Neonatal screening improves sickle cell disease clinical outcome in Belgium.

Objectives To compare the outcomes of sickle cell disease patients diagnosed through neonatal screening with those who were not. Methods In an observational multicenter study in Belgium, 167 screened and 93 unscreened sickle cell disease patients were analyzed for a total of 1116 and 958 patient-years of follow-up, respectively. Both groups were compared with propensity score analysis, with patients matched on three covariates (gender, genotype, and central Africa origin). Bonferroni correction was applied for all comparisons. Results Kaplan-Meier estimates of survival without bacteremia were... Mehr ...

Verfasser: Lê, Phu-Quoc
Ferster, Alina
Dedeken, Laurence
Vermylen, Christiane
Vanderfaeillie, Anna
Rozen, Laurence
Heijmans, Catherine
Huybrechts, Sophie
Devalck, Christine
Cotton, Frédéric
Ketelslegers, Olivier
Dresse, Marie-Françoise
Fils, Jean-François
Gulbis, Béatrice
Dokumenttyp: Artikel
Erscheinungsdatum: 2018
Verlag/Hrsg.: Sage Publications
Schlagwörter: Adolescent / Adult / Anemia / Sickle Cell / Belgium / Child / Preschool / Ethnic Groups / Female / Hospitalization / Humans / Infant / Newborn / Male / Neonatal Screening / Outcome Assessment (Health Care) / Propensity Score / Survival Analysis / Young Adult / Sickle cell disease / Infection / Neonatal screening programme
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26603482
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : http://hdl.handle.net/2078.1/222353