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Updated: Jul 17 2017

Coarctation of Aorta

Overview
 
               
Snapshot
  •  A 7-year-old-boy is seen for the first time by a primary care physician. His parents report that he tires easily and often complains of weakness in his legs. Physical exam shows a healthy boy with a blood pressure of 141/91 mmHg. His lower extremities are slightly atrophic with a mottling appearance.
Introduction
  • A congenital heart defect characterized by narrowing of the lumen of the aorta
    • usually occurs just distal to subclavian artery at the juntion of the ductus arteriosus and aortic arch
    • leads to decreased flow distal to the constriction and increased flow proximal to it 
  • Risk factors include
    • Turner syndrome   
    • affects males > females
    • associated with bicuspid aortic valve (~70%)
  • A cause of secondary HTN
Presentation
  • Symptoms 
    • patients present in childhood with
      • asymptomatic HTN
        • due to decreased blood flow to kidneys
        • when symptomatic may present with headaches or blurred vision
      • dyspnea on exertion
      • syncope
      • systemic hypoperfusion (shock state)
      • without cyanosis
  • Physical exam
    • shows systolic BP in the upper extremities greater than in the lower extremities
      • right arm BP may be greater than left arm BP
      • with weak femoral and distal pulses
    • continuous murmur over collateral vessels in the back
    • may have machine-like murmur due to a patent ductus arteriosus
    • lower extremity skin mottling
Evaluation
  • CXR may reveal:
    • "reverse 3 sign"
      • due to dilatation of the proximal and distal segments surrounding the coarctation
    • "rib notching" due to collateral circulation through intercostals
  • Diagnosis made by CT or aortogram
  • Echo shows
    • left ventricular hypertrophy (can also be seen sometimes on EKG) 
    • increased incidence of bicuspid aortic valves (70%)
Differential
  • Primary HTN, pheochromocytoma, aortic stenosis, renal artery syndrome, renal disease, Cushing's, and hyperaldostronism
Treatment
  • Surgical correction or balloon angioplasty +/- stent placement
    • repair ASAP to prevent heart failure, CAD, and intercerebral hemorrhage
  • Endocarditis prophylaxis
    • indicated prior to dental work before and after surgical repair of defect
Prognosis, Prevention, and Complications
  • 25% continue to have HTN even after repair
  • Condition often recurs

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