| Literature DB >> 27812348 |
Sebastien Laporte1, Danping Wang2, Jennyfer Lecompte1, Sophie Blancho3, Baptiste Sandoz1, Antoine Feydy4, Pavel Lindberg5, Julien Adrian6, Elodie Chiarovano7, Catherine de Waele7, Pierre-Paul Vidal7.
Abstract
The main concern with whiplash is that a large proportion of whiplash patients experience disabling symptoms or whiplash-associated disorders (WAD) for months if not years following the accident. Therefore, identifying early prognostic factors of WAD development is important as WAD have widespread clinical and economic consequences. In order to tackle that question, our study was specifically aimed at combining several methods of investigation in the same WAD patients at the acute stage and 6 months later. Our longitudinal, open, prospective, multi-center study included 38 whiplash patients, and 13 healthy volunteers matched for age, gender, and socio-economic status with the whiplash group. Whiplash patients were evaluated 15-21 days after road accident, and 6 months later. At each appointment, patients underwent a neuropsychological evaluation, a full clinical neurological examination, neurophysiological and postural tests, oto-neurological tests, cervical spine cord magnetic resonance imaging (MRI) with tractography (DTI). At 6 months, whiplash patients were categorized into two subgroups based on the results of the Diagnostic and Statistical Manual of Mental Disorders as having either favorable or unfavorable progression [an unfavorable classification corresponding to the presence of post-concussion symptom (PCS)] and we searched retrospectively for early prognostic factors of WAD predicting the passage to chronicity. We found that patients displaying high level of catastrophizing at the acute stage and/or post-traumatic stress disorder associated with either abnormalities in head or trunk kinematics, abnormal test of the otolithic function and at the Equitest or a combination of these syndromes, turned to chronicity. This study suggests that low-grade whiplash patients should be submitted as early as possible after the trauma to neuropsychological and motor control tests in a specialized consultation. In addition, they should be evaluated by a neuro-otologist for a detailed examination of vestibular functions, which should include cervical vestibular evoked myogenic potential. Then, if diagnosed at risk of WAD, these patients should be subjected to an intensive preventive rehabilitation program, including vestibular rehabilitation if required.Entities:
Keywords: biomechanics; cognition; neuro-otology; neuropsychological tests; tractography; whiplash outcome
Year: 2016 PMID: 27812348 PMCID: PMC5072109 DOI: 10.3389/fneur.2016.00177
Source DB: PubMed Journal: Front Neurol ISSN: 1664-2295 Impact factor: 4.003
Number of volunteers and whiplash patients included in the present study at 15–21 days (D15–21) and at 6 months (M6) after the whiplash.
| Volunteers | Whiplash patients | ||
|---|---|---|---|
| D15–21 | M6 | ||
| Neuropsychological analysis | 13 (7F/6M) | 38 (22F/16M) | 37 (21F/16M) |
| Kinematics analysis | 13 (7F/6M) | 38 (22F/16M) | 37 (21F/16M) |
| Otoneurorogical analysis | 8 (4F/4M) | 38 (21F/16M) | 17 (9F/8M) |
| Imagery analysis | 22 (12F/10M) | 22 (12F/10M) | |
| Early detection analysis | 13 (7F/6M) | 17 (9F/8M) | 17 (9F/8M) |
Repositioning absolute errors (AE) and root mean square errors (RMSE) in neutral position after head–neck extension (EXT), right (R) and left (L) axial rotation (AR) in whiplash patients at early (WAD D15–21) and chronic (WAD M6) stages compared to the control group.
| EXT (°) | R AR (°) | L AR (°) | ||||
|---|---|---|---|---|---|---|
| AE | RMSE | AE | RMSE | AE | RMSE | |
| WAD D15–21 | 2.6 ± 1.8 | 3.9 ± 2.5 | 2.6 ± 1.3 | 3.9 ± 2.1 | 2.6 ± 1.5 | 4.0 ± 2.3 |
| WAD M6 | 2.6 ± 1.8 | 4.1 ± 2.2 | 2.4 ± 1.5 | 4.3 ± 2.8 | 2.7 ± 1.5 | 4.0 ± 2.2 |
| Control | 2.2 ± 1.1 | 3.2 ± 1.2 | 2.3 ± 1.6 | 3.7 ± 1.9 | 2.2 ± 1.1 | 3.8 ± 2.1 |
Mean ± SD.
Figure 1Example of head movements during figure-eight test. (A) Control volunteer and (B) a selected Whiplash patient at early stage displaying impairment of head movement during the test.
Figure 2(A,B) CVEMPs induced by air conducted sound delivered for the right (A) and left (B) ears. (C,D) OVEMPs induced by air conducted sound delivered for the right (C) and left (D) ears. Note: decreased VEMP’s responses from the left ear compare to the right. (E) Illustration of a normal caloric test result.
Percentage of normal and abnormal cVEMPs in whiplash patients at early (WAD D15–21) and chronic (WAD M6) stages compared to the Control group.
| WAD D15–21 ( | WAD M6 ( | Control ( | |
|---|---|---|---|
| cVEMP 500 Hz STB abnormal EPr in % | 24.3 | 23.5 | 0 |
| cVEMP clicks abnormal EPr in % | 28.1 | 14.3 | 0 |
Latencies of the P13 and N23 potentials induced by 500 Hz and high level clicks in whiplash patients at early (WAD D15–21) and chronic (WAD M6) stages compared to the control group.
| Latency P13 | Latency N23 | |||||
|---|---|---|---|---|---|---|
| WAD D15–21 | WAD M5 | Control | WAD D15–21 | WAD M5 | Control | |
| cVEMP STB (ms) | 14.7 ± 1.3 | 14.6 ± 1.0 | 14.6 ± 0.9 | 21.7 ± 1.6 | 21.5 ± 1.5 | 22.3 ± 1.7 |
| cVEMP click (ms) | 11.8 ± 1.2 | 11.6 ± 1.5 | 11.9 ± 1.07 | 18.3 ± 1.6 | 18.1 ± 2.1 | 18.4 ± 1.8 |
Mean ± SD.
Percentage of normal and abnormal c-oVEMPs clicks in whiplash patients at early (WAD D15–21) and chronic (WAD M6) stages compared to the control group. NR patients to one of the ASC or BCV stimulation were excluded from this table.
| WAD D15–21 ( | WAD M6 ( | Control ( | |
|---|---|---|---|
| oVEMP STB abnormal EPr % | 40 | 38.4 | 0 |
| oVEMP FZ abnormal EPr % | 28.5 | 11.7 | 0 |
| oVEMP mastoid abnormal EPr % | 22.2 | 5.8 | 0 |
Latencies of the n1–p1 potentials clicks in whiplash patients at early (WAD D15–21) and chronic (WAD M6) stages compared to the control group.
| Latency n1 | Latency p1 | |||||
|---|---|---|---|---|---|---|
| WAD D15–21 | WAD M5 | Control | WAD D15–21 | WAD M5 | Control | |
| oVEMP STB (ms) | 11.2 ± 0.7 | 11.2 ± 0.6 | 10.5 ± 0.4 | 15.5 ± 1.3 | 15.3 ± 0.9 | 14.6 ± 1.0 |
| oVEMP FZ (ms) | 11.0 ± 0.8 | 10.8 ± 0.7 | 11.2 ± 0.9 | 15.1 ± 1.0 | 14.9 ± 0.7 | 14.7 ± 0.9 |
| oVEMP mastoid (ms) | 10.8 ± 0.8 | 10.7 ± 0.6 | 10.9 ± 0.8 | 15.0 ± 1.7 | 14.9 ± 0.9 | 15.1 ± 0.8 |
Mean ± SD.
Figure 3Example of comprehensive MRI in one WAD patient. (A,B) Sagittal T2and STIR images without any signs of traumatic lesions. (C) Spinal cord structural integrity qualitatively similar to control subjects. (D) Coronal T1 without traumatic signs in neck musculature. (E) Dynamic T2-weighted imaging without any signs of instability. (F) Axial T1 images also without traumatic lesions in neck muscles. (G,H) DTI group results. Fractional anisotropy (FA) values in WAD patients C1–C6 in acute (open circles) and chronic phase (filled triangles). No difference was present at any cervical level. Apparent diffusion coefficient (ADC) values show no changes with time in WAD patients.
Figure 4Comparison between the volunteers (Group V), non-chronic (Group NC), and chronic (Group C) groups. (A) %MC_IL: percentage of coupled movements in lateral bending. (B) Rom RA: range of motion in axial rotation. (C) HEADaS: mean values of the RMS of the rotational acceleration for the figure-eight pursuit. (D) Composite: percentage of composite score for the Equitest®.