Digitalni repozitorij raziskovalnih organizacij Slovenije

Izpis gradiva
A+ | A- | Pomoč | SLO | ENG

Naslov:Supplemental iron and recombinant erythropoietin for anemia in infants born very preterm : a survey of clinical practice in Europe
Avtorji:ID Reibel-Georgi, Nora J. (Avtor)
ID Scrivens, Alexandra (Avtor)
ID Heeger, Lisanne E. (Avtor)
ID Lopriore, Enrico (Avtor)
ID New, Helen V (Avtor)
ID Deschmann, Emöke (Avtor)
ID Stanworth, Simon J. (Avtor)
ID Aguar Carrascosa, Marta (Avtor)
ID Brække, Kristin (Avtor)
ID Cardona, Francesco Stefano (Avtor)
ID Lozar Krivec, Jana (Avtor), et al.
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (1,14 MB)
MD5: C418CC17A5D2078E35E0F2247CBB8000
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Objectives: To survey practices of iron and recombinant human erythropoietin (rhEpo) administration to infants born preterm across Europe. Study design: Over a 3-month period, we conducted an online survey in 597 neonatal intensive care units (NICUs) of 18 European countries treating infants born with a gestational age of <32 weeks. Results: We included 343 NICUs (response rate 56.3%) in the survey. Almost all NICUs (97.7%) routinely supplement enteral iron, and 74.3% of respondents to all infants born <32 weeks of gestation. We found that 65.3% of NICUs routinely evaluate erythropoiesis and iron parameters beyond day 28 after birth. Most NICUs initiate iron supplementation at postnatal age of 2 weeks and stop after 6 months (34.3%) or 12 months (34.3%). Routine use of rhEpo was reported in 22.2% of NICUs, and in individual cases in 6.9%. RhEpo was mostly administered subcutaneously (70.1%) and most frequently at a dose of 250 U/kg 3 times a week (44.3%), but the dose varied greatly between centers. Conclusions: This survey highlights wide heterogeneity in evaluating erythropoietic activity and iron deficiency in infants born preterm. Variation in iron supplementation during infancy likely reflects an inadequate evidence base. Current evidence on the efficacy and safety profile of rhEpo is only poorly translated into clinical practice. This survey demonstrates a need for standards to optimize patient blood management in anemia of prematurity
Ključne besede:neonate, prematurity, recombinant human erythropoietin, very low birth weight infant
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2025
Št. strani:str. 1-8
Številčenje:Vol. 276
PID:20.500.12556/DiRROS-28993 Novo okno
UDK:616-053.2
ISSN pri članku:0022-3476
DOI:10.1016/j.jpeds.2024.114302 Novo okno
COBISS.SI-ID:213510915 Novo okno
Datum objave v DiRROS:15.04.2026
Število ogledov:43
Število prenosov:14
Metapodatki:XML DC-XML DC-RDF
:
Kopiraj citat
  
Objavi na:Bookmark and Share


Postavite miškin kazalec na naslov za izpis povzetka. Klik na naslov izpiše podrobnosti ali sproži prenos.

Gradivo je del revije

Naslov:The Journal of pediatrics
Skrajšan naslov:J Pediatr
Založnik:C. V. Mosby.
ISSN:0022-3476
COBISS.SI-ID:245271 Novo okno

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Nazaj