefano Bellentani, on behalf of the HCC-NAFLD Italian Study Group [, Mauro Bernardi, Maurizio Biselli, Paolo Caraceni, Marco Domenicali, Francesca Garuti, Annagiulia Gramenzi, Barbara Lenzi, Donatella Magalotti, Matteo Cescon, Matteo Ravaioli, Emanuela Giampalma, Rita Golfieri, Cristina Mosconi, Luigi Bolondi, Marco Zoli, Alessandro Granito, Francesco Tovoli, Franco Trevisani, Laura Venerandi, Giovanni Brandi, Alessandro Cucchetti, ], DIPARTIMENTO DI MEDICINA SPECIALISTICA, DIAGNOSTICA E SPERIMENTALE, DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE, Facolta' di MEDICINA e CHIRURGIA, AREA MIN. 06 - Scienze mediche, Da definire, Croce', Saveria, and HCC NAFLD Italian Study, Group
- Subjects
Male ,Cirrhosis ,Survival ,Chronic liver disease ,Gastroenterology ,0302 clinical medicine ,Non-alcoholic Fatty Liver Disease ,Nonalcoholic fatty liver disease ,80 and over ,Prospective Studies ,Chronic ,Prospective cohort study ,Aged, 80 and over ,Medicine (all) ,Liver Neoplasms ,hepatocellular carcinoma ,Middle Aged ,Hepatitis C ,Liver Neoplasm ,030220 oncology & carcinogenesis ,Hepatocellular carcinoma ,Competing risk analysi ,030211 gastroenterology & hepatology ,Female ,Non Alcoholic SteatoHepatitis=NASH ,Human ,medicine.medical_specialty ,Aged ,Carcinoma, Hepatocellular ,Hepatitis C, Chronic ,Humans ,Hepatology ,Competing risk analysis ,Milan criteria ,03 medical and health sciences ,Internal medicine ,medicine ,Survival rate ,business.industry ,Settore MED/09 - MEDICINA INTERNA ,Carcinoma ,nutritional and metabolic diseases ,Hepatocellular ,medicine.disease ,digestive system diseases ,Nonalcoholic fatty liver disease, hepatocellular carcinoma, clinical patterns ,business ,clinical patterns - Abstract
none 31 no Nonalcoholic fatty liver disease (NAFLD) represents the hepatic manifestation of metabolic syndrome and may evolve into hepatocellular carcinoma (HCC). Only scanty clinical information is available on HCC in NAFLD. The aim of this multicenter observational prospective study was to assess the clinical features of patients with NAFLD-related HCC (NAFLD-HCC) and to compare them to those of hepatitis C virus (HCV)-related HCC. A total of 756 patients with either NAFLD (145) or HCV-related chronic liver disease (611) were enrolled in secondary care Italian centers. Survival was modeled according to clinical parameters, lead-time bias, and propensity analysis. Compared to HCV, HCC in NAFLD patients had a larger volume, showed more often an infiltrative pattern, and was detected outside specific surveillance. Cirrhosis was present in only about 50% of NAFLD-HCC patients, in contrast to the near totality of HCV-HCC. Regardless of tumor stage, survival was significantly shorter (P = 0.017) in patients with NAFLD-HCC, 25.5 months (95% confidence interval 21.9-29.1), than in those with HCV-HCC, 33.7 months (95% confidence interval 31.9-35.4). To eliminate possible confounders, a propensity score analysis was performed, which showed no more significant difference between the two groups. Additionally, analysis of patients within Milan criteria submitted to curative treatments did not show any difference in survival between NAFLD-HCC and HCV-HCC (respectively, 38.6 versus 41.0 months, P = nonsignificant) CONCLUSIONS: NAFLD-HCC is more often detected at a later tumor stage and could arise also in the absence of cirrhosis, but after patient matching, it has a similar survival rate compared to HCV infection; a future challenge will be to identify patients with NAFLD who require more stringent surveillance in order to offer the most timely and effective treatment. Fabio Piscagliaxxx; Gianluca Svegliati-Baroni; Andrea Barchetti; Anna Pecorellixxx; Sara Marinellixxx; Claudio Tiribelli; and; Stefano Bellentani; on behalf of the HCC-NAFLD Italian Study Group [;Mauro Bernardi; Maurizio Biselli; Paolo Caraceni; Marco Domenicali; Francesca Garuti; Annagiulia Gramenzi; Barbara Lenzi; Donatella Magalotti; Matteo Cescon; Matteo Ravaioli; Emanuela Giampalma; Rita Golfieri; Cristina Mosconi; Luigi Bolondi; Marco Zoli; Alessandro Granito; Francesco Tovoli; Franco Trevisani; Laura Venerandi; Giovanni Brandi; Alessandro Cucchetti;] Fabio Piscagliaxxx; Gianluca Svegliati-Baroni; Andrea Barchetti; Anna Pecorellixxx; Sara Marinellixxx; Claudio Tiribelli; and; Stefano Bellentani; on behalf of the HCC-NAFLD Italian Study Group [;Mauro Bernardi; Maurizio Biselli; Paolo Caraceni; Marco Domenicali; Francesca Garuti; Annagiulia Gramenzi; Barbara Lenzi; Donatella Magalotti; Matteo Cescon; Matteo Ravaioli; Emanuela Giampalma; Rita Golfieri; Cristina Mosconi; Luigi Bolondi; Marco Zoli; Alessandro Granito; Francesco Tovoli; Franco Trevisani; Laura Venerandi; Giovanni Brandi; Alessandro Cucchetti;]
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- 2016
7. External validation of the ITA.LI.CA prognostic system for patients with hepatocellular carcinoma: A multicenter cohort study
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Dionigi, E., primary, Borzio, M., additional, Rossini, A., additional, Marignani, M., additional, Sacco, R., additional, De sio, I., additional, Bertolini, E., additional, Francica, G., additional, Giacomin, A., additional, Parisi, G., additional, Vicari, S., additional, Toldi, A., additional, Salmi, A., additional, Boccia, S., additional, Maringhini, A., additional, and Fornari, F., additional
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- 2017
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8. External validation of the ITA.LI.CA prognostic system for patients with hepatocellular carcinoma: a multicenter cohort study
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Borzio, M., primary, Dionigi, E., additional, Rossini, A., additional, Marignani, M., additional, Sacco, R., additional, De Sio, I., additional, Bertolini, E., additional, Francica, G., additional, Giacomin, A., additional, Parisi, G., additional, Vicari, S., additional, Toldi, A., additional, Salmi, A., additional, Boccia, S., additional, Maringhini, A., additional, and Fornari, F., additional
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- 2017
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9. Clinical Patterns of hepatocellular carcinoma (HCC) in Non Alcoholic Fatty Liver Disease (NAFLD): a multicenter case-control study
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Piscaglia, F., Svegliati Baroni, G., Barchetti, A., Pecorelli, A., Marinelli, S., Tiribelli, C., Bellentani e. gruppo studio italiano HCC NAFLD composto da: L. Bolondi, S. Bellentani e. gruppo studio italiano HCC NAFLD composto da: L. Bolondi, Zoli, M., Malagotti, D., Vanni, Ester, Mezzabotta, Lavinia, Cabibbo, G., Petta, S., Fracanzani, A., Fargion, S., Marra, F., Fani, B., Sacco, R., Morisco, F., Caporaso, N., Guarino, M., Colombo, M., D’Ambrosio, R., Crocè, L. S., Patti, R., Giannini, E., Lonardo, A., Baldelli, E., Miele, L., Grieco, A., Farinati, F., Pozzan, C., Borzio, M., Dionigi, E., Soardo, G., Roselli, P., Ciccarese, F., Virdone, F., Affronti, A., Boschi, F. G., Borzio, F., Trevisani, F., and Bugianesi, Elisabetta
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- 2015
10. Therapeutic Strategies in the Real Life in BCLC-C Hepatocellular Carcinoma in Italy: Assessment in the Italian Liver Cancer and Validation in the Italian Association of Hospital Gastroenterologists Database
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Vanin, V., primary, Imondi, A., additional, Pozzan, C., additional, Murer, F., additional, Vitale, A., additional, Cillo, U., additional, Dionigi, E., additional, Borzio, M., additional, Trevisani, F., additional, and Farinati, F., additional
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- 2016
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11. Clinical patterns of hepatocellular carcinoma (HCC) in non alcoholic fatty liver disease (NAFLD): a multicenter case-control study
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Piscaglia, F., primary, Baroni, G. Svegliati, additional, Barchetti, A., additional, Pecorelli, A., additional, Marinelli, S., additional, Tiribelli, C., additional, Bellentani, S., additional, Bolondi, L., additional, Zoli, M., additional, Malagotti, D., additional, Brandi, G., additional, Bugianesi, E., additional, Vanni, E., additional, Mezzabotta, L., additional, Cabibbo, G., additional, Petta, S., additional, Fracanzani, A., additional, Fargion, S., additional, Marra, F., additional, Fani, B., additional, Sacco, R., additional, Morisco, F., additional, Caporaso, N., additional, Guarino, M., additional, Colombo, M., additional, D’Ambrosio, R., additional, Crocè, L.S., additional, Patti, R., additional, Giannini, E., additional, Lonardo, A., additional, Baldelli, E., additional, Miele, L., additional, Grieco, A., additional, Farinati, F., additional, Pozzan, C., additional, Borzio, M., additional, Dionigi, E., additional, Soardo, G., additional, Roselli, P., additional, Ciccarese, F., additional, Virdone, F., additional, Affronti, A., additional, Foschi, F.G., additional, Borzio, F., additional, and Trevisani, F., additional
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- 2015
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12. FRI-094 - External validation of the ITA.LI.CA prognostic system for patients with hepatocellular carcinoma: a multicenter cohort study
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Borzio, M., Dionigi, E., Rossini, A., Marignani, M., Sacco, R., De Sio, I., Bertolini, E., Francica, G., Giacomin, A., Parisi, G., Vicari, S., Toldi, A., Salmi, A., Boccia, S., Maringhini, A., and Fornari, F.
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- 2017
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13. PC.01.6 MANAGEMENT OF HCC IN ELDERLY PATIENTS: AN ITALIAN “IN FIELD” EXPERIENCE
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Dionigi, E., primary, Borzio, M., additional, Rossini, A., additional, Toldi, A., additional, Francica, G., additional, Fornari, F., additional, Salmi, A., additional, Farinati, F., additional, Vicari, S., additional, Marignani, M., additional, Andriulli, A., additional, Ginanni, B., additional, and Sacco, R., additional
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- 2014
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14. SAT-099 - Therapeutic Strategies in the Real Life in BCLC-C Hepatocellular Carcinoma in Italy: Assessment in the Italian Liver Cancer and Validation in the Italian Association of Hospital Gastroenterologists Database
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Vanin, V., Imondi, A., Pozzan, C., Murer, F., Vitale, A., Cillo, U., Dionigi, E., Borzio, M., Trevisani, F., and Farinati, F.
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- 2016
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15. 671 CLINICAL FEATURES OF NON ALCOHOLIC STEATOHEPATITIS (NASH)-RELATED HEPATOCELLULAR CARCINOMA (HCC) IN ITALY: A MULTICENTER PROSPECTIVE SURVEY
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Rossini, A., primary, Sacco, R., additional, Fornari, F., additional, De Sio, I., additional, Spinzi, G., additional, Francica, G., additional, Parisi, G., additional, Salmi, A., additional, Dionigi, E., additional, Farinati, F., additional, Di Fonzo, M., additional, Salvagnini, M., additional, Vicari, S., additional, and Borzio, M., additional
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- 2013
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16. 252 IMPROVING PROGNOSIS OF HCC IN THE REAL-WORLD CLINICAL PRACTICE: AN ITALIAN EXPERIENCE
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Borzio, M., primary, Sacco, R., additional, Fanigliulo, L., additional, Parisi, G., additional, Francica, G., additional, Dionigi, E., additional, Salvagnini, M., additional, Di Fonzo, M., additional, Salmi, A., additional, De Sio, I., additional, and Vicari, S., additional
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- 2013
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17. P.11.12 IMPROVING PROGNOSIS OF HCC ON THE REAL-WORLD CLINICAL PRACTICE IN ITALY
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Borzio, M., primary, Sacco, R., additional, Fanigliulo, L., additional, Parisi, G., additional, Dionigi, E., additional, Salvagnini, M., additional, Difonzo, M., additional, Vicari, S., additional, Salmi, A., additional, Desio, I., additional, and Francica, G., additional
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- 2013
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18. F-44 Improving prognosis of HCC in the real-world clinical practice: an Italian field experience
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Borzio, M., primary, Sacco, R., additional, Fanigliulo, L., additional, Parisi, G., additional, Francica, G., additional, Dionigi, E., additional, Salvagnini, M., additional, Di Fonzo, M., additional, Salmi, A., additional, De Sio, I., additional, and Vicari, S., additional
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- 2013
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19. 5 THE EMERGING IMPACT OF HEPATOCELLULAR CARCINOMA ARISING ON A BACKGROUND OF NAFLD
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Reeves, H., primary, Villa, E., additional, Bellentani, S., additional, Dionigi, E., additional, Dufour, J.-F., additional, de Oliveira, C., additional, Fracanzani, A., additional, Barcheti, A., additional, Merle, P., additional, Boursier, J., additional, Schattenberg, J., additional, Fedchuk, L., additional, Holst, C., additional, and Ratziu, V., additional
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- 2012
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20. CS.01.3 THE EMERGING IMPACT OF HCC-NAFLD IN ITALY
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Bellentani, S., primary, Barchetti, A., additional, Dionigi, E., additional, Fracanzani, A., additional, Brandi, G., additional, Miele, L., additional, Rigato, I., additional, Svegliati-Baroni, G., additional, Giannini, E.G., additional, Cabibbo, G., additional, Piscaglia, F., additional, Soardo, G., additional, Marra, F., additional, Farinati, F., additional, Trevisani, F., additional, and Villa, E., additional
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- 2012
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21. OC-26 The emerging impact of HCC-NAFLD in Italy
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Bellentani, S., primary, Brachetti, A., additional, Dionigi, E., additional, Fracanzani, A., additional, Brandi, G., additional, Miele, L., additional, Rigato, I., additional, Baroni, G. Svegliati, additional, Giannini, G., additional, Cabibbo, G., additional, Piscaglia, F., additional, Soardo, G., additional, Marra, F., additional, Farinati, F., additional, and Villa, E., additional
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- 2012
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22. P71 A model to improve performance of current category 9 UK listing criteria: early liver graft dysfunction. A single centre cohort
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Al-Freah, M. A. B., primary, Dionigi, E., additional, McPhail, M. J. W., additional, Foxton, M., additional, Auzinger, G., additional, Rela, M., additional, Heaton, N. D., additional, O'Grady, J. G., additional, Heneghan, M. A., additional, Bernal, W., additional, and Wendon, J. A., additional
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- 2011
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23. 162 BACTERIAL INFECTIONS IN CIRRHOSIS ARE ASSOCIATED WITH A POOR PROGNOSIS THAT IS NOT REFLECTED BY MELD AND UKELD SCORES
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Dionigi, E., primary, Garcovich, M., additional, Vemala, V., additional, Patch, D.W., additional, Thorburn, D., additional, Burroughs, A.K., additional, and O'Beirne, J.P., additional
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- 2010
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24. PTU-058 Histological liver collagen proportionate area predicts decompensation in patients with liver cirrhosis of mixed aetiologies
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Isgro, G, primary, Calvaruso, V, additional, Manousou, P, additional, Luong, T, additional, Alibrandi, A, additional, Garcovich, M, additional, Tsochatzis, E, additional, Dionigi, E, additional, Patch, D, additional, O'Beirne, J, additional, Dhillon, A, additional, and Burroughs, A, additional
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- 2010
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25. F.N.12 BACTERIAL INFECTIONS IN CIRRHOSIS ARE ASSOCIATED WITH A POOR PROGNOSIS THAT IS NOT REFLECTED BY MELD AND UKELD SCORES
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Dionigi, E., primary, Garcovich, M., additional, Patch, D.W., additional, Thorburn, D., additional, Burroughs, A.K., additional, and O'Beirne, J.P., additional
- Published
- 2010
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26. T.N.13 PREDICTORS OF OUTCOME IN CIRRHOTICS ADMITTED TO INTENSIVE CARE UNIT (ICU); SURVIVORS EXHIBITED SIGNIFICANT RISE OF SERUM SODIUM LEVELS AND A FALL IN LACTATE LEVELS AT 48 HOURS
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Garcovich, M., primary, Vemala, V., additional, Davenport, A., additional, Dionigi, E., additional, Shaw, S., additional, Agarwal, B., additional, and Burroughs, A.K., additional
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- 2010
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27. THE SYSTEMIC INFLAMMATORY RESPONSE SYNDROME (SIRS) PREDICTS THE IN-HOSPITAL OUTCOME IN CIRRHOTIC PATIENTS
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Cazzaniga, M., primary, Dionigi, E., additional, Fioretti, A., additional, Monti, V., additional, Gobbo, G., additional, and Salerno, F., additional
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- 2009
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28. The systemic inflammatory response syndrome (SIRS) in cirrhotic patients: Relationship with the in-hospital outcome
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Cazzaniga, M., primary, Dionigi, E., additional, Fioretti, A., additional, Monti, V., additional, Gobbo, G., additional, and Salerno, F., additional
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- 2009
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29. Diastolic dysfunction is associated with poor survival in patients with cirrhosis with transjugular intrahepatic portosystemic shunt
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Cazzaniga, M., primary, Salerno, F., additional, Pagnozzi, G., additional, Dionigi, E., additional, Visentin, S., additional, Cirello, I., additional, Meregaglia, D., additional, and Nicolini, A., additional
- Published
- 2007
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30. P99 Relation of donor risk index and model for end-stage liver disease score to outcome of elective liver transplantation; a single centre experience.
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Al-Freah, M, Al-Freah, M A B, Dionigi, E, Suddle, A, Aluvihare, V, Agarwal, K, Wendon, J, Auzinger, G, O'Grady, J, Rela, M, Heneghan, M, Heaton, N, and Bernal, W
- Abstract
Introduction Patients with advanced liver disease, reflected in high model for end-stage liver disease (MELD) scores have the lowest chances of survival without liver transplantation (LT) and yet, may derive greatest survival-benefit from LT. The use of extended criteria (EC) grafts in such patients has been advocated as a means of optimising the chances of successful transplantation. Aim To determine the effects of graft quality (using Donor Risk Index, DRI) and MELD score at the time of LT on the duration of post-LT intensive care unit (ICU) and hospital length of stay (LOS) and survival. Method Retrospective analysis of 898 adult patients who underwent elective LT (109 re-do LT) over the period 2000–2008. Pre-LT MELD scores were categorised as low (<15), intermediate (15–25), or High (>25). Graft quality was categorised as low (DRI >1.7) or High (DRI <1.7). Data are presented as median (IQR). Results Median age was 53 years (44–60) and 64% were male. Median pre-LT MELD was 15 (11–19) and median DRI in the high and low quality groups were 1.5 (1.3–1.6) and 2.0 (1.9–2.1). Increasing MELD score was associated with greater ICU and Hospital LOS (p<0.0001, Kruskal–Wallis test). However, within each MELD category there was no significant difference in ICU or hospital LOS between recipients of grafts with DRI < or >1.7. See . On multivariate regression analysis MELD was an independent predictor of LOS with no significant effect of DRI identified. Survival at 1-year in the overall cohort was 90%; in MELD <15 92.6%, 15–25 87.4% and >25 82.7%. There were no significant differences in 1 year survival between recipients with DRI < or >1.7 in the group as a whole or in the MELD sub-categories. Conclusion In this cohort, length of ICU and hospital stay related to pre-LT MELD score and not graft quality as evaluated by DRI. Hospital and ICU stay and consequently resource use was increased particularly in those patients with MELD of 25 and above, but not further prolonged by the use of ECD grafts in the range of DRI used in this cohort. [ABSTRACT FROM PUBLISHER]
- Published
- 2010
31. Comparison of three therapeutic regimens for genotype-3 hepatitis C virus infection in a large real-life multicentre cohort
- Author
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Sergio Lazzaroni, Paolo Grossi, Chiara Molteni, Maria Grazia Valsecchi, Pietro Lampertico, Luca Valenti, Alessio Aghemo, Alessia Giorgini, Antonella d'Arminio Monforte, Roberta D'Ambrosio, Federico Gatti, Omar Giglio, Daniele Bella, Davide Paolo Bernasconi, Giuseppe Lapadula, Sherrie Bhoori, Hamid Hasson, Monica Schiavini, Elisa Colella, Roberto Boldizzoni, A. Ciaccio, Simona Landonio, Andrea Capretti, Maria Cristina Vinci, Giuliano Rizzardini, Barbara Menzaghi, Elisabetta Degasperi, Caterina Uberti-Foppa, Chiara Baiguera, Andrea Lombardi, Gianpiero Aimo, Layla Pagnucco, Paolo Perini, Giuliana Cologni, Natalia Terreni, Paolo Bonfanti, Mauro Viganò, Paolo Viganò, Alessandro Soria, Roberto Rossotti, Massimo Puoti, Ombretta Spinelli, Canio Carriero, Silvia Polo, Guglielmo Marco Migliorino, Silvia Colombo, Riccardo Centenaro, Luisa Pasulo, Anna De Bona, E. Dionigi, Paolo Poggio, Franco Noventa, Isabella Carderi, Angelo Pan, Angiola Spinetti, Mariella Di Marco, Cecilia Liani, Stefano Fagiuoli, Marie Graciella Pigozzi, Marco Fava, Massimo Graffeo, Maria Grazia Rumi, Alberto Colombo, Soria, A., Fava, M., Bernasconi, D. P., Lapadula, G., Colella, E., Valsecchi, M. G., Migliorino, G. M., D'Ambrosio, R., Landonio, S., Schiavini, M., Spinetti, A., Carriero, C., Degasperi, E., Cologni, G., Gatti, F., Vigano, P., Hasson, H., Uberti-Foppa, C., Pasulo, L., Baiguera, C., Rossotti, R., Vinci, M., Puoti, M., Giorgini, A., Menzaghi, B., Lombardi, A., Pan, A., Aghemo, A., Grossi, P. A., Boldizzoni, R., Colombo, S., Vigano, M., Rumi, M. G., Del Poggio, P., Valenti, L., Giglio, O., De Bona, A., d'Arminio Monforte, A., Colombo, A., Spinelli, O., Pigozzi, M. G., Molteni, C., Bonfanti, P., Terreni, N., Perini, P., Capretti, A., Bella, D., Liani, C., Polo, S., Aimo, G., Pagnucco, L., Bhoori, S., Centenaro, R., Graffeo, M., Ciaccio, A., Dionigi, E., Lazzaroni, S., Carderi, I., Di Marco, M., Rizzardini, G., Noventa, F., Lampertico, P., Fagiuoli, S., Soria, A, Fava, M, Bernasconi, D, Lapadula, G, Colella, E, Valsecchi, M, Migliorino, G, D'Ambrosio, R, Landonio, S, Schiavini, M, Spinetti, A, Carriero, C, Degasperi, E, Cologni, G, Gatti, F, Vigano, P, Hasson, H, Uberti-Foppa, C, Pasulo, L, Baiguera, C, Rossotti, R, Vinci, M, Puoti, M, Giorgini, A, Menzaghi, B, Lombardi, A, Pan, A, Aghemo, A, Grossi, P, Boldizzoni, R, Colombo, S, Vigano, M, Rumi, M, Del Poggio, P, Valenti, L, Giglio, O, De Bona, A, d'Arminio Monforte, A, Colombo, A, Spinelli, O, Pigozzi, M, Molteni, C, Bonfanti, P, Terreni, N, Perini, P, Capretti, A, Bella, D, Liani, C, Polo, S, Aimo, G, Pagnucco, L, Bhoori, S, Centenaro, R, Graffeo, M, Ciaccio, A, Dionigi, E, Lazzaroni, S, Carderi, I, Di Marco, M, Rizzardini, G, Noventa, F, Lampertico, P, and Fagiuoli, S
- Subjects
Male ,medicine.medical_specialty ,Daclatasvir ,Genotype ,Sofosbuvir ,ribavirin ,pibrentasvir ,daclatasvir ,genotype 3 ,glecaprevir ,Hepatitis C ,sofosbuvir ,sustained virological response ,velpatasvir ,Hepacivirus ,Antiviral Agents ,Gastroenterology ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Internal medicine ,Ribavirin ,medicine ,Humans ,Univariate analysis ,Hepatology ,business.industry ,Glecaprevir ,Hepatitis C, Chronic ,medicine.disease ,Pibrentasvir ,Regimen ,Treatment Outcome ,chemistry ,030220 oncology & carcinogenesis ,Drug Therapy, Combination ,Female ,030211 gastroenterology & hepatology ,business ,medicine.drug - Abstract
Background & Aims: In the direct-acting antiviral era, treatment of genotype-3 HCV (HCV-GT3) is still challenging. Real-life comparisons between recommended regimens, sofosbuvir (SOF)+daclatasvir (DAC), SOF/velpatasvir (VEL), glecaprevir/pibrentasvir (GLE/PIB), are scarce. We aimed at filling this data gap. Methods: Sustained virological response 12weeks after treatment completion (SVR12) was assessed for all HCV-GT3 patients consecutively treated within the Lombardia web-based Navigatore HCV-Network; differences in SVR12 across regimens were evaluated by logistic regression. Results: Of the 2082 subjects with HCV-GT3, 1544 were evaluable for comparisons between regimens: SOF+DAC (1023, 66.2%), SOF/VEL (369, 23.9%), GLE/PIB (152, 9.8%). Patients treated with former regimens were more frequently male, cirrhotic, HIV-positive, pretreated, used ribavirin in their regimen, and had lower baseline HCV-RNA. SVR12 was similar across groups: 94.8% in SOF+DAC, 97.6% in SOF/VEL, 96.7% in GLE/PIB (P=.065). At univariate analysis, SVR12 was associated with female gender (97.9% vs 94.8%, P=.007) and lower median pretreatment Log10HCV-RNA (5.87 vs 6.20, P=.001). At multivariate logistic regression analysis, treatment with SOF/VEL was associated with a higher likelihood of SVR12 than SOF+DAC, but only in the absence of ribavirin (98% vs 90.3%). Female gender and lower pretreatment HCV-RNA were independently associated with SVR12. Conclusions: In a large real-life setting of HCV-GT3-infected patients with a high proportion of cirrhosis, the success rate was remarkable. The slight advantage of SOF/VEL on SOF+DAC was significant only without ribavirin. The current prescription shift towards novel regimens (ie SOF/VEL and GLE/PIB) in easier-to-treat patients allows ribavirin-free and shorter schedules without mining SVR12 in this <> genotype.
- Published
- 2020
32. Renal safety in 3264 HCV patients treated with DAA-based regimens: Results from a large Italian real-life study
- Author
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Alessandra Brocchieri, Marta Borghi, Angelo Pan, Mariella Di Marco, Silvia Colombo, Chiara Molteni, Natalia Terreni, Paolo Poggio, Alberto Colombo, De Silvestri Annalisa, Riccardo Centenaro, Luisa Pasulo, Paolo Viganò, Maria Cristina Vinci, Marie Graciella Pigozzi, Stefano Fagiuoli, Pietro Lampertico, Sergio Lazzaroni, Sherrie Bhoori, Massimo Zuin, Franco Noventa, Alessio Aghemo, Barbara Menzaghi, Andrea Lombardi, Franco Maggiolo, I. Fanetti, Alessia Giorgini, Massimo Puoti, Emanuela Messina, Paolo Grossi, Roberta D'Ambrosio, Pietro Invernizzi, Monia Mendeni, Daniele Bella, E. Dionigi, Ombretta Spinelli, Maria Teresa Taddei, Pietro Pozzoni, Antonella d'Arminio Monforte, Elisabetta Buscarini, Angiola Spinetti, Serena Zaltron, D'Ambrosio, R, Pasulo, L, Giorgini, A, Spinetti, A, Messina, E, Fanetti, I, Puoti, M, Aghemo, A, Vigano, P, Vinci, M, Menzaghi, B, Lombardi, A, Pan, A, Pigozzi, M, Grossi, P, Lazzaroni, S, Spinelli, O, Invernizzi, P, Maggiolo, F, Terreni, N, Monforte, A, Poggio, P, Taddei, M, Colombo, S, Pozzoni, P, Molteni, C, Brocchieri, A, Bhoori, S, Buscarini, E, Centenaro, R, Mendeni, M, Colombo, A, Di Marco, M, Dionigi, E, Bella, D, Borghi, M, Zuin, M, Zaltron, S, Noventa, F, Annalisa, D, Lampertico, P, and Fagiuoli, S
- Subjects
Male ,Sustained Virologic Response ,Sofosbuvir ,Hepacivirus ,Kidney ,urologic and male genital diseases ,Gastroenterology ,chemistry.chemical_compound ,0302 clinical medicine ,MED/12 - GASTROENTEROLOGIA ,eGFR ,Aged, 80 and over ,Hepatitis C ,Middle Aged ,medicine.anatomical_structure ,Italy ,030220 oncology & carcinogenesis ,Drug Therapy, Combination ,Female ,030211 gastroenterology & hepatology ,Glomerular Filtration Rate ,Cohort study ,medicine.drug ,Adult ,medicine.medical_specialty ,SVR ,Genotype ,Renal function ,CKD ,Antiviral Agents ,Young Adult ,03 medical and health sciences ,Internal medicine ,medicine ,Humans ,Renal Insufficiency, Chronic ,Aged ,Retrospective Studies ,Hepatology ,business.industry ,Ribavirin ,Retrospective cohort study ,Hepatitis C, Chronic ,medicine.disease ,Logistic Models ,chemistry ,business ,Kidney disease - Abstract
Background: Sofosbuvir (SOF)-based regimens have been associated with renal function worsening in HCV patients with estimated glomerular filtration rate (eGFR) ≤ 45 ml/min, but further investigations are lacking. Aim: To assess renal safety in a large cohort of DAA-treated HCV patients with any chronic kidney disease (CKD). Methods: All HCV patients treated with DAA in Lombardy (December 2014–November 2017) with available kidney function tests during and off-treatment were included. Results: Among 3264 patients [65% males, 67% cirrhotics, eGFR 88 (9–264) ml/min], CKD stage was 3 in 9.5% and 4/5 in 0.7%. 79% and 73% patients received SOF and RBV, respectively. During DAA, eGFR declined in CKD-1 (p < 0.0001) and CKD-2 (p = 0.0002) patients, with corresponding rates of CKD stage reduction of 25% and 8%. Conversely, eGFR improved in lower CKD stages (p < 0.0001 in CKD-3a, p = 0.0007 in CKD-3b, p = 0.024 in CKD-4/5), with 33–45% rates of CKD improvement. Changes in eGFR and CKD distribution persisted at SVR. Baseline independent predictors of CKD worsening at EOT and SVR were age (p < 0.0001), higher baseline CKD stages (p < 0.0001) and AH (p = 0.010 and p < 0.0001, respectively). Conclusions: During DAA, eGFR significantly declined in patients with preserved renal function and improved in those with lower CKD stages, without reverting upon drug discontinuation.
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- 2020
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33. Tra scultura e pittura: il paradosso di Brescia
- Author
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MARCO PIERATTILIO TANZI, a cura di R. Dionigi e F. M. Ferro, and Tanzi, Marco Pierattilio
- Published
- 2020
34. The impact of infection by multidrug-resistant agents in patients with cirrhosis. A multicenter prospective study
- Author
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Salerno, Francesco, Borzio, Mauro, Pedicino, Claudia, Simonetti, Rosa, Rossini, Angelo, Boccia, Sergio, Cacciola, Irene, Burroughs, Andrew K., Manini, Matteo A., La Mura, Vincenzo, Angeli, Paolo, Bernardi, Mauro, Dalla Gasperina, Daniela, Dionigi, Elena, Dibenedetto, Clara, Arghittu, Milena, Francavilla, Antonio, Trevisani, Franco, Salmi, Andrea, Fatuzzo, Filippo, Arvaniti, Vassiliki, Cambieri, Patrizia, Raguzzi, Ivana, Aghemo, Alessio, Trotta, Elisa, Cottone, Mario, Perricone, Giovanni, Giusti, Massimo, Cazzaniga, Massimo, Gobbo, Giulia, Monti, Valentina, Tejada, Milvana, Costa, Elena, Andriulli, Angelo, Grossi, Paolo, Salerno, F, Borzio, M, Pedicino, C, Simonetti, R, Rossini, A, Boccia, S, Cacciola, I, Burroughs, Ak, Manini, Ma, La Mura, V, Angeli, P, Bernardi, M, Dalla Gasperina, D, Dionigi, E, Dibenedetto, C, Arghittu, M, and Trevisani, F.
- Subjects
Liver Cirrhosis ,Male ,medicine.medical_specialty ,Cirrhosis ,bacterial resistance, cirrhosis, portal hypertension, survival ,medicine.drug_class ,Antibiotics ,survival ,03 medical and health sciences ,0302 clinical medicine ,Spontaneous bacterial peritonitis ,Antibiotic resistance ,Drug Resistance, Multiple, Bacterial ,Internal medicine ,medicine ,Humans ,Hospital Mortality ,Prospective Studies ,030212 general & internal medicine ,Prospective cohort study ,Aged ,Cross Infection ,Bacteria ,Hepatology ,business.industry ,cirrhosis ,Mortality rate ,portal hypertension ,Bacterial Infections ,bacterial resistance ,Middle Aged ,Prognosis ,medicine.disease ,Anti-Bacterial Agents ,Surgery ,Logistic Models ,Italy ,Hepatocellular carcinoma ,Multivariate Analysis ,Female ,030211 gastroenterology & hepatology ,business - Abstract
Background & Aims Bacterial strains resistant to antibiotics are a serious clinical challenge. We assessed the antibiotic susceptibility of bacteria isolated from infections in patients with cirrhosis by a multicentre investigation. Results Three hundred and thirteen culture-positive infections (173 community acquired [CA] and 140 hospital acquired [HA]) were identified in 308 patients. Urinary tract infections, spontaneous bacterial peritonitis and bacteremias were the most frequent. Quinolone-resistant Gram-negative isolates were 48%, 44% were extended-spectrum beta-lactamase producers and 9% carbapenem resistant. In 83/313 culture-positive infections (27%), multidrug-resistant agents (MDRA) were isolated. This prevalence did not differ between CA and HA infections. MDRA were identified in 17 of 37 patients on quinolone prophylaxis, and in 46 of 166 not on prophylaxis (45% vs 27%; P
- Published
- 2016
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35. Comparison of three therapeutic regimens for genotype-3 hepatitis C virus infection in a large real-life multicentre cohort.
- Author
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Soria A, Fava M, Bernasconi DP, Lapadula G, Colella E, Valsecchi MG, Migliorino GM, D'Ambrosio R, Landonio S, Schiavini M, Spinetti A, Carriero C, Degasperi E, Cologni G, Gatti F, Viganò P, Hasson H, Uberti-Foppa C, Pasulo L, Baiguera C, Rossotti R, Vinci M, Puoti M, Giorgini A, Menzaghi B, Lombardi A, Pan A, Aghemo A, Grossi PA, Boldizzoni R, Colombo S, Viganò M, Rumi MG, Del Poggio P, Valenti L, Giglio O, De Bona A, d'Arminio Monforte A, Colombo A, Spinelli O, Pigozzi MG, Molteni C, Bonfanti P, Terreni N, Perini P, Capretti A, Bella D, Liani C, Polo S, Aimo G, Pagnucco L, Bhoori S, Centenaro R, Graffeo M, Ciaccio A, Dionigi E, Lazzaroni S, Carderi I, Di Marco M, Rizzardini G, Noventa F, Lampertico P, and Fagiuoli S
- Subjects
- Antiviral Agents therapeutic use, Drug Therapy, Combination, Female, Genotype, Hepacivirus genetics, Humans, Male, Ribavirin therapeutic use, Sofosbuvir therapeutic use, Treatment Outcome, Hepatitis C drug therapy, Hepatitis C, Chronic drug therapy
- Abstract
Background & Aims: In the direct-acting antiviral era, treatment of genotype-3 HCV (HCV-GT3) is still challenging. Real-life comparisons between recommended regimens, sofosbuvir (SOF)+daclatasvir (DAC), SOF/velpatasvir (VEL), glecaprevir/pibrentasvir (GLE/PIB), are scarce. We aimed at filling this data gap., Methods: Sustained virological response 12 weeks after treatment completion (SVR12) was assessed for all HCV-GT3 patients consecutively treated within the Lombardia web-based Navigatore HCV-Network; differences in SVR12 across regimens were evaluated by logistic regression., Results: Of the 2082 subjects with HCV-GT3, 1544 were evaluable for comparisons between regimens: SOF + DAC (1023, 66.2%), SOF/VEL (369, 23.9%), GLE/PIB (152, 9.8%). Patients treated with former regimens were more frequently male, cirrhotic, HIV-positive, pretreated, used ribavirin in their regimen, and had lower baseline HCV-RNA. SVR12 was similar across groups: 94.8% in SOF + DAC, 97.6% in SOF/VEL, 96.7% in GLE/PIB (P = .065). At univariate analysis, SVR12 was associated with female gender (97.9% vs 94.8%, P = .007) and lower median pretreatment Log
10 HCV-RNA (5.87 vs 6.20, P = .001). At multivariate logistic regression analysis, treatment with SOF/VEL was associated with a higher likelihood of SVR12 than SOF + DAC, but only in the absence of ribavirin (98% vs 90.3%). Female gender and lower pretreatment HCV-RNA were independently associated with SVR12., Conclusions: In a large real-life setting of HCV-GT3-infected patients with a high proportion of cirrhosis, the success rate was remarkable. The slight advantage of SOF/VEL on SOF + DAC was significant only without ribavirin. The current prescription shift towards novel regimens (ie SOF/VEL and GLE/PIB) in easier-to-treat patients allows ribavirin-free and shorter schedules without mining SVR12 in this <> genotype., (© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.) - Published
- 2020
- Full Text
- View/download PDF
36. Renal safety in 3264 HCV patients treated with DAA-based regimens: Results from a large Italian real-life study.
- Author
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D'Ambrosio R, Pasulo L, Giorgini A, Spinetti A, Messina E, Fanetti I, Puoti M, Aghemo A, Viganò P, Vinci M, Menzaghi B, Lombardi A, Pan A, Pigozzi MG, Grossi P, Lazzaroni S, Spinelli O, Invernizzi P, Maggiolo F, Terreni N, Monforte AD, Poggio PD, Taddei MT, Colombo S, Pozzoni P, Molteni C, Brocchieri A, Bhoori S, Buscarini E, Centenaro R, Mendeni M, Colombo AE, Di Marco M, Dionigi E, Bella D, Borghi M, Zuin M, Zaltron S, Noventa F, Annalisa S, Lampertico P, and Fagiuoli S
- Subjects
- Adult, Aged, Aged, 80 and over, Antiviral Agents adverse effects, Drug Therapy, Combination, Female, Genotype, Glomerular Filtration Rate, Hepacivirus, Hepatitis C, Chronic pathology, Humans, Italy, Logistic Models, Male, Middle Aged, Renal Insufficiency, Chronic complications, Renal Insufficiency, Chronic physiopathology, Retrospective Studies, Sofosbuvir adverse effects, Sustained Virologic Response, Young Adult, Antiviral Agents therapeutic use, Hepatitis C, Chronic drug therapy, Sofosbuvir therapeutic use
- Abstract
Background: Sofosbuvir (SOF)-based regimens have been associated with renal function worsening in HCV patients with estimated glomerular filtration rate (eGFR) ≤ 45 ml/min, but further investigations are lacking., Aim: To assess renal safety in a large cohort of DAA-treated HCV patients with any chronic kidney disease (CKD)., Methods: All HCV patients treated with DAA in Lombardy (December 2014-November 2017) with available kidney function tests during and off-treatment were included., Results: Among 3264 patients [65% males, 67% cirrhotics, eGFR 88 (9-264) ml/min], CKD stage was 3 in 9.5% and 4/5 in 0.7%. 79% and 73% patients received SOF and RBV, respectively. During DAA, eGFR declined in CKD-1 (p < 0.0001) and CKD-2 (p = 0.0002) patients, with corresponding rates of CKD stage reduction of 25% and 8%. Conversely, eGFR improved in lower CKD stages (p < 0.0001 in CKD-3a, p = 0.0007 in CKD-3b, p = 0.024 in CKD-4/5), with 33-45% rates of CKD improvement. Changes in eGFR and CKD distribution persisted at SVR. Baseline independent predictors of CKD worsening at EOT and SVR were age (p < 0.0001), higher baseline CKD stages (p < 0.0001) and AH (p = 0.010 and p < 0.0001, respectively)., Conclusions: During DAA, eGFR significantly declined in patients with preserved renal function and improved in those with lower CKD stages, without reverting upon drug discontinuation., (Copyright © 2019 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2020
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37. External validation of the ITA.LI.CA prognostic system for patients with hepatocellular carcinoma: A multicenter cohort study.
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Borzio M, Dionigi E, Rossini A, Marignani M, Sacco R, De Sio I, Bertolini E, Francica G, Giacomin A, Parisi G, Vicari S, Toldi A, Salmi A, Boccia S, Mitra M, and Fornari F
- Subjects
- Aged, Cohort Studies, Female, Humans, Italy, Male, Middle Aged, Neoplasm Staging, Prognosis, Survival Rate, Carcinoma, Hepatocellular mortality, Carcinoma, Hepatocellular pathology, Liver Neoplasms mortality, Liver Neoplasms pathology
- Abstract
Several staging systems for hepatocellular carcinoma (HCC) have been developed. The Barcelona Clinic Liver Cancer staging system is considered the best in predicting survival, although limitations have emerged. Recently, the Italian Liver Cancer (ITA.LI.CA) prognostic system, integrating ITA.LI.CA tumor staging (stages 0, A, B1-3, C) with the Child-Turcotte-Pugh score, Eastern Cooperative Oncology Group performance status, and alpha-fetoprotein with a strong ability to predict survival, was proposed. The aim of our study was to provide an external validation of the ITA.LI.CA system in an independent real-life occidental cohort of HCCs. From September 2008 to April 2016, 1,508 patients with cirrhosis and incident HCC were consecutively enrolled in 27 Italian institutions. Clinical, tumor, and treatment-related variables were collected, and patients were stratified according to scores of the Barcelona Clinic Liver Cancer system, ITA.LI.CA prognostic system, Hong Kong Liver Cancer system, Cancer of the Liver Italian Program, Japanese Integrated System, and model to estimate survival in ambulatory patients with hepatocellular carcinoma. Harrell's C-index, Akaike information criterion, and likelihood-ratio test were used to compare the predictive ability of the different systems. A subgroup analysis for treatment category (curative versus palliative) was performed. Median follow-up was 44 months (interquartile range, 23-63 months), and median overall survival was 34 months (interquartile range, 13-82 months). Median age was 71 years, and patients were mainly male individuals and hepatitis C virus carriers. According to ITA.LI.CA tumor staging, 246 patients were in stage 0, 472 were in stage A, 657 were in stages B1/3, and 133 were in stage C. The ITA.LI.CA prognostic system showed the best discriminatory ability (C-index = 0.77) and monotonicity of gradients compared to other systems, and its superiority was also confirmed after stratification for treatment strategy., Conclusion: This is the first study that independently validated the ITA.LI.CA prognostic system in a large cohort of Western patients with incident HCCs. The ITA.LI.CA system performed better than other multidimensional prognostic systems, even after stratification by curative or palliative treatment. This new system appears to be particularly useful for predicting individual HCC prognosis in clinical practice. (Hepatology 2018;67:2215-2225)., (© 2017 by the American Association for the Study of Liver Diseases.)
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- 2018
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38. Management and prognosis of hepatocellular carcinoma in the elderly: Results of an in-field multicenter cohort study.
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Borzio M, Dionigi E, Vitale A, Rossini A, Marignani M, Fornari F, Vicari S, De Sio I, Farinati F, Bertolini E, Oliveri F, Leandro G, Francica G, Mitra M, Omazzi B, Boccia S, Salmi A, Toldi A, and Sacco R
- Subjects
- Age Factors, Aged, Carcinoma, Hepatocellular diagnosis, Carcinoma, Hepatocellular therapy, Cohort Studies, Female, Humans, Italy epidemiology, Liver Neoplasms diagnosis, Liver Neoplasms therapy, Male, Middle Aged, Prognosis, Survival Analysis, Carcinoma, Hepatocellular mortality, Liver Neoplasms mortality
- Abstract
Aims: This multicentre cohort study evaluated the role of ageing on clinical characteristics, treatment allocation and outcome of new hepatocellular carcinomas (HCCs), in clinical practice., Material & Methods: From September 2008, 541 patients >70 years old (elderly group), and 527 ≤70 years old (non-elderly group) with newly diagnosed HCC were consecutively enrolled in 30 Italian centres. Differences in clinical characteristics and treatment allocation between groups were described by a multivariable logistic regression model measuring the inverse probability weight to meet the elderly group. Survival differences were measured by unadjusted and adjusted (by inverse probability weight) survival analysis., Results: Elderly patients were mainly females, hepatitis C virus infected and with better conserved liver function (P<.001). At presentation, HCC median size was similar in both groups while, in youngers, HCC was more frequently multinodular (P=.001), and associated with neoplastic thrombosis (P=.009). Adjusted survival analysis showed that age did not predict short-mid-term survival (within 24 months), while it was a significant independent predictor of long-term survival. Moreover, age had a significant long-term survival impact mainly on early HCC stages (Barcelona Clinic for Liver Cancer [BCLC] 0-A), its impact on BCLC B stage was lower, while it was negligible for advanced-terminal stages., Conclusions: Age per se does not impact on short-mid-term prognosis (≤24 months) of HCC patients, and should not represent a limitation to its management., (© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2017
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39. Bacterial Infections Change Natural History of Cirrhosis Irrespective of Liver Disease Severity.
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Dionigi E, Garcovich M, Borzio M, Leandro G, Majumdar A, Tsami A, Arvaniti V, Roccarina D, Pinzani M, Burroughs AK, O'Beirne J, and Tsochatzis EA
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- Adult, Aged, Ascites epidemiology, Ascites etiology, Cohort Studies, Community-Acquired Infections epidemiology, Cross Infection epidemiology, Disease Progression, End Stage Liver Disease, Esophageal and Gastric Varices epidemiology, Esophageal and Gastric Varices etiology, Female, Gastrointestinal Hemorrhage epidemiology, Humans, Hypertension, Portal etiology, Incidence, Liver Cirrhosis complications, Liver Cirrhosis mortality, Liver Cirrhosis physiopathology, Male, Middle Aged, Prognosis, Proportional Hazards Models, Retrospective Studies, Severity of Illness Index, Survival Rate, Bacterial Infections epidemiology, Liver Cirrhosis epidemiology
- Abstract
Objectives: We assessed the prognostic significance of infections in relation to current prognostic scores and explored if infection could be considered per se a distinct clinical stage in the natural history of cirrhosis., Methods: We included consecutive patients with cirrhosis admitted to a tertiary referral liver unit for at least 48 h over a 2-year period. Diagnosis of infection was based on positive cultures or strict established criteria. We used competing risk analysis and propensity score matching for data analysis., Results: 501 patients (63% male, 48% alcoholic liver disease, median Model of End-stage Liver Disease (MELD)=17) underwent 781 admissions over the study period. Portal hypertensive bleeding and complicated ascites were the commonest reasons of admission. The incidence of proven bacterial infection was 25.6% (60% community acquired and 40% nosocomial). Survival rates at 3, 6, 12, and 30 months were 83%, 77%, 71%, and 62% in patients without diagnosis of infection, vs. 50%, 46%, 41%, and 34% in patients with diagnosis of infection. Overall survival was independently associated with MELD score (hazards ratio (HR) 1.099), intensive care (ITU) stay (HR 1.967) and bacterial infection (HR 2.226). Bacterial infection was an independent predictor of survival even when patients who died within the first 30 days were excluded from the analysis in Cox regression (HR 2.013) and competing risk Cox models in all patients (HR 1.46) and propensity risk score-matched infected and non-infected patients (HR 1.67)., Conclusions: Infection most likely represents a distinct prognostic stage of cirrhosis, which affects survival irrespective of disease severity, even after recovery from the infective episode.
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- 2017
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40. The impact of infection by multidrug-resistant agents in patients with cirrhosis. A multicenter prospective study.
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Salerno F, Borzio M, Pedicino C, Simonetti R, Rossini A, Boccia S, Cacciola I, Burroughs AK, Manini MA, La Mura V, Angeli P, Bernardi M, Dalla Gasperina D, Dionigi E, Dibenedetto C, and Arghittu M
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- Aged, Bacteria classification, Bacteria isolation & purification, Cross Infection microbiology, Female, Hospital Mortality, Humans, Italy, Logistic Models, Male, Middle Aged, Multivariate Analysis, Prognosis, Prospective Studies, Anti-Bacterial Agents therapeutic use, Bacterial Infections drug therapy, Cross Infection drug therapy, Drug Resistance, Multiple, Bacterial, Liver Cirrhosis complications
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Background & Aims: Bacterial strains resistant to antibiotics are a serious clinical challenge. We assessed the antibiotic susceptibility of bacteria isolated from infections in patients with cirrhosis by a multicentre investigation., Results: Three hundred and thirteen culture-positive infections (173 community acquired [CA] and 140 hospital acquired [HA]) were identified in 308 patients. Urinary tract infections, spontaneous bacterial peritonitis and bacteremias were the most frequent. Quinolone-resistant Gram-negative isolates were 48%, 44% were extended-spectrum beta-lactamase producers and 9% carbapenem resistant. In 83/313 culture-positive infections (27%), multidrug-resistant agents (MDRA) were isolated. This prevalence did not differ between CA and HA infections. MDRA were identified in 17 of 37 patients on quinolone prophylaxis, and in 46 of 166 not on prophylaxis (45% vs 27%; P<.03). In 287 cases an empiric antibiotic therapy was undertaken, in 37 (12.9%) this therapy failed. The in-hospital mortality rate of this subset of patients was significantly higher compared to patients who received an effective broad(er)-spectrum therapy (P=.038). During a 3-month follow-up, 56/203 culture-positive patients (27.6%) died, 24/63 who have had MDRA-related infections (38%) and 32/140 who have had antibiotic-susceptible infections (22.8%) (P=.025). Multivariate analysis disclosed MDRA infection, age, hepatocellular carcinoma, bilirubin, international normalized ratio and the occurrence of portal hypertension-related complications independent predictors of death., Conclusions: Infection by MDRA is frequent in patients with cirrhosis and the prognosis is severe, especially in patients unresponsive to empiric antibiotic therapy., (© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
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- 2017
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41. Management of hepatocellular carcinoma in the elderly.
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Borzio M, Dionigi E, Parisi G, Raguzzi I, and Sacco R
- Abstract
Mean age of hepatocellular carcinoma (HCC) patients has been progressively increasing over the last decades and ageing of these patients is becoming a real challenge in every day clinical practice. Unfortunately, international guidelines on HCC management do not address this problem exhaustively and do not provide any specific recommendation. We carried out a literature search in MEDLINE database for studies reporting on epidemiology, clinical characteristics and treatment outcome of HCC in elderly patients. Available data seem to indicate that in elderly patients the outcome of HCC is mostly influenced by liver function and tumor stage rather than by age and the latter should not influence treatment allocation. Age is not a risk for resection and older patients with resectable HCC and good liver function could gain benefit from surgery. Mild comorbidities do not seem a contraindication for surgery in aged patients. Conversely, major resection in elderly, even when performed in experienced high-volume centres, should be avoided. Both percutaneous ablation and transarterial chemoembolization are not contraindicated in aged patients and safety profile of these procedures is acceptable. Sorafenib is a viable option for advanced HCC in elderly provided that a careful evaluation of concomitant comorbidities, particularly cardiovascular ones, is taken into account. Available data seem to suggest that in either elderly and younger, treatment is a main predictor of outcome. Consequently, a nihilistic attitude of physicians towards under- or no-treatment of aged patients should not be longer justified.
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- 2015
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42. Trend of improving prognosis of hepatocellular carcinoma in clinical practice: an Italian in-field experience.
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Borzio M, Dionigi E, Rossini A, Toldi A, Francica G, Fornari F, Salmi A, Farinati F, Vicari S, Marignani M, Terracciano F, Ginanni B, and Sacco R
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- Aged, Carcinoma, Hepatocellular etiology, Carcinoma, Hepatocellular mortality, Female, Humans, Italy, Kaplan-Meier Estimate, Liver Cirrhosis diagnosis, Liver Cirrhosis mortality, Liver Neoplasms etiology, Liver Neoplasms mortality, Male, Middle Aged, Neoplasm Staging, Practice Patterns, Physicians' trends, Predictive Value of Tests, Quality Improvement trends, Quality Indicators, Health Care trends, Risk Factors, Time Factors, Treatment Outcome, Carcinoma, Hepatocellular diagnosis, Carcinoma, Hepatocellular therapy, Early Detection of Cancer trends, Liver Cirrhosis complications, Liver Neoplasms diagnosis, Liver Neoplasms therapy, Outcome Assessment, Health Care trends
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Background: Recent data suggest that outcome of hepatocarcinoma is improving., Aims: In order to explore whether survival is also increasing in clinical practice, we compared two multicenter independent in-field cohorts of cirrhotics with newly diagnosed HCCs., Methods: Cohort 1 (C1) consisted of 327 patients enrolled between January and December 1998, and cohort 2 (C2) included 826 patients enrolled between September 2008 and November 2012. Patients were stratified according to Child-Pugh score, MELD score, and HCC staged according to TNM, BCLC systems., Results: At baseline, C2 patients were significantly older, with more frequent comorbidities and better liver function. In C2, HCC was more frequently detected under regular ultrasound surveillance (P < 0.001), BCLC early stages were more frequent, and rates of smaller and uni/paucinodular tumors were significantly higher. Treatment of any type was more frequently offered to C2 patients (P < 0.001). Proportion of patients treated by TACE increased, and radiofrequency ablation was the most used ablative treatment. Survival rate was significantly higher in C2 being C1 and C2 survival at 1-3 years 72-25 and 75-44 %, respectively. Child-Pugh score A, BCLC stage A, single nodule, size ≤ 3 cm, belonging to cohort C2 and treatment per se independently predicted survival., Conclusions: This in-field study showed a trend on improved HCC outcomes over time, which seems to be mainly due to a better presentation thanks to the wider application of surveillance and increased propensity to treat patients. These encouraging data should support further efforts to implement such approach to HCC in everyday clinical practice.
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- 2015
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43. Adherence to American Association for the Study of Liver Diseases guidelines for the management of hepatocellular carcinoma: results of an Italian field practice multicenter study.
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Borzio M, Fornari F, De Sio I, Andriulli A, Terracciano F, Parisi G, Francica G, Salvagnini M, Marignani M, Salmi A, Farinati F, Carella A, Pedicino C, Dionigi E, Fanigliulo L, Cazzaniga M, Ginanni B, and Sacco R
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- Aged, Aged, 80 and over, Carcinoma, Hepatocellular epidemiology, Female, Humans, Italy, Liver Neoplasms epidemiology, Male, Middle Aged, Practice Guidelines as Topic, Prospective Studies, Carcinoma, Hepatocellular diagnosis, Carcinoma, Hepatocellular therapy, Guideline Adherence statistics & numerical data, Liver Neoplasms diagnosis, Liver Neoplasms therapy
- Abstract
Aim: Adherence to and the applicability of practice guidelines for the management of hepatocellular carcinoma (HCC) in field practice have not been fully addressed. We designed a multicenter field practice prospective study to evaluate the adherence to the 2005 American Association for the Study of Liver Diseases guidelines in Italy., Materials & Methods: The study began in September 2008 and consecutively enrolled cirrhotic patients with newly diagnosed HCC from 30 local, nonreference centers in Italy. Patients were stratified according to Child-Pugh, the model for end-stage liver disease, tumor-node metastasis, performance status and the Barcelona Clinic Liver Cancer (BCLC) classifications. The diagnostic and therapeutic strategies adopted in each individual patient were recorded. Statistical analysis was carried out on 536 patients using all of the valuable data., Results: A total of 286 (54.5%) patients were ≥70 years old. Comorbidities, recorded in 397 (74%) patients, were classified as moderate to severe in 170 patients (43%). Overall, 174 (59%) patients with early-stage BCLC were ≥70 years; 104 (35%) of these had moderate-to-severe comorbidities and 54% were under a regular US surveillance program. Diagnosis was performed by computed tomography in 93% of patients, contrast-enhanced ultrasound in 62% and MRI in 17%. In patients with nodules of ≤2 cm, adherence to noninvasive diagnostic criteria was 56%. Adherence to the BCLC classification was shown to be suboptimal overall, particularly regarding allocation to surgical procedures, and a total of 119 patients (40%) with BCLC stage A did not receive curative therapies., Conclusions: This multicenter survey showed that, in the 'real world', adherence to the both the diagnostic and therapeutic American Association for the Study of Liver Diseases 2005 algorithms was low, particularly in patients with early-stage HCC. Difficulties in applying the algorithms in routine clinical practice and the high prevalence of older patients with relevant comorbidities may account for our findings. Strategies to help improve adherence to international guidelines for HCC in field practice are required.
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- 2013
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44. The systemic inflammatory response syndrome in cirrhotic patients: relationship with their in-hospital outcome.
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Cazzaniga M, Dionigi E, Gobbo G, Fioretti A, Monti V, and Salerno F
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- Aged, Bilirubin blood, Cohort Studies, Creatinine blood, Female, Follow-Up Studies, Humans, Liver Cirrhosis diagnosis, Liver Failure physiopathology, Male, Middle Aged, Multiple Organ Failure physiopathology, Multivariate Analysis, Prognosis, Prospective Studies, Sepsis physiopathology, Systemic Inflammatory Response Syndrome diagnosis, Hospital Mortality, Liver Cirrhosis complications, Liver Cirrhosis physiopathology, Systemic Inflammatory Response Syndrome complications, Systemic Inflammatory Response Syndrome physiopathology
- Abstract
Background/aims: Some evidence suggests that the systemic inflammatory response syndrome (SIRS) contributes to the poor outcome of cirrhotic patients. We studied 141 cirrhotic patients consecutively admitted to a tertiary referral centre assessing prevalence of SIRS and its relationship with in-hospital outcome., Methods: Presence of SIRS was assessed on admission and during hospital stay. Main clinical outcomes were death and development of portal hypertension-related complications., Results: Thirty-nine patients met SIRS criteria. SIRS was present on admission in 20 of 141 patients (14.1%), whereas it occurred during hospital stay in 19 of 121 (15.7%). SIRS was correlated with bacterial infection at admission (p=0.02), jaundice (p=0.011), high serum creatinine levels (p=0.04), high serum bilirubin levels (p=0.002), high international normalized ratio (p=0.046), high model of end-stage liver disease (MELD) score (p=0.001), and high SOFA score (p=0.003). During a follow-up of 14+/-8 days, 16 patients died (11%), 7 developed portal hypertension-related bleeding (5%), 16 hepatic encephalopathy (11%), and 5 hepatorenal syndrome type-1 (3.5%). SIRS was correlated both to death (p<0.001) and to portal hypertension-related complications (p<0.001). On multivariate analysis, SIRS and MELD were independently associated with death., Conclusions: SIRS frequently occurs in patients with advanced cirrhosis and is associated with a poor outcome.
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- 2009
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