Cargando…
Predictors of quality of life among adolescents and young adults with a bleeding disorder
BACKGROUND: Health-related quality of life (HRQoL) in adolescents and young adults with bleeding disorders is under-researched. We aimed to describe factors related to HRQoL in adolescents and young adults with hemophilia A or B or von Willebrand disease. METHODS: A convenience sample of volunteers...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383972/ https://www.ncbi.nlm.nih.gov/pubmed/28388906 http://dx.doi.org/10.1186/s12955-017-0643-7 |
_version_ | 1782520380863283200 |
---|---|
author | McLaughlin, John M. Munn, James E. Anderson, Terry L. Lambing, Angela Tortella, Bartholomew Witkop, Michelle L. |
author_facet | McLaughlin, John M. Munn, James E. Anderson, Terry L. Lambing, Angela Tortella, Bartholomew Witkop, Michelle L. |
author_sort | McLaughlin, John M. |
collection | PubMed |
description | BACKGROUND: Health-related quality of life (HRQoL) in adolescents and young adults with bleeding disorders is under-researched. We aimed to describe factors related to HRQoL in adolescents and young adults with hemophilia A or B or von Willebrand disease. METHODS: A convenience sample of volunteers aged 13 to 25 years with hemophilia or von Willebrand disease completed a cross-sectional survey that assessed Physical (PCS) and Mental (MCS) Component Summary scores on the SF-36 questionnaire. Quantile regression models were used to assess factors associated with HRQoL. RESULTS: Of 108 respondents, 79, 7, and 14% had hemophilia A, hemophilia B, and von Willebrand disease, respectively. Most had severe disease (71%), had never developed an inhibitor (65%), and were treated prophylactically (68%). Half of patients were aged 13 to 17 years and most were white (80%) and non-Hispanic (89%). Chronic pain was reported as moderate to severe by 31% of respondents. Median PCS and MCS were 81.3 and 75.5, respectively. Quantile regression showed that the median PCS for women (61% with von Willebrand disease) was 13.1 (95% CI: 2.4, 23.8; p = 0.02) points lower than men. Ever developing an inhibitor (vs never) was associated with a 13.1-point (95% CI: 4.7, 21.5; p < 0.01) PCS reduction. MCS was 10.0 points (95% CI: 0.7, 19.3; p = 0.04) higher for prophylactic infusers versus those using on-demand treatment. Compared with patients with no to mild chronic pain, those with moderate to severe chronic pain had 25.5-point (95% CI: 17.2, 33.8; p < 0.001) and 10.0-point (95% CI: 0.8, 19.2; p = 0.03) reductions in median PCS and MCS, respectively. CONCLUSIONS: Efforts should be made to prevent and manage chronic pain, which was strongly related to physical and mental HRQoL, in adolescents and young adults with hemophilia and von Willebrand disease. Previous research suggests that better clotting factor adherence may be associated with less chronic pain. |
format | Online Article Text |
id | pubmed-5383972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53839722017-04-10 Predictors of quality of life among adolescents and young adults with a bleeding disorder McLaughlin, John M. Munn, James E. Anderson, Terry L. Lambing, Angela Tortella, Bartholomew Witkop, Michelle L. Health Qual Life Outcomes Research BACKGROUND: Health-related quality of life (HRQoL) in adolescents and young adults with bleeding disorders is under-researched. We aimed to describe factors related to HRQoL in adolescents and young adults with hemophilia A or B or von Willebrand disease. METHODS: A convenience sample of volunteers aged 13 to 25 years with hemophilia or von Willebrand disease completed a cross-sectional survey that assessed Physical (PCS) and Mental (MCS) Component Summary scores on the SF-36 questionnaire. Quantile regression models were used to assess factors associated with HRQoL. RESULTS: Of 108 respondents, 79, 7, and 14% had hemophilia A, hemophilia B, and von Willebrand disease, respectively. Most had severe disease (71%), had never developed an inhibitor (65%), and were treated prophylactically (68%). Half of patients were aged 13 to 17 years and most were white (80%) and non-Hispanic (89%). Chronic pain was reported as moderate to severe by 31% of respondents. Median PCS and MCS were 81.3 and 75.5, respectively. Quantile regression showed that the median PCS for women (61% with von Willebrand disease) was 13.1 (95% CI: 2.4, 23.8; p = 0.02) points lower than men. Ever developing an inhibitor (vs never) was associated with a 13.1-point (95% CI: 4.7, 21.5; p < 0.01) PCS reduction. MCS was 10.0 points (95% CI: 0.7, 19.3; p = 0.04) higher for prophylactic infusers versus those using on-demand treatment. Compared with patients with no to mild chronic pain, those with moderate to severe chronic pain had 25.5-point (95% CI: 17.2, 33.8; p < 0.001) and 10.0-point (95% CI: 0.8, 19.2; p = 0.03) reductions in median PCS and MCS, respectively. CONCLUSIONS: Efforts should be made to prevent and manage chronic pain, which was strongly related to physical and mental HRQoL, in adolescents and young adults with hemophilia and von Willebrand disease. Previous research suggests that better clotting factor adherence may be associated with less chronic pain. BioMed Central 2017-04-07 /pmc/articles/PMC5383972/ /pubmed/28388906 http://dx.doi.org/10.1186/s12955-017-0643-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research McLaughlin, John M. Munn, James E. Anderson, Terry L. Lambing, Angela Tortella, Bartholomew Witkop, Michelle L. Predictors of quality of life among adolescents and young adults with a bleeding disorder |
title | Predictors of quality of life among adolescents and young adults with a bleeding disorder |
title_full | Predictors of quality of life among adolescents and young adults with a bleeding disorder |
title_fullStr | Predictors of quality of life among adolescents and young adults with a bleeding disorder |
title_full_unstemmed | Predictors of quality of life among adolescents and young adults with a bleeding disorder |
title_short | Predictors of quality of life among adolescents and young adults with a bleeding disorder |
title_sort | predictors of quality of life among adolescents and young adults with a bleeding disorder |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383972/ https://www.ncbi.nlm.nih.gov/pubmed/28388906 http://dx.doi.org/10.1186/s12955-017-0643-7 |
work_keys_str_mv | AT mclaughlinjohnm predictorsofqualityoflifeamongadolescentsandyoungadultswithableedingdisorder AT munnjamese predictorsofqualityoflifeamongadolescentsandyoungadultswithableedingdisorder AT andersonterryl predictorsofqualityoflifeamongadolescentsandyoungadultswithableedingdisorder AT lambingangela predictorsofqualityoflifeamongadolescentsandyoungadultswithableedingdisorder AT tortellabartholomew predictorsofqualityoflifeamongadolescentsandyoungadultswithableedingdisorder AT witkopmichellel predictorsofqualityoflifeamongadolescentsandyoungadultswithableedingdisorder |