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Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data

Complex regional pain syndrome (CRPS) is a chronic pain disorder that typically follows trauma or surgery. Suspected CRPS reported after vaccination with human papillomavirus (HPV) vaccines led to temporary suspension of proactive recommendation of HPV vaccination in Japan. We investigated the poten...

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Autores principales: Huygen, Frank, Verschueren, Kristin, McCabe, Candida, Stegmann, Jens-Ulrich, Zima, Julia, Mahaux, Olivia, Van Holle, Lionel, Angelo, Maria-Genalin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587999/
https://www.ncbi.nlm.nih.gov/pubmed/26501109
http://dx.doi.org/10.1016/j.ebiom.2015.07.003
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author Huygen, Frank
Verschueren, Kristin
McCabe, Candida
Stegmann, Jens-Ulrich
Zima, Julia
Mahaux, Olivia
Van Holle, Lionel
Angelo, Maria-Genalin
author_facet Huygen, Frank
Verschueren, Kristin
McCabe, Candida
Stegmann, Jens-Ulrich
Zima, Julia
Mahaux, Olivia
Van Holle, Lionel
Angelo, Maria-Genalin
author_sort Huygen, Frank
collection PubMed
description Complex regional pain syndrome (CRPS) is a chronic pain disorder that typically follows trauma or surgery. Suspected CRPS reported after vaccination with human papillomavirus (HPV) vaccines led to temporary suspension of proactive recommendation of HPV vaccination in Japan. We investigated the potential CRPS signal in relation to HPV-16/18-adjuvanted vaccine (Cervarix®) by database review of CRPS cases with independent expert confirmation; a disproportionality analysis and analyses of temporality; an observed versus expected analysis using published background incidence rates; systematic reviews of aggregate safety data, and a literature review. The analysis included 17 case reports of CRPS: 10 from Japan (0.14/100,000 doses distributed) and seven from the United Kingdom (0.08/100,000). Five cases were considered by independent experts to be confirmed CRPS. Quantitative analyses did not suggest an association between CRPS and HPV-16/18-adjuvanted vaccine. Observed CRPS incidence after HPV-16/18 vaccination was statistically significantly below expected rates. Systematic database reviews using search terms varying in specificity and sensitivity did not identify new cases. No CRPS was reported during clinical development and no unexpected results found in the literature. There is not sufficient evidence to suggest an increased risk of developing CRPS following vaccination with HPV-16/18-adjuvanted vaccine. Post-licensure safety surveillance confirms the acceptable benefit-risk of HPV-16/18 vaccination.
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spelling pubmed-45879992015-10-23 Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data Huygen, Frank Verschueren, Kristin McCabe, Candida Stegmann, Jens-Ulrich Zima, Julia Mahaux, Olivia Van Holle, Lionel Angelo, Maria-Genalin EBioMedicine Research Paper Complex regional pain syndrome (CRPS) is a chronic pain disorder that typically follows trauma or surgery. Suspected CRPS reported after vaccination with human papillomavirus (HPV) vaccines led to temporary suspension of proactive recommendation of HPV vaccination in Japan. We investigated the potential CRPS signal in relation to HPV-16/18-adjuvanted vaccine (Cervarix®) by database review of CRPS cases with independent expert confirmation; a disproportionality analysis and analyses of temporality; an observed versus expected analysis using published background incidence rates; systematic reviews of aggregate safety data, and a literature review. The analysis included 17 case reports of CRPS: 10 from Japan (0.14/100,000 doses distributed) and seven from the United Kingdom (0.08/100,000). Five cases were considered by independent experts to be confirmed CRPS. Quantitative analyses did not suggest an association between CRPS and HPV-16/18-adjuvanted vaccine. Observed CRPS incidence after HPV-16/18 vaccination was statistically significantly below expected rates. Systematic database reviews using search terms varying in specificity and sensitivity did not identify new cases. No CRPS was reported during clinical development and no unexpected results found in the literature. There is not sufficient evidence to suggest an increased risk of developing CRPS following vaccination with HPV-16/18-adjuvanted vaccine. Post-licensure safety surveillance confirms the acceptable benefit-risk of HPV-16/18 vaccination. Elsevier 2015-07-06 /pmc/articles/PMC4587999/ /pubmed/26501109 http://dx.doi.org/10.1016/j.ebiom.2015.07.003 Text en © 2015 The Authors. Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Huygen, Frank
Verschueren, Kristin
McCabe, Candida
Stegmann, Jens-Ulrich
Zima, Julia
Mahaux, Olivia
Van Holle, Lionel
Angelo, Maria-Genalin
Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data
title Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data
title_full Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data
title_fullStr Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data
title_full_unstemmed Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data
title_short Investigating Reports of Complex Regional Pain Syndrome: An Analysis of HPV-16/18-Adjuvanted Vaccine Post-Licensure Data
title_sort investigating reports of complex regional pain syndrome: an analysis of hpv-16/18-adjuvanted vaccine post-licensure data
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4587999/
https://www.ncbi.nlm.nih.gov/pubmed/26501109
http://dx.doi.org/10.1016/j.ebiom.2015.07.003
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