Changes in factors associated with inhaled antibiotic prescriptions for people with cystic fibrosis over time in the U.S.

IF 5.4 2区 医学 Q1 RESPIRATORY SYSTEM Journal of Cystic Fibrosis Pub Date : 2024-10-09 DOI:10.1016/j.jcf.2024.09.017
Marianne S Muhlebach, Jane She, Eric Y Zhang, Jonathan D Cogen, Michael R Kosorok
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Abstract

Rationale: 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.

Objectives: 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.

Methods: 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.

Results: 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, (CI95 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)).

Conclusions: Factors predicting inhaled antibiotic prescription differed between 2011 and 2019 indicating changes in health and care for pwCF even prior to triple-modulators.

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美国囊性纤维化患者吸入抗生素处方相关因素随时间推移的变化。
依据:CF 护理指南推荐使用慢性吸入抗生素治疗慢性绿脓杆菌(Pa)肺部感染。这些药物成本高、耗时长,而且处方需求可能会随着治疗效果的改善而改变:我们确定了患有慢性、间歇性或阴性 Pa 感染类别的 pwCF 比例、他们的临床和人口统计学特征、与吸入式抗生素处方相关的因素以及 2011 年至 2019 年间的变化:这项队列研究使用了美国 CF 基金会患者登记处的数据,研究对象为年龄大于 2 岁、既往未进行过肺移植、呼吸道培养次数≥3 次/年的 pwCF,通过会诊数据确定慢性吸入抗生素(每个日历年≥3 个月)和 Pa 感染状态。使用广义估计方程模型评估了相关临床因素的结果和处方几率,并在预测因素和日历年之间添加了交互作用,以检查预测因素随时间的变化:结果:患有慢性和间歇性帕金森病的患儿比例下降,这些群体的抗生素处方率上升,帕金森病阴性患儿的抗生素处方率下降。西班牙裔、女性、胰腺功能不全、CF 糖尿病和 ivacaftor/lumacaftor 与每种 Pa 状态下的抗生素处方率较高有关。在 Pa 阴性 pwCF 中,伯克霍尔德氏菌(1.17,(CI95 1.03,1.34))或 MRSA(OR 1.45,(1.26,1.68))的处方量较高,但在 2011 年至 2019 年期间有所下降。曲霉菌 OR 在 2019 年增至 1.6,(1.3,1.8)。使用伊伐卡夫托的 pwCF 的处方量有所下降,2019 年慢性 pwCF(OR 0.7,(0.5,0.8))和 Pa 阴性 pwCF(OR 0.7,(0.5,0.8))的处方量有所下降:预测吸入抗生素处方的因素在 2011 年和 2019 年之间存在差异,表明即使在使用三联调节剂之前,pwCF 的健康和护理也发生了变化。
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来源期刊
Journal of Cystic Fibrosis
Journal of Cystic Fibrosis 医学-呼吸系统
CiteScore
10.10
自引率
13.50%
发文量
1361
审稿时长
50 days
期刊介绍: The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society. The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS.
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