Evidence map›Paper›PMID 41893841›Full record

ArticleJAMA network open2026

Discontinuation of RAS Inhibition After an Acute Decline in Estimated Glomerular Filtration Rate.

Elaine Ku, Navdeep Tangri, Ranveer Brar, Charles E McCulloch, Mark J Sarnak

Abstract read
In one paragraph

Article in JAMA network open, 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

5 authors.

Elaine KuDivision of Nephrology, Departments of Medicine and Pediatrics, University of California, San Francisco.
Navdeep TangriDepartment of Community Health Sciences, Max Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Ranveer BrarDepartment of Community Health Sciences, Max Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Charles E McCullochDepartment of Epidemiology and Biostatistics, University of California, San Francisco.
Mark J SarnakDivision of Nephrology, Department of Medicine, Tufts Medical Center, Boston, Massachusetts.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Although renin-angiotensin system inhibitors (RASIs) slow the progression of chronic kidney disease, these agents are frequently discontinued if acute declines in the estimated glomerular filtration rate (eGFR) occur after their initiation. Objective: To examine the risk for cardiovascular, kidney, and mortality outcomes associated with discontinuation vs continuation of RASIs in patients with an acute decline in eGFR after RASI initiation. Design, Setting, and Participants: This retrospective cohort study using a target trial emulation approach leveraged electronic health record data from the Manitoba Centre for Health Policy that were linked to vital statistics in the province of Manitoba, Canada. Propensity score matching was applied to identify adults (aged ≥18 years) receiving new prescriptions for RASIs between January 1, 2008, and December 31, 2021, who subsequently had an eGFR decline of more than 15% within 90 days of the prescription. Data were analyzed between January 14, 2024, and January 22, 2026. Exposure: RASI discontinuation (vs continuation) defined based on whether a RASI prescription was refilled within 90 days after a decline in eGFR of 15% had occurred. Main Outcomes and Measures: The primary outcomes of end-stage kidney disease (ESKD) or death, and secondary outcomes of major adverse cardiovascular events (MACEs) (including myocardial infarction, heart failure, stroke, or cardiovascular mortality) or acute kidney injury (AKI) were examined after 180 days. Cox proportional hazards models were used to compare the exposure with the outcomes in an intention-to-treat approach. Results: A total of 4233 patients (mean [SD] age, 64.6 [16.2] years; 2697 male [51.1%]) who had a more than 15% decline in eGFR after starting a RASI were included; 1411 patients (33.3%) discontinued RASIs, and 2822 (66.6%) continued RASIs . Patients who discontinued vs continued RASIs had a higher risk of death (hazard ratio [HR], 1.23; 95% CI, 1.07-1.41) and ESKD (HR, 1.74; 95% CI, 1.28-2.38). Their risk of MACEs (HR, 1.13; 95% CI, 0.99-1.28) and AKI (HR, 1.11; 95% CI, 0.90-1.37) was not significantly higher. Conclusions and Relevance: This cohort study found that discontinuation of RASIs after an acute decline in eGFR was associated with ESKD and death compared with continuing RASIs. These findings suggest that further study is needed to understand reasons for frequent discontinuation of RASIs and devise strategies to improve their persistent use.

Indexed as

Angiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsGlomerular Filtration RateRenal Insufficiency, ChronicRenin-Angiotensin SystemWithholding TreatmentAgedCardiovascular DiseasesDisease ProgressionFemaleHumansKidney Failure, ChronicMaleManitobaMiddle AgedRetrospective StudiesAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor Antagonists

Identifiers

PMID41893841
PMCPMC13032147

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.