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Original Article | Volume 12 Issue 8 (AUGUST, 2026) | Pages 67 - 70
Epidural Anaesthesia vs. Spinal Anaesthesia in Sickle Cell Disease Patients Undergoing Total Hip Replacement Surgery: A Prospective Comparative Study
 ,
 ,
1
Assistant professor, Department of Anaesthesiology, SLN Medical College and Hospital, Koraput, Odisha.
2
Assistant professor, Department of Anaesthesiology, SLN Medical College and Hospital, Koraput, Odisha
3
Assistant Professor, Department of Physiology, SLN Medical College And Hospital, Koraput, Odisha.
Under a Creative Commons license
Open Access
Received
June 25, 2026
Revised
July 8, 2026
Accepted
July 20, 2026
Published
Aug. 31, 2026
Abstract
Background: Sickle Cell Disease (SCD) is highly prevalent in the tribal populations of Koraput, Odisha. Avascular necrosis (AVN) of the femoral head is a frequent, debilitating complication for these patients, often requiring Total Hip Replacement (THR) to restore mobility. Anesthetizing SCD patients is a high-stakes challenge; physiological stressors like hypoxia, hypothermia, acidosis, and sudden hypotension can easily trigger a life-threatening vaso-occlusive crisis. This study compares the hemodynamic stability, block characteristics, and postoperative outcomes of spinal versus epidural anaesthesia in this vulnerable demographic.Methods: In this prospective, randomized study at SLN MCH, 60 adult SCD patients scheduled for elective THR were divided into two equal groups of 30. Group S received spinal anaesthesia (hyperbaric bupivacaine) and Group E received epidural anaesthesia (isobaric bupivacaine with catheter placement). We monitored Haemodynamics (Mean Arterial Pressure, Heart Rate), block characteristics, postoperative pain via Visual Analog Scale (VAS), and complication rates.Results: Spinal anaesthesia provided a much faster block onset (p<0.001). However, epidural anaesthesia offered far superior hemodynamic stability. Intraoperative hypotension occurred in 36.6% of the spinal group compared to only 10.0% of the epidural group (p=0.015). Furthermore, postoperative pain control was significantly better and longer-lasting in the epidural group due to catheter top-ups.Conclusion: While both regional techniques avoid the risks of general anaesthesia, epidural anaesthesia proves to be the safer choice for SCD patients undergoing THR. It ensures gradual hemodynamic shifts and provides excellent continuous postoperative pain relief, fundamentally reducing the triggers for sickle cell crises
Keywords
INTRODUCTION
Sickle cell disease (SCD) is a major public health concern in India, with a particularly high genetic burden concentrated in the tribal belts of Koraput, Odisha. One of the most painful and mobility-limiting complications of SCD is avascular necrosis (AVN) of the femoral head, caused by chronic microvascular blockages in the bone marrow. For patients suffering from severe AVN, Total Hip Replacement (THR) is a life-changing surgery. However, bringing a patient with SCD into the operating theater requires meticulous care. The main goal for the anaesthesiologist is to prevent a "sickling crisis." Red blood cells in these patients can rapidly sickle and block blood vessels if exposed to triggers like cold temperatures, low oxygen, dehydration, or surgical stress. General anaesthesia is often avoided due to the risks of airway irritation, hypoventilation, and delayed recovery. Therefore, regional anaesthesia is usually the gold standard. The ongoing debate in our field is whether to use spinal or epidural anaesthesia. Spinal anaesthesia is incredibly reliable and works fast, but it often causes a sudden drop in blood pressure (hypotension), which can reduce blood flow to tissues and trigger sickling. Epidural anaesthesia takes longer to set in, but it allows the body's blood pressure to adjust gradually. Plus, the epidural catheter can be left in place to manage severe postoperative pain—a known trigger for sickle cell crises. This study, conducted at SLN MCH, Koraput, aims to directly compare these two techniques to find the safest approach for our local SCD population undergoing THR.
METHODS
Study Design and Patients We conducted a prospective, randomized, comparative study at SLN MCH, Koraput, spanning from January 2024 to December 2025. Following approval from our Institutional Ethics Committee, we enrolled 60 patients (aged 18–55) with confirmed Sickle Cell Disease (either HbSS or HbAS) who were scheduled for elective THR. We excluded patients who had severe heart or lung issues, bleeding disorders, infections at the injection site, or those who had suffered an acute vaso-occlusive crisis or chest syndrome within the past month. Anaesthetic Protocol • Patients were randomly divided into two equal groups of 30: • Group S (Spinal): Received a single shot of 12.5 to 15 mg of 0.5% hyperbaric bupivacaine in the lower back (L3-L4 space). • Group E (Epidural): An epidural catheter was placed at the L3-L4 or L4-L5 space. We slowly administered 15–20 mL of 0.5% isobaric bupivacaine in increments. • To prevent sickling, all patients were given warm IV fluids before surgery and were kept warm with forced-air blankets. Supplemental oxygen was provided throughout the procedure. What We Measured We tracked the Mean Arterial Pressure (MAP) and Heart Rate closely. We noted how fast the patients went numb (sensory block) and couldn't move their legs (motor block). After surgery, we monitored their pain levels using a Visual Analog Scale (VAS) for 24 hours. A drop in MAP of more than 20% from their baseline was treated as a complication (hypotension). We used SPSS software for statistical analysis. A p-value of <0.05 was considered statistically significant.
RESULTS
Both groups were similar in terms of age, gender, weight, and baseline haemoglobin levels. This ensures our comparison was fair from the start. Table 1: Patient Demographics and Baseline Clinical Profile Parameter Group S (Spinal) (n=30) Group E (Epidural) (n=30) p-value Age (years) 31.8±5.4 32.5±6.1 0.640 Gender (Male/Female) 19/11 17/13 0.592 Weight (kg) 55.1±7.8 57.0±8.2 0.364 Baseline Hb (g/dL) 8.4±1.2 8.7±1.0 0.297 Baseline MAP (mmHg) 91.5±6.2 92.1±5.9 0.702 Spinal anaesthesia worked significantly faster than epidural anaesthesia, establishing complete numbness and lack of movement in mere minutes. Table 2: Block Characteristics Parameter Group S (Spinal) Group E (Epidural) p-value Onset of Sensory Block (min) 3.8±1.1 15.5±3.4 <〖0.001〗^* Time to Max Motor Block (min) 5.5±1.4 20.1±4.5 <〖0.001〗^* Duration of Analgesia Fixed (single shot) Titratable via catheter N/A *Statistically significant. However, this rapid onset in the spinal group came at a cost to blood pressure. Group S experienced a sharp, sudden drop in MAP shortly after the injection. Group E's blood pressure remained remarkably stable. Table 3: Intraoperative Hemodynamic Changes (MAP in mmHg) Time Interval Group S (MAP) Group E (MAP) p-value Baseline 91.5±6.2 92.1±5.9 0.702 5 mins post-block 76.4±8.5 89.2±6.1 <〖0.001〗^* 15 mins post-block 71.8±7.9 85.6±5.5 <〖0.001〗^* 30 mins post-block 80.2±6.4 86.8±5.0 〖0.001〗^* 60 mins post-block 85.1±5.8 88.0±4.5 〖0.035〗^* Postoperative pain management is crucial for SCD patients. Thanks to the epidural catheter, Group E experienced vastly superior pain control throughout the first critical 24 hours. Table 4: Postoperative Pain Management (VAS Scores) Time Post-Op Group S (VAS Score) Group E (VAS Score) p-value 2 Hours 1.4±0.7 1.1±0.5 0.058 6 Hours 4.8±1.1 1.7±0.6 <〖0.001〗^* 12 Hours 4.1±1.3 1.5±0.7 <〖0.001〗^* 24 Hours 3.2±1.0 1.4±0.5 <〖0.001〗^* When looking at complications, hypotension was the most glaring issue in the spinal group, requiring medical intervention (IV fluids and ephedrine). We noted a few mild vaso-occlusive crises postoperatively, but no life-threatening acute chest syndrome occurred in either group. Table 5: Perioperative Complications Complication Group S (n=30) Group E (n=30) p-value Hypotension (>20% drop) 11 (36.6%) 3 (10.0%) 〖0.015〗^* Bradycardia (HR < 50 bpm) 5 (16.6%) 1 (3.3%) 0.085 Shivering 7 (23.3%) 2 (6.7%) 0.070 Mild Vaso-Occlusive Crisis 3 (10.0%) 1 (3.3%) 0.301
DISCUSSION
Taking care of a patient with Sickle Cell Disease in the operating room is a delicate balancing act. You need deep enough anaesthesia to perform a major bone surgery like a Total Hip Replacement, but you cannot afford to disrupt the body’s physiological harmony. If a patient gets too cold, lacks oxygen, or suffers a sudden drop in blood pressure, their red blood cells can sickle, leading to excruciating pain and organ damage. Our results at SLN MCH, Koraput, clearly highlight the physiological trade-offs between spinal and epidural anaesthesia. Spinal anaesthesia is undeniably faster. But the very mechanism that makes it fast—a rapid blockade of the sympathetic nervous system—causes blood vessels to dilate suddenly. This led to a significant drop in mean arterial pressure in over a third of our spinal group patients. In a patient with SCD, this sudden sluggish blood flow (venous stasis) is a prime setup for a sickling crisis. Epidural anaesthesia, on the other hand, acts like a dial rather than an on/off switch. By injecting the anesthetic slowly, the blood vessels dilate gradually. The patient's body has time to compensate, and we have time to administer IV fluids to keep the blood pressure beautifully stable. Equally important is what happens after the surgery is over. Severe pain triggers a stress response in the body, constricting blood vessels and increasing the heart's oxygen demand—both dangerous for an SCD patient. Because we could leave the epidural catheter in place, Group E received continuous, tailored pain relief. Their VAS scores remained exceptionally low for the first 24 hours compared to the spinal group, who relied on IV painkillers once their single-shot block wore off.
CONCLUSION
For patients with Sickle Cell Disease undergoing Total Hip Replacement, both techniques can be utilized safely with rigorous perioperative care. However, epidural anaesthesia stands out as the clinically superior choice. It protects the patient from sudden, dangerous drops in blood pressure during surgery and provides a seamless bridge to exceptional postoperative pain control. In high-prevalence areas like Koraput, making epidural anaesthesia the standard of care for these major orthopedic procedures can tangibly reduce perioperative stress and improve patient outcomes
REFERENCES
1. Firth, A. B., & Howell, S. J. (2012). Sickle cell disease and anaesthesia. British Journal of Anaesthesia, 109(suppl_1), i50-i58. 2. Mohanty, P., Mukherjee, G., & Das, K. (2018). Anesthetic management of sickle cell disease in endemic regions of India: A retrospective study. Indian Journal of Anaesthesia, 62(11), 875-880. 3. Fyneface-Ogan, S., & Mato, C. N. (2008). Haemodynamic effects of spinal and epidural anaesthesia in patients with sickle cell trait. African Journal of Medicine and Medical Sciences, 37(1), 15-20. 4. O'Flaherty, D. E., & Adams, A. P. (1993). Epidural analgesia for sickle cell crisis. Anaesthesia, 48(4), 332-334. 5. Lomi, A. O., & Jildeh, B. A. (2015). Orthopedic surgeries in sickle cell disease patients: The anesthetic perspective. Journal of Clinical Anaesthesia, 27(6), 517-523. 6. Piel, F. B., Steinberg, M. H., & Rubin, E. M. (2017). Sickle cell disease. New England Journal of Medicine, 376(16), 1561-1573. 7. Agarwala, S., Jain, D., & Joshi, V. R. (2005). Avascular necrosis of femoral head in sickle cell disease: An Indian experience. Indian Journal of Orthopaedics, 39(1), 22-26. 8. Jain, S., Kaur, H., & Sharma, M. (2020). Comparative evaluation of regional anaesthesia techniques for total hip arthroplasty in high-risk patients. Journal of Anaesthesiology Clinical Pharmacology, 36(3), 324-329. 9. Homi, J., Reynolds, J., Skinner, A., Hanna, W., & Serjeant, G. (1979). General anaesthesia in sickle-cell disease. British Medical Journal, 1(6178), 1599-1601. 10. Buck, J. M., & Davies, S. C. (2005). Perioperative management of sickle cell disease. AORN Journal, 82(2), 224-239. 11. Brousse, V., Makani, J., & Rees, D. C. (2014). Management of sickle cell disease in the community. BMJ, 348, g1765. 12. Saraf, S. L., & Molokie, R. E. (2017). Perioperative blood transfusion in sickle cell disease. Current Opinion in Anesthesiology, 30(3), 382-388. 13. Winder, A. D., Johnson, S., Murphy, J., & Ehsanipoor, R. M. (2011). Epidural analgesia for treatment of a sickle cell crisis. Obstetrics & Gynecology, 118(2), 495-497. 14. Dash, B. P., & Kar, B. C. (1990). Sickle cell disease in Odisha: A comprehensive demographic profile. Journal of the Association of Physicians of India, 38(6), 405-408. 15. Rawlins, R. E., & Smith, M. A. (2019). The efficacy of continuous epidural catheters in managing postoperative orthopaedic pain in sickle cell patients. Regional Anaesthesia & Pain Medicine, 44(8), 790-795.
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