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Management strategies for gastrointestinal, erectile, bladder, and sudomotor dysfunction in patients with diabetes

dc.contributor.authorKempler, Peteren_US
dc.contributor.authorAmarenco, G.en_US
dc.contributor.authorFreeman, R.en_US
dc.contributor.authorFrontoni, Simonaen_US
dc.contributor.authorHorowitz, M.en_US
dc.contributor.authorStevens, Martin J.en_US
dc.contributor.authorLow, Phillip A.en_US
dc.contributor.authorPop‐busui, R.en_US
dc.contributor.authorTahrani, A. A.en_US
dc.contributor.authorTesfaye, Solomonen_US
dc.contributor.authorVárkonyi, T.en_US
dc.contributor.authorZiegler, D.en_US
dc.contributor.authorValensi, Paulen_US
dc.date.accessioned2011-11-10T15:37:19Z
dc.date.available2012-12-03T21:17:30Zen_US
dc.date.issued2011-10en_US
dc.identifier.citationKempler, P.; Amarenco, G.; Freeman, R.; Frontoni, S.; Horowitz, M.; Stevens, M.; Low, P.; Pop‐busui, R. ; Tahrani, A. A.; Tesfaye, S.; Várkonyi, T. ; Ziegler, D.; Valensi, P. (2011). "Management strategies for gastrointestinal, erectile, bladder, and sudomotor dysfunction in patients with diabetes." Diabetes/Metabolism Research and Reviews 27(7): 665-677. <http://hdl.handle.net/2027.42/87058>en_US
dc.identifier.issn1520-7552en_US
dc.identifier.issn1520-7560en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/87058
dc.description.abstractThere are substantial advances in understanding disordered gastrointestinal autonomic dysfunction in diabetes. It occurs frequently. The underlying pathogenesis is complex involving defects in multiple interacting cell types of the myenteric plexus as well. These defects may be irreversible or reversible. Gastrointestinal symptoms represent a major and generally underestimated source of morbidity for escalating health care costs in diabetes. Acute changes in glycaemia are both determinants and consequences of altered gastrointestinal motility. 35–90% of diabetic men have moderate‐to‐severe erectile dysfunction (ED). ED shares common risk factors with CVD. Diagnosis is based on medical/sexual history, including validated questionnaires. Physical examination and laboratory testing must be tailored to patient's complaints and risk factors. Treatment is based on PDE5‐inhibitors (PDE5‐I). Other explorations may be useful in patients who do not respond to PDE5‐I. Patients at high cardiovascular risk should be stabilized by their cardiologists before sexual activity is considered or ED treatment is recommended. Estimates on bladder dysfunction prevalence are 43–87% of type 1 and 25% of type 2 diabetic patients, respectively. Common symptoms include dysuria, frequency, urgency, nocturia and incomplete bladder emptying. Diagnosis should use validated questionnaire for lower urinary tract symptoms. The type of bladder dysfunction is readily characterized with complete urodynamic testing. Sudomotor dysfunction is a cause of dry skin and is associated with foot ulcerations. Sudomotor function can be assessed by thermoregulatory sweat testing, quantitative sudomotor axon reflex test, sympathetic skin response, quantitative direct/indirect axon reflex testing and the indicator plaster. Copyright © 2011 John Wiley & Sons, Ltd.en_US
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherGastroparesisen_US
dc.subject.otherGastrointestinal Autonomic Neuropathyen_US
dc.subject.otherErectile Dysfunctionen_US
dc.subject.otherSudomotor Dysfunctionen_US
dc.subject.otherBladder Dysfunctionen_US
dc.titleManagement strategies for gastrointestinal, erectile, bladder, and sudomotor dysfunction in patients with diabetesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Metabolism, Endocrinology and Diabetes, Brehm Center for Diabetes Research, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherI Department of Medicine, Semmelweis University, Budapest, Hungaryen_US
dc.contributor.affiliationotherService de Neuro‐Urologie, Hôpital Tenon, Assistance Publique‐Hôpitaux de Paris, Paris, Franceen_US
dc.contributor.affiliationotherBeth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USAen_US
dc.contributor.affiliationotherDepartment of Internal Medicine, University of Tor Vergata, Rome, Italyen_US
dc.contributor.affiliationotherDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australiaen_US
dc.contributor.affiliationotherDepartment of Medicine, University of Birmingham, Birmingham, UKen_US
dc.contributor.affiliationotherMayo Clinic, Rochester, MN, USAen_US
dc.contributor.affiliationotherDepartment of Diabetes and Endocrinology, Heart of England NHS Foundation Trust, Birmingham, UKen_US
dc.contributor.affiliationotherSchool of Clinical and Experimental Medicine, University of Birmingham, Birmingham, UKen_US
dc.contributor.affiliationotherDiabetes Research Unit, Sheffield Teaching Hospitals, Sheffield, UKen_US
dc.contributor.affiliationotherFirst Department of Medicine, University of Szeged, Szeged, Hungaryen_US
dc.contributor.affiliationotherInstitute for Clinical Diabetology, German Diabetes Center, Leibniz Center for Diabetes Research, Heinrich Heine University, Düsseldorf, Germanyen_US
dc.contributor.affiliationotherDepartment of Metabolic Diseases, University Hospital, Düsseldorf, Germanyen_US
dc.contributor.affiliationotherService d'Endocrinologie‐Diabétologie‐Nutrition, AP‐HP, Hôpital Jean Verdier, Paris‐Nord University, CRNH‐IdF, Bondy, Franceen_US
dc.contributor.affiliationotherI Department of Medicine, Semmelweis University, 1083 Budapest, Korányi Sándor u. 2/a, Hungary.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/87058/1/1223_ftp.pdf
dc.identifier.doi10.1002/dmrr.1223en_US
dc.identifier.sourceDiabetes/Metabolism Research and Reviewsen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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