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An association between infantile haemangiomas and erythropoietin treatment in preterm infants
Corinna Doege1, Maria Pritsch, Michael C Frühwald
1Department of Pediatrics, University Children's Hospital of Münster, Albert-Schweitzer Strasse 33, Münster, Germany.
Insights
Erythropoietin therapy may increase the risk of infantile haemangiomas in preterm infants. This study found a higher incidence of these benign vascular tumors in infants treated with erythropoietin, even after accounting for other risk factors.
Area of Science:
- Neonatology
- Pediatric Oncology
- Vascular Biology
Background:
- Infantile haemangiomas are common benign vascular tumors in premature infants.
- Gestational age and birth weight are known risk factors.
- The potential influence of erythropoietin therapy on haemangioma incidence was investigated.
Purpose of the Study:
- To determine if erythropoietin therapy is associated with an increased incidence of infantile haemangiomas in preterm infants.
- To identify erythropoietin therapy as an independent risk factor for haemangioma development.
Main Methods:
- Retrospective analysis of 2563 preterm infants admitted to a Neonatology division.
- Review of hospital charts for clinical data, including erythropoietin treatment and haemangioma diagnosis.
- Multivariable analysis to adjust for known risk factors and oxygen therapy.
Main Results:
- Haemangiomas were diagnosed in 4.3% of preterm infants.
- A higher incidence (12-15%) was observed in infants with lower gestational age (<31 weeks).
- Erythropoietin therapy was an independent risk factor (HR 2.82), particularly in male infants (HR 3.61).
Conclusions:
- Erythropoietin treatment is associated with an increased incidence of infantile haemangiomas.
- This association remains significant after adjusting for other known risk factors.
- Further research may be warranted to understand the underlying mechanisms.
Background:
Infantile haemangiomas are benign vascular neoplasms that occur frequently in premature infants. The authors hypothesised that in addition to gestational age and birth weight, erythropoietin therapy may influence the incidence of these soft tissue tumours in preterm infants.
Methods:
2563 infants born prematurely and admitted to the Division of Neonatology, University of Heidelberg Medical School were investigated in a retrospective analysis. Hospital charts for all infants were reviewed for clinical data. The primary endpoint was the percentage of infants who had received erythropoietin treatment and were diagnosed with a haemangioma.
Results:
Haemangiomas were diagnosed in 4.3% (n=110) of the 2563 preterm infants. These 110 infants had a median gestational age of 29 weeks (IQR 27-33 weeks) and the female:male ratio was 1.8:1. A higher incidence of haemangiomas (12-15%) was detected in premature infants with a lower gestational age (<31 weeks). Erythropoietin therapy was shown to be an independent risk factor after adjusting for all other known factors and oxygen therapy in multivariable analysis (HR 2.82, 95% CI 1.55 to 5.12). Subgroup analysis revealed that the effect was more pronounced in male than female infants (HR 3.61, 95% CI 1.52 to 8.57).
Conclusions:
This retrospective study demonstrates that erythropoietin treatment is associated with an increase in the incidence of these benign vascular tumours after adjusting for all other factors.
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