Cerebral and Endocrine Dysfunction Flashcards

(114 cards)

1
Q

Main functions/symptoms of endocrine dysfunction (4)

A

1) energy production
-fatigue, weakness

2) sexual reproduction
-delayed puberty, precocious puberty,

3) growth –> delayed

4) fluid and electrolyte balance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What does thyroid hormone regulate?

A

basal metabolic rate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

2 hormones that the thyroid secretes

A

1) thyroid hormone

2) calcitonin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

2 hormones that thyroid hormone is made up of

A

1) thyroxin (T4)

2) triiodothyronine (T3)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

thyroid hormone function

A

metabolism

growth and development of body tissues

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Juvenile hypothyroidism types (2)

A

1) congenital

2) acquired

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Risk factor for congenital juvenile hypothyroidism

A

mom taking antithyroid drugs during pregnancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Causes of acquired juvenile hypothyroidism

A

thyroidectomy

radiation (Hodgkin or other malignancy)

infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

When should hypothyroidism ideally be identified and treated by?

A

3 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What happens if the child is not treated by then

A

intellectual delay

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Clinical manifestations of junevile hypothyroidism (many)

A

cognitive decline

constipation

growth decline

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Therapeutic management of juvenile hypothyroidism

A

LIFELONG oral TH replacement

increase amount over 4 to 8 weeks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What happens if TH replacement therapy is increased too quickly?

A

hyperthyroidism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is important in the treatment of juvenile hypothyroidism?

A

prompt treatment

compliance

lifelong treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Goiter

A

hypertrophy of thyroid gland

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Types of goiter (2)

A

1) congenital

2) acquired

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Main cause of congenital goiter

A

maternal use of antithyroid drugs during pregnancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

If you know that child is at risk of being born with goiter, what should you be prepared to do?

A

be ready to intubate

increased risk of breathing difficulties

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Causes of acquired goiter (many)

A

neoplasm

inflammatory disease

increased secretion of pituitary thyrotropic hormone

dietary deficiency - rare in kids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Most common cause of hyperthyroidism in childhood

A

Graves disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Symptoms of hyperthyroidism (many)

A

enlarged thyroid gland

exophthalmos - bulging of the eyes

weight loss

diarrhea

hyperactivity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

T or F: Treatment for hyperthyroidism is firmly established.

A

FALSE

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Treatment for hyperthyroidism (3)

A

1) Antithyroid drugs (PTU and methimazole)

2) thyroidectomy
-if drugs don’t work

3) ablation with radioiodine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Which diabetes type is most common in children?
a) Type 1
b) Type 2

A

a) Type 1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Type 1 DM
destruction of beta cells, usually leading to absolute insulin deficiency onset usually in childhood and adolescence
26
Type 2 DM
insulin resistance usually later in life
27
Conditions that can lead to diabetes (2)
1) cystic fibrosis -pancreas messed up 2) acute lymphocytic leukemia (ALL) -steroid treatment
28
Main diabetes symptoms (4)
polyuria polydypsia fatigue weight loss
29
Diabetes diagnosis (2)
1) glucose levels 2) A1C
30
Why may children be diagnosed with diabetes on vacation?
parents are with them for an extended period of time for the first time in a while
31
Diabetes management
insulin pens insulin pumps
32
Diabetes is easier to control with: a) pens b) pumps
b) pumps moving towards this
33
Challenge with insulin administration in childhood
timing of insulin with meals child may not want to eat may have to administer halfway through meal
34
Challenge with diabetes management in adolescence
puberty, growth body image drugs and alcohol
35
Symptoms of cerebral dysfunction in infants
tone bulging fontanelles high-pitched cry* irritability sleepy feeding issues, uncoordinated suck difficult to consol
36
Big thing in assessment of cerebral function in infants and young children
observe spontaneous and elicited reflex responses what's present and what's not
37
Assessment of cerebral function
family history medical history head-to-toe neuro growth and development***
38
Pediatric Glasgow Coma Scale components (3)
eye opening motor response verbal response
39
Neuro exam components (many)
BP HR - tachy initially resp skin eyes - pupils, response to light motor function posture reflexes response to pain
40
What is a late sign of neuro issues?
hypertension*** bradycardia
41
T or F: Early signs and symptoms of increased ICP are obvious.
FALSE may be subtle
42
What is a major, late sign of increased ICP?
altered LOC
43
LATE signs of increased ICP
decreased LOC bradycardia decreased motor response to command decreased sensory response to painful stimuli alterations in pupil size and reactivity papilledema decerebrate or decorticate posturing Cheyne-Stokes respirations (periodic breathing)
44
Children with increased ICP will have vomiting a) WITH nausea b) WITHOUT nausea
b) WITHOUT nausea
45
Personality and Behavioral Signs of Increasing ICP
irritability, restlessness lethargy drowsiness, indifference decrease in physical activity and motor skills inability to follow commands memory loss
46
lethargy
VERY sleepy and drowsy but awaken to verbal or physical stimuli
47
obtunded
arouse with stimulation confused
48
stupor
only respond to vigorous and painful stimulation
49
coma
no motor or verbal response, even to painful stimulation
50
T or F: Most brain injuries are mild.
TRUE most are concussions, sustained during sports
51
Mild TBI - Pediatric Glasgow Coma Scale score
13 to 15 e.g. concussion
52
Moderate TBI - Pediatric Glasgow Coma Scale score
9 to 12
53
Severe TBI - Pediatric Glasgow Coma Scale score
< 8
54
Causes of TBI
falls MVA bicycle injuries shaken baby syndrome sports
55
Unique sign of shaken baby syndrome
retinal hemorrhages
56
Head traumas (3)
1) concussion 2) contusion and laceration -tearing of tissue 3) skull fractures -abnormal to see
57
Current protocol for concussions
do what you can tolerate
58
Complications of head trauma (many)
epidural hemorrhage subdural hemorrhage cerebral edema herniation
59
Epidural hemorrhage
between dura and skull can be LETHAL*
60
Subdural hemorrhage
in outermost meningeal layer
61
Cerebral edema
inadequate drainage accumulation
62
Herniation
very very high ICP shifts brain across structures FATAL*
63
If child is suspected to have spine issue, what precautions are they put on?
spine precaution C-spine collar on until excluded needs to be maintained until excluded by assessment and imaging
64
Diagnostic eval of TBI
detailed history ABCs evaluation for shock vital signs neuro exam LOC special tests: -CT scan -MRI -behavioral assessment
65
Care of the comatose child
neuro assessments - ICP* vital sign monitoring pain assessments/control calm, quiet environment family support
66
How to know if pain has decreased in comatose child
look at temp, HR, BP treat pain and see if they go down
67
Nervous system tumours
difficult to treat poor survival signs and symptoms vary
68
BIG sign of nervous system tumour
chronic headache! also ICP
69
Diagnostic eval of nervous system tumours
clinical signs lumbar puncture* MRI -most common but need to be sedated CT -quick but radiation EEG
70
Treatment of nervous system tumours
surgery chemo radiation (less so in children)
71
Cushing's Triad
signs of ICP 1) hypertension 2) bradycardia 3) irregular respirations
72
Intracranial infections
limited response to injury can affect meninges, brain, or spinal cord difficult to distinguish lab studies required*
73
Bacterial meningitis
acute inflammation of the meninges and CSF
74
Which vaccine targets bacterial meningitis?
Hib vaccine
75
Most common causative bacterial agents for meningitis (3)
1) Streptococcus pneumoniae 2) Group β streptococci 3) E. coli
76
Lab test signs of bacterial meningitis
white cells in CSF LOW blood sugar (bacteria eat sugar) HIGH protein
77
Definitive diagnostic test
lumbar puncture
78
Signs and symptoms of bacterial meningitis
increased ICP: bulging fontanelles nuchal rigidity fever N/V irritability photophobia no appetite headache
79
Transmission of bacterial meningitis
nasopharyngeal secretions
80
If a child under 1 month has a fever, what do you do?
assume they have bacterial meningitis until proven otherwise!! don't have BBB until 1 month
81
Therapeutic management of bacterial meningitis
isolation precautions antibiotics RESTRICT fluids* ventilation & perfusion hemodynamics systemic shock control of seizures and temp treat complications
82
Complications of bacterial meningitis
intellectual disability seizures hearing loss (antibiotics or disease itself)
83
How soon after the initiative of antibiotic therapy for meningitis should you see a response?
24 to 48 hours
84
Non-bacterial/aseptic meningitis
mainly caused by viruses
85
Symptoms of non-bacterial/aseptic meningitis (4)
meningeal irritation headache fever malaise
86
What other diseases is non-bacterial/aseptic meningitis associated with?
measles mumps herpes leukemia
87
Treatment for non-bacterial/aseptic meningitis
symptomatic pain, hydration, fever calm, quiet environment
88
Encephalitis
inflammatory process of CNS with altered function of brain and spinal cord
89
Causes of encephalitis (2)
1) direct invasion of CNS by a virus 2) post-infectious involves of the CNS after a viral infeciton
90
T or F: We usually know the cause of encephalitis.
FALSE most frequently viral though
91
Clinical manifestations of encephalitis
malaise fever headache/dizziness stiff neck nausea/vomiting ataxia speech difficulties poor feeding
92
Clinical manifestations of SEVERE encephalitis
high fever stupor/seizures disorientation/spasticity coma ocular palsies paralysis
93
Therapeutic management of encephalitis
hospitalization antimicrobial therapy: IV acyclovir & vancomycin nutrition* physio manage complications like seizures
94
Reye's syndrome
toxic encephalopathy associated with other characteristic organ involvement
95
What is Reye's syndrome usually caused by?
aspirin hepatic
96
Symptoms of Reye's syndrome
fever profoundly impaired consciousness disordered hepatic function
97
Etiology of seizures (4)
1) acute symptomatic -associated with head trauma or meningitis 2) remote symptomatic -prior brain injury such as encephalitis or stroke 3) cryptogenic -no clear cause 4) idiopathic -genetic in origin
98
Seizures linked with a fever are associated with: a) the temperature itself b) how fast the temperature rises
b) how fast the temperature rises
99
Seizure classification (3)
1) focal 2) generalized 3) epileptic spasms
100
Focal seizure
local onset and involves a relatively small location of the brain classified based on awareness during seizure
101
Generalized seizure
BOTH hemispheres, without local onset awareness impaired motor involved often bilateral seizures can be convulsive or nonconvulsive
102
Epileptic spasm seizure
spasms of muscles of neck, trunk & extremities mode of onset (focal vs. generalized not well understood)
103
Epilepsy criteria
at least 2 unprovoked seizures occurring MORE than 24h apart
104
Generalized absence seizures
formerly petit mal or absence seizures very brief can keep talking, walking minimal change in tone can be mistaken for daydreaming parent may not notice
105
Focal, Generalized, Unknown Onset Epileptic Spasms
onset in first 6 to 8 months of life associated with cognitive impairment spasm but then continue what they're doing, don't fall asleep
106
Febrile seizures
transient disorder - most will outgrow associated with a febrile illness that is not a CNS infection should return to alert mental status
107
Treatment of seizures
pharmacological keto diet vagus nerve stimulation device surgery avoid triggers
108
Considerations for seizures drugs
monitor therapeutic levels** increase dosage as child grows (weight-based) monitor for side effects DO NOT STOP ABRUPTLY
109
Nursing interventions during a seizure
cushions for bed rails oxygen and suction at bedside suction if they vomit time the seizure positioning maybe observe symptoms
110
Hydrocephalus
caused by an imbalance in the production and absorption of cerebrospinal fluid (CSF)
111
What type of seizure do people with hydrocephalus demonstrate?
pseudo-seizure somatic presentation very real to the patient
112
Etiology of Hydrocephalus
developmental abnormalities usually apparent in early infancy other causes include neoplasms, infection, and trauma often associated with myelomeningocele
113
Treatment of of hydrocephalus
surgical ventriculoperitoneal shunt complications
114
Signs and symptoms of shunt infection
risk greatest: 1 to 2 months after placement increased head circumference symptoms of ICP massive dose of antibiotics or shunt removal