Short-term and long-term response to pulmonary exacerbation treatment in cystic fibrosis

被引:48
作者
Heltshe, Sonya L. [1 ,2 ]
Goss, Christopher H. [1 ,3 ]
Thompson, Valeria [1 ]
Sagel, Scott D. [4 ,5 ]
Sanders, Don B. [6 ]
Marshall, Bruce C. [7 ]
Flume, Patrick A. [8 ]
机构
[1] Seattle Childrens Res Inst, Cyst Fibrosis Fdn Therapeut Dev Network Coordinat, Seattle, WA 98121 USA
[2] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Div Pulm & Crit Care Med, Seattle, WA USA
[4] Univ Colorado, Sch Med, Dept Pediat, Aurora, CO USA
[5] Childrens Hosp Colorado, Aurora, CO USA
[6] Univ Wisconsin, Dept Pediat, Sch Med & Publ Hlth, Madison, WI USA
[7] Cyst Fibrosis Fdn, Bethesda, MD USA
[8] Med Univ S Carolina, Dept Med & Pediat, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
INTRAVENOUS ANTIBIOTIC-TREATMENT; QUALITY-OF-LIFE; ADULT PATIENTS; PSEUDOMONAS-AERUGINOSA; LUNG-FUNCTION; THERAPY; HOME; CF; DECLINE; TIME;
D O I
10.1136/thoraxjnl-2014-206750
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background 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. Methods 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. Results 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. Conclusions 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.
引用
收藏
页码:223 / 229
页数:7
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