Safety of Drugs during Pregnancy and Breastfeeding in Cystic Fibrosis Patients
Author(s) -
Alice Panchaud,
Ermindo R. Di Paolo,
Angela Koutsokera,
Ursula Winterfeld,
Etienne Weisskopf,
David Baud,
Alain Sauty,
Chantal Csajka
Publication year - 2016
Publication title -
respiration
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.264
H-Index - 81
eISSN - 1423-0356
pISSN - 0025-7931
DOI - 10.1159/000444088
Subject(s) - medicine , cystic fibrosis , pregnancy , breastfeeding , lactation , obstetrics , intensive care medicine , breast feeding , pediatrics , genetics , biology
Health management of cystic fibrosis (CF) patients should be maximized during pregnancy and breastfeeding because of its significant impact on the maternal and newborn outcomes. Thus, numerous drugs will have to be continued during pregnancy and lactation. Most of the drugs representing CF treatment lines cross the placenta or are excreted into human milk. Research addressing the risks and benefits of drugs used in CF patients during pregnancy and lactation is often incomplete or challenged by limited methodology, which often leads to conflicting or inconclusive results. Yet, potential treatment benefits for CF pregnant patients most often outbalance potential risks for the unborn child.
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