1. Review article: the evidence that vancomycin is a therapeutic option for primary sclerosing cholangitis.
- Author
-
Damman JL, Rodriguez EA, Ali AH, Buness CW, Cox KL, Carey EJ, and Lindor KD
- Subjects
- Cholangitis, Sclerosing complications, Cholangitis, Sclerosing epidemiology, Colitis, Ulcerative complications, Colitis, Ulcerative drug therapy, Colitis, Ulcerative epidemiology, Colitis, Ulcerative pathology, Disease Progression, Humans, Inflammatory Bowel Diseases complications, Inflammatory Bowel Diseases drug therapy, Inflammatory Bowel Diseases epidemiology, Inflammatory Bowel Diseases pathology, Treatment Outcome, Cholangitis, Sclerosing drug therapy, Vancomycin therapeutic use
- Abstract
Background and Aims: PSC is an autoimmune biliary inflammatory disorder that is often associated with inflammatory bowel disease (IBD), with 50%-75% of patients with PSC having coexisting IBD, most commonly ulcerative colitis. Currently, no medical therapies have been shown to improve the disease course or slow its progression. However, ongoing research has resulted in a growing interest in the use of antibiotics for treatment of PSC, of which vancomycin is the most studied. In this review, we summarise the current evidence on the use of vancomycin in PSC and comment on future research areas of interest., Methods: A comprehensive PUBMED and EMBASE literature search for articles on vancomycin, PSC, therapeutic options and microbiome was performed., Results: Two randomised clinical trials, three case series and two case reports were included in the study. These include uncontrolled data from at least 98 patients that include promising improvements in biochemistry and imaging. Optimal dosing regimens are unclear., Conclusion: Vancomycin is one of the most studied antibiotics used in the treatment of PSC with promising results. There is not currently sufficient evidence to support treatment recommendations. Further research is needed to establish if vancomycin is a PSC treatment., (© 2018 John Wiley & Sons Ltd.)
- Published
- 2018
- Full Text
- View/download PDF