Impact of Non-invasive Ventilation in Hypercapnic COPD
Status: | Recruiting |
---|---|
Conditions: | Chronic Obstructive Pulmonary Disease, Pulmonary, Pulmonary |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 45 - 75 |
Updated: | 5/13/2018 |
Start Date: | April 23, 2018 |
End Date: | April 22, 2020 |
Contact: | Jeremy E Orr, MD |
Email: | sleepresearch@ucsd.edu |
Phone: | 858-246-2154 |
Impact of Non-invasive Ventilation on Biomarkers in Hypercapnic COPD
Chronic obstructive pulmonary disease (COPD) is a highly prevalent condition worldwide and is
a cause of substantial morbidity and mortality. Unfortunately, few therapies have been shown
to improve survival. The importance of systemic effects and co-morbidities in COPD has
garnered attention based on the observation that many patients with COPD die from causes
other than respiratory failure, including a large proportion from cardiovascular causes.
Recently, two high profile randomized trials have shown substantial improvements in morbidity
and mortality with use of nocturnal non-invasive ventilation (NIV) in COPD patients with
hypercapnia. Although the mechanisms by which NIV improves outcomes remain unclear, the
important benefits of NIV might be cardiovascular via a number of mechanisms. In contrast to
prior trials of NIV in COPD that did not show substantial benefit, a distinguishing feature
of these encouraging recent NIV clinical trials was a prominent reduction of hypercapnia,
which might be a maker or mediator of effective therapy. Alternatively, improvements might be
best achieved by targeting a different physiological measure. Additional mechanistic data are
therefore needed to inform future trials and achieve maximal benefit of NIV. Recent work in
cardiovascular biomarkers has identified high-sensitivity troponin to have substantial
ability to determine cardiovascular stress in a variety of conditions - even with only small
changes. In COPD, a number of observational studies have shown that high-sensitivity troponin
increases with worsening disease severity, and that levels increase overnight during sleep.
This biomarker therefore presents a promising means to study causal pathways regarding the
effect of NIV in patients with COPD. With this background, the investigator's overall goals
are: 1) To determine whether the beneficial effect of non-invasive ventilation might be due
to a reduction in cardiovascular stress, using established cardiovascular biomarkers, and 2)
To define whether a reduction in PaCO2 (or alternative mechanism) is associated with such an
effect.
a cause of substantial morbidity and mortality. Unfortunately, few therapies have been shown
to improve survival. The importance of systemic effects and co-morbidities in COPD has
garnered attention based on the observation that many patients with COPD die from causes
other than respiratory failure, including a large proportion from cardiovascular causes.
Recently, two high profile randomized trials have shown substantial improvements in morbidity
and mortality with use of nocturnal non-invasive ventilation (NIV) in COPD patients with
hypercapnia. Although the mechanisms by which NIV improves outcomes remain unclear, the
important benefits of NIV might be cardiovascular via a number of mechanisms. In contrast to
prior trials of NIV in COPD that did not show substantial benefit, a distinguishing feature
of these encouraging recent NIV clinical trials was a prominent reduction of hypercapnia,
which might be a maker or mediator of effective therapy. Alternatively, improvements might be
best achieved by targeting a different physiological measure. Additional mechanistic data are
therefore needed to inform future trials and achieve maximal benefit of NIV. Recent work in
cardiovascular biomarkers has identified high-sensitivity troponin to have substantial
ability to determine cardiovascular stress in a variety of conditions - even with only small
changes. In COPD, a number of observational studies have shown that high-sensitivity troponin
increases with worsening disease severity, and that levels increase overnight during sleep.
This biomarker therefore presents a promising means to study causal pathways regarding the
effect of NIV in patients with COPD. With this background, the investigator's overall goals
are: 1) To determine whether the beneficial effect of non-invasive ventilation might be due
to a reduction in cardiovascular stress, using established cardiovascular biomarkers, and 2)
To define whether a reduction in PaCO2 (or alternative mechanism) is associated with such an
effect.
Inclusion Criteria:
- Subjects with previously diagnosed severe COPD (FEV1 <50% predicted) and daytime
hypercapnia (PaCO2 or TcCO2 > 45 mmHg)
Exclusion Criteria:
- Lung disease besides COPD (e.g., pulmonary fibrosis, bronchiectasis, pulmonary
arterial hypertension) other than well controlled asthma
- Unrevascularized coronary artery disease, angina, prior heart attack or stroke,
congestive heart failure
- Uncontrolled hypertension (SBP >160, DBP >95)
- Unwilling or unable to withhold CPAP during polysomnography
- Presence of tracheostomy
- Hospitalization within the past 90 days
- Prior peptic ulcer disease, esophageal varicies, or gastrointestinal bleeding (< 5
years)
- Prior gastric bypass surgery
- Anticoagulant use (other than aspirin) or bleeding diathesis (only for esophageal
catheter placement)
- Chronic liver disease or end-stage kidney disease
- Allergy to any of the study medications
- Regular use of medications known to affect control of breathing (opioids,
benzodiazepines, theophylline)
- Insomnia or circadian rhythm disorder
- Active illicit substance use or >3 oz nightly alcohol use
- Psychiatric disease, other than controlled depression
- Pregnancy
- Prisoners
- Cognitive impairment, unable to provide consent, or unable to carry out research
procedures
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