TABLE 6.
GRADE quality grading of included SRs.
Author (year) | Outcomes (n) | Limitations | Inconsistency | Indirectness | Imprecision | Publication bias | Quality of evidence |
---|---|---|---|---|---|---|---|
Wang (2015) | WOMAC physical function score (3) | −1① | 0 | 0 | −1③ | 0 | L |
PGI-I scores (3) | −1① | −1② | 0 | 0 | 0 | L | |
30% pain reduction rate (3) | −1① | 0 | 0 | 0 | 0 | M | |
50% pain reduction rate (3) | −1① | −2② | 0 | −1③ | 0 | CL | |
BPI-S score (3) | −1① | 0 | 0 | 0 | 0 | M | |
Adverse events (3) | −1① | 0 | 0 | −1③ | 0 | L | |
Serious adverse events (3) | −1① | 0 | 0 | −1③ | 0 | L | |
Treatment emergent adverse events (3) | −1① | 0 | 0 | −1③ | 0 | L | |
Treatment discontinuation rate (3) | −1① | −1② | 0 | −1③ | 0 | CL | |
Chen (2019) | WOMAC stiffness score (6) | −1① | 0 | 0 | −1③ | −1④ | CL |
WOMAC physical function score (6) | −1① | −1② | 0 | −1③ | −1④ | CL | |
BPI-S score (5) | −1① | 0 | 0 | 0 | −1④ | L | |
30% pain reduction rate (4) | −1① | 0 | 0 | 0 | −1④ | L | |
50% pain reduction rate (4) | −1① | −1② | 0 | 0 | −1④ | CL | |
Weekly 24-h average pain score (3) | −1① | 0 | 0 | 0 | −1④ | L | |
Treatment emergent adverse events (5) | −1① | 0 | 0 | −1③ | −1④ | CL | |
Serious adverse events (5) | −1① | 0 | 0 | −1③ | −1④ | CL | |
Treatment discontinuation rate (5) | −1① | 0 | 0 | −1③ | −1④ | CL | |
Gao (2019) | WOMAC total score (5) | −1① | −1② | 0 | −1③ | −1④ | CL |
WOMAC pain score (4) | −1① | −2② | 0 | −1③ | −1④ | CL | |
WOMAC stiffness score (4) | −1① | −2② | 0 | −1③ | −1④ | CL | |
WOMAC physical function score (4) | −1① | −2② | 0 | −1③ | −1④ | CL | |
PGI-I scores (5) | −1① | −1② | 0 | 0 | −1④ | CL | |
BPI-S score (5) | −1① | −1② | 0 | 0 | −1④ | CL | |
30% pain reduction rate (5) | −1① | 0 | 0 | 0 | −1④ | L | |
50% pain reduction rate (4) | −1① | −2② | 0 | 0 | −1④ | CL | |
Treatment emergent adverse events (5) | −1① | 0 | 0 | 0 | −1④ | L | |
Serious adverse events (5) | −1① | 0 | 0 | −1③ | −1④ | CL | |
Treatment discontinuation rate (3) | −1① | −1② | 0 | −1③ | −1④ | CL | |
Osani (2019) | WOMAC pain score (5) | −1① | −1② | 0 | 0 | 0 | L |
WOMAC physical function score (5) | −1① | −1② | 0 | 0 | 0 | L | |
Treatment emergent adverse events (5) | −1① | −2② | 0 | 0 | 0 | CL | |
Serious adverse events (5) | −1① | 0 | 0 | 0 | 0 | M | |
Treatment discontinuation rate (5) | −1① | 0 | 0 | 0 | 0 | M | |
Gastrointestinal adverse event (5) | −1① | −1② | 0 | 0 | 0 | L | |
Quality of life improvement (3) | −1① | 0 | 0 | 0 | 0 | M | |
Improvement of depressive symptoms (2) | −1① | 0 | 0 | −1③ | 0 | L | |
Qu (2020) | WOMAC total score (2) | −1① | −1② | 0 | −1③ | −1④ | CL |
WOMAC pain score (3) | −1① | 0 | 0 | 0 | −1④ | L | |
WOMAC stiffness score (3) | −1① | −1② | 0 | −1③ | −1④ | CL | |
WOMAC physical function score (3) | −1① | −2② | 0 | 0 | −1④ | CL | |
BPI-S score (5) | −1① | 0 | 0 | 0 | −1④ | L | |
Dry mouth (2) | −1① | −1② | 0 | 0 | −1④ | CL | |
Drowsiness (2) | −1① | 0 | 0 | 0 | −1④ | L | |
Nausea (2) | −1① | −1② | 0 | 0 | −1④ | CL | |
Chen (2021) | 30% pain reduction rate (5) | −1① | 0 | 0 | −1③ | −1④ | CL |
50% pain reduction rate (5) | −1① | 0 | 0 | 0 | −1④ | L | |
Pain reduction average rate (5) | −1① | 0 | 0 | −1③ | −1④ | CL | |
WOMAC pain score (4) | −1① | −2② | 0 | 0 | −1④ | CL | |
WOMAC stiffness score (6) | −1① | −1② | 0 | −1③ | −1④ | CL | |
WOMAC physical function score (6) | −1① | −1② | 0 | 0 | −1④ | CL | |
SF-36 physical functional subscale (2) | −1① | −2② | 0 | −1③ | −1④ | CL | |
SF-36 bodily pain subscale (2) | −1① | −2② | 0 | 0 | −1④ | CL | |
SF-36 role physical subscale (3) | −1① | −2② | 0 | −1③ | −1④ | CL | |
PGI-I scores (5) | −1① | −1② | 0 | 0 | −1④ | CL | |
CGI-S scores (4) | −1① | −2② | 0 | −1③ | −1④ | CL | |
Treatment emergent adverse events (5) | −1① | −2② | 0 | −1③ | −1④ | CL | |
Serious adverse events (5) | −1① | 0 | 0 | −1③ | −1④ | CL | |
BPI-I score (3) | −1① | −1② | 0 | −1③ | −1④ | CL | |
BPI-S score (5) | −1① | 0 | 0 | 0 | −1④ | L |
Abbreviations: CL, critically low; L, low; M: moderate; H, high; ①, The design of the experiment with a large bias in random, distributive hiding or blind; ②, The confidence interval overlaps less, the heterogeneity test P is Critically small, and the I 2 is larger; ③, Confidence interval is not narrow enough; ④, Fewer studies are included and there may be greater publication bias.