A cost-effectiveness analysis comparing different strategies to implement noninvasive prenatal testing into a Down syndrome screening program

被引:43
作者
Ayres, Alice C. [1 ]
Whitty, Jennifer A. [2 ,3 ]
Ellwood, David A. [1 ]
机构
[1] Griffith Univ, Sch Med, Gold Coast, Qld 4222, Australia
[2] Griffith Univ, Sch Med, Ctr Appl Hlth Econ, Populat & Social Hlth Res Program,Griffith Hlth I, Logan, UT USA
[3] Univ Queensland, Sch Pharm, Brisbane, Qld, Australia
关键词
benefits; consequences; cost; implementation; noninvasive prenatal testing; CLINICAL UTILITY; DNA; TRISOMY-21; TRISOMIES;
D O I
10.1111/ajo.12223
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BackgroundCurrently, noninvasive prenatal testing (NIPT) is only recommended in high-risk women following conventional Down syndrome (DS) screening, and it has not yet been included in the Australian DS screening program. AimsTo evaluate the cost-effectiveness of different strategies of NIPT for DS screening in comparison with current practice. MethodsA decision-analytic approach modelled a theoretical cohort of 300,000 singleton pregnancies. The strategies compared were the following: current practice, NIPT as a second-tier investigation, NIPT only in women >35years, NIPT only in women >40years and NIPT for all women. The direct costs (low and high estimates) were derived using both health system costs and patient out-of-pocket expenses. The number of DS cases detected and procedure-related losses (PRL) were compared between strategies. The incremental cost per case detected was the primary measure of cost-effectiveness. ResultsUniversal NIPT costs an additional $134,636,832 compared with current practice, but detects 123 more DS cases (at an incremental cost of $1,094,608 per case) and avoids 90 PRL. NIPT for women >40years was the most cost-effective strategy, costing an incremental $81,199 per additional DS case detected and avoiding 95 PRL. ConclusionsThe cost of NIPT needs to decrease significantly if it is to replace current practice on a purely cost-effectiveness basis. However, it may be beneficial to use NIPT as first-line screening in selected high-risk patients. Further evaluation is needed to consider the longer-term costs and benefits of screening.
引用
收藏
页码:412 / 417
页数:6
相关论文
共 28 条
[1]   Noninvasive Prenatal Testing for Fetal Aneuploidy [J].
不详 .
OBSTETRICS AND GYNECOLOGY, 2012, 120 (06) :1532-1534
[2]  
[Anonymous], 2013, MED BEN SCHED BOOK
[3]  
[Anonymous], 2013, SONIC GENETICS VIA S
[4]  
[Anonymous], 2007, PREN SCREEN TSTS
[5]  
[Anonymous], 2013, WOMENS ULTR MELB OR
[6]  
[Anonymous], 2014, DNA BAS NONIN PREN T
[7]   Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: relation to maternal and fetal characteristics [J].
Ashoor, G. ;
Syngelaki, A. ;
Poon, L. C. Y. ;
Rezende, J. C. ;
Nicolaides, K. H. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2013, 41 (01) :26-32
[8]   Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18 [J].
Ashoor, Ghalia ;
Syngelaki, Argyro ;
Wagner, Marion ;
Birdir, Cahit ;
Nicolaides, Kypros H. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2012, 206 (04) :322.e1-322.e5
[9]   Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis [J].
Benn, Peter ;
Borell, Antoni ;
Chiu, Rossa ;
Cuckle, Howard ;
Dugoff, Lorraine ;
Faas, Brigitte ;
Gross, Susan ;
Johnson, Joann ;
Maymon, Ron ;
Norton, Mary ;
Odibo, Anthony ;
Schielen, Peter ;
Spencer, Kevin ;
Huang, Tianhua ;
Wright, Dave ;
Yaron, Yuval .
PRENATAL DIAGNOSIS, 2013, 33 (07) :622-629
[10]   Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing [J].
Bianchi, Diana W. ;
Platt, Lawrence D. ;
Goldberg, James D. ;
Abuhamad, Alfred Z. ;
Sehnert, Amy J. ;
Rava, Richard P. .
OBSTETRICS AND GYNECOLOGY, 2012, 119 (05) :890-901