Pituitary Disorders
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Transcript Pituitary Disorders
PITUITARY GLAND
Where is it located???
Name its’ 3 parts or sections.
What hormones are secreted by the
pituitary gland???
Pituitary Gland
ANTERIOR PITUITARY
SECRETES 6+ HORMONES:
ACTH (adrenocorticotropic hormone)
release of cortisol in adrenal glands
TSH (thyroid stimulating hormone)
release of T3 & T4 in thyroid gland
GH (growth hormone)
stimulates growth of bone/tissue
FSH (follicle stimulating hormone)
stimulates growth of ovarian follicles &
spermatogenesis in males
LH (lutenizing hormone)
regulates growth of gonads &
reproductive activities
Prolactin
promotes mammary gland growth
and milk secretion
ANTERIOR HYPER PITUITARY
DISORDERS
What would happen if you had TOO
MUCH secretion of prolactin?
Too much release of Lutenizing
Hormone (LH)?
ANTERIOR HYPER PITUITARY
DISORDERS
ETIOLOGY
Primary: the defect is in the gland itself
which releases that particular hormone
that is too much or too little.
Secondary: defect is somewhere outside
of gland
i.e. GHRH from hypothalamus
TRH from hypothalamus
PITUITARY TUMORS
10% OF ALL BRAIN TUMORS
What are the diagnostic tests to
diagnose a pituitary tumor?
tumors usually cause hyper release of
hormones
ANTERIOR PITUITARYHYPERfunctioning
Sing along
What would happen if you had too
much growth hormone secretion???
Which goolish character on the
Addam’s Family may have had too
much GH secretion?
TOO MUCH GROWTH
HORMONE
GIGANTISM IN CHILDREN
skeletal growth; may grow
up to 8 ft. tall and > 300 lbs
ACROMEGALY IN ADULTS
enlarged feet/hands, thickening of bones,
prognathism, diabetes, HTN, wt. gain, H/A,
Visual disturbances, diabetes mellitus
GIGANTISM IN CHILDREN
ACROMEGALY IN ADULTS
What assessment findings would the nurse
document?
What assessment findings would the nurse
document?
MEDICAL INTERVENTIONS
FOR PITUITARY TUMOR
Medications
Parlodel (bromocriptine) to
________ & GH levels.
Radiation therapy
external radiation will bring down GH
levels 80% of time
Transsphenoidal
Hypophysectomy
Neurosurgery:
procedure called “transsphenoidal
hypophysectomy”; New Method
Most common method: incision is
made thru floor of nose into the
sella turcica.
Nursing Management
Pre op hypophysectomy
Anxiety r/t
a. body changes
b. fear of unknown
c. brain involvement
d. chronic condition with life long care
Sharmyn
Sensory-perceptual alteration r/t
a. visual field cuts
b. diplopia
secondary to pressure on optic
nerve.
Alteration in comfort (headache) r/t
a. tumor growth/edema
Knowledge deficit r/t
Post-op teaching
pain control
ambulation
hormone replacement
activity
Post operative care
Post-op complications of hormone
insufficiency:
What would happen if you didn’t have
enough ADH?
What is that disorder called?
Other insuffciency:
Decrease ACTH will require cortisone
replacement due to decrease
glucocorticoid production.
Can you live without
glucocorticoids????
Other deficiency:
in sex hormones can lead to
infertility due to decrease production of
ova & sperm
What were those hormones called
again?-
Incisional disruption after
transsphenoidal
hypophysectomy
Avoid bending and straining X 2
months post transsphenoidal
hypophysectomy,
Use stool softeners
Avoid coughing
Saline mouth rinses
No toothbrushes for 7-10 days
Post-op CSF Leak where sella
turcica was entered
any clear rhinorrhea - test for glucose
+ glucose = CSF Leak
Notify physician
HOB 30 degrees
Bedrest
CSF leak usually resolves within 72
hrs.
If not - spinal taps done to decrease
pressure
Post op problems cont.
Periocular edema/ecchymosis
Headaches
Visual field cuts/diplopia
What is the most important nursing
intervention for these
problems????
ANTERIOR PITUITARYHypofunction
1. Etiology (rare disorder) may be due to
disease, tumor, or destruction of the gland.
Diagnostic tests
CT Scan
Serum hormone levels
S & S Anterior Pituitary
Hypofunctioning
GH
FSH/LH
Prolactin
ACTH
TSH
Medical Management
neurosurgery -- removal of tumor
radiation -
hormone replacement
tumor size
cortisol, thyroid, sex hormones
Nursing Management
Assessment of S & S of hypo or hyper
functioning hormone levels
Teaching-Compliance with hormone
replacement therapy
Counseling and referrals
Support medical interventions
Posterior Pituitary
(Neurohypophysis)
Question??? What hormones are
released by the posterior pituitary?
_____ & _____are released when
signaled by hypothalamus
ADH (Vasopressin)
secreted by cells in the hypothalmus
and stored in posterior pituitary
acts on distal & collecting tubules of
the kidneys making more permeable to
H20 -or
volume excreted?
Bonus Round...
Under what conditions is ADH
released???
ADH has vasoconstrictive or
vasodilation action???
ANSWERS:
released in response to decrease blood
volume, increase concentration of Na+
or other substances, pain, stress
ADH has vasocontrictive properties
Oxytocin
Controls lactation & stimulates uterine
contractions
‘Cuddle hormone’
Research links oxytocin and socio-sexual
behaviors
Posterior Hyper pituitary
Disorders
SIADH (TOO MUCH ADH!!)
lung cancer, Ca duodenum/pancreas,
trauma, pulmonary disease, CNS
disorders, drugs -- Vincristine,
nicotine, general anesthetics,
tricyclic antidepressants
Think tank:
If you are having too much ADH... What
would the clinical signs/symptoms be??
Clinical manifestations-SIADH
Weight gain or weight loss?
or
urine output?
or
serum Na levels?
weakness
muscle cramps
H/A
Diarrhea
If hyponatremia worsens will
develop neuro manifestations
lethargy
decrease tendon reflexes
seizures
Diagnostic Tests-SIADH
Serum Na+ <135meq/l
Serum osmolality <275 OSM/kg H2O
urine specific gravity
or normal BUN
Medical Treatment
***FLUID RESTRICTION
LIMIT TO 1000ML/24HRS
IV 3% NaCl to replace Na
IF CHF -- Lasix (temporary fix)
Treat underlying problem --Chemo,
radiation
Declomycin 600 po-1200mg/day
to inhibit ADH
Nursing Interventions-SIADH
Fluid restriction may be as little as 500600ml/24hrs
Daily weights...
1 lb. weight = 500ml fluid retention
Accurate I & Os
Nursing Management-SIADH
F & E imbalances
fluid intake
High risk for injury r/t complications of
fluid overload (seizures)
Posterior Hypopituitary
ADH disorders
Diabetes Insipidus
(too little ADH)
What do you think the S&S would be
if you had too little ADH???
Etiology
50% idiopathic
a. central -- i.e. brain tumors
b. nephrogenic - inability of tubules
to respond to ADH
Clinical Manifestations-DI
Polydipsia
Polyuria (10L in 24 hours)
Severe fluid volume deficit
wt loss
tachycardia
constipation
shock
Diagnostic Tests-DI
or
or
or
urine specific gravity
serum Na
serum osmolality
Dehydration test:
2 units of Vasopressin (ADH) mixed in saline
administered over 2 hrs then check urine
osmolality levels
Medical Management-DI
Identification of etiology, H & P
Tx of underlying problem
DDAVP (nasal spray)
Pitressin s.c. IM, nasal spray
Nursing Management-DI
Assess for F & E imbalances
High risk for sleep disturbances
Increase po/IV fluids
RF Injury (hypovolemic shock)
Knowledge deficit
High risk for ineffective coping