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. 2014 May 12;2014:804746. doi: 10.1155/2014/804746

Table 2.

Characteristics of the included studies: chemotherapy-induced nausea and vomiting (CINV).

Author Sample size (M/F)
Cancer type
Intervention (n) Control (n) Outcome measures Result
Intervention Control
Liu et al. 2011 [24] 51 (27/24)  
Hematologic cancer
Promethazine (25 mg) injection at bilateral ST36 (n = 26) Metoclopramide (10 mg), IV  (n = 25) Responder rate (%)a 96.2%* 68%
Yang et al. 2011 [25] 96 (50/46)  
Various
Metoclopramide (10 mg) injection at bilateral ST36 (n = 50) 
0.5 h before chemotherapy, qd
Tropisetron (5 mg), IV (n = 46) 
0.5 h before chemotherapy, bid
Responder rate (%)b 78%* 52.1%
You et al. 2009 [26] 142 (0/142)  
Ovarian cancer
Vit. B6 (50 mg) injection and MA at bilateral PC6 (n = 46) 
qod
(1) Vit. B6 (50 mg), IM  (n = 46) 
bid 
(2) MA at bilateral PC6 (n = 45)  
qod
(A) Total number of emesis episodes in 21 days (mean, 95% CI)  
(B) Proportion of emesis free days in 21 days (%, mean, 95% CI)
(A) 5.9, 3.8–7.0**  
(B) 59%, 48–69**
(1) (A) 13.2, 9.4–15.0 (B) 21%, 12–28 
(2) (A) 10.6, 7.4–11.8 (B) 30%, 21–39
Chen 2007 [27] 258 (0/258)  
Ovarian cancer
Metoclopramide injection (n = 98) 
10 mg, at left PC6 and CV10, 15 min before chemotherapy 
10 mg, at right PC6 and CV 10 after chemotherapy
(1) Metoclopramide, IV (n = 74) 
20 mg each, before and after chemotherapy 
(2) Granisetron (3 mg), IV (n = 86) 
before chemotherapy
Responder rate (%)c 95%** (1) 40.5% 
(2) 96.5%
Hu 2003 [28] 123 (86/37)  
Various
Huangqi or Danggui (4 mL) injection, alternately at bilateral ST36, SP10, and BL23 (n = 71) 
qd
Batilol (50 mg), leucogen (20 mg) and Vit. B6 (20 mg), po (n = 52) 
tid
Responder rate (%)b 71.8%** 44.2%
Tao et al. 2000 [29] 480 (343/137)  
Various
Metoclopramide (5 mg) and diazepam (1.25 mg) injection alternately at bilateral PC6 and ST36 (n = 160) 
30 min before chemotherapy 
Metoclopramide (10 mg) after chemotherapy
(1) Metoclopramide (20 mg) and diazepam (5 mg), IV (n = 160) 
30 min before chemotherapy 
Metoclopramide (20 mg) after chemotherapy 
(2) Ondansetron, IV (n = 160) 
8 mg, 30 min before chemotherapy 
8 mg, after chemotherapy
Responder rate (%)d 98.8%** (1) 43.1% 
(2) 94.4%

AEs: adverse events; bid: twice a day; CI: confidence interval; h: hour(s); IM: intramuscular injection; IV: intravenous injection; MA: manual acupuncture; min: minute(s); NR: not reported; po: orally; qd: everyday; qod: every other day; Vit.: vitamin; WHO: World Health Organization.

Acupuncture point ST36 refers to 36th point of stomach meridian and extra points have different nomenclature (e.g., Ex-UE7 means 7th extra point in upper extremity).

aResponder rate: (number of participants with any improvement from the intervention/total number of participants) ∗ 100(%).

bResponder rate: (number of participants with WHO grade [30] 0 + 1/total number of participants) ∗ 100(%).

cResponder rate: (number of participants with less than four emesis episodes per day/total number of participants) ∗ 100(%).

dResponder rate: (number of participants with less than three emesis episodes per day/total number of participants)∗100 (%).

*P < 0.05; **P < 0.01.