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27 Cards in this Set

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Addison's Disease
Hyposecreation of adrenal cortex hormones (glucocorticoids and mineralocorticoids) from the adreanal gland, resulting in deficiency of the corticosteriod hormones. THE CONDITION IS FATAL IF LEFT UNTREATED.
Adrenalectomy
The surgical removal of an adrenal gland. Lifelong replacement of glucococorticoids and mineralocorticoids is necessary with a bilateral adrenalectomy. Temporary replacement may be necessary for up to 2 yrs for a unilateral adrenalectomy.
Chvostek's Sign
A spasm of the facial muscles elicited by tapping the facial nerve just anterior to the ear. The sign is noted in hypocalcemia.
Cushing's Disease
A metabolic disorder characterized by abnormally increased secretion (endogenous) of cortisol, caused by increased amounts of adrencocrticotropic hormone (ACTH) secreated by the pituitary gland.
Cushing's Syndrome
A metabolic disorder resulting from the chronic and excessive production of cortisol by the adrenal cortex or by the administration of glucocorticoids in large doses for several weeks or longer (exogenous or iatrogenic).
Dawn Phenomenon
A nocturnal release of growth hormone, which may cause blood glucose level elevations before breakfast in the client with diabetes mellitus. Treatment includes administering an evening dose of intermediate-acting insulin at 10 PM.
Diabetes Insipidus
The hyposecreation of antidiuretic hormone (ADH) from the posterior pituitary gland, resulting in failure of tubular reabsorption of water in the kidneys and diuresis.
Diabetic Ketoacidosis
A life-threatening complication of the diabetes mellitus that develops when a severe insulin deficiency occurs. Hyperglycemia progresses to ketoacidosis over a period of seveal hrs to several days. Acidosis occures in clients with Type 1 diabetes mellitus, persons with undiagnosed diabetes, and person who stop prescribed treatment for diabetes.
Diabetes Mellitus
A chronic disorder of glucose intolerance and impaired carbohydrate, protein, and lipid metabolism caused by deficiency of insulin or resistance to the action of insulin. A deficiency of effective insulin results in hyperglycemia.
Hyperglycemia
Elevated blood glucose level > 250 mg/dL
Hyperglycemic Hyperosmolar Nonketotic Syndrome
Extreme hyperglycemia w/o acidosis. A complication of Type 2 DM, which may result in dehydration or vascular collapse but does not include the acidosis component of diabetic ketoacidosis. Onset is usually slow, taking from hours to days.
Hypoglycemia
Low blood glucose level (less than 70 mg/dL) that results from too much insulin, not enough food, or excess activity.
Hypophysectomy
The removal of the pituitary gland.
Hypothyroidism
A hypothyroid state resulting from a hyposecretion of thyroid hormone. The condition occurs in adulthood.
Myxedema
The most severe form of hypothyroidism characterized by swelling of the hands, face, feet, and periorbital tissues. At this stage, the disease may lead to coma and death.
Myxedema Coma
A rare but serious disorder that results from persistently low thyroid production. Coma can be precipitated by acute illness, rapid withdrawal of thyroid medication, anesthesia and surgery, hypothermia, and the use of sedatives and opiod analgesics.
Somogyl Phenomenon
A rebound phenomenon that occurs in clients with Type 1 DM. Normal or elevated blood glucose levels are present at bedtime; hypoglycemia occurs at about 2 - 3 AM. Counterregulatory hormones, produced to prevent furthur hypoglycemic, result in hyperglycemia (eveident in the prebreakfast blood glucose level). Treatment includes doses of intermediate - acting insulin or increasing the bedtime snack.
Thyroidectomy
Surgical removal of the thyroid gland to treat persistent hyperthyroidism or thyroid tumors.
Thyroid Storm
An acute, potentially fatal exacerbation of hyperthyroidism that may result from manipulation of the thyroid gland during surgery, severe infection, or stress.
Trousseau's Sign
A sign of hypocalcemia. Carpal spasm can be elicited by compressing the barachial artery with a blood pressure cuff for 3 minutes.
Functions of Endocrine Glands
1. Maintenance & Regulation of Vital Functions.
2. Response to stress & injury
3. Growth and development
4. Energy metabolism
5. Reproduction
6. Fluid, electrolyte, and acid-base balance
Risk Factors for Endocrine Gland Disorders
1. Age
2. Heredity
3. Congenital Factors
4. Trauma
5. Environmental Factors
6. Consequence of other disorders
Hypothalamus
Activates, controls, and integrates the peripheral autonomic nervous system, endocrine processes, and many somatic functions, such as body temperature, sleep, and appetite.
Located in the diencephalon of the brain.
Hypothalamus Hormones
1. Corticotropin - releasing hormone (CRH)
2. Gonadotropin-releasing hormone (GnRH)
3. Growth hormone-inhibiting hormone (GHIH)
4. Melanocyte-inhibiting hormone (MIH)
5. Prolactin-inhibiting hormone (PIH)
6. Thyrotropin-releasing hormone (TRH)
Pituitary Gland
1. The MASTER gland, located at the base of the brain.
2. Influenced by the hypothalamus
3. Directly affects the function of the other endocrine glands
4. Promotes growth of body tissue, influences water absorption by the kidney
5. Controls sexual development and function
Pituitary Gland Hormones
(Anterior Lobe Production)
1. Growth Hormone (GH)
2. Follicle-Stimulating Hormone (FSH)
3. Luteinizing Hormone (LH)
4. Thyroid-Stimulating Hormone (TSH)
5. Adrenocortioctropic Hormone (ACTH)
6. Melanocyte-Stimulating Hormone (MSH)
7. Prolactin (PRL)
8. Somatorophic growth-stimulating hormone
Pituitary Gland Hormones
(Posterior Lobe Production)
** These hormones are produced by the hypothalamus, stored in the posterior lobe, and secreted into the blood when needed.

1. Oxytocin
2. Vosopressin
3. Antidiuretic Hormone (ADH)