American Journal of Obstetrics & Gynecology
Volume 192, Issue 2 , Pages 452-457, February 2005

Severe fetal placental vascular lesions in term infants with neurologic impairment

Departments of Pathology and Reproductive Biology, Case School of Medicine and University Hospitals of Cleveland, Case Western Reserve University, Cleveland, Ohio

Received 19 May 2004; received in revised form 22 June 2004; accepted 19 July 2004.

Objective

This study tests the hypothesis that placental disease can identify antepartum processes that either progress into the intrapartum period or predispose to intrapartum brain injury.

Study design

Lesions that affect large fetal vessels were compared in the placentas of 125 neurologically impaired term infants who were the focus of clinical negligence litigation and 250 consecutive singleton deliveries of ≥36 weeks of gestation.

Results

One or more of 4 severe placental fetal vascular lesions (fetal thrombotic vasculopathy, chronic villitis with obliterative fetal vasculopathy, chorioamnionitis with severe fetal vasculitis, and meconium-associated fetal vascular necrosis) were found in 51% of index cases versus 10% of the comparison group (P <.0001). Prevalence of these lesions in the 64 infants with cerebral palsy was 52% (P <.0001).

Conclusion

Severe fetal placental vascular lesions are correlated highly with neurologic impairment and cerebral palsy. Their nature, duration, and anatomic location make them strong candidates for the antepartum processes that place fetuses at risk for brain injury during the intrapartum period.

Key words: Brain damage, Cerebral palsy, Neonatal encephalopathy, Placenta

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 30.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Reprints not available from the author.

PII: S0002-9378(04)00790-2

doi:10.1016/j.ajog.2004.07.030

American Journal of Obstetrics & Gynecology
Volume 192, Issue 2 , Pages 452-457, February 2005