Long-term study of one hundred five patients with cystic fibrosis; studies made over a five- to fourteen-year period.

Long-term study of one hundred five patients with cystic fibrosis; studies made over a five- to fourteen-year period.
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对一百五名囊性纤维化患者的长期研究;

DOI:
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发表时间:
1958
期刊:
A M A Journal of Diseases of Children
影响因子:
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通讯作者:
L. Kulczycki
L. Kulczycki
中科院分区:
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文献类型:
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作者:
H. Shwachman;L. Kulczycki

文献摘要

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囊性纤维化患者的儿童期后生存率越来越高。这是由于诊断方法的改进,早期识别轻微病例,以及采取有效的治疗措施。麦金托什的一份报告中包含的10岁以上幸存者人数最多。1然而,目前还没有关于向一大群囊性纤维化患者提供长期护理结果的报告。很明显,这种研究的最终结果将反映诊断的敏锐性,因为病例越早被发现,疾病越轻,最终结果就越好。正是出于这个原因,我们引入了一个临床评估系统,可以用作一个测量设备,比较一个病人与下一个。这是好的,也,指出一些
The survival beyond childhood of patients with cystic fibrosis is being noted with increasing frequency. This is explained by improved diagnostic methods, with the early recognition of mild cases, and by the application of effective therapeutic measures. The largest number of survivors beyond the age of 10 included in one report is in that of McIntosh.1However, there have been no reports dealing with the results of long-term care provided to a large group of patients with cystic fibrosis. It is obvious that the end-results of such a study would reflect diagnostic acumen, for the earlier the case is recognized and the milder the disease the better should be the end-result. It is for this reason that we have introduced a system of clinical evaluation which can be used as a measuring device to compare one patient with the next. It is well, also, to point out some of