Comparing the different oxycodone doses of prevent oxycodone for prevention of preventing fentanyl-induced cough during induction of general anaesthesia

被引:5
作者
Dai, Bizhao [1 ]
Cao, Xiaofei [2 ]
机构
[1] Xuzhou Med Univ, Peoples Hosp 1, Dept Anesthesiol, Xuzhou, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Anesthesiol, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
关键词
INTRAVENOUS DEXMEDETOMIDINE-MIDAZOLAM; LIDOCAINE;
D O I
10.1111/ijcp.13642
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Fentanyl-induced cough (FIC) usually occurs after the intravenous administration of fentanyl during general anaesthesia induction. It is a transient condition depending on the fentanyl administration dose and injection speed. Oxycodone can also prevent FIC because it has been proven to treat coughing. This study aimed to evaluate the efficacy of different oxycodone doses to prevent FIC during general anaesthesia induction. Methods In a double-blind randomised controlled trial, 210 adult patients who were undergoing elective surgery, classified as American Society of Anaesthesiologists physical status I-II, and aged 20-65 years were randomly assigned into five equally sized groups: Sham group, Group ROMAN NUMERAL ONE, Group II, Group III and Group IV. Groups ROMAN NUMERAL ONE-IV were each intravenously injected with oxycodone 0.025, 0.05, 0.075 and 0.100 mg/kg, while an equal volume of normal saline was given instead of oxycodone in the Sham group. Five minutes later, fentanyl 3 mu g/kg was intravenously injected within 5 seconds, then, 2 minutes later the other drugs were administered for general anaesthesia induction. The occurrence and severity of coughing were observed within 2 minutes of the fentanyl injection. Vital signs and intensities of coughing were recorded and analysed. Results Coughing incidences were each 57.1, 50, 42.8, 33.3 and 21.4% in the Sham group and Groups ROMAN NUMERAL ONE-IV. Significant differences were found in the incidences of coughing between the Sham group and Groups III-IV. No significant differences in FIC incidences have been detected between the Sham group and Groups ROMAN NUMERAL ONE-II. However, no significant difference in FIC incidence existed between Group III and Group IV. Cough severities in Groups III and IV were significantly lower than in Groups ROMAN NUMERAL ONE and II (P < .05). No significant differences existed in the hypotension or severe bradycardia incidences during anaesthesia induction among the five groups (P > .05). Conclusion Oxycodone 0.075 mg/kg provided more effective FIC prevention during general anaesthesia induction.
引用
收藏
页数:5
相关论文
共 23 条
[1]  
Du BX, 2014, INT J CLIN EXP MED, V7, P826
[2]  
Generali Joyce A, 2014, Hosp Pharm, V49, P23, DOI 10.1310/hpj4901-23
[3]  
Golmohammadi Mitra, 2018, Electron Physician, V10, P6877, DOI 10.19082/6877
[4]   Role of pre-emptive Huff's manoeuvre and acupressure in reducing the incidence of fentanyl induced cough; a risk factor for postoperative nausea vomiting in female patients: A prospective randomised controlled study [J].
Gupta, Parul ;
Jindal, Parul ;
Kumar, Nidhi .
INDIAN JOURNAL OF ANAESTHESIA, 2019, 63 (10) :834-840
[5]   Incidence of fentanyl-induced cough and injection speed [J].
Hung, K-C .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 2009, 53 (09) :1227-1227
[6]  
Iida Kazumi, 2009, Masui, V58, P962
[7]   Fentanyl-induced cough during general anesthesia: a different perspective [J].
Lawlor, D. A. ;
Chaudhri, R. ;
Shannon, J. .
IRISH JOURNAL OF MEDICAL SCIENCE, 2013, 182 (02) :307-307
[8]   Effects of oxycodone and diazepam alone and in combination on operant nociception [J].
Leonard, Michael Z. ;
Kangas, Brian D. .
BEHAVIOURAL PHARMACOLOGY, 2020, 31 (2-3) :168-173
[9]   Fentanyl-induced cough is a risk factor for postoperative nausea and vomiting [J].
Li, C. C. ;
Chen, S. S. ;
Huang, C. H. ;
Chien, K. L. ;
Yang, H. J. ;
Fan, S. Z. ;
Leighton, B. L. ;
Chen, L. K. .
BRITISH JOURNAL OF ANAESTHESIA, 2015, 115 (03) :444-448
[10]   Dezocine prevents sufentanil-induced cough during general anesthesia induction: A randomized controlled trial [J].
Liu, Xue-Sheng ;
Xu, Guang-Hong ;
Shen, Qi-Ying ;
Zhao, Qing ;
Cheng, Xin-Qi ;
Zhang, Jian ;
Gu, Er-Wei .
PHARMACOLOGICAL REPORTS, 2015, 67 (01) :52-55