Emerging clinical concerns in the ageing haemophilia patient

The availability of safe replacement clotting factor concentrates together with effective antiviral drugs to treat human immunodeficiency and hepatitis C viruses and the provision of care at designated haemophilia treatment centres have resulted in a new phenomenon in haemophilia management – the ag...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Haemophilia : the official journal of the World Federation of Hemophilia 2009-11, Vol.15 (6), p.1197-1209
Hauptverfasser: KONKLE, B. A., KESSLER, C., ALEDORT, L., ANDERSEN, J., FOGARTY, P., KOUIDES, P., QUON, D., RAGNI, M., ZAKARIJA, A., EWENSTEIN, B.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1209
container_issue 6
container_start_page 1197
container_title Haemophilia : the official journal of the World Federation of Hemophilia
container_volume 15
creator KONKLE, B. A.
KESSLER, C.
ALEDORT, L.
ANDERSEN, J.
FOGARTY, P.
KOUIDES, P.
QUON, D.
RAGNI, M.
ZAKARIJA, A.
EWENSTEIN, B.
description The availability of safe replacement clotting factor concentrates together with effective antiviral drugs to treat human immunodeficiency and hepatitis C viruses and the provision of care at designated haemophilia treatment centres have resulted in a new phenomenon in haemophilia management – the ageing patient. Today, increasing numbers of persons with haemophilia (PWH) are middle‐aged and older, and they face the same age‐related health issues as the general population. The impact of these risks on PWH is unclear, however, and there is a paucity of information about how to manage comorbidities in this patient population. This review focuses on five comorbidities that uniquely affect older PWH: cardiovascular disease, liver disease, cancer, renal disease and joint disease. Available research is summarized and potential management approaches are suggested.
doi_str_mv 10.1111/j.1365-2516.2009.02066.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_734231908</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>21172055</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4376-a2bdcf7999659ac3d8e3cb88782078cb40f10480d60d8e734dd134e8f7d141783</originalsourceid><addsrcrecordid>eNqNkF1LwzAUhoMobk7_gvRKr1rz0SYp6MUcc3MORVS8DGmabpn9sulw-_e2dsw7MTc58D7vOfAA4CDooeZdrTxEaODiAFEPQxh6EENKvc0B6O-Dw3YOkMsxoj1wYu0KQkQa7hj0UEg59Sntg-txpquFyReOSk1ulEwdVeRKV7l1TO7US-3IhW7zpdRZUS5NaqRTytrovD4FR4lMrT7b_QPwdjd-HU3d-dPkfjScu8onjLoSR7FKWBiGNAilIjHXREWcM44h4yryYYKgz2FMYRMx4scxIr7mCYuRjxgnA3DZ7S2r4nOtbS0yY5VOU5nrYm1FU8EEhbAlL_4kMUIMwyBoQN6BqiqsrXQiyspkstoKBEXrWKxEq1K0KkXrWPw4Fpumer67sY4yHf8Wd1Ib4KYDvkyqt_9eLKbDcTs1fbfrG1vrzb4vqw9BGWGBeH-cCPbyPBs9TGbilnwDhjOYGw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>21172055</pqid></control><display><type>article</type><title>Emerging clinical concerns in the ageing haemophilia patient</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>KONKLE, B. A. ; KESSLER, C. ; ALEDORT, L. ; ANDERSEN, J. ; FOGARTY, P. ; KOUIDES, P. ; QUON, D. ; RAGNI, M. ; ZAKARIJA, A. ; EWENSTEIN, B.</creator><creatorcontrib>KONKLE, B. A. ; KESSLER, C. ; ALEDORT, L. ; ANDERSEN, J. ; FOGARTY, P. ; KOUIDES, P. ; QUON, D. ; RAGNI, M. ; ZAKARIJA, A. ; EWENSTEIN, B.</creatorcontrib><description>The availability of safe replacement clotting factor concentrates together with effective antiviral drugs to treat human immunodeficiency and hepatitis C viruses and the provision of care at designated haemophilia treatment centres have resulted in a new phenomenon in haemophilia management – the ageing patient. Today, increasing numbers of persons with haemophilia (PWH) are middle‐aged and older, and they face the same age‐related health issues as the general population. The impact of these risks on PWH is unclear, however, and there is a paucity of information about how to manage comorbidities in this patient population. This review focuses on five comorbidities that uniquely affect older PWH: cardiovascular disease, liver disease, cancer, renal disease and joint disease. Available research is summarized and potential management approaches are suggested.</description><identifier>ISSN: 1351-8216</identifier><identifier>EISSN: 1365-2516</identifier><identifier>DOI: 10.1111/j.1365-2516.2009.02066.x</identifier><identifier>PMID: 19686466</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; ageing ; Blood Coagulation Factors - therapeutic use ; Cardiovascular Diseases - complications ; Cardiovascular Diseases - drug therapy ; Cardiovascular Diseases - epidemiology ; comorbidities ; Comorbidity ; Factor VIII - therapeutic use ; haemophilia ; Hemophilia A - complications ; Hemophilia A - drug therapy ; Hemophilia A - epidemiology ; Humans ; Joint Diseases - complications ; Joint Diseases - drug therapy ; Joint Diseases - epidemiology ; Kidney Failure, Chronic - complications ; Kidney Failure, Chronic - drug therapy ; Kidney Failure, Chronic - epidemiology ; Liver Diseases - complications ; Liver Diseases - drug therapy ; Liver Diseases - epidemiology ; Male ; Middle Aged ; Neoplasms - complications ; Neoplasms - drug therapy ; Neoplasms - epidemiology ; Practice Guidelines as Topic ; Risk Assessment</subject><ispartof>Haemophilia : the official journal of the World Federation of Hemophilia, 2009-11, Vol.15 (6), p.1197-1209</ispartof><rights>2009 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4376-a2bdcf7999659ac3d8e3cb88782078cb40f10480d60d8e734dd134e8f7d141783</citedby><cites>FETCH-LOGICAL-c4376-a2bdcf7999659ac3d8e3cb88782078cb40f10480d60d8e734dd134e8f7d141783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2516.2009.02066.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2516.2009.02066.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19686466$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KONKLE, B. A.</creatorcontrib><creatorcontrib>KESSLER, C.</creatorcontrib><creatorcontrib>ALEDORT, L.</creatorcontrib><creatorcontrib>ANDERSEN, J.</creatorcontrib><creatorcontrib>FOGARTY, P.</creatorcontrib><creatorcontrib>KOUIDES, P.</creatorcontrib><creatorcontrib>QUON, D.</creatorcontrib><creatorcontrib>RAGNI, M.</creatorcontrib><creatorcontrib>ZAKARIJA, A.</creatorcontrib><creatorcontrib>EWENSTEIN, B.</creatorcontrib><title>Emerging clinical concerns in the ageing haemophilia patient</title><title>Haemophilia : the official journal of the World Federation of Hemophilia</title><addtitle>Haemophilia</addtitle><description>The availability of safe replacement clotting factor concentrates together with effective antiviral drugs to treat human immunodeficiency and hepatitis C viruses and the provision of care at designated haemophilia treatment centres have resulted in a new phenomenon in haemophilia management – the ageing patient. Today, increasing numbers of persons with haemophilia (PWH) are middle‐aged and older, and they face the same age‐related health issues as the general population. The impact of these risks on PWH is unclear, however, and there is a paucity of information about how to manage comorbidities in this patient population. This review focuses on five comorbidities that uniquely affect older PWH: cardiovascular disease, liver disease, cancer, renal disease and joint disease. Available research is summarized and potential management approaches are suggested.</description><subject>Aged</subject><subject>ageing</subject><subject>Blood Coagulation Factors - therapeutic use</subject><subject>Cardiovascular Diseases - complications</subject><subject>Cardiovascular Diseases - drug therapy</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>comorbidities</subject><subject>Comorbidity</subject><subject>Factor VIII - therapeutic use</subject><subject>haemophilia</subject><subject>Hemophilia A - complications</subject><subject>Hemophilia A - drug therapy</subject><subject>Hemophilia A - epidemiology</subject><subject>Humans</subject><subject>Joint Diseases - complications</subject><subject>Joint Diseases - drug therapy</subject><subject>Joint Diseases - epidemiology</subject><subject>Kidney Failure, Chronic - complications</subject><subject>Kidney Failure, Chronic - drug therapy</subject><subject>Kidney Failure, Chronic - epidemiology</subject><subject>Liver Diseases - complications</subject><subject>Liver Diseases - drug therapy</subject><subject>Liver Diseases - epidemiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasms - complications</subject><subject>Neoplasms - drug therapy</subject><subject>Neoplasms - epidemiology</subject><subject>Practice Guidelines as Topic</subject><subject>Risk Assessment</subject><issn>1351-8216</issn><issn>1365-2516</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkF1LwzAUhoMobk7_gvRKr1rz0SYp6MUcc3MORVS8DGmabpn9sulw-_e2dsw7MTc58D7vOfAA4CDooeZdrTxEaODiAFEPQxh6EENKvc0B6O-Dw3YOkMsxoj1wYu0KQkQa7hj0UEg59Sntg-txpquFyReOSk1ulEwdVeRKV7l1TO7US-3IhW7zpdRZUS5NaqRTytrovD4FR4lMrT7b_QPwdjd-HU3d-dPkfjScu8onjLoSR7FKWBiGNAilIjHXREWcM44h4yryYYKgz2FMYRMx4scxIr7mCYuRjxgnA3DZ7S2r4nOtbS0yY5VOU5nrYm1FU8EEhbAlL_4kMUIMwyBoQN6BqiqsrXQiyspkstoKBEXrWKxEq1K0KkXrWPw4Fpumer67sY4yHf8Wd1Ib4KYDvkyqt_9eLKbDcTs1fbfrG1vrzb4vqw9BGWGBeH-cCPbyPBs9TGbilnwDhjOYGw</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>KONKLE, B. A.</creator><creator>KESSLER, C.</creator><creator>ALEDORT, L.</creator><creator>ANDERSEN, J.</creator><creator>FOGARTY, P.</creator><creator>KOUIDES, P.</creator><creator>QUON, D.</creator><creator>RAGNI, M.</creator><creator>ZAKARIJA, A.</creator><creator>EWENSTEIN, B.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200911</creationdate><title>Emerging clinical concerns in the ageing haemophilia patient</title><author>KONKLE, B. A. ; KESSLER, C. ; ALEDORT, L. ; ANDERSEN, J. ; FOGARTY, P. ; KOUIDES, P. ; QUON, D. ; RAGNI, M. ; ZAKARIJA, A. ; EWENSTEIN, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4376-a2bdcf7999659ac3d8e3cb88782078cb40f10480d60d8e734dd134e8f7d141783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>ageing</topic><topic>Blood Coagulation Factors - therapeutic use</topic><topic>Cardiovascular Diseases - complications</topic><topic>Cardiovascular Diseases - drug therapy</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>comorbidities</topic><topic>Comorbidity</topic><topic>Factor VIII - therapeutic use</topic><topic>haemophilia</topic><topic>Hemophilia A - complications</topic><topic>Hemophilia A - drug therapy</topic><topic>Hemophilia A - epidemiology</topic><topic>Humans</topic><topic>Joint Diseases - complications</topic><topic>Joint Diseases - drug therapy</topic><topic>Joint Diseases - epidemiology</topic><topic>Kidney Failure, Chronic - complications</topic><topic>Kidney Failure, Chronic - drug therapy</topic><topic>Kidney Failure, Chronic - epidemiology</topic><topic>Liver Diseases - complications</topic><topic>Liver Diseases - drug therapy</topic><topic>Liver Diseases - epidemiology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasms - complications</topic><topic>Neoplasms - drug therapy</topic><topic>Neoplasms - epidemiology</topic><topic>Practice Guidelines as Topic</topic><topic>Risk Assessment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KONKLE, B. A.</creatorcontrib><creatorcontrib>KESSLER, C.</creatorcontrib><creatorcontrib>ALEDORT, L.</creatorcontrib><creatorcontrib>ANDERSEN, J.</creatorcontrib><creatorcontrib>FOGARTY, P.</creatorcontrib><creatorcontrib>KOUIDES, P.</creatorcontrib><creatorcontrib>QUON, D.</creatorcontrib><creatorcontrib>RAGNI, M.</creatorcontrib><creatorcontrib>ZAKARIJA, A.</creatorcontrib><creatorcontrib>EWENSTEIN, B.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Haemophilia : the official journal of the World Federation of Hemophilia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KONKLE, B. A.</au><au>KESSLER, C.</au><au>ALEDORT, L.</au><au>ANDERSEN, J.</au><au>FOGARTY, P.</au><au>KOUIDES, P.</au><au>QUON, D.</au><au>RAGNI, M.</au><au>ZAKARIJA, A.</au><au>EWENSTEIN, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Emerging clinical concerns in the ageing haemophilia patient</atitle><jtitle>Haemophilia : the official journal of the World Federation of Hemophilia</jtitle><addtitle>Haemophilia</addtitle><date>2009-11</date><risdate>2009</risdate><volume>15</volume><issue>6</issue><spage>1197</spage><epage>1209</epage><pages>1197-1209</pages><issn>1351-8216</issn><eissn>1365-2516</eissn><abstract>The availability of safe replacement clotting factor concentrates together with effective antiviral drugs to treat human immunodeficiency and hepatitis C viruses and the provision of care at designated haemophilia treatment centres have resulted in a new phenomenon in haemophilia management – the ageing patient. Today, increasing numbers of persons with haemophilia (PWH) are middle‐aged and older, and they face the same age‐related health issues as the general population. The impact of these risks on PWH is unclear, however, and there is a paucity of information about how to manage comorbidities in this patient population. This review focuses on five comorbidities that uniquely affect older PWH: cardiovascular disease, liver disease, cancer, renal disease and joint disease. Available research is summarized and potential management approaches are suggested.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19686466</pmid><doi>10.1111/j.1365-2516.2009.02066.x</doi><tpages>13</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1351-8216
ispartof Haemophilia : the official journal of the World Federation of Hemophilia, 2009-11, Vol.15 (6), p.1197-1209
issn 1351-8216
1365-2516
language eng
recordid cdi_proquest_miscellaneous_734231908
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Aged
ageing
Blood Coagulation Factors - therapeutic use
Cardiovascular Diseases - complications
Cardiovascular Diseases - drug therapy
Cardiovascular Diseases - epidemiology
comorbidities
Comorbidity
Factor VIII - therapeutic use
haemophilia
Hemophilia A - complications
Hemophilia A - drug therapy
Hemophilia A - epidemiology
Humans
Joint Diseases - complications
Joint Diseases - drug therapy
Joint Diseases - epidemiology
Kidney Failure, Chronic - complications
Kidney Failure, Chronic - drug therapy
Kidney Failure, Chronic - epidemiology
Liver Diseases - complications
Liver Diseases - drug therapy
Liver Diseases - epidemiology
Male
Middle Aged
Neoplasms - complications
Neoplasms - drug therapy
Neoplasms - epidemiology
Practice Guidelines as Topic
Risk Assessment
title Emerging clinical concerns in the ageing haemophilia patient
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T00%3A35%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Emerging%20clinical%20concerns%20in%20the%20ageing%20haemophilia%20patient&rft.jtitle=Haemophilia%20:%20the%20official%20journal%20of%20the%20World%20Federation%20of%20Hemophilia&rft.au=KONKLE,%20B.%20A.&rft.date=2009-11&rft.volume=15&rft.issue=6&rft.spage=1197&rft.epage=1209&rft.pages=1197-1209&rft.issn=1351-8216&rft.eissn=1365-2516&rft_id=info:doi/10.1111/j.1365-2516.2009.02066.x&rft_dat=%3Cproquest_cross%3E21172055%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=21172055&rft_id=info:pmid/19686466&rfr_iscdi=true