Evaluating implementation of a hospital‐based cancer registry to improve childhood cancer care in low‐ and middle‐income countries

Author:

Maas Melissa R.1ORCID,Yang Allison1ORCID,Muir Michele A.2ORCID,Collins James B.12,Canter Courtney3,Tamamyan Gevorg45,Chitsike Inam6,Kouya Francine7,Nguyen Kim Hoa8ORCID,Ahmad Alia9,Alcasabas Ana Patricia10,Gao Yi‐Jin11ORCID,Johnson Kimberly J.12,Ferrara Gia13ORCID,Bhakta Nickhill13,Muluneh Benyam1ORCID

Affiliation:

1. Division of Pharmacotherapy and Experimental Therapeutics University of North Carolina Eshelman School of Pharmacy Chapel Hill North Carolina USA

2. GSK Durham North Carolina USA

3. North Carolina Translational and Clinical Sciences Institute Chapel Hill North Carolina USA

4. Pediatric Cancer and Blood Disorders Center of Armenia Yeolyan Hematology and Oncology Center Yerevan Armenia

5. Department of Hematology and Pediatric Oncology Yerevan State Medical University Yerevan Armenia

6. Parirenyatwa Group of Hospitals Harare Zimbabwe

7. Mbingo Baptist Hospital Cameroon

8. Hue Central Hospital Hue Vietnam

9. University of Child Health Sciences, The Children's Hospital Lahore Pakistan

10. University of Philippine—Philippine General Hospital Manila Philippines

11. Shanghai Children's Medical Center Shanghai China

12. Brown School at Washington University in St. Louis St. Louis Missouri USA

13. Department of Global Pediatric Medicine St. Jude Children's Research Hospital Memphis Tennessee USA

Abstract

AbstractPurposeCancer is a leading cause of global childhood mortality, affecting 400,000 children annually. While treatable with modern therapies, children living in low‐ and middle‐income countries (LMICs) have limited access to care and lower survival rates. Hospital‐based cancer registries (HBCRs) collect detailed patient information to critically evaluate and evolve care. The St. Jude Global Childhood Cancer Analytics Resource and Epidemiological Surveillance System (SJCARES) is a cloud‐based HBCR network facilitating quality data collection of pediatric cancer. Wide variation in the success of implementation has warranted further research into the implementation approach, to create a sustainable and adaptable HBCR in LMICs.MethodsSeven of 89 sites using the SJCARES registry were selected, stratified by global region and stage of implementation. Semi‐structured interviews were conducted with key groups (clinicians, administrators, data clerks) using an interview guide developed from the Consolidation Framework for Implementation Research (CFIR). Interviews were conducted via a video‐telephone software program and transcribed by a transcription service. Transcripts were thematically coded using rapid qualitative analysis.ResultsA total of 18 participants (11 clinicians, 4 administrators, 3 data clerks) were interviewed. Several barrier themes were identified, including: difficulty integrating the registry into existing workflow; lack of resources; lack of government or administrative support; and damaged, misplaced, or illegible medical records. Facilitator themes were identified, including: internal support for the registry; clear and extensive training; and dedicated support staff.ConclusionInterviewed participants identified key barriers and facilitators to the implementation of the SJCARES registry across multiple phases. We plan to use these results to develop targeted implementation strategies including a readiness assessment tool to help guide more successful implementation of the SJCARES registry and other HBCRs in LMICs.

Funder

Washington University in St. Louis

Publisher

Wiley

Reference17 articles.

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