Evidence Based Medicine on FHIR Implementation Guide, published by HL7 International / Clinical Decision Support. This guide is not an authorized publication; it is the continuous build for version 2.0.0-ballot built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/ebm/ and changes regularly. See the Directory of published versions
Active as of 2024-11-21 |
Generated Narrative: Citation 267246
version: 1; Last updated: 2024-08-01 12:35:46+0000
Profile: JournalArticleCitation
url: Citation 11232013 Rosiglitazone monotherapy is effective in patients with type 2 diabetes.
identifier: FEvIR Object Identifier/267246, https://pubmed.ncbi.nlm.nih.gov
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title: 11232013 Rosiglitazone monotherapy is effective in patients with type 2 diabetes.
status: Active
date: 2024-11-21 14:09:14+0000
publisher: HL7 International / Clinical Decision Support
contact: HL7 International / Clinical Decision Support: http://www.hl7.org/Special/committees/dss
description:
This Citation Resource is referenced in an example for the EBMonFHIR Implementation Guide.
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https://creativecommons.org/licenses/by-nc-sa/4.0/
approvalDate: 2001-04-12
lastReviewDate: 2018-11-30
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https://pubmed.ncbi.nlm.nih.gov
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/10.1210/jcem.86.1.7157Titles
Type Language Text Primary title English Rosiglitazone monotherapy is effective in patients with type 2 diabetes.
Abstracts
Text This study evaluated the efficacy and safety of rosiglitazone monotherapy in patients with type 2 diabetes. After a 4-week placebo run-in period, 493 patients with type 2 diabetes were randomized to receive rosiglitazone [2 or 4 mg twice daily (bd)] or placebo for 26 weeks. The primary end point was change in hemoglobin A(1c); other variables assessed included fasting plasma glucose, fructosamine, endogenous insulin secretion, urinary albumin excretion, serum lipids, and adverse events. Rosiglitazone (2 and 4 mg bd) decreased mean hemoglobin A(1c) relative to placebo by 1.2 and 1.5 percentage points, respectively, and reduced fasting plasma glucose concentrations relative to placebo by 3.22 and 4.22 mmol/L, respectively. Fasting plasma insulin and insulin precursor molecules decreased significantly. Homeostasis model assessment estimates indicate that rosiglitazone (2 and 4 mg bd) reduced insulin resistance by 16.0% and 24.6%, respectively, and improved ss-cell function over baseline by 49.5% and 60.0%, respectively. Urinary albumin excretion decreased significantly in the rosiglitazone (4 mg bd) group. There was no increase in adverse events with rosiglitazone. In the short-term, rosiglitazone is an insulin sensitizer that is effective and safe as monotherapy in patients with type 2 diabetes who are inadequately controlled by lifestyle interventions.
relatesTo
type: correction-in
classifier: Published Erratum
citation:
J Clin Endocrinol Metab 2001 Apr;86(4):1659
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classifier: Published Erratum
citation:
J Clin Endocrinol Metab. 2002 Feb;2(1):iv.
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identifier: Print ISSN Type/0021-972X, ISOAbbreviation/J Clin Endocrinol Metab, ISSN Linking/0021-972X, Medline Title Abbreviation/J Clin Endocrinol Metab, NLM Unique ID/0375362
title: The Journal of clinical endocrinology and metabolism
publisherLocation: United States
citedMedium: Print
volume: 86
issue: 1
articleDate: 2001-01
publicationDateText: 2001-Jan
language: English
pageString: 280-8
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contributor: Lebovitz HE
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affiliation: Department of Medicine, State University of New York, Brooklyn, New York 11203, USA. hlebovitz@attglobal.net
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contributor: Rosiglitazone Clinical Trials Study Group
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