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Strategies for secondary use of real-world clinical and administrative data for outcome ascertainment in pragmatic clinical trials.
Hau, Cynthia; Woods, Patricia A; Guski, Amanda S; Raju, Srihari I; Zhu, Liang; Alba, Patrick R; Cushman, William C; Glassman, Peter A; Ishani, Areef; Taylor, Addison A; Ferguson, Ryan E; Leatherman, Sarah M.
Afiliação
  • Hau C; Cooperative Studies Program Coordinating Center, VA Boston Healthcare System, Boston, MA, United States. Electronic address: cynthia.hau@va.gov.
  • Woods PA; Cooperative Studies Program Coordinating Center, VA Boston Healthcare System, Boston, MA, United States.
  • Guski AS; Cooperative Studies Program Coordinating Center, VA Boston Healthcare System, Boston, MA, United States.
  • Raju SI; Minneapolis VA Healthcare System, Minneapolis, MN, United States.
  • Zhu L; Cooperative Studies Program Coordinating Center, VA Boston Healthcare System, Boston, MA, United States.
  • Alba PR; VA Informatics and Computing Infrastructure, Salt Lake City VA Healthcare System, Salt Lake City, CT, United States; Division of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT, United States.
  • Cushman WC; Medical Service, Memphis VA Medical Center, Memphis, TN, United States; Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, United States.
  • Glassman PA; Pharmacy Benefits Management Services, Department of Veterans Affairs, Washington DC, United States; VA Greater Los Angeles Healthcare System, Los Angeles, CA, United States; David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
  • Ishani A; Minneapolis VA Healthcare System, Minneapolis, MN, United States; Department of Medicine, University of Minnesota, Minneapolis, MN, United States.
  • Taylor AA; Michael E. DeBakey VA Medical Center, Houston, TX, United States; Baylor College of Medicine, Department of Medicine, Houston, TX, United States.
  • Ferguson RE; Cooperative Studies Program Coordinating Center, VA Boston Healthcare System, Boston, MA, United States; Department of Medicine, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, United States.
  • Leatherman SM; Cooperative Studies Program Coordinating Center, VA Boston Healthcare System, Boston, MA, United States; Department of Biostatistics, Boston University School of Public Health, Boston, MA, United States.
J Biomed Inform ; 150: 104587, 2024 02.
Article em En | MEDLINE | ID: mdl-38244956
ABSTRACT

BACKGROUND:

Pragmatic trials are gaining popularity as a cost-effective way to examine treatment effectiveness and generate timely comparative evidence. Incorporating supplementary real-world data is recommended for robust outcome monitoring. However, detailed operational guidelines are needed to inform effective use and integration of heterogeneous databases.

OBJECTIVE:

Lessons learned from the Veterans Affairs (VA) Diuretic Comparison Project (DCP) are reviewed, providing adaptable recommendations to capture clinical outcomes from real-world data.

METHODS:

Non-cancer deaths and major cardiovascular (CV) outcomes were determined using VA, Medicare, and National Death Index (NDI) data. Multiple ascertainment strategies were applied, including claims-based algorithms, natural language processing, and systematic chart review.

RESULTS:

During a mean follow-up of 2.4 (SD = 1.4) years, 907 CV events were identified within the VA healthcare system. Slight delays (∼1 year) were expected in obtaining Medicare data. An additional 298 patients were found having a CV event outside of the VA in 2016 - 2021, increasing the CV event rate from 3.5 % to 5.7 % (770 of 13,523 randomized). NDI data required âˆ¼2 years waiting period. Such inclusion did not increase the number of deaths identified (all 894 deaths were captured by VA data) but enhanced the accuracy in determining cause of death.

CONCLUSION:

Our experience supports the recommendation of integrating multiple data sources to improve clinical outcome ascertainment. While this approach is promising, hierarchical data aggregation is required when facing different acquisition timelines, information availability/completeness, coding practice, and system configurations. It may not be feasible to implement comparable applications and solutions to studies conducted under different constraints and practice. The recommendations provide guidance and possible action plans for researchers who are interested in applying cross-source data to ascertain all study outcomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Pragmáticos como Assunto Tipo de estudo: Clinical_trials / Guideline Limite: Aged / Humans País/Região como assunto: America do norte Idioma: En Revista: J Biomed Inform Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ensaios Clínicos Pragmáticos como Assunto Tipo de estudo: Clinical_trials / Guideline Limite: Aged / Humans País/Região como assunto: America do norte Idioma: En Revista: J Biomed Inform Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article