Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Mar 16;6(1):e16.
doi: 10.2196/medinform.9680.

Effect of Seasonal Variation on Clinical Outcome in Patients with Chronic Conditions: Analysis of the Commonwealth Scientific and Industrial Research Organization (CSIRO) National Telehealth Trial

Affiliations

Effect of Seasonal Variation on Clinical Outcome in Patients with Chronic Conditions: Analysis of the Commonwealth Scientific and Industrial Research Organization (CSIRO) National Telehealth Trial

Ahmadreza Argha et al. JMIR Med Inform. .

Abstract

Background: Seasonal variation has an impact on the hospitalization rate of patients with a range of cardiovascular diseases, including myocardial infarction and angina. This paper presents findings on the influence of seasonal variation on the results of a recently completed national trial of home telemonitoring of patients with chronic conditions, carried out at five locations along the east coast of Australia.

Objective: The aim is to evaluate the effect of the seasonal timing of hospital admission and length of stay on clinical outcome of a home telemonitoring trial involving patients (age: mean 72.2, SD 9.4 years) with chronic conditions (chronic obstructive pulmonary disease coronary artery disease, hypertensive diseases, congestive heart failure, diabetes, or asthma) and to explore methods of minimizing the influence of seasonal variations in the analysis of the effect of at-home telemonitoring on the number of hospital admissions and length of stay (LOS).

Methods: Patients were selected from a hospital list of eligible patients living with a range of chronic conditions. Each test patient was case matched with at least one control patient. A total of 114 test patients and 173 control patients were available in this trial. However, of the 287 patients, we only considered patients who had one or more admissions in the years from 2010 to 2012. Three different groups were analyzed separately because of substantially different climates: (1) Queensland, (2) Australian Capital Territory and Victoria, and (3) Tasmania. Time series data were analyzed using linear regression for a period of 3 years before the intervention to obtain an average seasonal variation pattern. A novel method that can reduce the impact of seasonal variation on the rate of hospitalization and LOS was used in the analysis of the outcome variables of the at-home telemonitoring trial.

Results: Test patients were monitored for a mean 481 (SD 77) days with 87% (53/61) of patients monitored for more than 12 months. Trends in seasonal variations were obtained from 3 years' of hospitalization data before intervention for the Queensland, Tasmania, and Australian Capital Territory and Victoria subgroups, respectively. The maximum deviation from baseline trends for LOS was 101.7% (SD 42.2%), 60.6% (SD 36.4%), and 158.3% (SD 68.1%). However, by synchronizing outcomes to the start date of intervention, the impact of seasonal variations was minimized to a maximum of 9.5% (SD 7.7%), thus improving the accuracy of the clinical outcomes reported.

Conclusions: Seasonal variations have a significant effect on the rate of hospital admission and LOS in patients with chronic conditions. However, the impact of seasonal variation on clinical outcomes (rate of admissions, number of hospital admissions, and LOS) of at-home telemonitoring can be attenuated by synchronizing the analysis of outcomes to the commencement dates for the telemonitoring of vital signs.

Trial registration: Australian New Zealand Clinical Trial Registry ACTRN12613000635763; https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=364030&isReview=true (Archived by WebCite at http://www.webcitation.org/ 6xLPv9QDb).

Keywords: chronic disease; clinical trial; seasonal variation; telehealth; telemonitoring; vital signs.

PubMed Disclaimer

Conflict of interest statement

Conflicts of Interest: There was no conflict of interest during the planning and execution of the project. Six months after its completion, BGC, Chief Investigator and Project Director, was appointed to a part-time position at Telemedcare Pty Ltd as Director of Research.

Figures

Figure 1
Figure 1
Final cohort of seasonal variation group.
Figure 2
Figure 2
Length of stay (LOS) versus hospital admissions for 136 (test and control) patients in years 2010 to 2012. Correlation coefficient=0.86. Solid line is the linear regression line (slope=6.31, intercept=–11.17, R2=.73), and dotted lines are 95% prediction bounds (slope=4.98, 7.63 and intercept=–36.59, 14.24).
Figure 3
Figure 3
Length of stay for 37 (test and control) patients of Queensland subgroup in years 2010 to 2012. Solid line is the linear regression line (slope=1.12, intercept=6.32, R2=.33), and dotted lines are 95% prediction bounds (slope=0.56, 1.67 and intercept=–5.41, 18.06).
Figure 4
Figure 4
Deviation from baseline (fitted values) in length of stay of 37 (test and control) patients of Queensland subgroup in years 2010 to 2012.
Figure 5
Figure 5
Average deviation from baseline: seasonal variation trend of length of stay in hospital for Queensland patients.
Figure 6
Figure 6
Distribution of commencement dates for monitoring of vital signs.
Figure 7
Figure 7
Estimated seasonal variation impact on length of stay with synchronized commencement days at different trial sites in Australia. QLD: Queensland, TAS: Tasmania, ACT: Australian Capital Territory, VIC: Victoria.
Figure 8
Figure 8
The formula to obtain the synchronized seasonal profile.

Similar articles

Cited by

References

    1. Bashshur RL, Shannon GW, Smith BR, Alverson DC, Antoniotti N, Barsan WG, Bashshur N, Brown EM, Coye MJ, Doarn CR, Ferguson S, Grigsby J, Krupinski EA, Kvedar JC, Linkous J, Merrell RC, Nesbitt T, Poropatich R, Rheuban KS, Sanders JH, Watson AR, Weinstein RS, Yellowlees P. The empirical foundations of telemedicine interventions for chronic disease management. Telemed J E Health. 2014 Sep;20(9):769–800. doi: 10.1089/tmj.2014.9981. http://europepmc.org/abstract/MED/24968105 - DOI - PMC - PubMed
    1. Bashshur RL, Howell JD, Krupinski EA, Harms KM, Bashshur N, Doarn CR. The empirical foundations of telemedicine interventions in primary care. Telemed J E Health. 2016 May;22(5):342–375. doi: 10.1089/tmj.2016.0045. http://europepmc.org/abstract/MED/27128779 - DOI - PMC - PubMed
    1. Steventon A, Bardsley M, Billings J, Dixon J, Doll H, Hirani S, Cartwright M, Rixon L, Knapp M, Henderson C, Rogers A, Fitzpatrick R, Hendy J, Newman S, Whole System Demonstrator Evaluation Team BMJ. 2012. Jun 21, [2018-02-26]. Effect of telehealth on use of secondary care and mortality: findings from the Whole System Demonstrator cluster randomised trial https://sso.lib.uts.edu.au/cas/login?service=https%3A%2F%2Fwww.lib.uts.e... 6xWt9AoOR. - PMC - PubMed
    1. Brown EM. The Ontario Telemedicine Network: a case report. Telemed J E Health. 2013 May;19(5):373–376. doi: 10.1089/tmj.2012.0299. - DOI - PubMed
    1. Paré G, Jaana M, Sicotte C. Systematic review of home telemonitoring for chronic diseases: the evidence base. J Am Med Inform Assoc. 2007 May;14(3):269–277. doi: 10.1197/jamia.M2270. https://sso.lib.uts.edu.au/cas/login?service=https%3A%2F%2Fwww.lib.uts.e... - DOI - PMC - PubMed

LinkOut - more resources