Transmission of Ureaplasma urealyticum from mothers to full and preterm infants. 1995

M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
Department of Microbiology, St. Boniface General Hospital, Winnipeg, Manitoba, Canada.

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)

UI MeSH Term Description Entries
D007230 Infant, Low Birth Weight An infant having a birth weight of 2500 gm. (5.5 lb.) or less but INFANT, VERY LOW BIRTH WEIGHT is available for infants having a birth weight of 1500 grams (3.3 lb.) or less. Low Birth Weight,Low-Birth-Weight Infant,Birth Weight, Low,Birth Weights, Low,Infant, Low-Birth-Weight,Infants, Low-Birth-Weight,Low Birth Weight Infant,Low Birth Weights,Low-Birth-Weight Infants
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D007234 Infant, Premature A human infant born before 37 weeks of GESTATION. Neonatal Prematurity,Premature Infants,Preterm Infants,Infant, Preterm,Infants, Premature,Infants, Preterm,Premature Infant,Prematurity, Neonatal,Preterm Infant
D007235 Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS.
D008297 Male Males
D011247 Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. Gestation,Pregnancies
D011251 Pregnancy Complications, Infectious The co-occurrence of pregnancy and an INFECTION. The infection may precede or follow FERTILIZATION. Complications, Infectious Pregnancy,Infectious Pregnancy Complications,Maternal Sepsis,Pregnancy, Infectious Complications,Sepsis during Pregnancy,Sepsis in Pregnancy,Infectious Pregnancy Complication,Pregnancy Complication, Infectious,Sepsis in Pregnancies,Sepsis, Maternal
D001997 Bronchopulmonary Dysplasia A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS. Dysplasia, Bronchopulmonary
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
June 1990, The Pediatric infectious disease journal,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
September 1987, The Pediatric infectious disease journal,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
June 1999, The Medical journal of Malaysia,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
January 1999, Gynakologisch-geburtshilfliche Rundschau,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
October 1998, Acta paediatrica (Oslo, Norway : 1992),
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
November 2013, Korean journal of pediatrics,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
January 1994, Israel journal of medical sciences,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
November 2006, BMC infectious diseases,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
December 2011, Pediatrics,
M J Alfa, and J E Embree, and P Degagne, and N Olson, and J Lertzman, and K S Macdonald, and N T Macdonald, and P F Hall
November 1984, Fertility and sterility,
Copied contents to your clipboard!