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PNP cardiac

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Answer
Cardiac anomaly that results from failure of the endocardial cushion to develop properly. Has 3 components-ASD, VSD and formation of AV valves. L>R shunting.   AV (atrioventricular) canal  
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cardiac lesion-failure of primitive arterial trunk to divide into aorta and PA causing mix of systemic and pulm. blood flow   Truncus Arteriosis  
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Is truncus arteriosis (TA) cyanotic or non-cyanotic   cyanotic  
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Management for truncus arteriosis (TA)?   Prostaglandin administration, manage shock and CHF. Surgery when stable.  
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Aorta arises from RV and PA rises from LV   Transposition of the Great Vessels  
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Management of transposition of the great vessels (TGV)?   If no ASD or VSD, will require immediate prostaglandin infusion, balloon septostomy ASAP  
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Cardiac lesion with 4 findings: outlet type VSD, RVOT obstruction, overriding aorta, RVH. R>L shunting.   Tetrology of Fallot  
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What is the treatment for a TET spell?   Legs to chest will increase SVR, phenylephrine is drug.  
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What cardiac lesion can be diagnosed later in life?   Coarctation of the Aorta  
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How does a coarctation present in the older child?   Systemic hypertension  
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Assessment of hypertension involves   BP eval (repeated), heart sounds, dysmorphic features, abnormal retinal exam (papilledema) abnormal growth parameters.  
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Diagnostic test for hypertension   CBC, UA, UC, uric acid, BUN, creatinine, lytes, lipid panel, renal US, echocardiography  
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Management of mild essential hypertension   dietary, exercise, wt loss  
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management of essential hypertension   diuretics, vasodialators, beta blockers, ACE inhibitors (never first line)  
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Management of secondary hypertension   find and tx underlying cause, referral to cardiology or nephrology  
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Definition of hypertension in kids   BP consistently >95% for age, gender, height measured on 3 separate occasions  
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Def secondary hypertension   usually renal vascular or systemic vascular with genetic syndrome, endocrine disorder, excess endogenous catecholamine  
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Def essential hypertension   multifactorial, genetic, familiar, enviro, dietary factors  
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Def kawasaki syndrome   Aquired heart disease. Acute systemic vasculitis of unknown origin. Acute and subacute phases.  
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Diagnosis/ symptoms of kawasaki disease   PRI: fever x5d, indurated palms & soles, erythematous rash, conjunctivae injection, desquam lips, strawberry tongue, LAD. SEC: vasculitis as murmur, N/V/D, abd pain, proteinuria, cough, joint swelling, seizures. 5D FEVER +4/5 PRIMARY OR 3+ CARDIAC INVOL  
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Treatment of kawasaki disease   IVIG, high dose aspirin, chronic aspirin if indicated, cardiology & ID consults. LT f/u echo's  
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Def rheumatic fever   Aquired heart disease. Collagen vascular disease of connective tissue resulting in vasculitis. Inflammation of joints & heart. Complication of GAS pharyngitis.  
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Diagnosis/ symptoms of rheumatic fever   Presents as migratory polyarthritis with joint pain, rash & subq nodules. Jones criteria: 2 major (carditis, polyarthritis, chorea, erythea marginatum, subq nodules) OR 1major & 2 minor (arthralgia, fever, elevated CRP, ESR, WBC, prolonged PR interval.  
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Rx & treatment for Rheumatic fever   Acute: penicillin, aspirin therapy. Bed rest until fever and symptoms resolove. cardiology and ID consults. Then PCN prophylaxis for endocarditis.  
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Symptoms of cardiomyopathies   CHF & decreased CO =>SOB  
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Etiology of cardiomyopathies   Acute or chronic sequelae of atypical viral disease. Dilated cardiomyopathy is most often seen.  
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Diagnosis of cardiomyopathies   CXR reveals cardiomegaly. ECHO globally decreased function. Work up for anatomic abnormalities, metabolic causes, infectious causes.  
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Treatment of cardiomyopathies   Acute: support cardiac output with inotropes and vasodilators, diuretics. Treat causes (IVIG, antivirals, surgery for ALCAPA)  
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Etiology of hypertrophic obstructive cardiomyopathy   50% familial, often found on autopsy  
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Symptoms of hypertrophic obstructive cardiomyopathy   Acute decompensation, may be with sports or activity  
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Management of hypertrophic obstructive cardiomyopathy   Activity restriction, beta blocker, avoidance of catecholamines  
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Etiology of Long QT syndrome   Congenital disorders characterized by a prolongation of the QT interval on ECG and a propensity to ventricular tacharrhythmias, which may lead to syncope, cardiac arrest, or sudden death  
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Symptoms of Long QT syndrome   Typically diagnosed s/p cardiac event(syncope or arrest). Eval relatives: K+, mg+, thyroid. EKG & echo.  
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Management of Long QT syndrome   Treat with beta blockers. Implantable cardioverter/defibrillator. Avoid meds that prolong QT (inc amioderone, EES, zoles & most psyc meds)  
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Definition/description of ASD   Opening in atrial septum. Left -> right shunting.  
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Symptoms/ characteristics of ASD   Usually asymptomatic, with soft, systolic ejection murmur with fixed S2. EKG - may show right axis deviation, RVH, Echocardiogram.  
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Management of ASD   May close spontaneously. Echocardiogram is routine monitoring. Surgery for large lesions.  
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Definition/description VSD   Open in the ventricular septum. Left to right shunting.  
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Symptoms/ characteristics of VSD   Findings dependent on the size of lesion and pulmonary vascular resistance. Signs of CHF, holosystolic murmur, pulmonary hypertension. can occur.  
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Management of VSD   Control symptoms of CHF prior to surgical correction, nutrition. Surgical correction is usually after the age of one.  
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Diagnostic tests of VSD   Echo, CXR, B-type natriuretic peptide serum level, EKG, occasionally cardiac catheterization.  
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Definition/description of Atrioventricular canal   Results for failure of endocardial cushion to develop normally. 3 components: ASD, inlet VSD, abnormal AV valves. LEFT TO RIGHT SHUNTING.  
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Symptoms/ characteristics of Atrioventricular canal   Depend on type and configuration. Tachypnea, poor weight gain, other signs of CHF.  
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Management of Atrioventricular canal   Control CHF and encourage weight gain. Surgical management.  
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Diagnostic of Atrioventricular canal   Echocardiogram, CXR.  
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Definition/description of PDA   Vessel connects the left main pulmonary artery to the descending aorta, in utero is part of normal circulation, after birth, lesion closes, if remains open: LEFT TO RIGHT SHUNTING.  
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Symptoms/ characteristics of PDA   Symptoms depend on extent of shunting. Possible CHF or pulmonary HTN. Symptoms include murmur, widened pulse pressure, low diastolic pressure and bounding pulses.  
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Management of PDA   Allow spontaneous closure. Surgery can be used. NSAIDs and prostaglandin keep PDA open.  
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Definition/ description of Truncus Arteriosus   Rare lesion - failure of the primitive arterial truck to septate and divide into aorta and pulmonary artery causing mixture of systemic and pulmonary blood flow. RIGHT TO LEFT SHUNTING.  
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Symptoms/ characteristics of Truncus Arteriosus   Usually diagnosed prenatally. Symptoms occur soon after birth with normal fall of PVR and include shock. Bounding peripheral pulses, cyanosis, harsh systolic murmur. EKG _ left atrial enlargement and biventricular hypertrophy.  
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Management of Truncus Arteriosus   Prostaglandin administration managing shock and CHF. Surgery indicated once patient stable.  
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Definition/ description of Transposition of the Great Vessels   Aorta rises from the anatomic right ventricle and the pulmonary artery rises from the anatomic left ventricle. RIGHT TO LEFT SHUNTING.  
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Symptoms/ characteristics of Transposition of the Great Vessels   Two separate and parallel circulation present.  
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Management of Transposition of the Great Vessels   Infants with intact ventricular and atrial septums will require immediate prostaglandin infusion, balloon septostomy ASAP.  
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Definition/ description of Tetralogy of Fallot   4 findings: outlet type VSD, right ventricular outflow tract obstruction, overriding aorta, RVH. RIGHT TO LEFT SHUNTING.  
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Symptoms/ characteristics of Tetralogy of Fallot   Degree of cyanosis is related to the degree of RV outflow tract obstruction. Presentation varies. Typically- TET spells. EKG - persistence of RVH beyond 3 months of age. CXR - "boot shaped" heart.  
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Management of Tetralogy of Fallot   Medical management of symptoms, nutrition until surgical repair which is only definitive treatment.  
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4 Left to right shunting conditions   ASD, VSD, AV, PDA  
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4 Right to left shunting conditions   Truncus Arteriosus, transposition of the great vessels, tetralogy of fallot, total anomalous pulmonary venous return.  
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What congenital cardiac condition has a boot shaped heart on CXR   Tetralogy of Fallot  
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Definition/ description of Total Anomalous pulmonary venous return (TAPRV)   Drainage of the pulmonary veins into a systemic venous structure or right atrium instead of left atrium. RIGHT TO LEFT SHUNTING.  
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Symptoms/ characteristics of Total Anomalous pulmonary venous return (TAPRV)   symptoms differ depending on obstruction type. Pulmonary venous HTN & pulmonary edema can develop. Presentation = CHF or inadequate growth, frequent pulmonary infections, mild cyanosis. "snowman" sign on CXR, Echocardiogram indicated.  
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Management of Total Anomalous pulmonary venous return (TAPRV)   Treatment of symptoms. Surgical repair by age 2 or 3.  
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Definition/ description of Coarctation of the Aorta   Obstructive condition. Variety of conditions occurring along the aortic arch - either discrete or generalized narrowing.  
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Symptoms/ characteristics of Coarctation of the Aorta   NN or older child. Pul edema occurs in NN w/ LV failure. Systemic HTN in older child. HF or cardiogenic shock in infant. Asymptomatic murmur/ HTN in older child. EKG, CXR- not conclusive for diagnosis. Echo or doppler studies, MRI definitive.  
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Management of Coarctation of the Aorta   Surgical repair, stent placement.  
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Post cardiac surgery emergencies   Pulmonary artery hypertension, cardiac tamponade, dysrhythmias, post pericardiotomy syndrome.  
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Definition/ description of Myocarditis   Serious, acute inflammation / infection of the myocardium. Often secondary to viral illness such as coxsackie or adenovirus.  
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Symptoms/ characteristics of Myocarditis   Sudden cardiac failure, murmur, gallop, tachypnea, life threatening arrhythmia.  
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Management of Myocarditis   Support while critically ill. ACE inhibitors, digoxin, diuretics, IVIG.  
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Diagnosis of myocarditis   gold standard = biopsy. Elevated troponin, flat T-waves on ECG  
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Definition/ description of Pericarditis   Sequelae to acute viral illness, such as inflammation of the pericardium of the heart.  
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Symptoms/ characteristics of Pericarditis   Fever, tachypnea, tachycardia, pericardial friction rub. May present in tamponade, ECHO may show fluid in pericardial sac. CXR= cardiomegaly. ECG= ST elevation, depression.  
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Management of Pericarditis   If tamponade, emergent pericardiocentesis; Abx 2-4 weeks for weeks for Staph & H flu.  
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Definition/ description of Endocarditis   Acute sepsis presentation  
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Symptoms/ characteristics of Endocarditis   Fever, murmur, embolic phemomena such as petechiae, vasculitis, osler nodes. Echo= vegetation and small, 2mm lesions  
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Management of Endocarditis   *Strep: PCN, Ceftraixone or Vanc. *Enterococci: ampicillin. *Staph Aureus: Nafcillin. Surgery for persistent +blood cx, absecess of valves &/or embloic events during abx tx.  
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Assessment and diagnosis of acute hypertension   Assessment: History, Symptoms, 4 extremity BP, heart sounds Diagnostics: EKG, echocardiogram, renal function, determine underlying cause.  
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Post pericardiotomy syndrome:   Post operative problem: febrile illness secondary to an inflammatory reaction involving the pleura and pericardium.  
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Post cardiac surgery complications   Pulmonary artery hypertension Cardiac Tamponade Dysrhythmias Post pericardiotomy syndrome  
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Cardiac Tamponade   cardiac compression occurring when blood or fluid builds up in the space between the myocardium and the pericardium.  
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Pulmonary artery hypertension   physiologic consequences of RV pressure overload and ventricular dysfunction.  
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