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. 2016 May 3;5(2):e11.
doi: 10.2196/ijmr.5196.

Telemonitoring in Cystic Fibrosis: A 4-year Assessment and Simulation for the Next 6 Years

Irene Tagliente  1 , Leopoldo Trieste, Terje Solvoll, Fabrizio Murgia, Sergio Bella
Affiliations

Telemonitoring in Cystic Fibrosis: A 4-year Assessment and Simulation for the Next 6 Years

Irene Tagliente et al. Interact J Med Res. .

Abstract

Background: Innovative technologies and informatics offer a wide range of services to health districts, doctors, nurses, and patients, and is changing the traditional concept of health care. In the last few years, the availability of portable devices, their easiness to transport and use, and the capability to collect and transmit various clinical data have resulted in the fast development of telemedicine. However, despite its potential impact in improving patient conditions, and its cost effectiveness reported in literature, telemedicine is not in daily practice.

Objective: The aim of this study is to provide evidence of the positive impact of telemonitoring proving the sustainability of an application by sending spirometry outcomes from patients' homes to the hospital doctors via the Internet, and from doctors to patients by an additional phone call solution.

Methods: We examined collected data related to clinical improvement of patients with cystic fibrosis (CF). The patients were followed-up at home using telemonitoring for a period of 10 years, with the aims to prove the sustainability of the methodology (transmissions of spirometry from the patients' home to the doctors and feedback from the doctors to the patients by phone call from the hospital). We stored and analyzed all spirometry transmissions received, and tested the possible presence to decrease the costs between the standard clinical trial (only ambulatory visits) and standard clinical trial with telemonitoring for the follow-up of patients with CF (telemedicine). This was done through an economic analysis of the costs for patients followed at home by telemonitoring. We assessed four years of observation and a simulation of total long-term costs between 2010 and 2020.

Results: We discovered a potential saving of €40,397.00 per patient for 10 years, actualized at €36,802.97 for the follow-up of all patients enrolled.

Conclusions: The results from the study suggest that telemedicine can improve the health of patients with CF. It is a relatively cheap and potentially sustainable solution, compared to standard clinical trials. However, to establish and prove the long-term effectiveness and cost-effectiveness, more controlled psychological and behavioral studies are needed.

Keywords: cost effectiveness; cystic fibrosis; eHealth; follow-up; telemonitoring.

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Conflict of interest statement

Conflicts of Interest: None declared.

Figures

Figure 1
Figure 1
Screenshot of the software interface.
Figure 2
Figure 2
Economic equations used in the calculations. Equation (a) is the actualization of saving st (t < 2015), and equation (b) is the actualization of saving st (t > 2015).
See this image and copyright information in PMC

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