Table of Content - Volume 14 Issue 2 - May 2020
Comparative study of intrathecal buprenorphine and fentanyl along with 0.5% hyberbaric bupivacaine for postoperative analgesia in LSCS patients under spinal anaesthesia
Meena Padmaja Grandhi1, S Praveen Kumar Reddy2*
1Assistant Professor. Department Of Anesthesia, NRI Medical College,Andhra Pradesh, INDIA. 2consultant Anaesthesiologist, Surya Hospital, Sangareddy, Telangana, INDIA. Email: meenapadmaja27@gmail.com
Abstract Background: The common anaesthetic technique used in obstetric anaesthesia is spinal anesthesia. The main disadvantage is its limited duration of action and thus, lack of postoperative analgesia.Short acting Opioids like Fentanyl and Sufentanil have been used intrathecally to provide pain relief . It is an effective analgesic with low intrinsic activity and can also be administered safely in the subarachnoid space. Aim: To compare onset of sensory and motor blockade and post operative analgesia between intrathecal buprenorphine and fentanyl along with 0.5% Hyberbaric bupivacaine for postoperative analgesia in LSCS patients under spinal anaesthesia Materials and methods: Patients with ASA Grade I and II of age 18-35 years were included in this study. The study group were randomly divided into two groups with 26 patients in each group. Group B-1.6ml of 0.5% Heavy Bupivacaine + 0.2ml (60 microgram) Buprenorphine + 0.2(distilled water) – total volume 2ml and group F -1.6ml of 0.5% Heavy Bupivacaine + 0.4ml (20 microgram) Fentanyl – total volume 2ml Results : Buprenorphine 60mcg added to 1.6 ml of 0.5% Hyperbaric Bupivacaine has comparable clinical onset of sensory and motor blockade, time for two segment regression, total duration of motor blockade but longer effective analgesia time when compared to Fentanyl 20 microgram added to 1.6 ml of 0.5% Hyperbaric Bupivacaine in patients undergoing LSCS under spinal anaesthesia Conclusion: So buprenorphine can be used as an adjuvant to bupivacaine in spinal anesthesia in addition to Fentanyl as it gives better post operative analgesia Key words: Buprenorphine, Fentanyl, Bupivacaine, spinal anesthesia, post operative analgesia
INTRODUCTION The common anaesthetic technique used in obstetric anaesthesia is spinal anesthesia.. The main advantage with this is – relative simplicity, rapidity, certainty, low failure rates, minimal side effects, an awake mother. The main disadvantage is its limited duration of action and thus, lack of postoperative analgesia.Short acting Opioids like Fentanyl and Sufentanil have been used intrathecally to provide pain relief1 .Buprenorphine is a mixed agonist - antagonist Opioid with high affinity at both µ and kappa opiate receptors. It is an effective analgesic with low intrinsic activity and can also be administered safely in the subarachnoid space2. Aims and Objectives: To evaluate and compare the synergistic effect of Bupivacaine 0.5% with Fentanyl versus Bupivacaine 0.5% with Buprenorphine, in patients undergoing LSCS under spinal anaesthesia regarding:
MATERIALS AND METHODS The study was conducted in the department of Anaesthesiology, Rural development trust hospital, Bathalapalli, Anantapuramu Inclusion Criteria
Exclusion Criteria
Sixty three patients (will be selected based on inclusion and exclusion criteria) scheduled for LSCS under spinal anaesthesia will be randomly allocated (using sealed envelope technique) into one of the two groups of twenty six each. Group B -1.6ml of 0.5% Heavy Bupivacaine + 0.2ml (60 microgram) Buprenorphine + 0.2(distilled water) – total volume 2ml Group F -1.6ml of 0.5% Heavy Bupivacaine + 0.4ml (20 microgram) Fentanyl – total volume 2ml Procedure: After thorough pre-anaesthetic examination, consent was taken.Baseline vitals are noted.Upon arrival in the operation theatre, an IV line is secured .Monitors were connected – Base line Heart rate, Oxygen Saturation, blood pressure were recorded and ECG was monitored.With patient in the left lateral position each patient is premedicated with ondansetron 4mg and ranitidine 50 mg iv and pre-loaded with 15ml/kg Ringer lactate over a period of 10 minutes. In left lateral position subarachnoid block was given under aseptic precautions after local infiltration, by midline approach,with OT table in neutral position, with 25G lumbar puncture needle, in L3 – L4 intervertebral space.Immediately following the injection patients will be turned to supine position and left uterine displacement was given.All Patients were supplemented with O2 (4 L/min) via a facemask Vital parameters will be measured after SAB every 3 min for 20 min, every 5 min thereafter till the end of surgery.Post-operative analgesia will be evaluated using VAS score.Rescue analgesia in the form of Diclofenac sodium 1.5 mg/kg I.M. will be given at the VAS score of >4.
Parameters observed:
RESULTS: Demographic data like Age, Weight, Sex and ASA Grade were similar in both the groups. TABLE I: TIME TO ONSET OF SENSORY BLOCK
Time taken to the onset of sensory block in the Group B was 2.86 ± .503 min and in the Group F was 3.05 ± .551 min. The shortest duration was 2 min and the longest duration was 4 min in both the groups. The onset time of sensory block was comparable in both the groups as indicated by the (p value = 0.45)
TABLE II: Time to reach Highest Sensory Level
The mean time to reach the highest level in group B was 5.86 ± 0.503 min and in group F was 5.71 ± 0.490 min. The mean time to reach highest sensory level was comparable in both the groups (p value = 0.109).
TABLE III: Mean duration of onset of motor block
The mean time of onset of motor blockade was 4.79 ± 0.513 min in Group B and 4.68 ± 0.502 min in Group F respectively. Mean duration of onset of motor blockade was comparable in both the groups (p value- 0.222).
TABLE IV:Total duration of Motor blockade in the two groups
The total mean duration of motorblockade was 134.76 ± 20.780 min in Group B and 133.81 ± 19.296 min in Group F respectively. Mean duration of onset of motor blockade was comparable in both the groups (p value 0.801)
TABLE V: Time for two segment regression of sensory blockade
The mean time for two segment regression in the group B was 82.62 ± 16.797 minutes and in group F was 82.86 ± 15.676 minutes. There was no significant difference in the two groups(p value 0.935).
TABLE VI:Effective analgesia time
The mean effective analgesia time in group B was 547.60 ± 80.276 minutes and that in group F was 410.00 ±67.942. 57.1 % of patients in group F had 401-500 minutes of duration of analgesia. 65.1% of patients in group B had 501-600 minutes of duration of analgesia. The shortest duration of analgesia was 210 minutes and 360 minutes in group F and group B respectively. The longest duration of analgesia was 600 minutes and 720 minutes in group F and group B respectively. Significantly prolonged effective analgesia time was found in Buprenorphine group with ‘p’ value <0.001.
TABLE VII:Comparison of side effects/Complications
The incidence of hypotension considered to be present whenever systolic blood pressure decreased to less than 90mm of Hg or <20% of the baseline whichever appears first was 15.9% in group F (10 patients) and in group B was 15.9% (10 patients) which is equal in both the groups Other common side effects noted in all the patients under the study were pruritis, nausea and vomiting. 3 patients in group F experienced pruritis with the incidence of 4.8% and 1 patient in group B experienced pruritis with the incidence of 1.6%, but there was no statistical difference in the incidence of pruritis between the two groups (p > 0.05).
DISCUSSION Spinal subarachnoid block is one of the most versatile regional anaesthesia techniques available today especially in patients undergoing LSCS. Regional anaesthesia offers several advantages over general anaesthesia - blunts stress response to surgery, decreases intraoperative blood loss, lowers the incidence of postoperative thromboembolic events, and provides analgesia in early postoperative period. Spinal opioids and local anaesthetics have been shown to act synergistically at the spinal level in animal studies3 .The advantage of combining the two types of agents in this manner is thought to be explained by their different analgesic properties and their ability activating the opiate receptors in the substantia gelatinosa, whereas local anaesthetics provide analgesia by blocking impulse transmission at the nerve roots and dorsal root ganglia4 The studies conducted by Rahul Seewal et al.. and Gajanan Chavan, Aparna Chavan et al..5 on different doses of intrathecal fentanyl showed that even if we increase the dose of fentanyl after 25mcg, there is no much variation in the duration of analgesia. Hence, we chose 20 micrograms of Fentanyl as the optimal dose to be added as an adjuvant to Bupivacaine Studies conducted by Sandhya Gujar, Pradnya Jagtap et al..6, G. CAPOGNA et al.. and Sunil Dixit demonstrated that increasing doses of buprenorphine from 30mcg to 60mcg prolonged duration of analgesia without significant complications like respiratory depression.Hence we chose to use 60micrograms of buprenorphine as an optimal dose to be added to bupivacaine as an adjuvant. The mean time taken to the onset of sensory block in the Group B was 2.86 ± .503 minutes and in the Group F was 3.05 ± .551 minutes. Fauzia A. Khan, Gauhar A. Hamdani in a study titled found that onset of sensory blockade with fentanyl 10 microgram was 3.2±2.0min and with buprenorphine 30microgram was 3.15±1.0min which was statistically comparable with ‘p’ value 0.94. This is in accordance with our study.7 In our study, the mean time for two segment regression in the group B was 82.62 ± 16.797 minutes and in group B was 82.86 ± 15.676 minutes. There was no significant difference in the two groups as indicated by the ‘p’ value 0.935. Harbhej Singh et al.. found that the time for two segment regression from the highest sensory level was 93.4±22minutes in a group which received 25microgram of fentanyl with 3ml of 0.5% hyperbaric bupivacaine this is accordance with our study group fentanyl.8 G, Priyanka V et al.. found that the 2 segment regression time was 122.00±9.85 minutes in a group which received 3cc of 0.5% hyperbaric bupivacaine with 100 μg of buprenorphine which did not match with our study group buprenorphine.9 The mean time to onset of motor blockade (modified Bromage 2) was 4.79 ± 0.513 minutes in Group B and 4.68 ± 0.502 minutes in Group F respectively. Mahima Gupta et al.. found the onset time of motor blockade (Bromage 2) in a group who received 60μg of buprenorphine with 3ml of 0.5% hyperbaric bupivacaine was 3.30±0.97 minutes which did not match with our study as this is faster.10 In our study the mean effective analgesia time in group B was 547.60 ± 80.276 minutes and that in group F was 410.00 ±67.942. Significantly prolonged effective analgesia time was found in Buprenorphine group with ‘p’ value <0.001.Rashmi Pal, K. K. Arora et al.. in a study found that the duration of analgesia is more in buprenorphine group than in fentanyl which is in accordance with our study.11
CONCLUSION Buprenorphine 60mcg added to 1.6 ml of 0.5% Hyperbaric Bupivacaine has comparable clinical onset of sensory and motor blockade, time for two segment regression, total duration of motor blockade but longer effective analgesia time when compared to Fentanyl 20 microgram added to 1.6 ml of 0.5% Hyperbaric Bupivacaine in patients undergoing LSCS under spinal anaesthesia.
REFERENCES
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