Cardiovascular Flashcards

1
Q

Viral Myocarditis

  • -viral prodrome, then s/s of heart failure
  • -dyspnea, syncope, tachycardia, n/v, hepatomegaly

Two most common etiologies?

Tx: inotropes and ?

A

Viral Myocarditis
–Coxsackie B, adenovirus

direct viral injury, autoimmune inflammation –> myocyte necrosis –> impaired systolic/diastolic fxn

respiratory distress due to left HF
hepatomegaly due to right HF

Tx: diuretics, inotropes

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2
Q

Ventricular Septal Defect (VSD)

  • -left to right shunt
  • -dyspnea, feeding difficulties, poor growth

Harsh holosytolic murmur heard where?
Diastolic rumble heard across what valve?
Which type is more likely to close (muscular or membranous)?
What parameter is the main determinant of shunt severity?

A

Ventricular Septal Defect

  • -left to right shunt
  • -dyspnea, feeding difficulties, poor growth, sweating, pulmonary infection, heart failure
  • -harsh holosytolic murmur heard at left lower sternal border
  • -diastolic rumble across mitral valve heard at apex
  • -muscular VSD more likely to close than membranous VSD (more common)

Shunt severity

  • -shunt increases as PVR decreases during first few weeks of life
  • -increased PVR –> Eisenmenger Syndrome
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3
Q

Atrial Septal Defect

  • -ostium secundum defect
  • -exercise intolerance
  • -widely split and fixed S2
  • -ECG: RAD, RVH
  • -often asymptomatic until 3rd decade

Systolic ejection murmur heard where?

A

Atrial Septal Defect

  • -ostium secundum defect
  • -exercise intolerance
  • -systolic ejection murmur at left upper sternal border
  • -widely split and fixed S2
  • -ECG: RAD and RVH
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4
Q

Tetralogy of Fallot

Four components?

Where can the systolic ejection murmur be heard?

Rx to prevent closure of ductus arteriosus?

A

Tetraology of Fallot

  • -pulmonary stenosis
  • -RVH
  • -VSD
  • -overriding aorta

Systolic ejection murmur at left upper sternal border
*single S2

Pathophys Principles

  1. pulmonary stenosis, VSD –> R2L shunt
  2. hypercyanotic ‘tet’ spell: agitation, exertion –> increase PVR –> increase R2L shunt
  3. squatting –> increase SVR –> decrease R2L shunt

Diagnostic Features

  1. CXR: boot-shaped heart
  2. single S2

Tx

  1. lateral knee-chest position to increase SVR
  2. PGE-1 to prevent ductal closure
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5
Q

Dx?

  • -most common cause of secondary HTN in children
  • -causes renal HTN
  • -usually affects right renal artery
  • -“string of beads” appearance
  • -hum or bruit heard at costovertebral angle
A

Fibromuscular Dysplasia

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6
Q

Hypertrophic Obstructive Cardiomyopathy

Mode of inheritance?

LVH –> LVOT obstruction

  1. How does squatting affect preload/afterload?
  2. How does Valsalva affect preload/afterload?

Tx
–what two classes of drugs?

A

Hypertrophic Obstructive Cardiomyopathy

MoI: AD
–African Americans

Pathophys Principles
1. LVH –> LVOT obstruction

  1. Maneuvers to increase preload or afterload –> increase LV cavity size –> decrease LVOT obstruction –> decrease murmur
    - -squatting, hand grip, leg raise, supine
    * squatting –> increase preload and afterload
  2. Maneuvers to decrease preload –> decrease LV cavity size –> increase LVOT obstruction –> increase murmur
    - -Valsalva, abrupt standing, nitroglycerin

Features
–palpitations, dizziness, syncope, risk of sudden death

Tx

  • -beta blockers (propranolol)
  • -Ca chnl blockers (verapamil)
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7
Q

Most common cyanotic heart disease in immediate newborn period (usually first few hours of life)?

Most common cyanotic heart disease after neonatal period?

Most common overall congenital heart lesion?

Congenital lesion associated with maternal rubella infxn?

Regurgitant lesion seen in Marfan, Ehlers-Danlos?

A

Transposition of the great arteries (TGA)
–most common cyanotic HD in immediate newborn period

Tetralogy of Fallot
–most common cyanotic HD after neonatal period

VSD
–most common congenital heart lesion

PDA
–associated with maternal rubella infxn

MVP
–Marfan, Ehlers-Danlos

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8
Q

Transposition of the great arteries (TGA)

What is the main defect?

Initial tx?

NB: more common in infant with diabetic mother

A

Transposition of the great arteries (TGA)

Pathophys Principles

  • -aorta arises from RV; pulmonary artery from LV
  • -2 parallel circuits; need foramen ovale and PDA for mixture of blood

Features
–severe cyanosis and tachypnea with PDA closure

CXR
–“egg on a string” heart (narrow mediastinum)

Tx
–PGE-1 to keep open PDA

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9
Q

Dx?

  • -severe newborn cyanosis
  • -CXR: decreased pulmonary blood flow
  • -ECG: LAD, LVH
A

Tricuspid Atresia

Pathophys: no outlet from RA to RV
–systemic venous return enters LA thru PFO or ASD

Triad

  • -severe newborn cyanosis
  • -CXR: decreased pulmonary blood flow
  • -ECG: LAD, LVH
  • *LAD is specific to Tricuspid Atresia!

Tx
–PGE-1 to keep open PFO

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10
Q

Dx?
Association?

  • -HTN in the upper body; hypoperfusion in the lower body
  • -“differential cyanosis”
  • -leg muscle fatigue
  • -rib notching
A

Coarctation of the Aorta
(Infantile form)
*association with Turner Syndrome
*often involves bicuspid aortic valve

Pathophys

  1. narrowing is distal to aortic arch; proximal to PDA
  2. RV blood flows ax PDA to supply aorta
  3. collaterals develop between hypertensive and hypoperfused vessels

Presentation

  • -differential cyanosis: upper body is pink; lower body is cyanotic
  • -HTN in upper extremities
  • -leg muscle fatigue
  • -collaterals –> rib notching; continuous murmur heard all over chest well

Tx

  • -PGE-1 ti keep open PDA
  • -surgery
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11
Q
  • -hearing loss
  • -syncope, long QT
  • -normal vitals and exam
  • -family hx of sudden death

Dx?
MoI?
Tx (class)?

A

Jervell and Lange-Nielsen Syndrome
–form of congenital long QT syndrome
–AR
Tx: beta blockers

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12
Q

ECG

  • -delta wave
  • -shortened PR interval
  • -widened QRS

Dx?

A

Wolff-Parkinson-White Syndrome
–accessory AV conduction pathway

Features

  • -supraventricular tachycardia
  • -otherwise healthy adolescent
  • -chest pain, palpitations, syncope, cardiac arrest

ECG Triad

  • -delta wave (sloped initial portion of QRS)
  • -shortened PR interval
  • -widened QRS
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13
Q

Three clues for an innocent murmur

  • -asymptomatic (normal activity, eating, growth)
  • -no family hx
  • -what type of maneuvers will decrease murmur intensity?
A

Three clues for an innocent murmur

  • -asymptomatic (normal activity, eating, growth)
  • -no family hx
  • -maneuvers that decrease venous return –> decrease murmur intensity
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14
Q

Breath-Holding Spell
–brief period of apnea and skin color change associated with an emotional trigger (crying, anger)

Association?

A

Breath-Holding Spell

  • -brief period of apnea and skin color change associated with an emotional trigger
  • -assoc w Fe-deficiency anemia
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15
Q

Endocardial Cushion Defect

Association?

Main pathology re: septal defect?

A

Endocardial Cushion Defect
*assoc w Down Syndrome

Pathophysiology

  • -contiguous ASD and VSD
  • -AV valve insufficiency

Features

  • -heart failure in early infancy
  • -hyperdynamic precordium (precordial bulge and lift)
  • -diaphoresis and dyspnea with feeds
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16
Q

Presentation:
pallor –> syncope; seizure; no respiratory distress –> alert, flushing

Dx?

A

Adams-Stokes Attack

AV block –> asystole –> brain hypoxia –> syncope, seizure –> recovery –> flushing

17
Q

Infective Endocarditis

Etiologic Associations

  • -dental procedure?
  • -IVDU? (2)
A

Infective Endocarditis

Etiologies

  • -Strep viridans (dental procedure)
  • -S. aureus
  • -Pseudomonas, Serratia (IVDU)

Presentation

  • -fever (prolonged, intermittent)
  • -murmur (new or changing)
  • -Osler nodes, Janeway lesions, splinter hemorrhages
  • -Roth spots

Dx Tests: bcx, echo

Complications
–heart failure

18
Q

Murmurs DDx

  1. “continuous machine-like murmur”
  2. mid-systolic “click” with late systolic murmur
A

Murmurs DDx

  1. PDA
    - -continuous machine like murmur
  2. MVP
    - -mid-systolic “click” with late systolic murmur
19
Q

Which rx closes a PDA?

Which rx maintains patency of a PDA?

A

Indomethacin
–closes PDA

PGE-1

  • -maintains patency of PDA
  • -necessary in some cyanotic congenital heart dz
20
Q

5 Cyanotic Congential Heart Diseases

  1. ?
  2. Transposition
  3. Tricuspid atresia
  4. Tetralogy of fallot
  5. Total anomalous pulmonary venous return
A

5 Cyanotic Congenital Heart Diseases

  1. Truncus arteriosus (1 vessel)
  2. Transposition (2 switched vessels)
  3. Tricuspid atresia (3, tri)
  4. Tetralogy of fallot (4, tetra)
  5. TAPVR (5 letters)