| Literature DB >> 26587390 |
Pu-Wei Hou1, Pin-Kuei Fu2, Hsin-Cheng Hsu1, Ching-Liang Hsieh3.
Abstract
To evaluate whether the use of traditional Chinese medicine (TCM; zhōng yī) influences symptoms or functional outcomes in patients with osteoarthritis (OA) of the knee ( xī guān jié yán). A systematic review of randomized control trials was conducted. Searches for studies in PubMed that were performed between 1965 and August 2013, and retrieved studies were subjected to reference screening. The types of studies included in our review were 1) placebo-based or comparative studies; 2) open label, single-blinded or double-blinded studies; 3) studies evaluating the efficacy of TCM for treating OA of the knee; and 4) studies evaluating only TCM or combination preparations. Trials were conducted with participants over 18 years of age with knee pain and at least three of the following characteristics: 1) an age greater than 50 years; 2) morning stiffness lasting for fewer than 30 min; 3) a crackling or grating sensation; 4) bony tenderness of the knee; 5) bony enlargement of the knee; or 6) no detectable warmth of the joint to the touch. Studies were rated for risk of bias and graded for quality. After screening, 104 studies that satisfied the eligibility requirements were identified, and only 18 randomized control trials were included in the quantitative and qualitative synthesis. Upon review, we found "moderate-quality" evidence of effects from acupuncture ( zhēn jiǔ) on pain, which was measured using a visual analogue scale, and physical function, which was measured using qigong ( qì gōng) with motion. "Low-quality" evidence was found regarding the effects of acupuncture on physical function, and no evidence was found regarding the effects of herbal medicine on pain or physical function. Herbal patches ( yào bù) appeared to affect pain and physical and function, but these effects were not found to be significant. The initial findings included in this review suggest that acupuncture is a promising intervention according to the primary outcome measure, pain, and qigong with motion is an effective method for treating physical function. However, according to the Grades of Recommendation, Assessment, Development, and Evaluation criteria, only moderate-quality evidence was found in these studies. Further rigorous studies are warranted to investigate the application of TCM in treating OA of knee.Entities:
Keywords: acupuncture; knee; massage; osteoarthritis; qigong; traditional Chinese medicine
Year: 2015 PMID: 26587390 PMCID: PMC4624358 DOI: 10.1016/j.jtcme.2015.06.002
Source DB: PubMed Journal: J Tradit Complement Med ISSN: 2225-4110
Criteria for judging the quality of individual trials.
| High | >75% of the criteria have been fulfilled [≧10/12]. Where they have not been fulfilled the conclusions of the study or review are thought very unlikely to alter. |
| Moderate | 50–75% of the criteria have been fulfilled [6–9/12]. Those criteria that have not been fulfilled or not adequately described are thought unlikely to alter the conclusions. |
| Low | Less than 50% of the checklist criteria were fulfilled [<6/12]. The conclusions of the study are thought likely or very likely to alter. |
This table is adapted from Liddle et al.12, 16
The evidence grading system applied in this review.
| High | At least 75% of the RCTs with no limitations of study design have consistent findings, direct and precise data and no known or suspected publication bias. |
| Moderate | One of the domains is not met. |
| Low | Two of the domains are not met. |
| Very low | Three of the domains are not met. |
| No evidence | No RCTs were identified that addressed this outcome. |
This table shows the CBRG recommended quality of evidence grading system that was applied to each outcome measure.19, 20
Osteoarthritis (OA) of the knee intervention with “Acupuncture (針灸 zhēn jiǔ)”.
| Basic information of researches | Participants | Intervention | Outcome assessment | Results | The risk of bias |
|---|---|---|---|---|---|
| Ng MM et al | N = 24 (diagnosed with OA knee) Knee pain during the preceding month morning stiffness less than 30 min, crepitus, bony enlargement, stable condition under arthritis medication | EA treatment (N = 8): ST-35 and EX-LE-4, De-Qi (得氣 dé qì)”, EA TENS Group (N = 8): the procedures were the same as EA group except surface electrodes were used instead of needle insertion | Pain: numerical rating scale of pain Function: passive range of movement of the OA knee; the Timed Up-and-Go test (TUGT) | For the EA group, there was a significant reduction of mean NRS of knee pain (229%) after eight sessions of treatment (p = 0.01), and the effect was well maintained (231%) at the 2-week follow-up evaluation (p = 0.01). A reduction of mean NRS of knee pain (228%) was significant in the TENS group after eight sessions of treatment (p = 0.01) but at the 2-week follow-up evaluation, the effect became less pronounced. The total passive knee ROM was not significantly different among the three groups across the period of study. There was a significant improvement (11%) in the TUGT scores in the EA group after eight sessions of treatment. | 10/12 (High) |
| Berman BM et al | N = 570 Age ≧50 years, diagnosis of OA of the knee, K-L∗ grade ≧2, moderate or great knee pain during the past month, willingness to be randomly assigned | True acupuncture group (N = 190): acupoints (穴位 xué wèi) (5 local and 4 distal points) by TCM theory, De-Qi”, EA No needle insertion, the procedure is the same as true acupuncture group, 6 two hour group sessions based on the Arthritis Self-Management Program | Pain: WOMAC pain score Function: WOMAC function score; SF-36; the 6-min walk time; the patient global assessment | While WOMAC pain among participants who were receiving true acupuncture decreased more than in the sham group at all of the post baseline assessments (no statistically significant difference). The true acupuncture group's improvement in WOMAC function from baseline was significantly greater than that of the sham control group at weeks 8. Changes in overall physical component score did not statistically significantly differ between the true versus sham acupuncture groups. | 11/12 (High) |
| Tukmachi E et al | N = 30 Age ≧18 years, OA of the knee≧6 months, K-L, grade IV no response to previous treatment no previous acupuncture | Group A (N = 9): Acupuncture alone, stop NSAIDs and analgesic drugs, “De-Qi” 8 acupoints used traditionally with EA Acupuncture and their existing analgesic and anti-inflammatory medication week 1–5: current medications, week6–10: acupuncture plus medications | Pain: VAS(10-cm) Function: WOMAC; global assessment | Group C showed no change in pain score during the first five weeks while waiting for acupuncture. After acupuncture there was a large and statistically significant drop in the VAS pain score for all three treated groups. In groups A and B the significant improvement in pain score was maintained when the patients attended for the final visit. WOMAC stiffness scores decreased by more than half in groups B and C after the course of acupuncture. The reduction was less dramatic in group A, but still significant and still present one month later. | 7/12 (Moderate) |
| Vas J et al | N = 97 Diagnosed by ACR criteria written informed consent Age ≧45 years, pain more than 3 months, Grade 1 of Ahlback classification | Intervention group (N = 48) acupuncture plus diclofenac, Acupoints based on traditional treatment methods, “De-Qi” EA placebo acupuncture plus diclofenac the procedures were the same as true acupuncture no needle penetration. | Pain: WOMAC pain scale VAS(100-mm) Function: WOMAC stiffness and function scale Others: the dosage of diclofenac accumulated; the profile of quality of life in the chronically ill (PQLC) | The WOMAC index and VAS presented a greater, and significant, reduction in the intervention group than in the control group. A reduction of 53.9 was observed in the total accumulated number of diclofenac tablets for the intervention group compared with the control group. The PQLC results indicate that acupuncture treatment produces significant changes in physical capability and psychological functioning. | 10/12 (High) |
| Witt C et al | N = 300 age 50–75 years diagnosed by ACR criteria, K-L∗ grade ≧2 average VAS (100 mm) ≧40 in the 7 days before baseline assessment written informed consent | Acupuncture group (N = 150): semi-standardized (TCM), 6 local and 2 distal acupoints, “De-Qi” Minimal acupuncture group (N = 76): superficial insetion at non-acupuncture point, at least eight out of ten points No acupuncture for 8 weeks after randomization, recieve 12 sessions of acupuncture from week 9. | Pain and function: WOMAC Pain Disability Index (PDI) SF-36 (German version) Others: Schmerzempfindungs-Skala [SES]; Allgemeine; Depressionsskala [ADS]; questions about workdays lost | On all WOMAC subscales (pain, stiffness, and physical function), the acupuncture group showed significant improvements compared with the minimal acupuncture and the waiting list groups. Patients who received acupuncture had significantly better results for almost all secondary outcome measures than did those in the minimal acupuncture and waiting list groups. | 10/12 (High) |
| Scharf HP et al | N = 1039 signed informed consent age ≧40 years, diagnosed by ACR criteria chronic pain more than 6 months K-L grade 2 or 3 a chronic pain score of at least 1, according to the criteria of von Korff and colleagues | Conservative therapy (N = 342): diclofenac, up to 150 mg/d, or rofecoxib, 25 mg/d 6 Physiotherapy sessions 10 acupuncture sessions, 2 of 16 defined points were chosen and 4 Ashi points, consercative therapy was the same as above. minimal-depth needling without stimulation at 10 points at defined distances from TCA points. the other procedures were the same as above. | Pain: WOMAC pain scale Function: WOMAC function scale (Success rates were calculated according to a change of at least 36% from baseline WOMAC scores at 13 and 26 weeks after the start of treatment.) Others: The dichotomized global patient assessment; SF-12 physical subscale | Statistically significantly increased success rates in the TCA and sham acupuncture groups compared with the conservative therapy group (p < 0.001 for both comparisons) and no difference between the TCA and sham acupuncture groups (p = 0.48). Statistically significant changes with respect to total WOMAC score. The changes in the TCA and sham acupuncture groups were much more distinct than those measured in the conservative therapy group. The dichotomized global patient assessment showed statistically significant differences among treatment groups, with a higher rate of satisfaction in the TCA and sham acupuncture groups at week 26. The SF-12 physical subscale at week 26 was also greater with TCA and sham acupuncture than with conservative therapy. | 10/12 (High) |
| Williamson L et al | N = 181 (on the surgical list) on the surgical list for knee arthroplasty, bilateral or unilateral knee pain more than 3 months | Acupuncture group (N = 60): acupoints were used in previous reported research, “De-Qi”, left in-situ 20 min. exercise circuit supervised by the same physiotherapist, once a week, for 6 weeks. exercise and advice by consensus. | Pain: VAS(10-cm) Function:Oxford Knee Score (OKS); WOMAC; a 50-m timed walk Others:Hospital Anxiety and Depression score (HAD) | The During the 50-m timed walk, the physiotherapy group had a lowest mean walking time but no significant difference. No significant pre-operative changes in HAD and WOMAC between the groups. | 10/12 (High) |
| Jubb RW et al | N = 68 Age >18 year, symptoms of OA of the knee over than 6 months, inadequate response to conventional treatment, not on a surgical list | Acupuncture group (N = 34): distal and local acupoints, EA to anterior part for 10 min and then posterior part 10 min needle did not be inserted into the skin | Pain: VAS Function: WOMAC*; EuroQol Others: plasma ß-endorphin concentration | The comparison between the acupuncture and the sham group showed a statistically significant improvement (pain score) in the acupuncture group (p = 0.035). No significant difference between the groups for EuroQol and WOMAC stiffness or function either at the end of treatment at week five or at the final visit at week nine. Plasma ß-endorphin levels did not vary significantly during the study. | 8/12 (Moderate) |
| Itoh K et al | N = 30 (age >60 years, diagnosed OA according to ACR* criteria) pain over 6 months, K-L grade ≧2 no neurological sign, no acupuncture in the previous 6 months Inadequate response to conventional treatment | Standard acupuncture (N = 10): traditional acupoints for knee pain, De-Qi” Trigger points, local twitch by stimulation non-penerating needle, A simulation of needle insertion and extraction was performed. | Pain: VAS(100-mm) Function: WOMAC | The VAS of the TrP group was the lowest of the three, and the difference was statistically significant when compared with SH group (p = 0.025), but no significant difference was detected between TrP and SA (p = 0.47). The lowest WOMAC score was found in the TrP group, and a statistically significant difference was detected between TrP and SH groups (p = 0.031). No significant difference was detected between SA and SH groups. | 8/12 (Moderate) |
| Lu TW et al | N = 20 bilateral medial compartment knee OA, grade 2 or 3 of K-L∗, ability to walk without assistance | Experimental group (N = 10): a 30 min EA*, 5 acupoints, “De-Qi” sham EA (line connected to needle but no power), needle into the skin at points from 1 cm left to the acupoints, No “De-Qi” | Pain: VAS(10-cm)* Function: Gait analysis (Vicon 512, Oxford Metrics, UK) | The VAS scores were decreased significantly after acupuncture treatment in both groups (the mean change of experimental group was 2 times than that of sham group). The experimental group showed a great contrast to the sham group, with significant improvements in the gait variables (hip and knee flexion, ankle plantarflexion were increased significantly and hip extensor, knee extensor and ankle plantarflexor moments were all increased significantly). | 9/12 (Moderate) |
| Soni A et al | N = 56 Patients listed for knee arthroplasty due to OA who had unilateral or bilateral knee pain lasting more than 3 months. | Acupuncture and exercise therapy (N = 28): Acupoints according to previous study, exercise according to the procedures of standard exercise and advice leaflet. designed by consensus between the physiotherapy, rheumatology and orthopaedic departments. | Pain: VAS(10-cm) Function: Oxford Knee Score (OKS); 50 m timed walk Others: the Hospital Anxiety and Depression score (HAD) | Combined acupuncture and physiotherapy is a pragmatic therapeutic option for patients with moderate to severe knee OA. Patients in the treatment group were more likely to withdraw from the surgical waiting list due to sufficient symptomatic improvement although the effect was not statistically significant (OR 7.64, 95% CI 0.86 to 68.20). | 8/12 (Moderate) |
| Mavrommatis CI et al | N = 120 meet the ACR criteria K-L grade ≧2 chronic pain more than 3 months | Acupuncture and etoricoxib (N = 40): 6 local and 4 distal acupoints, “De-Qi”, EA in pairs ST36-SP9 and GB34-SP10 the procedures were the same as real acupuncture but no needle insertion, the same pairs of EA stimulation | Pain: WOMAC pain scale; VAS(100-mm); Pain Test; FDK 20 Algometer of Warner USA Function: WOMAC stifness and function scale; Short Form-36 version 2 Others: BMI, CBC, ESR, Rh factor, liver and kidney function, uric acid and arterial blood pressure | WOMAC index score and its subscales at the end, week 8, are significant differences at all group. Patients receiving acupuncture plus etoricoxib (group I) had significantly better results in all outcome measurements except for the WOMAC scales and the SF-36v2 mental component summary. No significant differences in the laboratory test results between groups at the beginning and at the end of the treatment. Follow-up (8–12 week), the superiority of response in the acupuncture plus pharmacological treatment group compared with responses in the other 2 groups remained statistically significant for all scales | 10/12 (High) |
*EA: electro-acupuncture.
*VAS: visual analogue scale.
*WOMAC: The Western Ontario and McMaster Universities Arthritis Index.
*ACR: American College of Rheumatology.
*K-L: Kellgren-Lawrence criteria.
Herbal patch for OA of the knee.
| Author/Year | Participants | Intervention | Outcome assessment | Results | The risk of bias |
|---|---|---|---|---|---|
| Wang X et al | N = 150 Age between 40-70 years, Diagnosed by the criteria of Chinese Orthopaedic Association and TCM syndrome evidence of idiopathic OA, Pain over 20/100 mm VAS | FNZG (N = 60) | Pain: VAS(100-mm) Function: WOMAC Others: TCM Syndrome Questionnaire | All three groups improved with respect to a decrease from baseline to day 1 and day 7 in the VAS score, the greatest in FNZG and the smallest in SJG group at day 7. Improvements from baseline to day 7 in the 3 WOMAC domains and total score were seen in three groups, the greatest in SJG without significant differences. FNZG group had a significantly greater decrease in the item of fear of coldness as assessed by TCMSQ than that in placebo group but SJG group did not reach a significant reduction. | 10/12 (High) |
Herbs for OA of the knee.
| Author/Year | Participants | Intervention | Outcome assessment | Results | The risk of bias |
|---|---|---|---|---|---|
| Park SH et al | N = 57 | AIF group (N = 31) | Pain: VAS(100-mm) Function: K-WOMAC | Decreases in VAS scores were significant in both study groups and the rate of response to AIF was 4.76 percentage points higher at 6 weeks than placebo group, however no significant difference was found between the two groups. Assessments of K-WOMAC scores showed significant improvements in pain, stiffness, physical function and total scores in the AIF group only. | 9/12 (Moderate) |
| Li XH et al | N = 100 | Chinese medicine for resolving phlegm and removing damp, orally taken twice a day, for 2 courses of treatment. Votalin tablet 25 mg each time and Vitamin C 20 mg each time, 3 times a day, for 2 courses of treatment. | Pain (0–3) Morning stiffness (0–3) Walking (0–3) Stand up from sitting position (0–3) Walk unrestrictedly (0–3) Lassitude in the loin and knees (0–3) Daily activity (0–3) Carry out all kinds of activities (0–3) | The total score for symptoms obviously declined after treatment in both groups. The decreased symptoms and effective rate were better in the treatment group but no statistic difference. X-ray manifestation on patients before and after treatment in the two groups was basically identical without obvious change. | 5/12 (Low) |
Qigong for OA of the knee.
| Author/Year | Participants | Intervention | Outcome assessment | Results | The risk of bias |
|---|---|---|---|---|---|
| Chen KW et al | N = 112 | EQT group (N = 60): Two qigong therapists were invited to perform EQT in this study. There is no standard procedure for EQT in the field. a sham healer to mimic EQT. | Pain: McGill Pain Questionnaire (MPQ-SF) Function: WOMAC; Time to walk a 15-m straight path; ROM when squatting down to the lowest position without pain Others: the Spielberger State Trait; Anxiety Scale; the Center for Epidemiologic Studies Depression Scale; an adopted general mood index | There are significant differences between healer 2 and the placebo group in reduced pain measured by MPQ (p < 0.05) and slightly reduced time for walking 15 m (p = 0.08) after treatment. Differences in pain reduction are smaller between healer 1 and the placebo group (p = 0.09) and are not statistically significant for reduced time in walking 15 m (p = 0.35). For psychological outcomes, no significant differences were found in depression or anxiety scales. | 10/12 (High) |
| An B et al | N = 28 (diagnosis according to ACR criteria) | Baduanjin intervention (N = 14): eight sections, and each section needs to be repeated 20 times. No intervention was undertaken for the control group. | Pain: WOMAC pain scale Function: WOMAC; SF-36; 6-MWT; ISKE | Compared with the control group, the participants in the Baduanjin group had statistically significant improvements in percentage changes of the WOMAC pain subscale, the WOMAC stiffness subscale, 0.029), the WOMAC physical function subscale, 6-MWT, and Peak Torque of the ISKE. The SF-36's General Health, Social Function, and Mental Health subscales had no significant changes between those in the Baduanjin and control groups. | 5/12 (Low) |
| Lee HJ et al | N = 41 | T'ai chi (太極拳 tài jí quán) (N = 28): 1 h, and repeated twice a week for eight weeks, 18 movements, focus on releasing tension in the physical body and mind acting in concert with breathing. no intervention during the study period. | Pain: No pain score. Function: WOMAC; The 6-m walking test Others: Short Form 36 (SF-36); Health Survey | The T'ai chi group showed significant improvements in the total SF-36 score compared with the control group. The T'ai chi group showed improvements in total WOMAC score compared with the control group. In the 6-m walking test, the T'ai chi group spent significantly shorter times. | 10/12 (High) |
Fig. 1Flow diagram of inclusion and exclusion of articles (PRISMA 2009 Flow Diagram).
Methodological quality assessment and risk-of-bias (Acupuncture (針灸 zhēn jiǔ)).
| Adequate randomization | Concealed allocation | Groups similar at baseline | Patient blinded | Care provider blinded | Outcome assessor blinded | Dropout rate described and acceptable | Intention to treat analysis | Co-interventions avoided or similar | Compliance acceptable | Timing outcome assessment similar | Report free of selective outcome reporting | Total | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ng MM et al 2003 | Yes | Unclear | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | Yes | Yes | 10/12 |
| Berman BM et al 2004 | Yes | Yes | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | Yes | Yes | 11/12 |
| Tukmachi E et al 2004 | Yes | Yes | No | No | No | No | Yes | Yes | No | Yes | Yes | Yes | 7/12 |
| Vas J et al 2004 | Yes | Yes | Yes | Yes | No | Yes | Yes | Yes | Yes | No | Yes | Yes | 10/12 |
| Witt C et al 2005 | Yes | Unclear | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | Yes | Yes | 10/12 |
| Scharf HP et al 2006 | Yes | Yes | Yes | Yes | No | Yes | Yes | Yes | No | Yes | Yes | Yes | 10/12 |
| Williamson L et al 2007 | Yes | Yes | Yes | Yes | No | Yes | Yes | Yes | Yes | Yes | Yes | No | 10/12 |
| Jubb RW et al 2008 | Unclear | Unclear | Yes | Yes | No | Yes | Yes | No | Yes | Yes | Yes | Yes | 8/12 |
| Itoh K et al 2008 | Unclear | Unclear | Yes | Yes | No | Yes | Yes | Unclear | Yes | Yes | Yes | Yes | 8/12 |
| Lu TW et al 2010 | Unclear | Yes | Yes | Yes | No | No | Yes | Yes | Yes | Yes | Yes | Yes | 9/12 |
| Soni A et al 2012 | Yes | Yes | No | No | No | Yes | No | Yes | Yes | Yes | Yes | Yes | 8/12 |
| Mavrommatis CI et al 2012 | Yes | Yes | Yes | Yes | No | Yes | Yes | Unclear | Yes | Yes | Yes | Yes | 10/12 |
Methodological quality assessment and risk-of-bias (Herbal patch).
| Adequate randomization | Concealed allocation | Groups similar at baseline | Patient blinded | Care provider blinded | Outcome assessor blinded | Dropout rate described and acceptable | Intention to treat analysis | Co-interventions avoided or similar | Compliance acceptable | Timing outcome assessment similar | Report free of selective outcome report in | Total | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Wang X et al 2012 | Unclear | Unclear | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | 10/12 |
Methodological quality assessment and risk-of-bias (Herbal medicine).
| Adequate randomization | Concealed allocation | Groups similar at baseline | Patient blinded | Care provider blinded | Outcome assessor blinded | Dropout rate described and acceptable | Intention to treat analysis | Co-interventions avoided or similar | Compliance acceptable | Timing outcome assessment similar | Report free of selective outcome reporting | Total | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Park SH et al 2009 | Unclear | Unclear | Yes | Yes | Yes | Unclear | Yes | Yes | Yes | Yes | Yes | Yes | 9/12 |
| Li XH et al 2010 | Unclear | Unclear | Yes | Unclear | Unclear | Unclear | Yes | Yes | Unclear | Yes | Unclear | Yes | 5/12 |
Methodological quality assessment and risk-of-bias (Qigong (氣功 qì gōng)).
| Adequate randomization | Concealed allocation | Groups similar at baseline | Patient blinded | Care provider blinded | Outcome assessor blinded | Dropout rate described and acceptable | Intention to treat analysis | Co-interventions avoided or similar | Compliance acceptable | Timing outcome assessment similar | Report free of selective outcome reporting | Total | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chen KW et al 2008 | Yes | Yes | Yes | Yes | No | Yes | Yes | No | Yes | Yes | Yes | Yes | 10/12 |
| An B et al 2008 | Unclear | Unclear | Yes | No | No | Unclear | No | No | Yes | Yes | Yes | Yes | 5/12 |
| Lee HJ et al 2009 | Yes | Yes | Yes | No | No | Yes | Yes | Yes | Yes | Yes | Yes | Yes | 10/12 |
Acupuncture (針灸 zhēn jiǔ) for osteoarthritis of the knee (膝關節炎 xī guān jié yán) (GRADE).
| Number of studies | Design | Limitation | Inconsistency | Indirectness | Imprecision | Publication bias | Other considerations | Quality |
|---|---|---|---|---|---|---|---|---|
| Pain after treatment | ||||||||
| 12 | RCT | Serious limitation | No serious inconsistency | No serious indirectness | No serious imprecision | Undetected | None | Moderate |
| Function after treatment | ||||||||
| 12 | RCT | Serious limitation | Serious | No serious indirectness | No serious imprecision | Undetected | None | Low |
Three studies were unclear random sequence generation. Four were unclear allocation concealment. Two were inadequate Selection of participants to groups. Three were no intention-to-treat principle. Three were inadequate blinding. Only two studies did not have serious limitations.
Nine studies were consistent with acupuncture to relief pain after treatment and had significant differences. One study achieved pain release without significant differences. The results of two studies without serious limitations were no significant differences about pain release.
Five studies had similar populations (age, diagnosis and severity) but patients of twelve studies were all diagnosed osteoarthritis. Eight studies used VAS for estimate the pain of the knee and four used other method to evaluate the severity of the pain.
Seven studies were consistent with acupuncture to improve function and had significant differences. The others did not achieve improved function. One study without serious limitations had improved function with significant differences.
Five studies had similar populations (age, diagnosis and severity) and patients of twelve studies were all diagnosed osteoarthritis. Nine studies used WOMAC as their outcome measurement of the function of the knee.
Herbs for osteoarthritis of the knee (膝關節炎 xī guān jié yán) (GRADE).
| Number of studies | Design | Limitation | Inconsistency | Indirectness | Imprecision | Publication bias | Other considerations | Quality |
|---|---|---|---|---|---|---|---|---|
| Pain after treatment | ||||||||
| 2 | RCT | Serious limitation | Serious inconsistency | Serious indirectness | Serious imprecision | Undetected | None | – |
| Function after treatment | ||||||||
| 2 | RCT | Serious limitation | Serious inconsistency | Serious indirectness | Serious imprecision | Undetected | None | – |
Two studies had both unclear random sequence generation and allocation concealment.
Two studies both had decreased pain after treatment but no significant differences.
One study had no reliability and validity of the outcome measurement.
One study had improved function with statistic difference but the other without statistic difference.
Qigong (氣功 qì gōng) for osteoarthritis of the knee (膝關節炎 xī guān jié yán) (GRADE).
| Number of studies | Design | Limitation | Inconsistency | Indirectness | Imprecision | Publication bias | Other considerations | Quality |
|---|---|---|---|---|---|---|---|---|
| Pain after treatment | ||||||||
| 3 | RCT | Serious limitation | Serious inconsistency | Serious indirectness | Serious imprecision | Undetected | None | – |
| Function after treatment | ||||||||
| 3 | RCT | Serious limitation | No serious inconsistency | No serious indirectness | No serious imprecision | Undetected | None | Moderate |
One study had both unclear random sequence generation and allocation concealment. Two studies had no intention-to-treat analysis.
One study did not have pain score but had the WOMAC index that has a subscale of the pain scale. Two studies had decreased pain scale with significant differences.
Two studies had improved function without significant differences and one with significant differences.