Continuous infusion of coagulation factor concentrates during intensive treatment
In clinical management of bleeds and surgical procedures in patients suffering from bleeding disorders either repetitive bolus injections (BI) or continuous infusion (CI) can be used for coagulation factor replacement. Continuous infusion seems to be an attractive route of administration and may be...
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Veröffentlicht in: | Haemophilia : the official journal of the World Federation of Hemophilia 2018-01, Vol.24 (1), p.24-32 |
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creator | Holme, P. A. Tjønnfjord, G. E. Batorova, A. |
description | In clinical management of bleeds and surgical procedures in patients suffering from bleeding disorders either repetitive bolus injections (BI) or continuous infusion (CI) can be used for coagulation factor replacement. Continuous infusion seems to be an attractive route of administration and may be considered if replacement therapy is required for more than 3 days. The strongest argument favouring continuous infusion is its superiority in providing the patient with a safe and constant level of the deficient coagulation factor by balancing input with clearance. Furthermore, several studies have shown that coagulation factor consumption may be reduced by CI compared to repetitive bolus injections (BI) since unnecessary peaks of factor level are avoided. Concerns have been raised whether continuous infusion of coagulation concentrates is associated with an increased risk of developing inhibitors. However, available data have so far not shown an increased risk for inhibitor development in severe haemophilia patients with more than 50 exposure days of coagulation factor concentrates. Further, previously reported complications when using CI such as phlebitis at the infusion site and pump failure are nowadays very seldom seen when small amounts of heparin are added to the infusion bag, and increased quality of the pumps are available. Over the last decades, numerous reports have confirmed CI to be a safe and effective mode of coagulation factor replacement even in the most challenging surgical procedures, such as total joint arthroplasties. |
doi_str_mv | 10.1111/hae.13331 |
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A. ; Tjønnfjord, G. E. ; Batorova, A.</creator><creatorcontrib>Holme, P. A. ; Tjønnfjord, G. E. ; Batorova, A.</creatorcontrib><description>In clinical management of bleeds and surgical procedures in patients suffering from bleeding disorders either repetitive bolus injections (BI) or continuous infusion (CI) can be used for coagulation factor replacement. Continuous infusion seems to be an attractive route of administration and may be considered if replacement therapy is required for more than 3 days. The strongest argument favouring continuous infusion is its superiority in providing the patient with a safe and constant level of the deficient coagulation factor by balancing input with clearance. Furthermore, several studies have shown that coagulation factor consumption may be reduced by CI compared to repetitive bolus injections (BI) since unnecessary peaks of factor level are avoided. Concerns have been raised whether continuous infusion of coagulation concentrates is associated with an increased risk of developing inhibitors. However, available data have so far not shown an increased risk for inhibitor development in severe haemophilia patients with more than 50 exposure days of coagulation factor concentrates. Further, previously reported complications when using CI such as phlebitis at the infusion site and pump failure are nowadays very seldom seen when small amounts of heparin are added to the infusion bag, and increased quality of the pumps are available. Over the last decades, numerous reports have confirmed CI to be a safe and effective mode of coagulation factor replacement even in the most challenging surgical procedures, such as total joint arthroplasties.</description><identifier>ISSN: 1351-8216</identifier><identifier>EISSN: 1365-2516</identifier><identifier>DOI: 10.1111/hae.13331</identifier><identifier>PMID: 28873263</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Catheters ; Coagulation ; coagulation factor concentrates ; continuous infusion ; haemophilia A ; haemophilia B ; Hemophilia ; Heparin ; Phlebitis ; rFVIIa</subject><ispartof>Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1), p.24-32</ispartof><rights>2017 John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons Ltd.</rights><rights>2018 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4191-85aababd3ca481f31b7dc2df2e8b83f4c306f9f04dcf9563fff3d5a9a44f05e53</citedby><cites>FETCH-LOGICAL-c4191-85aababd3ca481f31b7dc2df2e8b83f4c306f9f04dcf9563fff3d5a9a44f05e53</cites><orcidid>0000-0002-3888-2905</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhae.13331$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhae.13331$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28873263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Holme, P. A.</creatorcontrib><creatorcontrib>Tjønnfjord, G. E.</creatorcontrib><creatorcontrib>Batorova, A.</creatorcontrib><title>Continuous infusion of coagulation factor concentrates during intensive treatment</title><title>Haemophilia : the official journal of the World Federation of Hemophilia</title><addtitle>Haemophilia</addtitle><description>In clinical management of bleeds and surgical procedures in patients suffering from bleeding disorders either repetitive bolus injections (BI) or continuous infusion (CI) can be used for coagulation factor replacement. Continuous infusion seems to be an attractive route of administration and may be considered if replacement therapy is required for more than 3 days. The strongest argument favouring continuous infusion is its superiority in providing the patient with a safe and constant level of the deficient coagulation factor by balancing input with clearance. Furthermore, several studies have shown that coagulation factor consumption may be reduced by CI compared to repetitive bolus injections (BI) since unnecessary peaks of factor level are avoided. Concerns have been raised whether continuous infusion of coagulation concentrates is associated with an increased risk of developing inhibitors. However, available data have so far not shown an increased risk for inhibitor development in severe haemophilia patients with more than 50 exposure days of coagulation factor concentrates. Further, previously reported complications when using CI such as phlebitis at the infusion site and pump failure are nowadays very seldom seen when small amounts of heparin are added to the infusion bag, and increased quality of the pumps are available. Over the last decades, numerous reports have confirmed CI to be a safe and effective mode of coagulation factor replacement even in the most challenging surgical procedures, such as total joint arthroplasties.</description><subject>Catheters</subject><subject>Coagulation</subject><subject>coagulation factor concentrates</subject><subject>continuous infusion</subject><subject>haemophilia A</subject><subject>haemophilia B</subject><subject>Hemophilia</subject><subject>Heparin</subject><subject>Phlebitis</subject><subject>rFVIIa</subject><issn>1351-8216</issn><issn>1365-2516</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE9PwyAYh4nROJ0e_AKmiRc9dONPYe1xWaYzWWJM9EwohdmlhQlUs28vtdODiVxeeHn45eUB4ArBCYpr-ibUBBFC0BE4Q4TRFFPEjvs9RWmOERuBc--3ECKCITsFI5znM4IZOQPPC2tCbTrb-aQ2uvO1NYnVibRi0zUi9EctZLAutoxUJjgRlE-qztVmE58EZXz9oZLglAhtvL8AJ1o0Xl0e6hi83i9fFqt0_fTwuJivU5mhIo5FhShFWREpshxpgspZJXGlscrLnOhMEsh0oWFWSV1QRrTWpKKiEFmmIVWUjMHtkLtz9r1TPvC29lI1jTAq_oajgjDMaO9lDG7-oFvbOROni1SeI8RwlkXqbqCks947pfnO1a1we44g7z3z6Jl_e47s9SGxK1tV_ZI_YiMwHYDPulH7_5P4ar4cIr8AFAiIRQ</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Holme, P. A.</creator><creator>Tjønnfjord, G. E.</creator><creator>Batorova, A.</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3888-2905</orcidid></search><sort><creationdate>201801</creationdate><title>Continuous infusion of coagulation factor concentrates during intensive treatment</title><author>Holme, P. A. ; Tjønnfjord, G. E. ; Batorova, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4191-85aababd3ca481f31b7dc2df2e8b83f4c306f9f04dcf9563fff3d5a9a44f05e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Catheters</topic><topic>Coagulation</topic><topic>coagulation factor concentrates</topic><topic>continuous infusion</topic><topic>haemophilia A</topic><topic>haemophilia B</topic><topic>Hemophilia</topic><topic>Heparin</topic><topic>Phlebitis</topic><topic>rFVIIa</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holme, P. A.</creatorcontrib><creatorcontrib>Tjønnfjord, G. 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E.</au><au>Batorova, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Continuous infusion of coagulation factor concentrates during intensive treatment</atitle><jtitle>Haemophilia : the official journal of the World Federation of Hemophilia</jtitle><addtitle>Haemophilia</addtitle><date>2018-01</date><risdate>2018</risdate><volume>24</volume><issue>1</issue><spage>24</spage><epage>32</epage><pages>24-32</pages><issn>1351-8216</issn><eissn>1365-2516</eissn><abstract>In clinical management of bleeds and surgical procedures in patients suffering from bleeding disorders either repetitive bolus injections (BI) or continuous infusion (CI) can be used for coagulation factor replacement. Continuous infusion seems to be an attractive route of administration and may be considered if replacement therapy is required for more than 3 days. The strongest argument favouring continuous infusion is its superiority in providing the patient with a safe and constant level of the deficient coagulation factor by balancing input with clearance. Furthermore, several studies have shown that coagulation factor consumption may be reduced by CI compared to repetitive bolus injections (BI) since unnecessary peaks of factor level are avoided. Concerns have been raised whether continuous infusion of coagulation concentrates is associated with an increased risk of developing inhibitors. However, available data have so far not shown an increased risk for inhibitor development in severe haemophilia patients with more than 50 exposure days of coagulation factor concentrates. Further, previously reported complications when using CI such as phlebitis at the infusion site and pump failure are nowadays very seldom seen when small amounts of heparin are added to the infusion bag, and increased quality of the pumps are available. 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subjects | Catheters Coagulation coagulation factor concentrates continuous infusion haemophilia A haemophilia B Hemophilia Heparin Phlebitis rFVIIa |
title | Continuous infusion of coagulation factor concentrates during intensive treatment |
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