Skoči na glavni sadržaj

Pregledni rad

Treatment of Ovarian Hyperstimulation Syndrome: New Insights

Miro Kasum orcid id orcid.org/0000-0003-4896-1284
Slavko Orešković


Puni tekst: engleski pdf 124 Kb

str. 421-427

preuzimanja: 763

citiraj


Sažetak

Ovarian hyperstimulation syndrome is the most serious iatrogenic complication resulting from ovarian stimulation. Currently there is no clear evidence of absolute efficacy for most of standard preventive and curative methods. Recent studies indicate that human chorionic gonadotropin increases vascular endothelial growth factor, vascular endothelial cadherin and vascular permeability via endothelial adherence junctions. Vascular endothelial growth factor plays a pivotal role in the pathophysiology of the condition and therefore vascular endothelial factor antagonism has been suggested for the prevention of the syndrome. Since vascular endothelial growth factor is also a physiological regulator of folliculogenesis, progesterone secretion and endometrial angiogenesis, its complete inactivation by specific blockers could produce undesirable effects interfering with early pregnancy development and therefore they cannot be used clinically. Recently, low doses of dopamine agonists (cabergoline) have been shown to counteract vascular endothelial growth factor induced vascular hyperpermeability, reducing the incidence of the syndrome by prophylactic treatment without compromising pregnancy outcome. The absence of undesirable side effects could make cabergoline an effective and safe etiologic approach for the prevention and treatment of the syndrome. A novel approach has suggested that metformin may also be helpful in the syndrome prevention in women with or without polycystic ovary disease.

Ključne riječi

Ovarian hyperstimulation syndrome – therapy; Ovulation induction – adverse effects; Ovulation induction – risk factors; Dopamine agonists

Hrčak ID:

84791

URI

https://hrcak.srce.hr/84791

Datum izdavanja:

20.12.2010.

Podaci na drugim jezicima: hrvatski

Posjeta: 1.635 *