Optimizing the delivery and use of a new monoclonal antibody in children with congenital heart disease: A successful provincial respiratory syncytial virus prophylaxis program
Objectives To describe a program for passive immunization against respiratory syncytial virus infection in infants with hemodynamically significant congenital heart disease (CHD) in accordance with the Canadian Paediatric Society recommendations. Methods A provincial coordinating committee composed...
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Veröffentlicht in: | Canadian journal of cardiology 2007-05, Vol.23 (6), p.463-466 |
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description | Objectives To describe a program for passive immunization against respiratory syncytial virus infection in infants with hemodynamically significant congenital heart disease (CHD) in accordance with the Canadian Paediatric Society recommendations. Methods A provincial coordinating committee composed of specialists in pediatrics, cardiology, infectious diseases, neonatology and public health collaborated to develop and implement a program to identify children with hemodynamically significant heart disease and offer respiratory syncytial virus prophylaxis. Database records for all children younger than two years of age who were seen by the provincial pediatric cardiology referral service were reviewed. Children with hemodynamically significant heart disease, as determined by a clinical assessment and echocardiography, were considered to be eligible for monthly palivizumab prophylaxis for five winter months. All physicians in the province were notified that approval of the provincial cardiology service was required for prophylaxis to be administered. Immunization rates were compared with projected rates based on the expected population-based immunization rates in infants with CHD in other provinces. Results 401 children with any cardiac diagnoses were identified, representing 545 potential patient-seasons of prophylaxis over two years in a birth cohort of 20,173 and 19,227 children, in each respective season (13.8 patient-seasons per 1000 births). Of these, 21 children were eligible for palivizumab prophylaxis according to the Canadian Paediatric Society criteria. All eligible children were immunized, and no ineligible children received the immunization. A review of palivizumab use in other provinces revealed highly variable rates of prophylaxis. Conclusions The use of palivizumab for children with CHD can be optimized through a provincial model, in which children requiring prophylaxis are prospectively identified and reviewed by pediatric cardiologists – and to whom evidence-based guidelines developed by a multidisciplinary team – are applied. Such a model ensures that all patients requiring prophylaxis receive the appropriate immunization and avoids the immunization of low-risk children with CHD, in whom the benefits of palivizumab have not been proven. |
doi_str_mv | 10.1016/S0828-282X(07)70785-7 |
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Methods A provincial coordinating committee composed of specialists in pediatrics, cardiology, infectious diseases, neonatology and public health collaborated to develop and implement a program to identify children with hemodynamically significant heart disease and offer respiratory syncytial virus prophylaxis. Database records for all children younger than two years of age who were seen by the provincial pediatric cardiology referral service were reviewed. Children with hemodynamically significant heart disease, as determined by a clinical assessment and echocardiography, were considered to be eligible for monthly palivizumab prophylaxis for five winter months. All physicians in the province were notified that approval of the provincial cardiology service was required for prophylaxis to be administered. Immunization rates were compared with projected rates based on the expected population-based immunization rates in infants with CHD in other provinces. Results 401 children with any cardiac diagnoses were identified, representing 545 potential patient-seasons of prophylaxis over two years in a birth cohort of 20,173 and 19,227 children, in each respective season (13.8 patient-seasons per 1000 births). Of these, 21 children were eligible for palivizumab prophylaxis according to the Canadian Paediatric Society criteria. All eligible children were immunized, and no ineligible children received the immunization. A review of palivizumab use in other provinces revealed highly variable rates of prophylaxis. Conclusions The use of palivizumab for children with CHD can be optimized through a provincial model, in which children requiring prophylaxis are prospectively identified and reviewed by pediatric cardiologists – and to whom evidence-based guidelines developed by a multidisciplinary team – are applied. Such a model ensures that all patients requiring prophylaxis receive the appropriate immunization and avoids the immunization of low-risk children with CHD, in whom the benefits of palivizumab have not been proven.</description><identifier>ISSN: 0828-282X</identifier><identifier>EISSN: 1916-7075</identifier><identifier>DOI: 10.1016/S0828-282X(07)70785-7</identifier><identifier>PMID: 17487291</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Antibodies, Monoclonal - administration & dosage ; Antibodies, Monoclonal - therapeutic use ; Antibodies, Monoclonal, Humanized ; Antiviral Agents - administration & dosage ; Antiviral Agents - therapeutic use ; Canada - epidemiology ; Cardiovascular ; Child Health Services ; Congenital heart disease ; Databases, Factual ; Delivery of Health Care ; Female ; Health Outcomes/Policy ; Heart Defects, Congenital - complications ; Humans ; Infant ; Infant, Newborn ; Male ; Outcome Assessment (Health Care) ; Palivizumab ; Respiratory syncytial virus ; Respiratory Syncytial Virus Infections - complications ; Respiratory Syncytial Virus Infections - epidemiology ; Respiratory Syncytial Virus Infections - prevention & control ; Respiratory Syncytial Viruses - immunology</subject><ispartof>Canadian journal of cardiology, 2007-05, Vol.23 (6), p.463-466</ispartof><rights>Canadian Cardiovascular Society</rights><rights>2007 Canadian Cardiovascular Society</rights><rights>2007, Pulsus Group Inc. All rights reserved 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c520t-456f86100876bf28aeda5654a586e1a7cf9609e4f6c1e6f0d7daa1ab3b6a182b3</citedby><cites>FETCH-LOGICAL-c520t-456f86100876bf28aeda5654a586e1a7cf9609e4f6c1e6f0d7daa1ab3b6a182b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2650666/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0828-282X(07)70785-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,3537,27905,27906,45976,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17487291$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Warren, Andrew, MD</creatorcontrib><creatorcontrib>Langley, Joanne M., MD</creatorcontrib><creatorcontrib>Thomas, Wanda</creatorcontrib><creatorcontrib>Scott, Jeff, MD</creatorcontrib><title>Optimizing the delivery and use of a new monoclonal antibody in children with congenital heart disease: A successful provincial respiratory syncytial virus prophylaxis program</title><title>Canadian journal of cardiology</title><addtitle>Can J Cardiol</addtitle><description>Objectives To describe a program for passive immunization against respiratory syncytial virus infection in infants with hemodynamically significant congenital heart disease (CHD) in accordance with the Canadian Paediatric Society recommendations. Methods A provincial coordinating committee composed of specialists in pediatrics, cardiology, infectious diseases, neonatology and public health collaborated to develop and implement a program to identify children with hemodynamically significant heart disease and offer respiratory syncytial virus prophylaxis. Database records for all children younger than two years of age who were seen by the provincial pediatric cardiology referral service were reviewed. Children with hemodynamically significant heart disease, as determined by a clinical assessment and echocardiography, were considered to be eligible for monthly palivizumab prophylaxis for five winter months. All physicians in the province were notified that approval of the provincial cardiology service was required for prophylaxis to be administered. Immunization rates were compared with projected rates based on the expected population-based immunization rates in infants with CHD in other provinces. Results 401 children with any cardiac diagnoses were identified, representing 545 potential patient-seasons of prophylaxis over two years in a birth cohort of 20,173 and 19,227 children, in each respective season (13.8 patient-seasons per 1000 births). Of these, 21 children were eligible for palivizumab prophylaxis according to the Canadian Paediatric Society criteria. All eligible children were immunized, and no ineligible children received the immunization. A review of palivizumab use in other provinces revealed highly variable rates of prophylaxis. Conclusions The use of palivizumab for children with CHD can be optimized through a provincial model, in which children requiring prophylaxis are prospectively identified and reviewed by pediatric cardiologists – and to whom evidence-based guidelines developed by a multidisciplinary team – are applied. Such a model ensures that all patients requiring prophylaxis receive the appropriate immunization and avoids the immunization of low-risk children with CHD, in whom the benefits of palivizumab have not been proven.</description><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antibodies, Monoclonal, Humanized</subject><subject>Antiviral Agents - administration & dosage</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Canada - epidemiology</subject><subject>Cardiovascular</subject><subject>Child Health Services</subject><subject>Congenital heart disease</subject><subject>Databases, Factual</subject><subject>Delivery of Health Care</subject><subject>Female</subject><subject>Health Outcomes/Policy</subject><subject>Heart Defects, Congenital - complications</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Outcome Assessment (Health Care)</subject><subject>Palivizumab</subject><subject>Respiratory syncytial virus</subject><subject>Respiratory Syncytial Virus Infections - complications</subject><subject>Respiratory Syncytial Virus Infections - epidemiology</subject><subject>Respiratory Syncytial Virus Infections - prevention & control</subject><subject>Respiratory Syncytial Viruses - immunology</subject><issn>0828-282X</issn><issn>1916-7075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstu1DAUhiMEokPhEUBeIVgE7ExiZ1gUVRU3qVIXgMTOcuyTySmOHWxnSngpXpFkZlQuG1a-nM_fsfw7yx4z-oJRxl9-pHVR50VdfHlGxXNBRV3l4k62YhvG83lZ3c1Wt8hJ9iDGa0pLJgS_n50wUdai2LBV9vNqSNjjD3RbkjogBizuIExEOUPGCMS3RBEHN6T3zmvrnbJzLWHjzUTQEd2hNQEcucHUEe3dFhymGepAhUQMRlARXpFzEketIcZ2tGQIfodO44wFiAMGlfzcM05OT2nZ3WEY44IN3WTVd9zPt0H1D7N7rbIRHh3H0-zz2zefLt7nl1fvPlycX-a6KmjKy4q3NWeU1oI3bVErMKriVamqmgNTQrcbTjdQtlwz4C01wijFVLNuuGJ10axPs7ODdxibHowGl4KycgjYqzBJr1D-XXHYya3fyYJXlHM-C54eBcF_GyEm2WPUYK1y4McoBS0FrbiYweoA6uBjDNDeNmFULlHLfdRyyVFSIfdRy-Xckz9v-PvUMdsZeH0AYH6nHUKQUSM4DQYD6CSNx_-2OPvHoC061Mp-hQnitR_D_B2iZDIWkh4ki4OKvUGsfwFGOdXm</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Warren, Andrew, MD</creator><creator>Langley, Joanne M., MD</creator><creator>Thomas, Wanda</creator><creator>Scott, Jeff, MD</creator><general>Elsevier Inc</general><general>Pulsus Group Inc</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><scope>5PM</scope></search><sort><creationdate>20070501</creationdate><title>Optimizing the delivery and use of a new monoclonal antibody in children with congenital heart disease: A successful provincial respiratory syncytial virus prophylaxis program</title><author>Warren, Andrew, MD ; Langley, Joanne M., MD ; Thomas, Wanda ; Scott, Jeff, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-456f86100876bf28aeda5654a586e1a7cf9609e4f6c1e6f0d7daa1ab3b6a182b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Antibodies, Monoclonal - administration & dosage</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antibodies, Monoclonal, Humanized</topic><topic>Antiviral Agents - administration & dosage</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Canada - epidemiology</topic><topic>Cardiovascular</topic><topic>Child Health Services</topic><topic>Congenital heart disease</topic><topic>Databases, Factual</topic><topic>Delivery of Health Care</topic><topic>Female</topic><topic>Health Outcomes/Policy</topic><topic>Heart Defects, Congenital - complications</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Outcome Assessment (Health Care)</topic><topic>Palivizumab</topic><topic>Respiratory syncytial virus</topic><topic>Respiratory Syncytial Virus Infections - complications</topic><topic>Respiratory Syncytial Virus Infections - epidemiology</topic><topic>Respiratory Syncytial Virus Infections - prevention & control</topic><topic>Respiratory Syncytial Viruses - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Warren, Andrew, MD</creatorcontrib><creatorcontrib>Langley, Joanne M., MD</creatorcontrib><creatorcontrib>Thomas, Wanda</creatorcontrib><creatorcontrib>Scott, Jeff, MD</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Canadian journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Warren, Andrew, MD</au><au>Langley, Joanne M., MD</au><au>Thomas, Wanda</au><au>Scott, Jeff, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimizing the delivery and use of a new monoclonal antibody in children with congenital heart disease: A successful provincial respiratory syncytial virus prophylaxis program</atitle><jtitle>Canadian journal of cardiology</jtitle><addtitle>Can J Cardiol</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>23</volume><issue>6</issue><spage>463</spage><epage>466</epage><pages>463-466</pages><issn>0828-282X</issn><eissn>1916-7075</eissn><abstract>Objectives To describe a program for passive immunization against respiratory syncytial virus infection in infants with hemodynamically significant congenital heart disease (CHD) in accordance with the Canadian Paediatric Society recommendations. Methods A provincial coordinating committee composed of specialists in pediatrics, cardiology, infectious diseases, neonatology and public health collaborated to develop and implement a program to identify children with hemodynamically significant heart disease and offer respiratory syncytial virus prophylaxis. Database records for all children younger than two years of age who were seen by the provincial pediatric cardiology referral service were reviewed. Children with hemodynamically significant heart disease, as determined by a clinical assessment and echocardiography, were considered to be eligible for monthly palivizumab prophylaxis for five winter months. All physicians in the province were notified that approval of the provincial cardiology service was required for prophylaxis to be administered. Immunization rates were compared with projected rates based on the expected population-based immunization rates in infants with CHD in other provinces. Results 401 children with any cardiac diagnoses were identified, representing 545 potential patient-seasons of prophylaxis over two years in a birth cohort of 20,173 and 19,227 children, in each respective season (13.8 patient-seasons per 1000 births). Of these, 21 children were eligible for palivizumab prophylaxis according to the Canadian Paediatric Society criteria. All eligible children were immunized, and no ineligible children received the immunization. A review of palivizumab use in other provinces revealed highly variable rates of prophylaxis. Conclusions The use of palivizumab for children with CHD can be optimized through a provincial model, in which children requiring prophylaxis are prospectively identified and reviewed by pediatric cardiologists – and to whom evidence-based guidelines developed by a multidisciplinary team – are applied. Such a model ensures that all patients requiring prophylaxis receive the appropriate immunization and avoids the immunization of low-risk children with CHD, in whom the benefits of palivizumab have not been proven.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>17487291</pmid><doi>10.1016/S0828-282X(07)70785-7</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies, Monoclonal - administration & dosage Antibodies, Monoclonal - therapeutic use Antibodies, Monoclonal, Humanized Antiviral Agents - administration & dosage Antiviral Agents - therapeutic use Canada - epidemiology Cardiovascular Child Health Services Congenital heart disease Databases, Factual Delivery of Health Care Female Health Outcomes/Policy Heart Defects, Congenital - complications Humans Infant Infant, Newborn Male Outcome Assessment (Health Care) Palivizumab Respiratory syncytial virus Respiratory Syncytial Virus Infections - complications Respiratory Syncytial Virus Infections - epidemiology Respiratory Syncytial Virus Infections - prevention & control Respiratory Syncytial Viruses - immunology |
title | Optimizing the delivery and use of a new monoclonal antibody in children with congenital heart disease: A successful provincial respiratory syncytial virus prophylaxis program |
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