Gambazza Simone, Mariani Alessandra, Brivio Anna, Carta Federica, Blardone Chiara, Lisiero Saba, Russo Maria, Colombo Carla
Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico Milano, Healthcare Professions Department, Milan, Italy.
Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico Milano, Cystic Fibrosis Centre of Milan, Milan, Italy.
Front Pediatr. 2022 Jun 22;10:926248. doi: 10.3389/fped.2022.926248. eCollection 2022.
An exercise test combined with a multiple breath washout nitrogen test (MBWN) may offer a comprehensive clinical evaluation of cystic fibrosis (CF) disease in children with normal spirometry. The purpose of the present study is to explore whether information derived from spirometry, MBWN, and exercise tests can help the CF multidisciplinary team to characterize time free from hospitalization due to pulmonary exacerbation (PE) in a cohort of pediatric patients with CF.
This prospective observational study was carried out at the Lombardia Region Reference Center for Cystic Fibrosis in Milano, Italy. In 2015, we consecutively enrolled children and adolescents aged <18 years with spirometry, MBWN, and Godfrey exercise test performed during an outpatient visit.
Over a median follow-up time of 2.2 years (interquartile range [IQR], 2.01; 3.18), 28 patients aged between 13.0 and 17.4 years were included. When lung functions were outside the normal range, 50% of patients were hospitalized 4 months after the outpatient visit, and their response to exercise was abnormal (100%). Half of the individuals with normal forced expiratory volume in the first second (FEV) and abnormal lung clearance index (LCI) experienced the first hospital admission 9 months after the clinic visit, and 84.2% presented an abnormal response to exercise. Conversely, 15.8% had abnormal exercise responses when lung functions were considered normal, with half of the adolescents hospitalized at 11 months.
Maintaining ventilation homogeneity, along with a normal ability to sustain intense work, may have a positive impact on the burden of CF disease, here conceived as time free from hospitalization due to PE.
运动试验联合多次呼气氮清除试验(MBWN)可为肺活量测定正常的儿童囊性纤维化(CF)疾病提供全面的临床评估。本研究的目的是探讨来自肺活量测定、MBWN和运动试验的信息是否有助于CF多学科团队对一组CF儿科患者因肺部加重(PE)导致的无住院时间进行特征描述。
这项前瞻性观察性研究在意大利米兰的伦巴第地区囊性纤维化参考中心进行。2015年,我们连续纳入了年龄<18岁、在门诊就诊时进行了肺活量测定、MBWN和戈弗雷运动试验的儿童和青少年。
在中位随访时间2.2年(四分位间距[IQR],2.01;3.18)内,纳入了28例年龄在13.0至17.4岁之间的患者。当肺功能超出正常范围时,50%的患者在门诊就诊后4个月住院,且他们的运动反应异常(100%)。第一秒用力呼气量(FEV)正常但肺清除指数(LCI)异常的个体中,一半在门诊就诊后9个月首次住院,84.2%的患者运动反应异常。相反,当肺功能被认为正常时,15.8%的青少年运动反应异常,其中一半的青少年在11个月时住院。
维持通气均匀性以及维持高强度工作的正常能力,可能对CF疾病负担产生积极影响,这里将CF疾病负担定义为因PE导致的无住院时间。