Heltshe Sonya L, Goss Christopher H, Thompson Valeria, Sagel Scott D, Sanders Don B, Marshall Bruce C, Flume Patrick A
Cystic Fibrosis Foundation Therapeutics Development Network Coordinating Center, Seattle Children's Research Institute, Seattle, Washington, USA Department of Pediatrics, University of Washington, School of Medicine, Seattle, Washington, USA.
Cystic Fibrosis Foundation Therapeutics Development Network Coordinating Center, Seattle Children's Research Institute, Seattle, Washington, USA Division of Pulmonary and Critical Care Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
Thorax. 2016 Mar;71(3):223-9. doi: 10.1136/thoraxjnl-2014-206750. Epub 2015 Apr 24.
Treatment of pulmonary exacerbations (PEx) in cystic fibrosis (CF) varies widely with no consensus on management practices or best indicators of therapeutic success. To design trials evaluating PEx treatment factors, we characterise the heterogeneity of PEx care in adults and paediatrics, and correlate it with measures of clinical response including short-term and long-term lung function changes, change in symptom severity score and time to next intravenous antibiotic therapy.
Data were used from a prospective observational study of patients with CF ≥10 years of age enrolled at six sites between 2007 and 2010. All were started on intravenous antibiotics for a clinically diagnosed PEx. Analysis of variance, logistic and Cox regression were used to examine the association of treatment factors with short-term and long-term clinical response.
Of 123 patients with CF (60% women, aged 23.1±10.2 years), 33% experienced <10% relative improvement in FEV1 during treatment, which was associated with failing to recover baseline lung function 3 months after treatment (OR=7.8, 95% CI 1.9 to 31.6, p=0.004) and a longer time to next intravenous antibiotic (HR=0.48, 95% CI 0.27 to 0.85, p=0.011). Symptom improvement was observed but was not associated with subsequent lung function or time to next antibiotic therapy, which had a median recurrence time of 143 days.
Immediate symptomatic or respiratory response to PEx treatment did not have a clear relationship with subsequent outcomes such as lung function or intravenous antibiotic-free interval. These results can inform future research of treatment regimens for PEx in terms of interventions and outcome measures.
NCT00788359 (www.clinicaltrials.gov).
囊性纤维化(CF)患者肺部加重期(PEx)的治疗差异很大,对于管理措施或治疗成功的最佳指标尚无共识。为了设计评估PEx治疗因素的试验,我们描述了成人和儿童PEx护理的异质性,并将其与临床反应指标相关联,包括短期和长期肺功能变化、症状严重程度评分变化以及下次静脉使用抗生素治疗的时间。
数据来自于2007年至2010年间在六个地点招募的≥10岁CF患者的前瞻性观察性研究。所有患者均因临床诊断为PEx而开始静脉使用抗生素。采用方差分析、逻辑回归和Cox回归来检验治疗因素与短期和长期临床反应之间的关联。
123例CF患者(60%为女性,年龄23.1±10.2岁)中,33%在治疗期间FEV1相对改善<10%,这与治疗后3个月未能恢复基线肺功能相关(OR=7.8,95%CI 1.9至31.6,p=0.004),且下次静脉使用抗生素的时间更长(HR=0.48,95%CI 0.27至0.85,p=0.011)。观察到症状有所改善,但与随后的肺功能或下次抗生素治疗时间无关,下次抗生素治疗的中位复发时间为143天。
PEx治疗后的即时症状或呼吸反应与随后的结果如肺功能或无静脉使用抗生素间隔时间没有明确关系。这些结果可为未来PEx治疗方案的研究提供干预措施和结果测量方面的参考。
NCT00788359(www.clinicaltrials.gov)