National Emphysema Treatment Trial (NETT)
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Accession Number
HLB00560616a
Study Type
Clinical Trial
Collection Type
Open BioLINCC Study
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Study Period
1996-2005
NHLBI Division
DLD
Dataset(s) Last Updated
January 3, 2018
Clinical Trial URLs
https://clinicaltrials.gov/ct2/show/NCT00000606
Primary Publication URLs
https://www.ncbi.nlm.nih.gov/pubmed/12759479
Consent
Commercial Use Data Restrictions No
Data Restrictions Based On Area Of Research No
Available Data
The current release of the NETT study dataset includes follow-up data through May of 2013
Objectives
To compare lung-volume-reduction surgery with medical therapy for severe emphysema, and to identify patient selection criteria for lung volume reduction surgery.
Background
Lung-volume-reduction surgery has been proposed as a palliative treatment for severe emphysema. Effects on mortality, the magnitude and durability of benefits, and criteria for the selection of patients have not been established.
Participants
A total of 1,218 patients with severe emphysema underwent pulmonary rehabilitation and were randomly assigned at 17 centers to undergo lung-volume-reduction surgery (bilateral stapled wedge resection) or to receive continued medical treatment. Patients were randomized after a 6-10 week pulmonary rehabilitation period and patients with a forced expiratory volume in one second (FEV1) that was 20 percent or less of predicted and a homogeneous distribution of emphysema or carbon monoxide diffusing capacity 20 percent or less of predicted were not eligible for randomization due to poor post-surgery prognosis for death or functional improvement.
Conclusions
Overall, lung-volume-reduction surgery increases the chance of improved exercise capacity but does not confer a survival advantage over medical therapy. It does yield a survival advantage for patients with both predominantly upper-lobe emphysema and low base-line exercise capacity. Patients previously reported to be at high risk and those with non-upper-lobe emphysema and high base-line exercise capacity are poor candidates for lung-volume-reduction surgery, because of increased mortality and negligible functional gain. (NEJM 2003;348:2059-2073).
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Resources Available
Study Datasets OnlyStudy Documents
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