JOURNAL HOME CME HOME THIS MONTH PAST ISSUES ETOC COLLECTIONS
AUTHORS REVIEWERS EDITORIAL BOARD FEEDBACK RSS HELP
A&A International Anesthesia Research Society
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a colleague
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vranken, J. H.
Right arrow Articles by Dzoljic, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vranken, J. H.
Right arrow Articles by Dzoljic, M.
Related Collections
Right arrow Regional Anesthesia
Right arrow Pain

Anesth Analg 2002;95:1724-1725
© 2002 International Anesthesia Research Society


PAIN MEDICINE

Continuous Sacral Nerve Root Block in the Management of Neuropathic Cancer Pain

Jan H. Vranken, MD, Marinus H. van der Vegt, MD, Leon H. Ubags, PhD, Aarnout J. Pijl, PhD, and Misa Dzoljic, PhD

Department of Anesthesiology, Pain Relief Unit, Academic Medical Center, University of Amsterdam, The Netherlands

Address correspondence and reprint requests to Jan H. Vranken, MD, Department of Anesthesiology, Pain Relief Unit, Academic Medical Center, University of Amsterdam, PO Box 22700, 1100 DE Amsterdam, The Netherlands. Address e-mail to j.h.vranken{at}amc.uva.nl


    Abstract
 Top
 Abstract
 Introduction
 Case Report
 Discussion
 References
 

IMPLICATIONS: Neuropathic cancer pain caused by tumor infiltration in the sacral plexus is primarily treated by nonsteroidal antiinflammatory drugs, antidepressants, anticonvulsants, and opioids. In one patient with severe pain despite pharmacotherapy, a catheter for the continuous administration of local anesthetics was inserted along the first sacral root, resulting in markedly improved analgesia.


    Introduction
 Top
 Abstract
 Introduction
 Case Report
 Discussion
 References
 
The effective treatment of patients suffering from neuropathic pain caused by tumor infiltration in the sacral plexus remains a clinical challenge (1). In patients with poor pain control despite pharmacotherapy, including opioids, corticosteroids, antidepressants, and anticonvulsants, combined with antineoplastic therapies (2), reversible peripheral nerve catheterization techniques may be considered. In this paper, we present a patient with an ovarian carcinoma infiltrating the sacral plexus causing a sacral radiculopathy not reacting sufficiently to pharmacological treatment. To obtain adequate pain relief, a catheter for the continuous administration of local anesthetics was inserted along the first sacral root.


    Case Report
 Top
 Abstract
 Introduction
 Case Report
 Discussion
 References
 
A 37-yr-old woman presented with severe neuropathic pain and sensory impairment in the left leg. Computerized axial tomography revealed an ovarian carcinoma with malignant infiltration of the psoas muscle and invasion of the left foramen of S1 with possible nerve root compression. At the time of admission, the patient experienced a constant severe burning pain located in the posterior thigh and calf radiating to the great toe (i.e., dermatome S1). The pain was resistant to a combination of nonsteroidal antiinflammatory drugs, dexamethasone 12 mg, carbamazepine 900 mg, amitriptyline 50 mg, and slow-release morphine 400 mg per day. Increasing the opioid dose was impossible because of dose-limiting side effects.

An infiltration with 1.5 mL of bupivacaine 0.25% along the S1 root resulted in an almost complete resolution of the neuropathic pain in the left leg. To obtain long-lasting pain relief, a catheter was inserted along the S1 nerve root. The patient was placed in a prone position, and the left S1 foraminal opening on the posterior plate of the sacrum was identified using a C-arm fluoroscopic device. Subsequently, an 18-gauge, 110-mm, 15-degree short bevel cannula (Contiplex D®, Braun, Melsungen, Germany) was introduced at the inferior lip of the S1 foraminal opening and advanced parallel to the beam of the fluoroscopic tube. Needle placement was confirmed using electrical stimulation at <1.0 V at 50 Hz, which resulted in paraesthesias in the S1 dermatome. Contrast fluid was injected to outline the S1 root sleeve (Fig. 1). The needle was removed, and a catheter (20-gauge, Perifix®, Braun) was advanced 1–2 cm beyond the tip of the cannula. Finally, the catheter was tunneled subcutaneously to the hip and was fixed with transparent dressing. The administration of bupivacaine 0.125% at an initial rate of 2 mL/h resulted in a significant improvement in pain relief. The daily opioid dose could be reduced, and side effects disappeared. After 5 days, the patient was discharged from the hospital with a continuous infusion of bupivacaine 0.125% at a rate of 4 mL/h.



View larger version (107K):
[in this window]
[in a new window]
 
Figure 1. Posteroanterior radiograph of the sacrum. Arrows indicate the spread of contrast fluid outlining the S1 root sleeve. The S1 and S2 foraminal openings on both sides are marked.

 
However, after 5 wk, while the neuropathic pain in the left leg was still absent, the patient was readmitted with severe pelvic pain resistant to slow-release morphine. Increasing the opioid dose led again to unacceptable side effects. Spinal treatment with opioids and local anesthetics was now proposed, but the patient refused further treatment and died 2 days later.


    Discussion
 Top
 Abstract
 Introduction
 Case Report
 Discussion
 References
 
Opioid analgesics are the mainstay in the management of cancer pain. However, neuropathic pain caused by tumor infiltration in the brachial or lumbosacral plexus is inherently less responsive to morphine and other potent opioids (3). For treating neuropathic pain, adjuvant drugs such as corticosteroids, antidepressants, anticonvulsants, and N-methyl-d-aspartate antagonists are frequently used with variable results (4).

In these patients with severe pain despite pharmacological treatment, invasive pain therapies should be contemplated. Percutaneous cervical cordotomy may be a useful blockade in terminally ill patients suffering from sacral plexopathy. Complications and side effects, such as respiratory failure, ipsilateral hemiparesis, urinary dysfunction, and in bilateral cordotomies and sleep apnea, have been reported using this technique (5).

Before performing neuroablative procedures, reversible peripheral nerve catheterization techniques may be evaluated for the management of neuropathic cancer pain. A catheter placed within the psoas muscle sheath or in the psoas compartment (virtual space between the psoas and the quadratus muscles) can be used to block the lumbar plexus. However, a successful blockade of the sacral nerves is only possible when large volumes of injectant are administered, which makes the psoas compartment technique unfeasible for continuous blockade (6).

In our patient suffering from a radiculopathy in the S1 dermatome, a catheter for the continuous administration of local anesthetics was inserted along the S1 root. To reduce the risk of nerve damage, a blunt needle was used to perform the neural blockade (7). The main advantage of this technique is the possibility of relieving neuropathic pain localized in the somatosensoric distribution of sacral nerve roots. The application of this technique resulted in a significant improvement in pain relief and a significant reduction in opioid consumption with the disappearance of the opioid-induced side effects.

Local anatomic distortions because of tumor growth may interfere with proper placement of a sacral catheter. Additionally, long-term pain relief may be compromised because of catheter-related complications such as dislocation and leakage.

Moreover, progressive tumor invasion with involvement of the whole sacral plexus can result in neuropathic pain in more than one dermatome. In these patients, intrathecally administered morphine, alone or in combination with local anesthetics, can be more appropriate in controlling cancer pain (8). Complications such as meningitis discourage the indiscriminate use of neuraxial analgesic techniques, and such risks should always be considered before these techniques are applied (9).

In conclusion, our patient with severe neuropathic cancer pain caused by infiltration of a sacral nerve (single dermatome) was effectively treated using a continuous sacral root nerve block. Although this new technique is promising, more experience is required to determine the safety and efficacy of this approach in cancer pain management.


    References
 Top
 Abstract
 Introduction
 Case Report
 Discussion
 References
 

  1. Rigor BM. Pelvic cancer pain. J Surg Oncol 2000; 75: 280–300.[Web of Science][Medline]
  2. Jaeckle KA. Nerve plexus metastases. Neurol Clin 1991; 9: 857–66.[Web of Science][Medline]
  3. Portenoy RK, Lesage P. Management of cancer pain. Lancet 1999; 353: 1695–700.[Web of Science][Medline]
  4. Mercadante S, Portenoy RK. Opioid poorly-responsive cancer pain. III. Clinical strategies to improve opioid responsiveness. J Pain Symptom Manage 2001; 21: 338–54.[Web of Science][Medline]
  5. Sanders M, Zuurmond WWA. Safety of unilateral and bilateral percutaneous cervical cordotomy in 80 terminally ill cancer patients. J Clin Oncol 1995; 13: 1509–12.[Abstract]
  6. Vaghadia H, Kapnoudhis P, Jenkins LC, Taylor D. Continuous lumbosacral block using a Tuohy needle and catheter technique. Can J Anaesth 1992; 39: 75–8.[Web of Science][Medline]
  7. Selander D, Dhuner KG, Lundborg G. Peripheral nerve injury due to injection needles used for regional anesthesia. Acta Anaesthesiol Scand 1977; 21: 182–8.[Web of Science][Medline]
  8. Van Dongen RTM, Crul BJP, de Bock M. Long-term intrathecal infusion of morphine and morphine/bupivacaine mixtures in the treatment of cancer pain: a retrospective analysis of 51 cases. Pain 1993; 55: 119–23.[Web of Science][Medline]
  9. Mercadante S. Problems of long-term spinal opioid treatment in advanced cancer patients. Pain 1999; 79: 1–13.[Web of Science][Medline]
Accepted for publication July 30, 2002.




This article has been cited by other articles:


Home page
Anesth. Analg.Home page
L. Puljak, S. L. Kojundzic, Q. H. Hogan, and D. Sapunar
Lidocaine Injection into the Rat Dorsal Root Ganglion Causes Neuroinflammation
Anesth. Analg., March 1, 2009; 108(3): 1021 - 1026.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
J. W. Shin, C. Pancaro, C. F. Wang, and P. Gerner
Low-Dose Systemic Bupivacaine Prevents the Development of Allodynia After Thoracotomy in Rats
Anesth. Analg., November 1, 2008; 107(5): 1587 - 1591.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a colleague
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vranken, J. H.
Right arrow Articles by Dzoljic, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vranken, J. H.
Right arrow Articles by Dzoljic, M.
Related Collections
Right arrow Regional Anesthesia
Right arrow Pain


Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins with the assistance of Stanford University Libraries' HighWire Press®. Copyright 2006 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press