Assessment and Management of Patients with Endocrine Disorders 2,3

Assessment and Management of Patients with Endocrine Disorders

Overview

  • Prepared by Prof. Zeinab Al-Wahsh for Spring 2024-2025 Lectures 2-3

Endocrine Glands

  • Endocrine glands release hormones (chemical messengers) into the bloodstream to various organs and tissues.

  • Example: Pancreas secretes insulin; Thyroid gland regulates chemical activity levels via pituitary instructions.

Pituitary Gland

Location and Structure

  • Size: About the size of a pea (1.27 cm in diameter).

  • Often called the master gland.

  • Located on the inferior aspect of the brain, with anterior and posterior lobes.

  • Controlled by the hypothalamus.

Disorders of the Pituitary Gland

Acromegaly

  • Occurrence: About 6 in every 100,000 adults.

  • Cause: Abnormal growth hormone (GH) production after normal growth.

  • Typically caused by a benign tumor in the pituitary gland.

  • Risk factors: Prior history of a pituitary tumor.

Hyperpituitarism - Acromegaly

  • Elevated secretion of anterior pituitary hormones leading to excessive GH.

  • Causes include:

    • Pituitary or hypothalamus malfunction.

    • Primary adenoma of hormone-secreting cells.

    • Lack of feedback from target gland.

  • Two types:

    • Acromegaly: occurs in adulthood.

    • Gigantism: occurs in childhood with extreme height.

Assessment of Acromegaly

  • Symptoms include:

    • Enlarged hands and feet.

    • Visual problems, headaches.

    • Oily skin, hyperglycemia, jaw protrusion, joint pain.

    • Menstrual disturbances, impotence.

Complications of Acromegaly

  • May include:

    • Hypo-pituitarism, high blood pressure, glucose intolerance, diabetes.

    • Cardiovascular disease, carpal tunnel syndrome, sleep apnea, arthritis.

    • Other complications include uterine fibroids and vision abnormalities.

Diagnosis & Tests for Acromegaly

  • High levels of growth hormone and IGF-1.

  • Spine x-ray shows abnormal bone growth.

  • MRI or CT might reveal pituitary tumors.

Management of Acromegaly

  • Provide emotional support and encourage expression of feelings.

  • Frequent skin care and interventions for joint pain.

  • Prepare client for radiation therapy or hypophysectomy if needed.

Simmonds' Disease (Panhypopituitarism)

  • No hormones from anterior pituitary lobes due to various causes (tumors, surgery, etc.).

  • Leads to atrophy of several organs including heart, kidneys, and adrenal glands.

  • Symptoms include impotence, extreme weight loss, hypometabolism, amenorrhea.

  • Treatment involves hormone replacement therapy (HRT).

Diabetes Insipidus (DI)

  • Overview: Water metabolism issue due to ADH deficiency.

  • Classification includes primary neurogenic, secondary neurogenic, nephrogenic, and drug-related.

  • Symptoms of DI:

    • Polyuria (excessive urination), polydipsia (excessive thirst).

    • Dehydration, dry skin, headache.

Addison's Disease

  • Condition involves hypo-secretion of adrenal cortex hormones, commonly due to autoimmune destruction.

  • Symptoms include weakness, GI disturbances, bronze pigmentation, electrolyte imbalances (hyperkalemia).

  • Treatment involves monitoring vital signs, maintaining fluid/electrolyte balance, and educating on lifelong corticosteroid use.

Cushing's Syndrome

  • Caused by increased ACTH from tumors.

  • Symptoms: central obesity, hypertension, moon face, and muscle weakness.

  • Treatment may involve adrenalectomy and the need for lifelong steroid supplementation post-surgery.

Hypothyroidism & Myxedema

  • Myxedema: severe hypothyroid state often caused by Hashimoto's thyroiditis.

  • Symptoms: lethargy, cold intolerance, weight gain, dry skin.

  • Diagnosis includes T4 test, high TSH in primary cases, and thyroid function tests.

Graves' Disease (Hyperthyroidism)

  • Caused by hyper-secretion of thyroid hormone leading to increased metabolism.

  • Symptoms include exophthalmos, increased appetite, nervousness.

  • Diagnosis includes decreased TSH and elevated T3/T4 levels.

  • Treatment may involve medication, radioactive iodine, or surgery.

Parathyroid Disorders

Hypoparathyroidism

  • Caused by decreased parathyroid hormone, typically after thyroid surgery.

  • Symptoms: hypocalcemia, tingling, cramps, tetany.

Hyperparathyroidism

  • Caused by increased parathyroid hormone.

  • Symptoms: bone deformities, fractures, elevated calcium levels.

  • Management includes monitoring electrolytes and potential surgical intervention.

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