ArticleScientific reports2026
Novel biodegradable device for transcatheter closure of atrial septal defects.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.
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
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
- Global research trends and hotspots of bioresorbable occluders for congenital heart disease: a bibliometric analysis.Frontiers in cardiovascular medicine · 2026Pooled it
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
The long-term safety of transcatheter atrial septal defect (ASD) closure devices remains a concern, despite favorable short- and mid-term outcomes. We developed a fully biodegradable atrial septal occluder (ASO) delivered via femoral vein catheterization. The device comprises a double-disc main body of poly(L-lactide-co-ɛ-caprolactone) (P(LA/CL)) and a locking component of polylactic acid with palladium alloy markers. In vitro, pH decreased from 7.56 ± 0.01 to 6.58 ± 0.03 over 16 weeks, mechanical strength was lost by 12 weeks, and mass decreased to 60% at 48 weeks. Device weight declined from 268,002 ± 3,226 (Da) to 2,405.8 ± 159.2 (Da) by 36 weeks. ASDs were closed in twelve pigs in vivo using the Brockenbrough technique. No perioperative or postoperative deaths occurred. Echocardiography and angiography performed up to 18 months confirmed complete closure without residual shunt. Macroscopic examination revealed persistence at 6 months, marked degradation at 12 months, and near-complete resorption with tissue replacement at 18 months. Histological examination revealed cellular infiltration and neotissue formation. These findings indicate that the biodegradable ASO is safe and effective for ASD closure and promotes host tissue regeneration, supporting its translation into clinical trials.
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