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  1. Article ; Online: Evolution of liver fibrosis after interferon-based anti-hepatitis C virus therapy failure in 3,049 chronic hepatitis C patients without cirrhosis.

    Omar, Heba / Waked, Imam / Elakel, Wafaa / Salama, Rabab / Abdel-Razik, Wael / Elmakhzangy, Hesham / Abdel-Rahman, Yasser Omar / Saeed, Ramy / Elshafaey, Arwa / Ziada, Dina H / Ismail, Sohier Ahmed / Dabbous, Hany M / Esmat, Gamal

    Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology

    2023  Volume 24, Issue 1, Page(s) 65–72

    Abstract: Background and study aims: Liver fibrosis is the underlying causeof hepatitis C virus (HCV)-related disease progression to endpoints such as cirrhosis, liver failure, and hepatocellular carcinoma. The aim of our study was to assess changes in hepatic ... ...

    Abstract Background and study aims: Liver fibrosis is the underlying causeof hepatitis C virus (HCV)-related disease progression to endpoints such as cirrhosis, liver failure, and hepatocellular carcinoma. The aim of our study was to assess changes in hepatic fibrosis in patients with chronic HCV who had a fibrosis evaluation at two time points at least six months apart.
    Patients and methods: This was a retrospective cohort study that included patients who had failed interferon therapy and received HCV retreatment with direct-acting antivirals (DAAs) at least six months later. Patients were evaluated previously for fibrosis according to liver biopsy and fibrosis biomarkers were evaluated before pegylated interferon and ribavirin (PEG/RBV) therapy. Fibrosis was re-evaluated with fibrosis-4 (FIB-4) scores before starting DAAs.
    Results: A total of 3,049 patients were included [age 43.47 ± 9.07 years, 55.20 % males] and baseline histopathology showed F1, F2, and F3 in 16.86 %, 46.21 %, and 36.93 %, respectively. The mean time interval between the last dose of previously failed IFN-therapy to the first dose of DAAs was 2.38 (±1.07) years. Overall, there was a significant increase in FIB-4 scores at retreatment times (from 11.71 ± 1.13 to 22.26 ± 1.68, p < 0.001). Patients with baseline FIB-4 < 1.45 (n = 1,569) and between 1.45 and 3.25 (n = 1,237) had significant increases in their FIB-4 at the retreatment time point [median difference; 0.41 (0.91) and 0.24 (1.5), p < 0.001, respectively], whereas patients with FIB-4 > 3.25 had significant reduction of their FIB-4 score at a retreatment timepoint [-0.98 (2.93), p ≤ 0.001].
    Conclusion: Fibrosis progressed in most patients, even within six months for some patients, and this indicates retreatment of non-system vascular resistance patients even if they do not have significant fibrosis.
    MeSH term(s) Male ; Humans ; Adult ; Middle Aged ; Female ; Hepatitis C, Chronic/complications ; Hepatitis C, Chronic/drug therapy ; Antiviral Agents/adverse effects ; Retrospective Studies ; Ribavirin/therapeutic use ; Liver Cirrhosis/pathology ; Fibrosis ; Interferons/therapeutic use ; Hepacivirus ; Liver Neoplasms/drug therapy
    Chemical Substances Antiviral Agents ; Ribavirin (49717AWG6K) ; Interferons (9008-11-1)
    Language English
    Publishing date 2023-01-30
    Publishing country Egypt
    Document type Journal Article
    ZDB-ID 2502114-X
    ISSN 2090-2387 ; 1687-1979
    ISSN (online) 2090-2387
    ISSN 1687-1979
    DOI 10.1016/j.ajg.2023.01.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Impact of Sarcopenia on Short-Term Complications and Survival After Liver Transplant.

    Hassan, Elham Ahmed / Makhlouf, Nahed A / Ibrahim, Mohamed Eltaher / Dabbous, Hany M / Salah, Medhat A / Aboalam, Hani Sayed / Mohamed, Mohamed Zidan / Fadel, Bashir A / Salama, Marwa Abdel Razek

    Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation

    2022  Volume 20, Issue 10, Page(s) 917–924

    Abstract: Objectives: Sarcopenia is a common entity in cirrhosis with significant morbidity and mortality. However,the effects of sarcopenia on the risk of complications and survival after liver transplant remain controversial.We aimed to evaluate the effect of ... ...

    Abstract Objectives: Sarcopenia is a common entity in cirrhosis with significant morbidity and mortality. However,the effects of sarcopenia on the risk of complications and survival after liver transplant remain controversial.We aimed to evaluate the effect of sarcopenia on survival and complications after liver transplant.
    Materials and methods: Our study cohort included 61 adult patients with hepatitis C-related cirrhosis who underwent living donor liver transplant. Pretransplant clinical and anthropometric assessments included body mass index, hand grip, mid-arm circumference, triceps skin fold thickness, and gait speed. Sarcopenia was determined by computed tomography using the skeletal muscle index at the third lumbar vertebra cut-off value of <38.5 cm2/m2 for women and <52.4 cm2/m2 for men; these patients were then followed up for 6 months after transplant to determine survival and complications.
    Results: At time of liver transplant, sarcopenia was present in 27/61 patients (44.3%). At follow-up after transplant, sarcopenia was found in 14 patients (30.4%) among 46 survivors; all patients who survived were male patients. Among patients with sarcopenia posttransplant, 12 had sarcopenia before transplant and 2 developed sarcopenia after transplant. Liver dysfunction, lower triceps skin fold thickness, recent infections, and sarcopenia pretransplant were associatedwithposttransplant complications, especially infection(42.8%) and prolonged intensive careunit stay. Age and pretransplant sarcopenia were found to be independent predictors of posttransplant mortality.
    Conclusions: Sarcopenia is a common entity in patients with cirrhosis who are on liver transplant wait lists and may continue after liver transplant. De novo sarcopenia after liver transplant is also a common finding. Sarcopenia can affect patient outcomes, including prolonged intensive care unit stay and poor short-term survival.
    MeSH term(s) Humans ; Adult ; Male ; Female ; Sarcopenia/diagnosis ; Sarcopenia/diagnostic imaging ; Liver Transplantation/adverse effects ; Hand Strength ; Living Donors ; Treatment Outcome ; Liver Cirrhosis/complications ; Liver Cirrhosis/diagnosis ; Liver Cirrhosis/surgery
    Language English
    Publishing date 2022-08-08
    Publishing country Turkey
    Document type Journal Article
    ZDB-ID 2396778-X
    ISSN 2146-8427 ; 1304-0855
    ISSN (online) 2146-8427
    ISSN 1304-0855
    DOI 10.6002/ect.2022.0293
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Outcome of Colonoscopic Screening in Potential Liver Transplant Candidates.

    Sakr, Mohammad A / Ebada, Hend E / Abdelkader, Soheir / Dabbous, Hany M / Montasser, Iman F / Bassuny, Ahmed N / Massoud, Yasmeen M / Abdelmoaty, Ahmed S

    Transplantation proceedings

    2020  Volume 52, Issue 1, Page(s) 227–232

    Abstract: Background: Screening for neoplastic lesions is mandatory as a part of the evaluation process of potential candidates for liver transplant (LT). This work aimed at identifying the main findings in screening colonoscopy and their risk factors.: Methods! ...

    Abstract Background: Screening for neoplastic lesions is mandatory as a part of the evaluation process of potential candidates for liver transplant (LT). This work aimed at identifying the main findings in screening colonoscopy and their risk factors.
    Methods: Endoscopic and pathologic findings of the biopsied lesions of 311 potential candidates for living donor liver transplant were collected and analyzed.
    Results: Colorectal polyps (8.7%) were the most common colonoscopic finding, of which 4.18% were diagnosed as adenomas. Other findings included hemorrhoids (7.7%), portal hypertensive colopathies (3.5%), angiomatous malformations (2.6%), rectal varices (1.6%), and diverticulosis (1.6%). The univariate analysis revealed that the prevalence of colonic adenoma was significant in patients 50 years and older (P = .03; odds ratio, 1.178; 95% CI, 1.016-1.365) and in patients who had hepatocellular carcinoma (P = .043; odds ratio, 6.5; 95% CI, 1.002-42.172). In the multivariate analysis, age was found to be the single best predictor of the presence of adenoma (P = .044; odds ratio, 1.178; 95% CI, 1.005-1.382).
    Conclusion: We can conclude that a screening colonoscopy prior to liver donor liver transplant should be performed at least in every LT candidate 50 years or older. Colonic polyps were the most common findings on screening colonoscopy prior to LT.
    MeSH term(s) Adenoma/diagnosis ; Adenoma/epidemiology ; Aged ; Colonic Neoplasms/diagnosis ; Colonic Neoplasms/epidemiology ; Colonic Polyps/diagnosis ; Colonic Polyps/epidemiology ; Colonoscopy/methods ; Colonoscopy/statistics & numerical data ; Female ; Humans ; Liver Transplantation/methods ; Living Donors ; Male ; Mass Screening/methods ; Mass Screening/statistics & numerical data ; Middle Aged ; Odds Ratio ; Preoperative Care/methods ; Preoperative Care/statistics & numerical data ; Prevalence ; Retrospective Studies ; Risk Factors
    Language English
    Publishing date 2020-01-30
    Publishing country United States
    Document type Evaluation Study ; Journal Article
    ZDB-ID 82046-5
    ISSN 1873-2623 ; 0041-1345
    ISSN (online) 1873-2623
    ISSN 0041-1345
    DOI 10.1016/j.transproceed.2019.10.026
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Efficacy of favipiravir in COVID-19 treatment: a multi-center randomized study

    Dabbous, Hany M / Abd-Elsalam, Sherief / El-Sayed, Manal H / Sherief, Ahmed F / Ebeid, Fatma F. S / El Ghafar, Mohamed Samir Abd / Soliman, Shaimaa / Elbahnasawy, Mohamed / Badawi, Rehab / Tageldin, Mohamed Awad

    Archives of virology. 2021 Mar., v. 166, no. 3

    2021  

    Abstract: No specific antiviral drugs have been approved for the treatment of COVID-19. This study aimed to evaluate the efficacy of favipiravir in treatment of COVID-19. This was a multicenter randomized controlled study including 96 patients with COVID- 19 who ... ...

    Abstract No specific antiviral drugs have been approved for the treatment of COVID-19. This study aimed to evaluate the efficacy of favipiravir in treatment of COVID-19. This was a multicenter randomized controlled study including 96 patients with COVID- 19 who were randomly assigned into a chloroquine (CQ) group and a favipiravir group. None of the patients in the favipiravir group needed mechanical ventilation (p = 0.129). One patient (2.3%) in the favipiravir group and two patients (4.2%) in the CQ group died (p = 1.00). Favipiravir is a promising drug for COVID-19 that decreases the hospital stay and the need for mechanical ventilation.ClinicalTrials.gov Identifier NCT04351295.
    Keywords COVID-19 infection ; chloroquine ; patients ; virology
    Language English
    Dates of publication 2021-03
    Size p. 949-954.
    Publishing place Springer Vienna
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 7491-3
    ISSN 1432-8798 ; 0304-8608
    ISSN (online) 1432-8798
    ISSN 0304-8608
    DOI 10.1007/s00705-021-04956-9
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: Seroprevalence of HBV/HCV coinfection among patients with HCV screened during the national campaign for HCV eradication in Egypt.

    Gamal Eldeen, Hadeel / Hassany, Mohamed / Elakel, Wafaa / AbdAllah, Mohamed / Abdel-Razek, Wael / Elshazly, Yehia / Dabbous, Hany M / Hamdy El-Sayed, Manal / El-Serafy, Magdy / Waked, Imam / Esmat, Gamal / Doss, Wahid / Hashem, Ahmed

    Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology

    2022  Volume 23, Issue 4, Page(s) 259–262

    Abstract: Background and study aims: Little is known about the true prevalence of hepatitis B virus (HBV) coinfection in patients with hepatitis C virus (HCV). This multicenter nationwide study aimed to assess the seroprevalence of HBV among Egyptian patients ... ...

    Abstract Background and study aims: Little is known about the true prevalence of hepatitis B virus (HBV) coinfection in patients with hepatitis C virus (HCV). This multicenter nationwide study aimed to assess the seroprevalence of HBV among Egyptian patients with HCV and its possible risk factors.
    Patients and methods: This is a cross-sectional, multicenter, nationwide study. Data were extracted from the National Network of Viral Hepatitis Treatment Centers database. Baseline data of patients proved to be viremic during the national campaign for HCV eradication (October 2018-April 2019) were retrieved. Data included demographics, laboratory tests (HBsAg, CBC, liver biochemical profile, creatinine, AFP, HbA1c, and viral load), FIB-4 score calculation, and abdominal ultrasound results.
    Results: Results of 297,965 patients showed that HBsAg was positive in 2,347 (0.8%) patients. Patients with HBV/HCV were 57% females and had a mean age of 51 ± 13 years. Patients with positive HBsAg showed significantly more tobacco consumption, intravenous drug abuse, hypertension, and diabetes. No significant difference was noted in HCV viremia between patients with HCV and those with HBV/HCV. Only 14% of patients with HBV/HCV had cirrhosis compared with the 9% of those with HCV; two of them had HCC.
    Conclusion: Although Egypt has a heavy HCV burden, the overall prevalence of HBV is low among patients with HCV infection. Comorbid conditions seem to favor coinfection.
    MeSH term(s) Humans ; Adult ; Middle Aged ; Hepacivirus ; Hepatitis B virus ; Seroepidemiologic Studies ; Carcinoma, Hepatocellular ; Cross-Sectional Studies ; Liver Neoplasms
    Language English
    Publishing date 2022-11-03
    Publishing country Egypt
    Document type Multicenter Study ; Journal Article
    ZDB-ID 2502114-X
    ISSN 2090-2387 ; 1687-1979
    ISSN (online) 2090-2387
    ISSN 1687-1979
    DOI 10.1016/j.ajg.2022.06.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Retraction Note: Safety and efficacy of favipiravir versus hydroxychloroquine in management of COVID-19: A randomised controlled trial.

    Dabbous, Hany M / El-Sayed, Manal H / El Assal, Gihan / Elghazaly, Hesham / Ebeid, Fatma F S / Sherief, Ahmed F / Elgaafary, Maha / Fawzy, Ehab / Hassany, Sahar M / Riad, Ahmed R / TagelDin, Mohamed A

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 18983

    Language English
    Publishing date 2021-09-18
    Publishing country England
    Document type Journal Article ; Retraction of Publication
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-98683-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Safety and efficacy of favipiravir versus hydroxychloroquine in management of COVID-19: A randomised controlled trial.

    Dabbous, Hany M / El-Sayed, Manal H / El Assal, Gihan / Elghazaly, Hesham / Ebeid, Fatma F S / Sherief, Ahmed F / Elgaafary, Maha / Fawzy, Ehab / Hassany, Sahar M / Riad, Ahmed R / TagelDin, Mohamed A

    publication RETRACTED

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 7282

    Abstract: Favipiravir is considered a potential treatment for COVID-19 due its efficacy against different viral infections. We aimed to explore the safety and efficacy of favipiravir in treatment of COVID-19 mild and moderate cases. It was randomized-controlled ... ...

    Abstract Favipiravir is considered a potential treatment for COVID-19 due its efficacy against different viral infections. We aimed to explore the safety and efficacy of favipiravir in treatment of COVID-19 mild and moderate cases. It was randomized-controlled open-label interventional phase 3 clinical trial [NCT04349241]. 100 patients were recruited from 18th April till 18th May. 50 patients received favipiravir 3200 mg at day 1 followed by 600 mg twice (day 2-day 10). 50 patients received hydroxychloroquine 800 mg at day 1 followed by 200 mg twice (day 2-10) and oral oseltamivir 75 mg/12 h/day for 10 days. Patients were enrolled from Ain Shams University Hospital and Assiut University Hospital. Both arms were comparable as regards demographic characteristics and comorbidities. The average onset of SARS-CoV-2 PCR negativity was 8.1 and 8.3 days in HCQ-arm and favipiravir-arm respectively. 55.1% of those on HCQ-arm turned PCR negative at/or before 7th day from diagnosis compared to 48% in favipiravir-arm (p = 0.7). 4 patients in FVP arm developed transient transaminitis on the other hand heartburn and nausea were reported in about 20 patients in HCQ-arm. Only one patient in HCQ-arm died after developing acute myocarditis resulted in acute heart failure. Favipiravir is a safe effective alternative for hydroxychloroquine in mild or moderate COVID-19 infected patients.
    MeSH term(s) Adult ; Amides/adverse effects ; Amides/therapeutic use ; Antiviral Agents/adverse effects ; Antiviral Agents/therapeutic use ; COVID-19/etiology ; Female ; Ferritins/blood ; Fibrin Fibrinogen Degradation Products/analysis ; Humans ; Hydroxychloroquine/adverse effects ; Hydroxychloroquine/therapeutic use ; Male ; Middle Aged ; Oseltamivir/therapeutic use ; Pyrazines/adverse effects ; Pyrazines/therapeutic use ; Treatment Outcome ; COVID-19 Drug Treatment
    Chemical Substances Amides ; Antiviral Agents ; Fibrin Fibrinogen Degradation Products ; Pyrazines ; fibrin fragment D ; Oseltamivir (20O93L6F9H) ; Hydroxychloroquine (4QWG6N8QKH) ; Ferritins (9007-73-2) ; favipiravir (EW5GL2X7E0)
    Language English
    Publishing date 2021-03-31
    Publishing country England
    Document type Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't ; Retracted Publication
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-85227-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Efficacy of favipiravir in COVID-19 treatment: a multi-center randomized study.

    Dabbous, Hany M / Abd-Elsalam, Sherief / El-Sayed, Manal H / Sherief, Ahmed F / Ebeid, Fatma F S / El Ghafar, Mohamed Samir Abd / Soliman, Shaimaa / Elbahnasawy, Mohamed / Badawi, Rehab / Tageldin, Mohamed Awad

    publication RETRACTED

    Archives of virology

    2021  Volume 166, Issue 3, Page(s) 949–954

    Abstract: No specific antiviral drugs have been approved for the treatment of COVID-19. This study aimed to evaluate the efficacy of favipiravir in treatment of COVID-19. This was a multicenter randomized controlled study including 96 patients with COVID- 19 who ... ...

    Abstract No specific antiviral drugs have been approved for the treatment of COVID-19. This study aimed to evaluate the efficacy of favipiravir in treatment of COVID-19. This was a multicenter randomized controlled study including 96 patients with COVID- 19 who were randomly assigned into a chloroquine (CQ) group and a favipiravir group. None of the patients in the favipiravir group needed mechanical ventilation (p = 0.129). One patient (2.3%) in the favipiravir group and two patients (4.2%) in the CQ group died (p = 1.00). Favipiravir is a promising drug for COVID-19 that decreases the hospital stay and the need for mechanical ventilation.ClinicalTrials.gov Identifier NCT04351295.
    MeSH term(s) Adult ; Amides/therapeutic use ; Antiviral Agents/therapeutic use ; COVID-19/drug therapy ; Chloroquine/therapeutic use ; Female ; Humans ; Length of Stay ; Male ; Pyrazines/therapeutic use ; Respiration, Artificial/statistics & numerical data ; SARS-CoV-2/drug effects ; Treatment Outcome
    Chemical Substances Amides ; Antiviral Agents ; Pyrazines ; Chloroquine (886U3H6UFF) ; favipiravir (EW5GL2X7E0)
    Language English
    Publishing date 2021-01-25
    Publishing country Austria
    Document type Clinical Trial, Phase II ; Clinical Trial, Phase III ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Retracted Publication
    ZDB-ID 7491-3
    ISSN 1432-8798 ; 0304-8608
    ISSN (online) 1432-8798
    ISSN 0304-8608
    DOI 10.1007/s00705-021-04956-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Retraction Note to: Efficacy of favipiravir in COVID‑19 treatment: a multi‑center randomized study.

    Dabbous, Hany M / Abd-Elsalam, Sherief / El-Sayed, Manal H / Sherief, Ahmed F / Ebeid, Fatma F S / El Ghafar, Mohamed Samir Abd / Soliman, Shaimaa / Elbahnasawy, Mohamed / Badawi, Rehab / Tageldin, Mohamed Awad

    Archives of virology

    2021  Volume 167, Issue 1, Page(s) 277

    Language English
    Publishing date 2021-11-22
    Publishing country Austria
    Document type Journal Article ; Retraction of Publication
    ZDB-ID 7491-3
    ISSN 1432-8798 ; 0304-8608
    ISSN (online) 1432-8798
    ISSN 0304-8608
    DOI 10.1007/s00705-021-05307-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Efficacy of loco-regional treatment for hepatocellular carcinoma prior to living donor liver transplantation: a report from a single center in Egypt.

    Shaker, Mohammad Kamal / Montasser, Iman F / Sakr, Mohamed / Elgharib, Mohamed / Dabbous, Hany M / Ebada, Hend / Dorry, Ahmed El / Bahaa, Mohamed / Meteini, Mahmoud El

    Journal of hepatocellular carcinoma

    2018  Volume 5, Page(s) 29–36

    Abstract: Background and aim: The number of loco-regional therapies (LRTs) for hepatocellular carcinoma (HCC) has increased dramatically during the past decade, bridging or downstaging patients on the waiting list for liver transplantation. This study aimed to ... ...

    Abstract Background and aim: The number of loco-regional therapies (LRTs) for hepatocellular carcinoma (HCC) has increased dramatically during the past decade, bridging or downstaging patients on the waiting list for liver transplantation. This study aimed to analyze the outcomes of LRTs prior to living donor liver transplantation in patients with HCC.
    Methods: Sixty-two HCC patients received living donor liver transplantation at Ain Shams Center for Organ Transplantation over a 2-year period. Data from 29 HCC patients were analyzed. Twenty patients (68.97%) met the Milan Criteria and 4 patients (13.8%) exceeded the Milan Criteria, but met the University of California, San Francisco Criteria. Five patients (17.2%) exceeded the University of California, San Francisco Criteria. All patients underwent preoperative LRTs. The protocol of bridging/downstaging, methods, duration of follow-up, the number of patients who were successfully downstaged before liver transplantation (LT), and their outcomes after LT were recorded.
    Results: There was a decrease in the mean overall size of focal lesions (from mean 5.46 to 4.11 cm) in the last abdominal computed tomography (CT) scan after LRT (
    Conclusion: These results encouraged tumor bridging/downstaging as a potential treatment option among carefully selected patients with HCC beyond conventional criteria for LT. Further studies on a large number of patients are necessary.
    Language English
    Publishing date 2018-02-27
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 2780784-8
    ISSN 2253-5969
    ISSN 2253-5969
    DOI 10.2147/JHC.S147098
    Database MEDical Literature Analysis and Retrieval System OnLINE

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