Literature DB >> 20055688

Emerging drugs in sepsis.

Marc Leone1, Julien Textoris, Fabrice Michel, Sandrine Wiramus, Claude Martin.   

Abstract

IMPORTANCE OF THE FIELD: Sepsis remains a major cause of death in intensive care units. Despite an intense research, a new drug that is effective in reducing mortality in sepsis is still awaited. AREAS COVERED IN THIS REVIEW: The literature was analyzed with Pubmed() during the 2008 - 2009 period. If required, seminal articles published before 2008 were cited. Clinical trials focusing on 'sepsis' were first assessed. Next, relevant experimental data in this field were reported. WHAT THE READER WILL GAIN: The goal of the review is to determine the role for new licensed antibiotics, to give an insight into the conflict on adjuvant therapies and to disclose new experimental concepts. TAKE HOME MESSAGE: New licensed antibiotics will offer the opportunity to refine the treatment choices. Direct hemoperfusion using polymyxin B-immobilized fiber column may be an option in sepsis due to Gram-negative bacilli. Among non-antibiotic drugs, new ongoing studies will clarify the role of drotrecogin alfa (activated) and low dose hydrocortisone. The modulation of monocytic human leukocyte antigen-DR seems the most prominent treatment. The use of cardiovascular drugs requires well-conducted clinical trials. The regulation of high mobility group box 1, adenosine blockade or correction of the impaired energy production is still at the experimental level.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20055688     DOI: 10.1517/14728210903559860

Source DB:  PubMed          Journal:  Expert Opin Emerg Drugs        ISSN: 1472-8214            Impact factor:   4.191


  3 in total

Review 1.  Human recombinant protein C for severe sepsis and septic shock in adult and paediatric patients.

Authors:  Arturo J Martí-Carvajal; Ivan Solà; Christian Gluud; Dimitrios Lathyris; Andrés Felipe Cardona
Journal:  Cochrane Database Syst Rev       Date:  2012-12-12

2.  Kukoamine B, a novel dual inhibitor of LPS and CpG DNA, is a potential candidate for sepsis treatment.

Authors:  Xin Liu; Xinchuan Zheng; Ning Wang; Hongwei Cao; Yongling Lu; Yupeng Long; Kecen Zhao; Hong Zhou; Jiang Zheng
Journal:  Br J Pharmacol       Date:  2011-03       Impact factor: 8.739

3.  A novel imidazopyridine derivative, X22, attenuates sepsis-induced lung and liver injury by inhibiting the inflammatory response in vitro and in vivo.

Authors:  Xiangting Ge; Zhiguo Feng; Tingting Xu; Beibei Wu; Hongjin Chen; Fengli Xu; Lili Fu; Xiaoou Shan; Yuanrong Dai; Yali Zhang; Guang Liang
Journal:  Drug Des Devel Ther       Date:  2016-06-30       Impact factor: 4.162

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.