Consensus recommendations for use of central venous access devices in haemophilia
Venous access is essential for delivery of haemophilia factor concentrate. Wherever possible, peripheral veins remain the route of choice, and the use of central venous access devices (CVADs) should be limited to cases of clear need in patients with caregivers able to exercise diligence in CVAD care...
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Veröffentlicht in: | Haemophilia : the official journal of the World Federation of Hemophilia 2004-09, Vol.10 (5), p.629-648 |
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creator | Ewenstein, B. M. Valentino, L. A. Journeycake, J. M. Tarantino, M. D. Shapiro, A. D. Blanchette, V. S. Hoots, W. K. Buchanan, G. R. Manco-Johnson, M. J. Rivard, G.-E. Miller, K. L. Geraghty, S. Maahs, J. A. Stuart, R. Dunham, T. Navickis, R. J. |
description | Venous access is essential for delivery of haemophilia factor concentrate. Wherever possible, peripheral veins remain the route of choice, and the use of central venous access devices (CVADs) should be limited to cases of clear need in patients with caregivers able to exercise diligence in CVAD care and should continue no longer than necessary. CVADs are of recognized value for repeated administration of coagulation factors in haemophilia, particularly for prophylaxis and immune tolerance therapy and in young children. Evidence to guide best practices has been fragmentary, and standardized methods for CVAD usage have yet to be established. We have developed management recommendations based upon available published evidence as well as extensive clinical experience. These recommendations address patient and CVAD selection; CVAD placement, care and removal; caregiver/patient guidance; and complications, including infection and thrombosis. In the absence of inhibitors, ports are recommended, primarily because of fewer associated infections than with external catheters. For patients with inhibitors, ports also appear to be associated with fewer infections. Infection is the most frequent complication, and recommendations to prevent and treat infections are supported by extensive clinical data and experience. Strict adherence to handwashing and aseptic technique are essential elements of catheter care. Evidence‐based data regarding the detection and treatment of CVAD‐related thrombotic complications are limited. Caregiver education is an integral part of CVAD use and the procedural practices of users should be regularly re‐assessed. These recommendations provide a basis for sound current CVAD practice and are expected to undergo further refinements as new evidence is compiled and clinical experience is gained. |
doi_str_mv | 10.1111/j.1365-2516.2004.00943.x |
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M. ; Valentino, L. A. ; Journeycake, J. M. ; Tarantino, M. D. ; Shapiro, A. D. ; Blanchette, V. S. ; Hoots, W. K. ; Buchanan, G. R. ; Manco-Johnson, M. J. ; Rivard, G.-E. ; Miller, K. L. ; Geraghty, S. ; Maahs, J. A. ; Stuart, R. ; Dunham, T. ; Navickis, R. J.</creator><creatorcontrib>Ewenstein, B. M. ; Valentino, L. A. ; Journeycake, J. M. ; Tarantino, M. D. ; Shapiro, A. D. ; Blanchette, V. S. ; Hoots, W. K. ; Buchanan, G. R. ; Manco-Johnson, M. J. ; Rivard, G.-E. ; Miller, K. L. ; Geraghty, S. ; Maahs, J. A. ; Stuart, R. ; Dunham, T. ; Navickis, R. J.</creatorcontrib><description>Venous access is essential for delivery of haemophilia factor concentrate. Wherever possible, peripheral veins remain the route of choice, and the use of central venous access devices (CVADs) should be limited to cases of clear need in patients with caregivers able to exercise diligence in CVAD care and should continue no longer than necessary. CVADs are of recognized value for repeated administration of coagulation factors in haemophilia, particularly for prophylaxis and immune tolerance therapy and in young children. Evidence to guide best practices has been fragmentary, and standardized methods for CVAD usage have yet to be established. We have developed management recommendations based upon available published evidence as well as extensive clinical experience. These recommendations address patient and CVAD selection; CVAD placement, care and removal; caregiver/patient guidance; and complications, including infection and thrombosis. In the absence of inhibitors, ports are recommended, primarily because of fewer associated infections than with external catheters. For patients with inhibitors, ports also appear to be associated with fewer infections. Infection is the most frequent complication, and recommendations to prevent and treat infections are supported by extensive clinical data and experience. Strict adherence to handwashing and aseptic technique are essential elements of catheter care. Evidence‐based data regarding the detection and treatment of CVAD‐related thrombotic complications are limited. Caregiver education is an integral part of CVAD use and the procedural practices of users should be regularly re‐assessed. 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M.</creatorcontrib><creatorcontrib>Valentino, L. A.</creatorcontrib><creatorcontrib>Journeycake, J. M.</creatorcontrib><creatorcontrib>Tarantino, M. D.</creatorcontrib><creatorcontrib>Shapiro, A. D.</creatorcontrib><creatorcontrib>Blanchette, V. S.</creatorcontrib><creatorcontrib>Hoots, W. K.</creatorcontrib><creatorcontrib>Buchanan, G. R.</creatorcontrib><creatorcontrib>Manco-Johnson, M. J.</creatorcontrib><creatorcontrib>Rivard, G.-E.</creatorcontrib><creatorcontrib>Miller, K. L.</creatorcontrib><creatorcontrib>Geraghty, S.</creatorcontrib><creatorcontrib>Maahs, J. A.</creatorcontrib><creatorcontrib>Stuart, R.</creatorcontrib><creatorcontrib>Dunham, T.</creatorcontrib><creatorcontrib>Navickis, R. J.</creatorcontrib><title>Consensus recommendations for use of central venous access devices in haemophilia</title><title>Haemophilia : the official journal of the World Federation of Hemophilia</title><addtitle>Haemophilia</addtitle><description>Venous access is essential for delivery of haemophilia factor concentrate. Wherever possible, peripheral veins remain the route of choice, and the use of central venous access devices (CVADs) should be limited to cases of clear need in patients with caregivers able to exercise diligence in CVAD care and should continue no longer than necessary. CVADs are of recognized value for repeated administration of coagulation factors in haemophilia, particularly for prophylaxis and immune tolerance therapy and in young children. Evidence to guide best practices has been fragmentary, and standardized methods for CVAD usage have yet to be established. We have developed management recommendations based upon available published evidence as well as extensive clinical experience. These recommendations address patient and CVAD selection; CVAD placement, care and removal; caregiver/patient guidance; and complications, including infection and thrombosis. In the absence of inhibitors, ports are recommended, primarily because of fewer associated infections than with external catheters. For patients with inhibitors, ports also appear to be associated with fewer infections. Infection is the most frequent complication, and recommendations to prevent and treat infections are supported by extensive clinical data and experience. Strict adherence to handwashing and aseptic technique are essential elements of catheter care. Evidence‐based data regarding the detection and treatment of CVAD‐related thrombotic complications are limited. Caregiver education is an integral part of CVAD use and the procedural practices of users should be regularly re‐assessed. These recommendations provide a basis for sound current CVAD practice and are expected to undergo further refinements as new evidence is compiled and clinical experience is gained.</description><subject>catheterization</subject><subject>Catheterization, Central Venous - methods</subject><subject>Catheters, Indwelling</subject><subject>central venous</subject><subject>Choice Behavior</subject><subject>Contraindications</subject><subject>Device Removal</subject><subject>Equipment Contamination - prevention & control</subject><subject>haemophilia A</subject><subject>haemophilia B</subject><subject>Hemophilia A - complications</subject><subject>Humans</subject><subject>infection</subject><subject>Infection Control</subject><subject>Patient Selection</subject><subject>Postoperative Complications - prevention & control</subject><subject>practice guidelines</subject><subject>Risk Assessment</subject><subject>Thrombosis - prevention & control</subject><subject>venous thrombosis</subject><issn>1351-8216</issn><issn>1365-2516</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtP4zAUhS3EiNfMX0BesUu4tmMnkdigUigDGgRiNEvLcW6ESx7FbqH8e5xpBVu88ZHvOcdXHyGUQcriOZ2nTCiZcMlUygGyFKDMRLreIQefg91RS5YUnKl9chjCHIAJDmqP7DMpZJ6XcEDuJ0MfsA-rQD3aoeuwr83SxUfaDJ6uAtKhoRb7pTctfcV-iE5jLYZAa3x1UVDX0yeD3bB4cq0zP8mPxrQBf23vI_L3cvo4mSW3d1fXk_PbxGbARaKgalhuwPKKMZMLmRmmDLO2VLWFTKKoBMiaZVKYWpa8kpWV0PCa84arAsQROdn0LvzwssKw1J0LFtvW9BiX1EoVssyLMhqLjdH6IQSPjV541xn_rhnoEaee65GaHqnpEaf-j1OvY_R4-8eq6rD-Cm75RcPZxvDmWnz_drGenU-jiPFkE3dhievPuPHPWuUil_rfnyv9-HAzKy7y37HrA_nEkoI</recordid><startdate>200409</startdate><enddate>200409</enddate><creator>Ewenstein, B. 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J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Consensus recommendations for use of central venous access devices in haemophilia</atitle><jtitle>Haemophilia : the official journal of the World Federation of Hemophilia</jtitle><addtitle>Haemophilia</addtitle><date>2004-09</date><risdate>2004</risdate><volume>10</volume><issue>5</issue><spage>629</spage><epage>648</epage><pages>629-648</pages><issn>1351-8216</issn><eissn>1365-2516</eissn><abstract>Venous access is essential for delivery of haemophilia factor concentrate. Wherever possible, peripheral veins remain the route of choice, and the use of central venous access devices (CVADs) should be limited to cases of clear need in patients with caregivers able to exercise diligence in CVAD care and should continue no longer than necessary. CVADs are of recognized value for repeated administration of coagulation factors in haemophilia, particularly for prophylaxis and immune tolerance therapy and in young children. Evidence to guide best practices has been fragmentary, and standardized methods for CVAD usage have yet to be established. We have developed management recommendations based upon available published evidence as well as extensive clinical experience. These recommendations address patient and CVAD selection; CVAD placement, care and removal; caregiver/patient guidance; and complications, including infection and thrombosis. In the absence of inhibitors, ports are recommended, primarily because of fewer associated infections than with external catheters. For patients with inhibitors, ports also appear to be associated with fewer infections. Infection is the most frequent complication, and recommendations to prevent and treat infections are supported by extensive clinical data and experience. Strict adherence to handwashing and aseptic technique are essential elements of catheter care. Evidence‐based data regarding the detection and treatment of CVAD‐related thrombotic complications are limited. Caregiver education is an integral part of CVAD use and the procedural practices of users should be regularly re‐assessed. These recommendations provide a basis for sound current CVAD practice and are expected to undergo further refinements as new evidence is compiled and clinical experience is gained.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15357790</pmid><doi>10.1111/j.1365-2516.2004.00943.x</doi><tpages>20</tpages></addata></record> |
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subjects | catheterization Catheterization, Central Venous - methods Catheters, Indwelling central venous Choice Behavior Contraindications Device Removal Equipment Contamination - prevention & control haemophilia A haemophilia B Hemophilia A - complications Humans infection Infection Control Patient Selection Postoperative Complications - prevention & control practice guidelines Risk Assessment Thrombosis - prevention & control venous thrombosis |
title | Consensus recommendations for use of central venous access devices in haemophilia |
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