| Literature DB >> 24997149 |
Cornelia Zeidler1, Ulrike A H Grote2, Anna Nickel2, Beate Brand2, Göran Carlsson3, Emília Cortesão4, Carlo Dufour5, Caroline Duhem6, Gundula Notheis7, Helen A Papadaki8, Hannah Tamary9, Geir E Tjønnfjord10, Fabio Tucci11, Jan Van Droogenbroeck12, Christiane Vermylen13, Jaroslava Voglova14, Blanca Xicoy15, Karl Welte2.
Abstract
Long-term granulocyte-colony stimulating factor treatment has been shown to be safe and effective in severe chronic neutropenia patients. However, data on its use during pregnancy are limited. To address this issue, we analyzed all pregnancies reported to the European branch of the Severe Chronic Neutropenia International Registry since 1994. A total of 38 pregnancies in 21 women with chronic neutropenia (16 pregnancies in 10 women with congenital, 10 in 6 women with cyclic, 12 in 5 women with idiopathic neutropenia) were reported. Granulocyte-colony stimulating factor was administered throughout pregnancy in 16 women and for at least one trimester in a further 5 women. No major differences were seen between treated and untreated women with respect to pregnancy outcome, newborn complications and infections. In addition, we evaluated the genetic transmission of known or suspected genetic defects in 16 mothers having 22 newborns as well as in 8 men fathering 15 children. As a proof of inheritance, neutropenia was passed on to the newborn in 58% from female and in 62% from male patients with ELANE mutations, but also to some newborns from parents with unknown gene mutation. Based on our results, granulocyte-colony stimulating factor therapy has been shown to be safe for mothers throughout pregnancies and for newborns without any signs of teratogenicity. With an increasing number of adult patients, genetic counseling prior to conception and supportive care of mothers during pregnancy are crucial. The acceptance of having affected children may reflect the high quality of life obtained due to this treatment. Copyright© Ferrata Storti Foundation.Entities:
Mesh:
Year: 2014 PMID: 24997149 PMCID: PMC4116840 DOI: 10.3324/haematol.2013.099101
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941