Abstract
Background
There is ongoing controversy about who should be referred for bone mineral density (BMD) testing to estimate fracture risk and diagnose osteoporosis. The purpose of this study was to examine patterns of use of BMD testing in Ontario between 1992 and 1998.
Methods
All physician claims from the Ontario Health Insurance Plan (OHIP) claims database for BMD testing between Jan. 1, 1992, and Dec. 31, 1998, were categorized by age and sex of the patient and the specialty of the physician who ordered the test. Time trends and regional rate variation analyses were also performed. To examine the prevalence of repeat testing, an inception cohort of women who had a BMD test in 1996 was followed for 2 years from the date of first test.
Results
From 1992 to 1998 the number of BMD tests performed per year in women increased from 34 402 to 230 936 and in men from 2 162 to 13 579. In 1998 most tests were being ordered by family physicians (80.2% in 1998 v. 52.1% in 1992). Approximately 1 in 7 women aged 55–69 years had BMD tests done in 1998. Within a 2-year period 29.3% of these women had the test repeated; the mean time between tests was 16 months. Regional rate variation analyses of BMD tests performed in 1996–1998 indicated a 235-fold variation in BMD test rates across counties in Ontario, with a range from 0.2 to 47.1 per 1000 women in the population.
Interpretation
The number of BMD tests performed each year in Ontario is increasing rapidly. However, the significant variation between rates of testing in different regions indicates that the diffusion of this technology may not be taking place according to population need.
Osteoporosis predisposes to bone fractures at the hip, wrist and spine. It affects approximately 1.4 million Canadians, mostly postmenopausal women and elderly people.1 Osteoporosis-related fractures cause considerable morbidity and an enormous financial burden through the use of health services, at an estimated cost of $1.3 billion in 1993.1 To prevent osteoporotic fractures, individuals at risk for fractures must first be identified, and then the appropriate interventions to reduce this risk, such as lifestyle modifications and hormone or other drug therapies, must be implemented.2
Bone mass is a major determinant of bone strength and has an inverse relationship with fracture risk. Prospective studies3,4,5,6 have shown an increasing gradient of fracture risk with decreasing bone mineral density (BMD), a decrease in density of 1 standard deviation (SD) being associated with a 1.5- to 3.0-fold increase in risk of fracture. However, the use of densitometry for risk assessment remains controversial in Canada. The provincial offices of health technology assessment in both Alberta7 and British Columbia8 have concluded that bone densitometry is unsuitable for screening and is not recommended for use in “well women.” Yet, clinical practice guidelines published in Canada,9 the United States,10 Europe11 and Australia12 state that those at greatest risk for osteoporosis-related fractures should be identified on the basis of BMD measurements.
Given the differing perspectives, the purpose of our research was to examine patterns of use of BMD testing in Ontario. Time trends, the age and sex distribution of the population being tested, specialties of the physicians ordering the test, repeat testing rates and regional rate variations were examined.
Methods
The primary data source was the Ontario Health Insurance Plan (OHIP) Claims Database. To obtain the age and sex of the patient for each test ordered, OHIP files were linked to the Registered Persons Database using a unique identifier.
Currently, dual-energy x-ray absorptiometry (DXA) is the accepted method to measure BMD for estimating fracture risk and diagnosing osteoporosis in the hip and spine.9,10,11,12 Before DXA technology, dual-photon absorptiometry (DPA) was the standard. To calculate time trends, all physician claims for BMD measurement by DPA or DXA between Jan. 1, 1992, and Dec. 31, 1998, were selected from the OHIP database using the following codes: J888 or J688 for a single site (spine, proximal femur, radius, whole body) and J856 or J656 for 2 or more sites.13 Physicians were categorized as family physicians, obstetrician-gynecologists, internal medicine specialists or “other” (e.g., radiologists). To calculate age- and sex-adjusted rates, the number of BMD tests were standardized using the Ontario population in the year the test was ordered.
To examine repeat testing in women, we created an inception cohort of all women who had BMD testing in 1996 by excluding those who had 1 or more tests between 1992 and 1995. Each patient in the cohort was then followed through record linkage in the OHIP database for 2 years from the date of their 1996 test. We calculated the proportion of women who had the test repeated during the 2-year period and the mean duration between tests. If the patient had a DXA within 1 month of their initial DXA, this was not considered a repeat test — the test was probably done again because of a technical error.
To obtain stable rate estimates for the 49 regions in Ontario, the analysis of regional rate variations combined data over 2 time periods: 1992–1995 and 1996–1998. The tests were assigned to each region according to the location of the physician's office. All rates were adjusted to the age and sex distribution of the population.
Three measures were used to quantify regional rate variations: the extremal quotient (EQ), the weighted coefficient of variation (CV) and the systematic component of variation (SCV).14 The EQ is the ratio of the highest observed proportion to the lowest and measures the relative difference between extremes. The CV measures the ratio of the SD of BMD rates across the various geographic regions to the mean BMD rate, weighted by the number of billings in each region to account for the unequal sizes of the regions, multiplied by 100. The SCV allows for comparison of variation among rates, and it is obtained by subtracting the random component of variation from the estimate of total variance.15 The EQ and CV are descriptive statistics and cannot be used to test hypotheses. Therefore, we calculated the likelihood ratio χ2 statistic, which allowed us to test the hypothesis that the rate of BMD testing did not vary between regions. A p-value below 0.05 was considered statistically significant. To determine if the relative ranking of regional rates remained stable over the 2 time periods, we calculated a Spearman's rank-order correlation coefficient. This statistic was also used to determine whether the quantity and location of bone densitometers was associated with regional rates. The data on densitometer quantity and location were provided by the Osteoporosis Society of Canada.
Results
The number of BMD test billings for men and women in Ontario between 1992 and 1998 are presented in Table 1. The annual number of BMD tests increased approximately 6-fold between 1992 and 1998 for both men and women. The rate of increase was largest between 1995 and 1996, when the number of tests increased by approximately 1.6 times.
The proportion of BMD tests ordered by family physicians increased from 52.1% in 1992 to 80.2% in 1998, whereas the proportion ordered by internal medicine specialists, obstetrician-gynecologists and physicians in other specialties decreased in the same time span (Table 2).
Time trends in age-specific rates of BMD testing are presented in Fig. 1. For all age groups, the number of BMD tests increased each year between 1992 and 1998. The highest rates were seen for women between the ages of 55 and 69 years. In 1998 approximately 1 in 7 women in this age range had a BMD test.
Of the women who had their first test in 1996, 29.3% had a repeat test within 2 years. The average time between tests was 16 months (range 1–24 months).
For the 49 Ontario counties the average age-adjusted rate of BMD testing for the 1992–1995 interval ranged from 0 to 28.9 tests per 1000 women in the population (data not shown), and for the 1996–1998 interval from 0.2 to 47.1 per 1000 women in the population (Table 3). The 5 regions with the highest BMD rates — Hamilton, Toronto, Halton, Durham and Brant (concentrated in south-central Ontario) — were the same for both time intervals. Most of the regions with the lowest BMD rates were in northern Ontario.
Using the 1992–1995 data the EQ, CV and SCV were 564.5, 71.6 and 588.5, respectively. For 1996–1998 these values were 251.7, 48.3 and 355.1, respectively. These statistics indicate significant regional variations in the use of the BMD test in Ontario. The χ2 test was statistically significant (p < 0.001) for both time periods, indicating that the BMD rates were significantly different between regions. The Spearman's rank-order correlation coefficient between region-specific rates for the 2 time periods was 0.7 (p < 0.001), indicating regions with high rates of use in 1992–1995 also had high rates in 1996–1998. In 1995 there were 95 bone densitometers in Ontario; in 1998 the total had increased to 212. The regions with more densitometers in 1998 had higher rates of BMD testing (ρ = 0.8, p < 0.001).
Interpretation
The number of BMD tests performed in Ontario increased at least 6-fold between 1992 and 1998. One in 7 women between 55 and 69 years of age had BMD tests done in 1998, compared with 1 in 50 in 1992. The increase in the proportion of BMD tests ordered by family physicians, from 52.1% in 1992 to 80.2% in 1998, suggests that osteoporosis is primarily being managed by family physicians. Approximately 30% of women had a repeat test within 2 years of their first test. Together, these data suggest that the large increase in the number of tests since 1996 is not primarily because of repeat testing in a select group of patients, but rather that new patients are being tested.
There was significant variation in the use of BMD tests across Ontario. The difference between the highest area rates and the lowest area rates was 235-fold. This suggests that there may be both under- and over-utilization of this diagnostic test;15,16 patients in low-utilization areas may not be getting tests they need, whereas patients in high-utilization areas may be having too many (or inappropriate) tests ordered.17 The steady increase in rates over the 7-year period with little change in regional rate variations supports the premise that the increases are occurring in an uncoordinated fashion.
There was large regional variation in the access to and availability of bone densitometers. We noted that area rates were correlated with the location of bone densitometers, suggesting that access to technology was driving utilization. The increase in the use of densitometry services is not only happening in Ontario but also in the United Kingdom, where there were over 100 hospital-based osteoporosis clinics in operation in 1997, compared with only a handful 10 years ago.18 The number of densitometers in Ontario grew from 95 in 1997 to 212 in 1998, yet regional variation was still significant. This may be because areas with high rates in the earlier period simply continued to add more densitometers to their existing complement.
Although hormone replacement therapy remains the treatment of choice for skeletal protection, there has been much effort devoted to alternative treatments for the prevention of osteoporosis because of the possible increase in the risk for breast cancer and the side effects (bleeding, weight gain and breast tenderness) associated with hormone therapy. The sharp jump in BMD testing rates after 1995 might be explained by the introduction of the bisphosphonate family of medications to the marketplace in 1995 as an alternative to hormone replacement therapy.
This study is limited by the information available in the administrative databases. We do not know why the tests were ordered (i.e., risk factors for osteoporosis, secondary osteoporosis or to monitor treatment effects) or what the results of the tests were.
Although BMD testing has been increasing rapidly in Ontario, the significant variation between regional rates of BMD testing indicates the diffusion of this technology may not be taking place according to population need.
Footnotes
This article has been peer reviewed.
Acknowledgements: We acknowledge Dr. J.I. Williams for his helpful comments and Keyi Wu for assistance with data analysis.
Dr. Jaglal is a Career Scientist supported by the Ontario Ministry of Health, and Dr. Hawker is a Medical Research Council of Canada Scientist.
This research was supported by a grant from the Institute for Clinical Evaluative Sciences, Toronto, Ont.
Reprint request to: Dr. Susan Jaglal, Department of Physical Therapy, 2nd Flr., 256 McCaul St., University of Toronto, Toronto, ON M5T 1W5; fax 416 978-4363; susan.jaglal@utoronto.ca
References
- 1.Goeree R, O'Brien B, Pettitt D, Cuddy L, Ferraz M, Adachi J. An assessment of the burden of illness due to osteoporosis in Canada. J Soc Obstet Gynaecol Can 1996;18(Suppl):15-24.
- 2.Consensus Development Conference: diagnosis, prophylaxis and treatment of osteoporosis. Am J Med 1993;94:646-50. [DOI] [PubMed]
- 3.Jergas M, Gluer CC. Assessment of fracture risk by bone density measurements. Semin Nucl Med 1997;27:261-75. [DOI] [PubMed]
- 4.Schott AM, Cormier C, Hans D, Favier F, Hausherr E, Dargent-Molina P, et al. How hip and whole-body bone mineral density predict hip fracture in elderly women. The EPIDOS prospective study. Osteoporos Int 1998;8:247-54. [DOI] [PubMed]
- 5.Cummings SR, Black DM, Nevitt MC, Browner W, Cauley J, Ensrud K, et al. Bone density of various sites for prediction of hip fractures. Lancet 1993; 341:72-5. [DOI] [PubMed]
- 6.Nevitt MC, Johnell O, Black DM, Ensrud K, Genant HK, Cummings SR. Bone mineral density predicts non-spine fractures in very elderly women. Osteoporos Int 1994;4:325-31. [DOI] [PubMed]
- 7.Hailey D, Sampietro-Colom L, Marshall D, Rico R, Granados A, Asua J. Statement of findings. INAHTA project on the effectiveness of bone density measurement and associated treatments for prevention of hip fractures. Edmonton (AB): Alberta Heritage Foundation for Medical Research; 1996.
- 8.Green CJ, Bassett K, Foerster V, Kazanjian A. Bone mineral density testing: does the evidence support its selective use in well women? Vancover: British Columbia Office of Health Technology Assessment; BCOHTA report no.: 1997:2T; 1997.
- 9.Scientific Advisory Board, Osteoporosis Society of Canada. Clinical practice guidelines for the diagnosis and management of osteoporosis CMAJ 1996; 155:1113-33. Available: www.cma.ca/disease/osteo_p2/osteocpg.htm [PMC free article] [PubMed]
- 10.National Osteoporosis Foundation. Physician's guide to prevention and treatment of osteoporosis. Belle Mead (NJ): Excerpta Medica Inc; 1998. Available: www .nof.org/for_professionals/clinical/clinical.htm
- 11.Kanis JA, Delmas P, Burckhardt P, Cooper C, Torgerson D. Guidelines for diagnosis and management of osteoporosis. The European Foundation for Osteoporosis and Bone Disease. Osteoporos Int 1997;7:390-406. [DOI] [PubMed]
- 12.The prevention and management of osteoporosis. Consensus statement. Australian National Consensus Conference 1996. Med J Aust 1997;167(Suppl 1):1-15. [PubMed]
- 13.Ontario health insurance plan schedule of benefits. Toronto: Ontario Ministry of Health; 1992.
- 14.McPherson K, Wennberg JE, Hovind OB, Clifford P. Small-area rate variations in the use of common surgical procedures: an international comparison of New England, England and Norway. N Engl J Med 1982;307:1310-14. [DOI] [PubMed]
- 15.Blumenthal D. The variation phenomenon in 1994. N Engl J Med 1994;331: 1017-8. [DOI] [PubMed]
- 16.Phelps CE, Parente ST. Priority setting in medical technology and medical practice assessment. Med Care 1990;28:703-23. [DOI] [PubMed]
- 17.Wennberg J, Gittelson A. Variations in medical care among small areas. Sci Am 1982;246:120-34. [DOI] [PubMed]
- 18.Blake GM, Gluer CC, Fogelman I. Bone densitometry: current status and future prospects. Br J Radiol 1997;70:S177-86. [DOI] [PubMed]