Recurrence rate of infantile hemangioma after oral propranolol therapy

被引:15
作者
Frongia, Giovanni [1 ]
Byeon, Ji-Oun [1 ]
Mehrabi, Arianeb [2 ]
Guenther, Patrick [1 ]
机构
[1] Univ Hosp Heidelberg, Div Pediat Surg, Dept Gen Visceral & Transplantat Surg, Heidelberg, Germany
[2] Univ Hosp Heidelberg, Dept Gen Visceral & Transplantat Surg, Heidelberg, Germany
关键词
Infantile hemangioma; Propranolol; Recurrence; Relapse; RISK-FACTORS; SAFETY;
D O I
10.1007/s00431-020-03872-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Oral propranolol is the treatment of choice for infantile hemangiomas. The growth relapse rate following oral propranolol therapy is not well established in the literature. The present study aimed at determining predictors of growth relapse of infantile hemangiomas after discontinuation of oral propranolol therapy. A retrospective analysis was performed of all cases of infantile hemangiomas aged <= 12 months undergoing oral propranolol therapy in a 6-year period. Of the 198 cases, regrowth after oral propranolol therapy was observed in 35 patients (18%). Facial hemangiomas showed a higher (p = 0.003) relapse rate as compared with other hemangiomas (27 out of 107 facial cases vs. 8 out of 91 with other location, respectively 25% and 8.8%). Of 35 growth relapses cases, 66% of cases (23 in total, 18 facial and 5 otherwise located hemangiomas) underwent a second cycle of oral propranolol therapy (median length of treatment 3 months, interquartile range 2-3). All cases had a successful outcome, either after a single cycle oral propranolol therapy (163 cases, 82%), or in case of regrowth, after a second therapy cycle (23 cases, 12%) or further conservative management (12 cases, 6%). Conclusion: Facial infantile hemangiomas relapse earlier and more frequently after oral propranolol therapy. We suggest to closely monitor these patients, as a second cycle of propranolol may be indicated. Prolonged oral propranolol therapy might be considered for facial infantile hemangiomas.
引用
收藏
页码:585 / 590
页数:6
相关论文
共 32 条
  • [11] FINN MC, 1983, J PEDIATR SURG, V18, P894
  • [12] Adverse effects of systemic glucocorticosteroid therapy in infants with hemangiomas
    George, ME
    Sharma, V
    Jacobson, J
    Simon, S
    Nopper, AJ
    [J]. ARCHIVES OF DERMATOLOGY, 2004, 140 (08) : 963 - 969
  • [13] Propranolol treatment for severe infantile hemangiomas: a single-centre 3-year experience
    Georgountzou, Anastasia
    Karavitakis, Emmanouil
    Klimentopoulou, Alexandra
    Xaidara, Athina
    Kakourou, Talia
    [J]. ACTA PAEDIATRICA, 2012, 101 (10) : E469 - E474
  • [14] Long-Term Treatment with Oral Propranolol Reduces Relapses of Infantile Hemangiomas
    Giachetti, Ana
    Garcia-Monaco, Ricardo
    Sojo, Magdalena
    Scacchi, Maria F.
    Cernadas, Carolina
    Guerchicoff Lemcke, Marianna
    Dovasio, Fernanda
    [J]. PEDIATRIC DERMATOLOGY, 2014, 31 (01) : 14 - 20
  • [15] Incidence and treatment of infantile haemangioma in preterm infants
    Goelz, Rangmar
    Poets, Christian F.
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2015, 100 (01): : F85 - F91
  • [16] Dramatic Shift in the Infantile Hemangioma Treatment Paradigm at a Single Institution
    Gomulka, Jennifer
    Siegel, Dawn H.
    Drolet, Beth A.
    [J]. PEDIATRIC DERMATOLOGY, 2013, 30 (06) : 751 - 752
  • [17] Propranolol in a case series of 174 patients with complicated infantile haemangioma: indications, safety and future directions
    Hermans, D. J. J.
    Bauland, C. G.
    Zweegers, J.
    van Beynum, I. M.
    van der Vleuten, C. J. M.
    [J]. BRITISH JOURNAL OF DERMATOLOGY, 2013, 168 (04) : 837 - 843
  • [18] Infantile hemangiomas: How common are they? A systematic review of the medical literature
    Kilcline, Christine
    Frieden, Ilona J.
    [J]. PEDIATRIC DERMATOLOGY, 2008, 25 (02) : 168 - 173
  • [19] A Randomized, Controlled Trial of Oral Propranolol in Infantile Hemangioma
    Leaute-Labreze, C.
    Hoeger, P.
    Mazereeuw-Hautier, J.
    Guibaud, L.
    Baselga, E.
    Posiunas, G.
    Phillips, R. J.
    Caceres, H.
    Lopez Gutierrez, J. C.
    Ballona, R.
    Friedlander, S. F.
    Powell, J.
    Perek, D.
    Metz, B.
    Barbarot, S.
    Maruani, A.
    Szalai, Z. Z.
    Krol, A.
    Boccara, O.
    Foelster-Holst, R.
    Febrer Bosch, M. I.
    Su, J.
    Buckova, H.
    Torrelo, A.
    Cambazard, F.
    Grantzow, R.
    Wargon, O.
    Wyrzykowski, D.
    Roessler, J.
    Bernabeu-Wittel, J.
    Valencia, A. M.
    Przewratil, P.
    Glick, S.
    Pope, E.
    Birchall, N.
    Benjamin, L.
    Mancini, A. J.
    Vabres, P.
    Souteyrand, P.
    Frieden, I. J.
    Berul, C. I.
    Mehta, C. R.
    Prey, S.
    Boralevi, F.
    Morgan, C. C.
    Heritier, S.
    Delarue, A.
    Voisard, J-J
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (08) : 735 - 746
  • [20] Leaute-Labreze C, 2011, J EUR ACAD DERMATOL, V25, P11, DOI DOI 10.1111/j.1468-3083.2011.04105.x