Evaluation of fetal ventriculomegaly

Autor: Özgür Aydın, Nazan Tarhan, Sevcan Arzu Arınkan, Öykü Tosun, Yusuf Çakmak, Abdulkadir Turgut, Vedat Dayıcıoğlu
Rok vydání: 2013
Předmět:
Zdroj: Journal of Clinical and Experimental Investigations, Vol 4, Iss 2, Pp 141-147 (2013)
ISSN: 1309-6621
Popis: Objective: To evaluate the prenatal and postnatal follow up, treatment and the outcome of the patients with ventriculomegaly. Methods: Patients with lateral cerebral ventricle size 10mm and higher were included. 69 patients were considered but 8 patients refused to join our study. The patients were divided into two groups as they had additional anomalies (combined ventriculomegaly) or not (isolated ventriculomegaly). Each group was divided into three subgroups according to their lateral cerebral ventricle size as mild (10-12 mm), moderate (12.1-4.9 mm), severe (15 mm and more) ventriculomegaly. Results: 10 fetuses with isolated ventriculomegaly and combined ventriculomegaly died after birth. Neurosurgical operations were performed for ten patients. We performed chromosomal analysis for 16.7% of our patients. Caesarian delivery was higher (91.7%) in combined ventriculomegaly groups and all newborns went to NNICU. In isolated ventriculomegaly group 18 patients showed normal neurological development at sixth month. None of the patients with combined ventriculomegaly group showed normal neurological development at sixth month. In severe ventriculomegaly group termination ratio was higher (64.7%) than isolated ventriculomegaly group (11%). The survival rate was 90% in mild ventriculomegaly group and 42.9% in severe ventriculomegaly group.Conclusion: Termination is more often in isolated severe ventriculomegaly than mild and moderate ventriculomegaly group because the prognosis is worse. Because the prognosis of the patients with mild ventriculomegaly is good decision for termination will be well evaluated with the family. J Clin Exp Invest 2013; 4 (2): 141-147Key words: Prenatal diagnosis, growth & development,prognosis
Databáze: OpenAIRE