17 research outputs found
GRADE for outcomes of this meta-analysis.
<p>GRADE for outcomes of this meta-analysis.</p
The summary outcomes of this meta-analysis with exposure only during pregnancy.
<p>(including those of sensitivity analysis).</p
The Newcastle-Ottawa Scale (NOS) quality assessment of the included studies in this meta-analysis.
<p>The Newcastle-Ottawa Scale (NOS) quality assessment of the included studies in this meta-analysis.</p
Risk of neonatal congenital malformations between different groups with exposure only during pregnancy.
<p>Risk of neonatal congenital malformations between different groups with exposure only during pregnancy.</p
Data extraction from the 12 included studies in this meta-analysis.
<p>Data extraction from the 12 included studies in this meta-analysis.</p
GRADE for outcomes of this meta-analysis with exposure only during pregnancy.
<p>GRADE for outcomes of this meta-analysis with exposure only during pregnancy.</p
Characteristics of the 12 included studies in this meta-analysis.
<p>Characteristics of the 12 included studies in this meta-analysis.</p
Comparison of glyburide and insulin in the management of gestational diabetes: A meta-analysis
<div><p>Objective</p><p>The aim of this meta-analysis was to determine the efficacy and safety of glyburide as a treatment for gestational diabetes mellitus (GDM) compared to insulin.</p><p>Methods</p><p>A meta-analysis was conducted to compare the management of gestational diabetes with glyburide and insulin. Studies fulfilling all of the following inclusion criteria were included in this meta-analysis: subjects were women with gestational diabetes requiring drug treatment; the comparison treatment included glyburide vs insulin; one or more outcomes (maternal or neonatal) should be provided in the individual study; the study design should be a randomized control trial. Exclusion criteria: non-RCT studies; non-human data. PubMed, Embase and CENTRAL databases were searched from inception until 10 October 2016.</p><p>Results</p><p>Ten randomized control trials involving 1194 participants met the inclusion criteria and were included. 13 primary outcomes (6 maternal, 7 neonatal) and 26 secondary outcomes (9 maternal, 17 neonatal) were detected and analyzed in this study. Glyburide significantly increased the risk of any neonatal hypoglycemia [risk ratio (RR), 1.89; 95% confidence interval (95%CI), 1.26 to 2.82; p = 0.002]. Sensitivity analysis confirmed robustness of this result [RR, 2.29; 95%CI, 1.49 to 3.54; p = 0.0002]. No differences were observed between the two groups with respect to birth weights [mean difference (MD), 79; 95%CI, -64 to 221.99; p = 0.28] and the risk of macrosomia [RR, 1.69; 95%CI, 0.57 to 5.08; p = 0.35].</p><p>Conclusion</p><p>For women with gestational diabetes, no differences in maternal short term outcomes were observed in those treated with glyburide or insulin. However, the incidence of neonatal hypoglycemia was higher in the glyburide group compared to the insulin group.</p></div
Baseline characteristics of studies comparing glyburide and insulin in the treatment of GDM.
<p>Baseline characteristics of studies comparing glyburide and insulin in the treatment of GDM.</p
Neonatal outcomes comparing glyburide and insulin.
<p>Neonatal outcomes comparing glyburide and insulin.</p