Am J Perinatol 2013; 30(06): 505-512
DOI: 10.1055/s-0032-1329181
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

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

Elisa Llurba
1   Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Advanced Fetal Care, University of Maryland School of Medicine, Baltimore, Maryland
2   Department of Obstetrics, Fetal Medicine Unit, Vall d'Hebron Hospital, Universitat Autònoma de Barcelona, Barcelona, Spain
,
Ozhan Turan
1   Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Advanced Fetal Care, University of Maryland School of Medicine, Baltimore, Maryland
,
Tania Kasdaglis
1   Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Advanced Fetal Care, University of Maryland School of Medicine, Baltimore, Maryland
,
Chris R. Harman
1   Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Advanced Fetal Care, University of Maryland School of Medicine, Baltimore, Maryland
,
Ahmet A. Baschat
1   Department of Obstetrics, Gynecology, and Reproductive Sciences, Center for Advanced Fetal Care, University of Maryland School of Medicine, Baltimore, Maryland
› Author Affiliations
Further Information

Publication History

13 February 2012

27 July 2012

Publication Date:
19 December 2012 (online)

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Abstract

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)] × 100; ΔmUtA-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 (ΔmUtA PI) was similar for patients with PRD. However, the prevalence of PRD doubled with rising ΔmUtA-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.