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Effect of Elexacaftor/Tezacaftor/Ivacaftor on Acquisition and Chronic Infection at a Single Pediatric Cystic Fibrosis Care Center

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Specialty Pediatrics
Date 2024 Apr 10
PMID 38596420
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Abstract

Objectives: As cystic fibrosis (CF) lung disease progresses, the airways become infected with opportunistic pathogens, such as (PA). In October 2019, the US Food and Drug Administration approved elexacaftor/tezacaftor/ivacaftor (ETI), a highly effective modulator therapy (HEMT), for individuals 12 years and older with 1 copy of the F508del cystic fibrosis transmembrane conductance regulator () mutation. ETI increases the amount of and function of CFTR in the respiratory epithelium, improving mucociliary clearance and reducing static airway mucus, a major trigger for chronic infection and inflammation.

Methods: A retrospective analysis of inhaled tobramycin (iTOB) prescriptions between January 1, 2016, and December 31, 2021, was performed. This captured data before and after ETI approval at Children's Mercy Kansas City (CMKC). The number of individuals with new PA acquisition and individuals considered -chronically infected was analyzed.

Results: The number of eradication prescriptions declined in 2020 and 2021, with 15 (7%) and 12 (5%) -individuals prescribed therapy for those years, respectively. A similar pattern was observed for -prescriptions for chronic infection. A reduction was seen in 2020 and 2021, with 28 (13%) and 20 (9%) individuals -prescribed therapy for the respective years.

Conclusions: The CMKC experienced a decrease in the number of courses of iTOB prescribed during the last 6 years. The reasons for this are likely multifactorial and may include the implementation of standardized PA surveillance and eradication protocols, the effect of HEMT on mucociliary clearance and airway microbiology, and the poorly understood effects of the SARS-CoV-2 pandemic on the epidemiology of respiratory infections.

References
1.
Mall M, Mayer-Hamblett N, Rowe S . Cystic Fibrosis: Emergence of Highly Effective Targeted Therapeutics and Potential Clinical Implications. Am J Respir Crit Care Med. 2019; 201(10):1193-1208. PMC: 7233349. DOI: 10.1164/rccm.201910-1943SO. View

2.
Zampoli M, Pillay K, Carrara H, Zar H, Morrow B . Microbiological yield from induced sputum compared to oropharyngeal swab in young children with cystic fibrosis. J Cyst Fibros. 2016; 15(5):605-10. DOI: 10.1016/j.jcf.2016.01.001. View

3.
Lee T, Brownlee K, Conway S, Denton M, Littlewood J . Evaluation of a new definition for chronic Pseudomonas aeruginosa infection in cystic fibrosis patients. J Cyst Fibros. 2004; 2(1):29-34. DOI: 10.1016/S1569-1993(02)00141-8. View

4.
Heijerman H, McKone E, Downey D, Van Braeckel E, Rowe S, Tullis E . Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial. Lancet. 2019; 394(10212):1940-1948. PMC: 7571408. DOI: 10.1016/S0140-6736(19)32597-8. View

5.
Yeoh D, Foley D, Minney-Smith C, Martin A, Mace A, Sikazwe C . Impact of Coronavirus Disease 2019 Public Health Measures on Detections of Influenza and Respiratory Syncytial Virus in Children During the 2020 Australian Winter. Clin Infect Dis. 2020; 72(12):2199-2202. PMC: 7543326. DOI: 10.1093/cid/ciaa1475. View