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Movements after the clinical diagnosis of brain death: supraspinal motor responses or spinal reflexes

Critical Care201317:469

  • Published:


  • Compute Tomography Angiography
  • Brain Death
  • Accessory Nerve
  • Jugular Foramen
  • Spinal Nerve Root

In a recent issue of Critical Care, Wu and Orizaola Balaguer [1] hypothesized that nociceptive head turning after brain death (BD) is a spinal reflex. We argue that it can be a supraspinal response, which would invalidate a diagnosis of BD.

The sternocleidomastoid and trapezius are innervated by the spinal nucleus of the accessory nerve extending from the lower medulla to the ventral horn of the spinal cord (C1-C4) [2]. Lower motor neurons from the lower medulla to C2 project to the sternocleidomastoid [2], contributing to the reported motor responses.

The spinal nerve roots of the accessory nerve ascend through the foramen magnum and descend through the jugular foramen. Compression of the vertebral-basilar arteries (causing intracranial circulatory arrest) and the spinal nerve roots by cerebellar tonsillar herniation at the foramen magnum would abolish the spinal accessory nerve reflex as well as cause cervicomedullary infarction.

The pyramidal tract projecting from the telencephalon controls voluntary movements. Subcortical nuclei in the diencephalon, mesencephalon, and rhombencephalon control non-voluntary movements. Complex movements are generally explained as spinal reflexes rather than supraspinal motor responses, despite an incidence of 40% to 50% in heart-beating donors [3]. Dismissal of supraspinal motor responses is incongruent with the finding [4] that, on histopathological examination, about 60% of heart-beating donors have normal or minimal ischemic injury to the brainstem. If (as these histopathological findings show) the subcortical nuclei are possibly uninjured, then the supraspinal origin of movements cannot be excluded [5].

The absence of brainstem injury at autopsy raises doubt that all movements in BD are spinal motor reflexes. Additional histopathological data are needed to determine whether movements originate from supraspinal or spinal nuclei.

Authors’ response

Yunfen Wu and Pedro Orizaola Balaguer

We appreciate the comments from Rady and Verheijde in response to our reported case. However, we do not agree with their invalidation of the BD diagnosis in our patient. Our arguments are the following: first, the criteria for a clinical diagnosis of BD were fulfilled [6]; second, the electroencephalographic recording was isoelectric; and third, computed tomography angiography (CTA) showed signals of intracranial circulatory arrest (Figure 1). The sensitivity of CTA in detecting intracranial circulatory arrest has been shown to be comparable to that of other established techniques [7].
Figure 1
Figure 1

Computed tomography angiography (CTA) shows signals of intracranial circulatory arrest. (A) Axial-view CTA image of the arterial phase. Severe brain edema is shown. Both superficial temporal arteries are visualized. (B) Axial-view CTA image of the venous phase. In both frames, there is no enhancement of the middle cerebral arteries or the basilar artery.

Nevertheless, we agree with Rady and Verheijde that a supraspinal origin of head-turning movements in our patient cannot be ruled out. In regard to the involved source of such movements in BD, we suggested in our previous report that further studies (including hispatological examination) are needed for this to be clarified.



Brain death


Computed tomography angiography.



YW and POB thank the Radiology Department of Hospital Universitario de Marqués de Valdecilla for technical and analytical support with the CTA images. Written consent to publish was obtained from the patient’s next of kin.

Authors’ Affiliations

Department of Critical Care Medicine, Mayo Clinic, 5777 East Mayo Boulevard, 85054 Phoenix, AZ, USA
Departments of Physical Medicine and Rehabilitation, Mayo Clinic, 5777 East Mayo Boulevard, 85054 Phoenix, AZ, USA


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© BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd.