医学
囊性纤维化
疾病
多学科方法
儿科
重症监护医学
医疗保健
肺病
梅德林
家庭医学
肺
病理
内科学
社会学
经济
法学
经济增长
社会科学
政治学
作者
Thomas Lahiri,Sarah E. Hempstead,Cynthia Brady,Carolyn L. Cannon,Kelli Clark,Michelle Condren,Margaret F. Guill,R. Paul Guillerman,Christina G. Leone,Karen Maguiness,Lisa Monchil,Scott W. Powers,Margaret Rosenfeld,Sarah Jane Schwarzenberg,Connie L. Tompkins,Edith T. Zemanick,Stephanie D. Davis
出处
期刊:Pediatrics
[American Academy of Pediatrics]
日期:2016-04-01
卷期号:137 (4)
被引量:144
标识
DOI:10.1542/peds.2015-1784
摘要
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.
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