Designation, diligence and drift: understanding laboratory expenditure increases in British Columbia, 1996/97 to 2005/06
© Sivananthan et al.; licensee BioMed Central Ltd. 2012
Received: 3 May 2012
Accepted: 10 December 2012
Published: 21 December 2012
Laboratory testing is one of the fastest growing areas of health services spending in Canada. We examine the extent to which increases in laboratory expenditures might be explained by testing that is consistent with guidelines for the management of chronic conditions, by analyzing fee-for-service physician payment data in British Columbia from 1996/97 and 2005/06.
We used direct standardization to quantify the effect on laboratory expenditures from changes in: fee levels; population growth; population aging; treatment prevalence; expenditure on recommended tests for those conditions; and expenditure on other tests. The chronic conditions selected were those with guidelines containing laboratory recommendations developed by the BC Guidelines and Protocol Advisory Committee: diabetes, hypertension, congestive heart failure, renal failure, liver disease, rheumatoid arthritis, osteoarthritis and dementia.
Laboratory service expenditures increased by $98 million in 2005/06 compared to 1996/97, or 3.6% per year after controlling for population growth and aging. Testing consistent with guideline-recommended care for chronic conditions explained one-third (1.2% per year) of this growth. Changes in treatment prevalence were just as important, contributing 1.5% per year. Hypertension was the most common condition, but renal failure and dementia showed the largest changes in prevalence over time. Changes in other laboratory expenditure including for those without chronic conditions accounted for the remaining 0.9% growth per year.
Increases in treatment prevalence were the largest driver of laboratory cost increases between 1996/97 and 2005/06. There are several possible contributors to increasing treatment prevalence, all of which can be expected to continue to put pressure on health care expenditures.
KeywordsClinical Laboratory Techniques/utilization Clinical Laboratory Techniques/statistics & numerical data Guideline care Diagnostic Techniques and Procedures/economics Diagnostic Techniques and Procedures/trends Fee-for-Service Plans/trends Health Expenditures/trends Physician's Practice Patterns/trends Chronic Disease/Condition British Columbia Canada
Canadians are concerned about the rising cost of health care and particularly about whether the public model is “sustainable” in the face of these cost pressures . Health care was identified as the topic of highest priority for Canadian voters during the 2011 Federal election, as it has been in previous elections . Within the overall landscape of increasing health care costs, expenditures for physician/specialists services in Canada have risen sharply over the past five years, regaining a position as the second largest cost component (exceeded only by acute hospital costs) . Payments for laboratory services, especially for services provided to seniors, have seen particularly rapid increases in British Columbia .
The question this raises is what the causes are of laboratory spending increases. Administrative data cannot easily answer the question of health impact associated with this increase in laboratory spending, but it can be used to help diagnose the sources of cost pressure. Repeat testing and technological innovations are likely contributors but are unlikely to explain all of the increases [5–7]. Spending of health care dollars on chronic conditions and the tests associated both with diagnosing and managing those conditions may, on the other hand, help explain the upward trend.
More than half of the Canadian population has at least one chronic condition, and this rises to 81% of community-dwelling seniors . Previous studies have demonstrated that high users of health care services tend to be individuals with (often multiple) chronic conditions . In British Columbia, as in many other provinces, there are guidelines associated with the management of chronic conditions designed to assist physicians in providing consistent, evidence-based care . This includes recommendations for specific laboratory tests to diagnose and/or manage such conditions. It should be noted, the study intent is not an evaluation of adherence to guidelines. Instead, the guidelines are used simply to indicate the consensus on recommended laboratory testing for different chronic conditions. This paper addresses the question: to what extent can increases in laboratory expenditures be explained by testing that is consistent with guidelines for the management of chronic conditions?
Building on previous research, our analyses focus on British Columbia, as no national database exists to allow a more wide-ranging analysis. Our period of analysis is 1996/97 to 2005/06. We describe the extent to which population growth and aging, changes in chronic disease prevalence, and guideline-consistent ordering may explain increased expenditures for laboratory services.
Study population and data sources
Our analyses are of the entire population of British Columbia. The data were accessed through Population Data BC. Data were analyzed at the individual patient level using unique but study-specific codes that do not permit personal identification of either patients or physicians. Permission for data access was provided by the BC Ministry of Health. Ethics approval for this research was granted by the University of British Columbia Behavioural Research Ethics Board.
We accessed the following files: 1) a central demographics file for 1996/97 and 2005/06 providing information on age and sex of individuals and denominator information for the analyses; and 2) the fee-for-service payment files for 1995/96-1996/97 and 2004/05-2005/06 as a two year period is required to confirm a diagnosis. The fee-for-service data include the date of each visit, total amount paid, a unique study-specific physician identification number as well as a study-specific patient identification number, the physician specialty code, the diagnostic (ICD9) code most responsible for the visit, a fee item code which is a code used to identify each service provided by a practitioner, and a service code, which is a grouping of the fee items that indicates the type of services rendered by a practitioner. We removed the effects of fee changes over this period by valuing services provided in all years at the fee levels in effect on April 1, 2005/06, yielding fee-adjusted expenditures .
Classifying chronic conditions
The chronic conditions selected for this study were those for which specific guidelines developed by the BC Guidelines and Protocol Advisory Committee for the Medical Services Commission containing laboratory recommendations which came into place before 2006 . These were diabetes, hypertension, congestive heart failure, renal failure, liver disease, rheumatoid arthritis, osteoarthritis and dementia. Cancer was excluded because the spectrum of diseases encompassed by the term resulted in patient profiles with more widely varying patterns of use than those with the other chronic conditions. There are other chronic conditions not included in this analysis that will have associated laboratory tests. Increases in testing for those conditions will be captured as general increases, since our research question is focused on testing related to guidelines.
Chronic conditions were identified using the first 3 digits only of the International Classification of Disease (ICD-9) diagnosis codes from records of fee-for-service payments to general physicians, medical specialists and surgical specialists. Individuals were counted as having a chronic condition if they had at least two records showing a diagnosis for the same condition over a two-year period. This approach to determining treatment prevalence is consistent with prior research using administrative data to identify individuals with chronic conditions [8, 11, 12]. Treatment prevalence is used here to acknowledge the limitations of administrative data in identifying the prevalence of disease. While administrative data have been shown to be quite valid in for this purpose , we are only counting people as having disease if they received services from a physician who recorded relevant diagnoses on a billing record. Individuals with one record showing a diagnosis of a chronic condition were counted in a ‘potential’ category, as the diagnosis may have been recorded as something to be ruled out rather than being definitive. Payments from 1995/96 – 1996/97 were used to identify chronic conditions for the 1996/97 study population, and 2004/05-2005/06 payments were used to identify chronic conditions for the 2005/06 study population.
We summarized the information on chronic conditions and created five mutually exclusive groups to reflect an overall chronic disease profile for each individual: ‘No Guideline-Related Chronic Condition’, ‘Potential Chronic Condition’, ‘One’, ‘Two’ or ‘Three plus Chronic Conditions’. Individuals who had no record of a chronic condition diagnosis during the two-year period were classified in the first category. Those who received only one record showing a diagnosis for one or more conditions were classified into the “Potential Chronic Condition” group. Those with two or more records showing diagnoses for one condition (irrespective of “potential” conditions) were counted in the “one Chronic Condition” group, and so on. Individuals in these profile groups reflect categorization based on the chronic diseases with guidelines identified earlier, as per our research question, but may still have other chronic conditions outside of the scope of the study.
Medical laboratory testing in British Columbia is provided by community-based and hospital-based laboratories. This study included all laboratory tests paid for through the Medical Services Plan (MSP) of BC., i.e. not through hospital global budgets. The latter generally include only inpatient laboratory services, so this was not a major limitation.
Payments for laboratory testing were identified in the MSP data using service codes, regardless of the type of practitioner that billed for the item. A cluster of laboratory tests was created for each of the eight chronic conditions examined, based on the test recommendations made by the BC Guidelines and Protocol Advisory Committee (see Additional file 1 for details). All other tests were classified as not attributable to the chronic conditions we were examining. The primary base fee is an administrative cost (similar to a pharmacy dispensing fee) that is applicable under specified criteria to certain panel tests performed within the same facility. It could not be allocated to specific laboratory tests but consisted of a large portion of expenditure and therefore was treated separately. Total payments and payments for test subsets by chronic condition were then summed for each person in the study population. Some tests are associated with more than one chronic condition. Allocating individuals to the mutually exclusive chronic disease profile groups and summing separately avoided double-counting.
Where Total Lab Exp is the total expenditure on laboratory testing in a given year, Nc is the number of people with chronic conditions, Nnc is the number of people without guideline-related chronic conditions, $Testsr is the expenditure on recommended laboratory tests for chronic conditions and $Testso is the expenditure on other laboratory tests. Using this expression we can see that after controlling for changes in fees, overall population growth and population aging, changes in laboratory expenditures will come from changes in the number of people with chronic conditions (the treatment prevalence), changes in the expenditure on recommended tests for each person, or changes in per person expenditure on other tests. We isolate these three components in our analyses using direct standardization.
The cost of utilization
Dynamics of laboratory expenditures in British Columbia, 1996/97 and 2005/06
Total health care services expenditures (constant $)
Per capita health care services expenditures
Total lab expenditures (constant $)
Per capita lab expenditures
% Growth attributable
Growth attributable to change in age structure
Growth attributable to other changes
Demography, treatment prevalence and co-morbidities
In examining chronic condition guideline-consistent laboratory test expenditures, one factor that may contribute to overall expenditure growth is any population-level changes in the treatment prevalence of the identified conditions. If age-specific prevalence is increasing, then, laboratory-related expenditures would increase faster than what we would expect as a result of population aging alone.
Figure 1B then illustrates the rapid change in the proportion of individuals in the different chronic disease categories between 1996/97 and 2005/06. An increasing number of individuals were classified as having one or more chronic conditions in 2005/06. The largest percentage increase, which reached triple digits in all age categories except for the youngest age group of 0–24 years, was seen for individuals classified as having three or more chronic conditions.
Intensity of service use
The intensity of service use, as demonstrated by per capita costs, tells a more nuanced story. As expected, intensity of service use was higher among those with chronic conditions, and increased both with the number of co-morbidities and over time (Figure 2B). The pattern of care for individuals classified as having three or more chronic conditions is of particular note because this category had the most rapid change in expenditure over the period.
Chronic condition guideline-consistent laboratory expenditures
Disaggregation of laboratory expenditures in British Columbia, 1996/07 and 2005/06
Total expenditure for guideline-consistent laboratory tests
Total expenditure for other laboratory tests
Guideline-consistent lab expenditures by age group
Per capita guideline consistent laboratory tests
Per capita other laboratory tests
Per capita base fee
0 to 24
25 to 44
45 to 54
55 to 64
65 to 74
75 to 84
% Growth attributable
Growth attributable to other changes (from Table 1)
Growth attributable to changes in prevalence
Growth attributable to changes in utilization
Growth attributable to changes in guideline-consistent laboratory testing
Growth attributable to changes in other laboratory testing
Summing up the effects
As shown in Table 1, 37.4% (3.6% average annual increase) of growth in laboratory expenditures between 1996/9/7 and 2005/06 was attributable to changes other than aging and population growth. Of this, 13.9% (1.5% per year) was due to changes in treatment prevalence. Disaggregating the remaining 20.7% (2.1%) further, chronic condition guideline-consistent laboratory tests accounted for 11.3% (1.2%) of the growth and changes in other laboratory tests 8.5% (0.9%).
Spending on laboratory testing in BC increased 58.7% between 1996/97 and 2005/06. Many factors, including changes in technology, repeat testing and inappropriate utilization have been proposed as potential factors contributing to the increase in laboratory utilization . One additional explanation for expenditure increases is increased testing consistent with medical practice guidelines for diagnosing and monitoring patients with chronic conditions. We find that there was, indeed such an increase between 1996/97 and 2005/06, but that this explains only about one-third of the total increase, net of population growth and aging. Changes in treatment prevalence were equally important, and unexplained increases in other laboratory tests for people with and without the specific chronic conditions of interest were a large contributing factor.
Several changes in the clinical definition and screening of chronic conditions occurred between 1996/97 and 2005/06. For example, the clinical definition of diabetes shifted from a fasting plasma glucose level of greater than or equal to 7.8 to 7.0 mmol/L [13, 14]. For renal disease, serum creatinine levels of 176.8 μmol/L in men (eGFR of ~40 mL/min/1.73 m2 for a 40 year old man) resulting in referral to a renal team for dialysis assessment, changed to every patient with urine abnormalities and an eGFR <90 mL/min/1.73 m2 receiving immediate further assessment and management [15, 16]. Similarly, the recommended screening guidelines for Type 2 diabetes shifted to begin at age 41 instead of age 46 [13, 14]. There were no major changes in clinical definitions or screening guidelines for osteoarthritis or rheumatoid arthritis and for those conditions we see relatively stable prevalence across age groups over time11. These changes are only two factors that may be driving the increase in treatment prevalence for these chronic conditions, but they are surely significant ones. Once people are diagnosed with a condition, it should be no surprise that associated health care, and particularly guideline-consistent expenditures will follow.
There has also been a trend during this period toward diagnosing “pre-disease” states as part of screening guidelines, and a growing demand from patients for tests of their choosing even if the physician may not consider them beneficial. As previously mentioned, the first screen for diabetes is now recommended at earlier ages regardless of risk factors with a diagnosis of “impaired fasting glucose” as a “pre-diabetic” state at fasting plasma glucose levels of 6.1 mmol/L. These individuals being flagged as “at risk” subsequently require follow up tests until the disease manifests itself . So recommendations for increased population screening at ever earlier ages and the lower threshold for these pre-disease "conditions" that then leads to increased monitoring of individuals with no disease with testing could be another driver of the increase in other laboratory tests [14, 17, 18].
Much has been made of the aging population and its impact on the healthcare system. However, only 5.3% of the growth in laboratory expenditure over this period was actually attributable to a change in the age structure. More is spent on the elderly and this trend has continued between 1996/97 to 2005/06. However, the impact of an increasing treatment prevalence of age-specific chronic conditions, and particularly of an increasing age-specific prevalence of patients with multiple co-morbidities, is far more important.
There are some limitations to this study. The fee-for-service physician data do not include information on services paid for through alternative payment arrangements such as salaries, sessional payments, or contractual arrangements. This does not affect the laboratory payments, which are all by fee-for-service for patients outside of acute care, but may affect our classification of these individuals into the chronic disease categories. In addition, our analysis of chronic conditions was not exhaustive, but rather focused only on those conditions that became the subject of incentive programs for primary care in BC. The “other” laboratory tests, while not guideline-recommended for these specific chronic conditions, may still be appropriate for other conditions. Therefore individuals with other potentially prevalent chronic conditions that were outside the scope of the conditions selected for this study would be classified as ‘no guideline-related chronic condition’, which limits our interpretation of people in this category.
Laboratory testing is one of the fastest growing areas of physician service provision. In British Columbia, there was just under $100 million in “new” laboratory expenditures in 2005/06 compared to a 1996/97 base of $167 million. This amounts to a 5.3% average annual increase in expenditure, or 3.6% per year after removing the effects of population growth and aging. Our primary research question was the extent to which diligence – testing consistent with guideline-indicated care – could explain this increase. The answer is that about one-third of the increase, or about 1.2% per year, can be attributed to changes in guideline-consistent test ordering. Surprisingly important are designation – the increased likelihood of being diagnosed with a chronic condition – at 1.5% per year, and drift – the general increase in laboratory expenditures, including expenditures for people without these guideline-related chronic conditions - at 0.9% per year. This suggests that future research might productively focus on the last of these contributing components, with an emphasis on the extent to which the increase in designation and the general increase in testing affects diagnosis or subsequent treatment.
Medical Service Plan
International Classification of Diseases
Estimated glomerular filtration rate.
We acknowledge Dawn Mooney for her work on the development and design of the study figures and Margaret McGregor for her thoughtful and critical review of the manuscript. The research reported here and all its authors were supported by a Canadian Institutes of Health Research Operating Grant.
- Boileau L: Canadians Fear Rising Health Care Costs Unsustainable. 2010, Canada: News Wire
- Mayeda A, De Souza M, Cohen T: Conservatives and Liberals each say they care more about health care. 2011, Toronto, Canada: The National Post
- Canadian Institute for Health Information: National Health Expenditure Trends, 1975 to 2010. 2010, Ottawa: CIHI
- McGrail KM, Evans RG, Barer ML, Kerluke KJ, McKendry R: Diagnosing senescence: Contributions to physician expenditure increases in British Columbia, 1996/97 to 2005/06. Healthcare Policy. 2011, 7 (1): 41-54.PubMed CentralPubMed
- Van Walraven C, Cernat G, Austin PC: Effect of provider continuity on test repetition. Clin Chem. 2006, 52 (12): 2219-2228. 10.1373/clinchem.2006.072934.View ArticlePubMed
- Schwartz WB: The inevitable failure of current cost containment strategies. Why they can provide only temporary relief. JAMA. 1987, 257: 220-228. 10.1001/jama.1987.03390020086032.View ArticlePubMed
- Robinson A: Rationale for cost-effective laboratory medicine. Clinc Micro Rev. 1994, 7 (2): 185-199.
- Broemeling AM, Watson D, Black C: Centre for Health Services and Policy Research. Chronic conditions and co-morbidity among residents of British Columbia. 2005, Report No: chspr05-08. Sponsored by The BC Ministry of Health
- Broemeling AM, Watson D, Prebtani F: Population patterns of chronic health conditions, co-morbidity and healthcare use in Canada: implications for policy and practice. Healthc Q. 2008, 11 (3): 70-76.View ArticlePubMed
- BC Ministry of Health Chronic Disease Guidelines: Available from: http://www.bcguidelines.ca/submenu_chronic_disease.html
- Kopec J, Rahman M, Sayre E, Cibere J, Flanagan W, Aghajanian J, et al: Trends in physician diagnosed osteoarthritis incidence in an administrative database in British Columbia, Canada, 1996–1997 through 2003–04. Am College Rheum. 2008, 59 (7): 929-934.
- Lix L, Yogendran M, Mann J: Defining and Validating Chronic Diseases: An Administrative Data Approach. An Update with ICD-10-CA. 2008, Winnipeg, MB: Manitoba Centre for Health Policy, University of Manitoba
- Meltzer S, Leiter L, Daneman D, Gerstein H, Lau D, Ludwig S, et al: Clinical practice guidelines for the management of diabetes in Canada. Canadian Med Assoc J. 1998, 159 (8): 1-29.
- Canadian Diabetes Association Clinical Practice Guidelines Expert Committee: Canadian diabetes association 2003 clinical practice guidelines for the prevention and management of diabetes in Canada. Can J Diabetes. 2003, 27 (2): 1-163.
- Obrador G, Peirera B: Early referral to the nephrologist and timely initiation of renal replacement therapy: a paradigm shift in the management of patients with chronic renal failure. Am J Kidney Dis. 1998, 31 (3): 398-417. 10.1053/ajkd.1998.v31.pm9506677.View ArticlePubMed
- Craven N: Management of chronic kidney disease in the primary care setting. BC Med J. 2005, 47 (6): 296-299.
- Carlsen B, Norheim OF: "Saying no is no easy matter" a qualitative study of competing concerns in rationing decisions in general practice. BMC Health Serv Res. 2005, 5: 70-10.1186/1472-6963-5-70.PubMed CentralView ArticlePubMed
- Brett AS, McCullough LB: Addressing requests by patients for nonbeneficial interventions. JAMA. 2012, 307 (2): 149-150. 10.1001/jama.2011.1999.View ArticlePubMed
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6963/12/472/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.