Adherence to nebulised therapies in adolescents with cystic fibrosis is best on week-days during school term-time
Open accessAbstract
Objectives Treatment regimen for families of children with cystic fibrosis (CF) is considerable, particularly when nebulised therapies for chronic Pseudomonas aeruginosa airway infection are prescribed. Adherence to these regimens is variable, particularly in adolescence. Previously, we reported children to be more adherent in evenings compared to mornings, suggesting an association with time-pressure. The aim of this study was to determine whether adherence would be better in adolescent patients at weekends and during school holidays when time-pressures may be less.Study design 24 patients (14 male, median [range] age 13.9 [11.1-16.8] years) were enrolled from two regional paediatric CF centres in the United Kingdom. Data for a full scholastic year, were downloaded openly from a breath-activated data logging nebuliser (I-neb™). Adherence (% of doses taken÷expected number) was calculated during term-times, holidays, weekends and weekdays, for each patient.Results Large variations in adherence were seen between patients. However, adherence during term-time was significantly better than holidays (p<0.001). Weekday adherence was better than weekend adherence in term-time but not holidays. Interestingly, patients prescribed three daily treatments took on average 1.4 treatments/day, a similar number to those prescribed two daily treatments.Conclusion Overall adherence to inhaled therapies was reasonable, but significantly reduced during holiday periods. This suggests a need for families to have not only time, but also structure in their daily routine to maintain optimal adherence to long-term therapies. It is important for CF teams to appreciate these factors when supporting families.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Trials using objective recorded measures suggest that adherence to inhaled therapies in people with CF is around 65% to 67% in children or adolescents.
“and 65% to 67% in children or adolescents (Ball 2013;McNamara 2009).”
From Psychological interventions for improving adherence to inhaled therapies in people with cystic fibrosis (2023) · cites this paper as Ball 2013
Objective adherence data collected using date-and time-logging nebulisers have demonstrated that, amongst adolescents with CF, adherence to inhaled therapies is greater on school days compared to weekends or holidays.
“Objective adherence data, collected using date-and time-logging nebulisers, have demonstrated that, amongst adolescents with CF, adherence to inhaled therapies is greater on school days compared to weekends or holidays (Ball 2013), despite this being a time when adolescents are likely to be busiest and are therefore more susceptible to miss treatments due to burden (Hoo 2017).”
From Psychological interventions for improving adherence to inhaled therapies in people with cystic fibrosis (2023) · cites this paper as Ball 2013
The results may be consistent with previous research highlighting the role of habit on adherence to inhaled therapies in people with cystic fibrosis, and with the suggestion that habit may attenuate the relationship between treatment complexity and perceived treatment burden.
“This may be consistent with previous research highlighting the role of habit on adherence to inhaled therapies in people with CF (Arden 2019;Ball 2013;Hoo 2017;Hoo 2019a), and the suggestion that habit (i.e.”
From Psychological interventions for improving adherence to inhaled therapies in people with cystic fibrosis (2023) · cites this paper as Ball 2013
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Lee, T. W. R., Brownlee, K. G., Conway, S. P., Denton, M., & Littlewood, J. M. (2003) · Journal of Cystic Fibrosis · doi:10.1016/s1569-1993(02)00141-8 · Cited by 714 · see citing works
Self-citationMeasuring compliance with inhaled medication in asthma.
Coutts, J., GIBSON, N. A., & Paton, J. Y. (1992) · Archives of Disease in Childhood · doi:10.1136/adc.67.3.332 · Cited by 270 · see citing works
A multi-method assessment of treatment adherence for children with cystic fibrosis
Modi, A. C., Lim, C. S., Yu, N. S., Geller, D., Wagner, M. H., & Quittner, A. L. (2006) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2006.03.002 · Cited by 264 · see citing works
Treatment compliance in children and adults with Cystic Fibrosis
Llorente, R. P. A., García, C. B., & Díaz, J. J. (2008) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2008.01.003 · Cited by 169 · see citing works
Compliance with inhaled asthma medication in preschool children.
GIBSON, N. A., Ferguson, A. E., Aitchison, T. C., & Paton, J. Y. (1995) · Thorax · doi:10.1136/thx.50.12.1274 · Cited by 160 · see citing works
Adherence to treatment in children and adolescent patients with cystic fibrosis
Zindani, G. N., Streetman, D. D., Streetman, D. S., & Nasr, S. Z. (2005) · Journal of Adolescent Health · doi:10.1016/j.jadohealth.2004.09.013 · Cited by 117 · see citing works
Year-to-year changes in lung function in individuals with cystic fibrosis
Liou, T. G., Elkin, E. P., Pasta, D. J., Jacobs, J. R., Konstan, M. W., Morgan, W. J., & Wagener, J. S. (2010) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2010.04.002 · Cited by 117 · see citing works
New Aerosol Delivery Devices for Cystic Fibrosis
Kesser, K. C., & Geller, D. E. (2009) · Respiratory Care · doi:10.4187/002013209790983250 · Cited by 97 · see citing works
Butner, J., Berg, C. A., Osborn, P. G., Butler, J. M., Godri, C., Fortenberry, K., Barach, I. M., Le, H., & Wiebe, D. J. (2009) · Developmental Psychology · doi:10.1037/a0015363 · Cited by 96 · see citing works
McNamara, P. S., McCormack, P., McDonald, A. J., Heaf, L., & Southern, K. W. (2009) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2009.04.006 · Cited by 72 · see citing works
Self-citationQuittner, A. L., Drotar, D., Landis, C., Slocum, N., Seidner, D., & Jacobsen, J. (2000) · Cited by 68 · see citing works
Adherence to nebulised antibiotics in cystic fibrosis
Latchford, G. J., Duff, A. J. A., Quinn, J., Conway, S., & Conner, M. T. (2008) · Patient Education and Counseling · doi:10.1016/j.pec.2008.08.027 · Cited by 49 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Update on Key Emerging Challenges in Cystic Fibrosis
Jennings, M. T., Riekert, K. A., & Boyle, M. (2014) · Medical Principles and Practice · doi:10.1159/000357646 · Cited by 3,667 · see citing works
Pulmonary medication adherence and health-care use in cystic fibrosis
Quittner, A. L., Zhang, J., Marynchenko, M., Chopra, P. A., Signorovitch, J., Yushkina, Y., & Riekert, K. A. (2014) · Chest · doi:10.1378/chest.13-1926 · Cited by 250 · see citing works
Inhaled antimicrobial therapy – Barriers to effective treatment
Weers, J. G. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2014.08.013 · Cited by 129 · see citing works
Children's Experiences of Cystic Fibrosis: A Systematic Review of Qualitative Studies
Jamieson, N., Fitzgerald, D. A., Singh‐Grewal, D., Hanson, C. S., Craig, J. C., & Tong, A. (2014) · PEDIATRICS · doi:10.1542/peds.2014-0009 · Cited by 114 · see citing works
Adherence to therapies in cystic fibrosis: a targeted literature review
Narayanan, S., Mainz, J. G., Gala, S., Tabori, H., & Grossoehme, D. H. (2017) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2017.1280399 · Cited by 97 · see citing works
Fibrous dysplasia and cemento-ossifying fibroma. A histologic spectrum.
Voytek, T. M., Ro, J. Y., Edeiken, J., & Ayala, A. G. (1995) · PubMed · Cited by 91 · see citing works
Grossoehme, D. H., Szczesniak, R. D., Britton, L., Siracusa, C. M., Quittner, A. L., Chini, B. A., Dimitriou, S. M., & Seid, M. (2015) · Annals of the American Thoracic Society · doi:10.1513/annalsats.201408-379oc · Cited by 76 · see citing works
The impact of medication adherence on lung health outcomes in cystic fibrosis
Eakin, M. N., & Riekert, K. A. (2013) · Current Opinion in Pulmonary Medicine · doi:10.1097/mcp.0b013e3283659f45 · Cited by 71 · see citing works
Electronic monitoring reveals highly variable adherence patterns in patients prescribed ivacaftor
Siracusa, C. M., Ryan, J. L., Burns, L., Wang, Y., Zhang, N., Clancy, J. P., & Drotar, D. (2015) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2015.05.009 · Cited by 71 · see citing works
Inhaled therapy in cystic fibrosis: agents, devices and regimens
Agent, P., & Parrott, H. (2015) · Breathe · doi:10.1183/20734735.021014 · Cited by 64 · see citing works
Wildman, M. J., O’Cathain, A., Maguire, C., Arden, M. A., Hutchings, M., Bradley, J., Walters, S. J., Whelan, P., Ainsworth, J., Buchan, I., et al. (2022) · Thorax · doi:10.1136/thoraxjnl-2021-217594 · Cited by 54 · see citing works
Opportunities for cystic fibrosis care teams to support treatment adherence
Riekert, K. A., Eakin, M. N., Bilderback, A. L., Ridge, A. K., & Marshall, B. C. (2014) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2014.10.003 · Cited by 45 · see citing works
Impact of home spirometry on medication adherence among adolescents with cystic fibrosis
Shakkottai, A., Kaciroti, N., Kasmikha, L., & Nasr, S. Z. (2018) · Pediatric Pulmonology · doi:10.1002/ppul.23950 · Cited by 40 · see citing works
Mitchell, R. M., Jones, A. M., Stocking, K., Foden, P., & Barry, P. J. (2021) · Thorax · doi:10.1136/thoraxjnl-2020-215556 · Cited by 40 · see citing works
Fungal contamination of nebuliser devices used by people with cystic fibrosis
Peckham, D. G., Williams, K., Wynne, S., Denton, M., Pollard, K., & Barton, R. (2015) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2015.06.004 · Cited by 31 · see citing works
Calthorpe, R. J., Smith, S. J., Rowbotham, N. J., Leighton, P. A., Davies, G., Daniels, T. E., Gathercole, K., Allen, L. J., Elliott, Z. C., & Smyth, A. R. (2020) · BMJ Open Respiratory Research · doi:10.1136/bmjresp-2020-000601 · Cited by 29 · see citing works
Grossoehme, D. H., Szczesniak, R. D., Mrug, S., Dimitriou, S. M., Marshall, A., & McPhail, G. L. (2016) · Journal of Pediatric Psychology · doi:10.1093/jpepsy/jsw024 · Cited by 27 · see citing works
Rouzé, H., Viprey, M., Allemann, S. S., Dima, A. L., Caillet, P., Denis, A., Bourdy, S., Camara, B., Llerena, C., Reix, P., et al. (2019) · Patient Preference and Adherence · doi:10.2147/ppa.s211769 · Cited by 26 · see citing works
Enhancing adherence to inhaled therapies in cystic fibrosis
Lomas, P. (2014) · Therapeutic Advances in Respiratory Disease · doi:10.1177/1753465814524471 · Cited by 24 · see citing works
Schwarz, C., Schulte-Hubbert, B., Bend, J., Abele‐Horn, M., Baumann, I. G., Bremer, W., Brunsmann, F., Dieninghoff, D., Eickmeier, O., Ellemunter, H., et al. (2018) · Pneumologie · doi:10.1055/s-0044-100191 · Cited by 24 · see citing works
Managing cystic fibrosis alongside children’s schooling: Family, nurse and teacher perspectives
Gathercole, K. (2018) · Journal of Child Health Care · doi:10.1177/1367493518814930 · Cited by 23 · see citing works
Nicolais, C. J., Bernstein, R. M., Saez-Flores, E., McLean, K. A., Riekert, K. A., & Quittner, A. L. (2019) · Journal of Clinical Psychology in Medical Settings · doi:10.1007/s10880-018-9598-z · Cited by 23 · see citing works
Mikesell, C. L., Kempainen, R. R., Laguna, T. A., Menk, J. S., Wey, A. R., Gaillard, P. R., & Regelmann, W. E. (2017) · Respiratory Care · doi:10.4187/respcare.05349 · Cited by 22 · see citing works
Hoo, Z. H., Boote, J., Wildman, M. J., Campbell, M. J., & Gardner, B. (2017) · Health Psychology and Behavioral Medicine · doi:10.1080/21642850.2017.1338958 · Cited by 21 · see citing works
Eaton, C. K., Beachy, S., McLean, K. A., Nicolais, C. J., Bernstein, R. M., Saez-Flores, E., Quittner, A. L., & Riekert, K. A. (2020) · Patient Education and Counseling · doi:10.1016/j.pec.2020.02.025 · Cited by 18 · see citing works
Murray, T. S., O’Rourke, T. K., Feinn, R., Drapeau, G., & Collins, M. S. (2019) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2019.05.008 · Cited by 15 · see citing works
Dawson, S., Girling, C.-J., Cowap, L., & Clark-Carter, D. (2023) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd013766.pub2 · Cited by 14 · see citing works
Measuring adherence with medications: time is of the essence
Steiner, J. F. (2016) · Pharmacoepidemiology and Drug Safety · doi:10.1002/pds.3932 · Cited by 14 · see citing works
Leggett, C., Giles, L. C., Anderson, J. J. A., Doogue, M. P., Couper, J., & Peña, A. S. (2019) · Archives of Disease in Childhood · doi:10.1136/archdischild-2018-316303 · Cited by 13 · see citing works
Girón, R. M., Peláez, A., Ibáñez, A., Martínez-Besteiro, E., Gómez-Punter, R. M., Martínez-Vergara, A., Ancochea, J., & Morell, A. (2022) · Antibiotics · doi:10.3390/antibiotics11111637 · Cited by 12 · see citing works
Morton, R., Elphick, H., Edwards, E., Daw, W., & West, N. (2017) · Patient Preference and Adherence · doi:10.2147/ppa.s123723 · Cited by 12 · see citing works
Adherence and barriers to hyperinsufflation in children with congenital muscular dystrophy
Pascoe, J. E., Sawnani, H., Mayer, O. H., McConnell, K. B., McDonough, J. M., White, C., Rutkowski, A. M., Amin, R. S., & Modi, A. C. (2016) · Pediatric Pulmonology · doi:10.1002/ppul.23645 · Cited by 11 · see citing works
An empirical method to cluster objective nebulizer adherence data among adults with cystic fibrosis
Hoo, Z. H., Campbell, M. J., Curley, R., & Wildman, M. J. (2017) · Patient Preference and Adherence · doi:10.2147/ppa.s131497 · Cited by 11 · see citing works
van Velzen, A. J., Uges, J. W. F., Heijerman, H. G. M., Arets, B. G. M., Nuijsink, M., van der Wiel, E. C., van Maarseveen, E. M., van Zanten, G. A., Pullens, B., Touw, D. J., et al. (2019) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.13988 · Cited by 11 · see citing works
Psychological predictors of nutritional adherence in adolescents with cystic fibrosis
Borschuk, A. P., Filigno, S. S., Opipari‐Arrigan, L., Peugh, J., & Stark, L. J. (2019) · Clinical Nutrition ESPEN · doi:10.1016/j.clnesp.2019.06.004 · Cited by 10 · see citing works
Adherence pattern to study drugs in clinical trials by patients with cystic fibrosis
Pugatsch, T., Shoseyov, D., Cohen‐Cymberknoh, M., Hayut, B., Armoni, S., Griese, M., & Kerem, E. (2015) · Pediatric Pulmonology · doi:10.1002/ppul.23344 · Cited by 9 · see citing works
Dixon, E., Puckey, M., Collins, N., Marsh, G. S., & Pabary, R. (2019) · Paediatric Respiratory Reviews · doi:10.1016/j.prrv.2019.04.002 · Cited by 8 · see citing works
ÇAKIR, M. N., & Kızıler, E. (2022) · Türkiye Sağlık Bilimleri ve Araştırmaları Dergisi · doi:10.51536/tusbad.1128746 · Cited by 7 · see citing works
TREATMENT ADHERENCE AMONG CHILDREN AND ADOLESCENTS IN A CYSTIC FIBROSIS REFERENCE CENTER
Bonfim, B. S., Filho, V. M. D. M., Fontenelle, F. M., & Souza, E. L. (2020) · Revista Paulista de Pediatria · doi:10.1590/1984-0462/2020/38/2018338 · Cited by 7 · see citing works
Byrwa, D. J., Pérez, G. F., Roach, C. M., Prentice, S., & Goetz, D. (2023) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2023.01.006 · Cited by 6 · see citing works
A weekend/weekday comparison of adherence to daily treatment regimens in adults with cystic fibrosis
Keyte, R., Egan, H. H., Jackson, C. A., Nash, E. F., Regan, A., & Mantzios, M. (2017) · Health Psychology Report · doi:10.5114/hpr.2018.72331 · Cited by 6 · see citing works
Adults with cystic fibrosis: spiritual coping with lifelong disease
Grossoehme, D. H., Cole, A. G., Lewis, K., Stamper, S. M., Teeters, A., & Joseph, P. M. (2020) · Journal of Health Care Chaplaincy · doi:10.1080/08854726.2020.1713647 · Cited by 5 · see citing works
S3-Leitlinie: Lungenerkrankung bei Mukoviszidose – Pseudomonas aeruginosa
Schwarz, C., Bend, J., Hebestreit, H. U., Hogardt, M., Hügel, C., Illing, S., Mainz, J. G., Rietschel, E., Schmidt, S., Schulte-Hubbert, B., et al. (2024) · Pneumologie · doi:10.1055/a-2182-1907 · Cited by 5 · see citing works
Richtig inhalieren bei Mukoviszidose: Internet-verfügbare Videoclips der Deutschen Atemwegsliga e.V.
Dieninghoff, D., Knipel, V., Criée, C.-P., & Windisch, W. (2015) · Pneumologie · doi:10.1055/s-0034-1392490 · Cited by 4 · see citing works
Impact of Digital Technologies on Clinical Care for Adults with Cystic Fibrosis
Peckham, D. G., & Spoletini, G. (2022) · Seminars in Respiratory and Critical Care Medicine · doi:10.1055/s-0042-1758730 · Cited by 3 · see citing works
Understanding Treatment Adherence in Cystic Fibrosis: Challenges and Opportunities
Muther, E., Butcher, J. L., & Riekert, K. A. (2020) · Respiratory medicine · doi:10.1007/978-3-030-42382-7_22 · Cited by 2 · see citing works
Can clinical benefits of modulators effectively ‘modulate’ adherence in people with CF?
Davis, C. S., & Cogen, J. D. (2021) · Thorax · doi:10.1136/thoraxjnl-2021-216974 · Cited by 2 · see citing works
Dawson, S., Cowap, L., Clark-Carter, D. D., & Girling, C. (2020) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd013766 · Cited by 1 · see citing works
After a long wait, two arrive, one after the other!
Southern, K. W., McCormack, P., & McNamara, P. S. (2013) · Thorax · doi:10.1136/thoraxjnl-2012-202891 · Cited by 1 · see citing works
Self-citationNew and Evolving Therapies for Cystic Fibrosis Patients
Jabar, A., Raissy, H., & Blake, K. (2014) · Pediatric Allergy Immunology and Pulmonology · doi:10.1089/ped.2014.0364
Lifestyle treatments in cystic fibrosis: The NHS should pay
Ketchell, R. I. (2016) · Paediatric Respiratory Reviews · doi:10.1016/j.prrv.2016.06.006
The role of beliefs in predicting adherence to nebulised therapy in adolescents with cystic fibrosis
Stirzaker, B. M. (2020) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
Abramavičius, S., Akramienė, D., Tashfeen, T., Uždavinytė, D., & Stankevıčıus, E. (2026) · Life · doi:10.3390/life16081267
- Authors
- Ball, R., Southern, K. W., McCormack, P., Duff, A. J. A., Brownlee, K. G., & McNamara, P. S.
- Affiliations
- Leeds General Infirmary (GB)
- University of Liverpool (GB)
- Corresponding author
- McNamara, Paul S.
- Venue
- Journal of Cystic Fibrosis
- Publisher
- Elsevier BV
- Published
- 2013-09
- Volume
- 12
- Issue
- 5
- Pages
- 440-444
- ISSN
- 1569-1993 (ISSN-L)
- OpenAlex
- W2168257476
- Cited by
- 53
- References
- 12
- Citations by year
- 2026: 1 · 2024: 1 · 2023: 2 · 2022: 3 · 2021: 3 · 2020: 7 · 2019: 7 · 2018: 3 · 2017: 6 · 2016: 4 · 2015: 6 · 2014: 7 · 2013: 2
- FWCI
- 5.15
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Cystic Fibrosis (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
- Health Sciences › Medicine › Family Practice › Medication Adherence and Compliance
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Inhalation and Respiratory Drug Delivery
- Keywords
- medication adherence, adolescents, Pseudomonas aeruginosa, school holidays, weekends, time pressure, daily routine, inhalation therapy
- MeSH terms
- Assessment of Medication Adherence, Adolescent, Child, Cystic Fibrosis, Female, Humans, Male, Nebulizers and Vaporizers, Respiratory Therapy, Retrospective Studies, Schools, Drug Monitoring, Medication Adherence
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review