Comparative efficacy and safety of antihyperglycemic drug classes for patients with type 2 diabetes following failure with metformin monotherapy: A systematic review and network meta‐analysis of randomized controlled trials
Aims To compare the efficacy and safety of antihyperglycemic agents, taken in combination with metformin, for the treatment of type 2 diabetes mellitus (T2DM). Methods A previous 2016 comprehensive search of Ovid MEDLINE, PubMed, and Cochrane CENTRAL was updated to October 2018, and a systematic rev...
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Veröffentlicht in: | Diabetes/metabolism research and reviews 2022-05, Vol.38 (4), p.e3515-n/a |
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creator | Zheng, Hui Sigal, Ronald J. Coyle, Doug Bai, Zemin Johnston, Amy Elliott, Jesse Hsieh, Shuching Kelly, Shannon E. Chen, Li Skidmore, Becky Toupin‐April, Karine Wells, George A. |
description | Aims
To compare the efficacy and safety of antihyperglycemic agents, taken in combination with metformin, for the treatment of type 2 diabetes mellitus (T2DM).
Methods
A previous 2016 comprehensive search of Ovid MEDLINE, PubMed, and Cochrane CENTRAL was updated to October 2018, and a systematic review and network meta‐analysis (NMA) was conducted. Randomized controlled trials (RCTs) of patients with T2DM taking an antihyperglycemic agent in combination with metformin were included. Bayesian NMA was performed to assess the relative efficacy and safety of the antihyperglycemic classes.
Results
In total, 204 RCTs were included, which assessed the efficacy and safety of eight antihyperglycemic drug classes (i.e., sulfonylureas, meglitinides, alpha‐glucosidase inhibitors, thiazolidinediones, basal and biphasic insulin, dipeptidyl peptidase 4 inhibitors, glucagon‐like‐peptide‐1 receptor agonists and sodium‐glucose cotransport‐2 inhibitors). All drug classes significantly reduced haemoglobin A1c (HbA1c) compared to metformin monotherapy (mean reduction from 0.50 to 0.92). The drug classes varied in their relative effects on hypoglycemia, body weight, body mass index, systolic and diastolic blood pressure, total cholesterol, high and low density lipoprotein cholesterol, and the classes had differing safety profiles on total adverse events, urogenital adverse events, heart failure, serious adverse events, and withdraw due to adverse events.
Conclusions
All eight antihyperglycemic drug classes, taken in combination with metformin, reduced HbA1c levels; however, the effects of the agents on other outcomes varied among the classes. |
doi_str_mv | 10.1002/dmrr.3515 |
format | Article |
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To compare the efficacy and safety of antihyperglycemic agents, taken in combination with metformin, for the treatment of type 2 diabetes mellitus (T2DM).
Methods
A previous 2016 comprehensive search of Ovid MEDLINE, PubMed, and Cochrane CENTRAL was updated to October 2018, and a systematic review and network meta‐analysis (NMA) was conducted. Randomized controlled trials (RCTs) of patients with T2DM taking an antihyperglycemic agent in combination with metformin were included. Bayesian NMA was performed to assess the relative efficacy and safety of the antihyperglycemic classes.
Results
In total, 204 RCTs were included, which assessed the efficacy and safety of eight antihyperglycemic drug classes (i.e., sulfonylureas, meglitinides, alpha‐glucosidase inhibitors, thiazolidinediones, basal and biphasic insulin, dipeptidyl peptidase 4 inhibitors, glucagon‐like‐peptide‐1 receptor agonists and sodium‐glucose cotransport‐2 inhibitors). All drug classes significantly reduced haemoglobin A1c (HbA1c) compared to metformin monotherapy (mean reduction from 0.50 to 0.92). The drug classes varied in their relative effects on hypoglycemia, body weight, body mass index, systolic and diastolic blood pressure, total cholesterol, high and low density lipoprotein cholesterol, and the classes had differing safety profiles on total adverse events, urogenital adverse events, heart failure, serious adverse events, and withdraw due to adverse events.
Conclusions
All eight antihyperglycemic drug classes, taken in combination with metformin, reduced HbA1c levels; however, the effects of the agents on other outcomes varied among the classes.</description><identifier>ISSN: 1520-7552</identifier><identifier>EISSN: 1520-7560</identifier><identifier>DOI: 10.1002/dmrr.3515</identifier><identifier>PMID: 34951928</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adverse events ; Antidiabetics ; antihyperglycemic agents and classes ; Bayesian analysis ; Blood pressure ; Body mass index ; Body weight ; Cholesterol ; Clinical trials ; Congestive heart failure ; Diabetes ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 ; Dipeptidyl-Peptidase IV Inhibitors - therapeutic use ; Drug formularies ; Drug Therapy, Combination ; GLP-1 receptor agonists ; Glucagon ; Glycated Hemoglobin A ; Hemoglobin ; Humans ; Hypoglycemia ; Hypoglycemic Agents - adverse effects ; Insulin ; Low density lipoprotein ; Meta-analysis ; Metformin ; Metformin - adverse effects ; Network Meta-Analysis ; Patients ; Peptidase ; Randomized Controlled Trials as Topic ; Safety ; Sodium-glucose cotransporter ; Systematic review ; Thiazolidinediones ; type 2 diabetes</subject><ispartof>Diabetes/metabolism research and reviews, 2022-05, Vol.38 (4), p.e3515-n/a</ispartof><rights>2021 John Wiley & Sons Ltd.</rights><rights>2022 John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-6321c0d46fd0e9b391e7b3aecfbbb14d30a20b946aa2f7b8a3311638806fbcb73</citedby><cites>FETCH-LOGICAL-c3535-6321c0d46fd0e9b391e7b3aecfbbb14d30a20b946aa2f7b8a3311638806fbcb73</cites><orcidid>0000-0001-9985-3115 ; 0000-0003-1934-7867</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdmrr.3515$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdmrr.3515$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34951928$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheng, Hui</creatorcontrib><creatorcontrib>Sigal, Ronald J.</creatorcontrib><creatorcontrib>Coyle, Doug</creatorcontrib><creatorcontrib>Bai, Zemin</creatorcontrib><creatorcontrib>Johnston, Amy</creatorcontrib><creatorcontrib>Elliott, Jesse</creatorcontrib><creatorcontrib>Hsieh, Shuching</creatorcontrib><creatorcontrib>Kelly, Shannon E.</creatorcontrib><creatorcontrib>Chen, Li</creatorcontrib><creatorcontrib>Skidmore, Becky</creatorcontrib><creatorcontrib>Toupin‐April, Karine</creatorcontrib><creatorcontrib>Wells, George A.</creatorcontrib><title>Comparative efficacy and safety of antihyperglycemic drug classes for patients with type 2 diabetes following failure with metformin monotherapy: A systematic review and network meta‐analysis of randomized controlled trials</title><title>Diabetes/metabolism research and reviews</title><addtitle>Diabetes Metab Res Rev</addtitle><description>Aims
To compare the efficacy and safety of antihyperglycemic agents, taken in combination with metformin, for the treatment of type 2 diabetes mellitus (T2DM).
Methods
A previous 2016 comprehensive search of Ovid MEDLINE, PubMed, and Cochrane CENTRAL was updated to October 2018, and a systematic review and network meta‐analysis (NMA) was conducted. Randomized controlled trials (RCTs) of patients with T2DM taking an antihyperglycemic agent in combination with metformin were included. Bayesian NMA was performed to assess the relative efficacy and safety of the antihyperglycemic classes.
Results
In total, 204 RCTs were included, which assessed the efficacy and safety of eight antihyperglycemic drug classes (i.e., sulfonylureas, meglitinides, alpha‐glucosidase inhibitors, thiazolidinediones, basal and biphasic insulin, dipeptidyl peptidase 4 inhibitors, glucagon‐like‐peptide‐1 receptor agonists and sodium‐glucose cotransport‐2 inhibitors). All drug classes significantly reduced haemoglobin A1c (HbA1c) compared to metformin monotherapy (mean reduction from 0.50 to 0.92). The drug classes varied in their relative effects on hypoglycemia, body weight, body mass index, systolic and diastolic blood pressure, total cholesterol, high and low density lipoprotein cholesterol, and the classes had differing safety profiles on total adverse events, urogenital adverse events, heart failure, serious adverse events, and withdraw due to adverse events.
Conclusions
All eight antihyperglycemic drug classes, taken in combination with metformin, reduced HbA1c levels; however, the effects of the agents on other outcomes varied among the classes.</description><subject>Adverse events</subject><subject>Antidiabetics</subject><subject>antihyperglycemic agents and classes</subject><subject>Bayesian analysis</subject><subject>Blood pressure</subject><subject>Body mass index</subject><subject>Body weight</subject><subject>Cholesterol</subject><subject>Clinical trials</subject><subject>Congestive heart failure</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2</subject><subject>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</subject><subject>Drug formularies</subject><subject>Drug Therapy, Combination</subject><subject>GLP-1 receptor agonists</subject><subject>Glucagon</subject><subject>Glycated Hemoglobin A</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Hypoglycemia</subject><subject>Hypoglycemic Agents - adverse effects</subject><subject>Insulin</subject><subject>Low density lipoprotein</subject><subject>Meta-analysis</subject><subject>Metformin</subject><subject>Metformin - adverse effects</subject><subject>Network Meta-Analysis</subject><subject>Patients</subject><subject>Peptidase</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Safety</subject><subject>Sodium-glucose cotransporter</subject><subject>Systematic review</subject><subject>Thiazolidinediones</subject><subject>type 2 diabetes</subject><issn>1520-7552</issn><issn>1520-7560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctu1DAUhiMEohdY8ALIEhu6mNaXOJOwq4arVIRUwTqyneMZFzsOttMorHgEXhGeBGemdIHE6hzL3_l8rL8onhF8TjCmF50L4Zxxwh8Ux4RTvFrzCj-87zk9Kk5ivMEYs7IqHxdHrGw4aWh9XPzaeDeIIJK5BQRaGyXUjETfoSg0pBl5nU_J7OYBwtbOCpxRqAvjFikrYoSItA9oyALoU0STSTuUMowo6oyQkPaEtX4y_RZpYewY4IA5SHnWmR453_u0gyCG-RW6RHGOCVxWKhTg1sC0X6iHNPnwdRkTv3_8FL2wczRx2TDke-_Md-iQ8n0K-b3cpmCEjU-KRzoXeHpXT4svb9983rxfXX1692FzebVSjDO-qhglCndlpTsMjWQNgbVkApSWUpKyY1hQLJuyEoLqtawFY4RUrK5xpaWSa3ZavDx4h-C_jRBT60xUYK3owY-xpRUpKWuapszoi3_QGz-G_J-F4jWtGaU8U2cHSgUfYwDdDsE4EeaW4HbJvV1yb5fcM_v8zjhKB909-TfoDFwcgMlYmP9val9_vL7eK_8AwAO_-w</recordid><startdate>202205</startdate><enddate>202205</enddate><creator>Zheng, Hui</creator><creator>Sigal, Ronald J.</creator><creator>Coyle, Doug</creator><creator>Bai, Zemin</creator><creator>Johnston, Amy</creator><creator>Elliott, Jesse</creator><creator>Hsieh, Shuching</creator><creator>Kelly, Shannon E.</creator><creator>Chen, Li</creator><creator>Skidmore, Becky</creator><creator>Toupin‐April, Karine</creator><creator>Wells, George A.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9985-3115</orcidid><orcidid>https://orcid.org/0000-0003-1934-7867</orcidid></search><sort><creationdate>202205</creationdate><title>Comparative efficacy and safety of antihyperglycemic drug classes for patients with type 2 diabetes following failure with metformin monotherapy: A systematic review and network meta‐analysis of randomized controlled trials</title><author>Zheng, Hui ; Sigal, Ronald J. ; Coyle, Doug ; Bai, Zemin ; Johnston, Amy ; Elliott, Jesse ; Hsieh, Shuching ; Kelly, Shannon E. ; Chen, Li ; Skidmore, Becky ; Toupin‐April, Karine ; Wells, George A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-6321c0d46fd0e9b391e7b3aecfbbb14d30a20b946aa2f7b8a3311638806fbcb73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adverse events</topic><topic>Antidiabetics</topic><topic>antihyperglycemic agents and classes</topic><topic>Bayesian analysis</topic><topic>Blood pressure</topic><topic>Body mass index</topic><topic>Body weight</topic><topic>Cholesterol</topic><topic>Clinical trials</topic><topic>Congestive heart failure</topic><topic>Diabetes</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2</topic><topic>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</topic><topic>Drug formularies</topic><topic>Drug Therapy, Combination</topic><topic>GLP-1 receptor agonists</topic><topic>Glucagon</topic><topic>Glycated Hemoglobin A</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Hypoglycemia</topic><topic>Hypoglycemic Agents - adverse effects</topic><topic>Insulin</topic><topic>Low density lipoprotein</topic><topic>Meta-analysis</topic><topic>Metformin</topic><topic>Metformin - adverse effects</topic><topic>Network Meta-Analysis</topic><topic>Patients</topic><topic>Peptidase</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Safety</topic><topic>Sodium-glucose cotransporter</topic><topic>Systematic review</topic><topic>Thiazolidinediones</topic><topic>type 2 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Hui</creatorcontrib><creatorcontrib>Sigal, Ronald J.</creatorcontrib><creatorcontrib>Coyle, Doug</creatorcontrib><creatorcontrib>Bai, Zemin</creatorcontrib><creatorcontrib>Johnston, Amy</creatorcontrib><creatorcontrib>Elliott, Jesse</creatorcontrib><creatorcontrib>Hsieh, Shuching</creatorcontrib><creatorcontrib>Kelly, Shannon E.</creatorcontrib><creatorcontrib>Chen, Li</creatorcontrib><creatorcontrib>Skidmore, Becky</creatorcontrib><creatorcontrib>Toupin‐April, Karine</creatorcontrib><creatorcontrib>Wells, George A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes/metabolism research and reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Hui</au><au>Sigal, Ronald J.</au><au>Coyle, Doug</au><au>Bai, Zemin</au><au>Johnston, Amy</au><au>Elliott, Jesse</au><au>Hsieh, Shuching</au><au>Kelly, Shannon E.</au><au>Chen, Li</au><au>Skidmore, Becky</au><au>Toupin‐April, Karine</au><au>Wells, George A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative efficacy and safety of antihyperglycemic drug classes for patients with type 2 diabetes following failure with metformin monotherapy: A systematic review and network meta‐analysis of randomized controlled trials</atitle><jtitle>Diabetes/metabolism research and reviews</jtitle><addtitle>Diabetes Metab Res Rev</addtitle><date>2022-05</date><risdate>2022</risdate><volume>38</volume><issue>4</issue><spage>e3515</spage><epage>n/a</epage><pages>e3515-n/a</pages><issn>1520-7552</issn><eissn>1520-7560</eissn><abstract>Aims
To compare the efficacy and safety of antihyperglycemic agents, taken in combination with metformin, for the treatment of type 2 diabetes mellitus (T2DM).
Methods
A previous 2016 comprehensive search of Ovid MEDLINE, PubMed, and Cochrane CENTRAL was updated to October 2018, and a systematic review and network meta‐analysis (NMA) was conducted. Randomized controlled trials (RCTs) of patients with T2DM taking an antihyperglycemic agent in combination with metformin were included. Bayesian NMA was performed to assess the relative efficacy and safety of the antihyperglycemic classes.
Results
In total, 204 RCTs were included, which assessed the efficacy and safety of eight antihyperglycemic drug classes (i.e., sulfonylureas, meglitinides, alpha‐glucosidase inhibitors, thiazolidinediones, basal and biphasic insulin, dipeptidyl peptidase 4 inhibitors, glucagon‐like‐peptide‐1 receptor agonists and sodium‐glucose cotransport‐2 inhibitors). All drug classes significantly reduced haemoglobin A1c (HbA1c) compared to metformin monotherapy (mean reduction from 0.50 to 0.92). The drug classes varied in their relative effects on hypoglycemia, body weight, body mass index, systolic and diastolic blood pressure, total cholesterol, high and low density lipoprotein cholesterol, and the classes had differing safety profiles on total adverse events, urogenital adverse events, heart failure, serious adverse events, and withdraw due to adverse events.
Conclusions
All eight antihyperglycemic drug classes, taken in combination with metformin, reduced HbA1c levels; however, the effects of the agents on other outcomes varied among the classes.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34951928</pmid><doi>10.1002/dmrr.3515</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9985-3115</orcidid><orcidid>https://orcid.org/0000-0003-1934-7867</orcidid></addata></record> |
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subjects | Adverse events Antidiabetics antihyperglycemic agents and classes Bayesian analysis Blood pressure Body mass index Body weight Cholesterol Clinical trials Congestive heart failure Diabetes Diabetes mellitus (non-insulin dependent) Diabetes Mellitus, Type 2 Dipeptidyl-Peptidase IV Inhibitors - therapeutic use Drug formularies Drug Therapy, Combination GLP-1 receptor agonists Glucagon Glycated Hemoglobin A Hemoglobin Humans Hypoglycemia Hypoglycemic Agents - adverse effects Insulin Low density lipoprotein Meta-analysis Metformin Metformin - adverse effects Network Meta-Analysis Patients Peptidase Randomized Controlled Trials as Topic Safety Sodium-glucose cotransporter Systematic review Thiazolidinediones type 2 diabetes |
title | Comparative efficacy and safety of antihyperglycemic drug classes for patients with type 2 diabetes following failure with metformin monotherapy: A systematic review and network meta‐analysis of randomized controlled trials |
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