Top

Gepubliceerd in:

10-10-2018 | Brief Communication

Hearing loss and quality of life in survivors of paediatric CNS tumours and other cancers

Auteurs: Annette Weiss, Grit Sommer, Christina Schindera, Laura Wengenroth, Axel Karow, Manuel Diezi, Gisela Michel, Claudia E. Kuehni, Swiss Paediatric Oncology Group (SPOG)

Gepubliceerd in: Quality of Life Research | Uitgave 2/2019

Abstract

Purpose

Hearing loss, a complication of cancer treatment, may reduce health-related quality of life (HRQoL), especially in childhood cancer survivors of central nervous system (CNS) tumours who often have multiple late effects. We examined the effect of hearing loss on HRQoL in young survivors of CNS and other childhood cancers.

Methods

Within the Swiss Childhood Cancer Survivor Study, we sent questionnaires about hearing loss and HRQoL (KIDSCREEN-27) to parents of survivors aged 8–15 years. We stratified the effect of hearing loss on HRQoL by cancer diagnosis, using multivariable logistic regression and adjusting for sociodemographic and clinical factors.

Results

Hearing loss was associated with impaired physical well-being [unadjusted estimated differences − 4.6 (CI − 9.2, − 0.1); adjusted − 4.0 (CI − 7.6, − 0.3)] and peers and social support [unadjusted − 6.7 (CI − 13.0, − 0.3); adjusted − 5.0 (CI − 10.5, 0.9)] scores in survivors of CNS tumours (n = 123), but not in children diagnosed with other cancers (all p-values > 0.20, n = 577).

Conclusion

Clinicians should be alert to signs of reduced physical well-being and impaired relationships with peers. Especially survivors of CNS tumours may benefit most from strict audiological monitoring and timely intervention to mitigate secondary consequences of hearing loss on HRQoL.

vorige artikel Association between disaster experience and quality of life: the mediating role of disaster risk perception

volgende artikel Development and construct validation of a parent-proxy quality of life instrument in children with bronchopulmonary dysplasia aged 4–8 years old

Alleen toegankelijk voor geautoriseerde gebruikers

Landier, W. (2016). Ototoxicity and cancer therapy. Cancer, 122(11), 1647–1658. https://doi.org/10.1002/cncr.29779.CrossRefPubMed

Roland, L., Fischer, C., Tran, K., Rachakonda, T., Kallogjeri, D., & Lieu, J. (2016). Quality of life in children with hearing impairment: Systematic review and meta-analysis. Otolaryngol Head Neck Surg. https://doi.org/10.1177/0194599816640485.CrossRefPubMedPubMedCentral

Lin, C.-Y., & Fung, X. (2018). The impact of environmental support on health for children with hearing impairment in Taiwan. Social Health and Behavior, 1(1), 4–10. https://doi.org/10.4103/shb.shb_12_18.CrossRef

Gurney, J. G., Tersak, J. M., Ness, K. K., Landier, W., Matthay, K. K., Schmidt, M. L., et al. (2007). Hearing loss, quality of life, and academic problems in long-term neuroblastoma survivors: A report from the Children’s Oncology Group. [Comparative Study Research Support, N.IH., Extramural Research Support, Non-U.S. Gov’t]. Pediatrics, 120(5), e1229–e1236. https://doi.org/10.1542/peds.2007-0178. [).CrossRefPubMed

Wengenroth, L., Gianinazzi, M. E., Rueegg, C. S., Luer, S., Bergstraesser, E., Kuehni, C. E., et al. (2015). Health-related quality of life in young survivors of childhood cancer. Quality of Life Research, 24(9), 2151–2161. https://doi.org/10.1007/s11136-015-0961-3.CrossRefPubMed

Laverdiere, C., Cheung, N. K., Kushner, B. H., Kramer, K., Modak, S., LaQuaglia, M. P., et al. (2005). Long-term complications in survivors of advanced stage neuroblastoma. Pediatric Blood and Cancer, 45(3), 324–332. https://doi.org/10.1002/pbc.20331.CrossRefPubMed

Portwine, C., Rae, C., Davis, J., Teira, P., Schechter, T., Lewis, V., et al. (2016). Health-related quality of life in survivors of high-risk neuroblastoma after stem cell transplant: A national population-based perspective. Pediatric Blood and Cancer, 63(9), 1615–1621. https://doi.org/10.1002/pbc.26063.CrossRefPubMed

Weiss, A., Kuonen, R., Brockmeier, H., Grotzer, M., Candreia, C., Maire, R., et al. (2018). Audiological monitoring in Swiss childhood cancer patients. Pediatric Blood and Cancer. https://doi.org/10.1002/pbc.26877.CrossRefPubMed

Children’s Oncology Group (2013). Long-Term Follow-Up Guidelines for Survivors of Childhood, Adolescent and Young Adult Cancers, Version 4.0. http://www.survivorshipguidelines.org.

10.

Kuehni, C. E., Rueegg, C. S., Michel, G., Rebholz, C. E., Strippoli, M. P., Niggli, F. K., et al. (2012). Cohort profile: The Swiss childhood cancer survivor study [Research Support, Non-U.S. Gov’t]. International Journal of Epidemiology, 41(6), 1553–1564, https://doi.org/10.1093/ije/dyr142.CrossRefPubMed

11.

Michel, G., von der Weid, N. X., Zwahlen, M., Adam, M., Rebholz, C. E., Kuehni, C. E., et al. (2007). The Swiss Childhood Cancer Registry: Rationale, organisation and results for the years 2001–2005. [Research Support, Non-U.S Gov’t]. Swiss Medical Weekly, 137(35–36), 502–509.PubMed

12.

Schindler, M., Mitter, V., Bergstraesser, E., Gumy-Pause, F., Michel, G., & Kuehni, C. E. (2015). Death certificate notifications in the Swiss Childhood Cancer Registry: Assessing completeness and registration procedures. Swiss Medical Weekly, 145, w14225. https://doi.org/10.4414/smw.2015.14225.CrossRefPubMed

13.

Ravens-Sieberer, U., & Europe, K. G. (2006). The Kidscreen questionnaires: Quality of life questionnaires for children and adolescents; handbook. Lengerich: Pabst Science Publ.

14.

Ravens-Sieberer, U., Auquier, P., Erhart, M., Gosch, A., Rajmil, L., Bruil, J., et al. (2007). The KIDSCREEN-27 quality of life measure for children and adolescents: Psychometric results from a cross-cultural survey in 13 European countries. Quality of Life Research, 16(8), 1347–1356. https://doi.org/10.1007/s11136-007-9240-2.CrossRefPubMed

15.

Jervaeus, A., Kottorp, A., & Wettergren, L. (2013). Psychometric properties of KIDSCREEN-27 among childhood cancer survivors and age matched peers: A Rasch analysis. Health and Quality of Life Outcomes, 11, 96. https://doi.org/10.1186/1477-7525-11-96.CrossRefPubMedPubMedCentral

16.

Jervaeus, A., Lampic, C., Johansson, E., Malmros, J., & Wettergren, L. (2014). Clinical significance in self-rated HRQoL among survivors after childhood cancer—Demonstrated by anchor-based thresholds. Acta Oncology, 53(4), 486–492. https://doi.org/10.3109/0284186x.2013.844852.CrossRef

17.

Bisegger, C., Cloetta, B., & Europe Kidscreen Group (2005). Kidscreen: Fragebogen zur Erfassung der gesundheitsbezogenen Lebensqualität von Kindern und Jugendlichen. Manual der deutschsprachigen Versionen für die Schweiz. Bern: Universität Bern, Abteilung Gesundheitsforschung des Instituts für Sozial- und Präventivmedizin.

18.

Steliarova-Foucher, E., Stiller, C., Lacour, B., & Kaatsch, P. (2005). International Classification of Childhood Cancer, third edition. [Research Support, Non-U.S. Gov’t]. Cancer, 103(7), 1457–1467. https://doi.org/10.1002/cncr.20910.CrossRefPubMed

19.

Fuemmeler, B. F., Elkin, T. D., & Mullins, L. L. (2002). Survivors of childhood brain tumors: Behavioral, emotional, and social adjustment. Clinical Psychology Review, 22(4), 547–585.CrossRefPubMed

20.

Hocking, M. C., McCurdy, M., Turner, E., Kazak, A. E., Noll, R. B., Phillips, P., et al. (2015). Social competence in pediatric brain tumor survivors: Application of a model from social neuroscience and developmental psychology. Pediatric Blood & Cancer, 62(3), 375–384. https://doi.org/10.1002/pbc.25300.CrossRef

21.

Schulte, F., Wurz, A., Reynolds, K., Strother, D., & Dewey, D. (2016). Quality of life in survivors of pediatric cancer and their siblings: The consensus between parent-proxy and self-reports. Pediatric Blood & Cancer, 63(4), 677–683. https://doi.org/10.1002/pbc.25868.CrossRef

22.

van Dijk, J., Huisman, J., Moll, A. C., Schouten-van Meeteren, A. Y., Bezemer, P. D., Ringens, P. J., et al. (2007). Health-related quality of life of child and adolescent retinoblastoma survivors in the Netherlands. Health and Quality Life Outcomes, 5, 65. https://doi.org/10.1186/1477-7525-5-65.CrossRef

23.

Matziou, V., Perdikaris, P., Feloni, D., Moschovi, M., Tsoumakas, K., & Merkouris, A. (2008). Cancer in childhood: Children’s and parents’ aspects for quality of life. European Journal of Oncology Nursing, 12(3), 209–216. https://doi.org/10.1016/j.ejon.2007.10.005.CrossRefPubMed

24.

Laffond, C., Dellatolas, G., Alapetite, C., Puget, S., Grill, J., Habrand, J. L., et al. (2012). Quality-of-life, mood and executive functioning after childhood craniopharyngioma treated with surgery and proton beam therapy. Brain Injury, 26(3), 270–281. https://doi.org/10.3109/02699052.2011.648709.CrossRefPubMed

25.

Weiss, A., Sommer, G., Kuonen, R., Scheinemann, K., Grotzer, M., Kompis, M., et al. (2017). Validation of questionnaire-reported hearing with medical records: A report from the Swiss Childhood Cancer Survivor Study. PLoS ONE, 12(3), e0174479. https://doi.org/10.1371/journal.pone.0174479.CrossRefPubMedPubMedCentral

26.

Louie, A. D., Robison, L. L., Bogue, M., Hyde, S., Forman, S. J., & Bhatia, S. (2000). Validation of self-reported complications by bone marrow transplantation survivors. Bone Marrow Transplant, 25(11), 1191–1196. https://doi.org/10.1038/sj.bmt.1702419.CrossRefPubMed

27.

Brinkman, T. M., Bass, J. K., Li, Z., Ness, K. K., Gajjar, A., Pappo, A. S., et al. (2015). Treatment-induced hearing loss and adult social outcomes in survivors of childhood CNS and non-CNS solid tumors: Results from the St. Jude Lifetime Cohort Study. Cancer, 121(22), 4053–4061. https://doi.org/10.1002/cncr.29604.CrossRefPubMedPubMedCentral

28.

Engelen, V., Koopman, H. M., Detmar, S. B., Raat, H., van de Wetering, M. D., Brons, P., et al. (2011). Health-related quality of life after completion of successful treatment for childhood cancer. Pediatric Blood & Cancer, 56(4), 646–653. https://doi.org/10.1002/pbc.22795.CrossRef

29.

Barrera, M., Shaw, A. K., Speechley, K. N., Maunsell, E., & Pogany, L. (2005). Educational and social late effects of childhood cancer and related clinical, personal, and familial characteristics. Cancer, 104(8), 1751–1760. https://doi.org/10.1002/cncr.21390.CrossRefPubMed

Titel: Hearing loss and quality of life in survivors of paediatric CNS tumours and other cancers
Auteurs: Annette Weiss
Grit Sommer
Christina Schindera
Laura Wengenroth
Axel Karow
Manuel Diezi
Gisela Michel
Claudia E. Kuehni
Swiss Paediatric Oncology Group (SPOG)
Publicatiedatum: 10-10-2018
Uitgeverij: Springer International Publishing
Gepubliceerd in: Quality of Life Research / Uitgave 2/2019
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI: https://doi.org/10.1007/s11136-018-2021-2

Bohn Stafleu van Loghum

Deel dit onderdeel of sectie (kopieer de link)

Abstract

Purpose

Methods

Results

Conclusion

Log in om toegang te krijgen

Andere artikelen Uitgave 2/2019

Temporal changes in importance of quality of life domains: a longitudinal study in community-dwelling Swiss older people

Personal and environmental contextual factors as mediators between functional disability and quality of life in adults with serious mental illness: a cross-sectional analysis

Test–retest reliability and validity of a single-item Self-reported Family Happiness Scale in Hong Kong Chinese: findings from Hong Kong Jockey Club FAMILY Project

Anxiety, depression and quality of life in chronic obstructive pulmonary disease patients and caregivers: an actor–partner interdependence model analysis

Health state utility values measured using the EuroQol 5-dimensions questionnaire in adults with chronic hepatitis C: a systematic literature review and meta-analysis

Making a picture worth a thousand numbers: recommendations for graphically displaying patient-reported outcomes data