Death in Unverricht-Lundborg disease: Difference between revisions
Created page with "''Khiari HM, Franceschetti S, Jovic N, Mrabet A, and Genton P (2009) Death in Unverricht- Lundborg disease.'' '''[https://link-springer-com.ezp.welch.jhmi.edu/content/pdf/10...." |
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Khiari HM, Franceschetti S, Jovic N, Mrabet A, and Genton P (2009) Death in Unverricht- Lundborg disease. | |||
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= | https://link-springer-com.ezp.welch.jhmi.edu/content/pdf/10.1007%2Fs10072-009-0102-2.pdf | ||
|abstract= | |||
The objective of this study is to report cases of unexpected deaths in Unverricht-Lundborg disease (ULD) patients, a comparatively benign form of progressive myoclonus epilepsy. We performed a multicentric study of the circumstances of death in ULD patients seen in the last 16 years. We assessed age, sex, severity and duration of disease, antiepileptic drugs, circumstances and presumed cause of death. Nineteen observations (12 females, 7 males) were collected from four centers (Tunis, Marseille, Milan, Belgrade). The most common causes of death are (1) SUDEP (six cases, all female), with 4/6 on phenobarbital alone, and (2) complications of severe ULD (six cases). Two patients committed suicide. Only one death was clearly unrelated to ULD (car accident), while four patients died of stroke, drowning, complications of chronic alcoholism and Wernicke encephalopathy, respectively. In conclusion, although the prognosis of ULD has progressed, there are still spontaneously severe forms and high risk of early death, including SUDEP. | |||
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Multicentric study, Unverricht Lundborg disease, Epilepsy, Death, SUDEP | |||
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*Retrospective study over 16 years of 19 cases of unexpected death in patients with progressive myoclonic epilepsy from 4 European centers. 6 of 19 patient deaths were consistent with SUDEP, but it is difficult to to draw conclusions that extend to patients other than those diagnosed with this rare form of epilepsy. | *Retrospective study over 16 years of 19 cases of unexpected death in patients with progressive myoclonic epilepsy from 4 European centers. 6 of 19 patient deaths were consistent with SUDEP, but it is difficult to to draw conclusions that extend to patients other than those diagnosed with this rare form of epilepsy. | ||
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Latest revision as of 17:23, 17 June 2019
Khiari HM, Franceschetti S, Jovic N, Mrabet A, and Genton P (2009) Death in Unverricht- Lundborg disease.
Abstract: The objective of this study is to report cases of unexpected deaths in Unverricht-Lundborg disease (ULD) patients, a comparatively benign form of progressive myoclonus epilepsy. We performed a multicentric study of the circumstances of death in ULD patients seen in the last 16 years. We assessed age, sex, severity and duration of disease, antiepileptic drugs, circumstances and presumed cause of death. Nineteen observations (12 females, 7 males) were collected from four centers (Tunis, Marseille, Milan, Belgrade). The most common causes of death are (1) SUDEP (six cases, all female), with 4/6 on phenobarbital alone, and (2) complications of severe ULD (six cases). Two patients committed suicide. Only one death was clearly unrelated to ULD (car accident), while four patients died of stroke, drowning, complications of chronic alcoholism and Wernicke encephalopathy, respectively. In conclusion, although the prognosis of ULD has progressed, there are still spontaneously severe forms and high risk of early death, including SUDEP.
Keywords: Multicentric study, Unverricht Lundborg disease, Epilepsy, Death, SUDEP
Context
- Retrospective study over 16 years of 19 cases of unexpected death in patients with progressive myoclonic epilepsy from 4 European centers. 6 of 19 patient deaths were consistent with SUDEP, but it is difficult to to draw conclusions that extend to patients other than those diagnosed with this rare form of epilepsy.