Evidence map›Paper›PMID 41572868›Full record

Observational studyActa dermato-venereologica2026

Higher Doses of Oral Propranolol for Resistant Infantile Haemangio-mas.

Isabelle Dreyfus, Charlène Dénos, Olivia Boccara, Sébastien Barbarot, Véronique Gagey-Caron, Annabel Maruani, Juliette Miquel, Catherine Droitcourt, Michèle Bigorre, Ludovic Martin and 2 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Acta dermato-venereologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Isabelle DreyfusReference Center for rare diseases of the skin, CHU Toulouse Larrey, Toulouse, France. dreyfus.i@chu-toulouse.fr.
Charlène DénosReference Center for rare diseases of the skin, CHU Toulouse Larrey, Toulouse, France.
Olivia BoccaraDermatology Department, Necker Children's Hospital, Assistance publique-hôpitaux de Paris, Paris, France.
Sébastien BarbarotDepartment of Dermatology, Nantes Université, Nantes, France.
Véronique Gagey-CaronDermatology Cabinet, Nantes, France.
Annabel MaruaniDepartment of Dermatology, Unit of Pediatric Dermatology, University of Tours, Inserm 1246-SPHERE, CHRU Tours, Tours, France.
Juliette MiquelDepartment of Dermatology and Pediatric Dermatology, CHU La Réunion site Saint Pierre, La Réunion, France.
Catherine DroitcourtDepartment of Dermatology and Venereology, CHU Rennes, Rennes, France.
Michèle BigorreOrthopedic surgery and infantile plastic surgery, CHU Montpellier, Hôpital Lapeyronie, Montpellier, France.
Ludovic MartinDepartment of Dermatology and Venereology, CHU Angers, Angers, France.
Christine Leauté-LabrèzeDepartment of Dermatology and Pediatric Dermatology, CHU Bordeaux, Hôpital Pellegrin, Bordeaux, France.
Juliette Mazereeuw-HautierReference Center for rare diseases of the skin, CHU Toulouse Larrey, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Propranolol at 3 mg/kg/day is considered the gold standard for treating infantile haemangiomas. Nevertheless, the management of propranolol-resistant infantile haemangiomas (PRIH) remains challenging. This national multicentre retrospective observational study includes all PRIHs who received propranolol > 3 mg/kg/day. The study aims to investigate the pattern of PRIHs, assess the effects and tolerance of a higher dose, and identify predictive factors for response to this increased dosage. Fifteen PRIHs were included (prevalence 0.45%), mainly females, and most presented with a large lesion. Three distinct patterns of PRIH were identified: facial segmental lesions (47%), facial localized lesions with a subcutaneous component (40%), and body-localized mixed and ulcerated lesions (13%). Six PRIH (40%) responded to the higher dose (from 3.75 to 4 mg/kg/day). Three predictive factors were significantly associated with a good response: IGIc-IH1 at the end of 3 mg/kg/day regimen (OR = 22.9, 95% CI [1.2-1844.1]), a duration of 3.5 months or more at 3 mg/kg/day (OR = 17.5, 95% CI [1.22-250.37]), and 7 months or more at > 3 mg/kg/day (OR = 17.5, 95% CI [1.22-250.37]). Tolerance was generally good, although one patient experienced severe hypotension during dose escalation. Propranolol doses higher than 3 mg/kg/day may therefore be considered a potential treatment option for PRIHs.

Indexed as

Adrenergic beta-AntagonistsDrug Resistance, NeoplasmPropranololSkin NeoplasmsAdministration, OralFemaleHumansInfantMaleRetrospective StudiesTime FactorsTreatment OutcomeAdrenergic beta-AntagonistsPropranolol

Identifiers

PMID41572868
PMCPMC12836399

What OpenQuestion holds

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Registered trials

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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.