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Desmopressin, sold under the trade name DDAVP among others, is a medication used to treat diabetes insipidus, bedwetting, hemophilia A, von Willebrand disease, and high blood urea levels.
Common side effects include headaches, diarrhea, and low blood sodium.
Desmopressin was approved for medical use in the United States in 1978.
1 Medical uses
1.1 Bed wetting
1.2 Nighttime urination
1.3 Clotting disorders
1.4 Diabetes insipidus
2 Side effects
3 Mechanism of action
6 Further reading
Desmopressin is used to treat nocturnal enuresis (bedwetting). It is usually prescribed in the form of desmopressin acetate, by mouth. Children taking DDAVP have 2.2 fewer wet nights per week and are 4.5 times more likely to sleep without disruption compared with placebo.
Desmopressin has some benefit in adults who have problems with night time urination (known as nocturia).
Desmopressin (DDAVP) stimulates the release of von Willebrand factor (vWF) from the Weibel–Palade bodies of endothelial cells, thereby increasing the levels of vWF (as well as coagulant factor VIII) 3 to 5-fold.
Desmopressin can be used to promote the release of von Willebrand factor (with subsequent increase in factor VIII survival secondary to vWF complexing) in patients with coagulation disorders such as von Willebrand disease, mild hemophilia A (factor VIII deficiency), and thrombocytopenia. It can be used with uremic induced platelet dysfunction. It is not effective in the treatment of hemophilia B (factor IX deficiency) or severe hemophilia A.
The usefulness of desmopressin in hemophilia A depends predominantly on whether the deficiency involved is qualitative (i.e., there is a functional mutation of the protein itself) or quantitative (i.e., there is decreased production of a functionally normal protein). Desmopressin is most effective in patients with quantitative deficiencies, because by increasing the release of vWF, the circulating pool of functional factor VIII effectively increases, as well. In patients who have functional defects in factor VIII, the use of desmopressin is moot, because it will only increase the circulating levels of a nonfunctional protein.
Desmopressin is used in the treatment of central diabetes insipidus (DI) as a replacement for endogenous antidiuretic hormone (ADH) that is in insufficient quantity due to decreased or non-existent secretion or production of ADH by the posterior pituitary or hypothalamus, respectively. It is also used in the diagnostic workup for diabetes insipidus, in order to distinguish central from DI due to the kidneys. Desmopressin is not effective at treating nephrogenic DI, thus a positive response is generally indicative of central DI.
US drug regulators added warning to the nasal sprays after two people died and fifty-nine other people had seizures. This occurred due to hyponatremia, a deficit of the body’s sodium levels, and the nasal spray is no longer approved for use in children in the United States. However, US drug regulators have said that desmopressin tablets can still be considered safe for treatment of nocturnal enuresis in children as long as the person is otherwise healthy.
Patients must stop taking desmopressin if they develop severe vomiting and diarrhea, fever, the flu, or severe cold. Patients should also be very cautious about taking desmopressin during hot weather conditions or following strenuous exercise, as these conditions can place stress on the body’s electrolyte and water balance.
A body needs to maintain a balance of water and ( sodium ). If sodium levels become too low ( hyponatremia ) – either as a result of increased water take-up or reduced salt levels – a person may have seizures and, in extreme cases, may die.
Mechanism of action
Desmopressin works by limiting the amount of water that is eliminated in the urine; that is, it is an antidiuretic. It works at the level of the renal collecting duct by binding to V2 receptors, which signal for the translocation of aquaporin channels via cytosolic vesicles to the apical membrane of the collecting duct. The presence of these aquaporin channels in the distal nephron causes increasing water reabsorption from the urine, which becomes passively re-distributed from the nephron to systemic circulation by way of basolateral membrane channels. Desmopressin also stimulates release of von Willebrand factor from endothelial cells by acting on the V2 receptor.
Desmopressin is degraded more slowly than recombinant vasopressin, and requires less frequent administration. In addition, it has little effect on blood pressure, while vasopressin may cause arterial hypertension. Vasopressin stimulates the release of ACTH, which indirectly increases responsiveness of alpha-1 receptor in blood vessel smooth muscle, increasing vessel tone and blood pressure.
Desmopressin ( 1-deamino-8- D -arginine vasopressin ) is a man-made form of the normal human hormone arginine vasopressin (the antidiuretic hormone, or ADH), a peptide containing nine amino acids.
Compared to vasopressin, desmopressin’s first amino acid has been deaminated, and the arginine at the eighth position is in the dextro rather than the levo form (see stereochemistry ).
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