Osteoarthritis (OA) is the most common joint disease. Articular cartilage in OA has shown to lose its mechanical resistance, elasticity and smoothness, and is consequently worn out by the movements of the joint. This leads to reactive bone remodeling, forming osteophytes, microfractures, subchondral eburnation and pseudocysts, and exposure of the articular end of the bone 1. The consequent roughness of the articular cartilage surfaces elicits secondary inflammatory reactions of the synovial membrane and bone. Unlike rheumatoid arthritis and other inflammatory joint diseases, the inflammatory component of OA is relatively mild 23. Clinical manifestations of OA of the knee are joint pain, stiffness in the morning or after rest, pain at night, limited joint motion and/or joint deformity. Joint pain in OA may originate from not only synovitis, but also stretching of the joint capsule or ligaments, periosteal irritation due to osteophyte formation, trabecular microfractures, intraosseous hypertension, or muscle spasm 4567.

There are many treatment modalities for OA of the knee including nonpharmacologic (e.g. patient education, weight control, physical and occupational therapy, and aerobic exercise programs) and pharmacologic therapy (e.g. intraarticular steroid injections, paracetamol, topical analgesics, nonsteroidal anti-inflammatory drugs (NSAIDs) and opioid analgesics) 8. Although NSAIDs are the most widely prescribed drugs to reduce joint pain and stiffness, the inflammatory component of OA is usually minimal, therefore, the need for the anti-inflammatory effect of NSAIDs in this condition is controversial 2910. Moreover, inhibition of prostaglandin biosynthesis is directly related to many common and occasionally severe side effects including gastrointestinal bleeding, hypertension, congestive heart failure, hyperkalemia, and renal insufficiency 11121314. These disadvantages call for an evaluation of the risks and benefits of the therapy in comparison with a less toxic one for OA.

Since the efficacy of NSAIDs in symptomatic treatment of OA of the knee depends on the analgesic rather than anti-inflammatory effect, paracetamol (analgesic drug) has been recently recommended as the first-line oral drug in the management of OA of the knee 8. However, the long term use of paracetamol probably leads to hepatic and renal impairment 1516. Thus, less toxic pain managing procedures, e.g. electroacupuncture (EA), may be considered as an alternative treatment of this disease. Even though EA is safe and effective in combating pain 1718, its role in OA of the knee is still controversial and comparative studies between EA and NSAIDs in this disease are rare 19. Therefore, the aim of this study was to compare the efficacy of EA, diclofenac and their combination in short-term, symptomatic treatment of OA of the knee.

Of the 200 subjects considered eligible for the study, 5 dropped out and 2 were withdrawn during the run-in period due to hypersensitivity to paracetamol and spontaneous pain relief. The remaining 193 subjects constituted the study population and were randomized into four parallel groups, which were not significantly different in base-line characteristics (Table 2) and radiographic findings of affected knees (Table 3). Only 1 patient in each placebo, EA and combined group as well as 2 patients in the diclofenac group received acupuncture treatment prior to this study.

Of the 193 study patients, 186 (96.37%) completed the study. The remaining 7 patients were withdrawn from the trial due to flare of pain with joint swelling (2 in the placebo and 1 in the EA group), severe GI side effects (3 in the combined group), and flare of pain from an accidental fall not related to treatment (1 in the EA group). Since there were few patients withdrawn from the trial, the results were, therefore, not substantially affected, whether the analysis was performed by an intention to treat analysis or an analysis on available completers. Thus, the following data showed the findings in only 186 available completers.

During 4 weeks of treatment, change in body weight compared to the base-line values did not significantly differ among the four groups (one-way ANOVA calculated weekly, data not shown). The rates of compliance with medications (placebo or diclofenac) and acupuncture (placebo or EA) in each group were more than 90%, and comparable among the four groups.

At the end of the study, the improvement of symptoms, which were determined by the reduction in mean changes in most outcome parameters (except WOMAC pain index and WOMAC total score), was greatest in the EA group (Table 4). The mean changes in VAS were significantly different between the EA and placebo group as well as the EA and diclofenac group (Table 4 and Figure 2). The mean changes in the Lequesne's functional index also differed significantly between the EA and placebo group (Table 4, Figure 3). In addition, there were significant differences in mean changes in the subscale of standardized WOMAC (pain index) between the combined and placebo group (Table 4 and Figure 4). The proportion of patients with the orthopedist's and patient's overall opinion of "much better" was greatest in the EA group, followed by the diclofenac, combined and placebo group, respectively. In addition, the proportion of responders was also greatest in the EA group, followed by the combined, diclofenac and placebo group, respectively. However, statistical differences among the four groups were found only in the orthopedist's overall opinion and a number of responders (Table 5). There were no differences between the four groups in the remaining outcome parameters.

The percentage of patients who experienced adverse effects (e.g. gastrointestinal and central nervous system symptoms, rash, edema, and hypertension) during this study did not differ between the four groups (data not shown), whereas, local contusions around the knee were common in the EA and combined group (approximately 45%). However, the contusions usually disappeared within 5–7 days.

When the responders in each group were followed up for 2 months, the proportion of remaining responders was not significantly different between the four groups (Table 6).

Although there are several lines of evidence from many controlled and uncontrolled studies for the short-term and long-term effectiveness of acupuncture in relieving clinical pain 232425262728, the scientific data concerning the efficacy of acupuncture in OA are rare 19. In addition, there are several systemic flaws 29 among these studies due to inadequate statistical power, inadequate sessions of acupuncture treatment, failure to control concomitant therapies, or no sham/placebo acupuncture controlled group. In this study, we minimized the methodological limitations of previous studies by using the randomized, single-blind, placebo controlled design with a larger sample size of OA patients coupled with standard outcome assessments. By using the percentage of the responders as the main efficacy criterion, the comparison between true and sham acupuncture needs at least 61 patients per group, whereas, only 35 patients per group are needed to compare between true and placebo acupuncture performed by not puncturing the skin 2330. In order to increase the ability of differentiating true from placebo effects and minimize the sample size, we selected the procedure of attaching the acupuncture points with the patch electrodes as placebo EA, and at least 45 completers per group were treated in this trial. In this study, a double-blind design was considered inappropriate, since we used patch electrodes as placebo EA and our patients might have recognized the difference between true and placebo EA. A single blind was, therefore, a reasonable alternative.

The acupuncture points used were selected because we intended to determine only the effects of local points around the affected knee. This applied especially to the medial aspect, which related to the knee compartment that was frequently involved in OA. Using these local points coupled with the needling technique (developed by Chawal Kanchanakul, acupuncturist of Dhammanamai Foundation, Chiang Mai, Thailand) demonstrated a rather simple, convenient, less painful, and more acceptable method for Thai patients, and it was effective in our pilot study. The points selected here were therefore different from other trials 24252628, which also included the distal points at medial and lateral aspects of the leg. Low-frequency (2 Hz) EA was selected because it produces an analgesia of long duration, which outlasts the 20-min stimulation session by 30 min to many hours. In addition, its effects are cumulative after several sessions of treatment given either daily or less frequently (2–3 times a week) 30. For these reasons, the low-frequency EA in this study was therefore given 3 times a week for 4 weeks, as commonly recommended in EA practice. However, to balance the acupuncture point stimulation by positive and negative polarities, each point was stimulated 6 times with positive and negative polarities in an alternate sequence during 12 sessions of treatment. In addition, each pair of electrodes was connected to each pair of adjacent points in order to obtain equal electrical sensation in each point during stimulation.

In this study, the clinical responses observed in the placebo group might result from, 1) the placebo effect or natural fluctuations in the symptoms of OA that are unrelated to the analgesic effect of paracetamol, because some patients demonstrated reductions in these scores without or with minimal analgesic need, or 2) the direct effects of paracetamol as a rescue analgesic. The latter reason made the placebo group not absolutely inert because paracetamol is also the first-line drug in the treatment of OA of the knee. However, the use of a rescue analgesic could not be avoided due to ethical reasons.

At week 4, the improvement of symptom scores (except change in WOMAC pain index and WOMAC total score) and the number of responders/patients with the opinion of "much better" were greatest in the EA group. These data indicate the great potential of EA in the symptomatic treatment of OA of the knee. This study also demonstrated that EA was significantly more effective than placebo with respect to changes in VAS and Lequesne's functional index, and significantly more effective than diclofenac with respect to the changes in VAS. This superiority of EA indicates its genuine efficacy 172330, which was more effective than placebo (or diclofenac) in this study. A previous trial revealed 34% and 14% reductions in the mean values of WOMAC total score and Lequesne's index, respectively after 4 weeks of acupuncture treatment 28, whereas, our study demonstrated a 50% and 45% reduction, respectively. These discrepancies might be due to differences in acupuncture point selection, number of points and the electrical stimulation technique used, or electrical stimulation parameters.

The clinical responses in the combined group were slightly superior to the diclofenac group, but not to the EA group (except for the tendency of being superior with respect to a change in the subscale of the standardized WOMAC: pain index). These responses indicate that EA may exert an adequate analgesic effect, a combination with diclofenac may not be of further benefit. Although a combination was not more efficacious than EA alone, it was significantly more so compared to placebo in terms of improvement in the WOMAC pain index, while EA was not. However, the nonsignificant change in clinical scores between the diclofenac and placebo group indirectly suggests that diclofenac may be as effective as paracetamol (as needed) in symptomatic treatment of OA of the knee.

The nonsignificant change in paracetamol consumption among the four groups during treatment might result from the unnecessary use of paracetamol in a great majority of active treatment groups, despite a significant improvement in some parameters of the EA and combined group, and a tendency to improve parameters in the diclofenac group. Another possibility might be the large variation in paracetamol consumption in each group that contributed to a false negative result. The nonsignificant change in the 50 feet-walk time among the four groups suggests that this parameter may not be sensitive enough to demonstrate existing differences. Walk time determined during stair climbing should thus be a better alternative 31. The failure to demonstrate the differences in other parameters (i.e. change in WOMAC stiffness, disability, and total scores) between the active treatment and placebo group may be due mainly to the rescue analgesic and partly to inadequacy of the sample size.

This study demonstrated that EA treatment was safe and free from serious adverse effects. However, the indifference in adverse events between the diclofenac and placebo group might be due to the exclusion of patients who were at high risk to the adverse effects of NSAIDs during the screening visit or short-term trial. In this study, the rescue analgesic paracetamol contributed to several confounding effects. Therefore, the randomized placebo controlled trial without using rescue analgesic should be investigated further to confirm the effectiveness of this range of active treatment, especially in EA and its combination with NSAIDs.

In summary, EA was significantly more effective than placebo regarding reductions in 100 mm VAS and Lequesne's functional index, but was significantly more effective than diclofenac in only the reduction of 100 mm VAS. The combination of EA and diclofenac treatment was more effective than placebo with respect to the reduction in the subscale of standardized WOMAC (pain index), but not more effective than EA treatment alone. Local contusions were minor adverse effects commonly found in the EA and combined group. The positive effects far outweigh the serious adverse ones of EA, which make this procedure an attractive alternative treatment for patients with OA of the knee.

None declared.