Truncus Arteriosus

Clinical

Definition:Ā single arterial trunk and overriding VSD, arising from normally formed ventricles. Absent or diminutive PDA. 100% mortality within the first year if untreated.

Prevalence 3% in CHD.

Incidence 5-15:100.000.


Physiology:

Parallel circulation.

With decreasing PVR there is Ā increased PBF and increased flow to LA and LV, leading to CCF.


Diagnosis:

Presents usually 1-2 weeks postnatally (decreasing PVR) and subsequently CCF with failure to thrive, dyspnea, diaphoresis.

Diagnosis is by echo and in selected cases, cardiac catheterisation.


Preoperative management:


Preoperative preparation:

ECG, CXR, CUS, FBE, clotting, UECs, FISH, PRBC (4), FFP (2), platelets (2), cryoprecipitate (2).

Methylprednisolone 10mg/kg 12hrs and 6hrs pre surgery in neonates.


Surgery:

Detaching of the PAs, ventriculotomy to close the VSD, valved RV-PA conduit.

In severe truncal valve insufficiency there may be aortic homograft with reimplantation of the coronary arteries.


Postoperative management:


Specific problems:


Outcome:

Perioperative mortality: 10%

Long term survival after 5, 10, 15 years: 90%, 85%, 83%


References:

[1] Critical Heart Disease in Infants and Children; 2nd ed, Nichols et al: Peristent Truncus arteriosus

[2] Surg Clin North Am. 1949 Aug;29(4):1245-70: Collett et al: Persistent truncus arteriosus; a classification according to anatomic types

[3] Am J Cardiol. 1965 Sep;16(3):406-25: Van Praagh et al: The anatomy of common aorticopulmonary trunk (truncus arteriosus communis) and its embryologic implications. A study of 57 necropsy cases

[4] Cardiol Young. 2005 Feb;15 Suppl 1:125-31: Backer et al: Techniques for repairing the aortic and truncal valves


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