پديد آورندگان :
Jafarieh، Hanieh نويسنده , , Karimi-Nejad، Ariana نويسنده , , Rajaee، Ahmad نويسنده , , Mirza-Zadeh، Maryam نويسنده , , Nabavi-Nia، Nasrin نويسنده , , Azimi، Farnaz نويسنده , , Zanganeh، Maryam نويسنده , , Karimi-Nejad، Roxana نويسنده , , Ramezanzadeh، Fatemeh نويسنده , , Kariminejad، Mohammad Hassan نويسنده ,
كليدواژه :
Early amniocentesis , Chromosomal abnormality , Prenatal Diagnosis , Intra-uterine fetal death , abortion , Amniocentesis
چكيده فارسي :
Early amniocentesis is a new context in prenatal diagnosis. However, the consequences of this procedure are not known clearly. We compared cytogenetic results of 655 amniotic fluid samples obtained at 12-14 gestational weeks (early amniocentesis, EA) and 804 samples at 15-18 gestational weeks (mid-trimester amniocentesis, MA). The rate of chromosomal abnormalities for early amniocentesis was 3.2% (21 cases) and for mid-trimester amniocentesis was 5.3% (43 cases) (p=0.047). True mosaicism was seen in 2 cases of each group (0.3% vs. 0.2%, respectively; p=1.000). We did not have maternal cell contamination in either group. The ratio of repeat amniocentesis was 0.6 percent in the EA group compared with 0.2 percent in MA group (p=0.417). Procedure-related early abortion (within the first 30 days after amniocentesis) was seen in 4 cases of EA (2.2%) and 3 cases of MA (1.5%) (p=0.719). Hemorrhage was occurs in the same ratio. Intra-uterine fetal death (IUFD) was seen in 7 cases of MA, but not in any cases of EA (p=0.015). Our findings showed comparable outcome of two method of amniocentesis, except lower chromosomal abortion rate and IUFD.