ABTS Congenital Cardiac flashcards
ABTS Congenital Cardiac · Build recall with a focused review session.
32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Prostaglandin E1 infusion
- PGE1 at 0.01–0.05 mcg/kg/min maintains ductal patency in ductal-dependent lesions; monitor for apnea, hypotension, fever, and tachycardia.
- Arterial switch operation
- For d-transposition of the great arteries, the arterial switch is ideally performed within the first two weeks before left ventricular mass regresses; coronary transfer is critical.
- Norwood stage I
- Stage I palliation for hypoplastic left heart syndrome includes atrial septectomy, neoaortic reconstruction with arch repair, and a systemic-to-pulmonary shunt or RV-PA conduit.
- Obstructed TAPVC
- Obstructed total anomalous pulmonary venous connection is a surgical emergency; avoid prostaglandin E1 because increasing pulmonary blood flow can worsen pulmonary edema.
- PA/IVS with coronary sinusoids
- In pulmonary atresia with intact ventricular septum, coronary sinusoids may make RV decompression unsafe; a systemic-to-pulmonary shunt may be preferred to protect myocardial perfusion.
- Critical aortic stenosis
- Neonatal critical aortic stenosis is usually treated first with balloon aortic valvuloplasty; surgery is reserved for failed balloon dilation or associated severe regurgitation.
- Truncus arteriosus repair
- Neonatal repair closes the ventricular septal defect and establishes right ventricle-to-pulmonary artery continuity with a conduit; 22q11.2 deletion should be assessed.
- Bidirectional Glenn shunt
- Superior cavopulmonary connection is usually performed at 3–6 months; it requires low pulmonary artery pressure, unobstructed pulmonary arteries, and acceptable ventricular function.
- Fontan completion
- Total cavopulmonary connection is typically completed at 2–4 years; fenestration may be used in high-risk patients with elevated pulmonary pressure or ventricular dysfunction.
- Tetralogy of Fallot repair
- Repair closes the ventricular septal defect and relieves right ventricular outflow tract obstruction; preserving pulmonary valve function reduces late pulmonary regurgitation.
- AV septal defect repair
- Repair closes the atrial and ventricular septal defects and reconstructs the common atrioventricular valve; residual mitral regurgitation and pulmonary hypertension affect outcomes.
- Ebstein cone repair
- Cone repair reconstructs the tricuspid valve by mobilizing and reattaching leaflets; concomitant arrhythmia surgery is considered when accessory pathways or atrial arrhythmias are present.
- Marfan aortic root threshold
- Adults with Marfan syndrome generally warrant aortic root replacement when the root reaches about 50 mm or grows rapidly; lower thresholds apply with additional risk factors.
- Eisenmenger pregnancy
- Eisenmenger syndrome causes fixed pulmonary vascular resistance and cyanosis; pregnancy is contraindicated because maternal mortality is high, so effective contraception is essential.
- Qp/Qs formula
- Pulmonary-to-systemic flow ratio equals (SaO2 minus SvO2) divided by (pulmonary venous oxygen saturation minus pulmonary artery oxygen saturation).
- Milrinone infusion
- Milrinone, a phosphodiesterase-3 inhibitor, is infused at 0.25–0.75 mcg/kg/min to improve cardiac output; hypotension and thrombocytopenia are potential adverse effects.
- Pulmonary hypertensive crisis
- Management avoids hypoxia, acidosis, and agitation; inhaled nitric oxide at 20–40 ppm, sedation, and pulmonary vasodilators reduce right ventricular afterload during a crisis.
- Junctional ectopic tachycardia
- Junctional ectopic tachycardia after congenital heart surgery is treated by correcting electrolytes, treating fever, reducing catecholamines, and using amiodarone or pacing when needed.
- Delayed sternal closure
- The sternum may remain open after neonatal cardiac surgery when edema or hemodynamic instability prevents safe closure; delayed closure occurs after swelling resolves in the intensive care unit.
- Chest tube bleeding
- Output exceeding 3 mL/kg/hour for three consecutive hours after pediatric cardiac surgery warrants evaluation for coagulopathy, surgical bleeding, and possible reexploration.
- Single-ventricle oxygen target
- After a systemic-to-pulmonary shunt, target oxygen saturation is about 75–85%; avoid hyperoxia, keep PaCO2 near 35–45 mm Hg, and monitor systemic oxygen delivery.
- Qp/Qs by saturations
- The Fick-based shunt fraction uses oxygen saturation differences: Qp/Qs = (SaO2 − SvO2)/(SpvO2 − SpaO2), where SpvO2 is pulmonary venous and SpaO2 pulmonary arterial saturation.
- Oxygen content formula
- Arterial oxygen content equals 1.34 times hemoglobin times arterial oxygen saturation plus 0.003 times arterial oxygen tension; it estimates oxygen carried in blood.
- Fick principle
- The Fick principle states that cardiac output equals oxygen consumption divided by the arteriovenous oxygen content difference; it underlies invasive hemodynamic calculations.
- Eisenmenger physiology
- Long-standing left-to-right shunts can cause irreversible pulmonary vascular disease, reversing shunt flow and producing cyanosis; vasodilator testing does not usually restore operability.
- Cardiac MRI after TOF
- Cardiac magnetic resonance quantifies right ventricular volumes and pulmonary regurgitation after tetralogy of Fallot repair and helps time pulmonary valve replacement.
- CT for vascular rings
- Computed tomography angiography defines vascular rings, anomalous coronary arteries, and complex aortic arch anatomy when echocardiography is insufficient.
- Balloon atrial septostomy
- Balloon atrial septostomy enlarges an atrial communication in lesions such as d-transposition or hypoplastic left heart with restrictive atrial septum, improving mixing or pulmonary venous drainage.
- Informed consent in pediatrics
- Consent for a child's cardiac surgery is obtained from a parent or guardian; the child's assent is sought when developmentally appropriate, using risks, benefits, and alternatives.
- Best interest standard
- When a child cannot decide, surrogate decision-makers should choose the option that best serves the child's interests, considering medical benefit, burdens, and the family's values.
- I-PASS handoff
- I-PASS is a structured handoff covering illness severity, patient summary, action list, situation awareness, and synthesis by receiver; it improves communication and reduces preventable harm.
- Just culture
- Just culture distinguishes human error from at-risk or reckless behavior, encouraging error reporting and system improvement while retaining accountability for unsafe choices.