| Literature DB >> 30886746 |
Cathy Tuckey1, Susan Kohut2, Dale W Edgar1,3,4,5.
Abstract
INTRODUCTION: Anecdotally, acupuncture is used in the treatment of scar tissue in order to improve scar quality and reduce symptoms of pain and pruritus. Unlike conditions such as lower back pain, knee osteoarthritis and migraines, there are no systematic reviews to confirm treatment efficacy. This systematic literature review aims to assess the current level of evidence for the use of acupuncture for treating abnormal scars such as hypertrophic or other symptomatic scars.Entities:
Keywords: Acupuncture; burns; dry needling; hypertrophic scar; neurogenic inflammation; pruritus
Year: 2019 PMID: 30886746 PMCID: PMC6415480 DOI: 10.1177/2059513119831911
Source DB: PubMed Journal: Scars Burn Heal ISSN: 2059-5131
Figure 1.Search Results
Clinical trial details: Part A.
| Study design | Type of scar | Type of control | Participants (n) | Type of treatment | Needle location | |
|---|---|---|---|---|---|---|
| Cuignet et al. (2015)[ | Cohort | HTS – burn | N/A | 32 | MA + EA | EA on extremity points of shared meridian and inner bladder line of nerve root supplying meridian of the scar. MA to TCM acupoints including some/all of: SP6, 9, 10, ST40, LI4, 11, BL13, 17 |
| Huang et al. (1999)[ | Clinical trial | HTS – burn | Usual care | 30 (?+30 control) | MA | 3 main TCM points (SP10, ST36 and LI11), unclear whether local needles were also used |
| Kotani et al. (2001)[ | Clinical trial | Abdominal surgery | Sham | 70 | Indwelling | Local tender points along scar |
| Loskotova and Loskotova (2017)[ | Retrospective | Acute burns | Usual care | 1008 total individuals over 32 years; comparison made for 198 with acu and 63 without acu | MA | TCM acupoints bilaterally, with combination of: LI4, LI11 and LU7 depending on access to unburnt skin |
| Song et al. (2011)[ | Clinical trial | HTS –burn | Ultrasound and Scareducer ointment | 80 | MA | Local around scar |
HTS, hypertrophic scar; MA, manual acupuncture; EA, electroacupuncture; TCM, traditional Chinese medicine; VAS, visual analogue scale; QST, quantitative sensory testing; OCSI, Oregon CONSORT STRICTA Instrument; N/A, not available.
Clinical trial details: Part B.
| Frequency of treatment | Outcome measures | Results | Statistical analysis | OCSI score (%) | Risk of bias | |
|---|---|---|---|---|---|---|
| Cuignet et al. (2015)[ | 30 min, 1× week, duration 3 weeks | VAS pain and itch, QST | 4/10–1/10 decrease in itch for all participants; responders had decreased pain by 4 points, non-responders had no change in pain scores; QST revealed difference between responders and non-responders | Adequate use of statistical analysis, including use of | 28 | High risk of performance and detection bias |
| Huang et al. (1999)[ | Unclear, differed between participants | Unvalidated TCM diagnostic scale | Significant improvement in itch for all participants | Use of | 34 | High risk of selection, performance and detection bias |
| Kotani et al. (2001)[ | 4 weeks, 20 sessions of 24 h indwelling needles in situ | VAS pain, QST | 70% of participants in treatment group had good to excellent outcomes | Adequate statistical analysis including correlations and | 50 | Low risk of selection or detection bias; high risk of performance bias |
| Loskotova and Loskotova (2017)[ | Daily, 30 min; unclear number of sessions | Unclear, qualitative appearance of burn, colour and presence of HTS | Applying acupuncture within 48 h resulted in complete healing without HTS in 6 weeks | Some use of statistical analysis ( | 13 | Risk of detection and reporting bias |
| Song et al. (2011)[ | 30 min, ×10 days, 7-day break, ×4 | Unvalidated 3-point scale – measuring pain, itch and scar pliability | Total effective rate was 93.9% for the treatment group and 77.8% for the control group after 1 year | Unvalidated outcome measures, basic statistical analysis including | 26 | High risk of selection, performance and detection bias |
HTS, hypertrophic scar; MA, manual acupuncture; EA, electroacupuncture; TCM, traditional Chinese medicine; VAS, visual analogue scale; QST, quantitative sensory testing; OCSI, Oregon CONSORT STRICTA Instrument.
Case report details.
| Type of scar | Needle location | Treatments (n) | Outcomes | Quality rating (JBI checklist) | |
|---|---|---|---|---|---|
| Anderson (2014)[ | Dupuytrens contracture surgery | Local plus LI4 and HT7 | 7 treatments over 3 months | Improved joint ROM, colour and numbness of skin | 6/8 |
| Fang | Post-surgical on thigh | Local and distant – TCM diagnosis | 8 treatments over 5 weeks | Pain decreased from 7/10 to 1–2/10 | 6/8 |
| Hunter (2011)[ | Post-surgical on wrist | Local only | 9 treatments over 4 months | Symptom-free, flatter | 2/8 |
| McCowen (2006)[ | Burns on hand | Local with EA | Unclear, could be just one | Improved joint ROM, and appearance of scar, decreased pain | 1/8 |
| Stephenson (2002)[ | Post-surgical upper limb scars | Local and distant – LI4 and TE5 for pain, or spleen points for swelling | 5–16 treatments over 5–8 weeks | Reduced pain and itch on VAS, 75% cases had reduced scar tightness, 75% had improved scar appearance, improved function by 12–81% via DASH score | 5/8 |
TCM, traditional Chinese medicine; EA, electroacupuncture; ROM, range of motion; VAS, visual analogue scale; DASH, Disabilities of the Arm, Shoulder and Hand.
Recommended Research Intervention Protocol – comparing local versus distant needle placement.
| Study parameters | Recommendation |
|---|---|
| Age of scar | Six weeks to one year |
| Needle location | Local around the scar (same dermatome), compared with distant (no shared neuroanatomy to scar) |
| Needles (n) | To be calculated based on scar size/circumference to ensure equal stimulation between groups |
| Needle stimulation | Bi-directional rotation as per Langevin[ |
| Treatment duration | Acupuncture needles may be retained anywhere from 30 s to 30 min or more (i.e. indwelling)[ |
| Treatments (n) | Six treatments over four weeks |
| Outcome measures | Must be validated tools such as VAS and POSAS and include Quality of Life measures, i.e. SF-36 |
Reporting must follow STRICTA and CONSORT guidelines.