Comparison of surgical field visibility during propofol or desflurane anesthesia for middle ear microsurgery

被引:5
|
作者
Yuan, Xia [1 ]
Liu, Tingjie [1 ]
Hu, Chunbo [1 ]
Shen, Xia [1 ]
机构
[1] Fudan Univ, Dept Anesthesiol, Eye Ear Nose & Throat Hosp, 83 Fenyang Rd, Shanghai 200031, Peoples R China
来源
BMC ANESTHESIOLOGY | 2019年 / 19卷
关键词
Anesthetics; inhalation; Desflurane; intravenous; Propofol; Hypotension; controlled; Surgery; Otolaryngology; CONTROLLED HYPOTENSION; REMIFENTANIL; NITROPRUSSIDE; SEVOFLURANE; RECOVERY; ESMOLOL; AGE;
D O I
10.1186/s12871-019-0759-x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BackgroundTo compare surgical field visibility between patients given propofol/remifentanil (PR) or desflurane/remifentanil (DR) anesthesia.MethodsA total of 80 adult patients undergoing middle ear microsurgery due to cholesteatoma otitis media with American Society of Anesthesiologists physical status I and II were randomly assigned to the PR or DR groups. The depth of anesthesia was titrated to maintain a Bispectral index (BIS) between 40 and 50. Remifentanil was titrated to maintain the mean blood pressure within 30% change of the pre-induction value. Surgical field visibility was rated at several timepoints by the surgeons using the Boezaart scores.ResultsAverage Boezaart scores for surgical field visibility at different time points were<2 in both PR and DR groups. Surgical field visibility score was lower in the PR group than in the DR group. Requirement for remifentanil was higher in the PR group (850 (488/1330) g) than in the DR group (258 (143/399) g, P<0.0001). The site effect concentration of remifentanil was higher in the PR group (3.6(2.8/5.0)ng/ml) than in the DR group (1.7 (1.0/1.6) ng/ml, P<0.0001). Hemodynamic profile (i.e., heart rate and mean blood pressure) was similar between groups (P>0.05). Extubation time (PR group, 21min vs. DR group, 19min; P=0.199) and post-anesthesia care unit time (PR group, 37min vs. DR group, 34min; P=0.324) were comparable between groups.ConclusionAlthough PR anesthesia resulted in lower surgical field visibility scores than DR anesthesia, both groups had scores <2, meaning no clinical differences between the two groups. DR provided acceptable operative conditions as well, albeit more remifentanil consumption was noted in the DR group.Trial registration p id=Par5 China Clinical Research Information Service, ChiCTR-1,800,015,537. Registered 5 April 2018. Date of enrolment of the first participant to the trial: 2 May 2018.
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页数:6
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