Complicaţiile hemostazice ale sindromului hellp
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COJOCARU, Victor, CERNEŢCHI, Olga, COŞPORMAC, Viorica, SÂRBU, Zinaida, COTELNIC, Anatolie. Complicaţiile hemostazice ale sindromului hellp. In: Analele Ştiinţifice ale USMF „N. Testemiţanu”, 2011, nr. 4(12), pp. 103-108. ISSN 1857-1719.
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Analele Ştiinţifice ale USMF „N. Testemiţanu”
Numărul 4(12) / 2011 / ISSN 1857-1719

Complicaţiile hemostazice ale sindromului hellp

Pag. 103-108

Cojocaru Victor, Cerneţchi Olga, Coşpormac Viorica, Sârbu Zinaida, Cotelnic Anatolie
 
Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu“
 
 
Disponibil în IBN: 14 decembrie 2013


Rezumat

Haemostasis complications of hellp syndrome 52 women diagnosed with HELLP syndrome were included in this study. The risk factors of HELLP syndrome appearance are uterine bleedings (insofar of atonic causes, placental abruption defect, trauma, premature separation (abruption) of the normally implanted placenta). Coagulation disorders of HELLP syndrome can trigger thrombohaemorrhagic complications, thrombosis, massive bleeding or bloody suffosion at different organs level (brain, stomach, uterus), surgical wound and so on. Patients with HELLP syndrome present major risk of development of CID syndrome.

În studiul au fost incluse 52 femei cu sindromul HELLP stabilit. Factorii de risc în apariţia sindromului HELLP sunt hemoragiile uterine (atât din cauze atonice, defectul de decolare placentară, traumatism, decolarea (abrupţia) prematură a placentei normal înserate). Dereglările de coagulare din cadrul sindromului HELLP pot conduce la declanşarea complicaţiilor trombohemoragice, tromboze, hemoragiilor masive sau sufuziunilor sangvinolente la nivelul diferitor organe (creier, stomac, uter), din plaga operatorie, etc. Pacientele cu sindromul HELLP prezentă risc major de dezvoltare a sindromului de CID.

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