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Pronunciation |
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(des
moe PRES in AS e
tate) |
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U.S. Brand
Names |
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DDAVP®; Stimate®
Nasal |
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Generic
Available |
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No |
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Canadian Brand
Names |
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Octostim® |
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Synonyms |
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1-Deamino-8-D-Arginine Vasopressin |
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Pharmacological Index |
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Vasopressin Analog, Synthetic |
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Use |
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Treatment of diabetes insipidus and controlling bleeding in mild hemophilia,
von Willebrand disease, and thrombocytopenia (eg, uremia), nocturnal
enuresis |
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Pregnancy Risk
Factor |
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B |
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Contraindications |
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Hypersensitivity to desmopressin or any component; avoid using in patients
with type IIB or platelet-type von Willebrand disease, patients with <5%
factor VIII activity level |
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Warnings/Precautions |
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Avoid overhydration especially when drug is used for its hemostatic
effect |
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Adverse
Reactions |
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1% to 10%:
Cardiovascular: Facial flushing
Central nervous system: Headache, dizziness
Gastrointestinal: Nausea, abdominal cramps
Genitourinary: Vulval pain
Local: Pain at the injection site
Respiratory: Nasal congestion
<1%: Increase in blood pressure, hyponatremia, water intoxication
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Overdosage/Toxicology |
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Symptoms of overdose include drowsiness, headache, confusion, anuria, water
intoxication |
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Drug
Interactions |
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Decreased effect: Demeclocycline, lithium may decrease ADH effects
Increased effect: Chlorpropamide, fludrocortisone may increase ADH response
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Stability |
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Keep in refrigerator, avoid freezing; discard discolored solutions; nasal
solution stable for 3 weeks at room temperature; injection stable for 2 weeks at
room temperature |
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Mechanism of
Action |
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Enhances reabsorption of water in the kidneys by increasing cellular
permeability of the collecting ducts; possibly causes smooth muscle constriction
with resultant vasoconstriction; raises plasma levels of von Willebrand factor
and factor VIII |
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Pharmacodynamics/Kinetics |
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Intranasal administration:
Onset of ADH effects: Within 1 hour
Peak effect: Within 1-5 hours
Duration: 5-21 hours
I.V. infusion:
Onset of increased factor VIII activity: Within 15-30 minutes
Peak effect: 90 minutes to 3 hours
Absorption: Nasal: Slow; 10% to 20%
Metabolism: Unknown
Half-life: Elimination (terminal): 75 minutes |
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Usual Dosage |
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Children:
Diabetes insipidus: 3 months to 12 years: Intranasal (using 100 mcg/mL nasal
solution): Initial: 5 mcg/day (0.05 mL/day) divided 1-2 times/day; range: 5-30
mcg/day (0.05-0.3 mL/day) divided 1-2 times/day; adjust morning and evening
doses separately for an adequate diurnal rhythm of water turnover
Hemophilia: >3 months: I.V. 0.3 mcg/kg; may repeat dose if needed; begin
30 minutes before procedure; dilute I.V. dose in 50 mL 0.9% sodium chloride and
infuse over 15-30 minutes
Nocturnal enuresis: greater than or equal to 6 years: Intranasal (using 100
mcg/mL nasal solution): Initial: 20 mcg (0.2 mL) at bedtime; range: 10-40 mcg;
it is recommended that 1/2
of the dose be given in each nostril
Children 12 years and Adults:
Diabetes insipidus:
I.V., S.C.: 2-4 mcg/day in 2 divided doses or
1/10
of the maintenance intranasal dose; dilute I.V. dose in 50 mL 0.9% sodium
chloride and infuse over 15-30 minutes
Intranasal (using 100 mcg/mL nasal solution): 5-40 mcg/day (0.05-0.4 mL)
divided 1-3 times/day; adjust morning and evening doses separately for an
adequate diurnal rhythm of water turnover. Note: The nasal spray pump
can only deliver doses of 10 mcg (0.1 mL) or multiples of 10 mcg (0.1 mL), if
doses other than this are needed, the rhinal tube delivery system is preferred.
Hemophilia/uremic bleeding:
I.V.: 0.3 mcg/kg by slow infusion, begin 30 minutes before procedure; dilute
I.V. dose in 50 mL 0.9% sodium chloride and infuse over 15-30 minutes
Nasal spray: Using high concentration spray: <50 kg: 150 mcg (1 spray);
>50 kg: 300 mcg (1 spray each nostril); repeat use is determined by the
patient's clinical condition and laboratory work; if using preoperatively,
administer 2 hours before surgery
Oral: Begin therapy 12 hours after the last intranasal dose for patients
previously on intranasal therapy
Children: Initial: 0.05 mg; fluid restrictions are required in children to
prevent hyponatremia and water intoxication
Adults: 0.05 mg twice daily; adjust individually to optimal therapeutic dose.
Total daily dose should be increased or decreased (range: 0.1-1.2 mg divided 2-3
times/day) as needed to obtain adequate antidiuresis. |
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Monitoring
Parameters |
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Blood pressure and pulse should be monitored during I.V. infusion
Hemophilia: Factor VIII antigen levels, APTT, bleeding time (for von
Willebrand disease and thrombocytopathies) |
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Mental Health: Effects
on Mental Status |
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May cause dizziness |
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Mental Health:
Effects on Psychiatric
Treatment |
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May decrease lithium's effect on ADH, however, hydrochlorothiazide or
amiloride are better choices |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |
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Patient
Information |
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Use specific product as directed. Diabetes insipidus: Avoid overhydration.
Weigh yourself daily at the same time in the same clothes. Report increased
weight or swelling of extremities. If using intranasal product, inspect nasal
membranes regularly. Report swelling or increased nasal congestion. All uses:
Report unresolved headache, difficulty breathing, acute heartburn or nausea,
abdominal cramping, or vulval pain. Breast-feeding precautions: Consult
prescriber if breast-feeding. |
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Nursing
Implications |
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Parenteral: Dilute to a maximum concentration of 0.5 mcg/mL in normal saline
and infuse over 15-30 minutes |
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Dosage Forms |
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Injection (DDAVP®): 4 mcg/mL (1 mL)
Solution, nasal:
DDAVP®: 100 mcg/mL (2.5 mL, 5 mL)
Stimate™: 1.5 mg/mL (2.5 mL)
Tablet (DDAVP®): 0.1 mg, 0.2 mg |
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References |
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Asplund R and Aberg H,
"Desmopressin in Elderly Subjects With Increased Nocturnal Diuresis: A Two-Month Treatment Study,"
Scand J Urol Nephrol, 1993, 27(1):77-82.
Cattaneo M,
"Review of Clinical Experience of Desmopressin in Patients With Congenital and Acquire Bleeding Disorder,"
Eur J Anesthesiol Suppl, 1997, 14:10-4.
Chistolini A, Dragoni F, Ferrari A, et al,
"Intranasal DDAVP®: Biological and Clinical Evaluation in
Mild Factor VIII Deficiency," Haemostasis, 1991, 21(5):273-7.
Lindeman RD, Lee TD Jr, Yiengst MJ, et al,
"Influence of Age, Renal Disease, Hypertension, Diuretics, and Calcium on the Antidiuretic Responses to Suboptimal Infusions of Vasopressin,"
J Lab Clin Med, 1966, 68(2):206-23.
Lusher JM,
"Response to 1-Deamino-8-D-Arginine Vasopressin in von Willebrand Disease,"
Haemostasis, 1994, 24(5):276-84.
Mannucci PM and Cattaneo M,
"Desmopressin: A Nontransfusional Treatment of Hemophilia and von Willebrand Disease,"
Haemostasis, 1992, 22(5)276-80.
Richardson DW and Robinson AG, "Desmopressin," Ann Intern Med, 1985,
103(2):228-39.
Stenberg A and Läckgren G,
"Desmopressin Tablets in the Treatment of Severe Nocturnal Enuresis in Adolescents,"
Pediatrics, 1994, 94(6 Pt 1):841-46.
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