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Dive into the research topics where Keith D. Lindor is active.

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Featured researches published by Keith D. Lindor.


Gastrointestinal Endoscopy | 1999

A randomized prospective study comparing rigid to balloon dilators for benign esophageal strictures and rings

James S. Scolapio; Tousif M. Pasha; Christopher J. Gostout; Douglas W. Mahoney; Alan R. Zinsmeister; Beverly J. Ott; Keith D. Lindor

BACKGROUND The optimum choice of dilator (rigid vs. balloon) for benign esophageal strictures has not been well studied. The aim of this study was to compare the immediate relief of dysphagia and the incidence of repeat dilatation within the first year with the use of either a rigid (Savary) dilator or balloon dilator for benign lower esophageal strictures. METHODS Patients with dysphagia found to have benign esophageal strictures during endoscopy were randomized to undergo dilation with a rigid (Savary) or a balloon dilator (Microvasive or Bard). The 1-year incidence of repeat dilatation was estimated by the Kaplan-Meier method. RESULTS A total of 251 subjects were stratified at entry according to the type of stricture (peptic vs. Schatzki ring) and severity of stricture (mild vs. moderate/severe) and then randomized to either a Savary (n = 88), Microvasive (n = 81), or Bard (n = 82) dilator. There were no significant differences between the rigid dilator or the two balloons with regard to immediate relief of dysphagia or the need for repeat dilatation at one year. Patients with moderate/severe strictures required repeat dilatation at one year twice as often as those with mild strictures. There were no significant complications reported in these patients. CONCLUSIONS Both rigid and balloon dilators are equally effective and safe in the treatment of benign lower esophageal strictures caused by acid reflux and Schatzki rings.


Journal of Hepatology | 2000

Magnetic resonance cholangiography in patients with biliary disease: its role in primary sclerosing cholangitis

Paul Angulo; Dawn H Pearce; C. Daniel Johnson; Jessica J Henry; Nicholas F. LaRusso; Bret T. Petersen; Keith D. Lindor

BACKGROUND/AIM Magnetic resonance cholangiography (MRC) is a non-invasive diagnostic procedure whose role in the management of patients with primary sclerosing cholangitis (PSC) is unclear. The aim of this study was to determine the usefulness of MRC in the evaluation of the biliary tree in patients with suspected biliary disease, and in particular, PSC. METHODS MRC and invasive cholangiography (ERCP or PTC) were both performed in 73 patients, (33 male, 40 female, mean age 56 years) with clinical and/or biochemical evidence of cholestasis. Images were interpreted by two radiologists unaware of the results of other studies. RESULTS Forty-two patients (58%) had benign biliary disease, including 23 patients (32%) with PSC; 9 patients (12%) had malignant biliary disease; and 22 patients (30%) had a normal biliary tree. Diagnostic quality images were obtained in 73/73 (100%) of MRC, and in 70/73 (96%) of invasive cholangiography (68 ERCPs, 2 PTCs) procedures. Using ERCP/PTC findings as the reference standard, MRC had an accuracy greater than 90% in the diagnosis of normal bile ducts, biliary dilatation, biliary obstruction, bile duct stones, and PSC. Using the final diagnosis, MRC had an overall diagnostic accuracy of 90% in the detection of biliary disease compared to 97% for invasive cholangiography. Additional diagnostic/therapeutic interventions were performed during ERCP in 73% of patients with PSC and in 43% of patients without PSC (p=0.02). CONCLUSIONS MRC has excellent diagnostic accuracy in the presence of biliary disease. Because of its noninvasive nature, MRC may have advantages over invasive cholangiography when diagnosis is the major goal of the procedure.


Hepatology | 1995

The combination of ursodeoxycholic acid and methotrexate for patients with primary biliary cirrhosis: The results of a pilot study

Keith D. Lindor; E.Rolland Dickson; Roberta A. Jorgensen; Monte L. Anderson; Russell H. Wiesner; Gregory J. Gores; Stephen M. Lange; Steven S. Rossi; Alan F. Hofmann; William P. Baldus

Ursodeoxycholic acid (UDCA) and methotrexate (MTX) have both been proposed as treatments for patients with primary biliary cirrhosis (PBC). It has been suggested that a combination of the two drugs may offer advantages over either used separately. In this pilot study, we sought to evaluate the safety and efficacy of this combination for patients with PBC. Thirty-two patients with antimitochondrial antibody positive PBC were prospectively entered into a pilot study and received UDCA, 13 to 15 mg/kg/d, in conjunction with MTX, 0.25 mg/kg/wk, for a period of 2 years. The results of this treatment were compared with those obtained from 180 patients with PBC studied in a placebo-controlled trial of UDCA alone conducted during the same period. Patients in the pilot study and randomized study were comparable with regard to age, gender, and liver biochemistries. The UDCA/MTX-treated patients were of earlier histologic stage and had a lower mean Mayo risk score. During this period, seven patients in the UDCA/MTX group were withdrawn, four for pulmonary toxicity (two who required hospitalization), and one each with mouth ulcer, extreme fatigue, and hair loss. The use of UDCA/MTX was not associated with improvement in symptoms. In the patients receiving UDCA/MTX, biochemical changes were comparable to those of patients receiving UDCA alone but superior to those in the placebo group (P < .05). Histological changes were comparable in all groups at 2 years. Cessation of MTX while UDCA was continued led to no deterioration in liver biochemistries.(ABSTRACT TRUNCATED AT 250 WORDS)


Mayo Clinic Proceedings | 2003

Value of Determining Carbohydrate-Deficient Transferrin Isoforms in the Diagnosis of Alcoholic Liver Disease

Linda M. Stadheim; John F. O'Brien; Keith D. Lindor; Gregory J. Gores; Douglas B. McGill

OBJECTIVE To determine whether isoform separation of carbohydrate-deficient transferrin (CDT) is of value in the diagnosis of alcoholic liver disease (ALD) and is specific to ALD when compared with other liver diseases. PATIENTS AND METHODS During 1995 and 1996, 47 patients with ALD were evaluated with CDT at the Mayo Clinic in Rochester, Minn. The diagnosis of ALD was based on biochemical and histological analyses and on a history of drinking that exceeded 5 years with an average alcohol intake of more than 60 g/d. Disease controls included nonalcoholic steatohepatitis (NASH) (n = 26) and other liver disease (n = 22). Normal controls (n = 21) were healthy individuals without liver disease. Transferrin isoforms were quantified by densitometry of Coomassie-stained transferrins after affinity purification and isoelectric focusing. The pentasialo, tetrasialo, trisialo, disialo, monosialo, and asialo isoforms were quantified as percentages of total band densities. RESULTS Receiver operating characteristic (ROC) curves were constructed for each isoform. The curves for total desialated isoforms (sum of disialo, monosialo, and asialo) displayed the best relationship between sensitivity and specificity with an ROC-area under the curve (AUC) of 0.922. The ROC-AUC values for individual transferrin isoforms in ALD vs NASH for pentasialo, tetrasialo, trisialo, disialo, monosialo, and asialo were 0.806, 0.917, 0.885, 0.933, 0.804, and 0.785, respectively. Only 58% of patients with ALD were detected at a specificity that excluded ALD in 84% of those who did not have it. CONCLUSION Within alcohol ingestion times reported to us, no associations with recent drinking were observed. Alcohol as a cause of liver disease is not perfectly established by CDT analysis, although a high total CDT value favors ALD over NASH.


The American Journal of Gastroenterology | 2000

Defining the relationship between autoimmune disease and primary sclerosing cholangitis

Jayant A. Talwalkar; Nicholas F. LaRusso; Keith D. Lindor

1. Bartlett JG, Chang TW, Gurwith M, et al. Antibiotic-associated pseudomembranous colitis due to toxin-producing clostridia. N Engl J Med 1978;298:531–7. 2. Viscidi R, Willey S, Bartlett JG. Isolation rates and toxigenic potential forClostridium difficileisolates from various patient populations. Gastroenterology 1981;81:5–10. 3. Gilligan PH, McCarthy LR, Genta VM. Relative frequency of Clostridium difficile in patients with diarrheal disease. J Clin Microbiol 1981;14:26–34. 4. Lipsett PA, Samantaray DK, Tam ML, et al. Pseudomembranous colitis: A surgical disease? Surgery 1994;116:491–7. 5. Bulusu M, Narayan S, Shetler K, Triadafilopoulos G. Leukocytosis as a harbinger and surrogate marker of Clostridium difficile infection in hospitalized patients with diarrhea. Am J Gastroenterol 2000;95:3137–41. 6. Bartlett JG. Antibiotic-associated diarrhea. Clin Infect Dis 1992;15:573–80. 7. Gilbert DN. Aspects of the safety profile of oral antimicrobial agents. Infect Dis Clin Pract 1995:4(suppl 2):S103–S109. 8. Gurwith M, Rabin HR, Love K. Diarrhea associated with clindamycin and ampicillin therapy. J Infect Dis 1977;135:S104– S109. 9. Flegel WA, Miller F, Daubener W, et al. Cytokine response by human monocytes to Clostridium difficiletoxin A and toxin B. Infect Immun 1991;59:3659–64.


Archive | 1994

Use of ursodeoxycholic acid to treat nonalcoholic steatohepatitis

Keith D. Lindor


Hepatology Communications | 2018

Dominant strictures in primary sclerosing cholangitis: A multicenter survey of clinical definitions and practices

Moira Hilscher; James H. Tabibian; Elizabeth J. Carey; Christopher J. Gostout; Keith D. Lindor


Archive | 2012

EDUCATION PRACTICE A 42-Year-Old Woman With a New Diagnosis of Sclerosing Cholangitis

Andrea A. Gossard; Keith D. Lindor


Archive | 2012

LIVER, PANCREAS, AND BILIARY TRACT Prevalence and Indicators of Portal Hypertension in Patients With Nonalcoholic Fatty Liver Disease

Flavia Mendes; Ayako Suzuki; Schuyler O. Sanderson; Keith D. Lindor; Paul Angulo


Archive | 2011

ORIGINAL ARTICLES—LIVER, PANCREAS, AND BILIARY TRACT Patients With Typical Laboratory Features of Autoimmune Hepatitis Rarely Need a Liver Biopsy for Diagnosis

Einar S. Björnsson; Jayant A. Talwalkar; Sombat Treeprasertsuk; Matthias Neuhauser; Keith D. Lindor

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Paul Angulo

University of Rochester

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