Publication

Childhood cancer survivorship care during the COVID-19 pandemic: an international report of practice implications and provider concerns

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Last modified
  • 05/22/2025
Type of Material
Authors
    Selina R van den Oever, Princess Máxima Center for Pediatric OncologySaskia MF Pluijm, Princess Máxima Center for Pediatric OncologyRod Skinner, Newcastle UniversityAdam Glaser, University of LeedsRenée L Mulder, Princess Máxima Center for Pediatric OncologySaro Armenian, City of Hope Comprehensive Cancer CenterEdit Bardi, St Anna Childrens HospitalClaire Berger, University Hospital Saint-EtienneMatthew J Ehrhardt, St. Jude Children’s Research HospitalJordan Marchak, Emory UniversityGabrielle M Haeusler, Paediatric Integrated Cancer CentreJaap den Hartogh, Dutch Childhood Cancer Parent Organization VOKK NetherlandsLars Hjorth, Lund UniversityTomas Kepak, Masaryk UniversityIzolda Kriviene, Republican Siauliai County HospitalThorsten Langer, University Hospital of Schleswig-HolsteinMiho Maeda, Nippon Medical SchoolCatalina Márquez-Vega, Hosp Virgen del RocioGisela Michel, University of LucerneMonica Muraca, IRCCS Istituto Giannina GasliniMohamed Najib, Hospital Tunku AzizahPaul C Nathan, The Hospital for Sick ChildrenAnna Panasiuk, Medical University of WroclawMaya Prasad, Tata Memorial HospitalJelena Roganovic, University of RijekaAnne Uyttebroeck, University Hospital LeuvenJeanette F Winther, Danish Cancer SocietyLorna Zadravec Zaletel, Institute of Oncology, ZaloskaElvira C van Dalen, Princess Máxima Center for Pediatric OncologyHelena JH van der Pal, Princess Máxima Center for Pediatric OncologyMelissa M Hudson, St. Jude Children’s Research HospitalLeontien CM Kremer, Princess Máxima Center for Pediatric Oncology
Language
  • English
Date
  • 2022-01-12
Publisher
  • SPRINGER
Publication Version
Copyright Statement
  • © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 16
Issue
  • 6
Start Page
  • 1390
End Page
  • 1400
Supplemental Material (URL)
Abstract
  • Purpose: Long-term follow-up (LTFU) care is essential to optimise health outcomes in childhood cancer survivors (CCS). We aimed to assess the impact of the COVID-19 pandemic on LTFU services and providers. Methods: A COVID-19 working group within the International Late Effects of Childhood Cancer Guideline Harmonization Group (IGHG) distributed a questionnaire to LTFU service providers in 37 countries across Europe, Asia, North America, Central/South America, and Australia. The questionnaire assessed how care delivery methods changed during the pandemic and respondents’ level of worry about the pandemic’s impact on LTFU care delivery, their finances, their health, and that of their family and friends. Results: Among 226 institutions, providers from 178 (79%) responded. Shortly after the initial outbreak, 42% of LTFU clinics closed. Restrictions during the pandemic resulted in fewer in-person consultations and an increased use of telemedicine, telephone, and email consultations. The use of a risk assessment to prioritise the method of LTFU consultation for individual CCS increased from 12 to 47%. While respondents anticipated in-person consultations to remain the primary method for LTFU service delivery, they expected significantly increased use of telemedicine and telephone consultations after the pandemic. On average, respondents reported highest levels of worry about psychosocial well-being of survivors. Conclusions: The pandemic necessitated changes in LTFU service delivery, including greater use of virtual LTFU care and risk-stratification to identify CCS that need in-person evaluations. Implications for Cancer Survivors: Increased utilisation of virtual LTFU care and risk stratification is likely to persist post-pandemic.
Author Notes
Keywords
Research Categories
  • Health Sciences, Oncology
  • Health Sciences, Epidemiology

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