» Articles » PMID: 25754096

Treatment and Demographic Factors Affecting Time to Next Pulmonary Exacerbation in Cystic Fibrosis

Overview
Journal J Cyst Fibros
Publisher Elsevier
Specialty Pulmonary Medicine
Date 2015 Mar 11
PMID 25754096
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Pulmonary exacerbations (PEx) are important CF clinical events.

Methods: We studied time to next PEx following intravenous (IV) antibiotic PEx treatment among Cleveland Ohio CF center patients occurring between January 2010 and September 2014. Patient demographics, clinical presentations, and treatments were modeled by Cox proportional hazards regression to identify covariates associated with time to next PEx.

Results: 193 patients were treated for PEx; 155 had a subsequent IV-treated PEx. Six covariates were associated with future PEx hazard: number of PEx in the prior year (hazard ratio 25.1 for ≥3 and 4.4 for 1-2 prior-year PEx versus none; P<.0001), IV treatment duration in weeks (1.2; P=.0004), percent hospital treatment (1.1; P=.0018), and chronic inhaled aminoglycosides (2.5; P<.0001), leukotriene modifiers (1.8; P=.0031), and high dose ibuprofen (0.52; P=.0006).

Conclusions: Time to next PEx was profoundly associated with prior-year PEx, suggestive of high-risk PEx phenotypes that warrant recognition and further study.

Citing Articles

Vitamin D deficiency in patients with cystic fibrosis: a systematic review and meta-analysis.

Farahbakhsh N, Fatahi S, Shirvani A, Motaharifard M, Mohkam M, Tabatabaii S J Health Popul Nutr. 2024; 43(1):11.

PMID: 38233891 PMC: 10795301. DOI: 10.1186/s41043-024-00499-2.


Pulmonary exacerbations in early cystic fibrosis lung disease are marked by strong modulation of CD3 and PD-1 on luminal T cells.

Giacalone V, Giraldo D, Silva G, Hosten J, Peng L, Guglani L Front Immunol. 2023; 14:1194253.

PMID: 37809107 PMC: 10551126. DOI: 10.3389/fimmu.2023.1194253.


Diagnosis and Management of Cystic Fibrosis Exacerbations.

Milinic T, McElvaney O, Goss C Semin Respir Crit Care Med. 2023; 44(2):225-241.

PMID: 36746183 PMC: 10131792. DOI: 10.1055/s-0042-1760250.


Role of inhaled antibiotics in the era of highly effective CFTR modulators.

Elborn J, Blasi F, Burgel P, Peckham D Eur Respir Rev. 2023; 32(167).

PMID: 36631132 PMC: 9879329. DOI: 10.1183/16000617.0154-2022.


Autogenic drainage for airway clearance in cystic fibrosis.

Burnham P, Stanford G, Stewart R Cochrane Database Syst Rev. 2021; 12:CD009595.

PMID: 34910295 PMC: 8672941. DOI: 10.1002/14651858.CD009595.pub3.


References
1.
Goss C, Burns J . Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis. Thorax. 2007; 62(4):360-7. PMC: 2092469. DOI: 10.1136/thx.2006.060889. View

2.
Murphy T, Anbar R, Lester L, Nasr S, Nickerson B, VanDevanter D . Treatment with tobramycin solution for inhalation reduces hospitalizations in young CF subjects with mild lung disease. Pediatr Pulmonol. 2004; 38(4):314-20. DOI: 10.1002/ppul.20097. View

3.
Konstan M, Morgan W, Butler S, Pasta D, Craib M, Silva S . Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr. 2007; 151(2):134-9, 139.e1. DOI: 10.1016/j.jpeds.2007.03.006. View

4.
Sequeiros I, Jarad N . Factors associated with a shorter time until the next pulmonary exacerbation in adult patients with cystic fibrosis. Chron Respir Dis. 2012; 9(1):9-16. DOI: 10.1177/1479972311433575. View

5.
Ferkol T, Rosenfeld M, Milla C . Cystic fibrosis pulmonary exacerbations. J Pediatr. 2006; 148(2):259-64. DOI: 10.1016/j.jpeds.2005.10.019. View