National Heart & Lung Institute, Imperial College London
Doi
Abstract
The purpose of this thesis was to describe the rate of forced expiratory volume in 1 second (FEV1) decline
in COPD patients seen in primary care and investigate factors associated with the rate to help identify COPD
patients who might decline faster and who may benefit from interventions to slow the rate of FEV1 decline.
The aims of this research were:
i. To describe and explore the rate of FEV1 decline in a primary care COPD population,
ii. To investigate the relationship between inhaled corticosteroids (ICS) and rate of FEV1 decline
in a primary care COPD population, and
iii. To investigate the relationship between the rate of FEV1 decline and future risk of CVD in a
primary care COPD population.
Firstly, other than increasing age, COPD patients who were current smokers, had low BMI, high mMRC
dyspnoea, low baseline FEV1 percent predicted, and more frequent or severe AECOPD were more likely to
have accelerated FEV1 decline. Secondly, a systematic review revealed that COPD patients enrolled in
randomised control trials (RCTs) treated with ICS had reduced rates of FEV1 decline compared to patients
not treated with ICS over short follow-up periods. However, over longer follow-up periods the rate of FEV1
decline in patients in ICS and non-ICS trial arms were similar. In addition, using primary care data, COPD
patients who initiated ICS showed an increase in FEV1, notably in patients with high blood eosinophils,
compared to patients who were not prescribed ICS however, prevalent ICS users had a clinically similar rate
of FEV1 decline compared to those not prescribed ICS, regardless of blood eosinophil level, echoing the
findings of the systematic review. Similarly, COPD patients who withdrew from ICS (from triple therapy)
showed a similar mean rate of FEV1 decline compared to patients who remained on triple therapy. Thirdly,
the rate of FEV1 decline, including accelerated FEV1 decline, was not associated with future risk of CVD
disease and mortality in CVD naïve COPD patients.
These results suggest that rate of FEV1 decline is heterogeneous and both patient related and disease
related characteristics should be monitored to identify COPD patients with faster disease progression
earlier. Whilst these patients may not have an increased risk of CVD, it is still important to identify these
patients to intervene with better treatments or other possible interventions to reduce the risk of all-cause
mortality and other potential morbidities. ICS treatment is a common intervention used to slow the
progression of COPD however, results suggest that its long-term use does not significantly slow down the
rate of FEV1 decline compared to non-ICS medications, but initiation of ICS treatment does improve FEV1
in the short-term. Proactive identification of fast FEV1 decliners and the implementation of effective
interventions in COPD patients by primary care providers may help to improve patient outcomes.Open Acces