Table 1.
A summary of the randomized controlled trials of acupuncture for spinal cord injury.
| First author (ref) (year) Country |
Study design | Patient population Type of SCI Target state Duration of SCI (mean (range)) |
Experimental treatment (regimen) | Control treatment (regimen) |
Main outcomes | Intergroup differences Experimental versus control |
|---|---|---|---|---|---|---|
| Functional recovery | ||||||
| Chen [3] (1995), China | Parallel 2 arms | 67 n.r. Lower extremity spasticity (A) 11.3 ± 10.0 (1–53) mo (B) 15.5 ± 16.7 (1–81) mo |
(A) EA, (n = 32) |
(B) Rehabilitation, (n = 35) |
Total efficacy rate (Ashworth scale) |
RR; P = 0.05, 1.86 (1.00, 3.45) |
| Wong [4] (2003), Taiwan | Parallel 2 arms Assessor blind |
100 Traumatic SCI Complete motor paralysis n.r. |
(A) EA + AA, plus (B), (n = 50) |
(B) Rehabilitation, (n = 50) |
(1) ASIA score (1) Motor (2) Sensory (3) Pain (2) Total FIM score |
(1) (1) MD, P = 0.003, 0.61 (0.21, 1.01) (2) MD, P = 0.005, 0.58 (0.18, 0.98) (3) MD, P = 0.009, 0.54 (0.14, 0.94) (2) MD, P = 0.02, 0.49 (0.09, 0.89) |
| Cui [5] (2004), China | Parallel 2 arms | 72 Traumatic SCI n.r. (A) 12.9 ± 5.1 d (B) 13.4 ± 6.2 d |
(A) EA, plus (B), (n = 37) |
(B) Rehabilitation, (n = 35) |
(1) FIM score (complete independent rate) (1) 3 sessions (2) 6 sessions |
(1) (1) RR, P = 0.36, 2.84 (0.31, 26.01) (2) RR, P = 0.34, 1.89 (0.51, 6.99) |
| Xu [6] (2004), China |
Parallel 2 arms | 62 Traumatic SCI n.r. n.r. |
(A) EA, plus (B), (n = 32) |
(B) Rehabilitation, (n = 30) |
Total FIM score |
MD, P = 0.08, 0.44 (−0.06, 0.95) |
| Chen [7] (2005), China | Parallel 2 arms | 56 Nontraumatic SCI Acute SCI n.r. |
(A) EA + AA, plus (B), (n = 28) |
(B) Rehabilitation, (n = 28) |
(1) ASIA score (1) Motor (2) Sensory (3) Pain (2) FIM score (locomotion ability) |
(1) (1) MD, P = 0.0003, 1.05 (0.48, 1.61) (2) MD, P < 0.00001, 1.91 (1.27, 2.55) (3) MD, P < 0.00001, 1.85 (1.22, 2.48) (2) MD, P < 0.00001, 2.13 (1.46, 2.79)* |
| Gu [8] (2005)a, China | Parallel 2 arms | 62 Traumatic SCI n.r. (A) 30.3 ± 17.6 d (B) 28.8 ± 11.7 d |
(A) EA, plus (B), (n = 32) |
(B) Rehabilitation + neurotropic oral drugs, (n = 30) |
(1) Total FIM score (2) Rehabilitation effectiveness (= (FIM discharge − FIM admission)/hospitalization day) |
(1) MD, P = 0.08, 0.44 (−0.06, 0.95) (2) MD, P = 0.05, 0.51 (0.01, 1.02) |
| Ma [9] (2005), China | Parallel 2 arms Assessor blind |
30 n.r. SCI (walking function) n.r. |
(A) EA + AT, plus (B), (n = 15) |
(B) Rehabilitation, (n = 15) |
(1) Fugl-Meyer's score (2) Lindmark's score |
(1) MD, P = 0.008, 1.04 (0.27, 1.81) (2) MD, P < 0.00001, 8.55 (6.12, 10.98) |
| Sheng [10] (2009), China |
Parallel 2 arms | 48 Traumatic SCI n.r. n.r. |
(A) EA, plus (B), (n = 24) |
(B) IV (BPH 120 mg + 0.9% NaCl 250 mL, daily for 3 months), (n = 24) |
(1) Total efficacy rate |
(1) RR, P = 0.003, 2.10 (1.28, 3.45) |
|
| ||||||
| Bladder dysfunction | ||||||
| Huang [11] (2002), China | Parallel 2 arms | 64 n.r. Urinary retention (A) 11.0 (5–20) d (B) 10.5 (5–20) d |
(A) EA, (n = 32) |
(B) IM (Neostigmine methylsulfate, (1 mg/2 mL), 2 hours after catheter removal) + IC + BT (n = 32) |
Total efficacy rate | RR, P = 0.02, 1.50 (1.07, 2.11) |
| Zhang [12] (2008), China | Parallel 2 arms | 89 n.r. Neurogenic bladder (A) 2~3 m (B) n.r. |
(A) EA, (n = 45) |
(B) IM (Neostigmine 0.5~1 mg, once a day) + IC + BT, (n = 44) |
Total efficacy rate | RR, P = 0.11, 1.12 (0.95, 1.32) |
| Zhou [13] (2007), China | Parallel 2 arms | 111 Traumatic SCI Neurogenic bladder (A) 45.62 ± 6.23 d (B) 43.76 ± 8.23 d |
(A) EA (n = 56) |
(B) IC + BT, (n = 55) |
(1) Total efficacy rate (2) Residual urine (mL) |
(1) RR, P = 0.006, 1.47 (1.12, 1.94) (2) MD, P < 0.00001, −1.16 (−1.56, −0.76) |
| Cheng [14] (1998), Taiwan | Parallel 4 arms | 80†
n.r. Neurogenic bladder (A) 23.7 ± 12.8 d (B) 26.1 ± 12.1 d |
(A) EA, plus (B) (1) above T11 (n = 18) (2) below T11 (n = 14) |
(B) IC + BT, (1) above T11 (n = 16) (2) below T11 (n = 12) |
Total days needed to reach bladder balance (1) Above T11 (2) Below T11 |
(1) MD, P = 0.003, 1.10 (0.37, 1.83) (2) MD, P = 0.009, 1.12 (0.28, 1.96) |
| Gu [15] (2005)b, China |
Parallel 2 arms | 64 mixed Bladder dysfunction n.r. |
(A) EA, plus (B), (n = 32) |
(B) IC, (n = 32) |
Total efficacy rate | RR, P = 0.007, 1.53 (1.12, 2.08) |
| Liu [16] (2009), China | Parallel 2 arms | 40 n.r. Bladder dysfunction 14 days~90 d |
(A) EA, plus (B), (n = 20) |
(B) IC + BT, (n = 20) |
Bladder voiding function parameters (1) Frequency of urination (times) (2) Maximum voided volume (mL) (3) Bladder capacity (mL) (4) Residual urine (mL) (5) Quality of life score |
(1) MD, P = 0.012, −0.49 (−1.12, 0.14) (2) MD, P = 0.024, 0.37 (−0.25, 1.00) (3) MD, P = 0.06, 0.61 (−0.02, 1.25) (4) MD, P = 0.32, −0.32 (−0.94, 0.31) (5) MD, P = 0.30, −0.33 (−0.96, 0.29) |
|
| ||||||
| Pain condition | ||||||
| Dyson-Hudson [17] (2007), USA | Parallel 2 arms Patient blind Assessor blind |
17 n.r. Chronic shoulder pain (A) 9.3 ± 10.5 y (B) 13.1 ± 7.7 y |
(A) AT, (n = 8) |
(B) Sham AT, (n = 9) |
(1) PC-WUSPI (2) NRS (11 points scale, shoulder pain) |
(1) MD, P = 0.19, −0.65 (−1.64, 0.33) (2) MD, P = 0.19, −0.67 (−1.69, 0.34) |
| Dyson-Hudson [18] (2001), USA | Parallel 2 arms | 18 n.r. Chronic SCI and shoulder pain (A) 16.2 ± 9.7 y (B) 13.4 ± 6.2 y |
(A) AT, (n = 9) |
(B) Trager Approach, (n = 9) |
(1) PC-WUSPI (2) NRS (10 points VAS, shoulder pain) (3) VRS (shoulder pain) |
(1) MD, P = 0.91, −0.05 (−0.98, 0.87) (2) No significant difference (P > 0.05)‡ (3) RR, P = 0.46, 0.89 (0.67, 1.20) |
AA: auricular acupuncture; ASIA score: American spinal injury association neurologic and functional score; AT: acupuncture; BPH: brain protein hydrolysate; BT: bladder training; EA: electrical AT; FIM score: functional independence measure score; IC: intermittent catheterization; IM: intramuscular; IV: intravenous; n.r.: not reported; NRS: numeric rating scale; PC-WUSPI score: performance-corrected wheelchair user's shoulder pain index score; SCI: spinal cord injury; VAS: visual analog scale; VRS: verbal response score.
*The author did not report total FIM score but did each of 6 domains.
†80 patients were randomized, but 60 were analyzed.
‡Each group had a significant effect after therapy (P < 0.01).