Non-invasive screening: The probability of events

2011
Authors
Lončar, D.Janković, Saša
Milovanović, D.
Milošević-Đorđević, Olivera

Stojadinović, M.
Lončar, S.
Article (Published version)
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Congenital anomalies are the cause of 20.0-25.0% of cases of perinatal death, while 3.0% of children are born with malformations of varying size. We examined the predictive values and defined the credibility ratio of the combined test results. Sensitivity of the test is 94.0%, and specificity is 99.0%. The positive likelihood ratio [likelihood ratio test (LR+)] is 94.00; a negative likelihood ratio [likelihood ratio test (LR-)] is 0.06. The pretest probability that pregnant women carry a fetus with chromosomal abnormality is 1:250. Posttest odds after the combined test to discover this abnormality are 0.3760, and probability of the same case is 0.2732 if it happens that the test result is positive. The result of our study confirms the justification of combined test usage in routine clinical practice, since the posttest odds rate in the case of a positive screening increases several times over (almost 90 times); the probability of detecting a chromosomal abnormality was about 70 times.
Keywords:
predictive value / combined test / ultrasonography / biochemical markersSource:
Archives of Biological Sciences, 2011, 63, 3, 609-615Publisher:
- Srpsko biološko društvo, Beograd, i dr.
DOI: 10.2298/ABS1103609L
ISSN: 0354-4664
WoS: 000294400500012
Scopus: 2-s2.0-79961200216
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Stomatološki fakultetTY - JOUR AU - Lončar, D. AU - Janković, Saša AU - Milovanović, D. AU - Milošević-Đorđević, Olivera AU - Stojadinović, M. AU - Lončar, S. PY - 2011 UR - https://smile.stomf.bg.ac.rs/handle/123456789/1636 AB - Congenital anomalies are the cause of 20.0-25.0% of cases of perinatal death, while 3.0% of children are born with malformations of varying size. We examined the predictive values and defined the credibility ratio of the combined test results. Sensitivity of the test is 94.0%, and specificity is 99.0%. The positive likelihood ratio [likelihood ratio test (LR+)] is 94.00; a negative likelihood ratio [likelihood ratio test (LR-)] is 0.06. The pretest probability that pregnant women carry a fetus with chromosomal abnormality is 1:250. Posttest odds after the combined test to discover this abnormality are 0.3760, and probability of the same case is 0.2732 if it happens that the test result is positive. The result of our study confirms the justification of combined test usage in routine clinical practice, since the posttest odds rate in the case of a positive screening increases several times over (almost 90 times); the probability of detecting a chromosomal abnormality was about 70 times. PB - Srpsko biološko društvo, Beograd, i dr. T2 - Archives of Biological Sciences T1 - Non-invasive screening: The probability of events VL - 63 IS - 3 SP - 609 EP - 615 DO - 10.2298/ABS1103609L ER -
@article{ author = "Lončar, D. and Janković, Saša and Milovanović, D. and Milošević-Đorđević, Olivera and Stojadinović, M. and Lončar, S.", year = "2011", abstract = "Congenital anomalies are the cause of 20.0-25.0% of cases of perinatal death, while 3.0% of children are born with malformations of varying size. We examined the predictive values and defined the credibility ratio of the combined test results. Sensitivity of the test is 94.0%, and specificity is 99.0%. The positive likelihood ratio [likelihood ratio test (LR+)] is 94.00; a negative likelihood ratio [likelihood ratio test (LR-)] is 0.06. The pretest probability that pregnant women carry a fetus with chromosomal abnormality is 1:250. Posttest odds after the combined test to discover this abnormality are 0.3760, and probability of the same case is 0.2732 if it happens that the test result is positive. The result of our study confirms the justification of combined test usage in routine clinical practice, since the posttest odds rate in the case of a positive screening increases several times over (almost 90 times); the probability of detecting a chromosomal abnormality was about 70 times.", publisher = "Srpsko biološko društvo, Beograd, i dr.", journal = "Archives of Biological Sciences", title = "Non-invasive screening: The probability of events", volume = "63", number = "3", pages = "609-615", doi = "10.2298/ABS1103609L" }
Lončar, D., Janković, S., Milovanović, D., Milošević-Đorđević, O., Stojadinović, M.,& Lončar, S.. (2011). Non-invasive screening: The probability of events. in Archives of Biological Sciences Srpsko biološko društvo, Beograd, i dr.., 63(3), 609-615. https://doi.org/10.2298/ABS1103609L
Lončar D, Janković S, Milovanović D, Milošević-Đorđević O, Stojadinović M, Lončar S. Non-invasive screening: The probability of events. in Archives of Biological Sciences. 2011;63(3):609-615. doi:10.2298/ABS1103609L .
Lončar, D., Janković, Saša, Milovanović, D., Milošević-Đorđević, Olivera, Stojadinović, M., Lončar, S., "Non-invasive screening: The probability of events" in Archives of Biological Sciences, 63, no. 3 (2011):609-615, https://doi.org/10.2298/ABS1103609L . .