Middle cerebral artery peak systolic velocity in fetuses with homozygous alpha-thalassemia-1: case series

J Med Assoc Thai. 2010 Feb:93 Suppl 2:S114-7.

Abstract

Objectives: The objective of this study is to evaluate the potential usefulness of middle cerebral artery peak systolic velocity (MCA-PSV) as a non-invasive means of detecting an anemic fetus from homozygous alpha-thalassemia-1.

Material and method: We observed four cases of referrals with complicated pregnancies in which the fetuses were suspected with homozygous alpha-thalassemia-1. Three out of four cases involved hydrop fetalis, detected through previous ultrasounds, while the remaining case was referred for prenatal diagnosis. Subsequently, we performed a detailed ultrasound and fetal MCA-PSV in all cases, and to confirm the diagnosis, we also performed cordocentesis.

Results: With all the four cases having the gestational age range from 18 to 27 weeks, three showed hydrop fetalis. The remaining case, the 18-week gestational age fetus referred for prenatal diagnosis, showed an increase in the cardiothoracic ratio without other signs of hydrop fetalis. MCA-PSV suggested the presence of fetal anemia in all cases (with the velocity ranging from 37.3 to 62.2 cm/sec). The results obtained from cordocentesis confirmed fetal anemia and homozygous alpha-thalassemia-1 in all cases.

Conclusion: Peak systolic velocity of fetal middle cerebral artery can predict anemia in fetus affected with homozygous alpha-thalassemia-1 disease.

Publication types

  • Case Reports

MeSH terms

  • Blood Flow Velocity / physiology
  • Cerebrovascular Circulation
  • Cordocentesis
  • Female
  • Fetus / physiology*
  • Gestational Age
  • Homozygote
  • Humans
  • Middle Cerebral Artery / diagnostic imaging*
  • Middle Cerebral Artery / physiopathology
  • Placenta / diagnostic imaging*
  • Placenta / physiopathology
  • Predictive Value of Tests
  • Pregnancy
  • Systole
  • Ultrasonography, Prenatal / methods
  • alpha-Thalassemia / diagnostic imaging*
  • alpha-Thalassemia / genetics
  • alpha-Thalassemia / physiopathology