Evidence map›Paper›PMID 27576368›Full record

ArticleRheumatology (Oxford, England)2016

A microcosting study of immunogenicity and tumour necrosis factor alpha inhibitor drug level tests for therapeutic drug monitoring in clinical practice.

Meghna Jani, Sean Gavan, Hector Chinoy, William G Dixon, Beverley Harrison, Andrew Moran, Anne Barton, Katherine Payne

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
0.6field-weighted citation impact, top 30% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Article
  8. Economics and Precision Medicine.Handbook of experimental pharmacology · 2023
    Article
  9. Assessing Immunogenicity of Biologic Drugs in Inflammatory Joint Diseases: Progress Towards Personalized Medicine.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2022
    Review
  10. Article
  11. Immunogenicity of biologic agents in rheumatology.Nature reviews. Rheumatology · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. The economic case for precision medicine.Expert review of precision medicine and drug development · 2018
    Article
  16. Article
  17. Article
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

8 authors at 5 institutions in 1 country.

Meghna JaniCentre for Musculoskeletal Research.
Sean GavanManchester Centre for Health Economics, Institute of Population Health, Manchester Academic Health Science Centre University of Manchester.
Hector ChinoyCentre for Musculoskeletal Research.
William G DixonCentre for Musculoskeletal Research.
Beverley HarrisonDepartment of Rheumatology, Salford Royal NHS Foundation Trust, Salford.
Andrew MoranDepartment of Immunology.
Anne BartonCentre for Musculoskeletal Research.
Katherine PayneManchester Centre for Health Economics, Institute of Population Health, Manchester Academic Health Science Centre University of Manchester, katherine.payne@manchester.ac.uk.
Salford Royal NHS Foundation Trust · GBUniversity of Manchester · GBCentre for Inflammation Research · GBManchester Academic Health Science Centre · GBNIHR Oxford Musculoskeletal Biomedical Research Centre · GB

Funding

Medical Research Council G1000417Medical Research Council MR/K015346/1
6 · The paper itself

Abstract

objectivesTo identify and quantify resource required and associated costs for implementing TNF-α inhibitor (TNFi) drug level and anti-drug antibody (ADAb) tests in UK rheumatology practice.

methodsA microcosting study, assuming the UK National Health Service perspective, identified the direct medical costs associated with providing TNFi drug level and ADAb testing in clinical practice. Resource use and costs per patient were identified via four stages: identification of a patient pathway with resource implications; estimation of the resources required; identification of the cost per unit of resource (2015 prices); and calculation of the total costs per patient. Univariate and multiway sensitivity analyses were performed using the variation in resource use and unit costs.

resultsTotal costs for TNFi drug level and concurrent ADAb testing, assessed using ELISAs on trough serum levels, were £152.52/patient (range: £147.68-159.24) if 40 patient samples were tested simultaneously. For the base-case analysis, the pre-testing phase incurred the highest costs, which included booking an additional appointment to acquire trough blood samples. The additional appointment was the key driver of costs per patient (67% of the total cost), and labour accounted for 10% and consumables 23% of the total costs. Performing ELISAs once per patient (rather than in duplicate) reduced the total costs to £133.78/patient.

conclusionThis microcosting study is the first assessing the cost of TNFi drug level and ADAb testing. The results could be used in subsequent cost-effectiveness analyses of TNFi pharmacological tests to target treatments and inform future policy recommendations.

Indexed as

AntibodiesCost-Benefit AnalysisDirect Service CostsDrug MonitoringEnzyme-Linked Immunosorbent AssayHumansRheumatologyState MedicineTumor Necrosis Factor-alphaUnited KingdomAntibodiesTumor Necrosis Factor-alphahealth economicsimmunogenicitymicrocostingopportunity costsTNFi drug levels

Identifiers

PMID27576368
PMCPMC5144665
OpenAlexW2508008033

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.