Literature DB >> 30032962

Development of a tool for comprehensive evaluation of population-based cancer registries.

Abbas Sheikhtaheri1, Azin Nahvijou2, Zahra Sedighi2, Maryam Hadji2, Mohammad Golmahi2, Gholamreza Roshandel3, Omid Beiki4, Zahra Ravankhah5, Kazem Zendehdel6.   

Abstract

OBJECTIVE: Several methods have been suggested for evaluation of population-based cancer registries (PBCR) worldwide. However, most of these methods evaluate the data and outputs of the cancer registries. This study aimed to develop a comprehensive tool and protocol for evaluation of inputs, processes and outputs of a PBCR.
METHODS: The standards of the North American Association of Central Cancer Registries (NAACCR) were used to draft a comprehensive checklist. In addition, the national guidelines of PBCR were used to develop a questionnaire for evaluation of knowledge and practice of the PBCR personnel. Furthermore, a protocol for evaluation of the completeness and validity of the PBCR data was developed according to the International Agency for Research on Cancer (IARC) and the NAACCR guidelines. A 0-4 Likert based score and expert opinions (10 experts) were used to assess validity of the eight questionnaires/checklists. A modified Delphi method was applied to validate the checklists and questionnaires. Questions with a score higher than 3 remained in the final tools.
RESULTS: The final package consists of 546 questions including 108 (19.8%) for evaluation of guidelines, 54 (9.9%) for analysis and reports, 87 (15.9%) for governance and infrastructure, 155 (28.4%) for information technology, 21 (3.8%) for personnel knowledge and 121 (22.2%) for their practice. Additionally, data quality indicators were also considered for evaluation of PBCRs.
CONCLUSION: This comprehensive tool can be used to show the gaps and limitations of the PBCR programs and provide informative clues for their improvement.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Assessment; Cancer registry; Disease registry; Evaluation; Population based cancer registry

Mesh:

Year:  2018        PMID: 30032962     DOI: 10.1016/j.ijmedinf.2018.06.006

Source DB:  PubMed          Journal:  Int J Med Inform        ISSN: 1386-5056            Impact factor:   4.046


  5 in total

1.  Barriers and facilitators for the implementation of health condition and outcome registry systems: a systematic literature review.

Authors:  Mina Lazem; Abbas Sheikhtaheri
Journal:  J Am Med Inform Assoc       Date:  2022-03-15       Impact factor: 4.497

2.  Lessons learned from hemolytic uremic syndrome registries: recommendations for implementation.

Authors:  Mina Lazem; Abbas Sheikhtaheri; Nakysa Hooman
Journal:  Orphanet J Rare Dis       Date:  2021-05-25       Impact factor: 4.123

3.  Regional COVID-19 registry in Khuzestan, Iran: A study protocol and lessons learned from a pilot implementation.

Authors:  Javad Zarei; Maryam Dastoorpoor; Amir Jamshidnezhad; Maria Cheraghi; Abbas Sheikhtaheri
Journal:  Inform Med Unlocked       Date:  2021-01-19

4.  Barriers and facilitators for disease registry systems: a mixed-method study.

Authors:  Mina Lazem; Abbas Sheikhtaheri
Journal:  BMC Med Inform Decis Mak       Date:  2022-04-11       Impact factor: 2.796

5.  National and Subnational Cancer Incidence for 22 Cancer Groups, 2000 to 2016: A Study Based on Cancer Registration Data of Iran.

Authors:  Javad Khanali; Ali-Asghar Kolahi
Journal:  J Cancer Epidemiol       Date:  2021-07-12
  5 in total

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