Evidence map›Paper›PMID 42246961›Full record

ArticlePediatric cardiology2026

Adenosine Dose and Cardioversion in Pediatric Supraventricular Tachycardia: A Systematic Review and Meta-Analysis.

Laís Dos Santos, Thaís Martins Shehan, Candela Lang, Ricardo Sanchez Algarin, Ingrid Bezerra de Oliveira Ribeiro, Paulo Cesar Mattos Dourado de Mesquita, Guilherme Dagostin de Carvalho

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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.

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0citing papers in PubMed
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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

5 · Who and what money

Authors and funding

7 authors.

Laís Dos SantosUniversidade Federal do Ceará, Fortaleza, Brazil. dralaisdossantos@gmail.com.
Thaís Martins ShehanUniversidade Federal Fluminense, Niterói, Brazil.
Candela LangUniversidad Austral, Pilar, Argentina.
Ricardo Sanchez AlgarinUniversidad Simón Bolívar, Barranquilla, Colombia.
Ingrid Bezerra de Oliveira RibeiroUniversidade Estadual do Piauí, Teresina, Brazil.
Paulo Cesar Mattos Dourado de MesquitaFaculdade de Medicina Nova Esperança, Mossoró, Brazil.
Guilherme Dagostin de CarvalhoInstituto Dante Pazzanese de Cardiologia, São Paulo, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

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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.