Your browser doesn't support javascript.
loading
A study on early-onset neonatal group B streptococcal infection, Bulgaria, 2007-2011.
Todorova-Christova, M; Vacheva, R; Decheva, A; Nikolov, A; Slancheva, B; Stoichkova, D; Christova, E; Shopova, E; Hitrova, S; Masseva, A; Yarakova, N; Kraleva, I; Takova, T S; Dimitrova, N; Dobreva, A.
Afiliação
  • Todorova-Christova M; National center of infectious and parasitic diseases, 26, Yanko Sakazov boulevard, 1504 Sofia, Bulgaria. Electronic address: maria.christova@gmail.com.
  • Vacheva R; University hospital "Queen Yoanna", 8, Byalo More street, 1527 Sofia, Bulgaria.
  • Decheva A; National center of infectious and parasitic diseases, 26, Yanko Sakazov boulevard, 1504 Sofia, Bulgaria.
  • Nikolov A; University hospital of obstetrics and gynecology "Маitchin Dom", 2, Zrave street, 1431 Sofia, Bulgaria.
  • Slancheva B; University hospital of obstetrics and gynecology "Маitchin Dom", 2, Zrave street, 1431 Sofia, Bulgaria.
  • Stoichkova D; First obstetrics & gynecology hospital "Sveta Sofiya", 2, Mihalaki Tashev street, 1330 Sofia, Bulgaria.
  • Christova E; Faculty of public health, medical university, 8, Byalo More street, 1527 Sofia, Bulgaria.
  • Shopova E; University hospital of obstetrics and gynecology "Маitchin Dom", 2, Zrave street, 1431 Sofia, Bulgaria.
  • Hitrova S; University hospital of obstetrics and gynecology "Маitchin Dom", 2, Zrave street, 1431 Sofia, Bulgaria.
  • Masseva A; University hospital of obstetrics and gynecology "Маitchin Dom", 2, Zrave street, 1431 Sofia, Bulgaria.
  • Yarakova N; University hospital of obstetrics and gynecology "Маitchin Dom", 2, Zrave street, 1431 Sofia, Bulgaria.
  • Kraleva I; First obstetrics & gynecology hospital "Sveta Sofiya", 2, Mihalaki Tashev street, 1330 Sofia, Bulgaria.
  • Takova TS; First obstetrics & gynecology hospital "Sveta Sofiya", 2, Mihalaki Tashev street, 1330 Sofia, Bulgaria.
  • Dimitrova N; First obstetrics & gynecology hospital "Sveta Sofiya", 2, Mihalaki Tashev street, 1330 Sofia, Bulgaria.
  • Dobreva A; Multi-Profile Acute Care Hospital "Vita" SPLLC, 9, Dragovitsa street, 1505 Sofia, Bulgaria.
Arch Pediatr ; 21(9): 953-60, 2014 Sep.
Article em En | MEDLINE | ID: mdl-25066700
ABSTRACT
This study examines neonatal group B streptococcal (GBS) colonization and its relation to early-onset GBS disease (EOGBSD), based upon the experience of leading obstetrics and gynecology centers in Bulgaria. The objectives of the study were to update neonatal colonization rates and to assess relationships between clinically differentiated cases (culture-proven GBS newborns) and risk factors inherent to the infant and mother, using a computerized file. The neonatal GBS colonization rate ranged from 5.48 to 12.19 per 1000 live births. Maternal-fetal infection (MFI, a provisional clinical diagnosis in culture-proven colonized infants with initial signs of infection that is usually overcome with antibiotic treatment) and/or intrapartum asphyxia (IA) have been demonstrated as the most frequent clinical manifestations, with significant correlations for the primary diagnosis, but not affirmative for the final diagnosis at discharge, resulting from adequate treatment of neonates. MFI and IA were significantly related to prematurity, and reciprocally, prematurity was associated with the risk of MFI, indirectly suggesting that preterm birth or PPROM (preterm premature rupture of membranes, an obstetric indication associated with early labor and delivery, one of the major causes of preterm birth) is a substantial risk factor for EOGBSD. The regression analysis indicated that in the case of a newborn with MFI, a birth weight 593.58 g lower than the birth weight of an infant without this diagnosis might be expected. Testing the inverse relationship, i.e., the way birth weight influences a certain diagnosis (logistic regression) established the presence of a relationship between birth weight categories (degree of prematurity) and the diagnosis of MFI. The proportions and odds ratios, converted into probabilities that a baby would develop MFI, indicate the particularly high risk for newborns with extremely low and very low birth weight extremely low birth weight (≤1000 g), the probability of developing a MFI is 66%; very low birth weight (1001-1500 g), 81%; low birth weight (the birth weight category including premature and small for gestational age term infants 1501-2500 g), 40%; normal birth weight (term infants) (>2500 g), 32%. In conclusion, the need to introduce separate categories for early- and late-onset GBS disease in the registration nomenclature of neonatal infectious diseases is highlighted by these results. Drawing up intrapartum antibiotic prophylaxis (IAP) guidelines is also strongly recommended.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Estreptocócicas / Streptococcus agalactiae Tipo de estudo: Etiology_studies / Guideline / Risk_factors_studies Limite: Female / Humans / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Arch Pediatr Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções Estreptocócicas / Streptococcus agalactiae Tipo de estudo: Etiology_studies / Guideline / Risk_factors_studies Limite: Female / Humans / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Arch Pediatr Ano de publicação: 2014 Tipo de documento: Article