Aldana-Valenzuela Carlos, Rodriguez-López Andrea Marina, Blancas Erika Guillén-
Department of Neonatology.
Department of Epidemiology, Mothers and Children Hospital of León, Guanajuato, México.
Pediatr Rep. 2019 Mar 27;11(1):7953. doi: 10.4081/pr.2019.7953. eCollection 2019 Feb 26.
is a rare cause of neonatal sepsis, and it is associated with significant morbidity and a very high fatality rate. The infection is usually acquired intrapartum, from the colonization of the maternal genital tract. Most affected neonates have an early-onset presentation of symptoms, usually within the first 48 hours after birth, which is similar to other causes of neonatal sepsis such as or . However, the virulence seems to be higher for , which has in addition a higher infant invasion/ maternal colonization ratio than . Pneumococcal vaccination has not resulted in a significant decline of neonatal cases. Many cases included ours, involved serotypes not present in the vaccine. Other strategies to protect these infants are necessary. We describe a late preterm infant with a fatal, early-onset sepsis caused by serotype 28 A. Maternal vaginal culture grew the same bacteria.
是新生儿败血症的罕见病因,与显著的发病率和极高的死亡率相关。感染通常在分娩期间获得,源于母体生殖道的定植。大多数受影响的新生儿有早期症状表现,通常在出生后的头48小时内,这与新生儿败血症的其他病因如或相似。然而,的毒力似乎更高,此外其婴儿侵袭/母体定植率也高于。肺炎球菌疫苗接种并未导致新生儿病例显著下降。许多病例包括我们的病例,涉及疫苗中不存在的血清型。保护这些婴儿需要其他策略。我们描述了一例晚期早产儿,患有由28 A血清型引起的致命性早发型败血症。母体阴道培养物培养出了相同的细菌。