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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Clinical Practice Guidelines From the Cystic Fibrosis Foundation for Preschoolers With Cystic Fibrosis
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Clinical Practice Guidelines From the Cystic Fibrosis Foundation for Preschoolers With Cystic Fibrosis

机译：囊性纤维化基金会针对囊性纤维化学龄前儿童的临床实践指南

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Cystic fibrosis (CF) clinical care guidelines exist for the care of infants up to age 2 years and for individuals >= 6 years of age. An important gap exists for preschool children between the ages of 2 and 5 years. This period marks a time of growth and development that is critical to achieve optimal nutritional status and maintain lung health. Given that disease often progresses in a clinically silent manner, objective and sensitive tools that detect and track early disease are important in this age group. Several challenges exist that may impede the delivery of care for these children, including adherence to therapies. A multidisciplinary committee was convened by the CF Foundation to develop comprehensive evidence-based and consensus recommendations for the care of preschool children, ages 2 to 5 years, with CF. This document includes recommendations in the following areas: routine surveillance for pulmonary disease, therapeutics, and nutritional and gastrointestinal care.
机译：囊性纤维化（CF）临床护理指南适用于2岁以下婴儿和6岁以上婴儿的护理。对于2至5岁的学龄前儿童，存在一个重要的差距。这个时期标志着生长和发育的时期，这对于实现最佳营养状况和维持肺部健康至关重要。鉴于疾病通常以临床上无声的方式发展，因此检测和追踪早期疾病的客观且敏感的工具在该年龄组中很重要。存在一些挑战，可能会阻碍对这些儿童的照料，包括坚持治疗。 CF基金会召集了一个多学科委员会，以针对循证医学为2至5岁的学龄前儿童提供全面的循证和共识性建议。该文件包括以下方面的建议：肺部疾病的常规监测，治疗以及营养和胃肠道护理。

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