Document Detail

Pregnancy and beta-thalassemia: an Italian multicenter experience.
MedLine Citation:
PMID:  19903676     Owner:  NLM     Status:  MEDLINE    
BACKGROUND: Recent advances in the management of thalassemia have significantly improved life expectancy and quality of life of patients with this hemoglobinopathy, with a consequent increase in their reproductive potential and desire to have children.
DESIGN AND METHODS: We describe the methods of conception and delivery, as well as the course and outcome of pregnancy including transfusions, iron overload and chelation in 46 women with thalassemia major (58 pregnancies) and in 11 women with thalassemia intermedia (17 pregnancies). Conception was achieved after gonadotrophin-induced ovulation in 33 of the women with thalassemia major and spontaneously in all of those with thalassemia intermedia.
RESULTS: Among the women with thalassemia major, 91% of the pregnancies resulted in successful delivery of 45 singleton live-born neonates, five sets of twins and one set of triplets. No secondary complications of iron overload developed or worsened during pregnancy. When considering only the singleton pregnancies, the proportion of babies with intrauterine growth retardation did not differ from that reported in the general Italian population. The high prevalence of pre-term births (32.7%) was mostly related to multiple pregnancies and precautionary reasons. Pregnancy was safe in most women with thalassemia major or intermedia. However, women with thalassemia intermedia who had never previously been transfused or who had received only minimal transfusion therapy were at risk of severe alloimmune anemia if blood transfusions were required during pregnancy.
CONCLUSIONS: Provided that a multidisciplinary team is available, pregnancy is possible, safe and usually has a favorable outcome in patients with thalassemia. In women with hypogonadotropic hypogonadism, gonadal function is usually intact and fertility is usually retrievable.
Raffaella Origa; Antonio Piga; Giovanni Quarta; Gian Luca Forni; Filomena Longo; Angela Melpignano; Renzo Galanello
Related Documents :
2127286 - Transplacental passage of digoxin in severe rhesus immunization.
24075376 - Blastocyst morphology score as an indicator of embryo competence for women aged younger...
8063266 - Is the hellp syndrome due to inherited factors? report of two cases.
16354976 - Intravenous immunoglobulins without initial and follow-up cordocentesis in alloimmune f...
20061276 - Adrenocorticotropic hormone-independent cushing syndrome manifesting during pregnancy.
12871446 - Thromboprophylaxis improves the live birth rate in women with consecutive recurrent mis...
Publication Detail:
Type:  Journal Article; Multicenter Study     Date:  2009-11-10
Journal Detail:
Title:  Haematologica     Volume:  95     ISSN:  1592-8721     ISO Abbreviation:  Haematologica     Publication Date:  2010 Mar 
Date Detail:
Created Date:  2010-03-08     Completed Date:  2010-07-08     Revised Date:  2013-05-31    
Medline Journal Info:
Nlm Unique ID:  0417435     Medline TA:  Haematologica     Country:  Italy    
Other Details:
Languages:  eng     Pagination:  376-81     Citation Subset:  IM    
Ospedale Regionale Microcitemie, ASL Cagliari, Dipartimento di Scienze Biomediche e Biotecnologie, Università di Cagliari, Via Jenner s/n, 09121 Cagliari, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Blood Transfusion
Chelation Therapy
Ferritins / blood
Gonadotropins / administration & dosage
Infant, Newborn
Iron Overload / prevention & control
Pregnancy Complications, Hematologic / therapy*
Pregnancy Outcome
Reproductive Techniques, Assisted
Treatment Outcome
Young Adult
beta-Thalassemia / complications*,  therapy
Reg. No./Substance:
0/Gonadotropins; 9007-73-2/Ferritins

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Class II-associated invariant chain peptide down-modulation enhances the immunogenicity of myeloid l...
Next Document:  IgA and IgG hypogammaglobulinemia in Waldenström's macroglobulinemia.