Evidence map›Paper›PMID 37628313›Full record

ArticleChildren (Basel, Switzerland)2023

Infantile Haemangioma in the Romanian Paediatric Population-Characteristics and Therapeutic Approaches.

Anca-Maria Raicu, George-Florin Danila, Ionut Fernando Secheli, Eugenia Claudia Bratu, Dana Galieta Minca

Abstract read
In one paragraph

Article in Children (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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

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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.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Anca-Maria RaicuDepartment of Public Health and Management, "Carol Davila" University of Medicine and Pharmacy, 050463 Bucharest, Romania.ORCID 0009-0002-7267-9967
George-Florin DanilaDepartment of Paediatric Surgery, Emergency Hospital for Children "M.S.Curie", 041451 Bucharest, Romania.
Ionut Fernando SecheliDepartment of Paediatric Surgery, Emergency Hospital for Children "M.S.Curie", 041451 Bucharest, Romania.
Eugenia Claudia BratuDepartment of Public Health and Management, "Carol Davila" University of Medicine and Pharmacy, 050463 Bucharest, Romania.ORCID 0000-0002-9162-6425
Dana Galieta MincaDepartment of Public Health and Management, "Carol Davila" University of Medicine and Pharmacy, 050463 Bucharest, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infantile haemangioma (IH) is the most common benign tumour in childhood, with an incidence of 4% to 12%. Aim: to describe the characteristics of infantile haemangioma in a sample of Romanian children <2 years old at diagnosis, types of treatment applied, recorded complications and the response to the therapeutic approach. A two-year prospective case series study (August 2019 to August 2021) was carried out. Sample: 117 patients <24 months of age diagnosed with IH at the Emergency Hospital for Children "Marie Sklodowska Curie", in Bucharest, Romania. Five therapeutic approaches were used: oral treatment with propranolol, local treatment with timolol, surgical treatment, topical treatment with steroids and no treatment ("wait and see"). Recorded factors mentioned in the literature were also present in this study population: female patients-68.4%; phototype I-58%. In 53% of cases, IHs had a head and neck location and 10% developed local complications (traumatic bleeding). The majority of patients (86%) required one type of therapy: oral propranolol (51%). A low relapse rate was recorded (4%). We consider that any child with a vascular anomaly should be referred to a highly specialised medical service for therapeutic approach.

Indexed as

infantile haemangiomapaediatric surgerypropranololtimololvascular anomalies

Identifiers

PMID37628313
PMCPMC10453925

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