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首页> 外文期刊>Neuromuscular disorders: NMD >Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols.
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Deflazacort in Duchenne muscular dystrophy: a comparison of two different protocols.

机译:杜氏肌营养不良症中的Deflazacort:两种不同方案的比较。

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We compare the long-term benefits and side effects of deflazacort using two treatment protocols from Naples (N) and Toronto (T). Boys with Duchenne muscular dystrophy between the ages of 8 and 15 years and who had four or more years of deflazacort treatment were reviewed. Diagnostic criteria included males with proximal muscle weakness evident before 5 years, increased serum creatine kinase and genetic testing and/or a muscle biopsy consistent with Duchenne muscular dystrophy. Thirty-seven boys were treated with protocol-N using deflazacort at a dose of 0.6 mg/kg per day for the first 20 days of the month and no deflazacort for the remainder of the month. Boys with osteoporosis received daily vitamin D and calcium. Deflazacort treatment started between 4 and 8 years of age. Thirty-two were treated with protocol-T using deflazacort at a dose of 0.9 mg/kg per day, plus daily vitamin D and calcium. Treatment started between 6 and 8 years of age. All boys were monitored every 4-6 months. The results were compared with age-matched controls in the two groups (19 for protocol-N and 30 for protocol-T). For the boys treated with protocol-N, 97% were ambulatory at 9 years (control, 22%), 35% at 12 years (control, 0%), 25% at 15 years (control, 0%). For the 32 boys treated with protocol-T, 100% were ambulatory at 9 years (control, 48%), 83% at 12 years (control, 0%) and 77% at 15 years (control, 0%). No aids or leg braces were used for ambulation. In boys 13 years and older, a scoliosis of >20 degrees developed in 30% of the boys on protocol-N, 16% on protocol-T and 90% of controls. For protocol-N, no cataracts were observed while in protocol-T, 30% of boys had asymptomatic cataracts that required no treatment. Fractures occurred in 19% (control 16%) of boys on protocol-N and 16% (control, 20%) of boys on protocol-T. This report illustrates: (a) the importance of collaborative studies in developing treatment protocols in Duchenne muscular dystrophy and (b) the long-term beneficial effects of deflazacort treatment inboth protocols. However, the protocol-T seems to be more effective and frequently is associated with asymptomatic cataracts.
机译:我们使用那不勒斯(N)和多伦多(T)的两种治疗方案比较了去黄藻的长期益处和副作用。回顾了8至15岁之间患有杜兴氏肌营养不良症的男孩,并接受了四年或更长时间的黄褐素治疗。诊断标准包括5岁之前明显有近端肌无力的男性,血清肌酸激酶增加和基因检测和/或与Duchenne肌营养不良症一致的肌肉活检。在该月的前20天内,每天以0.6 mg / kg的剂量服用去黄索,对37名男孩进行了方案N的治疗,而在该月的剩余时间中,未使用去黄索。患有骨质疏松症的男孩每天接受维生素D和钙。 Deflazacort治疗开始于4至8岁之间。 32例患者接受了方案T的治疗,每天使用0.9毫克/千克的除草剂加维生素D和钙。治疗开始于6至8岁之间。每4-6个月对所有男孩进行一次监测。将结果与两组年龄匹配的对照组进行比较(方案N为19,方案T为30)。对于接受方案N治疗的男孩,有9%的儿童在9岁时能走动(对照组,22%),12岁的35%(对照组,0%),15岁的25%(对照组,0%)。对于接受方案-T治疗的32名男孩,在9岁时有100%的门诊(对照组,48%),在12岁时有83%的门诊(对照组,0%)和在15岁时有77%的门诊(对照组,0%)。步行过程中不使用辅助工具或大括号。在13岁及13岁以上的男孩中,接受协议N的男孩中有30%发生了脊柱侧弯,接受协议T的男孩中有16%发生了脊柱侧弯,而对照组的90%出现了脊柱侧弯。对于方案N,未观察到白内障,而在方案T中,有30%的男孩患有无症状白内障,无需治疗。方案N的男孩中发生骨折的比例为19%(对照组为16%),方案T的男孩中发生骨折的比例为16%(对照组为20%)。该报告说明:(a)合作研究在制定杜兴氏肌营养不良症治疗方案中的重要性,以及(b)两种方案均对去黄索治疗具有长期有益作用。但是,方案-T似乎更有效,并且经常与无症状性白内障相关。

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