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. 2024 Jun 3;7(6):e2418808.
doi: 10.1001/jamanetworkopen.2024.18808.

Concordance With Screening and Treatment Guidelines for Chronic Kidney Disease in Type 2 Diabetes

Affiliations

Concordance With Screening and Treatment Guidelines for Chronic Kidney Disease in Type 2 Diabetes

Daniel Edmonston et al. JAMA Netw Open. .

Abstract

Importance: Chronic kidney disease (CKD) is an often-asymptomatic complication of type 2 diabetes (T2D) that requires annual screening to diagnose. Patient-level factors linked to inadequate screening and treatment can inform implementation strategies to facilitate guideline-recommended CKD care.

Objective: To identify risk factors for nonconcordance with guideline-recommended CKD screening and treatment in patients with T2D.

Design, setting, and participants: This retrospective cohort study was performed at 20 health care systems contributing data to the US National Patient-Centered Clinical Research Network. To evaluate concordance with CKD screening guidelines, adults with an outpatient clinician visit linked to T2D diagnosis between January 1, 2015, and December 31, 2020, and without known CKD were included. A separate analysis reviewed prescription of angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) and sodium-glucose cotransporter 2 (SGLT2) inhibitors in adults with CKD (estimated glomerular filtration rate [eGFR] of 30-90 mL/min/1.73 m2 and urinary albumin-to-creatinine ratio [UACR] of 200-5000 mg/g) and an outpatient clinician visit for T2D between October 1, 2019, and December 31, 2020. Data were analyzed from July 8, 2022, through June 22, 2023.

Exposures: Demographics, lifestyle factors, comorbidities, medications, and laboratory results.

Main outcomes and measures: Screening required measurement of creatinine levels and UACR within 15 months of the index visit. Treatment reflected prescription of ACEIs or ARBs and SGLT2 inhibitors within 12 months before or 6 months following the index visit.

Results: Concordance with CKD screening guidelines was assessed in 316 234 adults (median age, 59 [IQR, 50-67] years), of whom 51.5% were women; 21.7%, Black; 10.3%, Hispanic; and 67.6%, White. Only 24.9% received creatinine and UACR screening, 56.5% received 1 screening measurement, and 18.6% received neither. Hispanic ethnicity was associated with lack of screening (relative risk [RR], 1.16 [95% CI, 1.14-1.18]). In contrast, heart failure, peripheral arterial disease, and hypertension were associated with a lower risk of nonconcordance. In 4215 patients with CKD and albuminuria, 3288 (78.0%) received an ACEI or ARB; 194 (4.6%), an SGLT2 inhibitor; and 885 (21.0%), neither therapy. Peripheral arterial disease and lower eGFR were associated with lack of CKD treatment, while diuretic or statin prescription and hypertension were associated with treatment.

Conclusions and relevance: In this cohort study of patients with T2D, fewer than one-quarter received recommended CKD screening. In patients with CKD and albuminuria, 21.0% did not receive an SGLT2 inhibitor or an ACEI or an ARB, despite compelling indications. Patient-level factors may inform implementation strategies to improve CKD screening and treatment in people with T2D.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Edmonston reported receiving grant funding from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study. Dr Mulder reported receiving institutional fees from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study. Dr Lampron reported receiving grant funding from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study. Dr Marsolo reported receiving grant funding from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study and grant funding from Bayer AG, Bristol Myers Squibb, Amgen Inc, Novartis AG, CSL Seqirus, and Genentech Inc outside the submitted work. Dr Chang reported consulting for Novartis AG and Amgen Inc and receiving grant funding from Novo Nordisk A/S, Bayer AG, Novartis AG, and Boehringer Ingelheim Pharmaceuticals Inc outside the submitted work. Dr Ford reported receiving grant funding from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study. Dr Fonseca reported receiving personal fees from Bayer AG, Boehringer Ingelheim Pharmaceuticals Inc, and AstraZeneca outside the submitted work. Dr Machineni reported receiving personal fees from Novo Nordisk A/S and Eli Lilly and Co outside the submitted work. Dr Butler reported receiving personal fees from Abbott Laboratories, American Regent Inc, Amgen Inc, Applied Therapeutics, Asklepios BioPharmaceutical Inc, Astellas Pharma US Inc, AstraZeneca, Bayer AG, Boehringer Ingelheim Pharmaceuticals Inc, Boston Scientific Corp, Bristol Myers Squibb, Cardiac Dimensions, CardioCell, Cardior Pharmaceuticals GmbH, CSL Behring, CVRx Inc, Cytokinetics Incorporated, Daxor Corporation, Edwards Lifesciences, Element Science Inc, Faraday Pharmaceuticals, Foundery, G3P, Innolife Pharma Inc, Impulse Dynamics, Imbria, Inventiva Pharma, Ionis Pharmaceuticals Inc, Lexicon Pharmaceuticals Inc, Eli Lilly and Co, LivaNova PLC, Janssen Global Services LLC, Medtronic PLC, Merck & Co Inc, Occlutech, Owkin, Novartis AG, Novo Nordisk A/S, Pharmacosmos, PharmaIN, Pfizer Inc, Prolaio, Regeneron Pharmaceuticals Inc, Renibus Therapeutics Inc, Roche, Salamandra, Sanofi SA, scPharmaceuticals Inc, Secretome Therapeutics, Sequana Medical NV, SQ Innovation Inc, Tenex Health, Tricog Health, Ultromics, CSL Vifor, and ZOLL Medical Corp outside the submitted work. Dr Hunt reported receiving grant funding from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study and grant funding from the BlueCross BlueShield Foundation of South Carolina; the National Heart, Lung, and Blood Institute; the US Environmental Protection Agency; the National Institutes of Health; the National Institute of Arthritis and Musculoskeletal and Skin Diseases; the US Department of Veterans Affairs (VA) Clinical Sciences Research and Development; and the VA Health Services Research and Development Service outside the submitted work. Dr Ahmad reported receiving personal fees from Pfizer Inc and Teladoc Health Inc, editorial support for abstracts and manuscript submissions from Pfizer Inc, and grant funding from Atman Health Inc outside the submitted work. Dr Gordon reported receiving grant funding from the Duke Clinical Research Institute during the conduct of the study. Dr Bosworth reported receiving grant funding from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study and grant funding from Sanofi SA, Boehringer Ingelheim Pharmaceuticals Inc, Novo Nordisk A/S, Better Therapeutics Inc, Walmart Inc, Otsuka Pharmaceutical, Novartis AG, Improved Patient Outcomes, Esperion Therapeutics Inc, Janssen Global Services Inc, Pfizer Inc, and the Elton John Foundation and personal fees from WebMD outside the submitted work. Dr Pagidipati reported receiving grant funding and personal fees from Boehringer Ingelheim Pharmaceuticals Inc during the conduct of the study and research support from Alnylam Pharmaceuticals Inc, Amgen Inc, Bayer AG, Boehringer Ingelheim Pharmaceuticals Inc, Eggland’s Best, Eli Lilly and Co, Novartis AG, Novo Nordisk A/S, and Merck & Co Inc; consulting or serving on the advisory panels for Amgen Inc, Bayer AG, Boehringer Ingelheim Pharmaceuticals Inc, CRISPR Therapeutics AG, Eli Lilly and Co, Esperion Therapeutics Inc, AstraZeneca, Merck & Co Inc, Novartis AG, and Novo Nordisk A/S; serving as executive committee member for trials sponsored by Novo Nordisk A/S and Amgen Inc; serving on the Data and Safety Monitoring Board for trials sponsored by Johnson & Johnson and Novartis AG; and serving on the medical advisory board for Miga Health. No other disclosures were reported.

Figures

Figure.
Figure.. Study Flow Diagrams
ACEI indicates angiotensin-converting enzyme inhibitor; ARB, angiotensin receptor blocker; CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate; FDA, US Food and Drug Administration; PCORnet, Patient-Centered Clinical Research Network; SGLT2, sodium-glucose cotransporter 2; T2D, type 2 diabetes; UACR, urine albumin-to-creatinine ratio.

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