Online reporting system for transfusion-related adverse events to enhance recipient haemovigilance in Japan: A pilot study
Abstract Background A surveillance system for transfusion-related adverse reactions and infectious diseases in Japan was started at a national level in 1993, but current reporting of events in recipients is performed on a voluntary basis. A reporting system which can collect information on all trans...
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| Veröffentlicht in: | Transfusion and apheresis science 2013-02, Vol.48 (1), p.95-102 |
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| creator | Odaka, Chikako Kato, Hidefumi Otsubo, Hiroko Takamoto, Shigeru Okada, Yoshiaki Taneichi, Maiko Okuma, Kazu Sagawa, Kimitaka Hoshi, Yasutaka Tasaki, Tetsunori Fujii, Yasuhiko Yonemura, Yuji Iwao, Noriaki Tanaka, Asashi Okazaki, Hitoshi Momose, Shun-ya Kitazawa, Junichi Mori, Hiroshi Matsushita, Akio Nomura, Hisako Yasoshima, Hitoshi Ohkusa, Yasushi Yamaguchi, Kazunari Hamaguchi, Isao |
| description | Abstract Background A surveillance system for transfusion-related adverse reactions and infectious diseases in Japan was started at a national level in 1993, but current reporting of events in recipients is performed on a voluntary basis. A reporting system which can collect information on all transfusion-related events in recipients is required in Japan. Methods We have developed an online reporting system for transfusion-related events and performed a pilot study in 12 hospitals from 2007 to 2010. Results The overall incidence of adverse events per transfusion bag was 1.47%. Platelet concentrates gave rise to statistically more adverse events (4.16%) than red blood cells (0.66%) and fresh-frozen plasma (0.93%). In addition, we found that the incidence of adverse events varied between hospitals according to their size and patient characteristics. Conclusion This online reporting system is useful for collection and analysis of actual adverse events in recipients of blood transfusions and may contribute to enhancement of the existing surveillance system for recipients in Japan. |
| doi_str_mv | 10.1016/j.transci.2012.07.008 |
| format | Article |
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A reporting system which can collect information on all transfusion-related events in recipients is required in Japan. Methods We have developed an online reporting system for transfusion-related events and performed a pilot study in 12 hospitals from 2007 to 2010. Results The overall incidence of adverse events per transfusion bag was 1.47%. Platelet concentrates gave rise to statistically more adverse events (4.16%) than red blood cells (0.66%) and fresh-frozen plasma (0.93%). In addition, we found that the incidence of adverse events varied between hospitals according to their size and patient characteristics. Conclusion This online reporting system is useful for collection and analysis of actual adverse events in recipients of blood transfusions and may contribute to enhancement of the existing surveillance system for recipients in Japan.</description><identifier>ISSN: 1473-0502</identifier><identifier>EISSN: 1878-1683</identifier><identifier>DOI: 10.1016/j.transci.2012.07.008</identifier><identifier>PMID: 22954634</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adverse effects ; Blood Safety - instrumentation ; Blood Safety - methods ; Blood transfusions ; Data Collection ; Haemovigilance ; Health technology assessment ; Hematology, Oncology and Palliative Medicine ; Humans ; Incidence ; Japan ; Online system ; Online Systems ; Pilot Projects ; Pilot study ; Transfusion Reaction</subject><ispartof>Transfusion and apheresis science, 2013-02, Vol.48 (1), p.95-102</ispartof><rights>2012</rights><rights>Copyright © 2012. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-3cddbc7ead51193b3311194d84bcb8738f0cabb16d0cfa047e30e1e0b484dcbc3</citedby><cites>FETCH-LOGICAL-c420t-3cddbc7ead51193b3311194d84bcb8738f0cabb16d0cfa047e30e1e0b484dcbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1473050212001802$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22954634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Odaka, Chikako</creatorcontrib><creatorcontrib>Kato, Hidefumi</creatorcontrib><creatorcontrib>Otsubo, Hiroko</creatorcontrib><creatorcontrib>Takamoto, Shigeru</creatorcontrib><creatorcontrib>Okada, Yoshiaki</creatorcontrib><creatorcontrib>Taneichi, Maiko</creatorcontrib><creatorcontrib>Okuma, Kazu</creatorcontrib><creatorcontrib>Sagawa, Kimitaka</creatorcontrib><creatorcontrib>Hoshi, Yasutaka</creatorcontrib><creatorcontrib>Tasaki, Tetsunori</creatorcontrib><creatorcontrib>Fujii, Yasuhiko</creatorcontrib><creatorcontrib>Yonemura, Yuji</creatorcontrib><creatorcontrib>Iwao, Noriaki</creatorcontrib><creatorcontrib>Tanaka, Asashi</creatorcontrib><creatorcontrib>Okazaki, Hitoshi</creatorcontrib><creatorcontrib>Momose, Shun-ya</creatorcontrib><creatorcontrib>Kitazawa, Junichi</creatorcontrib><creatorcontrib>Mori, Hiroshi</creatorcontrib><creatorcontrib>Matsushita, Akio</creatorcontrib><creatorcontrib>Nomura, Hisako</creatorcontrib><creatorcontrib>Yasoshima, Hitoshi</creatorcontrib><creatorcontrib>Ohkusa, Yasushi</creatorcontrib><creatorcontrib>Yamaguchi, Kazunari</creatorcontrib><creatorcontrib>Hamaguchi, Isao</creatorcontrib><title>Online reporting system for transfusion-related adverse events to enhance recipient haemovigilance in Japan: A pilot study</title><title>Transfusion and apheresis science</title><addtitle>Transfus Apher Sci</addtitle><description>Abstract Background A surveillance system for transfusion-related adverse reactions and infectious diseases in Japan was started at a national level in 1993, but current reporting of events in recipients is performed on a voluntary basis. A reporting system which can collect information on all transfusion-related events in recipients is required in Japan. Methods We have developed an online reporting system for transfusion-related events and performed a pilot study in 12 hospitals from 2007 to 2010. Results The overall incidence of adverse events per transfusion bag was 1.47%. Platelet concentrates gave rise to statistically more adverse events (4.16%) than red blood cells (0.66%) and fresh-frozen plasma (0.93%). In addition, we found that the incidence of adverse events varied between hospitals according to their size and patient characteristics. Conclusion This online reporting system is useful for collection and analysis of actual adverse events in recipients of blood transfusions and may contribute to enhancement of the existing surveillance system for recipients in Japan.</description><subject>Adverse effects</subject><subject>Blood Safety - instrumentation</subject><subject>Blood Safety - methods</subject><subject>Blood transfusions</subject><subject>Data Collection</subject><subject>Haemovigilance</subject><subject>Health technology assessment</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Incidence</subject><subject>Japan</subject><subject>Online system</subject><subject>Online Systems</subject><subject>Pilot Projects</subject><subject>Pilot study</subject><subject>Transfusion Reaction</subject><issn>1473-0502</issn><issn>1878-1683</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0Eou3CRwD5yCXB_5J4OYCqqhRQpR6As-XYk9ZLYgfbWWn59DjdhQMXTmPZM--Nfw-hV5TUlND27a7OUftkXM0IZTXpakLkE3ROZScr2kr-tJxFxyvSEHaGLlLaEUI7um2fozPGto1ouThHv-786DzgCHOI2fl7nA4pw4SHEPGjw7AkF3wVYdQZLNZ2DzEBhj34nHAOGPyD9maVMG525RY_aJjC3t278fHBefxFz9q_w5d4dmPIOOXFHl6gZ4MeE7w81Q36_vH629Wn6vbu5vPV5W1lBCO54sba3nSgbUPplvec01KFlaI3vey4HIjRfU9bS8ygieiAE6BAeiGFNb3hG_TmqDvH8HOBlNXkkoGxLAdhSYoyKVrWtAXWBjXHVhNDShEGNUc36XhQlKgVu9qpE3a1YlekUwV7mXt9slj6CezfqT-cS8OHYwOUj-4dRFUkoMCxrmDLygb3X4v3_yiYEpwzevwBB0i7sERfKCqqUplRX9fs1-gpK7FLwvhvgyeugg</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Odaka, Chikako</creator><creator>Kato, Hidefumi</creator><creator>Otsubo, Hiroko</creator><creator>Takamoto, Shigeru</creator><creator>Okada, Yoshiaki</creator><creator>Taneichi, Maiko</creator><creator>Okuma, Kazu</creator><creator>Sagawa, Kimitaka</creator><creator>Hoshi, Yasutaka</creator><creator>Tasaki, Tetsunori</creator><creator>Fujii, Yasuhiko</creator><creator>Yonemura, Yuji</creator><creator>Iwao, Noriaki</creator><creator>Tanaka, Asashi</creator><creator>Okazaki, Hitoshi</creator><creator>Momose, Shun-ya</creator><creator>Kitazawa, Junichi</creator><creator>Mori, Hiroshi</creator><creator>Matsushita, Akio</creator><creator>Nomura, Hisako</creator><creator>Yasoshima, Hitoshi</creator><creator>Ohkusa, Yasushi</creator><creator>Yamaguchi, Kazunari</creator><creator>Hamaguchi, Isao</creator><general>Elsevier Ltd</general><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>7X8</scope></search><sort><creationdate>20130201</creationdate><title>Online reporting system for transfusion-related adverse events to enhance recipient haemovigilance in Japan: A pilot study</title><author>Odaka, Chikako ; Kato, Hidefumi ; Otsubo, Hiroko ; Takamoto, Shigeru ; Okada, Yoshiaki ; Taneichi, Maiko ; Okuma, Kazu ; Sagawa, Kimitaka ; Hoshi, Yasutaka ; Tasaki, Tetsunori ; Fujii, Yasuhiko ; Yonemura, Yuji ; Iwao, Noriaki ; Tanaka, Asashi ; Okazaki, Hitoshi ; Momose, Shun-ya ; Kitazawa, Junichi ; Mori, Hiroshi ; Matsushita, Akio ; Nomura, Hisako ; Yasoshima, Hitoshi ; Ohkusa, Yasushi ; Yamaguchi, Kazunari ; Hamaguchi, Isao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-3cddbc7ead51193b3311194d84bcb8738f0cabb16d0cfa047e30e1e0b484dcbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adverse effects</topic><topic>Blood Safety - instrumentation</topic><topic>Blood Safety - methods</topic><topic>Blood transfusions</topic><topic>Data Collection</topic><topic>Haemovigilance</topic><topic>Health technology assessment</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Incidence</topic><topic>Japan</topic><topic>Online system</topic><topic>Online Systems</topic><topic>Pilot Projects</topic><topic>Pilot study</topic><topic>Transfusion Reaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Odaka, Chikako</creatorcontrib><creatorcontrib>Kato, Hidefumi</creatorcontrib><creatorcontrib>Otsubo, Hiroko</creatorcontrib><creatorcontrib>Takamoto, Shigeru</creatorcontrib><creatorcontrib>Okada, Yoshiaki</creatorcontrib><creatorcontrib>Taneichi, Maiko</creatorcontrib><creatorcontrib>Okuma, Kazu</creatorcontrib><creatorcontrib>Sagawa, Kimitaka</creatorcontrib><creatorcontrib>Hoshi, Yasutaka</creatorcontrib><creatorcontrib>Tasaki, Tetsunori</creatorcontrib><creatorcontrib>Fujii, Yasuhiko</creatorcontrib><creatorcontrib>Yonemura, Yuji</creatorcontrib><creatorcontrib>Iwao, Noriaki</creatorcontrib><creatorcontrib>Tanaka, Asashi</creatorcontrib><creatorcontrib>Okazaki, Hitoshi</creatorcontrib><creatorcontrib>Momose, Shun-ya</creatorcontrib><creatorcontrib>Kitazawa, Junichi</creatorcontrib><creatorcontrib>Mori, Hiroshi</creatorcontrib><creatorcontrib>Matsushita, Akio</creatorcontrib><creatorcontrib>Nomura, Hisako</creatorcontrib><creatorcontrib>Yasoshima, Hitoshi</creatorcontrib><creatorcontrib>Ohkusa, Yasushi</creatorcontrib><creatorcontrib>Yamaguchi, Kazunari</creatorcontrib><creatorcontrib>Hamaguchi, Isao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transfusion and apheresis science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Odaka, Chikako</au><au>Kato, Hidefumi</au><au>Otsubo, Hiroko</au><au>Takamoto, Shigeru</au><au>Okada, Yoshiaki</au><au>Taneichi, Maiko</au><au>Okuma, Kazu</au><au>Sagawa, Kimitaka</au><au>Hoshi, Yasutaka</au><au>Tasaki, Tetsunori</au><au>Fujii, Yasuhiko</au><au>Yonemura, Yuji</au><au>Iwao, Noriaki</au><au>Tanaka, Asashi</au><au>Okazaki, Hitoshi</au><au>Momose, Shun-ya</au><au>Kitazawa, Junichi</au><au>Mori, Hiroshi</au><au>Matsushita, Akio</au><au>Nomura, Hisako</au><au>Yasoshima, Hitoshi</au><au>Ohkusa, Yasushi</au><au>Yamaguchi, Kazunari</au><au>Hamaguchi, Isao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Online reporting system for transfusion-related adverse events to enhance recipient haemovigilance in Japan: A pilot study</atitle><jtitle>Transfusion and apheresis science</jtitle><addtitle>Transfus Apher Sci</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>48</volume><issue>1</issue><spage>95</spage><epage>102</epage><pages>95-102</pages><issn>1473-0502</issn><eissn>1878-1683</eissn><abstract>Abstract Background A surveillance system for transfusion-related adverse reactions and infectious diseases in Japan was started at a national level in 1993, but current reporting of events in recipients is performed on a voluntary basis. A reporting system which can collect information on all transfusion-related events in recipients is required in Japan. Methods We have developed an online reporting system for transfusion-related events and performed a pilot study in 12 hospitals from 2007 to 2010. Results The overall incidence of adverse events per transfusion bag was 1.47%. Platelet concentrates gave rise to statistically more adverse events (4.16%) than red blood cells (0.66%) and fresh-frozen plasma (0.93%). In addition, we found that the incidence of adverse events varied between hospitals according to their size and patient characteristics. Conclusion This online reporting system is useful for collection and analysis of actual adverse events in recipients of blood transfusions and may contribute to enhancement of the existing surveillance system for recipients in Japan.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22954634</pmid><doi>10.1016/j.transci.2012.07.008</doi><tpages>8</tpages></addata></record> |
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| ispartof | Transfusion and apheresis science, 2013-02, Vol.48 (1), p.95-102 |
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| subjects | Adverse effects Blood Safety - instrumentation Blood Safety - methods Blood transfusions Data Collection Haemovigilance Health technology assessment Hematology, Oncology and Palliative Medicine Humans Incidence Japan Online system Online Systems Pilot Projects Pilot study Transfusion Reaction |
| title | Online reporting system for transfusion-related adverse events to enhance recipient haemovigilance in Japan: A pilot study |
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