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Acupuncture (PDQ®)
Patient VersionHealth Professional VersionLast Modified: 09/26/2008
Table 4. Clinical Studies of Acupuncture: Nausea and Vomitinga

Reference Citation(s)  Type of Study  Condition Treated  No. of Patients: Enrolled; Treated; Controlb  Strongest Benefit Reportedc  Concurrent Therapyd  Level of Evidence Scoree 
[20] RCT N/V related to high-dose chemotherapy for breast cancer 104; 37; 67 (sham EA or no EA) Less N/V in EA groupf Yes (prochlorperazine, lorazepam, and diphenhydramine) 1iiC
[18,24,25] RCT N/V from chemotherapy 10; 10 (EA); 10 sham EA (crossover study) Significantly less N/V than controlg Yes (metoclopramide) 1iiC
[21] RCT N/V from chemotherapy 100 (these patients were used more than once because of nature of crossover study); 27 surface electrodes; 11 rubber electrodes; 14 crossover study; 24 transcutaneous electrical stimulation 75% achieved considerable benefith Yes (metoclopramide, thiethylperazine, prochlorperazine, cyclizine, lorazepam, and steroid) 1iiC
[28] RCT N/V from chemotherapy 16 (the same 16 patients treated twice in a crossover study); 16 ondansetron plus transcutaneous electrical stimulation; 16 cross-over treatment ondansetron only Symptom-free patient days: 58.8%i Yes (ondansetron) 1iiC
[26] RCT N/V from chemotherapy 53 enrolled; 38 completed; 38 acupressure; 38 crossover to acupressure at a sham point 55% reduction in N/Vj Yes (antiemetics) 1iiC
[30] RCT N/V from high-dose chemotherapy 80; 41 acupuncture; 39 noninvasive placebo acupuncture Nonek Yes (ondansetron) 1iiC
[29] RCT N/V from chemotherapy 739; 233 bilateral acupressure bands and 234 transcutaneous electrical stimulation bands; 233 no bands; 39 not evaluable Less N/V in treatment groups than in controll Yes (5-HT3 receptor antagonist, prochlorperazine, and/or others) 1iiC
[32] RCT N/V from chemotherapy 36; 17 acupressure; 19 control Significantly lower N/V Yes (antiemetics) 1iiC
[19] Nonrandomized controlled trial N/V from chemotherapy 105; EA at P6 63%, complete relief, at least 8 h Yes (metoclopramide; prednisolone) 2C
[22,24] Consecutive case study N/V from chemotherapy 40; 40 acupressure 8–24 h relief Yes (not specified) 3iiC
[19] CT N/V from chemotherapy 43; 38 10 Hz EA; 5 sham (crossover subset) 8–10 h relief; 32 patients had complete relief Yes (antiemetics) 2C
[27] CT N/V from chemotherapy 18; 18 acupressure bands; 18 (crossover study—incorrect placement of acupressure bands) Effective for N/V Yes (antiemetics: prochlorperazine, maxalon, and domperidone suppository) 2C
[23] Nonconsecutive case series N/V from chemotherapy 26; 26 acupuncture; 51 historical controls—no acupuncture Mean no. of episodes and duration of N/V reduced Yes (metoclopramide,dexamethasone, and diphenhydramine) 3iiiC
[18] Nonconsecutive case series (pilot study) N/V from chemotherapy 15; 15 EA; none 12 patients—no symptoms for 8 h Yes (antiemetic: metoclopramide) 3iiiC
[33] Consecutive, uncontrolled case series N/V from chemotherapy mean no. of emesis 7–3 27; no controls 10 patients had complete response to EA and had no vomiting Yes (antiemetics: either ondansetron 8 mg or granisetron 3 mg) 3iiiC
[31] RCT N/V from moderate to highly emetogenic chemotherapy 160; 96; 54 Decreased delayed N/V for acupressure Yes; (anthracycline and cyclophosphamide and an antiemetic) 1iiC

CT = controlled trial; EA = electroacupuncture; h = hour; No. = number; N/V = nausea and vomiting; RCT = randomized controlled trial.
aSee text and the NCI Dictionary for additional information and definition of terms.
bNumber of patients treated plus number of patients control may not equal number of patients enrolled; number of patients enrolled equals number of patients initially considered by the researcher who conducted a study; number of patients treated equals number of enrolled patients who were given the treatment being studied AND for whom results were reported; historical control subjects are not included in number of patients enrolled.
cStrongest evidence reported that the treatment under study has activity or improves the well-being of cancer patients.
dConcurrent therapy for symptoms treated (not cancer).
eFor information about levels of evidence analysis and an explanation of the level of evidence scores, see Levels of Evidence for Human Studies of Cancer Complementary and Alternative Medicine.
f P < .001, low-frequency EA at classical antiemetic acupuncture points daily versus minimal needling at control points with sham EA versus no adjunct needling.
g P < .001, EA versus sham EA.
h P < .001, surface electrodes versus rubber electrodes.
i P < .00059.
j P < .02, acupressure versus acupressure at a sham point.
k P < .05, acupuncture versus noninvasive placebo acupuncture.
l P < .05, acupressure and acustimulation wrist bands versus no treatment.

References

  1. Dundee JW, Ghaly RG, Fitzpatrick KT, et al.: Acupuncture prophylaxis of cancer chemotherapy-induced sickness. J R Soc Med 82 (5): 268-71, 1989.  [PUBMED Abstract]

  2. Dundee JW, Ghaly RG, Fitzpatrick KT, et al.: Optimising antiemesis in cancer chemotherapy. Br Med J (Clin Res Ed) 294 (6565): 179, 1987.  [PUBMED Abstract]

  3. Shen J, Wenger N, Glaspy J, et al.: Electroacupuncture for control of myeloablative chemotherapy-induced emesis: A randomized controlled trial. JAMA 284 (21): 2755-61, 2000.  [PUBMED Abstract]

  4. Dundee JW, Yang J, McMillan C: Non-invasive stimulation of the P6 (Neiguan) antiemetic acupuncture point in cancer chemotherapy. J R Soc Med 84 (4): 210-2, 1991.  [PUBMED Abstract]

  5. Dundee JW, Yang J: Prolongation of the antiemetic action of P6 acupuncture by acupressure in patients having cancer chemotherapy. J R Soc Med 83 (6): 360-2, 1990.  [PUBMED Abstract]

  6. Aglietti L, Roila F, Tonato M, et al.: A pilot study of metoclopramide, dexamethasone, diphenhydramine and acupuncture in women treated with cisplatin. Cancer Chemother Pharmacol 26 (3): 239-40, 1990.  [PUBMED Abstract]

  7. Dundee JW, McMillan CM: Clinical uses of P6 acupuncture antiemesis. Acupunct Electrother Res 15 (3-4): 211-5, 1990.  [PUBMED Abstract]

  8. Dundee JW, Ghaly RG, Fitzpatrick KT, et al.: Acupuncture to prevent cisplatin-associated vomiting. Lancet 1 (8541): 1083, 1987.  [PUBMED Abstract]

  9. Price H, Lewith G, Williams C: Acupressure as an antiemetic in cancer chemotherapy. Complementary Medical Research 5 (2): 93-4. 

  10. Stannard D: Pressure prevents nausea. Nurs Times 85 (4): 33-4, 1989 Jan 25-31.  [PUBMED Abstract]

  11. McMillan C, Dundee JW, Abram WP: Enhancement of the antiemetic action of ondansetron by transcutaneous electrical stimulation of the P6 antiemetic point, in patients having highly emetic cytotoxic drugs. Br J Cancer 64 (5): 971-2, 1991.  [PUBMED Abstract]

  12. Roscoe JA, Morrow GR, Hickok JT, et al.: The efficacy of acupressure and acustimulation wrist bands for the relief of chemotherapy-induced nausea and vomiting. A University of Rochester Cancer Center Community Clinical Oncology Program multicenter study. J Pain Symptom Manage 26 (2): 731-42, 2003.  [PUBMED Abstract]

  13. Streitberger K, Friedrich-Rust M, Bardenheuer H, et al.: Effect of acupuncture compared with placebo-acupuncture at P6 as additional antiemetic prophylaxis in high-dose chemotherapy and autologous peripheral blood stem cell transplantation: a randomized controlled single-blind trial. Clin Cancer Res 9 (7): 2538-44, 2003.  [PUBMED Abstract]

  14. Dibble SL, Luce J, Cooper BA, et al.: Acupressure for chemotherapy-induced nausea and vomiting: a randomized clinical trial. Oncol Nurs Forum 34 (4): 813-20, 2007.  [PUBMED Abstract]

  15. Molassiotis A, Helin AM, Dabbour R, et al.: The effects of P6 acupressure in the prophylaxis of chemotherapy-related nausea and vomiting in breast cancer patients. Complement Ther Med 15 (1): 3-12, 2007.  [PUBMED Abstract]

  16. Choo SP, Kong KH, Lim WT, et al.: Electroacupuncture for refractory acute emesis caused by chemotherapy. J Altern Complement Med 12 (10): 963-9, 2006.  [PUBMED Abstract]


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