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引用次数: 0
摘要
针对囊性纤维化跨膜传导调节蛋白缺陷的新型药物疗法有可能显著提高众多囊性纤维化患者的生活质量。然而,在一些国家,社会保险并不支付调节剂的费用,因为这些药物非常昂贵。本研究旨在了解因法律程序和交付过程而中断调节剂治疗的儿童的健康状况。我们的研究发现,与调节剂疗法相关的预测用力呼气容积百分比(FEV1)和体重指数(BMI)z-score 值的显著增加随着调节剂疗法的中断而急剧下降。在停药 1 个月后的首次随访中,发现 FEV1、BMI z 分数和体重 z 分数显著恶化。有 8 名患者的 FEV1 下降了 10%以上。研究结果表明,继续进行调节性治疗非常重要,关键是不能中断治疗。
Impact of interruption of CFTR modulator therapies
Novel drug therapy targeting the defective cystic fibrosis transmembrane conductance regulator protein has the potential to significantly enhance the quality of life for numerous patients with cystic fibrosis. However, in some countries social insurance does not pay for modulators because these drugs are extremely expensive. This study sought to understand the impact on the health of children whose modulator treatments were interrupted because of legal procedures and delivery processes. Our study identified that the significant increase in percent-predicted forced expiratory volume levels (FEV1) and BMI z-score values associated with modulator therapies decreased sharply with their discontinuation. Significant worsening in FEV1, BMI z-scores, and BW z-scores were detected in the first follow-up visit after therapy discontinuation within 1 month. Eight patients had a reduction of FEV1 of more than 10%. The findings suggest that modulatory treatment continuation is important, and it is crucial that treatment is not interrupted.
期刊介绍:
The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.