Evidence map›Paper›PMID 35915738›Full record

ArticleInternational journal of chronic obstructive pulmonary disease2022

Single-Inhaler Triple Therapy in Patients with Advanced COPD: Bayesian Modeling of the Healthcare Resource Utilization Data and Associated Costs from the IMPACT Trial.

Andrea Gabrio, Necdet B Gunsoy, Gianluca Baio, Alan Martin, Victoria F Paly, Nancy Risebrough, David M G Halpin, Dave Singh, Robert A Wise, MeiLan K Han and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in International journal of chronic obstructive pulmonary disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02164513 (A Phase III, 52 Week, Randomized, Double-blind, 3-arm Parallel Group Study, Comparing the Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination FF/UMEC/VI With the Fixed Dose Dual Combinations of FF/VI and UMEC/VI, All Administered Once-daily in the Morning Via a Dry Powder Inhaler in Subjects With Chronic Obstructive Pulmonary Disease), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02164513 phase3completednot on this map

A Phase III, 52 Week, Randomized, Double-blind, 3-arm Parallel Group Study, Comparing the Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination FF/UMEC/VI With the Fixed Dose Dual Combinations of FF/VI and UMEC/VI, All Administered Once-daily in the Morning Via a Dry Powder Inhaler in Subjects With Chronic Obstructive Pulmonary Disease

TypeinterventionalSponsorGlaxoSmithKlineRan2014 to 2017Enrolled10,355ConditionsPulmonary Disease, Chronic ObstructiveArmsfluticasone furoate (FF), vilanterol (VI), umeclidinium bromide (UMEC)
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 9 institutions in 3 countries.

Andrea GabrioUCL Statistical Science, University College London, London, UK.
Necdet B GunsoyValue Evidence & Outcomes, GlaxoSmithKline, Brentford, UK.
Gianluca BaioUCL Statistical Science, University College London, London, UK.ORCID 0000-0003-4314-2570
Alan MartinValue Evidence and Outcomes, GlaxoSmithKline, Uxbridge, UK.ORCID 0000-0002-3673-3383
Victoria F PalyGlobal HTA, Health Economics, Reimbursement & Outcomes, ICON Plc., Philadelphia, PA, USA.ORCID 0000-0003-3508-1296
Nancy RisebroughGlobal HTA, Health Economics, Reimbursement & Outcomes, ICON plc., Toronto, ON, Canada.
David M G HalpinUniversity of Exeter Medical School, College of Medicine and Health, University of Exeter, Exeter, UK.ORCID 0000-0003-2009-4406
Dave SinghThe Centre for Respiratory Medicine and Allergy, Institute of Inflammation and Repair, Manchester Academic Health Science Centre, University of Manchester, Manchester University NHS Foundation Trust, Manchester, UK.
Robert A WiseThe Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-8353-2349
MeiLan K HanUniversity of Michigan, Pulmonary & Critical Care, Ann Arbor, MI, USA.
Fernando J MartinezJoan and Sandy Weill Department of Medicine, New York-Presbyterian Hospital/Weill Cornell Medical Center, New York, NY, USA.ORCID 0000-0002-2412-3182
Gerard J CrinerLewis Katz School of Medicine, Temple University, Philadelphia, PA, USA.
Neil MartinGlobal Medical Affairs, GlaxoSmithKline, Uxbridge, UK.
David A LipsonDevelopment Clinical Sciences, GlaxoSmithKline, Collegeville, PA, USA.ORCID 0000-0001-6732-4593
Afisi S IsmailaValue Evidence and Outcomes, GlaxoSmithKline, Collegeville, PA, USA.ORCID 0000-0002-2876-8308
GlaxoSmithKline (United Kingdom) · GBGlaxoSmithKline (United States) · USUniversity College London · GBJohns Hopkins University · USManchester Academic Health Science Centre · GBNewYork–Presbyterian Hospital · USTemple University · USUniversity of Exeter · GBUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: In the IMPACT trial (NCT02164513), triple therapy with fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) showed clinical benefit compared with dual therapy with either FF/VI or UMEC/VI in the treatment of chronic obstructive pulmonary disease (COPD). We used data from IMPACT to determine whether this translated into differences in COPD-related healthcare resource utilization (HRU) costs in a United Kingdom (UK) setting. Methods: In a within-trial analysis, individual patient data from the IMPACT intention-to-treat (ITT) population were analyzed to estimate rates of COPD-related HRU with FF/UMEC/VI, FF/VI, or UMEC/VI. A Bayesian approach was applied to address issues typically encountered with this kind of data, namely data missing due to early study withdrawal, subjects with zero reported HRU, and skewness. Rates of HRU were estimated under alternate assumptions of data being missing at random (MAR) or missing not at random (MNAR). UK-specific unit costs were then applied to estimated HRU rates to calculate treatment-specific costs. Results: Under each MNAR scenario, per patient per year (PPPY) rates of COPD-related HRU were lowest amongst those patients who received treatment with FF/UMEC/VI compared with those receiving either FF/VI or UMEC/VI. Although absolute HRU rates and costs were typically higher for all treatment groups under MNAR scenarios versus MAR, final economic conclusions were robust to patient withdrawals. Conclusions: PPPY rates were typically lower with FF/UMEC/VI versus FF/VI or UMEC/VI.

Indexed as

Pulmonary Disease, Chronic ObstructiveAdministration, InhalationAndrostadienesBayes TheoremBenzyl AlcoholsBronchodilator AgentsChlorobenzenesDelivery of Health CareDouble-Blind MethodDrug CombinationsFluticasoneHumansNebulizers and VaporizersQuinuclidinesAndrostadienesBenzyl AlcoholsBronchodilator AgentsChlorobenzenesDrug CombinationsFluticasoneQuinuclidinesCOPDcosthealthcare resource usesingle-inhaler triple therapy

Identifiers

PMID35915738
PMCPMC9338436
OpenAlexW4287222255

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.