4.5 Article

Prognostic value of short-term decline of forced expiratory volume in 1 s over height cubed (FEV1/Ht3) in a cohort of adults aged 80 and over

Journal

AGING CLINICAL AND EXPERIMENTAL RESEARCH
Volume 30, Issue 5, Pages 507-516

Publisher

SPRINGER
DOI: 10.1007/s40520-017-0792-x

Keywords

Adults aged 80 and over; FEV1/Ht(3) decline; Mortality; Hospitalization; Disability

Funding

  1. Fondation Louvain, Brussels, Belgium [B40320084685]
  2. ERAWEB 2, Erasmus Mundus program at Katholieke Universiteit Leuven (KU Leuven)

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Background Forced expiratory volume in 1 s over height cubed (FEV1/Ht(3)) is an FEV1 expression that uses no reference values and is independently associated with adverse outcomes in older adults. No studies have reported on the prognostic value of its decline over time in adults aged 80 and over. Aim To investigate the prognostic value of FEV1/Ht(3) decline for adverse outcomes in a cohort of adults aged 80 and over. Methods 328 community-dwelling adults aged 80 and over of the BELFRAIL prospective cohort had two valid FEV1 measurements as part of their comprehensive geriatric assessment at baseline and follow-up (after 1.7 +/- 0.21 years). Kaplan-Meier survival curves, Cox and logistic multivariable regression, assessed association of excessive decline of FEV1/Ht(3) (lowest quintile of percentage change) with all-cause mortality (3 years after follow-up assessment), time to first hospitalization (1 year), and new/worsened disability in activities of daily living (ADL) at the follow-up assessment. Results Participants with excessive FEV1/Ht(3) decline had increased adjusted hazard ratio for all-cause death 1.61 (95% CI 1.01-2.55) and first hospitalization 1.71 (1.08-2.71) and increased odds ratio for new/worsened ADL disability at follow-up 2.02 (1.10-3.68) compared to the rest of the study population. Conclusions Excessive, short-term decline in FEV1/Ht(3) was independently associated with all-cause mortality, time to first, unplanned hospitalization, and ADL disability in a cohort of adults aged 80 and over. This FEV1 expression should be further investigated in studies of longitudinal FEV1 change in older adults.

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