- Research article
- Open Access
Development and feasibility of a personalized, interactive risk calculator for knee osteoarthritis
BMC Musculoskeletal Disorders volume 16, Article number: 312 (2015)
The incidence of knee osteoarthritis (OA) is rising. While several risk factors have been associated with the development of knee OA, this information is not readily accessible to those at risk for osteoarthritis. Risk calculators have been developed for several prevalent chronic conditions but not for OA. Using published evidence on established risk factors, we developed an interactive, personalized knee OA risk calculator (OA Risk C) and conducted a pilot study to evaluate its acceptability and feasibility.
We used the Osteoarthritis Policy (OAPol) Model, a validated, state-transition simulation of the natural history and management of OA, to generate data for OA Risk C. Risk estimates for calculator users were based on a set of demographic and clinical factors (age, sex, race/ethnicity, obesity) and select risk factors (family history of knee OA, occupational exposure, and history of knee injury). OA Risk C presents personalized risk of knee OA in several ways to maximize understanding among a wide range of users. We conducted a study of 45 subjects in a primary care setting to establish the feasibility and acceptability of the OA risk calculator. Pilot study participants were asked several questions regarding ease of use, clarity of presentation, and clarity of the graphical representation of their risk. These questions used a five-level agreement scale ranging from strongly disagree to strongly agree.
OA Risk C depicts information about users’ risk of symptomatic knee OA in 5 year intervals. Study participants estimated their lifetime risk at 38 %, while their actual lifetime risk, as estimated by OA Risk C, was 25 %. Eighty-four percent of pilot study participants reported that OA Risk C was easy to understand, and 89 % agreed that the graphs depicting their risk were clear and comprehensible.
We have developed a personalized, computer-based OA risk calculator that is easy to use. OA Risk C may be utilized to estimate individuals’ knee OA risk and to deliver educational and behavioral interventions focused on osteoarthritis risk reduction.
Knee osteoarthritis (OA) is a condition that affects the bones, cartilage, and other tissues in the knee and often leads to pain and physical limitation. While the severity of pain fluctuates during the course of the disease that lasts on average 26 years from the time of diagnosis, it is unlikely that symptoms disappear completely [1, 2]. The disease affects nearly 9.3 million US adults, accounting for $27 billion in annual health care expenses [3, 4]. While generally considered a disorder of aging, the incidence of knee OA in younger adults is rising, with about 50 % of diagnoses occurring in patients younger than 55 . While not every radiographic change leads to the development of the symptomatic disease, those with symptoms often seek medical care and ultimately consider total knee replacement, due to limited non-surgical treatment options [6, 7].
A number of risk factors have been identified for knee OA. Older age, female sex, obesity, occupational exposure, and history of knee injury have been associated with the development of the disease [8–10]. With the greater obesity epidemic  and an increasing number of traumatic knee injuries , the clinical and economic burden of knee OA will likely continue to grow. In addition to accumulation of risk factors, aging of the population plays a key role in the increasing prevalence of knee OA. Despite the increasing incidence of OA and the substantial disability associated with the disease, to our knowledge, few studies have focused on primary prevention efforts [13–17]. While OA prevention across all ages is important, preventive interventions focused primarily on older populations may have a limited effect due to prolonged exposure to risk factors earlier in life. Primary prevention efforts that raise awareness of modifiable OA risk factors in younger populations may offer a greater impact.
Online risk calculators have been developed for several diseases, including heart disease, cancer, diabetes, stroke, emphysema, and osteoporosis [18–22]. These tools request that users enter demographic and risk factor information. The tools then provide an estimate of the user’s risk for developing a particular illness. The American Heart Association and American College of Cardiology have published online and mobile versions of their risk calculator for public use.
Websites hosting risk calculators are highly trafficked. In 2006, the Your Disease Risk website , which estimates visitors’ risk of developing seven different diseases, including cancer, diabetes, and heart disease, recorded 2000 visitors per day on average . In a 2013 survey of over 3000 US adults, the Pew Research Internet Project found that 72 % of internet users had consulted online sources for health information in the past year . To our knowledge, there is no online risk calculator for osteoarthritis. The availability of a risk assessment tool for OA would raise awareness of modifiable risk factors for the condition. We sought to develop an interactive, personalized, computer-based risk calculator for knee OA (OA Risk C). We tested the feasibility and acceptability of the calculator in a sample of OA-free patients in a primary care setting.
Risk calculator development and derivation of OA risk
We used data generated by the Osteoarthritis Policy (OAPol) Model to create a computer-based risk calculator for knee OA (OA Risk C). OA Risk C allows users to enter their demographic and risk factor information, including family history of osteoarthritis, exposure to occupational risk factors (such as squatting and kneeling), and history of knee injury. Users are matched to one of 2016 OAPol simulations, which provides an estimate of their 5, 10, 15, 20, 25, 30-year, and lifetime risk of knee OA and total knee replacement (TKR).
Structure of the OAPol model
OAPol is a validated, published, state-transition, Monte Carlo model of the natural history and management of knee OA [5, 6, 26, 27]. “State transition” implies that the model follows each person’s history as a sequence of annual transitions from one health state to another. Health states are designed to be predictive of clinical prognosis related to knee OA, risk for developing comorbidities, and mortality. The OAPol Model considers five major comorbidities (cardiovascular disease, diabetes mellitus, cancer, chronic obstructive pulmonary disease, and other musculoskeletal diseases). The prevalence and incidence of each of these comorbidities are stratified by age, sex, race/ethnicity, and obesity. Prevalence of cardiovascular disease is further stratified by diabetes mellitus status. Persons who develop comorbidities have higher risk for death. The explicit accounting for competing risks from other comorbidities is a special feature of the OAPol model.
Each person is followed from the time of entry into the OAPol Model until death. Upon entry into the model, a person is randomly assigned age, sex, race/ethnicity, and body mass index (BMI) from a set of user-specified probability distributions. At the start of each annual cycle, the model records the patient’s age, obesity status (defined by BMI), symptomatic knee osteoarthritis status, and presence of specific comorbidities. The model then uses these characteristics, in addition to sex and race/ethnicity, to determine the probabilities that indicate development of symptomatic knee osteoarthritis, progression of symptomatic knee osteoarthritis, development of a new comorbidity, and death in the subsequent year. Transition probabilities are derived from literature or secondary analyses of data from national- or population-based cohorts and translated into risk functions for the model. Details of transitional probabilities derivation have been previously published . Upon the person’s death, summary statistics are recorded and a new person enters the model. A large number of individual simulations are aggregated to obtain stable estimates of OA and TKR rates. The size of the hypothetical cohort, N, is selected to ensure stable population estimates. For the purposes of establishing stable estimates for risk of knee OA, we used N = 1,000,000 for each model run.
We conducted 2016 model simulations using each unique combination of seven input parameters. These included starting age (25–45), sex (male, female), race/ethnicity (White, Black, Hispanic), obesity status (obese, non-obese), family history of knee OA (present, absent), occupational exposure to OA risk (present, absent), and history of knee injury (present, absent) (Table 1).
We defined incident knee osteoarthritis as Kellgren-Lawrence (K-L) grade 2 accompanied by knee pain. Base incidence rates were derived from the National Health Interview Survey and stratified by age, sex, and obesity. Details on incidence rates derivation have been previously published . Upon development of symptomatic knee OA, subjects could progress through K-L grades 2 through 4 based on probabilities derived from the Johnston County Osteoarthritis Project, a cohort study of OA  and calibrated to published rates of annual knee OA progression . Progression probabilities were stratified by sex, obesity, and current K-L grade (Table 1). Annual incidence of TKR was derived from two multi-centered longitudinal studies: MOST (Multicenter Osteoarthritis Study) and OAI (Osteoarthritis Initiative) [31, 32]. Further details of incidence rate derivation have been published elsewhere .
To account for increased risk of developing knee OA for those with a family history of knee OA, occupational exposure, obesity, or history of knee injury, we used the published data from Zhang et al. . Based on the data from Zhang et al., knee injury increased OA incidence by a factor of 2.39. Family history of OA increased OA incidence by a factor of 1.72, and occupational risks by a factor of 1.28 (Table 1). Risk factors were assumed to be independent and multiplicative. As noted above, age, sex and obesity status were estimated directly based upon National Health Interview Survey data . For example, to incorporate the impact of obesity, we first derived the incidence of knee OA among those who are not obese. This was done by dividing the age/sex stratified incidence of knee OA by the sum of the prevalence of obesity multiplied by the increased risk of OA due to obesity and prevalence of non-obesity. To ensure that we did not overinflate the risk of OA among obese persons, we applied increase in risk to the incidence of OA among those who are non-obese persons, derived as described above. We used the incidence rate among non-obese individuals as the basis for the risk adjustment for other risk factors.
Risk calculator design and user interface
OA Risk C users input demographic and risk factor information, including age, sex, race/ethnicity, height, and weight. Questions about risk factors are asked in such a way that someone unfamiliar with OA could answer them. Family history of osteoarthritis is determined by asking: “Do your parents, siblings, or grandparents have any of the following: Arthritis (osteoarthritis), Knee or hip replacement, Finger nodes?” Users are asked to check all that apply, including “Don’t Know” (Fig. 1). Users have the option of viewing a popup image of finger nodes if they are unfamiliar with the term. If the user selects any of the first three options (arthritis, knee or hip replacement, finger nodes), he or she is considered to have a family history of OA. Occupational risk is determined using the question: “Have you been exposed to occupational risk factors associated with knee OA such as kneeling, squatting, or lifting?” History of knee injury is determined by asking: “Have you previously had a serious knee injury that limited your ability to walk for at least 7 days?” This question conforms to the definition of knee injury used in the Osteoarthritis Initiative, a multi-center cohort study of knee OA .
Users are shown the results of their risk calculation in several different ways. The first page contains a simple graphical representation of their 5, 10, 15, 20, 25, 30-year, and lifetime risk of developing knee osteoarthritis and total knee replacement (Fig. 2). We also present risk information in icon array form, which users can access by clicking “What does my risk mean?” An example of this pictorial representation of the risk of developing knee OA is shown in Fig. 3. Then, users are taken to the interactive component of the risk calculator, where they can learn how different factors contribute to their risk of developing knee OA. Users are able to adjust their risk factors on an interactive graph. Four dropdown menus allow users to add or remove each risk factor and see how their risk assessment changes (Fig. 4). For example, a non-obese person can view their risk of developing osteoarthritis if they were obese. Users are also able to see which component of their risk is due to added risk factors, and which component simply reflects the underlying risk experienced by someone of their demographic group with no additional risk factors. As on the previous page, users are given the option to view this information in icon array form. Finally, users are shown a graphical comparison of how their personal risk of developing knee OA and undergoing TKR compares to that of the average American with no risk factors (Fig. 5).
Pilot study of risk calculator clinical implementation
In order to determine the feasibility and acceptability of the OA Risk Calculator, we enrolled 45 subjects at a primary care clinic within a tertiary medical center. Both patients and non-patients in the waiting room of the clinic were invited to participate. Those who spoke English, were between the ages of 25 and 45 years, had not been diagnosed with arthritis by a physician, had access to a computer and the Internet, and were willing to provide their email address were eligible for the study. After agreeing to participate, eligible subjects read and signed a digital consent form. They were given a convertible laptop (which functions as both a laptop computer and tablet) and instructed to follow the directions on the computerized risk calculator until the completion page appeared. Because the aim of pilot testing was to determine the usability of the calculator, the research assistant administering the calculator asked subjects to refrain from commenting or asking questions until the end of the survey if possible. After using OA Risk C, we provided study participants with a brochure about OA that included suggestions for minimizing exposure to modifiable OA risk factors. Patients were given a 2-h parking voucher for their participation or an Amazon gift card of equivalent value ($9) if they did not park.
To measure feasibility and acceptability of the calculator, we asked subjects to rate its ease of use and comprehensibility on a 5-point agreement scale with the following options: Strongly Disagree, Disagree, Neutral, Agree, and Strongly Agree. Participants were also asked for suggestions for improvement and general feedback. This study was approved by the Partners Healthcare Institutional Review Board (protocol 2014P000844).
We asked 227 people in the clinic waiting room to take part in the study. Two-hundred and nine (92 %) were English-speakers, and of those, 118 (56 %) agreed to participate. Seventy-three (62 %) of those who agreed were ineligible: 7 were not patients at the clinic and were approached before we gained approval to recruit non-patients for the study; 47 were not between the ages of 25 and 45 years; 15 had been diagnosed with arthritis; 3 were excluded because of lapses in wireless internet access; and 1 was excluded because they had insufficient time to complete the study (Fig. 6).
Forty-five patients were enrolled and completed the OA Risk C assessment. Average age was 34 (standard deviation [SD] 6) years, and 87 % were females. Thirty-one percent identified themselves as White, 27 % as Black, and 36 % as Hispanic. Forty-six percent had a Bachelor’s degree or higher. Forty-four percent reported having a family member with arthritis; 36 % reported having an occupational exposure, shown to be associated with higher incidence of osteoarthritis; and 7 % reported history of knee injury (Table 2). More than one third of subjects (38 %) had at least two risk factors for knee OA, and about two thirds had at least one risk factor. On average, study participants overestimated their lifetime risk of developing knee OA. The average lifetime risk estimate was 38 %, while average lifetime risk as determined by the calculator was 25 %.
Overall, participants responded favorably to questions about the usability and clarity of the risk calculator. Eighty-seven percent of participants reported agreement with the statement, “The risk calculator was easy to use.” Eighty-four percent agreed that their risk of developing knee osteoarthritis was clear and easy to understand, and 89 % stated that the graphical representation of OA risk was clear and easy to understand (Fig. 7).
Rated ease of use was high across all age, sex, and race/ethnicity groups. Self-reported understanding of OA risk was generally high, ranging from 100 % in Whites to 87 % in Hispanics and 75 % in Blacks. Men reported more difficulty understanding the graphical representation of their OA risk – 17 % of men compared to 3 % of women did not agree that the graphical representation of their risk of developing knee OA was clear and easy to understand.
We have developed an Osteoarthritis Risk Calculator and assessed its ease of use and feasibility in a primary care setting. Overall, subjects found that the calculator was clear and that the results were comprehensible. These findings suggest that OA Risk C may be utilized successfully by a wider audience.
Risk calculators have been developed for several conditions, including heart disease, cancer, diabetes, stroke, emphysema, and osteoporosis [18–22]. Many of these risk calculators have been integrated into clinical practice. Recommendations for statin utilization were updated in 2013 to account for calculated risk [34, 35], and the American Heart Association and American College of Cardiology have encouraged public use of their risk calculator. The Carotid Risk Assessment Tool, which allows physicians to view estimated 2-year mortality for patients with carotid artery stenosis, was incorporated into an electronic medical record. Overall, physicians felt that the tool was useful when weighing the risks and benefits of revascularization surgery for patients with carotid artery stenosis and that the tool aided patients in their decision-making .
While most risk calculators have been well received by patients, reactions to the results of risk calculators vary. One study showed that diabetic patients using a cardiovascular risk calculator had a diverse range of responses to viewing their risk of experiencing a heart attack and/ or stroke; some reported feeling distressed when their risk was substantially higher than expected . Another study found that in cohort of 50 patients ranging in age from 27 to 84 years old, many had suboptimal understanding of the connection between high cholesterol and cardiovascular disease (CVD) risk. When presented with results from a cardiovascular risk-adjusted age calculator, some study participants felt that their newfound knowledge would motivate positive behavior change . Krones et al. conducted a randomized trial to assess the effect of an intervention including a paper-based CVD risk calculator and information booklet on shared decision-making between patients and physicians in a primary care setting. Compared to the control arm, patients in the intervention group had higher satisfaction and involvement in decision-making , indicating that personalized health information may serve to activate patients. Taken together, these previous studies suggest that viewing personalized risk information may lead to a more educated and activated patient population that is motivated for behavior change.
The OA Risk Calculator was well-received overall. Patients reported verbally that learning about their risk of developing OA was helpful and interesting, and the majority of participants believed the calculator was easy to use and that the results were easy to understand. Research suggests that even highly educated individuals are poor at converting between percentages and proportions in the context of risk . Therefore, we used multiple presentations of OA risk, including an icon array form, which shows a pictorial representation of each user’s risk of developing knee OA (Fig. 3).
Primary prevention interventions focused on middle-aged and older populations may have a limited effect due to prolonged exposure to risk factors earlier in life. Educating younger populations about modifiable knee OA risk factors may have an even greater impact by prompting younger persons to minimize their exposure to risk factors. Injury prevention programs have been shown to reduce the number of traumatic knee injuries in sports participants [41–43] and might be more widely used if younger persons were aware that knee injury is a risk factor for OA. Similarly, several weight management interventions developed within the context of OA [13, 44, 45] may be extended to younger persons who are overweight or obese and who wish to lose weight to reduce their risk of developing knee OA.
This study has certain limitations. Because the OAPol model does not contain data for persons younger than 25 or for those identifying as a race/ethnicity other than Black, White, or Hispanic, we were unable to accurately estimate risk for these populations. Only those aged 25 to 45 years were included in this pilot study, and those who identified as a race/ethnicity other than Black, White, or Hispanic were able to participate in the study with the knowledge that the risk information presented would be that of someone with their risk factors who identifies as White. The data used in the OAPol model to generate our risk estimates were derived from multiple data sources. In the analysis we used the best available data. While our current risk ratios are derived from the 2011 report from the Nottingham study, these observations have been confirmed in the most recent meta-analysis published in 2015 . All estimates carry some uncertainty. We minimized uncertainty by conducting a large number of simulations and using data from large cohort studies.
Since the increase in risk due to occupational exposure, history of knee injury, or family history of knee OA was applied to basic incidence rates of non-obese persons, it may lead to some overestimation. The prevalence of these risk factors in the population does not exceed 10 %, so the bias due to overestimation is not substantial. It ranges from 2 % for those with the occupational exposure to 14 % among those with history of knee injury. Additionally, we have assumed that risk factors are independent and multiplicative. If this assumption is not satisfied, the estimated risk among persons with multiple risk factors may be overestimated. To address this limitation, we will include a disclaimer at the footnote of the calculator. Lastly, there is limited information available showing that reducing exposure to risk factors of knee OA will impact risk in a meaningful way. To address this limitation, we carefully described the impact of the risk factor by stating that the comparison is between persons with and without the risk factor. In addition, we will include a disclaimer stating that there is limited data on the reduction of the risk among those who modify a risk factor such as obesity.
Despite these limitations, this study has certain strengths. It is the first to our knowledge that describes the development and acceptability of a risk calculator for osteoarthritis. OA Risk C is unique in its flexibility and adaptability over time. Because it relies on outputs from the OAPol model, it can be updated whenever we update or change the model as new data become available. Moreover, we have illustrated the feasibility and comprehensibility of OA Risk C in a pilot study of 45 subjects in a primary care setting. This suggests that the OA risk calculator may be successfully used by a wider audience. Future research may focus on determining whether or not viewing personalized risk of developing knee OA prompts behavior change to minimize modifiable risk factors.
We have developed an Osteoarthritis Risk Calculator (OA Risk C) and illustrated its acceptability and feasibility in a pilot study of 45 subjects. This risk assessment tool may be disseminated to a wider audience in order to educate the general population about their personalized risk of developing knee OA and present interventions to minimize exposure to risk factors. Doing so may motivate behavior changes that reduce the incidence and burden of knee OA.
- OA Risk C:
Osteoarthritis risk calculator
Total knee replacement
Collins JE, Katz JN, Dervan EE, Losina E. Trajectories and risk profiles of pain in persons with radiographic, symptomatic knee osteoarthritis: data from the osteoarthritis initiative. Osteoarthritis Cartilage. 2014;22(5):622–30. doi:10.1016/j.joca.2014.03.009.
Felson D, Niu J, Sack B, Aliabadi P, McCullough C, Nevitt MC. Progression of osteoarthritis as a state of inertia. Ann Rheum Dis. 2013;72(6):924–9. doi:10.1136/annrheumdis-2012-201575.
Lawrence RC, Felson DT, Helmick CG, Arnold LM, Choi H, Deyo RA, et al. Estimates of the prevalence of arthritis and other rheumatic conditions in the United States, Part II. Arthritis Rheum. 2008;58(1):26–35. doi:10.1002/art.23176.
Losina ENN, Holt HL, Reichmann WM, Hunter DJ, Suter LG, Solomon DH. Cost-Effectiveness of ACR Guideline-Based Care and Lifetime Direct Medical Costs Attributable to Knee OA Management in the US [abstract]. Arthritis Rheum. 2009;60(10):1177.
Losina E, Weinstein AM, Reichmann WM, Burbine SA, Solomon DH, Daigle ME, et al. Lifetime risk and age at diagnosis of symptomatic knee osteoarthritis in the US. Arthritis Care Res (Hoboken). 2013;65(5):703–11. doi:10.1002/acr.21898.
Losina E, Paltiel AD, Weinstein AM, Yelin E, Hunter DJ, Chen SP, et al. Lifetime medical costs of knee osteoarthritis management in the United States: impact of extending indications for total knee arthroplasty. Arthritis Care Res (Hoboken). 2015;67(2):203–15. doi:10.1002/acr.22412.
Weinstein AM, Rome BN, Reichmann WM, Collins JE, Burbine SA, Thornhill TS, et al. Estimating the burden of total knee replacement in the United States. J Bone Joint Surg Am. 2013;95(5):385–92. doi:10.2106/JBJS.L.00206.
Felson DT, Anderson JJ, Naimark A, Walker AM, Meenan RF. Obesity and knee osteoarthritis. The Framingham Study. Ann Intern Med. 1988;109(1):18–24.
Blagojevic M, Jinks C, Jeffery A, Jordan KP. Risk factors for onset of osteoarthritis of the knee in older adults: a systematic review and meta-analysis. Osteoarthritis Cartilage. 2010;18(1):24–33. doi:10.1016/j.joca.2009.08.010.
Felson DT, Hannan MT, Naimark A, Berkeley J, Gordon G, Wilson PW, et al. Occupational physical demands, knee bending, and knee osteoarthritis: results from the Framingham Study. J Rheumatol. 1991;18(10):1587–92.
Kelly T, Yang W, Chen CS, Reynolds K, He J. Global burden of obesity in 2005 and projections to 2030. Int J Obes (Lond). 2008;32(9):1431–7. doi:10.1038/ijo.2008.102.
Louw QA, Manilall J, Grimmer KA. Epidemiology of knee injuries among adolescents: a systematic review. Br J Sports Med. 2008;42(1):2–10. doi:10.1136/bjsm.2007.035360.
Messier SP, Mihalko SL, Legault C, Miller GD, Nicklas BJ, DeVita P, et al. Effects of intensive diet and exercise on knee joint loads, inflammation, and clinical outcomes among overweight and obese adults with knee osteoarthritis: the IDEA randomized clinical trial. JAMA. 2013;310(12):1263–73. doi:10.1001/jama.2013.277669.
Wang C, Schmid CH, Hibberd PL, Kalish R, Roubenoff R, Rones R, et al. Tai Chi is effective in treating knee osteoarthritis: a randomized controlled trial. Arthritis Rheum. 2009;61(11):1545–53. doi:10.1002/art.24832.
Pavelka K, Gatterova J, Olejarova M, Machacek S, Giacovelli G, Rovati LC. Glucosamine sulfate use and delay of progression of knee osteoarthritis: a 3-year, randomized, placebo-controlled, double-blind study. Arch Intern Med. 2002;162(18):2113–23.
Tanaka R, Ozawa J, Kito N, Moriyama H. Effects of exercise therapy on walking ability in individuals with knee osteoarthritis: A systematic review and meta-analysis of randomised controlled trials. Clin Rehabil. 2015. doi:10.1177/0269215515570098.
Runhaar J, van Middelkoop M, Reijman M, Willemsen S, Oei EH, Vroegindeweij D, et al. Prevention of knee osteoarthritis in overweight females; the first preventive randomized controlled trial in osteoarthritis. Am J Med. 2015. doi:10.1016/j.amjmed.2015.03.006.
Nobel L, Mayo NE, Hanley J, Nadeau L, Daskalopoulou SS. MyRisk_Stroke Calculator: A Personalized Stroke Risk Assessment Tool for the General Population. J Clin Neurol. 2014;10(1):1–9. doi:10.3988/jcn.2014.10.1.1.
Levy AG, Sonnad SS, Kurichi JE, Sherman M, Armstrong K. Making sense of cancer risk calculators on the web. J Gen Intern Med. 2008;23(3):229–35. doi:10.1007/s11606-007-0484-x.
Sheridan S, Pignone M, Mulrow C. Framingham-based tools to calculate the global risk of coronary heart disease: a systematic review of tools for clinicians. J Gen Intern Med. 2003;18(12):1039–52.
Heikes KE, Eddy DM, Arondekar B, Schlessinger L. Diabetes Risk Calculator: a simple tool for detecting undiagnosed diabetes and pre-diabetes. Diabetes Care. 2008;31(5):1040–5. doi:10.2337/dc07-1150.
Harle CA, Downs JS, Padman R. A clustering approach to segmenting users of internet-based risk calculators. Methods Inf Med. 2011;50(3):244–52. doi:10.3414/ME09-01-0080.
Your Disease Risk. Washington University in St. Louis School of Medicine. http://www.yourdiseaserisk.wustl.edu/. Accessed 24 April 2015.
Waters EA, Sullivan HW, Nelson W, Hesse BW. What is my cancer risk? How internet-based cancer risk assessment tools communicate individualized risk estimates to the public: content analysis. J Med Internet Res. 2009;11(3), e33. doi:10.2196/jmir.1222.
Fox S, Duggan M. Health Online 2013. Pew Research Center. 2013. http://www.pewinternet.org/2013/01/15/health-online-2013/. Accessed 24 April 2015.
Losina E, Walensky RP, Reichmann WM, Holt HL, Gerlovin H, Solomon DH, et al. Impact of obesity and knee osteoarthritis on morbidity and mortality in older Americans. Ann Intern Med. 2011;154(4):217–26. doi:10.7326/0003-4819-154-4-201102150-00001.
Losina E, Burbine SA, Suter LG, Hunter DJ, Solomon DH, Daigle ME, et al. Pharmacologic regimens for knee osteoarthritis prevention: can they be cost-effective? Osteoarthritis Cartilage. 2014;22(3):415–30. doi:10.1016/j.joca.2014.01.005.
National Health Interview Survey 2007–2008. Centers for Disease Control and Prevention, National Center for Health Statistics, US Department of Health and Human Services. Available from: http://www.cdc.gov/nchs/nhis.htm. Accessed: 13 Mar 2014.
Jordan JM, Helmick CG, Renner JB, Luta G, Dragomir AD, Woodard J, et al. Prevalence of knee symptoms and radiographic and symptomatic knee osteoarthritis in African Americans and Caucasians: the Johnston County Osteoarthritis Project. J Rheumatol. 2007;34(1):172–80.
Cooper C, Snow S, McAlindon TE, Kellingray S, Stuart B, Coggon D, et al. Risk factors for the incidence and progression of radiographic knee osteoarthritis. Arthritis Rheum. 2000;43(5):995–1000. doi:10.1002/1529-0131(200005)43:5<995::AID-ANR6>3.0.CO;2-1.
Osteoarthritis Initiative (OAI). Available from: http://oai.epi-ucsf.org/datarelease/default.asp. Accessed: 3 Jan 2012.
Multicenter Osteoarthritis Study (MOST). Cordinating Center, University of California San Francisco. Available from: http://most.ucsf.edu/. Accessed: 3 Jan 2012.
Zhang W, McWilliams DF, Ingham SL, Doherty SA, Muthuri S, Muir KR, et al. Nottingham knee osteoarthritis risk prediction models. Ann Rheum Dis. 2011;70(9):1599–604. doi:10.1136/ard.2011.149807.
Goff Jr DC, Lloyd-Jones DM, Bennett G, Coady S, D'Agostino Sr RB, Gibbons R, et al. 2013 ACC/AHA guideline on the assessment of cardiovascular risk: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2014;63(25 Pt B):2935–59. doi:10.1016/j.jacc.2013.11.005.
Goff Jr DC, Lloyd-Jones DM, Bennett G, Coady S, D'Agostino RB, Gibbons R, et al. 2013 ACC/AHA guideline on the assessment of cardiovascular risk: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2014;129(25 Suppl 2):S49–73. doi:10.1161/01.cir.0000437741.48606.98.
Faerber AE, Horvath R, Stillman C, O'Connell ML, Hamilton AL, Newhall KA, et al. Development and pilot feasibility study of a health information technology tool to calculate mortality risk for patients with asymptomatic carotid stenosis: the Carotid Risk Assessment Tool (CARAT). BMC Med Inform Decis Mak. 2015;15(1):20. doi:10.1186/s12911-015-0141-y.
Nolan T, Dack C, Pal K, Ross J, Stevenson FA, Peacock R, et al. Patient reactions to a web-based cardiovascular risk calculator in type 2 diabetes: a qualitative study in primary care. Br J Gen Pract. 2015;65(632):e152–60. doi:10.3399/bjgp15X683953.
Goldman RE, Parker DR, Eaton CB, Borkan JM, Gramling R, Cover RT, et al. Patients' perceptions of cholesterol, cardiovascular disease risk, and risk communication strategies. Ann Fam Med. 2006;4(3):205–12. doi:10.1370/afm.534.
Krones T, Keller H, Sonnichsen A, Sadowski EM, Baum E, Wegscheider K, et al. Absolute cardiovascular disease risk and shared decision making in primary care: a randomized controlled trial. Ann Fam Med. 2008;6(3):218–27. doi:10.1370/afm.854.
Lipkus IM, Samsa G, Rimer BK. General performance on a numeracy scale among highly educated samples. Med Decis Making. 2001;21(1):37–44.
Hewett TE, Lindenfeld TN, Riccobene JV, Noyes FR. The effect of neuromuscular training on the incidence of knee injury in female athletes. A prospective study. Am J Sports Med. 1999;27(6):699–706.
LaBella CR, Huxford MR, Grissom J, Kim KY, Peng J, Christoffel KK. Effect of neuromuscular warm-up on injuries in female soccer and basketball athletes in urban public high schools: cluster randomized controlled trial. Arch Pediatr Adolesc Med. 2011;165(11):1033–40. doi:10.1001/archpediatrics.2011.168.
van Beijsterveldt AM, van de Port IG, Krist MR, Schmikli SL, Stubbe JH, Frederiks JE, et al. Effectiveness of an injury prevention programme for adult male amateur soccer players: a cluster-randomised controlled trial. Br J Sports Med. 2012;46(16):1114–8. doi:10.1136/bjsports-2012-091277.
Miller GD, Rejeski WJ, Williamson JD, Morgan T, Sevick MA, Loeser RF, et al. The Arthritis, Diet and Activity Promotion Trial (ADAPT): design, rationale, and baseline results. Control Clin Trials. 2003;24(4):462–80.
Bliddal H, Leeds AR, Christensen R. Osteoarthritis, obesity and weight loss: evidence, hypotheses and horizons - a scoping review. Obes Rev. 2014;15(7):578–86. doi:10.1111/obr.12173.
Silverwood V, Blagojevic-Bucknall M, Jinks C, Jordan JL, Protheroe J, Jordan KP. Current evidence on risk factors for knee osteoarthritis in older adults: a systematic review and meta-analysis. Osteoarthritis Cartilage. 2015;23(4):507–15. doi:10.1016/j.joca.2014.11.019.
Dr. Katz is the President-Elect of the Osteoarthritis Research Society International. Drs. Katz and Losina are Deputy Editors for Biostatistics and Methodology for the Journal of Bone and Joint Surgery. All other authors have no conflicts of interest to report.
EL conceived of the study and participated in its design, in data analysis, and in manuscript drafting. KK recruited subjects for the clinical pilot study and participated in drafting the manuscript. GM participated in the design of OA Risk C, in data analysis, and in manuscript drafting. JC and JK contributed to the study design and revised the manuscript critically for intellectual content. All authors have read and approved the final manuscript.
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Losina, E., Klara, K., Michl, G.L. et al. Development and feasibility of a personalized, interactive risk calculator for knee osteoarthritis. BMC Musculoskelet Disord 16, 312 (2015). https://doi.org/10.1186/s12891-015-0771-3
- Knee OA
- Risk calculator
- OA risk