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Once daily insulin detemir in cystic fibrosis with insulin deficiency

机译:每日一次胰岛素地特米尔治疗伴有胰岛素缺乏的囊性纤维化

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The aim of this study was to determine if once daily insulin detemir reverses decline in weight and lung function in patients with cystic fibrosis (CF). 12 patients with early insulin deficiency and six with CF related diabetes (aged 7.2-18.1 years) were treated for a median of 0.8 years. Changes in weight and lung function following treatment were compared to pretreatment changes. Before treatment, the change in weight SD score (ΔWtSDS), percentage of predicted forced expiratory volume in 1 s (Δ%FEV 1) and percentage of predicted forced vital capacity (Δ%FVC) declined in the whole study population (-0.45±0.38, -7.9±12.8%, -5.8±14.3%) and in the subgroup with early insulin deficiency (-0.41±0.43, -9.8±9.3%, -6.8±10.3%). Following treatment with insulin ΔWtSDS, Δ%FEV 1 and Δ%FVC significantly improved in the whole study population (+0.18±0.29 SDS, p=0.0001; +3.7±10.6%, p=0.007; +5.2±12.7%, p=0.013) and in patients with early insulin deficiency (+0.22±0.31 SDS, p=0.003; +5.3±11.5%, p=0.004; +5.8±13.4%, p=0.024). Randomised controlled trials are now needed.
机译:这项研究的目的是确定每日一次地特胰岛素是否能逆转患有囊性纤维化(CF)患者的体重和肺功能下降。治疗12例早期胰岛素缺乏患者和6例CF相关糖尿病(年龄7.2-18.1岁),中位治疗0.8年。将治疗后体重和肺功能的变化与治疗前的变化进行比较。治疗前,在整个研究人群中,体重SD得分(ΔWtSDS),1秒内预计的强制呼气量百分比(Δ%FEV 1)和预计的强制肺活量百分比(Δ%FVC)的变化均下降了(-0.45± 0.38,-7.9±12.8%,-5.8±14.3%)和早期胰岛素缺乏的亚组(-0.41±0.43,-9.8±9.3%,-6.8±10.3%)。用胰岛素ΔWtSDS治疗后,整个研究人群中的Δ%FEV 1和Δ%FVC显着改善(+ 0.18±0.29 SDS,p = 0.0001; + 3.7±10.6%,p = 0.007; + 5.2±12.7%,p = 0.013)和早期胰岛素缺乏症患者(+ 0.22±0.31 SDS,p = 0.003; + 5.3±11.5%,p = 0.004; + 5.8±13.4%,p = 0.024)。现在需要随机对照试验。

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