Cardiac Stuff Flashcards

1
Q

Complate atrioventricular septal defect murmur?

A
  • Loud S2 (Pulm HTN)
  • hyperdynamic precordium
  • systolic ejection murmur at Left Upper sternal Border (hearing the turbulence over the pulmonary valve where there is a BUNCH of blood flowing due to the L –> R Shunt)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

ASD Murmur?

A
  • fixed, split S2
  • systolic ejection murmur at Left upper sternal border (turbulence over tons of blood over the pulm valve)

(remember S2 split comes because the Pulm valve will stay open a tad bit longer because you have a rush of venous return and the valve stays open longer, but with an ASD, there’s still tons of extra R heart return from the L–> shunt)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

PDA

A

continuous machineline murmur @ ALL OVER left sternal border

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Tetralogy of Fallot Classic murmur? Findings on X-ray

A
  1. Single second heart sound (S2)
  2. harsh, crescendo-decrescendo murmur (due to RVOT obstruction) @ LUSB

X-ray = “boot-shaped” heart due to RVH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Murmur of VSD

A

harsh, holosystolic murmur @ the Left LOWER sternal border

diabstolic rumble over the apex (increased flow across the mitral valve)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how to treat a tet spell? What are the 4

A
  1. Overriding aortic arch
  2. RVOT (Pulmonary Valve stenosis or even atresia!)
  3. Ventral Septal Defect
  4. Right Ventricular hypertrophy

tx:

  • Knee-chest position to increase Systemic vascular resistance and decrease the amount of R==> L shunting.
  • oxygen to stimulate pulmonary vasodilation
  • morphine to relax patient and depress HR
  • Fluids to improve R ventricular filling
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Mitral Valve prolapse murmur

A
  1. midsystolic click

2. late systolic murmur

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the 5 CYANOTIC heart defects? Most common? What type of shunts are these?

A
  1. Truncus arteriosus
  2. Transposition of the great vessels
  3. Tricuspid atresia
  4. Tetralogy of Fallot
  5. total anomalous Pulmonary venous return

Most common is transposition of the great vessels

These are Left-to-right shunts which make them totally cyanotic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the X-ray finding on transposition of the great vessels?

A

“Egg-on-a-string” heart (narrow medistinum)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How does total anomalous pulmonary venous return present? X-ray?

A

Severe cyanosis, respiratory distress

X-ray -
enlarge supracardiac veins & SVC (“snowman” sign)

pulmonary edema

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

VSD Presentation?

A

failure to thrive, easy fatiguability, heart failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the characteristic findings of tricuspid valve atresia? What is the pathology

A
  1. Left axis deviation in the neonate
  2. small or absent R waves in the precordial leads

Basically, the fact that there is no valve means that there is no communication and the right ventricle becomes hypoplastic as well as the pulmonary valve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Presentation of laryngomalacia and vascular rings and pathology? How to tell the difference?

A

Laryngomalacia

  • 4-8 months
  • laxity of the supraglottic structures during inspiratory phase –> inspiratory stridor
  • WORSENS IN SUPINE AND GETS BETTER IN THE PRONE OR WITH SITTING UP

vascular rings

  • before 1 years
  • abnormal development of the aortic arch leading to tracheal, bronchial, and esophageal compression
  • IMPROVES WITH NECK EXTENSION (throwing your head back)
  • 50% HAVE CARDIAC ABNORMALITIES
  • does not improve with epi or bronchodilators
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Presentation of viral myocarditis? X-ray and echo? dx? Bugs?

A

Presentation:

  • viral prodrome
  • heart failure: dyspnea, syncope, tachycardia
  • nausea and vomiting
  • hepatomegaly

X-ray

  • cardiomegaly
  • pulmonary edema

Echo:

  • diffuse hypokinesis
  • decreased EF

dx: endomyocardial biopsy

bugs:

  • Coxsackie B
  • adenovirus
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is found after rheumatic fever? What the murmur? what is the tx?

A

after rheumatic fever you get persistent mitral valve disease.

Murmur:

  1. LOUD S1
  2. mid-systolic rumble

tx: Anyone with a history of rheumatic fever gets continuous antibioic prophylaxis to prevent Group A. Strep and persistent damage. so Penicillin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Murmur of Hypertrophic Cardiomyopathy? What makes it louder?

A

systolic

  • ejection murmur at the left sternal border.
  • pulse has a dual upstroke, strong apical pulse

Louder is anything that decreases preload (thus making the left ventricle cavity smaller and thus increases the murmur)

  • valsalva
  • abrupt standing
  • nitro

Softer is anything that increases afterload

  • squatting
  • hand grip
17
Q

What do you see on EKG with WPW? What is the presentation? pathology

A
  1. widened QRS
  2. with a delta wave
  3. shortened PR interval

Presentation: Most asymptomatic, some will present with chest pain, palpitations, syncope, or cardiac arrest.

Path: there is an accessory pathway that conducts antegrade from the atria to the ventricles faster than conduction through AV node

18
Q

What are features of Jervell and Lange-Nielsen Syndrome? What is the inheritance pattern?

A
  1. sudden death in family
  2. QT interval greater than 600 ms
  3. CONGENITAL SENSORINEURAL DEAFNESS

inheritance - autosomal recessive

19
Q

What is dx of long Qt syndrome? What is risk? What is presentation?

What is tx?

A

QT longer than 440 ms in males and 460 in femals.

Risk: torsade de pointes (ventricular arrythmia leading to death)

presentation of long Qt: fainting, lightheadedness, palpitations

tx; propranolol and long-term pacemaker placement

20
Q

Cardiac condition associated with

Down’s Syndrome

A

Complete endocardial cushion defect (ASD and VSD)
then VSD
Then ASD

21
Q

Cardiac condition associated with

congenital rubella

A

PDA

22
Q

Cardiac condition associated with

Turner’s Syndrome

A

coarctation of the aorta

biscupid aortic valve

23
Q

Cardiac condition associated with

Kawasaki Disease

A

Coronary artery aneurysms

24
Q

Cardiac condition associated with

Neonatal Lupus

A

congenital heart block

25
Q

Cardiac condition associated with

supravalvular aortic stenosis

A

Williams syndrome

26
Q

Cardiac condition associated with

maternal lithium

A

ebstein’s anomaly (abnormalities of the tricuspid valve)

27
Q

Cardiac condition associated with

neonatal thyrotoxicosis

A

Heart failure

28
Q

Cardiac condition associated with

Maternal diabetes

A

asymmetric septal hypertrophy and transposition of the great vessels