Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries

Abbey Diaz; Shafkat Jahan; Neal A. Palafox; Ian Ring; Lisa Whop; Danica Cossio; Kalinda Griffiths; Gail Garvey

doi:10.1007/978-3-031-56806-0_12

Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries

Abbey Diaz, Shafkat Jahan, Neal A. Palafox, Ian Ring, Lisa Whop, Danica Cossio, Kalinda Griffiths, Gail Garvey

College of Medicine and Public Health

Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

26 Downloads (Pure)

Abstract

Population-based cancer registries (PBCRs) are data information systems that systematically collect, record, and manage data of cancer patients within a defined population [1]. They play a valuable role in cancer surveillance within a given population, identifying changes in cancer incidence over time, across regions, and among diverse population groups, and, when linked to death registration data, enable the analysis of survival patterns [2]. These data are critical for assessing the need for and effectiveness of national cancer control programs, identifying possible cancer causes, and assisting patients and their healthcare professionals to make informed care decisions.

Original language	English
Title of host publication	Indigenous and Tribal Peoples and Cancer
Editors	Gail Garvey, Linda Burhansstipanov, Lea Bill, Nina Scott, Lisa Whop
Place of Publication	Switzerland
Publisher	Springer Science+Business Media
Chapter	12
Pages	59-63
Number of pages	5
ISBN (Electronic)	9783031568060
ISBN (Print)	9783031568053
DOIs	https://doi.org/10.1007/978-3-031-56806-0_12
Publication status	Published - 2024

Keywords

Population-based cancer registries (PBCRs)
indigenous identification
Cancer registries
Indigenous people

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1007/978-3-031-56806-0_12Licence: CC BY-NC-ND

Published versionFinal published version, 452 KBLicence: CC BY-NC-ND

Cite this

Diaz, A., Jahan, S., Palafox, N. A., Ring, I., Whop, L., Cossio, D., Griffiths, K., & Garvey, G. (2024). Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries. In G. Garvey, L. Burhansstipanov, L. Bill, N. Scott, & L. Whop (Eds.), Indigenous and Tribal Peoples and Cancer (pp. 59-63). Springer Science+Business Media. https://doi.org/10.1007/978-3-031-56806-0_12

@inbook{bccaa55d1f9c4ed5b61c5c5a2891ac68,

title = "Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries",

abstract = "Population-based cancer registries (PBCRs) are data information systems that systematically collect, record, and manage data of cancer patients within a defined population [1]. They play a valuable role in cancer surveillance within a given population, identifying changes in cancer incidence over time, across regions, and among diverse population groups, and, when linked to death registration data, enable the analysis of survival patterns [2]. These data are critical for assessing the need for and effectiveness of national cancer control programs, identifying possible cancer causes, and assisting patients and their healthcare professionals to make informed care decisions.",

keywords = "Population-based cancer registries (PBCRs), indigenous identification, Cancer registries, Indigenous people",

author = "Abbey Diaz and Shafkat Jahan and Palafox, {Neal A.} and Ian Ring and Lisa Whop and Danica Cossio and Kalinda Griffiths and Gail Garvey",

year = "2024",

doi = "10.1007/978-3-031-56806-0_12",

language = "English",

isbn = "9783031568053",

pages = "59--63",

editor = "Gail Garvey and Linda Burhansstipanov and Lea Bill and Nina Scott and Lisa Whop",

booktitle = "Indigenous and Tribal Peoples and Cancer",

publisher = "Springer Science+Business Media",

}

Diaz, A, Jahan, S, Palafox, NA, Ring, I, Whop, L, Cossio, D, Griffiths, K & Garvey, G 2024, Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries. in G Garvey, L Burhansstipanov, L Bill, N Scott & L Whop (eds), Indigenous and Tribal Peoples and Cancer. Springer Science+Business Media, Switzerland, pp. 59-63. https://doi.org/10.1007/978-3-031-56806-0_12

Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries. / Diaz, Abbey; Jahan, Shafkat; Palafox, Neal A. et al.
Indigenous and Tribal Peoples and Cancer. ed. / Gail Garvey; Linda Burhansstipanov; Lea Bill; Nina Scott; Lisa Whop. Switzerland: Springer Science+Business Media, 2024. p. 59-63.

Research output: Chapter in Book/Report/Conference proceeding › Chapter › peer-review

TY - CHAP

T1 - Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries

AU - Diaz, Abbey

AU - Jahan, Shafkat

AU - Palafox, Neal A.

AU - Ring, Ian

AU - Whop, Lisa

AU - Cossio, Danica

AU - Griffiths, Kalinda

AU - Garvey, Gail

PY - 2024

Y1 - 2024

N2 - Population-based cancer registries (PBCRs) are data information systems that systematically collect, record, and manage data of cancer patients within a defined population [1]. They play a valuable role in cancer surveillance within a given population, identifying changes in cancer incidence over time, across regions, and among diverse population groups, and, when linked to death registration data, enable the analysis of survival patterns [2]. These data are critical for assessing the need for and effectiveness of national cancer control programs, identifying possible cancer causes, and assisting patients and their healthcare professionals to make informed care decisions.

AB - Population-based cancer registries (PBCRs) are data information systems that systematically collect, record, and manage data of cancer patients within a defined population [1]. They play a valuable role in cancer surveillance within a given population, identifying changes in cancer incidence over time, across regions, and among diverse population groups, and, when linked to death registration data, enable the analysis of survival patterns [2]. These data are critical for assessing the need for and effectiveness of national cancer control programs, identifying possible cancer causes, and assisting patients and their healthcare professionals to make informed care decisions.

KW - Population-based cancer registries (PBCRs)

KW - indigenous identification

KW - Cancer registries

KW - Indigenous people

UR - http://www.scopus.com/inward/record.url?scp=105003360363&partnerID=8YFLogxK

U2 - 10.1007/978-3-031-56806-0_12

DO - 10.1007/978-3-031-56806-0_12

M3 - Chapter

AN - SCOPUS:105003360363

SN - 9783031568053

SP - 59

EP - 63

BT - Indigenous and Tribal Peoples and Cancer

A2 - Garvey, Gail

A2 - Burhansstipanov, Linda

A2 - Bill, Lea

A2 - Scott, Nina

A2 - Whop, Lisa

PB - Springer Science+Business Media

CY - Switzerland

ER -

Barriers and Enablers to Collecting Indigenous Identification Information by Cancer Registries

Abstract

Keywords

UN SDGs

Access to Document

Other files and links

Fingerprint

Cite this