Literature DB >> 25418756

Contemporary roles of registries in clinical cardiology: when do we need randomized trials?

Francesca Ieva1, Chris P Gale, Linda D Sharples.   

Abstract

Clinical registries are established as tools for auditing clinical standards and benchmarking quality improvement initiatives. They also have an emerging role (as electronic health records) in cardiovascular research and, in particular, the conduct of RCTs. While the RCT is accepted as the most robust experimental design, observational data from clinical registries has become increasingly valuable for RCTs. Data from clinical registries may be used to augment results from RCTs, identify patients for recruitment and as an alternative when randomization is not practically possible or ethically desirable. Here the authors appraise the advantages and disadvantages of both methodologies, with the aim of clarifying when their joint use may be successful.

Entities:  

Keywords:  clinical cardiology; clinical practice; clinical registries; evidence based medicine; observational data; randomized controlled trials; routinely collected data

Mesh:

Year:  2014        PMID: 25418756     DOI: 10.1586/14779072.2015.982096

Source DB:  PubMed          Journal:  Expert Rev Cardiovasc Ther        ISSN: 1477-9072


  9 in total

Review 1.  Determining the Suitability of Registries for Embedding Clinical Trials in the United States: A Project of the Clinical Trials Transformation Initiative.

Authors:  J Stephen Mikita; Jules Mitchel; Nicolle M Gatto; John Laschinger; James E Tcheng; Emily P Zeitler; Arlene S Swern; E Dawn Flick; Christopher Dowd; Theodore Lystig; Sara B Calvert
Journal:  Ther Innov Regul Sci       Date:  2020-06-22       Impact factor: 1.778

Review 2.  Addressing the Heterogeneity of Heart Failure in Future Randomized Trials.

Authors:  Annamaria Iorio; Andrea Pozzi; Michele Senni
Journal:  Curr Heart Fail Rep       Date:  2017-06

3.  Dynamic clustering of hazard functions: an application to disease progression in chronic heart failure.

Authors:  Francesca Ieva; Anna Maria Paganoni; Teresa Pietrabissa
Journal:  Health Care Manag Sci       Date:  2016-02-04

4.  Multi-state modelling of repeated hospitalisation and death in patients with heart failure: The use of large administrative databases in clinical epidemiology.

Authors:  Francesca Ieva; Christopher H Jackson; Linda D Sharples
Journal:  Stat Methods Med Res       Date:  2015-03-26       Impact factor: 3.021

5.  Methodological issues on the use of administrative data in healthcare research: the case of heart failure hospitalizations in Lombardy region, 2000 to 2012.

Authors:  Cristina Mazzali; Anna Maria Paganoni; Francesca Ieva; Cristina Masella; Mauro Maistrello; Ornella Agostoni; Simonetta Scalvini; Maria Frigerio
Journal:  BMC Health Serv Res       Date:  2016-07-08       Impact factor: 2.655

6.  Multi-state modelling of heart failure care path: A population-based investigation from Italy.

Authors:  Francesca Gasperoni; Francesca Ieva; Giulia Barbati; Arjuna Scagnetto; Annamaria Iorio; Gianfranco Sinagra; Andrea Di Lenarda
Journal:  PLoS One       Date:  2017-06-07       Impact factor: 3.240

Review 7.  Defining key design elements of registry-based randomised controlled trials: a scoping review.

Authors:  Bill Karanatsios; Khic-Houy Prang; Ebony Verbunt; Justin M Yeung; Margaret Kelaher; Peter Gibbs
Journal:  Trials       Date:  2020-06-22       Impact factor: 2.279

8.  Patient focused registries can improve health, care, and science.

Authors:  Eugene C Nelson; Mary Dixon-Woods; Paul B Batalden; Karen Homa; Aricca D Van Citters; Tamara S Morgan; Elena Eftimovska; Elliott S Fisher; John Ovretveit; Wade Harrison; Cristin Lind; Staffan Lindblad
Journal:  BMJ       Date:  2016-07-01

Review 9.  Establishing Patient Registries for Rare Diseases: Rationale and Challenges.

Authors:  Vanessa Boulanger; Marissa Schlemmer; Suzanne Rossov; Allison Seebald; Pamela Gavin
Journal:  Pharmaceut Med       Date:  2020-06
  9 in total

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