Health and treatment outcomes of patients with hemophilia in the Netherlands, 1972–2019
Introduction We conducted six cross‐sectional nationwide questionnaire studies among all patients with hemophilia in the Netherlands from 1972 until 2019 to assess how health outcomes have changed, with a special focus on patients >50 years of age. Methods Data were collected on patient character...
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Veröffentlicht in: | Journal of thrombosis and haemostasis 2021-10, Vol.19 (10), p.2394-2406 |
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creator | Hassan, Shermarke Balen, Erna C. Smit, Cees Mauser‐Bunschoten, Evelien P. Vulpen, Lize F. D. Eikenboom, Jeroen Beckers, Erik A. M. Hooimeijer, Louise Ypma, Paula F. Nieuwenhuizen, Laurens Coppens, Michiel Schols, Saskia E. M. Leebeek, Frank W. G. Driessens, Mariëtte H. Rosendaal, Frits R. Bom, Johanna G. Gouw, Samantha C. |
description | Introduction
We conducted six cross‐sectional nationwide questionnaire studies among all patients with hemophilia in the Netherlands from 1972 until 2019 to assess how health outcomes have changed, with a special focus on patients >50 years of age.
Methods
Data were collected on patient characteristics, treatment, (joint) bleeding, joint impairment, hospitalizations, human immunodeficiency virus and hepatitis C infections, and general health status (RAND‐36).
Results
In 2019, 1009 patients participated, of whom 48% had mild, 15% moderate, and 37% severe hemophilia. From 1972 to 2019, the use of prophylaxis among patients with severe hemophilia increased from 30% to 89%. Their median annual bleeding rate decreased from 25 to 2 bleeds. Patients with severe hemophilia aged 40 years joint status did not improve. In 2019, 5% of all 1009 patients were positive for the human immunodeficiency virus. The proportion of patients with an active hepatitis C infection drastically decreased from 45% in 2001 to 2% in 2019 due to new anti‐hepatitis C treatment options. Twenty‐five percent had significant liver fibrosis even after successful therapy. Compared to the general male population, patients aged >50 years reported much lower scores on the RAND‐36, especially on physical functioning.
Discussion/Conclusion
Our study shows that increased use of prophylactic treatment and effective hepatitis C treatment have improved joint health and nearly eradicated hepatitis C infection in patients with hemophilia in the Netherlands. However, patients still suffer from hemophilia‐related complications, especially patients aged >50 years. |
doi_str_mv | 10.1111/jth.15424 |
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We conducted six cross‐sectional nationwide questionnaire studies among all patients with hemophilia in the Netherlands from 1972 until 2019 to assess how health outcomes have changed, with a special focus on patients >50 years of age.
Methods
Data were collected on patient characteristics, treatment, (joint) bleeding, joint impairment, hospitalizations, human immunodeficiency virus and hepatitis C infections, and general health status (RAND‐36).
Results
In 2019, 1009 patients participated, of whom 48% had mild, 15% moderate, and 37% severe hemophilia. From 1972 to 2019, the use of prophylaxis among patients with severe hemophilia increased from 30% to 89%. Their median annual bleeding rate decreased from 25 to 2 bleeds. Patients with severe hemophilia aged <16 years reported joint impairment less often over time, but in those aged >40 years joint status did not improve. In 2019, 5% of all 1009 patients were positive for the human immunodeficiency virus. The proportion of patients with an active hepatitis C infection drastically decreased from 45% in 2001 to 2% in 2019 due to new anti‐hepatitis C treatment options. Twenty‐five percent had significant liver fibrosis even after successful therapy. Compared to the general male population, patients aged >50 years reported much lower scores on the RAND‐36, especially on physical functioning.
Discussion/Conclusion
Our study shows that increased use of prophylactic treatment and effective hepatitis C treatment have improved joint health and nearly eradicated hepatitis C infection in patients with hemophilia in the Netherlands. However, patients still suffer from hemophilia‐related complications, especially patients aged >50 years.</description><identifier>ISSN: 1538-7933</identifier><identifier>ISSN: 1538-7836</identifier><identifier>EISSN: 1538-7836</identifier><identifier>DOI: 10.1111/jth.15424</identifier><identifier>PMID: 34117710</identifier><language>eng</language><publisher>England: Elsevier Limited</publisher><subject>Bleeding ; clinical outcomes ; Cross-Sectional Studies ; Factor VIII ; Fibrosis ; HAEMOSTASIS ; Hemophilia ; Hemophilia A - diagnosis ; Hemophilia A - drug therapy ; Hemophilia A - epidemiology ; Hepatitis C ; HIV ; Human immunodeficiency virus ; Humans ; Immune system ; joint damage ; Male ; Netherlands - epidemiology ; Original ; Patients ; Prophylaxis ; quality of life ; Treatment Outcome</subject><ispartof>Journal of thrombosis and haemostasis, 2021-10, Vol.19 (10), p.2394-2406</ispartof><rights>2021 The Authors. published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.</rights><rights>2021 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4434-4728802ad07cc859921adb84e32da5c30640091750675c69c418fe7a4d7465ad3</citedby><cites>FETCH-LOGICAL-c4434-4728802ad07cc859921adb84e32da5c30640091750675c69c418fe7a4d7465ad3</cites><orcidid>0000-0002-3678-6581 ; 0000-0002-1957-4122 ; 0000-0002-5045-636X ; 0000-0001-5677-1371 ; 0000-0001-9095-2475 ; 0000-0003-2558-7496 ; 0000-0002-3268-5759 ; 0000-0003-2423-2829 ; 0000-0003-3242-5524</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34117710$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hassan, Shermarke</creatorcontrib><creatorcontrib>Balen, Erna C.</creatorcontrib><creatorcontrib>Smit, Cees</creatorcontrib><creatorcontrib>Mauser‐Bunschoten, Evelien P.</creatorcontrib><creatorcontrib>Vulpen, Lize F. D.</creatorcontrib><creatorcontrib>Eikenboom, Jeroen</creatorcontrib><creatorcontrib>Beckers, Erik A. M.</creatorcontrib><creatorcontrib>Hooimeijer, Louise</creatorcontrib><creatorcontrib>Ypma, Paula F.</creatorcontrib><creatorcontrib>Nieuwenhuizen, Laurens</creatorcontrib><creatorcontrib>Coppens, Michiel</creatorcontrib><creatorcontrib>Schols, Saskia E. M.</creatorcontrib><creatorcontrib>Leebeek, Frank W. G.</creatorcontrib><creatorcontrib>Driessens, Mariëtte H.</creatorcontrib><creatorcontrib>Rosendaal, Frits R.</creatorcontrib><creatorcontrib>Bom, Johanna G.</creatorcontrib><creatorcontrib>Gouw, Samantha C.</creatorcontrib><title>Health and treatment outcomes of patients with hemophilia in the Netherlands, 1972–2019</title><title>Journal of thrombosis and haemostasis</title><addtitle>J Thromb Haemost</addtitle><description>Introduction
We conducted six cross‐sectional nationwide questionnaire studies among all patients with hemophilia in the Netherlands from 1972 until 2019 to assess how health outcomes have changed, with a special focus on patients >50 years of age.
Methods
Data were collected on patient characteristics, treatment, (joint) bleeding, joint impairment, hospitalizations, human immunodeficiency virus and hepatitis C infections, and general health status (RAND‐36).
Results
In 2019, 1009 patients participated, of whom 48% had mild, 15% moderate, and 37% severe hemophilia. From 1972 to 2019, the use of prophylaxis among patients with severe hemophilia increased from 30% to 89%. Their median annual bleeding rate decreased from 25 to 2 bleeds. Patients with severe hemophilia aged <16 years reported joint impairment less often over time, but in those aged >40 years joint status did not improve. In 2019, 5% of all 1009 patients were positive for the human immunodeficiency virus. The proportion of patients with an active hepatitis C infection drastically decreased from 45% in 2001 to 2% in 2019 due to new anti‐hepatitis C treatment options. Twenty‐five percent had significant liver fibrosis even after successful therapy. Compared to the general male population, patients aged >50 years reported much lower scores on the RAND‐36, especially on physical functioning.
Discussion/Conclusion
Our study shows that increased use of prophylactic treatment and effective hepatitis C treatment have improved joint health and nearly eradicated hepatitis C infection in patients with hemophilia in the Netherlands. However, patients still suffer from hemophilia‐related complications, especially patients aged >50 years.</description><subject>Bleeding</subject><subject>clinical outcomes</subject><subject>Cross-Sectional Studies</subject><subject>Factor VIII</subject><subject>Fibrosis</subject><subject>HAEMOSTASIS</subject><subject>Hemophilia</subject><subject>Hemophilia A - diagnosis</subject><subject>Hemophilia A - drug therapy</subject><subject>Hemophilia A - epidemiology</subject><subject>Hepatitis C</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immune system</subject><subject>joint damage</subject><subject>Male</subject><subject>Netherlands - epidemiology</subject><subject>Original</subject><subject>Patients</subject><subject>Prophylaxis</subject><subject>quality of life</subject><subject>Treatment Outcome</subject><issn>1538-7933</issn><issn>1538-7836</issn><issn>1538-7836</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc1KBSEYhiWK_hfdQAhtCjrl7-hsgjhUp4ja1KKVmONpPMyMJ3WKdt1Dd9iVZJ2KCnKhog_P9328AGxgtIfz2p-keg9zRtgcWMacyoGQtJj_upeULoGVGCcI4ZITtAiWKMNYCIyWwc3I6ibVUHcVTMHq1NouQd8n41sboR_DqU4uv0X46DJX29ZPa9c4DV0HU23hhc17aLIg7kJcCvL6_EJypTWwMNZNtOuf5yq4Pj66Go4G55cnp8PD84FhjLIBE0RKRHSFhDGSlyXBurqVzFJSaW4oKhhCJRYcFYKbojQMy7EVmlWCFVxXdBUczLzT_ra1lcm9Bt2oaXCtDk_Ka6d-_3SuVnf-QUmOJZI0C7Y_BcHf9zYm1bpobJNHsr6PinCGOCZEkIxu_UEnvg9dHi9TghcFYeSd2plRJvgYgx1_N4OReg9M5cDUR2CZ3fzZ_Tf5lVAG9mfAo2vs0_8mdXY1minfAI7Dnpc</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Hassan, Shermarke</creator><creator>Balen, Erna C.</creator><creator>Smit, Cees</creator><creator>Mauser‐Bunschoten, Evelien P.</creator><creator>Vulpen, Lize F. D.</creator><creator>Eikenboom, Jeroen</creator><creator>Beckers, Erik A. M.</creator><creator>Hooimeijer, Louise</creator><creator>Ypma, Paula F.</creator><creator>Nieuwenhuizen, Laurens</creator><creator>Coppens, Michiel</creator><creator>Schols, Saskia E. M.</creator><creator>Leebeek, Frank W. G.</creator><creator>Driessens, Mariëtte H.</creator><creator>Rosendaal, Frits R.</creator><creator>Bom, Johanna G.</creator><creator>Gouw, Samantha C.</creator><general>Elsevier Limited</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3678-6581</orcidid><orcidid>https://orcid.org/0000-0002-1957-4122</orcidid><orcidid>https://orcid.org/0000-0002-5045-636X</orcidid><orcidid>https://orcid.org/0000-0001-5677-1371</orcidid><orcidid>https://orcid.org/0000-0001-9095-2475</orcidid><orcidid>https://orcid.org/0000-0003-2558-7496</orcidid><orcidid>https://orcid.org/0000-0002-3268-5759</orcidid><orcidid>https://orcid.org/0000-0003-2423-2829</orcidid><orcidid>https://orcid.org/0000-0003-3242-5524</orcidid></search><sort><creationdate>202110</creationdate><title>Health and treatment outcomes of patients with hemophilia in the Netherlands, 1972–2019</title><author>Hassan, Shermarke ; Balen, Erna C. ; Smit, Cees ; Mauser‐Bunschoten, Evelien P. ; Vulpen, Lize F. D. ; Eikenboom, Jeroen ; Beckers, Erik A. M. ; Hooimeijer, Louise ; Ypma, Paula F. ; Nieuwenhuizen, Laurens ; Coppens, Michiel ; Schols, Saskia E. M. ; Leebeek, Frank W. G. ; Driessens, Mariëtte H. ; Rosendaal, Frits R. ; Bom, Johanna G. ; Gouw, Samantha C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4434-4728802ad07cc859921adb84e32da5c30640091750675c69c418fe7a4d7465ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Bleeding</topic><topic>clinical outcomes</topic><topic>Cross-Sectional Studies</topic><topic>Factor VIII</topic><topic>Fibrosis</topic><topic>HAEMOSTASIS</topic><topic>Hemophilia</topic><topic>Hemophilia A - diagnosis</topic><topic>Hemophilia A - drug therapy</topic><topic>Hemophilia A - epidemiology</topic><topic>Hepatitis C</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immune system</topic><topic>joint damage</topic><topic>Male</topic><topic>Netherlands - epidemiology</topic><topic>Original</topic><topic>Patients</topic><topic>Prophylaxis</topic><topic>quality of life</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hassan, Shermarke</creatorcontrib><creatorcontrib>Balen, Erna C.</creatorcontrib><creatorcontrib>Smit, Cees</creatorcontrib><creatorcontrib>Mauser‐Bunschoten, Evelien P.</creatorcontrib><creatorcontrib>Vulpen, Lize F. D.</creatorcontrib><creatorcontrib>Eikenboom, Jeroen</creatorcontrib><creatorcontrib>Beckers, Erik A. M.</creatorcontrib><creatorcontrib>Hooimeijer, Louise</creatorcontrib><creatorcontrib>Ypma, Paula F.</creatorcontrib><creatorcontrib>Nieuwenhuizen, Laurens</creatorcontrib><creatorcontrib>Coppens, Michiel</creatorcontrib><creatorcontrib>Schols, Saskia E. M.</creatorcontrib><creatorcontrib>Leebeek, Frank W. G.</creatorcontrib><creatorcontrib>Driessens, Mariëtte H.</creatorcontrib><creatorcontrib>Rosendaal, Frits R.</creatorcontrib><creatorcontrib>Bom, Johanna G.</creatorcontrib><creatorcontrib>Gouw, Samantha C.</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hassan, Shermarke</au><au>Balen, Erna C.</au><au>Smit, Cees</au><au>Mauser‐Bunschoten, Evelien P.</au><au>Vulpen, Lize F. D.</au><au>Eikenboom, Jeroen</au><au>Beckers, Erik A. M.</au><au>Hooimeijer, Louise</au><au>Ypma, Paula F.</au><au>Nieuwenhuizen, Laurens</au><au>Coppens, Michiel</au><au>Schols, Saskia E. M.</au><au>Leebeek, Frank W. G.</au><au>Driessens, Mariëtte H.</au><au>Rosendaal, Frits R.</au><au>Bom, Johanna G.</au><au>Gouw, Samantha C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Health and treatment outcomes of patients with hemophilia in the Netherlands, 1972–2019</atitle><jtitle>Journal of thrombosis and haemostasis</jtitle><addtitle>J Thromb Haemost</addtitle><date>2021-10</date><risdate>2021</risdate><volume>19</volume><issue>10</issue><spage>2394</spage><epage>2406</epage><pages>2394-2406</pages><issn>1538-7933</issn><issn>1538-7836</issn><eissn>1538-7836</eissn><abstract>Introduction
We conducted six cross‐sectional nationwide questionnaire studies among all patients with hemophilia in the Netherlands from 1972 until 2019 to assess how health outcomes have changed, with a special focus on patients >50 years of age.
Methods
Data were collected on patient characteristics, treatment, (joint) bleeding, joint impairment, hospitalizations, human immunodeficiency virus and hepatitis C infections, and general health status (RAND‐36).
Results
In 2019, 1009 patients participated, of whom 48% had mild, 15% moderate, and 37% severe hemophilia. From 1972 to 2019, the use of prophylaxis among patients with severe hemophilia increased from 30% to 89%. Their median annual bleeding rate decreased from 25 to 2 bleeds. Patients with severe hemophilia aged <16 years reported joint impairment less often over time, but in those aged >40 years joint status did not improve. In 2019, 5% of all 1009 patients were positive for the human immunodeficiency virus. The proportion of patients with an active hepatitis C infection drastically decreased from 45% in 2001 to 2% in 2019 due to new anti‐hepatitis C treatment options. Twenty‐five percent had significant liver fibrosis even after successful therapy. Compared to the general male population, patients aged >50 years reported much lower scores on the RAND‐36, especially on physical functioning.
Discussion/Conclusion
Our study shows that increased use of prophylactic treatment and effective hepatitis C treatment have improved joint health and nearly eradicated hepatitis C infection in patients with hemophilia in the Netherlands. However, patients still suffer from hemophilia‐related complications, especially patients aged >50 years.</abstract><cop>England</cop><pub>Elsevier Limited</pub><pmid>34117710</pmid><doi>10.1111/jth.15424</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-3678-6581</orcidid><orcidid>https://orcid.org/0000-0002-1957-4122</orcidid><orcidid>https://orcid.org/0000-0002-5045-636X</orcidid><orcidid>https://orcid.org/0000-0001-5677-1371</orcidid><orcidid>https://orcid.org/0000-0001-9095-2475</orcidid><orcidid>https://orcid.org/0000-0003-2558-7496</orcidid><orcidid>https://orcid.org/0000-0002-3268-5759</orcidid><orcidid>https://orcid.org/0000-0003-2423-2829</orcidid><orcidid>https://orcid.org/0000-0003-3242-5524</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bleeding clinical outcomes Cross-Sectional Studies Factor VIII Fibrosis HAEMOSTASIS Hemophilia Hemophilia A - diagnosis Hemophilia A - drug therapy Hemophilia A - epidemiology Hepatitis C HIV Human immunodeficiency virus Humans Immune system joint damage Male Netherlands - epidemiology Original Patients Prophylaxis quality of life Treatment Outcome |
title | Health and treatment outcomes of patients with hemophilia in the Netherlands, 1972–2019 |
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