2015
DOI: 10.1016/j.jns.2015.08.490
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Use of epinet database for observational study of status epilepticus in Auckland, New Zealand

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Cited by 3 publications
(5 citation statements)
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“…The EpiNet study group was established to provide a platform to undertake multicenter collaborative research studies in epilepsy . We undertook a population‐based epidemiological incidence study of SE in greater Auckland, New Zealand (population = 1.614 million), using the EpiNet platform, with comprehensive data collection based on the new ILAE SE classification …”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…The EpiNet study group was established to provide a platform to undertake multicenter collaborative research studies in epilepsy . We undertook a population‐based epidemiological incidence study of SE in greater Auckland, New Zealand (population = 1.614 million), using the EpiNet platform, with comprehensive data collection based on the new ILAE SE classification …”
Section: Introductionmentioning
confidence: 99%
“…13,14 We undertook a population-based epidemiological incidence study of SE in greater Auckland, New Zealand (population = 1.614 million), 15 using the EpiNet platform, with comprehensive data collection based on the new ILAE SE classification. 16 We also compared population incidence using previous ILAE classifications.…”
Section: Introductionmentioning
confidence: 99%
“…14 The form contains subforms focused on SE Onset, Patient Care, History, and Outcome. 14 The form contains subforms focused on SE Onset, Patient Care, History, and Outcome.…”
Section: Se Form In Epinetmentioning
confidence: 99%
“…A structured online clinical record was created in EpiNet to collect comprehensive information regarding an episode of SE. 14 This study was approved by the Northern B New Zealand Ethics Committee and the research governance committees of Auckland District Health Board, Waitemata District Health Board, and Counties Manukau District Health Board. Informed consent was obtained from patients after they had recovered from their episode of SE; if patients did not or could not give informed consent retrospectively, the ethics committee gave us permission to record deidentified data in the EpiNet database.…”
Section: Se Form In Epinetmentioning
confidence: 99%
“…First described in early writings of Antiquity and subsequently recognised by French physicians as a clinical entity ( état de mal épileptique ) since 1824, SE is a complex, heterogeneous condition which carries a high morbidity‐mortality depending on the cause, age of onset, seizure severity, and medical co‐morbidities, and where management remains a major challenge largely due to lack of evidence. Whilst ongoing trials will hopefully advance our status quo in the management of SE, its incidence, causes, responses to treatment and outcomes are also being determined in a New Zealand study . In the meantime, a clear therapeutic plan focusing on the initial stages (where evidence exists) by way of implementing integrated algorithms such as the suggested one is essential, for a prompt and accurate diagnosis will usually result in a better outcome.…”
mentioning
confidence: 99%