Use of Stellate Ganglion Local Anesthetic Blockade for Treatment of Complex Regional Pain Syndrome Type-II of the Upper Extremity: A Case Report of One Patient's Experience after Traumatic Hand Injury

Case Report

Austin J Anesthesia and Analgesia. 2021; 9(1): 1094.

Use of Stellate Ganglion Local Anesthetic Blockade for Treatment of Complex Regional Pain Syndrome Type-II of the Upper Extremity: A Case Report of One Patient’s Experience after Traumatic Hand Injury

Ahmad S* and Sabia M

Department of Anesthesiology, Cooper University Hospital, USA

*Corresponding author: Ahmad S, Department of Anesthesiology, Cooper University Hospital, 1 Cooper Plz, Camden, NJ 08103, USA

Received: December 21, 2020; Accepted: January 12, 2021; Published: January 19, 2021

Abstract

Background: Complex Regional Pain Syndrome (CRPS) is a neuropathic pain syndrome associated with edema, muscle weakness, and hyperhidrosis. It can be precipitated by fracture, surgery, and spinal cord injury and usually involves the ipsilateral and sometimes contralateral extremity.

Case Details: A 47-year-old male with CRPS Type-II involving the upper extremity had severe neuropathic pain that was limiting his ADLs despite medical, physical and occupational therapy. This case discusses the use of stellate ganglion block in the treatment of upper extremity CRPS Type-II.

Conclusion: Stellate ganglion blockade is an effective adjuvant therapy in the treatment of CRPS Type-II when conservative therapy has failed to provide improvement in pain, highlighting a need for a multimodal therapeutic strategy.

Keywords: Stellate ganglion block; Chronic pain; Complex regional pain syndrome type-II; Bupivacaine

Abbreviations

CRPS: Complex Regional Pain Syndrome; ADLs: Activities of Daily Living; IASP: International Association for the Study of Pain; MCPJ: Metacarpophalangeal Joint; ROM: Range of Motion; PT: Physical Therapy; VAS: Visual Analogue Scale; SGB: Stellate Ganglion Block

Introduction

Complex Regional Pain Syndrome (CRPS) is a chronic relapsing pain condition described by disturbances in pain, motor, sensory, autonomic, and trophic influences. Symptom severity is not related to the degree of precipitating event. The International Association for the Study of Pain (IASP) defines CRPS as a collection of locally appearing painful conditions following a trauma, which chiefly occur distally and exceed in intensity and duration the expected course of the original trauma. The Budapest criteria, described in (Table 1), was just as sensitive but more specific than the IASP definition for the clinical diagnosis of CRPS [1,2]. There are two subtypes of CRPS. In CRPS Type-I, formerly known as reflex sympathetic dystrophy, the inciting event does not cause an overt nerve injury but symptoms are manifested as pain disproportionate to that expected of the injury. The pain and autonomic instability can affect parts of the extremity that are not involved in the inciting event and even include the contralateral extremity. In CRPS Type-II, formerly known as causalgia, the inciting event leads to an identifiable nerve injury resulting in allodynia, burning pain that is regional and not bound by a particular dermatome [3]. Though multiple models have been proposed, the exact pathophysiology of CRPS remains unclear. Consequently, there is wide variation in treatment of CRPS, for which no drug has yet been specifically approved by the US Food and Drug Administration. Increased sympathetic activity manifested by elevated circulating levels of free radicals, inflammatory mediators, cytokines, and glutamate has been observed in patients with CRPS [4]. When conservative management, including pharmacotherapy and Physical Therapy (PT), does not offer relief of symptoms, treatment can be escalated to include interventions such as sympathetic nerve blocks, brachial plexus blocks, epidural drug administration and spinal cord stimulation. This case report adds to the body of literature that supports the use of Stellate Ganglion Block (SGB) of the lower cervical and upper thoracic sympathetic ganglia in the treatment of CRPS [4,5].