Abstract | OBJECTIVE: METHOD: We recruited 60 patients into the study. All subjects were randomly allocated into 3 groups. Group 1 received 0.9% sodium chloride (saline group), group 2 received 0.25% bupivacaine ( bupivacaine group) and group 3 received 2% lidocaine ( lidocaine group), infiltrated around each tonsil. Pain was evaluated with McGrath's face scale. RESULT: The postoperative pain scores at 2 and 6 hours were similar among the groups (P>0.05). The pain scores in the bupivacaine group were lower than those in the saline group at 12 h (P<0.05). The pain scores in the bupivacaine and lidocaine groups were significantly lower than those in the saline group from 18 to 24 hours until day 7 (P<0.05). There was no difference between the bupivacaine and lidocaine groups (P> 0.05). CONCLUSION:
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Authors | Xin Zhang, Yu Xu, Peizhong Li |
Journal | Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery
(Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi)
Vol. 28
Issue 3
Pg. 148-50
(Feb 2014)
ISSN: 2096-7993 [Print] China |
PMID | 24826447
(Publication Type: English Abstract, Journal Article, Randomized Controlled Trial)
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Chemical References |
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Topics |
- Analgesia
(methods)
- Bupivacaine
- Child
- Child, Preschool
- Female
- Humans
- Lidocaine
- Male
- Pain Measurement
- Pain, Postoperative
(prevention & control)
- Snoring
(surgery)
- Tonsillectomy
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