Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management

Detalhes bibliográficos
Autor(a) principal: Pinto, Patrícia Jesus Ribeiro
Data de Publicação: 2020
Outros Autores: Paredes, Ana Cristina, Almeida, Armando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/1822/62450
Resumo: Background. Hemophilia is a rare disorder characterized by spontaneous bleeding, with pain being a critical aspect. However, a systematic assessment of hemophilia-related pain in Portugal has never been conducted. Objective. To understand the pain experience among Portuguese people with hemophilia (PWH) by describing its prevalence, characteristics, and impact and uncovering intervention needs in the realm of hemophilia-related pain care. Methods. A cross-sectional observational survey, with age-adapted versions of questions concerning pain, emotional distress, and quality of life, was answered by 104 adults, 21 children/teenagers (10-17 years), and 19 children (1-9 years). Results. Pain was reported by 82 (78.8%) adults, 16 (76.2%) children/teenagers, and 13 (68.4%) children, with 65 (62.5%), 13 (61.9%), and eight (42.1%) of them reporting pain lasting more than three months, respectively. The mean number of pain locations (SD) was 5.23 (3.95) for adults, 4.13 (3.48) for children/teenagers, and 3.15 (1.99) for children age 1-9 years, with lower limbs pain causing the greatest negative impact. More frequent pain-triggering factors were physical effort/movements (61, 74.4%) for adults and hemarthrosis for younger groups (children/teenagers: 14, 87.5%; children: 9, 69.2%). Bleeds yielded the highest mean pain intensity (adults: M [SD] = 5.67 [2.09]; children/teenagers: M [SD] = 5.69 [2.15]). Adults with pain revealed more anxiety (odds ratio [OR] =1.698, P= 0.003) and depression (OR = 1.961, P= 0.025) and lower quality of life (OR = 0.928, P= 0.001). Conclusions. The current findings highlight the high prevalence, duration, and frequency of pain at all ages, its potentially simultaneous acute and chronic nature, its likelihood to affect multiple locations concurrently, and its detrimental impact. Important insights concerning intervention needs are presented, ultimately contributing to the improvement of hemophilia-related pain management and patient care.
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spelling Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain managementHemophiliaHemarthrosisChronic arthropathyEmotional DistressHealth-Related Quality of LifeCiências Médicas::Medicina BásicaScience & TechnologyBackground. Hemophilia is a rare disorder characterized by spontaneous bleeding, with pain being a critical aspect. However, a systematic assessment of hemophilia-related pain in Portugal has never been conducted. Objective. To understand the pain experience among Portuguese people with hemophilia (PWH) by describing its prevalence, characteristics, and impact and uncovering intervention needs in the realm of hemophilia-related pain care. Methods. A cross-sectional observational survey, with age-adapted versions of questions concerning pain, emotional distress, and quality of life, was answered by 104 adults, 21 children/teenagers (10-17 years), and 19 children (1-9 years). Results. Pain was reported by 82 (78.8%) adults, 16 (76.2%) children/teenagers, and 13 (68.4%) children, with 65 (62.5%), 13 (61.9%), and eight (42.1%) of them reporting pain lasting more than three months, respectively. The mean number of pain locations (SD) was 5.23 (3.95) for adults, 4.13 (3.48) for children/teenagers, and 3.15 (1.99) for children age 1-9 years, with lower limbs pain causing the greatest negative impact. More frequent pain-triggering factors were physical effort/movements (61, 74.4%) for adults and hemarthrosis for younger groups (children/teenagers: 14, 87.5%; children: 9, 69.2%). Bleeds yielded the highest mean pain intensity (adults: M [SD] = 5.67 [2.09]; children/teenagers: M [SD] = 5.69 [2.15]). Adults with pain revealed more anxiety (odds ratio [OR] =1.698, P= 0.003) and depression (OR = 1.961, P= 0.025) and lower quality of life (OR = 0.928, P= 0.001). Conclusions. The current findings highlight the high prevalence, duration, and frequency of pain at all ages, its potentially simultaneous acute and chronic nature, its likelihood to affect multiple locations concurrently, and its detrimental impact. Important insights concerning intervention needs are presented, ultimately contributing to the improvement of hemophilia-related pain management and patient care.This work was supported by the Novo Nordisk HERO Research Grant 2015. PRP is the recipient of a postdoctoral grant (SFRH/BPD/103529/2014) from the Portuguese Foundation of Science and Technology.Oxford University PressUniversidade do MinhoPinto, Patrícia Jesus RibeiroParedes, Ana CristinaAlmeida, Armando20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/62450engPinto, P. R., Paredes, A. C., & Almeida, A. (2019). Pain Prevalence, Characteristics, and Impact Among People with Hemophilia: Findings from the First Portuguese Survey and Implications for Pain Management. Pain Medicine.1526-23751526-463710.1093/pm/pny30930812031https://academic.oup.com/painmedicine/advance-article-abstract/doi/10.1093/pm/pny309/5366314info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:52:28Zoai:repositorium.sdum.uminho.pt:1822/62450Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:51:36.578949Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
title Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
spellingShingle Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
Pinto, Patrícia Jesus Ribeiro
Hemophilia
Hemarthrosis
Chronic arthropathy
Emotional Distress
Health-Related Quality of Life
Ciências Médicas::Medicina Básica
Science & Technology
title_short Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
title_full Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
title_fullStr Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
title_full_unstemmed Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
title_sort Pain prevalence, characteristics, and impact among people with hemophilia: findings from the first portuguese survey and implications for pain management
author Pinto, Patrícia Jesus Ribeiro
author_facet Pinto, Patrícia Jesus Ribeiro
Paredes, Ana Cristina
Almeida, Armando
author_role author
author2 Paredes, Ana Cristina
Almeida, Armando
author2_role author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Pinto, Patrícia Jesus Ribeiro
Paredes, Ana Cristina
Almeida, Armando
dc.subject.por.fl_str_mv Hemophilia
Hemarthrosis
Chronic arthropathy
Emotional Distress
Health-Related Quality of Life
Ciências Médicas::Medicina Básica
Science & Technology
topic Hemophilia
Hemarthrosis
Chronic arthropathy
Emotional Distress
Health-Related Quality of Life
Ciências Médicas::Medicina Básica
Science & Technology
description Background. Hemophilia is a rare disorder characterized by spontaneous bleeding, with pain being a critical aspect. However, a systematic assessment of hemophilia-related pain in Portugal has never been conducted. Objective. To understand the pain experience among Portuguese people with hemophilia (PWH) by describing its prevalence, characteristics, and impact and uncovering intervention needs in the realm of hemophilia-related pain care. Methods. A cross-sectional observational survey, with age-adapted versions of questions concerning pain, emotional distress, and quality of life, was answered by 104 adults, 21 children/teenagers (10-17 years), and 19 children (1-9 years). Results. Pain was reported by 82 (78.8%) adults, 16 (76.2%) children/teenagers, and 13 (68.4%) children, with 65 (62.5%), 13 (61.9%), and eight (42.1%) of them reporting pain lasting more than three months, respectively. The mean number of pain locations (SD) was 5.23 (3.95) for adults, 4.13 (3.48) for children/teenagers, and 3.15 (1.99) for children age 1-9 years, with lower limbs pain causing the greatest negative impact. More frequent pain-triggering factors were physical effort/movements (61, 74.4%) for adults and hemarthrosis for younger groups (children/teenagers: 14, 87.5%; children: 9, 69.2%). Bleeds yielded the highest mean pain intensity (adults: M [SD] = 5.67 [2.09]; children/teenagers: M [SD] = 5.69 [2.15]). Adults with pain revealed more anxiety (odds ratio [OR] =1.698, P= 0.003) and depression (OR = 1.961, P= 0.025) and lower quality of life (OR = 0.928, P= 0.001). Conclusions. The current findings highlight the high prevalence, duration, and frequency of pain at all ages, its potentially simultaneous acute and chronic nature, its likelihood to affect multiple locations concurrently, and its detrimental impact. Important insights concerning intervention needs are presented, ultimately contributing to the improvement of hemophilia-related pain management and patient care.
publishDate 2020
dc.date.none.fl_str_mv 2020
2020-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/1822/62450
url https://hdl.handle.net/1822/62450
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pinto, P. R., Paredes, A. C., & Almeida, A. (2019). Pain Prevalence, Characteristics, and Impact Among People with Hemophilia: Findings from the First Portuguese Survey and Implications for Pain Management. Pain Medicine.
1526-2375
1526-4637
10.1093/pm/pny309
30812031
https://academic.oup.com/painmedicine/advance-article-abstract/doi/10.1093/pm/pny309/5366314
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Oxford University Press
publisher.none.fl_str_mv Oxford University Press
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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