4.2 Article

Emergence of Late-Onset Placental Dysfunction: Relationship to the Change in Uterine Artery Blood Flow Resistance between the First and Third Trimesters

Journal

AMERICAN JOURNAL OF PERINATOLOGY
Volume 30, Issue 6, Pages 505-511

Publisher

THIEME MEDICAL PUBL INC
DOI: 10.1055/s-0032-1329181

Keywords

constitutionally small neonates; fetal growth restriction; preeclampsia; uterine artery Doppler; third trimester

Funding

  1. Maternal and Child Health and Development Network SAMID [RD 08/0072]
  2. Department of Human Resources of Carlos III Institute of Health, Madrid, Spain
  3. AGAUR (Agencia gestio d'Ajuts Universitaris i per a la Recerca) from Generalitat de Catalunya, Spain [BE 2010]
  4. [BAE-11/00071]

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Objectives To test if emergence of third-trimester (T3) placental dysfunction is related to the impedance change in uterine artery blood flow resistance between the first trimester (T1) and T3. Study Design Mean T1 and T3 uterine artery (mUtA) pulsatility index (PI) was measured in 1098 singletons. Each patient's individual mUtA-PI change was calculated ([(T3 PI - T1 PI/interval in days)] x 100; Delta mUtA-PI). This parameter and T1 and T3 mUtA-PI z-scores were related to placenta-related disease (PRD) and to constitutionally small neonates (CS). Results Forty-seven (5%) women had PRD and 83 (8.7%) delivered a CS neonate. T1 and T3 mUtA-PI z-scores were higher with PRD (0.418 versus -0.097 and 1.06 versus -0.13, p < 0.001 for all). Change in mUtA-PI (Delta mUtA PI) was similar for patients with PRD. However, the prevalence of PRD doubled with rising Delta mUtA-PI (11.1% versus 5.2%, p = 0.041). Conclusion T3 uterine artery Doppler performs significantly better in detecting patients at risk for late-onset PRD than T1 or the gestational age change in uterine artery Doppler resistance This suggests that a proportion of late emerging PRD is not amenable to early screening by uterine artery Doppler. Further research is essential to identify the optimal screening strategy for late-onset placental dysfunction.

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