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. 2017 Jul 3;318(1):68–81. doi: 10.1001/jama.2017.7918

Table 4. Successful Treatment Effects for Pain Intensity by Study Among Participants With Chronic Low Back Pain.

Intervention Group,
No.With Treatment Success/Total No. (%)
Control Group,
No. With Treatment Success/Total No. (%)
Relative Risk (95% CI)a P Value Risk Difference (95% CI) NNT
Facet Joint Trial
Pain intensity reduction >30%
3 wk 40/102 (39.22) 27/100 (27.00) 1.33 (0.80 to 1.97) .25 12.22 (−0.65 to 25.08) NA
6 wk 45/112 (40.17) 36/114 (31.57) 1.13 (0.70 to 1.63) .59 8.60 (−3.86 to 21.06) NA
3 mo 52/114 (45.61) 40/111 (36.03) 1.16 (0.76 to 1.60) .46 9.58 (−3.20 to 22.36) NA
6 mo 60/108 (55.56) 53/105 (50.47) 1.02 (0.71 to 1.33) .88 5.09 (−8.31 to 18.47) NA
9 mo 52/102 (50.98) 50/102 (49.02) 1.09 (0.75 to 1.42) .60 1.88 (−11.76 to 15.68) NA
12 mo 47/100 (47.00) 53/99 (53.53) 0.78 (0.50 to 1.09) .16 −6.53 (−20.40 to 7.33) NA
Pain intensity reduction ≥2 points
3 wk 56/102 (54.90) 44/100 (44.00) 1.17 (0.81 to 1.53) .36 10.90 (−2.81 to 24.61) NA
6 wk 57/112 (50.89) 47/114 (41.23) 1.09 (0.74 to 1.46) .65 9.66 (−3.27 to 22.60) NA
3 mo 64/111 (57.65) 52/111 (46.85) 1.07 (0.75 to 1.39) .68 10.80 (−2.25 to 23.87) NA
6 mo 68/108 (62.96) 61/105 (58.09) 1.00 (0.73 to 1.25) .98 4.84 (−8.25 to 17.98) NA
9 mo 56/102 (54.90) 58/102 (56.86) 0.90 (0.62 to 1.17) .47 −1.96 (−15.59 to 11.66) NA
12 mo 55/100 (55.00) 55/99 (55.56) 0.76 (0.49 to 1.05) .11 −0.56 (−14.37 to 13.26) NA
Sacroiliac Joint Trial
Pain intensity reduction >30%
3 wk 41/90 (45.56) 16/83 (19.27) 2.35 (1.45 to 3.32) .001 26.29 (12.94 to 39.62) 4
6 wk 43/104 (41.35) 25/91 (27.47) 1.49 (0.94 to 2.18) .08 13.88 (0.69 to 27.05) 7
3 mo 48/105 (45.71) 29/84 (34.52) 1.33 (0.87 to 1.81) .16 11.19 (−2.74 to 25.13) NA
6 mo 50/99 (50.51) 42/85 (49.41) 1.01 (0.69 to 1.34) .94 1.10 (−13.40 to 15.58) NA
9 mo 39/98 (39.79) 33/76 (43.42) 0.88 (0.54 to 1.27) .53 −3.63 (−18.39 to 11.14) NA
12 mo 48/97 (49.48) 31/75 (41.33) 1.15 (0.75 to 1.56) .48 8.15 (−6.79 to 23.09) NA
Pain intensity reduction ≥2 points
3 wk 56/90 (62.22) 30/83 (36.14) 1.68 (1.25 to 2.05) .002 26.08 (11.68 to 40.47) 4
6 wk 59/104 (56.73) 40/91 (43.95) 1.29 (0.97 to 1.59) .08 12.78 (−1.18 to 26.73) NA
3 mo 62/105 (59.05) 40/84 (47.61) 1.25 (0.94 to 1.52) .11 11.44 (−2.80 to 25.66) NA
6 mo 61/99 (61.61) 47/85 (55.29) 1.12 (0.85 to 1.35) .37 6.32 (−7.94 to 20.59) NA
9 mo 51/98 (52.04) 41/76 (53.95) 0.96 (0.68 to 1.22) .76 −1.91 (−16.85 to 13.04) NA
12 mo 57/97 (58.76) 41/75 (54.67) 1.04 (0.76 to 1.30) .77 4.09 (−10.83 to 19.03) NA
Combination Trial
Pain intensity reduction >30%
3 wk 23/75 (30.67) 7/48 (14.58) 2.39 (1.08 to 4.16) .03 16.09 (1.64 to 30.53) 6
6 wk 32/88 (36.36) 21/72 (29.17) 1.16 (0.63 to 1.84) .60 7.19 (−7.34 to 21.73) NA
3 mo 43/86 (50.00) 19/72 (26.38) 1.92 (1.19 to 2.65) .01 23.62 (8.94 to 38.28) 4
6 mo 36/82 (43.90) 38/68 (55.88) 0.77 (0.44 to 1.11) .19 −11.98 (−27.94 to 3.98) NA
9 mo 38/81 (46.91) 26/61 (42.62) 1.05 (0.62 to 1.52) .83 4.29 (−12.21 to 20.79) NA
12 mo 37/75 (49.33) 32/56 (57.14) 0.86 (0.52 to 1.21) .47 −7.81 (−25.02 to 9.40) NA
Pain intensity reduction ≥2 points
3 wk 32/75 (42.67) 12/48 (25.00) 1.67 (0.89 to 2.57) .10 17.67 (1.04 to 34.26) 5
6 wk 44/88 (50.00) 33/72 (45.83) 0.96 (0.58 to 1.37) .83 4.17 (−11.38 to 19.71) NA
3 mo 48/86 (55.81) 28/72 (38.88) 1.32 (0.85 to 1.79) .20 16.93 (1.53 to 32.32) 5
6 mo 49/82 (59.76) 43/68 (63.23) 0.91 (0.59 to 1.19) .54 −3.47 (−19.10 to 12.14) NA
9 mo 48/81 (59.25) 34/61 (55.73) 0.98 (0.62 to 1.31) .91 3.52 (−12.91 to 19.95) NA
12 mo 41/75 (54.67) 37/56 (66.07) 0.80 (0.50 to 1.10) .21 −11.40 (−28.16 to 5.35) NA

Abbreviations: NA, not applicable; NNT, number needed to treat.

a

Relative risk was estimated based on the method of Zhang et al.31