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1.
Am J Obstet Gynecol ; 211(6): 665.e1-7, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24949536

ABSTRACT

OBJECTIVE: We sought to analyze whether maternal intravenous fluid therapy prior to external cephalic version (ECV) increases the amount of amniotic fluid and the success rate of the procedure. STUDY DESIGN: This was a prospective single-center cohort study of 200 women with a consecutive cohort of 100 pregnant women with a breech presentation at term who were administered intravenous fluid therapy with 2 L of hypotonic saline before the version attempt, compared to a control cohort of 100 pregnant women not given hydration treatment. RESULTS: The mean increase in the amniotic fluid index (AFI) after intravenous maternal hydration was 3.75 ± 2.71 cm. The amount of fluid before hydration was the only variable found to be associated with increases in amniotic fluid levels, both in absolute and relative terms (odds ratio, -0.21; 95% confidence interval, -0.37 to -0.05 and odds ratio, -4.62; 95% confidence interval, -6.17 to -3.06; P < .01, respectively). We did not observe any severe complications secondary to the intravenous fluid therapy. The ECV success rate was 43% in the study group compared to 47% in the control group (P = .67). The success rate was significantly lower the larger the relative increase in the AFI, although no correlation was found in absolute terms (χ(2) for linear trend = 0.03 and 0.34, respectively). CONCLUSION: Maternal intravenous fluid therapy with 2 L of hypotonic saline prior to ECV is an effective and safe technique for increasing the AFI. However, its use in ECV does not increase the success rate of the procedure.


Subject(s)
Amniotic Fluid , Breech Presentation/therapy , Fluid Therapy/methods , Version, Fetal/methods , Adult , Cohort Studies , Female , Humans , Infusions, Intravenous , Pregnancy , Prospective Studies , Treatment Outcome
2.
J Matern Fetal Neonatal Med ; 26(4): 407-11, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23025564

ABSTRACT

OBJECTIVE: To analyze morbidity and mortality in twin pregnancies as a function of the type of delivery and chorionicity. DESIGN: Retrospective cohort study. METHODS: Analysis of the type of delivery, intertwin time interval, and perinatal variables of >1000 twin deliveries during a 10-year period. MAIN OUTCOME MEASURE: Influence of delivery type and chorionicity on perinatal outcome. RESULTS: The rate of cesarean sections was 42.4%. No differences were found as a function of chorionicity or as a function of presentation of the second twin. Cesarean sections were performed after vaginal delivery of the first twin in 1.8% of cases, being more common if the second baby was in a non-cephalic presentation (6.9% vs. 0.4%, p < 0.05). The average twin-to-twin delivery time interval was longer in the cases where the second had a cephalic presentation (8.26 ± 7.75 min vs. 6.81 ± 5.97 min, p < 0.05). The umbilical artery pH was lower the longer the interval between the birth of the twins, both in monochorionic and dichorionic. CONCLUSIONS: According to the results, vaginal delivery is as safe as elective caesarean section in twin pregnancies where the first twin is in cephalic presentation and the intrapartum management should not vary due to chorionicity.


Subject(s)
Chorion , Delivery, Obstetric/methods , Pregnancy, Twin , Cesarean Section/statistics & numerical data , Cohort Studies , Female , Gestational Age , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Labor Presentation , Parity , Pregnancy , Pregnancy Outcome , Retrospective Studies , Time Factors , Umbilical Arteries
3.
J Perinat Med ; 38(1): 23-8, 2010.
Article in English | MEDLINE | ID: mdl-20047524

ABSTRACT

OBJECTIVE: To compare the success rate of external cephalic version (ECV) at term using ritodrine or atosiban as a tocolytic agent. STUDY DESIGN: Prospective cohort study with a sample of 236 pregnant women with a breech presentation at term, from November 2006 to March 2008. Data have been analyzed from the moment the cephalic version is performed until the time of delivery. RESULTS: ECV success rate using ritodrine as a tocolytic agent was 56.8% compared to 31.4% with atosiban. Ritodrine increases the version success potential more significantly than atosiban (P<0.05). In both cases, the use of ECV reduced the rate of cesarean sections, although a higher number of versions are required with atosiban [numbers needed to treat (NNT)=9.08] to avoid a cesarean section compared to ritodrine (NNT=3.41). CONCLUSIONS: Ritodrine seems better than atosiban as tocolytic agent for ECVs.


Subject(s)
Ritodrine/administration & dosage , Tocolysis , Tocolytic Agents/administration & dosage , Vasotocin/analogs & derivatives , Version, Fetal , Adult , Female , Humans , Pregnancy , Prospective Studies , Treatment Outcome , Vasotocin/administration & dosage
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