Endoscopic Ultrasound Guided Celiac Plexus Neurolysis

Manoop S. Bhutani, M.D.

 

Keywords

Celiac plexus block, Endoscopic Ultrasound

Introduction

Chronic abdominal pain can be a disabling symptom in patients with pancreatic cancer and chronic pancreatitis. When conservative therapy fails to adequately control the patient's pain, celiac plexus neurolysis or block may provide significant relief from pain. Celiac plexus block has traditionally been performed percutaneously under radiologic guidance (1). EUS provides an alternative method for performing celiac plexus neurolysis. The celiac plexus is not visible by EUS. However, the celiac ganglion is consistently located at the origin of the celiac artery from the aorta. Since celiac artery is well visualized during EUS, celiac plexus neurolysis can be performed using a trans-gastric anterior approach.

Body

Efficacy and Patient Selection

The most appropriate candidates for EUS guided celiac plexus neurolysis are patients with unresectable pancreatic cancer with significant pain that are completely or partially refractory to narcotic pain medications. EUS guided celiac plexus neurolysis may provide effective palliation of pancreatic cancer pain in 78-88% of patients (2, 3).

The efficacy of celiac plexus block in patients with chronic pancreatitis is less well established and the results are not as favorable in patients with pancreatic cancer. There is some data suggesting that the efficacy of celiac block under EUS guidance may be slightly better than CT guided percutaneous block in patients with chronic pancreatitis (4). Thus, celiac nerve block may be an option in selected cases of chronic pancreatitis with disabling pain that is refractory to narcotics and other medical measures. The decision to perform EUS guided celiac nerve block in patients with chronic pancreatitis should be made on a case-to-case basis with informed consent explaining the risk of complications and somewhat limited efficacy.

Figure 1

Figure 2A

Figure 2B

Figure 3A

Figure 3B

Figure 3C

Equipment

1. Curved linear array echoendoscope ( GF-UC3OP Olympus Corp, Melville, NY, FG 36UX Pentax Corp., Orangeburg, NY).
2. Twenty two gauge EUS guided fine needle aspiration needle (Wilson Cook, Winston-Salem NC; Olympus Corp, Melville, NY; Mediglobe Corp, Temple, AZ.
3. 0.25% Bupivacaine for nerve block.
4. 98% dehydrated alcohol for injection or Triamcinolone acetonide (40mg/ ml).

Technique

1. Patient fasting post midnight.
2. Informed consent.
3. Continuous normal saline infusion through an intravenous line.
4. Conscious sedation with demerol and midazolam.
5. Per-oral insertion of a curved linear array echoendoscope.
6. The aorta is identified along its longitudinal axis while imaging through the distal esophagus.
7. While maintaining the longitudinal view of the aorta on the ultrasonic screen(Figure 1), the echoendoscope is gently advanced towards the cardia/proximal stomach until the take off of the celiac artery from the aorta is identified(Figure 2A, 2B).
8. The echoendoscope is slowly rotated clockwise or anti-clockwise so that the celiac artery take-off is not visible. Color Doppler is used to rule out major vessels between the transducer and the peri-aortic space in this position.
9. A-22-gauge EUS guided FNA needle is connected to a 10cc syringe (containing 5cc of normal saline) after removing the stylet.
10. The needle with its outer sheath is loaded through the biopsy channel of the echoendoscope and is slowly advanced through the gastric wall into the peri-aortic space on the side of the celiac artery(Figure 3A). An aspiration test is preformed by gently pulling the plunger of the syringe. If no blood return is seen in the syringe, the plunger is pushed forward expelling a few cc of saline to clear the needle of any tissue material.
11. The syringe with saline is disconnected and 3 cc's of 0.25% bupivacaine is injected slowly with a syringe(figure 3B). This is followed by injection of 10cc. of 98% dehydrated alcohol for injection. In patients with chronic pancreatitis, 10cc of 0.25% bupivacaine mixed with 40mg of triaimcinolone may be injected instead of the bupivacaine and alcohol combination suggested above(Figure 3C).
12. The needle is then withdrawn from the peri-aortic space into its outer sheath. The echoendoscope is then rotated to the opposite side (clockwise or anti-clockwise) and similar procedure is repeated as in step 11.
13. In selected cases when it is technically difficult to find a good avascular window on either side of the celiac artery, a single midline injection may be made in the peri-aortic space at the angle between the take off of the celiac artery and the aorta (Figure 2A).
14. The patient is then transported to the recovery room.

Post Procedure Recovery

1. Normal saline infusion is continued in the recovery room.
2. The patient is observed for about 2 hours and monitored especially for hypotension.
3. The patient is checked for the presence of orthostatic hypotension prior to discharge.

Complications

A small percentage of patients undergoing EUS guided celiac plenus neurolysis or block may experience postural hypotension and diarrhea (2). These complications are due to the sympathetic blockade and are usually self limited and / or easily treatable by saline infusion (postural hypotension) and anti-diarrheals. A single case of pseudoaneurysm of the splenic artery after EUS guided celiac neurolysis using bupivacaine and alcohol has been reported (5). There has also been a case report of an intra-abdominal abscess occurring after EUS guided celiac plexus block in a patient with chronic pancreatitis using bupivacaine and steroids (5). This patient was on a chronic proton pump inhibitors (PPIs), and the authors have postulated that overgrowth of bacteria in the stomach due to the PPI may have contributed to this complication. I prefer to have patients stop their PPIs at least 5-7 days prior to a planned EUS guided celiac neurolysis or block. In addition, I give a single dose of IV antibiotic(usually of the quinolone group) during or immediately after the procedure followed by followed by the same antibiotic per orally for 5 days. Some authors have suggested that antibiotics are not necessary when bupivacaine and alcohol are used due to the bactericidal properties of alcohol. The most dreaded complication of celiac plexus neurolysis is paraplegia. This complication is seen in about 1% of patients undergoing percutaneous radiology guided celiac plexus neurolysis through a posterior approach (1,6). Since EUS guided celiac plexus neurolysis is preformed through an anterior approach with a short needle track it has been theorized that the chances of paraplegia may be less by using EUS as compared to a posterior percataneous approach(7). Although no cases of paraplegia during celiac block have been reported with the EUS approach, a theoretical risk of this complication should still be kept in mind (and explained to the patient during informed consent).

References

1. Lillemoe KD, Cameron JL, Kaufman HS, et al Chemical Spanchnicectomy in patients with unresectable pancreatic cancer: A prospective randomized trial Ann Surg 1993: 217:447-457

2. Wiersema MJ, Wiersema LM Endosonography guided celiac plexus neurolysis Gastrointest Endosco 1996;44:656-662

3. Gunartanam NT, Sarma AV, Norton ID, et al A prospective study of EUS-guided celiac plexus neurolysis for pancreatic cancer pain Gastrointest Endosc 2001;54:316-24

4. Gress F, Schmitt C, Sherman S, et al A prospective randomized comparison of endoscopic ultrasound and computed tomography guided celiac plexus block for the management of chronic pancreatitis. Am J Gastroeneterol 1999; 94: 900-905

5. Gress F, Ciaccia D, Kiel J, Sherman S, et al. Endoscopic ultrasound guided celiac plexus block for management Gastroinestinal Endoscopy 1997;45:173(abstract)

6. Van Dongen RT, Crul BJP Paraplegia following celiac plexus block Anesthesia 1991;46:862-863

7. Wiersema MJ Endosonography guided celiac plexus neurolysis In: Bhutani MS (ed). Interventional Endoscopic Ultrasonography, Harwood Academic Publishers, Amstedam, 1999;p117-123

 




Editorial Board:
Manoop S. Bhutani, M.D.
Galveston, TX
William R. Brugge, M.D.
Boston, MA
Peter R. McNally, D.O.
Denver, CO
Iqbal S. Sandhu, M.D.
Salt Lake City, UT
Thomas J. Savides, M.D.
San Diego, CA

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