Endocrine - Pituitary Flashcards

(53 cards)

1
Q

Endocrine Glands

A

Secrete hormones DIRECTLY into surrounding extracellular fluid

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2
Q

Exocrine Glands

A

Products are discharged via ducts

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3
Q

What mediates the endocrine system?

A

HORMONES

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4
Q

What are hormones?

A

Chemical messengers that transport information from initial cells to target cells

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5
Q

Hormone Secretion Regulation

A
  • Neural control
  • Biorhythms
  • Feedback mechanisms
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6
Q

Hormone Neural Control

A

Suppress or stimulate hormone secretion
Stimuli include pain, smell, touch, stress, sight, taste
Catecholamines, ADH, & cortisol are hormones under neural control

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7
Q

Hormone Biorhythms

A

Genetically encoded or acquired biorhythms
Intrinsic hormonal oscillations - circadian, weekly, or seasonal
Potential to vary w/ life stages

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8
Q

Hormone Feedback Mechanisms

A

Negative or positive

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9
Q

Anterior Pituitary

A
Adenohypophysis
80% pituitary
Secretes 6 hormones 
- Growth hormone
- Adrenocorticotropic ACTH
- Thyroid-stimulating TSH
- Follicle-stimulating FSH
- Luteinizing hormone
- Prolactin
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10
Q

TSH

A

Thyrotropin-releasing hormone TRH → TSH

Target site = thyroid glands

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11
Q

ACTH

A

Corticotropin-releasing hormone CRH → ACTH
Target site = adrenal cortex zona fasiculata & reticularis
CORTISOL

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12
Q

FSH/LH

A

Gonadotropin-releasing hormone → FSH/LH
Target site = gonads (testes/ovaries)
Estrogen, progesterone, testosterone

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13
Q

Prolactin

A

Anterior pituitary hormone
Prolactin releasing & inhibitory hormone/factor
Lactotroph
Target site = breasts

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14
Q

Growth Hormone

A

Anterior pituitary hormone
Growth hormone releasing & inhibitory hormone/factor
Somatotroph
Target site = all tissues

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15
Q

Primary Pituitary Disorder

A

Defect to the peripheral endocrine gland (target organ)

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16
Q

Secondary Pituitary Disorder

A
Pituitary defect
(ex: tumor)
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17
Q

Tertiary Pituitary Disorder

A

Hypothalamus defect (not common)

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18
Q

Panhypopituitarism

A

Generalized pituitary hypofunction

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19
Q

Panhypopituitarism Causes

A
Non-functioning tumors compress & destroy normal pituitary tissue
Hypophysectomy
Postpartum shock
Irradiation
Trauma
Infiltrative disorders
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20
Q

Anterior Pituitary Hyposecretion

Treatment

A

Surgical tumor removal

Hormone replacement therapy - thyroid hormone, glucocorticoids, vasopressin

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21
Q

Anterior Pituitary Hypersecretion

A

Usually caused by benign adenomas
Prolactin → amenorrhea, infertility, ↓libido, impotence
ACTH → Cushing’s disease
Growth hormone → promotes growth all tissues capable to grow
Tumors that secrete thyrotropin or gonadotropin are rare

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22
Q

Growth Hormone Normal Secretion

A

Secretion increases during stress, hypoglycemia, exercise, & deep sleep
Stimulate insulin-like growth factor type 1 (IGF-1) production that mediates GH effects
Skeletal muscle, heart, skin, & visceral organ undergo hypertrophy & hyperplasia d/t GH & IGF-1

23
Q

Growth Hormone Hypersecretion

A

Usually caused by GH secreting pituitary adenoma

24
Q

Gigantism

A

GH hypersecretion prior to puberty or before growth plates closure
8-9’ tall

25
Acromegaly
GH hypersecretion in adults after growth plates closed (adolescence) Sustained GH hypersecretion → tissue growth
26
Acromegaly S/S
``` Skeletal & soft tissue overgrowth Large mandible & tongue → potential difficult intubation Tissue hypertrophy around vocal cords Visceromegaly Osteoarthritis Glucose intolerance Skeletal muscle weakness Extrasellar tumor excision ```
27
Acromegaly Comorbidities
HTN, cardiomyopathy, & ischemic heart disease Diabetes Osteoarthritis & skeletal muscle weakness/fatigue ↑lung volumes & sleep apnea Organ enlargement - liver, spleen, kidneys, heart
28
Acromegaly Treatment
Restore normal GH levels Preferred initial treatment - microsurgical tumor removal w/ gland preservation Small tumors transsphenoid approach Large tumors intracranial approach Irradiation and/or suppressant drug therapy as adjunct to shrink tumor for non-surgical candidates
29
Acromegaly Anesthetic Considerations
Difficult mask/airway Sleep apnea Postop respiratory obstruction or failure Systemic HTN, ischemic heart disease, arrhythmias Monitor blood glucose Stress-level glucocorticoid therapy & thyroid replacement
30
Pituitary Surgery | Preop Evaluation
Check electrolytes, hormone levels, & glucose Imaging to assess tumor extent EKG to assess LV hypertrophy or arrhythmias Consider echo w/ cardiac dysfunction patients Optimize cardiac function prior to surgery Check collateral wrist circulation prior to A-line insertion (potential ulnar flow impede d/t carpal tunnel ligament hypertrophy)
31
Transsphenoid Approach
``` Elevate HOB 15° A-line Lumbar drain VAE risk Submucosal epi injections to vasoconstrict → HTN Intraop hypotension d/t inadequate cortisol secretion Muscle relaxation & smooth extubation Neurological exam postop ```
32
Transsphenoid Approach Complications
``` Cranial nerve damage Epistaxis Hyponatremia CSF leak Diabetes insipidus ```
33
Posterior Pituitary
Neurohypophysis 20% pituitary Secretes ADH (vasopressin) & oxytocin (Pitocin)
34
ADH
Antidiuretic hormone or vasopressin Controls renal water reabsorption Regulates serum osmolarity
35
Oxytocin
Stimulates uterine contractions Breast myoepithelia cells - milk ejection during lactation Induces labor & decreases postpartum bleeding
36
Vasopressin Receptors
V1 - mediates vasopressin (refractory hypotension) V2 - mediates water reabsorption in renal collecting ducts (DDAVP target site) V3 - located in CNS & stimulates corticotrophin secretion modulation
37
Stimuli to release ADH:
``` ↑plasma Na+ ↑serum osmolality ↓blood volume Smoking (nicotine) Pain or stress Nausea Vasovagal reaction ANG II PPV ```
38
Diabetes Insipidus
Cause: surgical trauma to posterior pituitary Reversible Insufficient ADH ↑UOP ↓urine osmolarity & specific gravity ↑serum electrolytes Hypernatremia
39
DI Types
Neurogenic or central caused by inadequate ADH release | Nephrogenic - renal tubular resistance to ADH
40
Neurogenic DI Causes
Head trauma Brain tumors Neurosurgery Infiltrating pituitary lesions
41
Nephrogenic DI
Associated w/ - Hypo/hyperkalemia - Genetic mutations - Hypercalcemia - Medication induced nephrotoxicity
42
ADH Deficiency S/S
Polyuria >2mL/kg/hr Dilute unconcentrated urine Dehydration Hypernatremia Na+ >145mEq/L ↑serum plasma osmolarity >290mOsm/L ↓urine osmolarity <300mOsm/L & specific gravity <1.01 Neurological hyperreflexia, weakness, lethargy, seizures, & coma
43
Significant/Complete DI
Plasma osmolarity >290mOsm/L
44
DI Treatment
``` Monitor UOP & electrolytes DDAVP or vasopressin Restrict Na+ intact Adequate fluid replacement UO 1:1 ```
45
DDAVP
``` Desmopressin ↑factor VIII Selective V2 agonist Admin 30-90min before surgery DOA 8-12 hours Less V1 (vasopressor) activity Enhanced antidiuretic properties Nasal 5-40mcg/day SQ 0.5-2mcg/day BID ```
46
Posterior Pituitary Preop Assess
Assess plasma electrolytes, renal function, & plasma osmolarity Dehydration → sensitive to general anesthesia hypotensive effects Replace intravascular volume w/ isotonic fluids over 24-48hrs
47
ADH Deficiency Preop Treatment
Surgery stress increases ADH secretion Complete DI pre-treat w/ DDAVP 1-2mcg IV Q12H Vasopressin 5-10 units IM/SQ Q8-12H Caution w/ CAD patients → HTN d/t arterial vasoconstriction Measure UOP, plasma osmolarity, & serum Na+ Admin isotonic fluids
48
SIADH
Syndrome inappropriate antidiuretic hormone ↑ADH ↑renal H2O reabsorption despite hyponatremia & plasma hypotonicity Intracellular & extracellular fluid expansion Hemodilution & weight gain UOP hypertonic/concentrated related to plasma
49
SIADH Causes
``` Hypothyroidism Pulmonary infection Small cell lung carcinoma Head trauma Intracranial tumors Pituitary surgery Medications ```
50
SIADH S/S
``` Water intoxication ↓serum osmolarity <270mOsm/L Dilutional hyponatremia <130mOsm/L ↓UOP Hypertonic/concentrated urine Neurological cerebral edema → lethargy, headache, nausea, confusion, seizures, & coma ```
51
SIADH Treatment
Mild - fluid restriction 800-1,000mL/day NS Consider hypertonic saline (symptomatic patients or serum Na+ <115-120mEq/L) w/ or w/o loop diuretic Monitor serum Na+ Q2H
52
Sodium Replacement
SLOWLY 1-2mEq/L/hr or 6-12mEq/L/day Prevent acute loss brain H2O Central pontine demyelination syndrome → permanent neurological damage
53
SIADH Anesthetic Considerations
Isotonic solution w/ fluid restriction CVP to help monitor fluid status & guide replacement therapy Closely monitor UOP, urine osmolarity, plasma osmolarity, & serum Na+ concentration Prevent nausea → triggers ADH release