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. 2016 Jul 28;2016(7):CD004598. doi: 10.1002/14651858.CD004598.pub4

Summary of findings 1. LASB for pain intensity and duration of pain relief in adults with CRPS.

Patient or population: adults with CRPS
Setting: secondary care
Intervention/comparison: LASB vs various comparisons
Outcome: pain intensity 0‐10 (VAS or NRS)
Comparison Studies No of participants(studies) Result (effect estimates reported where available from study report) Quality of the evidence(GRADE)
LASB vs placebo Aydemir 2006; Price 1998 23 (2) No significant between‐group difference ⊕⊕⊕⊝ Moderatea
Thoracic LASB + steroid vs subcutaneous local anaesthetic+ steroid Rocha 2014 36 (1) Favours LASB
Mean difference (0‐10 scale)
One month −1.25 (95% CI −3.2 to 0.7)
One year −2.39 (95% CI −4.72 to −0.06)
⊕⊝⊝⊝ Very lowb
LASB vs ultrasound block Aydemir 2006 18 (1) No significant between‐group difference ⊕⊕⊝⊝ Lowc
LASB vs IVRB guanethidine Bonelli 1983 19 (1) No significant between‐group difference ⊕⊝⊝⊝ Very lowb
LASB lumbar plexus vs pulsed radiofrequency lumbar plexus Freitas 2013 40 (1) No significant between‐group difference ⊕⊝⊝⊝ Very lowb
LASB (lidocaine + clonidine) vs IVRB (lidocaine + clonidine) Nascimento 2010 43 (1) No significant between‐group difference ⊕⊝⊝⊝ Very lowb
LASB + PT+ pharmacological vs PT + pharmacological Rodriguez 2005 82 (1) Favours SGB group ⊕⊝⊝⊝ Very lowb
LASB + PT vs PT Zeng 2003 60 (1) No significant between‐group difference ⊕⊝⊝⊝ Very lowb
Continuous LASB vs continuous brachial plexus block Toshniwal 2012 33 (1) Favours brachial plexus block ⊕⊕⊝⊝ Lowc
Image‐guided LASB vs nonimage‐guided LASB Yoo 2012 42 (1) Mean difference
2 weeks postinjection −0.58 (95% CI −1.51 to 0.35)
4 weeks postinjection −0.74 (95% CI −1.36 to −0.12)
⊝⊝⊝⊝ Very lowd
Outcome: hand pain 0‐3 scale
LASB vs oral corticosteroids Lim 2007 38 (1) 15 day follow‐up, no significant between‐group difference at
30 day follow‐up 0.4 (95% CI −0.69 to −0.11), favours LASB with steroid
⊝⊝⊝⊝ Very lowd
Outcome: duration of pain relief
LASB bupivacaine + BTA vs LASB bupivacaine Carroll 2009 9 (1) Increased duration of relief with BTA
Median time to analgesic failure (days):
LASB bupivacaine + BTA 71 (95% CI 12 to 253)
LASB bupivacaine 10 (95%CI 0 to 12)
⊕⊕⊝⊝ Lowc

a Downgraded once for imprecision.
b Downgraded three times for limitations, inconsistency, and imprecision.
cDowngraded twice for inconsistency and imprecision.
dDowngraded four times for limitations, inconsistency, indirectness, and imprecision.