Cardiology Flashcards
Warfarin and pregnancy
Warfarin is associated with teratogenicity (eg, skeletal abnormalities) and can cross the placental barrier, leading to fetal bleeding.
Low-dose warfarin ≤5 mg/day appears to provide a higher safety margin, and continuing this regimen throughout pregnancy (including the first trimester) is a potential option for pregnant patients with mechanical heart valves.
However, pregnant patients with any other indication for anticoagulation (eg, atrial fibrillation, venous thromboembolism) and those with higher dose requirements (>5 mg/day) should be managed with subcutaneous LMWH
Statin myopathy
Statin myopathy commonly occurs due to drug-drug interactions and usually resolves after discontinuing the statin.
After resolution of myopathy, patients requiring aggressive cholesterol lowering should be restarted on an alternate statin with a lower myopathic potential (eg, rosuvastatin, pravastatin, fluvastatin).
Post CABG mediastinitis
Postoperative mediastinitis typically occurs within the first 2 weeks after surgery and presents with fever, tachycardia, chest pain, and signs of sternal wound infection, such as purulent discharge.
Post cardiac injury syndrome
likely an autoimmune reaction, causing inflammation and presenting with the typical symptoms of pericarditis. Treatment includes NSAIDs or steroids. Prophylactic colchicine after cardiac surgery significantly decreases the incidence of PCIS.
Aortic dissection complications
Stroke (carotid artery)
• Horner syndrome (carotid sympathetic plexus)
• Acute aortic regurgitation (aortic root/valve)
• Myocardial ischemia/infarction (coronary artery ostia)
• Pericardial effusion/tamponade (pericardium)
• Hemothorax (pleural cavity)
• Renal infarction (renal arteries)
• Intestinal ischemia (mésenteric arteries)
• Lower extremity paralysis (spinal arteries)
Mitral stenosis
Percutaneous mitral balloon valvotomy indications
Severe mitral stenosis (valve area ≤1.5 cm²) & ≥1 of the following:
• Symptoms (eg, dyspnea, orthopnea)
• Pulmonary artery systolic pressure >50 mm Hg
Mitral valve stenosis
Percutaneous mitral valve balloon valvotomy contraindications
• Moderate or severe mitral regurgitation
• Complex valve anatomy
• Extensive valve calcification
• Left atrial thrombus
They should proceed with surgical mitral valve repair/replacement
Anti platelets post coronary stenting
Recommended duration
• DAPT for minimum of 6-12 months after BMS or DES placement
• DAPT for minimum of 4 weeks in select patients after BMS
• Continue DAPT for a total of 30 months if possible (eg, low bleeding risk)
• Continue aspirin indefinitely
Dual anti platelets perioperative management
• Elective surgery: defer procedure until after minimum DAPT duration
• Urgent surgery: continue P2Y12 receptor blocker or hold for shortest duration possible
• Continue aspirin unless high risk of severe surgical bleeding
Plavix pre CABG
The use of P2Y12 inhibitors within 5-7 days of coronary artery bypass graft (CABG) is associated with an increased risk of significant bleeding, with increased requirements for blood transfusion and possible reoperation; current guidelines recommend that these agents be discontinued at least 5-7 days before CABG
Peripheral arterial disease management (Part 1)
-Modifying risk factors (especially smoking cessation)
-adding graded exercise therapy can improve symptoms and decrease the progression of disease.
-Antiplatelet therapy is the preferred initial therapy for PAD, and aspirin is the preferred drug .
-Clopidogrel is typically used in patients who cannot tolerate aspirin.
Peripheral arterial disease management (Part 2)
-Patients who are still symptomatic on antiplatelet therapy require second-line agents such as cilostazol, a phosphodiesterase inhibitor and vasodilator that inhibits platelet aggregation and significantly increases maximal and pain-free walking distances.
-Cilostazol is contraindicated in patients with heart failure due to increased mortality in these patients.
Choice of stress testing in intermediate risk CAD
Pharmacologic radionuclide perfusion imaging should be performed to evaluate suspected coronary heart disease in patients with paced ventricular rhythm or left bundle branch block.
Papillary muscles rupture
Papillary muscle rupture may occur acutely or within 3-5 days of acute myocardial infarction, most commonly one that affects the inferior wall. Patients have rapid-onset pulmonary edema and cardiogenic shock due to acute mitral regurgitation. A new holosystolic murmur is often, but not always, present
Hypertrophic cardiomyopathy definition
Defined as left ventricular wall thickness ≥15 mm (1.5 cm) at any location in the absence of other potential causes (eg, hypertension, valvular heart disease).
Hypertrophic cardiomyopathy presentation
Patients with HCM may remain asymptomatic, or they may develop dyspnea, orthopnea, palpitations, chest pain, dizziness, or syncope.
Exertional myocardial ischemia can lead to sustained ventricular arrhythmia and sudden cardiac death (SCD);
HCM is the most common cause of SCD in young athletes.
Hypertrophic cardiomyopathy initial management
To lower the risk of SCD, patients with probable or definite HCM should not participate in high-intensity competitive sports regardless of the presence of symptoms, degree of wall thickness or left ventricular outflow tract (LVOT) obstruction, or prior treatment.
Hypertrophic cardiomyopathy ICD indication
An implantable cardioverter defibrillator (ICD) is generally indicated for primary prevention in patients with risk factors for SCD (eg, left ventricular wall thickness >30 mm, family history of SCD due to HCM) and for secondary prevention in patients who survive an episode of sustained ventricular arrhythmia.
Hypertrophic cardiomyopathy medical management
Medical therapy with negative inotropic agents (eg, beta blockers, nondihydropyridine calcium channel blockers, disopyramide) is recommended in patients with LVOT obstruction and symptoms of heart failure.
Dihydropyridine calcium channel blockers (eg, amlodipine, nifedipine) as well as other vasodilators (eg, ACE inhibitors) and diuretics should be avoided in patients with HCM as they decrease afterload and can worsen LVOT obstruction and symptoms.
Hypertrophic cardiomyopathy surgical management
Alcohol septal ablation or surgical septal myectomy is indicated for HCM patients with severe LVOT obstruction (resting or Valsalva gradient >50 mm Hg) and heart failure symptoms that are refractory to optimal medical therapy
Central sleep apnea
Central sleep apnea with Cheyne-Stokes breathing is a potential complication in patients with heart failure. Treatment includes positive airway pressure therapy and supplemental oxygen.
Peripartum cardiomyopathy Risk factors
• Maternal age >30
• Multiple gestation
• Eclampsia or preeclampsia
- maternal cocaine use
- African descent
Peripartum cardiomyopathy presentation
• Left ventricular ejection fraction <45%
• Onset at ≥36 weeks gestation or ≤5 months postdelivery
• No other causes of heart failure
Peripartum cardiomyopathy management
• Urgent delivery if hemodynamic instability present
• Standard management of heart failure with reduced ejection fraction (eg, beta blocker, diuretics) Avoid ARBs/ACEI during pregnancy
• Patients who recover LV function to normal have a lower risk of complications during subsequent pregnancies, but their risk is still elevated when compared to the general population.
Patients with persistent LV dysfunction have a substantially higher risk of complications such as significant decline in LVEF, recurrent heart failure, and death and should avoid subsequent pregnancies.
Atrial flutter management
Radiofrequency ablation has an excellent success rate in restoring and maintaining sinus rhythm in patients with typical atrial flutter. It is generally preferred over long-term antiarrhythmic agents as a safe and effective first-line treatment in such patients.
Congenital long QT syndrome
-Jervell & Lange-Nielsen syndrome (autosomal recessive)
-Romano-Ward syndrome (autosomal dominant)
Management
Management includes avoidance of conditions (eg, strenuous exercise, electrolyte abnormalities such as hypokalemia or hypomagnesemia) and medications (eg, antipsychotics, fluoroquinolones) that may prolong the QT interval. Current guidelines also recommend that all patients with congenital LQTS (symptomatic or asymptomatic) be treated with beta blockers (eg, propanolol, nadolol) to decrease the risk of symptomatic arrhythmias and sudden cardiac death