Ara

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Dergi Kimliği

Online ISSN
1305-3132

Yayın Dönemi
1993 - 2021

Editor-in-Chief
​Cihat Şen, ​Nicola Volpe

Editors
Daniel Rolnik, Mar Gil, Murat Yayla, Oluş Api

Künye

2000 Amniocentesis results of chromosome studies. Perinatoloji Dergisi 2002;10(3):222-222

Yazar Bilgileri

M. Bogavac 1,
N. Prapas 2,
I. Prapas 2,
A. Gkoutzioulis 2,
A. Labreli 2,
S. Prapa 3

  1. Clinic Centre Novi Sad Department of Obstetrics and Gynecology Novi Sad YU
  2. Aristotelian University of Thessaloniki Fourth Department for Obstetrics and Gynecology Thessaloniki GR
  3. Iakentron - Thessaloniki GR
Yayın Geçmişi
Çıkar Çakışması

Çıkar çakışması bulunmadığı belirtilmiştir.

Amaç

Amniocentesis is the most common invasive prenatal diagnostic technique in pregnant women at increased risk of chromosomal abnormalities and fetal anomalies. The aim of this study was to present our experience from a material of 2000 amniocenteses.

Yöntem

2000 women with indication for amniocenlesis were studied at the Aristotelian University of Thessaloniki, Greece and lakentron medical center, during a five-year period.

Bulgular


The most common indicalion for amniocentesis was advanced maternal age and positive Triple test for which we had 1806 patients (90,3%). The mean age was 34.01 years (17-48 years).The prevalence of chromosomal abnormalities was 3 %. Successful sampling of amniotic fluid in the first attempt for amniocentesis was done in 98% of the women.

Sonuç

 Amniocentesis is a safe, reliable and relatively easy method, which must be performed by specialized obstetricians.
Anahtar Kelimeler

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