Diabetes Insipidus Flashcards

1
Q

How much decrease in AVP in DI?

A

≥ 75% in the secretion or action of AVP

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2
Q

Urine volume and Urine Osmolality in DI

A

24h urine volume >40 mL/kg BW
Uosm < 300mosmol/kg

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3
Q

Polyuria leads to what symptoms in DI

A

Urine frequency
Enuresis
Nocturia - may disturb sleep, cause mild daytime fatigue or somnolence
Slight rise in Posm stimulates THIRST and POLYDIPSIA
Clinical signs of dehydration uncommon unless fluid intake is impaired

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4
Q

Primary secretory deficiency in AVP results from what?

A

Results from a genesis or irreversible destruction of the neurohypophysis
Aka neurohypophyseal DI, neurogenic DI, pituitary DI, cranial DI or central DI

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5
Q

Post-surgical Pituitary DI

A

Results from surgery in or around the neurohypophysis
Generally appears within 24h which transitions i a few days to 2-3 week period of inappopriate anti diuretics, after which DI may or may not recur permanently

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6
Q

Gestational DI

A

Results from increased metabolism by an N-terminal aminopeptidase produced by the placenta;
S/sx manifest during pregnancy and usually remit several weeks after delivery

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7
Q

Most common primary secretory AVP deficiency genetic form

A

Autosomal dominant mutations in the coding region of on e allele of the AVP-neurophysin II (AVP-NPII) gene with DI developing over several months to years that may occasionally remit spontaneously in late middle age

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8
Q

What kind of secretory deficiency of AVP results form inhibition of secretion by excessive intake of fluids?

A

Secondary secretory deficiency
** Primary Polydipsia

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9
Q

3 categories of Primary Polydipsia

A
  1. Dipsogenic DI - inappropriate increase in thirst caused by altered set point in osmoredulation
  2. Psychogenic Polydipsia - feature of psychosis or OCD
  3. Iatrogenic Polydipsia
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10
Q

Primary deficiencies in the antidiuretic action of AVP result in what?

A

NEPHROGENIC DI

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11
Q

3 causes of NEPHROGENIC DI

A
  1. Genetic:
    A. x-linked: mutations in the coding region of the V2 receptor gene
    B. AR: mutations in the gene encoding the aquaporin protein
  2. Acquired
  3. Exposure to drugs
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12
Q

Secondary Deficiencies in the antidiuretic response o AVP results in what

A

Polyuria - causes a washout in the medullary concentration gradient, resolves in 24-48h after correction of Polyuria

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13
Q

In a patient with Polyuria but 24 hour urine osmolality is > 300 mosm.kg, what should we evaluate for?

A

Uncontrolled DM

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14
Q

If plasma AVP is >1pg/ml:______
If <1 pg/ml:______

A

> 1pg/mlL NEPHROGENIC DI
<1 pg/mlL do BRAIN MRI
IF with pituitary bright spot: PRIMARY POLYDIPSIA
IF no pituitary bright spot: PITUITARY DI

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15
Q

What to do if with <40ml/kg and Uosm of >300mosm/L/

A

Do GU EVALUATION

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16
Q

TREATMENT FOR CENTRAL DI

A

DDAVP (Desmopressin)

17
Q

What is DDAVP

A

A synthetic analogue of AVP that acts selectively at V2 receptors to increase urine concentration and decrease urine flow in a dose-dependent manner

18
Q

Treatment of NEPHROGENIC DI

A

Thiazide diuretic and/or amiloride in conjunction with a low-sodium diet.
Inhibitors of prostaglandin synthesis (eg indomethacin) are also effective in many patients

19
Q

Treatment of Primary Polydipsia

A

No effective treatment
Advise about the use of drugs that can impair urinary free-water excretion: thiazides, carbamazepine