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1.
J Stroke Cerebrovasc Dis ; 31(8): 106510, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35605386

ABSTRACT

BACKGROUND AND PURPOSE: Progressive lacunar syndromes (PLS) occur in up to 20-30% of patients with lacunar strokes, increasing the risk of long term dependency. Our aim is to develop a predictive score to identify patients at high risk of presenting PLS. METHODS: We derived a risk score for PLS in a cohort of consecutive patients (n=187) presenting with one of the five classic lacunar syndromes (LS) and absence of vascular occlusion, perfusion deficit or symptomatic stenosis. A risk score was developed using the coefficients from the logistic regression model, and receiver operating characteristic (ROC) analysis was conducted to assess the prognostic value of the risk score. Sensitivity, specificity and accuracy were estimated for each total point score. RESULTS: Out of 187 patients included in our sample, 52 (27.8%) presented PLS. Previous history of diabetes mellitus (1 point), diastolic blood pressure at admission (2 points), clinical deficits consistent with a pure motor syndrome (1 point) and asymptomatic intracranial atheromatosis or stenosis in non-symptomatic territory (1 point) were independent predictors for PLS. The estimated area under the ROC curve for this model was 0.77 (95% CI,0.68 - 0.84). CONCLUSION: This score could be a useful tool in routine clinical practice to predict the occurrence of PLS, allowing the identification of those patients with LS who are at high risk of long term dependency due to early neurological worsening, and who would benefit the most from an intensive treatment.


Subject(s)
Stroke, Lacunar , Cohort Studies , Constriction, Pathologic , Humans , Prognosis , Risk Factors , Stroke, Lacunar/diagnostic imaging , Stroke, Lacunar/etiology
3.
Article in English | MEDLINE | ID: mdl-37152624

ABSTRACT

Background: A 61-year-old male patient presented with cerebellar syndrome, which had progressively worsened for 10 days, followed by a tonic-clonic seizure. Phenomenology Shown: Blood analysis showed severe hypomagnesemia and a brain MRI showed T2 hyperintensity in the cerebellar hemispheres (Figure 1). Therefore, the final diagnosis was cerebellar syndrome and epileptic seizures secondary to severe hypomagnesemia. Educational Value: In cases of subacute onset of ataxia, the possibility of ataxia secondary to hypomagnesemia should be considered, as it can be diagnosed with a basic blood test and there are potentially life-threatening outcomes in the absence of treatment, with a reversible course following early supplementation.


Subject(s)
Cerebellar Ataxia , Male , Humans , Middle Aged , Cerebellar Ataxia/diagnostic imaging , Cerebellar Ataxia/etiology , Ataxia/diagnostic imaging , Ataxia/etiology , Seizures/diagnostic imaging , Seizures/drug therapy , Seizures/etiology , Magnetic Resonance Imaging , Neuroimaging
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