» Articles » PMID: 10364024

Unfractioned Heparin in the Therapy of Patients with Highly Active Inflammatory Bowel Disease

Overview
Specialty Gastroenterology
Date 1999 Jun 11
PMID 10364024
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Unfractioned heparin reportedly improves severe ulcerative colitis and Crohn's disease, but most of the few observations made have been published as abstracts. This prospective study evaluated whether heparin results in improvement of disease activity in patients with highly active, refractory ulcerative colitis or Crohn's disease.

Methods: Thirteen patients with ulcerative colitis and four patients with Crohn's disease received continuous intravenous heparin, aiming at a partial thromboplastin time of about 60 s for 2 wk. The following 6 wk, patients injected 12,500 units of heparin twice daily. All patients received sulphasalzine (1 g t.i.d.). Clinical and laboratory data were assessed weekly during the first month of treatment and every other week thereafter.

Results: A significant decline of clinical activity (p = 0.0059), C-reactive protein (p = 0.0119), and erythrocyte sedimentation rate (p = 0.0096) was observed in the ulcerative colitis patients. In Crohn's disease clinical activity and laboratory values remained unchanged. Seven patients with ulcerative colitis but none of the Crohn's disease patients achieved complete remission after an average of 4 wk. In ulcerative colitis the histology (p = 0.0431) but not the endoscopic score (p = 0.1088) improved significantly. In one patient with ulcerative colitis, massive colonic bleeding was observed on day 11 of the study.

Conclusions: These data are further evidence of a beneficial effect of unfractioned heparin in the therapy of patients with highly active ulcerative colitis. Because of possible serious bleeding, intravenous heparin should be administered in hospitalized patients only.

Citing Articles

Unfractionated or low-molecular weight heparin for induction of remission in ulcerative colitis.

Chande N, Wang Y, McDonald J, MacDonald J Cochrane Database Syst Rev. 2022; 8:CD006774.

PMID: 35658167 PMC: 9392958. DOI: 10.1002/14651858.CD006774.pub4.


Role of the gut microbiome in cardiovascular drug response: The potential for clinical application.

Steiner H, Gee K, Giles J, Knight H, Hurwitz B, Karnes J Pharmacotherapy. 2021; 42(2):165-176.

PMID: 34820870 PMC: 10321137. DOI: 10.1002/phar.2650.


Necessity of heparin for maintaining peripheral venous catheters: A systematic review and meta-analysis.

You T, Jiang J, Chen J, Xu W, Xiang L, Jiao Y Exp Ther Med. 2017; 14(2):1675-1684.

PMID: 28810636 PMC: 5526172. DOI: 10.3892/etm.2017.4706.


Protein losing enteropathy: comprehensive review of the mechanistic association with clinical and subclinical disease states.

Levitt D, Levitt M Clin Exp Gastroenterol. 2017; 10:147-168.

PMID: 28761367 PMC: 5522668. DOI: 10.2147/CEG.S136803.


Histologic scoring indices for evaluation of disease activity in Crohn's disease.

Novak G, Parker C, Pai R, MacDonald J, Feagan B, Sandborn W Cochrane Database Syst Rev. 2017; 7:CD012351.

PMID: 28731502 PMC: 6483549. DOI: 10.1002/14651858.CD012351.pub2.