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- author "me"
- fileName "Fn2 test 4"
- tags "Endo"
- description ""
- causes of pituitary problems
- Overrsecretion
- Undersectrion
- Receptor site failure
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What is hypopituitarism
- Deficiency of one or more anterior pituitary hormones
- Deficiencies of ACTH and TSH and the most life threatening (result in corresponding dec in secretion of vital hormones from the adrenal and thyroid gland)
- Defic. Of gonadotropins (LH,FSH) change sexual function
- Def of growth hormone
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Growht hormone deficiensy (somatropin)
- Normal at birth
- Growth patterns progressively deviate, often beginning in infancy
- Short stature
- Growth retardation: dwarfisim"
- Sexual development usually normal but delayed
- Appear younger than age and others frequently relate to them in childish ways
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G.H. Deficiency teatment
- Recombinant growth hormone
- Somatroping (genotropin, nutropin)
- Typically show immediate inc in growth and may inc 12 in or ore in ht over several years of treatment
- Ultimately, resistance develops to the PRO and growth tapers off
- SC or IM
- Given at bedtime to most closely approximate physiologic release of GH
- Should not be given to adolescents whose epiphyses have sealed
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Causes of hyperpituitarism
- Hormone oversecretion
- Hypothalmic dyffunction
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Hormone oversectretion
- Primary cause is the presence of pituitary adenoma
- Causes: gigantism and acromegaly
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Hypothalmic dysfunction
Excessive amounts of releasing hormones are produced and then overstimulate the normal pituitary gland
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gigantism
- Onset occurs before puberty
- Rapid proportional growth in the length of this bones
- May have delayed closure of fontanels
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Acromegaly
- Continues past puberty
- Early diagnosis and treatment essential to prevent irreversible changes in soft tissue
- Skeletal changes permanent
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Manifesttions of overproduction of gh
- Changes in facial features
- Arthritic changes
- Vision changes
- Inc perspiration and oil secretion
- Organomegaly
- Htn
- Dysphagia
- Deepening of voice
- Hypersescretion of PRL
- Hypogonadism
- Galactorrhea
- Hypertrophy of skin
- In skeletal thickness
- Hyperglycemia
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Changes in facial features
- Inc lip and nose size
- Inc head, hand and foot size
- Prominent supraorbital ridge
- Prognathism(lower jaw protrudes out
- Difficulty chewing
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Arthritic changes
- Degeneration of joint cartilage
- Joint pain
- Dec mobility
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therapeutic management of over production of gh
- Surgical
- External ratiation
- Radioactive implants
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Nursing considerations for overproduction of gh
- Early identification of excessive growth rates
- Emotional support
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Precocious puberty
- Manifestations of sexual development before age 9 in boys and 8 in girls
- Monthly SC luteinizing hormone-releasing hormone(Lupron)
- --regulates pituitary secretions
- --slows prepubertal growth to normal rates
- --discontinued in time to allow normal pubertal changes to occur
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Primary hypothyroidism
Thyroid cant produce amount of hormones pituitary calls for
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Secondary hypothyroidism
Thyroid isnt being stimulted by pituitary to produce hormones
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Hypothyroidism---congenital cretinism
- Apear normal at birth
- If not detected irreversible brain damage and physical signs of develop
- Neonatal screening mandatory
- Hormone replacement
- Bone age surveys so ensure optimum treatment
- Normal physical growth and intelligence if treatment started shortly after birth
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Nursing care for cretinism
- Early ID
- Be suspicious of:
- --unusally wuiet and good baby
- --prolonged jaundice
- --constipation
- --umbilical hernia
- Life long therapy
- Synthroid
- Breast feeding acceptable
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Drug therapy for cretinism
Signs of overdose
Inadequate tx
- S.o.: rapid pulse
- --dyspnea
- --irritability
- --insomnia
- --fever
- --sweating
- --wt loss
- I,t,--fatigue
- --sleepiness
- --dec appetite
- --constipation
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Juvenile hypothyroidism: manifestations
- Develops after neonatal period but before puberty
- Stunted growth (earliest sign)**
- Dry skin
- Puffiness around eyes
- Sparse hai
- Constipation
- Sleepiness
- Mental decline
- Tx:lthyroxine
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Lymphocytic thyroiditis
Chronic: hashimotos disease
- Autoimmune diorder
- Strong genetic predisposition
- Thyroid becomes invaded with antithyroid antibodies and lymphocytes, causing thyroid tissue destrcution (replaced with fibrous tissue)
- More freq after 6 years reaching peak in adolescence
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Manifestations of lymphocytic throiditis
- Painless goiter
- Tracheal compression*****
- --sense of fullenss
- --hoarseness
- --dysphagia
- Most children euthyroid, but may be hypo- or hyper-thyroid
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Thyroiditis management
- In many cases, goiter regresses spontaneously within a yr or two
- Thyroid hormone**
- --supresses TSHsecretion
- --surgery (subtotal thyroidectomy) if goiter does not respond to thyroid horone if it compresses other structures
- Reassure that condition is probably temporary
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Goiter
- May be mild and noticeable when inc demand TH(rapid growth)
- Can cause resp distress
- --if born with it, immediate precautions instituted for emergency vent
- --position neck hyperextended to breath
- Immediate surgery to remover part of glane may be life saving
- THreplacement tx the hypothyroidism and reverse the TSH effect on the gland
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