Analytical Piece
Received: 25 January 2022 - Revised: 20 April 2022 - Accepted: 20 April 2022
DOI: 10.1002/pd.6155
R E S E A RCH NOT E
Insurance and geographic variations in non‐invasive prenatal testing
Jacqueline Ellison1 | Catharine Wang2 | Christina Yarrington3 | Philip Connors3 |
Amresh Hanchate4
1Department of Health Services, Policy, and Practice, Brown University School of Public Health, Providence, Rhode Island, USA
2Department of Community Health Sciences, Boston University School of Public Health, Boston, Massachusetts, USA
3Department of Obstetrics and Gynecology, Boston Medical Center, Boston, Massachusetts, USA
4Department of Social Sciences and Health Policy, Wake Forest School of Medicine, Boston, Massachusetts, USA
Correspondence
Jacqueline Ellison, Department of Health
Services, Policy, and Practice, Brown
University School of Public Health, 121 South
Main St, Providence, RI 02912, USA.
Email: [email protected]
Funding information
National Human Genome Research Institute,
Grant/Award Number: R21 HG009567;
Healthcare Research and Quality National
Research Service Award, Grant/Award
Number: 5T32 HS000011
Key points
What is already known about this topic?
� Single‐site studies suggest racial, ethnic, and insurance disparities in use of Non‐invasive
prenatal testing (NIPT).
� Population‐level research from outside the U.S. highlights significant geographic variations
in NIPT uptake.
What does this study add?
� Enrollees living in zip‐codes with a higher proportion of Black and Hispanic/Latino residents
were significantly less likely to receive NIPT.
� Enrollees living in zip‐codes with a higher proportion of people living below the federal
poverty level (FPL) were significantly less likely to receive NIPT.
� Birthing people with Medicaid were five times less likely to receive NIPT than those with
commercial coverage.
Non‐invasive prenatal testing (NIPT) during pregnancy is a highly
sensitive and specific screening tool for chromosomal aneuploidy.
This screening has the highest detection rate for Down syndrome,
and unlike invasive methods, carries no risk for miscarriage or other
pregnancy complications.1,2 In 2012, the American College of
Obstetrician‐Gynecologists (ACOG) recommended that pregnant
people at increased risk for aneuploidy, including those aged 35 and
older, be offered NIPT.3 Because this relatively new technology has
advantages over both traditional serum marker screening and inva-
sive diagnostics with improved detection rate and lower obstetric
risk respectively, quantifying disparities in uptake is particularly
important.
As with other prenatal services in the U.S., inequities in invasive
prenatal testing are well‐established.4,5 Single‐site studies have also
demonstrated disparities in NIPT based on insurance type, race, and
ethnicity, however findings on the role of insurance are
inconclusive.6,7 While important, single‐site studies may not be
generalizable. Given pervasive inequities in access to prenatal care in
the U.S., understanding geographic and insurance coverage dispar-
ities in NIPT use at the population‐level is critical.
Massachusetts (MA) has one of the highest insurance coverage
rates in the country and, by 2015, NIPT was reimbursed by both
public and commercial payers for pregnant residents aged 35 and
older. The state is therefore a ‘best case scenario’ context from
which to understand variations in NIPT uptake. Our objective was to
estimate the population‐level rate of NIPT uptake in Massachusetts
and identify disparities based on insurance type and patient zip‐ code.
We used the 2015 Massachusetts All‐Payer Claims Database,
which represents nearly all healthcare utilization records of Massa-
chusetts residents under the age of 65.8 These data capture service
use, patient age, insurance type, and 5‐digit zip‐code at the time of
1004 - Prenatal Diagnosis. 2022;42:1004–1007. wileyonlinelibrary.com/journal/pd © 2022 John Wiley & Sons Ltd.
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billing. We used 2015 data as this was the first year a specific NIPT
billing code (CPT 81420) was adopted. Using ICD‐9 codes for de-
livery, we identified pregnant patients aged 35 years or older at their
delivery between 7/1/2015 to 12/31/2015 who were eligible for
NIPT use per ACOG guidelines.
Our outcome, NIPT uptake, was defined as the number of
patients who received NIPT per 1000 eligible (i.e., pregnant people
aged 35 and older). We estimated NIPT rates by insurance type,
admission to a teaching hospital, and at the zip‐code level, the
proportion of residents living below 100% of the federal poverty
level (FPL), and the proportion of Black or Hispanic residents.
Focusing on delivery hospital allowed us to capture potential dif-
ferences in practice patterns between affiliates of teaching and
non‐teaching hospitals. Because of documented racial/ethnic and
income disparities in invasive diagnostic testing, and in the absence
of individual sociodemographic information, we used census data
to characterize patient zip‐codes by the proportion of Black/His-
panic and low‐income residents (high vs. low). Our goal was to
assess the role of area‐level sociodemographic characteristics
and NIPT uptake. To distinguish between the high and low cate-
gories, we ranked all zip‐codes in Massachusetts by the overall
proportion of Black/Hispanic and low‐income residents, and
defined zip‐codes in the top 25% of each category as a "high" zip‐ code. We initially examined the proportion of Black and Hispanic
residents separately, however because there was substantial
overlap between the two, we chose to combine these groups.
Finally, we estimated adjusted odds of NIPT using logistic regres-
sion, accounting for insurance type, delivery at a teaching hospital,
and zip‐code sociodemographic composition, and including hospital
random effects and clustered standard errors at the hospital‐level.
Individuals with missing data were dropped from the analysis
(n = 403).
There were 4506 non‐invasive prenatal tests performed on
22,393 pregnant patients aged 35+ (201.2 per 1000) in 2015 (Ta-
ble 1). We observed considerable geographic variation. Patients living
in zip‐codes within and surrounding the Boston metropolitan area
were more likely to receive NIPT, as were those living in Eastern MA
(Figure 1). The observed NIPT rate (per 1000 pregnant individuals
aged 35+) was 48.7 for Medicaid enrollees and 272.1 for commercial
enrollees; 123.0 and 223.2 for patients living in a zip‐code with a high
versus low proportion of Black/Hispanic residents; and 107.7 and
218.4 for those in a zip‐code with a high versus low proportion of
low‐income residents. In adjusted models, pregnant people living in a
zip‐code with a high Black/Hispanic population were significantly less
likely to receive NIPT (aOR:0.80; 95% CI: 0.59–0.95) then people
living outside these zip‐codes, as were those living in low‐income zip‐ codes (aOR:0.80; 95% CI: 0.70–0.93). Medicaid enrollees were less
likely than commercial enrollees to receive NIPT (aOR:0.18; 95% CI:
0.16–0.20).
In this population‐level analysis of NIPT uptake in Massachu-
setts, we found that birthing people covered by Medicaid were over
five times less likely to receive NIPT than their counterparts with
commercial coverage. Lower NIPT rates in zip‐codes with a high
proportion of low‐income or Black/Hispanic residents also suggests
that geographic variations in uptake may reflect racial/ethnic and
income disparities independent of insurance coverage. We found
no significant association between NIPT uptake and delivery at a
teaching hospital.
Our findings on geographic variation are consistent with research
from Australia and the Netherlands which found that people living in
socioeconomically disadvantaged neighborhoods were less likely to
receive NIPT.9,10 The finding that people with Medicaid coverage
were less likely to receive NIPT is inconsistent with a single‐site study
in Wisconsin which found that pregnant people with Medicaid were
more likely to receive NIPT than those with commercial coverage.6
This discrepancy is likely due to the fact that commercial payers in
Wisconsin were not required to reimburse for NIPT. As with the
present study, a single‐site study in Massachusetts also found lower
NIPT uptake among Medicaid enrollees.7 A study performed in Col-
orado which evaluated all prenatal genetic testing found no differ-
ence in uptake between Medicaid and commercial enrollees.11
Inconsistent findings on variation by insurance status highlight the
fundamental role of payer coverage on financial barriers to NIPT, and
how these may drive regional variations in use. In addition to within‐ state variation identified in the present study, there is likely
substantial between‐state variation due to differences in state pol-
icies governing commercial payers and Medicaid programs.
Research is needed to understand reasons for lower NIPT uptake
by Medicaid enrollees in the state, despite coverage of this screening
by the Massachusetts Medicaid program. It is possible that the fa-
cilities where patients with Medicaid receive prenatal care are less
likely to offer NIPT. For example, federally qualified health centers
which serve low‐income populations may not have a lab on site or a
relationship with an NIPT company, both of which are necessary to
offer testing. It is also possible that pregnant Medicaid patients do
not know about, prefer not to undergo, or are not offered NIPT.
Interpersonal racism via clinician discrimination and bias perpetuates
inequities in perinatal service delivery and outcomes.12,13 Structural
racism includes policies governing the distribution of healthcare re-
sources and is another fundamental cause of perinatal health in-
equities.14 Medicaid typically reimburses services at lower rates than
commercial payers, and clinical implementation of NIPT was pre-
dominantly led by industry.15 Consequently, profit‐driven decisions
in the early diffusion of this technology likely prioritized higher‐ income populations.16 Because Black, Hispanic, and low‐income
birthing people are more likely to be covered by Medicaid, discrep-
ancies in NIPT uptake among Medicaid enrollees disproportionately
affect these populations.
This study has limitations. First, we were unable to capture
patient‐level sociodemographic characteristics with insurance claims
data. Zip‐code level proxies are crude measures of patient charac-
teristics and should be interpreted as such. We were also unable to
capture NIPT use by enrollees with coverage through the Veterans
Administration, Tricare, or Medicare, which may offer less generous
coverage for pregnancy‐related services. Given established varia-
tions in state Medicaid programs, our findings may not generalize
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outside of Massachusetts. This study also used data from the early
days of NIPT, and increased awareness of the technology may have
improved uptake since then. Finally, because we could not observe
patient preferences for NIPT, we were unable to determine whether
disparities are a consequence of patient preferences or access bar-
riers. Black patients and those presenting for prenatal care at a later
gestational age are less likely to receive genetic counseling, sug-
gesting that discrepancies in NIPT may be due to provider counseling,
not patient choice.11 It is also important to note that people who did
not receive NIPT may have received other serum screening tests,
such as first trimester or quad screens, or undergone invasive pro-
cedures such as amniocentesis or chorionic villus sampling.
Our findings highlight substantial disparities in NIPT uptake
based on insurance and zip‐code of residence. These disparities likely
reflect established inequities in prenatal care. Research is needed to
identify barriers and facilitators to uptake and to evaluate
TAB L E 1 Rates (per 1000 eligible patients) and adjusted odds of Non‐invasive prenatal testing (NIPT) use
Cohort NIPT rate Adjusted OR (95% CI) P
Total patients (n = 22,393) 201.2
Insurance
Medicaid (n = 7106) 48.7 0.18 (0.16–0.20) <0.001
Commercial (n = 15,287) 272.1 Ref
Teaching hospital
Yes (n = 5025) 182.1 1.15 (0.80–1.67) 0.453
No (n = 17,368) 206.8 Ref
Zip‐code sociodemographicsa
Proportion of Black/Hispanic residents
High (n = 4886) 123.0 0.80 (0.70–0.90) <0.001
Low (n = 14,586) 223.2 Ref
Proportion living below the FPL
High (n = 3584) 107.7 0.80 (0.70–0.93) 0.003
Low (n = 15,886) 218.4 Ref
Note: The model included hospital random effects and clustered standard errors at the hospital level.
Abbreviations: CI, confidence interval; NIPT, non‐invasive prenatal testing; OR, odds ratio; Ref, referent.
The model included hospital random effects and clustered standard errors at the hospital level. aZip‐code sociodemographic indicators were derived from the Census Bureau's American Community Survey and defined based on patient zip‐code at
time of delivery and the population proportion of Black/Hispanic residents or residents living below 100% the FPL within each zip‐code.
F I GUR E 1 Zip‐code variation in Non‐invasive prenatal testing (NIPT) rates (per 1000 eligible patients) [Colour figure can be viewed at wileyonlinelibrary.com]
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interventions to address inequities in NIPT use. Specifically, survey
research to determine which patients are and are not offered NIPT
versus traditional serum screening will be critical moving forward.
Ultimately, our findings suggest that the benefits of NIPT availability
have not been realized in a substantial portion of the population‐ particularly among pregnant people who disproportionately experi-
ence barriers to care.
ACKNOWLEDGMENT
Funding for this study was provided to Amresh Hanchate and
Catharine Wang by the National Institute of Health Human Genome
Research Institute (R21 HG009567). Jacqueline Ellison was sup-
ported by the Agency for Healthcare Research and Quality National
Research Service Award (5T32 HS000011).
CONFLICT OF INTEREST
The authors declare no conflict of interest.
DATA AVAILABILITY STATEMENT
The data that support the findings of this study are available from the
Massachusetts Center for Health Information Analysis. Restrictions
apply to the availability of these data, which were used under license
for this study.
ORCID
Jacqueline Ellison https://orcid.org/0000-0003-1346-0965
REFERENCES
1. Akolekar R, Beta J, Picciarelli G, Ogilvie C, D’Antonio F. Procedure‐ related risk of miscarriage following amniocentesis and chorionic
villus sampling: a systematic review and meta‐analysis. Ultrasound Obstet Gynecol. 2015;45(6):16‐26. https://doi.org/10.1097/ogx.
0000000000000214
2. Goldwaser T, Klugman S. Cell‐free DNA for the detection of fetal
aneuploidy. Fertil Steril. 2018;109(2):195‐200. https://doi.org/10.
1016/j.fertnstert.2017.12.019
3. American College of Obstetricians and Gynecologists Committee on
Genetics. Committee Opinion No. 545: noninvasive prenatal testing
for fetal aneuploidy. Obstet Gynecol. 2012;120:1532‐1534.
4. Kuppermann M, Learman LA, Gates E, et al. Beyond race or ethnicity
and socioeconomic status: predictors of prenatal testing for Down
syndrome. Obstet Gynecol. 2006;107(5):1087‐1097. https://doi.org/
10.1097/01.aog.0000214953.90248.db
5. Kuppermann M, Gates E, Eugene Washington A. Racial‐ethnic dif-
ferences in prenatal diagnostic test use and outcomes: preferences,
socioeconomics, or patient knowledge? Obstet Gynecol. 1996;87:675
‐682. https://doi.org/10.1016/0029‐7844(96)00017‐8 6. Benoy ME, Iruretagoyena JI, Birkeland LE, Petty EM. The impact of
insurance on equitable access to non‐invasive prenatal screening
(NIPT): private insurance may not pay. J Community Genet. 2021;12(1):185‐197. https://doi.org/10.1007/s12687‐020‐00498‐w
7. Yarrington CD, Smith‐Lin C, Neuhalfen R, Hanchate A, Connors P,
Wang C. Racial and ethnic differences in uptake of cell‐free fetal
DNA aneuploidy screening in an urban safety net hospital. Prenat Diagn, 2021;41(11):1389‐1394. https://doi.org/10.1002/pd.6029
8. Massachusetts All Payer Claims Database. https://www.chiamass.gov/
ma‐apcd/
9. Hui L, Barclay J, Poulton A, Hutchinson B, Halliday JL. Prenatal
diagnosis and socioeconomic status in the non‐invasive prenatal
testing era: a population‐based study. Aust N Z J Obstet Gynaecol. 2018;58(4):404‐410. https://doi.org/10.1111/ajo.12778
10. van der Meij KRM, Kooij C, Bekker MN, Galjaard RH, Henneman L,
Dutch NIPT Consortium. Non‐invasive prenatal test uptake in so-
cioeconomically disadvantaged neighborhoods. Prenat Diagn. 2021;41(11):1395‐1400. https://doi.org/10.1002/pd.6043
11. Christopher D, Fringuello M, Fought AJ, et al. Evaluating for
disparities in prenatal genetic counseling. Am J Obstet Gynecol MFM. 2022;4(1):100494. https://doi.org/10.1016/j.ajogmf.2021.10
0494
12. Tucker Edmonds B, Schmidt A, Walker VP. Addressing bias and
disparities in periviable counseling and care. Semin Perinatol. 2021;
151524. https://doi.org/10.1016/j.semperi.2021.151524
13. Altman MR, Oseguera T, McLemore MR, Kantrowitz‐Gordon I,
Franck LS, Lyndon A. Information and power: women of color’s ex-
periences interacting with health care providers in pregnancy and
birth. Soc Sci Med. 2019;238:112491. https://doi.org/10.1016/j.
socscimed.2019.112491
14. Crear‐Perry J, Correa‐de‐Araujo R, Lewis Johnson T, McLemore MR,
Neilson E, Wallace M. Social and structural determinants of health
inequities in maternal health. J Womens Health. 2021;30(2):230‐235.
https://doi.org/10.1089/jwh.2020.8882
15. Agarwal A, Sayres LC, Cho MK. Commercial landscape of noninva-
sive prenatal testing in the United States. Prenat Diagn. 2013
(6):521‐531. Wiley Online Library https://obgyn.onlinelibrary.wiley.
com/doi/10.1002/pd.4101
16. Denbow JM. Prenatal nondiscrimination laws: disability, social
conservatism, and the political Economy of genetic screening. Disabil Stud Q. 2020;40(4). https://doi.org/10.18061/dsq.v40i4.7124
How to cite this article: Ellison J, Wang C, Yarrington C,
Connors P, Hanchate A. Insurance and geographic variations
in non‐invasive prenatal testing. Prenat Diagn.
2022;42(8):1004‐1007. https://doi.org/10.1002/pd.6155
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nloaded from https://obgyn.onlinelibrary.w
iley.com /doi/10.1002/pd.6155 by T
echnical U niversity O
strava, W iley O
nline L ibrary on [06/03/2023]. See the T
erm s and C
onditions (https://onlinelibrary.w iley.com
/term s-and-conditions) on W
iley O nline L
ibrary for rules of use; O A
articles are governed by the applicable C reative C
om m
ons L icense
- Insurance and geographic variations in non‐invasive prenatal testing
- ACKNOWLEDGMENT
- CONFLICT OF INTEREST
- DATA AVAILABILITY STATEMENT