ISOLATED ABERRANT RIGHT SUBCLAVIAN ARTERY: SHOULD INVASIVE INTERVENTION BE RECOMMENDED IN THE ERA OF NONINVASIVE PRENATAL TESTS?

被引:0
作者
Sivrikoz, Tugba Sarac [1 ]
Erzincan, Selen Gursoy [2 ]
Uygur, Lutfiye Selcuk [3 ]
Isguder, Cigdem Kunt [4 ]
Telek, Savci Bekir [1 ]
Has, Recep [1 ]
Kalelioglu, Ibrahim Halil [1 ]
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Obstet & Gynecol, Istanbul, Turkiye
[2] Bakirkoy Dr Sadi Konuk Training & Res Hosp, Dept Obstet & Gynecol, Istanbul, Turkiye
[3] Zeynep Kamil Women & Children Hlth Educ & Res Hos, Dept Obstet & Gynecol, Istanbul, Turkiye
[4] Prof Dr Ilhan Varank Educ & Res Hosp, Dept Obstet & Gynecol, Istanbul, Turkiye
来源
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI | 2023年 / 86卷 / 01期
关键词
Aberrant right subclavian artery; Cell-Free DNA; Down syndrome; 22q11; 2; microdeletion; prenatal diagnosis; ul-trasound; CELL-FREE DNA; MATERNAL BLOOD; DOWN-SYNDROME; 2ND-TRIMESTER; FETUSES; FETAL; METAANALYSIS; ASSOCIATION; GESTATION; MARKERS;
D O I
10.26650/IUITFD.1202881
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: An aberrant right subclavian artery (ARSA) is an aor-tic arch anomaly isolated or associated with other ultrasound markers and/or congenital anomalies. This study aimed to eval-uate the necessity of invasive prenatal tests (PIT) in cases with isolated ARSA (iARSA) in prenatal sonography.Materials and Methods: The presence of ARSA was evaluated retrospectively in 7690 fetuses who underwent a second -trimes-ter ultrasonography evaluation between March 2015 and Feb-ruary 2021. PIT was recommended for patients with non-iARSA. cfDNA test (including 22q11.2 microdeletion/duplication syn-drome (MMS) or PIT was suggested for patients with iARSA.Results: The mean week of gestation was 20.26 +/- 3.93 in 95 fetus-es diagnosed with ARSA. Of the fetuses, fourty-two (44%) had iARSA, and 53 (56%) had additional findings. No chromosomal abnormality was found in any of the isolated cases. Trisomy 21 in 14, Trisomy 18 in one, 47,XX,+i(9)(p10) in one of 53 were found in non-isolated cases. Additional abnormalities and/or soft ul-trasound markers were accompanied in all fetuses with chromo-somal abnormalities. Conclusion: When iARSA is detected in prenatal ultrasonogra-phy, cfDNA testing may be sufficient, including 22q11.2 MMS. However, PIT should be recommended in the presence of structural abnormalities, soft ultrasound markers, or increased risk in the antenatal screening test.
引用
收藏
页码:37 / 43
页数:7
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