The Australian Youth Cancer Service: Developing and Monitoring the Activity of Nationally Coordinated Adolescent and Young Adult Cancer Care
Adolescents and young adults (aged 15–25 years) diagnosed with cancer have unique medical and psychosocial experiences and care needs, distinct from those of paediatric and older adult patients. Since 2011, the Australian Youth Cancer Services have provided developmentally appropriate, multidiscipli...
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Veröffentlicht in: | Cancers 2021-05, Vol.13 (11), p.2675 |
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creator | Patterson, Pandora Allison, Kimberley R. Bibby, Helen Thompson, Kate Lewin, Jeremy Briggs, Taia Walker, Rick Osborn, Michael Plaster, Meg Hayward, Allan Henney, Roslyn George, Shannyn Keuskamp, Dominic Anazodo, Antoinette |
description | Adolescents and young adults (aged 15–25 years) diagnosed with cancer have unique medical and psychosocial experiences and care needs, distinct from those of paediatric and older adult patients. Since 2011, the Australian Youth Cancer Services have provided developmentally appropriate, multidisciplinary and comprehensive care to these young patients, facilitated by national service coordination and activity data collection and monitoring. This paper reports on how the Youth Cancer Services have conceptualised and delivered quality youth cancer care in four priority areas: clinical trial participation, oncofertility, psychosocial care and survivorship. National activity data collected by the Youth Cancer Services between 2016–17 and 2019–20 are used to illustrate how service monitoring processes have facilitated improvements in coordination and accountability across multiple indicators of quality youth cancer care, including clinical trial participation, access to fertility information and preservation, psychosocial screening and care and the transition from active treatment to survivorship. Accounts of both service delivery and monitoring and evaluation processes within the Australian Youth Cancer Services provide an exemplar of how coordinated initiatives may be employed to deliver, monitor and improve quality cancer care for adolescents and young adults. |
doi_str_mv | 10.3390/cancers13112675 |
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Since 2011, the Australian Youth Cancer Services have provided developmentally appropriate, multidisciplinary and comprehensive care to these young patients, facilitated by national service coordination and activity data collection and monitoring. This paper reports on how the Youth Cancer Services have conceptualised and delivered quality youth cancer care in four priority areas: clinical trial participation, oncofertility, psychosocial care and survivorship. National activity data collected by the Youth Cancer Services between 2016–17 and 2019–20 are used to illustrate how service monitoring processes have facilitated improvements in coordination and accountability across multiple indicators of quality youth cancer care, including clinical trial participation, access to fertility information and preservation, psychosocial screening and care and the transition from active treatment to survivorship. Accounts of both service delivery and monitoring and evaluation processes within the Australian Youth Cancer Services provide an exemplar of how coordinated initiatives may be employed to deliver, monitor and improve quality cancer care for adolescents and young adults.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13112675</identifier><identifier>PMID: 34071622</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Adolescents ; Age ; Cancer ; Clinical trials ; Collaboration ; COVID-19 ; Data collection ; Health care policy ; Health services ; Hospitals ; Integrated approach ; Jurisdiction ; Oncology ; Pandemics ; Participation ; Patients ; Pediatrics ; Peer tutoring ; Survival ; Teenagers ; Young adults</subject><ispartof>Cancers, 2021-05, Vol.13 (11), p.2675</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. 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Since 2011, the Australian Youth Cancer Services have provided developmentally appropriate, multidisciplinary and comprehensive care to these young patients, facilitated by national service coordination and activity data collection and monitoring. This paper reports on how the Youth Cancer Services have conceptualised and delivered quality youth cancer care in four priority areas: clinical trial participation, oncofertility, psychosocial care and survivorship. National activity data collected by the Youth Cancer Services between 2016–17 and 2019–20 are used to illustrate how service monitoring processes have facilitated improvements in coordination and accountability across multiple indicators of quality youth cancer care, including clinical trial participation, access to fertility information and preservation, psychosocial screening and care and the transition from active treatment to survivorship. Accounts of both service delivery and monitoring and evaluation processes within the Australian Youth Cancer Services provide an exemplar of how coordinated initiatives may be employed to deliver, monitor and improve quality cancer care for adolescents and young adults.</description><subject>Adolescents</subject><subject>Age</subject><subject>Cancer</subject><subject>Clinical trials</subject><subject>Collaboration</subject><subject>COVID-19</subject><subject>Data collection</subject><subject>Health care policy</subject><subject>Health services</subject><subject>Hospitals</subject><subject>Integrated approach</subject><subject>Jurisdiction</subject><subject>Oncology</subject><subject>Pandemics</subject><subject>Participation</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Peer tutoring</subject><subject>Survival</subject><subject>Teenagers</subject><subject>Young adults</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdUU1vEzEQtRCIVqVnrpa4cEnrr3hjDkjRAi1SaQ-UAyfLa882rhw72N5I-Q_90ThpQVBfxqN5783HQ-gtJWecK3JuTbSQC-WUMtnNX6BjRjo2k1KJl__8j9BpKfekPc5pJ7vX6IgL0lHJ2DF6uF0BXk6lZhO8ifhnmuoK9wdl_B3y1lv4gD_BFkLa-HiHTXT4W4q-prxP655uq9_6usNpxNem-hRNCDvcp5Sdj6aCw0uXAhQLsR4EWpfGXbop1D-9epPhDXo1mlDg9CmeoB9fPt_2l7Orm4uv_fJqZoUUdQaj4FYuiJHUDI6Ds2xQRDgFzDFDuBjng1XdOMDYWauc4Eyp0XSOKWZG6vgJ-viou5mGdaO3sdr6epP92uSdTsbr_yvRr_Rd2uoFVYt2uCbw_kkgp18TlKrXvm0XgomQpqLZnEvRLKG8Qd89g96nKbcLHVBKEknYoqHOH1E2p1IyjH-HoUTvzdbPzOa_AeXuoA8</recordid><startdate>20210528</startdate><enddate>20210528</enddate><creator>Patterson, Pandora</creator><creator>Allison, Kimberley R.</creator><creator>Bibby, Helen</creator><creator>Thompson, Kate</creator><creator>Lewin, Jeremy</creator><creator>Briggs, Taia</creator><creator>Walker, Rick</creator><creator>Osborn, Michael</creator><creator>Plaster, Meg</creator><creator>Hayward, Allan</creator><creator>Henney, Roslyn</creator><creator>George, Shannyn</creator><creator>Keuskamp, Dominic</creator><creator>Anazodo, Antoinette</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4446-5868</orcidid><orcidid>https://orcid.org/0000-0002-1288-9930</orcidid><orcidid>https://orcid.org/0000-0001-6623-2611</orcidid></search><sort><creationdate>20210528</creationdate><title>The Australian Youth Cancer Service: Developing and Monitoring the Activity of Nationally Coordinated Adolescent and Young Adult Cancer Care</title><author>Patterson, Pandora ; 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Since 2011, the Australian Youth Cancer Services have provided developmentally appropriate, multidisciplinary and comprehensive care to these young patients, facilitated by national service coordination and activity data collection and monitoring. This paper reports on how the Youth Cancer Services have conceptualised and delivered quality youth cancer care in four priority areas: clinical trial participation, oncofertility, psychosocial care and survivorship. National activity data collected by the Youth Cancer Services between 2016–17 and 2019–20 are used to illustrate how service monitoring processes have facilitated improvements in coordination and accountability across multiple indicators of quality youth cancer care, including clinical trial participation, access to fertility information and preservation, psychosocial screening and care and the transition from active treatment to survivorship. 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subjects | Adolescents Age Cancer Clinical trials Collaboration COVID-19 Data collection Health care policy Health services Hospitals Integrated approach Jurisdiction Oncology Pandemics Participation Patients Pediatrics Peer tutoring Survival Teenagers Young adults |
title | The Australian Youth Cancer Service: Developing and Monitoring the Activity of Nationally Coordinated Adolescent and Young Adult Cancer Care |
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