Development of an Ordinal Scale Treatment Endpoint for Adults Hospitalized With Influenza

Author:

Lee Nelson1ORCID,Smith Stephanie W1,Hui David S C23,Ye Ming4,Zelyas Nathan5,Chan Paul K S36,Drews Steven J5,Zapernick Lori1,Wong Rity2,Labib Mary1,Shokoples Sandy7,Eurich Dean T4

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Canada

2. Department of Medicine, Chinese University of Hong Kong, HKSAR, PRC

3. Stanley Ho Centre for Emerging Infectious Diseases, Chinese University of Hong Kong, HKSAR, PRC

4. School of Public Health, University of Alberta, Edmonton, Canada

5. Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Canada

6. Department of Microbiology, Chinese University of Hong Kong, Hong Kong Special Administrative Region, People’s Republic of China

7. Provincial Laboratory for Public Health, Edmonton, Canada

Abstract

Abstract Background An obstacle in influenza therapeutics development is the lack of clinical endpoints, especially in hospitalized patients. A single time-point binary outcome measure is limited by patients’ diverse clinical trajectories and low event rates. Methods A 6-point ordinal scale with ascending clinical status severity (scoring: discharged; subacute care; acute care without/with respiratory failure; intensive care unit [ICU]; death) was proposed to study outcomes of adults hospitalized with influenza. Individual patient data from 2 active surveillance cohorts’ datasets (2015/2016−2017/2018; Edmonton, Hong Kong) was used for evaluation. The impact of neuraminidase inhibitor (NAI) treatment on longitudinal ordinal outcome changes over 30 days was analyzed using mixed-effects ordinal logistic regression and group-based trajectory models. Results Patient (n = 1226) baseline characteristics included age (mean 68.0 years), virus-type (A 78.1%, B 21.9%), respiratory failure (57.2%), ICU admittance (14.4%), and NAI treatment within 5 days of illness (69.2%). Outcomes at 30 days included discharged (75.2%), subacute care (13.7%), acute care (4.5%), and death (6.6%). Two main clinical trajectories were identified, predictive by baseline scoring (mean ± SD, 4.3 ± 0.6 vs 3.5 ± 0.6, P < .001). Improved outcomes with NAI treatment within 5 days were indicated by significantly lower clinical status scores over time (unadjusted odds ratio [OR], 0.53; 95% confidence interval [CI], .41−.69; P < .001; adjusted OR, 0.62; 95% CI, .50−.77; P < .001, for baseline score, age, and within-patient correlations). In subanalysis, influenza vaccination was also associated with lower scores (adjusted OR, 0.67; 95% CI, .50−.90; P = .007). Analyses of binary endpoints showed insignificant results. Conclusions The ordinal outcome scale is a potentially useful clinical endpoint for influenza therapeutic trials, which could account for the diverse clinical trajectories of hospitalized patients, warranting further development.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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