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Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study
BACKGROUND: Cancer-induced bone pain (CIBP) is considered to have both nociceptive and neuropathic components. However, the prevalence, risk factors, and impact of the neuropathic components are yet poorly understood. METHODS: We estimate the prevalence of neuropathic pain (NP) features in patients...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Pain Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043784/ https://www.ncbi.nlm.nih.gov/pubmed/36973971 http://dx.doi.org/10.3344/kjp.22392 |
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author | Zinboonyahgoon, Nantthasorn Luansritisakul, Choopong |
author_facet | Zinboonyahgoon, Nantthasorn Luansritisakul, Choopong |
author_sort | Zinboonyahgoon, Nantthasorn |
collection | PubMed |
description | BACKGROUND: Cancer-induced bone pain (CIBP) is considered to have both nociceptive and neuropathic components. However, the prevalence, risk factors, and impact of the neuropathic components are yet poorly understood. METHODS: We estimate the prevalence of neuropathic pain (NP) features in patients with CIBP at a tertiary care pain clinic setting using the Douleur Neuropathique 4 questionnaire and evaluate their associated factors and their impact after 4 weeks of treatment using the Brief Pain Inventory questionnaire and the Edmonton Symptom Assessment System. RESULTS: A total of 133 patients were recruited. The estimated prevalence of NP was 30.8% (95% confidence interval 23.6%–39.1%). Initially, the patients with NP had significantly higher average pain scores (6.00 vs. 5.05, P = 0.006), higher total interference scores (5.84 vs. 4.89, P = 0.033), and symptom distress scores (35.88 vs. 26.52, P = 0.002). After 4 weeks of treatment, patients in both groups reported significantly decreased pain intensity and improved quality of life. However, the patients with NP still reported significantly higher average pain (4.61 vs. 3.58, P = 0.048), trending toward higher total interference scores (3.52 vs. 2.99, P = 0.426), and symptom distress scores (23.30 vs. 20.77, P = 0.524). From multivariate analysis, the independent risk factors for NP were younger age, pain in the extremities, and higher average pain scores. CONCLUSIONS: NP are common in patients with CIBP. These conditions negatively affect pain intensity and the patient’s quality of life before and after treatment. |
format | Online Article Text |
id | pubmed-10043784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Korean Pain Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100437842023-04-01 Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study Zinboonyahgoon, Nantthasorn Luansritisakul, Choopong Korean J Pain Clinical Research Articles BACKGROUND: Cancer-induced bone pain (CIBP) is considered to have both nociceptive and neuropathic components. However, the prevalence, risk factors, and impact of the neuropathic components are yet poorly understood. METHODS: We estimate the prevalence of neuropathic pain (NP) features in patients with CIBP at a tertiary care pain clinic setting using the Douleur Neuropathique 4 questionnaire and evaluate their associated factors and their impact after 4 weeks of treatment using the Brief Pain Inventory questionnaire and the Edmonton Symptom Assessment System. RESULTS: A total of 133 patients were recruited. The estimated prevalence of NP was 30.8% (95% confidence interval 23.6%–39.1%). Initially, the patients with NP had significantly higher average pain scores (6.00 vs. 5.05, P = 0.006), higher total interference scores (5.84 vs. 4.89, P = 0.033), and symptom distress scores (35.88 vs. 26.52, P = 0.002). After 4 weeks of treatment, patients in both groups reported significantly decreased pain intensity and improved quality of life. However, the patients with NP still reported significantly higher average pain (4.61 vs. 3.58, P = 0.048), trending toward higher total interference scores (3.52 vs. 2.99, P = 0.426), and symptom distress scores (23.30 vs. 20.77, P = 0.524). From multivariate analysis, the independent risk factors for NP were younger age, pain in the extremities, and higher average pain scores. CONCLUSIONS: NP are common in patients with CIBP. These conditions negatively affect pain intensity and the patient’s quality of life before and after treatment. The Korean Pain Society 2023-04-01 2023-04-01 /pmc/articles/PMC10043784/ /pubmed/36973971 http://dx.doi.org/10.3344/kjp.22392 Text en © The Korean Pain Society, 2023 https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Research Articles Zinboonyahgoon, Nantthasorn Luansritisakul, Choopong Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study |
title | Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study |
title_full | Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study |
title_fullStr | Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study |
title_full_unstemmed | Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study |
title_short | Neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study |
title_sort | neuropathic pain feature in cancer-induced bone pain: does it matter? a prospective observational study |
topic | Clinical Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043784/ https://www.ncbi.nlm.nih.gov/pubmed/36973971 http://dx.doi.org/10.3344/kjp.22392 |
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