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解脲脲原体从母亲传播至足月儿和早产儿。

Transmission of Ureaplasma urealyticum from mothers to full and preterm infants.

作者信息

Alfa M J, Embree J E, Degagne P, Olson N, Lertzman J, Macdonald K S, Macdonald N T, Hall P F

机构信息

Department of Microbiology, St. Boniface General Hospital, Winnipeg, Manitoba, Canada.

出版信息

Pediatr Infect Dis J. 1995 May;14(5):341-5. doi: 10.1097/00006454-199505000-00001.

Abstract

This study assessed maternal genital colonization and subsequent neonatal transmission rate of Ureaplasma urealyticum in pregnant women in an average socioeconomic population. In addition very low birth weight infants were assessed to determine whether the presence of U. urealyticum correlated with increased risk of developing respiratory problems. The study group consisted of 108 sequential full term mothers and 104 preterm mothers delivering in a tertiary care hospital in central Canada. The genital carriage rates (assessed using placental sampling) of ureaplasmas in term and preterm mothers were 25.9 and 19.2%, respectively (P = 0.3185). Acquisition of ureaplasmas in the neonatal respiratory tract of neonates occurred significantly (P = 0.0182) more often in preterm neonates (11 of 130; 8.5%) than in term neonates (2 of 110; 0.9%). Very low birth weight (VLBW) infants (< or = 1500 g) were at greater risk (P = 0.042) of acquiring ureaplasmas in their respiratory tracts (5 of 26; 19%) than larger preterm neonates (6 of 104; 5.8%). All VLBW infants with respiratory colonization by ureaplasmas (5 of 5) developed bronchopulmonary dysplasia compared with 33% (7 of 21) of VLBW neonates without ureaplasmas (P = 0.028). This difference in bronchopulmonary dysplasia development among VLBW infants was independent of further stratification by birth weight. These VLBW neonates with ureaplasmas also stayed significantly (P = 0.037) longer in the neonatal intensive care unit (43.6 +/- 10.4 days) than did other preterm neonates (22.1 +/- 20.8 days). Our results demonstrate that VLBW preterm neonates have increased risk of acquiring U. urealyticum.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究评估了平均社会经济水平人群中孕妇解脲脲原体的生殖道定植情况及随后的新生儿传播率。此外,对极低出生体重儿进行评估,以确定解脲脲原体的存在是否与发生呼吸问题的风险增加相关。研究组由在加拿大中部一家三级护理医院分娩的108名连续足月母亲和104名早产母亲组成。足月和早产母亲中脲原体的生殖道携带率(通过胎盘取样评估)分别为25.9%和19.2%(P = 0.3185)。早产新生儿(130例中有11例;8.5%)在新生儿呼吸道中获得脲原体的情况明显(P = 0.0182)比足月新生儿(110例中有2例;0.9%)更常见。极低出生体重(VLBW)婴儿(≤1500 g)呼吸道获得脲原体的风险(P = 0.042)高于较大的早产新生儿(104例中有6例;5.8%)(26例中有5例;19%)。所有呼吸道被脲原体定植的VLBW婴儿(5例中的5例)均发生了支气管肺发育不良,而未感染脲原体的VLBW新生儿中这一比例为33%(21例中有7例)(P = 0.028)。VLBW婴儿中支气管肺发育不良的这种差异与出生体重的进一步分层无关。这些感染脲原体的VLBW新生儿在新生儿重症监护病房的停留时间(43.6±10.4天)也明显(P = 0.037)长于其他早产新生儿(22.1±20.8天)。我们的结果表明,VLBW早产新生儿获得解脲脲原体的风险增加。(摘要截短于250字)

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