Efficacy of Epidural Dexmedetomidine as an Adjuvant to 0.75% Ropivacaine in Lower Abdominal Surgeries: A Comparative Study

Authors:
  • Dr Adithya R , Assistant Professor, Department of Anaesthesiology, BGS Medical College and Hospital, Bengaluru, Karnataka
  • Dr Akshay Shetty , Associate Professor, Department of Anaesthesiology, BGS Medical College and Hospital, Bengaluru, Karnataka
  • Dr Monika Vidyasagar D , Senior Resident, Department of Anaesthesiology, Sapthagiri Institute of Medical Sciences and Research Centre, Bengaluru, Karnataka.

Article Information:

Published:March 10, 2026
Article Type:Original Research
Pages:719 - 722
Received:January 15, 2026
Accepted:February 10, 2026

Abstract:

Introduction: Epidural anaesthesia is widely used for lower abdominal surgeries due to its ability to provide effective intraoperative anaesthesia and postoperative analgesia. Ropivacaine, a long-acting amide local anesthetic, is preferred because of its favorable safety profile. Dexmedetomidine, a highly selective α2-adrenergic agonist, has emerged as an effective adjuvant to enhance block characteristics and prolong analgesia. Materials and Methods: This prospective, randomized, double-blind study was conducted in the Department of Anaesthesiology, Sapthagiri Institute of Medical Sciences and Research Centre, Bengaluru, Karnataka from November 2024 to October 2025. A total of 100 patients (ASA I–II), aged 18–60 years, undergoing elective lower abdominal surgeries under epidural anaesthesia were included in the study. Patients were randomly allocated into two groups (n=50 each). Group R received 20 mL of 0.75% ropivacaine, while Group RD received 20 mL of 0.75% ropivacaine with dexmedetomidine (1 µg/kg). Parameters assessed included onset of sensory and motor block, duration of block, duration of analgesia, hemodynamic changes, and adverse effects. Results: Group RD showed significantly faster onset of sensory and motor block (p<0.001), prolonged duration of analgesia (p<0.001), and better postoperative pain scores compared to Group R. Hemodynamic parameters remained stable in both groups, though mild bradycardia was observed in the RD group. Conclusion: Addition of dexmedetomidine to 0.75% ropivacaine significantly improves block quality and prolongs postoperative analgesia without major adverse effects.

Keywords:

Epidural anaesthesia Ropivacaine Dexmedetomidine Lower abdominal surgery Analgesia α2 agonist

Article :

INTRODUCTION:

Epidural anaesthesia is a cornerstone technique in lower abdominal surgeries because it provides excellent surgical anaesthesia, reduces stress response, and offers prolonged postoperative analgesia¹. Compared to general anaesthesia, epidural blockade decreases perioperative morbidity, enhances early ambulation, and improves patient satisfaction². Ropivacaine, a pure S-enantiomer amide local anesthetic, has gained widespread acceptance due to its lower cardiotoxicity and neurotoxicity compared to bupivacaine³. Its differential block characteristic allows preferential sensory blockade with minimal motor impairment⁴.

 

Despite its favorable pharmacological profile, the duration of analgesia with plain ropivacaine may be limited, necessitating the use of adjuvants⁵. Various adjuvants such as opioids, clonidine, and magnesium have been evaluated to enhance epidural block quality⁶. However, opioid-related side effects such as pruritus, respiratory depression, and nausea limit their widespread use⁷.

Dexmedetomidine is a highly selective α2-adrenergic receptor agonist with sedative, analgesic, and sympatholytic properties⁸. It acts at the locus coeruleus and dorsal horn of the spinal cord, reducing nociceptive transmission⁹. Epidural dexmedetomidine enhances local anesthetic effects by hyperpolarizing interneurons and inhibiting substance P release¹⁰. It prolongs sensory and motor blockade without causing significant respiratory depression¹¹.

 

Recent clinical studies have shown that adding dexmedetomidine to ropivacaine improves onset time, prolongs duration of analgesia, and provides hemodynamic stability¹²–¹⁴. Furthermore, its anti-inflammatory and stress-attenuating effects may contribute to improved postoperative recovery¹⁵.

 

Lower abdominal surgeries require adequate intraoperative anaesthesia and prolonged postoperative analgesia to facilitate early mobilization and reduce complications¹⁶. Therefore, evaluating the efficacy of dexmedetomidine as an epidural adjuvant with ropivacaine is clinically relevant.

 

This study aims to compare 0.75% ropivacaine alone versus 0.75% ropivacaine with dexmedetomidine in lower abdominal surgeries with respect to onset and duration of block, analgesic efficacy, hemodynamic stability, and adverse effects.

MATERIALS AND METHODS:

This prospective, randomized, double-blind study was conducted in the Department  of Anaesthesiology, Sapthagiri Institute of Medical Sciences and Research Centre, Bengaluru,  Karnataka, from November 2024 to October 2025. A total of 100 patients scheduled for elective lower abdominal surgeries under epidural anaesthesia were enrolled.

 

Inclusion Criteria

             Age 18–60 years

             ASA physical status I and II

             Elective lower abdominal surgery

             BMI 18–30 kg/m²

 

Exclusion Criteria

             Patient refusal

             Coagulopathy

             Infection at puncture site

             Severe cardiac, hepatic, renal disease

             Known allergy to study drugs

             Pregnancy

 

Randomization

Patients were randomly divided into:

             Group R (n=50): 20 mL of 0.75% ropivacaine

             Group RD (n=50): 20 mL of 0.75% ropivacaine + dexmedetomidine (1 µg/kg)

 

Procedure

Epidural catheter was inserted at L2–L3 or L3–L4 interspace. After negative aspiration and test dose, study drug was administered.

 

Parameters Assessed

             Onset of sensory block (T10 level)

             Onset of motor block (Modified Bromage scale)

             Duration of sensory and motor block

             Duration of analgesia (VAS >4)

             Hemodynamic parameters

             Sedation score

             Adverse effects

Statistical analysis was performed using SPSS software. P-value < 0.05 considered was considered statistically significant.

RESULTS:

Table 1: Demographic Data

Parameter

Group R

Group RD

p-value

Age (years)

42 ± 10

41 ± 9

0.62

Weight (kg)

64 ± 8

66 ± 7

0.41

Duration of Surgery (min)

95 ± 20

98 ± 18

0.53

No significant difference in baseline demographic characteristics.

 

Table 2: Onset of Block

Parameter

Group R

Group RD

p-value

Sensory Onset (min)

12.4 ± 2.1

8.3 ± 1.5

<0.001

Motor Onset (min)

18.6 ± 2.8

12.5 ± 2.0

<0.001

Faster onset in RD group.

 

Table 3: Duration of Block

Parameter

Group R

Group RD

p-value

Sensory Duration (min)

210 ± 25

340 ± 30

<0.001

Motor Duration (min)

180 ± 20

300 ± 28

<0.001

Significant prolongation in RD group.

 

Table 4: Duration of Analgesia

Group

Duration (min)

R

230 ± 22

RD

420 ± 35

p < 0.001

RD provided prolonged postoperative analgesia.

 

Table 5: Hemodynamic Changes

Parameter

Bradycardia

Hypotension

R

2 (4%)

3 (6%)

RD

6 (12%)

5 (10%)

Slightly higher bradycardia in RD group but manageable.

 

Table 6: Adverse Effects

Side Effect

R

RD

Nausea

3

2

Sedation

1

8

Respiratory depression

0

0

Sedation higher in RD but no respiratory depression.

DISCUSSION:

The present study demonstrates that the addition of dexmedetomidine to 0.75% ropivacaine for epidural anaesthesia significantly enhances the block characteristics and prolongs postoperative analgesia in patients undergoing lower abdominal surgeries. The findings indicate a faster onset of both sensory and motor blockade, significantly prolonged duration of anaesthesia, and superior postoperative analgesic quality in the dexmedetomidine group compared to ropivacaine alone.

 

The faster onset of sensory and motor block observed in the dexmedetomidine group can be attributed to the synergistic interaction between α2-adrenergic agonists and local anesthetics. Dexmedetomidine enhances local anesthetic action by inhibiting the release of substance P in the dorsal horn and by hyperpolarizing interneurons, thereby facilitating earlier conduction blockade. Similar findings were reported by Gupta et al., who demonstrated reduced onset time when dexmedetomidine was added to epidural ropivacaine. Sharma et al. also observed significantly quicker attainment of T10 sensory level with α2 agonist supplementation.

 

One of the most clinically relevant findings of this study is the significant prolongation of sensory block and postoperative analgesia in the dexmedetomidine group. The duration of analgesia was nearly doubled compared to ropivacaine alone. This prolonged effect is consistent with previous studies by Bajwa et al. and Al-Mustafa et al., who reported extended analgesic duration due to spinal α2 receptor activation. Dexmedetomidine acts by decreasing sympathetic outflow and attenuating nociceptive transmission at the spinal cord level. This mechanism allows sustained analgesia without increasing the concentration of local anesthetic, thereby avoiding toxicity.

 

Hemodynamic stability was maintained in both groups throughout the perioperative period. Although a slightly higher incidence of bradycardia was observed in the dexmedetomidine group, it was mild and responsive to atropine. This sympatholytic effect is well documented in the literature and reflects central inhibition of norepinephrine release. Importantly, no episodes of significant hypotension or respiratory depression were recorded. The absence of respiratory depression is a major advantage over opioid adjuvants, which are associated with pruritus, nausea, vomiting, and ventilatory compromise.

 

Sedation scores were higher in the dexmedetomidine group, but the sedation was cooperative and arousable, which may be advantageous in regional anaesthesia settings. The sedative effect is mediated through action on the locus coeruleus and provides patient comfort without respiratory compromise. Similar observations were made in multiple randomized trials evaluating epidural dexmedetomidine.

 

Our findings support the growing body of evidence that dexmedetomidine is an effective and safe epidural adjuvant. Compared to clonidine, dexmedetomidine exhibits greater α2 receptor selectivity, resulting in improved analgesic efficacy with fewer side effects. The prolonged analgesic effect also reduces the need for rescue analgesics, contributing to enhanced postoperative recovery and patient satisfaction.

 

However, certain limitations must be acknowledged. The study was conducted at a single center with a relatively modest sample size. Long-term outcomes such as chronic pain and recovery profiles were not evaluated. Future multicenter trials with larger populations would provide stronger evidence.

CONCLUSION:

The findings of this study suggest that dexmedetomidine is an effective and reliable adjuvant to epidural 0.75% ropivacaine in lower abdominal surgeries. Its ability to enhance block quality, prolong analgesic duration, maintain hemodynamic stability, and avoid opioid-related adverse effects makes it a valuable addition to regional anaesthesia practice. It is a safe and effective epidural adjuvant in lower abdominal surgeries.

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