Hidroksiprogesteron kaproat enjeksiyonu, ikinci trimester tarama belirteçlerini ve yenidoğan sonuçlarını değiştirir mi?

Year 2019, Volume: 3 Issue: 1, 74 - 77, 27.01.2019

Yusuf Madendağ , İlknur Çöl Madendağ

https://doi.org/10.28982/josam.516877

Abstract

Amaç: İkinci trimesterde, alfa-fetoprotein (AFP), konjuge olmayan estriol (uE3) ve insan koryonik gonadotropin (hCG) gibi maternal serum markırlarını biyokimyasal olarak değerlendirerek; nöral tüp defekti (NTD) ve bazı fetal anöploidi taraması yapılabilmektedir. İkinci trimesterde düşük tedavisi için 17-hidroksiprogesteron kaproat (17OHPC) takviyesinin bu markerleri etkileyip etkilemediğini değerlendirmek. Ayrıca, gebelerde 17OHPC kullanımının gebelik sonuçlarına etkisini değerlendirmektir.

Yöntemler: Bu retrospektif çalışma Aralık 2014 ile Mart 2018 arasında 1275 gebe içermekteydi. Annelik yaşı, tarama sırasındaki vücut kitle indeksi (VKİ), tarama sırasındaki gebelik yaşı, maternal serum AFP, uE3 ve hCG düzeyleri, fetal cinsiyet, fetal doğum ağırlığı, Apgar skoru 5. dakika <7 ve yenidoğan yoğun bakım ünitesine (NICU) giriş değerlendirildi.

Bulgular: Anne yaşı, VKİ, gebelik yaşı, fetal cinsiyet, fetal doğum ağırlığı, Apgar skoru 5. dakika <7 ve NICU'ya kabul edilmesinde istatistiksel olarak anlamlı bir fark yoktu. Ortalama maternal serum uE3 ve AFP düzeyleri progesteron grubunda kontrol grubuna göre anlamlı derecede düşüktü (sırasıyla p=0,008, p=0,046). Bununla birlikte, ortalama maternal serum hCG düzeyleri progesteron grubunda kontrol grubundan anlamlı derecede yüksekti (p=0,033).

Sonuçlar: Fetal anöploidi ve NTD'ler için yapılan ikinci trimester tarama testleri, 17OHPC kullanan hamile kadınlarda yanlış sonuçlar verebilir. Bu yanlış sonuçlar yanlış tanı ve aşırı yönetime neden olabilir. 17OHPC kullanan gebelerde bu belirteçler için yeni eşik değerleri tanımlanmalıdır.

Keywords

17-hidroksiprogesteron-kaproat, Doğum öncesi tarama testleri, Progesteron tedavisi, Erken doğum

Does hydroxyprogesterone caproate injection alter second trimester screening markers and neonatal outcomes?

Abstract

Aim: In the second trimester, biochemically evaluating maternal serum markers such as alpha-fetoprotein (AFP), unconjugated estriol (uE3), and human chorionic gonadotropin (hCG) may be performed as prenatal screening for neural tube defects (NTDs) and fetal aneuploidy and anomalies. We evaluated whether supplementation of 17-hydroxyprogesteronecaproate (17OHPC) in the second trimester can effect these markers. In addition, we evaluated pregnancy outcomes in pregnant women using 17OHPC. 

Methods: This case control study included 1275 pregnant women between December 2014 and March 2018. The progesterone (study) group included women with a previous preterm birth and cervical length >25 mm. The control group included healthy pregnant women with a cervical length >25 mm and no previous preterm birth. Maternal age, body mass index (BMI) at the time of screening, gestational age at the time of screening, levels of maternal serum AFP, uE3, and hCG, fetal sex, fetal birth weight, Apgar score 5th minute <7, and admission to the neonatal intensive care unit (NICU) were evaluated.

Results: There was no statistically significant difference for maternal age, BMI, gestational age, fetal sex, fetal birth weight, Apgar score 5th minute <7, and admission to the NICU. The mean maternal serum uE3 and AFP levels were significantly less in the study group than in control group (P=0.008 and P=0.046, respectively). However, the mean maternal serum hCG levels were significantly higher in the study (P=0.033).

Conclusions: Second trimester screening tests for fetal aneuploidy and NTDs can give incorrect results in pregnant women using 17OHPC. These incorrect results may cause misdiagnosis and over-management. New threshold values for these markers in pregnant women using 17OHPC should be identified.

Keywords

17-hydroxyprogesterone caproate, Prenatal screening tests, Progesterone therapy, Preterm delivery

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