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1.
JCO Clin Cancer Inform ; 4: 929-937, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-33104389

RESUMO

PURPOSE: ASCO, through its wholly owned subsidiary, CancerLinQ LLC, developed CancerLinQ, a learning health system for oncology. A learning health system is important for oncology patients because less than 5% of patients with cancer enroll in clinical trials, leaving evidence gaps for patient populations not enrolled in trials. In addition, clinical trial populations often differ from the overall cancer population with respect to age, race, performance status, and other clinical parameters. MATERIALS AND METHODS: Working with subscribing practices, CancerLinQ accepts data from electronic health records and transforms the local representation of a patient's care into a standardized representation on the basis of the Quality Data Model from the National Quality Forum. CancerLinQ provides this information back to the subscribing practice through a series of tools that support quality improvement. CancerLinQ also creates de-identified data sets for secondary research use. RESULTS: As of March 2020, CancerLinQ includes data from 63 organizations across the United States that use nine different electronic health records. The database includes 1,426,015 patients with a primary cancer diagnosis, of which 238,680 have had additional information abstracted from unstructured content. CONCLUSION: As CancerLinQ continues to onboard subscribing practices, the breadth of potential applications for a learning health care system widen. Future practice-facing tools could include real-world data visualization, recommendations for treatment of patients with actionable genetic variations, and identification of patients who may be eligible for clinical trials. Feeding these insights back into oncology practice ensures that we learn how to treat patients with cancer not just on the basis of the selective experience of the 5% that enroll in clinical trials, but from the real-world experience of the entire spectrum of patients with cancer in the United States.


Assuntos
Registros Eletrônicos de Saúde , Neoplasias , Confiabilidade dos Dados , Humanos , Oncologia , Neoplasias/epidemiologia , Neoplasias/terapia , Sociedades Médicas , Estados Unidos/epidemiologia
2.
JCO Clin Cancer Inform ; 2: 1-10, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30652592

RESUMO

PURPOSE: A joint data quality initiative between the Cancer Treatment Centers of America and the ASCO big data health technology platform CancerLinQ® was initiated to document and codify the steps taken to evaluate, stratify, and determine the potential effect of data elements used for electronic clinical quality measures as captured within structured fields in electronic health records. METHODS: The processes involved the identification of clinical concepts required in measure population criteria and then to map these to the corresponding components of the CancerLinQ data model. A quantitative assessment of mappings between electronic clinical quality measure clinical concepts and attributes from the CancerLinQ clinical database was performed. In parallel, a qualitative analysis of high-impact data elements from the Cancer Treatment Centers of America clinical measures was made using local, expert consensus. RESULTS: An impact assessment was derived using a count of the data elements across measures and the specific population criteria affected. CONCLUSION: A list of putative high-impact data elements can provide guidance for clinicians to facilitate specific data element capture related to quality metrics in an electronic environment.


Assuntos
Registros Eletrônicos de Saúde/normas , Oncologia/organização & administração , Sociedades Médicas/organização & administração , Confiabilidade dos Dados , Atenção à Saúde , Estudos de Avaliação como Assunto , Humanos
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