ArticleJCEM case reports2026
The use of automated insulin delivery system in people with type 1 diabetes and end stage kidney disease on hemodialysis.
Article in JCEM case 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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Managing patients with type 1 diabetes (T1D) with end stage kidney disease (ESKD) on hemodialysis presents unique challenges due to altered insulin kinetics and rapid glucose fluxes. We report the case of a 48-year-old female with long-standing T1D and ESKD who suffered from severe glycemic variability and recurrent hypoglycemia despite intensive insulin management. The patient was transitioned to the Medtronic MiniMed™ 780G automated insulin delivery (AID) system. Although glycemic control generally improved, she experienced frequent intradialytic hypoglycemia and hypotension. A specialized protocol was implemented to mitigate these risks: setting a temporary glucose target of 150 mg/dL (SI: 8.3 mmol/L) (reference range, 70-180 mg/dL [SI: 3.9-10 mmol/L]) two hours prior to dialysis, suspending the pump upon dialysis initiation, and resuming delivery only when sensor glucose exceeded 200 mg/dL (SI: 11.1 mmol/L). Following this adjustment, intradialytic adverse events were resolved, and the patient achieved a time in range of 69% with a glucose management indicator (GMI) of 7.0%. This case demonstrates that while standard AID algorithms are not calibrated for dialysis, they can be safely employed in ESKD patients through tailored modifications, specifically strategic pump suspension and proactive target elevation.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.