PEDS ASSESSMENT Flashcards

1
Q

What is the hole between R & L atria that must close at birth

A

Foramen ovale

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2
Q

What must close at birth to allow blood flow to the lungs?

A

Ductus anteriosus

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3
Q

What must close at birth to allow blood flow to the liver?

A

Ductus venosus

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4
Q

Defects that increase pulmonary blood flow

A
  1. Patent ductus arteriosus
  2. Atrial septal deficits
  3. Ventricular septal deficits
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5
Q

Patent ductus arteriosus is

A

Common in premature
- leads to heart failure, inadequate oxygen to brain

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6
Q

What causes “wet lungs”

A

Atrial septal deficits

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7
Q

Atrial septal deficits

A

Opening in septum between R & L atrial chambers
- wet lungs (too much blood in lungs)
- lead to respiratory infection, R ventricle working too hard —- heart failure, poor exercise tolerance, being small for age

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8
Q

Deficits that decrease pulmonary blood flow

A

Tetralogy of Fallot

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9
Q

Ventricular septal deficits

A

1+ openings in muscular/membranous portions of ventricular septum
- 50% cases of resolve by 5yrs otherwise surgery needed
- feeding difficulties, SOB, increased perspiration, increased respiratory infections, fatigue with increased activity, delayed growth

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10
Q

Can result in Eisenmenger’s complex of pulmonary vascular obstruction

A

Ventricular septal deficits

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11
Q

Tetralogy of Fallot

A
  • pulmonary valve/artery stenosis, ventricular septal deficit, R ventricular hypertrophy, override of ventricular septum
  • central cyanosis, coagulation deficits, clubbing of fingers/toes, feeding difficulties, failure to thrive, dyspnea
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12
Q

Result in feeding difficulties

A

Tetralogy of Fallot, ventricular septal deficits

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13
Q

Results in clubbing of fingers/toes

A

Tetralogy of Fallot

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14
Q

Deficits with mixed pulmonary blood flow

A

Transposition of great arteries

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15
Q

Transposition of great arteries

A
  • no communication between systemic & pulmonary circulations
  • result of coexisting congenital transposition of the ventricles
  • cyanosis, congestive heart failure, respiratory distress
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16
Q

Result in heart failure

A
  • transposition of great arteries
  • patent ductus arteriosus
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17
Q

Result in cyanosis

A
  • transposition of great arteries
  • tetralogy of Fallot
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18
Q

Results in delayed growth

A

Ventricular septal deficits

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19
Q

Abnormally slow HR below 60 mph

A

Bradydysrhythmia

20
Q

Pacemaker is used for

A

Bradydysrthemia

21
Q

Abnormal fast HR more than 100 BPM

A

Tachydysrthymia

22
Q

Tachydysrthymia results in

A
  • can lead to CHF
  • irritability, poor eating habits, pallor
23
Q

Treatment for sickle cell anemia

A

Pain management

24
Q

Treatment for osteogenesis imperfeca

A
  • parent education in handling/positioning to prevent fx
  • encourage monitored activity promoting WBering
25
Deficiency of surfactant
Respiratory distress syndrome
26
Result of prolonged mechanical ventilation use to treat acute respiratory problems
Bronchopulmonary dysplasia
27
Bronchial smooth muscle hyperactivity that causes airway constriction in lower respiratory tract, difficulty breathing, wheezing
Asthma
28
Degenerative condition caused by inherited autosomal recessive disorder related to chromosome 7 gene
Cystic fibrosis
29
Too many red blood cells, elevated levels of white blood cells
Erythrocytosis/ transient leukemia - Down syndrome children
30
Absence/reduction of one of clottingblood proteins
Hemophilia
31
Bleeding episodes after traumatic events
Mild hemophilia
32
bleeding episodes after minor injury
Moderate hemophilia
33
Bleeding after injuries or without apparent cause, may affect muscles/joints
Severe hemophilia
34
signs of hemophilia
1. Excessive bleeding 2. Excessive bruising 3. Spontaneous bruising/bleeding without known cause 4. Nosebleeds
35
Iron deficiency in blood
Anemia
36
How is anemia treated?
Diet
37
Abnormally shaped red blood cells
Sickle cell anemia
38
Brittle bones, decreased bone deposition caused by inability to form type I collagen
OI
39
Most severe OT
Fetal: fx occur in utero, during birth, high mortality
40
Moderate severe OI
Infantile: fx in early childhood, severe limb deformity, growth disturbances
41
Least severe OI
Juvenile: fx in late childhood, by puberty, bones begin to harden & fewer fx occur
42
Excessive growth at ephiphyseal plate
Marfan’s syndrome
43
Presentation of marfan’s syndrome
1. Long slender fingers (arachnodactyly) 2. Skull asymmetries 3. Tall stature 4. Joint, eye, heart differences 5. Lax, hyper mobile joints 6. Poorly developed, striated muscles
44
Comorbidities of marfans
1. Dislocation of lenses 2. Scoliosis 3. Coxa vara 4. Depressed sternum 5. Stooped shoulders 6. Fragility of blood vessels 7. Delayed walking
45
Stunting of epiphyseal growth plate & cartilage formation
Achondroplasia (chnondrodystrophia or dwarfism)
46
Presentation & comorbidities of achondroplasia
- grow less than 4ft tall - limbs shorter in length - prominent forehead - small nose, jaw Comorbidities: lumbar lordosis, coxa vara, cubitus Vargas, back and leg pain
47
Reduced anterior horn cells in spinal cord
Arthrogryposis multiplex congenital