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1.
Gastroenterology ; 157(4): 967-976.e1, 2019 10.
Article in English | MEDLINE | ID: mdl-31158369

ABSTRACT

BACKGROUND & AIMS: The efficacy of prophylactic placement of hemoclips to prevent delayed bleeding after removal of large colonic polyps has not been established. We conducted a randomized equivalence study to determine whether prophylactic placement of hemoclips affects incidence of delayed post-polypectomy bleeding (PPB). METHODS: During elective colonoscopy performed at 4 Veterans Affairs Medical Centers, 1098 patients who had polyps ≥1 cm removed were randomly assigned to groups that received prophylactic hemoclips (n = 547) or no hemoclips (n = 551), from September 2011 through September 2018. Data on PPB (rectal bleeding resulting in hemoglobin decreases ≥2 g/dL, hemodynamic instability, colonoscopy, angiography, or surgery) within 30 days of colonoscopy (called delayed PPB) were collected during telephone interviews or hospital visits 7 and 30 days after colonoscopy. The primary outcome was the incidence of important post-polypectomy bleeding. RESULTS: Twelve patients in the hemoclip group (2.3%) and 15 patients in the no hemoclip group (2.9%) had important delayed PPB. There were no deaths, and no patients in either group required angiography or surgery. In intention-to-treat analysis, two 1-sided test's lower and upper confidence interval limits were -2.07 and 1.01, indicating that the data approached but did not meet equivalence criteria. On multiple logistic regression analysis, significant predictors of PPB included use of warfarin with bridging, thienopyridines, polyp size, and polyp location, but hemoclip placement did not associate with important delayed PPB. CONCLUSIONS: In a randomized trial, we found that prophylactic placement of hemoclips after removal of large colon polyps does not affect the proportion of important delayed PPB events, compared with no hemoclip placement. These findings call into question the widespread, expensive practice of routinely placing prophylactic hemoclips after polypectomy. ClinicalTrials.gov ID: NCT01647581.


Subject(s)
Colectomy/adverse effects , Colonic Polyps/surgery , Colonoscopy/adverse effects , Hemostatic Techniques/instrumentation , Postoperative Hemorrhage/prevention & control , Surgical Instruments , Colectomy/methods , Colonic Polyps/pathology , Equipment Design , Female , Hemostatic Techniques/adverse effects , Humans , Male , Middle Aged , Postoperative Hemorrhage/etiology , Prospective Studies , Risk Factors , Time Factors , Treatment Outcome , United States , United States Department of Veterans Affairs
2.
J Clin Transl Hepatol ; 5(1): 67-75, 2017 Mar 28.
Article in English | MEDLINE | ID: mdl-28507929

ABSTRACT

Nonalcoholic fatty liver disease (NAFLD) represents a major public health epidemic. Pharmacologic therapies for this condition are scarce, but multiple agents with novel mechanisms of action are in development. Here we review the pathophysiology and natural history of NALFD, diagnostic testing and data for currently available treatment strategies. We then turn our attention to promising developmental drugs and their respective trials. As the prevalence of fatty liver disease increases, clinicians will have more tools at hand for management of this condition. We conclude the horizon is bright for patients and doctors who deal with NAFLD.

3.
Clin Liver Dis ; 19(4): 707-16, vii, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26466657

ABSTRACT

The treatment of chronic hepatitis C virus (HCV) has undergone a period of rapid evolution. The era of combination direct antivirals has led to high rates of sustained viral response (SVR), limited toxicities, and more broad applicability across patient demographics. Even current therapies have their limitations, however, including genotype specificity and variable durations of treatment depending on the presence or absence of cirrhosis. Developing a fixed-duration pangenotypic regimen that can broadly treat all stages of fibrosis with equal rates of SVR in all patients, irrespective of treatment experience, is the goal of future therapies. This article reviews antivirals in development.


Subject(s)
Antiviral Agents/therapeutic use , Hepacivirus , Hepatitis C, Chronic/drug therapy , Nucleic Acid Synthesis Inhibitors/therapeutic use , Amides , Benzazepines/therapeutic use , Benzofurans/therapeutic use , Carbamates/therapeutic use , Clinical Trials, Phase I as Topic , Clinical Trials, Phase II as Topic , Clinical Trials, Phase III as Topic , Cyclopropanes , Drug Discovery , Drug Therapy, Combination , Forecasting , Hepacivirus/genetics , Heterocyclic Compounds, 4 or More Rings/therapeutic use , Humans , Imidazoles/therapeutic use , Indoles/therapeutic use , Isoquinolines/therapeutic use , MicroRNAs , Molecular Targeted Therapy , Protease Inhibitors/therapeutic use , Pyrrolidines , Quinoxalines/therapeutic use , RNA, Viral/biosynthesis , Sofosbuvir/therapeutic use , Sulfonamides/therapeutic use , Valine/analogs & derivatives , Viral Nonstructural Proteins/antagonists & inhibitors
4.
Therap Adv Gastroenterol ; 8(3): 143-59, 2015 May.
Article in English | MEDLINE | ID: mdl-25949527

ABSTRACT

Crohn's disease (CD) is a debilitating, systemic inflammatory disorder with both gastrointestinal and extraintestinal manifestations. Its existence predates modern medicine, but its precise etiology remains incompletely understood. Most authorities suggest a multifactorial pathogenesis owing to a mixture of genetic disorders, immunologic dysregulation, microbiota disequilibrium and environmental influences. Of these factors, the overactive immunologic response seen in CD appears to be the most promising target of medical therapy. Biological agents comprise a relatively new class of drugs that can induce and maintain remission in moderate to severe CD, as well as in ulcerative colitis. This review will provide an overview of CD, its history, clinical features, pathophysiology, and treatment options focusing on current and future biological agents with an emphasis on drug development, dosage and administration.

5.
Best Pract Res Clin Gastroenterol ; 26(5): 601-10, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23384805

ABSTRACT

Diarrhoea is a common manifestation of Crohn's disease (CD). We advocate an evidence-based approach to treat the underlying disease and reduce symptoms. This article reviews disease grading systems, current concepts in medical therapy, and other treatments that may become available in the future. While some drug classes (e.g. salicylates, immunomodulators) have been studied for many decades, newer approaches including anti-TNF monoclonal antibodies (biologics), and gut selective agents are changing the paradigm we use to treat this debilitating condition.


Subject(s)
Crohn Disease/drug therapy , Anti-Bacterial Agents/therapeutic use , Antibodies, Monoclonal/therapeutic use , Crohn Disease/diagnosis , Gastrointestinal Agents/therapeutic use , Humans , Immunologic Factors/therapeutic use , Salicylates/therapeutic use , Steroids/therapeutic use
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