Economic Evaluation of Molecular Testing for Pulmonary Tuberculosis Diagnosis: A Systematic Review

Abstract

Purpose

Rapid molecular assays such as Xpert MTB/RIF and TB-LAMP accelerate pulmonary tuberculosis (TB) diagnosis but are more expensive than smear microscopy. This study provided an updated economic synthesis for presumptive adult pulmonary TB in high-burden settings, broadening the evidence from Xpert MTB/RIF to other WHO endorsed tests compared to conventional strategies.

Methods

Medline, Embase and Scopus were searched through March 2025. The strategy combined search terms related to molecular diagnostic tests, pulmonary tuberculosis, and economic evaluation study designs. Full economic evaluations comparing molecular tests with smear microscopy, culture or passive case-finding were eligible. Two reviewers independently screened articles, extracted data, and adjusted costs to 2025 US dollars (USD) using average exchange rates. Reporting quality was appraised using the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) 2022 checklist. Due to heterogeneity in evaluation criteria, model structures, time horizons, and outcome measures, meta-analysis were not feasible. Therefore, results were synthesized narratively, and incremental cost-effectiveness ratios (ICERs) were contextualized against country-specific cost-effectiveness thresholds to enable meaningful cross-study interpretation.

Results

Eight studies conducted in low- and middle-income countries with high TB burdens were included. All evaluated Xpert MTB/RIF and the Thai studies also examined TB-LAMP. Five studies reported cost per disability-adjusted life years (DALYs) averted or quality-adjusted life years (QALYs) gained, while three used TB cases detected or years of life saved (YLS). CHEERS reporting quality was high (median is 23/28 items). Reported ICERs for molecular testing were either cost-saving or highly cost-effective compared with country-specific thresholds. Probabilistic sensitivity analyses (five studies) indicated ≥90% probability of cost-effectiveness in four studies and 6% in one.

Conclusion

Recent evidence supports the cost-effectiveness and cost-saving of Xpert MTB/RIF and TB-LAMP for diagnosing adult pulmonary TB. Policymakers should prioritize reducing cartridge costs and implementing models that capture patient-level benefits to maximize economic benefits.

Introduction

Tuberculosis (TB) remains a major global health challenge. In 2024, the World Health Organization (WHO) estimated approximately 10.8 million new cases equivalent to 133 per 100,000 population and 1.25 million TB-related deaths.¹ Over 80% of this burden occurred in low- and middle-income countries.¹ Achieving the End TB Strategy targets, which aim for an 80% reduction in TB incidence and a 90% reduction in mortality by 2030, will require timely and accurate diagnosis as a critical component.² Conventional sputum-smear microscopy detects fewer than half of active pulmonary TB cases, and mycobacterial culture generally requires several weeks to yield results. Health economic evaluations are essential tools that provide policymakers with the evidence needed to guide resource allocation for TB diagnostics.

Consequently, the WHO now recommends rapid nucleic acid amplification tests (NAATs), including Xpert MTB/RIF Ultra, Truenat, TB-LAMP, and line-probe assays (LPA), as the initial diagnostic options for individuals with presumptive TB.³ These assays demonstrate pooled sensitivities of ≥85% and specificities >95%, significantly reducing the median time from patient presentation to treatment initiation from weeks to days.^4,5 However, the substantial capital investment, high cartridge costs, and ongoing maintenance requirements raise concerns about affordability in resource-constrained settings. Table S1 summarizes the strengths and weaknesses of these diagnostic tools.

Two systematic reviews have previously evaluated the economic value of Xpert MTB/RIF. Sagili et al concluded that Xpert MTB/RIF was highly cost-effective across high-burden settings, while noting considerable heterogeneity in costing methods, price-year adjustments, and outcome measures.⁶ Subsequently, Hao et al updated the evidence to mid-2019 and reached similar conclusions but highlighted a lack of economic evaluations for alternative molecular tests such as TB-LAMP or LPA.⁷ Although Xpert MTB/RIF, TB-LAMP, and LPA differ in technical performance, infrastructure requirements, and intended use cases, they are frequently considered alternative or complementary options within national TB diagnostic algorithms, particularly in high-burden settings. Since 2019, several comprehensive economic evaluations have emerged, incorporating dynamic transmission or program-level models and accounting for recent reductions in cartridge price.

In response to this evidence gap, we conducted a systematic review to synthesize economic evaluations of all WHO-endorsed rapid molecular diagnostics, ie, Xpert MTB/RIF, TB-LAMP, and LPA compared with conventional diagnostic strategies in presumptive adult pulmonary TB, including individuals with or without HIV infection, using literature published through March 2025. Although operationally distinct, these tests are WHO-recommended initial diagnostics and are often weighed as comparable policy alternatives. By standardizing monetary inputs to 2025 local prices and evaluating reporting quality using the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) 2022 checklist, this review provides an up-to-date, methodologically consistent synthesis to guide policymakers in scaling-up rapid molecular testing in high-burden, resource-constrained settings.

Methods

This systematic review was conducted in accordance with a pre-registered protocol (PROSPERO registration number: CRD 42022362042) and reported following the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) 2020 statement, an updated guideline for reporting systematic reviews.⁸

Data Sources and Searches

Electronic databases were performed across three electronic databases: MEDLINE (via PubMed), Scopus and Embase, covering all literature published up to March 2025. The search strategy included terms related to interventions (I), outcomes (O) and study design (S), while population (P) and comparators (C) were excluded to allow broader sensitivity and irrelevant results were manually excluded during the selection process. The full search strategies were shown in Table S2.

Search terms for the intervention (I) included: (“Xpert” OR “Cepheid” OR “Genexpert” OR “MTB/RIF”) OR (“loop mediated isothermal amplification” OR “LAMP”) OR (“line probe assay” OR “LPA”). For the population (P), the term used was “tuberculosis”. For the study design (S), terms include: “economic evaluation” OR “cost-effectiveness analysis” OR “cost-utility analysis” OR “cost-benefit analysis” OR “cost-minimization analysis”. Within each domain, search terms were combined using the Boolean operator “OR”, and terms across domains were combined using “AND”.

Selection of Studies

Two independent reviewers (NC and PY) evaluated the eligibility of studies based on titles and abstracts. When eligibility could not be determined, full texts were retrieved and reviewed. Disagreements were resolved through discussion and, if necessary, consultation with a third reviewer (UC). Studies were included if they met the following criteria. Firstly, they were full economic evaluation studies including cost-effectiveness, cost-utility, cost-benefit, or cost-minimization analyses comparing the cost-effectiveness of molecular testing with conventional culture-based strategies considered as a gold standard for diagnosing pulmonary TB. Secondly, studies were included if they involved adult participants (aged ≥15 years, as defined by WHO¹) with presumptive pulmonary TB with or without HIV infection. Studies were excluded if they met any of following criteria. Firstly, they were review articles, editorials, or commentaries. Secondly, they lacked both cost and outcome data for the evaluated interventions. Lastly, the full text was not available in English or Thai. These eligibility criteria are summarized in Table 1.

Table 1.

Inclusion and Exclusion Criteria for Study Selection

Criteria Type	Description
Inclusion Criteria	Full economic evaluation studies (cost-effectiveness, cost-utility, cost-benefit, or cost-minimization analysis) comparing molecular testing (eg, Xpert MTB/RIF, TB-LAMP, or LPA) with conventional culture-based strategies Conducted in adult populations (aged ≥15 years) with presumptive pulmonary TB with or without HIV infection Published in English or Thai Full text
Exclusion Criteria	Review articles, editorials, or commentaries Participants with external pulmonary TB

Abbreviations: LPA, Line Probe Assay; TB, Tuberculosis.

Data Extraction and Quality Assessment

Two independent reviewers (NC and PY) used standardized data extraction forms to collect information relevant to the research question, methodology, and study characteristics. Extracted data were cross-checked and validated for completeness and accuracy. Three key domains were assessed for each included study: methodological variations, transparency of reporting, and quality of input parameters. Extracted study characteristics included first author’s affiliation, funding sources, study setting, type of economic evaluation, models used, cost inputs, perspective, time horizon, cycle length, discount rate, and sensitivity analysis methods.

To evaluate the quality and transparency of reporting, the reviewers applied the CHEERS 2022 checklist,⁹ the current international standard for health economic evaluations. This updated framework reflects recent methodological advances, provides clearer guidance for consistent and transparent reporting, and ensures comparability across studies, making it preferable to earlier versions of CHEERS or other reporting tools. Detailed results of CHEERS assessment are presented in Table S3.

Data Synthesis and Analysis

This review aimed to compare the cost-effectiveness of Xpert MTB/RIF, TB-LAMP, and LPA in the diagnosis of pulmonary TB across the included studies. However, direct comparison was not feasible due to substantial heterogeneity among studies. Contributing factors included variations in perspectives (eg, societal, healthcare provider, governmental), time horizons, intervention and comparator combinations (eg, Xpert MTB/RIF alone vs Xpert MTB/RIF combined with other diagnostic tools) and outcome measures. Given this heterogeneity, a meta-analysis was not appropriate. Instead, the findings were summarized narratively. In accordance with established systematic review guidelines (eg, PRISMA), a narrative synthesis is an accepted approach when quantitative pooling is not feasible.⁸ While the synthesis is narrative, this review was conducted using rigorous systematic review methodology, including a registered protocol, comprehensive search strategy, dual independent screening, and formal quality appraisal.

For each study, the reported incremental cost-effectiveness ratios (ICERs) and corresponding cost-effectiveness (CE) thresholds were extracted and presented. These values were contextualized based on the country-specific thresholds or other willingness-to-pay (WTP) benchmarks employed by the study authors. Because the included studies varied in time horizons and outcome measures, eg, quality adjusted life years (QALYs), disability adjusted life years (DALYs), life years (LYs), years of life saved (YLS), we standardized all reported costs to 2025 United States dollars (USD) and compared ICERs against country-specific cost-effectiveness thresholds. This approach enabled consistent interpretation of cost-effectiveness across studies, despite heterogeneity in model structures, time horizons, and outcome metrics. Additionally, the WHO’s list of high TB burden countries¹ was used for country classification. For studies that did not explicitly report the year of cost analysis, the year of publication was used as a proxy.

Results

Study Information

The database search identified 260 records (PubMed=82, Embase=78, Scopus=100). After removing 135 duplicates, 125 titles/abstracts were screened, resulting in the exclusion of 69 records. Of the 56 full-text articles accessed for eligibility, 48 were excluded, leaving eight studies for qualitative synthesis. The full PRISMA 2020 flow chart is presented in Figure 1. Table 2 presents characteristics of the included studies. Most of the included economic evaluations were conducted in low- and lower-middle-income countries with a high TB burden. Six studies were based in sub-Saharan Africa and South-East Asia—Mozambique,¹⁰ India,¹¹ South Africa/Zambia/Zimbabwe/Tanzania,¹² Ethiopia,¹³ Zambia¹⁴ and Thailand¹⁵—while two additional studies focused on Thailand’s national TB control context.^16,17 All eight studies assessed Xpert MTB/RIF as the primary molecular diagnostic. The two Thai studies also examined TB-LAMP as an alternative or add-on diagnostic test.^16,17 Of the articles assessed for eligibility, none were economic evaluations of LPA that met the inclusion criteria. In seven of the studies,^{10–13,15–17} sputum-smear microscopy served as the primary comparator, whereas one Zambian study compared a mobile X-ray plus Xpert screening strategy to passive case finding.¹⁴

Figure 1.

PRISMA 2020 flow diagram of study selection process.

Note: Adapted from Page MJ, McKenzie JE, Bossuyt PM et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71.⁸

Abbreviations: EE, economic evaluation; HTA, health technology assessment.

Table 2.

Characteristics of Included Studies

Author (Year)	Country	Study Setting	Funding Source	Intervention	Comparator	Target Population	Model Type	Perspective	Discount Rate	Sensitivity Analysis
Orlando (2018)10	Mozambique	HIV+ patients in Mozambique	DREAM program and Global Fund	Xpert MTB/RIF	Symptom Screening and Sputum smear microscopy	HIV-positive, antiretroviral treatment-naïve adults	Decision model	Health provider perspective	3%	One-way sensitivity analysis
Lee et al (2019)11	India	Public sector (DMCs and PHCs)	NIH (NIDA, NIAID, NIMH)	Xpert MTB/RIF	Sputum smear microscopy	HIV-negative adults with presumptive TB (≥15 years old)	CEPAC-I microsimulation model	Health provider perspective	3%	One-way, two-way, and scenario sensitivity analyses
Pooran (2019)12	South Africa, Zambia, Zimbabwe, Tanzania	Primary health-care clinics	EDCTP, South African MRC, National Research Foundation	Xpert MTB/RIF (point of care)	Sputum smear microscopy	Adults with presumptive tuberculosis	no simulation model	Health provider perspective	Not specified	One-way sensitivity analysis and probabilistic sensitivity analyses
Khumsri (2020)15	Thailand	Outpatient department of tertiary care hospital	Not specified	Xpert MTB/RIF	Sputum smear microscopy	Adults ≥18 years with presumptive pulmonary TB	Decision tree	Societal perspective	Not applied	One-way and probabilistic sensitivity analyses
Kaso & Hailu (2021)13	Ethiopia	Public health facilities in Arsi Zone (8 facilities: hospitals and health centers)	Addis Ababa University & Gates Foundation	Xpert MTB/RIF	Sputum smear microscopy	Suspected pulmonary TB patients	no simulation model	Health provider perspective	3%	Scenario analysis on cost drivers (eg, cartridge cost, machine lifespan)
Jo et al (2021)14	Zambia	Community-level mass screening via mobile units	Stop TB Partnership’s TB REACH initiative	X-ray with CAD + Xpert MTB/RIF	Passive Case Finding (PCF)	Adults in Zambia, including people with HIV	Decision tree and Markov model	Health provider perspective	3%	one-way, three-way, and probabilistic sensitivity analyses
Chitpim et al (2022)16	Thailand	General population suspected of having pulmonary TB	Thailand Science Research and Innovation, HSRI, Mahidol University	Initial Xpert MTB/RIF, Initial TB-LAMP Add-on Xpert MTB/RIF, Add-on TB-LAMP	Sputum Smear Microscopy + Culture and Drug Susceptibility Testing (DST)	Thai adults over 15 years with suspected pulmonary TB	Hybrid Decision Tree-Markov model	Societal perspective	3%	One-way and Probabilistic Sensitivity Analysis
Chitpim et al (2025)17	Thailand	General Thai population, national TB program	Thailand Science Research and Innovation, HSRI, Mahidol University	Initial Xpert MTB/RIF, Initial TB-LAMP Add-on Xpert MTB/RIF, Add-on TB-LAMP	Sputum Smear Microscopy with Culture and Drug Susceptibility Testing (conventional method)	Suspected TB cases aged ≥15 years in Thailand	Dynamic transmission model	Societal perspective	3%	One-way and probabilistic sensitivity analysis (Monte Carlo simulation)

Abbreviations: DALY, Disability-Adjusted Life Year; ICER, Incremental Cost-Effectiveness Ratio; LY, Life Year; NA, Not Available; YLS, Years of Life Saved.

In terms of methodology, five studies adopted a cost-utility analysis, reporting outcomes in terms of DALYs or QALYs,^{10,12,15–17} while three studies presented cost-effectiveness in natural units such as TB cases detected or YLS.^11,13,14 Most studies adopted a healthcare provider perspectives,^10–14 while three applied a societal perspective to account for patient-incurred costs.^15–17 Decision-tree frameworks were the most commonly used modelling approach, employed in three studies.^10,13,15 These were complemented by a microsimulation model,¹¹ a hybrid decision-tree–Markov structure,¹⁶ a dynamic transmission model¹⁷ and pragmatic trial-based or program-specific model.^12,14 Time horizons varied: four studies focused on the diagnostic episode or a one-year period,^10,12,13,15 one assessed a five-year program cycle;¹⁴ another modelled a 15-year horizon;¹⁷ and two projected outcomes over a lifetime period.^11,16 A 3% annual discount rate was applied in six studies, while two studies did not discount due to short analytic time horizons.^12,15 All studies conducted one-way sensitivity analysis, and five included probabilistic sensitivity analyses (PSA) to explore parameter uncertainty.^11,14–17

Cost-Effectiveness Analysis Results

Table 3 presents the cost-effectiveness analysis results of all included studies. Rapid molecular testing primarily Xpert MTB/RIF was found to be either economically dominant or highly cost-effective relative to smear microscopy or passive case finding. Three analyses^10,13,15 reported that Xpert was cost-saving, reducing total costs by 35–70 USD per patient while improving outcomes in terms of DALYs averted or TB cases detected. The remaining five studies reported favorable ICERs. In low-income, high-burden settings, the cost per DALY averted ranged from cost-saving to 57 USD¹² and from 222 USD to 340 USD per YLS,¹¹ well below commonly used WTP thresholds, typically 0.5–1 x GDP per capita. In Thailand, two studies comparing both Xpert and TB-LAMP reported ICERs between 1,290 USD and 1,340 USD per QALY gained,^16,17 which remain comfortably within the national threshold of 4,500 USD per QALY gained. A single Zambian study¹⁴ evaluating a mobile digital-X-ray combined with Xpert yielded an ICER of 4,254 USD per additional bacteriologically confirmed TB initiation, which is below the country’s WTP threshold.

Table 3.

Cost-Effectiveness Results of Included Studies

Author (Year)	Type of EE	Time Horizon	Currency & Year	Outcome Measures	Effectiveness Results	Total Cost (Intervention)	Total Cost (Comparator)	ICER*	CE Threshold Used	CE Results
Orlando (2018)10	CUA	1 year	USD, 2016	DALY	NA	$92,263	$147,226	$ 56.54/ DALYs averted	Not provided	NA
Pooran (2019)12	CUA	1 year	USD 2014	Number of treatment initiation, number of treatment completion	NA	Tanzania $304,051 Zambia $192,113 Zimbabwe $261,975 South Africa $171,145	Tanzania: $250,772 Zambia: $155,010 Zimbabwe: $233,468 South Africa: $139,306 All sites: $215,346	Tanzania: $4254 Zambia: Dominated Zimbabwe: $1675 South Africa: $1373 ALL sites: $4185	3x GDP per capita per DALY averted Tanzania: $2637 Zambia: $3534 Zimbabwe: $3027 South Africa: $15,822 ALL sites: $8412	Cost-effective
Khumsri (2020)15	CUA	1 year	USD	Correct diagnosis, Time to diagnosis, QALYs gained	Xpert MTB/RIF had 947.14 QALYs vs 939.84 for AFB smear	$143,110.64	$196,666.84	Dominant (more effective and less costly)	160,000 THB per QALY ($5079.36)	Cost-saving
Kaso & Hailu (2021)13	CEA	1 year	USD, 2018	Number of TB case detected	221 TB cases detected by Gene Xpert, 74 by smear microscopy	$77.9 (per case detected)	$55.8 (per case detected)	$20 per TB case detected	No WTP threshold used (intermediate outcome)	NA
Jo et al (2021)14	CEA	5 years	USD, 2019	TB death averted, number of TB case diagnosed	Incrementally diagnose 407 (7207 versus 6800) TB patients and avert 502 (611 versus 1113) TB-associated deaths compared to the status quo (passive case finding)	$3,897,000	$2,787,000	$2,284 per death averted	$4800 per TB death averted (about three times Zambia’s GDP per capita in 2018)	Cost-effective
Chitpim et al (2025)17	CUA	15 years	Thai Baht, 2023	LY, QALY	-Initial Xpert MTB/RIF: increased 9671 QALYs per population -Initial TB-LAMP: increased 14,115 QALYs per population -Add-on Xpert MTB/RIF: increased 24,073 QALYs per population -Add-on TB-LAMP: 9135 increased 24,073 QALYs per population	-Initial Xpert MTB/RIF: 1,292,192,150 Baht per population -Initial TB-LAMP: 1,411,099,374 Baht per population -Add-on Xpert MTB/RIF: 1,408,692,323 Baht per population -Add-on TB-LAMP: 1,352,902,142 Baht per population	1,320,355,676 Baht per population	-Initial Xpert MTB/RIF: Dominant -Initial TB-LAMP: 6429 Baht/QALY gained -Add-on Xpert MTB/RIF: 3670 Baht/QALY gained -Add-on TB-LAMP: 3563 Baht/QALY gained	160,000 Baht per QALY gained	Cost-effective
Lee et al (2019)11	CEA	Lifetime	USD, 2017	YLS, number of TB cases detected/linked to care	Xpert increased life expectancy by 0.18 years	$120	$80	$222/YLS	$990/YLS (50% of India’s 2017 GDP per capita)	Cost-effective
Chitpim et al (2022)16	CUA	Lifetime	Baht, 2021	LYs, QALYs	-Initial Xpert MTB/RIF: increased 0.84 years -Initial TB-LAMP: increased 0.94 years -Add-on Xpert MTB/RIF: increased 0.53 years -Add-on TB-LAMP: increased 0.79 years	-Initial Xpert MTB/RIF: 7010 Baht -Initial TB-LAMP: 7626 Baht -Add-on Xpert MTB/RIF: 8924 Baht -Add-on TB-LAMP: 6565 Baht	6845 Baht	-Initial Xpert MTB/RIF: 197 Baht/QALY gained -Initial TB-LAMP: Dominant -Add-on Xpert MTB/RIF: 3940 Baht/QALY gained -Add-on TB-LAMP: 993 Baht/QALY gained	160,000 Baht per QALY gained	Cost-saving or Cost-effective

Abbreviations: DALY, Disability-Adjusted Life Year; ICER, Incremental Cost-Effectiveness Ratio; LY, Life Year; NA, Not Available; YLS, Years of Life Saved; CE, Cost-Effectiveness.

PSA conducted in five studies consistently supported the base-case results. For example, Jo¹⁴ demonstrated a 97% probability that the mobile-X-ray plus Xpert intervention would be cost-effective at a WTP of 4,800 USD per TB death averted in Zambia. Both Thai studies^16,17 revealed more than 95% probability of cost-effectiveness below the national threshold of 4,500 USD per QALY gained. Khumsri¹⁵ found Xpert to be economically dominant in all 1,000 Monte-Carlo simulations. Moreover, the analysis by Pooran¹² was comparatively more uncertain, demonstrating a 61% probability of cost-effectiveness at its DALY-based WTP threshold. Across all PSA, the parameters with the greatest influence on ICERs were the price of diagnostic cartridge, the underlying prevalence of TB, and the costs associated with downstream treatment. Nevertheless, even under plausible variations in these parameters, molecular testing rarely exceeded country-specific WTP thresholds.

Quality Assessment of Reporting

Reporting quality was generally high among the included studies. Application of the 28-item CHEERS 2022 checklist revealed a median compliance of 23 items (82%), with individual scores ranging from 21/28 (75%) to 25/28 (89%). The most comprehensive reporting was observed in Lee,¹¹ which fulfilled 25 items (89%), followed by Jo¹⁴ with 24 items (86%). Five studies^{10,11,13,14,16,17} exceeded the 80% “good” reporting threshold, whereas two studies^12,15 were categorized as “moderate” at 75% (Table S3).

All studies consistently reported key elements, including the title, abstract, background and objectives, study population, setting, comparators, perspective, time horizon, currency and price date, resource-use measurement, and uncertainty analysis. However, no study provided a pre-published health-economic analysis plan (item 4) or discussed stakeholder engagement (item 20). Only one study¹¹ mentioned the public availability of analytic code or data (item 28). Justification of model structure (item 16) and formal assessment of heterogeneity (item 18) were either missing or only briefly addressed in approximately half of the studies. Additionally, two studies with short time horizon did not report discounting.^12,15

Discussion

This study presents the most-updated systematic review of economic evaluations of all WHO-endorsed molecular TB diagnostics, specifically Xpert MTB/RIF, TB-LAMP and LPA compared to conventional diagnostic strategies in presumptive adult pulmonary TB. Building upon previous systematic reviews, including those by Sagili et al and Hao et al, this review extends the evidence base to include studies published through March 2025.^6,7 Notably, it significantly updates the last comprehensive review by Hao et al,⁷ which included studies only up to mid-2020. Over the past five years, the evidence base has become more refined. While earlier reviews included numerous heterogeneous conference abstracts, our analysis incorporated eight peer-reviewed journal articles, five of which were published after 2020. These studies provide more robust and detailed evaluations of both cost and effectiveness. Importantly, this review is the first to include dynamic transmission models and programmatic-level evaluations for TB-LAMP and for mobile X-ray combined with Xpert MTB/RIF, providing a more nuanced perspective on large scale implementation scenarios and their long-term public health impact.

Our review revealed that all eight eligible economic evaluation studies were conducted in Mozambique,¹⁰ India,¹¹ South Africa, Zambia, Zimbabwe, Tanzania,¹² Ethiopia,¹³ Zambia¹⁴ and Thailand,^15–17 countries classified as low-, lower-middle-, or middle-income countries with a high-TB-burden. According to the WHO’s latest classification for 2021–2025, 30 countries are designated as high-burden for TB, accounting for nearly 87% of global TB cases.¹⁸ However, only nine of these countries have conducted economic evaluations of diagnostic tests for pulmonary TB. This highlights a significant gap in the evidence base and raises concerns about the lack of such studies in many high-burden countries.

To enable meaningful cross-country comparisons, an element lacking in previous reviews, we adjusted all ICER values to local prices, converted to 2025 USD, and compared them against country specific cost-effectiveness thresholds. Although our findings indicated that rapid molecular testing was either cost-saving or highly cost-effective across all studies,^10–17 the key drivers of parameter uncertainty were cartridge price, underlying TB prevalence, and downstream treatment costs. These findings underscore the need for caution when generalizing economic evaluation results across countries, as differences in epidemiological contexts, health system capacity, and cost structures can significantly influence outcomes. Beyond the methodological considerations of the economic models, real-world implementation faces significant challenges, including infrastructural needs, logistical hurdles with supply chains, and the requirement for trained personnel. Overcoming these barriers is crucial to ensure the effective uptake of these molecular tests.

In addition, all included studies assessed Xpert MTB/RIF as the primary molecular diagnostic test,^10–17 while two studies from Thailand^16,17 also examined TB-LAMP, either as an alternative or as an add-on test compared with sputum-smear microscopy. These findings are consistent with WHO recommendations, which advocate the use of Xpert MTB/RIF Ultra, Truenat, and TB-LAMP as the initial diagnostic options for individuals with presumptive TB.³ Remarkably, our reviewed suggested that the majority of studies (5 out of 6 studies) applied a cost-utility analysis, reporting outcomes in terms of DALYs or QALYs, which are particularly relevant for informing policy decisions regarding the inclusion of TB diagnostic tests in healthcare benefit packages.^{10,12,15–17} Moreover, decision-tree models were the most commonly used modelling approach,^10,13,15 followed by pragmatic trial-based or program-specific model,^12,14 microsimulation model,¹¹ a hybrid decision-tree–Markov structure,¹⁶ and a dynamic transmission model.¹⁷ Despite TB being an infectious disease with person-to-person transmission, only one study applied a dynamic transmission model to account for both the direct and indirect effects of TB transmission.¹⁷ This model specifically evaluated the potential impact of diagnostic delays such as differences in turnaround time between testing with molecular diagnostic tests and sputum-smear microscopy on disease spread within the community.¹⁷ However, conducting such dynamic models is often challenging due to their significant complexity and extensive data requirements, particularly for country-specific transmission parameters that are frequently unavailable. These findings suggest that future economic evaluation studies should incorporate dynamic transmission models to more accurately reflect the epidemiological and public health implications of diagnostic strategies.

In terms of quality assessment based on the 28-item CHEERS 2022 checklist, we excluded grey literature that did not meet minimum methodological standards, resulting in a more reliable evidence base. Overall, the reporting quality was generally high among the included studies. However, several important elements consistently lacking, including a pre-published health-economic analysis plan (item 4), stakeholder engagement (item 20), justification of model structure (item 16) and a formal assessment of heterogeneity (item 18). Future economic evaluations should aim to incorporate these components to enhance the transparency, methodological rigor and relevance to decision-makers.

It is important to acknowledge the limitations of our study. First, we included only English-language full-text articles and excluded grey literatures, which may contain valuable local insights on economic evaluation of molecular tests. Second, we assessed reporting quality solely using the CHEERS 2022 checklist. Although existing guidelines for quality assessment of health economics models have been published by the International Society of Pharmacoeconomics and Outcomes Research (ISPOR) and the National Institute for Health and Care Excellence (NICE),^19–21 we did not apply them in this review. Future studies should consider incorporating multiple quality appraisal tools to strengthen the robustness of their assessments.

Conclusion

In summary, this systematic review synthesized current evidence on the cost-effectiveness of rapid molecular diagnostics for presumptive adult pulmonary TB, including Xpert MTB/RIF, TB-LAMP and LPA, compared with conventional strategies, covering studies published up to March 2025. Eight studies were identified, all from high TB burden low- and lower-middle-income countries. Across diverse settings, these molecular tests were consistently found to be cost-saving or highly cost-effective. By contextualizing ICERs against country-specific thresholds, our review enabled meaningful interpretation across studies despite heterogeneity in time horizons, model structures, and outcome measures. In addition, key drivers of parameter uncertainty included cartridge prices, TB prevalence and downstream treatment costs. Based on the CHEERS 2022 checklist, the overall reporting quality of included studies was relatively high. However, our review also highlights a continued lack of economic evaluation studies of molecular diagnostic tests in many high-burden countries. Moreover, the generalizability of economic evaluation results across different settings should be approached with caution in policy decision making, given variations in epidemiological and health system contexts. Overall, our findings provide evidence to guide national TB programs in adopting rapid molecular diagnostics as cost-effective tools to optimize resource allocation in high-burden settings. This offers a strong economic rationale for policymakers to prioritize funding and scale-up of these diagnostics over conventional methods. To strengthen the evidence base, future research should incorporate dynamic transmission models and assess the equity implications of diagnostic strategies to ensure benefits reach the most vulnerable populations. Linking such evidence into national policy frameworks and donor funding priorities will be critical to accelerate adoption, maximize health gains, and support sustainable investments in TB control.

Funding Statement

This research was supported by multiple funding sources. The Royal Golden Jubilee Ph.D. Scholarship (Grant No. PHD/0104/2559) was awarded to N.C. and U.C. by the Thailand Science Research and Innovation (TSRI), Ministry of Higher Education, Science, Research and Innovation. Additional support was provided by the Health Systems Research Institute (HSRI) and Mahidol University (Fundamental Fund: fiscal year 2024 by the National Science Research and Innovation Fund (NSRF)).

Disclosure

The authors report no conflicts of interest in this work.