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WH and Pedi > Pedi Neuro > Flashcards

Pedi Neuro Flashcards

1
Q

Premature closure of one or more cranial sutures. Common in certain syndromes. Simple (1 suture) vs complex (multiple sutures). Abnormal head shape. Can cause increased ICP and/or brain/facial/eye abnormalities.

A

Craniosynostosis

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2
Q

Treatment: Surgery. Endoscopic before 6 months. Helmet post op- 23 hours/day x 3-4 months (open surgery- no helmet)
Nursing: Neuro baseline, CBC, wound care, post-op pain, helmet adherence

A

Craniosynostosis Treament and Nursing Care

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3
Q 
Asymmetry and flattening of the head due to external forces on skull. Supine for long periods ("Back to Sleep" campaign, prematurity...)
Skull deformity (R occiput greater than L). May cause uneven facial features. Determine cause 
(? Decreased ROM, ? torticollis - SCM muscle)
A

Deformational Plagiocephaly (DP)

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4
Q

Treatment: Positioning, orthotics (helmet less than 12 mo)
Nursing: Helmet 20-23 hours/day x 2-6 mo. Tummy time; limit car seats, swings

A

Deformational Plagiocephaly (DP) Treatment and Nursing Care

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5
Q

Abnormally small head. Head circumference 2 SDs below mean. Primary (genetic, chromosomal or hereditary cause). Secondary (exposure to irradiation, maternal infection or ETOH/tobacco). Varying degrees of cognitive impairment and motor delays.

A

Microcephaly

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6
Q

No cure: Supportive treatment.
Nursing care: Support for special needs child and family. Services, resources, equipment
Coping with appearance and raising a special needs child.

A

Microcephaly Treatment and Nursing Care

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7
Q

Build up of CSF in brain- imbalance between production and absorption. Increased production of CSF, decreased absorption of CSF, obstruction of flow (non communicating) (no LP) leads to increased ICP.

A

Hydrocephalus

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8
Q

Common cause: Arnold-Chiari malformation Types 1 & 2. Narrow foramen magnum and low cerebellar tonsils (blowing flow). Other causes: Abnormal CNS development, tumors, lesions, bleeding, head injury.

A

Hydrocephalus Causes

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9
Q

Treatment: Relieve ICP leads to VP shunt (lateral ventricle - peritoneum)
Complications: infected, clogged, kinked, clotted; need replacement with growth.
Monitor neuro status closely; head circ, temp, lethargy, feeding, N & V, seizure, skin. No contact sports

A

Hydrocephalus Treatment, Complications, and Nursing Care

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10
Q

Part of the cerebellum at the back of the skull bulges through the opening in the skull and extends into spinal canal.
Headache, neck ache, difficulty swallowing, balance, hearing issues; other neuro S/s

A

Arnold Chiari Malformation

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11
Q

Treatment only if symptomatic: Posterior fossa decompression. Applies to both types

A

Arnold Chiari Malformation Treament

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12
Q

Congenital vascular lesions- failure of vessels to differentiate. Bypass of capillaries; higher pressure causes dilation/weakening/susceptibility. Most common cause of spontaneous hemorrhage in children. Headache, weakness, seizure activity, cognitive impairment, sudden change in LOC.

A

Arteriovenous Malformation

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13
Q

Diagnosis: Neuroimaging; CT, MRI
Treatment: surgical resection; evacuation.
Outcomes depend on severity, time elapsed.
Post op: frequent neuro checks; ICU management. Serious complications common leading to disability and death. Rehab and family support

A

Ateriovenous Malformation Treatment, Complications, and Nursing Care

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14
Q

Infection of the meninges (membranes protecting brain). Spread through respiratory secretions. Bacterial/septic (or viral). S. pneumoniae, N meningitidis, E. coli or HiB. Pathogen disseminates; through CSF into brain.

A

Meningitis

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15
Q

S/s include inflammatory response: fever, headache, stiff neck, lethargy, photophobia, purpuric rash (treat immediately). Brudzinki’s and Kernig’s signs; Lumbar Puncture

A

S/s and Diagnosis of Meningitis

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16
Q

Isolation! Neuro checks; antibiotics; supportive care. Prophylaxis for those near

A

Nursing interventions for Meningitis

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17
Q

Very rare, potentially fatal toxic metabolic encephalopathic condition. Mitochondrial injury related to aspirin given during VIRAL illness. Influenza A or B, varicella; (paraflu, CMV, Coxsackie, EBV, HIV, Hep A and B, rota). Imcreased ammonia levels leading to acute encephalitis and liver failure.

A

Reyes Syndrome

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18
Q

Stages 0-6- vomiting, lethargy, disorientation - rapid progression (3-5 days): fulminant liver failure, encephalopathy, organ failure.
Diagnosis: liver biposy, LP, blood (ammonia) (specific CDC diagnostic criteria)

A

Reyes Syndrome S/s and Diagnosis

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19
Q

PICU care: specifically neuro and resp
Increased risk of bleeding due to liver involement.
Diuretics, corticosteroids, insulin, electrolytes
Teach prevention: no ASA in children over 19.
NO ASPIRIN

A

Reyes Syndrome Nursing Interventions

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20
Q

Infection surrounding meninges with CEREBRAL EDEMA. Usually viral; associated with mosquito bite-based and herpes type 1. Similar to meningitis

A

Encephalitis

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21
Q

Similar presentation to meningitis (stiff neck, lethargy, photophobia) but s/s can progress rapidly to decreased LOC, seizures.
Confirmed with MRI

A

Encephalitis S/s and Diagnosis

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22
Q

Interventions include close monitoring, IV antibiotics/antivirals, antipyretics, anti-inflammatories, anti epileptics. NOT a seizure disorder

A

Encephalitis Nursing Interventions

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23
Q

Electrical disturbance in the brain. Large # of brain cells abnormally activated at once. Causes motor, sensory/language/motor and cognitive changes.
Classified according to where they begin/area of brain affected, altered LOC and type of activity, frequency and duration.
Focal (1 hemisphere) vs generalized (both hemispheres)

A

Seizure Disorders

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24
Q

Causes include: Structural (tumor, cyst, brain defect), genetic, infectious, metabolic derangement, abnormal immune response, unknown

A

Causes of Seizure Disorders

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25
Q

Motor manifestations: Impaired awareness vs unconsciousness. Jerking in 1 extremity. Stiffness on 1 side. Lip smacking
Non-motor: Tingling, buzzing sounds, flashing lights. Feeling anxious, fearful, angry

A

Focal Manifestations of Seizure Disorders

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26
Q

Loss of consciousness
Motor manifestations: tonic (stiff, increased tone), clonic (rhythmic jerking x 4 extrem), tonic-clonic (loss of conscience), myoclonic (looks like tics, tremors), atonic (“drop attack” injury risk).
Non motor: challenging to diagnose (ADD), can look like daydreaming. Can look like daydreaming. Absence seizures: eyes flutter, lip smacking, rubbing fingers together

A

Generalized Manifestations of Seizure Disorders

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27
Q

0.5- 1% of pediatric population. Recurrent and unprovoked seizures. 2 seizures more than 24 hours apart. Probability of another (EEG activity)

A

Epilepsy

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28
Q

EMERGENCY. Prolonged seizures or series of seizures with no recovery in between. More than 5 minutes or multiple within 5 minutes. Convulsive or non convulsive. Medically induced coma.

A

Status Epilepticus

29
Q

Seizures triggered by fever over 101.2 (Fever may follow seizure). Most common 6mos to 3 years.
Simple: less than 10 mins, happens once
Complex: More than 10 minutes, more than 1x

A

Febrile Seizures

30
Q

Diagnose: CT/MRI (r/o lesion, mass, bleed), EEG; labs (lytes, infection, levels)
Assess/Document: Start time, length, preceding activity, clinical manifestations (deat?), post ictal (state/behavior after)
Treatment: Anti-epileptics, seizure precautions (O2, pads, meds at bedside), pt adherence to meds; “grids and strips” - locate focus area, safety (no swim alone), individualized plan at school

A

Epilepsy Diagnosis, Treatment, and Nursing Interventions

31
Q

(TBI). Blow/jolt to head, disrupts normal brain function. Once of leading preventable causes of death in children. Infants and toddlers at greatest risk (large head); teenagers. Primary and secondary

A

Accidental head trauma

32
Q

Injury cause directly from trauma at time of injury. Skull fracture, bleed (epidural, subdural, intracerebral), concussion, contusion (“brain bruise)

A

Primary head trauma

33
Q

Indirectly from trauma, later.

Ischemia/hypoxia, cerebral edema, increased ICP

A

Secondary head trauma

34
Q

Includes Shaken Baby Syndrome (SBS)/Abusive.
Infant or small child shaken or beaten by adult. #1 cause of brain damage in infants in US. 1300 cases reported yearly, 25% result in death. 80% of survivors have permanent, severe disability. Silent condition. S/s similar to other conditions. Vomiting, irritability, increased sleeping leading to apnea. Retinal hemorrhage, skeletal survery. RN is a mandated reporter

A

Non-Accidental Head trauma

35
Q

S/s include: Photophobia, N/v, headache, vertigo, irritability, lethargy, poor feeding, amnesia/confusion, apnea, altered LOC, drainage from ears/nose (CSF)

A

Early signs of head trauma

36
Q

Increased ICP, hydrocephalus, seizure activity, posturing, unequal or nonreactive pupils, ecchymosis around eyes, diminished reflexes, herniation, cushing’s triad, coma. RED FLAGS

A

Late signs of head trauma

37
Q

Rapid recognition, diagnosis, treatment critical for good outcomes. Classification based on GCS score. Exam/LOC/Q1hr neuro checks. CT/MRI, ICP monitoring, Central Perfusion Pressure = MAP - ICP. Posturing? Decorticate or decebrate (brainstem)

A

Diagnosis of head trauma

38
Q

Treatment: Supportive; neuroprotective - HOB, Na+, cool, quiet. Period of peak swelling- 72 hours.
Priorities: Maintain adequate Bp, O2 sat, ventilation. Antiseizures, prevent hypoglycemia, Mannitol and 3% saline, keep electrolytes WNL, Monitor urine output (DI, SIADH), nutrition
Discharge: rehab, trach, helmet?

A

Head Trauma treatment and Nursing Interventions

39
Q

Common complaint, mild to severe. Acute. If its acute and recurrent its a migraine. Girls more often than boys. Paroxysmal.
Chronic - tension; psych.
Chronic non-progressive- abnormal, increased ICP tumor

A

Headaches

40
Q

Assess location and accompanying symptoms.
Treat underlying cause: OTC meds, relaxation, triggers, keep journal.
If reported needs immediate follow up: Increase in frequency and severity, awaken a child from sleep, occur early in AM, become worse on arising, persistent in frontal or occipital areas, change in gait personality/behavior, made worse by Valsalva

A

Headaches Nursing interventions

41
Q

Umbrella term- complex, multifactorial non progressive disorder of the brain.
Developing brain does not form properly or insult damages brain. Impaired control of muscles/movement. Impaired sensory functions, perception, cognitive ability, communication. Feeding difficulties.

A

Cerebral Palsy

42
Q

Varying degrees of disability: spastic (80%), dyskinetic (increased/decreased tone), ataxic (coordination/gait), mixed.
Support- patient and family; in school/community: El, multiple therapies
Meds- prevent spasticity, seizures (gum hyperplasia).
Adaptive devices? WC, braces, assistive technology

A

Cerebral Palsy S/s and Nursing Interventions

43
Q

Incomplete formation of spinal cord. Nervous tissue not encased/protected. Open vs closed. Associated with folate deficiency

A

Neural Tube Defects (NTDs)

44
Q

1600 children/year (most common NTD) 80% also have hydrocephalus (serial measurements). 3 types. Neurological impairment and paralysis below level of defect

A

Spina Bifida

45
Q

Interventions include: C section- minimize birth trauma; surgical repair 24-36 hours old (protect lesion before: sterile, moist drape)

A

Spina Bifida Nursing Interventions

46
Q

No visual defect, vertebral arch abnormality. Type of spinal bifida

A

Spina bifida occulta

47
Q

Protrusion of meninges. Type of spina bifida

A

Spina bifida with Meningocele

48
Q

sac with meninges and spinal cord. Associated with chiari type 2. Type of spina bifida

A

Spina bifida with myelomeningocele

49
Q

Skull fails to fuse in week 3-4 of gestation: brain and cranial membranes protrude anywhere along skull midline (nose-neck) 1 in 12000

A

Encephalocele

50
Q

Failure of major parts of brain to develop; neural tube does not close at cranial end. More than 1.2 in 10,000. Fatal, no treatment (most stillborn or die within a few hours)

A

Ancephaly

51
Q

Progressive muscle weakness due to muscle fiber degeneration, caused by genetic defect. Dystrophin (protein)- muscle fibers break down and lose function (Duschenne MD and Becker MD)

A

Muscular Dystrophy

52
Q

Generalized weakness in proximal muscles of arms/legs. Not keeping up with peers, toe walk, difficulty getting up/with stairs. Gower sign.
Eventual impairment in ambulation then respiratory and cardiac function.
Treatment: Glucocorticoids can delay loss of function but affect bone health. Physical therapy. Monitor respiratory and heart function; nutrition

A

Muscular Dystrophy S/s and Treatment

53
Q

Genetically inherited mutation in survival motor neuron 1 (SMN1) gene. Causes loss of motor function in all muscles. Degeneration of nerve cells/motor neurons in anterior horn of spinal cord. Muscles don’t receive signals from the nerve cells; atrophy. 4 types. Children present with varying degrees of motor delay, hypotonia,. and absent reflexes.

A

Spinal Muscular Atrophy (SMA)

54
Q

Infantile onset less than 6 months; most severe; 50%; cant sit, swallow. Type of SMA

A

Type 1 Spinal Muscular Atrophy

55
Q

6-12 mos: sit/stand, never walk. Type of SMA

A

Type 2 Spinal Muscular Atrophy

56
Q

2-3 years; trouble with stairs, lose ability to walk. Type of SMA

A

Type 3 Spinal Muscular Atrophy

57
Q

Diagnosis after 18 years. Type of SMA

A

Type 4 Spinal Muscular Atrophy

58
Q

Interventions include: Pulmonary interventions, PT; assistive devices. Feeding/nutrition. Skin/positioning. Surgery for scoliosis

A

Nursing Interventions for Spinal muscular atrophy

59
Q

Damage to spinal cord resulting is loss of physical and or sensory function. Over 50% due to MVA. Determined by mechanism of injury and direction of forces. Injury types: Hyperflexion, rotational, hyperextension, compression

A

Spinal Cord Injury

60
Q

Absence of sensory, motor, and autonomic function below level of injury.

A

Complete spinal cord injury

61
Q

Some motor/sensory/autonomic function below level of injury

A

Incomplete spinal cord injury

62
Q

Xray, CT/MRI to determine level and extent of injury. Immobilization to prevent further injury; prevent sequelae.
Interventions: managing spasticity with splints, stretching PT. Baclofen, valium, clonidine. Dysautonomia (bladder and temp)- monitor; decrease triggers (catheterization. Neurogenic bladder/bowel- intermittent cath; bowel regimen. Skin integrity. Nutrition/feeding (swallowing). Family support; rehab, home modifications, home care needs, adaptive devices, services.

A

Spinal Cord Injury Diagnosis and Nursing Interventions

63
Q

transient suppression of nerve function

A

Spinal shock

64
Q

loss of vasomotor tone and sympathetic innervation of the heart

A

Neurogenic shock

65
Q

Increased BP, decreased HR, sweating, full bladder/bowels

A

Autonomic dysreflexia

66
Q

AKA acute inflammatory demyelinating polyradiculoneuropathy. Triggered by recent viral or bacterial infection. Autoimmune response: attack on PNS (CNS unaffected). Inflammation and demyelination of peripheral nerves. Causes progressive weakness, can lead to neuromuscular paralysis and resp failure. ASCENDING (feet up to check and neck) hypotonia, numbness, pain (over a few days- weeks).

A

Guillain-Barre Syndrome

67
Q

Diagnosis: CSF = increased protein (more than 2x normal)
Treatment: IVIG x 5 days or phasmapheresis.
Nursing: Extended hospitalization. Monitor resp status (intubation?) Skin/immobility, nutrition

A

Guillian Barre Syndrome Diagnosis, Treatment and Nursing Interventions

68
Q

Type of Arnold Chiari. Affects only cerebellum

A

Arnold Chiari 1

69
Q

Type of Arnold Chiari. Affects cerebellum and brainstem.

A

Arnold Chiari 2

WH and Pedi (20 decks)

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