Pregled bibliografske jedinice broj: 465825
Influence of the inherited glucose-6-phosphate dehydrogenase deficiency on the appearance and the course of neonatal hyperbilirubinemia
Influence of the inherited glucose-6-phosphate dehydrogenase deficiency on the appearance and the course of neonatal hyperbilirubinemia // Croatia 32nd UMEMPS Congress (UMEMPS 2009) : abstracts ; u: Paediatria Croatica 53 (2009) (S) / Barišić, Ingeborg (ur.).
Zagreb, 2009. str. 49-49 (poster, nije recenziran, sažetak, stručni)
CROSBI ID: 465825 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Influence of the inherited glucose-6-phosphate dehydrogenase deficiency on the appearance and the course of neonatal hyperbilirubinemia
Autori
Glavinić, Robert ; Marušić, Eugenija ; Krželj, Vjekoslav ; Pleština-Borjan, Ivna ; Škrabić, Veselin ; Unić, Ivana ; Bilić, Ivana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Croatia 32nd UMEMPS Congress (UMEMPS 2009) : abstracts ; u: Paediatria Croatica 53 (2009) (S)
/ Barišić, Ingeborg - Zagreb, 2009, 49-49
Skup
Croatia UMEMPS Congress (32 ; 2009)
Mjesto i datum
Dubrovnik, Hrvatska, 30.09.2009. - 03.10.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
G-6-PD deficiency; neonatal hyperbilirubinemia; florescent spot test; Central Dalmatia
Sažetak
Aim: The aim of this study was to determine the influence of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency on the appearance and the course of neonatal hyperbilirubinemia in Central Dalmatia region. Methods: The florescent spot test was used in the retrospective study to screen blood samples of 513 male children which had neonatal hyperbilirubinemia higher than 240µmol/L. Florescence reading was performed at the beginning and at the 5th, 10th and 20th minutes of incubation and was classified into three groups: bright florescence, weak florescence and no florescence. Samples with no florescence and weak florescence reading in 5th minute were quantitatively measured using spectrophotometric method. Results: Bright florescence in 5th, 10th, and 20th minute were present in 461 samples (90%). The rest 52 samples (10%) were quantitatively measured using spectrophotometric method and in 32 of them there were normal G-6-PD activity but 20 samples (3, 9%) were G-6-PD deficient. The average of hospitalization of the children with newborn jaundice and G-6-PD deficiency were 15, 8 days, and 9 days for the same children with normal G-6-PD activity. Conclusion: Prevalence rate of G-6-PD deficiency among newborns in Central Dalmatia region is significantly higher (p< 0, 001) compared to the prevalence rate among men in Central Dalmatia region (0, 75% in males). We can also conclude that G-6PD deficiency has an influence on a course of newborn jaundice. The children with newborn jaundice and G-6-PD deficiency have had a significantly longer hospitalization then children with neonatal hyperbilirubinemia and normal G-6-PD.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
216-0000000-3464 - Genske, kliničke i populacijske osobitosti deficita G-6-PD u Hrvatskoj (Krželj, Vjekoslav, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Split
Profili:
Robert Glavinić
(autor)
Vjekoslav Krželj
(autor)
Ivana Unić
(autor)
Veselin Škrabić
(autor)
Ivna Pleština-Borjan
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus