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CMAJ : Canadian Medical Association Journal logoLink to CMAJ : Canadian Medical Association Journal
. 2010 Feb 9;182(2):143–151. doi: 10.1503/cmaj.090979

Proliferation of prenatal ultrasonography

John J You 1,, David A Alter 1, Therese A Stukel 1, Sarah D McDonald 1, Andreas Laupacis 1, Ying Liu 1, Joel G Ray 1
PMCID: PMC2817321  PMID: 20048009

Abstract

Background

The extent to which temporal increases in the use of prenatal ultrasonography reflect changes in maternal risk is unknown. In this population-based study, we examined the use of prenatal ultrasonography from 1996 to 2006 in Ontario.

Methods

With fiscal year 1996/97 as the baseline, we evaluated the relative risk (RR) and 95% confidence interval (CI) for the change in rates of ultrasonography for each subsequent year. The RR was adjusted for maternal age, income, rural residence, maternal comorbidities, receipt of genetics consultation or amniocentesis — all in the index pregnancy — and history of complications in a prior pregnancy.

Results

The study sample consisted of 1 399 389 singleton deliveries. The rate of prenatal ultrasonography increased from 2055 per 1000 pregnancies in 1996 to 3264 per 1000 in 2006 (adjusted RR 1.55, 95% CI 1.54–1.55). The rate increased among both women with low-risk pregnancies (adjusted RR 1.54, 95% CI 1.53–1.55) and those with high-risk pregnancies (adjusted RR 1.55, 95% CI 1.54–1.57). The proportion of pregnancies with at least four ultrasound examinations in the second or third trimesters rose from 6.4% in 1996 to 18.7% in 2006 (adjusted RR 2.68, 95% CI 2.61–2.74). Paradoxically, this increase was more pronounced among low-risk pregnancies (adjusted RR 2.92, 95% CI 2.83–3.01) than among high-risk pregnancies (adjusted RR 2.25, 95% CI 2.16–2.35).

Interpretation

Substantial increases in the use of prenatal ultrasonography over the past decade do not appear to reflect changes in maternal risk. Nearly one in five women now undergo four or more ultrasound examinations during the second and third trimesters. Efforts to promote more appropriate use of prenatal ultrasonography for singleton pregnancies appear warranted.


The rapid proliferation of diagnostic imaging is a challenge for the containment of health care expenditures and for system sustainability in many countries.1 The ensuing debate among clinicians, researchers and policy-makers has become increasingly contentious and highly politicized.2,3 In Canada, the annual operational costs for diagnostic imaging now total more than $2.2 billion.4 Prenatal ultrasonography is one of the most rapidly proliferating imaging tests, this expansion being marked most strikingly by an increase in the proportion of women undergoing multiple pre-natal examinations for a single pregnancy.5 Although guidelines generally recommend that two ultrasound examinations be performed in a pregnancy without complications — one in the first trimester, for measurement of nuchal translucency to screen for aneuploidy, and one in the second trimester to screen for fetal anomalies — it is conceivable that the proliferation of prenatal ultrasonography reflects changes in maternal risk over time.610

In other areas of health care, interventions that are most beneficial to high-risk individuals are frequently directed to low-risk populations.1113 We hypothesized that increasing trends in the use of prenatal ultrasonography could not be explained solely by pregnancy risk and would be evident among low-risk pregnancies. Accordingly, we performed a population-based study to examine the annual rates of prenatal ultrasonography, adjusted for maternal risk profiles.

Methods

Study design

We conducted a repeated cross-sectional population-based study of all women with a singleton obstetric delivery during the period 1996/97 to 2006/07 in Ontario, Canada’s most populous province (12 million people).

Data sources

For this study, we used two linked administrative databases. We obtained records of hospital admissions from the Canadian Institute for Health Information Discharge Abstract Database. We used these records to identify obstetric deliveries and maternal comorbidities. The anonymized discharge abstracts contained a unique encrypted identifier, the patient’s age, sex, date of admission, up to 16 diagnoses from the International Classification of Diseases, 9th revision, and up to 25 diagnoses from the International Classification of Diseases, 10th revision. Outpatient data were obtained from the database of the Ontario Health Insurance Plan, which contains billing information for physician services, including a service date and a single diagnosis. We used the Ontario Health Insurance Plan database to identify all outpatient claims for prenatal ultrasonography.9 We also used this database to identify maternal comorbidities, because some of these conditions may be diagnosed on an outpatient basis. Neighbourhood income quintile for each patient was defined according to postal code, using census data from Statistics Canada.14

Participants

For the period Apr. 1, 1996, to Mar. 31, 2007, we identified all deliveries across all Ontario hospitals in each fiscal year. To do this, we used a main patient service code for obstetric delivery in the Discharge Abstract Database.15 Participants were women with an admission to hospital for delivery of a liveborn or stillborn singleton infant after at least 20 weeks’ gestation. We excluded women younger than 15 years or older than 54 years at the date of admission to hospital for delivery and women with deliveries associated with an abortive procedure. If a woman had more than one delivery in a given fiscal year, we included only the first eligible delivery. The hospital admission date was used to define the date of the index delivery.

Maternal risk profile

We classified a pregnancy as “high-risk” if it was associated with a maternal comorbidity, genetics consultation, amniocentesis or history of complications in a prior pregnancy (see Appendix 1, available at www.cmaj.ca/cgi/content/full/cmaj.090979/DC1). We deemed all other index pregnancies to be “low-risk.” We considered a maternal comorbidity to be present if any of the following diagnoses could be identified in the Ontario Health Insurance Plan database or the Discharge Abstract Database within the 12 months before (and during) the hospital stay for the index delivery: any diabetes mellitus (gestational or prepregnancy), any hypertension, thyroid disease, cardiac disease, rheumatologic disease, venous thromboembolism, renal disease or epilepsy; we also considered hospital admission for supervision of a high-risk pregnancy to represent maternal comorbidity. Similarly, we used the Ontario Health Insurance Plan database to identify claims for genetics consultation and amniocentesis during the 12 months before (and during) the hospital stay for the index delivery. Finally, we defined a history of a prior pregnancy with complications as any pregnancy in the preceding five years that had been associated with stillbirth or with a genetics consultation, amniocentesis or hospital admission for supervision of a high-risk pregnancy during the 12 months before delivery.

Prenatal ultrasonography

The main study outcome was the annual rate of utilization of prenatal ultrasonography. For each woman’s index delivery in a given fiscal year, we considered all prenatal ultrasonography examinations performed during the 40-week period before her delivery date. We ascribed each examination to the fiscal year during which she delivered. Ultrasound examinations performed on an inpatient basis are not captured by the Ontario Health Insurance Plan database.

We classified prenatal ultrasound examinations according to estimated gestational age at the time of the procedure: first trimester (0 to 14 weeks), second trimester (15 to 27 weeks) or third trimester (28 to 40 weeks). We estimated gestational age at the time of ultrasonography by calculating the number of days between the date of the ultrasound examination and the delivery date and assuming that the delivery occurred at 40 weeks’ gestation. For example, if a woman delivered on Aug. 30, 2004, and had undergone ultrasonography on Aug. 10, 2004 (20 days before), the examination would be categorized as having taken place during the third trimester. This approach has a reported sensitivity of 90% and specificity of 99%.16

Data analysis

For each fiscal year, we computed the rate of prenatal ultrasonography by dividing the number of examinations attributed to that fiscal year by the corresponding number of inhospital singleton deliveries. We used Poisson regression to estimate the crude increase in the rate of prenatal ultrasonography within each fiscal year, relative to 1996, expressed as a relative risk (RR) and 95% confidence interval (CI). In a multivariate model, we then adjusted for maternal age, neighbourhood income quintile, rural place of residence, any diabetes mellitus (gestational or prepregnancy), any hypertension, any other maternal comorbidity (i.e., one or more of thyroid disease, cardiac disease, rheumatologic disease, venous thromboembolism, renal disease, epilepsy or admission to hospital for supervision of high-risk pregnancy), a genetics consultation and amniocentesis — all in the index pregnancy — as well as history of a prior pregnancy with complications, as defined above. We then restricted these multivariate analyses to women with a low-risk pregnancy, as well as to ultrasonography examinations performed in the second or third trimesters (to lessen the effect of a high uptake of first-trimester ultrasonography for measurement of nuchal translucency in recent years).17

In secondary analyses, we used the same multivariate model to generate the RR for undergoing prenatal ultrasonography in 2006 relative to 1996, stratified by maternal age at delivery, neighbourhood income quintile, place of residence (urban v. rural), any maternal diabetes mellitus (yes v. no) and any maternal hypertension (yes v. no). To evaluate whether the number of ultrasound examinations performed during pregnancy changed over time, we categorized all index pregnancies in 1996 into approximate quartiles, according to the number of second- and third-trimester ultrasound examinations per pregnancy. First-trimester examinations were excluded from this particular analysis to remove the potential effect of the recent introduction of first-trimester ultrasound testing for nuchal translucency. We used the same regression models as above to estimate the adjusted RR for the proportion of women receiving the fixed categorized number of ultrasound examinations in each year relative to 1996, both for the entire cohort and stratified by low-risk versus high-risk status.

The study was approved by the Sunnybrook Health Sciences Centre Research Ethics Board.

Results

We captured data for 1 424 767 in-hospital deliveries over the 11-year study period. A total of 25 378 deliveries were excluded because of multiple-gestation pregnancies (n = 22 785), a second delivery within the same fiscal year (n = 1628), extremes of maternal age (n = 665) or delivery after 20 weeks’ gestation in association with an abortive procedure (n = 300). The final study sample was 1 399 389 singleton deliveries (Table 1).

Table 1.

Characteristics of singleton pregnancies in Ontario, 1996 to 2006, n = 1 399 389

Characteristic Fiscal year; no. (%) of singleton deliveries*
1996
131 746
1997
128 976
1998
126 841
1999
126 078
2000
122 019
2001
126 062
2002
123 502
2003
127 086
2004
127 610
2005
128 721
2006
130 748
Maternal age, yr, mean (SD) 28.9 (5.4) 29.1 (5.5) 29.1 (5.5) 29.2 (5.5) 29.3 (5.6) 29.5 (5.5) 29.6 (5.5) 29.7 (5.5) 29.7 (5.5) 29.8 (5.5) 29.8 (5.5)
15–19 6 990 (5.3) 6 577 (5.1) 6 621 (5.2) 6 010 (4.8) 5 730 (4.7) 5 519 (4.4) 5 233 (4.2) 5 148 (4.1) 4 808 (3.8) 4 834 (3.8) 5 029 (3.8)
20–24 20 683 (15.7) 20 038 (15.5) 19 990 (15.8) 19 465 (15.4) 18 762 (15.4) 18 562 (14.7) 17 959 (14.5) 17 900 (14.1) 17 861 (14.0) 17 903 (13.9) 18 480 (14.1)
25–29 40 814 (31.0) 39 576 (30.7) 38 150 (30.1) 37 795 (30.0) 35 824 (29.4) 36 829 (29.2) 35 674 (28.9) 36 675 (28.9) 36 836 (28.9) 36 796 (28.6) 36 684 (28.1)
30–34 43 346 (32.9) 42 247 (32.8) 40 707 (32.1) 40 608 (32.2) 39 271 (32.2) 41 677 (33.1) 41 188 (33.4) 42 744 (33.6) 43 201 (33.9) 43 459 (33.8) 43 874 (33.6)
35–54 19 913 (15.1) 20 538 (15.9) 21 373 (16.9) 22 200 (17.6) 22 432 (18.4) 23 475 (18.6) 23 448 (19.0) 24 619 (19.4) 24 904 (19.5) 25 729 (20.0) 26 681 (20.4)
Income quintile
Q1 (lowest) 29 414 (22.3) 28 376 (22.0) 28 355 (22.4) 28 492 (22.6) 27 558 (22.6) 27 491 (21.8) 26 340 (21.3) 26 341 (20.7) 26 078 (20.4) 25 995 (20.2) 26 040 (19.9)
Q2 27 744 (21.1) 26 978 (20.9) 26 040 (20.5) 25 659 (20.4) 24 495 (20.1) 24 986 (19.8) 23 934 (19.4) 24 477 (19.3) 23 966 (18.8) 24 249 (18.8) 24 564 (18.8)
Q3 26 413 (20.0) 25 542 (19.8) 25 262 (19.9) 24 704 (19.6) 24 045 (19.7) 24 732 (19.6) 24 083 (19.5) 24 725 (19.5) 24 571 (19.3) 24 522 (19.1) 24 935 (19.1)
Q4 26 247 (19.9) 26 191 (20.3) 25 213 (19.9) 23 807 (18.9) 23 150 (19.0) 25 045 (19.9) 25 243 (20.4) 26 137 (20.6) 26 928 (21.1) 27 208 (21.1) 27 799 (21.3)
Q5 (highest) 21 133 (16.0) 21 196 (16.4) 20 765 (16.4) 20 400 (16.2) 19 841 (16.3) 20 798 (16.5) 20 766 (16.8) 22 048 (17.3) 22 498 (17.6) 23 197 (18.0) 23 664 (18.1)
Rural place of residence 17 565 (13.3) 16 810 (13.0) 16 072 (12.7) 14 756 (11.7) 14 094 (11.6) 14 315 (11.4) 13 792 (11.2) 14 143 (11.1) 13 929 (10.9) 13 813 (10.7) 14 167 (10.8)
Maternal comorbidities
Any hypertension 5 691 (4.3) 5 994 (4.6) 5 592 (4.4) 5 601 (4.4) 5 598 (4.6) 5 486 (4.4) 5 743 (4.7) 6 035 (4.7) 6 210 (4.9) 6 305 (4.9) 6 189 (4.7)
Any diabetes mellitus 6 688 (5.1) 6 410 (5.0) 6 331 (5.0) 6 267 (5.0) 6 433 (5.3) 7 241 (5.7) 7 495 (6.1) 7 750 (6.1) 8 685 (6.8) 8 875 (6.9) 9 596 (7.3)
Other comorbidity 4 169 (3.2) 3 991 (3.1) 3 998 (3.2) 4 343 (3.4) 4 161 (3.4) 4 449 (3.5) 4 038 (3.3) 4 313 (3.4) 4 001 (3.1) 4 069 (3.2) 4 202 (3.2)
Genetics consultation 564 (0.4) 698 (0.5) 758 (0.6) 884 (0.7) 907 (0.7) 969 (0.8) 914 (0.7) 920 (0.7) 944 (0.7) 953 (0.7) 876 (0.7)
Amniocentesis 1 488 (1.1) 1 682 (1.3) 1 861 (1.5) 1 916 (1.5) 1 852 (1.5) 1 868 (1.5) 1783 (1.4) 1 723 (1.4) 1 638 (1.3) 1 592 (1.2) 1 364 (1.0)
Pregnancy in prior 5 yr
None 75 279 (57.1) 74 231 (57.6) 73 421 (57.9) 74 089 (58.8) 72 919 (59.8) 75 287 (59.7) 75 137 (60.8) 77 816 (61.2) 78 231 (61.3) 77 758 (60.4) 79 133 (60.5)
Without complications 53 466 (40.6) 51 459 (39.9) 49 792 (39.3) 48 139 (38.2) 45 071 (36.9) 46 584 (37.0) 44 379 (35.9) 45 273 (35.6) 45 338 (35.5) 46 784 (36.3) 47 556 (36.4)
With complications§ 3 001 (2.3) 3 286 (2.5) 3 628 (2.9) 3 850 (3.1) 4 029 (3.3) 4 191 (3.3) 3 986 (3.2) 3 997 (3.1) 4 041 (3.2) 4 179 (3.2) 4 059 (3.1)
High-risk pregnancy 20 634 (15.7) 20 629 (16.0) 20 596 (16.2) 21 002 (16.7) 21 050 (17.3) 22 160 (17.6) 22 060 (17.9) 22 958 (18.1) 23 888 (18.7) 24 385 (18.9) 25 178 (19.3)

Note: Q = quintile, SD = standard deviation.

*

Unless indicated otherwise.

Income quintiles for each fiscal year do not sum to 100% because of missing data for up to 3% of patients.

Thyroid disease, cardiac disease, rheumatologic disease, venous thromboembolism, renal disease, epilepsy or admission to hospital for supervision of high-risk pregnancy.

§

Defined as prior pregnancy associated with genetics consultation, amniocentesis, admission to hospital for supervision of high-risk pregnancy or pregnancy ending in stillbirth.

Defined as any hypertension, any diabetes mellitus, any other comorbidity (as defined above), genetics consultation or amniocentesis during index pregnancy or history of pregnancy with complications (as defined above).

The annual number of ultrasound examinations increased linearly over the study period (p for trend < 0.001; Figure 1). The rate rose from 2055 per 1000 pregnancies in 1996 to 3264 per 1000 in 2006, which represents a crude 11-year RR (i.e., increase in utilization) of 1.59 (95% CI 1.58–1.60) and an adjusted RR of 1.55 (95% CI 1.54–1.55) (Table 2).

Figure 1.

Figure 1

Relative risk (RR) of undergoing obstetric ultrasonography from fiscal year 1996/97 to fiscal year 2006/07. Increases in the annual rate of prenatal ultrasonography are expressed as relative risk, with fiscal year 1996/97 as the referent. Data were adjusted for maternal age, income quintile, rural versus urban place of residence, any diabetes mellitus, any hypertension, any other maternal comorbidity, genetics consultation and amniocentesis — all in the index pregnancy — and a history of complications in a prior pregnancy. For all trends, p < 0.001. CI = confidence interval.

Table 2.

Use of prenatal ultrasonography for women with a singleton pregnancy in Ontario, 1996 to 2006, according to trimester

Timing of procedure Measure Fiscal year Adjusted RR (95% CI)*
1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006
All women Total no. 131 746 128 976 126 841 126 078 122 019 126 062 123 502 127 086 127 610 128 721 130 748
Any trimester No. US 270 687 278 089 270 185 278 068 285 758 312 527 323 216 352 815 377 852 398 905 426 757 -
Rate/1000 2 055 2 156 2 130 2 206 2 342 2 479 2 617 2 776 2 961 3 099 3 264 1.55 (1.54–1.55)
First trimester No. US 48 613 48 562 47 459 45 296 49 077 55 455 61 233 71 378 81 853 90 027 98 451 -
Rate/1000 369 377 374 359 402 440 496 562 641 699 753 1.98 (1.96–2.00)
Second trimester No. US 133 759 136 486 136 004 140 925 142 388 152 736 154 847 165 883 171 887 177 599 185 847 -
Rate/1000 1 015 1 058 1 072 1 118 1 167 1 212 1 254 1 305 1 347 1 380 1 421 1.38 (1.37–1.39)
Third trimester No. US 88 315 93 041 86 722 91 847 94 293 104 336 107 136 115 554 124 112 131 279 142 459 -
Rate/1000 670 721 684 728 773 828 867 909 973 1 020 1 090 1.55 (1.54–1.56)
Low-risk pregnancy Total no. 111 112 108 347 106 245 105 076 100 969 103 902 101 442 104 128 103 722 104 336 105 570
Any trimester No. US 216 673 222 299 214 726 219 193 222 805 241 873 248 628 270 827 286 855 302 103 321 185 -
Rate/1000 1 950 2 052 2 021 2 086 2 207 2 328 2 451 2 601 2 766 2 895 3 042 1.54 (1.53–1.55)
First trimester No. US 39 808 39 739 38 650 36 544 39 417 44 395 48 929 57 123 65 392 71 841 78 628 -
Rate/1000 358 367 364 348 390 427 482 549 630 689 745 2.03 (2.00–2.05)
Second trimester No. US 110 692 112 718 111 718 115 163 115 433 123 097 124 295 132 464 135 685 139 672 145 566 -
Rate/1000 996 1 040 1 052 1 096 1 143 1 185 1 225 1 272 1 308 1 339 1 379 1.37 (1.36–1.38)
Third trimester No. US 66 173 69 842 64 358 67 486 67 955 74 381 75 404 81 240 85 778 90 590 96 991 -
Rate/1000 596 645 606 642 673 716 743 780 827 868 919 1.53 (1.51–1.55)
High-risk pregnancy Total no. 20 634 20 629 20 596 21 002 21 050 22 160 22 060 22 958 23 888 24 385 25 178
Any trimester No. US 54 014 55 790 55 459 58 875 62 953 70 654 74 588 81 988 90 997 96 802 105 572 -
Rate/1000 2 618 2 704 2 693 2 803 2 991 3 188 3 381 3 571 3 809 3 970 4 193 1.55 (1.54–1.57)
First trimester No. US 8 805 8 823 8 809 8 752 9 660 11 060 12 304 14 255 16 461 18 186 19 823 -
Rate/1000 427 428 428 417 459 499 558 621 689 746 787 1.80 (1.76–1.85)
Second trimester No. US 23 067 23 768 24 286 25 762 26 955 29 639 30 552 33 419 36 202 37 927 40 281 -
Rate/1000 1 118 1 152 1 179 1 227 1 281 1 338 1 385 1 456 1 515 1 555 1 600 1.42 (1.39–1.44)
Third trimester No. US 22 142 23 199 22 364 24 361 26 338 29 955 31 732 34 314 38 334 40 689 45 468 -
Rate/1000 1 073 1 125 1 086 1 160 1 251 1 352 1 438 1 495 1 605 1 669 1 806 1.60 (1.57–1.62)

Note: CI = confidence interval, RR = relative risk, US = ultrasonography examination.

*

For 2006 v. 1996, adjusted for maternal age, income quintile, rural place of residence, diabetes mellitus, hypertension, other maternal comorbidity, genetics consultation and amniocentesis — all in the index pregnancy — and for history of complications of pregnancy.

The magnitude of the increase in ultrasonography rates over the 11-year study period was similar for women with low-risk pregnancies (adjusted RR 1.54, 95% CI 1.53–1.55, 2006 relative to 1996) and those with high-risk pregnancies (adjusted RR 1.55, 95% CI 1.54–1.57) (Figure 1, Table 2) and for examinations performed in the second and third trimesters (adjusted RR 1.45, 95% CI 1.44–1.46) (Figure 1). Although within-stratum interactions were statistically significant (p < 0.001), the magnitude of the adjusted RRs was comparable upon stratification by maternal characteristics (Figure 2). The relative increase in ultrasonography across the 11-year study period was evident in all trimesters, but was most pronounced for examinations performed in the first trimester (Figure 2).

Figure 2.

Figure 2

Relative risk (RR) of undergoing obstetric ultrasonography in fiscal year 2006/07 relative to fiscal year 1996/97. Data were adjusted for maternal age, income quintile, rural versus urban place of residence, any diabetes mellitus, any hypertension, any other maternal comorbidity, genetics consultation and amniocentesis — all in the index pregnancy — and a history of complications in a prior pregnancy. For all within-stratum interaction terms, p < 0.001. CI = confidence interval.

In 1996, the quartiles for the number of ultrasound examinations performed in the second and third trimesters were zero or one, two, three, and four or more (Table 3). Among all women, the proportion of pregnancies with four or more fetal ultrasound examinations in the second or third trimester rose from 6.4% in 1996 to 18.7% in 2006, corresponding to an adjusted RR of 2.68 (95% CI 2.61–2.74) across the decade. This change was more pronounced among low-risk pregnancies (adjusted RR, 2.92, 95% CI 2.83–3.01) than among high-risk pregnancies (adjusted RR 2.25, 95% CI 2.16–2.35). By 2006, more than one-third (37.2%) of all women were receiving three or more ultrasound examinations during the second and third trimesters of pregnancy (Table 3).

Table 3.

Use of prenatal ultrasonography during the second and third trimesters among women with a singleton pregnancy in Ontario, 1996 to 2006

All participants, by quartile Fiscal year
1996, n = 131 746 1997, n = 128 976 1998, n = 126 841 1999, n = 126 078 2000, n = 122 019 2001, n = 126 062 2002, n = 123 502 2003, n = 127 086 2004, n = 127 610 2005, n = 128 721 2006, n = 130 748
All participants

Q1 (0 or 1 US examinations)

No. (%) 71 645 (54.4) 65 522 (50.8) 66 709 (52.6) 62 518 (49.6) 55 868 (45.8) 53 793 (42.7) 49 590 (40.2) 47 620 (37.5) 44 998 (35.3) 42 234 (32.8) 39 448 (30.2)

Adjusted RR (95% CI)* 1.00 (ref) 0.94 (0.93–0.95) 0.97 (0.96–0.98) 0.92 (0.91–0.93) 0.85 (0.84–0.86) 0.79 (0.79–0.80) 0.75 (0.74–0.76) 0.70 (0.69–0.71) 0.66 (0.65–0.67) 0.62 (0.61–0.62) 0.57 (0.56–0.57)

Q2 (2 US examinations)

No. (%) 38 100 (28.9) 39 194 (30.4) 37 250 (29.4) 37 816 (30.0) 38 429 (31.5) 40 509 (32.1) 40 103 (32.5) 41 367 (32.6) 41 239 (32.3) 41 908 (32.6) 42 590 (32.6)

Adjusted RR (95% CI)* 1.00 (ref) 1.05 (1.04–1.07) 1.02 (1.00–1.03) 1.04 (1.03–1.06) 1.09 (1.08–1.11) 1.12 (1.10–1.13) 1.13 (1.11–1.14) 1.13 (1.11–1.14) 1.12 (1.11–1.14) 1.13 (1.12–1.15) 1.13 (1.12–1.15)

Q3 (3 US examinations)

No. (%) 13 516 (10.3) 14 538 (11.3) 13 721 (10.8) 15 029 (11.9) 16 094 (13.2) 17 959 (14.2) 18 809 (15.2) 20 714 (16.3) 21 542 (16.9) 22 981 (17.9) 24 204 (18.5)

Adjusted RR (95% CI)* 1.00 (ref) 1.10 (1.07–1.12) 1.05 (1.03–1.08) 1.16 (1.13–1.19) 1.28 (1.25–1.31) 1.38 (1.34–1.41) 1.47 (1.44–1.50) 1.57 (1.53–1.60) 1.62 (1.58–1.65) 1.71 (1.67–1.75) 1.77 (1.74–1.81)

Q4 (≥ 4 US examinations)

No. (%) 8 485 (6.4) 9 722 (7.5) 9 161 (7.2) 10 715 (8.5) 11 628 (9.5) 13 801 (10.9) 15 000 (12.1) 17 385 (13.7) 19 831 (15.5) 21 598 (16.8) 24 506 (18.7)

Adjusted RR (95% CI)* 1.00 (ref) 1.16 (1.13–1.20) 1.11 (1.08–1.14) 1.29 (1.25–1.33) 1.43 (1.39–1.47) 1.63 (1.58–1.67) 1.79 (1.75–1.84) 2.00 (1.95–2.05) 2.25 (2.19–2.31) 2.41 (2.35–2.47) 2.68 (2.61–2.74)

Low-risk subgroup n = 111 112 n = 108 347 n = 106 245 n = 105 076 n = 100 969 n = 103 902 n = 101 442 n = 104 128 n = 103 722 n = 104 336 n = 105 570

Q4 (≥ 4 US examinations)

No. (%) 5 485 (4.9) 6 486 (6.0) 5 977 (5.6) 7 085 (6.7) 7 481 (7.4) 8 884 (8.6) 9 643 (9.5) 11 213 (10.8) 12 719 (12.3) 13 845 (13.3) 15 687 (14.9)

Adjusted RR (95% CI)* 1.00 (ref) 1.20 (1.16–1.25) 1.13 (1.09–1.17) 1.35 (1.30–1.39) 1.47 (1.42–1.53) 1.70 (1.64–1.76) 1.89 (1.83–1.95) 2.12 (2.05–2.19) 2.42 (2.34–2.50) 2.61 (2.53–2.69) 2.92 (2.83–3.01)

High-risk subgroup n = 20 634 n = 20 629 n = 20 596 n = 21 002 n = 21 050 n = 22 160 n = 22 060 n = 22 958 n = 23 888 n = 24 385 n = 25 178

Q4 (≥ 4 US examinations)

No. (%) 3 000 (14.5) 3 236 (15.7) 3 184 (15.5) 3 630 (17.3) 4 147 (19.7) 4 917 (22.2) 5 357 (24.3) 6 172 (26.9) 7 112 (29.8) 7 753 (31.8) 8 819 (35.0)
Adjusted RR (95% CI)* 1.00 (ref) 1.08 (1.03–1.14) 1.07 (1.02–1.12) 1.19 (1.13–1.24) 1.34 (1.28–1.41) 1.48 (1.42–1.55) 1.61 (1.54–1.68) 1.78 (1.70–1.86) 1.94 (1.86–2.03) 2.06 (1.97–2.15) 2.25 (2.16–2.35)

Note: CI = confidence interval, Q = quartile, RR = relative risk, US = ultrasonography examination.

*

Adjusted for maternal age, income quintile, rural place of residence, diabetes mellitus, hypertension, other maternal comorbidity, genetics consultation, amniocentesis – all in the index pregnancy – and for history of complications of pregnancy.

Interpretation

In a health care system with universal access to prenatal services, we observed a 55% relative increase (adjusted) in the use of outpatient obstetric ultrasonography among singleton pregnancies over the decade from 1996/97 to 2006/07. This change was statistically significant and robust across subgroups, regardless of pregnancy risk, maternal demographic characteristics or maternal comorbidities. By 2006, over one-third of women with a singleton pregnancy were undergoing three or more outpatient ultrasound examinations during the second and third trimesters.

Our findings are consistent with a growing body of evidence suggesting that some health interventions most beneficial to high-risk individuals are frequently directed at apparently low-risk populations. This “treatment–risk paradox” has been described for statin therapy in high-risk elderly patients,11 for pharmacotherapy in patients with congestive heart failure12 and for temporal trends in the utilization of non-invasive cardiac testing.13 Although the use of prenatal ultrasonography among women with low-risk pregnancies may not account for a large proportion of total expenditures for medical imaging, it serves as a test case of a rapidly proliferating diagnostic technology. As such, it is a microcosm of a much bigger phenomenon that may be occurring with many other diagnostic imaging tests and that, cumulatively, may account for billions of dollars of health care expenditures.1,2

Others have documented substantial regional differences in utilization of obstetric ultrasonography and evidence of inappropriate use of this technology.5,1820 In our study, rising utilization could not be explained solely by increases in maternal age, changes in maternal risk profiles or increases in uptake of first-trimester scanning for nuchal translucency. Hence, it would appear that nonclinical factors may largely explain the increases in prenatal ultrasonography that we observed. These factors may include the practice of defensive medicine, the desire to reassure a patient that her pregnancy is progressing normally, patient demand and even the “entertainment” value of seeing one’s fetus.2124 Although the benefits of prenatal ultrasonography in high-risk pregnancies may be clearer, the value of repeat ultrasonography in low-risk patients is not.25,26 Prenatal ultrasonography is widely regarded as safe.27 However, some studies have suggested that frequent prenatal ultrasonography may be associated with intrauterine growth restriction, delayed speech and non–right-handedness.2831 Moreover, when a prenatal ultrasound examination is performed in a low-risk pregnancy, unintended harmful consequences may outweigh any potential benefits. For example, incidental benign findings — which are becoming increasingly prevalent with advances in technology —can cause anxiety and can lead to additional investigations, some of which may be invasive, such as amniocentesis.32

More than one-third of women now undergo three or more ultrasound examinations during the second and third trimesters of a singleton pregnancy, a rate that appears to be climbing for reasons unrelated to changes in maternal risk. As such, there is a need for patients, clinicians and policy-makers to carefully consider the optimal number of obstetric ultrasound examinations per pregnancy. Assuming an average cost of $64 per examination (based on the 2008 fee schedule in Ontario33), we estimate that the cumulative amount in fees for additional prenatal ultrasound examinations performed since 1996 was $30 million. Given the high aggregate costs of prenatal ultrasonography (because pregnancy is so common) and the evidence of potential overuse in populations not at high risk, health policy-makers could make a legitimate argument that costs be contained in groups for whom there is no documented benefit. Indeed, after the first trimester, most current guidelines recommend only a single second-trimester anatomic ultrasound examination during a pregnancy without complications.6,7 However, obstetricians function in the highest-risk medico-legal environment, where the implicit rules governing practice may differ from those in other domains of medicine, including the need to reassure patients through safe and relatively inexpensive tests like ultrasonography.21,22 In publicly funded health systems, citizens are key stakeholders in this debate, and efforts to engage citizens in deliberations about setting health care priorities should be encouraged.34 Various options for optimizing the use of obstetric ultrasonography, such as preauthorization of claims and changes to the fee schedule, will require debate and will necessarily demand a balance between policy pragmatism and an honest acknowledgement of defensive practice styles among individual providers.

Our study has some limitations. First, we had to estimate the trimester in which ultrasonography had been performed. Therefore, for preterm deliveries, some examinations actually completed in the first or second trimester would have been ascribed to a later period in the pregnancy, which would have led us to underestimate the number of first-trimester examinations. To counter this effect, we excluded multifetal pregnancies and adjusted for maternal risk, each of which is more likely to result in preterm delivery. Second, we excluded women who aborted before 20 weeks’ gestation, some of whom might have been considered to be at high risk. The remaining women in our study cohort whose pregnancies were defined as “high-risk” might have had a lower disease burden than the entire population of women with high-risk pregnancies, which might have limited somewhat the generalizability of our findings to pregnancies extending beyond 20 weeks’ gestation. Third, we did not have data about trends in the locations where the prenatal ultrasound examinations were performed, such as private physicians’ offices versus hospital-based facilities. Future studies will be needed to examine potential system-level reasons for the trends we observed. Finally, since the Ontario Health Insurance Plan database does not provide the indications for prenatal ultrasonography, we could not directly assess the appropriateness of the patterns of use that we observed. A detailed chart review, combined with surveys or interviews of mothers and their pregnancy caregivers, might better elucidate the underlying reasons for the rising use of prenatal ultrasonography.

In conclusion, there has been a substantial increase in the use of prenatal ultrasonography in the past decade, and more than one-third of women with a singleton pregnancy now receive three or more ultrasound examinations during the second and third trimesters. Efforts to promote more appropriate use of prenatal ultrasonography in low-risk groups appear warranted, but careful debate will be required to determine the most effective and acceptable approaches to achieve this goal.

Supplementary Material

[Online Appendix]
090979_index.html (748B, html)

Footnotes

Funding: John You is supported by a Career Scientist Award from the Ontario Ministry of Health and Long-Term Care. Joel Ray is supported by a New Investigator Award from the Canadian Institutes of Health Research. The Institute for Clinical Evaluative Sciences receives core operating funding in the form of an annual grant from the Ontario Ministry of Health and Long-Term Care. This study was funded by an operating grant from the Canadian Institutes of Health Research and was supported by the Institute for Clinical Evaluative Sciences. None of the funding sources had a role in the design and conduct of the study; the collection, management, analysis or interpretation of the data; or the preparation, review or approval of the manuscript. The opinions, results and conclusions reported in this paper are those of the authors and are independent from the funding sources. No endorsement by the Institute for Clinical Evaluative Sciences or the Ontario Ministry of Health and Long-Term Care is intended or should be inferred.

Previously published at www.cmaj.ca

Competing interests: None declared.

Contributors: All authors contributed to the concept and design of the study. Drs. You and Ray drafted the manuscript. All authors contributed to the analysis and interpretation of data, critically revised the manuscript for important intellectual content and approved the final version.

This article has been peer reviewed.

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Supplementary Materials

[Online Appendix]
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090979_1.pdf (33.8KB, pdf)

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