Antibiotic Regimen Changes during Cystic Fibrosis Pediatric Pulmonary Exacerbation Treatment

被引:3
|
作者
Cogen, Jonathan D. [1 ]
Sanders, Don B. [2 ]
Slaven, James E. [3 ]
Faino, Anna V. [4 ]
Somayaji, Ranjani [5 ]
Gibson, Ron L. [1 ]
Hoffman, Lucas R. [1 ]
Ren, Clement L. [6 ]
机构
[1] Univ Washington, Div Pulm & Sleep Med, Dept Pediat, Seattle Childrens Hosp, Seattle, WA USA
[2] Indiana Univ Sch Med, Div Pediat Pulmonol Allergy & Sleep Med, Indianapolis, IN USA
[3] Indiana Univ Sch Med, Dept Biostat & Hlth Data Sci, Indianapolis, IN USA
[4] Seattle Childrens Res Inst, Core Biostat Epidemiol & Analyt Res, Seattle, WA USA
[5] Univ Calgary, Dept Med, Cumming Sch Med, Calgary, AB, Canada
[6] Univ Penn, Div Pulm & Sleep Med, Dept Pediat, Childrens Hosp Philadelphia,Perelman Sch Med, Philadelphia, PA USA
基金
美国国家卫生研究院;
关键词
CF; antibacterial agents; hospitalization;
D O I
10.1513/AnnalsATS.202301-078OC
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Rationale/Objectives: Antibiotic selection for in-hospital treatment of pulmonary exacerbations (PEx) in people with cystic fibrosis (CF) is typically guided by previous respiratory culture results or past PEx antibiotic treatment. In the absence of clinical improvement during PEx treatment, antibiotics are frequently changed in search of a regimen that better alleviates symptoms and restores lung function. The clinical benefits of changing antibiotics during PEx treatment are largely uncharacterized. Methods: This was a retrospective cohort study using the Cystic Fibrosis Foundation Patient Registry Pediatric Health Information System. PEx were included if they occurred in children with CF from 6 to 21 years old who had been treated with intravenous antibiotics between January 1, 2006, and December 31, 2018. PEx with lengths of stay <5 or >21 days or for which treatment was delivered in an intensive care unit were excluded. An antibiotic change was defined as the addition or subtraction of any intravenous antibiotic between Hospital Day 6 and the day before hospital discharge. Inverse probability of treatment weighting was used to adjust for disease severity and indication bias, which might influence a decision to change antibiotics. Results: In all, 4,099 children with CF contributed 18,745 PEx for analysis, of which 8,169 PEx (43.6%) included a change in intravenous antibiotics on or after Hospital Day 6. The mean change in pre- to post-treatment percent predicted forced expiratory volume in 1 second (ppFEV(1)) was 11.3 (standard error, 0.21) among events in which an intravenous antibiotic change occurred versus 12.2 (0.18) among PEx without an intravenous antibiotic change (P = 0.001). Similarly, the odds of return to >= 90% of baseline ppFEV(1) were less for PEx with antibiotic changes than for those without changes (odds ratio [OR], 0.89 [95% confidence interval (CI), 0.80-0.98]). The odds of returning to >= 100% of baseline ppFEV(1) did not differ between PEx with versus without antibiotic changes (OR, 0.94 [95% CI, 0.86-1.03]). In addition, PEx treated with intravenous antibiotic changes were associated with higher odds of future PEx (OR, 1.17 [95% CI, 1.12-1.22]). Conclusions: In this retrospective study, changing intravenous antibiotics during PEx treatment in children with CF was common and not associated with improved clinical outcomes.
引用
收藏
页码:1293 / 1298
页数:6
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