Final Blueprint Pt. 3 Flashcards

1
Q

what are the congenital problems?

A

cerebral palsy, neural tube defects, spina bifida, hydrocephalus, and hypotonia

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2
Q

what is important to know about hydrocephalus?

A

Cause: primary (Arnold Chiari Syndrome) and secondary (acquired).

S/S: sunset sign, increased head circumference, high-pitched cry, poor feeding if ICP is too high

Surgical treatment with shunt placement/biggest complication is infection

Nursing care: support child and family, teach signs of infection, and skin care.

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3
Q

what is hypotonia?

A

floppy infant syndrome, when supine is frog legged. Head lag, poor suck, and EMG key diagnostic test. Management by the cause.

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4
Q

convex curve, secondary to disease such as TB, chronic arthritis, compression FX, postural: noted when skeletal growth outpaces muscle, and treated with exercises (shoulder and abd) and bracing

A

Kyphosis

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5
Q

lateral curvature, spiral rotation, thoracic hypokyphosis, classified by age on onset: infantile, juvenile, adolescent, usually no cause, but may be in association with neuromuscular conditions, and observed undressed-shoulder height, scapular or flank shape or hip height and alignment

A

scoliosis

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6
Q

cervical or lumbar curve beyond physiologic limits, secondary to disease, the result of trauma, or idiopathic, associated with contracture of hip, scoliosis, obesity, DDH and SCFE, and treated with wt loss if contributing exercises and bracing.

A

lordosis

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7
Q

what is important to know about scoliosis?

A

Bracing = Gold Standard treatment

Compliance difficult: body image

Boston or Wilmington: plastic – underarm

Milwaukee: with neck brace

Charleston nighttime: prevents walking

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8
Q

what is hypoglycemia and its S/S?

A

monitor often and treat with 15 gm carbohydrate or glucagon. Recheck BG 15 M. Repeat the cycle until glucose >70 and continue to monitor for 2 H.

S/S:
Clammy skin
Irritability
Decreased LOC
Stroke like S/S
Slurred speech
Hungry
Grouchy
Sleepy
Sweating
Shakey
Pallor
Confusion

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9
Q

what are the S/S and important to know for hyperglycemia?

A

S/S:
Polydipsia
Polyuria
Polyphagia

Type 1 DM: your body does not make insulin, so you take insulin. Typically, not diagnosed until they are teens.

Exercise burns up extra glucose. So, if you have a kid who has T1DM, and he goes to PE pat should have snack b4 exercise. In order to prevent hypoglycemia attack. That is also why they get a 9pm snack like PB and crackers.

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10
Q

what is the NIPS pain scale?

A

maximal score of 7 points, considering pain > 4

Facial expression (relaxed = 0 pts, contracted = 1 pt, (–) = 2 pts)

Cry (absent = 0 pts, mumbling = 1 pt, vigorous = 2 pts)

Breathing (relaxed = 0 pts, different than basal = 1 pt, (–) = 2)

Arms (relaxed = 0 pts, flexed/stretched = 1 pt, (–) = 2 pts)

Legs (relaxed = 0 pts, flexed/stretched = 1 pt, (–) = 2 pts)

Alertness (sleeping/calm = 0 pts, uncomfortable = 1 pt, (–) = 2 pts)

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11
Q

what is the FLACC pain scale?

A

(2 months – 7 years): behaviors are scored 0-2 for each of 5 behaviors for a total of 0 (no pain) to 10 (worst pain)

Face: no expression or smile = 0, occasional grimace or frown, withdrawn, disinterested = 1, frequent to constant quivering chin, clenched jaw = 2

Legs: normal position/relaxed = 0, uneasy, restless, tense = 1, kicking or legs drawn up = 2

Activity: lying quietly, normal position, moves easy = 0, squirming, shifting back and forth, tense = 1, arched, rigid or jerking = 2

Cry: no cry (awake or asleep) = 0, moans or whimpers, occasional complaint = 1, crying steadily, screams or sobs, frequent complaints = 2

Consolability: content, relaxed = 0, reassured by occasional touch, hug or being talked to, distractible = 1, difficult to console or comfort = 2

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12
Q

what is the FACES pain scale?

A

(3 years and older): rating scales uses drawings of happy and sad faces to depict levels of pain

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13
Q

what is the HUS triad?

A

anemia, thrombocytopenia, and renal failure

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14
Q

what is the patho and treatment for HUS?

A

Patho: primary site endothelial lining of the small glomerular arterioles-swell and occluded with deposits of platelets and fibrin clots. RBC are damaged moving through partially occluded blood vessels. Damaged cells removed by spleen causing acute hemolytic anemia = thrombocytopenia

Treat: hemodialysis or peritoneal dialysis (for those anuric for 24 H, or oliguria with uremia or HTN and seizures), FFP and plasmapheresis, fresh/washed packed cells, and emergency support for family and child.

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15
Q

what are the CM for HUS?

A

primarily in infant 6 mos to 5 yo, acquired hemolytic anemia, thrombocytopenia, renal injury, and CNS symptoms, associated with e.coli (undercooked ground beef), unpasteurized milk or fruit juice (apple), sprouts, lettuce, salami or drinking – swimming in sewage-contaminated H2O, and begins with gastro or URI.

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16
Q

what is the patho and etiology of nephrotic syndrome?

A

Patho: predominately 2-7 yo (rare under 6 mos, uncommon under 1 yo, usually after 8 yo), may be metabolic, biochemical, physiochemical, or immune-mediated disturbance: basement membrane increasingly permeable to protein- albumin leaks and is lost in urine (reduces serum albumin level), fluid accumulates in interstitial spaces (edema) and body cavities (ascites).

Etiology: massive proteinuria, hypoalbuminemia, hyperlipidemia, and edema, primary (idiopathic nephrosis, childhood nephrosis, or minimal change nephrotic syndrome), secondary (after glomerular damage), and congenital (autosomal recessive).

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17
Q

what are the CM, therapy goals, and TX for nephrotic syndrome?

A

CM: wt gain, edema around eyes, scrotum, labia, ankles – especially in the AM, ascites, poor appetite, elevated BP, tired, and urine is frothy and decreased in volume.

Therapy goals: reduce excretion of urinary protein and fluid retention in tissues and prevent infection and minimize therapy complications.

Treatment: low salt diet, severe cases fluid restriction, edema (diuretics), 25% albumin, and corticosteroids.

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18
Q

what is important to know about reflexes?

A

Absent corneal reflex and presence of tonic neck reflex associated with severe brain damage. Neuro “health” in young infants: presence of Moro, tonic neck, and withdrawal reflexes.

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19
Q

dorsiflexion of big toe and fanning of toes should be absent after 1 YO or locomotion.

A

babinski reflex

20
Q

a normal reflex of an infant when he or she is startled or feels like they are falling

A

moro reflex

21
Q

when a baby’s head is turned to one side, the arm on that side stretches out and the opposite arm bends up at the elbow. This is often called the fencing position.

A

tonic neck reflex

22
Q

upon stimulation of the feel or hands of the extended limb, the infant reacts with a total flexion pattern of withdrawal. It assists in the early balancing of muscle tone between the flexors and extensors.

A

withdrawal reflex

23
Q

stiff in hamstrings that prevents ability to straighten leg, indicates bacterial meningitis (NOT GOOD).

A

kerning’s reflex

24
Q

major stiff in neck that causes flexing in hips and knees when neck is flexed, indicates bacterial meningitis (NOT GOOD).

A

brudzinski nuchal rigidity

25
Q

dysfunction of cerebral cortex/ brainstem (tumor).

A

flexion (decorticate)

26
Q

dysfunction of midbrain to brainstem (stroke).

A

extension (decerebrate)

27
Q

focused on dominating and control, care more about obedience than nurturing or protecting their kid

A

authoritarian

28
Q

think of their kids as = or friends, kids make own rules, parents give them little responsibilities or expectations

A

permissive

29
Q

nurturing, responsive, but still set boundaries and expectations of their kids

A

authoritative

30
Q

married couple with biological/adopted kids

A

traditional nuclear family

31
Q

couple with dependent kids

A

nuclear family

32
Q

couple with @ least 1 kid of both parents, plus step-kids

A

blended family

33
Q

included grandparents, aunts/uncles, cousins, etc.

A

extended family

34
Q

1 parent with kids

A

single parent family

35
Q

divorced or separated into 2 separate families, 1 headed by each parent

A

binuclear family

36
Q

“it takes a village”

A

communal family

37
Q

what are the most common signs for infection?

A

Elevated WBC (norm range 5000 – 10000)
Positive blood cultures
Fever
Persistent cry
Irritability
Sleeping more than usual
Lethargy (inactive)
Refusing to take a bottle or breastfeed
Breathing problems
Rash

38
Q

what are the S/S that suggest bleeding?

A

Low Hgb (norm range 10-15)
Low Hct (norm range 32-44%)
High PT (norm range 11-12.5 seconds)
High PTT (norm range 60-70 seconds)
Pain at the injured site
Swollen, tight abd
N/V
Pale, clammy, sweaty skin
Breathlessness
Extreme thirst
Unconsciousness

39
Q

what is graves disease?

A

Hyperthyroidism: excess of thyroid hormone, often hereditary, most common cause of hyperthyroidism in kids, thyrotoxic mom = probable positive neonate, and 5x more likely in girls than boys.

40
Q

what is the DX, TX, and nursing for graves disease?

A

Diagnosis: labs = low TSH, increased T4 and T3

Treatment: antithyroid drugs, thyroidectomy, and radioiodine ablation.

Nursing considerations: treat the S/S, calm environment for patients, monitor for hypothyroidism and treatment SE “thyroid storm”, no vigorous exercise until therapy is complete, and education: signs of hypothyroidism/thyroid storm and when to call HCP.

41
Q

what is osteogenesis imperfecta (OI)?

A

“brittle bone” disease (multiple types)

Clinical features include fragile bones, deformity, fractures, blue sclerae, hearing loss, hypoplastic, discolored teeth.

Care given to protect from fracture, may be mistaken for abuse

Biphosphate therapy with IV pamidronate to promote density

42
Q

what are the goals and types of OI?

A

Goals to prevent contractures, muscle weakness, malalignment.

Types: I, II, III, IV, V- XIX:

Type I: mildest form, most common; fractures but no bone deformities (best kind to have)

Type II: most severe, babies often do not survive birth due to fractures, inability to breathe (worst kind to have)

Type III: broken bones at birth, severe physical disabilities

Type IV: bones break easily, 1st is often before puberty; mild to moderate bone deformities (like type 1)

Types V-XIX: varying degrees, very similar, far less common

43
Q

what is spina bifida?

A

Myelodysplasia: Occulta/not visible externally/ dimple and cystic/ visible with sac like protrusion. Meningocele (not associated with a neuro deficit) and myelomeningocele (spina bifida meninges, spinal fluid and nerves). Neural tube fails to close in utero, usually lumbar area.

44
Q

what are the S/S for spina bifida?

A

paralysis of legs, loss of bowel and bladder function, hip dislocation and clubbed feet. Frequently associated with hydrocephalus.

45
Q

what are the dx and complications for spina bifida?

A

Maternal AFP, US, CT, MRI.

Complications: urinary and bowel continence (self-cath), not all mentally deficient, wheel chair, and latex allergy.