An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.

BACKGROUND:Structural chromosome abnormalities can cause significant negative reproductive outcomes as they typically result in morbidity and mortality of newborns. The prevalence of structural chromosomal abnormalities in live births is at least 0.05%, of which many of them have parental origins. I...

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Main Authors: Kittiphong Thiboonboon, Wantanee Kulpeng, Yot Teerawattananon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC6007916?pdf=render
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spelling doaj-7c6661f1faf14fb4afaf28850c47e0312020-11-25T02:35:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01136e019931810.1371/journal.pone.0199318An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.Kittiphong ThiboonboonWantanee KulpengYot TeerawattananonBACKGROUND:Structural chromosome abnormalities can cause significant negative reproductive outcomes as they typically result in morbidity and mortality of newborns. The prevalence of structural chromosomal abnormalities in live births is at least 0.05%, of which many of them have parental origins. It is uncommon to predict structural chromosome abnormalities at birth in the first child but it is possible to prevent repeated abnormalities through screening and diagnostic programmes. This study will provide an economic analysis of the prenatal detection of these abnormalities. METHODS:A cost-benefit analysis using a decision analytic model was employed to compare the status quo (doing nothing) with two interventional strategies. The first strategy (Strategy I) is preconceptional screening plus amniocentesis, and the second strategy (Strategy II) is amniocentesis alone. The monetary values in Thai baht (THB) were adjusted to international dollars (I$) using purchasing power parity (PPP) (I$1 = THB 17.60 for the year 2013). The robustness of the results was tested by applying a probabilistic sensitivity analysis. RESULTS:Both diagnostic strategies can reduce approximately 10.7-11.1 births with abnormal chromosomes per 1,000 diagnosed couples. The benefit cost ratios were 1.62 for Strategy I and 1.24 for Strategy II. Net present values per 1,000 diagnoses in couples were I$464,000 for Strategy I and I$267,000 for Strategy II. The probabilistic sensitivity analysis suggested that the cost-benefit analysis was sufficiently robust, confirming that both strategies provided higher benefits than costs. CONCLUSIONS:Since the benefits of both diagnostic strategies exceeded their costs, both strategies are economical-with Strategy I being more economically attractive. Strategy I is superior to Strategy II because it decreases the risk of normal children potentially dying from the amniocentesis process.http://europepmc.org/articles/PMC6007916?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kittiphong Thiboonboon
Wantanee Kulpeng
Yot Teerawattananon
spellingShingle Kittiphong Thiboonboon
Wantanee Kulpeng
Yot Teerawattananon
An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.
PLoS ONE
author_facet Kittiphong Thiboonboon
Wantanee Kulpeng
Yot Teerawattananon
author_sort Kittiphong Thiboonboon
title An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.
title_short An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.
title_full An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.
title_fullStr An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.
title_full_unstemmed An economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.
title_sort economic analysis of chromosome testing in couples with children who have structural chromosome abnormalities.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description BACKGROUND:Structural chromosome abnormalities can cause significant negative reproductive outcomes as they typically result in morbidity and mortality of newborns. The prevalence of structural chromosomal abnormalities in live births is at least 0.05%, of which many of them have parental origins. It is uncommon to predict structural chromosome abnormalities at birth in the first child but it is possible to prevent repeated abnormalities through screening and diagnostic programmes. This study will provide an economic analysis of the prenatal detection of these abnormalities. METHODS:A cost-benefit analysis using a decision analytic model was employed to compare the status quo (doing nothing) with two interventional strategies. The first strategy (Strategy I) is preconceptional screening plus amniocentesis, and the second strategy (Strategy II) is amniocentesis alone. The monetary values in Thai baht (THB) were adjusted to international dollars (I$) using purchasing power parity (PPP) (I$1 = THB 17.60 for the year 2013). The robustness of the results was tested by applying a probabilistic sensitivity analysis. RESULTS:Both diagnostic strategies can reduce approximately 10.7-11.1 births with abnormal chromosomes per 1,000 diagnosed couples. The benefit cost ratios were 1.62 for Strategy I and 1.24 for Strategy II. Net present values per 1,000 diagnoses in couples were I$464,000 for Strategy I and I$267,000 for Strategy II. The probabilistic sensitivity analysis suggested that the cost-benefit analysis was sufficiently robust, confirming that both strategies provided higher benefits than costs. CONCLUSIONS:Since the benefits of both diagnostic strategies exceeded their costs, both strategies are economical-with Strategy I being more economically attractive. Strategy I is superior to Strategy II because it decreases the risk of normal children potentially dying from the amniocentesis process.
url http://europepmc.org/articles/PMC6007916?pdf=render
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