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Department of Anesthesiology, University Medical Center, State University of New York at Stony Brook, Stony Brook, New York
Address correspondence and reprint requests to Joy E. Schabel, MD, Department of Anesthesiology, State University of New York at Stony Brook, Stony Brook, New York 11794-8480.
| Abstract |
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Implications: We report a case of a patient experiencing severe arm pain after dural puncture. This complication has not been reported previously. The patient was successfully treated with an epidural patch.
| Introduction |
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| Case Report |
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Spinal anesthesia was administered at the L3-4 vertebral interspace with a 24-gauge Sprotte needle. Three milliliters of hyperbaric lidocaine 1.5% was injected. A T6 sensory level was obtained. After the procedure, the patient recovered uneventfully, and she was discharged home the same day.
On postoperative Day 1, the patient developed a dull, postural neck ache that was only present when she was upright. She denied having any headache, visual changes, tinnitus, or other symptoms. She was told to drink caffeinated beverages, which did not help.
On postoperative Day 2, she began having sharp, bilateral forearm pain associated with tingling and numbness. There was no associated weakness. The symptoms were postural in nature, occurring only when she was upright and disappearing when she was supine. She again denied headache or visual changes. An anesthesiologist was called to evaluate the patient in the emergency room. The patients chief complaint was positional, excruciating, bilateral forearm pain. The pain corresponded to the C5-6 dermatomes and was unchanged by neck flexion, extension, or rotation. On physical examination, the patient was afebrile, and her vital signs were stable. There were no signs of facial or skull asymmetry. Her neck did not appear abnormally short. It was supple and nontender with full range of motion. There was no evidence of upper extremity injury. Her arms and shoulders were nontender with full range of motion. A neurological examination was attempted with the patient in the sitting position, but she was unable to hold the position for more than a minute because of the excruciating arm pain. Therefore, most of the examination was performed with the patient supine. Evaluation of cranial nerves IIXII was normal. Upper and lower extremity motor examinations revealed 5/5-muscle strength. There were no sensory deficits to light touch, pinprick, or cold. Her deep tendon reflexes were 2+ throughout. Her gait could not be assessed secondary to the postural pain. Because the arm pain was completely relieved with the supine position, it was felt to be related to the dural puncture. Cervical spine radiographs, magnetic resonance imaging (MRI), and computed tomography were not taken at the time of the examination based on her specific history and physical examination findings.
A lumbar epidural blood patch was performed with 22 mL of sterile autologous blood. The patient experienced immediate relief of the arm pain and numbness. Her neck ache resolved within 24 h. Follow-up revealed no recurrence of the arm pain or neck ache.
| Discussion |
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Dysfunction of cranial nerves III, IV, V, VI, VII, and VIII has been reported after dural puncture (11). Permanent abducens palsy has been reported (12). It has been suggested that the intracranial hypotension causes the abducens nerve to be stretched along the sharp edge of the petrous bone (12). Lumbar nerve root irritation during lumbar puncture can occur secondary to needle contact with the sensory roots. Transient dysesthesias are reported by 13% of patients in one series (13). We add cervical dysesthesias to the list of potential complications of dural puncture.
Other possible diagnoses for the symptoms of arm pain include cervical disk herniation and tumor. To spare the patient additional cost and delay in treatment, we postponed ordering a cervical spine MRI until after an attempt at an epidural blood patch. We felt that risks of a lumbar epidural blood patch in this patient were small. Also, because her symptoms only began after the spinal anesthetic and were clearly postural, we felt strongly that they were related to the dural puncture rather than to a cervical spine tumor or disk herniation.
Another theoretical possibility was the preexistence of a basilar impression deformity in this patient. This can cause weakness and paresthesias in the limbs. Basilar impression deformity is either a congenital or acquired abnormality of the craniocervical junction, which causes the odontoid to be more cephalad than normal. It can be associated with other vertebral defects such as an Arnold-Chiari malformation, Klippel-Feil syndrome, atlantooccipital fusion, syringomyelia, odontoid anomalies, hypoplasia of the atlas, and a bifid posterior arch of the atlas (14). The workup before the blood patch could have included cervical spine films, MRI, and computed tomography to eliminate these rare abnormalities. The omission of these studies is an acknowledged limitation of this case report. In the clinical setting, we did not obtain these studies before the blood patch, not only for the reasons cited earlier; but also, because the patients history was negative for any history of neck symptoms. She also did not show any of the physical findings that are usually associated with these rare congenital anomalies: a short neck, asymmetry of the face and skull, or a history of torticollis. Furthermore, she had a negative medical history for all of the systemic diseases that can cause softening of the cervicocranial structures and lead to an acquired basilar impression deformity. These diseases include Pagets disease, osteomalacia, rickets, osteogenesis imperfecta, rheumatoid arthritis, neurofibromatosis, and ankylosing spondylitis (14).
Hysteria can also be considered in the differential diagnosis, especially because her neurological examination was normal. Hysteria has been reported as the cause of deafness, blindness, paralysis, sensory disturbances, and various pain syndromes (15). However, this patient denied any medical or family history of psychiatric illness, and her medical record revealed no history of psychogenic disorders. There also appeared to be no prodromal stress, which is often present with somatoform conversion disorders. In addition, not all nerve root irritation causes numbness that can be documented on physical examination. Perhaps had we been able to keep the patient in the sitting position for a longer time, we would have been able to identify neurologic deficits.
In summary, this is the first reported case of intracranial hypotension secondary to dural puncture resulting in upper extremity dysesthesias, presumably from nerve traction. A caveat is that no radiographic studies were performed to eliminate basal impression deformity as a possible contributing diagnosis. An epidural blood patch should be considered part of the treatment of a patient experiencing postural arm pain after recent dural puncture.
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