Abstract
Objective:
While opioids are known to cause unintended adverse effects, they are being utilized by a number of patients with osteoarthritis (OA). The aim of this study was to evaluate the association of patient familiarity and perceptions regarding efficacy and risks with opioid medication use for OA.
Methods:
A total of 362 adults with knee and/or hip OA were surveyed in this cross-sectional study. Patients’ familiarity with and perceptions of benefits/risks of opioid medications were measured to evaluate potential associations with the utilization of opioid medications for OA within the last 6 months. Logistic regression models were adjusted for sociodemographic and clinical variables.
Results:
In this sample, 28.7% (100/349) reported use of an opioid medication for OA-related symptoms in the last 6 months. Those who were on an opioid medication, compared to those who were not, were younger (mean age 62.5 vs. 64.8), more likely to have ≤ a high school education (48.0% vs. 35.3%), and had higher mean depression (PHQ-8 7.2 vs. 4.9) and OA-related pain (WOMAC 54.8 vs. 46.8) scores. After adjustment for sociodemographic and clinical variables, the following were associated with opioid medication use: higher perception of medication benefit (OR 1.68 [95% CI 1.18, 2.41]), lower perception of medication risk (OR 0.67 [95% CI 0.51, 0.88]), and having family/friends that received the medication for OA (OR 3.88 [95% CI 1.88, 8.02]).
Conclusion:
Among adults with knee/hip OA, opioid use was associated with believing that the medication was beneficial and low risk and being familiar with the treatment.
KEY INDEXING TERMS: osteoarthritis, opioids, treatment utilization, familiarity, perceptions
INTRODUCTION
Osteoarthritis (OA) is the most common form of arthritis and disease management includes pain control and functional improvement1, 2. Exercise, physical therapy, acetaminophen, and non-steroidal anti-inflammatory drugs (NSAIDs) are considered first-line treatments1, 2. Initial non-pharmacologic and pharmacologic OA therapies maybe insufficient to control the symptoms, however. Pain-relieving effects of NSAIDs and acetaminophen can be small and short-lasting2, 3. Prescription of NSAIDs may not be appropriate due to drug intolerance and/or the presence of particular comorbidities (e.g., gastrointestinal bleeding history). Joint replacement surgery may be an option among those with severe disease1, 2. However, those with multiple comorbidities may be poor surgical candidates, and some patients have a preference against surgery4. The 2019 American College of Rheumatology/Arthritis Foundation Guidelines conditionally recommend against the use of non-tramadol opioid agents in patients with knee and/or hip OA.1 However, the Guidelines acknowledge that opioids may be used under certain instances, particularly when alternative therapies have failed or are contraindicated.
Indeed, opioids have been increasingly used to treat chronic pain conditions including those caused by musculoskeletal disorders in the United States (US) and worldwide5, 6. From 2001 and 2010, opioid prescribing in the US for acute and chronic musculoskeletal pain visits increased by 50% and 79%, respectively5. In a recent study, there was an observed decrease in the use of opioids between 2013 and 2016 among men and those who were less educated; however, there was a significant overall increase in opioid use from 1999 to 20167. In Sweden from 2013–2015, the one year prevalence of opioid use among OA patients was 24%, two-fold higher compared to those without OA8. Yet, opioid medications can cause nausea, constipation, drowsiness, and vomiting9. The chronic use of opioids has been associated with increased risk for fractures, cardiovascular events, and greater mortality10. There is also concern regarding the dangers of opioid dependence and overdose11. In response to the opioid epidemic crisis, rheumatologists have advocated for the use of alternate methods of pain control and the focus on the treatment of concomitant psychiatric diseases12.
With recognition of the necessity to minimize potential risks while maintaining adequate pain management among OA patients with chronic pain, there is a need to understand factors that are associated with the use of opioids for OA-related symptoms.13–17. Younger age, female sex, White race, depression, and greater OA disease severity have all been associated with opioid use13–15, 18, 19. In addition, patient-level factors such as attitudes and beliefs about treatment options may influence treatment choices. Patient familiarity and perceptions about non-pharmacologic treatments have been associated with utilization of exercise and joint replacement surgery for OA20–22. Yet, the potential association of these patient-level factors with utilization of opioids for OA is poorly understood. While many of the known determinants of opioid use are relatively immutable, patient familiarity and perceptions about medications are also modifiable at the point of care23.
The primary objective of this study is to investigate the association of familiarity, perceived benefits, and perceived risks with opioid medication use for OA treatment, controlling for patient demographic and clinical characteristics. The secondary objective is to examine the association of demographic factors with familiarity, perceived benefits, and perceived risks of opioid use for OA.
METHODS
Setting and Participants
Participants for this cross-sectional study were recruited from the University of Arizona Arthritis Center research registry and Banner University Medical Center (BUMC) Rheumatology, Orthopedic Surgery/Sports Medicine and Internal Medicine Clinics located in Tucson, Arizona from July 2015 through April 2018. The target sample included patients with knee or hip OA. A diagnosis of knee OA was confirmed by radiographic evidence of OA, presence of chronic frequent knee pain, and age ≥ 50 years24. A confirmed diagnosis of hip OA depended on the presence of hip pain and femoral and/or acetabular osteophytes on radiograph25. The presence of chronic frequent pain due to knee or hip OA was evaluated according to questions from the Arthritis Supplement of the National Health and Nutrition Exam Survey26, 27. Patients with any of the following diagnoses were excluded: disease associated with inflammatory arthritis (e.g., rheumatoid arthritis), total hip and knee arthroplasty history, or moderate to severe cognitive dysfunction.
Screening and Recruitment
Medical records and the University of Arizona Arthritis Center research registry were reviewed to identify patients with knee and/or hip OA. Patients were then screened by telephoned to evaluate eligibility. Those who were eligible and willing to participate in the study were subsequently consented and given a questionnaire to complete on site. They were given a private room where they individually filled out the paper survey by themselves, without assistance. They were also offered the option to complete the survey at home and return the survey by mail. English and Spanish language versions of surveys were offered.
Primary Study Outcome
The primary study outcome was opioid medication use for treatment of pain from OA within the last 6 months. Participants were asked if they “used or participated” in various different “treatments for joint pain of arthritis in the last 6 months.” Treatment option included “strong pain medications, you get with a prescription, including opioids, such as Morphine (MS Contin, Astramorph, Duramorph), Acetaminophen with codeine (Tylenol with codeine #3) or Hydrocodone with acetaminophen (Vicodin, Lorcet, Lortab).”
Exposure Variables
Familiarity with Opioid Medications for OA Treatment.
Participants’ familiarity with opioid medications as treatment for OA was determined by asking if they: 1) have heard of it as OA treatment; 2) have family/friends that received it for treatment; and 3) have a good understanding of what happens after treatment. Response options for all questions were “yes” or “no”. There were items used in previous studies20, 28, but modified to measure familiarity with opioid medications for OA.
Perceptions of Benefit and Risk of Opioid Medications.
Perceived benefit and risk of opioid medications were assessed using previously used measures of perceived benefit (4 item) and risk (3 item) of joint replacement surgery21, but adapted for opioids. The perception of benefit was measured by determining the extent to which participants believed that an opioid medication treatment: 1) was beneficial for people with arthritis; 2) was beneficial for them; 3) could lead to pain relief; and 4) could cause functional improvement. The perception of risk was measured by determining the extent to which participants: 1) believe in the risk/danger with (very harmless-very harmful); 2) believe in serious complications with (not at all-very serious); and 3) showed concern for potential complications from opioid medication treatment use (not at all-very concerned). Possible ordinal responses ranged from 1 to 5 for each question. Responses to each set of questions were averaged to obtain a scale of 1 to 5, with higher values indicating greater perception of benefit/risk. Both perceived benefit and perceived risk of opioid medication measures had good internal reliability scores (Cronbach α = 0.8250 and 0.8517, respectively).
Study Covariates
Sociodemographic.
The following were included as covariates: age, sex, race, ethnicity, educational attainment, employment, marital status, household income, and medical insurance.
Clinical.
Quality of life was assessed using the following question: “How would you rate your overall quality of life?” which was scored on a 5-point ordinal scale ranging from poor to excellent29. Depression was assessed using the Patient Health Quetionnaire-8 (PHQ-8, range: 0–24)30. Medical comorbidity was assessed using a modified self-reported Charlson Comorbidity Index31. Health literacy was determined by asking, “How confident are you filling out medical forms by yourself?”32 Study participants were dichotomized between those with adequate (extremely, quite a bit) versus inadequate (somewhat, a little bit, or not at all) health literacy. OA-related disease severity was measured using the 24-item Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)33. The WOMAC has three subscales: pain, stiffness, and disability. Each subscale score was normalized to a range from 0 to 100.
The full study protocol was approved by the University of Arizona Institutional Review Board (#1502663769) and was previously described20, 34.
Statistical Methods
Demographic information, clinical characteristics, and psychosocial variables were compared by opioid treatment group using two-sided Fisher’s exact test or χ2 test for categorical variables, and two-sided t-test for continuous variables.
Familiarity with opioid medication statements were compared by opioid treatment group and by various sociodemographic characteristics using two-sided Fisher’s exact test or χ2 test. Perceived benefit and risk of opioid medications were also compared by the same variables using two-sided t-test.
A logistic regression model was used to estimate the adjusted odds ratio (OR) of using an opioid medication, comparing participants by levels of perceived benefit and perceived risk of opioid medicines and by familiarity with opioids. The model was adjusted for age, sex, race (White vs. not), education, Patient Health Questionnaire-8 (Depression) score, and WOMAC total score. All demographic (age, sex, race, education, income) and clinical variables (quality of life, OA disease severity, number of comorbidities, depression) that were previously associated with opioid medication use in other OA studies were considered as covariates13–17. Income was considered but dropped from the model due to significant overlap with education. To account for missing data, multiple imputation using chained equation was used to build the multivariable model35.
Analyses were performed using STATA IC 16.0 (StataCorp LP, College Station, TX, USA).
RESULTS
Among the 1430 considered for study eligibility, 320 were excluded during screening, 269 declined study participation (prior to screening), and 331 could not be contacted. A total of 510 were deemed eligible for the study, and 408 consented to participate (Figure 1). Among those who consented, 34 never returned a survey and 12 changed their mind about participating or had subsequent joint replacement surgery. Overall, 362 surveys were received, but 13 had missing opioid medication use information and were therefore excluded.
Figure 1.

Study flow chart
*Exclusionary diagnoses: rheumatoid arthritis, systemic lupus erythematosus, a seronegative spondyloarthropathy, gout, pseudogout, senile dementia, vascular dementia, alcohol-induced dementia, drug-induced dementia
Sociodemographic & Clinical Characteristics by Treatment Use
A total of 100 study participants out of 349 were on an opioid medication for OA in the last 6 months. Those who had used an opioid medication, compared to those who had not, were younger (mean age 62.5 vs. 64.8, p=0.019), but the two medication treatment groups did not significantly differ by sex, race, or ethnicity (Table 1).
Table 1.
Patient sociodemographic and clinical characteristics by opioid medication use in the last 6 months
| Has NOT Used (n = 249) | Has Used (n = 100) | p-value a | |
|---|---|---|---|
| Age, Mean (SD) | 64.8 (8.3) | 62.5 (8.1) | 0.019 |
| Sex, n (%) Female | 180 (72.6) | 69 (69.0) | 0.503 |
| Race, n (%) | 0.646 | ||
| White | 171 (68.7) | 67 (67.0) | |
| Black or African-American | 16 (6.4) | 9 (9.0) | |
| American Indian or Alaskan Native | 8 (3.2) | 2 (2.0) | |
| Other | 38 (15.3) | 11 (11.0) | |
| Missing/Refuse to answer | 16 (6.4) | 11 (11.0) | |
| Ethnicity, n(%) Hispanic | 84 (33.7) | 37 (37.0) | 0.562 |
| Education, n (%) | 0.013 | ||
| Less than a high school diploma | 15 (6.0) | 14 (14.0) | |
| High school/GED | 73 (29.3) | 34 (34.0) | |
| Associate’s Degree or higher | 127 (51.0) | 34 (34.0) | |
| Other | 31 (12.5) | 18 (18.0) | |
| Missing/Refuse to answer | 3 (1.2) | 0 (0.0) | |
| Employment, n (%) | <0.001 | ||
| Full-time | 52 (21.1) | 12 (12.0) | |
| Part-time | 17 (6.8) | 11 (11.0) | |
| Unemployed | 16 (6.4) | 7 (7.0) | |
| Disabled | 40 (16.1) | 34 (34.0) | |
| Retired | 122 (49.0) | 28 (28.0) | |
| Missing/Refuse to answer | 2 (0.8) | 8 (8.0) | |
| Marital Status, n (%) Married | 120 (48.4) | 36 (36.7) | 0.059 |
| Annual Income, n (%) | 0.001 | ||
| <$20,000 | 71 (28.5) | 52 (52.0) | |
| $20,000 – 39,999 | 37 (14.9) | 15 (15.0) | |
| ≥$40,000 | 113 (45.4) | 25 (25.0) | |
| Missing/Refuse to answer/Don’t know | 26 (11.2) | 8 (8.0) | |
| Insurance, n (%) | |||
| Medicaid | 37 (14.9) | 33 (33.0) | 0.003 |
| Medicare | 134 (53.8) | 53 (53.0) | 0.247 |
| Medigap | 50 (20.1) | 18 (18.0) | 0.450 |
| Private | 63 (25.3) | 19 (19.0) | 0.170 |
| HMO | 27 (10.8) | 7 (7.0) | 0.208 |
| Other | 40 (16.1) | 16 (16.0) | 0.082 |
| Overall quality of life, n (%) | <0.001 | ||
| Excellent | 33 (13.3) | 7 (7.0) | |
| Very Good | 101 (40.6) | 27 (27.0) | |
| Good | 66 (26.5) | 27 (27.0) | |
| Fair | 34 (13.7) | 31 (31.0) | |
| Poor | 15 (6.0) | 7 (7.0) | |
| PHQ-8, Mean (SD) | 4.9 (5.3) | 7.2 (5.6) | 0.002 |
| Confidence filling medical forms, n(%) | 0.321 | ||
| Extremely, Quite a bit | 212 (85.1) | 86 (86.0) | |
| Somewhat, a little bit, or not at all | 34 (13.6) | 14 (14.0) | |
| Comorbidity Score, Mean (SD) | 3.2 (1.8) | 4.1 (1.9) | <0.001 |
| WOMAC-Pain, Mean (SD) | 46.8 (21.1) | 54.8 (20.3) | 0.002 |
| WOMAC-Disability, Mean (SD) | 44.9 (21.5) | 56.6 (19.4) | <0.001 |
GED=General Education Development; HMO=Health maintenance organization; PHQ-8: Patient Health Questionnaire-8; WOMAC= Western Ontario and McMaster Universities Osteoarthritis Index
Fisher’s exact or χ2 test for categorical variables. T-test for continuous variables.
Having a high school education or less (48.0% vs. 35.3%, p=0.013), not having full-time employment, and a household income of <$20,000 per year (52.0% vs. 28.5%, p=0.001) were more common among those who were on an opioid medication compared to those who were not (Table 1). Having Medicaid insurance was also more common among those who had used an opioid medication compared to those who had not (33.0% vs. 14.9%, p=0.003). Neither marital status nor having other types of medical insurance differed by opioid medication treatment group (Table 1).
Those who had used an opioid medication for OA, compared to those who had not, were more likely to report having only “fair” or “poor health” (31.0% vs. 13.7%, 7.0% vs. 6.0%, p<0.001), had higher number of comorbidities (mean 4.1 vs. 3.2, p<0.001), and had higher PHQ-8 scores (mean 7.2 vs. 4.9, p=0.002). Mean WOMAC pain and disability scores were also higher among them compared to those who were not on an opioid medication for OA (54.8 vs. 46.8, p=0.002; 56.6 vs. 44.9, p<0.001; respectively).
Knowledge and Attitudes about Opioid Medications
Study participants who were on an opioid medication for OA had greater familiarity with opioid medications than those were not on the medication the last 6 months (Table 2A). They were more likely to have heard of its use for OA (95.9% vs. 71.4%, p<0.001), to have family/friends that received it for OA (77.4% vs. 40.4%, p<0.001), and to have a good understanding of the consequences of its use (92.2% vs. 64.7%, p<0.001). They also had higher perceived benefit (mean 3.9 vs. 3.3, p<0.001) and lower perceived risk (mean 3.2 vs. 3.8, p<0.001) of taking opioid medications for OA. After adjustment for age, sex, race, education, PHQ-8 score, and WOMAC total score, odds of opioid medication treatment use remained significantly higher among those with higher perceived medication benefit (OR 1.68 [95% CI 1.18, 2.41]) or had family/friends that received the medication for OA (OR 3.88 [95% CI 1.88, 8.02]). Odds of opioid medication treatment use were lower among those who perceived greater medication risk (OR 0.67 [95% CI 0.51, 0.88]) (Table 3).
Table 2.
Patient knowledge and attitudes about opioid medications
| A. By opioid medication use in the last 6 months | |||
|---|---|---|---|
|
| |||
| Has NOT Used (n = 249) | Has Used (n = 100) | p-value a | |
| Familiarity with Opioid Medications, n(%) | |||
| Heard of use of it to treat osteoarthritis | 170 (71.4) | 94 (95.9) | <0.001 |
| Have family/friends that received it for OA treatment | 80 (40.4) | 65 (77.4) | <0.001 |
| Have a good understanding of what happens after treatment | 145 (64.7) | 83 (92.2) | <0.001 |
| Perception of benefit of Opioid Medications, mean (SD) | 3.3 (0.9) | 3.9 (0.9) | <0.001 |
| Perception of risk of Opioid Medications, mean (SD) | 3.8 (1.1) | 3.2 (1.18) | <0.001 |
| B. By education | |||
|
| |||
| ≤High School Education (n = 145) | >High School Education (n = 162) | p-value a | |
|
| |||
| Familiarity with Opioid Medications, n(%) | |||
| Heard of use of it to treat osteoarthritis | 100 (71.9) | 127 (82.5) | 0.031 |
| Have family/friends that received it for OA treatment | 51 (43.6) | 69 (53.9) | 0.107 |
| Have a good understanding of what happens after treatment | 88 (69.8) | 103 (70.1) | 0.968 |
| Perception of benefit of Opioid Medications, mean (SD) | 2.38 (1.1) | 2.52 (0.9) | 0.236 |
| Perception of risk of Opioid Medications, mean (SD) | 2.12 (1.2) | 3.03 (1.0) | <0.001 |
| C. By annual household income | |||
|
| |||
| <$40,000 (n = 185) | ≥$40,000 (n = 139) | p-value a | |
|
| |||
| Familiarity with Opioid Medications, n(%) | |||
| Heard of use of it to treat osteoarthritis | 135 (77.1) | 108 (80.0) | 0.545 |
| Have family/friends that received it for OA treatment | 82 (55.4) | 58 (51.8) | 0.562 |
| Have a good understanding of what happens after treatment | 121 (74.7) | 91 (70.5) | 0.429 |
| Perception of benefit of Opioid Medications, mean (SD) | 2.47 (1.0) | 2.49 (0.9) | 0.855 |
| Perception of risk of Opioid Medications, mean (SD) | 2.34 (1.2) | 3.00 (1.0) | <0.001 |
Fisher’s exact or χ2 test for categorical variables. T-test for continuous variables.
Table 3.
Patient knowledge and attitudes towards opioid medications associated with opioid medication use (vs. no opioid medication use) in the last 6 months adjusted for sociodemographic and clinical variables.
| Independent Variable | Odds Ratio | 95% CI |
|---|---|---|
| Outcome: Opioid medication use (vs. No opioid medication use) a | ||
| Perception of benefit b | 1.68 c | 1.18, 2.41 |
| Perception of risk b | 0.67 c | 0.51, 0.88 |
| Have family/friends that received it for OA treatment | 3.88 c | 1.88, 8.02 |
| Have a good understanding of what happens after treatment | 2.40 | 0.94, 6.14 |
Logistic regression model adjusted for age, sex, race (White vs. not), education, Patient Health Questionnaire-8 (Depression) score, WOMAC Total score. N= 271
OR for a one-point increase in a scale ranging from 1 to 5.
p<0.05
Those with a high school education or less, compared to those with more than a high school education, were less likely to have heard of the use of opioid medications for OA (71.9% vs. 82.5%, p=0.031) and perceived opioid medications as less risky (mean 2.1 vs. 3.0, p<0.001). Other familiarity with opioid medication statements and perception of medication benefit, however, did not differ by educational level (Table 2B).
Those with an income less than $40,000 per year, compared to those with an annual household income of at least $40,000, had perceived opioid medications as less risky (mean 2.3 vs. 3.0, p<0.001). However, perceived medication benefit and familiarity with opioid medications did not differ by annual household income level (Table 2C).
DISCUSSION
In this sample of patients with OA, patient knowledge and attitudes regarding opioid medications were significantly associated with use of opioids in the management of pain. We specifically found that having family/friends who have used opioid medications and having higher perceived benefit and lower perceived risk of opioid medications were all independently associated with their use. Perceived risk of the use of opioid medications was lower while opioid medication use for OA was higher among those with lower educational attainment and less income. Use of the treatment was also more common among those with fair/poor health, higher levels of depression, and higher OA disease severity.
Knowledge, attitudes and beliefs about treatments may influence perceptions of need and use of health treatments, including treatments for OA36, 37. In a previous study, patients’ familiarity with exercise and higher perceived benefits of exercise were associated with exercise use for OA treatment20. Patients’ familiarity with, along with lower perceived risk and higher perceived benefits, of joint replacement surgery were also strongly linked to OA patients’ willingness to undergo joint replacement surgery21. In turn, willingness to have the surgical procedure had been tightly linked to actual joint replacement22. The current study, albeit cross-sectional and therefore unable to establish direction of causality, found positive associations between patient knowledge and attitudes about opioid medications and utilization of an opioid medication for knee/hip OA.
Patients’ perceptions about the effects of opioid medications may or may not reflect the treatment’s actual effects, however. While higher perceived benefit may be linked to more use of an opioid medication, pain and disability may only be minimally relieved with an opioid drug. In a meta-analysis, treatment of OA patients with opioids compared to placebo was associated with a mere 12% improvement in pain and 11% improvement in function38. A systematic review found that non-steroidal anti-inflammatory drugs and opioids offer comparable levels of pain relief in OA39. In a randomized trial, treatment with opioids was not superior to treatment with non-opioid medications for improving pain-related function due to chronic back or joint pain, and adverse medication-related symptoms were more common among opioid users40. Perceived risk about opioid medicines may also be underestimated or overestimated. Up to 22% of people with OA who use opioids experience a side effect, and 1.3% have adverse events that result in hospitalization, permanent disability, or death38. Use of opioids compared to placebo was also previously associated with higher risk of having an adverse event affecting the upper and lower gastrointestinal, dermatologic, and central nervous systems41.
Similarly, familiarity with a medication may not be helpful when the information about the medication is incomplete or imprecise. It was not surprising to find that having family or friends who used an opioid medication was associated with self-reported use of the drug. An individual’s social network often influences utilization of various treatments20, 42. When the treatment is high risk, however, the effect may be detrimental to the individual’s health and can lead to drug misuse or overuse. In a qualitative study of 30 non-medical opioid users, most admitted that they initiated recreational use when they were able to access the medication through a family member/friend43. Regardless, patient knowledge and beliefs about opioid medications may be changed through patient education.44, 45.
Lower educational attainment and income were both associated with greater use of an opioid medication for OA treatment in our study. Educational level was not significantly associated with opioid use in other studies of patients with arthritis15, 16, 46. However, lower income was consistently associated with current use of an opioid medication in several OA studies14, 46. It is possible that those with lower income have less access to other OA treatments that require financial resources and/or time commitment (e.g., exercise, complementary/alternative therapies). Our study additionally found that those with a lower levels of education and income were less likely to perceive an opioid medication as risky compared to those with higher levels of education and income. Less educated study participants were also found to have lower awareness of its use as a treatment in OA.
Our cross-sectional study found an association between greater OA disease severity (which was based on patient-reported measures) and opioid use. This association was also found in other studies.14, 15, 18 The finding also suggests that patient perspectives are likely taken into account when providers consider prescribing these types of medications and that some OA patients may truly benefit from opioid use. However, while disease severity may lead to increased use of an opioid therapy, it is also possible that opioid use may worsen OA symptoms. Prospective studies may be useful in clarifying these relationships. The association between OA disease severity and opioid use may also be an example of confounding by indication; those with more severe joint pain might have been more likely to be offered opioids by providers. OA-related pain severity was controlled for in our multivariable analysis, regardless (Table 3).
More than 25% of the study participants reported opioid use for OA in the last 6 months. In contrast, in a study of veterans with OA from 1998–1999, 41% of subjects had at least one opioid prescription13. In a study of community-dwelling elders with OA from 2002–2003, prescription opioids were taken by <10% of participants15. In a national study of patients with knee OA, opioid prescription was received by 31% in 2003, 39% in 2006, and 40% in 200947. An administrative claims database study from 2007–2014 found that 13% of hip OA and 16% of knee OA patients were prescribed an opioid48. Differences in the reported rates of opioid use are likely from various reasons: varying times of study administration, different data sources, different study designs, and sample differences (e.g., radiographic vs. non-radiographic OA).
There are several limitations to consider in interpreting our results. First, this is a cross-sectional study; only associations, and not causal relationships, between patient knowledge/beliefs about opioids and opioid medication use could be made. Second, all measures used for this study were based on self-report, including opioid medication use. Although self-reported measures are vulnerable to memory and social desirability biases49, self-reported medication use tends to correlate well with pharmacy data confirming high validity and utility for analysis50. Third, our sample is composed of a population primarily residing in Tucson, Arizona. The generalizability of our findings to other OA patients who reside in other geographic regions is unknown. Future studies should consider replicating our study in other geographic areas. Fourth, we do not have details on patients’ more specific and explicit reasons for opioid use or non-use. Future research should examine the role of other patient-related variables that may affect opioid medication use for OA, such as previous experiences with opioids, perceived financial burden associated with medical care, and perceived benefits/risks of other therapies for OA. Fifth, provider-related characteristics (e.g., recognition of appropriateness of opioid use, bias for/against opioid use) could also affect the associations observed in our main analyses; these should be studied as well. Finally, our sample was limited to people who were successfully contacted and could fill out a questionnaire. Treatment use patterns and beliefs about opioid medications may differ among those who could not or chose not to participate in the research study. The Health Insurance Portability and Accountability Act prevents us from gathering data from non-study participants, so we cannot compare our study sample from screened but non-consented OA patients.
Conclusion
In this cross-sectional study, we found that patient knowledge and beliefs about opioids were associated with use of opioid medications in the management of OA-related pain symptoms. Among patients with knee or hip OA, those who were on an opioid medication, compared to those who were not, were more familiar with opioids, were more likely to believe in their efficacy, and perceived them as less risky. Perceived medication efficacy and risk as well as having family/friends who use the medication were associated with opioid medication use even after controlling for patient sociodemographic and clinical characteristics. Use of an opioid medication for OA was also more common among those with lower education, lower income, poorer physical and mental health, and more OA-related symptoms. Patients’ perceptions and beliefs about opioids should be evaluated and discussed when considering these medications for OA treatment.
Acknowledgements
We would like to thank Andrea Arellano and Jazmin Dagnino for assistance with patient recruitment. We would also like to thank all BUMC patients and University of Arizona Arthritis Center research registry members who participated in the study.
The current study and Dr. Vina were funded in part by NIH/National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) (K23AR067226). Dr. Kwoh’s work was supported by the NIH/NIAMS (R01AR066601). Dr. Ibrahim was supported in part by a K24 Mid-Career Development Award from NIAMS (K24AR055259)
REFERENCES
- 1.Kolasinski SL, Neogi T, Hochberg MC, Oatis C, Guyatt G, Block J, et al. 2019 American College of Rheumatology/Arthritis Foundation Guideline for the Management of Osteoarthritis of the Hand, Hip, and Knee. Arthritis Care Res (Hoboken) 2020;72:149–62. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Zhang W, Nuki G, Moskowitz RW, Abramson S, Altman RD, Arden NK, et al. OARSI recommendations for the management of hip and knee osteoarthritis: part III: Changes in evidence following systematic cumulative update of research published through January 2009. Osteoarthritis Cartilage 2010;18:476–99. [DOI] [PubMed] [Google Scholar]
- 3.Bjordal JM, Ljunggren AE, Klovning A, Slordal L. Non-steroidal anti-inflammatory drugs, including cyclo-oxygenase-2 inhibitors, in osteoarthritic knee pain: meta-analysis of randomised placebo controlled trials. BMJ 2004;329:1317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Vina ER, Cloonan YK, Ibrahim SA, Hannon MJ, Boudreau RM, Kwoh CK. Race, sex, and total knee replacement consideration: role of social support. Arthritis Care Res (Hoboken) 2013;65:1103–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Larochelle MR, Zhang F, Ross-Degnan D, Wharam JF. Trends in opioid prescribing and co-prescribing of sedative hypnotics for acute and chronic musculoskeletal pain: 2001–2010. Pharmacoepidemiol Drug Saf 2015;24:885–92. [DOI] [PubMed] [Google Scholar]
- 6.Birke H, Kurita GP, Sjogren P, Hojsted J, Simonsen MK, Juel K, et al. Chronic non-cancer pain and the epidemic prescription of opioids in the Danish population: trends from 2000 to 2013. Acta Anaesthesiol Scand 2016;60:623–33. [DOI] [PubMed] [Google Scholar]
- 7.Stokes A, Berry KM, Hempstead K, Lundberg DJ, Neogi T. Trends in Prescription Analgesic Use Among Adults With Musculoskeletal Conditions in the United States, 1999–2016. JAMA Netw Open 2019;2:e1917228. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Thorlund JB, Turkiewicz A, Prieto-Alhambra D, Englund M. Opioid use in knee or hip osteoarthritis: a region-wide population-based cohort study. Osteoarthritis Cartilage 2019;27:871–7. [DOI] [PubMed] [Google Scholar]
- 9.Avouac J, Gossec L, Dougados M. Efficacy and safety of opioids for osteoarthritis: a meta-analysis of randomized controlled trials. Osteoarthritis Cartilage 2007;15:957–65. [DOI] [PubMed] [Google Scholar]
- 10.Solomon DH, Rassen JA, Glynn RJ, Lee J, Levin R, Schneeweiss S. The comparative safety of analgesics in older adults with arthritis. Arch Intern Med 2010;170:1968–76. [DOI] [PubMed] [Google Scholar]
- 11.Centers for Disease C, Prevention. Vital signs: overdoses of prescription opioid pain relievers---United States, 1999--2008. MMWR Morb Mortal Wkly Rep 2011;60:1487–92. [PubMed] [Google Scholar]
- 12.Lee YC, Kremer J, Guan H, Greenberg J, Solomon DH. Chronic Opioid Use in Rheumatoid Arthritis: Prevalence and Predictors. Arthritis Rheumatol 2019;71:670–7. [DOI] [PubMed] [Google Scholar]
- 13.Dominick KL, Bosworth HB, Dudley TK, Waters SJ, Campbell LC, Keefe FJ. Patterns of opioid analgesic prescription among patients with osteoarthritis. J Pain Palliat Care Pharmacother 2004;18:31–46. [PubMed] [Google Scholar]
- 14.Abbate LM, Jeffreys AS, Coffman CJ, Schwartz TA, Arbeeva L, Callahan LF, et al. Demographic and Clinical Factors Associated with Non-Surgical Osteoarthritis Treatment Use Among Patients in Outpatient Clinics. Arthritis Care Res (Hoboken) 2017. [DOI] [PMC free article] [PubMed]
- 15.Marcum ZA, Perera S, Donohue JM, Boudreau RM, Newman AB, Ruby CM, et al. Analgesic use for knee and hip osteoarthritis in community-dwelling elders. Pain Med 2011;12:1628–36. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Vina ER, Hausmann LRM, Obrosky DS, Youk A, Ibrahim SA, Weiner DK, et al. Social & psychological factors associated with oral analgesic use in knee osteoarthritis management. Osteoarthritis Cartilage 2019;27:1018–25. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Power JD, Perruccio AV, Gandhi R, Veillette C, Davey JR, Lewis SJ, et al. Factors Associated With Opioid Use in Presurgical Knee, Hip, and Spine Osteoarthritis Patients. Arthritis Care Res (Hoboken) 2019;71:1178–85. [DOI] [PubMed] [Google Scholar]
- 18.Kingsbury SR, Hensor EM, Walsh CA, Hochberg MC, Conaghan PG. How do people with knee osteoarthritis use osteoarthritis pain medications and does this change over time? Data from the Osteoarthritis Initiative. Arthritis Res Ther 2013;15:R106. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Sharma A, Kudesia P, Shi Q, Gandhi R. Anxiety and depression in patients with osteoarthritis: impact and management challenges. Open Access Rheumatol 2016;8:103–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Vina ER, Hannon MJ, Hausmann LRM, Ibrahim SA, Dagnino J, Arellano A, et al. Modifiable Determinants of Exercise Use in a Diverse Ethnic Population with Osteoarthritis. Arthritis Care Res (Hoboken) 2019. [DOI] [PMC free article] [PubMed]
- 21.Suarez-Almazor ME, Souchek J, Kelly PA, O’Malley K, Byrne M, Richardson M, et al. Ethnic variation in knee replacement: patient preferences or uninformed disparity? Arch Intern Med 2005;165:1117–24. [DOI] [PubMed] [Google Scholar]
- 22.Hausmann LR, Mor M, Hanusa BH, Zickmund S, Cohen PZ, Grant R, et al. The effect of patient race on total joint replacement recommendations and utilization in the orthopedic setting. J Gen Intern Med 2010;25:982–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.House JS. Understanding social factors and inequalities in health: 20th century progress and 21st century prospects. J Health Soc Behav 2002;43:125–42. [PubMed] [Google Scholar]
- 24.Altman R, Asch E, Bloch D, Bole G, Borenstein D, Brandt K, et al. Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association. Arthritis Rheum 1986;29:1039–49. [DOI] [PubMed] [Google Scholar]
- 25.Altman R, Alarcon G, Appelrouth D, Bloch D, Borenstein D, Brandt K, et al. The American College of Rheumatology criteria for the classification and reporting of osteoarthritis of the hip. Arthritis Rheum 1991;34:505–14. [DOI] [PubMed] [Google Scholar]
- 26.Davis MA, Ettinger WH, Neuhaus JM. Obesity and osteoarthritis of the knee: evidence from the National Health and Nutrition Examination Survey (NHANES I). Semin Arthritis Rheum 1990;20:34–41. [DOI] [PubMed] [Google Scholar]
- 27.Christmas C, Crespo CJ, Franckowiak SC, Bathon JM, Bartlett SJ, Andersen RE. How common is hip pain among older adults? Results from the Third National Health and Nutrition Examination Survey. J Fam Pract 2002;51:345–8. [PubMed] [Google Scholar]
- 28.Ibrahim SA, Siminoff LA, Burant CJ, Kwoh CK. Understanding ethnic differences in the utilization of joint replacement for osteoarthritis: the role of patient-level factors. Med Care 2002;40:I44–51. [DOI] [PubMed] [Google Scholar]
- 29.Covinsky KE, Wu AW, Landefeld CS, Connors AF Jr., Phillips RS, Tsevat J, et al. Health status versus quality of life in older patients: does the distinction matter? Am J Med 1999;106:435–40. [DOI] [PubMed] [Google Scholar]
- 30.Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med 2001;16:606–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Chaudhry S, Jin L, Meltzer D. Use of a self-report-generated Charlson Comorbidity Index for predicting mortality. Med Care 2005;43:607–15. [DOI] [PubMed] [Google Scholar]
- 32.Chew LD, Griffin JM, Partin MR, Noorbaloochi S, Grill JP, Snyder A, et al. Validation of screening questions for limited health literacy in a large VA outpatient population. J Gen Intern Med 2008;23:561–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Bellamy N, Buchanan WW, Goldsmith CH, Campbell J, Stitt LW. Validation study of WOMAC: a health status instrument for measuring clinically important patient relevant outcomes to antirheumatic drug therapy in patients with osteoarthritis of the hip or knee. J Rheumatol 1988;15:1833–40. [PubMed] [Google Scholar]
- 34.Vina ER, Hannon MJ, Masood HS, Hausmann LRM, Ibrahim SA, Dagnino J, et al. Nonsteroidal Anti-Inflammatory Drug Use in Chronic Arthritis Pain: Variations by Ethnicity. Am J Med 2019. [DOI] [PMC free article] [PubMed]
- 35.White IR, Royston P, Wood AM. Multiple imputation using chained equations: Issues and guidance for practice. Stat Med 2011;30:377–99. [DOI] [PubMed] [Google Scholar]
- 36.Andersen RM. Revisiting the behavioral model and access to medical care: does it matter? J Health Soc Behav 1995;36:1–10. [PubMed] [Google Scholar]
- 37.Papandony MC, Chou L, Seneviwickrama M, Cicuttini FM, Lasserre K, Teichtahl AJ, et al. Patients’ perceived health service needs for osteoarthritis (OA) care: a scoping systematic review. Osteoarthritis Cartilage 2017;25:1010–25. [DOI] [PubMed] [Google Scholar]
- 38.da Costa BR, Nuesch E, Kasteler R, Husni E, Welch V, Rutjes AW, et al. Oral or transdermal opioids for osteoarthritis of the knee or hip. Cochrane Database Syst Rev 2014:CD003115. [DOI] [PMC free article] [PubMed]
- 39.Smith SR, Deshpande BR, Collins JE, Katz JN, Losina E. Comparative pain reduction of oral non-steroidal anti-inflammatory drugs and opioids for knee osteoarthritis: systematic analytic review. Osteoarthritis Cartilage 2016;24:962–72. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Krebs EE, Gravely A, Nugent S, Jensen AC, DeRonne B, Goldsmith ES, et al. Effect of Opioid vs Nonopioid Medications on Pain-Related Function in Patients With Chronic Back Pain or Hip or Knee Osteoarthritis Pain: The SPACE Randomized Clinical Trial. JAMA 2018;319:872–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Fuggle N, Curtis E, Shaw S, Spooner L, Bruyere O, Ntani G, et al. Safety of Opioids in Osteoarthritis: Outcomes of a Systematic Review and Meta-Analysis. Drugs Aging 2019;36:129–43. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Gelberg L, Andersen RM, Leake BD. The Behavioral Model for Vulnerable Populations: application to medical care use and outcomes for homeless people. Health Serv Res 2000;34:1273–302. [PMC free article] [PubMed] [Google Scholar]
- 43.Rigg KK, McLean K, Monnat SM, Sterner GE 3rd, Verdery AM. Opioid misuse initiation: Implications for intervention. J Addict Dis 2018;37:111–22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Yajnik M, Hill JN, Hunter OO, Howard SK, Kim TE, Harrison TK, et al. Patient education and engagement in postoperative pain management decreases opioid use following knee replacement surgery. Patient Educ Couns 2019;102:383–7. [DOI] [PubMed] [Google Scholar]
- 45.Hero JO, McMurtry C, Benson J, Blendon R. Discussing Opioid Risks With Patients to Reduce Misuse and Abuse: Evidence From 2 Surveys. Ann Fam Med 2016;14:575–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Mikuls TR, Mudano AS, Pulley L, Saag KG. The association of race/ethnicity with the receipt of traditional and alternative arthritis-specific health care. Med Care 2003;41:1233–9. [DOI] [PubMed] [Google Scholar]
- 47.Wright EA, Katz JN, Abrams S, Solomon DH, Losina E. Trends in prescription of opioids from 2003–2009 in persons with knee osteoarthritis. Arthritis Care Res (Hoboken) 2014;66:1489–95. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.DeMik DE, Bedard NA, Dowdle SB, Burnett RA, McHugh MA, Callaghan JJ. Are We Still Prescribing Opioids for Osteoarthritis? J Arthroplasty 2017;32:3578–82 e1. [DOI] [PubMed] [Google Scholar]
- 49.Stirratt MJ, Dunbar-Jacob J, Crane HM, Simoni JM, Czajkowski S, Hilliard ME, et al. Self-report measures of medication adherence behavior: recommendations on optimal use. Transl Behav Med 2015;5:470–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Fujita M, Sato Y, Nagashima K, Takahashi S, Hata A. Validity assessment of self-reported medication use by comparing to pharmacy insurance claims. BMJ Open 2015;5:e009490. [DOI] [PMC free article] [PubMed] [Google Scholar]
