Comparison of general practitioners and rheumatologists' prescription patterns for patients with knee osteoarthritis
© Richette et al; licensee BioMed Central Ltd. 2011
Received: 10 November 2010
Accepted: 12 April 2011
Published: 12 April 2011
To compare the prescription modalities of general practitioners (GPs) and rheumatologists (RHs) for symptomatic knee osteoarthritis (OA) and to determine correlates with prescription of low-dose NSAIDs.
This observational, prospective, national survey was carried out among a national representative sample of GPs (n = 808) and RHs (n = 134). Each physician completed a medical questionnaire for the 2 most recent patients fulfilling the ACR criteria for knee OA.
GPs and RHs included 1,570 and 251 patients, respectively. Mean pain level of the knee (on a VAS, 0-100 mm) was greater for GP patients than for RH patients (49.8 ± 16.3 vs. 46.2 ± 17.1 mm, respectively; p < 0.01). As compared with patients of RHs, those of GPs more frequently had another joint affected by OA: 71.2% vs. 63.7% (p < 0.0001) and more often had hypertension and diabetes mellitus (p < 0.05).
As compared with RHs, GPs more frequently prescribed low-dose NSAIDs (p < 0.0001), oral NSAIDs (p < 0.05), and topical NSAIDs (p < 0.0001) but less frequently symptomatic slow-acting drugs for OA (p < 0.01). Moreover, GPs more frequently recommended rehabilitation (p < 0.01) and loss of weight (p < 0.0001). Logistic regression analysis revealed an association of low-dose NSAIDs prescription and prescription by GPs, prescription of topical NSAIDs, no prescription of oral NSAIDs or coxibs and no intra-articular injection of steroids.
This study identified speciality-related variability in some aspects of the management of knee OA. The clinical profile of patients with knee OA differed between GPs and RHs.
Osteoarthritis (OA) is the most prevalent joint disease worldwide and a leading cause of chronic disability . The prevalence of symptomatic knee OA has been recently estimated to be 9% in the general population. This estimate was computed with a Kellgren-Lawrence score of ≥1 used to define OA . France has about 40-fold more general practitioners (GPs; n = 101,667 in 2009) than rheumatologists (RHs; n = 2,625 in 2007) and thus, most symptomatic knee OA is managed by GPs.
Several recommendations have been published for the treatment of knee OA, including non pharmacological and pharmacological treatments, for both GPs and RHs [3–5]. Use of these treatments may differ among GPs and RHs, but few studies  have investigated the prescription patterns of these two types of physicians for the treatment of knee OA.
Because the prevalence of knee OA increases with age, the safety of prescribed drugs deserves special consideration, and the benefits and risks of prescribing nonsteroidal anti-inflammatory drugs (NSAIDs) must be cautiously evaluated for each patient. Indeed, serious side effects occur with the long-term use of NSAIDs by elderly people with OA. The drugs can cause severe gastrointestinal complications, such as bleeding or perforation . Several studies and meta-analyses have also suggested an association of increased cardiovascular risk and the use of traditional NSAIDs and coxibs [8, 9]. Because of the dose-dependent elevation in cardiovascular and gastrointestinal risks [7, 9], NSAIDs should be used at the lowest effective dose for the shortest possible time . Use of NSAIDs at a low dose, such as ibuprofen at up to 1200 mg or naproxen at up to 500 mg, may be associated with decreased cardiovascular risk  and may be an interesting alternative to alleviate pain in patients with OA. Indeed ibuprofen (400 mg 3 times daily) has been shown to be more effective than acetaminophen (1000 mg 3 times daily) in reducing pain and improving function in patients with knee or hip OA .
We designed this national observational prospective study to compare the prescription patterns of GPs and RHs for patients with knee OA, with a special emphasis on low-dose NSAIDs prescriptions.
We found that there is speciality-related variability in some aspects of the management of knee OA and that the clinical profile of patients with knee OA differed between GPs and RHs.
The study took the form of a cross-sectional survey by questionnaires completed by GPs and RHs working full- or part-time in different areas of France. This study was conducted in accordance with the recommendations of the Helsinki declaration. Ethical approval was not required for this study, in accordance with national guidelines.
Selection of physicians
GPs were randomly selected from the CEGEDIM registry and RHs from the French Society of Rheumatology registry. In total, 7,451 GPs and 1,777 RHs in private practice were asked to participate; 1,194 GPs (16.0%) and 225 RHs (12.7%) agreed and were sent questionnaires in May 2008. Finally, 808 GPs (67.6%) and 134 RHs (59.5%) recruited patients. This rate of participation was expected and is usual for this kind of survey. The demographics of these GPs and RHs did not significantly differ from those of GPs and RHs in France in general in terms of sex, age and number of years of practice.
Participating GPs and RHs were asked to record data for 2 consecutive patients presenting symptomatic knee OA according to the American College of Rheumatology criteria . Eligible patients with knee OA were ≥ 18 years old and did not have another condition that might have interfered with the assessment of knee OA.
After a clinical examination, physicians were asked to complete a questionnaire covering the clinical characteristics of OA, co-morbidities, current medications and the different treatments prescribed for knee OA at the end of the consultation. In France, low-dose NSAIDs are sold over the counter and are ibuprofen (up to 1200 mg), ketoprofen (up to 75 mg/j) and naproxen (up to 660 mg/j). Additionally, available SYSADOA are avocado/soybean unsaponifiable, chondroitin, glucosamine and diacerein. The questionnaire was pragmatic and did not provide the definition of the recorded co-morbidities (hypertension, diabetes mellitus, peptic ulcer, cardiovascular risk, history of cancer, anxiety, depression) to avoid any bias in the prescription. Pain intensity was assessed by a 100-mm visual analog scale (VAS). The patients were also asked to report the presence or absence of daily disability due to knee OA (yes/no) and the presence or absence of pain at night (yes/no). A pilot study included a group of 2 GPs and 2 RHs, as well as a group of 4 clinical and non-clinical researchers experienced in this type of survey, to test the questionnaire for comprehensibility and relevance.
Data are reported as mean ± standard deviation (SD) or percentages. Comparisons between the data for GPs and RHs involved the chi-square test or t test, as appropriate. Multiple regression analysis was used to assess the independent association of the prescription of low-dose NSAIDs and other variables. Because the study was exploratory, the sample size was calculated to provide a satisfying precision in the worst situation for ordinal data (rate of 50%). With an alpha risk of 5% and an expected precision of 2.5%, the number of patients needed was 1,536 and therefore 768 practitioners (who would each recruit 2 patients). Because the expected rate of practitioners actively recruiting patients among those giving their consent to participate was 55%, we invited 1,400 physicians (1,200 GPs and 200 RHs) to participate. A P value < 0.05 was considered statistically significant. All analyses involved use of SAS v9.2 (SAS Inst., Cary, NC).
Demographic characteristics of GPs and RHs
Characteristics of general practitioners (GPs) and rheumatologists (RHs)
n = 808
n = 134
52.2 ± 6.8
52.7 ± 7.5
Sex, % male
Practice location: % metropolitan/rural
Number of patients seen per week
141.1 ± 39.3
91.2 ± 30.0
Number of patients with knee OA seen per week
11.1 ± 8.6
16.7 ± 8.5
Demographic characteristics of patients with knee OA
Characteristics of patients with knee OA seen by general practitioners (GPs) and rheumatologists (RHs)
n = 1,821
n = 1,570
n = 251
67.3 ± 9.7
67.0 ± 9.7
69.8 ± 9.7
Sex, % female
28.9 ± 4.7
29.1 ± 4.6
28.0 ± 4.9
Duration of disease, years
7.7 ± 5.7
7.8 ± 5.6
6.8 ± 5.4
Pain (VAS, 0-100 mm)
On movement over the last 24 hr
61.6 ± 17.9
62.4 ± 17.6
57.3 ± 19.0
32.7 ± 20.0
33.9 ± 20.5
25.3 ± 20.6
49.3 ± 16.4
49.8 ± 16.3
46.2 ± 17.1
Pain at night, %
Daily disability, %
Presence of SF effusion, %
Co-morbidities in patients with knee OA seen by general practitioners (GPs) and rheumatologists (RHs)
n = 1,821
n = 1,570
n = 251
History of cancer
Prescription modalities of GPs and RHs
Frequency of non pharmacological and oral pharmacological treatments prescribed during the consultation for knee OA for general practitioners (GPs) and rheumatologists (RHs)
n = 1,821
n = 1,570
n = 251
Weak opioid analgesics
Strong opioid analgesics
Proton pump inhibitor
Symptomatic slow-acting drugs
Non pharmacological treatments
Weight loss (if obese)
Information and education
Frequency of local treatments performed during the consultation for knee OA by general practitioners (GPs) and rheumatologists (RHs)
n = 1,821
n = 1,570
n = 251
Correlates with prescription of low-dose NSAIDs
Frequency of low-dose NSAIDS, NSAIDS or coxib prescriptions according to the presence or absence of cardiovascular risk in patients with knee OA
Absence of CV risk
Presence of CV risk
Low-dose NSAIDs (n = 250)
NSAIDs (n = 613)
Coxibs (n = 155)
This national observational prospective study was designed to compare the prescription patterns of GPs and RHs for their patients with knee OA, with a special emphasis on the prescription of low-dose NSAIDs.
The results of our study are consistent with published data showing that physicians in private practice in general follow the international recommendations [3, 5, 12] for the pharmacological treatment of OA [6, 13–15]. GPs and RHs preferentially prescribed acetaminophen, and conventional NSAIDs were more frequently prescribed than were coxibs and low-dose NSAIDs. By contrast, topical NSAIDs, which should be considered ahead of oral NSAIDs according to the National Institute for Health and Clinical Excellence guidelines , were less frequently prescribed than were standard oral NSAIDs [6, 14].
Of interest, our study identified variability by medical specialty in some aspects of the pharmacological treatment of knee OA. Indeed, GPs more frequently prescribed NSAIDs (conventional, low-dose and topical), whereas RHs more often prescribed SYSADOAs and more frequently gave intra-articular injections of steroids and hyaluronic acid. This variability is similar to what was found in the AMICA survey, which suggested that the pharmacological management of knee OA differs between GPs and RHs [6, 16]. Another explanation could be the different clinical profile of patients seen by GPs or RHs. Indeed, in our study, as compared with RH patients, GP patients had longer duration of disease, more frequently had another joint affected by OA and the disease was more painful, as was previously noted in other studies [6, 17]. Although in France patients can directly consult a specialist, these differences might be due to patients' more limited access to RHs, which leads patients with painful disease to consult GPs more often. Moreover, as shown in a previous British survey , a mixture of physical, social and psychological factors might predict visits to GPs, that may explain the different clinical profile of patients with knee OA who consulted GPs.
Our GPs and RHs did not differ in the prescription of analgesics. Acetaminophen was prescribed for only 43% of patients with chronic knee OA, which is far less that the 95.8% recorded by Denoeud et al., who assessed the pharmacological modalities prescribed by GPs as first-line treatment for knee OA . This relatively low use of acetaminophen for chronic knee OA might be due to the modest efficacy of long-term intake of this drug to alleviate pain .
GPs and RHs did not often recommend nonpharmacological modalities such as information, physical therapy, exercise or weight loss (for obese people). For example, weight reduction, which has been showed to be effective in alleviating pain in patients with knee OA , was recommended by only about half of the RHs and 65% of the GPs. These figures, which are close to those obtained from a recent survey of GPs , highlight the need to improve the dissemination of recommendations for nonpharmacological treatment of OA .
Another interesting finding is the high proportion of patients with knee OA who had hypertension (57.3%) or another cardiovascular risk factor (27.5%). These results are in accordance with results of a large survey showing that 40% of patients with OA have hypertension as compared with 25% in the general population . This point is of importance given the known increased cardiovascular risk associated with the use of traditional NSAIDs and coxibs, in particular for patients with established cardiovascular conditions. Of note, hypertension and diabetes mellitus were more frequent in GP patients, who were more often prescribed NSAIDs to alleviate OA pain. Cyclooxygenase inhibition causes adverse effects, in particular blood pressure elevation, mainly by impairing the systemic and renal vasodilatatory benefits of prostacyclin . GPs and RHs seem to be aware of this key notion, and it affects their prescription practice because we found that NSAIDs and coxibs were prescribed less for patients with a known cardiovascular risk.
A recent large-scale study has also demonstrated a dose-dependant relation between the use of conventional NSAIDs or coxibs and risk of death and myocardial infarction in healthy individuals . By contrast, use of low-dose ibuprofen was associated with decreased risk of cardiovascular events, which could be due to an antithrombotic effect comparable to that of aspirin .
In our survey, as compared with the prescription of classical NSAIDs and coxibs, that of low-dose NSAIDs did not depend on the perceived presence of cardiovascular risk factors and was associated with prescription by GPs, prescription of topical NSAIDs and no prescription of NSAIDs or coxibs. Thus, these practitioners prescribe low-dose NSAIDs as an alternative to conventional NSAIDs or coxibs for patients with knee OA, regardless of their cardiovascular profile.
Our study contains some limitations. Although the response rate was high (67%), participants may not have been representative of all GPs and RHs. Moreover, the proportion of GPs was much higher than that of RHs, for demographic reasons.
Our study found that GPs and RHs see a different clinical profile of patients with knee OA. GP patients more often exhibit severe conditions and more often have vascular comorbidities. GPs and RHs show some variability in their management of knee OA in that GPs more frequently prescribe NSAIDs. Finally, low-dose NSAIDs, a medication prescribed more often by GPs than RHs, is used as an alternative to conventional NSAIDs or coxibs, independent of the perceived presence of cardiovascular risk factors.
This study was performed with the support of an independent grant provided by Wyeth-Santé Familiale France, which was not involved in the statistical analysis.
The authors thank all the physicians and all people with knee OA who took part in the study.
- Lohmander LS, Roos EM: Clinical update: treating osteoarthritis. Lancet. 2007, 370: 2082-2084. 10.1016/S0140-6736(07)61879-0.View ArticlePubMedGoogle Scholar
- Roux CH, Saraux A, Mazieres B, Pouchot J, Morvan J, Fautrel B, Testa J, Fardellone P, Rat AC, Coste J, Guillemin F, Euller-Ziegler L: Screening for hip and knee osteoarthritis in the general population: predictive value of a questionnaire and prevalence estimates. Ann Rheum Dis. 2008, 67: 1406-1411. 10.1136/ard.2007.075952.View ArticlePubMedGoogle Scholar
- Jordan KM, Arden NK, Doherty M, Bannwarth B, Bijlsma JW, Dieppe P, Gunther K, Hauselmann H, Herrero-Beaumont G, Kaklamanis P, Lohmander S, Leeb B, Lequesne M, Mazieres B, Martin-Mola E, Pavelka K, Pendleton A, Punzi L, Serni U, Swoboda B, Verbruggen G, Zimmerman-Gorska I, Dougados M: EULAR Recommendations 2003: an evidence based approach to the management of knee osteoarthritis: Report of a Task Force of the Standing Committee for International Clinical Studies Including Therapeutic Trials (ESCISIT). Ann Rheum Dis. 2003, 62: 1145-1155. 10.1136/ard.2003.011742.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang W, Moskowitz RW, Nuki G, Abramson S, Altman RD, Arden N, Bierma-Zeinstra S, Brandt KD, Croft P, Doherty M, Dougados M, Hochberg M, Hunter DJ, Kwoh K, Lohmander LS, Tugwell P: OARSI recommendations for the management of hip and knee osteoarthritis, Part II: OARSI evidence-based, expert consensus guidelines. Osteoarthritis Cartilage. 2008, 16: 137-162. 10.1016/j.joca.2007.12.013.View ArticlePubMedGoogle Scholar
- Conaghan PG, Dickson J, Grant RL: Care and management of osteoarthritis in adults: summary of NICE guidance. Bmj. 2008, 336: 502-503. 10.1136/bmj.39490.608009.AD.View ArticlePubMedPubMed CentralGoogle Scholar
- Scarpa R, Sarzi-Puttini P, Cimmino MA, Caporali R, Parazzini F, Zaninelli A, Canesi B: Analysis of pharmacologic and nonpharmacologic prescription patterns of general practitioners and specialists in the AMICA study. Semin Arthritis Rheum. 2005, 35: 24-30. 10.1016/j.semarthrit.2005.02.001.View ArticlePubMedGoogle Scholar
- Masso Gonzalez EL, Patrignani P, Tacconelli S, Garcia Rodriguez LA: Variability among nonsteroidal antiinflammatory drugs in risk of upper gastrointestinal bleeding. Arthritis Rheum. 2010, 62: 1592-1601. 10.1002/art.27412.View ArticlePubMedGoogle Scholar
- McGettigan P, Henry D: Cardiovascular risk and inhibition of cyclooxygenase: a systematic review of the observational studies of selective and nonselective inhibitors of cyclooxygenase 2. Jama. 2006, 296: 1633-1644. 10.1001/jama.296.13.jrv60011.View ArticlePubMedGoogle Scholar
- Fosbol EL, Gislason GH, Jacobsen S, Folke F, Hansen ML, Schramm TK, Sorensen R, Rasmussen JN, Andersen SS, Abildstrom SZ, Traerup J, Poulsen HE, Rasmussen S, Kober L, Torp-Pedersen C: Risk of myocardial infarction and death associated with the use of nonsteroidal anti-inflammatory drugs (NSAIDs) among healthy individuals: a nationwide cohort study. Clin Pharmacol Ther. 2009, 85: 190-197. 10.1038/clpt.2008.204.View ArticlePubMedGoogle Scholar
- Boureau F, Schneid H, Zeghari N, Wall R, Bourgeois P: The IPSO study: ibuprofen, paracetamol study in osteoarthritis. A randomised comparative clinical study comparing the efficacy and safety of ibuprofen and paracetamol analgesic treatment of osteoarthritis of the knee or hip. Ann Rheum Dis. 2004, 63: 1028-1034. 10.1136/ard.2003.011403.View ArticlePubMedPubMed CentralGoogle Scholar
- Altman R, Asch E, Bloch D, Bole G, Borenstein D, Brandt K, Christy W, Cooke TD, Greenwald R, Hochberg M: 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: 1039-1049. 10.1002/art.1780290816.View ArticlePubMedGoogle Scholar
- Zhang W, Nuki G, Moskowitz RW, Abramson S, Altman RD, Arden NK, Bierma-Zeinstra S, Brandt KD, Croft P, Doherty M, Dougados M, Hochberg M, Hunter DJ, Kwoh K, Lohmander LS, Tugwell P: 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: 476-499. 10.1016/j.joca.2010.01.013.View ArticlePubMedGoogle Scholar
- Denoeud L, Mazieres B, Payen-Champenois C, Ravaud P: First line treatment of knee osteoarthritis in outpatients in France: adherence to the EULAR 2000 recommendations and factors influencing adherence. Ann Rheum Dis. 2005, 64: 70-74. 10.1136/ard.2003.015263.View ArticlePubMedPubMed CentralGoogle Scholar
- Conrozier T, Marre JP, Payen-Champenois C, Vignon E: National survey on the non-pharmacological modalities prescribed by French general practitioners in the treatment of lower limb (knee and hip) osteoarthritis. Adherence to the EULAR recommendations and factors influencing adherence. Clin Exp Rheumatol. 2008, 26: 793-798.PubMedGoogle Scholar
- Chevalier X, Marre JP, de Butler J, Hercek A: Questionnaire survey of management and prescription of general practitioners in knee osteoarthritis: a comparison with 2000 EULAR recommendations. Clin Exp Rheumatol. 2004, 22: 205-212.PubMedGoogle Scholar
- Chard J, Dickson J, Tallon D, Dieppe P: A comparison of the views of rheumatologists, general practitioners and patients on the treatment of osteoarthritis. Rheumatology (Oxford). 2002, 41: 1208-1210. 10.1093/rheumatology/41.10.1208-a.View ArticleGoogle Scholar
- Mitchell HL, Carr AJ, Scott DL: The management of knee pain in primary care: factors associated with consulting the GP and referrals to secondary care. Rheumatology (Oxford). 2006, 45: 771-776. 10.1093/rheumatology/kei214.View ArticleGoogle Scholar
- Towheed TE, Maxwell L, Judd MG, Catton M, Hochberg MC, Wells G: Acetaminophen for osteoarthritis. Cochrane Database Syst Rev. 2006, CD004257-1
- Christensen R, Bartels EM, Astrup A, Bliddal H: Effect of weight reduction in obese patients diagnosed with knee osteoarthritis: a systematic review and meta-analysis. Ann Rheum Dis. 2007, 66: 433-439. 10.1136/ard.2006.065904.View ArticlePubMedPubMed CentralGoogle Scholar
- Roberts C, Adebajo AO, Long S: Improving the quality of care of musculoskeletal conditions in primary care. Rheumatology (Oxford). 2002, 41: 503-508. 10.1093/rheumatology/41.5.503.View ArticleGoogle Scholar
- Singh G, Miller JD, Lee FH, Pettitt D, Russell MW: Prevalence of cardiovascular disease risk factors among US adults with self-reported osteoarthritis: data from the Third National Health and Nutrition Examination Survey. Am J Manag Care. 2002, 8: S383-391.PubMedGoogle Scholar
- Moore RA, Derry S, McQuay HJ: Cyclo-oxygenase-2 selective inhibitors and nonsteroidal anti-inflammatory drugs: balancing gastrointestinal and cardiovascular risk. BMC Musculoskelet Disord. 2007, 8: 73-10.1186/1471-2474-8-73.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2474/12/72/prepub
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