Spinal anaesthesia for ambulatory arthroscopic surgery of the knee: a comparison of low-dose prilocaine and fentanyl with bupivacaine and fentanyl

被引:26
作者
Black, A. S. [1 ]
Newcombe, G. N. [1 ]
Plummer, J. L. [1 ]
McLeod, D. H. [1 ]
Martin, D. K. [2 ]
机构
[1] Flinders Med Ctr, Dept Anaesthesia & Pain Med, Bedford Pk, SA 5042, Australia
[2] Sportsmed SA, Stepney, SA 5069, Australia
关键词
ambulatory; prilocaine; spinal anaesthesia; TNS; TRANSIENT NEUROLOGIC SYMPTOMS; MINIDOSE LIDOCAINE-FENTANYL; INTRATHECAL FENTANYL; PROLONGING RECOVERY; PLAIN ARTICAINE; 5-PERCENT; PROCAINE; VOLUNTEERS; TRIAL;
D O I
10.1093/bja/aeq272
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background. Prospective data on the use of prilocaine for ambulatory spinal anaesthesia remain limited. We compared the behaviour and characteristics of subarachnoid block using prilocaine and fentanyl with that of bupivacaine and fentanyl. Methods. In a prospective, double-blind, randomized controlled trial, 50 patients undergoing elective ambulatory arthroscopic knee surgery received subarachnoid anaesthesia, with either prilocaine 20 mg and fentanyl 20 mg (Group P) or plain bupivacaine 7.5 mg and fentanyl 20 mg (Group B). Primary endpoints included times for onset of maximum sensory block level and regression of sensory block to L4, and also motor block at 1 and 2 h, and levels of haemodynamic stability. Comparisons between the groups were made by chi(2) test for proportions and the Mann-Whitney test for ordinal data. Time-to-event data were analysed by the Mann-Whitney test for uncensored data or the logrank test for censored data. Results. At 2 h, motor block in Group P had fully resolved in 86% of patients, compared with 27% in Group B (P<0.001). Median time to regression of sensory block to L4 was significantly shorter in Group P (97 min) than in Group B (280 min) (P<0.001). A clinically significant decrease in arterial pressure was more common in Group B (73%) than in Group P (32%) (P=0.004). Two patients in Group P required conversion to general anaesthesia, but for reasons unrelated to prilocaine itself. Conclusions. The combination of prilocaine and fentanyl is a better alternative to that of low-dose bupivacaine and fentanyl, for spinal anaesthesia in ambulatory arthroscopic knee surgery.
引用
收藏
页码:183 / 188
页数:6
相关论文
共 27 条
[1]   Comparison of hyperbaric and plain articaine in spinal anaesthesia for open inguinal hernia repair [J].
Bachmann, M. ;
Pere, P. ;
Kairaluoma, P. ;
Rosenberg, P. H. ;
Kallio, H. .
BRITISH JOURNAL OF ANAESTHESIA, 2008, 101 (06) :848-854
[2]   A comparison of minidose lidocaine-fentanyl and conventional-dose lidocaine spinal anesthesia [J].
Ben-David, B ;
Maryanovsky, M ;
Gurevitch, A ;
Lucyk, C ;
Solosko, D ;
Frankel, R ;
Volpin, G ;
DeMeo, PJ .
ANESTHESIA AND ANALGESIA, 2000, 91 (04) :865-870
[3]   A comparison of minidose lidocaine-fentanyl spinal anesthesia and local anesthesia/propofol infusion for outpatient knee arthroscopy [J].
Ben-David, B ;
DeMeo, PJ ;
Lucyk, C ;
Solosko, D .
ANESTHESIA AND ANALGESIA, 2001, 93 (02) :319-325
[4]   Intrathecal fentanyl with small-dose dilute bupivacaine: Better anesthesia without prolonging recovery [J].
BenDavid, B ;
Solomon, E ;
Levin, H ;
Admoni, H ;
Goldik, Z .
ANESTHESIA AND ANALGESIA, 1997, 85 (03) :560-565
[5]   Spinal bupivacaine in ambulatory surgery: The effect of saline dilution [J].
BenDavid, B ;
Levin, H ;
Solomon, E ;
Admoni, H ;
Vaida, S .
ANESTHESIA AND ANALGESIA, 1996, 83 (04) :716-720
[6]   Intrathecal fentanyl does not modify the duration of spinal procaine block [J].
Boucher, C ;
Girard, M ;
Drolet, P ;
Grenier, Y ;
Bergeron, L ;
Le Truong, HH .
CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE, 2001, 48 (05) :466-469
[7]   The incidence of transient neurological symptoms after spinal anaesthesia with lidocaine compared to prilocaine [J].
de Weert, K ;
Traksel, M ;
Gielen, M ;
Slappendel, R ;
Weber, E ;
Dirksen, R .
ANAESTHESIA, 2000, 55 (10) :1020-1024
[8]   Spinal anaesthesia with articaine 5% vs bupivacaine 0.5% for day-case lower limb surgery:: a double-blind randomized clinical trial [J].
Dijkstra, T. ;
Reesink, J. A. ;
Verdouw, B. C. ;
Van der Pol, W. S. C. J. M. ;
Feberwee, T. ;
Vulto, A. G. .
BRITISH JOURNAL OF ANAESTHESIA, 2008, 100 (01) :104-108
[9]   Chloroprocaine spinal anesthesia: Back to the future? [J].
Drasner, K .
ANESTHESIA AND ANALGESIA, 2005, 100 (02) :549-552
[10]   Should intrathecal lidocaine be used in the 21st century? [J].
Gaiser, RR .
JOURNAL OF CLINICAL ANESTHESIA, 2000, 12 (06) :476-481