Detail information
ID ENCL000069
Year 2013
Surgery Cardiac Surgical Procedures
Acupoint
Acupoint Code
Hegu LI4
Yanglao SI6
Kunlun BL60
Yintang GV29
Baihui GV20
Erdian
Shuanijue
Touwei ST8
Neiguan PC6
Liangqiu ST34
Xuehai SP10
Neiting ST44
Taixi KI3
Xingjian LR2
Side
Description Hegu;Yanglao;Kunlun;Yintang;Baihui;Erdian/Shuanijue;Touwei;Neiguan;Liangqiu;Xuehai;Neiting;Taixi;Xingjian
Experimental Description We performed a prospective, randomized, controlled, observer-blinded, three-armed clinical trial with 100 patients. Group 1 (n = 33) and Group 2 (n = 34) received one 20 min session of standardized acupuncture treatment with two different sets of acupoints. Group 3 (n = 33) served as standard analgesia control without additional intervention.
Sample Count 100
Control
Std
Group 3(standard analgesia control without additional intervention)(n=33)
Experiment standardized acupuncture treatment with two different sets of acupoints Group 1 (n=33);Group 2 (n=34)
Indicator Forced vital capacity(FVC) Percentile pain reduction(PPR)
Auxiliary Medication Patients were included in the study if they had undergone conventional on-bypass surgery via median sternotomy and reported pain during deep inspiration with an intensity of at least 3 on a 1-10 numeric rating scale under standard analgesia with tNSARs and high-dose opioids.
Stimulation Method MS
Induction Method
Electroacupuncture Instrument Model Manufacturer Frequency Waveform Strength Induction Time
- - - - - 20 min

Acupuncture_Needle Needle_Manufacturer Needle_Depth
0.25×40 mm - -

Description Group 1 and 2 received one single 20 min session of standardized verum acupuncture treatment in addition to standard analgesia. Acupuncture was performed on 12 acupoints using sterile 0.25 × 40 mm surgical stainless steel needles.
Anesthesia Method
AAA
Clinical Trial Type random
Contraindications Intolerance to acupuncture treatment or sudden worsening of the physical condition
Effector Primary endpoint analysis revealed a statistically significant analgesic effect for both acupuncture treatments. Group 1 showed a mean percentile pain reduction (PPR) of 18% (SD 19, P < 0.001). Group 2 yielded a mean PPR of 71% (SD 13, P < 0.001). In Group 1, acupuncture resulted in a mean forced vital capacity (FVC) increase of 30 cm3 (SD 73) without statistical significance (P = 0.303). In Group 2, posttreatment FVC showed a significant increase of 306 cm3 (SD 215, P < 0.001).
Literature
PMID 23573118
Title Objectifying acupuncture effects by lung function and numeric rating scale in patients undergoing heart surgery.
Abstract Rationale. Poststernotomy pain and impaired breathing are common clinical problems in early postoperative care following heart surgery. Insufficiently treated pain increases the risk of pulmonary complications. High-dose opioids are used for pain management, but they may cause side effects such as respiratory depression. Study Design. We performed a prospective, randomized, controlled, observer-blinded, three-armed clinical trial with 100 patients. Group 1 (n = 33) and Group 2 (n = 34) received one 20 min session of standardized acupuncture treatment with two different sets of acupoints. Group 3 (n = 33) served as standard analgesia control without additional intervention. Results. Primary endpoint analysis revealed a statistically significant analgesic effect for both acupuncture treatments. Group 1 showed a mean percentile pain reduction (PPR) of 18% (SD 19, P < 0.001). Group 2 yielded a mean PPR of 71% (SD 13, P < 0.001). In Group 1, acupuncture resulted in a mean forced vital capacity (FVC) increase of 30 cm(3) (SD 73) without statistical significance (P = 0.303). In Group 2, posttreatment FVC showed a significant increase of 306 cm(3) (SD 215, P < 0.001). Conclusion. Acupuncture revealed specific analgesic effects after sternotomy. Objective measurement of poststernotomy pain via lung function test was possible."
Souce Evid Based Complement Alternat Med. 2013;2013:219817. doi: 10.1155/2013/219817. Epub 2013 Mar 14.