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ultrasound diagnosis of fatal anomalies

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TETRALOGY OF FALLOT

Extrasystoles (Supraventricular)

Definition: This is defined as heart beats occurring

additionally to the sinus rhythm. The most

frequent cause of extrasystoles is premature

contractions of the atrium, which appear more

than 8 ms prior to the expected atrial contractions.

The stimulation arises mostly from an ectopic

focus within the atrium and not from the

sinoatrial node.

Procedure after birth: If the arrhythmia is present

until just before birth, then 24-h monitoring

of the heart frequency of the newborn is recommended.

ECG is useful.

Prognosis: Spontaneous remission in the late

stages of pregnancy or just after birth is the usual

course.

Incidence: Seen often in the early stage of the

third trimester.

Clinical history/genetics: Caffeine intake by the

mother has been described as a possible cause.

Certain drugs may also be responsible (fenoterol

and some vasoactive substances such as those in

nasal sprays).

Associated malformations: Structural cardiac

anomalies; 1% of cases may be complicated by

development of supraventricular tachycardia.

Ultrasound findings: The arrhythmic contractions

are first diagnosed in B-mode. They can be

differentiated further using M-mode.

Clinical management: Further sonographic

screening, including fetal echocardiography, to

exclude cardiac anomaly. Weekly control of the

heart frequency is necessary for early detection

and treatment of supraventricular tachycardia,

before the development of cardiac failure with

fetal hydrops. Abstinence from caffeine is advised

and β-mimetics should be avoided.

Tetralogy of Fallot

Definition: A combined cardiac malformation

consisting of four anomalies: VSD, pulmonary

stenosis, hypertrophy of the right heart (postnatal)and

overriding of the aorta (over VSD).

Incidence: One in 2000 births, 6–10% of all congenital

heart malformations.

Clinical history/genetics: Mostly a sporadic,

multifactorial inheritance. Recurrence rate of

2.5% with one affected sibling and of 8% when

two siblings are affected; in case of an affected

References

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M, Pahl L. Prenatal diagnosis and management of

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

fetal cardiac arrhythmias. Semin Ultrasound CT MR

1993; 14: 286–97.

Goraya JS, Parmar VR. Fetal and neonatal extrasystoles.

Indian Pediatr 2000; 37: 784–6.

Hata T, Takamori H, Hata K, Takamiya O, Murao F, Kitao

M. Antenatal diagnosis of congenital heart disease

and fetal arrhythmia by ultrasound: prospective

study. Gynecol Obstet Invest 1988; 26: 118–25.

Kleinman CS, Hobbies JC, Jaffe CC, Lynch DC, Talner

NS. Echocardiographic studies of the human fetus:

prenatal diagnosis of congenital heart disease and

cardiac dysrhythmias. Pediatrics 1980; 65: 1059–67.

Pál A, Gembruch U, Hansmann M. Practical importance

of the exact diagnosis of fetal arrhythmias. Orv Hetil

1991; 132: 1359–62.

Southall DP, Richards J, Hardwick RA, et al. Prospective

study of fetal heart rate and rhythm patterns. Arch

Dis Child 1980; 55: 506–11.

Tsujimoto H, Takeshita S, Kawamura Y, Nakatani K, Sato

M. Isolated congenital left ventricular diverticulum

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9.

mother the probability of recurrence is 2.5 %,

and with an affected father it is 1.5%. Autosomaldominant

inheritance has also been reported in

rare cases.

Teratogens: High doses of Vitamin A, thalidomide,

trimethadione, sexual steroids and alcohol.

Associated malformations: Extracardiac malformations

are seen in a total of 16%.

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