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Comparative efficacy and complications of long-acting and intermediate-acting insulin regimens for adults with type 1 diabetes: an individual patient data network meta-analysis
ObjectiveTo examine the comparative efficacy and complications of long-acting and intermediate-acting insulin for different patient characteristics for type 1 diabetes mellitus (T1DM).DesignSystematic review and individual patient data (IPD) network meta-analysis (NMA).Data sourcesMEDLINE, EMBASE an...
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Published in: | BMJ open 2022-11, Vol.12 (11), p.e058034 |
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description | ObjectiveTo examine the comparative efficacy and complications of long-acting and intermediate-acting insulin for different patient characteristics for type 1 diabetes mellitus (T1DM).DesignSystematic review and individual patient data (IPD) network meta-analysis (NMA).Data sourcesMEDLINE, EMBASE and the Cochrane Central Register of Controlled Trials were searched through June 2015.Eligibility criteriaRandomised controlled trials (RCTs) on adults with T1DM assessing glycosylated haemoglobin (A1c) and severe hypoglycaemia in long-acting and intermediate-acting insulin regimens.Data extraction and synthesisWe requested IPD from authors and funders. When IPD were not available, we used aggregate data. We conducted a random-effects model, and specifically a one-stage IPD-NMA for those studies providing IPD and a two-stage IPD-NMA to incorporate those studies not providing IPD.ResultsWe included 28 RCTs plus one companion report, after screening 6680 titles/abstracts and 205 full-text articles. Of the 28 RCTs, 27 studies provided data for the NMA with 7394 participants, of which 12 RCTs had IPD on 4943 participants. The IPD-NMA for A1c suggested that glargine once daily (mean difference [MD]=−0.31, 95% confidence interval [CI]: −0.48 to −0.14) and detemir once daily (MD=−0.25, 95% CI: –0.41 to −0.09) were superior to neutral protamine Hagedorn (NPH) once daily. NPH once/two times per day improved A1c compared with NPH once daily (MD=−0.30, 95% CI: –0.50 to −0.11). Results regarding complications in severe hypoglycaemia should be considered with great caution due to inconsistency in the evidence network. Accounting for missing data, there was no evidence of inconsistency and long-acting insulin regimens ranked higher regarding reducing severe hypoglycaemia compared with intermediate-acting insulin regimens (two-stage NMA: glargine two times per day SUCRA (Surface Under the Cumulative Ranking curve)=89%, detemir once daily SUCRA=77%; one-stage NMA: detemir once daily/two times per day SUCRA=85%). Using multiple imputations and IPD only, complications in severe hypoglycaemia increased with diabetes-related comorbidities (regression coefficient: 1.03, 95% CI: 1.02 to 1.03).ConclusionsLong-acting insulin regimens reduced A1c compared with intermediate-acting insulin regimens and were associated with lower severe hypoglycaemia. Of the observed differences, only glargine once daily achieved a clinically significant reduction of 0.30%. Results should be interpreted wit |
doi_str_mv | 10.1136/bmjopen-2021-058034 |
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When IPD were not available, we used aggregate data. We conducted a random-effects model, and specifically a one-stage IPD-NMA for those studies providing IPD and a two-stage IPD-NMA to incorporate those studies not providing IPD.ResultsWe included 28 RCTs plus one companion report, after screening 6680 titles/abstracts and 205 full-text articles. Of the 28 RCTs, 27 studies provided data for the NMA with 7394 participants, of which 12 RCTs had IPD on 4943 participants. The IPD-NMA for A1c suggested that glargine once daily (mean difference [MD]=−0.31, 95% confidence interval [CI]: −0.48 to −0.14) and detemir once daily (MD=−0.25, 95% CI: –0.41 to −0.09) were superior to neutral protamine Hagedorn (NPH) once daily. NPH once/two times per day improved A1c compared with NPH once daily (MD=−0.30, 95% CI: –0.50 to −0.11). Results regarding complications in severe hypoglycaemia should be considered with great caution due to inconsistency in the evidence network. Accounting for missing data, there was no evidence of inconsistency and long-acting insulin regimens ranked higher regarding reducing severe hypoglycaemia compared with intermediate-acting insulin regimens (two-stage NMA: glargine two times per day SUCRA (Surface Under the Cumulative Ranking curve)=89%, detemir once daily SUCRA=77%; one-stage NMA: detemir once daily/two times per day SUCRA=85%). Using multiple imputations and IPD only, complications in severe hypoglycaemia increased with diabetes-related comorbidities (regression coefficient: 1.03, 95% CI: 1.02 to 1.03).ConclusionsLong-acting insulin regimens reduced A1c compared with intermediate-acting insulin regimens and were associated with lower severe hypoglycaemia. Of the observed differences, only glargine once daily achieved a clinically significant reduction of 0.30%. Results should be interpreted with caution due to very low quality of evidence.PROSPERO registration numberCRD42015023511.</description><identifier>ISSN: 2044-6055</identifier><identifier>EISSN: 2044-6055</identifier><identifier>DOI: 10.1136/bmjopen-2021-058034</identifier><identifier>PMID: 36332950</identifier><language>eng</language><publisher>England: British Medical Journal Publishing Group</publisher><subject>Adult ; Bias ; Clinical significance ; Diabetes ; DIABETES & ENDOCRINOLOGY ; Diabetes and Endocrinology ; Diabetes Mellitus, Type 1 - drug therapy ; EPIDEMIOLOGY ; Funding ; Glycated Hemoglobin ; Humans ; Hypoglycemia ; Hypoglycemia - chemically induced ; Hypoglycemic Agents - therapeutic use ; Insulin ; Insulin - therapeutic use ; Insulin Glargine - therapeutic use ; Insulin, Isophane ; Insulin, Long-Acting - therapeutic use ; Meta-analysis ; Network Meta-Analysis ; Patients ; PUBLIC HEALTH ; Systematic review</subject><ispartof>BMJ open, 2022-11, Vol.12 (11), p.e058034</ispartof><rights>Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. 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Published by BMJ. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b539t-4d6d521abaef7455d9b9ab71f423c7be1292249ed1fd0867783585568a7016893</citedby><cites>FETCH-LOGICAL-b539t-4d6d521abaef7455d9b9ab71f423c7be1292249ed1fd0867783585568a7016893</cites><orcidid>0000-0001-6680-6507 ; 0000-0002-2926-7257 ; 0000-0002-4114-8971 ; 0000-0001-6388-4825 ; 0000-0003-0856-1892 ; 0000-0003-3051-1445 ; 0000-0003-1041-4592</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2732031508/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2732031508?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3194,25753,27924,27925,37012,37013,44590,53791,53793,55341,55350,75126,77596,77597,77660,77686</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36332950$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Veroniki, Areti Angeliki</creatorcontrib><creatorcontrib>Seitidis, Georgios</creatorcontrib><creatorcontrib>Stewart, Lesley</creatorcontrib><creatorcontrib>Clarke, Mike</creatorcontrib><creatorcontrib>Tudur-Smith, Catrin</creatorcontrib><creatorcontrib>Mavridis, Dimitris</creatorcontrib><creatorcontrib>Yu, Catherine H</creatorcontrib><creatorcontrib>Moja, Lorenzo</creatorcontrib><creatorcontrib>Straus, Sharon E</creatorcontrib><creatorcontrib>Tricco, Andrea C</creatorcontrib><title>Comparative efficacy and complications of long-acting and intermediate-acting insulin regimens for adults with type 1 diabetes: an individual patient data network meta-analysis</title><title>BMJ open</title><addtitle>BMJ Open</addtitle><addtitle>BMJ Open</addtitle><description>ObjectiveTo examine the comparative efficacy and complications of long-acting and intermediate-acting insulin for different patient characteristics for type 1 diabetes mellitus (T1DM).DesignSystematic review and individual patient data (IPD) network meta-analysis (NMA).Data sourcesMEDLINE, EMBASE and the Cochrane Central Register of Controlled Trials were searched through June 2015.Eligibility criteriaRandomised controlled trials (RCTs) on adults with T1DM assessing glycosylated haemoglobin (A1c) and severe hypoglycaemia in long-acting and intermediate-acting insulin regimens.Data extraction and synthesisWe requested IPD from authors and funders. When IPD were not available, we used aggregate data. We conducted a random-effects model, and specifically a one-stage IPD-NMA for those studies providing IPD and a two-stage IPD-NMA to incorporate those studies not providing IPD.ResultsWe included 28 RCTs plus one companion report, after screening 6680 titles/abstracts and 205 full-text articles. Of the 28 RCTs, 27 studies provided data for the NMA with 7394 participants, of which 12 RCTs had IPD on 4943 participants. The IPD-NMA for A1c suggested that glargine once daily (mean difference [MD]=−0.31, 95% confidence interval [CI]: −0.48 to −0.14) and detemir once daily (MD=−0.25, 95% CI: –0.41 to −0.09) were superior to neutral protamine Hagedorn (NPH) once daily. NPH once/two times per day improved A1c compared with NPH once daily (MD=−0.30, 95% CI: –0.50 to −0.11). Results regarding complications in severe hypoglycaemia should be considered with great caution due to inconsistency in the evidence network. Accounting for missing data, there was no evidence of inconsistency and long-acting insulin regimens ranked higher regarding reducing severe hypoglycaemia compared with intermediate-acting insulin regimens (two-stage NMA: glargine two times per day SUCRA (Surface Under the Cumulative Ranking curve)=89%, detemir once daily SUCRA=77%; one-stage NMA: detemir once daily/two times per day SUCRA=85%). Using multiple imputations and IPD only, complications in severe hypoglycaemia increased with diabetes-related comorbidities (regression coefficient: 1.03, 95% CI: 1.02 to 1.03).ConclusionsLong-acting insulin regimens reduced A1c compared with intermediate-acting insulin regimens and were associated with lower severe hypoglycaemia. Of the observed differences, only glargine once daily achieved a clinically significant reduction of 0.30%. Results should be interpreted with caution due to very low quality of evidence.PROSPERO registration numberCRD42015023511.</description><subject>Adult</subject><subject>Bias</subject><subject>Clinical significance</subject><subject>Diabetes</subject><subject>DIABETES & ENDOCRINOLOGY</subject><subject>Diabetes and Endocrinology</subject><subject>Diabetes Mellitus, Type 1 - drug therapy</subject><subject>EPIDEMIOLOGY</subject><subject>Funding</subject><subject>Glycated Hemoglobin</subject><subject>Humans</subject><subject>Hypoglycemia</subject><subject>Hypoglycemia - chemically induced</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin</subject><subject>Insulin - therapeutic use</subject><subject>Insulin Glargine - therapeutic use</subject><subject>Insulin, Isophane</subject><subject>Insulin, Long-Acting - therapeutic use</subject><subject>Meta-analysis</subject><subject>Network Meta-Analysis</subject><subject>Patients</subject><subject>PUBLIC HEALTH</subject><subject>Systematic review</subject><issn>2044-6055</issn><issn>2044-6055</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9ks1u1DAUhSMEolXpEyAhS2zYhPonTmIWSGjET6VKbGBt3cQ3Uw-JHWyn1bxVHxG3mZaWBd7Yvj7ns691iuI1o-8ZE_VZN-38jK7klLOSypaK6llxzGlVlTWV8vmj9VFxGuOO5lFJJSV_WRyJWgiuJD0ubjZ-miFAsldIcBhsD_2egDOkzwdj3ibrXSR-IKN32xL6ZN32TmBdwjChsZDwvm5dXEbrSMCtnTD7Bh8ImGVMkVzbdEnSfkbCSDZ1mDB-yKRsMvbKmgVGMufr0CViIAFxmK59-EUmTFCCg3EfbXxVvBhgjHh6mE-Kn18-_9h8Ky--fz3ffLooOylUKitTG8kZdIBDU0lpVKega9hQcdE3HTKuOK8UGjYY2tZN0wrZSlm30FBWt0qcFOcr13jY6TnYCcJee7D6ruDDVkNIth9RcyZEVVNYkYqD4UPeY992omUtZNbHlTUvXf6wPncYYHwCfXri7KXe-iutaqFoU2fAuwMg-N8LxqQnG3scR3Dol6h5I7isuBIiS9_-I935JeTPW1VUMEnbrBKrqg8-xoDDw2MY1bcB04eA6duA6TVg2fXmcR8Pnvs4ZcHZKsjuv_f-D_kHxKHfqw</recordid><startdate>20221104</startdate><enddate>20221104</enddate><creator>Veroniki, Areti Angeliki</creator><creator>Seitidis, Georgios</creator><creator>Stewart, Lesley</creator><creator>Clarke, Mike</creator><creator>Tudur-Smith, Catrin</creator><creator>Mavridis, Dimitris</creator><creator>Yu, Catherine H</creator><creator>Moja, Lorenzo</creator><creator>Straus, Sharon E</creator><creator>Tricco, Andrea C</creator><general>British Medical Journal Publishing Group</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6680-6507</orcidid><orcidid>https://orcid.org/0000-0002-2926-7257</orcidid><orcidid>https://orcid.org/0000-0002-4114-8971</orcidid><orcidid>https://orcid.org/0000-0001-6388-4825</orcidid><orcidid>https://orcid.org/0000-0003-0856-1892</orcidid><orcidid>https://orcid.org/0000-0003-3051-1445</orcidid><orcidid>https://orcid.org/0000-0003-1041-4592</orcidid></search><sort><creationdate>20221104</creationdate><title>Comparative efficacy and complications of long-acting and intermediate-acting insulin regimens for adults with type 1 diabetes: an individual patient data network meta-analysis</title><author>Veroniki, Areti Angeliki ; Seitidis, Georgios ; Stewart, Lesley ; Clarke, Mike ; Tudur-Smith, Catrin ; Mavridis, Dimitris ; Yu, Catherine H ; Moja, Lorenzo ; Straus, Sharon E ; Tricco, Andrea C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b539t-4d6d521abaef7455d9b9ab71f423c7be1292249ed1fd0867783585568a7016893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Bias</topic><topic>Clinical significance</topic><topic>Diabetes</topic><topic>DIABETES & ENDOCRINOLOGY</topic><topic>Diabetes and Endocrinology</topic><topic>Diabetes Mellitus, Type 1 - drug therapy</topic><topic>EPIDEMIOLOGY</topic><topic>Funding</topic><topic>Glycated Hemoglobin</topic><topic>Humans</topic><topic>Hypoglycemia</topic><topic>Hypoglycemia - chemically induced</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin</topic><topic>Insulin - therapeutic use</topic><topic>Insulin Glargine - therapeutic use</topic><topic>Insulin, Isophane</topic><topic>Insulin, Long-Acting - therapeutic use</topic><topic>Meta-analysis</topic><topic>Network Meta-Analysis</topic><topic>Patients</topic><topic>PUBLIC HEALTH</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Veroniki, Areti Angeliki</creatorcontrib><creatorcontrib>Seitidis, Georgios</creatorcontrib><creatorcontrib>Stewart, Lesley</creatorcontrib><creatorcontrib>Clarke, Mike</creatorcontrib><creatorcontrib>Tudur-Smith, Catrin</creatorcontrib><creatorcontrib>Mavridis, Dimitris</creatorcontrib><creatorcontrib>Yu, Catherine H</creatorcontrib><creatorcontrib>Moja, Lorenzo</creatorcontrib><creatorcontrib>Straus, Sharon E</creatorcontrib><creatorcontrib>Tricco, Andrea C</creatorcontrib><collection>BMJ Open Access Journals</collection><collection>BMJ Journals:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMJ open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Veroniki, Areti Angeliki</au><au>Seitidis, Georgios</au><au>Stewart, Lesley</au><au>Clarke, Mike</au><au>Tudur-Smith, Catrin</au><au>Mavridis, Dimitris</au><au>Yu, Catherine H</au><au>Moja, Lorenzo</au><au>Straus, Sharon E</au><au>Tricco, Andrea C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative efficacy and complications of long-acting and intermediate-acting insulin regimens for adults with type 1 diabetes: an individual patient data network meta-analysis</atitle><jtitle>BMJ open</jtitle><stitle>BMJ Open</stitle><addtitle>BMJ Open</addtitle><date>2022-11-04</date><risdate>2022</risdate><volume>12</volume><issue>11</issue><spage>e058034</spage><pages>e058034-</pages><issn>2044-6055</issn><eissn>2044-6055</eissn><abstract>ObjectiveTo examine the comparative efficacy and complications of long-acting and intermediate-acting insulin for different patient characteristics for type 1 diabetes mellitus (T1DM).DesignSystematic review and individual patient data (IPD) network meta-analysis (NMA).Data sourcesMEDLINE, EMBASE and the Cochrane Central Register of Controlled Trials were searched through June 2015.Eligibility criteriaRandomised controlled trials (RCTs) on adults with T1DM assessing glycosylated haemoglobin (A1c) and severe hypoglycaemia in long-acting and intermediate-acting insulin regimens.Data extraction and synthesisWe requested IPD from authors and funders. When IPD were not available, we used aggregate data. We conducted a random-effects model, and specifically a one-stage IPD-NMA for those studies providing IPD and a two-stage IPD-NMA to incorporate those studies not providing IPD.ResultsWe included 28 RCTs plus one companion report, after screening 6680 titles/abstracts and 205 full-text articles. Of the 28 RCTs, 27 studies provided data for the NMA with 7394 participants, of which 12 RCTs had IPD on 4943 participants. The IPD-NMA for A1c suggested that glargine once daily (mean difference [MD]=−0.31, 95% confidence interval [CI]: −0.48 to −0.14) and detemir once daily (MD=−0.25, 95% CI: –0.41 to −0.09) were superior to neutral protamine Hagedorn (NPH) once daily. NPH once/two times per day improved A1c compared with NPH once daily (MD=−0.30, 95% CI: –0.50 to −0.11). Results regarding complications in severe hypoglycaemia should be considered with great caution due to inconsistency in the evidence network. Accounting for missing data, there was no evidence of inconsistency and long-acting insulin regimens ranked higher regarding reducing severe hypoglycaemia compared with intermediate-acting insulin regimens (two-stage NMA: glargine two times per day SUCRA (Surface Under the Cumulative Ranking curve)=89%, detemir once daily SUCRA=77%; one-stage NMA: detemir once daily/two times per day SUCRA=85%). Using multiple imputations and IPD only, complications in severe hypoglycaemia increased with diabetes-related comorbidities (regression coefficient: 1.03, 95% CI: 1.02 to 1.03).ConclusionsLong-acting insulin regimens reduced A1c compared with intermediate-acting insulin regimens and were associated with lower severe hypoglycaemia. Of the observed differences, only glargine once daily achieved a clinically significant reduction of 0.30%. Results should be interpreted with caution due to very low quality of evidence.PROSPERO registration numberCRD42015023511.</abstract><cop>England</cop><pub>British Medical Journal Publishing Group</pub><pmid>36332950</pmid><doi>10.1136/bmjopen-2021-058034</doi><orcidid>https://orcid.org/0000-0001-6680-6507</orcidid><orcidid>https://orcid.org/0000-0002-2926-7257</orcidid><orcidid>https://orcid.org/0000-0002-4114-8971</orcidid><orcidid>https://orcid.org/0000-0001-6388-4825</orcidid><orcidid>https://orcid.org/0000-0003-0856-1892</orcidid><orcidid>https://orcid.org/0000-0003-3051-1445</orcidid><orcidid>https://orcid.org/0000-0003-1041-4592</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2044-6055 |
ispartof | BMJ open, 2022-11, Vol.12 (11), p.e058034 |
issn | 2044-6055 2044-6055 |
language | eng |
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source | BMJ Open Access Journals; Publicly Available Content Database (Proquest) (PQ_SDU_P3); BMJ; PubMed Central |
subjects | Adult Bias Clinical significance Diabetes DIABETES & ENDOCRINOLOGY Diabetes and Endocrinology Diabetes Mellitus, Type 1 - drug therapy EPIDEMIOLOGY Funding Glycated Hemoglobin Humans Hypoglycemia Hypoglycemia - chemically induced Hypoglycemic Agents - therapeutic use Insulin Insulin - therapeutic use Insulin Glargine - therapeutic use Insulin, Isophane Insulin, Long-Acting - therapeutic use Meta-analysis Network Meta-Analysis Patients PUBLIC HEALTH Systematic review |
title | Comparative efficacy and complications of long-acting and intermediate-acting insulin regimens for adults with type 1 diabetes: an individual patient data network meta-analysis |
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