Matias 1998.
Clinical features and settings | High‐risk referral for invasive testing | |
Participants | 486 participants UK and Portugal Dates not reported Pregnant women Singleton pregnancies Median age 35 years (17‐46 years) 10‐14 weeks' gestation |
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Study design | Prospective cohort study | |
Target condition and reference standard(s) | Down's syndrome: 38 cases Reference standard: fetal karyotyping. In cases where NT above 95th percentile or abnormal ductus venousus flow, follow‐up scan conducted at 14‐16 weeks |
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Index and comparator tests | Maternal age First trimester NT (SSD, Aloka) First trimester ductus venosus flow velocity: measured transabdominally (5‐MHz curvilinear probe, Ecocee, Toshiba) or transvaginally (SSD 2000, Aloka) |
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Follow‐up | 100% karyotyping | |
Aim of study | To assess the possible role of Doppler ultrasound assessment of ductus venous blood flow in screening for chromosomal abnormalities at 11 to 14 weeks of gestation | |
Notes | ||
Table of Methodological Quality | ||
Item | Authors' judgement | Description |
Representative spectrum? All tests | Yes | Selective testing of high‐risk women as done in practice |
Acceptable reference standard? All tests | Yes | Karyotyping |
Partial verification avoided? All tests | Yes | All women received a reference standard |
Differential verification avoided? All tests | Yes | All women had the same reference standard |
Incorporation avoided? All tests | Yes | Reference standard was independent of the index test |
Reference standard results blinded? All tests | No | Reference standard interpreted with knowledge of index test results |
Index test results blinded? All tests | Yes | Index test interpreted without knowledge of reference standard results |
Relevant clinical information? All tests | Yes | Information available as would be in standard clinical practice |
Uninterpretable results reported? All tests | Yes | Reported that measurements made successfully in all cases |
Withdrawals explained? All tests | No | No details of withdrawals given |