Cost-Effectiveness of a Proteomic Test for Preterm Birth Prediction.
cost effectiveness
preterm birth
progesterone
prognostic test
Journal
ClinicoEconomics and outcomes research : CEOR
ISSN: 1178-6981
Titre abrégé: Clinicoecon Outcomes Res
Pays: New Zealand
ID NLM: 101560564
Informations de publication
Date de publication:
2021
2021
Historique:
received:
21
06
2021
accepted:
15
08
2021
entrez:
22
9
2021
pubmed:
23
9
2021
medline:
23
9
2021
Statut:
epublish
Résumé
Preterm birth (PTB) carries increased risk of short- and long-term health problems as well as higher healthcare costs. Current strategies using clinically accepted maternal risk factors (prior PTB, short cervix) can only identify a minority of singleton PTBs. We modeled the cost-effectiveness of a risk-screening-and-treat strategy versus usual care for commercially insured pregnant US women without clinically accepted PTB risk factors. The risk-screening-and-treat strategy included use of a novel PTB prognostic blood test (PreTRM We built a cost-effectiveness model using a combined decision-tree/Markov approach and a US payer perspective. We modeled 1-week cycles of pregnancy from week 19 to birth (preterm or term) and assessed costs throughout the pregnancy, and further to 12-months post-delivery in mothers and 30-months in infants. PTB rates and costs were based on >40,000 mothers and infants from the HealthCore Integrated Research Database In the base case, the risk-screening-and-treat strategy dominated usual care with an estimated 870 fewer PTBs (20% reduction) and $54 million less in total cost ($863 net savings per pregnant woman). Reductions were projected for neonatal intensive care admissions (10%), overall length-of-stay (7%), and births <32 weeks (33%). Treatment effectiveness had the strongest influence on cost-effectiveness estimates. The risk-screening-and-treat strategy remained dominant in the majority of probabilistic sensitivity analysis simulations and model scenarios. Use of a novel prognostic test during pregnancy to identify women at risk of PTB combined with evidence-based treatment is estimated to reduce total costs while preventing PTBs and their consequences.
Sections du résumé
BACKGROUND
BACKGROUND
Preterm birth (PTB) carries increased risk of short- and long-term health problems as well as higher healthcare costs. Current strategies using clinically accepted maternal risk factors (prior PTB, short cervix) can only identify a minority of singleton PTBs.
OBJECTIVE
OBJECTIVE
We modeled the cost-effectiveness of a risk-screening-and-treat strategy versus usual care for commercially insured pregnant US women without clinically accepted PTB risk factors. The risk-screening-and-treat strategy included use of a novel PTB prognostic blood test (PreTRM
METHODS
METHODS
We built a cost-effectiveness model using a combined decision-tree/Markov approach and a US payer perspective. We modeled 1-week cycles of pregnancy from week 19 to birth (preterm or term) and assessed costs throughout the pregnancy, and further to 12-months post-delivery in mothers and 30-months in infants. PTB rates and costs were based on >40,000 mothers and infants from the HealthCore Integrated Research Database
RESULTS
RESULTS
In the base case, the risk-screening-and-treat strategy dominated usual care with an estimated 870 fewer PTBs (20% reduction) and $54 million less in total cost ($863 net savings per pregnant woman). Reductions were projected for neonatal intensive care admissions (10%), overall length-of-stay (7%), and births <32 weeks (33%). Treatment effectiveness had the strongest influence on cost-effectiveness estimates. The risk-screening-and-treat strategy remained dominant in the majority of probabilistic sensitivity analysis simulations and model scenarios.
CONCLUSION
CONCLUSIONS
Use of a novel prognostic test during pregnancy to identify women at risk of PTB combined with evidence-based treatment is estimated to reduce total costs while preventing PTBs and their consequences.
Identifiants
pubmed: 34548799
doi: 10.2147/CEOR.S325094
pii: 325094
pmc: PMC8449551
doi:
Types de publication
Journal Article
Langues
eng
Pagination
809-820Informations de copyright
© 2021 Grabner et al.
Déclaration de conflit d'intérêts
Michael Grabner, Chi Nguyen, Haechung Chung, Nilesh Gangan, and Eric Stanek are employees of HealthCore, Inc., an independent research organization that received funding from Sera Prognostics Inc. for the conduct of the study. Michael Grabner and Eric Stanek are stockholders of Anthem, Inc., which has a financial interest in Sera Prognostics. Julja Burchard and Jay Boniface are employees and stockholders of Sera Prognostics Inc. John Zupancic is a consultant to Sera Prognostics Inc. The authors report no other conflicts of interest in this work.
Références
J Am Heart Assoc. 2018 Jan 15;7(2):
pubmed: 29335319
Semin Perinatol. 2021 Apr;45(3):151390
pubmed: 33541716
J Pediatr. 2017 Feb;181:309-318.e1
pubmed: 27806833
Science. 2014 Aug 15;345(6198):760-5
pubmed: 25124429
J Clin Endocrinol Metab. 2012 Aug;97(8):E1429-39
pubmed: 22689691
Am J Obstet Gynecol. 2018 Feb;218(2):161-180
pubmed: 29157866
Natl Vital Stat Rep. 2019 Nov;68(13):1-47
pubmed: 32501202
Am J Obstet Gynecol. 2012 Nov;207(5):390.e1-8
pubmed: 23010094
Am J Obstet Gynecol. 2014 Feb;210(2):131.e1-8
pubmed: 24036403
J Matern Fetal Neonatal Med. 2007 Feb;20(2):89-112
pubmed: 17437208
Obstet Gynecol. 2007 Oct;110(4):865-72
pubmed: 17906021
Am J Obstet Gynecol. 2011 Apr;204(4):320.e1-6
pubmed: 21345407
Arch Dis Child. 2019 May;104(5):456-465
pubmed: 30413489
J Perinatol. 2020 Jul;40(7):1091-1099
pubmed: 32103158
Ultrasound Obstet Gynecol. 2011 Jul;38(1):18-31
pubmed: 21472815
PLoS One. 2015 Apr 16;10(4):e0122341
pubmed: 25881289
Reprod Biol Endocrinol. 2014 Dec 04;12:123
pubmed: 25475528
Dis Manag. 2006 Aug;9(4):236-41
pubmed: 16893336
J Steroid Biochem Mol Biol. 1993 Oct;46(4):497-505
pubmed: 8217880
Am J Obstet Gynecol. 2008 Oct;199(4):393.e1-8
pubmed: 18928985
Lancet. 2016 May 21;387(10033):2106-2116
pubmed: 26921136
J Matern Fetal Neonatal Med. 2006 Dec;19(12):773-82
pubmed: 17190687
JAMA. 2017 Mar 14;317(10):1047-1056
pubmed: 28291893
N Engl J Med. 2003 Jun 12;348(24):2379-85
pubmed: 12802023
Matern Child Health J. 2016 Apr;20(4):808-18
pubmed: 26740227
Health Technol Assess. 2019 Mar;23(13):1-226
pubmed: 30917097
Am J Perinatol. 2021 Aug 16;:
pubmed: 34399434
J Endocrinol. 2010 Oct;207(1):1-16
pubmed: 20817666
Am J Obstet Gynecol. 2012 May;206(5):376-86
pubmed: 22542113
J Pediatr. 2019 Jan;204:118-125.e14
pubmed: 30297293
Am J Obstet Gynecol. 2016 May;214(5):633.e1-633.e24
pubmed: 26874297
Annu Rev Biochem. 2012;81:379-405
pubmed: 22439968
AJP Rep. 2016 Oct;6(4):e407-e416
pubmed: 27917307
J Am Coll Cardiol. 2020 Jul 7;76(1):57-67
pubmed: 32616164
Matern Child Health J. 2015 Jan;19(1):121-7
pubmed: 24770956
Biol Reprod. 2011 Sep;85(3):431-41
pubmed: 21613632
Am J Obstet Gynecol. 2014 Nov;211(5):530.e1-4
pubmed: 24844852
Value Health. 2012 Sep-Oct;15(6):812-20
pubmed: 22999130
Trends Endocrinol Metab. 2015 Jul;26(7):376-83
pubmed: 26044465
Semin Fetal Neonatal Med. 2018 Apr;23(2):126-132
pubmed: 29229486
Teratology. 1983 Oct;28(2):201-8
pubmed: 6648824
Am J Obstet Gynecol. 2016 Jul;215(1):103.e1-103.e14
pubmed: 26772790
Pharmacoeconomics. 2014 May;32(5):467-78
pubmed: 24715602
JAMA Netw Open. 2021 Jan 4;4(1):e2033361
pubmed: 33416881
Obstet Gynecol. 2019 Dec;134(6):1333-1338
pubmed: 31764747
N Engl J Med. 2014 Jan 16;370(3):254-61
pubmed: 24428470
Am J Obstet Gynecol MFM. 2020 Aug;2(3):100140
pubmed: 33345877
Am J Perinatol. 2020 Jan;37(2):127-136
pubmed: 31652479