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. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: J Matern Fetal Neonatal Med. 2017 Oct 11;32(4):527–541. doi: 10.1080/14767058.2017.1384460

Table 4.

Neonatal outcomes of study population

Characteristics Intra-amniotic
inflammation (−)/
MIAC (−)
(Group 1, n=102)
P* Adjusted
P*,§
Intra-amniotic
inflammation (+)/
MIAC (−)
(Group 2, n=48)
P Intra-amniotic
inflammation (+)/
MIAC (+)
(Group 3; n=18)
P Adjusted
P,§
Neonatal death 5/102 (5%) NS NS 6/48 (13%) NS 4/18 (22%) NS NS
Significant morbidity**,†† 19/101 (19%) .006 .012 21/42 (50%) NS 8/15 (53%) NS NS
    Respiratory distress syndrome 13/101 (13%) NS NS 5/42 (12%) NS 3/15 (20%) NS NS
    Bronchopulmonary dysplasia 10/97 (10%) .002 .015 18/42 (43%) NS 4/15 (27%) NS NS
    Intraventricular hemorrhage 8/101 (8%) NS NS 2/42 (5%) NS 4/15 (27%) NS NS
    Necrotizing enterocolitis 3/101 (3%) NS NS 4/42 (10%) NS 0/15 NS NS
    Proven early neonatal sepsis 1/101 (1%) NS NS 1/42 (2%) NS 0/15 NS NS
Neonatal death and/or any significant morbidity 21/102 (21%) .002 .007 27/48 (56%) NS 11/18 (61%) .011 NS

Data presented as n/N (%).

MIAC, microbial invasion of amniotic cavity; NS, not significant.

*

Comparison between groups 1 and 2.

Comparison between groups 2 and 3.b

Comparison between groups 1 and 3.

§

Adjusted for gestational age at amniocentesis and the cervical dilatation (generalized estimation equation models).

**

Defined as the presence of any of the following conditions: proven early neonatal sepsis, respiratory distress syndrome, bronchopulmonary dysplasia, intraventricular hemorrhage, and necrotizing enterocolitis.

††

Ten cases were excluded from the analysis because they died shortly after delivery as a result of extreme prematurity and thus could not be evaluated with respect to the presence or absence of neonatal morbidity.