dc.contributor.author
Radauer‐Plank, Anne‐Catherine
dc.contributor.author
Diesch‐Furlanetto, Tamara
dc.contributor.author
Schneider, Monika
dc.contributor.author
Sommerhäuser, Greta
dc.contributor.author
Friedrich, Lucía Alácan
dc.contributor.author
Salow, Vivienne
dc.contributor.author
Dülberg, Jill
dc.contributor.author
Diepold, Miriam
dc.contributor.author
Rovó, Alicia
dc.contributor.author
Njue, Linet Muthoni
dc.contributor.author
Drexler, Beatrice
dc.contributor.author
Infanti, Laura
dc.contributor.author
Kroiss, Sabine
dc.contributor.author
Merki, Ramona
dc.contributor.author
Scheinemann, Katrin
dc.contributor.author
Eisenreich, Bernhard
dc.contributor.author
Hegemann, Inga
dc.contributor.author
Mandic, Ljubica
dc.contributor.author
Kager, Leo
dc.contributor.author
Borgmann‐Staudt, Anja
dc.contributor.author
Schilling, Ralph
dc.contributor.author
Roll, Stephanie
dc.contributor.author
Balcerek, Magdalena
dc.date.accessioned
2025-12-10T11:02:24Z
dc.date.available
2025-12-10T11:02:24Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/50774
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-50501
dc.description.abstract
Background: Both diagnosis and treatment of hemoglobinopathies have been associated with an increased risk of fertility impairment. German guidelines recommend annual monitoring of fertility parameters to enable early detection of fertility impairment and/or to offer fertility preservation (FP) when indicated. We explored the general desire for parenthood, the frequency of recalling fertility counseling and testing, and the utilization of FP in adolescents and adults with hemoglobinopathies. Procedure: In a cross-sectional study, patients aged 12-50 years, treated in Germany, Austria, or Switzerland, were surveyed on fertility-related aspects. Medical data, including fertility testing results, were collected from patient records. Results: Overall, 116/121 eligible patients, diagnosed with sickle cell disease (70.7%), thalassemia (27.6%), or other hemoglobinopathy (1.7%), participated in our study (57.8% female, median age 17.0 years, range 12-50 years). All participants required treatment of the underlying hemoglobinopathy: 68.1% received hydroxyurea, 25.9% required regular blood transfusions, and 6.0% underwent hematopoietic stem cell transplantation (HSCT). Most patients (82/108, 75.9%) stated a considerable to strong desire for (future) parenthood, independent of sex, education, diagnosis, or subjective health status. Fertility counseling was only recalled by 32/111 patients (28.8%) and least frequently by younger patients (12-16 years) or those treated with regular blood transfusions or hydroxyurea. While fertility testing was documented for 59.5% (69/116) in medical records, only 11.6% (13/112) recalled previous assessments. FP was only used by 5.4% (6/111) of patients. Conclusion: Most patients with hemoglobinopathies wish to have biological children, yet only few recalled fertility counseling and testing. Adequate patient counseling should be offered to all patients at risk for infertility.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
congenital anemias
en
dc.subject
fertility impairment
en
dc.subject
fertility preservation
en
dc.subject
hemoglobinopathies
en
dc.subject
patient counseling
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Desire for biological parenthood and patient counseling on the risk of infertility among adolescents and adults with hemoglobinopathies
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e30359
dcterms.bibliographicCitation.doi
10.1002/pbc.30359
dcterms.bibliographicCitation.journaltitle
Pediatric Blood & Cancer
dcterms.bibliographicCitation.number
7
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.volume
70
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
37057367
dcterms.isPartOf.issn
1545-5009
dcterms.isPartOf.eissn
1545-5017