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2015 ; 19
(81
): 1-246
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gab.com Text
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English Wikipedia
The cost-effectiveness of domiciliary non-invasive ventilation in patients with
end-stage chronic obstructive pulmonary disease: a systematic review and economic
evaluation
#MMPMID26470875
Dretzke J
; Blissett D
; Dave C
; Mukherjee R
; Price M
; Bayliss S
; Wu X
; Jordan R
; Jowett S
; Turner AM
; Moore D
Health Technol Assess
2015[Oct]; 19
(81
): 1-246
PMID26470875
show ga
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a chronic progressive
lung disease characterised by non-reversible airflow obstruction. Exacerbations
are a key cause of morbidity and mortality and place a considerable burden on
health-care systems. While there is evidence that patients benefit from
non-invasive ventilation (NIV) in hospital during an acute exacerbation, evidence
supporting home use for more stable COPD patients is limited. In the U.K.,
domiciliary NIV is considered on health economic grounds in patients after three
hospital admissions for acute hypercapnic respiratory failure. OBJECTIVE: To
assess the clinical effectiveness and cost-effectiveness of domiciliary NIV by
systematic review and economic evaluation. DATA SOURCES: Bibliographic databases,
conference proceedings and ongoing trial registries up to September 2014.
METHODS: Standard systematic review methods were used for identifying relevant
clinical effectiveness and cost-effectiveness studies assessing NIV compared with
usual care or comparing different types of NIV. Risk of bias was assessed using
Cochrane guidelines and relevant economic checklists. Results for primary
effectiveness outcomes (mortality, hospitalisations, exacerbations and quality of
life) were presented, where possible, in forest plots. A speculative Markov
decision model was developed to compare the cost-effectiveness of domiciliary NIV
with usual care from a UK perspective for post-hospital and more stable
populations separately. RESULTS: Thirty-one controlled effectiveness studies were
identified, which report a variety of outcomes. For stable patients, a modest
volume of evidence found no benefit from domiciliary NIV for survival and some
non-significant beneficial trends for hospitalisations and quality of life. For
post-hospital patients, no benefit from NIV could be shown in terms of survival
(from randomised controlled trials) and findings for hospital admissions were
inconsistent and based on limited evidence. No conclusions could be drawn
regarding potential benefit from different types of NIV. No cost-effectiveness
studies of domiciliary NIV were identified. Economic modelling suggested that NIV
may be cost-effective in a stable population at a threshold of £30,000 per
quality-adjusted life-year (QALY) gained (incremental cost-effectiveness ratio
£28,162), but this is associated with uncertainty. In the case of the
post-hospital population, results for three separate base cases ranged from usual
care dominating to NIV being cost-effective, with an incremental
cost-effectiveness ratio of less than £10,000 per QALY gained. All estimates were
sensitive to effectiveness estimates, length of benefit from NIV (currently
unknown) and some costs. Modelling suggested that reductions in the rate of
hospital admissions per patient per year of 24% and 15% in the stable and
post-hospital populations, respectively, are required for NIV to be
cost-effective. LIMITATIONS: Evidence on key clinical outcomes remains limited,
particularly quality-of-life and long-term (>?2 years) effects. Economic
modelling should be viewed as speculative because of uncertainty around effect
estimates, baseline risks, length of benefit of NIV and limited
quality-of-life/utility data. CONCLUSIONS: The cost-effectiveness of domiciliary
NIV remains uncertain and the findings in this report are sensitive to emergent
data. Further evidence is required to identify patients most likely to benefit
from domiciliary NIV and to establish optimum time points for starting NIV and
equipment settings. FUTURE WORK RECOMMENDATIONS: The results from this report
will need to be re-examined in the light of any new trial results, particularly
in terms of reducing the uncertainty in the economic model. Any new randomised
controlled trials should consider including a sham non-invasive ventilation arm
and/or a higher- and lower-pressure arm. Individual participant data analyses may
help to determine whether or not there are any patient characteristics or
equipment settings that are predictive of a benefit of NIV and to establish
optimum time points for starting (and potentially discounting) NIV. STUDY
REGISTRATION: This study is registered as PROSPERO CRD42012003286. FUNDING: The
National Institute for Health Research Health Technology Assessment programme.