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Secondary non-invasive prenatal screening for fetal trisomy: an effectiveness study in a public health setting
被引:12
作者:
Guy, G. P.
[1
,2
]
Hargrave, J.
[1
,3
]
Dunn, R.
[3
]
Price, K.
[3
]
Short, J.
[3
]
Thilaganathan, B.
[1
,2
,3
]
机构:
[1] St Georges Univ Hosp NHS Fdn Trust, Fetal Med Unit, Blackshaw Rd, London SW17 0RE, England
[2] St Georges Univ London, Vasc Biol Res Ctr, Mol & Clin Sci Res Inst, London, England
[3] St Georges Univ London, St Georges Antenatal Fetal Evaluat SAFE Lab, St Georges Hosp, London, England
关键词:
Cell-free DNA;
failed sample;
fetal fraction;
first-trimester screening;
no-call rate;
non-invasive prenatal testing;
trisomy;
13;
18;
21;
twin pregnancy;
CELL-FREE DNA;
MATERNAL BLOOD;
IONA TEST;
IMPACT;
D O I:
10.1111/1471-0528.16464
中图分类号:
R71 [妇产科学];
学科分类号:
100211 ;
摘要:
Objective To evaluate the effectiveness of secondary screening using non-invasive prenatal testing (NIPT) in a routine NHS setting including test performance, turn-around times (TATs) and no-call (failure to obtain result) rates. To examine the influence of maternal and fetal characteristics on test performance. Design Retrospective cohort. Setting London teaching hospital. Sample A total of 8651 pregnancies undergoing screening for fetal trisomy using NIPT provided by an NHS cell-free DNA screening laboratory - the SAFE laboratory. Methods Screening test evaluation and TATs. Univariate and multivariate logistic regression analysis to identify significant predictors of no-call results and reported by low fetal fraction (<2%), very high fetal fraction (>40%) and processing failure. Main outcome measures Test performance, TATs and no-call rates, factors affecting no-call results. Results Average TAT was 4.0 days (95% CI 4.0-4.2 days). Test sensitivities for trisomies 21 and 13/18 were 98.9% (95% CI 95.9-99.9%) and 90.4% (95% CI 80.0-96.8%), respectively. The overall no-call rate was 32/8651 (0.37%, 95% CI 0.26-0.52%). The overall risk of a no-call result was influenced by gestational age, dichorionic twin pregnancy, history of malignancy and pregnancies affected by trisomy 13/18, but not by maternal weight or use of low-molecular-weight heparin. Conclusions High-throughput NIPT can be effectively embedded into a public health NHS setting. TATs of 4 days and no-calls of <0.5% were well within clinically desirable tolerances. Gestational age, maternal weight, assisted reproductive techniques, use of low-molecular-weight heparin and past history of malignancy did not have major impacts on test no-call rates and should not constitute reasons for withholding the option of NIPT from women. Tweetable abstract Turn-around times of 4 days, no-call (test failure) rates of 0.37% and highly accurate NIPT can be successfully embedded in the NHS.
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页码:440 / 446
页数:7
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