Pituitary and Adrenal Gland Disorders
Pituitary Hormones
Anterior Lobe
TSH-Thyroid Stimulating Hormone
ACTH-Adrenocorticotropic Hormone
FSH-Follicle Stimulating Hormone
LH-Luteinizing Hormone
GH-Growth Hormone
Prolactin
Posterior Lobe
ADH-Anti-Diuretic Hormone
aka Arginine Vasopressin (AVP) or simply vasopressin
Oxytocin
Anterior Pituitary Disorders
Acromegaly
GH
Overgrowth of soft tissues and bone

6/1,000,000 Adults
Shortens life span 5-10 yrs
Clinical Manifestations
Enlarged Hand and Feet
Thickening of bony and soft tissue of the face
Leather, thick, and oily skin
Visual disturbances
Peripheral neuropathy
Headaches
Menstrual changes
Acromegaly Diagnostic
H&P
Abnormal tissue growth
Increase in hat, ring, glove, shoe size
Growth Factor levels
Oral glucose tolerance test (OGTT)
Growth Hormone response to oral glucose challenge
MRI/CT with contrast
Acromegaly Treatment
Surgery (Hypophysectomy)
Treatment of Choice
Transsphenoidal Approach
Permanent Loss of Pituitary Hormones
Target organ hormone replacement for
lifetime
Radiation Therapy
Used when surgery failed to produce complete remission/high risk surgery
candidate
Offered in combo with drug therapy
Drug Therapy
Used for inadequate response to/cannot be treated with surgery or radiation
therapy
Most common medication is octreotide (Sandostatin) given IM. Reduces GH
levels within norm range
Nursing Management- Surgical
Post-Surgical
Head of Bed 30 degrees
Neuro Assessment
Pupillary Response, Speech Patterns, Extremity Movement and Strength
Q 4hr Mouth Care, No teeth brushing for 10 days
Hemorrhage
Avoid Coughing, Sneezing, or Straining

CFS (glucose test)
Nursing Management- Radiation
Stereotactic Radiosurgery
Specialized Radiation Neuro ICU
Headaches, Seizures, Nausea, Vomiting
Pin Site Care
Diabetes Insipidus (Loss ADH)
Infertility (FSH, LH)
Increased Risk for Colon Polyps and Colorectal Cancer
Nursing Management-Medication
Octreotide (Sandostatin) lowers GH
Subcutaneous three times a week
Dopamine agonist reduces secretion of GH
Combination Drugs
Hormonal Therapy
Life Long Therapy
ADH
Cortisol
Thyroid
Hypopituitarism
Selective Hypopituitarism verses Panhypopituitarism
Causes
Pituitary tumor
Autoimmune disorders
Infections
Pituitary Infarction (Sheehan Syndrome)
Destruction of Pituitary (trauma, radiation, surgery)
Anterior pituitary hormone deficiency = end organ failure.
Life Threatening
Hypopituitarism Clinical Manifestations
Vary with the Pituitary dysfunction.
Headache, visual changes, anosmia, seizures
Growth hormone deficiency
Truncal obesity
Decreased muscle mass
Decreased energy
Reduced exercise capability.


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- Fall '18
- Mrs.Fair
- Cortisol, ADH, Growth Hormone response, Treatment of Choice, Infertility, Increased Risk