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Cardiovascular: Brief reports

‘Real-life’ information on pulmonary arterial hypertension: the iPHnet Project

, , , , , , , , & show all
Pages 2409-2414 | Accepted 28 Aug 2014, Published online: 24 Sep 2014
 

Abstract

Background:

Over the last two decades the development and analysis of a number of registries have enhanced the knowledge of the epidemiology, presentation, natural history, and pathophysiology of pulmonary arterial hypertension (PAH). The understanding of the effectiveness of available treatments has also been greatly improved. However, most of the registries present some methodological issues, such as differences in the classification of patients and presence of confounding factors or missing values, that can impact on the generalizability of the results.

Objective:

The aim of this study is to present the Italian Pulmonary Hypertension Network (iPHnet) Project, a database used to collect health records on patients with PAH that can also be used for research purposes to retrieve ad hoc information.

Results:

iPHnet presents various characteristics such as facilitated access, data sharing and interoperability, update, patient’s anonymity and data integrity. The system also enables the creation of patients’ electronic health records (EHRs), the exportation and personalization of data and the possibility to design clinical report forms (CRFs) and collect information usable in clinical trials. In addition, it is possible to analyze the information present in the registry, creating graphs or other immediately available charts to evaluate the trends of a specific data and perform therapeutic or clinic adjustments. Treatment of data in the iPHnet database complies with FDA requirements, backup and disaster recovery policies and patients’ privacy.

Conclusions:

iPHnet is a flexible tool that integrates the capabilities of an EHR for PAH patients with those of a PAH registry. The ability to retrieve relevant information – although with all the limitations of any registry-based analysis – and to create appropriate CRFs will facilitate the development of prospective and retrospective trials aimed at providing new ‘real-life’ evidence on PAH.

Transparency

Declaration of funding

The authors confirm that the study has no third party funding/sponsorship. Editorial assistance was supported by internal funds.

Declaration of financial/other relationships

R.P., S.G., M.D’A., P.V., M.M., C.A., F.P., R.B., F.F. and C.D.V. have disclosed that they have no significant relationships with or financial interests in any commercial companies related to this study or article.

CMRO peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

Acknowledgments

Editorial assistance for the preparation of this manuscript was provided by Sara Marceglia PhD, Ambra Corti, and Luca Giacomelli PhD, this latter as attendee of the event: ‘Ipertensione Polmonare: il network come strumento per l’appropriatezza diagnostica-terapeutica’ held in Rome, 29 November 2013, on behalf of Content Ed Net.

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