Synthesizing evidence in health care transforms large volumes of data into actionable knowledge, enabling decisions based on the best available information. This process integrates findings from multiple sources to produce clear, accurate, and accessible summaries for clinicians, policy makers, and patients alike [1]. As a core component of knowledge translation, evidence synthesis bridges research and practice, and is essential for developing effective health policies [2,3].

Yet limited statistical and health literacy among professionals and the public often hampers the effective use of synthesized evidence [4-6]. This highlights the need for tools that democratize access to high-level information and support meaningful stakeholder participation in health care decisions [7].

In recent years, tertiary evidence synthesis, commonly known as umbrella reviews, has emerged as a third tier in the evidence hierarchy, building on primary studies and systematic reviews with or without meta-analyses (SRs/MAs). Also referred to as overviews, meta-reviews, or meta-epidemiological studies [8,9], umbrella reviews (hereafter referred to as traditional umbrella reviews [TURs]) are particularly valuable for addressing broad questions, generating rapid insights, or navigating resource constraints. Despite structured guidance from organizations such as Cochrane and the Joanna Briggs Institute [10-14], methodological inconsistency across TURs persists due to variations in implementation.

The COVID-19 pandemic underscored the need for faster synthesis methods, even at the expense of some precision [15]. In this context, The Umbrella Collaboration (TU) introduces a novel artificial intelligence (AI)–assisted approach to tertiary synthesis, combining automation and human oversight. Although tools such as Covidence, Rayyan, and DistillerSR have improved aspects of secondary synthesis [16], the application of AI to tertiary synthesis remains largely unexplored. Large language models (LLMs) such as ChatGPT show potential for automating SRs [17], but dedicated software for tertiary synthesis has yet to be established.

TU addresses this gap by offering a structured, reproducible, and fully digital alternative to TURs. It is a patent-pending software system that automates tertiary evidence synthesis through a combination of algorithmic processes, natural language processing (NLP), and selective use of LLMs. TU retrieves abstracts of SRs/MAs from MEDLINE via PubMed, using LLMs (eg, ChatGPT-4 [18]) to suggest related terms, validated by a human reviewer, to enhance search sensitivity without sacrificing specificity. Crucially, AI is limited to this initial phase; subsequent steps are fully managed by rule-based software to ensure transparency and auditability.

TU extracts and synthesizes key information, including outcomes of interest (OoIs), effect sizes (ESs), direction, statistical significance, and a certainty estimate derived from sentiment analysis, and presents results in plain language through an interactive web platform. The system updates daily, supporting the principles of living SRs [19]. Unlike tools that assist in isolated stages of secondary synthesis, TU delivers an end-to-end solution tailored specifically for tertiary synthesis. A schematic diagram (Figure 1) illustrates the overall architecture, from automated literature retrieval to final result visualization. A more detailed technical description of the algorithms and processes is available in Multimedia Appendix 1.

As AI evolves, fully automated synthesis workflows may become feasible, but rigorous validation is essential to ensure trust, transparency, and scientific integrity.

The implementation of new methodologies in the scientific field requires a comparative validation process with established methods to confirm their reliability and effectiveness. TU, being an innovative methodology still in its theoretical-conceptual stage, must be evaluated against established methodologies. Therefore, this study aims to validate TU by comparing its performance and outcomes with the gold standard, TURs, to establish its credibility and potential superiority.

This study aims to evaluate whether TU, a software-driven and AI-assisted system, can produce results comparable to TURs, while offering a faster, more efficient, and potentially more comprehensive approach.

Figure 2 outlines the study design. Using a structured comparative approach, 8 TURs in geriatrics were selected as reference models. Each was replicated in TU using the same research questions. Key variables, including OoI, ES, certainty, and execution time, were systematically collected and compared across both methodologies.

To compare both methodologies, we conducted a targeted PubMed search to identify representative TURs in geriatrics. Rather than aiming for an exhaustive review, this focused approach was designed to select suitable benchmarks for parallel evaluation. Given the study’s aim, methodological comparison rather than comprehensive coverage, this simplified strategy was both appropriate and intentional.

TU estimates the certainty of evidence for each OoI using automated sentiment analysis (SA) applied to SR/MA abstracts. While this approach, based on NLP and a model trained on Twitter/X data, does not replicate the multidimensional Grading of Recommendations Assessment, Development, and Evaluation (GRADE) framework [20], it offers a rapid and scalable approximation. GRADE ratings from TURs were categorized as very low to high, while TU’s SA scores (ranging from −1 to +1) were normalized to a 0‐1 scale using the following formula: (SA score + 1)/2. GRADE levels were similarly mapped to enable direct comparison and statistical concordance analysis.

The execution time of each methodology was assessed, with TU providing exact time measurements and TURs relying on an estimated time frame of 6-12 months based on existing literature.

A targeted PubMed search using the terms “umbrella” AND “geriatric” was conducted to identify suitable TURs, which served as benchmarks. Their research questions were replicated in TU without modification. TU then applied automated searches and synthesis using NLP, web scraping, sentiment analysis, and machine learning, with human oversight for verification and extraction. Data from both methodologies were systematically collected to compare outcomes, ESs, certainty, and execution time.

TU relied solely on abstracts due to practical constraints, such as limited access to full texts and the aim to minimize language bias, as all MEDLINE abstracts are in English. Although abstracts may omit methodological details, TU uses structured extraction criteria to capture key information. This study explicitly evaluates whether abstract-based synthesis in TU can yield conclusions comparable to those from full-text TURs.

Results from TU and TURs were compared using contingency tables for outcomes and ESs. Certainty scores from both methods were transformed to a 0‐1 scale for direct comparison. Chi-square tests assessed differences between methodologies, and Spearman correlations evaluated the association between TU certainty estimates and GRADE ratings.

This study did not involve human participants, personal data, or animals. All data were obtained from previously published studies and analyzed in accordance with established ethical standards for secondary data analysis. Therefore, ethical review or approval was not required. This is consistent with the institutional policy of Universidad Alfonso X El Sabio (Villanueva de la Cañada, Madrid, Spain), which exempts research based solely on publicly available, nonidentifiable data from review by the institutional review board.

To establish reference models, we conducted a PubMed search on March 5, 2023, using the terms “umbrella” AND “geriatric,” which yielded 111 results. After excluding 75 records for irrelevance or ineligibility, 36 TURs remained. From these, 8 were randomly selected, with a preference for recent publications, to serve as comparators for TU [21-28]. The selection process is summarized in Figure 3 and Multimedia Appendix 2.

Across the 8 comparative projects, TURs identified 86 OoIs, while TU identified 410 for the same research questions. TU replicated 73 of the 86 (85%) TUR OoIs and missed 13 (15%). Conversely, only 73 out of 410 (17.8%) TU’s OoIs were reported by TURs, leaving 337 (82.2%) additional OoIs uniquely identified by TU (Table 2).

The identification gain factor, calculated as the ratio of OoIs identified by TU to those identified by TURs, quantifies TU’s broader retrieval capacity. TU consistently identified more OoIs across all projects, with an overall gain factor of 4.77 (ie, nearly 5 times more outcomes). Project-specific gain factors ranged from 1.87 to 18.63 (Table 3).

To assess agreement, ESs for 48 matched OoIs were compared between TURs and TU. TUR-reported ESs were standardized (Cohen d) for comparison with TU’s R_TU metric. TURs classified most OoIs as small (n=23, 48%) or trivial (n=16, 33%). TU showed a similar pattern, with 26 (54%) classified as small and 17 (35%) classified as trivial. Moderate effects were less frequent—TUR: n=7 (15%); TU: n=5 (10%)—and large effects were rare, with TUR reporting 2 (4%) and TU reporting none.

Table 4 summarizes the categorical agreement in ES classification. TU labeled 17 out of 48 (35%) OoIs as trivial; of these, 10 out of 17 (59%) matched TUR classifications, while 7 out of 17 (41%) were classified as small. Among OoIs, TU classified as small (26/48, 54%), half-matched TURs, with the rest spread across trivial (5/26, 19%), moderate (6/23, 23%), and large (2/26, 8%) classifications. For the 5 of 48 (10%) OoIs labeled as moderate by TU, TURs agreed in only 1 case, classifying most as small or trivial.

Of the 48 OoIs analyzed, full concordance in ES classification was found in 24 (50%) cases and partial concordance (1-level difference) in 21 (44%) cases. Only 3 (6%) cases showed major discordance. Overall, consistent classification (full + partial) was observed in 45 out of 48 (94%) samples (Table 5).

A Spearman correlation assessed the relationship between TU and TUR ESs (R_TU vs Cohen d), yielding ρ=0.399 (P=.005), indicating a statistically significant, low-to-moderate positive correlation. The nonparametric approach was chosen to ensure robustness against outliers and deviations from normality, as both the TU and TUR ES distributions significantly deviated from normality according to the Shapiro-Wilk test (W=0.874 and 0.847, respectively; P<.001 for both cases). The nonparametric approach ensures robustness against outliers and nonnormality. A scatter plot with a regression line (Figure 4) confirmed this trend, although the explained variance was modest (R^²=0.111).

We compared transformed certainty scores between TU and TURs using GRADE in 5 of the 8 included reviews, yielding 25 matched OoIs. Figure 5 illustrates the relationship between GRADE-based scores (x-axis) and TU’s sentiment-based estimates (y-axis), both normalized to a 0‐1 scale for direct comparison.

A Spearman correlation assessed the relationship between transformed certainty scores from TURs (GRADE) and TU (sentiment analysis). Due to nonnormal distributions of the transformed certainty scores, Shapiro-Wilk W=0.874 (P=.005) for TUR and W=0.928 (P=.049) for TU, a nonparametric test was used. A Spearman correlation between the transformed certainty scores assigned by TURs and TU yielded ρ=0.446 (P=.02), indicating a statistically significant, moderate positive association that supports concordance between both approaches.

Execution time was assessed only for TU, as none of the selected TURs reported this metric. While TURs typically take 6‐12 months, TU projects were completed in a mean time of 4 hours and 46 minutes (SD 2 hours and 30 minutes), with a median of 4 hours and 36 minutes. Completion times ranged from 1 hour and 34 minutes [28] to 10 hours and 8 minutes [24] (Table 6).

The findings of this study support the validity of the TU as a robust and efficient methodology for tertiary evidence synthesis. TU demonstrated a high level of concordance with TURs in identifying OoIs, successfully replicating the majority of those reported in TURs while also identifying a substantial number of additional outcomes. The experimental ES metric employed by TU (R_TU) showed a statistically significant correlation with standardized measures such as Cohen d and SMD, reinforcing its methodological soundness for estimating the magnitude of interventions or exposures. In addition, TU’s automated, sentiment-based certainty assessment exhibited an acceptable level of agreement with GRADE, the most widely adopted system for evaluating certainty in evidence synthesis. One of the most notable advantages of TU lies in its execution time: while TURs typically require several months to complete, TU was able to generate comprehensive results within hours. This efficiency, combined with TU’s demonstrated consistency and methodological coherence, highlights its potential value in settings where rapid evidence synthesis is essential or where resources are limited.

The development of TU aligns with the growing interest in AI-assisted tools for evidence synthesis, an emerging field likely to shape the future of scientific research. Rather than replacing TURs, TU is intended to complement them by offering a methodologically sound alternative in contexts where conventional approaches may be impractical or untimely. As a semiautomated platform, TU leverages NLP, sentiment analysis, and machine learning to streamline tertiary synthesis while maintaining methodological rigor. Despite its potential, TU represents a paradigm shift that may require time and educational efforts for widespread understanding and adoption. During the initial dissemination of this project, a general unfamiliarity with automated tertiary synthesis was observed, underscoring the need for clearer conceptual frameworks and greater engagement with the research community.

The identification of OoIs represents a central axis in the comparison between TU and TURs. In the context of tertiary evidence synthesis, an OoI reflects a specific finding previously evaluated in 1 or more SRs/MAs and integrated to answer a defined research question. The validity of a synthesis model depends not only on aggregating relevant data but also on faithfully capturing the main conclusions emerging from the primary literature.

Given the limited literature on tertiary synthesis, this analysis draws from well-established principles in secondary synthesis, where many of the same strengths and limitations apply. These include challenges in outcome selection, variability in inclusion criteria, and the balance between breadth and precision.

The comparative analysis revealed substantial differences in the number and breadth of OoIs identified. Across the 8 matched projects, TURs identified a total of 86 OoIs, whereas TU detected 410, yielding an identification gain factor of 4.77. TU replicated 73 out of 86 (85%) OoIs reported by TURs and contributed 337 additional OoIs. This difference does not appear to stem solely from broader search strategies or inclusion criteria. According to the Cochrane Handbook [29], umbrella reviews can pursue either broad or narrow questions [30]. While both methodologies support both approaches, several TURs in this study applied restrictive filters. For example, project 6 [24] limited both its search strategy and inclusion criteria, while projects 3 [23] and 4 [21] also applied inclusion restrictions. Nevertheless, even when only unrestricted TURs are considered, TU maintained a gain factor of 4.93, suggesting an intrinsic property of TU in capturing a greater volume of outcomes.

One explanation lies in TU’s automated and systematic extraction process, which minimizes human bias and ensures that any OoI mentioned in an abstract is captured, regardless of its perceived importance. By contrast, traditional reviews often apply subjective judgment in prioritizing outcomes, potentially omitting secondary findings. Moreover, TU is not constrained by human workload, allowing it to process larger volumes of data and extract multiple OoIs per review without sacrificing comprehensiveness.

A second consideration is the differing approach to quality assessment. TURs often prioritize high-quality SRs/MAs, limiting scope but potentially increasing rigor. TU, by relying on abstracts, does not perform formal quality appraisals. While this design choice increases the number of included studies, it should not be interpreted as a methodological flaw. Notably, up to 30% of SRs/MAs fail to report study quality assessments, and only 12.9% set quality thresholds for meta-analysis inclusion [31,32]. Furthermore, tools such as PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses)-Abstract could be integrated into future versions of TU to address this limitation, though prior research has shown that abstracts often score low on PRISMA quality indicators [33-36]. Nonetheless, TU consistently identifies more OoIs based solely on abstracts than TURs do using full-text reviews.

Another factor is the role of cognitive bias in outcome selection. Human reviewers may unconsciously favor familiar or hypothesis-confirming outcomes, limiting variability. While TU still involves human oversight in the final output selection, its core processes are software-driven, applying uniform parameters across all included studies and thereby reducing cognitive distortions. For instance, whereas TURs tended to report outcomes only in 1 direction, TU captured both positive and negative effects, aligning with best-practice guidelines from the Joanna Briggs Institute and the Cochrane Collaboration, which emphasize the importance of presenting balanced results for informed decision-making [29,37].

Finally, while it is possible that TU identifies outcomes of limited clinical relevance, this risk appears minimal. All OoIs extracted by TU are derived from published SRs/MAs indexed in MEDLINE, which are assumed to meet minimum standards of relevance and methodological quality. According to the Cochrane Handbook [30], reviews should focus on critical and important outcomes, excluding trivial ones.

While a higher number of outcomes may raise concerns about information overload, it is important to consider the primary purpose of tertiary synthesis: to provide a comprehensive and structured overview of the available evidence landscape. TU does not aim to guide individual clinical decisions but rather to inform stakeholders of the full scope of existing research. In this context, the inclusion of a larger set of outcomes enhances transparency and facilitates a more complete understanding of the literature. A formal qualitative appraisal of these additional outcomes, although beyond the scope of this study, represents a valuable direction for future research.

The study examined the concordance and correlation of ES metrics for OoIs between TU and TURs, using a unified set of outcomes assessed by both methodologies. TU incorporates a novel metric, R_TU, specifically developed to standardize and synthesize ESs from SRs/MAs within a tertiary synthesis framework. Unlike conventional metrics such as Cohen d or the SMD, R_TU was designed to allow direct aggregation of heterogeneous ES measures and requires empirical validation. This analysis represents the first formal evaluation of R_TU against traditional metrics.

In the qualitative comparison of ES categories (trivial, small, moderate, and large), TU demonstrated a high level of agreement with TURs. Full concordance, defined as an exact categorical match between the 2 methods, was observed in 24 out of 48 (50%) cases, while consistent concordance (full plus 1-level deviation) was reached in 45 out of 48 (94%) cases. Only 3 out of 48 (6%) cases showed discordance, meaning the categorical classifications differed by more than 1 level. These findings suggest that TU approximates the classification logic of TURs with a high degree of reliability, reinforcing the potential of R_TU to align with established interpretive frameworks.

The strength of the association between ES categorizations assigned by each methodology was evaluated using Cramér V, which yielded a value of 0.339. This indicates a moderate association and supports the notion that TU and TURs tend to classify the strength of associations in a comparable manner. Although the chi-square test did not reach statistical significance, likely due to the limited sample size and sparse contingency cells, Cramér V remains a valid ES measure and is less sensitive to these limitations [38]. In applied research, the strength of association can often be more informative than statistical significance, particularly when evaluating the practical utility of an experimental method [39]. It is worth noting that the statistical power of the chi-square test may have been reduced by the small number of observations and the presence of empty cells in the contingency table, both of which are known to limit test sensitivity. In line with recent critiques of overreliance on P values in biomedical research [40-43], the observed concordance rates and ES association offer more meaningful insights into the comparability of methods than statistical significance alone.

The quantitative comparison of ES values further supports the validity of TU. The Spearman correlation coefficient between TU and TUR values was positive and statistically significant, indicating a consistent directional relationship. Additionally, the slope of the regression line approached 1.0 (β=.8), suggesting that the R_TU metric yields ES of similar magnitude to those reported in TURs using standard metrics. This represents a marked improvement in proportionality compared with earlier regression slopes reported in other validation contexts.

However, the coefficient of determination (R²) remained modest (R²=0.11), indicating that a substantial portion of the variance in TUR ES is not explained by TU estimates. This implies that, while TU captures general trends in effect magnitude, additional factors, such as differences in underlying metric types, weighting procedures, or reviewer judgments, may influence the exact values. It also highlights the limitations of linear models in fully explaining the relationship between these 2 methods.

These findings provide preliminary but encouraging evidence for the validity of R_TU as a useful metric for tertiary synthesis. Despite its experimental nature, R_TU appears to closely approximate established metrics such as Cohen d and the SMD in both categorical classification and magnitude. Future studies will be needed to further evaluate the sensitivity, specificity, and contextual performance of R_TU across diverse synthesis domains. Nonetheless, this initial validation suggests that TU can offer a consistent and efficient alternative for evaluating and categorizing ES in large-scale evidence synthesis.

While the observed correlation between TU and TUR ESs was moderate (ρ=0.399), this result is consistent with the structural differences between the R_TU metric and conventional measures such as Cohen d and SMD. R_TU is a proprietary, automated metric specifically developed for abstract-level synthesis, prioritizing scalability and consistency over statistical precision at the study level. It does not incorporate weighting by sample size or variance and relies on normalized effect descriptors extracted from secondary sources. These foundational differences partly account for the limited shared variance (R²=0.11). However, in the context of tertiary synthesis, where the goal is to identify trends and prioritize outcomes across a broad evidence base, R_TU provides an acceptable and interpretable proxy. Moreover, this divergence has limited implications for clinical decision-making, as TU is designed to support synthesis and orientation at the field level, rather than to inform individual patient decisions. Future work may explore hybrid models that integrate additional contextual parameters to enhance concordance while preserving automation.

In this study, certainty assessments were compared exclusively among those TURs that applied the GRADE framework, a well-established and widely endorsed method for evaluating the certainty of evidence [44]. Although other appraisal tools exist, such as the statistical grading criteria proposed by Papatheodorou [45] or the methodological assessment framework AMSTAR 2 [46], these differ conceptually from the certainty model implemented in TU. Papatheodorou’s system, despite its structure, has been criticized for relying on arbitrary statistical thresholds and for lacking sensitivity to clinical relevance and risk of bias [47]. AMSTAR 2, in turn, focuses on the methodological quality of the SRs/MAs themselves, rather than the certainty of individual outcomes. By contrast, TU’s approach aligns more closely with GRADE principles by estimating certainty at the outcome level, albeit through an innovative method based on an automated sentiment analysis of SR/MA abstracts. Originally, the GRADE system referred to “quality of evidence,” which denoted the degree of confidence in the validity of study findings to inform clinical decisions. Over time, this evolved to “confidence in estimates,” and more recently, to “certainty of evidence,” a term now widely accepted as it better reflects both the trust in effect estimates and their applicability in practice [20,48].

The comparison between transformed certainty scores, standardized to a 0‐1 scale, for outcomes evaluated by TU and those rated using the GRADE framework provides important insights into the potential validity of TU’s automated approach. The observed positive and statistically significant correlation suggests that TU is capable of approximating GRADE-based judgments, thereby reinforcing the conceptual alignment between the 2 methodologies. However, this result must be interpreted with caution. The number of matched outcomes was limited, which restricts generalizability and underscores the need for further validation in broader domains and larger datasets. Crucially, we recognize that TU’s sentiment-based certainty estimation cannot replicate the multidimensional rigor of GRADE, which accounts for factors such as study limitations, inconsistency, indirectness, imprecision, and publication bias. The use of a general sentiment analysis model, originally trained on nonmedical texts, represents a methodological limitation. In this context, TU’s certainty scoring should be viewed as a preliminary proxy, not a substitute for comprehensive manual assessments. Nevertheless, the approach offers a scalable and fully automated alternative capable of supporting rapid synthesis at low resource costs. Despite its current limitations, TU provides a complementary framework that aligns with the growing need for efficient, transparent, and reproducible tools in evidence synthesis. The correlation observed with GRADE invites further research into the integration of automated text-based analyses with established appraisal frameworks. As these technologies evolve, ongoing refinement and external validation will be critical to define their appropriate role in supporting scientific practice.

Execution time is a critical but often overlooked dimension in the evaluation of evidence synthesis methodologies. TURs rarely document their execution timelines, a pattern that was consistent among the TURs included in this study. By contrast, the TU methodology records execution time precisely, from the initiation of the first search term to the completion of the first version of the synthesis project, excluding any subsequent updates in this study. This level of detail in time tracking is unprecedented in both secondary and tertiary syntheses and represents a methodological innovation that may become increasingly relevant with the integration of automation tools. As a result, traditional timelines measured in months or years may soon be replaced by more accurate, time-stamped process metrics.

Given the lack of concrete time data from TURs, direct comparisons were not feasible. However, the execution times recorded for TU are sufficiently notable to highlight its efficiency. TU projects were completed within a range of 1.5-10 hours, substantially shorter than the typical duration for TURs, which is estimated to range between 6 and 12 months. This is also well below the average time frames reported for SRs/MAs, which commonly take 1-2 years [49], or for accelerated alternatives such as rapid reviews, which range from 5 to 12 weeks [50], and even the Two-Week SR approach, which targets completion in 11 working days [51]. The remarkable speed of TU is a key strength, particularly in light of the growing international demand for agile evidence synthesis methods. Organizations such as the WHO [52], Cochrane Collaboration [53], and Joanna Briggs Institute [15] have emphasized the need for rapid yet valid synthesis approaches, an objective that TU appears to fulfill effectively in the context of tertiary reviews.

It is important to note that the time measured in this study refers solely to the initial execution phase of TU projects and does not account for later updates. However, TU includes a novel updating system that keeps projects active beyond their initial completion. The platform automatically checks daily for new SRs/MAs that match the predefined search criteria. When new studies are identified, a human reviewer is notified and can assess their eligibility. If approved, the system integrates the new results into the existing synthesis following revision and confirmation. While no equivalent system currently exists in traditional tertiary synthesis, the need for regular updates is well documented in evidence-based practice. In SRs/MAs, updates are typically recommended every 2 years or in response to emerging evidence, yet compliance with this standard is often poor [54-57]. TU’s automated updating mechanism represents a major advantage in maintaining the relevance and accuracy of results, particularly in fast-evolving fields.

Notably, projects with a higher number of included references required longer execution times, which is expected given the additional workload involved in processing more SRs/MAs. Although TU significantly streamlines the synthesis process, the complexity and volume of information remain factors that influence total execution time, particularly when human oversight is still involved. Looking ahead, TU is being developed to support full automation of SR/MA data analysis, eliminating the need for human intervention. This transition will depend on training algorithms through semiautomated projects, progressively improving accuracy via machine learning.

Interestingly, the number of search terms used did not appear to correlate with execution time (unpublished data), suggesting that TU’s algorithms can manage variable search complexity efficiently. In traditional methodologies, the search phase is often complex and conducted by specialized information professionals using advanced Boolean strategies across multiple databases [58-60]. By contrast, TU simplifies this process by using basic search terms exclusively in PubMed, automatically generated and refined through generative AI. This shift toward simplified, automated search strategies opens new avenues for exploring the adequacy and efficiency of noncomplex methods in evidence synthesis. It also raises important questions about the continued necessity of highly complex search protocols, suggesting that AI-assisted models may offer comparable effectiveness in certain contexts [61-63].

Ultimately, the short execution times observed with TU not only improve the efficiency of tertiary synthesis but also enhance the feasibility of rapidly delivering high-level evidence. In settings where timeliness is essential, this temporal advantage may outweigh minor trade-offs in other methodological dimensions. This capability holds particular promise for public health and health care decision-making, where fast access to up-to-date, high-quality evidence is crucial. TU, therefore, emerges as a promising tool in scenarios where speed is a priority, offering a pragmatic balance between rapid synthesis and analytical depth, while still requiring further validation against established gold standards.

One key limitation is the small number of TURs included—only 8, randomly selected from 36 eligible reviews. Although intended to be representative, the lack of formal randomization introduces potential selection bias. The limited sample may not reflect the full methodological or topical diversity of umbrella reviews in geriatrics. However, all selected TURs were recent (2021‐2023), which enhances comparability by aligning with current evidence synthesis standards. Another limitation is the lack of blinding: the lead investigator selected and analyzed the TURs, potentially introducing bias. Prior knowledge of TUR findings could have influenced TU outputs. However, the heterogeneity of outcomes across TURs reduces this risk, and TU’s algorithm-driven, semiautomated workflow limits subjective influence. Results were largely determined by predefined rules, adding neutrality to the process.

The decision to utilize only 1 database, MEDLINE via PubMed, in TU is both a recognized limitation and a deliberate choice shaped by resource constraints and technical considerations. Although SRs typically require searching multiple databases to capture all relevant literature [64], our approach focuses on testing whether TU can achieve outcomes comparable to TURs despite this limitation. A pilot study provided preliminary evidence of PubMed’s strong coverage, but further validation through TU is necessary to confirm its applicability across different domains. Although searching multiple databases is often recommended to reduce language and indexing biases, particularly regarding non-English literature [65,66], TU mitigates some of these biases by focusing on abstracts in English, as all PubMed abstracts are provided in English regardless of the original publication’s language. Nonetheless, the absence of Chinese databases in our approach remains a notable limitation, given that only a small proportion of Chinese journals are indexed in MEDLINE.

Relying solely on abstracts in TU was a deliberate choice to test whether tertiary synthesis can be performed efficiently, with minimal resources, and without requiring advanced methodological expertise. While abstracts may omit key details (eg, certainty ratings, ES calculations, risk of bias), TU’s structured, automated approach aims to generate clinically useful insights under standardized conditions. This approach offers 2 main advantages: (1) reduced language bias because all MEDLINE abstracts are in English; and (2) greater feasibility, as full-text access often requires costly subscriptions.

This pilot study focused on geriatrics to ensure methodological clarity and feasibility during initial validation. Limiting the scope allowed for controlled comparisons between TU and TURs. Future research should expand TU’s application to other medical fields (eg, cardiology, psychiatry) and to nonmedical domains such as education or sociology, enabling stepwise validation before broader implementation.

This study provides preliminary evidence supporting the validity of the TU as a complementary, semiautomated tool for tertiary evidence synthesis. In a set of comparative projects, TU demonstrated a high level of concordance with TURs in identifying OoIs, estimating ESs, and assessing certainty, while offering substantially shorter execution times.

Although the methodology remains experimental and further validation is required across broader contexts, the results suggest that semiautomated approaches such as TU may represent a promising step toward more efficient, scalable, and continuously updatable models of evidence synthesis. TU does not aim to replace traditional methods but to provide a practical alternative in settings where time, resources, or responsiveness are critical.

Future studies with larger datasets, enhanced blinding procedures, and expanded topic areas will be essential to confirm these findings and further explore the potential role of TU in the evolving landscape of evidence-based research.