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Rapid Communication|Articles in Press

Association between nebuliser therapies adherence and visit-to-visit variability of FEV1 in patients with cystic fibrosis

  • David Drummond
    Correspondence
    Corresponding author at: University of Manchester, Vaughan House, Manchester M13 9GB, UK.
    Affiliations
    Division of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health, United Kingdom

    Service de Pneumologie et Allergologie Pédiatriques, Hôpital Necker Enfants Malades, AP-HP Centre Université de Paris, France

    Heka Team, Centre de Recherche des Cordeliers, INSERM, Université Paris Cité, Paris, France
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  • Pauline Whelan
    Affiliations
    Centre for Health Informatics, Division of Imaging, Informatics and Data Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, United Kingdom
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  • Matthew Sperrin
    Affiliations
    Division of Informatics, Imaging and Data Science, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health, United Kingdom
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Published:March 14, 2023DOI:https://doi.org/10.1016/j.jcf.2023.03.006

      Highlights

      • We hypothesised that lower adherence was associated with higher FEV1 variability.
      • Objective adherence data from data-logging nebulisers were used.
      • We found a statistically significant association between lower adherence and higher FEV1 variability.
      • The clinical implications of this result need to be further investigated.

      Abstract

      At the same level of lung function, some patients with cystic fibrosis have large variations in their FEV1 percent predicted (FEV1pp) values while others have stable values. We hypothesised that lower adherence to nebuliser therapies was associated with higher FEV1pp variability. We conducted a post hoc analysis of the ACtiF trial data. Adherence was calculated using data from data-logging nebulisers, and FEV1pp variability using the coefficient of variation equation. Amongst the 543 patients included in the analysis, those poorly adherent (adherence < 50%) had a higher FEV1pp variability than patients moderately (50 to < 80%) and highly adherent (≥ 80%), with median values (IQR1–3) of 8.1% (4.9–13.7), 6.3% (3.9–9.8), and 6.3% (3.9–9.3) respectively (p < 0.01). This result was confirmed by a multiple linear regression including adherence as a continuous variable (p < 0.01). Further studies are needed to determine the implications of these differences in FEV1pp variability on the prognosis of patients.

      Keywords

      Abbreviations:

      BMI (body mass index), CF (cystic fibrosis), CFTR (cystic fibrosis transmembrane regulator), DAG (directed acyclic graph), FEV1 (forced expiratory volume in one second), UK (United Kingdom)
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      References

      1. European Cystic Fibrosis Society. ECFS patient registry; Annual Data Report 2019.

        • Castellani C.
        • Duff A.J.A.
        • Bell S.C.
        • Heijerman H.G.M.
        • Munck A.
        • Ratjen F.
        • et al.
        ECFS best practice guidelines: the 2018 revision.
        J Cyst Fibros Off J Eur Cyst Fibros Soc. 2018; 17: 153-178https://doi.org/10.1016/j.jcf.2018.02.006
        • Szczesniak R.
        • Heltshe S.L.
        • Stanojevic S.
        • Mayer-Hamblett N.
        Use of FEV1 in cystic fibrosis epidemiologic studies and clinical trials: a statistical perspective for the clinical researcher.
        J Cyst Fibros. 2017; 16: 318-326https://doi.org/10.1016/j.jcf.2017.01.002
        • Morgan W.J.
        • VanDevanter D.R.
        • Pasta D.J.
        • Foreman A.J.
        • Wagener J.S.
        • Konstan M.W.
        • et al.
        Forced expiratory volume in 1 s variability helps identify patients with cystic fibrosis at risk of greater loss of lung function.
        J Pediatr. 2016; 169 (e2): 116-121https://doi.org/10.1016/j.jpeds.2015.08.042
        • Vandenbranden S.L.
        • McMullen A.
        • Schechter M.S.
        • Pasta D.J.
        • Michaelis R.L.
        • Konstan M.W.
        • et al.
        Lung function decline from adolescence to young adulthood in cystic fibrosis.
        Pediatr Pulmonol. 2012; 47: 135-143https://doi.org/10.1002/ppul.21526
        • Dasenbrook E.C.
        • Fink A.K.
        • Schechter M.S.
        • Sanders D.B.
        • Millar S.J.
        • Pasta D.J.
        • et al.
        Rapid lung function decline in adults with early-stage cystic fibrosis lung disease.
        J Cyst Fibros. 2020; 19 (Off J Eur Cyst Fibros Soc): 527-533https://doi.org/10.1016/j.jcf.2019.12.005
        • Hong K.
        • Muntner P.
        • Kronish I.
        • Shilane D.
        • Chang T.I.
        Medication adherence and visit-to-visit variability of systolic blood pressure in African Americans with chronic kidney disease in the AASK trial.
        J Hum Hypertens. 2016; 30: 73-78https://doi.org/10.1038/jhh.2015.26
        • Muntner P.
        • Levitan E.B.
        • Joyce C.
        • Holt E.
        • Mann D.
        • Oparil S.
        • et al.
        Association between antihypertensive medication adherence and visit-to-visit variability of blood pressure.
        J Clin Hypertens. 2013; 15 (Greenwich Conn): 112-117https://doi.org/10.1111/jch.12037
        • McGillicuddy J.W.
        • Chandler J.L.
        • Sox L.R.
        • Taber D.J.
        Exploratory analysis of the impact of an mhealth medication adherence intervention on tacrolimus trough concentration variability: post hoc results of a randomized controlled trial.
        Ann Pharmacother. 2020; 54: 1185-1193https://doi.org/10.1177/1060028020931806
        • White H.
        • Shaw N.
        • Denman S.
        • Pollard K.
        • Wynne S.
        • Peckham D.G
        Variation in lung function as a marker of adherence to oral and inhaled medication in cystic fibrosis.
        Eur Respir J. 2017; 491600987https://doi.org/10.1183/13993003.00987-2016
        • Anghel L.A.
        • Farcas A.M.
        • Oprean R.N.
        An overview of the common methods used to measure treatment adherence.
        Med Pharm Rep. 2019; 92: 117-122https://doi.org/10.15386/mpr-1201
        • Wildman M.J.
        • O'Cathain A.
        • Maguire C.
        • Arden M.A.
        • Hutchings M.
        • Bradley J.
        • et al.
        Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial.
        Thorax. 2021; (thoraxjnl-2021-217594)https://doi.org/10.1136/thoraxjnl-2021-217594
        • Earnest A.
        • Salimi F.
        • Wainwright C.E.
        • Bell S.C.
        • Ruseckaite R.
        • Ranger T.
        • et al.
        Lung function over the life course of paediatric and adult patients with cystic fibrosis from a large multi-centre registry.
        Sci Rep. 2020; 10: 17421https://doi.org/10.1038/s41598-020-74502-1
        • Wildman M.J.
        • Hoo Z.H.
        Moving cystic fibrosis care from rescue to prevention by embedding adherence measurement in routine care.
        Paediatr Respir Rev. 2014; 15: 16-18https://doi.org/10.1016/j.prrv.2014.04.007
        • El-Gheryani M.S.A.
        • Hoo Z.H.
        • Curley R.
        • Wildman M.J.
        S136 Understanding longitudinal changes in%FEV1 variability and its role as an indicator of care quality among adults with cystic fibrosis.
        Thorax. 2018; 73 (A85–A85)https://doi.org/10.1136/thorax-2018-212555.142
        • Morgan W.J.
        • VanDevanter D.R.
        • Pasta D.J.
        • Foreman A.J.
        • Wagener J.S.
        • Konstan M.W.
        Corrigendum to FEV1 variability helps identify patients with cystic fibrosis at risk of greater loss of lung Function.
        J Pediatr. 2023; ([The Journal of Pediatrics (2016) 116–121]) (0)https://doi.org/10.1016/j.jpeds.2022.12.017