{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,12]],"date-time":"2025-11-12T20:39:10Z","timestamp":1762979950641},"reference-count":8,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2013,2,26]],"date-time":"2013-02-26T00:00:00Z","timestamp":1361836800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J Paediatrics Child Health"],"published-print":{"date-parts":[[2013,3]]},"abstract":"<jats:sec><jats:title>Aims<\/jats:title><jats:p>Fully implantable central venous access devices (<jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>s) can offer long\u2010term reliable venous access to facilitate regular factor replacement therapy in haemophilia. However, <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related infection remains a major deterrent to the optimal use of <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> in this population. This report represents the first review of <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> use in haemophilia in <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>ustralia and aims to examine the rate of complications including <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related infections.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>A retrospective review of medical records was conducted of all haemophilic patients with fully implantable <jats:styled-content style=\"fixed-case\">CVADs<\/jats:styled-content> at the <jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>oyal <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>hildren's <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>ospital (<jats:styled-content style=\"fixed-case\">RCH<\/jats:styled-content>), Melbourne, between 1 <jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>une 1992 and 30 <jats:styled-content style=\"fixed-case\">J<\/jats:styled-content>une 2009. <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related bloodstream infection was defined based on the guidelines from the <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>entre of <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>isease <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>ontrol and <jats:styled-content style=\"fixed-case\">V<\/jats:styled-content>ictoria <jats:styled-content style=\"fixed-case\">N<\/jats:styled-content>ational <jats:styled-content style=\"fixed-case\">N<\/jats:styled-content>osocomial <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>nfection <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>urveillance. To further enhance identification of <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related infection in this study, a third criterion of \u2018suspected infection\u2019 was added by the authors.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Eighty\u2010one <jats:styled-content style=\"fixed-case\">CVADs<\/jats:styled-content> in 56 patients were managed at the <jats:styled-content style=\"fixed-case\">RCH<\/jats:styled-content> during this time period resulting in a combined study period of 94\u2009756 <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> days. Median age at first <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> insertion = 2.16 years (range 0.66 to 13.98 years). <jats:styled-content style=\"fixed-case\">CVADs<\/jats:styled-content> were inserted predominantly due to difficult venous access and prophylaxis initiation (70.4%). Median life\u2010span of a <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> was 1227 days, equivalent to 3.36 years (<jats:italic>n<\/jats:italic> = 50; range 0.22 to 9.44 years). Fifty\u2010seven <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related infections occurred in 37 <jats:styled-content style=\"fixed-case\">CVADs<\/jats:styled-content> (46.3%) in 29 patients (51.8%). Overall incidence of confirmed <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related bloodstream infection = 0.42 per 1000 <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> days (95% confidence interval (<jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>): 0.31 to 0.58 per 1000 <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> days) and indicate better performance compared with the published benchmark of 0.66 per 1000 <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> days (0.44 to 0.97 per 1000 <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> days). The incidence of both confirmed (criteria 1, 2) and suspected (criterion 3) <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related infection is 0.60 per 1000 <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> days (95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>: 0.46 to 0.78), which is comparable to the international benchmark. The majority of <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related infections (73.7%) were successfully treated with intravenous antimicrobials without necessitating <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> removal. <jats:italic><jats:styled-content style=\"fixed-case\">K<\/jats:styled-content>lebsiella pneumoniae<\/jats:italic> was the most common organism found in positive blood cultures.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content>\u2010related infection in this Australian population was comparable to rates described in the medical literature. Ongoing surveillance for infection rates is important to provide an up\u2010to\u2010date assessment of risks associated with <jats:styled-content style=\"fixed-case\">CVAD<\/jats:styled-content> use in this population.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jpc.12112","type":"journal-article","created":{"date-parts":[[2013,2,26]],"date-time":"2013-02-26T12:09:36Z","timestamp":1361880576000},"page":"242-245","update-policy":"http:\/\/dx.doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["Central venous access device\u2010related infections in patients with haemophilia"],"prefix":"10.1111","volume":"49","author":[{"given":"Zhi Han","family":"Yeoh","sequence":"first","affiliation":[{"name":"Henry Ekert Haemophilia Treatment Centre Royal Children's Hospital  Melbourne Victoria Australia"},{"name":"Melbourne Medical School University of Melbourne  Melbourne Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Janine","family":"Furmedge","sequence":"additional","affiliation":[{"name":"Henry Ekert Haemophilia Treatment Centre Royal Children's Hospital  Melbourne Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Julia","family":"Ekert","sequence":"additional","affiliation":[{"name":"Henry Ekert Haemophilia Treatment Centre Royal Children's Hospital  Melbourne Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Joe","family":"Crameri","sequence":"additional","affiliation":[{"name":"Department of Surgery  Melbourne Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nigel","family":"Curtis","sequence":"additional","affiliation":[{"name":"Infectious Diseases Unit Department of General Medicine Royal Children's Hospital  Melbourne Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Chris","family":"Barnes","sequence":"additional","affiliation":[{"name":"Henry Ekert Haemophilia Treatment Centre Royal Children's Hospital  Melbourne Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2013,2,26]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00270-006-0021-z"},{"key":"e_1_2_7_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(97)10006-X"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa067659"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2141.2007.06703.x"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.2003.00840.x"},{"key":"e_1_2_7_7_1","first-page":"s12","article-title":"Barriers to primary prophylaxis in haemophilic children: the issue of the venous access","volume":"6","author":"Santagostino E","year":"2008","journal-title":"Blood Transfus."},{"key":"e_1_2_7_8_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11908-005-0042-9"},{"key":"e_1_2_7_9_1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1365-2516.2003.00793.x"}],"container-title":["Journal of Paediatrics and Child Health"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fjpc.12112","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fjpc.12112","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/jpc.12112","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,15]],"date-time":"2023-10-15T04:27:54Z","timestamp":1697344074000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/jpc.12112"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,2,26]]},"references-count":8,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2013,3]]}},"alternative-id":["10.1111\/jpc.12112"],"URL":"https:\/\/doi.org\/10.1111\/jpc.12112","archive":["Portico"],"relation":{},"ISSN":["1034-4810","1440-1754"],"issn-type":[{"value":"1034-4810","type":"print"},{"value":"1440-1754","type":"electronic"}],"subject":[],"published":{"date-parts":[[2013,2,26]]},"assertion":[{"value":"2012-06-09","order":1,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2013-02-26","order":2,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}]}}