Literature DB >> 21840788

Therapeutic strategies for severe alcoholic hepatitis.

Yoshinori Horie1, Yoshiyuki Yamagishi, Hirotoshi Ebinuma, Toshifumi Hibi.   

Abstract

BACKGROUND AND AIMS: Severe alcoholic hepatitis (SAH) is an inflammatory response with multiple morbidity factors like leucocytosis, hepatomegaly, renal failure, hepatic encephalopathy, endotoxemia, and has a high mortality rate. Accordingly, identifying therapeutic interventions that can support prognosis is the goal of research.
METHODS: Questionnaires were sent to 1234 medical institutions asking for information on patients with SAH during 2004 to 2008 including patients' demography, disease profile and the therapeutic interventions patients had received during hospitalization.
RESULTS: Twenty-nine hospitals had treated SAH patients, and provided full demographic data on 62 patients. Twenty-seven patients had received no treatment, 10 patients had received granulocytes/monocytes apheresis (GMA) to deplete elevated myeloid linage leucocytes, the rest had received one or more of the following treatments, corticosteroids, plasma exchange (PE) and haemodialysis (HD). Further, 23 patients had died and 39 had survived within 100 days of hospitalization. Serum creatinine (Cr) was higher in patients who had died vs patients who had survived (P=0.026). Likewise, patients with white blood cells (WBC) ≥ 10(4)/μL had higher mortality rate vs patients with WBC<10(4)/μL (P=0.039). GMA in patients with WBC ≥ 10(4)/μL showed 100% prognosis vs patients with WBC ≥ 10(4)/μL who did not receive GMA (P=0.0007). Corticosteroids, PE and HD did not significantly impact prognosis of SAH patients.
CONCLUSIONS: Our perception is that, patients with elevated myeloid leucocytes benefit most from GMA, while PE appears to support patients with coagulation deficiency or high plasma bilirubin and HD has indication in patients with high Cr.
Copyright © 2011 Elsevier Masson SAS. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21840788     DOI: 10.1016/j.clinre.2011.07.005

Source DB:  PubMed          Journal:  Clin Res Hepatol Gastroenterol        ISSN: 2210-7401            Impact factor:   2.947


  6 in total

1.  Sequential therapy consisting of glucocorticoid infusions followed by granulocyte-monocyte absorptive apheresis in patients with severe alcoholic hepatitis.

Authors:  Kazuhiro Watanabe; Yoshihito Uchida; Kayoko Sugawara; Kayoko Naiki; Mie Inao; Nobuaki Nakayama; Satoshi Mochida
Journal:  J Gastroenterol       Date:  2016-11-17       Impact factor: 7.527

Review 2.  Granulocytapheresis for the treatment of severe alcoholic hepatitis: a case series and literature review.

Authors:  Kenya Kamimura; Michitaka Imai; Akira Sakamaki; Shigeki Mori; Masaaki Kobayashi; Ken-Ichi Mizuno; Manabu Takeuchi; Takeshi Suda; Minoru Nomoto; Yutaka Aoyagi
Journal:  Dig Dis Sci       Date:  2013-09-20       Impact factor: 3.199

3.  Preventive effects of indole-3-carbinol against alcohol-induced liver injury in mice via antioxidant, anti-inflammatory, and anti-apoptotic mechanisms: Role of gut-liver-adipose tissue axis.

Authors:  Youngshim Choi; Mohamed A Abdelmegeed; Byoung-Joon Song
Journal:  J Nutr Biochem       Date:  2017-12-10       Impact factor: 6.048

4.  Case of severe alcoholic hepatitis treated with granulocytapheresis.

Authors:  Yukari Watanabe; Kenya Kamimura; Tomohiro Iwasaki; Hiroyuki Abe; Shunsaku Takahashi; Ken-Ichi Mizuno; Manabu Takeuchi; Atsushi Eino; Ichiei Narita; Shuji Terai
Journal:  World J Clin Cases       Date:  2016-11-16       Impact factor: 1.337

5.  Disease spectrum of alcoholic liver disease in Beijing 302 Hospital from 2002 to 2013: A large tertiary referral hospital experience from 7422 patients.

Authors:  Ang Huang; Binxia Chang; Yin Sun; Huiming Lin; Baosen Li; Guangju Teng; Zheng-Sheng Zou
Journal:  Medicine (Baltimore)       Date:  2017-02       Impact factor: 1.889

6.  Human neutrophil peptide-1 promotes alcohol-induced hepatic fibrosis and hepatocyte apoptosis.

Authors:  Rie Ibusuki; Hirofumi Uto; Kohei Oda; Akihiko Ohshige; Kazuaki Tabu; Seiichi Mawatari; Kotaro Kumagai; Shuji Kanmura; Tsutomu Tamai; Akihiro Moriuchi; Hirohito Tsubouchi; Akio Ido
Journal:  PLoS One       Date:  2017-04-12       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.