Comparison of the risk of acute outcomes between patients with type 2 diabetes exposed to dapagliflozin and those exposed to other antidiabetic treatments

Study type
Protocol
Date of Approval
Study reference ID
15_220
Lay Summary

The overall goal of this research study is to estimate the risk of hospitalization for acute kidney injury (AKI), hospitalization for acute liver injury (ALI), and severe complications of urinary tract infections (UTI) in patients who are prescribed dapagliflozin compared to patients prescribed other oral antidiabetic drugs (ADs). Dapagliflozin and other antidiabetic drugs are used to treat type 2 diabetes mellitus. Because of the way dapagliflozin works in the body, there is interest in further evaluating its safety in a large population. The study will be implemented in three administrative health care data sources in two countries: in the United Kingdom, the Clinical Practice Research Datalink (CPRD); and in the United States, the Centers for Medicare and Medicaid Services (CMS) Medicare databases and the HealthCore Integrated Research Database (HIRD). Individuals in the databases will be included in the study if they meet the following age criteria; 18 years and older (CPRD and HIRD), or 65 years or older (Medicare). The final study report will be submitted for review to the European Medicines Agency to ensure the continued safety of the drug and will be submitted for publication in a scientific journal.

Technical Summary

This cohort study compares the incidences of hospitalization for AKI, hospitalization for ALI, and sex-specific incidence of severe complications of UTI among new users of dapagliflozin, a sodium-glucose cotransporter 2 (SGLT2) inhibitor medication, with those among new users of other specific ADs. The study duration is 5 years. Follow-up will start on the date a patient has a first prescription recorded in CPRD or dispensing recorded in the other data sources for a study drug, and will continue until first occurrence of any acute end-point, death, discontinuation from the study database, or the end of the study. The study will be implemented in adults in three administrative health care data sources in two countries: United Kingdom: the Clinical Practice Research Datalink; and the United States: the Centers for Medicare and Medicaid Services Medicare databases and the HealthCore Integrated Research Database. Propensity scores will be estimated at cohort entry by logistic regression models. Incidence rates of each outcome will be determined in each cohort. Propensity score stratification will be used to estimate adjusted incidence rate ratios comparing dapagliflozin with comparator ADs for each outcome of interest with 95% confidence intervals. Analyses will be conducted in each data source, and a pooled estimate will be calculated using aggregate data, if deemed appropriate.

Collaborators

Kay Johannes - Chief Investigator - RTI Health Solutions ( USA )
Leah McGrath - Corresponding Applicant - RTI Health Solutions ( USA )
Alejandro Arana Navarro - Collaborator - RTI Health Solutions ( USA )
Alicia Gilsenan - Collaborator - RTI Health Solutions ( USA )
Brian Calingaert - Collaborator - RTI Health Solutions ( USA )
David Martinez - Collaborator - RTI Health Solutions ( USA )
Elizabeth Andrews - Collaborator - RTI Health Solutions ( USA )
Estel Plana Hortoneda - Collaborator - RTI Health Solutions ( USA )
Heather Danysh - Collaborator - RTI Health Solutions ( USA )
J. Bradley Layton - Collaborator - RTI Health Solutions ( USA )
Jaume Aguado - Collaborator - RTI Health Solutions ( USA )
Jennifer Bartsch - Collaborator - RTI Health Solutions ( USA )
Joan Fortuny - Collaborator - RTI Health Solutions ( USA )
Jordi Castellsague - Collaborator - RTI Health Solutions ( USA )
Karolina Andersson Sundell - Collaborator - Astra Zeneca R&D Molndal Sweden
Lia Gutierrez - Collaborator - RTI Health Solutions ( USA )
Lisa McQuay - Collaborator - RTI Health Solutions ( USA )
MANEL PLADEVALL - Collaborator - RTI Health Solutions ( USA )
Maria Reynolds - Collaborator - RTI Health Solutions ( USA )
Ryan Ziemiecki - Collaborator - RTI Health Solutions ( USA )
Shannon Hunter - Collaborator - RTI Health Solutions ( USA )
Sophie Shen - Collaborator - Bristol-Myers Squibb Pharmaceuticals Limited - UK ( BMS )
Zhou Xiaolei - Collaborator - RTI Health Solutions ( USA )

Linkages

HES Admitted Patient Care;HES Admitted Patient Care;HES Outpatient;HES Outpatient;ONS Death Registration Data;ONS Death Registration Data;Patient Level Index of Multiple Deprivation;Patient Level Index of Multiple Deprivation;Practice Level Index of Multiple Deprivation;Practice Level Index of Multiple Deprivation