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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.
Pollock, Carol; Sanchez, Juan Jose Garcia; Carrero, Juan-Jesus; Kumar, Supriya; Pecoits-Filho, Roberto; Lam, Carolyn S P; Chen, Hungta; Kanda, Eiichiro; Lainscak, Mitja; Wheeler, David C.
Afiliação
  • Pollock C; Royal North Shore Hospital, Kolling Institute, University of Sydney, St Leonards, New South Wales, Australia.
  • Sanchez JJG; Global Market Access and Pricing, BioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.
  • Carrero JJ; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Kumar S; Real World Data Science, BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, Maryland, USA.
  • Pecoits-Filho R; School of Medicine, Pontifical Catholic University of Parana, Curitiba, Brazil.
  • Lam CSP; Arbor Research Collaborative for Health, Ann Arbor, Michigan, USA.
  • Chen H; Department of Cardiology, National Heart Centre Singapore, Singapore City, Singapore.
  • Kanda E; Duke-NUS Medical School, Singapore City, Singapore.
  • Lainscak M; Medical and Payer Evidence Statistics, BioPharmaceuticals Medical, AstraZeneca, Gaithersburg, Maryland, USA.
  • Wheeler DC; Kawasaki Medical School, Kurashiki, Japan.
Diabet Med ; 41(2): e15200, 2024 Feb.
Article em En | MEDLINE | ID: mdl-37578188
ABSTRACT

AIMS:

To 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).

METHODS:

Data 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.

RESULTS:

Of 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.

CONCLUSIONS:

Individuals with CKD and T2D had many combinations of therapies and substantial follow-up time on therapy. These results highlight opportunities for improved CKD management.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Insuficiência Renal Crônica / Metformina Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adolescent / Adult / Humans Idioma: En Revista: Diabet Med Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Insuficiência Renal Crônica / Metformina Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Adolescent / Adult / Humans Idioma: En Revista: Diabet Med Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália