Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel; Paediatric Infectious Disease Unit, Soroka University Medical Centre, Beer Sheva, Israel.
Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel; Paediatric Infectious Disease Unit, Soroka University Medical Centre, Beer Sheva, Israel.
J Hosp Infect. 2018 Sep;100(1):40-46. doi: 10.1016/j.jhin.2017.12.024. Epub 2018 Jan 10.
Preterm infants are at high risk for extended-spectrum-beta-lactamase-producing Enterobacteriaceae (ESBL-E) sepsis and neonatal intensive care unit (NICU) outbreaks. Maternal colonization with ESBL-E may be precursory to mother-to-child transmission. However, there is no consensus regarding surveillance of pregnant women for ESBL-E colonization.
To identify pairs of mothers and infants harbouring same-strain ESBL-E colonization and to determine whether maternal transmission may play a role in increasing ESBL-E carriage in preterm infants.
This was a one-year analysis from an ongoing, prospective ESBL-E surveillance of mothers of premature infants and their offspring. Mother-infant pairs colonized with the same bacteria underwent strain analysis using pulsed-field gel electrophoresis (PFGE). Clinical parameters were collected from the hospital computerized records.
Between January 2015 and January 2016, 313/409 (76.5%) mothers and all 478 (100%) infants were screened for ESBL-E colonization; carriage rates were 21.5% and 14.8%, respectively. Four (5.6%) colonized infants developed late-onset sepsis and two (2.8%) died. Twenty-five mother-infant pairs colonized with the same bacterial strain were identified; a subgroup of 10 pairs of isolates underwent PFGE, and 70% displayed an identical PFGE fingerprint. No similarities were found between isolates recovered from unrelated neonates and mothers. ESBL-E colonization was found significantly earlier in infants of mothers colonized at birth (P<0.001) compared with infants of non-colonized mothers.
ESBL-E carriage rates in mothers and NICU infants with non-negligible maternal-neonatal ESBL-E transmission in the study region indicate that maternal colonization surveillance and/or further infection control interventions should be considered.
早产儿患产超广谱β-内酰胺酶(ESBL-E)肠杆菌科细菌败血症和新生儿重症监护病房(NICU)爆发的风险很高。产妇携带 ESBL-E 可能是母婴传播的先兆。然而,对于孕妇是否应进行 ESBL-E 定植筛查,目前尚无共识。
确定携带相同 ESBL-E 定植的母婴对,并确定产妇传播是否可能在增加早产儿 ESBL-E 定植方面发挥作用。
这是一项正在进行的前瞻性 ESBL-E 监测早产儿母亲及其后代的为期一年的分析。使用脉冲场凝胶电泳(PFGE)对携带相同细菌的母婴对进行菌株分析。从医院计算机记录中收集临床参数。
2015 年 1 月至 2016 年 1 月,对 313/409(76.5%)位母亲及其 478(100%)名婴儿进行了 ESBL-E 定植筛查;定植率分别为 21.5%和 14.8%。4 名(5.6%)定植婴儿发生晚发性败血症,2 名(2.8%)死亡。确定了 25 对携带相同细菌株的母婴对;10 对分离株的亚组进行了 PFGE,70%显示出相同的 PFGE 指纹。从无关的新生儿和母亲中分离出的分离株之间没有发现相似性。与未定植的母亲相比,在出生时定植的母亲的婴儿中发现 ESBL-E 定植的时间明显更早(P<0.001)。
研究地区存在不容忽视的母婴 ESBL-E 传播,表明应考虑进行产妇定植监测和/或进一步的感染控制干预。