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Use and perceived effectiveness of non-analgesic medical therapies for chronic pancreatitis in the United States

dc.contributor.authorBurton, F.en_US
dc.contributor.authorAlkaade, S.en_US
dc.contributor.authorCollins, D.en_US
dc.contributor.authorMuddana, V.en_US
dc.contributor.authorSlivka, A.en_US
dc.contributor.authorBrand, R. E.en_US
dc.contributor.authorGelrud, A.en_US
dc.contributor.authorBanks, P. A.en_US
dc.contributor.authorSherman, S.en_US
dc.contributor.authorAnderson, M. A.en_US
dc.contributor.authorRomagnuolo, J.en_US
dc.contributor.authorLawrence, C.en_US
dc.contributor.authorBaillie, J.en_US
dc.contributor.authorGardner, T. B.en_US
dc.contributor.authorLewis, M. D.en_US
dc.contributor.authorAmann, S. T.en_US
dc.contributor.authorLieb, J. G.en_US
dc.contributor.authorO’connell, M.en_US
dc.contributor.authorKennard, E. D.en_US
dc.contributor.authorYadav, D.en_US
dc.contributor.authorWhitcomb, David C.en_US
dc.contributor.authorForsmark, C. E.en_US
dc.date.accessioned2011-01-31T17:29:57Z
dc.date.available2012-03-05T15:30:01Zen_US
dc.date.issued2011-01en_US
dc.identifier.citationBurton, F.; Alkaade, S.; Collins, D.; Muddana, V.; Slivka, A.; Brand, R. E.; Gelrud, A.; Banks, P. A.; Sherman, S.; Anderson, M. A.; Romagnuolo, J.; Lawrence, C.; Baillie, J.; Gardner, T. B.; Lewis, M. D.; Amann, S. T.; Lieb, J. G.; O’connell, M.; Kennard, E. D.; Yadav, D.; Whitcomb, D. C.; Forsmark, C. E.; (2011). "Use and perceived effectiveness of non-analgesic medical therapies for chronic pancreatitis in the United States." Alimentary Pharmacology & Therapeutics 33(1): 149-159. <http://hdl.handle.net/2027.42/79114>en_US
dc.identifier.issn0269-2813en_US
dc.identifier.issn1365-2036en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/79114
dc.description.abstractAliment Pharmacol Ther 2011; 33: 149–159Effectiveness of medical therapies in chronic pancreatitis has been described in small studies of selected patients.To describe frequency and perceived effectiveness of non-analgesic medical therapies in chronic pancreatitis patients evaluated at US referral centres.Using data on 516 chronic pancreatitis patients enrolled prospectively in the NAPS2 Study, we evaluated how often medical therapies [pancreatic enzyme replacement therapy (PERT), vitamins/antioxidants (AO), octreotide, coeliac plexus block (CPB)] were utilized and considered useful by physicians.Oral PERT was commonly used (70%), more frequently in the presence of exocrine insufficiency (EI) (88% vs. 61%, P  < 0.001) and pain (74% vs. 59%, P  < 0.002). On multivariable analyses, predictors of PERT usage were EI (OR 5.14, 95% CI 2.87–9.18), constant (OR 3.42, 95% CI 1.93–6.04) or intermittent pain (OR 1.98, 95% CI 1.14–3.45). Efficacy of PERT was predicted only by EI (OR 2.16, 95% CI 1.36–3.42). AO were tried less often (14%) and were more effective in idiopathic and obstructive vs. alcoholic chronic pancreatitis (25% vs. 4%, P  = 0.03). Other therapies were infrequently used (CPB – 5%, octreotide – 7%) with efficacy generally <50%.Pancreatic enzyme replacement therapy is commonly utilized, but is considered useful in only subsets of chronic pancreatitis patients. Other medical therapies are used infrequently and have limited efficacy.en_US
dc.format.extent139103 bytes
dc.format.extent3106 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.titleUse and perceived effectiveness of non-analgesic medical therapies for chronic pancreatitis in the United Statesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOtolaryngologyen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, MI, USA.en_US
dc.contributor.affiliationotherSt. Louis University, St. Louis, MO, USA.en_US
dc.contributor.affiliationotherUniversity of Florida, Gainesville, FL, USA.en_US
dc.contributor.affiliationotherUniversity of Pittsburgh, Pittsburgh, PA, USA.en_US
dc.contributor.affiliationotherBrigham and Women’s Hospital, Boston, MA, USA.en_US
dc.contributor.affiliationotherIndiana University Medical Center, Indianapolis, IN, USA.en_US
dc.contributor.affiliationotherDigestive Disease Center, Medical University of South Carolina, Charleston, SC, USA.en_US
dc.contributor.affiliationotherDuke University Medical Center, Durham, NC, USA.en_US
dc.contributor.affiliationotherDartmouth-Hitchcock Medical Center, Lebanon, NH, USA.en_US
dc.contributor.affiliationotherMayo Clinic, Jacksonville, FL, USA.en_US
dc.contributor.affiliationotherNorth Mississippi Medical Center, Tupelo, MS, USA.en_US
dc.contributor.affiliationotherUniversity of Pennsylvania School of Medicine, Philadelphia, PA, USA.en_US
dc.contributor.affiliationotherEpidemiology Data Center, University of Pittsburgh, Pittsburgh, PA, USA.en_US
dc.identifier.pmid21083584en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/79114/1/j.1365-2036.2010.04491.x.pdf
dc.identifier.doi10.1111/j.1365-2036.2010.04491.xen_US
dc.identifier.sourceAlimentary Pharmacology & Therapeuticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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