ArticlePediatric cardiology2026
Adenosine Dose and Cardioversion in Pediatric Supraventricular Tachycardia: A Systematic Review and Meta-Analysis.
Article in Pediatric cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.
What it found
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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.
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Corrections and comments
- Erratum issued
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Although adenosine is recommended as first-line therapy for pediatric supraventricular tachycardia (SVT), the optimal weight-based dose for reliable first-pass cardioversion remains uncertain. To evaluate the association between weight-based adenosine dosing and cardioversion probability in children with SVT. PubMed, Embase, Scopus, and the Cochrane Library were searched from inception through July 2025. Of 3,195 records identified, 9 observational studies including 480 patients and 1,369 intravenous adenosine bolus administrations met inclusion criteria. Two reviewers independently screened studies and extracted bolus-level cardio version data. Risk of bias was assessed with ROBINS-I and certainty of evidence with GRADE. Logit-transformed cardioversion proportions were pooled using a three-level random-effects model to account for clustering of multiple bolus administrations within studies. Successful cardioversion to sinus rhythm following an individual intravenous adenosine bolus. Conversion probability increased across prespecified weight-based dose categories: 25% (95% CI, 14%-40%) at doses < 100 µg/kg, 38% (95% CI, 31%-46%) at 100 µg/kg, 47% (95% CI, 39%-55%) at 150-225 µg/kg, and 59% (95% CI, 48%-69%) at 250-400 µg/kg. In the three-level model, overall conversion probability was 41% (95% CI, 35% to 47%). Increasing dose was associated with higher odds of cardioversion (β = 0.0054 per µg/kg; OR per 100 µg/kg, 1.72 [95% CI, 1.43 to 2.07]; P < .001), with residual heterogeneity primarily attributable to between-study variability. Higher weight-based adenosine doses were consistently associated with greater conversion probability across observational cohorts. These findings suggest that commonly used initial doses may underperform in many children and justify prospective trials evaluating mechanism-specific initial dosing strategies.
Identifiers
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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.