Evidence map›Paper›PMID 37743931›Full record

ArticleMDM policy & practice

The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling Analysis.

Pamela P Pei, Kieran P Fitzmaurice, Mylinh H Le, Christopher Panella, Michelle L Jones, Ankur Pandya, C Robert Horsburgh, Kenneth A Freedberg, Milton C Weinstein, A David Paltiel and 1 more

Abstract read
In one paragraph

Article in MDM policy & practice. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Pamela P PeiMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.ORCID https://orcid.org/0000-0002-6095-8494
Kieran P FitzmauriceMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Mylinh H LeMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Christopher PanellaMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Michelle L JonesMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Ankur PandyaDepartment of Health Policy and Management, Harvard T.H. Chan School of Public Health, Boston, MA, USA.ORCID https://orcid.org/0000-0002-6130-2286
C Robert HorsburghSchool of Public Health and School of Medicine, Boston University, Boston, MA, USA.
Kenneth A FreedbergMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Milton C WeinsteinDepartment of Health Policy and Management, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
A David PaltielPublic Health Modeling Unit, Yale School of Public Health, New Haven, CT, USA.
Krishna P ReddyMedical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.

Funding

Novel Methods to Inform HIV/TB Clinical Trial DevelopmentR01AI093269 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI REDDY, KRISHNA P · 2011 to 2024
$6.8M
NIAID NIH HHS R01 AI093269
6 · The paper itself

Abstract

Highlights: In conventional VOI analysis, it is assumed that the optimal decision will always be adopted even without a trial. This can potentially lead to an underestimation of the value of trials when adoption requires new clinical trial evidence. To capture the influence that a trial may have on decision makers' willingness to adopt the optimal decision, we also consider value-of-implementation (VOM), a metric quantifying the benefit of new study information in promoting wider adoption of the optimal strategy. The overall value-of-a-trial (VOT) includes both VOI and VOM.Our model-based analysis suggests that the information obtained from a trial of screening strategies for HIV-associated tuberculosis in South Africa would have no value, when measured using traditional methods of VOI assessment. A novel strategy, which includes the urine FujiLAM test, is optimal from a health economic standpoint but is underutilized. A trial would reduce uncertainties around downstream health outcomes but likely would not change the optimal decision. The high VOT (nearly $700 million over 5 y) lies solely in promoting uptake of FujiLAM, represented as VOM.Our results highlight the importance of employing a more comprehensive approach for evaluating prospective trials, as conventional VOI methods can vastly underestimate their value. Trialists and funders can and should assess the VOT metric instead when considering trial designs and costs. If VOI is low, the VOM and cost of a trial can be compared with the benefits and costs of other outreach programs to determine the most cost-effective way to improve uptake.

Indexed as

HIVtuberculosisvalue-of-implementationvalue-of-information

Identifiers

PMID37743931
PMCPMC10517616

What OpenQuestion holds

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LicenceCC BY-NC
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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.