| Literature DB >> 36091598 |
Boram Lee1, Chan-Young Kwon2, Man Young Park3.
Abstract
Background: Chronic rhinosinusitis (CRS) is a highly prevalent disease associated with poor quality of life. In this paper, we appraised the role of acupuncture in the treatment of CRS.Entities:
Year: 2022 PMID: 36091598 PMCID: PMC9451955 DOI: 10.1155/2022/6429836
Source DB: PubMed Journal: Evid Based Complement Alternat Med ISSN: 1741-427X Impact factor: 2.650
Figure 1A PRISMA flow diagram of the literature screening and selection processes.
General characteristics of the included studies.
| Study ID | Sample size (A) : (B) (enrolled ⟶ analyzed) | Mean age (range) (yr) | CRS disease period | CRS diagnosis | Population | (A) Treatment intervention | (B) Control intervention | Outcome |
|---|---|---|---|---|---|---|---|---|
| Chen [ | 57 (27 : 30)⟶53 (24 : 29) | (A) 46.33 ± 15.871 | Not reported | Not reported | Clear pain in the nose, forehead, and head within 48 hr after FESS (VAS 4–7) | Manual acupuncture | Ibuprofen sustained-release capsule | (1) VAS (0–10) |
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| Chen et al. [ | 70 (35 : 35) ⟶ 70 (35 : 35) | (A) 42.18 ± 5.30 (20–57) | Not reported | Not reported | CRS, population after FESS | Transcutaneous electrical acupoint stimulation + (B) | Routine perioperative nursing | (1) VAS (0–10) |
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| Guo et al. [ | 120 (60 : 60) ⟶ 120 (60 : 60) | (A) 22–61 | >12 wk | Clinical symptom, nasal endoscopy, and/or sinus CT | CRS, excluded population with nasal polyps | Moxibustion | Budesonide nasal spray, roxithromycin tablets | (1) TER |
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| He et al. [ | 72 (36 : 36) ⟶ 65 (32 : 33) | (A) 38.23 ± 1.32 (26–71) | >12 wk (A) 13.64 ± 2.01 yr (1–26) | Clinical symptom, nasal endoscopy, and/or sinus CT | CRS | Electroacupuncture + (B) | Amoxicillin capsule, topical furosemide nasal drops | (1) TER |
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| Huang et al. [ | 687 (367 : 320) ⟶ 687 (367 : 320) | (A) 16–80 | (A) 6 mo–25 yr | Clinical symptom, nasal endoscopy, and sinus CT or MRI | CRS, excluded population with indications for surgery | Moxibustion + roxithromycin | Budesonide nasal spray, roxithromycin tablets | (1) TER |
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| Li and Fu [ | 100 (50 : 50) ⟶ 100 (50 : 50) | (A) 48.79 ± 6.47 (20–70) | Not reported | Not reported | CRS | Manual acupuncture + (B) | 1% ephedrine saline into the turbinate, antibiotics | (1) TER |
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| Ma et al. [ | 100 (50 : 50) ⟶ 100 (50 : 50) | (A) 30.0 ± 11.6 | >3 mo | Clinical symptom, sinus radiology, and/or endoscopy | CRS | Manual acupuncture | Antibiotics (roxithromycin, penicillin, or cephalosporin), chlorpheniramine, furosemide nasal drops | (1) TER |
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| Rossberg et al. [ | 55 (25 : 19 : 21) ⟶ 39 (16 : 13 : 10) | (A) 41.1 ± 14.7 | >3 mo | Clinical symptom, and sinus CT | CRS, excluded population with nasal polyps and pansinusitis | Manual acupuncture | (B1) minimal acupuncture at non-acupoints | (1) Sinus soft tissue swelling as assessed by CT (mm) (change) |
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| Sun [ | 80 (40 : 40) ⟶ 80 (40 : 40) | (A) 37.5 ± 5.5 (19–60) | Not reported | Clinical symptom, nasal endoscopy, and/or sinus CT | CRS, population after FESS under local anesthesia | Manual acupuncture | Ibuprofen sustained-release capsule | (1) TER |
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| Zhang et al. [ | 120 (60 : 60) ⟶ 120 (60 : 60) | (A) 40 | Not reported | Clinical symptom, and sinus CT | CRS, conservative treatment is not effective and has no contraindications to FESS | Electroacupuncture + (B) | FESS under intravenous general anesthesia combined with endotracheal intubation | (1) Additional doses of propofol during operation (mg/kg) |
CRS: chronic rhinosinusitis; CT: computer tomography; FESS: functional endoscopic sinus surgery; MCS: mental component summary; PCS: physical component summary; SF-MPQ: the short-form McGill pain questionnaire; SF-36: the 36-item short-form survey; SNOT: sinonasal outcome test; TER: total effective rate; and VAS: visual analogue scale.
Details of acupuncture methods.
| Study ID | Style of acupuncture | Number of needles | Acupuncture points | Depth of insertion | Response sought | Needle stimulation | Retention time | Needle type | Number of treatment sessions | Frequency | Treatment duration | Follow-up period |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chen [ | Manual acupuncture | 13 | Bilateral LI20, BL2, EX-HN5, LI4, ST36, EX-HN3, GV20, GV24 | Not reported | Perform needle manipulation so that there is a sense of acupuncture | Needle manipulation every 10 min | 30 min | Disposal sterile acupuncture needle (Suzhou Tianxie acupuncture equipment Co., ltd.) | 1-2 | Once or twice a day (if there was no effect within 4 hours after the initial acupuncture, acupuncture was performed once more.) | 1 day | None |
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| Chen et al. [ | Transcutaneous electrical acupoint stimulation | Not applicable | Bilateral LI4, LI20 | Not applicable | Slight tingling sensation | 2/100 Hz, intensity 4 | 30 min | A low-frequency electronic pulse therapy device (Wuxi Jiajian medical instrument Co., ltd.) | 4 | 1, 13, 25, 37 hours after surgery | 37 hours | None |
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| Guo et al. [ | Moxibustion | Not applicable | Bilateral LI20, EX-HN3 | Not applicable | Feel the local skin warm and slightly hot without burning pain, and the local skin is slightly red without blistering | Not applicable | 30 min | Ginger-separated moxibustion | 14 | Once a day | 14 days | None |
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| He et al. [ | Electroacupuncture | 2 | ST7, SI18 (CRS affected side) | ST7: 45–60 mm | Deqi (soreness, numbness, heaviness or distension) | Not reported | 20 min | 0.3 mm × 75 mm filiform acupuncture needle | 10 | 5 times a week | 2 weeks | 1, 3 months |
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| Huang et al. [ | Moxibustion | Not applicable | EX-HN3, EX-HN8 (no data on side) | Not applicable | Feel the local skin warm and slightly hot without burning pain, and the local skin is slightly red without blistering | Not applicable | 30–40 min | Ginger-separated moxibustion | 14–70 | Once or twice a day | 14–70 days | None |
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| Li and Fu [ | Manual acupuncture | Not reported | LI20, EX-HN3, GV20, LI4, GB20, LU5, LU7 (no data on side) | LI20: 0.1–0.3 cun | Not reported | Needle manipulation every 5 min | 25 min | Not reported | 15 | Once a day | 15 days | None |
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| Ma et al. [ | Manual acupuncture | Not reported | ST7 (no data on side) | 2.5 cun | Deqi (soreness, numbness, heaviness or distension) | Strong twirling and trembling method | No retention | 3 cun filiform acupuncture needle | 6 | Once a week | 6 weeks | 6 months |
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| Rossberg et al. [ | Manual acupuncture | Not reported | According to the four TCM diagnosis-retention of damp in the yangming channel, damp combined with heat: (bilateral) LI4, LI11, ST40, ST44-retention of phlegm in the shaoyang channel, liver fire: (Bilateral) GB34, LR2, LI4, LR3 | Facial/hand/feet: 0.5 cun arms/legs/trunk: 1.3 cun | Deqi (soreness, numbness, heaviness or distension) | Stimulated manually using reducing or reinforcing methods | 25 min | 0.28 mm × 25–40 mm filiform acupuncture needle | 10 | Not reported | 4 weeks | 11 months |
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| Sun [ | Manual acupuncture | Not reported | LI20, BL2, EX-HN5, EX-HN3, GV20, GV24, LI4, ST36 (no data on side) | Not reported | Not reported | Needle manipulation every 10 min | 30 min | Not reported | Not reported | Once or twice a day (if there was no effect within 4 hours after the initial acupuncture, acupuncture was performed once more.) | Not reported | None |
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| Zhang et al. [ | Electroacupuncture | 4 | Bilateral LI4, PC6 | Not reported | Not reported | Wave of condensation and rarefaction, 2/100 Hz, 8–12 mA, neutral supplementation and draining methods | 30 min | Not reported | 1 | Once | 1 day | 6 hours |
Figure 2Risk-of-bias summary for all included studies. Low, unclear, and high risk, respectively, are represented by the following symbols: “+,” “?,” and “−.”
Figure 3Forest plot of total effective rate: acupuncture versus conventional treatment.
Figure 4Forest plot of visual analogue scale: acupuncture versus conventional treatment.
Summary of findings.
| Outcomes | Subgroup | No. of participants (RCTs) | Anticipated absolute effects (95% CI) | Relative effect (95% CI) |
| Quality of evidence (grade) | Comments | |
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| Risk with control group | Risk with treatment group | |||||||
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| TER | Total | 1040 (5) | 739 per 1000 | 865 per 1000 (776 to 961) | RR 1.17 (1.05, 1.30) | 59 | Moderate | Risk of bias (−1) |
| Manual acupuncture | 233 (3) | 815 per 1000 | 864 per 1000 (791 to 954) | RR 1.06 (0.97, 1.17) | 0 | Moderate | Risk of bias (−1) | |
| Moxibustion | 807 (2) | 716 per 1000 | 909 per 1000 (845 to 973) | RR 1.27 (1.18, 1.36) | 0 | Moderate | Risk of bias (−1) | |
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| VAS | Total | 253 (3) | — | MD 2.04 lower (2.1 to 1.98 lower) | — | 89 | Moderate | Risk of bias (−1) |
| Manual acupuncture | 133 (2) | — | MD 0.91 lower (1.48 to 0.34 lower) | — | 65 | Moderate | Risk of bias (−1) | |
| Moxibustion | 120 (1) | — | MD 2.05 lower (2.11 to 1.99 lower) | — | NA | Moderate | Risk of bias (−1) | |
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| SNOT-20 | Total (moxibustion) | 120 (1) | — | MD 3.48 lower (3.58 to 3.38 lower) | — | NA | Moderate | Risk of bias (−1) |
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| Lund-kennedy endoscopic score | Total (moxibustion) | 120 (1) | — | MD 1.25 lower (1.82 to 0.68 lower) | — | NA | Moderate | Risk of bias (−1) |
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| Lund-Mackay CT score | Total (moxibustion) | 120 (1) | — | MD 1.23 lower (1.8 to 0.66 lower) | — | NA | Moderate | Risk of bias (−1) |
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| Recurrence rate (after 6 months) | Total (manual acupuncture) | 65 (1) | 320 per 1000 | 176 per 1000 (74 to 422) | RR 0.55 (0.23, 1.32) | NA | Low | Risk of bias (−1) |
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| Adverse events | Total (manual acupuncture) | 53 (1) | 69 per 1000 | 41 per 1000 (4 to 432) | RR 0.60 (0.06, 6.26) | NA | Low | Risk of bias (−1) |
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| TER | Total | 165 (2) | 783 per 1000 | 979 per 1000 (869 to 1000) | RR 1.25 (1.11, 1.40) | 0 | Moderate | Risk of bias (−1) |
| Manual acupuncture | 100 (1) | 800 per 1000 | 984 per 1000 (848 to 1000) | RR 1.23 (1.06, 1.41) | NA | Low | Risk of bias (−1) | |
| Electroacupuncture | 65 (1) | 758 per 1000 | 970 per 1000 (788 to 1000) | RR 1.28 (1.04, 1.57) | NA | Low | Risk of bias (−1) | |
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| VAS | Total | 195 (2) | — | MD 1.07 lower (1.27 to 0.87 lower) | — | 98 | Moderate | Risk of bias (−1) |
| Electroacupuncture | 120 (1) | — | MD 0.19 higher (0.2 lower to 0.58 higher) | — | NA | Moderate | Risk of bias (−1) | |
| TEAS | 75 (1) | — | MD 1.50 lower (1.73 to 1.27 lower) | NA | Moderate | Risk of bias (−1) | ||
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| Adverse events | Total (electroacupuncture) | 65 (1) | 0 per 1000 | 0 per 1000 (0 to 0) | RR 3.09 (0.13, 73.19) | NA | Low | Risk of bias (−1) |
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| Adverse events | Total (manual acupuncture) | 42 (1) | 294 per 1000 | 441 per 1000 (185 to 1000) | RR 1.50 (0.63, 3.53) | NA | Low | Risk of bias (−1) |
CI: confidence interval; CT: computer tomography; MD: mean difference; NA: not applicable; RCT: randomized controlled trial; RR: risk ratio; SNOT: sinonasal outcome test; TEAS: transcutaneous electrical acupoint stimulation; TER: total effective rate; and VAS: visual analogue scale.