TY - JOUR
T1 - Database and registry research in thyroid cancer
T2 - Striving for a new and improved national thyroid cancer database
AU - Mehra, Saral
AU - Tuttle, R. Michael
AU - Milas, Mira
AU - Orloff, Lisa
AU - Bergman, Donald
AU - Bernet, Victor
AU - Brett, Elise
AU - Cobin, Rhoda
AU - Doherty, Gerard
AU - Judson, Benjamin L.
AU - Klopper, Joshua
AU - Lee, Stephanie
AU - Lupo, Mark
AU - Machac, Josef
AU - Mechanick, Jeffrey I.
AU - Randolph, Gregory
AU - Ross, Douglas S.
AU - Smallridge, Robert
AU - Terris, David
AU - Tufano, Ralph
AU - Alon, Eran
AU - Clain, Jason
AU - Dosreis, Laura
AU - Scherl, Sophie
AU - Urken, Mark L.
N1 - Publisher Copyright:
© Copyright 2015, Mary Ann Liebert, Inc. 2015.
PY - 2015/2/1
Y1 - 2015/2/1
N2 - Background: Health registries have become extremely powerful tools for cancer research. Unfortunately, certain details and the ability to adapt to new information are necessarily limited in current registries, and they cannot address many controversial issues in cancer management. This is of particular concern in differentiated thyroid cancer, which is rapidly increasing in incidence and has many unknowns related to optimal treatment and surveillance recommendations. Summary: In this study, we review different types of health registries used in cancer research in the United States, with a focus on their advantages and disadvantages as related to the study of thyroid cancer. This analysis includes population-based cancer registries, health systems-based cancer registries, and patient-based disease registries. It is important that clinicians understand the way data are collected in, as well as the composition of, these different registries in order to more critically interpret the clinical research that is conducted using that data. In an attempt to address shortcoming of current databases for thyroid cancer, we present the potential of an innovative web-based disease management tool for thyroid cancer called the Thyroid Cancer Care Collaborative (TCCC) to become a patient-based registry that can be used to evaluate and improve the quality of care delivered to patients with thyroid cancer as well as to answer questions that we have not been able to address with current databases and registries. Conclusion: A cancer registry that follows a specific patient, is integrated into physician workflow, and collects data across different treatment sites and different payers does not exist in the current fragmented system of healthcare in the United States. The TCCC offers physicians who treat thyroid cancer numerous time-saving and quality improvement services, and could significantly improve patient care. With rapid adoption across the nation, the TCCC could become a new paradigm for database research in thyroid cancer to improve our understanding of thyroid cancer management.
AB - Background: Health registries have become extremely powerful tools for cancer research. Unfortunately, certain details and the ability to adapt to new information are necessarily limited in current registries, and they cannot address many controversial issues in cancer management. This is of particular concern in differentiated thyroid cancer, which is rapidly increasing in incidence and has many unknowns related to optimal treatment and surveillance recommendations. Summary: In this study, we review different types of health registries used in cancer research in the United States, with a focus on their advantages and disadvantages as related to the study of thyroid cancer. This analysis includes population-based cancer registries, health systems-based cancer registries, and patient-based disease registries. It is important that clinicians understand the way data are collected in, as well as the composition of, these different registries in order to more critically interpret the clinical research that is conducted using that data. In an attempt to address shortcoming of current databases for thyroid cancer, we present the potential of an innovative web-based disease management tool for thyroid cancer called the Thyroid Cancer Care Collaborative (TCCC) to become a patient-based registry that can be used to evaluate and improve the quality of care delivered to patients with thyroid cancer as well as to answer questions that we have not been able to address with current databases and registries. Conclusion: A cancer registry that follows a specific patient, is integrated into physician workflow, and collects data across different treatment sites and different payers does not exist in the current fragmented system of healthcare in the United States. The TCCC offers physicians who treat thyroid cancer numerous time-saving and quality improvement services, and could significantly improve patient care. With rapid adoption across the nation, the TCCC could become a new paradigm for database research in thyroid cancer to improve our understanding of thyroid cancer management.
UR - http://www.scopus.com/inward/record.url?scp=84922558757&partnerID=8YFLogxK
U2 - 10.1089/thy.2014.0270
DO - 10.1089/thy.2014.0270
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C2 - 25517683
AN - SCOPUS:84922558757
SN - 1050-7256
VL - 25
SP - 157
EP - 168
JO - Thyroid
JF - Thyroid
IS - 2
ER -