Acupuncture is a method of producing analgesia or altering the function of a body system by inserting fine, wire-thin needles (about the diameter of a strand of hair) into acupoints along a specific meridian (meridians are channels in the body that transport energy) on the body. The needles are twirled or energized electronically or are warmed and left in place for approximately 20–30 minutes. The acupuncture point P6 is most commonly used for treatment of nausea and vomiting. Acupuncture has been evaluated in anxiety, chemotherapy-induced nausea and vomiting, dyspnea, pain, hot flashes, depression, lymphedema, sleep-wake disturbances, peripheral neuropathy, and fatigue.
Effectiveness Not Established
Chao, L.F., Zhang, A.L., Liu, H.E., Cheng, M.H., Lam, H.B., & Lo, S.K. (2009). The efficacy of acupoint stimulation for the management of therapy-related adverse events in patients with breast cancer: A systematic review. Breast Cancer Research and Treatment, 118, 255–267.doi: 10.1007/s10549-009-0533-8
To scrutinize the evidence of using acupoint stimulation (APS) by any modality on managing adverse events related to anticancer therapies in patients with breast cancer
English databases searched were PubMed, Cochrane library, Embase, the Cumulative Index to Nursing and Allied Health, and PsycINFO.
Chinese databases searched were CNKI, CEPS, and WanFang as well as manual searching.
Search keywords were medical terms of breast cancer (e.g., breast neoplasm, breast carcinoma, breast tumor) combined separately with at least one of the following: acupuncture, acupressure, auricular acupuncture, ear acupuncture, acupuncture points, electroacupuncture, acupoint, transcutaneous electric nerve stimulation, moxibustion.
Studies were included if they
- Were in English or Chinese language.
- Reported on adults diagnosed with breast cancer at any stage and undergoing treatments such as surgery, radiotherapy, chemotherapy, hormonal therapy, or palliative treatment and experiencing treatment-induced adverse events.
- Utilized an intervention that involved stimulation of acupuncture points by any modality.
- Had at least one clinically related outcome variable, as well as condition-specific outcomes or generic health status outcomes.
Studies were excluded if they were
- Animal studies.
- Case reports and anecdotal evidence.
- Qualitative studies or descriptive surveys.
- Reports available only in abstract form.
- Trials that included diagnosis other than breast cancer unless separate data was available for the breast cancer group.
Initial review involved 843 titles and abstracts and 51 full-text articles. Of those, 26 studies were included in the report.
Study evaluation began with two independent reviewers using a modified Jadad scale, assessing 3 aspects: randomization procedure (2 points); dropout and withdrawal discussion (1 point); and blinding (2 points). Studies were classified as high quality if they attained a score of 3 or higher.
Evaluated literature included 18 randomized controlled trials (RCTs) and eight controlled clinical trials published between 1999 and 2008. Nine trials included conventional acupuncture, 6 included electroacupuncture, 5 included drug injection in acupoints, 3 included self-acupressure, and 3 included acupoint stimulation by wristbands or acumagnet. Eighteen were in English, and 8 were in Chinese.
- The total sample size was 1,548.
- Age range across across studies was 28–76 years.
- Five studies reported the participant’s body mass index, which ranged from 23.1 to 28.8.
- Information on participants’ education, background of acupuncturists, symptom distress before management, and measurement tool reliability was reported in too few studies to provide a meaningful summary.
Nine of the 26 studies were rated as high quality. Adverse effects (outcomes) of the APS included vasomotor syndrome, chemotherapy-induced nausea and vomiting (CINV), post-mastectomy pain, joint symptoms, lymphedema, leukopenia, and adverse events.
Eleven studies investigated CINV and APS with acupoints P6 and ST36. Ten of the CINV studies reported APS significantly improved emesis caused by breast cancer therapy.
The most common outcome evaluated by APS in the studies was CINV. APS was noted to be effective in reducing acute emesis caused by breast cancer therapy. Authors reported that APS is beneficial in the management of CINV, especially in the acute phase.
Healthcare providers should consider using APS as an option for the management of CINV.
Collins, K.B., & Thomas, D.J. (2004). Acupuncture and acupressure for the management of chemotherapy-induced nausea and vomiting. Journal of the American Association of Nurse Practitioners, 16(2), 80-84.doi: 10.1111/j.1745-7599.2004.tb00376.x
To review existing research on the use of acupuncture and acupressure in the management of nausea and vomiting in order to provide nurses the information required to assist their patients receiving chemotherapy and experiencing chemotherapy-induced nausea and vomiting (CINV)
Databases searched were described as scientific and internet sources, Institutes of Health Consensus statement, and federal regulations.
Search keywords included acupuncture and acupressure in combination with chemotherapy-induced nausea and vomiting.
Numerous studies tested the effectiveness of acupressure, acupuncture, and the combination. Few focused on acupressure alone for managing CINV.
A total of five studies were found, representing a total of 409 patients.
Very few studies were found, but, overall, results indicated improvement in nausea and vomiting, supporting the use of acupressure and acupuncture of the treatment of CINV. Acupuncture and acupressure were found to be safe and effective for the relief of CINV in combination with current antiemetic drugs.
The sample sizes were small in the studies; therefore, determining applicability to various practice settings and populations is difficult.
Ezzo, J., Vickers, A., Richardson, M.A., Allen, C., Dibble, S.L., Issell, B., … Zhang, G. (2005). Acupuncture-point stimulation for chemotherapy-induced nausea and vomiting. Journal of Clinical Oncology, 23, 7188-7198.doi: 10.1200/JCO.2005.06.028
Database searched was MEDLINE (1966-Dec 2003).
Search keywords were acupuncture, alternative medicine, electroacupuncture, moxibustion, “injections, intramuscular”, “Medicine, Traditional Chinese”, acupressure, transcutaneous electrical nerve stimulation (TENS), and TENS. These were combined with nausea, vomiting, emesis, antiemetic therapy, and antineoplastic agents/adverse effects.
Studies were included in the review if they
- Were randomized.
- Involved patients receiving chemotherapy.
- Included an intervention that stimulated acupuncture points.
- Reported on nausea or vomiting as outcomes.
Studies were excluded from the review if they had a high possibility of bias.
In all, 14 studies were identified and reviewed.
In the nine studies that evaluated acute vomiting management via acupuncture-point stimulation, acute vomiting was reduced but nausea severity was not.
In the seven studies that assessed acute nausea via acupressure, acute nausea severity was reduced.
Three studies that evaluated delayed vomiting did not support the intervention.
In the five studies using acupuncture-point stimulation, the intervention did not reduce delayed vomiting.
The pooled results of 11 studies using acupuncture-point stimulation plus antiemetics for chemotherapy-induced nausea and vomiting (CINV) showed significant reduction in acute vomiting and marginal statistical significance for reducing acute nausea.
Electroacupuncture provided protective effects for acute vomiting, but acupuncture did not. Acupressure was effective for acute nausea in patients using “state-of-the-art” antiemetics. However, placebo effects may have influenced results.
Garcia, M. K., McQuade, J., Haddad, R., Patel, S., Lee, R., Yang, P., . . . Cohen, L. (2013). Systematic review of acupuncture in cancer care: a synthesis of the evidence. Journal of Clinical Oncology, 31, 952–960.doi: 10.1200/JCO.2012.43.5818
To evaluate the effectiveness of acupuncture for symptom control in patients with cancer.
Databases searched were MEDLINE, EMBASE, CINAHL, Cochrane Collaboration, Scopus, and PubMed through December 2011.
Search keywords were acupuncture, electroacupuncture, moxibustion, Chinese medicine, Asian medicine, and keywords that included cancer and cancer symptoms.
Studies were included in the review if they
- Were randomized, clinical trials (RCTs)
- Involved acupuncture with needle insertion
- Compared acupuncture to control, placebo, or sham acupuncture.
Studies were excluded from the review if they
- Compared two active acupuncture forms, acupressure, or other interventions similar to acupuncture that did not involve needle insertion
- Did not measure the effect of acupuncture on symptoms
- Were considered gray literature (i.e., not generally accessible).
In total, 3,494 references were retrieved and evaluated according to the Cochrane Handbook for Systematic Reviews of Interventions.
- The final number of studies included was 41.
- The authors did not provide the sample range across studies, total number of patients, disease types, or characteristics.
Studies addressed potential management of the following symptoms:
- Pain: Eleven RCTs met the criteria for analysis. No large trials reported positive results or were of good quality.
- Chemotherapy-Induced Nausea and Vomiting (CINV): Eleven RCTs met the criteria for analysis. One large study with a low risk of bias showed between-group effect sizes for acupuncture versus sham (0.80) and for acupuncture versus usual care (1.10).
- Fatigue: Three RCTs met the criteria for analysis. All had high risks of bias, and two had negative outcomes.
- Hot Flashes: Seven RCTs met the criteria for analysis. None had a low risk of bias.
- Anxiety or Depression: Five of the six RCTs analyzed showed positive results. All five had high risks of bias.
- Sleep: Three RCTs met the criteria for analysis, and all three reported positive outcomes and had high risks of bias.
The strongest evidence that the study produced showed that acupuncture may be effective for the management of CINV. The study did not show acupuncture to be efficacious in the treatment of other symptoms.
The studies included were of low quality.
Available evidence, which was limited, did not support the claim that acupuncture is effective in alleviating various adverse symptoms in adults with cancer. Additional research is needed to determine the efficacy. The findings of this analysis suggested that patients with uncontrolled CINV may be appropriate candidates for acupuncture referral. For the treatment of other symptoms, the efficacy is undetermined.
Mayer, D.J. (2000). Acupuncture: An evidence-based review of the clinical literature. Annual Review of Medicine, 51, 49-63.doi: 10.1146/annurev.med.51.1.49
MEDLINE was searched for the 14 medical conditions for which the National Institutes of Health Acupuncture Consensus Development Panel (NIHCDP) concluded acupuncture was effective or could be useful. The two conditions in which acupuncture was found to be effective are the treatment of chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea and vomiting. The remaining 12 conditions reviewed in the article were the effect of acupuncture on pain and the treatment of other conditions (e.g., addiction, stroke rehabilitation, and asthma).
Three of the studies reviewed examined the effect of P6 acupuncture on CINV. Although the chemotherapy agents were variable and various carcinomas were studied, strong evidence supported the use of acupuncture for greater antiemetic effect than antiemetics alone.
Evidence supports the use of acupuncture in the treatment of CINV and postoperative nausea and vomiting.
Miller, M., & Kearney, N. (2004). Chemotherapy-related nausea and vomiting—Past reflections, present practice and future management. European Journal of Cancer Care, 13(1), 71-81.doi: 10.1111/j.1365-2354.2004.00446.x
- Databases searched were MEDLINE and CINAHL (1990-2002).
- Search keywords were nausea, vomiting, chemotherapy and neoplasm, assessment, management, complementary therapies, pharmacological, and nonpharmacological.
- Studies were included in the review if they included primary research, literature reviews, opinion articles, and information leaflets/booklets.
- Studies were excluded if they involved anticipatory nausea and vomiting associated with chemotherapy, because the authors felt that symptoms with a psychological basis should be addressed in a separate paper.
- Nonpharmacologic management interventions were reviewed with the intention that they do not replace standard antiemetic therapies but, rather, are adjuncts to improve quality of life (QOL).
- Intervention articles were reviewed for progressive muscle relaxation, guided imagery, self-hypnosis, acupressure/acupuncture, transcutaneous electrical nerve stimulation, biofeedback, cognitive distraction, and music therapy.
Support for the use of nonpharmacologic interventions for the treatment of chemotherapy-induced nausea and vomiting (CINV) was weak.
Many studies were flawed because of small sample sizes and confounding variables (e.g., stage of disease, various chemotherapy regimens, culture, patient compliance).
Preliminary available evidence suggests positive benefits through nonpharmacologic techniques; however, larger randomized trials are needed to demonstrate the exact benefits, including economic.
Silva, D.R.F., dos Reis, P.E.D., Gomes, I.P., Funghetto, S.S., & Ponce de Leon, C.G.R.M. (2009). Non pharmacological interventions for chemotherapy induced nausea and vomits: Integrative review. Online Brazilian Journal of Nursing, 8(1).doi: 10.5935/1676-4285.20092098
To identify the evidence in scientific literature related to nonpharmacologic interventions for the treatment of chemotherapy-induced nausea and vomiting (CINV)
Databases searched were Cochrane, PubMed, Latin American and Caribbean Health Sciences Literature (LILACSO), and Brazilian Nursing Database (BDENF).
Search keywords were nausea, vomiting, chemotherapy, nursing care, cursing care protocols for cancer chemotherapy, and chemotherapy induced nausea and vomiting.
Studies were included in the review if they
- Addressed nonpharmacological interventions for nausea and vomiting.
- Were completed within the past 10 years (1998–2008).
- Were conducted in English or Spanish.
- An initial set of 111 articles were identified. Of these, 102 were related to pharmacological management and were eliminated. A final sample of nine studies was included in the review.
- The authors developed an instrument to analyze the literature related to method, journal type, and author.
- The articles were published in English (78%), Portuguese (11%), and Spanish (11%).
- The majority of the articles (67%) were written by physicians in collaboration with psychologists and pharmacists.
- Across the nine studies, a total sample of 1,635 patients were studied.
- The majority of studies involved the use acupuncture, acupressure, or electroacupuncture (5 trials and 1 meta-analysis).
- Studies involved patients receiving highly emetogenic chemotherapy or those with refractory CINV.
- One of the studies involved patient dietary education and adherence to antiemetic therapy in which patients reported a better sense of security with the provision of written information.
- One study, which had 16 participants, found hypnosis to be effective in reducing anticipatory CINV.
- One randomized, controlled trial of 62 patients using a yoga program showed no decrease in frequency or intensity of CINV with the intervention.
- Findings among studies of acupuncture and acupressure had mixed results, with most showing no significant difference in symptoms with the intervention.
- The meta-analysis showed a reduction in the proportion of patients with acute vomiting but not in the severity of nausea.
- Electrical stimulation did not improve results.
This review demonstrated no substantial effects among the interventions included. Findings regarding the use of acupuncture, acupressure, and electroacupuncture were mixed. Most studies using acupuncture and acupressure involved use of the p6 point on the wrist.
This review included a limited number of studies.
The evidence does not demonstrate significant effect of these interventions for CINV. However, these interventions may be useful as adjuncts to pharmacologic treatment. Nonpharmacologic interventions appear to be most effective in the prevention of acute vomiting rather than symptoms of nausea.
Research Evidence Summaries
Choo, S.P., Kong, K.H., Lim, W.T., Gao, F., Chua, K., & Leong, S.S. (2006). Electroacupuncture for refractory acute emesis caused by chemotherapy. The Journal of Alternative and Complementary Medicine, 12, 963-969.doi: 10.1089/acm.2006.12.963
To evaluate the use of electroacupuncture in preventing anthracycline-based chemotherapy-related nausea and vomiting (CINV) refractory to combination 5-HT3-antagonist and dexamethasone
Intervention Characteristics/Basic Study Process:
Patients received electroacupuncture in addition to standard antiemetic prophylaxis. Acupuncture was started 10 minutes prior to start of chemotherapy infusion and then continued for an additional 20 minutes. The P6 acupuncture point was used, a second needle was inserted at a different point, and electrical stimulation was delivered.
- The study consisted of 27 patients with breast cancer.
- All patients were receiving their second cycles of doxorubicin and cyclophosphamide; cyclophosphamide, doxorubicin, and prednisone; or doxorubicin only.
- Patients were defined as having refractory emesis (defined as vomiting three or more times, 24-48 hours after cycle one).
- Patients received standard antemetic prophylaxis.
This was a prospective trial.
- Patients completed a questionnaire assessing their attitudes toward acupuncture.
- Patients recorded frequency of vomiting in diaries.
- A trained doctor interviewed patients via telephone 24-48 hours after chemotherapy to grade nausea and vomiting using the National Cancer Institute Common Toxicity Criteria (NCI-CTC).
- Ten patients (37%) reported no vomiting after the second cycle of chemotherapy with the addition of electroacupuncture.
- The majority of patients (96%) reported significantly less nausea and vomiting, but one patient experienced increased vomiting after electroacupuncture.
- Overall, mean emetic episodes decreased from 7 to 3 after the intervention (p < 0.0001).
- NCI grade of vomiting decreased significantly (p = 0.0120).
- The number of patients reporting grade 3-4 vomiting dropped from 14 prior to the electroacupuncture to 5 after the electroacupuncture.
- NCI grade of nausea improved as well after the intervention (p < 0.0001).
- Most patients (93%) reported that they thought that electroacupuncture was an acceptable procedure and helpful in reducing emesis.
- All patients participated in the intervention group; no control group was provided.
- Two subjects complained of severe headaches after the electroacupuncture, lasting for several days; otherwise it was well-tolerated.
- The intervention was delivered by trained acupuncturists.
Gottschling, S., Reindl, T.K., Meyer, S., Berrang, J., Henze, G., Graeber, S., … Graf, N. (2008). Acupuncture to alleviate chemotherapy-induced nausea and vomiting in pediatric oncology—A randomized multicenter crossover pilot trial. Klinische Padiatrie, 220, 365–370.doi: 10.1055/s-0028-1086039
To evaluate the efficacy and acceptance of acupuncture as an additive antiemetic treatment during highly emetogenic chemotherapy (HEC) in pediatric patients with cancer
Intervention Characteristics/Basic Study Process:
Patients receiving chemotherapy were randomized to receive antiemetic medication plus acupuncture or antiemetic medication alone.
- Group 1 participants received acupuncture before chemotherapy, were offered acupuncture daily during chemotherapy, and received no acupuncture in their subsequent chemotherapy.
- Group 2 received treatments in the opposite order.
Acupuncture points were based on the acupuncturists’ decision, until the patient reported a “de Qi” sensation.
Antiemetic rescue medication, number of retching and vomiting episodes, and a short essay of the acupuncture experience were recorded.
- The sample consisted of 23 participants.
- The patients' ages ranged from 6-18 years with a mean of 13.6 years and standard deviation of 2.9 years.
- The sample was 56.5% female and 43.5% male.
- Diagnoses were Ewing sarcoma, rhabdomyosarcoma, osteosarcoma, undifferentiated sarcoma, and synovial sarcoma.
- Patients who had full control of chemotherapy-induced nausea and vomiting (CINV) without need for antiemetic rescue medication during the first chemotherapy course were excluded from the study.
This study was conducted in multiple inpatient settings in five German cancer centers.
This was a prospective, randomized, crossover clinical trial pilot study.
An open-form essay was used to document the subjective experience of acupuncture.
In evaluating chemotherapy courses, overall, no significant differences were found in retching or vomiting episodes. In evaluating differences between group 1 and group 2, no significant effect was found with dexamethasone (p = 0.145); however, the acupuncture group was associated with lower phenothiazine medication use (p = 0.001) and less retching and vomiting episodes (p = 0.01).
Acupuncture with baseline antiemetic medication was associated with less phenothiazine use and less retching and vomiting among children receiving HEC.
- The sample was small.
- The number of times that the children received acupuncture depended on individual patient requests and was not recorded.
- Acupuncture sessions did not follow a standard procedure of needle placement, and differences among acupuncturists may provide differing results.
- The methods for recording retching and vomiting episodes were not documented.
- Although one of the study aims was to evaluate acceptance of acupuncture, the authors did not specify how this was measured.
- The title suggests that the study evaluated nausea, but this was not discussed.
Acupuncture may provide some relief of retching or vomiting episodes associated with HEC, but the intervention should be used in combination with standard antiemetic treatment.
Melchart, D., Ihbe-Heffinger, A., Leps, B., von Schilling, C., & Linde, K. (2006). Acupuncture and acupressure for the prevention of chemotherapy-induced nausea: A randomised cross-over pilot study. Supportive Care in Cancer, 14, 878-882.doi: 10.1007/s00520-006-0028-7
To study the effectiveness of acupuncture and acupressure in reducing chemotherapy-induced nausea
Intervention Characteristics/Basic Study Process:
Patients were treated for one cycle of chemotherapy with acupuncture and acupressure at point P6 and for one cycle at a close sham point. Participants were randomized to acupuncture at P6 or at a close nonacupuncture point, and it was delivered by one of two physicians with training and experience in acupuncture. Participants wore acupressure bands for 72 hours at the same points on both arms and could wear them for an additional four days if needed. The bands were covered with a mull bandage to blind the staff. Participants completed diaries for seven days, documenting intensity (on a 0-6 rating scale), frequency, and duration of nausea and vomiting; additional antiemetics taken; and, on day 7, rate the effectiveness of side effects or impairment by acupuncture or acupressure. Patients completed the Morrow Assessment of Nausea and Emesis (MANE). Oncology staff checked that the diaries were completed accurately, standard antiemetics regimens were followed, and if any adverse reactions related to acupuncture occurred.
- The study consisted of 28 patients receiving moderately emetogenic chemotherapy (MEC) or highly emetogenic chemotherapy (HEC).
Patients were eligible for the study if they
- Were 18-75 years old.
- Were scheduled to receive MEC or HEC and standard antiemesis additional medication for rescue predefined for two cycles of chemotherapy.
- Had a Karnofsky index of 50%.
Patients were excluded from the study if they had
- Received chemotherapy within the last three months.
- Experienced anticipatory nausea and vomiting, cerebral metastasis, chronic ileus or subileus, or lymphedema in arms.
- Prior knowledge of acupressure points.
The study was conducted by the hematology and gastroenterology departments of a large university hospital in Germany.
This was a randomized, crossover pilot study.
- The MANE, shortened version, was used to measure nausea.
- Patients recorded the Intensity, frequency, and duration of nausea in patient diaries.
- No difference was found between combined acupuncture and acupressure at the P6 point and at the sham point.
- The study was stopped early because of recruitment problems and low incidence of nausea and vomiting in the sham group.
- Half of the participants reported an irradiating feeling, which is a sign of effective acupuncture.
- The sample size was small.
- Incidence of nausea was low in the sham group.
- No acupuncture control group was included.
- No control was included for type of cancer or chemotherapy regimen.
- The sham point may have been too close to P6 or the needle was too deep.
Shen, J., Wenger, N., Glaspy, J., Hays, R.D., Albert, P.S., Choi, C., & Shekelle, P.G. (2000). Electroacupuncture for control of myeloablative chemotherapy-induced emesis: A randomized controlled trial. JAMA, 284, 2755-2761.doi: 10.1001/jama.284.21.2755
To compare the effectiveness of electroacupuncture, minimal needling and mock electrical stimulation, or antiemetic medications alone in controlling emesis among patients undergoing highly emetogenic chemotherapy
Intervention Characteristics/Basic Study Process:
Participants were randomly assigned to one of three groups.
- Low-frequency electroacupuncture at classic antiemetic acupuncture points once daily for five days
- Minimal needling at control points with mock electrostimulation once daily for five days
- No adjunct needling
- The study consisted of 104 patients.
- The mean age was 46 years with a range of 18–62 years.
- All participants were women with histologically proven resected breast cancer undergoing myeloablative chemotherapy, Karnofsky scores of 80 or more (on a 0–100 scale), and life expectancy of at least six months. All participants were appropriate candidates for bone marrow transplantation.
- Patients were excluded from the study if they had brain metastases, cardiac pacemakers, life-threatening concurrent nonmalignant conditions, or active skin infections over the proposed treatment area.
Participants were from an inpatient unit at a tertiary hospital with a comprehensive cancer center. Patients were recruited from oncology clinics.
The study design was random, without stratification.
Investigators recorded the total number of emetic episodes during the five-day study period and the proportion of emesis-free days across the treatment groups.
- The electroacupuncture group had significantly fewer emesis episodes than the minimal needling group or the pharmacotherapy group alone (p < 0.001).
- The minimal needling group had significantly fewer episodes of emesis than the pharmacotherapy group alone (p = 0.01).
- The electroacupuncture group had a greater proportion of emesis-free days than the other groups (p < 0.001).
- No significant difference existed between the groups over days 6–14.
- Homogeneity of sample (standard chemotherapy and supportive care) helped to increase the precision in measurement; however, generalizability is limited.
- The study did not include 5-HT3 antagonists or corticosteroids.
- Training is required for electroacupuncture and minimal needling. The two investigators administered the procedure (training completed with 3–20 years of experience).
- Time commitment was 30 minutes a day for five days.
- This was a grant-funded project.
- The beneficial effect of electroacupuncture may be related to attention and clinician-patient interaction.
- Minimal needling led to a reduction in emesis, which could have been a placebo effect.
- Electroacupuncture has been thought to modulate serotonin, substance P, and endogenous opioids (similar to drugs that are available now).
Yeh, C.H., Chien, L.C., Chiang, Y.C., Lin, S.W., Huang, C.K., & Ren, D. (2012). Reduction in nausea and vomiting in children undergoing cancer chemotherapy by either appropriate or sham auricular acupuncture points with standard care. Journal of Alternative and Complementary Medicine, 18, 334-340.doi: 10.1089/acm.2011.0102
To report the findings of a feasibility and pilot study using auricular point acupressure for chemotherapy-induced nausea and vomiting (CINV) in a small group of children in Taiwain
- To examine the feasibility of recruiting children with cancer into a larger study
- To assess the feasibility of successfully completing each of the three protocols (standard care, auricular acupressure using sham auricular points [SAP], and auricular acupressure intervention [AAP])
- To analyze the longitudinal CINV data
- To determine the effect size for use in a future study of the efficacy of the intervention.
Intervention Characteristics/Basic Study Process:
Subjects were entered into the study for three successive rounds of chemotherapy. Round one was used as the standard care (SC) group and provided baseline data. Subjects were then randomized to one of two treatments: auricular acupressure intervention (AAP) or auricular acupressure using sham points (SAP). In the third cycle, participants were crossed over to the other treatment. Patients had a seed application prior to their round of chemotherapy and seeds remained for seven days. They were instructed to press their acupoints three times a day for three-minute periods. They also were instructed to press the seeds as soon as they felt nausea. Each participant received a booklet with a diary to keep track of stimulation times, sites stimulation, duration, and whether or not the child felt relief. Data was collected prior to chemotherapy administration and daily for seven days.
- The study consisted of 10 participants.
- Mean age of participants was 13.29 years (SD = 3.31).
- The smaple was 60% male and 40% female.
- Cancer diagnoses was 30% leukemia and 70% “other solid tumor."
This was a single site study conducted at a large children’s hospital in Taiwan.
Phase of Care and Clinical Applications:
All patients were pediatric and in active antitumor treatment.
This was a crossover, randomized design feasibility study.
The study used the Morrow Assessment of Nausea and Emetics (MANE), a 17-item, self-report questionnaire that measures occurrence, duration, and severity of nausea and vomiting. Demographic data was collection from medical chart review. Patients and their parents kept study booklets to record stimulation times, the number of acupoints stimulated, and stimulation duration at each of the acupoints, as well as whether or not the child felt relief from symptoms.
The authors were able to recruit 10 patients from a possible 22, all of whom were able to complete the entire study. Subjects kept the taped seeds on for 88% of the possible treatment days, suggesting the intervention is feasible and acceptable to children and their families.
The SC group reported more nausea overall than either the AAP or SAP groups, with 30% still reporting nausea on day 7. The SAP group reported the same nausea as the SC during the first two days, but declining nausea after day 2, with only 20% still reporting nausea on day 6. The AAP group reported less nausea on day 1, similar nausea on day 2, and no nausea by day 5. Although analysis did not show statistical significance, the authors described this trend as clinically significant.
Vomiting followed similar trends with most vomiting in the SC group, followed by SCA, and then AAP, but the difference was not statistically significant.
Because of the small sample size, comparison of the efficacy of the acupuncture intervention group and the sham acupuncture point group is not possible. The intervention group did demonstrate lower occurrence of acute and delayed nausea and shorter duration of nausea, but these results varied. A larger study using a similar design would be necessary to evaluate this question.
- The sample size was small sample with fewer than 30 patients.
- A risk of bias exists because of the sample characteristics and the lack of blinding.
- The measurement validity and reliability was questionable.
- The increased presence of research staff may have had a potential psychologic benefit, impacting results.
Acupuncture is an acceptable intervention to children and their parents for CINV. Potential clinical trends toward efficacy exist, but the small sample size limits the ability to draw definitive conclusions regarding its effectiveness.
National Comprehensive Cancer Network. (2011). NCCN Clinical Practice Guidelines in Oncology: Antiemesis [v.3.2011]. Retrieved from http://www.nccn.org/professionals/physician_gls/pdf/antiemesis.pdf
Purpose & Patient Population:
To provide guidance for treatment selection for the prevention and management of nausea and vomiting in adult patients with cancer receiving chemotherapy or radiation therapy
Type of Resource/Evidence-Based Process:
- Databases searched were not stated.
- Search keywords were not stated.
- This was a panel member consensus. The specific process was not described.
Results Provided in the Reference:
- These guidelines provide dose- and timing-specific recommendations for the prevention of acute and delayed emesis for chemotherapeutic regimens with high-, moderate- and low-emetic risk.
- These guidelines address the use of nonpharmacologic interventions related to anticipatory nausea, and they address the prevention and management of nausea and vomiting for multiday and oral chemotherapy regimens.
- These guidelines provide a table of classification of chemotherapy agents according to emetic risk.
Guidelines & Recommendations:
These guidelines stress the goal of prevention in all cases.
- For highly emetogenic chemotherapy (HEC) risk, use a combination of serotonin antagonist, steroid, neurokinin 1 (NK1) antagonist, and, potentially, lorazepam with or without H2 blocker, or proton pump inhibitor. Specific dosage and duration of treatment recommendations are provided for each medication that fits into these types.
For moderate emetic risk prevention, recommendation is
- Day 1, serotonin antagonist and steroid, with or without an NK1 antagonist and with or without lorazepam and H2 blocker or proton pump inhibitor. For both of these levels of emetic risk, drug dosages and frequency are the same. With moderate risk, all medications other than the serotonin antagonist are suggested as optional.
- Daily therapy is varied after day one in these recommendations.
- For low- and minimal-risk chemotherapy, dexamethasone, metoclopramide, or prochlorperazine with or without lorazepam and H2 blockers or proton pump inhibitors are recommended.
- The principle of breakthrough treatment is to add one agent from a different class of drugs to the current regimen. This might include antipsychotics, cannabinoids, phenothiazines, steroids. or other drugs.
- Behavioral therapies, acupuncture or acupressure, and either alprazolam or lorazepam beginning the night before treatment are suggested for prevention and treatment of anticipatory emesis.
- All evidence is considered strength of lower level with complete panel consensus for recommendations.
- These guidelines provide a very specific, but individualized, recipe for antiemetic drug combinations.
- Ongoing evaluation of effectiveness is emphasized, and management strategies for breakthrough emesis and prevention enhancement with subsequent chemotherapy cycles are provided.