Prospective, longitudinal, multicenter study on the provision of information regarding sudden unexpected death in epilepsy to adults with epilepsy

被引:8
作者
Wadle, Nora-Elena [1 ,2 ]
Schwab, Christina [1 ,2 ]
Seifart, Carola [3 ]
von Podewils, Felix [4 ,5 ]
Knake, Susanne [6 ,7 ]
Willems, Laurent M. [1 ,2 ]
Menzler, Katja [6 ,7 ]
Schulz, Juliane [4 ,5 ]
Conradi, Nadine [1 ,2 ]
Rosenow, Felix [1 ,2 ]
Strzelczyk, Adam [1 ,2 ,6 ,7 ,8 ,9 ]
机构
[1] Univ Hosp Frankfurt, Epilepsy Ctr Frankfurt Rhine Main, Dept Neurol, Frankfurt am Main, Germany
[2] Goethe Univ, Frankfurt am Main, Germany
[3] Philipps Univ Marburg, Med Fac, Inst Review Board, Marburg, Germany
[4] Univ Greifswald, Epilepsy Ctr, Greifswald, Germany
[5] Univ Greifswald, Dept Neurol, Greifswald, Germany
[6] Philipps Univ Marburg, Epilepsy Ctr Hessen, Marburg, Germany
[7] Philipps Univ Marburg, Dept Neurol, Marburg, Germany
[8] Univ Hosp Frankfurt, Epilepsy Ctr Frankfurt Rhine Main, Dept Neurol, Schleusenweg 2-16,Haus 95, D-60528 Frankfurt, Germany
[9] Goethe Univ, Schleusenweg 2-16,Haus 95, D-60528 Frankfurt, Germany
关键词
counseling; depression; mortality; quality of life; SUDEP; RISK-FACTORS REPORT; QUALITY-OF-LIFE; AMERICAN EPILEPSY; IMPLEMENTATION SUBCOMMITTEE; GUIDELINE DEVELOPMENT; RAPID DETECTION; INCIDENCE RATES; GERMAN VERSION; TASK-FORCE; SUDEP;
D O I
10.1111/epi.17481
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveDespite increased awareness of the serious epilepsy complication sudden unexpected death in epilepsy (SUDEP), a substantial population of people with epilepsy (PWE) remain poorly informed. Physicians indicate concern that SUDEP information may adversely affect patients' health and quality of life. We examined SUDEP awareness and the immediate and long-term effects of providing SUDEP information to PWE. MethodsBaseline knowledge and behaviors among PWE and behavioral adjustments following the provision of SUDEP information were evaluated in a prospective, multicenter survey using the following validated scales: Neurological Disorders Depression Inventory for Epilepsy for depression symptoms, the EuroQoL five-dimension scale for health-related quality of life (HRQoL), a visual analog scale for overall health, the revised Epilepsy Stigma Scale for perceived stigma, and the Seizure Worry Scale for seizure-related worries. The prospective study collected data through semiquantitative interviews before (baseline), immediately after, and 3 months after the provision of SUDEP information. ResultsIn total, 236 participants (mean age = 39.3 years, range = 18-77 years, 51.7% women) were enrolled, and 205 (86.9%) completed long-term, 3-month follow-up. One patient died from SUDEP before follow-up. No worsening symptoms from baseline to 3-month follow-up were observed on any scale. At baseline, 27.5% of participants were aware of SUDEP. More than 85% of participants were satisfied with receiving SUDEP information. Three quarters of participants were not concerned by the information, and >80% of participants recommended the provision of SUDEP information to all PWE. Although most patients reported no behavioral adjustments, 24.8% reported strong behavioral adjustments at 3-month follow-up. SignificanceThe provision of SUDEP information has no adverse effects on overall health, HRQoL, depressive symptoms, stigma, or seizure worry among PWE, who appreciate receiving information. SUDEP information provision might improve compliance among PWE and reduce but not eliminate the increased mortality risk.
引用
收藏
页码:406 / 419
页数:14
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