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Long Term Treatment of Intractable Reflex Sympathetic Dystrophy With Intrathecal Morphine

Published online by Cambridge University Press:  18 September 2015

W.J. Becker*
Affiliation:
Department of Clinical Neurosciences, The University of Calgary and The Calgary General Hospital, Calgary
D.P. Ablett
Affiliation:
Department of Clinical Neurosciences, The University of Calgary and The Calgary General Hospital, Calgary
C.J. Harris
Affiliation:
Department of Clinical Neurosciences, The University of Calgary and The Calgary General Hospital, Calgary
O.N. Dold
Affiliation:
Department of Clinical Neurosciences, The University of Calgary and The Calgary General Hospital, Calgary
*
Department of Clinical Neurosciences, Calgary General Hospital, M6-012, 841 Centre Avenue E., Calgary. Alberta. Canada T2E0A1
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Abstract

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Background:

Some patients with reflex sympathetic dystrophy (RD) develop intractable symptoms unresponsive to conventional therapy. Recently, intrathecal morphine therapy has been used with some success in such patients.

Methods:

The clinical course of two patients with intractable reflex sympathetic dystrophy (RSD) is described. Both patients developed intractable leg pain, swelling and autonomic changes after a leg injury. Numerous medical treatments and surgical sympathectomies failed to provide long term relief.

Results:

Relatively satisfactory symptom control was achieved only with the use of long term intrathecal morphine therapy delivered by subcutaneously implanted infusion pumps. Exacerbations of the RSD continued to occur, at times in association with further leg trauma, but these could be controlled by a temporary escalation of the intrathecal morphine dose. Complications of morphine therapy were relatively minor. A red rash appearing over the pump site was the first sign that a drug catheter break had occurred, necessitating surgical catheter revision.

Conclusion:

Long term intrathecal morphine therapy is a useful treatment option for patients with intractable severe RSD who have failed other therapies and remain markedly disabled.

Type
Original Articles
Copyright
Copyright © Canadian Neurological Sciences Federation 1995

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