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TABLE OF CONTENTS
HEADER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ABSTRACT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
PLAIN LANGUAGE SUMMARY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
SUMMARY OF FINDINGS FOR THE MAIN COMPARISON . . . . . . . . . . . . . . . . . . .
BACKGROUND . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
OBJECTIVES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
METHODS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
RESULTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Figure 1.
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Figure 2.
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ADDITIONAL SUMMARY OF FINDINGS . . . . . . . . . . . . . . . . . . . . . . . . . .
DISCUSSION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
AUTHORS CONCLUSIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ACKNOWLEDGEMENTS
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
REFERENCES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
CHARACTERISTICS OF STUDIES . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
DATA AND ANALYSES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 1.1. Comparison 1 Acupuncture versus sham treatment, Outcome 1 Pain intensity (VAS) immediate post
treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 1.2. Comparison 1 Acupuncture versus sham treatment, Outcome 2 Pain intensity (VAS) short term. . . .
Analysis 1.3. Comparison 1 Acupuncture versus sham treatment, Outcome 3 Pain intensity (VAS) intermediate term.
Analysis 1.4. Comparison 1 Acupuncture versus sham treatment, Outcome 4 Pain intensity (VAS) long term. . . .
Analysis 1.5. Comparison 1 Acupuncture versus sham treatment, Outcome 5 Disability (NDI) immediate post
treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 1.6. Comparison 1 Acupuncture versus sham treatment, Outcome 6 Disability (NPQ) immediate post
treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 1.7. Comparison 1 Acupuncture versus sham treatment, Outcome 7 Disability (NPQ) short term. . . . .
Analysis 1.8. Comparison 1 Acupuncture versus sham treatment, Outcome 8 Disability (NDI) short term. . . . .
Analysis 1.9. Comparison 1 Acupuncture versus sham treatment, Outcome 9 Disability (NDI) intermediate term. .
Analysis 1.10. Comparison 1 Acupuncture versus sham treatment, Outcome 10 Quality of life (SF-36) immediate post
treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 1.11. Comparison 1 Acupuncture versus sham treatment, Outcome 11 Quality of life (SF-36) short term. .
Analysis 2.1. Comparison 2 Acupuncture versus inactive control, Outcome 1 Pain intensity (VAS) immediate post
treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 2.2. Comparison 2 Acupuncture versus inactive control, Outcome 2 Pain intensity (VAS) short term. . . .
Analysis 2.3. Comparison 2 Acupuncture versus inactive control, Outcome 3 Pain intensity (VAS) intermediate term.
Analysis 2.4. Comparison 2 Acupuncture versus inactive control, Outcome 4 Pain intensity (VAS) long term. . . .
Analysis 2.5. Comparison 2 Acupuncture versus inactive control, Outcome 5 Pain pressure threshold immediate post
treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 2.6. Comparison 2 Acupuncture versus inactive control, Outcome 6 Pain pressure threshold short term. . .
Analysis 2.7. Comparison 2 Acupuncture versus inactive control, Outcome 7 Pain intensity (proportion pain relief )
immediate post treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 2.8. Comparison 2 Acupuncture versus inactive control, Outcome 8 Disability (NDI) short term. . . . .
Analysis 2.9. Comparison 2 Acupuncture versus inactive control, Outcome 9 Disability (NDI) intermediate term. .
Analysis 2.10. Comparison 2 Acupuncture versus inactive control, Outcome 10 Disability (NDI) long term. . . .
Analysis 2.11. Comparison 2 Acupuncture versus inactive control, Outcome 11 Function (NHP) immediate post
treatment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 2.12. Comparison 2 Acupuncture versus inactive control, Outcome 12 Function (NHP) intermediate term.
Analysis 2.13. Comparison 2 Acupuncture versus inactive control, Outcome 13 Function (NPQ) short term. . . .
Analysis 2.14. Comparison 2 Acupuncture versus inactive control, Outcome 14 Quality of life (SF-36, Functional
Component) short term. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Acupuncture for neck disorders (Review)
Copyright 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
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Analysis 3.1. Comparison 3 Acupuncture versus wait-list, Outcome 1 Pain intensity (VAS) short term. . . . . .
Analysis 3.2. Comparison 3 Acupuncture versus wait-list, Outcome 2 Disability (neck and pain disability scale) short
term. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 3.3. Comparison 3 Acupuncture versus wait-list, Outcome 3 Disability (neck and pain disability scale) intermediate
term. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 3.4. Comparison 3 Acupuncture versus wait-list, Outcome 4 Quality of life (SF-36 mental score) short term.
Analysis 3.5. Comparison 3 Acupuncture versus wait-list, Outcome 5 Quality of life (SF-36 mental score) intermediate
term. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Analysis 3.6. Comparison 3 Acupuncture versus wait-list, Outcome 6 Quality of life (SF-36 physical score) intermediate
term. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
APPENDICES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
WHATS NEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
HISTORY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
CONTRIBUTIONS OF AUTHORS . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
DECLARATIONS OF INTEREST . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
SOURCES OF SUPPORT . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
DIFFERENCES BETWEEN PROTOCOL AND REVIEW . . . . . . . . . . . . . . . . . . . . .
INDEX TERMS
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[Intervention Review]
McMaster University, Hamilton, Canada. 3 Department of Anesthesiology, University of Munich, Munich, Germany. 4 John Walsh
Centre for Rehabilitation Research, Kolling Institute, Northern Sydney Local Health District, St Leonards, Australia. 5 Canadian Forces
Health Services Group/Groupe de Services de Sant des Forces Canadiennes, National Defence/Dfense Nationale, Government of
Canada/Gouvernement du Canada, Kingston, Canada
Contact address: Kien Trinh, DeGroote School of Medicine, Office of MD Admissions, McMaster University, 1200 Main Street West,
MDCL-3112, Hamilton, ON, L8N 3Z5, Canada. trinhk@mcmaster.ca.
Editorial group: Cochrane Back and Neck Group.
Publication status and date: New search for studies and content updated (conclusions changed), published in Issue 5, 2016.
Review content assessed as up-to-date: 25 August 2015.
Citation: Trinh K, Graham N, Irnich D, Cameron ID, Forget M. Acupuncture for neck disorders. Cochrane Database of Systematic
Reviews 2016, Issue 5. Art. No.: CD004870. DOI: 10.1002/14651858.CD004870.pub4.
Copyright 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
ABSTRACT
Background
Neck pain is one of the three most frequently reported complaints of the musculoskeletal system. Treatments for neck pain are varied,
as are perceptions of benefit. Acupuncture has been used as an alternative to more conventional treatment for musculoskeletal pain.
This review summarises the most current scientific evidence on the effectiveness of acupuncture for acute, subacute and chronic neck
pain. This update replaces our 2006 Cochrane review update on this topic.
Objectives
To determine the effects of acupuncture for adults with neck pain, with focus on pain relief, disability or functional measures, patient
satisfaction and global perceived effect.
Search methods
We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, the Manual, Alternative and
Natural Therapy Index System (MANTIS), the Cumulative Index to Nursing and Allied Health Literature (CINAHL) and the Index to
Chiropractic Literature (ICL) from their beginning to August 2015. We searched reference lists, two trial registers and the acupuncture
database Traditional Chinese Medical Literature Analysis and Retrieval System (TCMLARS) in China to 2005.
Selection criteria
We included published trials that used random assignment to intervention groups, in full text or abstract form. We excluded quasirandomised controlled trials (RCTs).
Data collection and analysis
Two review authors made independent decisions for each step of the review: article inclusion, data abstraction and assessment of quality
of trial methods. We assessed study quality by using the Cochrane Back Review Group Risk of bias tool. We used consensus to resolve
disagreements, and when clinical heterogeneity was absent, we combined studies by using random-effects meta-analysis models.
Acupuncture for neck disorders (Review)
Copyright 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Main results
Of the 27 included studies, three represented individuals with whiplash-associated disorders (WADs) ranging from acute to chronic (205
participants), five explored chronic myofascial neck pain (186 participants), five chronic pain due to arthritic changes (542 participants),
six chronic non-specific neck pain (4011 participants), two neck pain with radicular signs (43 participants) and six subacute or chronic
mechanical neck pain (5111 participants).
For mechanical neck pain, we found that acupuncture is beneficial at immediate-term follow-up compared with sham acupuncture for
pain intensity; at short-term follow-up compared with sham or inactive treatment for pain intensity; at short-term follow-up compared
with sham treatment for disability; and at short-term follow-up compared with wait-list control for pain intensity and neck disability
improvement. Statistical pooling was appropriate for acupuncture compared with sham for short-term outcomes due to statistical
homogeneity (P value = 0.83; I2 = 20%). Results of the meta-analysis favoured acupuncture (standardised mean difference (SMD) 0.23, 95% confidence interval (CI) -0.20 to -0.07; P value = 0.0006). This effect does not seem sustainable over the long term. Whether
subsequent repeated sessions would be successful was not examined by investigators in our primary studies.
Acupuncture appears to be a safe treatment modality, as adverse effects are minor. Reported adverse effects include increased pain,
bruising, fainting, worsening of symptoms, local swelling and dizziness. These studies reported no life-threatening adverse effects and
found that acupuncture treatments were cost-effective.
Since the time of our previous review, the quality of RCTs has improved, and we have assessed many of them as having low risk of bias.
However, few large trials have provided high-quality evidence.
Authors conclusions
Moderate-quality evidence suggests that acupuncture relieves pain better than sham acupuncture, as measured at completion of treatment
and at short-term follow-up, and that those who received acupuncture report less pain and disability at short-term follow-up than those
on a wait-list. Moderate-quality evidence also indicates that acupuncture is more effective than inactive treatment for relieving pain at
short-term follow-up.
Individuals with chronic neck pain who received acupuncture reported better pain relief immediately after treatment and in the short
term compared to those who received sham treatments. Individuals with chronic neck pain who received acupuncture reported better
pain relief and improvement in disability in the short term than those who were on a wait-list.
Acupuncture treatments appear to be safe, and investigators have reported only minor and short-lasting side effects.
Quality of the evidence
The quality of the evidence used to determine whether acupuncture is helpful remains low or moderate. Limitations in the evidence
include few study participants, the tendency of researchers to not keep track of who dropped out of the study and they did not make
sure that patients who entered the study were randomly assigned to a group. These types of flaws introduce bias into the studies and
therefore affect how strongly we believe the results.
S U M M A R Y O F F I N D I N G S F O R T H E M A I N C O M P A R I S O N [Explanation]
Assumed risk
Corresponding risk
Sham
Acupuncture
Relative effect
(95% CI)
560
(8 studies)
M oderate
Lim itations: -1
Inconsistency: 0
Indirectness: 0
Im precision: 0
Other: 0
290
(2 studies)
Low
Lim itations: -1
Inconsistency: 0
Indirectness: 0
Im precision: -1
Other: 0
173
(3 studies)
N/ A
178
(1 study)
Low
Lim itations: 0
Inconsistency: 0
Indirectness: -1
Im precision: -1
Other: 0
* The basis f or the assumed risk (e.g. m edian control group risk across studies) is provided in f ootnotes. The corresponding risk (and its 95% conf idence interval) is based on
the assum ed risk in the com parison group and the relative effect of the intervention (and its 95% CI)
CI: conf idence interval; RR: risk ratio
Adverse ef f ects were reported in 14 studies and included increased pain, bruising, f ainting, worsening of sym ptom s, local swelling and dizziness. No lif e-threatening adverse
ef f ects were noted by these studies
GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our conf idence in the estim ate of ef f ect
M oderate quality: Further research is likely to have an im portant im pact on our conf idence in the estim ate of ef f ect and m ay change the estim ate
Low quality: Further research is very likely to have an im portant im pact on our conf idence in the estim ate of ef f ect and is likely to change the estim ate
Very low quality: We are very uncertain about the estim ate
BACKGROUND
play a role in central mechanisms of acupuncture-induced analgesia. In the peripheral nervous system, -endorphin seems to be
released from keratinocytes when activated by increased extracellular endocannabinoid concentrations after acupuncture in an inflammatory pain model (Chen 2009).
Likewise, serotonin is known to be involved in the analgesic effect
of acupuncture by affecting transmission of pain signals at central
and peripheral levels. Similar to oestrogen, serotonin seems to be
indirectly involved in the antinociceptive effect of acupuncture by
sensitising peripheral afferents and thereby activating endogenous
pain control. In contrast, an increase in extracellular ATP concentration may act directly on afferent neurons expressing purinergic
receptors, leading to nerve fibre activation, which in turn causes
antinociceptive spinal or supraspinal reactions.
Such mechanisms of endogenous pain control triggered by Aand C-fiber activation are generally distinguished according to the
respective neural structures and neurotransmitters involved and
are termed diffuse noxious inhibitory control (DNIC), segmental
inhibition and descending pain control pathways (Zhao 2008).
Effects of acupuncture on muscles and fascia have also been described (Langevin 2006). When effects of acupuncture are approached from the perspective of mechanical tissue manipulation, it can be concluded that existing evidence shows effects of
acupuncture on structure and alignment of connective tissue or
fasciae (Langevin 2006). Conversely, a reduction in muscle tone
through acupuncture has been proposed, but this proposal is based
mainly on observations of clinical improvement after acupuncture, such as increased cervical range of motion in patients with
neck pain (Irnich 2001). Moreover, recent brain imaging studies
have revealed that acupuncture alters brain activation patterns in
areas associated with pain processing (Huang 2012SR).
OBJECTIVES
To determine the effects of acupuncture for adults with neck pain,
with focus on pain relief, disability or functional measures, patient
satisfaction and global perceived effect.
Types of interventions
Studies must have used acupuncture techniques involving insertion of needles. Stimulation of needles may involve manual, electrical, heat, laser or other forms of stimulation. Control groups
were treated with sham acupuncture (some form of mock or pretend), wait-list control or inactive treatment control (e.g. sham
transcutaneous electrical nerve stimulation (TENS)).
METHODS
Types of outcome measures
Types of studies
We included published randomised controlled trials (RCTs) in full
text or abstract form. We included abstracts if sufficient information for analyses could be obtained from study authors. We excluded quasi-RCTs and clinical controlled trials (CCTs) because
we found numerous RCTs for this update. This is different from
the approach presented in the protocol.
Types of participants
Participants were adults (18 years or older) with the following neck
disorders.
Mechanical neck disorders (MNDs), including whiplashassociated disorders (WADs) categories 1 and 2 (Spitzer 1987;
Spitzer 1995), myofascial pain syndrome (MPS) and
degenerative changes (DCs) (Schumacher 1993).
Neck disorder with headache (Olesen 1988; Olesen 1997;
Sjaastad 1990).
Neck disorders with radicular symptoms (NDRs),
including WAD category 3 (Spitzer 1987; Spitzer 1995).
For the purposes of this review, we defined symptom duration as
acute (< 30 days), subacute (30 days to 90 days) or chronic ( 90
days).
We excluded studies if they investigated neck disorders with:
definite or possible long tract signs (e.g. myelopathies);
neck pain caused by other pathological entities
(Schumacher 1993);
neck pain related to neurological disease (e.g. spasmodic
torticollis);
neck pain related to fracture and dislocation;
headache not of cervical origin;
co-existing headache when neck pain was not dominant or
when headache was not provoked by neck movement or
sustained neck posture; or
mixed headache.
Primary outcomes
Pain relief (e.g. visual analogue scale (VAS), numerical rating scale
(NRS)), disability or functional measures (e.g. Neck Disability
Index (NDI), quality of life (e.g. Short Form (SF)-36), activities of
daily living (ADLs)), patient satisfaction questionnaires and global
perceived effect were the outcomes of interest.
Secondary outcomes
China in September 2005. We did not further update the TCMLARS search, as this search yielded no RCTs previously.
See Appendix 1 for the search strategies used for CENTRAL,
MEDLINE, EMBASE, MANTIS, CINAHL and ICL. Subject
headings (MeSHs) and keywords included anatomical terms, disorder or syndrome terms, treatment terms and methodological
terms consistent with those advised by the CBRG (Furlan 2009).
Searching other resources
We also screened references, communicated with the Trials Search
Co-ordinator of the CBRG, contacted identified content experts
and reviewed our own personal files.
A P value for the Chi2 test (test of heterogeneity) less than 0.05 or
an I2 value greater than 25% would indicate significant statistical
heterogeneity. However, because an acupuncture review includes
few studies, the test of heterogeneity might not have the power to
detect a difference even when one exists; therefore, we determined
that subgroups were statistically heterogeneous if I2 values were
greater than 25% despite failure to reject the null hypothesis with
the Chi2 test.
Assessment of reporting biases
When a published protocol was available, we compared outcomes
reported a priori with outcomes of interest in the RCT.
Data synthesis
Before calculating a pooled effect measure, we assessed the appropriateness of pooling on clinical grounds. We planned to combine
outcome measures from individual trials by performing a metaanalysis when possible (clinical comparability of populations, interventions and outcomes between trials). We planned to use a
random-effects model for these meta-analyses.
We considered each subgroup (e.g. 1.1) to be clinically homogeneous. We meta-analysed each subgroup unless we noted statistical heterogeneity. When a meta-analysis was not possible, we described qualitatively in the text the results of clinically comparable
trials.
Regardless of whether available data were sufficient for use in
quantitative analyses to summarise the data, we assessed the overall quality of the evidence for each outcome. To accomplish this,
we used the GRADE (Grades of Recommendation, Assessment,
Development and Evaluation Working Group) approach, as recommended in the Cochrane Handbook for Systematic Reviews of
Interventions (Higgins 2011) and adapted in the updated CBRG
method guidelines (Furlan 2009). We considered that the following factors may decrease the quality of the evidence, study design
and risk of bias, inconsistency of results, indirectness (not generalisable), imprecision (sparse data) and other factors (e.g. reporting
bias). We reduced our rating of the quality of the evidence for
RESULTS
Description of studies
We selected 27 trials (N = 5462) for inclusion in this review (Figure
1). Duration of the disorder and disorder subtypes were as follow.
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Included studies
Of the 27 included studies, three represented individuals with
WAD (205 participants), five chronic myofascial neck pain (186
participants), five chronic pain due to arthritic changes (n = 506),
six chronic non-specific neck pain (4011 participants), two neck
Excluded studies
We excluded 103 trials after reviewing the full report. Of these, we
excluded 13 studies on the basis of participant characteristics: Two
RCTs included participants with a neck disorder excluded from
this review (i.e. ankylosing spondylitis) (Emery 1986) and spinal
cord stenosis (Li 2006); three included headaches not of cervical
origin (Coeytaux 2005; Venancio 2008; Venancio 2009); seven included participants with pain from other areas as well (head, shoulder or back) (Gallacchi 1981; Gallacchi 1983; Gaw 1975; Giles
2003; Kisiel 1996; Lundeburg 1988; Muller 2005); and one included participants who did not have neck pain (Sato 2014). Furthermore, we excluded two abstracts (Johnson 2000; Teng 1973)
because they did not appear to describe RCTs. We excluded 64
studies on the basis of the comparison performed: Six studies included acupuncture as the control (Fernandez-Carnero 2014; Guo
2013; Harvey 2015; Li 2013; Wang G 2014; Zhang J 2013); 31
compared acupuncture types (Ceccherelli 2006; Ceccherilli 2014;
Dong 2012; Fu 2007; Gil 2015; Huang 2008; Jia 2007; Jin 2012;
Kai 2008; Li 2004; Liu 2008; Lixing 2000; Lu 2006; Myburgh
2012; Nakajima 2015; Pecos-Martin 2015; Sator-Katzenschlager
2003; Shang 2002; Shuangquan 2003; Sun 2013; Wan 2013;
Wang 2007; Wang 2008; Xu 2012; Yang 2009; Yoon 2009; Yu
2003; Zeng 2005; Zhao 2004; Zhu 2006; Zhuang 2004); 27 compared acupuncture versus active treatment (Bahadir 2009; Cho
2014; David 1998; Edwards 2003; Eroglu 2013; Falkenberg 2007;
Franca 2008; Fu 2005; Fu 2014; Ga 2007b; Giles 1999; Hu 2014;
Huang 2012; Hudson 2010; Li 2006; Liu 2013; MacPherson
2013; McLean 2013; Rayegani 2014; Salter 2006; Tobbackx 2013;
Yang 2013; Yoshimizu 2012; Zhang 2003; Zhang J 2008; Zhou
2014; Ziaeifar 2014). In addition, we excluded 15 RCTs on the
basis of the intervention provided: eight by type (i.e. EMG needle,
mini-scalpel, injection needle) (Calvo-Trujillo 2013; Chu 1997;
Lin 2004; Ma 2010; Seo 2014; Zhang X-Z 2013; Zheng 2014; Zhi
2008) and seven additional studies that used acupuncture as part
of a multi-modal approach (Cohen 2014; Gallego Sendarrubias
2015; Guanygue 2001; Hayek 2014; Hudson 2010; Lundeburg
1991; Soderlund 2001) and could not isolate the acupuncture effect. We excluded eight studies because they were not randomised
or were quasi-randomised (Ga 2007a; Hua 2009; Loy 1983; Luo
2010; Pan 2008; Peng 1987; Xue 2007; Zhang 1996). We excluded one study because investigators did not perform betweengroup comparisons (Zhu 2002). (See Characteristics of excluded
studies tables.)
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Figure 2. Risk of bias summary: review authors judgements about each risk of bias item for each included
study.
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Allocation
We found that six of the 27 included studies had low risk of bias
on the basis of allocation; 19 had uncertain risk of bias; and two
had high risk of bias. We discussed effects of risks of bias on review
results for each subgroup separately under Effects of interventions.
Blinding
We found that 12 of the 27 included studies had low risk of bias
on blinding of participants; 12 studies had uncertain risk of bias,
and three had high risk of bias. We discussed effects of risks of
bias on review results for each subgroup separately under Effects
of interventions.
Incomplete outcome data
We found that two of the 27 included studies had low risk of bias
on drop-out rate; four studies had uncertain risk of bias, and one
had high risk of bias. We discussed effects of risks of bias on review
results for each subgroup separately under Effects of interventions.
Selective reporting
We found that three of the 27 included studies had low risk of
bias; 24 studies had uncertain risk of bias, and no study had high
risk of bias. We discussed effects of risks of bias on review results
for each subgroup separately under Effects of interventions.
Effects of interventions
See: Summary of findings for the main comparison; Summary
of findings 2; Summary of findings 3
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No convincing evidence favoured acupuncture in all other measures such as disability (NDI) or quality of life over the short
term, the intermediate term or the long term. (Please see Analysis
1.5, Analysis 1.6, Analysis 1.7, Analysis 1.8, Analysis 1.9, Analysis
1.10, and Analysis 1.11.) Statistical pooling for Analysis 1.6 and
Analysis 1.8 were inappropriate in this instance because of heterogeneity.
Some evidence suggests that acupuncture may be more beneficial
than sham acupuncture for disability (Northwick Park Pain Questionnaire (NPQ)). Two studies (n = 290) involved participants
with mechanical neck disorders, one with low risk of bias (Liang
2011) and the other with high risk of bias (Fu 2009). Meta-analysis favoured acupuncture (P value = 0.001). (Please see Analysis
1.7.) Statistical pooling was appropriate in this instance because
of statistical homogeneity (P value = 0.88; I2 = 0%). On the basis
of the GRADE scale, we downgraded the quality level of evidence
to moderate because only one of the two studies (50%) presented
low risk.
Acupuncture versus inactive treatment
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No convincing evidence favoured acupuncture in all other measures such as disability (NDI) and quality of life over the short
term, the intermediate term or the long term. (Please see Analysis
2.5, Analysis 2.6, Analysis 2.7, Analysis 2.8, Analysis 2.9, Analysis
2.10, Analysis 2.11, Analysis 2.12, Analysis 2.13 and Analysis
2.14.) Statistical pooling for Analysis 2.5, Analysis 2.6 and Analysis
2.14 were inappropriate in this instance because of heterogeneity.
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A D D I T I O N A L S U M M A R Y O F F I N D I N G S [Explanation]
Assumed risk
Corresponding risk
Inactive treatment
Acupuncture
Relative effect
(95% CI)
404
(5 studies)
M oderate
Lim itations: 0
Inconsistency: 0
Indirectness: 0
Im precision: -1
Other: 0
132
(2 studies)
N/ A
17
118
(1 study)
123
(1 study)
N/ A
Low
Lim itations: 0
Inconsistency: 0
Indirectness: -1
Im precision: -1
Other: 0
143
(2 studies)
N/ A
* The basis f or the assumed risk (e.g. m edian control group risk across studies) is provided in f ootnotes. The corresponding risk (and its 95% conf idence interval) is based on
the assum ed risk in the com parison group and the relative effect of the intervention (and its 95% CI)
CI: conf idence interval; RR: risk ratio
Adverse ef f ects were reported in 14 studies and included increased pain, bruising, f ainting, worsening of sym ptom s, local swelling and dizziness. No lif e-threatening adverse
ef f ects were noted by these studies
GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our conf idence in the estim ate of ef f ect
M oderate quality: Further research is likely to have an im portant im pact on our conf idence in the estim ate of ef f ect and m ay change the estim ate
Low quality: Further research is very likely to have an im portant im pact on our conf idence in the estim ate of ef f ect and is likely to change the estim ate
Very low quality: We are very uncertain about the estim ate
18
Acupuncture compared with wait- list control for chronic neck pain
Patient or population: patients with chronic neck pain (pain f or m ore than 90 days)
Settings: prim ary care newspaper advertisem ent or recruited through participating physicians
Intervention: acupuncture
Comparison: wait-list control
Outcomes
Assumed risk
Corresponding risk
Acupuncture
Relative effect
(95% CI)
30
(1 study)
M oderate
Lim itations: 0
Inconsistency: 0
Indirectness: -1
Im precision: 0
Other: 0
3451
(1 study)
M oderate
Lim itations: 0
Inconsistency: 0
Indirectness: -1
Im precision: 0
Other: 0
3451
(1 study)
N/ A
19
* The basis f or the assumed risk (e.g. m edian control group risk across studies) is provided in f ootnotes. The corresponding risk (and its 95% conf idence interval) is based on
the assum ed risk in the com parison group and the relative effect of the intervention (and its 95% CI)
CI: conf idence interval; RR: risk ratio
Adverse ef f ects were reported in 14 studies and included increased pain, bruising, f ainting, worsening of sym ptom s, local swelling and dizziness. No lif e-threatening adverse
ef f ects were noted by these studies Cost of care was calculated in 1 study, which f ound that acupuncture treatm ent was cost-ef f ective
GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our conf idence in the estim ate of ef f ect
M oderate quality: Further research is likely to have an im portant im pact on our conf idence in the estim ate of ef f ect and m ay change the estim ate
Low quality: Further research is very likely to have an im portant im pact on our conf idence in the estim ate of ef f ect and is likely to change the estim ate
Very low quality: We are very uncertain about the estim ate
xxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxxx
20
DISCUSSION
AUTHORS CONCLUSIONS
Implications for practice
For mechanical neck pain, we found that acupuncture is beneficial immediately following treatment and at short-term follow-up
21
ine the long-term efficacy or effectiveness of acupuncture compared with sham acupuncture.
ACKNOWLEDGEMENTS
Thank you to the primary authors who responded to requests for
information. We also thank our volunteers, our translators and the
Cochrane Back Review Group editors.
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31
CHARACTERISTICS OF STUDIES
RCT
Number analysed/randomised: 36/46
Intention-to-treat: NR
Power analysis: NR
Funding source: intramural grant from the Anesthesia Department of Brigham and
Womens Hospital, Boston, MA
Participants
Interventions
INDEX TREATMENT
Group 1 - relevant acupuncture (believed to be effective for the condition treated)
Pre-determined relevant points; shallow needling (2 to 3 mm) used with copper wire
containing silicone diode applied for stage 1 of session (10 minutes); infrared lamp also
used over points during stage 2 of treatment (10 minutes). Treatment done without Deqi
by a licensed acupuncturist with 13 years of experience
COMPARISON TREATMENT 1
Group 2 - irrelevant acupuncture
Same treatment dosage and duration as Group 1, using pre-determined irrelevant points
with copper wire attached but connections severed (stage 1) and placebo light (no heat
during stage 2)
COMPARISON TREATMENT 2
Group 3 - medical control
NSAID 500 mg OD Trilisate, no acupuncture
CO-INTERVENTION
Avoided
Treatment schedule: 14 sessions over 12 weeks, with each session averaging 30 minutes
in duration
Duration of follow-up: immediate post treatment
Outcomes
Notes
--
32
Birch 1998
(Continued)
Risk of bias
Bias
Authors judgement
Not reported
Not reported
Unclear risk
Adequately described
Not possible
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
Unclear risk
Not reported
Compliance acceptable?
Low risk
Low risk
Fatal Flaw
Low risk
Acceptable
33
Cameron 2011
Methods
RCT
Number analysed/randomised: 116/124
Intention-to-treat: reported but not done
Power analysis: calculated
Funding source: government organisational funds
Participants
Interventions
INDEX TREATMENT
Group 1 - real electroacupuncture (EAP)
Acupuncture points = GB39, GB20, L114, SI6 bilaterally 1 to 1.5 cm depth; electrodes
attached to needles at 2 acupuncture points in the cervical area, plus 1 in each wrist and
ankle 2 to 5 Hz 1.5 v; unable to feel the current
COMPARISON TREATMENT
Group 2 - simulated EAP
Same treatment dosage and duration as Group 1, points 20 to 30 mm from selected
points; same attachment of electrodes but machine not turned on
CO-INTERVENTION
Comparable between groups; included medication, physiotherapy and chiropractic therapy
Treatment schedule: 2 sessions/wk over 6 weeks, with each session averaging 30 minutes
in duration
Duration of follow-up: 3 and 6 months
Outcomes
34
Cameron 2011
(Continued)
Notes
--
Risk of bias
Bias
Authors judgement
Low risk
Adequately blinded
Not possible
Low risk
Low risk
Low risk
Reported to be similar
Unclear risk
Compliance acceptable?
Low risk
Low risk
Fatal Flaw
Low risk
Acceptable
35
Chou 2009
Methods
RCT
Number Analysed/randomised: 10/10
Intention-to-treat: calculated
Power analysis: NR
Funding source: none
Participants
Interventions
INDEX TREATMENT
Remote acupuncture group (RA)
Acupuncture points - TE5, LI11; the needle was manipulated for the Deqi. First, TE5
was inserted and manipulated for 15 seconds; after 5 minutes, LI11 was treated in the
same way. Five minutes later, both needles were manipulated for 15 seconds at the same
time; manipulation stopped and needles remained inserted for 3 minutes
COMPARISON TREATMENT
Sham acupuncture
Sham acupuncture needle inserted into rubber connector taped onto skin at TE5 and
LI11; needle contacted skin but did not penetrate. No manipulation of needle
CO-INTERVENTION
Avoided
Treatment schedule: 1 session
Duration of follow-up: immediate post treatment
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
36
Chou 2009
(Continued)
Not possible
No drop-outs
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
Low risk
Compliance acceptable?
Low risk
Low risk
Immediate post
Fatal Flaw
High risk
Coan 1982
Methods
RCT
Number analysed/randomised: 30/30
Intention-to-treat: NR
Power analysis: NR
Funding source: NR
Participants
37
Coan 1982
(Continued)
Interventions
INDEX TREATMENT
Acupuncture (treatment group)
Technique according to classical oriental meridian theory healing by stimulating energy
flow in the body; acupuncture points varied between participants and varied from day
to day; electroacupuncture and moxibustion were used in some participants; other treatment parameters were not specified
COMPARISON
Wait-list (control group)
Treatment schedule: 3 to 4 sessions/wk over 4 weeks
Duration of follow-up: 8 weeks
CO-INTERVENTION
Comparable between index and control groups for medication use only
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
High risk
Not blinded
Not possible
No drop-outs
Low risk
38
Coan 1982
(Continued)
No missing data
Unclear risk
No protocol
Low risk
Reported to be similar
High risk
Compliance acceptable?
High risk
Not reported
Low risk
Fatal Flaw
Low risk
Acceptable
Fu 2009
Methods
RCT
Number Analysed/randomised: 112/117
Intention-to-treat: NR
Power analysis: NR
Funding source: State Ministry of Science and Technology
Participants
Interventions
INDEX TREATMENT
Acupuncture group
Acupuncture points - Du14, ExHN15, SI15 needles inserted to muscle layer manipulated
for Deqi, then remained inserted for 20 minutes; infrared radiation
COMPARISON TREATMENT
Sham
Superficial insertion 1 cm apart laterally from acupuncture points. Remained for 20
minutes, no manipulation; infrared radiation
CO-INTERVENTION
NR
Treatment schedule: once every other day for 9 sessions over 18 days
Duration of follow-up: immediate post treatment, 4 weeks, 3 months
Outcomes
39
Fu 2009
(Continued)
--
Risk of bias
Bias
Authors judgement
Low risk
Not possible
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
40
Fu 2009
(Continued)
Unclear risk
Not reported
Compliance acceptable?
Unclear risk
Not reported
Low risk
Fatal Flaw
High risk
He 2004
Methods
RCT
Number analysed/randomised: 24/24
Intention-to-treat: NR
Power analysis: NR
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Acupuncture
16 body points, 6 ear points, electrostimulation
COMPARISON TREATMENT
Placebo
10 to 14 mm distal to real points or 4 to 6 mm for ear points; electrostimulation set up
but no voltage
CO-INTERVENTION
Reported, see Risk of bias
Treatment schedule: 3 times per week, over 3 to 4 weeks, for a total of 10 treatments,
with each session averaging 45 minutes in duration
Duration of follow-up: immediate post treatment, 6 months, 3 years
Outcomes
41
He 2004
(Continued)
Costs of care: NR
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
Described in report
Not possible
Described in report
No drop-outs
Low risk
Unclear risk
No protocol
High risk
Not similar with respect to PPT and duration of symptoms; also headache baseline
information not provided
High risk
Compliance acceptable?
Low risk
Low risk
Fatal Flaw
Low risk
Acceptable
42
He 2005
Methods
RCT
Number analysed/randomised: 24/24
Intention-to-treat: NR
Power analysis: NR
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Acupuncture
16 body points, 6 ear points, electrostimulation
COMPARISON TREATMENT
Placebo
10 to 14 mm distal to real points or 4 to 6 mm for ear points; electrostimulation but no
voltage
CO-INTERVENTION
Reported, see Risk of bias
Treatment schedule: 3 times/wk over 3 to 4 weeks for a total of 10 treatments, with each
session averaging 45 minutes in duration
Duration of follow-up: immediate post treatment, 6 months, 3 years
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
43
He 2005
(Continued)
Not possible
No drop-outs
Low risk
Not reported
Unclear risk
No protocol
Low risk
Reported to be similar
Low risk
Reported to be similar
Compliance acceptable?
Low risk
Low risk
Fatal Flaw
Low risk
Acceptable
Ilbuldu 2004
Methods
RCT
Number analysed/randomised: 60/60
Intention-to-treat: NR
Power analysis: NR
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Dry needling (dn) upper trapezius
COMPARISON TREATMENT
Placebo laser
CO-INTERVENTION
Paracetamol as needed
Treatment schedule: dn once/wk over 4 weeks, placebo laser 3 sessions/wk over 4 weeks
Duration of follow-up: immediate post treatment and 6 months
44
Ilbuldu 2004
(Continued)
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Not reported
Unclear risk
Not possible
High risk
Not reported
45
Ilbuldu 2004
(Continued)
Unclear risk
No protocol
Low risk
Reported to be similar
Unclear risk
Compliance acceptable?
Unclear risk
Not reported
Low risk
Fatal Flaw
High risk
Irnich 2001
Methods
RCT
Number analysed/randomised: 177/177
Intention-to-treat: reported
Power analysis: NR
Funding source: German Ministry for Education and Research. Manuscript preparation
supported by German Medical Acupuncture Association
Participants
Interventions
INDEX TREATMENT
Acupuncture
TCM plus ear acupuncture and dry needling of myofascial points. Local points - UB10,
active myofascial trigger points were located predominantly in the trapezius (nearby
GB20) and levator scapulae (nearby SI14). Distal points - SI3, UB60, Liv3, GB34,
TW5, ear point (cervical spine)
COMPARISON TREATMENT
Sham laser acupuncture (control)
Laser pen inactivated - each point treated for 2 minutes
CO-INTERVENTION
Not reported
Treatment schedule: 5 sessions over 3 weeks, each session 30 minutes in duration
Duration of follow-up: 12 weeks
Outcomes
46
Irnich 2001
(Continued)
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
Not possible
Low risk
Reported in text
Unclear risk
No protocol
Low risk
Reported to be similar
Unclear risk
Not reported
47
Irnich 2001
(Continued)
Compliance acceptable?
Unclear risk
Not reported
Low risk
Fatal Flaw
Low risk
Acceptable
Irnich 2002
Methods
RCT, cross-over
Number analysed/randomised: 34/36
Intention-to-treat: NA
Power analysis: NR
Funding source: German Ministry for Education and Research
Participants
Interventions
INDEX TREATMENT 1
Non-local needle acupuncture (NLA) at distant points according to the theory of channels of TCM and varied individually by therapist
INDEX TREATMENT 2
Dry needling (dn) of local myofascial trigger points with strong manual stimulation of
ah shi points
COMPARISON TREATMENT
Sham laser acupuncture (SHAM)
CO-INTERVENTION
Not reported
Treatment schedule: each participant treated once with all interventions with a 1-week
wash-out period and each session averaging 30 minutes in duration
Duration of follow-up: immediately following completion of each treatment
Outcomes
Notes
--
Risk of bias
Acupuncture for neck disorders (Review)
Copyright 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
48
Irnich 2002
(Continued)
Bias
Authors judgement
Fully concealed
Low risk
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
Unclear risk
Not reported
Compliance acceptable?
Low risk
Low risk
Fatal Flaw
Low risk
Acceptable
49
Itoh 2007
Methods
RCT
Number analysed/randomised: 31/40
Intention-to-treat: not calculated
Power analysis: not calculated
Location: Japan
Funding source: Japan Society of Acupuncture and Moxibustion
Participants
Interventions
INDEX TREATMENT 1
Standard acupuncture (SA)
Acupuncture points local: GB20, GB21, BL10, BL11, SI12, SI13; distal TE5, LI4, SI3
Inserted needles into the muscle (depth of 20 mm) using sparrow pecking technique;
manipulation stopped when participants reached Deqi, and needles were left in place
for an additional 10 minutes
INDEX TREATMENT 2
Trigger point acupuncture (TrP)
Local needling of myofascial trigger points (mean number of insertions 2.3)
Needles were inserted 20 mm into the skin over the trigger point by the sparrow pecking
technique. Manipulation was stopped when the local twitch response was elicited, and
the needle was left in place for an additional 10 minutes
INDEX TREATMENT 3:
Non-trigger point acupuncture (non-TrP)
Non-TrP group received the same treatment as above but at non-tender points (mean
number of insertions 2.4). The non-tender point chosen had no tenderness nor taut
muscle band. However, the point was selected in the same muscle but away from the
trigger point by 50 mm
COMPARISON TREATMENT
Sham acupuncture (SH)
SH groups received treatment at trigger points. Similar stainless steel needles were used,
but the tips had been cut off and smoothed to prevent penetration of the skin by the needle
with the sparrow pecking technique. Simulation of needle extraction was performed
after 10 minutes (mean number of insertions 2.6)
CO-INTERVENTION
Not specified
Treatment schedule:
6 treatments within 10 weeks; applied in 2 phases of 3 treatments:
3 treatments within first 3 weeks, no treatment from week 4 to 7 and 3 treatments from
week 7 to 10
Duration of follow-up: 3 weeks
Outcomes
Groups
PAIN INTENSITY (VAS 0 to 100 mm)
Baseline mean: SA 69.5, TrP 67.0, non-TrP 70.9, SH 64.1
End of study mean: SA 51.6, TrP 11.0, non-TrP 57.6, SH 53.9
Absolute benefit: SA 17.9, TrP 56.0, non-TrP 13.3, SH 10.2
Reported results: statistically significant improvement in the TrP group only
SA vs SH: SMD -0.24 (95% CI random -1.26 to 0.78) immediate post treatment
50
Itoh 2007
(Continued)
--
Risk of bias
Bias
Authors judgement
Computer-generated randomisation
Not reported
Unclear risk
Not possible
High risk
51
Itoh 2007
(Continued)
Unclear risk
No protocol
Unclear risk
Unclear risk
Not reported
Compliance acceptable?
Unclear risk
Not reported
Low risk
Fatal Flaw
High risk
Kwak 2012
Methods
RCT
Number analysed/randomised: 40/40
Intention-to-treat: reported
Power analysis: NR
Funding source: University of Tsukuba, Japan
Participants
Interventions
INDEX TREATMENT
Acupuncture
Acupuncture points from the gallbladder (GB), small intestine (SI), bladder (BL), triple
energiser (TE) and large intestine (LI) meridian systems located on shoulder, neck, head
and upper limbs. Needles (length 40 mm; diameter 0.16 mm, SEIRIN Co. Ltd) were
inserted perpendicularly to a depth of 1.0 to 2.0 cm in place for 15 minutes
COMPARISON
Wait-list
CO-INTERVENTION
Both groups maintained their usual care, including physiotherapy, exercise and sufficient
rest
Treatment schedule: Treatment consisted of 6 sessions, 3/wk for 2 weeks
No follow-up
Outcomes
52
Kwak 2012
(Continued)
Risk of bias
Bias
Authors judgement
Unclear risk
No drop-outs
Low risk
Acceptable
Low risk
See registration
Low risk
Unclear risk
Not reported
Compliance acceptable?
Unclear risk
Not reported
Low risk
53
Kwak 2012
Fatal Flaw
(Continued)
High risk
Liang 2009
Methods
RCT
Number analysed/randomised: 53/54
Intention-to-treat: NA
Power analysis: NR
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Routine acupuncture
Treated with routine acupuncture at GV 14, Ex-HN 15 and SI 15 with 40 mm long
needles (diameter of 0.30 mm). Needles were retained for 20 minutes after Deqi was
achieved
COMPARISON TREATMENT
Sham acupuncture
Sham acupuncture. Needled at 1 cm lateral to Ex-HN 15 and SI 15 (needles were 40
mm long with a diameter of 0.22 mm). Needles were retained for 20 minutes
CO-INTERVENTION
Infrared radiation as adjuvant treatment, comparable between index and control groups
Treatment schedule: Treatment consisted of 9 sessions, applied 3 times a week (every
other day) over a period of 3 weeks
No follow-up
Outcomes
QUALITY OF LIFE: Northwick Park Neck Pain Questionnaire (up to 100, low score
= better)
Baseline mean: routine acupuncture 35.32, sham acupuncture 31.96
End of study mean: routine acupuncture 19.16, sham acupuncture 23.76
Absolute benefit: routine acupuncture 16.16, sham acupuncture 8.2
Reported results: Both groups showed improvement
SMD -0.39 (95% CI random -0.77 to -0.00) immediate post treatment
Adverse effects: NR
Costs of care: NR
Notes
--
Risk of bias
Bias
Authors judgement
54
Liang 2009
(Continued)
Unclear risk
Not described
Not described
Not described
Not described
No drop-outs
Low risk
As described
Low risk
None reported
Unclear risk
Not described
Unclear risk
Not described
Compliance acceptable?
Unclear risk
Not described
Low risk
Fatal Flaw
High risk
Reporting flaws
Liang 2011
Methods
RCT, pilot
Number analysed/randomised: 178/190
Intention-to-treat: Not all randomised participants were analysed
Power analysis: calculated 90%
Funding source: NR
Participants
55
Liang 2011
(Continued)
Interventions
INDEX TREATMENT
Acupuncture group
Acupuncture points - Du14, SI15 and Ex-HN15 bilaterally manually stimulated on
insertion for Deqi. Needles were inserted into the muscle (to a depth of 20 mm), left
in place for 20 minutes. During treatment, participants received infrared irradiation on
the cervical region
COMPARISON TREATMENT
Sham
Participants in the control group received placebo acupuncture on the sham points,
which were 1 cm lateral to the standard acupuncture points selected in the study group.
Needles were inserted into the skin to a depth of approximately 3 mm and remained in
the subcutaneous tissues with no manual stimulation. During treatment, participants in
the control group also received infrared irradiation on the cervical region
CO-INTERVENTION
NR
Treatment schedule: 3 weeks, total 9 sessions, with each session averaging 20 minutes in
duration
Duration of follow-up: immediate post, 4 weeks, 3 months
Outcomes
56
Liang 2011
(Continued)
adverse events transient and resolved, although those who fainted decided to withdraw
from the study
Costs of care: NR
Notes
--
Risk of bias
Bias
Authors judgement
Low risk
Reported as blinded
Not possible
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
Unclear risk
Not reported
Compliance acceptable?
Unclear risk
Not reported
Low risk
Fatal Flaw
Low risk
Acceptable
57
Nabeta 2002
Methods
RCT
Number analysed/randomised: 34/34
Intention-to-treat: calculated
Power analysis: NR
Funding source: NR
Participants
Interventions
Treatment was provided to tender points on the posterior aspect of the neck and upper
back
All tender points were carefully detected where the subjects felt dull pain and stiffness
(neck, shoulder, and back) and were used for the acupuncture treatment. All tender
points were treated in each group
INDEX TREATMENT
Sparrow pecking acupuncture
Disposable stainless needles (0.2 mm 40 mm) were inserted into the muscle to a depth
of about 20 mm, and the sparrow pecking technique was applied. When the participant
felt Deqi, the manipulation was stopped and the needle was retained for 5 more minutes
COMPARISON TREATMENT
Simulated sparrow pecking acupuncture with no needle insertion
For sham acupuncture, similar stainless needles (0.2 mm 40 mm) were used, but the
tips had previously been cut off to prevent the needle from penetrating the skin. The cut
ends were smoothed with sandpaper manually under clean conditions. The acupuncturist
pretended to insert the needle and to use the sparrow pecking technique, then removed
the needles. Simulation of needle extraction was performed after 5 minutes
CO-INTERVENTION
Not specified
Duration of treatment: once/wk for 3 weeks
Duration of follow-up: 9 days
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
58
Nabeta 2002
(Continued)
Unclear risk
Not reported
Reported as blinded
Not possible
Low risk
No drop-outs
No drop-outs
Unclear risk
No protocol
Low risk
Unclear risk
Not reported
Compliance acceptable?
High risk
Low risk
9 days
Fatal Flaw
Low risk
Acceptable
Petrie 1983
Methods
RCT
Number analysed/randomised: 13/13
Intention-to-treat: NR
Power analysis: NR
Funding source: NR
Participants
59
Petrie 1983
(Continued)
Interventions
INDEX TREATMENT
Acupuncture group
5 standard points used - Du14, GB20 bilateral, GB21 bilateral; 28 g needle used to
achieve sensation of Teh Chi (Deqi); needles manipulated after insertion and on removal
COMPARISON
Placebo TNS group
Sham electrical stimulation with lead electrode applied to each side of the neck, 5 cm
lateral to C7
CO-INTERVENTION
Comparable between index and control groups
Treatment schedule: 4 weeks (2 times/wk), with each session averaging 20 minutes
Duration of follow-up: none
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
Not possible
No drop-outs
Low risk
60
Petrie 1983
(Continued)
Unclear risk
No protocol
Low risk
Appears similar
Unclear risk
Not reported
Compliance acceptable?
Low risk
Low risk
Fatal Flaw
High risk
Petrie 1986
Methods
RCT
Number analysed/randomised: 25/26
Intention-to-treat: NR
Power analysis: reported
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Acupuncture group
5 predetermined acupuncture points - Du14, GB20 and GB21 bilaterally manually
stimulated on insertion to Teh Chi (Deqi) and at 5-minute intervals
COMPARISON TREATMENT
Sham TNS
TNS electrodes placed at the base of the neck connected to an oscilloscope display
without a currentExaminer re-entered the room at 5 minute intervals to check display
CO-INTERVENTION
Analgesics comparable between groups
Treatment schedule: 2 sessions/wk for 4 weeks, with each session averaging 20 minutes
in duration
Duration of follow-up: 4 weeks
Outcomes
61
Petrie 1986
(Continued)
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
Not possible
Low risk
Unclear risk
No protocol
High risk
High risk
Not reported
Compliance acceptable?
High risk
Low risk
62
Petrie 1986
Fatal Flaw
(Continued)
High risk
Sahin 2010
Methods
RCT
Number analysed/randomised: 29/31
Intention-to-treat: NR
Power analysis: NR
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Electroacupuncture group (EAP)
7 acupuncture points - Du14 and GB20, GB21, LI4, UB10, UB60, TE5 all bilaterally
and manually stimulated on insertion to Teh Chi (Deqi), EAP added after 1 to 4 Hz,
200 s
COMPARISON TREATMENT
Sham EAP
Same points as the treatment group; needles inserted 1 to 2 cm away from the meridian
points. No Deqi. EAP stimulated, then turned off
CO-INTERVENTION
NR
Treatment schedule: 10 sessions over 3 weeks, with each session averaging 30 minutes
in duration
Duration of follow-up: immediate post treatment, 3 months
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
63
Sahin 2010
(Continued)
Not described
Names sealed in opaque envelopes. Envelopes were then allocated randomly into
2 groups. After the doctor examined participants, she gave the names of those who
were included in the study to someone else,
who prepared the envelopes
High risk
Reported as blinded
Not possible
Low risk
Unclear risk
No protocol
High risk
Unclear risk
Not reported
Compliance acceptable?
Unclear risk
Not reported
Low risk
Fatal Flaw
High risk
64
Seidel 2002
Methods
RCT
Number Analysed/randomised: 48/51
Intention-to-treat: NR
Power analysis: NR
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Conventional meridian acupuncture (Acu)
15 minutes per session; maximum 15 needles per session. Option of 15 acupuncture
points was available. Seirin needles 7, 0.3 30 mm and 0.2 15 mm. Insertion until
the Deqi response was achieved
COMPARISON TREATMENT
Placebo LASER (LLLT0)
Outcome power: 0 mV, Meridian acupuncture points same as acupuncture group
CO-INTERVENTION
Avoided in trial design
Treatment schedule: 4 weeks, 2 sessions per week - total 8 sessions
Duration of follow-up: 4 weeks
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
65
Seidel 2002
(Continued)
Unclear risk
Possibly adequate
Reported as blinded
Not possible
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
Low risk
Avoided
Compliance acceptable?
High risk
Not acceptable
Low risk
Assessed at 4 weeks
Fatal Flaw
Low risk
Acceptable
Sun 2010
Methods
RCT
Number analysed/randomised: 34/35
Intention-to-treat: calculated
Power analysis: calculated 90%
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Acupuncture group
5 predetermined acupuncture points - TE14, GB20, SI3 bilaterally manually stimulated
66
Sun 2010
(Continued)
on insertion to Qi
COMPARISON TREATMENT
Sham acupuncture
Same points as treatment group. Inserted into subcutaneous tissue at 2 mm depth. No
manual stimulation
CO-INTERVENTION
NR
Treatment schedule: 2 sessions/wk for 3 consecutive weeks, with each session averaging
20 minutes in duration
Duration of follow-up: immediate post, 4 weeks, 12 weeks
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
Not possible
Low risk
67
Sun 2010
(Continued)
Unclear risk
No protocol
Low risk
Reported to be similar
Unclear risk
Not reported
Compliance acceptable?
Unclear risk
Low risk
Fatal Flaw
High risk
Thomas 1991
Methods
RCT cross-over
Number analysed/randomised: 132/132
Power analysis: Post hoc analysis suggested 70 participants per group were needed
Intention-to-treat analysis: NA
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Acupuncture (Acu): LI3 and GB20 bilaterally, DU14, DU16, DU20 with manual stimulation for 10s for Deqi every 5 minutes, 40 minute session
COMPARISON TREATMENT
Sham acupuncture: needles inserted superficially, not manually stimulated
CO-INTERVENTION
Instructed to take no pain medication 24 hours before trials
Duration of treatment: 1 session
Duration of follow-up: 2 hours
Outcomes
68
Thomas 1991
(Continued)
ture but statistically significant when acupuncture was compared with placebo diazepam
vs placebo acupuncture: SMD 0.17 (95% CI random -0.25 to 0.59) immediate post
treatment
vs placebo diazepam: SMD 0.09 (95% CI random -0.33 to 0.51) immediate post treatment
Adverse effects: NR
Costs of care: NR
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
Not possible
No drop-outs
Low risk
Unclear risk
No protocol
Low risk
Low risk
Avoided
Compliance acceptable?
Low risk
Low risk
69
Thomas 1991
Fatal Flaw
(Continued)
High risk
Tough 2010
Methods
Participants
Interventions
INDEX TREATMENT
Acupuncture group
Trigger point needling using 0.25 mm 30 to 40 mm length, 6 to 7 sparrow pecking
into each MTrP (muscles treated not described)
COMPARISON
Sham acupuncture
Same procedure as treatment group; however, a sham needle 0.30 mm 50 mm cut,
and blunted end was tapped against the skin, with sparrow pecking motion
CO-INTERVENTION
Participant education, heat, analgesics and exercise (home therapy)
Treatment schedule: 1 session/wk, total 2 to 6 treatments depending on participant
response
Duration of follow-up: 6 weeks
Outcomes
Notes
--
70
Tough 2010
(Continued)
Risk of bias
Bias
Authors judgement
Held centrally by the pharmacy department at the research site; allocation concealed from the investigator until after participant enrolment
Low risk
Acceptable at 17%
Low risk
Unclear risk
No protocol available
Low risk
Unclear risk
Not reported
Compliance acceptable?
Unclear risk
Exercise booklet given; unsure whether participants received all acupuncture treatment prescribed
Low risk
Fatal Flaw
Low risk
Acceptable
71
Tsai 2010
Methods
RCT
Number analysed/randomised: 35/35
Intention-to-treat: NA
Power analysis: NR
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Acupuncture group
Dry needling, used a 25-hypodermic needle (0.5 mm in diameter). Manual stimulation
of the needle to the MTrP region of the extensor carpi radialis longus muscle to elicit a
local twitch response. 1 to 2 minutes
COMPARISON
Sham acupuncture
Same procedure as treatment group; however, needle was maintained in the subcutaneous
tissue
CO-INTERVENTION
Avoided
Treatment schedule: 1 session
Duration of follow-up: immediate post treatment
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Unclear risk
72
Tsai 2010
(Continued)
Reported in text
Not possible
No drop-outs
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
Low risk
Compliance acceptable?
Low risk
Acceptable by design
Low risk
Fatal Flaw
Low risk
Acceptable
Vas 2006
Methods
RCT
Number analysed/randomised: 85/123
Intention-to-treat: calculated (although ITT stated, not all analysed at T2, only T1)
Power analysis: calculated (90% power, alpha = 5%, 49 participants needed for experimental group and 46 for control group)
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Acupuncture
Points were selected according to pain characteristics and accompanying symptoms on
73
Vas 2006
(Continued)
the basis of traditional Chinese treatment methods. Puncture was bilateral, with sterile,
single-use needles (25 mm 0.25 mm or 40 mm 0.25 mm). Puncture was effected
by determining the Deqi. Needles were kept in place for 30 minutes and were manually
stimulated every 10 minutes. After the needles were removed, Vaccaria seeds were applied
in the ear auricle and were taped there until the following treatment session. Participants
were told to apply pressure to each ear point for a series of 10 repeats 3 times per day
COMPARISON TREATMENT
TENS placebo
Applied using TRANSMED 911 transcutaneous nerve stimulation units that had been
adjusted beforehand to prevent current through the electrodes. Electrodes were placed
at Jianjing (GB 21) bilateral acupuncture point for 30 minutes. Participants state was
checked every 10 minutes, and the TENS-placebo potentiometer adjusted
CO-INTERVENTION
Not avoided but comparable; both groups were provided with analgesic rescue medications once weekly
Duration of treatment: 3 weeks
Treatment consisted of 5 sessions over 3 weeks (2 in each of first 2 weeks and once in
the third week)
Duration of follow-up: 6 months
Outcomes
Notes
--
74
Vas 2006
(Continued)
Risk of bias
Bias
Authors judgement
Unclear risk
Not possible
High risk
Unclear risk
No protocol
Low risk
Reported to be similar
High risk
Compliance acceptable?
Unclear risk
Low risk
Fatal Flaw
Low risk
Acceptable
75
White 2000
Methods
RCT/cross-over
Number analysed/randomised: 68/68
Intention-to-treat: NR
Power analysis: NR
Funding source: Forest Park Institute, Ambulatory Anesthesia Research Foundation,
White Mountain Institute
Participants
Interventions
INDEX TREATMENT 1
Local dermatomal stimulation
10 acupuncture-like needle probes inserted 2 to 4 cm into soft tissue/paraspinous muscles
in the cervical region, alternating frequency of 15 Hz to 30 Hz to produce gentle tapping
sensation without muscle contraction
COMPARISON TREATMENT 1
Remote dermatomal stimulation
10 acupuncture-like needle probes inserted into soft tissue/paraspinous muscle in the
lower back region with identical electrical therapy characteristics of the local dermatomal
stimulation group
COMPARISON TREATMENT 2
Control needles only
Needles inserted into the cervical region without electrical stimulation
CO-INTERVENTION
Analgesics comparable between groups
Treatment schedule: 3 times/wk for 3 consecutive weeks, with 1 week off between modalities and each session averaging 30 minutes in duration
Duration of follow-up: 24 hours after completion of each 3 week treatment period
Outcomes
Notes
--
Risk of bias
Bias
Authors judgement
Not reported
Not reported
Unclear risk
76
White 2000
(Continued)
Not possible
Inadequate description
Unclear risk
Unclear risk
No protocol
High risk
High risk
Compliance acceptable?
Low risk
Acceptable
Low risk
Fatal Flaw
High risk
Inadequate reporting
White 2004
Methods
RCT
Number analysed/randomised: 124/135
Intention-to-treat: NR
Power analysis: calculated
Funding source: Henry Smiths Charity, Hospital Savings Association, Laing Foundation
Participants
Interventions
INDEX TREATMENT
Acupuncture with single-use needles, points based on individualised western acupuncture
techniques previously reported as effective in neck pain, 6 points on average, with each
session averaging 20 minutes in duration. Manual stimulation to Deqi. 8 treatments
77
White 2004
(Continued)
Notes
--
Risk of bias
Bias
Authors judgement
Adequate
Unclear risk
78
White 2004
(Continued)
Not possible
Acceptable
Low risk
Unclear risk
No protocol
Low risk
Reported to be similar
High risk
Compliance acceptable?
Unclear risk
Not described
Low risk
Fatal Flaw
Low risk
Acceptable
Witt 2006
Methods
RCT
Number analysed/randomised: 3036/3766
Intention-to-treat: calculated
Power analysis: calculated
Funding source: NR
Participants
Interventions
INDEX TREATMENT
Immediate acupuncture treatment plus additional conventional treatment as needed
Participants could be treated individually, and numbers of needles and acupuncture
points used were chosen at the discretion of physicians. Only needle acupuncture (with
79
Witt 2006
(Continued)
disposable 1-time needles) and manual stimulation were allowed, whereas other forms
of acupuncture treatment were not allowed
COMPARISON TREATMENT
Conventional treatment; delayed acupuncture treatment 3 months after study onset
Control group was not allowed to use any kind of acupuncture during first 3 months
CO-INTERVENTION
Comparable between index and control groups. Participants were free to use conventional
routine medical care as offered by German social health insurance funds
Treatment schedule: Each participant in the randomised acupuncture group received up
to 15 acupuncture sessions during first 3 months and no acupuncture sessions between
3 and 6 months
Duration of treatment: 3 months
Duration of follow-up: 3 months after treatment
Outcomes
80
Witt 2006
(Continued)
29% other
Costs of care: acupuncture treatment associated with higher costs (EURO925.53
1551.06 vs EURO648.06 1459.13); however according to assumed threshold values
beyond 3 month follow-up, acupuncture appears cost-effective. Also, over-the-counter
medications were not included in the cost of routine care
Notes
--
Risk of bias
Bias
Authors judgement
Low risk
Not possible
Not possible
High risk
Unclear risk
No protocol
Low risk
Reported to be similar
Unclear risk
Not reported
Compliance acceptable?
Low risk
Low risk
81
Witt 2006
Fatal Flaw
(Continued)
Low risk
Acceptable
Abbreviations:
BL = bladder
CI = confidence interval
cm = centimetre
dn = dry needling
EAP = electroacupuncture
g = gauge
GB = gallbladderITT = intention-to-treat
LI = large intestine
LLLT0 = placebo intestine
mg = milligram
mm = millimetreMPS = myofascial neck pain syndrome
MTrP = muscles treated not described
NA = not applicable
NDI = Neck Disability Index
NLA = non-local needle electroacupuncture
NPQ = Northwick Park Pain Questionnaire
NR = not reported
NSAID = non-steroidal anti-inflammatory drug
NTPA = non-trigger point acupuncture
OD = daily
PPT = pain pressure threshold
RA = remote acupuncture
RCT = randomised controlled trial
SA = standard acupuncture
SD = standard deviation
SF-36 = Short Form-36
SH = sham treatment
SI = small intestine
SMD = standardised mean difference
TCM = Traditional Chinese Medicine
TE = triple energiser
TENS = transcutaneous electrical nerve stimulation
TNS = transcutaneous nerve stimulation
TPA = trigger point acupuncture
TrP = trigger point acupuncture
VAS = visual analogue scale
WAD = whiplash-associated disorder
82
Study
Bahadir 2009
Calvo-Trujillo 2013
Ceccherelli 2006
Ceccherilli 2014
Cho 2014
Chu 1997
Coeytaux 2005
Cohen 2014
David 1998
Dong 2012
Edwards 2003
Emery 1986
Eroglu 2013
Falkenberg 2007
Fernandez-Carnero 2014
Franca 2008
Fu 2005
Fu 2007
Fu 2014
Ga 2007a
Design: quasi-RCT
Comparison: acupuncture vs active treatment (lidocaine)
Ga 2007b
83
(Continued)
Gallacchi 1981
Gallacchi 1983
Gaw 1975
Gil 2015
Giles 1999
Giles 2003
Guanygue 2001
Comparison: included other treatments with acupuncture; the effect of acupuncture could not be
isolated
Guo 2013
Harvey 2015
Hayek 2014
Comparison: acupuncture may be part of multi-modal treatment vs epidural steroid injections (ESI)
with depo-methylprednisolone
Hu 2014
Hua 2009
Design: quasi-RCT
Comparison: electroacupuncture portion of control
Huang 2008
Huang 2012
Hudson 2010
Jia 2007
Jin 2012
Johnson 2000
Kai 2008
Kisiel 1996
84
(Continued)
Li 2004
Li 2006
Li 2013
Lin 2004
Liu 2008
Liu 2013
Comparison: acupuncture vs active treatment (intravenous drip with 5% glucose 250 mL and compound Salvia miltiorrhiza injection and mechanical traction)
Lixing 2000
Llamas-Ramas 2014
Loy 1983
Design: quasi-RCT
Comparison: acupuncture vs active treatment (traction and shortwave diathermy)
Lu 2006
Lundeburg 1988
Population: head and neck pain included; unable to obtain split data
Lundeburg 1991
Luo 2010
Design: non-RCT
Ma 2010
Intervention: mini-scalpel
MacPherson 2013
Comparison: acupuncture vs active treatment (Alexander lessons, postural awareness, usual care)
McLean 2013
Muller 2005
Myburgh 2012
Nakajima 2015
Pan 2008
Design: quasi-RCT
Population: occipital neuralgia
Pecos-Martin 2015
Peng 1987
Design: non-RCT
85
(Continued)
Rayegani 2014
Comparison: acupuncture vs active treatment (physiotherapy including heat, TENS, ultrasound, passive
and self stretching)
Salter 2006
Sato 2014
Population: individuals with latent trigger points in upper trapezius, no neck pain
Sator-Katzenschlager 2003
Seo 2014
Shang 2002
Shuangquan 2003
Soderlund 2001
Sun 2013
Takakura 2014
Teng 1973
Tobbackx 2013
Venancio 2008
Venancio 2009
Wan 2013
Comparison: 1 acupuncture type vs another vs active treatment (oral Jing fukang granule)
Wang 2007
Wang 2008
Wang G 2014
Xu 2012
Xue 2007
Design: quasi-RCT
Comparison: 1 acupuncture type vs another
Yang 2009
86
(Continued)
Yang 2013
Yoon 2009
Yoshimizu 2012
Yu 2003
Zeng 2005
Zhang 1996
Zhang 2003
Zhang J 2008
Zhang J 2013
Zhao 2004
Zheng 2014
Zhi 2008
Zhou 2014
Zhu 2002
Zhu 2006
Zhuang 2004
Ziaeifar 2014
87
Participants
Interventions
Outcomes
Numeric Rating Scale (NRS), ROM, Symptom Checklist (SCL) questionnaire and overall satisfaction
Notes
Bar-Haim 2012
Methods
RCT
Participants
Interventions
Outcomes
Pain (NPS)
Notes
clinicaltrials.gov
Cerezo-Tellez 2014
Methods
RCT
Participants
Interventions
Outcomes
Notes
clinicaltrials.gov
Choi 2011
Methods
RCT
Participants
Interventions
Acupuncture vs wait-list
Outcomes
Pain (VAS), post-needling pain, pressure pain threshold, range of motion, quality of life (SF-36), Depression Scale,
Cornell Medical Index (CMI)
88
Choi 2011
Notes
(Continued)
clinicaltrials.gov
Guo 2014
Methods
Guo Y
Participants
Interventions
Outcomes
Notes
http://apps.who.int/trialsearch/AdvSearch.aspx
Liguori 2012
Methods
Participants
Interventions
Outcomes
Notes
Mejuto-Vzquez 2014
Methods
RCT
Participants
Interventions
Outcomes
Numeric Pain Rating Scale (NPRS), pressure pain threshold (PPT) for pain, range of motion
Notes
--
Simma-Kletscha 2009
Methods
RCT
Participants
Interventions
89
Simma-Kletscha 2009
(Continued)
Outcomes
Pain intensity (VAS), functional muscle test, ability to open the mouth, axiographic evaluation
Notes
Sterling 2015
Methods
Participants
Interventions
Dry needling, advice and exercise vs sham dry needling, advice and exercise
Outcomes
Notes
--
Wilke 2014
Methods
Participants
Interventions
Outcomes
Mechanical pain threshold, motion-related pain (visual analogue scale - VAS) and cervical range of motion, range of
motion
Notes
--
Zhang SP 2013
Methods
RCT
Participants
Interventions
Outcomes
Neck Pain Disability Northwick Park Neck Pain Questionnaire (NPQ), Quality of Life SF-36 health survey, use of
medication for neck pain, sick leave
Notes
--
90
Evaluation of immediate effect of acupuncture on pain, cervical range of motion and electromyographic
activity of the upper trapezius muscle in patients with non-specific neck pain: study protocol for a randomised
controlled trial
Methods
Participants
Interventions
Outcomes
EMG activity of upper trapezius, NPRS for neck pain and cervical range of motion (CROM)
Starting date
--
Contact information
--
Notes
--
Kim 2014
Trial name or title
Acupuncture as analgesia for non-emergent acute non-specific neck pain, ankle sprain and primary headache
in an emergency department setting: a protocol for a parallel-group, randomised, controlled pilot trial
Methods
Participants
40 patients with non-emergent acute neck pain, ankle sprain or primary headache
Interventions
Outcomes
Numeric Rating Scale for pain (NRS), Neck Disability Index (NDI), participant-reported overall improvement
Starting date
--
Contact information
--
Notes
To be determined if number of participants with neck pain is sufficient and extractable data are available and/
or if primary headaches are of cervical origin
91
Liang 2012
Trial name or title
Optimised acupuncture treatment for neck pain caused by cervical spondylosis: a study protocol of a multicentre randomised controlled trial
Methods
Participants
Interventions
Outcomes
Northwick Park Pain Questionnaire (NPQ), McGill Pain Questionnaire (MPQ) and SF-36 for pain and
disability
Starting date
--
Contact information
--
Notes
--
Que 2013
Trial name or title
Effectiveness of acupuncture intervention for neck pain caused by cervical spondylosis: study protocol for a
randomised controlled trial
Methods
Participants
Interventions
Outcomes
Starting date
--
Contact information
--
Notes
--
Sun 2014
Trial name or title
Acupuncture at Houxi (SI 3) acupoint for acute neck pain caused by stiff neck: study protocol for a pilot
randomised controlled trial
Methods
Participants
Interventions
92
Sun 2014
(Continued)
Outcomes
NPQ, SF-MPQ
Starting date
--
Contact information
--
Notes
--
93
No. of
studies
No. of
participants
Statistical method
Effect size
11
8
1
560
34
34
319
124
34
15
1
1
94
4
1
1
1
2
2
290
290
No. of
studies
No. of
participants
Statistical method
Effect size
95
5
5
1
1
1
1
1
1
1
1
96
No. of
studies
No. of
participants
Statistical method
Effect size
1
1
97
Analysis 1.1. Comparison 1 Acupuncture versus sham treatment, Outcome 1 Pain intensity (VAS)
immediate post treatment.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
10
3.3 (1.1)
10
7.1 (0.9)
Tsai 2010
17
5.2 (1.6)
18
6.4 (1)
14
15 (5)
10
36 (8)
White 2000
23
-38 (17)
23
-9 (16)
Fu 2009
57
3.19 (1.92)
55
4.14 (1.59)
Liang 2011
88
3.48 (2.04)
90
4.01 (1.45)
15
1.87 (1.9)
16
3.37 (2.14)
46.1 (19)
51.4 (23.3)
1.8 (1.2)
44
1.6 (1.1)
44
13
4.31 (1.61)
16
5.46 (2.26)
Sun 2010
17
30 (25.4)
17
40 (20.4)
-10
-5
[Acupuncture]
10
[Sham Treatment]
(1) eg. Rendant 2011: Exercise therapy vs Wait list control; duration: 18 sessions over 6 months; follow-up: none; instrument: VAS:
98
Analysis 1.2. Comparison 1 Acupuncture versus sham treatment, Outcome 2 Pain intensity (VAS) short
term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Weight
IV,Random,95% CI
Std.
Mean
Difference
IV,Random,95% CI
17
30 (15.5)
17
17
30 (20.55)
17
6.1 %
6.1 %
6.1 %
6.1 %
17
43.3 (19.7)
17
17
46.8 (25.4)
17
57
2.89 (1.81)
55
3.28 (1.48)
20.1 %
Liang 2011
88
2.88 (1.72)
90
3.19 (1.31)
32.0 %
Sahin 2010
13
4 (2.97)
16
3.54 (3.13)
5.2 %
57.2 %
22.0 %
22.0 %
5.8 %
5.8 %
2.7 %
2.7 %
158
161
64
3.7 (2.4)
64
60
4.6 (2.32)
60
17
1.7 (2)
17
17
3.2 (2.8)
17
51.6 (22)
53.9 (23)
-2
-1
[Acupuncture]
[Sham Treatment]
(Continued . . . )
99
(. . .
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Continued)
Std.
Mean
Difference
Weight
IV,Random,95% CI
IV,Random,95% CI
281
279
100.0 %
-2
-1
[Acupuncture]
[Sham Treatment]
Analysis 1.3. Comparison 1 Acupuncture versus sham treatment, Outcome 3 Pain intensity (VAS)
intermediate term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Std.
Mean
Difference
Mean(SD)
IV,Random,95% CI
IV,Random,95% CI
24 (7)
12
36 (8)
4.1 (2.4)
60
5.5 (2.32)
12
64
-20
-10
[Acupuncture]
10
20
[Sham Treatment]
100
Analysis 1.4. Comparison 1 Acupuncture versus sham treatment, Outcome 4 Pain intensity (VAS) long
term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
12
44 (11)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
12
19 (6)
-100
-50
[Acupuncture]
50
100
[Sham Treatment]
Analysis 1.5. Comparison 1 Acupuncture versus sham treatment, Outcome 5 Disability (NDI) immediate
post treatment.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
9.4 (5.8)
10.4 (3.7)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
-4
-2
[Acupuncture]
[Sham Treatment]
101
Analysis 1.6. Comparison 1 Acupuncture versus sham treatment, Outcome 6 Disability (NPQ) immediate
post treatment.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Std.
Mean
Difference
Mean(SD)
Mean(SD)
IV,Random,95% CI
IV,Random,95% CI
Fu 2009
57
19.98 (11.3)
55
25.02 (13.03)
Liang 2009
53
19.16 (11.49)
53
23.76 (12.15)
Liang 2011
88
20.71 (11.91)
90
24.04 (11.83)
-2
-1
[Acupuncture]
[Sham Treatment]
Analysis 1.7. Comparison 1 Acupuncture versus sham treatment, Outcome 7 Disability (NPQ) short term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Weight
IV,Random,95% CI
Std.
Mean
Difference
IV,Random,95% CI
57
20.55 (10.2)
55
25.77 (15.05)
38.5 %
Liang 2011
88
19.09 (9.94)
90
23.53 (13.67)
61.5 %
100.0 %
145
145
-1
-0.5
[Acupuncture]
0.5
[Sham Treatment]
102
Analysis 1.8. Comparison 1 Acupuncture versus sham treatment, Outcome 8 Disability (NDI) short term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Std.
Mean
Difference
Mean(SD)
IV,Random,95% CI
IV,Random,95% CI
11.1 (5)
60
14.7 (6.2)
10.9 (6.6)
64
13.3 (6.4)
17
8.4 (7.8)
17
11.9 (8.8)
17
-3.8 (0.8)
18
-2.9 (0.6)
-2
-1
[Acupuncture]
[Sham Treatment]
103
Analysis 1.9. Comparison 1 Acupuncture versus sham treatment, Outcome 9 Disability (NDI) intermediate
term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
60
16.8 (7.75)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
64
14.5 (7.2)
-100
-50
50
[Acupuncture]
100
[Sham Treatment]
Analysis 1.10. Comparison 1 Acupuncture versus sham treatment, Outcome 10 Quality of life (SF-36)
immediate post treatment.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
88
86.02 (13.19)
90
78.94 (22.66)
Std.
Mean
Difference
IV,Fixed,95% CI
IV,Fixed,95% CI
-1
-0.5
[Acupuncture]
0.5
[Sham Treatment]
104
Analysis 1.11. Comparison 1 Acupuncture versus sham treatment, Outcome 11 Quality of life (SF-36) short
term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
90
85.88 (14.01)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
88
84.26 (15.24)
-2
-1
[Acupuncture]
[Sham Treatment]
Analysis 2.1. Comparison 2 Acupuncture versus inactive control, Outcome 1 Pain intensity (VAS)
immediate post treatment.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Std.
Mean
Difference
Mean(SD)
Mean(SD)
IV,Random,95% CI
IV,Random,95% CI
20
7.62 (1.5)
20
7.65 (1.57)
19.1 (16.11)
34
28 (19.36)
34
13
-36.59 (22.95)
12
-32.88 (18.55)
Seidel 2002
12
7 (11.4)
12
25.2 (26.6)
1.8 (1.2)
44
1.7 (1)
44
-10
-5
Favours treatment
10
Favours control
105
Analysis 2.2. Comparison 2 Acupuncture versus inactive control, Outcome 2 Pain intensity (VAS) short
term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
51
-24.22 (27.98)
57
-17.28 (28.1)
Petrie 1986
13
-31.77 (24.1)
12
-24.72 (20.6)
Seidel 2002
12
9.4 (17.8)
12
19.6 (24.57)
Vas 2006
61
-42.1 (21.1)
62
-14 (15.7)
White 2004
63
20.39 (20.26)
61
30.69 (22)
-10
-5
Favours acupuncture
10
Favours sham
106
Analysis 2.3. Comparison 2 Acupuncture versus inactive control, Outcome 3 Pain intensity (VAS)
intermediate term.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Std.
Mean
Difference
Mean(SD)
Mean(SD)
IV,Random,95% CI
IV,Random,95% CI
4.24 (2.93)
20
4.22 (3.06)
20
45
-41.1 (26.9)
40
-26.8 (25.9)
White 2004
57
19.21 (24.22)
54
21.02 (24.38)
-10
-5
Favours treatment
10
Favours control
Analysis 2.4. Comparison 2 Acupuncture versus inactive control, Outcome 4 Pain intensity (VAS) long term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
53
24.36 (26.68)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
54
20.91 (25.69)
-4
-2
Favours experimental
Favours control
107
Analysis 2.5. Comparison 2 Acupuncture versus inactive control, Outcome 5 Pain pressure threshold
immediate post treatment.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
51
0.06 (0.58)
57
-0.03 (0.51)
Seidel 2002
12
5.75 (1.59)
12
6.12 (3.11)
-2
-1
Favours experimental
Favours control
Analysis 2.6. Comparison 2 Acupuncture versus inactive control, Outcome 6 Pain pressure threshold short
term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
51
0.19 (0.77)
57
0.03 (0.62)
Seidel 2002
12
6.68 (2.18)
12
7.32 (3.32)
-2
-1
Favours experimental
Favours control
108
Analysis 2.7. Comparison 2 Acupuncture versus inactive control, Outcome 7 Pain intensity (proportion
pain relief) immediate post treatment.
Review:
Study or subgroup
Treatment
Control
n/N
n/N
1/7
6/6
Risk Ratio
MH,Random,95%
CI
Risk Ratio
MH,Random,95%
CI
0.02
0.1
Favours treatment
10
50
Favours control
Analysis 2.8. Comparison 2 Acupuncture versus inactive control, Outcome 8 Disability (NDI) short term.
Review:
Study or subgroup
White 2004
Treatment
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
59
10.98 (6.27)
59
12.68 (7.79)
IV,Random,95% CI
IV,Random,95% CI
-0.24 [ -0.60, 0.12 ]
-1
-0.5
Favours treatment
Std.
Mean
Difference
0.5
Favours control
109
Analysis 2.9. Comparison 2 Acupuncture versus inactive control, Outcome 9 Disability (NDI) intermediate
term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
53
10.64 (8.3)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
56
9.91 (6.96)
-1
-0.5
Favours treatment
0.5
Favours control
Analysis 2.10. Comparison 2 Acupuncture versus inactive control, Outcome 10 Disability (NDI) long term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
53
10.72 (9.11)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
53
8.89 (6.57)
-100
-50
Favours experimental
50
100
Favours control
110
Analysis 2.11. Comparison 2 Acupuncture versus inactive control, Outcome 11 Function (NHP) immediate
post treatment.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
20
23.07 (19.09)
20
19.35 (14.14)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
-2
-1
Favours acupuncture
Analysis 2.12. Comparison 2 Acupuncture versus inactive control, Outcome 12 Function (NHP)
intermediate term.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
13.68 (16.62)
20
16.08 (17.43)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
20
-4
-2
Favours acupuncture
111
Analysis 2.13. Comparison 2 Acupuncture versus inactive control, Outcome 13 Function (NPQ) short term.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
61
-30.2 (13.6)
62
-12.7 (14.9)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
-2
-1
Favours acupuncture
Analysis 2.14. Comparison 2 Acupuncture versus inactive control, Outcome 14 Quality of life (SF-36,
Functional Component) short term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
45
9.3 (11)
40
5.3 (8)
White 2004
59
42.49 (9.75)
59
43.75 (10.04)
-2
-1
Favours acupuncture
112
Analysis 3.1. Comparison 3 Acupuncture versus wait-list, Outcome 1 Pain intensity (VAS) short term.
Review:
Study or subgroup
Treatment
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
3.63 (2.21)
15
5.36 (2.32)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
15
-2
-1
Favours experimental
Favours control
Analysis 3.2. Comparison 3 Acupuncture versus wait-list, Outcome 2 Disability (neck and pain disability
scale) short term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
1698
-5.8 (0.65)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
1753
-28.9 (0.65)
-2
-1
Favours treatment
Favours control
113
Analysis 3.3. Comparison 3 Acupuncture versus wait-list, Outcome 3 Disability (neck and pain disability
scale) intermediate term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
1698
25.1 (0.7)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
1753
28 (0.7)
-100
-50
Favours experimental
50
100
Favours control
Analysis 3.4. Comparison 3 Acupuncture versus wait-list, Outcome 4 Quality of life (SF-36 mental score)
short term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
1698
1 (0.25)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
1753
4.2 (0.25)
-100
-50
Favours experimental
50
100
Favours control
114
Analysis 3.5. Comparison 3 Acupuncture versus wait-list, Outcome 5 Quality of life (SF-36 mental score)
intermediate term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
1698
3.1 (0.3)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
1753
4 (0.3)
-100
-50
Favours experimental
50
100
Favours control
Analysis 3.6. Comparison 3 Acupuncture versus wait-list, Outcome 6 Quality of life (SF-36 physical score)
intermediate term.
Review:
Study or subgroup
Treatment
N
Std.
Mean
Difference
Control
Mean(SD)
Mean(SD)
1698
5 (0.2)
Std.
Mean
Difference
IV,Random,95% CI
IV,Random,95% CI
1753
5.6 (0.2)
-100
-50
Favours experimental
50
100
Favours control
115
APPENDICES
Appendix 1. Computerised search strategy
CENTRAL-OVID
August 25, 2015
1. Neck Pain/
2. exp Brachial Plexus Neuropathies/
3. exp neck injuries/ or exp whiplash injuries/
4. cervical pain.mp.
5. neckache.mp.
6. whiplash.mp.
7. cervicodynia.mp.
8. cervicalgia.mp.
9. brachialgia.mp.
10. brachial neuritis.mp.
11. brachial neuralgia.mp.
12. neck pain.mp.
13. neck injur*.mp.
14. brachial plexus neuropath*.mp.
15. brachial plexus neuritis.mp.
16. thoracic outlet syndrome/ or cervical rib syndrome/
17. Torticollis/
18. exp brachial plexus neuropathies/ or exp brachial plexus neuritis/
19. cervico brachial neuralgia.ti,ab.
20. cervicobrachial neuralgia.ti,ab.
21. (monoradicul* or monoradicl*).tw.
22. or/1-21
23. exp headache/ and cervic*.tw.
24. exp genital diseases, female/
25. genital disease*.mp.
26. or/24-25
27. 23 not 26
28. 22 or 27
29. neck/
30. neck muscles/
31. exp cervical plexus/
32. exp cervical vertebrae/
33. atlanto-axial joint/
34. atlanto-occipital joint/
35. Cervical Atlas/
36. spinal nerve roots/
37. exp brachial plexus/
38. (odontoid* or cervical or occip* or atlant*).tw.
39. axis/ or odontoid process/
40. Thoracic Vertebrae/
41. cervical vertebrae.mp.
42. cervical plexus.mp.
43. cervical spine.mp.
44. (neck adj3 muscles).mp.
45. (brachial adj3 plexus).mp.
Acupuncture for neck disorders (Review)
Copyright 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
116
117
118
MEDLINE-OVID
August 25, 2015
1. Neck Pain/
2. exp Brachial Plexus Neuropathies/
3. exp neck injuries/ or exp whiplash injuries/
4. cervical pain.mp.
5. neckache.mp.
6. whiplash.mp.
7. cervicodynia.mp.
8. cervicalgia.mp.
9. brachialgia.mp.
Acupuncture for neck disorders (Review)
Copyright 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
119
120
62. pain.mp.
63. ache.mp.
64. sore.mp.
65. stiff.mp.
66. discomfort.mp.
67. injur*.mp.
68. neuropath*.mp.
69. or/60-68
70. 59 and 69
71. Radiculopathy/
72. exp temporomandibular joint disorders/ or exp temporomandibular joint dysfunction syndrome/
73. myofascial pain syndromes/
74. exp Sprains and Strains/
75. exp Spinal Osteophytosis/
76. exp Neuritis/
77. Polyradiculopathy/
78. exp Arthritis/
79. Fibromyalgia/
80. spondylitis/ or discitis/
81. spondylosis/ or spondylolysis/ or spondylolisthesis/
82. radiculopathy.mp.
83. radiculitis.mp.
84. temporomandibular.mp.
85. myofascial pain syndrome*.mp.
86. thoracic outlet syndrome*.mp.
87. spinal osteophytosis.mp.
88. neuritis.mp.
89. spondylosis.mp.
90. spondylitis.mp.
91. spondylolisthesis.mp.
92. or/71-91
93. 59 and 92
94. exp neck/
95. exp cervical vertebrae/
96. Thoracic Vertebrae/
97. neck.mp.
98. (thoracic adj3 vertebrae).mp.
99. cervical.mp.
100. cervico*.mp.
101. 99 or 100
102. exp genital diseases, female/
103. genital disease*.mp.
104. exp *Uterus/
105. or/102-104
106. 101 not 105
107. (thoracic adj3 spine).mp.
108. cervical spine.mp.
109. 94 or 95 or 96 or 97 or 98 or 106 or 107 or 108
110. Intervertebral Disk/
111. (disc or discs).mp.
112. (disk or disks).mp.
113. 110 or 111 or 112
114. 109 and 113
Acupuncture for neck disorders (Review)
Copyright 2016 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
121
115. herniat*.mp.
116. slipped.mp.
117. prolapse*.mp.
118. displace*.mp.
119. degenerat*.mp.
120. (bulge or bulged or bulging).mp.
121. 115 or 116 or 117 or 118 or 119 or 120
122. 114 and 121
123. intervertebral disk degeneration/ or intervertebral disk displacement/
124. intervertebral disk displacement.mp.
125. intervertebral disc displacement.mp.
126. intervertebral disk degeneration.mp.
127. intervertebral disc degeneration.mp.
128. 123 or 124 or 125 or 126 or 127
129. 109 and 128
130. 28 or 70 or 93 or 122 or 129
131. animals/ not (animals/ and humans/)
132. 130 not 131
133. exp *neoplasms/
134. exp *wounds, penetrating/
135. 133 or 134
136. 132 not 135
137. Neck Pain/rh, th [Rehabilitation, Therapy]
138. exp Brachial Plexus Neuropathies/rh, th
139. exp neck injuries/rh, th or exp whiplash injuries/rh, th
140. thoracic outlet syndrome/rh, th or cervical rib syndrome/rh, th
141. Torticollis/rh, th
142. exp brachial plexus neuropathies/rh, th or exp brachial plexus neuritis/rh, th
143. or/137-142
144. Radiculopathy/rh, th
145. exp temporomandibular joint disorders/rh, th or exp temporomandibular joint dysfunction syndrome/rh, th
146. myofascial pain syndromes/rh, th
147. exp Sprains and Strains/rh, th
148. exp Spinal Osteophytosis/rh, th
149. exp Neuritis/rh, th
150. Polyradiculopathy/rh, th
151. exp Arthritis/rh, th
152. Fibromyalgia/rh, th
153. spondylitis/rh, th or discitis/rh, th
154. spondylosis/rh, th or spondylolysis/rh, th or spondylolisthesis/rh, th
155. or/144-154
156. 59 and 155
157. acupuncture/ or chiropractic/
158. exp Musculoskeletal Manipulations/
159. massage.tw.
160. mobili?ation.tw.
161. Acupuncture Therapy/
162. (acupuncture or acu-puncture or needling or acupressure or mox?bustion).tw.
163. ((neck or spine or spinal or cervical or chiropractic* or musculoskeletal* or musculo-skeletal*) adj3 (adjust* or manipulat* or
mobiliz* or mobilis*)).tw.
164. (manual adj therap*).tw.
165. (manipulati* adj (therap* or medicine)).tw.
166. (massag* or reflexolog* or rolfing or zone therap*).tw.
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167. Nimmo.mp.
168. exp Vibration/tu [Therapeutic Use]
169. (vibration adj5 (therap* or treatment*)).tw.
170. (Chih Ya or Shiatsu or Shiatzu or Zhi Ya).tw.
171. (flexion adj2 distraction*).tw.
172. (myofascial adj3 (release or therap*)).tw.
173. muscle energy technique*.tw.
174. trigger point.tw.
175. proprioceptive Neuromuscular Facilitation*.tw.
176. cyriax friction.tw.
177. (lomilomi or lomi-lomi or trager).tw.
178. aston patterning.tw.
179. (strain adj counterstrain).tw.
180. (craniosacral therap* or cranio-sacral therap*).tw.
181. (amma or ammo or effleuurage or petrissage or hacking or tapotment).tw.
182. Complementary Therapies/
183. ((complement* or alternat* or osteopthic*) adj (therap* or medicine)).tw.
184. (Tui Na or Tuina).tw.
185. or/157-184
186. 136 and 185
187. 143 or 156 or 186
188. animals/ not (animals/ and humans/)
189. 187 not 188
190. exp randomized controlled trials as topic/
191. randomized controlled trial.pt.
192. controlled clinical trial.pt.
193. (random* or sham or placebo*).tw.
194. placebos/
195. random allocation/
196. single blind method/
197. double blind method/
198. ((singl* or doubl* or trebl* or tripl*) adj25 (blind* or dumm* or mask*)).ti,ab.
199. (rct or rcts).tw.
200. (control* adj2 (study or studies or trial*)).tw.
201. or/190-200
202. 189 and 201
EMBASE-OVID
August 25, 2015
1. neck pain/
2. brachial plexus neuropathy/
3. neck injury/ or whiplash injury/
4. cervical pain.mp.
5. neckache.mp.
6. whiplash.mp.
7. cervicodynia.mp.
8. cervicalgia.mp.
9. brachialgia/
10. brachialgia.mp.
11. brachial neuritis.mp.
12. brachial neuralgia.mp.
13. neck pain.mp.
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124
67. injur*.mp.
68. neuropath*.mp.
69. or/60-68
70. radiculopathy/
71. temporomandibular joint disorder/
72. myofascial pain/
73. spondylosis/ or cervical spondylosis/
74. neuritis/
75. exp arthritis/
76. fibromyalgia/
77. exp spondylitis/
78. diskitis/
79. spondylolisthesis/
80. radiculopathy.mp.
81. radiculitis.mp.
82. temporomandibular.mp.
83. myofascial pain syndrome*.mp.
84. spinal osteophytosis.mp.
85. neuritis.mp.
86. spondylosis.mp.
87. spondylitis.mp.
88. spondylolisthesis.mp.
89. or/70-88
90. 59 and 89
91. neck/
92. cervical spine/
93. neck.mp.
94. (thoracic adj3 vertebra?).mp.
95. cervical.mp.
96. cervico*.mp.
97. exp gynecologic disease/
98. genital disease*.mp.
99. exp *uterine cervix/
100. or/97-99
101. 95 or 96
102. 101 not 100
103. (thoracic adj3 spine).mp.
104. cervical spine.mp.
105. 91 or 92 or 93 or 94 or 102 or 103 or 104
106. intervertebral disk/
107. (disc or discs).mp.
108. (disk or disks).mp.
109. 106 or 107 or 108
110. 105 and 109
111. herniat*.mp.
112. slipped.mp.
113. prolapse*.mp.
114. displace*.mp.
115. degenerat*.mp.
116. (bulge or bulged or bulging).mp.
117. 110 or 111 or 112 or 113 or 114 or 115 or 116
118. 110 and 117
119. intervertebral disk hernia/
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MANTIS-OVID
November 2013 (last available access)
1 neck pain.mp. [mp=title, abstract, descriptors]
2 brachial plexus neuropathies.mp. [mp=title, abstract, descriptors]
3 neck injuries.mp. [mp=title, abstract, descriptors]
4 cervical pain.mp. [mp=title, abstract, descriptors]
5 neckache.mp. [mp=title, abstract, descriptors]
6 whiplash.mp. [mp=title, abstract, descriptors]
7 cervicodynia.mp. [mp=title, abstract, descriptors]
8 cervicalgia.mp. [mp=title, abstract, descriptors]
9 brachialgia.mp. [mp=title, abstract, descriptors]
10 brachial neuritis.mp. [mp=title, abstract, descriptors]
11 brachial neuralgia.mp. [mp=title, abstract, descriptors]
12 brachial plexus neuropath*.mp. [mp=title, abstract, descriptors]
13 brachial plexus neuritis.mp. [mp=title, abstract, descriptors]
14 (thoracic outlet syndrome or cervical rib syndrome).mp. [mp=title, abstract, descriptors]
15 torticollis.mp. [mp=title, abstract, descriptors]
16 cervico brachial neuralgia.mp. [mp=title, abstract, descriptors]
17 (monoradicul* or monoradicl*).tw.
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18 or/1-17
19 headache.mp. and cervic*.tw. [mp=title, abstract, descriptors]
20 genital diseases, female.mp. [mp=title, abstract, descriptors]
21 genital disease*.mp. [mp=title, abstract, descriptors]
22 or/20-21
23 19 not 22
24 18 or 23
25 neck.mp. [mp=title, abstract, descriptors]
26 neck muscles.mp. [mp=title, abstract, descriptors]
27 cervical plexus.mp. [mp=title, abstract, descriptors]
28 cervical vertebrae.mp. [mp=title, abstract, descriptors]
29 atlanto-axial joint.mp. [mp=title, abstract, descriptors]
30 atlanto-occipital joint.mp. [mp=title, abstract, descriptors]
31 cervical atlas.mp. [mp=title, abstract, descriptors]
32 spinal nerve roots.mp. [mp=title, abstract, descriptors]
33 brachial plexus.mp. [mp=title, abstract, descriptors]
34 (odontoid* or cervical or occip* or atlant*).tw.
35 (axis or odontoid process).mp. [mp=title, abstract, descriptors]
36 thoracic vertebrae.mp. [mp=title, abstract, descriptors]
37 cervical vertebrae.mp. [mp=title, abstract, descriptors]
38 cervical plexus.mp. [mp=title, abstract, descriptors]
39 cervical spine.mp. [mp=title, abstract, descriptors]
40 (neck adj3 muscles).mp. [mp=title, abstract, descriptors]
41 (brachial adj3 plexus).mp. [mp=title, abstract, descriptors]
42 (thoracic adj3 vertebrae).mp. [mp=title, abstract, descriptors]
43 (thoracic adj3 spine).mp. [mp=title, abstract, descriptors]
44 (thoracic adj3 outlet).mp. [mp=title, abstract, descriptors]
45 trapezius.mp. [mp=title, abstract, descriptors]
46 cervical.mp. [mp=title, abstract, descriptors]
47 cervico*.mp. [mp=title, abstract, descriptors]
48 46 or 47
49 genital diseases, female.mp. [mp=title, abstract, descriptors]
50 genital disease*.mp. [mp=title, abstract, descriptors]
51 uterus.mp. [mp=title, abstract, descriptors]
52 49 or 50 or 51
53 48 not 52
54 25 or 26 or 27 or 28 or 29 or 30 or 31 or 32 or 33 or 34 or 35 or 36
or 37 or 38 or 39 or 40 or 41 or 42 or 43 or 44 or 45 or 53
55 pain.mp. [mp=title, abstract, descriptors]
56 injuries.mp. [mp=title, abstract, descriptors]
57 ache.mp. [mp=title, abstract, descriptors]
58 sore.mp. [mp=title, abstract, descriptors]
59 stiff.mp. [mp=title, abstract, descriptors]
60 discomfort.mp. [mp=title, abstract, descriptors]
61 injur*.mp. [mp=title, abstract, descriptors]
62 neuropath*.mp. [mp=title, abstract, descriptors]
63 or/55-62
64 54 and 63
65 radiculopathy.mp. [mp=title, abstract, descriptors]
66 (temporomandibular joint disorders or temporomandibular joint dysfunction syndrome).mp. [mp=title, abstract, descriptors]
67 myofascial pain syndromes.mp. [mp=title, abstract, descriptors]
68 sprains and strains.mp. [mp=title, abstract, descriptors]
69 spinal osteophytosis.mp. [mp=title, abstract, descriptors]
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129
130
CINAHL-EBSCO
August 2015
S151 S90 or S104 or S150
S150 S82 and S149
S149 S105 or S106 or S107 or S108 or S109 or S110 or S111 or S112 or S113 or S114 or S115 or S116 or S117 or S118 or S119 or
S120 or S121 or S122 or S123 or S124 or S125 or S126 or S127 or S128 or S129 or S130 or S131 or S132 or S133 or S134 or S135
or S136 or S137 or S138 or S139 or S140 or S141 or S142 or S143 or S144 or S145 or S146 or S147 or S148
S148 TX faradic
S147 MH biofeedback
S146 TX Relaxation Therapy
S145 MH Relaxation Therapy
S144 TX alexander N3 technique OR TX alexander N3 method
S143 TX Feldenkrais
S142 TX postur* correction
S141 MH ice
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S140 TX Cryoanesthesia
S139 MH Cryoanesthesia
S138 TX vapocoolant spray
S137 (MH Hyperthermia, Induced)
S136 MH Hydrotherapy
S135 MH cryotherapy
S134 TX repetitive magnetic stimulation
S133 (MH Physical Therapy+)
S132 (MH Physical Therapy Modalities+)
S131 MH lasers
S130 (MH Phototherapy+)
S129 MH Ultrasonic Therapy
S128 (MH Rehabilitation+)
S127 TX Laser Therapy
S126 (MH Laser Therapy)
S125 TX traction
S124 MH traction
S123 TX pillow* OR TX collar*
S122 Occlusal Splints
S121 TX oral splints
S120 (MH Periodontal Splints)
S119 TX taping
S118 TX kinesiotaping
S117 (MH Orthoses)
S116 (MH Electric Stimulation)
S115 (MH Magnet Therapy)
S114 MH electromagnetics
S113 (MH Electromagnetic Fields)
S112 pulsed electromagnetic field
S111 TX pulsed electro magnetic field
S110 (MH Electrical Stimulation, Functional) OR (MH Electrical Stimulation, Neuromuscular)
S109 (MH Therapeutic Exercise+)
S108 (MH Exertion)
S107 (MH Exercise+)
S106 (MH Exercise+)
S105 (MH Combined Modality Therapy+)
S104 S34 and S103
S103 S91 or S92 or S93 or S94 or S95 or S96 or S97 or S98 or S99 or S100 or S101 or S102
S102 (MH Spondylolisthesis/RH)
S101 (MH Spondylolysis/RH) OR (MH Spondylosis/RH)
S100 (MH Spondylitis, Ankylosing/RH)
S99 (MH Fibromyalgia/RH)
S98 (MH Arthritis+/RH)
S97 (MH Polyradiculopathy/RH)
S96 (MH Neuritis/RH)
S95 (MH Spinal Osteophytosis/RH)
S94 (MH Sprains and Strains/RH)
S93 (MH Myofascial Pain Syndromes/RH)
S92 (MH Temporomandibular Joint Syndrome/RH) OR (MH Temporomandibular Joint Diseases/RH)
S91 (MH Radiculopathy/RH)
S90 S83 or S84 or S85 or S86 or S87 or S88 or S89
S89 (MH Brachial Plexus Neuritis/RH)
S88 (MH Torticollis/RH)
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ICL
August 2015
S1 Subject:Neck Pain OR Subject:Brachial Plexus Neuritis OR All Fields:brachial plexus neuropathies
S2 All Fields:brachial plexus neuropathy
S4 Subject:Neck Injuries OR Subject:Whiplash Injuries OR Subject:Cervical Vertebrae / abnormalities
S5 All Fields:cervical pain OR All Fields:neckache OR All Fields:whiplash
S6 All Fields:cervicodynia OR All Fields:cervicalgia OR All Fields:brachialgia
S7 All Fields:brachial neuritis OR All Fields:brachial neuralgia OR All Fields:neck pain
S8 Subject:Thoracic Outlet Syndrome OR Subject:Torticollis OR All Fields:cervical rib syndrom*
S11 All Fields:cerv* AND All Fields:headache*
S12 All Fields:monoradicul* OR All Fields:monoradicl*
S13 S1 OR S2 OR S4 OR S5 OR S6 OR S7 OR S8 OR S11 OR S12
S14 Subject:Neck OR Subject:Neck Muscles OR Subject:Cervical Vertebrae
S16 Subject:Cervical Atlas OR Subject:Atlanto-Axial Joint OR Subject:Atlanto-Occipital Joint
S17 Subject:Atlas OR Subject:Spinal Nerve Roots OR All Fields:brachial plexus
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Selection bias (biased allocation to interventions) due to inadequate generation of a randomised sequence
Risk of selection bias is low if investigators describe a random component in the sequence generation process such as referring to a
random number table, using a computer random number generator, tossing a coin, shuffling cards or envelopes, throwing dice, drawing
lots and minimising (minimisation may be implemented without a random element, and this is considered to be equivalent to being
random).
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Risk of selection bias is high if investigators describe a non-random component in the sequence generation process such as sequence
generated by odd or even date of birth, date (or day) of admission, hospital or clinic record number; or allocation by judgement of the
clinician, preference of the participant, results of a laboratory test or series of tests, or availability of the intervention.
Selection bias (biased allocation to interventions) due to inadequate concealment of allocations before assignment
Risk of selection bias is low if participants and investigators enrolling participants could not foresee assignment because one of the
following, or an equivalent method, was used to conceal allocation: central allocation (including telephone, web-based and pharmacycontrolled randomisation); sequentially numbered drug containers of identical appearance; or sequentially numbered, opaque, sealed
envelopes.
Risk of bias is high if participants or investigators enrolling participants could possibly foresee assignments and thus introduce selection
bias, such as allocation based on using an open random allocation schedule (e.g. list of random numbers); assignment envelopes were
used without appropriate safeguards (e.g. if envelopes were unsealed or non-opaque or not sequentially numbered); alternation or
rotation; date of birth; case record number; or other explicitly unconcealed procedures.
Blinding of participants
Performance bias due to knowledge of allocated interventions by participants during the study
Risk of performance bias is low if blinding of participants was ensured and it was unlikely that blinding could have been broken; or if
no blinding or incomplete blinding was provided but the review authors judged that the outcome is not likely to be influenced by lack
of blinding.
Performance bias due to knowledge of allocated interventions by personnel/care providers during the study
Risk of performance bias is low if blinding of personnel was ensured and it was unlikely that blinding could have been broken; or if no
blinding or incomplete blinding was provided but the review authors judged that the outcome is not likely to be influenced by lack of
blinding.
Risk of detection bias is low if blinding of the outcome assessment was ensured and it was unlikely that blinding could have been
broken; or if no blinding or incomplete blinding was provided but the review authors judged that the outcome is not likely to be
influenced by lack of blinding, or:
for patient-reported outcomes in which the participant was the outcome assessor (e.g. pain, disability): Risk of bias for outcome
assessors is low if risk of bias for participant blinding is low (Boutron 2005);
for outcome criteria that are clinical or therapeutic events that will be determined by the interaction between participants and
care providers (e.g. co-interventions, length of hospitalisation, treatment failure), in which the care provider is the outcome assessor:
Risk of bias for outcome assessors is low if risk of bias for care providers is low (Boutron 2005); and
for outcome criteria that are assessed from data from medical forms: Risk of bias is low if the treatment or adverse effects of the
treatment could not be noticed in the extracted data (Boutron 2005).
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Risk of attrition bias is low if no outcome data were missing; reasons for missing outcome data were unlikely to be related to the
true outcome (for survival data, censoring is unlikely to be introducing bias); missing outcome data were balanced in numbers, with
similar reasons for missing data across groups; for dichotomous outcome data, the proportion of missing outcomes compared with the
observed event risk was not enough to have a clinically relevant impact on the intervention effect estimate; for continuous outcome
data, the plausible effect size (difference in means or standardised difference in means) among missing outcomes was not enough to have
a clinically relevant impact on observed effect size, or missing data were imputed using appropriate methods (if drop-outs were very
large, imputation using even acceptable methods may still suggest high risk of bias) (van Tulder 2003). The percentage of withdrawals
and drop-outs should not exceed 20% for short-term follow-up and 30% for long-term follow-up and should not lead to substantial
bias (these percentages are commonly used but arbitrary and are not supported by the literature) (van Tulder 2003).
Risk of reporting bias is low if the study protocol is available and all of the studys pre-specified (primary and secondary) outcomes of
interest in the review have been reported in the pre-specified way, or if the study protocol is not available but it is clear that published
reports include all expected outcomes, including those that were pre-specified (convincing text of this nature may be uncommon).
Risk of reporting bias is high if not all of the studys pre-specified primary outcomes have been reported; one or more primary outcomes
were reported using measurements, analysis methods or subsets of the data (e.g. subscales) that were not pre-specified; one or more
reported primary outcomes were not pre-specified (unless clear justification for their reporting is provided, such as an unexpected
adverse effect); one or more outcomes of interest in the review were reported incompletely so that they cannot be entered into a metaanalysis; or the study report fails to include results for a key outcome that would be expected to have been reported for such a study.
Risk of bias is low if no co-interventions were provided, or if they were similar between index and control groups (van Tulder 2003).
Risk of bias is low if compliance with the interventions was acceptable and was based on reported intensity/dosage, duration, number
and frequency for both index and control intervention(s). For single-session interventions (e.g. surgery), this item is irrelevant (van
Tulder 2003).
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Intention-to-treat analysis
Risk of bias is low if all randomised participants were reported/analysed in the group to which they were allocated by randomisation.
Timing of outcome assessments (detection bias)
Bias because important outcomes were not measured at the same time across groups
Risk of bias is low if all important outcome assessments for all intervention groups were measured at the same time (van Tulder 2003).
Other bias
Risk of bias is low if the study appears to be free of other sources of bias not addressed elsewhere (e.g. study funding).
WHATS NEW
Last assessed as up-to-date: 25 August 2015.
Date
Event
Description
31 December 2015
The previous version of this review included 10 studies that focused on chronic neck pain. In this review,
we included 27 studies representing acupuncture for a
variety of acute and chronic neck disorders
31 December 2015
138
HISTORY
Protocol first published: Issue 3, 2004
Review first published: Issue 3, 2006
Date
Event
Description
22 May 2014
Amended
19 June 2008
Amended
CONTRIBUTIONS OF AUTHORS
Primary reviewers for this review - Trinh K, Graham N, Irnich D, Cameron ID, Forget M.
Statistician - Trinh K, Goldsmith CH (Cervical Overview Group - COG).
Methodological quality assessment - COG Validity Team; Burnie S, Empey B, Forget M, Goldsmith CH, Graham N, LeBlanc F, Szeto
G.
Study identification and selection - Brunarski D, Graham N, Gross A, Haines T (COG).
Research librarian - Rice M.
Data abstraction, synthesis, manuscript preparation, public responsibility, grants, administration - primary review authors.
Final synthesis - primary review authors.
DECLARATIONS OF INTEREST
D Irnich is an author of two included studies. He did not take part in data extraction.
Use of raters from diverse professional backgrounds (sports medicine physician, rheumatologist, occupational health physician, physiatrist, statistician, physiotherapist, manual therapist, chiropractor, massage therapist) should serve to limit any conflicts of interest that
might have been present during the review process.
SOURCES OF SUPPORT
Internal sources
No sources of support supplied
139
External sources
Candian Institute of Health Research, Canada.
Knowledge Synthesis Grant Synthesizing Research Evidence into Clinical Recommendations for Managing Neck Pain
INDEX TERMS
Medical Subject Headings (MeSH)
Acupuncture
Therapy; Chronic Disease; Neck Pain [ therapy]; Randomized Controlled Trials as Topic; Treatment Outcome
140