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

Objectives. Conventional value-of-information (VOI) analysis assumes complete uptake of an optimal decision. We employed an extended framework that includes value-of-implementation (VOM)—the benefit of encouraging adoption of an optimal strategy—and estimated how future trials of diagnostic tests fo...

Full description

Bibliographic Details
Main Authors: 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, Krishna P. Reddy
Format: Article
Language:English
Published: SAGE Publishing 2023-09-01
Series:MDM Policy & Practice
Online Access:https://doi.org/10.1177/23814683231198873
_version_ 1797676751262842880
author 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
Krishna P. Reddy
author_facet 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
Krishna P. Reddy
author_sort Pamela P. Pei
collection DOAJ
description Objectives. Conventional value-of-information (VOI) analysis assumes complete uptake of an optimal decision. We employed an extended framework that includes value-of-implementation (VOM)—the benefit of encouraging adoption of an optimal strategy—and estimated how future trials of diagnostic tests for HIV-associated tuberculosis could improve public health decision making and clinical and economic outcomes. Methods. We evaluated the clinical outcomes and costs, given current information, of 3 tuberculosis screening strategies among hospitalized people with HIV in South Africa: sputum Xpert ( Xpert ), sputum Xpert plus urine AlereLAM ( Xpert+AlereLAM ), and sputum Xpert plus the newer, more sensitive, and costlier urine FujiLAM ( Xpert+FujiLAM ). We projected the incremental net monetary benefit (INMB) of decision making based on results of a trial comparing mortality with each strategy, rather than decision making based solely on current knowledge of FujiLAM’s improved diagnostic performance. We used a validated microsimulation to estimate VOI (the INMB of reducing parameter uncertainty before decision making) and VOM (the INMB of encouraging adoption of an optimal strategy). Results. With current information, adopting Xpert+FujiLAM yields 0.4 additional life-years/person compared with current practices (assumed 50% Xpert and 50% Xpert+AlereLAM ). While the decision to adopt this optimal strategy is unaffected by information from the clinical trial (VOI = $ 0 at $3,000/year-of-life saved willingness-to-pay threshold), there is value in scaling up implementation of Xpert+FujiLAM , which results in an INMB (representing VOM) of $650 million over 5 y. Conclusions. Conventional VOI methods account for the value of switching to a new optimal strategy based on trial data but fail to account for the persuasive value of trials in increasing uptake of the optimal strategy. Evaluation of trials should include a focus on their value in reducing barriers to implementation. 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.
first_indexed 2024-03-11T22:34:50Z
format Article
id doaj.art-6824d4747a2a40a097a453d64002c1c4
institution Directory Open Access Journal
issn 2381-4683
language English
last_indexed 2024-03-11T22:34:50Z
publishDate 2023-09-01
publisher SAGE Publishing
record_format Article
series MDM Policy & Practice
spelling doaj.art-6824d4747a2a40a097a453d64002c1c42023-09-22T20:33:32ZengSAGE PublishingMDM Policy & Practice2381-46832023-09-01810.1177/23814683231198873The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling AnalysisPamela P. PeiKieran P. FitzmauriceMylinh H. LeChristopher PanellaMichelle L. JonesAnkur PandyaC. Robert HorsburghKenneth A. FreedbergMilton C. WeinsteinA. David PaltielKrishna P. ReddyObjectives. Conventional value-of-information (VOI) analysis assumes complete uptake of an optimal decision. We employed an extended framework that includes value-of-implementation (VOM)—the benefit of encouraging adoption of an optimal strategy—and estimated how future trials of diagnostic tests for HIV-associated tuberculosis could improve public health decision making and clinical and economic outcomes. Methods. We evaluated the clinical outcomes and costs, given current information, of 3 tuberculosis screening strategies among hospitalized people with HIV in South Africa: sputum Xpert ( Xpert ), sputum Xpert plus urine AlereLAM ( Xpert+AlereLAM ), and sputum Xpert plus the newer, more sensitive, and costlier urine FujiLAM ( Xpert+FujiLAM ). We projected the incremental net monetary benefit (INMB) of decision making based on results of a trial comparing mortality with each strategy, rather than decision making based solely on current knowledge of FujiLAM’s improved diagnostic performance. We used a validated microsimulation to estimate VOI (the INMB of reducing parameter uncertainty before decision making) and VOM (the INMB of encouraging adoption of an optimal strategy). Results. With current information, adopting Xpert+FujiLAM yields 0.4 additional life-years/person compared with current practices (assumed 50% Xpert and 50% Xpert+AlereLAM ). While the decision to adopt this optimal strategy is unaffected by information from the clinical trial (VOI = $ 0 at $3,000/year-of-life saved willingness-to-pay threshold), there is value in scaling up implementation of Xpert+FujiLAM , which results in an INMB (representing VOM) of $650 million over 5 y. Conclusions. Conventional VOI methods account for the value of switching to a new optimal strategy based on trial data but fail to account for the persuasive value of trials in increasing uptake of the optimal strategy. Evaluation of trials should include a focus on their value in reducing barriers to implementation. 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.https://doi.org/10.1177/23814683231198873
spellingShingle 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
Krishna P. Reddy
The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling Analysis
MDM Policy & Practice
title The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling Analysis
title_full The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling Analysis
title_fullStr The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling Analysis
title_full_unstemmed The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling Analysis
title_short The Value-of-Information and Value-of-Implementation from Clinical Trials of Diagnostic Tests for HIV-Associated Tuberculosis: A Modeling Analysis
title_sort value of information and value of implementation from clinical trials of diagnostic tests for hiv associated tuberculosis a modeling analysis
url https://doi.org/10.1177/23814683231198873
work_keys_str_mv AT pamelappei thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT kieranpfitzmaurice thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT mylinhhle thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT christopherpanella thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT michelleljones thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT ankurpandya thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT croberthorsburgh thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT kennethafreedberg thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT miltoncweinstein thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT adavidpaltiel thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT krishnapreddy thevalueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT pamelappei valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT kieranpfitzmaurice valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT mylinhhle valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT christopherpanella valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT michelleljones valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT ankurpandya valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT croberthorsburgh valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT kennethafreedberg valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT miltoncweinstein valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT adavidpaltiel valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis
AT krishnapreddy valueofinformationandvalueofimplementationfromclinicaltrialsofdiagnostictestsforhivassociatedtuberculosisamodelinganalysis