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ultrasound diagnosis of fatal anomalies

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TRANSPOSITION OT THE GREAT ARTERIES

Ventricular tachycardia: normal atrial rhythm

with an increased frequency in the heart chamber.

Mostly benign.

Clinical management: Further sonographic

screening, including fetal echocardiography. Intermittent

ultrasound monitoring. M-mode

echocardiography. Depending on the form and

cause of the tachyarrhythmia, initially therapy

with transplacental medication (e.g., digoxin

and flecainide, possibly sotalol). If this therapy is

not successful, or in case of fetal hydrops, direct

administration of agents into the umbilical vein

(e.g., amiodarone is favorable due to its long halflife;

side effects include hypothyroidism in the

fetus). This treatment option should only be

used in units with experience in prenatal cardiology.

In a mature fetus, delivery and postnatal

therapy is an option. Vaginal delivery is possible.

Procedure after birth: After birth, facilities for

intensive medical treatment are required. In

severe cases that do not respond to this, electrophysiological

diagnosis and intervention with

ablation of extra conduction points or other

structures determining the cardiac rhythm using

a catheter can be an option as the last resort.

Prognosis: Fetal hydrops develops within 48 h in

case of fetal tachycardia of 220–240 bpm. The

mortality is very high in these cases. The tachycardias

are usually well treatable using medications.

Transposition of the Great Arteries (TGA)

Definition: In D-TGA, the aorta arises from the

right ventricle and lies ventral and to the right

(D, dextro-)of the pulmonary artery. The pulmonary

artery arises posteriorly from the left ventricle.

In L-TGA (corrected transposition; L,

levo-), the atrioventricular and ventriculoarterial

connections are discordant, so that the

hemodynamic situation is corrected.

Incidence: One in 2000 births, 5% of all congenital

heart disease.

Clinical history/genetics: Recurrence rate in case

of one affected sibling is 1.5%, in case of two affected

siblings 5%.

References

Chang CL, Chao AS, Wu CD, Lien R, Cheng PJ. Ultrasound

recognition and treatment of fetal supraventricular

tachycardia with hydrops: a case report. Chang Keng

I Hsueh Tsa Chih 1998; 21: 217–21.

Fyfe DA, Meyer KB, Case CL. Sonographic assessment of

fetal cardiac arrhythmias. Semin Ultrasound CT MR

1993; 14: 286–97.

Gembruch U, Bald R, Hansmann M. Color-coded M-

mode Doppler echocardiography in the diagnosis of

fetal arrhythmia. Geburtshilfe Frauenheilkd 1990;

50: 286–90.

Gembruch U, Hansmann M, Bald R, Redel BA. Supraventricular

tachycardia of the fetus in the 3rd

trimester of pregnancy following persistent supraventricular

extrasystole. Geburtshilfe Frauenheilkd

1987; 47: 656–9.

John JB, Bricker JT, Fenrich AL, et al. Fetal diagnosis of

right ventricular aneurysm associated with supraventricular

tachycardia with left bundle-branch

block aberrancy. Circulation 2002; 106: 141–2.

Jouannic JM, Le Bidois J, Fermont L, et al. Prenatal ultrasound

may predict fetal response to therapy in nonhydropic

fetuses with supraventricular tachycardia.

Fetal Diagn Ther 2002; 17: 120–3.

King CR, Mattioli L, Goertz KK, Snodgrass W. Successful

treatment of fetal supraventricular tachycardia with

maternal digoxin therapy. Chest 1984; 85: 573–5.

Krapp M, Baschat AA, Gembruch U, Geipel A, Germer U.

Flecainide in the intrauterine treatment of fetal supraventricular

tachycardia. Ultrasound Obstet Gynecol

2002; 19: 158–64.

Kühl PG, Ulmer HE, Schmidt W, Wille L. Non-immunologic

hydrops fetalis: report of 14 cases and literature

review. Klin Pädiatr 1985; 197: 282–7.

Shirley IM, Richards BA, Ward RH. Ultrasound diagnosis

of hydrops fetalis due to fetal tachycardia. Br J Radiol

1981; 54: 815–7.

Simpson LL, Marx GR. Diagnosis and treatment of structural

fetal cardiac abnormality and dysrhythmia.

Semin Perinatol 1994; 18: 215–27.

Wester HA, Grimm G, Lehmann F. Echocardiographic diagnosis

of fetal heart insufficiency caused by supraventricular

tachycardia. Z Kardiol 1984; 73: 405–8.

Teratogens: High doses of vitamin A, amphetamines,

trimethadione, sexual steroids.

Associated malformations: Situs inversus.

Ultrasound findings: The two great vessels run

parallel to each other instead of crossing. The

aorta arises from the right ventricle and runs

ventral to the pulmonary trunk, which arises

from the left ventricle. The aorta is identified because

of its arch and the branches arising from it.

The pulmonary trunk is recognized due to its bifurcation

into the right and left pulmonary arteries.

The isthmus of the aorta may show stenosis.

In 40% of cases, a concomitant VSD and

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