Comprehensive care of children with Dravet syndrome

被引:13
作者
Granata, Tiziana [1 ]
机构
[1] IRCCS Fdn Neurol Inst C Besta, Dept Pediat Neurosci, I-20133 Milan, Italy
关键词
Severe myoclonic epilepsy of infancy; Management; Cognitive development; Social problems; Treatment; Comorbidities; SEVERE MYOCLONIC EPILEPSY; INFANCY;
D O I
10.1111/j.1528-1167.2011.03011.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P>The comprehensive care of a patient with Dravet syndrome encompasses both the "care" and the "cure" of the patient, and requires cooperation among family, doctors, and several other specialized caregivers to search for the attainment of the best quality of life for the patients and their families. Several issues peculiar to the disease to be faced while dealing with the patient are: (1) SMEI is an "evolving" disease that appears in an otherwise healthy child with symptoms that appear and mutate throughout the course of the disease; (2) the severity of the disease is not fully predictable at onset and appears to be individual-specific; (3) the seizures are invariably drug resistant and seizure freedom is not a realistic goal; and (4) in addition to seizures many other invalidating clinical problems, including cognitive impairment, behavior disorders, and a number of comorbidities characterize the disease course. The comprehensive caring must be physician-guided and patient-centered and implies a multidisciplinary approach to be built around the children and caregivers, who need to be guided through the steps of the diagnosis, treatments, and managements of the various comorbidities.
引用
收藏
页码:90 / 94
页数:5
相关论文
共 14 条
  • [1] Casse-Perrot Catherine, 2001, VVolume 50, P131
  • [2] Severe myoclonic epilepsy in infancy: Toward an optimal treatment
    Ceulemans, B
    Boel, M
    Claes, L
    Dom, L
    Willekens, H
    Thiry, P
    Lagae, L
    [J]. JOURNAL OF CHILD NEUROLOGY, 2004, 19 (07) : 516 - 521
  • [3] De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
    Claes, L
    Del-Favero, J
    Ceulemans, B
    Lagae, L
    Van Broeckhoven, C
    De Jonghe, P
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) : 1327 - 1332
  • [4] Dalla Bernardina B, 1987, ADV EPILEPTOL, P175
  • [5] Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
    Depienne, C.
    Trouillard, O.
    Saint-Martin, C.
    Gourfinkel-An, I.
    Bouteiller, D.
    Carpentier, W.
    Keren, B.
    Abert, B.
    Gautier, A.
    Baulac, S.
    Arzimanoglou, A.
    Cazeneuve, C.
    Nabbout, R.
    LeGuern, E.
    [J]. JOURNAL OF MEDICAL GENETICS, 2009, 46 (03) : 183 - 191
  • [6] Dravet C., 1982, Advances in Epileptology, P135
  • [7] DULAC O, 1990, Neurophysiologie Clinique, V20, P115, DOI 10.1016/S0987-7053(05)80366-1
  • [8] Dravet syndrome: The long-term outcome
    Genton, Pierre
    Velizarova, Reana
    Dravet, Charlotte
    [J]. EPILEPSIA, 2011, 52 : 44 - 49
  • [9] Living with a brother or sister with epilepsy: Siblings' experiences
    Hames, Annette
    Appleton, Richard
    [J]. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2009, 18 (10): : 699 - 701
  • [10] Coping with a child with Dravet syndrome: Insights from families
    Nolan, Kathleen
    Camfield, Carol S.
    Camfield, Peter R.
    [J]. JOURNAL OF CHILD NEUROLOGY, 2008, 23 (06) : 690 - 694