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characteristics and outcomes were collected. Quantitative and Our objective was to determine whether fetal presentation at the
qualitative variables were compared by Wilcox, t-test or Fisher test diagnosis of PPROM has an effect on the latency period and other
respectively. perinatal outcomes.
RESULTS: Among 3068 women (1497 nullipara and 1571 para), 208 STUDY DESIGN: All cases of PPROM after 20 weeks of gestation
(6.8%) had a second stage > 2 hours. OP position was diagnosed in delivered at our institution from January 2014 though May 2017.
76 (36.5%) of these women. Vaginal delivery occurred in 74.1% (43/ Inclusion criteria: singleton gestations. Exclusion criteria: PPROM at
58) and 83.3% (15/18) of nulliparous and parous women, respectively, less than 20 wks gestational age (GA), multiple gestations and fetal
when the second stage of labor was extended. Length of second stage anomalies. The analysis was stratified based on GA at time of
was longer in nulliparous women with a fetus in an OP position than rupture: 20 - 26 wks, 26 wks+1d - 28 wks, 28 wks+1d - 30 wks, 30
in nulliparous women with a fetus in an occiput anterior position. wks+1d - 32 wks and 32 wks+1d - 36 wks+6d. We calculated that 20
However, perineal tears of 3rd and 4th degree, postpartum hemorrhage women with noncephalic and 80 with cephalic presentations would
and neonatal outcomes were similar (Table 1). give the study 80% power to detect HR of 1.3 for latency measured
CONCLUSION: Extending the second stage of labor with a fetus in days.
in an OP position is safe and reduce the risk of CD whatever the RESULTS: 120 cases of PPROM were reviewed: 100 were cephalic
parity. and 20 noncephalic at presentation. There were no differences in
maternal age, race, smoking status, infection on admission,
bleeding in pregnancy, history of preterm delivery or the use of
latency antibiotics between fetal presentation. There was no dif-
ference noted in latency period based on fetal presentation (HR ¼
1.17, CI: 0.66, 2.07). Noncephalic presentation at PPROM was
associated with delivery for nonreassuring fetal status, lower
Apgar scores at 1 and 5 minutes and fetal anemia. A fetal/
neonatal composite morbidity composite variable consisting of
sepsis, IUFD, RDS and neonatal demise showed a trend toward
worse outcomes for fetuses in noncephalic presentation however
it did not reach statistical significance (OR ¼ 4.62, CI 0.94, 22.71,
P¼0.06).
CONCLUSION: Fetal presentation at the time of PPROM does not
appear to affect the length of the latency period. However, there may
be increased maternal and fetal/neonatal morbidity associated with
fetal malpresentation and closer fetal monitoring may be warranted
for non-vertex presenting fetuses in cases of PPROM.