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dc.contributor.author Ferencz, Viktória
dc.contributor.author Domjan B
dc.contributor.author Gerő, László
dc.contributor.author Tänczer, Tímea
dc.contributor.author Tabák, Ádám
dc.date.accessioned 2015-12-17T10:02:32Z
dc.date.available 2015-12-17T10:02:32Z
dc.date.issued 2015
dc.identifier.citation pagination=1443-1450; journalVolume=156; journalIssueNumber=36; journalTitle=ORVOSI HETILAP;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2274
dc.identifier.uri doi:10.1556/650.2015.30239
dc.description.abstract Insulin therapy is the most effective treatment of diabetes. It is proven to prevent microvascular disease and likely to decrease the risk of cardiovascular complications. However, these benefits are associated with a 2-3 times increased risk of hypoglycaemia and a faster weight gain compared to other antidiabetic medications. In addition, one study found elevated all-cause mortality among patients on intensive therapy (requiring more frequent insulinisation). Insulin has growth factor properties that may translate to increased mitogenicity. These factors could prevent the medical team or the patient from initiation or intensification of insulin therapy. The authors describe evidence on long-term remission related to transient intensified insulin therapy at diabetes diagnosis. The currently recommended method of insulin initiation is once daily basal insulin treatment that offers different schedules for intensification. The authors review the pharmacokinetics of analogue insulins that translate to similar efficacy to human insulins with a 20-30% lower risk of hypoglycaemia. Orv. Hetil., 2015, 156(36), 1443-1450.
dc.relation.ispartof urn:issn:0030-6002
dc.title A normoglykaemia elérésének korlátai inzulinkezelt 2-es tipusú cukorbetegekben
dc.type Journal Article
dc.date.updated 2015-11-05T10:27:55Z
dc.language.rfc3066 hu
dc.identifier.mtmt 2945132
dc.identifier.pubmed 26320598
dc.contributor.department SE/AOK/K/I. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem


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