Cardio Flashcards

1
Q

Cyanotic heart defects

A

The 5 T’s that have right-to-left shunts

Truncus arteriosus = ONE arterial vessel overriding ventricles

Transposition of the great vessels = TWO arteries switched

Tricuspid atresia (THREE)

Tetralogy of Fallot (FOUR)

Total anomalous pulmonary venous return = FIVE words

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2
Q

presents with severe cyanosis within the first few hours of life.

A

Transposition of great arteries

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3
Q

Noncyanotic heart defects—

The 3 D’s

A

VSD

ASD

PDA

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4
Q

Down syndrome heart defects

A

ASD

Endocardial cushion defects

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5
Q

Congenital rubella heart defect

A

PDA

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6
Q

Turner’s syndrome heart defect

A

Coarctation of the aorta

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7
Q

Coronary artery aneurysms associated disease

A

Kawasaki disease

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8
Q

Associated with maternal lithium use

A

Ebstein’s anomaly

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9
Q

Neonatal lupus is associated with this heart problem

A

Congenital heart block

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10
Q

Neonatal thyrotoxicosis effect

A

Heart failure

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11
Q

Heart diseases of newborn associated with maternal diabetes

A

TGA

Asymmetric septal hyper trophy

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12
Q

Suprvalvular aortic stenosis seen in

A

William’s disease

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13
Q

most common cause of congenital heart disease.

A

VSD

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14
Q

Small versus large VSD

A

Small
-harsh holosystolic murmur

Large
-frequent respiratory infections, dyspnea, FTT, and CHF

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15
Q

Surgical indications of VSD

A
  1. symptomatic patients who fail medical management

2. children

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16
Q

VSD ECG

A

ECG: LVH and may show both LVH and RVH with larger VSD

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17
Q

Heart defect that has a fixed, widely split S2

A

ASD

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18
Q

Examination reveals a right ventricular heave; a wide and fixed, split S2; and a systolic ejection murmur at the left upper sternal border (from ↑ flow across the pulmonary valve). There may also be a mid-diastolic rumble at the left lower sternal border.

19
Q

ASD ECG ABD CXR findings

A

ECG may show RVH and right atrial enlargement. PR prolongation is common.
CXR reveals cardiomegaly and ↑ pulmonary vascular markings.

20
Q

Failure of the ductus arteriosus to close in the first few days of life, leading to an acyanotic left-to-right shunt from the aorta to the pulmonary artery. Risk factors include maternal first-trimester rubella infection, prematurity, and female gender

A

Patent ductus arteriosus

21
Q

In infants presenting in a shocklike state within the first few weeks of life, look for:

A
  1. Sepsis
  2. Inborn errors of metabolism
  3. Ductal-dependent congenital heart disease, usually left-sided lesions (as the ductus is closing)
  4. Congenital adrenal hyperplasia
22
Q

Examination reveals a continuous “machinery murmur” at the second left intercostal space at the sternal border, a loud S2, wide pulse pressure, and bounding peripheral pulses.

A

patent Ductus arteriosus

23
Q

Indomethacin is to ____ Pda

A

Come IN and CLOSE the door: give INdomethacin to CLOSE a PDA.

24
Q

Constriction of a portion of the aorta, leading to ↑ flow proximal to and ↓ flow distal to the coarctation.

A

Coarctation of the aorta

25
Most common site of coarctation
Occurs just below the left subclavian artery in 98% of patients
26
More than two-thirds of patients have a bicuspid aortic valve.
Coarctation
27
Coarctation of the aorta
The condition is associated with Turner’s syndrome, berry aneurysms, and male gender.
28
Heart defects that require a patent PDA for survival
transposition of the great vessels tetralogy of Fallot hypoplastic left heart Critical coarctation
29
Differential cyanosis may be seen with lower O₂ saturation in the left arm and lower extremities (postductal areas) as compared to the right arm (preductal area).
Coarctation of the aorta
30
CXR and ECG of coarctation
LVH on ECG the “3” sign on CXR due to pre- and postdilatation of the coarctation segment with aortic wall indentation "rib notching” due to collateral circulation through the intercostal arteries
31
Without a septal defect (ASD or VSD) and a PDA, it is incompatible with life The most common cyanotic congenital heart lesion in the newborn
TGA
32
Examination reveals tachypnea, progressive hypoxemia, and extreme cyanosis. Some patients have signs of CHF, and a single loud S2 is often present. There may not be a murmur if no VSD is present. If a VSD is present, a systolic murmur may be heard at the left sternal border.
TGA
33
DiGeorge syndrome— CATCH 22
Cardiac abnormalities (transposition) Abnormal facies Thymic aplasia Cleft palate Hypocalcemia 22q11 deletion
34
CXR may show a narrow heart base, absence of the main pulmonary artery segment, an “egg-shaped silhouette,” and ↑ pulmonary vascular markings
TGA
35
__________ is the most common cyanotic heart disease of newborns __________ is the most common cyanotic heart disease of childhood
TGA | TOF
36
Tetralogy of Fallot components
Consists of pulmonary stenosis, overriding aorta, RVH, and VSD
37
Children often squat for relief during hypoxemic episodes called “tet spells,” which ↑ systemic vascular resistance.
TOF
38
CXR shows a “boot-shaped” heart with ↓ pulmonary vascular markings. Remember that a VSD may result in ↑ pulmonary vascular markings. ECG shows right-axis deviation and RVH.
TOF
39
Treat hypercyanotic “tet spells” with
O₂, propranolol, phenylephrine, the knee-chest position, fluids, and morphine.
40
Infants with FTT will first fall off of the ______ curve, then the ______ curve, and finally the _______ curve.
Infants with FTT will first fall off of the weight curve, then the height curve, and finally the head circumference curve.
41
Order of sexual development in a female
Thelarche Pubarche Growth spurt Menarche
42
Precocious puberty in males | In females
8 | 9
43
Delayed puberty boys | Girls
14 | 13
44
Pattern of sexual development in males
Gonadarche Pubarche Adrenarche Growth spurt