Prednisone 10 days on/10 days off in patients with Duchenne muscular dystrophy

被引:0
|
作者
Chiara S. M. Straathof
W. C. G.(Truus) Overweg-Plandsoen
Gert Jan van den Burg
Anneke J. van der Kooi
Jan J. G. M. Verschuuren
Imelda J. M. de Groot
机构
[1] Leiden University Medical Centre,Department of Neurology
[2] Hospital Gelderse Vallei,Department of Pediatry
[3] Academic Medical Centre,Department of Neurology
[4] Radboud University Medical Centre,Department of Rehabilitation Medicine
来源
Journal of Neurology | 2009年 / 256卷
关键词
Muscle disorders; Muscular dystrophy;
D O I
暂无
中图分类号
学科分类号
摘要
Corticosteroids are effective in improving motor function in Duchenne muscular dystrophy (DMD) patients within 6 months–2 years of treatment initiation, but there is as yet no consensus on which treatment scheme is the best. We retrospectively analyzed data of 35 DMD patients who were treated with prednisone 0.75 mg/kg per day intermittently 10 days on/10 days off. Prednisone was started during the ambulant phase at age 3.5–9.7 years (median 6.5 years). The median period of treatment was 27 months (range 3–123 months). The median age at which ambulation was lost was 10.8 years (mean 10.9 years; 95% confidence interval 10.0–11.8 years). Nine patients (26%) had excessive weight gain. Eight boys (21%) had a bone fracture, which was when four of these eight children lost the ability to walk. Treatment was stopped in two obese patients, two hyperactive boys and one patient following a fracture. Our data suggest that prednisone 10 on/10 off has relatively few side effects and extends the ambulant phase by 1 year compared to historical controls.
引用
收藏
页码:768 / 773
页数:5
相关论文
共 50 条
  • [21] 10 marathons, 10 days, £10,000
    不详
    VETERINARY RECORD, 2017, 180 (08) : 192 - 192
  • [22] MYOCARDIAL-INFARCTION IN A CHILD AGED 10 WITH DUCHENNE MUSCULAR-DYSTROPHY
    FIORISTA, F
    BRAMBILLA, G
    SAVIOTTI, M
    DIACO, T
    MORPURGO, M
    ZEITSCHRIFT FUR KARDIOLOGIE, 1981, 70 (10): : 784 - 788
  • [23] The 10th Oligonucleotide Therapy Approved: Golodirsen for Duchenne Muscular Dystrophy
    Aartsma-Rus, Annemieke
    Corey, David R.
    NUCLEIC ACID THERAPEUTICS, 2020, 30 (02) : 67 - 70
  • [24] A 6-MONTH TRIAL OF PREDNISONE IN DUCHENNE MUSCULAR-DYSTROPHY
    BROOKE, MH
    GRIGGS, RC
    MOXLEY, R
    MENDELL, J
    FENICHEL, G
    MILLER, JP
    ANNALS OF NEUROLOGY, 1987, 22 (01) : 120 - 120
  • [25] ON and OFF Electroretinography and Contrast Sensitivity in Duchenne Muscular Dystrophy
    Salgueiro Barboni, Mirella Telles
    Nagy, Balazs Vince
    de Araujo Moura, Ana Laura
    Damico, Francisco Max
    da Costa, Marcelo Fernandes
    Kremers, Jan
    Ventura, Dora Fix
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 54 (05) : 3195 - 3204
  • [26] Deflazacort vs prednisone in Duchenne muscular dystrophy: Trends of an ongoing study
    Reitter, B
    BRAIN & DEVELOPMENT, 1995, 17 : 39 - 43
  • [27] Effect of Deflazacort and Prednisone on Muscle Enzymes in the Treatment of Duchenne Muscular Dystrophy
    Dubow, Jordan
    Wanaski, Stephen
    Cunniff, Timothy
    Meyer, James
    NEUROLOGY, 2016, 86
  • [28] 10 MEMORABLE DAYS - DAYS OF BULGARIAN CULTURE IN CUBA
    RADILOV, N
    OBZOR-A BULGARIAN QUARTERLY REVIEW OF LITERATURE AND ARTS, 1982, (60): : 100 - 101
  • [29] Intermittent prednisone therapy in Duchenne muscular dystrophy - A randomized controlled trial
    Beenakker, EAC
    Fock, JM
    Van Tol, MJ
    Maurits, NM
    Koopman, HM
    Brouwer, OF
    Van der Hoeven, JH
    ARCHIVES OF NEUROLOGY, 2005, 62 (01) : 128 - 132