Factors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort study

Author:

Emiralioğlu Nagehan1,Çakır Banu2,Sertçelik Ahmet2,Yalçın Ebru1,Kiper Nural1,Şen Velat3,Altıntaş Derya Ufuk4,Serbes Mahir4,Çokuğraş Haluk5,Kılınç Ayşe Ayzıt5ORCID,Başkan Azer Kılıç5,Hepkaya Evrim5,Yazan Hakan6ORCID,Türel Özden6,Kafi Hale Molla6,Yılmaz Aslı İmran7,Ünal Gökçen7,Çağlar Tuğçe7ORCID,Damadoğlu Ebru8,Irmak İlim8,Demir Esen9,Öztürk Gökçen9ORCID,Bingöl Ayşen10,Başaran Erdem10ORCID,Sapan Nihat11,Aslan Ayşe Tana12,Asfuroğlu Pelin12,Harmancı Koray13,Köse Mehmet14ORCID,Hangül Melih14,Özdemir Ali15ORCID,Tuğcu Gökçen16ORCID,Polat Sanem Eryılmaz16ORCID,Özcan Gizem17ORCID,Gayretli Zeynep Gökçe18,Keskin Özlem19,Bilgiç Sevgi19,Yüksel Hasan20,Özdoğan Şebnem21ORCID,Topal Erdem22,Çaltepe Gönül23,Can Demet24,Ekren Pervin Korkmaz25,Kılıç Mehmet26,Süleyman Ayşe27,Eyüboğlu Tuğba Şişmanlar12ORCID,Cinel Güzin16ORCID,Pekcan Sevgi7ORCID,Çobanoğlu Nazan17ORCID,Çakır Erkan28ORCID,Özçelik Uğur1,Doğru Deniz1ORCID

Affiliation:

1. Department of Pediatric Pulmonology Hacettepe University Faculty of Medicine Ankara Turkey

2. Department of Public Health, Division of Epidemiology Hacettepe University Faculty of Medicine Ankara Turkey

3. Department of Pediatric Pulmonology Dicle University Faculty of Medicine Diyarbakır Turkey

4. Department of Pediatric Allergy and Immunology Çukurova University Faculty of Medicine Adana Turkey

5. Department of Pediatric Pulmonology Cerrahpaşa Faculty of Medicine İstanbul University‐Cerrahpaşa İstanbul Turkey

6. Department of Pediatric Pulmonology Bezmi Alem University Faculty of Medicine İstanbul Turkey

7. Department of Pediatric Pulmonology Necmettin Erbakan University Faculty of Medicine Konya Turkey

8. Department of Adult Pulmonology Hacettepe University Faculty of Medicine Ankara Turkey

9. Department of Pediatric Pulmonology Ege University Faculty of Medicine İzmir Turkey

10. Department of Pediatric Allergy, Immunology and Pulmonology Akdeniz University Faculty of Medicine Antalya Turkey

11. Department of Pediatric Allergy Uludağ University Faculty of Medicine Bursa Turkey

12. Department of Pediatric Pulmonology Gazi University Faculty of Medicine Ankara Turkey

13. Department of Pediatric Allergy Osmangazi University Faculty of Medicine Eskişehir Turkey

14. Department of Pediatric Pulmonology Erciyes University Faculty of Medicine Kayseri Turkey

15. Department of Pediatric Pulmonology Mersin City Hospital Mersin Turkey

16. Department of Pediatric Pulmonology Ankara City Hospital Ankara Turkey

17. Department of Pediatric Pulmonology Ankara University Faculty of Medicine Ankara Turkey

18. Department of Pediatric Infectious Disease Karadeniz Technical University Faculty of Medicine Trabzon Turkey

19. Department of Pediatric Allergy and Immunology Gaziantep University Faculty of Medicine Gaziantep Turkey

20. Department of Pediatric Allergy, Immunology and Pulmonology Celal Bayar University Faculty of Medicine Manisa Turkey

21. Department of Pediatric Pulmonology Sarıyer Hamidiye Etfal Hospital İstanbul Turkey

22. Department of Pediatric Allergy and Immunology İnönü University Faculty of Medicine Malatya Turkey

23. Department of Pediatric Gastroenterology Ondokuz Mayıs University Faculty of Medicine Samsun Turkey

24. Department of Pediatric Pulmonology Balıkesir University Faculty of Medicine Balıkesir Turkey

25. Department of Adult Pulmonology Ege University Faculty of Medicine İzmir Turkey

26. Department of Pediatric Allergy and Immunology Fırat University Faculty of Medicine Elazığ Turkey

27. Department of Pediatric Allergy and Immunology İstanbul University İstanbul Faculty of Medicine İstanbul Turkey

28. Department of Pediatric Pulmonology İstinye University Faculty of Medicine Istanbul Turkey

Abstract

AbstractBackgroundThe decline in pulmonary function is a predictor of disease progression in patients with cystic fibrosis (CF). This study aimed to determine the decline rate of percent predicted forced expiratory volume in 1 s (ppFEV1) based on the data of the CF Registry of Turkey. The secondary aim was to investigate the risk factors related to the decline in ppFEV1.MethodsA retrospective cohort study of CF patients over 6 years old, with pulmonary function data over at least 2 years of follow‐up was extracted from the national CF registry for years 2017–2019. Patients were classified according to disease severity and age groups. Multivariate analysis was used to predict the decline in ppFEV1 and to investigate the associated risk factors.ResultsA total of 1722 pulmonary function test results were available from 574 patients over the study period. Mean diagnostic age was older and weight for age, height for age, and body mass index z scores were significantly lower in the group of ppFEV1 < 40, while chronic Pseudomonas aeruginosa (p < .001) and mucoid P. aeruginosa colonization (p < .001) were significantly higher in this group (p < .001). Overall mean annual ppFEV1 decline was −0.97% (95% confidence interval [CI] = −0.02 to −1.92%). The mean change of ppFEV1 was significantly higher in the group with ppFEV1 ≥ 70 compared with the other (ppFEV1 < 40 and ppFEV1: 40–69) two groups (p = .004). Chronic P. aeruginosa colonization (odds ratio [OR] = 1.79 95% CI = 1.26–2.54; p = .01) and initial ppFEV1 ≥ 70 (OR = 2.98 95% CI = 1.06‐8.36), p = .038) were associated with significant ppFEV1 decline in the whole cohort.ConclusionsThis data analysis recommends close follow‐up of patients with normal initial ppFEV1 levels at baseline; advocates for early interventions for P. aeruginosa; and underlines the importance of nutritional interventions to slow down lung disease progression.

Publisher

Wiley

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