Q. A CXR done in a cyanotic infant showed the typical boot-shaped heart. Which next investigation will be helpful to see if it's TOF or Tricuspid Atresia, if echocardiography is not available immediately?
Ans.
When a CXR showing a boot-shaped heart is obtained, echocardiography is immediately performed. Since it is not available, an ECG is performed. If the ECG shows
Features of RVH → Tetralogy of Fallot
Features of LVH → Tricuspid Atresia.
Q. Which of the following is a ductus-dependent lesion?
TGA
TAPVC
ECD
Supracristal VSD
Ans. A) TGA
Q. Which of the following is a ductus-dependent lesion?
TGA
Tricuspid atresia
ECD
Supracristal VSD
Since most varieties of TGA have VSD. TGA with intact ventricularseptum – only ductus-dependent form of TGA.
Ans. B) Tricuspid atresia
Q. A neonate developed shock, absent pulses, and poor perfusion on day 2 of life. Sepsis markers were negative, and there was a poor response to Dopamine & Epinephrine. On doing echocardiography, a specific abnormality in the heart was detected, for which Alprostadilinfusion was started, and there was a dramatic improvement in his clinical status. What could not have been the likely CHD?
Q. Why is PDA more common in preterm and LBW babies?
Ans. The smooth muscle in the wall of the pretermductus is less responsive to high PO2 . Thus, it is less likely to constrict after birth.. The valve structure of DA is normal in preterm newborns. Only its reactivity to oxygen is reduced
Q. Which age group shows maximum chances of restenosis or re-coarctation?
Ans. Surgery done in infancy (before 1 year) shows maximum chances of restenosis, but this does not mean that you delay the surgery.
Q. What is the procedure of choice if re-coarctation occurs?
Ans. Balloon angioplasty is the first-line treatment performed.
Balloon angioplasty as a secondary procedure after initial surgery does not increase the chance of damage, rupture, or aneurysm formation.
It is, therefore, the method of choice once post-surgical re-coarctation has happened.
Q. What are the CNS complications associated with CoA?
Ans. They are related to the formation of CNS haemorrhage, including haemorrhagic stroke.
Q. If the CoA is uncorrected, how long will the patient survive?
Ans. The patient will survive for 20-40 years. There are cases where they have survived for longer, but there are LV dysfunctions seen, due to which the patient will die because of uncorrected cardiac failure. The patients have been candidates for cardiac transplants.
Ans. A heart-lung transplant is needed. If some of the patients benefit from heart transplants alone or, in the case of cirrhosis, a liver transplant can be carried out.
Q. Look at the Echo image of the parasternal long-axis view in a 7-month-old infant showing Multiple ventricular masses and tell the likely diagnosis?
Ans. The most likely diagnosis is Rhabdomyoma.
Q. IE is strongly suspected in a child. But blood cultures sterile possibilities?
Ans.
Antimicrobial given prior to presentation.
Fungal sepsis.
Infection with fastidious/Atypical microbes: Brucella, Bartonella, HACEK group and Chlamydia.
Improper blood collection for culture.
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