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Development and Validation of a Nomogram Based on the Epidemiology-Based Mortality Score in Status Epilepticus (EMSE) Parameters to Predict 30-day Mortality in Status Epilepticus.
Brigo, Francesco; Turcato, Gianni; Lattanzi, Simona; Orlandi, Niccolò; Turchi, Giulia; Zaboli, Arian; Giovannini, Giada; Meletti, Stefano.
Affiliation
  • Brigo F; Department of Neurology, Hospital of Merano-Meran (SABES-ASDAA), Merano-Meran, Italy.
  • Turcato G; Department of Internal Medicine, Hospital of Santorso, AULSS-7), Santorso, Italy.
  • Lattanzi S; Neurological Clinic, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.
  • Orlandi N; Neurology Department, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
  • Turchi G; Department of Biomedical, Metabolic, and Neural Sciences, University of Modena and Reggio-Emilia, Modena and Reggio-Emilia, Italy.
  • Zaboli A; Neurology Department, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
  • Giovannini G; Department of Emergency Medicine, Hospital of Merano-Meran (SABES-ASDAA), Merano-Meran, Italy.
  • Meletti S; Neurology Department, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
Neurocrit Care ; 37(3): 754-760, 2022 12.
Article in En | MEDLINE | ID: mdl-35778648
ABSTRACT

BACKGROUND:

To develop a nomogram using the parameters of the Epidemiology-Based Mortality Score in Status Epilepticus (EMSE) and to evaluate its accuracy compared with the EMSE alone in the prediction of 30-day mortality in patients with status epilepticus (SE).

METHODS:

We included a cohort of patients with SE aged ≥ 21 years admitted from 2013 to 2021. Regression coefficients from the multivariable logistic regression model were used to generate a nomogram predicting the risk of 30-day mortality. Discrimination of the nomogram was evaluated using the area under the receiver operating characteristic curve (AUCROC) with 95% confidence interval. Internal validation was performed by bootstrap resampling.

RESULTS:

Among 698 patients with SE, the 30-day mortality rate was 28.9% (202 of 698). On the multivariable analysis, all EMSE parameters (except for the comorbidity group including metastatic solid tumor or AIDS) were associated with a significantly higher risk of 30-day mortality and were included in the nomogram. The discriminatory capability of the nomogram with bootstrap resampling (5000 resamples) had an AUCROC of 0.830 (95% confidence interval 0.798-0.862). Conversely, the AUCROC of the EMSE was 0.777 (95% confidence interval 0.742-0.813). Thus, the probability that a patient who died within 30 days from SE had a higher score than a patient who survived was 83%, indicating good discriminatory power of the nomogram. Conversely, the risk predicted using the EMSE alone was 77%. The nomogram was well calibrated.

CONCLUSIONS:

A nomogram based on EMSE parameters appears superior to the EMSE in predicting the risk of 30-day mortality after SE. The discrimination and calibration of the nomogram shows a better predictive accuracy than the EMSE alone.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Status Epilepticus / Nomograms Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Humans Language: En Journal: Neurocrit Care Journal subject: NEUROLOGIA / TERAPIA INTENSIVA Year: 2022 Type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Status Epilepticus / Nomograms Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Humans Language: En Journal: Neurocrit Care Journal subject: NEUROLOGIA / TERAPIA INTENSIVA Year: 2022 Type: Article Affiliation country: Italy