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Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective
BACKGROUND: Chronic nonbacterial osteomyelitis (CNO) is an autoinflammatory bone disorder that if left untreated can result in bone destruction and severe continuing pain due to persistent inflammation. The impact this chronic disease has on the daily lives of affected children and their families is...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295016/ https://www.ncbi.nlm.nih.gov/pubmed/30547806 http://dx.doi.org/10.1186/s12969-018-0294-1 |
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author | Oliver, Melissa Lee, Tzielan C. Halpern-Felsher, Bonnie Murray, Elizabeth Schwartz, Rebecca Zhao, Yongdong |
author_facet | Oliver, Melissa Lee, Tzielan C. Halpern-Felsher, Bonnie Murray, Elizabeth Schwartz, Rebecca Zhao, Yongdong |
author_sort | Oliver, Melissa |
collection | PubMed |
description | BACKGROUND: Chronic nonbacterial osteomyelitis (CNO) is an autoinflammatory bone disorder that if left untreated can result in bone destruction and severe continuing pain due to persistent inflammation. The impact this chronic disease has on the daily lives of affected children and their families is not well known. The purpose of this study is to understand the disease burden and socioeconomic and psychological impact of CNO from the patients’ and families’ perspectives and identify areas of improvement for patient care and reduced disease burden based on patients’ and families’ responses. METHODS: Participants were invited through a social media platform group and at clinic visits at Stanford Children’s Health. An online survey was administered to patients with a diagnosis of CNO made at < 22 years of age and/or the parent/guardian of a patient with CNO diagnosis made at < 22 years of age. RESULTS: There was a total of 284 survey participants. The median age at CNO diagnosis was 10 years (range 2–22+). Median time from first CNO symptom to diagnosis was 2 years. Antibiotics were used in 35% of patients prior to CNO diagnosis; of these, 24% received antibiotics for greater than 6 months. Between 25 and 61% reported a negative effect of CNO on relationships, school/work performance, or finances; and 19–50% reported effects on psychosocial well-being. The majority agreed patients’ performance with daily tasks and hobbies was challenged by pain, fatigue and physical limitation related to CNO. CONCLUSIONS: Patients with CNO experienced on average a 2-year delay in diagnosis and receiving effective treatments. At least 25% reported problems with relationships, school, work, finances and well-being due to CNO. Recognition of these challenges emphasizes the need to increase awareness of this disease and address the socioeconomic stressors and mental health issues in order to provide optimal care of children with CNO. |
format | Online Article Text |
id | pubmed-6295016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62950162018-12-18 Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective Oliver, Melissa Lee, Tzielan C. Halpern-Felsher, Bonnie Murray, Elizabeth Schwartz, Rebecca Zhao, Yongdong Pediatr Rheumatol Online J Research Article BACKGROUND: Chronic nonbacterial osteomyelitis (CNO) is an autoinflammatory bone disorder that if left untreated can result in bone destruction and severe continuing pain due to persistent inflammation. The impact this chronic disease has on the daily lives of affected children and their families is not well known. The purpose of this study is to understand the disease burden and socioeconomic and psychological impact of CNO from the patients’ and families’ perspectives and identify areas of improvement for patient care and reduced disease burden based on patients’ and families’ responses. METHODS: Participants were invited through a social media platform group and at clinic visits at Stanford Children’s Health. An online survey was administered to patients with a diagnosis of CNO made at < 22 years of age and/or the parent/guardian of a patient with CNO diagnosis made at < 22 years of age. RESULTS: There was a total of 284 survey participants. The median age at CNO diagnosis was 10 years (range 2–22+). Median time from first CNO symptom to diagnosis was 2 years. Antibiotics were used in 35% of patients prior to CNO diagnosis; of these, 24% received antibiotics for greater than 6 months. Between 25 and 61% reported a negative effect of CNO on relationships, school/work performance, or finances; and 19–50% reported effects on psychosocial well-being. The majority agreed patients’ performance with daily tasks and hobbies was challenged by pain, fatigue and physical limitation related to CNO. CONCLUSIONS: Patients with CNO experienced on average a 2-year delay in diagnosis and receiving effective treatments. At least 25% reported problems with relationships, school, work, finances and well-being due to CNO. Recognition of these challenges emphasizes the need to increase awareness of this disease and address the socioeconomic stressors and mental health issues in order to provide optimal care of children with CNO. BioMed Central 2018-12-14 /pmc/articles/PMC6295016/ /pubmed/30547806 http://dx.doi.org/10.1186/s12969-018-0294-1 Text en © The Author(s). 2018 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 Article Oliver, Melissa Lee, Tzielan C. Halpern-Felsher, Bonnie Murray, Elizabeth Schwartz, Rebecca Zhao, Yongdong Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective |
title | Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective |
title_full | Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective |
title_fullStr | Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective |
title_full_unstemmed | Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective |
title_short | Disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective |
title_sort | disease burden and social impact of pediatric chronic nonbacterial osteomyelitis from the patient and family perspective |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295016/ https://www.ncbi.nlm.nih.gov/pubmed/30547806 http://dx.doi.org/10.1186/s12969-018-0294-1 |
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