| Literature DB >> 31649617 |
Brian L Edlow1,2, Zachary D Threlkeld3, Katie P Fehnel4, Yelena G Bodien1,5.
Abstract
Historically, Duret hemorrhages have conferred a devastating prognosis. However, recent case reports suggest that cognitive and functional recovery are possible after Duret hemorrhages. Here, we describe a patient who recovered consciousness, communication, and functional independence after Duret hemorrhages caused by traumatic transtentorial herniation. We performed prospective, standardized behavioral assessments, structural MRI scans and stimulus-based functional MRI (fMRI) scans during the first 2 years of recovery. The multimodal assessments revealed reintegration of neural networks mediating language and consciousness, concurrent with the reemergence of functional independence. These observations provide insights into network-based mechanisms of recovery from coma and add to a growing body of evidence indicating that Duret hemorrhages are not invariably associated with a poor prognosis.Entities:
Keywords: Duret hemorrhage; brainstem; coma; herniation; traumatic brain injury
Year: 2019 PMID: 31649617 PMCID: PMC6794605 DOI: 10.3389/fneur.2019.01077
Source DB: PubMed Journal: Front Neurol ISSN: 1664-2295 Impact factor: 4.003
Figure 1Duret hemorrhages due to traumatic transtentorial herniation. Representative axial images are shown at the levels of the caudal midbrain (top row) and rostral pons (bottom row). In the caudal midbrain, a Duret hemorrhage is indicated by curvilinear hypointense signal at the midline on the susceptibility-weighted angiography (SWAN) image, which corresponds with a hyperintensity on the T2-weighted image (T2) and diffusion-weighted image (DWI), as well as a hypointensity on the apparent diffusion coefficient (ADC) map (solid arrows). A second hypointense lesion is seen in the rostral pons on the SWAN image. The signal properties of this second lesion are similar on the diffusion-weighted image and apparent diffusion coefficient map (dashed arrows), but no corresponding hyperintensity is seen on the T2-weighted image. A T2-hyperintense lesion within the right cerebral peduncle (arrow head) at the level of the caudal midbrain likely represents injury to the descending corticospinal tract fibers due to compression against the tentorium during the herniation event.
Figure 2Multifocal infarctions due to vascular compression during transtentorial herniation. Representative diffusion-weighted images (DWI; top row) and apparent diffusion coefficient (ADC; bottom row) images demonstrate ischemic infarctions with the anterior cerebral artery, middle cerebral artery, and posterior cerebral artery territories. The infarctions are indicated by hyperintense signal on DWI and corresponding hypointense signal on ADC. At the time of this MRI scan (post-herniation day 6), the patient's behavioral assessment indicated a minimally conscious state.
Cognitive, behavioral, and functional assessments.
| Event | Admission through discharge after initial fall | Readmission through transfer to | Study participation | LTACH admission through discharge | IRF admission through discharge | Clinical and research follow-up | Clinical follow-up | Clinical follow-up |
| Diagnosis | No cognitive deficits | Coma-VS/MCS | PTCS | PTCS | PTCS- recovered from PTCS | Recovered from PTCS | Recovered from PTCS | Recovered from PTCS |
| Level of consciousness/ cognition | GCS = 15 | GCS = 4 (E1M2V1); | GCS = 11 | CRSR = 13–23 | Cognition could not be validly assessed due to aphasia | Oriented, unable to count from 20 to 1, or recite the months. CAP = 3 symptoms-not confused; TMT A: severely impaired TMT B: unable to complete | Not formally assessed | Brief test of Adult cognition by telephone: impaired abstract reasoning and processing speed |
| DRS | 5 | 28–23 | 21 | 18–6 | 6 | 6 | 5 | 5 |
| GOSE | 5 | 3 | 3 | 3 | 3 | 3 | 5 | 5 |
| Subjective observations | Headache, nausea, peripheral injuries | Fluctuating arousal, inconsistent command following, no expressive language | Reproducible command- following, expresses himself via writing | Non-fluent aphasia; cognitive- linguistic deficits in attention, recall, problem solving, and executive functioning | Requires 24-h supervision; speaking in short sentences; ongoing impairments in comprehension, expression, and cognition | Near fluent speech, short- term memory impairment, states that thoughts remain fast, but has difficulty expressing himself | Ongoing difficulty with memory (i.e., occasionally misses doses of medications) | Starting to complete tasks that resembled his prior career as a carpenter; ongoing difficulties with reasoning, processing speed, attention |
Timeline of behavioral recovery: A, auditory; Ar, arousal; C, communication; CRSR, Coma Recovery Scale-Revised; CAP, Confusion Assessment Protocol; DRS, Disability Rating Scale; E, eyes; GCS, Glasgow Coma Scale; GOSE, Glasgow Outcome Scale-Extended; IRF, inpatient rehabilitation facility; LTACH, Long Term Acute Care Hospital; M, motor; MCS, minimally conscious state; 0, oromotor; PTCS, post-traumatic confusional state; TBI, traumatic brian injury; TMT, trail making test; V, verbal; Vi, visual; VS, vegetative state.
Figure 3Mapping the Duret hemorrhage lesions to the ascending arousal network atlas. The Duret hemorrhages were manually traced on the Harvard Ascending Arousal Network (AAN) Atlas (www.martinos.org/resources/aan-atlas). Hypointense lesions seen in the caudal midbrain and rostral pons on the susceptibility-weighted angiography (SWAN) images (solid red arrow and dashed red arrow, respectively), were traced in red on the atlas template. These hemorrhages overlapped the dorsal raphe (DR) nucleus and ventral tegmental area (VTA) in the caudal midbrain, as well as the right parabrachial complex (PBC) in the rostral pons. All other AAN nuclei were spared: mRt, mesencephalic reticular formation; PTg, pedunculotegmental nucleus; PAG, periaqueductal gray; LC, locus coeruleus; LDTg, laterodorsal tegmental nucleus; MnR, median raphe; PnO, pontis oralis.
Figure 4Longitudinal reorganization of the language network after traumatic transtentorial herniation. Stimulus-based functional MRI (fMRI) was performed on post-herniation day 14 in the intensive care unit (ICU; top row) and at 5-month follow up (bottom row). Representative fMRI activation Z-score maps are shown from a sagittal, coronal, and axial perspective, superimposed upon the patient's T1-weighted images. At the time of the ICU fMRI scan, the patient's behavioral assessment indicated that he had recovered to a post-traumatic confusional state, but he remained mute and was unable to consistently follow commands. FMRI revealed a small region of activation in response to spoken language within the right superior temporal gyrus (STG). At 5-month follow up, he was consistently following commands, oriented, and with near fluent language. Repeat stimulus-based fMRI using the same spoken language stimulus demonstrated a larger region of activation in the right STG, as well as new regions of activation within the left STG and right inferior frontal gyrus (IFG). The T1-weighted images demonstrated encephalomalacia of the left hemisphere, with ex vacuo dilatation of the left lateral ventricle. Given that the patient is left-handed and that he did not undergo fMRI before his injury, it is unknown whether he was right-hemisphere dominant or left-hemisphere dominant for language before the injury. Nevertheless, these longitudinal fMRI data indicate that his language network underwent recovery and/or reorganization after the injury and was right-hemisphere dominant post-injury. A, Anterior, L, Left, P, Posterior, R, Right.