Effect of placenta previa on fetal growth restriction and stillbirth

Aim To examine the association between placenta previa and adverse perinatal outcomes such as low birth weight, preterm delivery, stillbirth and fetal growth restriction (FGR). Methods This retrospective cohort study includes 12,034 delivered pregnant women who were recruited for the study between 2...

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Veröffentlicht in:Archives of gynecology and obstetrics 2012-08, Vol.286 (2), p.295-298
Hauptverfasser: Yeniel, A. Ozgur, Ergenoglu, A. Mete, Itil, Ismail Mete, Askar, Niyazi, Meseri, Reci
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Sprache:eng
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Zusammenfassung:Aim To examine the association between placenta previa and adverse perinatal outcomes such as low birth weight, preterm delivery, stillbirth and fetal growth restriction (FGR). Methods This retrospective cohort study includes 12,034 delivered pregnant women who were recruited for the study between 2004 and 2010 in Ege University Hospital. Data were collected by browsing the clinic’s archives. The association between placenta previa and adverse perinatal outcomes was determined via Chi-square tests and Student’s t test. Logistic regression analysis was used to adjust for confounding factors in evaluating the association between placenta previa and the adverse perinatal outcomes. Results There was no significant relationship between placenta previa and FGR or stillbirth. Low birth weight and preterm delivery were significantly higher in the placenta previa group. According to logistic regression analysis, low birth weight was associated with an OR of 3.01 (95 % CI 2.05–4.52) and preterm delivery was associated with an OR of 8.14 (95 % CI 5.60–11.83); while, placenta previa did not affect FGR and stillbirth significantly. Conclusion Although there is no consensus on the association between placenta previa and FGR in previous studies, we suggest that placenta previa is not a reason for placental insufficiency. Management of placenta previa especially depends on maternal hemodynamic parameters such as heavy hemorrhage and hypotensive shock rather than fetal well-being protocols based on serial growth ultrasound and fetal Doppler investigation.
ISSN:0932-0067
1432-0711
DOI:10.1007/s00404-012-2296-4