Endocrine Disorder Flashcards

1
Q

What is the endocrine system composed of?

A

glands, tissues, or clusters of cells that produce and release hormones

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

What is the gold standard for making the diagnosis of GH excess?

A

Failure to suppress serum GH levels after an oral glucose challenge test

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

Lab/Diagnostic Studies for Diabetes Insipidus

A
  • Radiographic studies
  • Urinalysis
  • Serum Osmolarity
  • Serum Sodium
  • Fluid Deprivation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the two types of pituitary disorders?

A

Anterior and Posterior

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

Anterior Pituitary Disorders

A
  • Growth Hormone Deficiency
  • Hyperpituitarism
  • Precocious Puberty
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Posterior Pituitary Disorders

A
  • Diabetes Insipidus

- Syndrome of Inappropriate Antidiuretic Hormone Secretion

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

When is Growth Hormone typically released?

A

-throughout the day, mostly secreted during sleep

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

What is growth hormone deficiency usually a result of?

A

Failure of the anterior pituitary or hypothalamic stimulation on the pituitary to produce sufficient GH

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

GH Deficiency is also known as what?

A

Hypopituitarism or Dwarfism

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

What is GH Deficiency characterized by?

A

poor growth and short stature

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

Complications for GH Deficiency Include?

A

unable to metabolize protein, fat, and carbohydrates effectively

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

What is the primary cause of GH Deficiency?

A

Injury to pituitary gland or hypothalamus

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

What may cause injury to the pituitary gland or hypothalamus resulting in GHD?

A
  • tumor
  • infection/infarction
  • CNS irradiation
  • abnormal formation in utero
  • birth trauma
  • Genetics (Prader-Willi or Turner)
  • Psychosocial
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Therapeutic Management for GHD

A
  • supplement GH
  • removal of tumors
  • continue treatment until near final height
  • physical exam
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What would you see on a Physical Exam for a child w/ GHD?

A
  • height at or < 3rd percentile
  • higher weight to height ratio
  • prominent abdominal fat
  • large forehead
  • high pitched voice
  • delayed sexual maturity, dentition, skeletal maturation
  • decreased muscle mass
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Teaching Plan for GHD

A
  • promoting growth
  • enhancing the child’s self esteem
  • providing appropriate education on disorder
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

When does treatment stop for GHD?

A

With fusion of growth plates

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

How often should you measure a child’s height w/ GHD?

A

q 3-6 months

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

What should the child notify the physician about during treatment?

A
  • headaches
  • rapid weight gain
  • increased thirst/urination
  • joint pain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Complications of GHD

A
  • altered carbohydrate, protein, fat metabolism
  • hypoglycemia
  • glucose intolerance/diabetes
  • slipped capital femoral epiphysis
  • pseudotumor cerebri
  • leukemia
  • recurrence of CNS tumors
  • Infection at injection site
  • edema and sodium retention
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Precocious Puberty

A

Development of sexual characteristics before the usual age of pubertal onset

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

When does Precocious Puberty begin for boys and girls?

A

Younger than 8 for girls and 9 for boys

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

What is the most common form of Precocious Puberty?

A

Central Precocious Puberty

24
Q

Central Precocious Puberty develops as a result of what?

A

Increase in hormones w/ development of sexual characteristics, increased growth, and reproductive capability

25
What happens if Precocious Puberty is left untreated?
The child may become fertile
26
S/S of Precocious Puberty?
- headaches - vision probs - behavior changes/mood swings - acne, body odor - accelerated growth - bone age is advanced - size of uterus increased
27
Goals of Nursing Management of Precocious Puberty
- educating about physical changes - teaching on meds - self esteem issues - promoting age appropriate physical dev and pubertal progression
28
Delayed Puberty for Girls
- breasts not developed by 12 - pubic hair not produced by 14 - menarche not occurred by 15
29
Delayed Puberty for Boys
- no testicular enlargement or scrotal changes by 14 | - no pubic hair by 15
30
What is the most common cause of Delayed Puberty?
Constitutional Delay-"Late Bloomer"
31
What are the 2 types of Diabetes Insipidus?
Nephrogenic and Central
32
How does Nephrogenic occur?
- transmitted genetically | - acquired from renal disease, hypercalcemia, hypokalemia, drugs-lithium, rifampin
33
Therapeutic Management for Nephrogenic DI
- diuretics - high fluid intake - restricted sodium - high-protein diet
34
What is the most common form of Diabetes Insipidus?
Central
35
Central DI is a disorder of what?
the pituitary gland
36
Central DI is characterized by what?
Polydipsia and polyuria
37
When does SIADH occur?
when the feedback mechanism that regulates ADH does not function properly
38
Diabetes Insipidus
- "high and dry" - increased urination - Hypernatremia - serum osmolarity > 300 - decreased urine osmolarity - dehydration, thirst
39
Syndrome of Inappropriate ADH
- "low and wet" - decreased urination - hyponatremia - serum osmolarity <280 - increased urine osmolarity - fluid retention - weight gain - HTN
40
Graves Disease
autoimmune disorder that causes excessive amounts of thyroid hormone to be released in response to human thyroid stimulator immunoglobin
41
Congenital Hypothyroidism
"Cretinism" - failure of the thyroid gland to migrate during fetal development which causes malfunction/malformation of thyroid gland - insufficient production of thyroid hormone
42
What happens if Congenital Hypothyroidism is left untreated?
- intellectual disability - short stature - growth failure - delayed physical maturity
43
What is the most common cause of preventable intellectual disability?
Congenital Hypothyroidism
44
How often should you measure thyroid levels until target is reached on stabilized dose of meds?
q 2-4 weeks
45
Hyperthyroidism
- nervousness/anxiety - diarrhea - heat intolerance - weight loss - smooth, velvety skin
46
Hypothyroidism
- tiredness, fatigue - constipation - cold intolerance - weight gain - dry, thick skin, edema of face, eyes and hands - decreased growth
47
Signs of Thyroid Storm
- sudden onset of severe restlessness and irritability - fever - diaphoresis - severe tachycardia - increased BP, HR, body temp to dangerous levels
48
Thyroid Storm
life-threatening health condition of untreated or undertreated hyperthyroidism
49
Addison's Disease
deficiency in the adrenal steroids, glucocorticoids-cortisol, and mineralcorticoids,-aldosterone
50
S/S of Addison's Disease
- hyponatremia - hyperkalemia - water loss - hypoglycemia - hypotension - hyperpigmentation - adrenal crisis
51
Cushing Syndrome
excess levels of one or all hormones, but most commonly glucocorticoid excess
52
S/S of Cushing Syndrome
- rapid weight game - decreased linear growth - weakness/fatigue - irritability - sleep problems - HTN - missed menstrual period
53
Congenital Adrenal Hyperplasia
autosomal recessive disorder in which there is an inefficient supply of the enzymes required for the synthesis of cortisol and aldosterone
54
What is the most common type of adrenocortical insufficiency?
Congenital Adrenal Hyperplasia
55
What is the obvious sign of Congenital Adrenal Hyperplasia?
Ambiguous genitalia