Evidence map›Paper›PMID 36705724›Full record

ArticleEuropean journal of pediatrics2023

Management of infantile hemangiomas-experience of a tertiary hospital.

Rita Gomes, Luís Salazar, Carolina Fraga, Mário Rui Correia, Joana Barbosa-Sequeira, Alexandre Fernandes, Sílvia Álvares, José Banquart Leitão, Margarida Paiva Coelho

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Article in European journal of pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Off-label use of medicines in South Africa: a review.Orphanet journal of rare diseases · 2024
    Review
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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

9 authors at 2 institutions in 1 country.

Rita GomesPediatrics Department, Centro Materno Infantil Do Norte Albino Aroso, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Porto, Portugal. ritagomesmoreira02@gmail.com.ORCID http://orcid.org/0000-0003-1246-194X
Luís SalazarPediatrics Department, Centro Materno Infantil Do Norte Albino Aroso, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Porto, Portugal.ORCID http://orcid.org/0000-0002-3760-5121
Carolina FragaPediatrics Department, Centro Materno Infantil Do Norte Albino Aroso, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Porto, Portugal.ORCID http://orcid.org/0000-0002-9782-3999
Mário Rui CorreiaPediatric Surgery Department, Centro Materno Infantil Do Norte Albino Aroso, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Porto, Portugal.ORCID http://orcid.org/0000-0002-0999-6524
Joana Barbosa-SequeiraPediatric Surgery Department, Centro Hospitalar Universitário São João, Porto, Portugal.ORCID http://orcid.org/0000-0002-2776-7055
Alexandre FernandesPediatrics Department, Centro Materno Infantil Do Norte Albino Aroso, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Porto, Portugal.
Sílvia ÁlvaresPediatric Cardiology Department, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Unit for Multidisciplinary Research in Biomedicine (UMIB), School of Medicine and Biomedical Sciences (ICBAS), Centro Materno Infantil Do Norte Albino Aroso, Porto, Portugal.ORCID http://orcid.org/0000-0002-2222-5943
José Banquart LeitãoPediatric Surgery Department, Centro Materno Infantil Do Norte Albino Aroso, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Porto, Portugal.
Margarida Paiva CoelhoPediatrics Department, Centro Materno Infantil Do Norte Albino Aroso, Centro Hospitalar Universitário Do Porto (CMIN-CHUPorto), Porto, Portugal.
Universidade do Porto · PTHospital de São João · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of the study is to describe the experience of a multidisciplinary team in a tertiary hospital regarding the management of Infantile Hemangiomas (IH). The method employed is a retrospective analysis of patients with IH followed in a tertiary pediatric hospital between January 2010 and May 2022. A total of 393 IH were diagnosed (56.7% female), with a median age of 5 months (interquartile range (IQR), 3-10). Imaging investigation was necessary for diagnosis and for exclusion of other IH in 9.2% and 14.3%, respectively. Focal (74.0%) and superficial (59.7%) lesions were more frequent as was facial location (35.9%). Pre-treatment ulceration or hemorrhage occurred in 6.6%. At follow-up, 87.4% regressed partially and 12.6% completely; 2.7% relapsed. Propranolol was started in 30.0% of cases for a median period of 9 months (IQR, 6-12), mainly due to esthetic concerns (41.9%). Side effects occurred in 8.3% (sleep disturbance in 5.1%). Only 1.7% were refractory and 5.9% had a rebound effect. Eleven patients were treated with topical timolol and 41 underwent surgery. Patients that were treated with propranolol had more risk factors (p = 0.016) and presented deeper lesions (p < 0.001) with a larger diameter (p < 0.001); total IH regression was less frequent (p < 0.001). Since 2020, twice-daily dosage was more frequently prescribed than three times daily (p = 0.007) and inpatient initiation of propranolol decreased (p = 0.750), without significant difference in the incidence of adverse reactions, duration of treatment, and lesion evolution.  Conclusions: Our protocol proved to be safe and feasible in an outpatient setting and twice daily administration of propranolol was effective. The majority of IH showed at least partial regression. Early detection of high-risk IH is paramount and a multidisciplinary assessment by a specialized team is essential for adequate management. What is Known: • IH are the most common vascular tumors in childhood. Although the majority evolves favorably, treatment may be warranted in selected cases. • Early detection of high-risk IH is paramount, and a multidisciplinary assessment by a specialized team is essential for adequate management. What is New: • One-third of our sample was treated with propranolol. These patients had more risk factors and presented deeper lesions with a larger diameter, and tumor total regression was less frequent. • Our results reinforce safety and feasibility of propranolol initiation in an outpatient setting, including twice daily dosage.

Indexed as

HemangiomaSkin NeoplasmsAdministration, OralAdrenergic beta-AntagonistsChildFemaleHumansInfantMalePropranololRetrospective StudiesTertiary Care CentersTreatment OutcomeAdrenergic beta-AntagonistsPropranololChildrenHemangiomaNeoplasmsPropranololVascular tissue

Identifiers

PMID36705724
OpenAlexW4318241097

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.