Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study

AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and...

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Veröffentlicht in:BMJ (Online) 2020-04, Vol.369, p.m1186
Hauptverfasser: Pasternak, Björn, Wintzell, Viktor, Melbye, Mads, Eliasson, Björn, Svensson, Ann-Marie, Franzén, Stefan, Gudbjörnsdottir, Soffia, Hveem, Kristian, Jonasson, Christian, Svanström, Henrik, Ueda, Peter
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container_start_page m1186
container_title BMJ (Online)
container_volume 369
creator Pasternak, Björn
Wintzell, Viktor
Melbye, Mads
Eliasson, Björn
Svensson, Ann-Marie
Franzén, Stefan
Gudbjörnsdottir, Soffia
Hveem, Kristian
Jonasson, Christian
Svanström, Henrik
Ueda, Peter
description AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and Norway, 2013-18.ParticipantsCohort of 29 887 new users of SGLT2 inhibitors (follow-up time: dapagliflozin 66.1%; empagliflozin 32.6%; canagliflozin 1.3%) and 29 887 new users of an active comparator, dipeptidyl peptidase-4 inhibitors, matched 1:1 on the basis of a propensity score with 57 variables. Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events.
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Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events.</description><identifier>ISSN: 1756-1833</identifier><identifier>ISSN: 0959-8138</identifier><identifier>ISSN: 0959-535X</identifier><identifier>EISSN: 1756-1833</identifier><identifier>DOI: 10.1136/bmj.m1186</identifier><identifier>PMID: 32349963</identifier><language>eng</language><publisher>England: BMJ Publishing Group LTD</publisher><subject>Acute Kidney Injury - epidemiology ; Adult ; Aged ; Aged, 80 and over ; Benzhydryl Compounds - therapeutic use ; Blood pressure ; Body mass index ; Canagliflozin - therapeutic use ; Cardiovascular diseases ; Cardiovascular Diseases - epidemiology ; cardiovascular outcomes ; Case-Control Studies ; Clinical Medicine ; Clinical trials ; Cohort analysis ; Cohort Studies ; Comorbidity ; Denmark - epidemiology ; Diabetes ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Mellitus, Type 2 - epidemiology ; diabetes-mellitus ; Dipeptidyl-peptidase IV ; Dipeptidyl-Peptidase IV Inhibitors - therapeutic use ; Female ; General &amp; Internal Medicine ; Glomerular filtration rate ; Glucose transporter ; Glucosides - therapeutic use ; Hemoglobin ; Hospitalization - statistics &amp; numerical data ; Hospitals ; Humans ; Kidney diseases ; Kidney Diseases - epidemiology ; Kidney Diseases - mortality ; Kidney Diseases - therapy ; Klinisk medicin ; Male ; Middle Aged ; Norway - epidemiology ; Patients ; Peptidase ; Population studies ; Prescription drugs ; Proportional Hazards Models ; Renal Insufficiency, Chronic - epidemiology ; Renal Replacement Therapy - statistics &amp; numerical data ; Sensitivity analysis ; Sodium-Glucose Transporter 2 Inhibitors - therapeutic use ; Sweden - epidemiology ; type-2</subject><ispartof>BMJ (Online), 2020-04, Vol.369, p.m1186</ispartof><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2020 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. BMJ 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 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)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2020 BMJ</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b574t-65219967cf9640d76bb30ca4e8b60ca3da35b6c59b83c3b6888ee7b2bd4923ad3</citedby><cites>FETCH-LOGICAL-b574t-65219967cf9640d76bb30ca4e8b60ca3da35b6c59b83c3b6888ee7b2bd4923ad3</cites><orcidid>0000-0002-3275-8743</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,550,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32349963$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/293615$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:143624602$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Pasternak, Björn</creatorcontrib><creatorcontrib>Wintzell, Viktor</creatorcontrib><creatorcontrib>Melbye, Mads</creatorcontrib><creatorcontrib>Eliasson, Björn</creatorcontrib><creatorcontrib>Svensson, Ann-Marie</creatorcontrib><creatorcontrib>Franzén, Stefan</creatorcontrib><creatorcontrib>Gudbjörnsdottir, Soffia</creatorcontrib><creatorcontrib>Hveem, Kristian</creatorcontrib><creatorcontrib>Jonasson, Christian</creatorcontrib><creatorcontrib>Svanström, Henrik</creatorcontrib><creatorcontrib>Ueda, Peter</creatorcontrib><title>Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study</title><title>BMJ (Online)</title><addtitle>BMJ</addtitle><description>AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and Norway, 2013-18.ParticipantsCohort of 29 887 new users of SGLT2 inhibitors (follow-up time: dapagliflozin 66.1%; empagliflozin 32.6%; canagliflozin 1.3%) and 29 887 new users of an active comparator, dipeptidyl peptidase-4 inhibitors, matched 1:1 on the basis of a propensity score with 57 variables. Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events.</description><subject>Acute Kidney Injury - epidemiology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Benzhydryl Compounds - therapeutic use</subject><subject>Blood pressure</subject><subject>Body mass index</subject><subject>Canagliflozin - therapeutic use</subject><subject>Cardiovascular diseases</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>cardiovascular outcomes</subject><subject>Case-Control Studies</subject><subject>Clinical Medicine</subject><subject>Clinical trials</subject><subject>Cohort analysis</subject><subject>Cohort Studies</subject><subject>Comorbidity</subject><subject>Denmark - epidemiology</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - epidemiology</subject><subject>diabetes-mellitus</subject><subject>Dipeptidyl-peptidase IV</subject><subject>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</subject><subject>Female</subject><subject>General &amp; 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Wintzell, Viktor ; Melbye, Mads ; Eliasson, Björn ; Svensson, Ann-Marie ; Franzén, Stefan ; Gudbjörnsdottir, Soffia ; Hveem, Kristian ; Jonasson, Christian ; Svanström, Henrik ; Ueda, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b574t-65219967cf9640d76bb30ca4e8b60ca3da35b6c59b83c3b6888ee7b2bd4923ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acute Kidney Injury - epidemiology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Benzhydryl Compounds - therapeutic use</topic><topic>Blood pressure</topic><topic>Body mass index</topic><topic>Canagliflozin - therapeutic use</topic><topic>Cardiovascular diseases</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>cardiovascular outcomes</topic><topic>Case-Control Studies</topic><topic>Clinical Medicine</topic><topic>Clinical trials</topic><topic>Cohort analysis</topic><topic>Cohort Studies</topic><topic>Comorbidity</topic><topic>Denmark - epidemiology</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - epidemiology</topic><topic>diabetes-mellitus</topic><topic>Dipeptidyl-peptidase IV</topic><topic>Dipeptidyl-Peptidase IV Inhibitors - therapeutic use</topic><topic>Female</topic><topic>General &amp; Internal Medicine</topic><topic>Glomerular filtration rate</topic><topic>Glucose transporter</topic><topic>Glucosides - therapeutic use</topic><topic>Hemoglobin</topic><topic>Hospitalization - statistics &amp; numerical data</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Kidney diseases</topic><topic>Kidney Diseases - epidemiology</topic><topic>Kidney Diseases - mortality</topic><topic>Kidney Diseases - therapy</topic><topic>Klinisk medicin</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Norway - epidemiology</topic><topic>Patients</topic><topic>Peptidase</topic><topic>Population studies</topic><topic>Prescription drugs</topic><topic>Proportional Hazards Models</topic><topic>Renal Insufficiency, Chronic - epidemiology</topic><topic>Renal Replacement Therapy - statistics &amp; numerical data</topic><topic>Sensitivity analysis</topic><topic>Sodium-Glucose Transporter 2 Inhibitors - therapeutic use</topic><topic>Sweden - epidemiology</topic><topic>type-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pasternak, Björn</creatorcontrib><creatorcontrib>Wintzell, Viktor</creatorcontrib><creatorcontrib>Melbye, Mads</creatorcontrib><creatorcontrib>Eliasson, Björn</creatorcontrib><creatorcontrib>Svensson, Ann-Marie</creatorcontrib><creatorcontrib>Franzén, Stefan</creatorcontrib><creatorcontrib>Gudbjörnsdottir, Soffia</creatorcontrib><creatorcontrib>Hveem, Kristian</creatorcontrib><creatorcontrib>Jonasson, Christian</creatorcontrib><creatorcontrib>Svanström, Henrik</creatorcontrib><creatorcontrib>Ueda, Peter</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>Nursing &amp; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</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 Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Göteborgs universitet</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>BMJ (Online)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pasternak, Björn</au><au>Wintzell, Viktor</au><au>Melbye, Mads</au><au>Eliasson, Björn</au><au>Svensson, Ann-Marie</au><au>Franzén, Stefan</au><au>Gudbjörnsdottir, Soffia</au><au>Hveem, Kristian</au><au>Jonasson, Christian</au><au>Svanström, Henrik</au><au>Ueda, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study</atitle><jtitle>BMJ (Online)</jtitle><addtitle>BMJ</addtitle><date>2020-04-29</date><risdate>2020</risdate><volume>369</volume><spage>m1186</spage><pages>m1186-</pages><issn>1756-1833</issn><issn>0959-8138</issn><issn>0959-535X</issn><eissn>1756-1833</eissn><abstract>AbstractObjectiveTo assess the association between use of sodium-glucose co-transporter 2 (SGLT2) inhibitors and risk of serious renal events in data from routine clinical practice.DesignCohort study using an active comparator, new user design and nationwide register data.SettingSweden, Denmark, and Norway, 2013-18.ParticipantsCohort of 29 887 new users of SGLT2 inhibitors (follow-up time: dapagliflozin 66.1%; empagliflozin 32.6%; canagliflozin 1.3%) and 29 887 new users of an active comparator, dipeptidyl peptidase-4 inhibitors, matched 1:1 on the basis of a propensity score with 57 variables. Mean follow-up time was 1.7 (SD 1.0) years.ExposuresSGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors, defined by filled prescriptions and analysed according to intention to treat.Main outcome measuresThe main outcome was serious renal events, a composite including renal replacement therapy, death from renal causes, and hospital admission for renal events. Secondary outcomes were the individual components of the main outcome.ResultsThe mean age of the study population was 61.3 (SD 10.5) years; 11 108 (19%) had cardiovascular disease, and 1974 (3%) had chronic kidney disease. Use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a reduced risk of serious renal events (2.6 events per 1000 person years versus 6.2 events per 1000 person years; hazard ratio 0.42 (95% confidence interval 0.34 to 0.53); absolute difference −3.6 (–4.4 to −2.8) events per 1000 person years). In secondary outcome analyses, the hazard ratio for use of SGLT2 inhibitors versus dipeptidyl peptidase-4 inhibitors was 0.32 (0.22 to 0.47) for renal replacement therapy, 0.41 (0.32 to 0.52) for hospital admission for renal events, and 0.77 (0.26 to 2.23) for death from renal causes. In sensitivity analyses in each of the Swedish and Danish parts of the cohort, the model was further adjusted for glycated haemoglobin and estimated glomerular filtration rate (Sweden and Denmark) and for blood pressure, body mass index, and smoking (Sweden only); in these analyses, the hazard ratio moved from 0.41 (0.26 to 0.66) to 0.50 (0.31 to 0.81) in Sweden and from 0.42 (0.32 to 0.56) to 0.55 (0.41 to 0.74) in Denmark.ConclusionsIn this analysis using nationwide data from three countries, use of SGLT2 inhibitors, compared with dipeptidyl peptidase-4 inhibitors, was associated with a significantly reduced risk of serious renal events.</abstract><cop>England</cop><pub>BMJ Publishing Group LTD</pub><pmid>32349963</pmid><doi>10.1136/bmj.m1186</doi><orcidid>https://orcid.org/0000-0002-3275-8743</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1756-1833
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issn 1756-1833
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0959-535X
1756-1833
language eng
recordid cdi_swepub_primary_oai_swepub_ki_se_471656
source Jstor Complete Legacy; MEDLINE; SWEPUB Freely available online
subjects Acute Kidney Injury - epidemiology
Adult
Aged
Aged, 80 and over
Benzhydryl Compounds - therapeutic use
Blood pressure
Body mass index
Canagliflozin - therapeutic use
Cardiovascular diseases
Cardiovascular Diseases - epidemiology
cardiovascular outcomes
Case-Control Studies
Clinical Medicine
Clinical trials
Cohort analysis
Cohort Studies
Comorbidity
Denmark - epidemiology
Diabetes
Diabetes Mellitus, Type 2 - drug therapy
Diabetes Mellitus, Type 2 - epidemiology
diabetes-mellitus
Dipeptidyl-peptidase IV
Dipeptidyl-Peptidase IV Inhibitors - therapeutic use
Female
General & Internal Medicine
Glomerular filtration rate
Glucose transporter
Glucosides - therapeutic use
Hemoglobin
Hospitalization - statistics & numerical data
Hospitals
Humans
Kidney diseases
Kidney Diseases - epidemiology
Kidney Diseases - mortality
Kidney Diseases - therapy
Klinisk medicin
Male
Middle Aged
Norway - epidemiology
Patients
Peptidase
Population studies
Prescription drugs
Proportional Hazards Models
Renal Insufficiency, Chronic - epidemiology
Renal Replacement Therapy - statistics & numerical data
Sensitivity analysis
Sodium-Glucose Transporter 2 Inhibitors - therapeutic use
Sweden - epidemiology
type-2
title Use of sodium-glucose co-transporter 2 inhibitors and risk of serious renal events: Scandinavian cohort study
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