Background: Postoperative pain management in cesarean deliveries presents unique challenges, with effective pain relief being essential for patient satisfaction and recovery. The use of Transverse Abdominis Plane (TAP) block has been increasingly favored as a part of multimodal analgesia strategies. This study aims to compare the analgesic efficacy of Bupivacaine alone versus Bupivacaine combined with Dexamethasone in TAP blocks, specifically focusing on the duration of analgesia, pain intensity, and the need for additional analgesic interventions. Methodology This study was conducted as a randomized controlled trial involving 172 women undergoing elective cesarean sections under spinal anesthesia. Patients were randomly assigned to two groups: Group A Received Bupivacaine and Dexamethasone, while Group B received Bupivacaine in the TAP block. The primary outcome measures included the duration of effective postoperative analgesia, visual analog scale (VAS) pain scores at specified intervals, and the frequency of rescue analgesic requirements. Secondary outcomes included the incidence of postoperative complications and overall patient satisfaction. Results The addition of Dexamethasone to Bupivacaine significantly extended the duration of postoperative analgesia by approximately 7 hours compared to Bupivacaine alone. Group B patients reported lower VAS pain scores at all-time points postoperatively and required fewer rescue analgesics. The combination therapy was also associated with a reduced incidence of opioid-related side effects and enhanced patient comfort. Conclusion The combination of Bupivacaine and Dexamethasone in TAP blocks offers a superior analgesic profile for cesarean deliveries, providing prolonged pain relief and reducing the need for additional analgesics. This approach should be considered a standard component of enhanced recovery protocols in obstetric surgery.
Cesarean delivery is one of the most commonly performed surgical procedures worldwide, and effective postoperative pain management is crucial for the well-being of the mother. Inadequate pain control can lead to delayed recovery, increased risk of chronic pain, and negative impacts on the ability to care for the newborn.[1-3] Traditionally, opioid-based analgesia has been the cornerstone of postoperative pain management. However, the adverse effects associated with opioids, including nausea, vomiting, respiratory depression, and delayed recovery, have prompted a shift toward multimodal analgesia strategies that minimize or eliminate the need for opioids.[4] The Transverse Abdominis Plane (TAP) block is a regional anesthesia technique that provides targeted analgesia to the anterior abdominal wall by delivering local anesthetic into the plane between the transversus abdominis and internal oblique muscles. This technique has been widely adopted due to its efficacy in reducing postoperative pain and opioid consumption. The addition of adjuvants, such as corticosteroids, to local anesthetics in TAP blocks has been explored to prolong the duration of analgesia and enhance patient outcomes.[5] The primary objective of this study is to compare the efficacy of Bupivacaine alone versus Bupivacaine combined with Dexamethasone in TAP blocks for postoperative pain management in women undergoing cesarean sections. This comparison focuses on key outcomes such as the duration of analgesia, pain intensity as measured by VAS scores, the need for rescue analgesics, and the incidence of postoperative complications.[6]
The findings of this study have the potential to inform clinical practice by identifying an optimal analgesic regimen that enhances postoperative pain control, reduces the reliance on opioids, and promotes faster recovery in cesarean deliveries. The use of TAP blocks with adjuvants like Dexamethasone could become a cornerstone of enhanced recovery protocols, leading to better patient outcomes and overall satisfaction.[7-9].
A randomized controlled trial, conducted at the Department of Anesthesia, D.Y. Patil Medical College Hospital and Research Institute, Kolhapur. The trial aimed to provide high-quality evidence on the effectiveness of adding Dexamethasone to Bupivacaine in TAP blocks for cesarean deliveries. A total of 172 women scheduled for elective cesarean sections under spinal anesthesia were enrolled in the study. Participants were randomly assigned to one of two groups using a computer-generated randomization sequence to ensure unbiased allocation. Group A consisted of 86 patients who received Bupivacaine and Dexamethasone, while Group B included 86 patients who received Bupivacaine alone. Inclusion criteria were women aged 18 years and older, classified as ASA physical status I or II, and willing to participate in the study. Exclusion criteria included refusal to participate, known allergies to local anesthetics or corticosteroids, significant cardiac disease, suspected coagulopathy, and local infections at the site of injection. Following informed consent and preoperative evaluation, all participants underwent standard spinal anesthesia for their cesarean section. After the surgical procedure, the TAP block was administered bilaterally using an ultrasound-guided technique. Group A patients received 20 ml of 0.25% Bupivacaine combined with 8 mg of Dexamethasone on each side, while Group B patients received the same dose of Bupivacaine alone. The block was performed by an experienced anesthesiologist using a 22G Echoplex needle under aseptic conditions
Characteristic |
Group A (Bupivacaine + Dexamethasone) |
Group B (Bupivacaine) |
Number of Patients |
86 |
86 |
Mean Age (years) |
29.5 ± 4.2 |
30.1 ± 3.8 |
ASA Grade I (%) |
78% |
76% |
ASA Grade II (%) |
22% |
24% |
Mean Duration of Surgery (minutes) |
55.3 ± 10.5 |
54.7 ± 11.2 |
Table 1: Patient Demographics and Baseline Characteristics |
The study enrolled a total of 172 women, with both groups well-matched in terms of age, ASA physical status, and the duration of surgery. The mean age of participants was approximately 30 years, and the majority of patients were classified as ASA grade I, indicating that they were in good health apart from their surgical condition. The duration of surgery was similar between the two groups, with no statistically significant differences observed.
Group |
Mean Duration of Analgesia (hours) |
Group A (Bupivacaine + Dexamethasone) |
10.34 ± 1.56 |
Group B (Bupivacaine) |
17.22 ± 2.34 |
P-value |
< 0.001 |
Table 2: Duration of Postoperative Analgesia |
The duration of postoperative analgesia was significantly longer in Group B, with an average duration of 17.22 hours, compared to 10.34 hours in Group A. This substantial difference highlights the efficacy of Dexamethasone as an adjuvant in extending the pain-relief benefits of the TAP block, providing patients with prolonged comfort during the critical postoperative period.
Time Interval (Hours Post-Op) |
Group A (Bupivacaine + Dexamethasone) |
Group B (Bupivacaine) |
P-value |
4 |
4.17 ± 1.12 |
2.85 ± 0.98 |
0.001 |
8 |
5.23 ± 1.34 |
3.19 ± 1.01 |
<0.001 |
12 |
6.02 ± 1.45 |
4.10 ± 1.13 |
<0.001 |
24 |
6.98 ± 1.55 |
5.22 ± 1.24 |
<0.001 |
Table 3: VAS Pain Scores at Different Time Intervals |
VAS pain scores, a subjective measure of pain intensity, were consistently lower in Group B at all-time points assessed. The addition of Dexamethasone not only prolonged analgesia but also significantly reduced the intensity of pain experienced by patients in the first 24 hours postoperatively. This reduction in pain intensity was statistically significant across all time points, indicating a robust analgesic effect.
Group |
Patients Requiring Rescue Analgesics (%) |
Group A (Bupivacaine + Dexamethasone) |
65% |
Group B (Bupivacaine) |
35% |
P-value |
0.002 |
Table 4: Requirement for Rescue Analgesics |
The need for rescue analgesics was significantly lower in Group B, with only 35% of patients requiring additional pain relief compared to 65% in Group A. This difference underscores the enhanced analgesic efficacy of the combination therapy, which provided more consistent and longer-lasting pain relief, reducing the reliance on additional medications.
Complication |
Group A (Bupivacaine + Dexamethasone) |
Group B (Bupivacaine) |
Nausea and Vomiting (%) |
12% |
8% |
Infection at Injection Site (%) |
2% |
1% |
Postoperative Headache (%) |
5% |
3% |
Allergic Reactions (%) |
1% |
0% |
Table 5: Complications and Adverse Events |
The incidence of complications and adverse events was slightly lower in Group B, although the differences were not statistically significant. Nausea and vomiting were the most common side effects observed, followed by postoperative headache and minor infections at the injection site. The lower rates of complications in the Dexamethasone group may contribute to the overall better patient experience.
The study's findings demonstrate that the addition of Dexamethasone to Bupivacaine in TAP blocks significantly enhances postoperative pain control in cesarean deliveries. The extended duration of analgesia, combined with lower pain intensity and reduced need for rescue analgesics, highlights the superiority of this combination therapy over Bupivacaine alone. These benefits are particularly relevant in the context of cesarean deliveries, where effective pain management is crucial for enabling early mobility, facilitating breastfeeding, and improving overall maternal satisfaction.[6-9]
The results of this study have important clinical implications for the management of postoperative pain in obstetric patients. The enhanced analgesic profile of the Bupivacaine-Dexamethasone combination suggests that it should be considered a preferred option in TAP blocks for cesarean deliveries. By providing longer-lasting and more effective pain relief, this approach can help reduce the reliance on opioids, thereby minimizing the risk of opioid-related side effects and promoting a smoother recovery process.[10]
Despite the positive findings, the study has several limitations that should be acknowledged. The focus on cesarean sections means that the results may not be generalizable to other types of surgeries or patient populations. Additionally, the study did not assess the impact of the analgesic regimen on long-term outcomes, such as the development of chronic pain or patient satisfaction beyond the immediate postoperative period. Future research should address these gaps by including a broader range of surgical procedures and evaluating long-term outcomes. To build on the findings of this study, future research should consider multi-center trials with larger, more diverse patient populations. Such studies could provide more comprehensive data on the safety and efficacy of Bupivacaine-Dexamethasone combinations in various surgical contexts. Additionally, exploring the potential benefits of other adjuvants in TAP blocks could further optimize pain management strategies in obstetric and non-obstetric surgeries.[11]
In conclusion, this study provides compelling evidence that the addition of Dexamethasone to Bupivacaine in TAP blocks significantly improves postoperative analgesia in cesarean deliveries. The combination therapy not only extends the duration of pain relief but also reduces pain intensity and the need for additional analgesics, leading to better patient outcomes. These findings support the use of Bupivacaine-Dexamethasone TAP blocks as a standard practice in enhanced recovery protocols for cesarean sections, with the potential to improve both patient satisfaction and clinical efficiency.