Evidence Based Medicine on FHIR Implementation Guide
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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

Example Citation: 11232013 Rosiglitazone monotherapy is effective in patients with type 2 diabetes.

Active as of 2024-11-21

Generated Narrative: Citation 267246

version: 1; Last updated: 2024-08-01 12:35:46+0000

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url: Citation 11232013 Rosiglitazone monotherapy is effective in patients with type 2 diabetes.

identifier: FEvIR Object Identifier/267246, https://pubmed.ncbi.nlm.nih.gov/11232013, Uniform Resource Identifier (URI)/urn:oid:2.16.840.1.113883.4.642.40.44.15.44

version: 2.0.0-ballot

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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identifier: https://pubmed.ncbi.nlm.nih.gov/11232013, https://doi.org/10.1210/jcem.86.1.7157

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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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citation:

J Clin Endocrinol Metab. 2002 Feb;2(1):iv.

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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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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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