Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35608
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dc.contributor.authorGao, Frank M-
dc.contributor.authorAli, Aleena S-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorGaca, Michele Jane-
dc.contributor.authorLecamwasam, Ashani-
dc.contributor.authorChurilov, Leonid-
dc.contributor.authorEkinci, Elif I-
dc.date.accessioned2024-12-02T04:05:25Z-
dc.date.available2024-12-02T04:05:25Z-
dc.date.issued2024-12-01-
dc.identifier.citationDiabetes care 2024-12-01; 47(12)en_US
dc.identifier.issn1935-5548-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35608-
dc.description.abstractThe safety and efficacy of sodium-glucose cotransporter 2 (SGLT2) inhibitors in hospitalized patients are unclear. To evaluate outcomes of inpatient SGLT2 inhibitor use. MEDLINE, Embase, Emcare, and Cochrane databases were searched through 29 May 2024. Randomized controlled trials (RCTs) and observational cohort studies with assessment of SGLT2 inhibitor use in patients hospitalized for any reason were included. Study characteristics and clinical outcomes were extracted. We performed a random-effects meta-analysis analyzing RCTs and cohort studies separately. Heterogeneity was quantified with the I2 statistic. Twenty-three RCTs comprising 19,846 participants (29.5% with type 2 diabetes) with comparison of SGLT2 inhibitors with placebo or active comparator were included. Ketoacidosis rates were 0.210 per 100 person-years (95% CI 0.119, 0.370) for SGLT2 inhibitors and 0.140 per 100 person-years (95% CI 0.070, 0.280) for control (rate ratio 1.50 [95 CI 0.56, 4.23], P = 0.38). SGLT2 inhibitor use was associated with fewer readmissions and urgent visits (odds ratio [OR] 0.64 [95 CI 0.47, 0.86], P < 0.01) and lower mortality rates (OR 0.74 [95% CI 0.56, 0.98], P = 0.03) in heart failure trials and lower incidence of acute kidney injury (OR 0.76 [95% CI 0.60, 0.97], P = 0.03) among all RCTs. Twenty observational studies were included and did not show increased adverse events. Ketoacidosis rates were low, likely leading to lack of power to detect significant differences. SGLT2 inhibitor use among hospitalized patients was associated with numerically higher rates of ketoacidosis, although further studies are required.en_US
dc.language.isoeng-
dc.titleA Systematic Review and Meta-analysis on the Safety and Efficacy of Sodium-Glucose Cotransporter 2 Inhibitor Use in Hospitalized Patients.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleDiabetes careen_US
dc.identifier.affiliationEndocrinologyen_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.;Australian Centre for Accelerating Diabetes Innovations, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.;Department of Diabetes and Metabolism, Barts Health NHS Trust, London, U.K.en_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.;Department of Critical Care, Melbourne Medical School, The University of Melbourne, Austin Hospital, Melbourne, Australia.;Department of Intensive Care, Austin Hospital, Melbourne, Australia.;Data Analytics Research and Evaluation Centre, Austin Hospital, Melbourne, Australia.;Department of Intensive Care, Royal Melbourne Hospital, Melbourne, Australia.en_US
dc.identifier.affiliationData Analytics Research and Evaluation (DARE) Centreen_US
dc.identifier.affiliationDepartment of Medicine, Austin Health, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.;Department of Nephrology, Northern Health, Melbourne, Australia.en_US
dc.identifier.affiliationAustralian Centre for Accelerating Diabetes Innovations, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.;Department of Medicine, Royal Melbourne Hospital, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.en_US
dc.identifier.affiliationDepartment of Endocrinology, Austin Hospital, Melbourne, Australia.;Department of Medicine, Austin Health, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.;Australian Centre for Accelerating Diabetes Innovations, Melbourne Medical School, The University of Melbourne, Melbourne, Australia.en_US
dc.identifier.doi10.2337/dc24-0946en_US
dc.type.contentTexten_US
dc.identifier.orcid0009-0005-0789-307Xen_US
dc.identifier.orcid0000-0002-1485-9153en_US
dc.identifier.orcid0000-0003-2372-395Xen_US
dc.identifier.pubmedid39602586-
dc.description.volume47-
dc.description.issue12-
dc.description.startpage2275-
dc.description.endpage2290-
dc.subject.meshtermssecondarySodium-Glucose Transporter 2 Inhibitors/therapeutic use-
dc.subject.meshtermssecondarySodium-Glucose Transporter 2 Inhibitors/adverse effects-
dc.subject.meshtermssecondaryHospitalization/statistics & numerical data-
dc.subject.meshtermssecondaryDiabetes Mellitus, Type 2/drug therapy-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptEndocrinology-
crisitem.author.deptSurgery-
crisitem.author.deptOffice for Research-
crisitem.author.deptEndocrinology-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptEndocrinology-
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