Spinal anaesthesia with 0.25 % hyperbaric bupivacaine for Caesarean section: effects of volume

Similar documents
EFFECTS OF POSTURE AND BARICITY ON SPINAL ANAESTHESIA WITH 0.5 % BUPIVACAINE 5 ML

COMPARISON OF INCREMENTAL SPINAL ANAESTHESIA USING A 32-GAUGE CATHETER WITH EXTRADURAL ANAESTHESIA FOR ELECTIVE CAESAREAN SECTION

INTRATHECAL FENTANYL ADDED TO LIDOCAINE FOR CESAREAN DELIVERY UNDER SPINAL ANESTHESIA

Intrathecal 0.75% Isobaric Ropivacaine Versus 0.5% Heavy Bupivacaine for Elective Cesarean Delivery: A Randomized Controlled Trial

Comparison Of Intrathecal Hyperbaric Ropivacaine And Bupivacaine For Caesarean Delivery

Spread of subarachnoid hyperbaric amethocaine in adolescents

Beneficial effects of the addition of intrathecal fentanyl to bupivacaine for spinal anesthesia in cesarean section

Efficacy Of Ropivacaine - Fentanyl In Comparison To Bupivacaine - Fentanyl In Epidural Anaesthesia

ISSN X (Print) Research Article

OBSTETRICS Effects of intrathecal and i.v. small-dose sufentanil on the median effective dose of intrathecal bupivacaine for Caesarean section

Effects of IV Ondansetron during spinal anaesthesia with Ropivacaine and Fentanyl

COMPARATIVE ANAESTHETIC PROPERTIES OF VARIOUS LOCAL ANAESTHETIC AGENTS IN EXTRADURAL BLOCK FOR LABOUR

Hyperbaric 2% Lignocaine In Spinal Anaesthesia An Excellent Option For Day Care Surgeries

COMPARISON OF THE EFFECT OF TWO DIFFERENT DOSES OF 0.75% GLUCOSE-FREE ROPIVACAINE FOR SPINAL ANESTHESIA FOR LOWER LIMB AND LOWER ABDOMINAL SURGERY

*Correspondence: P Gupta E mail: Received: 15/05/2017 Accepted: 04/07/2017 DOI: /slja.v26i1.

ABSTRACT INTRODUCTION METHODS

Combination of Ultra-low Dose Bupivacaine and Fentanyl for Spinal Anaesthesia in Out-patient Anorectal Surgery

Intrathecal infusion of bupivacaine with or without morphine for postoperative analgesia after hip and knee arthroplasty

Addition of Adrenaline to Chloroprocaine Provides a Moderate Duration Time for Epidural Anaesthesia in Elective Caesarean Section

Comparison of ropivacaine and bupivacaine in extradural analgesia for the relief of pain in labour

Mhamed S. Mebazaa *, Sonia Ouerghi **

Comparision of Intravenous Bolus Phenylephrine and Ephedrine for Prevention of Post Spinal Hypotension in Cesarean Sections

The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters. doi:10.

Epidural Volume Extension In Combined Spinal Epidural Anaesthesia For Rapid Motor Recovery After Elective Caesarean SectionA Comparative Study

Induction position for spinal anaesthesia: Sitting versus lateral position

OBSTETRICS Effect of i.v. phenylephrine or ephedrine on the ED50 of intrathecal bupivacaine with fentanyl for Caesarean section

ORIGINAL ARTICLE A COMPARATIVE STUDY BETWEEN 0.5% HYPERBARIC BUPIVACAINE AND 0.5% HYPERBARIC BUPIVACAINE WITH

Controlled Trial of Wound Infiltration with Bupivacaine for Post Operative Pain Relief after Caesarean Section

COMPARISON OF EXTRADURAL ROPIVACAINE AND BUPIVACAINE

Original Article. MA Qadeer Khan 1, B Syamasundara Rao 2, SA Aasim 3 INTRODUCTION MATERIALS AND METHODS

Evaluation of Effective Low Dose Bupivacaine with Fentanyl in Spinal Anaesthesia for Lower Segment Caesarean Section Surgeries

PROPHYLACTIC ORAL EPHEDRINE IN PREVENTION OF HYPOTENSION FOLLOWING SPINAL ANAESTHESIA R. Vasanthageethan 1, S. Ramesh Kumar 2, Ilango Ganesan 3

Regional Anaesthesia for Caesarean Section

Head Elevation in Spinal-Epidural Anesthesia Provides Improved Hemodynamics and Appropriate Sensory Block Height at Caesarean Section

Sri Lankan Journal of Anaesthesiology 17(2) : (2009)

Factors in patient dissatisfaction and refusal regarding spinal anesthesia

Spinal anaesthesia with lidocaine 2% Caesarean section

Comparison of spinal anesthesia dosage based on height and weight versus height alone in patients undergoing elective cesarean section

Closed-loop Double-pump Automated System Manual Boluses

Original Article. Moinul Hossain 1*, Abu Hasanat Md. Ahsan Habib 2, Md. Mustafa Kamal 3, Md. Mizanur Rahman 4

EXTRADURAL BLOCK WITH BUPIVACAINE: INFLUENCE OF DOSE, VOLUME, CONCENTRATION AND PATIENT CHARACTERISTICS

Original Article The spread of spinal anesthesia in term parturient: effect of hip/shoulder width ratio and vertebral column length

Regional Anaesthesia for Caesarean Section Warwick D. Ngan Kee

Although intrathecal (IT) sufentanil provides effective

Original Article. anaesthetic for spinal anaesthesia was first introduced into clinical practice in 1979 with intrathecal morphine (6)

Section: Anaesthesia. Original Article INTRODUCTION

International Journal of Health Sciences and Research ISSN:

International Journal of Medical and Health Sciences

Comparative Study of Intrathecal Ropivacaine and Levobupivacaine With Fentanyl And Magnesium As Adjuvants For Lower Abdominal Surgeries

Combined spinalepidural. epidural analgesia in labour (review) By Neda Taghizadeh

Transient neurological symptoms after spinal anaesthesia with 4% mepivacaine and 0.5% bupivacaine

A comparative study of Ropivacaine and Bupivacaine in combined spinal epidural anaesthesia and Post- operative analgesia

Hemodynamic changes of intrathecal hyperbaric ropivacaine and bupivacaine in

A Randomised Controlled Study Comparing Intrathecal Hyperbaric Bupivacaine And Isobaric Bupivacaine In Common Urological Procedures

The Temperature of Bupivacaine 0.5% Affects the Sensory Level of Spinal Anesthesia

EPIDURAL ANALGESIA FOR THE SURGICAL INDUCTION OF LABOUR

Cesarean Section Should be Managed: Low Dose / CSE versus High Dose Spinals with Vasopressors

F Sheikh, M Ahmed, M Ommid, S Gurcoo, N Shakoor, S Nazir, G Nisa

An Epidural Initial Dose is Unnecessary in Combined Spinal Epidural Anesthesia for Caesarean Section

Y. Lim, 1 A. T. Sia 2 and C. E. Ocampo 3

Evaluation of pre-emptive intramuscular phenylephrine and ephedrine for reduction of spinal anaesthesia-induced hypotension during Caesarean section

CESAREAN delivery is most commonly performed under

Time duration to safety sitting in parturient receiving spinal anesthesia for cesarean section with 0.5% Bupivacaine and morphine

Evaluation of the Effect of Magnesium Sulphate as Adjunct to Epidural Bupivacaine: An Institutional Based Study

Combined Spinal epidural with Levobupivacaine or Ropivacaine with Fentanyl for Labor Analgesia: A Comparative Study

* ** *** **** ***** Assistant Professor Anesthesiology & ICU, Liaquat University of Medical and Health Sciences Jamshoro **

Efficacy of intrathecal fentanyl along with bupivacaine and bupivacaine alone in lower segment caesarean section

ABSTRACT. Keywords: Hypotension, Spinal Anaesthesia, Caesarean Section, Crystalloid Preloading, Coloading.

OBSTETRICS Intrathecal morphine reduces breakthrough pain during labour epidural analgesia

Comparative Study of Role of Fentanyl and Dexmedetomidine as an Adjuvant to Bupivacaine in Controlling Post-operative Pain

Comparison of intrathecal isobaric bupivacaine±morphine and ropivacaine±morphine for Caesarean delivery ²

Original article Pravara Med Rev 2010; 2(3)

COMPARISON OF % BUPIVACAINE WITH % FENTANYL V/S % BUPIVACAINE IN AMBULATORY LABOR EPIDURAL ANALGESIA

Labor Epidural: Local Anesthetics and Beyond

Study of Failed Spinal Anesthesia Undergoing Caesarean Section and Its Management

COMBINED SPINAL AND EPIDURAL ANAESTHESIA (CSEA) USING SEPARATE INTERSPACE TECHNIQUE

Sonia Ouerghi *, Mohamed A. Bougacha **,

Comparison of Haemodynamic, block level and patient comfort by using 0.75% & 0.5% Hyperbaric Bupivacaine in Caesarean Section

MD (Anaesthesiology) Title (Plan of Thesis) (Session )

RIA ABSTRACT INTRODUCTION /jp-journals

Original contribution. Department of Anesthesiology, Sapporo Medical University, School of Medicine, Sapporo, Hokkaido, Japan

CHA Gumi Medical Center, CHA University, Gumi, Korea

International Journal of Clinical And Diagnostic Research ISSN Volume 3, Issue 6, Nov-Dec 2015.

Comparative Study of Low Doses of Intrathecal Bupivacaine Admixed With Fentanyl Citrate in Caesarean Section Deliveries

Association of lipophilic opioids and hyperbaric bupivacaine in spinal anesthesia for elective cesarean section. Randomized controlled study 1

Crystalloid prehydration versus cohydration for prevention of hypotension during spinal anaesthesia for elective caesarean section

REGIONAL/LOCAL ANESTHESIA and OBESITY

MATERNAL AND FETAL HAEMODYNAMIC EFFECTS OF SPINAL AND EXTRADURAL ANAESTHESIA FOR ELECTIVE CAESAREAN SECTION

Original Research Article

jorapain ABSTRACT INTRODUCTION /jp-journals

ANESTHESIA FOR CESAREAN DELIVERY

Effect of Clonidine Addition To Hyperbaric 0.5% Bupivacaine For Spinal Anaesthesia In Lower Limb Surgery [A Comparative Study]

Abstract. Ahmed Gamassy and Ayad Saleh

Effects of Adding Intrathecal Magnesium Sulphate To Bupivacaine And Fentanyl in Lower Abdominal And Lower Limb Surgeries

British Journal of Anaesthesia 103 (5): (2009) doi: /bja/aep263 Advance Access publication September 28, 2009

Epidural Analgesia in Labor - Whats s New

Yuko Kondo, Kaoru Sakatani, Noriya Hirose, Takeshi Maeda, Jitsu Kato, Setsuro Ogawa, and Yoichi Katayama

Original Article INTRODUCTION. Abstract

Keywords: Bupivacaine, Haemodynamic Alteration, Levobupivacaine, Spinal Anaesthesia, Transurethral Resection of Prostate

prilocaine hydrochloride 2% hyperbaric solution for injection (Prilotekal ) SMC No. (665/10) Goldshield Group

Transcription:

British Journal of Anaesthesia 1996; 77: 145 149 Spinal anaesthesia with 0.25 % hyperbaric bupivacaine for Caesarean section: effects of volume C. J. CHUNG, S. H. BAE, K. Y. CHAE AND Y. J. CHIN Summary To investigate the safety and efficacy of 0.25 % hyperbaric bupivacaine for spinal anaesthesia in Caesarean section, we studied 60 parturients allocated randomly to one of three groups. According to the patient s height, groups 1, 2 and 3 received 3.2 3.6 ml (8 9 mg), 3.6 4.0 ml (9 10 mg) and 4.0 4.4 ml (10 11 mg) of 0.25 % bupivacaine in 5 % glucose, respectively. Subarachnoid injection was performed in the right lateral decubitus position, and parturients were then turned immediately supine with left uterine displacement. Mean spread of sensory analgesia was significantly higher in group 3 (T2 3) than in groups 1 and 2 (T4 5 in each group). Duration of sensory analgesia was significantly longer in groups 2 and 3 than in group 1. Complete motor block of the lower extremities occurred in all patients but in only one in group 1. Onset time and duration of motor block were not significantly different between the three groups. The incidence of hypotension was significantly higher in group 3 (75 %) than in groups 1 and 2 (40 % in each group). The efficacy of intraoperative analgesia was significantly greater in groups 2 and 3 than in group 1. The incidence of patients requiring analgesics during operation was significantly lower in groups 2 (25 %) and 3 (10 %) than in group 1 (70 %). There was no difference in neonatal condition between the three groups. Spinal anaesthesia with 3.6 4.0 ml of 0.25 % bupivacaine in 5 % glucose was satisfactory for Caesarean section. (Br. J. Anaesth. 1996; 77: 145 149) Key words Anaesthetics local, bupivacaine. Anaesthetic techniques, subarachnoid. Anaesthesia, obstetric. Amylocaine is a drug used frequently for spinal anaesthesia in Caesarean section. However, this agent often fails to provide good maternal sensory block [1, 2]. Recently, bupivacaine has gained popularity in obstetric anaesthesia but 0.5 % plain bupivacaine has been shown to be unreliable and produced occasional high block [3, 4]. Therefore, hyperbaric bupivacaine has been used more often than plain bupivacaine for spinal anaesthesia in Caesarean section. The total dose of bupivacaine is more important than volume or concentration of anaesthetic solution in determining spread of anaesthetic solution in the CSF [5 7]. However, the effect of volume of hyperbaric spinal anaesthetic solution injected may be additive to the effects of gravity, position and dose [8 10]. Almost all parturients given 0.5 % hyperbaric bupivacaine 7.5 10 mg for spinal anaesthesia in Caesarean section required supplementary analgesia because of visceral pain during surgery [11, 12]. When hyperbaric bupivacaine 10 15 mg was used for spinal anaesthesia in Caesarean section, good sensory block developed and the incidence of supplementary analgesia was decreased [2, 12]. However, the volume exceeded 3 ml in those cases. When 0.25 % hyperbaric bupivacaine solution 10 15 mg is used for spinal anaesthesia in Caesarean section, the volume reaches 4 6 ml, which may influence spinal anaesthesia because of easily cephalad spread of local anaesthetic solution in CSF. The aim of this investigation was to assess the safety and efficacy of 0.25 % bupivacaine in 5 % glucose for spinal anaesthesia in Caesarean section. Sensory and motor block, haemodynamic changes, quality of intraoperative analgesia and complications were compared. Patients and methods We studied 60 term parturients, ASA I or II, chosen to have spinal anaesthesia for elective Caesarean section. The study was approved by the Hospital Ethics Committee and written informed consent was obtained from all patients at the preoperative visit. Parturi ents who had obstetri c compli cati ons or evidence of fetal compromise were excluded. Hyperbaric bupivacaine solution 0.25 % was made with the same volume of 0.5 % bupivacaine hydrochloride (Marcaine, Astra, Sweden) and 10 % glucose monohydrate (Daehan Pharmaceutical Co., Seoul, Korea). The specific gravity of 0.25 % bupivacaine in 5 % glucose was 1.022 at 23 C. Patients were allocated randomly to one of three groups. Each group had 10 mothers who were 156 160 cm tall and 10 mothers 161 165 cm tall. mothers (156 160 cm tall) were given 3.2 ml of 0.25 % bupivacaine in 5 % glucose, and those 161 165 cm received 3.6 ml. CHAN JONG CHUNG*, MD, SEUNG HWAN BAE, MD, KI YOUNG CHAE, MD, YOUNG JHOON CHIN, MD, Department of Anesthesiology, College of Medicine, Dong-A University, Pusan, Korea. Accepted for publication: March 13, 1996. * Address for correspondence: Department of Anaesthesiology, Dong-A Medical Centre, 1-3 ga Tongdaesin-dong, Seo-gu, Pusan, 602-103, Korea.

146 British Journal of Anaesthesia In groups 2 and 3, the corresponding bupivacaine volumes were 3.6 and 4.0 ml, and 4.0 and 4.4 ml, respectively. All subarachnoid blocks were performed by one anaesthetist and data were collected by two registrars who were blinded to the solutions used. All parturients received ranitidine 10 mg and glycopyrronium 0.2 mg i.m., 1 h before arrival in the operating room. All patients received an infusion of lactated Ringer s solution 1000 ml over 10 20 min before induction. They were also given ephedrine 40 mg i.m., approximately 10 min before subarachnoid injection. Subarachnoid injection was performed in the right lateral decubitus position with a 25-gauge Quincke spinal needle, using a midline approach at the L2 3 or L3 4 interspace. The predetermined volume of local anaesthetic was injected over 20 30 s without barbotage. After subarachnoid injection, mothers were immediately turned supine with left uterine displacement. The parturient s head was rested on a pillow. The spread of sensory block to pinprick was measured at 2-min intervals during the first 10 min and then at 5-min intervals. The degree of motor block of the lower extremities was also assessed at the same interval, using the modified Bromage scale: 0 no paralysis; 1 unable to raise the extended leg; 2 unable to flex knee; 3 unable to flex ankle. Maternal arteri al pressure and heart rate were recorded every minute until delivery and every 5 min thereafter, using an automated, non-invasive device (Sirecust 404, Simens, Germany). If hypotension (systolic arterial pressure less than 100 mm Hg or a 20 % reduction in systolic arterial pressure) occurred, it was treated promptly by increasing uterine displacement and the rate of fluid administration. If hypotension persisted despite these measures, ephedrine 10 mg was given i.v. and repeated as needed. Oxygen was administered routinely by face mask at 6 litre min 1 until the end of operation. When sensory block at or above T6 was established, surgery were commenced. The incidence and frequency of complications were noted. The efficacy of intraoperative analgesia was assessed by the following four categories: excellent no discomfort during the procedure; good mild discomfort but required no systemic analgesia; fair pain that required additional analgesia; and poor moderate or severe pain that needed more than fentanyl 100 g or general anaesthesia. When the patient complained of pain, fentanyl 50 g was given i.v. and repeated as needed. I.v. midazolam 2.5 mg was administered if the patient requested to sleep after the birth of the baby. I.v. droperidol 0.625 mg was used to treat nausea or vomiting. The times of bupivacaine injection, start of surgery, delivery and termination of surgery were recorded. The condition of the neonates was assessed by Apgar score at 1 and 5 min after delivery. All mothers received oxytocin by continuous infusion after delivery. Return of sensory and motor function was assessed at 15-min intervals until complete recovery from anaesthesia. All data are expressed as number or mean (SD or range). The results were analysed using one-way and two-way ANOVA followed by Tukey s test for parametric data, and the chi-square test with Yates correction, the Kruskall-Wallis followed by the Mann Whitney U test for non-parametric data. P 0.05 was considered statistically significant. Results There were no statistically significant differences in mean age, weight, height and gestational age between the three groups (table 1). In four patients in group 1, the spinal was converted to general anaesthesia 10 15 min after delivery of the neonate because surgical anaesthesia was inadequate. These patients were excluded from further analysis of sensory and motor block. Onset and segmental spread of sensory analgesia are shown in figure 1. Cephalad spread of sensory analgesia was increased significantly with an increase in volume, and the differences between groups 1 and 3 and between groups 2 and 3 were significant. Onset time of sensory analgesia to T6 was significantly faster in group 3 than in group 1. The mean maximal level of analgesia in group 3 (T2 3) was significantly higher than that in groups 1 and 2 (T4 5 in each), and the times to achieve the maximal level were similar, with an average of 10 15 min between the three groups. Sensory analgesia at or above T6 was obtained in all patients, but sensory analgesia below Table 1 Patient characteristics (mean (SD or range)) Age (yr) 30.0 (23 34) 29.9 (25 35) 29.4 (24 36) Height (cm) 159.5 (2.4) 158.8 (2.2) 160.6 (2.7) Weight (kg) 65.0 (8.5) 65.6 (5.9) 68.4 (8.5) Gestation (weeks) 37.8 (0.9) 38.3 (0.8) 37.9 (2.1) Figure 1 Onset and segmental spread of sensory analgesia after subarachnoid injection of 0.25 % bupivacaine in 5 % glucose for term parturients in group 1 (3.2 3.6 ml ( )), group 2 (3.6 4.0 ml ( )) and group 3 (4.0 4.4 ml ( ). *P 0.05 vs group 1, P 0.05 vs groups 1 and 2.

Spinal anesthesia for Caesarean section 147 Table 2 Comparison of times of onset and regression of subarachnoid block (mean (SD)). *P 0.05 vs group 1 Table 3 Incision direction and surgical times (mean (SD) or number). Long/trans Longitudinal/transverse (n 16) Sensory block (min) T6 7.7 (2.4) 6.9 (1.8) 5.5 (2.4)* maximal level 13.8 (3.2) 12.7 (2.7) 11.9 (3.0) Regression time to T10 85.0 (15.3) 103.0 (14.3)* 108.5 (20.8)* Regression time to L5 164.0 (20.3) 185.5 (20.9)* 198.0 (26.8)* Motor block (min) complete block 11.6 (3.7) 12.1 (3.2) 10.7 (3.7) complete regression 122.0 (25.9) 137.3 (24.5) 142.2 (33.3) Incision direction Long/trans 6/14 7/13 6/14 Induction to operative start time (min) 16.6 (4.5) 16.5 (3.2) 15.9 (3.5) Induction to operative end time (min) 82.3 (9.3) 84.6 (10.3) 83.2 (8.1) Uterine incision to delivery time (s) 91.6 (23.2) 78.3 (33.0) 82.5 (26.7) Table 4 Efficacy of sensory block during surgery (number). *P 0.05 vs group 1 Category * * Excellent 4 10 16 Good 2 5 2 Fair 9 5 2 Poor 5 0 0 Figure 2 Changes in maternal systolic arterial pressure (SAP) during the first 30 min after subarachnoid injection of 0.25 % bupivacaine in 5 % glucose for term parturients in group 1 (3.2 3.6 ml ( )), group 2 (3.6 4.0 ml ( )) and group 3 (4.0 4.4 ml ( )). C Control. *P 0.05 compared with control value in each group. T4 was obtained significantly more in group 1 (70 %) Figure 3 Changes in maternal heart rate during the first 30 min after subarachnoid injection of 0.25 % bupivacaine in 5 % glucose for term parturients in group 1 (3.2 3.6 ml ( )), group 2 (3.6 4.0 ml ( )) and group 3 (4.0 4.4 ml ( )). C Control. than in groups 2 and 3 (30 % and 10 %, respectively). Two patients in group 3 had a block up to C6 and C7, respectively. Total time for regression of sensory analgesia to T10 and L5 was significantly longer in groups 2 and 3 than in group 1 (table 2). Complete motor block of the lower extremities was obtained in all patients at an average time of 10 13 min, except for one patient in group 1 (Bromage scale 2). Duration of complete motor block was longer with an increase in volume, but this was not statistically significant (table 2). There were no significant differences in systolic arterial pressure and heart rate during the first 30 min between the three groups (figs 2, 3). Compared with control preanaesthetic values, systolic arterial pressure was significantly decreased at 4 min in groups 1 and 2, and at 4 and 6 min in group 3. The percentage maximal decreases in systolic arterial pressure were 16.1 (9.9) %, 17.8 (10.1) % and 25.7 (13.2) % in groups 1, 2 and 3, respectively, recorded 4 6 min after induction of spinal anaesthesia. Hypotension developed in eight of 20 patients in group 1 (40 %), and six required i.v. ephedrine, compared with eight of 20 patients in group 2 (40 %), and seven required i.v. ephedrine and 15 of 20 patients in group 3 (75 %), and 14 required i.v. ephedrine. The incidence of hypotension and need for ephedrine were significantly greater in group 3 than in groups 1 and 2. The various time intervals from induction of anaesthesia to end of surgery are shown in table 3. There were no significant differences in these times between the groups. No patient in any group complained of discomfort at incision from skin to the uterus. The efficacy of intraoperative analgesia was significantly greater in groups 2 and 3 than in group 1 (table 4). In group 1, only four patients (20 %) were totally painless; 14 patients (70 %) required supplementary analgesia 40 50 min after induction, four of whom required general anaesthesia about 10 15 min after delivery. Five patients in group 2 (25 %) and two in group 3 (10 %) required supplementary analgesia 50 60 min after induction of spinal anaesthesia. Neonatal weight and Apgar scores at 1 and 5 min were similar between the three groups (table 5). The condition of the neonates was good. Two infants in group 3 had an Apgar score of 5 and 6, but more than 8 at 5 min.

148 British Journal of Anaesthesia Table 5 Neonatal status (mean (SD)) Neonatal weight (kg) 3.3 (0.3) 3.2 (0.2) 3.4 (0.3) Apgar score 1 min 8.3 (0.5) 8.4 (0.5) 8.2 (0.8) 5 min 9.5 (0.4) 9.6 (0.3) 9.4 (0.7) Table 6 Intraoperative complications (number). Patients in whom droperidol was used. *P 0.05 vs groups 1 and 2 Hypotension 8 8 15* Bradycardia 4 5 7 Nausea/vomiting 2 3 6 Dyspnoea 1 2 4 Transient headache 0 0 2 The incidences of complications after spinal anaesthesia are shown in table 6. Complications occurred more in group 3 than in groups 1 and 2, but this was not significant. Discussion Our data indicated that 0.25 % bupivacaine in 5 % glucose could be used safely and effectively for spinal anaesthesia in Caesarean section. Lignocaine, amylocaine and bupivacaine can be used for spinal anaesthesia in Caesarean section but some mothers who received amylocaine spinal anaesthesia needed supplementary analgesia because of intraoperative visceral pain [1, 2]. Recently, bupivacaine has gained popularity in obstetric anaesthesia for extradural and also spinal anaesthesia. Hyperbaric bupivacaine provided better intraoperative analgesia and produced shorter duration of motor block than hyperbaric amylocaine [2]. Within the range of 7.5 12 mg of 0.5 % hyperbaric bupivacaine, similar levels of sensory block to T3 occurred, despite the varying doses of drug injected, but the duration of sensory block was longer with the large than the small dose. Increasing the dose increased the intensity of motor block, but the duration of motor block was similar [11, 12]. In our study, increasing the dose increased the level and duration of sensory block, but the intensity and duration of motor block were similar between the three groups. Several reports [5 7] have suggested that the total dose of bupivacaine is more important than volume or concentration of anaesthetic solution in determining spread of anaesthetic solution in the CSF. The relationship between volume of anaesthetic injected for spinal anaesthesia and final level of block have not been defined clearly. Baricity determines primarily the spread of subarachnoid local anaesthetic in the CSF. In recent studies of plain spinal infusion in pregnancy, final levels of block were similar with volumes and concentrations ranging from 3 ml of 0.5 % to 18 ml of 0.083 % plain bupivacaine [13 15]. However, increasing the vol- ume administered into the subarachnoid space, especially in a hyperbaric solution, resulted in significantly greater cephalad spread [8 10]. The effect of volume of hyperbaric spinal anaesthetic solution injected may be additive to the effects of gravity, position and dose. High volumes of hyperbaric local anaesthetic solution may influence the spread of local anaesthetic in CSF and final block. In the clinical dose range (10 15 mg) of 0.5 % or 0.75 % hyperbaric bupivacaine, the volume does not exceed 3 ml. When 0.25 % hyperbaric bupivacaine solution is used, the dose of 10 15 mg reaches 3.0 6.0 ml. The large volume itself may influence the spread of local anaesthetic in CSF and final block, especially in the narrow subarachnoid space of term parturients. In our preliminary study with 5 6 ml of 0.25 % bupivacaine in 5 % glucose, sensory block occurred at the cervical level of dermatome in a few minutes after subarachnoid injection in all parturients. Severe hypotension developed and nausea or vomiting, dyspnoea, and transient headache occurred in all patients. The one cause limiting the choice of spinal anaesthesia for Caesarean section is the possibility of neonatal depression because of severe hypotension after spinal anaesthesia. Petersen and co-workers [12] reported incidences of hypotension in patients given 7.5 10 mg and 10 12.5 mg of 0.5 % hyperbaric bupivacaine solution of 24 % and 26 %, respectively. In our study, despite adequate hydration and i.m. ephedrine before induction of spinal anaesthesia, the incidence of hypotension in the 4.0 4.4-ml group (75 %) was significantly greater than in the 3.2 3.6- ml and 3.6 4.0-ml groups (40 % in each group). The percentage maximal decrease in systolic arterial pressure and the incidence of patients requiring supplementary ephedrine were significantly greater in the 4.0 4.4-ml group than in the two other groups. The condition of the neonates, assessed by Apgar score, was good and similar in the three groups. Two neonates in the 4.0 4.4-ml group had an Apgar score of 5 and 6 at 1 min, respectively, but the scores at 5 min were more than 8. In these two neonates, maternal systolic arterial pressure decreased transiently to 70 and 75 mm Hg a few minutes after induction of spinal anaesthesia. A large volume of 0.25 % hyperbaric bupivacaine solution could easily spread in a cephalad direction in CSF and influence sensory block and also sympathetic block. Therefore, simply increasing the volume of 0.25 % hyperbaric bupivacaine solution to increase the dose must be considered for spinal anaesthesia for Caesarean section. It is generally accepted that sensory analgesia to at least the fourth thoracic dermatome is necessary for Caesarean section. However, despite seemingly adequate levels of sensory block regardless of the local anaesthetic used, many parturients required supplementary analgesia during exteriorization of the uterus and traction on the abdominal viscera [11, 12]. In our study, all parturients experienced a block at or above T6 in sensory analgesia. Sensory block above T4 was obtained significantly more often in the 3.6 4.0-ml and 4.0 4.4-ml groups than in the 3.2 3.6-ml group. No patient complained of dis-

Spinal anesthesia for Caesarean section 149 comfort at incision from skin to the uterus. Petersen and co-workers [12] reported that similar spread of sensory block to above T3 developed in patients who received 7.5 10 mg and 10 12.5 mg of 0.5 % hyperbaric bupivacaine solution, but the use of a larger dose of bupivacaine resulted in a lesser frequency of moderate to severe visceral pain. In our study, the frequency of visceral pain and requirement for supplementary opioids were significantly less in the 3.6 4.0-ml and 4.0 4.4-ml groups than in the 3.2 3.6-ml group. A variety of ways have been tried to improve the quality of spinal anaesthesia during Caesarean section. Injecting larger doses of local anaesthetic can improve the quality of sensory block [12, 16]. In 0.25 % hyperbaric bupivacaine solution, increasing volume to increase the dose is not recommended because the large volume itself would cause cervical spinal block and severe hypotension. The addition of adrenaline [17], morphine [18] or fentanyl [19] to hyperbaric bupivacaine solution improved the quality of bupivacaine intraoperative analgesia. In our study with 0.25 % hyperbaric bupivacaine, a larger dose improved the quality of sensory analgesia, but the incidence of hypotension and its severity were greater with volumes exceeding 4.0 ml. Acknowledgements This work was supported in part by a grant from Dong-A University, Korea. References 1. Schnider SM. Anesthesia for elective cesarean section. In: Schnider SM, ed. Obstetrical Anesthesia. Baltimore: Williams and Wilkins, 1970; 94. 2. Michie AR, Freeman, Dutton DA, Howie HB. Subarachnoid anaesthesia for elective Caesarean section. Anaesthesia 1988; 43: 96 99. 3. Russell IF. Spinal anaesthesia for Caesarean section: the use of 0.5 % bupivacaine. British Journal of Anaesthesia 1983; 55: 309 314. 4. Russell IF. Inadvertent total spinal for Caesarean section. Anaesthesia 1985; 40: 199 200. 5. Sheskey MC, Rocco AG, Bizzarri-Schmid M, Francis DM, Edstrom H, Covino BG. A dose response study of bupivacaine for spinal anesthesia. Anesthesia and Analgesia 1983; 62: 931 935. 6. Bengtsson M, Malmqvist L-A, Edstrom HH. Spinal analgesia with glucose-free bupivacaine: effect of volume and concentration. Acta Anaesthesiologica Scandinavica 1984; 28: 583 586. 7. Mukkada TA, Bridenbaugh PO, Singh PM, Edstrom HH. Effects of dose, volume, and concentration of glucose-free bupivacaine in spinal anesthesia. Regional Anesthesia 1986; 11: 98 101. 8. Axelsson KH, Edstrom HH, Sundberg AEA, Widman GB. Spinal anaesthesia with hyperbaric bupivacaine: effects of volume. Acta Anaesthesiologica Scandinavica 1982; 26: 439 454. 9. Chambers WA, Littlewood DG, Edstrom HH, Scott DB. Spinal anaesthesia with hyperbaric bupivacaine: effects of concentration and volume administered. British Journal of Anaesthesia 1982: 54; 75 80. 10. Stienstra R, Greene NM. Factors affecting the subarachnoid spread of local anesthetic solution. Regional Anesthesia 1991; 16: 1 6. 11. Santos S, Pedersen H, Finster M, Edstrom H. Hyperbaric bupivacaine for spinal anesthesia in cesarean section. Anesthesia and Analgesia 1984; 63: 1009 1013. 12. Pedersen H, Santos AC, Steinberg ES, Schapiro HM. Harmon TW, Finster M. Incidence of visceral pain during cesarean section: the effect of varying doses of spinal bupivacaine Anesthesia and Analgesia 1989; 69: 46 49. 13. Van Zundert AA, De Woff AM, Vaes L, Soetens M. High volume spinal anesthesia with bupivacaine 0.125 % for cesarean section. Anesthesiology 1988; 69: 998 1003. 14. Russell IF. Spinal anesthesia for cesarean delivery with dilute solutions of plain bupivacaine: the relationship between infused volume and spread. Regional Anesthesia 1991; 16: 130 136. 15. Vucevic M, Russell IF. Spinal anaesthesia for Caesarean section: 0.125 % plain bupivacaine 12 ml compared with 0.5 % plain bupivacaine 3 ml. British Journal of Anaesthesia 1992; 68: 590 559. 16. DeSimone CA, Norris MC, Leighton B, Epstein R, Palmer C, Kaplan S, Goodman D. Spinal anesthesia with hyperbaric bupivacaine for cesarean section: a comparison of two doses. Anesthesiology 1988; 69: A670. 17. Abouleish EI. Epinephrine improves the quality of spinal hyperbaric bupivacaine for cesarean section. Anesthesia and Analgesia 1987; 66: 395 400. 18. Abouleish E, Rawal N, Fallon K, Hernandez. Combined intrathecal morphine and bupivacaine for cesarean section. Anesthesia and Analgesia 1988; 67: 370 374. 19. Hunt CO, Naulty JS, Bader AB, Hauch MA, Vartikar J, Datta S, Hertwig LM, Ostheimer GW. Perioperative analgesia with subarachnoid fentanyl bupivacaine for cesarean delivery. Anesthesiology 1989; 71: 535 540.