Muhlebach Marianne S, She Jane, Zhang Eric Y, Cogen Jonathan D, Kosorok Michael R
Marsico Lung Institute and Division of Pediatric Pulmonary Medicine, University of North Carolina at Chapel Hill, USA.
Department of Biostatistics University of North Carolina at Chapel Hill, USA.
J Cyst Fibros. 2025 Jan;24(1):98-104. doi: 10.1016/j.jcf.2024.09.017. Epub 2024 Oct 10.
CF care guidelines recommend chronic inhaled antibiotics for chronic Pseudomonas aeruginosa (Pa) lung infection. These medications are costly, time consuming and prescription needs may change with improved outcomes.
We determined the proportion of pwCF with chronic, intermittent or negative Pa infection categories, their clinical and demographic characteristics, factors associated with inhaled antibiotic prescription and changes between 2011 and 2019.
This cohort study using the U.S. CF Foundation patient registry for pwCF >2 years, no prior lung transplant, and with ≥3 respiratory cultures/year determined chronic inhaled antibiotics (≥3 months per calendar year) and Pa infection status from encounter level data. Outcomes and odds of prescription for relevant clinical factors were evaluated using generalized estimating equation models with additional interaction between the predictor and the calendar year to examine changes of predictors over time.
Proportion of pwCF with chronic and intermittent Pa decreased and antibiotic prescription rates increased for these groups and decreased for Pa negative pwCF. Hispanic ethnicity, female sex, pancreatic insufficiency, CF diabetes, and ivacaftor/lumacaftor were associated with higher antibiotic prescriptions for each Pa status. Among Pa-negative pwCF prescriptions were higher with Burkholderia spp. (1.17, (CI 1.03,1.34)) or MRSA (OR 1.45, (1.26,1.68)) but decreased between 2011 and 2019. For Aspergillus OR increased to 1.6,(1.3,1.8) in 2019. Prescriptions for pwCF on ivacaftor decreased, becoming lower in 2019 for chronic (OR 0.7, (0.5,0.8)) and Pa-negative pwCF (OR 0.7, (0.5,0.8)).
Factors predicting inhaled antibiotic prescription differed between 2011 and 2019 indicating changes in health and care for pwCF even prior to triple-modulators.
囊性纤维化(CF)护理指南推荐对慢性铜绿假单胞菌(Pa)肺部感染使用慢性吸入性抗生素。这些药物成本高昂、耗时,且随着治疗效果的改善,处方需求可能会发生变化。
我们确定了患有慢性、间歇性或阴性Pa感染类型的CF患者的比例、他们的临床和人口统计学特征、与吸入性抗生素处方相关的因素以及2011年至2019年期间的变化。
这项队列研究使用了美国CF基金会患者登记系统,纳入年龄大于2岁、未曾接受过肺移植且每年有≥3次呼吸道培养结果的CF患者,根据就诊水平数据确定慢性吸入性抗生素(每年≥3个月)和Pa感染状况。使用广义估计方程模型评估相关临床因素的处方结局和几率,并在预测因素和日历年之间进行额外交互分析,以研究预测因素随时间的变化。
患有慢性和间歇性Pa的CF患者比例下降,这些组的抗生素处方率上升,而Pa阴性的CF患者的抗生素处方率下降。西班牙裔、女性、胰腺功能不全、CF相关性糖尿病以及依伐卡托/鲁马卡托与每种Pa状态下较高的抗生素处方相关。在Pa阴性的CF患者中,伯克霍尔德菌属(1.17,(CI 1.03,1.34))或耐甲氧西林金黄色葡萄球菌(OR 1.45,(1.26,1.68))感染时处方率较高,但在2011年至2019年期间有所下降。2019年,曲霉感染的OR值增至1.6,(1.3,1.8)。接受依伐卡托治疗的CF患者的处方率下降,2019年慢性(OR 0.7,(0.5,0.8))和Pa阴性CF患者(OR 0.7,(0.5,0.8))的处方率更低。
2011年至2019年期间,预测吸入性抗生素处方的因素有所不同,这表明在三联调节剂出现之前,CF患者的健康状况和治疗情况就已经发生了变化。