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透明质酸酶对局部麻醉的影响:一项前瞻性、随机、对照、双盲研究。

The effects of hyaluronidase on local anesthesia: a prospective, randomized, controlled, double-blind study.

作者信息

Courtiss E H, Ransil B J, Russo J

机构信息

Newton-Wellesley Hospital, Boston, Mass, USA.

出版信息

Plast Reconstr Surg. 1995 Apr;95(5):876-83.

PMID:7708872
Abstract

Hyaluronidase, an enzyme that breaks down intercellular cement, has been advocated as an additive to local anesthetics because it allows injected solutions to spread and penetrate tissues. Because epinephrine is commonly used in conjunction with local anesthetics, the combined effects of both hyaluronidase and epinephrine were studied in a prospective, controlled, double-blind manner. The forearms of volunteers ranging in number from 15 to 23 were injected with 0.5 ml of lidocaine to which graded doses of hyaluronidase and epinephrine had been added. At various intervals after injection, the areas of anesthesia were measured. From these data, the time to reach peak area of anesthesia (onset), the size of the peak area of anesthesia, and the time until disappearance of anesthesia (duration) were computed and analyzed. We found that epinephrine has a more profound effect on the onset, area, and duration of anesthesia than hyaluronidase. Epinephrine delayed the time to reach peak area of anesthesia (onset) relative to lidocaine alone more than hyaluronidase (0.28 h versus 0.04 h). When both agents were used together, the effect was subtractive (0.28-0.04 = 0.24 h, compared with 0.22 h observed). This suggests a negative interaction (inhibition) because hyaluronidase decreased the epinephrine effect by 21 percent. Concerning the size of peak area of anesthesia, epinephrine increased the area relative to lidocaine alone more than hyaluronidase (626 versus 221 mm2). When both agents were used together, the effect was additive (626 + 221 = 847 mm2, compared with 848 mm2 observed). This suggests that the two agents acted independently of each other in relation to area of anesthesia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

透明质酸酶是一种能够分解细胞间黏合剂的酶,它被提倡用作局部麻醉剂的添加剂,因为它能使注射的溶液在组织中扩散和渗透。由于肾上腺素通常与局部麻醉剂联合使用,因此以前瞻性、对照、双盲的方式研究了透明质酸酶和肾上腺素的联合作用。给15至23名志愿者的前臂注射0.5毫升利多卡因,并添加了不同剂量的透明质酸酶和肾上腺素。在注射后的不同时间间隔,测量麻醉区域。根据这些数据,计算并分析达到麻醉峰值区域的时间(起效时间)、麻醉峰值区域的大小以及麻醉消失的时间(持续时间)。我们发现,肾上腺素对麻醉的起效时间、区域和持续时间的影响比透明质酸酶更为显著。相对于单独使用利多卡因,肾上腺素使达到麻醉峰值区域的时间(起效时间)延迟得比透明质酸酶更多(分别为0.28小时和0.04小时)。当两种药物一起使用时,效果是相减的(0.28 - 0.04 = 0.24小时,而观察到的是0.22小时)。这表明存在负相互作用(抑制),因为透明质酸酶使肾上腺素的效果降低了21%。关于麻醉峰值区域的大小,相对于单独使用利多卡因,肾上腺素使该区域增大得比透明质酸酶更多(分别为626平方毫米和221平方毫米)。当两种药物一起使用时,效果是相加的(626 + 221 = 847平方毫米,而观察到的是848平方毫米)。这表明在麻醉区域方面,这两种药物相互独立起作用。(摘要截选至250字)

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