1992
DOI: 10.1016/0020-7292(92)90297-v
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Prenatal microbiological risk factors associated with preterm birth

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Cited by 29 publications
(44 citation statements)
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“…Gestational ages were equivalent (68 to 70%), and lung development at this time in gestation is similar. It is possible that events leading to human premature birth, specifically the high incidence of chorioamniotic infection with fetal inflammatory response, could alter the subsequent pulmonary cytokine response of the human premature as compared with that of premature baboons delivered by elective hysterotomy (54)(55)(56)(57). The significant differences in pulmonary mechanics present throughout the course of this study suggest that the histologic differences between HFOV and LV-PPV animals could be related to differences in how these two techniques maintain lung inflation.…”
Section: Time-dependent Changes For Tracheal Cytokines In Immature Bamentioning
confidence: 89%
“…Gestational ages were equivalent (68 to 70%), and lung development at this time in gestation is similar. It is possible that events leading to human premature birth, specifically the high incidence of chorioamniotic infection with fetal inflammatory response, could alter the subsequent pulmonary cytokine response of the human premature as compared with that of premature baboons delivered by elective hysterotomy (54)(55)(56)(57). The significant differences in pulmonary mechanics present throughout the course of this study suggest that the histologic differences between HFOV and LV-PPV animals could be related to differences in how these two techniques maintain lung inflation.…”
Section: Time-dependent Changes For Tracheal Cytokines In Immature Bamentioning
confidence: 89%
“…In a cross-sectional study of reproductive age women in 2001 the National Health and Nutrition Examination Survey (NHANES) found that the prevalence of BV in the U.S. was 29.2% (59). BV has been shown to be an independent risk factor for the acquisition of sexually transmitted infections (19; 69; 83; 118), the acquisition and transmission of HIV (20–22; 69; 103; 105), the development of pelvic inflammatory disease (PID) (76), as well as reproductive tract and obstetric sequelae (37; 39; 49; 71; 72). Numerous investigations have been performed to identify factors that increase a woman’s risk to BV.…”
Section: Bacterial Vaginosismentioning
confidence: 99%
“…In a study of 534 pregnant women, cervical infection with Chlamydia trachomatis BV was independently associated with PPROM, SPTL and LBW (Gravett et al 1986). Th e presence of Gardnerella vaginalis and Ureaplasma urealyticum during the 2nd trimester increased the risk of PTB two-fold (McDonald et al 1992). …”
Section: Can Abnormal Genital Tract Colonisation Identify Women At Rimentioning
confidence: 96%
“…Th e main cohort studies from Europe, North America and the Far East (Gravett et al 1986;Kurki et al 1992;Riduan et al 1993;Hay et al 1994;McGregor et al 1994;Hillier et al 1995;Meis et al 1995;Gratacos et al 1998) and three case -control studies from the USA, Sweden and Australia (Eschenbach et al 1984;McDonald et al 1992;Holst et al 1994) have used diff erent methodologies to examine the association between abnormal genital tract fl ora, either in the form of BV or the presence of BV associated organisms, and adverse outcomes of pregnancy. Th e majority of these studies show a statistically signifi cant association between abnormal genital tract fl ora and PTB and the degree of risk was greater the earlier in pregnancy at which the abnormal fl ora was detected (Lamont et al 2004).…”
Section: Treatment Timingmentioning
confidence: 98%