SynthesisEuropean journal of pediatrics2025
Early vs. late initiation of long-acting basal insulin during IV insulin in pediatric diabetic ketoacidosis: a GRADE-assessed systematic review and meta-analysis.
Synthesis in European journal of pediatrics, 2025. 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
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The effectiveness of starting long-acting basal insulin during the intravenous (IV) phase of pediatric diabetic ketoacidosis (DKA) is still a topic of debate. We question whether it can improve outcomes without causing additional harm. We performed a systematic review following PRISMA guidelines and a random-effects meta-analysis (PROSPERO: CRD420251155626) of studies involving patients under 18 years with DKA. We defined "early basal" as starting subcutaneous glargine or detemir while IV insulin was still being administered, with a planned overlap of four hours or more. Comparators began basal insulin at or after stopping IV insulin or had less than 4 h of overlap. The main outcome was the time to resolution of DKA/acidosis. Secondary outcomes included the duration of IV insulin, hospital length of stay (LOS), hypoglycemia, and hypokalemia. We assessed the risk of bias using RoB-2 and NOS, and we evaluated the certainty of evidence using GRADE. Eight studies (3 RCTs, 5 cohorts; n = 1325) met our criteria (695 early-basal, 630 comparator). Early basal insulin reduced the time to DKA/acidosis resolution (4 studies; n = 445), showing a mean difference (MD) of - 3.58 h (95% CI - 6.13 to - 1.03; p = 0.006; I
conclusionsIn pediatric DKA, starting long-acting basal insulin during IV insulin administration with an overlap of four hours or more speeds up metabolic resolution by about 3 to 5 h without raising the risk of hypoglycemia or hypokalemia. The effects on the duration of IV insulin and LOS are inconsistent. These findings support the use of early basal insulin as a safe transition strategy. Further multicenter pragmatic RCTs with standardized definitions for overlap are needed. WHAT IS KNOWN: • Diabetic ketoacidosis (DKA) in children is a major medical emergency requiring prompt treatment to avoid severe complications, with the standard treatment involving intravenous (IV) insulin administration. • Long-acting basal insulin has been shown in adult populations to hasten recovery from DKA without increasing the risk of hypoglycemia or hypokalemia. WHAT IS NEW: • This meta-analysis emphasizes the effects on the pediatric population, providing high-certainty evidence that early initiation of long-acting basal insulin during IV insulin infusion in pediatric DKA significantly reduces the time to DKA resolution. • The study confirms that early basal insulin does not increase the risk of hypoglycemia or hypokalemia, supporting its safety as a transition strategy in pediatric DKA management.
Indexed as
Identifiers
41296041What 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.