The difference in the false positive rate of the quadruple test for Down syndrome screening between advanced maternal age group and the young age group at Bangplee hospital

Main Article Content

Haruthaitip Bhatharavidthaya

Abstract

Background: Thailand’s policy recommends screening all pregnant Thai women for Down syndrome using the quadruple test. While this increases the detection rate, it also raises false positives, leading to unnecessary amniocentesis   


Objectives: To compare the false positive rate of the quadruple test between advanced maternal age (≥35 years) and younger age (<35 years) pregnant women.


Methods: This retrospective chart review analyzed data from pregnant women screened for Down syndrome using the quadruple test. Results were reported as means, percentages, sensitivity, specificity, and false positive rates. A Z-test for two proportions was used to compare the groups.


Results: Among 393 women screened, 327 (83.2%) were <35 years, and 66 (16.8%) were ≥35 years. The overall false positive rate was 5.3%. The false positive rate was significantly higher in the advanced maternal age group (18.1%) compared to the younger group (2.7%) (Z = 5.08, p < 0.0001).


Conclusion: Women of advanced maternal age show a significantly higher false positive rate in Down syndrome screening using the quadruple test. Adjusting screening strategies for this group may reduce unnecessary procedures and resource wastage.

Article Details

Section
Research Article

References

Cunningham FG, Leveno KJ, Dashe JS, Hoffman BL, Spong CY, Casey BM. Williams Obstetrics. 26th ed. New York: McGraw-Hill; 2022. p. 332-5.

American College of Obstetricians and Gynecologists. Screening for fetal chromosomal abnormalities. ACOG Practice Bulletin No. 226. Obstet Gynecol. 2020;136(4):e48-69.

Chaipongpun N, Wanapirak C, Sirichotiyakul S, Tongprasert F, Srisupundit K, Luewan S, et al. Performance of serum quad test in screening for fetal Down syndrome in a large-scale unselected population in a developing country. Int J Public Health. 2023;68:1605903.

Siriwipat A. Outcome of Down syndrome screening using quadruple test at Phatthalung Hospital. Reg 11 Med J. 2022;37(2):93-102.

Wongkrajang P, Jittikoon J, Sangroonggruangsri S, Talungchit P, Ruangvutilert P, Tachjaree P, et al. Prenatal screening tests and prevalence of fetal aneuploidies in a tertiary hospital in Thailand. PLoS One. 2023;18(4):e0284829.

Wald NJ, Hackshaw AK. Antenatal screening for Down’s syndrome with the quadruple test. Lancet. 2003;361(9360):835-6.

Pranpanus S, Kor-anantakul O, Suntharasaj T, Suwanrath C, Hanprasertpong T, Pruksanusak N, et al. Ethnic-specific reference range affects the efficacy of quadruple test as a universal screening for Down syndrome in a developing country. PLoS One. 2021;16(5):e0251553.

Somsri S. Down syndrome screening outcomes in advanced maternal age pregnant women at Roi Et Hospital. Srinagarind Med J. 2021;36(5):570-7.

American College of Obstetricians and Gynecologists. Screening for fetal chromosomal abnormalities. ACOG Practice Bulletin No. 77. Obstet Gynecol. 2007;109(1):217-27.

American College of Obstetricians and Gynecologists. Prenatal diagnosis of fetal chromosomal abnormalities. ACOG Practice Bulletin No. 27. Obstet Gynecol. 2001;97(5 Pt 1):1-12.

Norwitz ER, Levy B. Noninvasive prenatal testing: the future is now. Rev Obstet Gynecol. 2013;6(2):48-62.

Gekas J, Langlois S, Ravitsky V, Audibert F, van den Berg DG, Haidar H, et al. Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma. Appl Clin Genet. 2014;7:127-31.

American College of Obstetricians and Gynecologists. Cell-free DNA screening for fetal aneuploidy. ACOG Committee Opinion No. 640. Obstet Gynecol. 2015;126(3):e31-7.

Ehrich M, Deciu C, Zwiefelhofer T, Tynan JA, Cagasan L, Tim R, et al. Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting. Am J Obstet Gynecol. 2011;204(3):205.e1-11.

Zimmermann B, Hill M, Gemelos G, Demko Z, Banjevic M, Baner J, et al. Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci. Prenat Diagn. 2012;32(13):1233-41.

Palomaki GE, Kloza EM, Lambert-Messerlian GM, Haddow JE, Neveux LM, Ehrich M, et al. DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study. Genet Med. 2011;13(11):913-20.