Abstract
Background: We aimed to critically evaluate the effectiveness and safety of acupuncture as an add-on therapy to conventional Western medication (WM) and assess the quality of evidence (QoE) of these findings.
Methods: A total of 12 English, Korean, and Chinese databases were searched on December 18, 2020. Randomized controlled trials (RCTs) assessing the effectiveness of acupuncture as an add-on therapy to conventional WM for functional dyspepsia (FD) were included. The primary outcome was the symptom score of FD. The risk of bias of the included studies and QoE were evaluated using the Cochrane Collaboration's risk of bias tool and Grading of Recommendations, Assessment, Development, and Evaluation method, respectively.
Results: A total of 22 RCTs were included. The total and individual FD symptom scores were significantly improved in the acupuncture combined with WM groups compared with the WM alone groups, except for in one study. The Nepean dyspepsia index score and total effective rate mostly improved significantly in the acupuncture group, regardless of the WM used and acupuncture type. FD-related biomarkers, such as ghrelin and gastrin levels, showed mixed results. The acupuncture group showed a significantly lower recurrence rate after 3–6 months of follow-up than the WM alone group. There were no differences in the incidence of adverse events between the two groups. The included studies generally had low methodological quality. The QoE for the main findings was generally very low to moderate.
Conclusion: Limited evidence suggests that acupuncture has the potential to improve FD treatment in combination with conventional WM. Furthermore, the methodological quality of the included studies and QoE of the main findings were generally low. Therefore, RCTs with a rigorous methodology, including sham acupuncture and multiethnic subjects, should be performed.
Systematic Review Registration: OSF registries [https://osf.io/mxren], PROSPERO [CRD42021226608].
Keywords: acupuncture, functional dyspepsia, dyspepsia, systematic review, meta-analysis
Introduction
Functional dyspepsia (FD) is a common functional gastrointestinal disorder. Its main symptoms include postprandial fullness, early satiation, epigastric pain, and epigastric burning, which are not fully explained by routine clinical evaluation (1). Generally, FD can be classified into postprandial distress syndrome (PDS) and epigastric pain syndrome (EPS) (1). Although the underlying pathology of FD is not fully understood, it is considered to be multifactorial. Moreover, upper gastrointestinal inflammation, gastric and duodenal disturbances, Helicobacter pylori infection, increased duodenal eosinophils, and psychological distress have been reported to be involved (2, 3). The prevalence of FD is reported at various levels around the world, ranging from 5 to 40%. Furthermore, based on the Rome III criteria, the prevalence rate has been reported as 9.8–20.2% in Western countries and 5.3–12.8% in Eastern countries (4). The main symptoms of FD are digestive and abdominal discomfort. While FD is not a life-threatening disease, it seriously impairs the quality of life (QoL) of patients and can be an economic and social burden (5, 6). Thus, FD poses serious public health problems at both individual and societal levels.
Conventional approaches to FD include proton pump inhibitors, Helicobacter pylori eradication treatment, antidepressants, and psychotherapy (3). However, interest in complementary and alternative medicine (CAM) approaches, such as herbal medicine or acupuncture, is increasing (7). For example, the Japanese Society of Gastroenterology's evidence-based clinical practice guidelines for FD published in 2015 recommend using herbal medicine along with anxiolytics and antidepressants as a second-line treatment (8). In addition, some researchers have suggested that acupuncture could be considered when constructing a comprehensive management strategy for FD, particularly for the management of EPS (9). The growing interest in CAM approaches for FD maybe because they are characterized as “holistic” approaches (7). In addition, the CAM approach is expected to play a role in complementing the limitations of conventional medicine in FD treatment (7). Therefore, if conventional medicine and CAM approaches are appropriately integrated, better treatment may be able to be provided to patients with FD. However, as many studies have pointed out, this process requires a careful, evidence-based approach (7).
Although several systematic reviews have already reported the effectiveness and safety of acupuncture (a typical non-pharmacological CAM treatment) for FD (10–13) a rigorous evaluation of the strength of evidence using the Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) has not been performed. This approach is essential for promoting the development of integrative medicine for FD in terms of evidence-based medicine (EBM) (8). Therefore, we aimed to comprehensively review randomized controlled trials (RCTs) of acupuncture as an add-on treatment to conventional Western medication (WM) for FD, critically evaluate the effectiveness and safety, and assess the quality of evidence (QoE). Through this, we expect to promote the development of integrative medicine for FD in terms of EBM and provide clinical evidence that is helpful in decision-making for clinicians, patients, and policymakers.
Materials and Methods
Protocol and Registration
The protocol of this study was published as a research paper (14) and we conducted this review accordingly. We registered our study with PROSPERO (registration number: CRD42021226608) and OSF registries (URL: https://osf.io/mxren). This study was reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2010 checklist (Supplementary File 1) (15).
Eligibility Criteria
Only RCTs evaluating the effectiveness and safety of acupuncture as an adjunctive therapy to conventional WM for FD were included without limitation of the publication status (not only studies published in journals but also gray literature such as theses and conference proceedings) or language. In the study design, we included only parallel-group studies. Only those diagnosed with FD based on standardized diagnostic criteria, such as Rome criteria or clinical symptoms, were included regardless of age, sex, or ethnicity. Studies involving patients with organic causes of dyspepsia were excluded. As treatment interventions, we included all types of acupuncture (manual acupuncture, electroacupuncture, auriculotherapy, and acupressure) as add-on therapies to conventional WM for FD, such as acid suppressants, prokinetics, Helicobacter pylori eradication, fundic relaxants, or antidepressants. For the control interventions, we included only conventional WM for FD.
The primary outcome of our study was the symptom score of FD, measured using such as the Nepean dyspepsia index (NDI) (16), gastrointestinal symptom rating scale (17), dyspepsia symptom severity index (18), and visual analog scale. The secondary outcome measures were (a) total effective rate (TER); (b) QoL measured by factors such as the FD-QoL (19) and the 36-item Short-Form Health Survey (SF-36) (20); (c) level of gut peptide hormones such as motilin, ghrelin, and gastrin; (d) incidence of adverse events during the treatment period; and (e) recurrence rate. Among them, TER is a non-validated outcome measure that is processed secondarily according to evaluation criteria such as the improvement rates of other quantified outcomes or clinical symptom improvement. Regarding the outcome, participants are generally classified as “cured,” “markedly improved,” “improved,” or “non-responder” after treatment. The following formula is generally used to calculate TER: N1 + N2 + N3/N, where N1, N2, and N3 are the number of cured, markedly improved, and improved patients, respectively, and N is the total sample size.
Information Sources and Search Strategy
The following 12 English, Korean, and Chinese electronic databases were searched from their inception to December 18, 2020, Medline (via PubMed), EMBASE (via Elsevier), the Cochrane Central Register of Controlled Trials, Allied and Complementary Medicine Database (via EBSCO), Cumulative Index to Nursing and Allied Health Literature (via EBSCO), Oriental Medicine Advanced Searching Integrated System, Korean studies Information Service System, Research Information Service System, Korean Medical Database, Korea Citation Index, China National Knowledge Infrastructure, and Wanfang data. We searched the reference lists of the included studies and trial registries, such as clinicaltrials.gov, to include all possible relevant literature. In addition, we set the search strategy as comprehensively as possible through consultation with FD and systematic review experts. The detailed search strategies for each database are described in Supplementary File 2.
Study Selection and Data Extraction
Using EndNote X8 (Clarivate Analytics, Philadelphia, USA), we imported documents retrieved from each database and other sources. After removing any duplicates, we examined the eligibility of the searched articles by reviewing the titles and abstracts for the first inclusion. Subsequently, the full text of each article was reviewed for final inclusion.
The following information was extracted from the included studies using a standardized, pre-defined, pilot-tested Excel form: basic research information (the first author's name, year of publication, country, or study setting), sample size, details of participants, treatment and control intervention, duration of intervention, outcome measures, adverse events, and information for the assessment of the risk of bias. In addition, we used the Standards for Reporting Interventions in Clinical Trials of Acupuncture checklist to extract detail on the acupuncture treatment methods used in each study. We contacted the corresponding authors of the included studies via e-mail for further information if the data were insufficient or ambiguous. Study selection and data extraction were independently conducted by two researchers (CYK and BL). In case of disagreement between them, a consensus was reached through discussions with another researcher (SJK).
Risk of Bias Assessment
We assessed the risk of bias of the included studies using the Cochrane Collaboration's risk of bias tool (21). We evaluated the random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessors, completeness of outcome data, selective reporting, and other biases as “low risk,” “unclear risk,” or “high risk” (21). For the other bias, we evaluated it based on the statistical homogeneity of the baseline clinical characteristics such as mean age, sex, or disease severity between the treatment and control groups. The risk of bias assessment was independently conducted by two researchers (CYK and BL). In case of disagreement between them, a consensus was reached through discussions with another researcher (SJK).
Data Analysis and Synthesis
Details of the participants, treatment and control interventions, and outcomes from all included studies are descriptively summarized. For studies that used the same type of treatment and control intervention, we quantitatively synthesized them with the same outcome measures using Review Manager software (version 5.4; Cochrane, London, UK). We presented continuous and binary outcomes using the mean difference (MD) and risk ratio (RR) with 95% confidence intervals (CIs). We assessed the heterogeneity between the studies included in the meta-analysis using the χ2 test and the I2 statistic. I2 values >50 and >75% were considered indicative of substantial and considerable heterogeneity, respectively. We pooled the results using a random-effects model if the included studies had significant heterogeneity (I2 value > 50%). In contrast, we used a fixed-effects model if the heterogeneity was not significant or if the number of studies included in the meta-analysis was less than five. This was done due to the estimate of the between-study variance being imprecise (22).
We conducted subgroup analyses according to the following to interpret the cause of heterogeneity: (a) type of conventional WM (acid suppressants, prokinetics, Helicobacter pylori eradication, fundic relaxants, or antidepressants), and (b) type of acupuncture (manual acupuncture, electroacupuncture, auriculotherapy, or acupressure). A sensitivity analysis was performed to identify the robustness of the results of the meta-analysis by excluding (a) studies with a high risk of bias and (b) outliers that were numerically distant from the rest of the data. If more than ten studies were included in each meta-analysis, we evaluated the evidence of publication bias using funnel plots.
QoE Assessment
We used the GRADE method to evaluate the QoE for the main findings of the synthesized study results (23). The risk of bias, inconsistency, indirectness, imprecision of the results, and publication bias of the main findings were evaluated via https://gradepro.org/ as “very low,” “low,” “moderate,” or “high.” The QoE assessment was independently conducted by two researchers (CYK and BL). Any discrepancies were resolved by discussion with another researcher (SJK).
Results
Study Selection
A total of 5,967 studies were identified in our initial search. After any duplicates were removed, 4,652 studies remained. Then, using title and abstract screening, 72 potentially relevant articles were selected for inclusion. Following a full-text review, one, three, 11, one, 12, 13, one, two, two, one, and three studies were excluded due to being a study protocol, non-clinical studies, non-RCTs, did not use acupuncture, used acupuncture only, combined with other traditional Chinese medicine treatments, did not use WM, no details of WM compared to two different traditional Chinese medicine treatments, compared two different WM only, and unable to acquire the full text, respectively (Supplementary File 3). Finally, 22 RCTs were included in this review (Figure 1) (24–44).
Study Characteristics
All included studies were conducted between 2008 and 2020. All studies were conducted by Chinese authors and were published in Chinese, except for one study (42) that was published in English in an international journal. Three studies were dissertations (24, 30, 31). Except for one article not mentioned (25), the study setting of all included studies was a hospital. Most studies used the Rome criteria to diagnose FD, including four studies (28, 29, 32, 34) using the Rome II criteria and 13 studies (24, 26, 27, 30–33, 35–39, 42) using the Rome III criteria. In eight studies, pattern identification was used and reflected in acupuncture treatment (24, 31–33, 37, 39, 40, 43). Han and Chen (44) performed a four-armed RCT and used two different WM protocols (protocol (A): mosapride and pantoprazole; protocol (B): mosapride, pantoprazole, and agomelatine) (44). Therefore, this study was classified into electroacupuncture combined with protocol (A) vs. protocol (A) and electroacupuncture combined with protocol (B) vs. protocol (B), which was named part one and part two of Han and Chen (44), respectively. Since these two parts do not overlap participants, we analyzed this study as two separate trials. (1) Eleven trials (27, 29–33, 35, 37, 38, 40, 41) compared acupuncture combined with prokinetics to prokinetics alone; (2) one trial (32) compared acupuncture combined with acid suppressants to acid suppressants alone; (3) seven trials (24–26, 28, 34, 43, 44) compared acupuncture combined with prokinetics and acid suppressants to prokinetics and acid suppressants; (4) two trials (36, 39) compared acupuncture combined with prokinetics and antidepressants to prokinetics and antidepressants; (5) one trial (44) compared acupuncture combined with prokinetics, acid suppressants, and antidepressants to prokinetics, acid suppressants, and antidepressants; and (6) one trial (42) compared acupuncture combined with gastrocaine (a potent local anesthetic for gastric pain) to gastrocaine alone. In addition, 17 trials used manual acupuncture (24–30, 32–36, 38, 39, 41, 43, 45), five used electroacupuncture (31, 40, 42, 44), and one used auricular acupuncture (37) (Table 1).
Table 1.
References | Sample size (included → analyzed) | Mean age (yr) | Disease period | Diagnosis criteria | Pattern identification | (A) Treatment intervention | (B) Control intervention | Outcomes |
---|---|---|---|---|---|---|---|---|
Chen et al. (26) | 128 (62:66) | 42.0 ± 5.23 | NR | Rome III | NR | (B) + MA | Rabeprazole + mosapride | 1. TER (dyspepsia symptom) |
Chen et al. (28) | 112 (54:58) | 38 (18–58) | 8 mon−12 yr | Rome II | NR | (B) + MA | Lansoprazole + mosapride | 1. TER (dyspepsia symptom) |
Chen et al. (37) | 90 (45:45) | (A) 67.1 ± 6.3 (62–74) (B) 66.8 ± 5.9 (60–75) |
(A) 2.6 ± 1.1 yr (10 mon−4 yr) (B) 2.7 ± 0.8 yr (1–5 yr) |
Rome III | Spleen-stomach weakness | (B) + EA | Mosapride | 1. FD symptom score 2. Functional digestive disorder quality of life scale 3. TER (dyspepsia symptom) |
Chen et al. (41) | 100 (50:50) | (A) 50.82 ± 6.61 (B) 50.50 ± 6.58 |
(A) 2.10 ± 0.33 yr (B) 2.07 ± 0.31 yr |
Consensus opinion on the diagnosis and treatment of functional dyspepsia with integrated TCM and Western medicine 2017 | NR | (B) + MA | Mosapride | 1. Serum motilin 2. Serum gastrin 3. FD symptom score 4. TER (dyspepsia symptom) |
Chung et al. (42) | 132 (66:66) | (A) 50.8 ± 11.2 (B) 47.6 ± 12.8 |
(A) 9.5 ± 9.3 yr (B) 9.3 ± 10.0 yr |
Rome III | NR | (B) + EA | On-demand gastrocaine | 1. Responder 2. Patient-reported global symptoms 3. Individual PDS symptoms 4. Other FD symptoms (epigastric pain, epigastric burning, and postprandial nausea) 5. Change of NDI score 6. Nutrient Drink Test 7. PHQ-9 8. GAD-7 |
Fan (33) | 112 (56:56) | (A) 38.9 ± 7.9 (22–70) (B) 38.3 ± 7.8 (21–70) |
(A) median 2.1 yr (0.7–6) (B) median 1.9 yr (0.5–5) |
Rome III | Acupuncture treatment according to deficiency/excess pattern | (B) + MA | Mosapride | 1. TER (dyspepsia symptom) 2. FD Symptom score 3. Electrogastrography |
Gao (34) | 100 (50:50) | (A) 38.24 ± 5.14 (19–56) (B) 38.19 ± 5.08 (20–57) |
(A) 5.16 ± 1.24 yr (8 mon−12 yr) (B) 5.21 ± 1.33 yr (9 mon−13 yr) |
Rome II | NR | (B) + MA | Lansoprazole + mosapride | 1. TER (dyspepsia symptom) 2. SF-36 |
Han (44) | 90 (45:45) → 79 (39:40) | NR | NR | NR | NR | (B) + EA | Mosapride + pantoprazole | 1. PSQI 2. FD symptom score 3. SAS 4. SDS 5. Serum estrogen level 6. Plasma motilin level 7. TER (dyspepsia symptom) |
Han (44) | 90 (45:45) → 84 (43:41) | NR | NR | NR | NR | (B) + EA | Mosapride + pantoprazole + agomelatine | 1. PSQI 2. FD symptom score 3. SAS 4. SDS 5. Serum estrogen level 6. Plasma motilin level 7. TER (dyspepsia symptom) |
He (29) | 260 (130:130) | (A) 46.2 ± 9.47 (B) 38.7 ± 9.86 |
(A) 2.7 ± 1.3 yr (B) 2.6 ± 1.4 yr |
Rome II | NR | (B) + MA | Mosapride | 1. TER (dyspepsia symptom) 2. FD symptom score 3. Recurrence rate (f/u for 3 mon after treatment) |
Jiang (38) | 90 (45:45) | (A) 50.15 ± 12.69 (B) 49.79 ± 13.75 |
(A) 16.53 ± 5.29 mon (B) 16.61 ± 4.75 mon |
Rome III | NR | (B) + MA | Mosapride | 1. PAGI-SYM 2. SF-36 3. Electrogastrography 4. TER (dyspepsia symptom) |
Liu and Shu (27) | 78 (40:38) | (A) 48.3 ± 4.8 (B) 46.0 ± 5.0 |
(A) 6.8 ± 1.1 mon (B) 7.0 ± 0.5 mon |
Rome III | NR | (B) + MA | Clebopride | 1. TER (dyspepsia symptom) |
Mao (31) | 80 (40:40) | (A) 45.28 ± 9.15 (B) 44.78 ± 10.20 |
(A) 19.18 ± 6.32 mon (B) 18.83 ± 7.48 mon |
Rome III | Liver qi invading the stomach | (B) + EA | Mosapride | 1. TCM symptom score 2. TER (TCM syndrome score) 3. FD symptom score 4. TER (dyspepsia symptom) 5. SAS 6. SDS 7. SF-36 |
Mei (40) | 80 (40:40) | (A) 37.2 ± 5.3 (20–61) (B) 37.5 ± 4.8 (22–65) |
(A) 6.3 ± 1.2 yr (1–18) (B) 6.8 ± 1.5 yr (1–15) |
8th edition of the “Internal Medicine” textbook | Acupuncture treatment according to deficiency/excess pattern | (B) + EA | Domperidone | 1. LDQ 2. NDI 3. Karnofsky performance scale |
Wang (43) | 42 (21:21) | (A) 34.52 ± 6.79 (B) 34.49 ± 6.72 |
(A) 4.52 ± 1.83 yr (B) 4.49 ± 1.79 yr |
Consensus opinion on the diagnosis and treatment of functional dyspepsia with integrated TCM and western medicine 2010 | Liver depression and spleen deficiency | (B) + MA | Domperidone + cimetidine | 1. TER (dyspepsia symptom) 2. FD symptom score |
Yan (35) | 136 (68:68) | (A) 40.35 ± 6.41 (27–63) (B) 41.58 ± 7.34 (25–64) |
(A) 6.68 ± 2.23 yr (6 mon−10 yr) (B) 6.87 ± 2.51 yr |
Rome III | NR | (B) + MA | Mosapride | 1. FD symptom score 2. TER (dyspepsia symptom) 3. Gastric emptying rate 4. Plasma motilin 5. Plasma ghrelin 6. Plasma 5-hydroxytryptamine |
Yang et al. (36) | 100 (50:50) | (A) 42.1 ± 13.9 (B) 40.8 ± 15.1 |
(A) 19.6 ± 10.3 mon (B) 23.6 ± 15.7 mon |
Rome III PSQI ≥ 8 | NR | (B) + MA | Itopride + deanxit | 1. PSQI 2. Serum gastrin 3. TER (TCM syndrome score) |
Yang and Huang (39) | 100 (50:50) | (A) 43.5 ± 3.5 (21–65) (B) 44.2 ± 3.3 (22–65) |
(A) 19.5 ± 5.5 mon (10 mon−3 yr) (B) 19.7 ± 5.3 mon (11 mon−3 yr) |
Rome III PSQI ≥ 8 | (A) liver qi depression (16), spleen-stomach qi deficiency (14), liver qi invading the stomach (13), dampness-heat stagnating in stomach (7) (B) liver qi depression (17), spleen-stomach qi deficiency (13), liver qi invading the stomach (12), dampness-heat stagnating in stomach (8) |
(B) + MA | Itopride + flupentixol and melitroxine | 1. PSQI 2. TER (sleep disorder) 3. SAS 4. SDS 5. SF-36 6. Serum motilin 7. Serum somatostatin8 Serum gastrin |
Yu (24) | 73 (37:36) → 70 (36:34) | (A) 39.7 ± 15.2 (18–66) (B) 41.4 ± 11.8 (18–65) |
NR | Rome III depression and anxiety attacks (CCMD-3) 10 ≤ HAMD ≤ 30 7 ≤ HAMA ≤ 29 | (A) liver qi stagnation (17), liver depression and spleen deficiency (8), spleen deficiency and phlegm-dampness (7), food accumulation and stagnation (2), cold-heat complex (2) (B) liver qi stagnation (16), liver depression and spleen deficiency (9), spleen deficiency and phlegm-dampness (7), food accumulation and stagnation (1), cold-heat complex (1) |
(B) + MA | Domperidone + sucralfate | 1. HAMD 2. HAMA 3. FD symptom score 4. TER (dyspepsia symptom) |
Zhang (25) | 61 (31:30) | (A) 47.3 ± 7.6 (B) 46.3 ± 8.1 |
NR | 6th edition of the “Internal Medicine” textbook | NR | (B) + MA | Domperidone + omeprazole | 1. TER (dyspepsia symptom) |
Zhang (30) | 72 (36:36) | (A) 30.63 ± 7.83 (B) 31.63 ± 7.84 |
(A) 17.27 ± 7.12 mon (B) 18.75 ± 6.9 mon |
Rome III | NR | (B) + MA | Mosapride | 1. FD symptom score 2. SF-36 3. TER (dyspepsia symptom) |
Zhang (45) | 58 (30:28) | (A) 33.60 ± 9.15 (21–60) (B) 31.78 ± 10.35 (18–58) |
(A) 4.81 ± 2.67 yr (9 mon−12 yr) (B) 4.14 ± 1.80 yr (1–9 yr) |
Rome III | liver qi invading the stomach | (B) + MA | Mosapride | 1. FD symptom score 2. TER (dyspepsia symptom) 3. Recurrence rate (f/u for 3 mon after treatment) |
Zhang (32) | 76 (40:36) | NR | NR | Rome II | NR | (B) + MA | Rabeprazole | 1. TER (dyspepsia symptom) 2. FD symptom score 3. Recurrence rate (f/u for 6 mon after treatment) |
EA, electro-acupuncture; FD, functional dyspepsia; GAD-7, general anxiety disorder-7; HAMA, Hamilton anxiety rating scale; HAMD, Hamilton depression rating scale; LDQ, Leeds indigestion symptom scores; MA, manual acupuncture; NDI, Nepean dyspepsia index; NR, not recorded; PAGI-SYM, patient assessment of upper gastrointestinal symptom severity; PDS, postprandial distress syndrome; PHQ-9, Patient health questionnaire-9; PSQI, Pittsburgh sleep quality index; SAS, self-rating anxiety scale; SDS, self-rating depression scale; SF-36, 36-item short-form health survey; TCM, traditional Chinese medicine; TER, total effective rate.
Except for one trial (39) which set the main acupoints according to pattern identification, a total of 36 acupoints were used as the main acupoints in 22 trials. Among them, ST36 was used the most in 18 trials, followed by PC6 (16 trials), CV12 (13 trials), ST25 (six trials), BL20 (five trials), and LR3 (five trials). As a response to acupuncture, 13 trials acquired De qi, such as numbness, soreness, distention, and heaviness. In the study that used electroacupuncture, the frequency was varied from 2 to 100 Hz, and the intensity was performed to the extent that the participants could tolerate it. Continuous waves were used as the waveform in two trials (31, 42) and sparse and dense waves were used in one trial (40). The needle retention time was between 15 and 30 min, with 30 min the most commonly used (14 trials). The duration of treatment varied from 2 to 10 weeks, with 4 weeks the most common. The number of treatment sessions varied from 12 to 56, with 28 sessions being the most common (7 trials). In one trial (42) a full license from the Chinese Medicine Council of Hong Kong was presented as a qualification for acupuncture therapists (Table 2).
Table 2.
References | Style of acupuncture | Number of needle (main acupoints) | Treatment points | Depth of insertion | Response sought | Needle stimulation | Needle retention time | Needle type | Number of treatment session | Frequency and duration | Qualification or experiences on acupuncture |
---|---|---|---|---|---|---|---|---|---|---|---|
Chen et al. (26) | MA | Unclear | ST36, PC6 | NR | NR | NR | 30 min | NR | 28 | 1 session/day for 4 wks | NR |
Chen et al. (28) | MA | Unclear | ST36, PC6 | NR | NR | NR | 30 min | NR | 28 | 1 session/day for 4 wks | NR |
Chen et al. (37) | Auricular acupuncture | 5 | Spleen, stomach, large intestine, triple energizers, cardia |
NR | NR | Press once every 4 h about 1 min, 3 times a day to the extent that the soreness or fever can be tolerated | 2 days | 0.20 × 1.5 mm | 14 | Every other day for 4 wks (alternating the left and right ears) |
NR |
Chen et al. (41) | MA | Unclear | CV6, CV4, CV11, ST36, CV12, PC6 -liver qi invading the stomach: LR3, LR14 -food damage to spleen: CV10, ST21 -spleen-stomach deficiency cold: SP6, LR13, BL20, BL21 |
NR | NR | NR | NR | NR | 30 | 1 session/day for 1 mon | NR |
Chung et al. (42) | EA | 15 | Bilateral ST34, ST36, ST40, ST42, CV12, PC6, BL20, BL21 | Depends on the patient's body type | De qi | EA for all acupoints except BL20, BL21, ST42, and CV12. 2 Hz, continuous wave, acceptable to the patient (0.5–1.5 mA) |
30 min, no retention for BL20 and BL21 |
0.20 × 25–40 mm | 20 | 2 sessions/wk for 10 wks | Full licensure from the Chinese Medicine Council of Hong Kong |
Fan (33) | MA | Unclear | BL21, BL20, CV11, ST36, ST23 -deficiency pattern: SP9, SP4 -excess pattern: ST44, LR3 |
NR | NR | Neutral supplementation and draining, needle manipulation every 15 min | 30 min | Disposable acupuncture needle | 24 | 1 session/day, 6 day/wk for 4 wks | NR |
Gao (34) | MA | Unclear | ST36, PC6 | NR | NR | NR | 30 min | NR | 28 | 1 session/day for 4 wks | NR |
Han (44) | EA | 9 | Bilateral ST36, CV12, SP6, LR3, PC6 | 15–45 mm | De qi | G6805 EA therapy device, 2–100 Hz, patient's perception of mild muscle tremor | 15 min | Huatuo needles, 0.38 × 50–80 mm, 28 gauge acupuncture |
56 | 2 sessions/day for 4 wks | NR |
Han (44) | MA | Unclear | ST36, ST44, LR3, PC6, BL20, BL21, BL18, BL15, CV12, et al. | NR | De qi | NR | 15–30 min | NR | 28 | 1 session/day for 4 wks | NR |
He (29) | MA | 15 | Bilateral BL20, BL21, PC6, CV12, ST25, ST36, ST34, ST40 -deficiency pattern: Bilateral GB34, SP4 -excess pattern: Bilateral ST44, LR3 |
NR | De qi | NR | 30 min | NR | 20 | 5 sessions/wk for 4 wks |
NR |
Jiang (38) | MA | 6 | Bilateral ST36, PC6, ST25 | NR | De qi | NR | 20–30 min | NR | NR | 4 wks | NR |
Liu and Shu (27) | EA | 7 or 9 | CV12, bilateral PC6, ST36, CV6, LR3, LR14, BL18, ST37, ST25 | NR | De qi | 20 Hz, continuous wave, acceptable to the patient | 20 min | 0.25 × 40 mm | 24 | 6 sessions/wk for 4 wks | NR |
Mao (31) | EA | Unclear | ST36, PC6 -deficiency pattern: SP4, SP9 -excess pattern: LR3, ST44 |
NR | De qi | Sparse and dense wave, 2/100 Hz, 0.1–1.0 mA | 30 min | Disposable acupuncture needle, 0.25 × 40 mm | 30 | 1 session/day for 1 mon | NR |
Mei (40) | Abdomen acupuncture | 6 | CV10, CV12, CV4, CV6, bilateral ST25 | NR | Not de qi | NR | 30 min | NR | 12 | 6 sessions/wk for 2 wks | NR |
Wang (43) | MA | 8 | CV12, CV10, bilateral ST36, ST21, PC6 | NR | NR | Neutral supplementation and draining, needle manipulation for 1 min every 10 min | 30 min | Disposable acupuncture needles, Huatuo needles, 0.30 × 50 mm | 28 | 1 session/day for 4 wks | NR |
Yan (35) | MA | Unclear | CV12, CV13, CV10, CV6, ST25, ST36, PC6, GV20, GV24, EX-HN3 -liver qi stagnation: LR3 -liver qi invading the stomach: SP4 -spleen-stomach weakness: CV4 -dampness-heat stasis and stagnation: GB34 |
NR | De qi | NR | 30 min | NR | 20 | 5 sessions/wk for 1 mon |
NR |
Yang et al. (36) | MA | Unclear | CV12, ST25, ST36, HT7, PC6, EX-HN1, SP6 -liver qi depression: CV17, LR13 -spleen-stomach qi deficiency: BL20, BL21 -liver qi invading the stomach: LR14, LR3 -dampness-heat stagnating in stomach: SP9, ST44 |
NR | Numbness, soreness, distention, and heaviness | 60–90 times/min (lifting frequency), 90–180°(twisting angle), 60–90 times/min (twisting frequency) | 30 min | Disposable stainless steel acupuncture needle | 14 | 1 session/day for 2 wks | NR |
Yang and Huang (39) | MA | 12 | Bilateral BL13, BL15, BL18, BL20, BL23, BL17 | 0.5–0.8 cun (寸) | De qi | Neutral supplementation and draining | 30 min | Stainless steel acupuncture needles, Huatuo needles, 0.32 × 50–70 mm | 24 | 3 sessions/wk for 8 wks |
NR |
Yu (24) | MA | Unclear | CV12, ST36 -liver qi stagnation, stomach qi failing to bear downward: BL18, LR14, ST34, PC6 -spleen deficiency: CV10, ST25 |
NR | NR | NR | NR | NR | NR | 2 wks | NR |
Zhang (25) | Abdomen acupuncture | 7 | CV4, CV12, CV10, bilareral ST25, SP15 -liver qi invading the stomach: Right CV4, ST23, up wind-dampness -spleen deficiency and qi stagnation, spleen-stomach deficiency cold: Left CV4, ST23, ST28, ST26 -vomiting: KI18, ST24 -insomnia: KI19, bilareral down wind-dampness |
To the abdominal wall | Diffuse pain in the abdominal wall | NR | 25 min | 0.22 × 40 mm, 0.22 × 25 mm | 15 | 1 session/day for 15 days |
NR |
Zhang (30) | MA | 7 | CV12, bilateral ST36, PC6, LR3 | 1–1.5 cun (寸) | De qi | Neutral supplementation and draining | 30 min | Disposable sterile filiform needle | 28 | 1 session/day for 4 wks | NR |
Zhang (46) | MA | Unclear | PC6, ST36 | NR | NR | NR | 30 min | NR | 28 | 7 sessions/wk for 4 wks | NR |
EA, electro-acupuncture; MA, manual acupuncture; NR, not recorded.
Risk of Bias Assessment
Sixteen studies using proper randomization method such as random number tables were evaluated as having a low risk of bias in the random sequence generation domain (24, 25, 27, 30, 31, 33, 34, 36–43, 45) and the remaining six studies were evaluated as having an unclear risk of bias because there was no mention of the randomization method (26, 28, 29, 32, 35, 44). There was no mention of allocation concealment, except for one study in which allocation concealment was performed using an opaque sealed envelope (42). All studies did not mention the blinding of participants and personnel. However, this was evaluated as having a high risk of bias in all studies due to all comparing the treatment and control interventions (acupuncture as add-on therapies to conventional WM vs. WM alone). As for the blinding of the outcome assessment, only one study mentioned that this was performed (42) while the other studies did not mention this. In two studies, dropouts occurred during the trial period, but the statistical analysis was performed using a per-protocol analysis method, and the risk of attrition bias was evaluated as high (24, 44). Four studies that presented only the TER without raw data were evaluated as having a high risk of reporting bias (25–28). All studies were evaluated as sufficiently homogeneous between the treatment and control groups in terms of the baseline characteristics (Figure 2).
Effectiveness and Safety of Acupuncture as an Add-On Treatment for FD
Symptom Score (Primary Outcome)
A meta-analysis was not performed because of the heterogeneity of the symptom score scales used in the included studies. The results of each study are summarized in Table 3. In addition to the total score, ten individual symptoms including epigastric pain, epigastric burning, decreased food intake, postprandial fullness, belching, acid reflux, early satiation, nausea and/or vomiting, obstruction of the throat, and loss of appetite were evaluated. In one study that compared manual acupuncture combined with mosapride and mosapride alone, it was found that there was no significant difference in the symptom scores between the two groups (30). One study found that the total symptom score of manual acupuncture combined with domperidone and sucralfate was higher than the control group. However, they did not statistically analyze the score (24). All other studies found that the individual symptoms of FD were significantly improved in the acupuncture combined with the WM group compared to the WM alone group (29, 31–33, 35–37, 39–45).
Table 3.
References | Study design | Total score | Epigastric pain | Epigastric burning | Decreased food intake | Postprandial fullness | Belching | Acid reflux | Early satiation | Nausea and/or vomiting | Obstruction of throat | Loss of appetite | Motilin | Ghrelin | 5-HT | Gastrin | Somatostatin |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Chen et al. (37) | AA + prokinetics | (A) < (B)* | – | – | – | – | – | – | – | – | – | – | – | – | – | – | – |
Chen et al. (41) | MA + prokinetics | – | (A) < (B)+ | (A) < (B)+ | – | (A) < (B)+ | – | – | (A) < (B)+ | – | – | – | (A) > (B)+ | – | – | (A) > (B)+ | – |
Chung et al. (42) | EA + gastrocaine | – | (change value) (A) > (B)* |
(change value) N.S |
– | (change value) (A) > (B)+ |
– | – | (change value) (A) > (B)* |
(change value) (A) > (B)* |
– | – | – | – | – | – | – |
Fan (33) | MA + prokinetics | – | (A) < (B)* | (A) < (B)* | – | (A) < (B)* | – | – | (A) < (B)* | – | – | – | – | – | – | – | – |
Han (44) | EA + prokinetics + acid suppressants | (A) < (B)* | – | – | – | – | – | – | – | – | – | – | (A) > (B)* | – | – | – | – |
Han (44) | EA + prokinetics + acid suppressants + antidepressants | (A) < (B)* | – | – | – | – | – | – | – | – | – | – | (A) > (B)* | – | – | – | – |
He (29) | MA + prokinetics | (A) < (B)* | – | – | – | – | – | – | – | – | – | – | – | – | – | – | – |
Mao (31) | EA + prokinetics | (A) < (B)* | (A) < (B)* | N.S | – | (A) < (B)* | – | – | (A) < (B)* | – | – | – | – | – | – | – | – |
Mei (40) | EA + prokinetics | (A) < (B)* | – | – | – | – | – | – | – | – | – | – | – | – | – | – | – |
Wang (43) | MA + prokinetics + acid suppressants | – | (A) < (B)+ | (A) < (B)+ | (A) < (B)+ | (A) < (B)+ | – | – | (A) < (B)+ | – | – | – | – | – | – | – | – |
Yan (35) | MA + prokinetics | – | (A) < (B)* | – | – | (A) < (B)* | – | – | (A) < (B)* | (A) < (B)* | – | (A) < (B)* | (A) > (B)* | (A) < (B)* | (A) < (B)* | – | – |
Yang et al. (36) | MA + prokinetics + antidepressants | – | – | – | – | – | – | – | – | – | – | – | – | – | – | (A) < (B)+ | – |
Yang and Huang (39) | MA + prokinetics + antidepressants | – | – | – | – | – | – | – | – | – | (A) < (B)* | – | – | (A) < (B)* | (A) < (B)* | ||
Yu (24) | MA + prokinetics + acid suppressants | (A) < (B) (no statistical data) | – | – | – | – | – | – | – | – | – | – | – | – | – | – | – |
Zhang (30) | MA + prokinetics | – | N.S | – | N.S | N.S | N.S | N.S | N.S | N.S | N.S | – | – | – | – | – | – |
Zhang (45) | MA + prokinetics | (A) < (B)* | – | – | – | – | – | – | – | – | – | – | – | – | – | – | – |
Zhang (32) | MA + acid suppressants | – | (A) < (B)* | (A) < (B)* | – | – | (A) < (B)* | – | – | – | – | – | – | – | – | - | - |
AA, auricular acupuncture; EA, electro-acupuncture; MA, manual acupuncture; N.S, not significant; 5-HT, 5-Hydroxytryptamine.
p < 0.05,
+p < 0.01, (A) treatment group, (B) control group.
NDI Score (Primary Outcome)
Only one study reported the NDI scores (40). According to Mei (40), electroacupuncture combined with domperidone showed a significantly lower NDI score than the control group (1 study; MD −7.92, 95% CI −11.84 to −4.00) (Table 4) (40).
Table 4.
Outcomes | No. participants (RCTs) | Anticipated absolute effects (95% CI) | Relative effect (95% CI) | I2 value | Quality of evidence (GRADE) | Comments | ||
---|---|---|---|---|---|---|---|---|
Risk with control group | Risk with acupuncture group | |||||||
NDI | Total (prokinetics; electro-acupuncture) | 80 (1) | – | MD 7.92 lower (11.84–4 lower) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Total effective rate | Total | 1,960 (20) | 702 per 1,000 | 906 per 1,000 (864–941) |
RR 1.29 (1.23–1.34) |
14 | ⊕⊕○○ LOW |
Risk of bias (−1) Indirectness (−1) |
Subgroup 1 | Prokinetics | 1,076 (10) | 741 per 1,000 | 926 per 1,000 (881–978) |
RR 1.25 (1.19–1.32) |
18 | ⊕⊕○○ LOW |
Risk of bias (−1) Indirectness (−1) |
Acid suppressants | 76 (1) | 722 per 1,000 | 924 per 1,000 (744–1,000) |
RR 1.28 (1.03–1.60) |
Not applicable | ⊕○○○ VERY LOW |
Risk of bias (−1) Indirectness (−1) Imprecision (−1) |
|
Prokinetics + Acid suppressants | 592 (7) | 739 per 1,000 | 917 per 1,000 (850–983) |
RR 1.24 (1.15–1.33) |
0 | ⊕⊕○○ LOW |
Risk of bias (−1) Indirectness (−1) |
|
Prokinetics + Acid suppressants + Antidepressants | 84 (1) | 780 per 1,000 | 976 per 1,000 (827–1,000) |
RR 1.25 (1.06–1.48) |
Not applicable | ⊕○○○ VERY LOW |
Risk of bias (−1) Indirectness (−1) Imprecision (−1) |
|
Gastrocaine | 132 (1) | 167 per 1,000 | 592 per 1,000 (332–1,000) |
RR 3.55 (1.99–6.30) |
Not applicable | ⊕○○○ VERY LOW |
Risk of bias (−1) Indirectness (−1) Imprecision (−1) |
|
Subgroup 2 | Manual acupuncture | 1,495 (15) | 755 per 1,000 | 936 per 1,000 (891–974) |
RR 1.24 (1.18–1.29) |
0 | ⊕⊕○○ LOW |
Risk of bias (−1) Indirectness (−1) |
Electro-acupuncture | 375 (4) | 487 per 1,000 | 779 per 1,000 (667–910) |
RR 1.60 (1.37–1.87) |
85 | ⊕○○○ VERY LOW |
Risk of bias (−1) Inconsistency (−2) Indirectness (−1) |
|
Auricular acupuncture | 90 (1) | 733 per 1,000 | 909 per 1,000 (748–1,000) |
RR 1.24 (1.02–1.52) |
Not applicable | ⊕○○○ VERY LOW |
Risk of bias (−1) Indirectness (−1) Imprecision (−1) |
|
SF-36 (total) | Total (manual acupuncture) | 190 (2) | – | MD 6.89 higher (5.32–8.47 higher) |
– | 86 | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Prokinetics | 90 (1) | – | MD 5.94 higher (4.22–7.66 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Acid suppressants | 100 (1) | – | MD 11.78 higher (7.87–15.69 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
SF-36 (vitality) | Total | 180 (2) | – | MD 4.72 higher (2.57–6.87 higher) |
– | 72 | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Prokinetics, Electro-acupuncture | 80 (1) | – | MD 8.5 higher (4–13 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 3.6 higher (1.15–6.05 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
SF-36 (physical functioning) | Total | 180 (2) | – | MD 4.64 higher (1.64–7.64 higher) |
– | 0 | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Prokinetics, Electro-acupuncture | 80 (1) | – | MD 5.38 higher (0.45–10.31 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 4.2 higher (0.42–7.98 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
SF-36 (bodily pain) | Total | 180 (2) | – | MD 2.85 higher (0.4–5.3 higher) |
– | 18 | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Prokinetics, Electro-acupuncture | 80 (1) | – | MD 5.4 higher (0.27–10.53 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 2.1 higher (0.68 lower−4.88 higher) |
– | Not applicable | ⊕⊕⊕○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
SF-36 (general health perceptions) | Total | 180 (2) | – | MD 3.74 higher (1.45–6.03 higher) |
– | 76 | ⊕○○○ VERY LOW |
Risk of bias (−1) Inconsistency (−2) |
Prokinetics, Electro-acupuncture | 80 (1) | – | MD 0.88 lower (5.84 lower−4.08 higher) |
– | Not applicable | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 5 higher (2.41–7.59 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
SF-36 (physical role functioning) | Total | 180 (2) | – | MD 3.23 higher (0.84–5.62 higher) |
– | 62 | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Prokinetics, Electro-acupuncture | 80 (1) | – | MD 9.38 higher (1.54–17.22 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 2.6 higher (0.09–5.11 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
SF-36 (emotional role functioning) | Total | 180 (2) | – | MD 3.34 higher (0.81–5.87 higher) |
– | 82 | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Prokinetics, Electroacupuncture | 80 (1) | – | MD 17.5 higher (5.36–29.64 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 2.7 higher (0.11–5.29 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
SF-36 (social role functioning) | Total | 180 (2) | – | MD 2.31 higher (0.22 lower−4.84 higher) |
– | 55 | ⊕○○○ VERY LOW |
Risk of bias (−1) Inconsistency (−1) Imprecision (−1) |
Prokinetics, Electro-acupuncture | 80 (1) | – | MD 6.87 higher (0.37–13.37 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 1.5 higher (1.24 lower−4.24 higher) |
– | Not applicable | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
SF-36 (mental health) | Total | 180 (2) | – | MD 8.36 higher (5.86–10.86 higher) |
– | 0 | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) |
Prokinetics, Electro-acupuncture | 80 (1) | – | MD 11 higher (5.04–16.96 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Antidepressants, Manual acupuncture | 100 (1) | – | MD 7.8 higher (5.05–10.55 higher) |
– | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Incidence of adverse events | Total | 1,209 (12) | 65 per 1,000 | 73 per 1,000 (33–165) |
RR 1.13 (0.50–2.54) |
64 | ⊕○○○ VERY LOW |
Risk of bias (−1) Inconsistency (−1) Imprecision (−1) |
Subgroup 1 | Prokinetics | 738 (7) | 76 per 1,000 | 71 per 1,000 (43–118) |
RR 0.93 (0.56–1.55) |
0 | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
Acid suppressants | 76 (1) | 83 per 1,000 | 50 per 1,000 (9–283) |
RR 0.60 (0.11–3.39) |
Not applicable | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
Prokinetics + Acid suppressants | 79 (1) | 25 per 1,000 | 9 per 1,000 (0–204) |
RR 0.34 (0.01–8.14) |
Not applicable | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
Prokinetics + Antidepressants | 100 (1) | 0 per 1,000 | 0 per 1,000 (0–0) |
Not estimable | Not applicable | ⊕⊕⊕○ MODERATE |
Risk of bias (−1) | |
Prokinetics + Acid suppressants + Antidepressants | 84 (1) | 24 per 1,000 | 8 per 1,000 (0–185) | RR 0.32 (0.01–7.59) |
Not applicable | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
Gastrocaine | 132 (1) | 91 per 1,000 | 621 per 1,000 (283–1,000) |
RR 6.83 (3.11–14.99) |
Not applicable | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
Subgroup 2 | Manual acupuncture | 834 (8) | 70 per 1,000 | 62 per 1,000 (38–104) |
RR 0.89 (0.54–1.48) |
0 | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
Electro-acupuncture | 375 (4) | 53 per 1,000 | 76 per 1,000 (14–422) |
RR 1.43 (0.26–7.90) |
65 | ⊕○○○ VERY LOW |
Risk of bias (−1) Inconsistency (−1) Imprecision (−1) |
|
Recurrence rate | Total (manual acupuncture) | 394 (3) | 170 per 1,000 | 75 per 1,000 (43–129) | RR 0.44 (0.25–0.76) |
0 | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
Prokinetics | 318 (2) | 190 per 1,000 | 80 per 1,000 (44–142) | RR 0.42 (0.23–0.75) |
0 | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
|
Acid suppressants | 76 (1) | 83 per 1,000 | 50 per 1,000 (9–283) | RR 0.60 (0.11–3.39) |
Not applicable | ⊕⊕○○ LOW |
Risk of bias (−1) Imprecision (−1) |
CI, confidence interval; MD, mean difference; NDI, Nepean dyspepsia index; RCT, randomized controlled trial; RR, risk ratio; SF-36, 36-item short-form health survey.
TER (Secondary Outcome)
According to the meta-analysis, the acupuncture combined with WM group showed a significantly higher TER than the WM group (20 studies; RR 1.29, 95% CI 1.23–1.34; I2 = 14%). The superiority of acupuncture combined with WM remained significant in all subgroup analyses according to the WM type: (1) prokinetics (10 studies; RR 1.25, 95% CI 1.19–1.32; I2 = 18%); (2) acid suppressants (1 study; RR 1.28, 95% CI 1.03–1.60); (3) prokinetics and acid suppressants (seven studies; RR 1.24, 95% CI 1.15–1.33; I2 = 0%); (4) prokinetics, acid suppressants, and antidepressants (one study; RR 1.25, 95% CI 1.06–1.48); and (5) gastrocaine (one study; RR 3.55, 95% CI 1.99–6.30), as well as, according to acupuncture type: (1) manual acupuncture (15 studies; RR 1.24, 95% CI 1.18–1.29; I2 = 0%); (2) electroacupuncture (four studies; RR 1.60, 95% CI 1.37–1.87; I2 = 85%); and (3) auricular acupuncture (one study; RR 1.24, 95% CI 1.02–1.52) (Table 4, Supplementary File 4).
Short-Form Health Survey (Secondary Outcome)
Although SF-36 was used, one study with a different symptom score range was not included in the meta-analysis (30). Overall, the acupuncture combined with WM group showed significantly higher scores than the control group in terms of the total score (2 studies; MD 6.89, 95% CI 5.32–8.47; I2 = 86%) as well as almost SF-36 subscales including vitality (two studies; MD 4.72, 95% CI 2.57–6.87; I2 = 72%), physical functioning (two studies; MD 4.64, 95% CI 1.64–7.64; I2 = 0%), bodily pain (two studies; MD 2.85, 95% CI 0.40–5.30; I2 = 18%), general health perception (two studies; MD 3.74, 95% CI 1.45–6.03; I2 = 76%), physical role functioning (two studies; MD 3.23, 95% CI 0.84–5.62; I2 = 62%), emotional role functioning (two studies; MD 3.34, 95% CI 0.81–5.87; I2 = 82%), and mental health (two studies; MD 8.36, 95% CI 5.86–10.86; I2 = 0%), but not in social role functioning (two studies; MD 2.31, 95% CI −0.22 to 4.84; I2 = 55%). In the subscale of social role functioning, when a subgroup analysis was performed according to acupuncture type, manual acupuncture combined with WM showed no significant difference with the WM group (1 study; MD 1.50, 95% CI −1.24 to 4.24), but electroacupuncture combined with WM showed significantly superior results compared to the WM group (1 study; MD 6.87, 95% CI 0.37–13.37) (Table 4, Supplementary File 4).
Biomarkers Related to FD (Secondary Outcome)
A meta-analysis was not performed for the biomarkers related to FD because of the heterogeneity of the measurement unit. The most frequently measured biomarker was the serum motilin level, and four (35, 41, 44) out of five studies (35, 39, 41, 44) reported that the level was significantly higher in the acupuncture combined with WM group after treatment compared to the control group (P < 0.05, P < 0.01). In addition, other biomarkers such as ghrelin (35) 5-Hydroxytryptamine (5-HT) (35), gastrin (36, 39, 41) and somatostatin (39) were measured. However, their levels were measured only in a single study or showed inconsistent results (Table 3).
Safety Data (Secondary Outcome)
A total of 12 trials reported the safety profile of the interventions (27, 29–32, 36, 38, 41, 42, 44, 45). Generally, there was no significant difference in the incidence of adverse events between acupuncture combined with WM and WM alone (12 studies; RR 1.13, 95% CI 0.50–2.54; I2 = 64%). The only individual study that showed a statistically significant difference between the two groups was Chung et al. (42). This study reported that the incidence of adverse events was significantly higher in the acupuncture combined with the WM group (62.12 vs. 10.91%) (42). This difference was attributed to local pain, local bruising, and local numbness due to acupuncture stimulation. No severe adverse events were reported with respect to the interventions used (Table 4, Supplementary File 5).
Recurrence Rate (Secondary Outcome)
Three studies reported the recurrence rate of FD after the end of treatment (29, 32, 32). As a result, manual acupuncture combined with WM group had a significantly lower recurrence rate after 3–6 months of follow-up than the control group (three studies; RR 0.44, 95% CI 0.25–0.76; I2 = 0%). In the subgroup analysis according to WM type, the significant superiority remained in combination with prokinetics (two studies; RR 0.42, 95% CI 0.23–0.75; I2 = 0%), but not in combination with acid suppressants (one study; RR 0.60, 95% CI 0.11–3.39). All studies only used manual acupuncture (Table 4, Supplementary File 4).
Sensitivity Analysis
In a meta-analysis of most outcomes other than TER, the number of studies was not sufficient to perform a sensitivity analysis excluding outliers. In the case of TER, even when an outlier (42) that was considered to be the main cause of statistical heterogeneity in the meta-analysis, was excluded from the sensitivity analysis, the existing results were not significantly affected (acupuncture combined with WM vs. WM alone, 19 studies, RR 1.25, 95% CI 1.20–1.30; I2 = 0%; and electroacupuncture combined WM vs. WM alone, three studies, RR 1.34, 95% CI 1.16–1.54; I2 = 39%). The results were similar in the sensitivity analysis, except for RCTs whose randomization method was unclear (28, 29, 32, 35, 44) or dissertation (24, 30, 31). The results of former were as follows: acupuncture combined with WM vs. WM alone (14 studies; RR 1.33, 95% CI 1.25–1.41; I2 = 57%), acupuncture combined with prokinetics vs. prokinetics alone (eight studies; RR 1.28, 95% CI 1.19–1.38; I2 = 35%), acupuncture combined with prokinetics and acid suppressants vs. prokinetics and acid suppressants (five studies; RR 1.25, 95% CI 1.15–1.36; I2 = 0%), manual acupuncture combined with WM vs. WM alone (11 studies; RR 1.25, 95% CI 1.17–1.32; I2 = 0%), and electroacupuncture combined with WM vs. WM alone (two studies; RR 2.31, 95% CI 1.71–3.13; I2 = 84%). The results of the latter were as follows: acupuncture combined with WM vs. WM alone (17 studies; RR 1.27, 95% CI 1.21–1.32; I2 = 31%), acupuncture combined with prokinetics vs. prokinetics alone (eight studies; RR 1.22, 95% CI 1.15–1.29; I2 = 0%), acupuncture combined with prokinetics and acid suppressants vs. prokinetics and acid suppressants (six studies; RR 1.23, 95% CI 1.13–1.33; I2 = 0%), manual acupuncture combined with WM vs. WM alone (13 studies; RR 1.22, 95% CI 1.17–1.28; I2 = 0%), and electroacupuncture combined with WM vs. WM alone (three studies; RR 1.58, 95% CI 1.33–1.88; I2 = 90%).
Publication Bias
Four funnel plots were generated for the TER, adverse events, and secondary outcomes. Except for one outlier (42), which was excluded from the sensitivity analysis, no apparent asymmetry was observed overall. However, the funnel plot of the adverse events showed apparent asymmetry, suggesting a potential publication bias (Figure 3).
QoE
The QoE of the NDI score, the primary outcome, was “moderate,” which was due to the high risk of bias of the included studies. The QoE for the TER ranged from “low” to “very low,” depending on the type of WM or the method of acupuncture used. This was due to the high risk of bias and the indirectness, inconsistency, and imprecision of the results. For SF-36, the QoE was generally evaluated as “moderate” or “low” due to the high risk of bias and imprecise results. Regarding the incidence of adverse events and recurrence rates, the QoE was generally low due to the high risk of bias and imprecise results (Table 4).
Discussion
Summary of Evidence
This systematic review was conducted to assess the effectiveness and safety of acupuncture as an add-on treatment to conventional WM for FD and critically evaluate the QoE. A total of 22 RCTs were included (24–45).
For the symptom scores, a meta-analysis was not performed due to the heterogeneity of the scales used. The studies included results for the total symptom score and ten individual FD symptom scores. Except for one study that did not find a significant difference between manual acupuncture combined with prokinetics and prokinetics alone in all evaluated symptom scores (30), the remaining studies supported the superiority of acupuncture combined with WM. The symptoms frequently improved with combined therapy were epigastric pain, epigastric burning, postprandial fullness, and early satiation. Only one study reported the NDI score, another primary outcome (40). In that study, electroacupuncture combined with domperidone showed significant superiority in terms of the NDI score after treatment compared to domperidone alone. In the secondary outcome TER, the most frequently reported outcome in the included studies, the acupuncture combined with WM group showed significantly higher TER than the WM group in both the meta-analysis and sensitivity analysis after removing outliers. Moreover, the superiority of acupuncture combined with WM remained significant in all subgroup analyses according to WM type (prokinetics, acid suppressants, prokinetics and acid suppressants, prokinetics and acid suppressants and antidepressants, and gastrocaine) as well as acupuncture type (manual acupuncture, electroacupuncture, and auricular acupuncture). In addition, the funnel plots did not suggest a potential publication bias. Acupuncture combined with WM showed superiority in most SF-36 results, but few studies have reported this outcome. As biomarkers related to FD, the levels of ghrelin, 5-HT, gastrin, and somatostatin showed mixed results, but motilin levels were significantly higher in the combined therapy group in most cases. Only three studies have reported the recurrence rate of FD after the end of treatment, and acupuncture combined with WM showed a significantly lower recurrence rate after 3–6 months of follow-up than WM alone. According to the subgroup analysis, it was particularly meaningful when combined with prokinetics but not with acid suppressants. Overall, acupuncture combined with WM did not show any significant difference in the incidence of adverse events compared to WM alone. However, the funnel plot suggests a potential publication bias.
The included studies had methodological flaws, especially those with a high risk of selection and performance bias. Most studies did not report proper allocation concealment or outcome assessment blinding procedures. In addition, no studies blinded the participants and personnel, suggesting potential performance bias. None of the studies were evaluated as having a low risk of bias in any of the seven bias items. In addition, the QoE evaluated by GRADE was often “moderate,” but there were still a number of studies evaluated as “low” or “very low.” No studies were rated as having high QoE. In particular, the QoE of TER, the most frequently reported outcome in the included studies, were all “very low” or “low.” This suggests that acupuncture combined with WM is likely to have potential therapeutic benefits in FD treatment, but the level of evidence is not high. Thus, interpretation of the findings requires caution.
Comparison With Previous Studies
The findings of this review can be compared with those of some previous systematic reviews. Zhou et al. reported that acupuncture significantly improved FD symptoms as a monotherapy or add-on therapy and improved FD-related QoL as monotherapy but had no significant effect on plasma motilin with borderline significance (six studies; standardized mean difference 0.67, 95% CI −0.07 to 1.42; I2 = 95%) (10). However, our review focuses on acupuncture as an add-on treatment and emphasizes that there was insufficient evidence for QoL improvement with acupuncture. In addition, according to the presents findings, acupuncture as an add-on treatment is associated with a significant increase in plasma motilin levels; however, this finding may be influenced by the results of studies published after the systematic review by Zhou et al. In an overview of systematic reviews performed by Ho et al. using network meta-analysis (NMA), it was concluded that the combination of manual acupuncture and clebopride was most effective in alleviating FD symptoms (11). In this NMA, other acupuncture types such as electroacupuncture or auricular acupuncture were not considered as add-on therapies (11). However, the subgroup analysis of our review showed that we should continue considering acupuncture types other than manual acupuncture as add-on therapies. Guo et al. reported that acupuncture and electroacupuncture potentially help improve FD symptoms and QoL (12), which is consistent the present review findings; in particular, this review focused on the therapeutic mechanisms of acupuncture and electroacupuncture for FD and suggested the regulation of gastric motility, gastric accommodation, mental status, gastrointestinal hormones, and central and autonomic functions as one of the underlying mechanisms (12), which supports the findings of our review. Finally, Mao et al. focused on electroacupuncture as a monotherapy for FD and reported that the therapeutic effect of electroacupuncture on FD is equivalent to that of WM on FD (13). As a monotherapy, acupuncture can be suggested as a treatment option for FD; however, as an add-on therapy, which was the scope of our study, it can be considered as a promising treatment option for FD. The implementation of treatment options may be selected based on factors such as resources in clinical settings, symptoms of patients, values and preferences of patients, clinical evidence for the effectiveness and safety of treatment options, and cost-effectiveness, if possible. Given the above findings, further studies comparing acupuncture as a monotherapy and acupuncture combined with conventional medication for FD in FD treatment may be helpful in the practical application of acupuncture-based treatment options.
Clinical Implications
FD is a common functional gastrointestinal disorder that causes impaired QoL in patients and socioeconomic burden (5, 6). Acupuncture, a non-pharmacological CAM treatment, has been reported to be effective and safe for the treatment of FD (10–13), and has the potential to improve the management of FD in combination with conventional WM. Acupuncture is also clinically useful because it is non-pharmacological and free of potential interactions with conventional WM.
Despite the studies not providing the best evidence, this review's findings generally suggest that acupuncture improves the symptoms of FD and some FD-related biomarkers when combined with conventional WM. In particular, in terms of TER, which has been reported frequently, acupuncture showed significant benefits in combination with prokinetics or acid suppressants. In addition, the therapeutic benefits of TER were maintained regardless of the type of acupuncture, namely manual acupuncture, electroacupuncture, and auricular acupuncture. The acupuncture method for FD showed inconsistency between the included studies, but ST36, PC6, and CV12 were the most frequently used acupoints, and De qi was generally performed. The treatment duration and number of sessions were the most common at four and 28 sessions, respectively. This was consistent with the results of the most frequently chosen acupoints in FD treatment in a recent survey by clinicians (47). In the acupuncture procedure, although stimulation for several acupoints produces the therapeutic effects in combination, the mechanism by which each acupoint stimulation contributes to the improvement of dyspepsia has also been reported. For example, improvement in dyspepsia symptoms associated with ST36 stimulation may be related to vagal and gastrointestinal hormonal mechanisms and inhibition of excessive autophagy of interstitial cells of Cajal (48, 49). There is clinical evidence that a combination of ST36 and PC6 stimulation improves gastric accommodation and gastric emptying in patients with FD (50, 51). One scholar also asserted that antinociceptive effects could be expected with ST36 and PC6 stimulation, while the inhibitory effect of gastric acid secretion through the somatosympathetic pathway can be expected with CV12 stimulation (52). In acupuncture, FD is usually treated using several acupoints. If the mechanism of stimulation of each acupoint is elucidated in more detail, it is expected that more effective treatment strategies can be established according to the subtype of FD and the predominant symptoms of patients.
Strengths and Limitations
This systematic review evaluated the role of acupuncture as an add-on therapy for FD treatment in terms of EBM. A subgroup analysis according to conventional WM and acupuncture type was conducted to resolve potential heterogeneity. The QoE of the findings of this review was strictly evaluated using the GRADE approach.
However, the following limitations should be considered. First, all studies included in this systematic review were conducted in China, and their risk of bias was not low enough to be reliable. This suggests that the findings could be challenging to generalize, particularly in countries other than China. As a country that has been using acupuncture for a long time, the Chinese may have a more favorable attitude toward acupuncture than other ethnicities, potentially contributing to placebo effects. In particular, the studies included in this review may be more susceptible to this problem because they are flawed in terms of performance bias. This suggests that further research using sham acupuncture is required. Moreover, only studies conducted in China were included, which could be a source of potential publication bias (53). Therefore, further studies evaluating the effectiveness and safety of add-on acupuncture in FD treatment should be conducted in countries other than China. Second, the diversity of the acupuncture methods used in the included studies may have contributed to the heterogeneity of the findings. Although CAM treatment, such as acupuncture, may emphasize customized treatment according to the individual patient's characteristics, developing a basic treatment standard that allows for some modifications could improve the quality of clinical evidence in this field. Third, the outcome most often reported in the included studies was TER. Although the gold standard evaluation tool for FD has not been determined, it is necessary to use a validated evaluation scale for gastrointestinal symptoms. In addition, although FD is a condition that seriously impairs the QoL of patients, only a small number of the included studies evaluated the effect of acupuncture on QoL. Therefore, further studies should be conducted that evaluate patients' QoL. Finally, other outcomes that can be objectively evaluated, such as FD-related biomarkers or detection of gastric myoelectrical activity using electrogastrography, could also be undertaken.
Conclusion
In combination with conventional WM, acupuncture may be able to improve the symptoms of patients with FD. However, the methodological quality of the included studies and the QoE of the main findings were generally low. In addition, all of the included studies were conducted in China, which makes generalization of the findings difficult and infers potential publication bias. Therefore, RCTs with a rigorous methodology, including sham acupuncture and multiethnic subjects, should be performed.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.
Author Contributions
The study was conceptualized by S-JK and J-WP. The study search, study screening, data extraction, and quality assessment were conducted by C-YK and BL. The manuscript was drafted by C-YK and BL and revised by S-JK, J-WP, JY, and JC. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Glossary
Abbreviations
- CAM
complementary and alternative medicine
- CI
confidence interval
- EBM
evidence-based medicine
- EPS
epigastric pain syndrome
- FD
functional dyspepsia
- GRADE
Grading of Recommendations, Assessment, Development, and Evaluation
- MD
mean difference
- NDI
Nepean dyspepsia index
- PDS
postprandial distress syndrome
- PRISMA
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
- QoE
quality of evidence
- QoL
quality of life
- RCT
randomized controlled trial
- RR
risk ratio
- SF-36
36-item short-form health survey
- TER
total effective rate
- WM
Western medication
- 5-HT
5-Hydroxytryptamine.
Footnotes
Funding. This research was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (grant number: HI20C1405).
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2021.682783/full#supplementary-material
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author/s.