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NBME CBSE

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Exam of 28 pages for the course NBME CBSE at NBME CBSE (NBME CBSE)

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NBME CBSE
Study online at https://quizlet.com/_8dlr9r

1. Bulbus cordis: Smooth parts (outflow tract) of left and right ventricles
2. endocardial cushions: Atrial septum, membranous interventricular septum; AV and semilunar valves

neural crest
3. left horn of the sinus venosus: coronary sinus
4. posterior, sub cardinal, and supra cardinal veins: IVC
5. Right common cardinal vein and right anterior cardinal vein: SVC
6. Right horn of sinus venosus: Smooth part of right atrium (sinus venarum)
7. Patent foramen ovale: failure of septum primum and septum secundum to fuse after birth
8. Transposition of the great vessels
Tetralogy of Fallot
Persistent truncus arteriosus: Conotruncal abnormalities associated with failure of neural crest cells
to migrate
9. ductus venosus: connects the umbilical vein to the inferior vena cava, bypassing the liver

becomes ligamentum venosum
10. phrenic nerve: innervates the diaphragm and pericardium
11. S3 heart sound: Increased ventricular filling pressure (e.g., mitral regurgitation, HF), common in dilated
ventricles

normal in kids and pregnant women
12. S4 heart sound: atrial kick late diastole, right before S1

best heard at apex in LLD position

High atrial pressure.

Stiff/hypertrophic ventricle (aortic stenosis, restrictive cardiomyopathy)

Always abnormal
13. atria contract: a wave of JVP
14. c wave: RV contraction (closed tricuspid valve bulging into atrium) wave of JVP




, NBME CBSE
Study online at https://quizlet.com/_8dlr9r

15. x descent: JVP wave corresponding to downward displacement of closed tricuspid valve during rapid
ventricular ejection phase

reduced or absent in tricuspid regurge
16. V wave: JVP wave corresponding to inc'd RA pressure due to filling against closed tricuspid valve
17. y descent: JVP wave corresponding to RA emptying into RV

absent in cardiac tamponade
18. plusus parvus et tardus: pulses are weak with delayed peak

Aortic stenosis
19. PR interval: 0.12-0.20 seconds

120 milliseconds
20. QT interval length: 9 - 11 squares = .36 to .44 seconds
21. Hypokalemia: U wave present on ECG
22. Mg sulfate: for torsades de pointe, hypokalemia (can lengthen QT and cause torsades), and pre-eclampsia
(prevent seizures)
23. Romano-Ward syndrome: -Congenital long QT syndrome
-Autosomal dominant, pure cardiac phenotype (no deafness).
24. Jervell and Lange-Nielsen syndrome: -Congenital long QT syndrome
-Autosomal recessive, sensorineural deafness
25. Brugada syndrome: -Autosomal dominant disorder affecting Na channels most common in Asian
males.
-ECG pattern of pseudo-right bundle branch block and ST elevations in V1-V3 (anterior ventricular septum)
-inc risk of ventricular tachyarrhythmias and sudden cardiac deatgh

Prevent SCD with implantable cardioverter-defibrillator (ICD).
26. Wolff-Parkinson-White Syndrome: Most common type of ventriuclar pre-excitation sydnrome.
Abnormal fast accessory conduction pathway from atria to venricle bypasses the rate-slowing AV node causing a delta
wave and widening QRS with shortened PR interval. Could lead to a reentrant circuit and suprvaventicular tachy.
27. First degree AV block: - PRI >5 boxes/.20 sec (200 msec)
- Fixed but prolonged PRI


, NBME CBSE
Study online at https://quizlet.com/_8dlr9r

(consistent but long)
- normally get bradycardia here
28. second degree AV block mobitz type 2: -PR interval is constant
-atrial conduction to ventricle is intermittent: dropped QRS without increasing PR interval length
-disease below AV node in His bundle

may progress to 3rd degree/complete AV block
29. Second Degree AV Block Mobitz Type 1 (wenckebach): Progressive lengthening of pr
interval leading to dropped QRS
30. third degree AV block: The atria and Ventricles are totally dissociated.
-So, the QRSs and the P waves have no relation to each other.
31. PCWP: 4-12 mmHg
est of LA pressure
32. Williams Syndrome: a genetic condition characterized by mental retardation in most regards but
surprisingly good use of language relative to their other abilities, elfin facies
Chromosome 7
assoc with supravalvular aortic stenosis
33. DiGeorge Syndrome: Maldevelopment of 3 and 4 pharyngeal pouches, fascial dysmorphia, cardiac
shunt (trunks arteriosus, tetralogy of Fallot), lack of T-cells, undeveloped paracortex
34. Corneal arcus: Lipid deposits in the cornea. Common in the elderly, but appears earlier in life with
hypercholesterolemia

35. Stanford A aortic dissection: Dissection of the ascending aorta
Tx with surgery
36. Stanford B aortic dissection: Dissection of the descending aorta below the level o the left subclavian
artery
Tx: Beta Blockers then vasodilators
37. Left bundle branch block: QRS> 120 msec
Deep, broad S waves in V1 and V2
Broad R waves in in V5 and V6

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