Glucose‐lowering treatment pathways of individuals with chronic kidney disease and type 2 diabetes according to the Kidney Disease: Improving Global Outcomes 2012 risk classification

Author:

Pollock Carol1,Sanchez Juan Jose Garcia2,Carrero Juan‐Jesus3,Kumar Supriya4,Pecoits‐Filho Roberto56,Lam Carolyn S. P.78,Chen Hungta9,Kanda Eiichiro10,Lainscak Mitja11,Wheeler David C.12ORCID

Affiliation:

1. Royal North Shore Hospital, Kolling Institute University of Sydney St Leonards New South Wales Australia

2. Global Market Access and Pricing BioPharmaceuticals Medical, AstraZeneca Cambridge UK

3. Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden

4. Real World Data Science BioPharmaceuticals Medical, AstraZeneca Gaithersburg Maryland USA

5. School of Medicine Pontifical Catholic University of Parana Curitiba Brazil

6. Arbor Research Collaborative for Health Ann Arbor Michigan USA

7. Department of Cardiology National Heart Centre Singapore Singapore City Singapore

8. Duke‐NUS Medical School Singapore City Singapore

9. Medical and Payer Evidence Statistics BioPharmaceuticals Medical, AstraZeneca Gaithersburg Maryland USA

10. Kawasaki Medical School Kurashiki Japan

11. Division of Cardiology, General Hospital Murska Sobota, and Faculty of Medicine University of Ljubljana Ljubljana Slovenia

12. Department of Renal Medicine University College London London UK

Abstract

AbstractAimsTo describe treatment pathways for key glucose‐lowering therapies in individuals with chronic kidney disease (CKD) and type 2 diabetes (T2D) using retrospective data from DISCOVER CKD (NCT04034992).MethodsData were extracted from the UK Clinical Practice Research Datalink (CPRD) linked to Hospital Episode Statistics data (2008–2020) and the US integrated Limited Claims and Electronic Health Records Database (LCED; 2012–2019). Eligible individuals were aged ≥18 years with CKD, identified by two consecutive estimated glomerular filtration rate (eGFR) measures (15–<75 mL/min/1.73 m2; 90–730 days apart; index date was the second measurement) and T2D. Chronological treatment pathways for glucose‐lowering therapies prescribed on or after CKD index to end of follow‐up were computed. Median time and proportion of overall follow‐up time on treatment were described for each therapy by database and by eGFR and urinary albumin‐to‐creatinine ratio (UACR) categories.ResultsOf 36,951 and 4339 eligible individuals in the CPRD and LCED, respectively, median baseline eGFR was 67.8 and 64.9 mL/min/1.73 m2; 64.2 and 63.9% received metformin prior to index; and median (interquartile range) time on metformin during follow‐up was 917 (390–1671) and 454 (192–850) days (accounting for ~75% of follow‐up time in both databases). The frequency of combination treatment increased over time. There were trends towards decreased metformin prescriptions with decreasing eGFR and increasing UACR within each eGFR category.ConclusionsIndividuals with CKD and T2D had many combinations of therapies and substantial follow‐up time on therapy. These results highlight opportunities for improved CKD management.

Funder

AstraZeneca

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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