Evidence map›Paper›PMID 42318531›Full record

ArticleKidney international reports2026

Modelled CKD Benefits of Broad Sodium-Glucose Cotransporter-2 Inhibitor Eligibility in the UK.

Navdeep Tangri, Stacey Priest, Anthony Zara, Bo Ren Long, Naveen Rao, Clélia-Elsa Froguel, Fiona Adshead, Steven Chadban

Abstract read
In one paragraph

Article in Kidney international reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Navdeep TangriUniversity of Manitoba, Winnipeg, Manitoba, Canada.
Stacey PriestValue & Evidence, EVERSANA, Burlington, Ontario, Canada.
Anthony ZaraValue & Evidence, EVERSANA, Burlington, Ontario, Canada.
Bo Ren LongValue & Evidence, EVERSANA, Burlington, Ontario, Canada.
Naveen RaoBioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.
Clélia-Elsa FroguelBioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.
Fiona AdsheadSustainable Healthcare Coalition, Devon, UK.
Steven ChadbanRoyal Prince Alfred Hospital, Camperdown, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Chronic kidney disease (CKD) affects >10% of the UK population and is expected to increase. Sodium-glucose cotransporter-2 inhibitors (SGLT-2is) are effective at slowing CKD progression; however, they are underprescribed because of barriers, including the need for urine albumin-creatinine ratio (UACR) testing and lack of guideline alignment. This study sought to quantify the clinical, economic, and environmental trade-offs of broad and restrictive SGLT-2i access in the UK. Methods: Five scenarios exploring a range of SGLT-2i eligibility criteria for patients with CKD were modelled over 10 years, beginning from 2025, using the validated IMPACT CKD individual-level microsimulation model. SGLT-2i treatment was modelled to improve estimated glomerular filtration rate (eGFR) decline and reduce cardiovascular (CV) events and acute kidney injury. A 3.5%/yr discount was applied to economic outcomes. Results: A maximally inclusive SGLT-2i scenario was compared with each of the less inclusive SGLT-2i eligibility criteria scenarios. Increasingly restrictive scenarios were projected to increase dialysis and all-cause mortality by 4.0% to 17.2% and 1.3% to 4.3%, respectively. Resulting from higher mortality, CKD prevalence was projected to decrease by 0.5% to 1.4%. Non-kidney replacement therapy (KRT) CKD costs and KRT costs were projected to increase by 0.7% to 2.1% and 2.4% to 10.6%, respectively, with increasingly restrictive scenarios. Total costs were projected to decrease by 15.2% to 33.9% because fewer patients are treated. Because of shifts to later stages, KRT-related environmental burden was projected to increase by 3.1% to 14.9%. Conclusion: Broad SGLT-2i eligibility criteria would likely reduce the holistic burden of CKD for patients, the National Health Service (NHS), and the environment.

Indexed as

chronic kidney diseasedisease burdenhealth policy modelkidney replacement therapysodium-glucose transporter 2 inhibitortreatment eligibility

Identifiers

PMID42318531
PMCPMC13273866

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.