Applying the ILAE diagnostic criteria for Lennox-Gastaut syndrome in the real-world setting: A multicentre retrospective cohort study.
Russell NightscalesZhibin Chen MBiostatSarah N BarnardClarissa AuvrezGerard TaoShobi SivathambooCaitlin BennettMaria RychkovaWendyl D'SouzaSamuel Frank BerkovicJohn-Paul NicoloTerence J O'BrienPiero PeruccaIngrid Eileen SchefferPatrick KwanPublished in: Epilepsia open (2023)
Up to 52% of patients diagnosed with LGS following VEM may not meet recently accepted ILAE criteria for LGS diagnosis. This may reflect both the limitations of retrospective medical record review and a historical tendency of applying the LGS diagnosis to a broad spectrum of severe, early-onset drug-resistant epilepsies with drop attacks. The ILAE criteria allow delineation of LGS based on distinct electroclinical features, potentiating accurate diagnosis, prognostication, and management formulation. Nonetheless, mortality outcomes between those who did and did not meet ILAE diagnostic criteria for LGS were similarly poor, and both groups suffered high rates of seizure-related injury.
Keyphrases
- early onset
- drug resistant
- end stage renal disease
- late onset
- multidrug resistant
- ejection fraction
- newly diagnosed
- chronic kidney disease
- healthcare
- clinical trial
- prognostic factors
- cross sectional
- high resolution
- risk factors
- randomized controlled trial
- study protocol
- type diabetes
- patient reported outcomes
- cardiovascular events
- skeletal muscle
- pseudomonas aeruginosa
- coronary artery disease
- insulin resistance
- mass spectrometry
- glycemic control
- weight loss
- drug induced