| Autor: |
Vargas-Cañas, Edwin Steven, Galnares-Olalde, Javier Andrés, León-Velasco, Fausto, García-Grimshaw, Miguel, Gutiérrez, Alonso, López-Hernández, Juan Carlos |
| Zdroj: |
The Canadian Journal of Neurological Sciences; September 2023, Vol. 50 Issue: 5 p745-750, 6p |
| Abstrakt: |
ABSTRACT:Background:Half of Guillain–Barré syndrome (GBS) present elevated cerebrospinal fluid (CSF) protein levels within 1 week since symptom onset and 80% within 2 weeks. Our objective was to determine the clinical and prognostic implication of albuminocytological dissociation in early GBS.Methods:An ambispective cohort study was conducted. Good outcome was considered if the patient was able to walk unaided (Guillain-Barré disability score [GDS] ≤ 2 points) at 3-month follow-up. Patients were classified into two groups: with and without albuminocytological dissociation; we compared clinical and paraclinic characteristics between the groups. We analyzed clinical and electrophysiological factors related to presenting early dissociation through a multivariate model.Results:We included 240 patients who fulfilled Asbury criteria for GBS. On further selection, only 94 patients fulfilled inclusion. Mean age was 45.94 ± 17.1 years and 67% were male. Median time from symptom onset to admission was 5 days (IQR 3–6). Regarding albuminocytological dissociation and electrophysiological variants, we found a significant difference: acute inflammatory demyelinating polyneuropathy (AIDP) [60.6% vs 26.2%, p= 0.002], acute motor axonal neuropathy (AMAN) [21.2% vs 49.1%, p= 0.009] and acute motor sensory axonal neuropathy (AMSAN) [12.1% vs 1.6%, p= 0.05]. We did not observe significant differences in recovery of independent walking in short term between both groups. The presence of conduction block in any variant (OR 3.21, 95% CI 1.12–9.16, p= 0.02) and absence of sural registration (OR 5.69, 95% CI 1.48–21.83, p= 0.011) were independent factors related to early dissociation.Conclusions:Early dissociation (<7 days) is not associated with any particular clinical feature or unfavorable outcome. It is more common to see in AIDP rather than axonal variants. |
| Databáze: |
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