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Pr enatal
dia gnosis of fetal
hear t anomalies

  Ultrasound screening

  Bogdan M. Muresan
The incidence of CHD (Congenital Heart
Disease) is around 8 to 9 per 1000 live
births



  If all subtle cardiac anomalies are
   counted (bicuspid Ao valve, aneurysm of
   atrial septum and LSVC persistent) may
   be in order of 50 per 1000 live births.
  The suspicion for CHD during a routine
   ultrasound is a risk factor with highest
   yield for CHD (40 to 50%)
The majority of fetuses with CHD have no known
risk factors.

SCREENING for CHD to every pregnant women -
routine scan: nuchal scan (12 weeks) and
anomalies scan (20-22 weeks)


 Risk factors for CHD
  Fetal: chromosomal abnormalities, extracardiac anatomic
   abnormalities, fetal cardiac arrhytmia, suspected cardiac anomaly
   on routine ultrasound, thickened nuchal translucency,
   monochorionic placentation;
  Maternal: family history of CHD, maternal metabolic disorders
   (diabetes, phenylketonuria), maternal teratogen exposure,
   pregnancy from assisted reproduction techniques, maternal
   obesity



    Alferd Abuhamad, Rabih Chaoui: A Practical Guide to Fetal Echocardiography
Nuchal scan (11-13WG)
soft markers for aneuploidies and CHD (in
             euploid cases):
  NT thickened; TR regurgitation; DV with “a”
                   reverse
CASE: 8 weeks pregnancy -
 refferal for a “problem”?
Is here a normal pregnancy ???
Routine exam at 8 weeks         search for: localisation / number of fetus-placenta
(intrauterine pregnancy), presence of FHR (normal FHR), embryon adnexa (normal
yolk sac)
Is there a possible
     problem ?
Embryo anatomy: heart is almost complete
developed; but it is impossible to asses
heart anatomy
-   look to heart position in thorax??
Untill 10-11 weeks there is a normal
 exomphalos (with bowel contents)
Transverse view of embryo thorax
“ Ectopia cordis” ????
http://www.sonoworld.com/TheFetus/page.aspx?
                  id=2687
Patient was reevaluated at 11
     weeks (nuchal scan)
unfortunately CRL < 45 mm (42,2mm)
               but:……
Normal fetal anatomy at this age
3D image revealed normal fetal
         anterior wall
(there is no place for “ectopia
            cordis”)
Nuchal scan
(CRL between 45-84 mm or 11-13
             WG)
Normal midsagital view – fetal profile (NT, FMF
angle, nasal bone, intracerebral translucency)
Normal fetal anterior wall:
 umbilical cord insertion and heart
            localisation
Good result at nuchal
         scan:
      PAPP-A, freeBetaHCG, NT
   Combined risk assessment (risk for
chromosomal abnormalities under 1/1000)
New soft markers in nuchal scan: nasal
bone, FMF angle, Tricuspid and DV flow
(routinely)

The presence of Tricuspid regurgitation –
it is associated with chromosomal
abnormalities and high risk for CHD in
euploid fetuses)
Possible AVSD
(if it is present - increases T21 risk
to ¼ and karyotyping is necessary)
After 10 days we performed
 a fetal echocardiography
         AVSD ???
or Mitral atresia with VSD
Great vessel outflow
      tract ???
Outflow Tract:
- Ao and Pulmonary Trunk have common origin in Right
Ventricle
- They are parallel at origin
- Pulmonary Trunk smaller than Ao
DORV (VSD included) with
mitral atresia/stenosis (or
  AVSD) and Pulmonary
  stenosis (possible ?)
DORV diferential diagnosis: conotrunkal anomalies
Extracardiac anomalies -
    ventriculomegaly
Management
 We offer karyotyping
  (CVS or                   If karyotype is normal:
  amniocentesis)            search for 22q11
  because it is frequent     microdeletion (di
  associated with            George)
  chromosomal
  abnormalities –           Cardiologist solution
  T13,18). Poor              (search for real CHD at
  prognosis:                 18-20 weeks and
  extracardiac anomalies     prognosis depends on
                             possible
 Abnormal karyotype:        lesions/extracardiac
      we offer TOP           anomalies
“ Ultrasound anomalies
scan” at any pregnancy
ages ?
  Patient was referred for other reason (in
   this case)
  Look and question for every possible
   anomalies
  Have always suspicions
  To recognize the limits of ultrasound to
   asses fetal anatomy at every age of
   gestation
Multumesc!
T hank you!
www.medicinafetala.ro

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ANATOMY AND PHYSIOLOGY OF REPRODUCTIVE SYSTEM.pptx
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Fetal Ecocardiography Screening

  • 1. Pr enatal dia gnosis of fetal hear t anomalies Ultrasound screening Bogdan M. Muresan
  • 2. The incidence of CHD (Congenital Heart Disease) is around 8 to 9 per 1000 live births  If all subtle cardiac anomalies are counted (bicuspid Ao valve, aneurysm of atrial septum and LSVC persistent) may be in order of 50 per 1000 live births.  The suspicion for CHD during a routine ultrasound is a risk factor with highest yield for CHD (40 to 50%)
  • 3. The majority of fetuses with CHD have no known risk factors. SCREENING for CHD to every pregnant women - routine scan: nuchal scan (12 weeks) and anomalies scan (20-22 weeks) Risk factors for CHD  Fetal: chromosomal abnormalities, extracardiac anatomic abnormalities, fetal cardiac arrhytmia, suspected cardiac anomaly on routine ultrasound, thickened nuchal translucency, monochorionic placentation;  Maternal: family history of CHD, maternal metabolic disorders (diabetes, phenylketonuria), maternal teratogen exposure, pregnancy from assisted reproduction techniques, maternal obesity  Alferd Abuhamad, Rabih Chaoui: A Practical Guide to Fetal Echocardiography
  • 4. Nuchal scan (11-13WG) soft markers for aneuploidies and CHD (in euploid cases): NT thickened; TR regurgitation; DV with “a” reverse
  • 5. CASE: 8 weeks pregnancy - refferal for a “problem”?
  • 6. Is here a normal pregnancy ???
  • 7. Routine exam at 8 weeks search for: localisation / number of fetus-placenta (intrauterine pregnancy), presence of FHR (normal FHR), embryon adnexa (normal yolk sac)
  • 8. Is there a possible problem ?
  • 9. Embryo anatomy: heart is almost complete developed; but it is impossible to asses heart anatomy - look to heart position in thorax??
  • 10. Untill 10-11 weeks there is a normal exomphalos (with bowel contents)
  • 11. Transverse view of embryo thorax
  • 14. Patient was reevaluated at 11 weeks (nuchal scan) unfortunately CRL < 45 mm (42,2mm) but:……
  • 15. Normal fetal anatomy at this age
  • 16. 3D image revealed normal fetal anterior wall (there is no place for “ectopia cordis”)
  • 17. Nuchal scan (CRL between 45-84 mm or 11-13 WG) Normal midsagital view – fetal profile (NT, FMF angle, nasal bone, intracerebral translucency)
  • 18. Normal fetal anterior wall: umbilical cord insertion and heart localisation
  • 19. Good result at nuchal scan: PAPP-A, freeBetaHCG, NT Combined risk assessment (risk for chromosomal abnormalities under 1/1000)
  • 20. New soft markers in nuchal scan: nasal bone, FMF angle, Tricuspid and DV flow (routinely) The presence of Tricuspid regurgitation – it is associated with chromosomal abnormalities and high risk for CHD in euploid fetuses)
  • 21. Possible AVSD (if it is present - increases T21 risk to ¼ and karyotyping is necessary)
  • 22. After 10 days we performed a fetal echocardiography AVSD ???
  • 23. or Mitral atresia with VSD
  • 24. Great vessel outflow tract ???
  • 25. Outflow Tract: - Ao and Pulmonary Trunk have common origin in Right Ventricle - They are parallel at origin - Pulmonary Trunk smaller than Ao
  • 26. DORV (VSD included) with mitral atresia/stenosis (or AVSD) and Pulmonary stenosis (possible ?)
  • 27. DORV diferential diagnosis: conotrunkal anomalies
  • 28. Extracardiac anomalies - ventriculomegaly
  • 29. Management  We offer karyotyping (CVS or  If karyotype is normal: amniocentesis)  search for 22q11 because it is frequent microdeletion (di associated with George) chromosomal abnormalities –  Cardiologist solution T13,18). Poor (search for real CHD at prognosis: 18-20 weeks and extracardiac anomalies prognosis depends on possible  Abnormal karyotype: lesions/extracardiac we offer TOP anomalies
  • 30. “ Ultrasound anomalies scan” at any pregnancy ages ?  Patient was referred for other reason (in this case)  Look and question for every possible anomalies  Have always suspicions  To recognize the limits of ultrasound to asses fetal anatomy at every age of gestation