Diagnostic, Prognostic, and Therapeutic Value of Droplet Digital PCR (ddPCR) in COVID-19 Patients: A Systematic Review

Accurate detection of SARS-CoV-2, the pathogen causing the global pandemic of COVID-19, is essential for disease surveillance and control. Quantitative reverse transcription PCR (RT-qPCR) is considered the reference standard test for the diagnosis of SARS-CoV-2 by the World Health Organization and Centers for Disease Control and Prevention. However, its limitations are a prompt for a more accurate assay to detect SARS-CoV-2, quantify its levels, and assess the prognosis. This article aimed to systematically review the literature and assess the diagnostic performance of droplet digital PCR (ddPCR), also to evaluate its potential role in prognosis and management of COVID-19 patients. PubMed and Scopus databases were searched to identify relevant articles published until 13 July 2021. An additional PubMed search was performed on 21 October 2021. Data from the 39 eligible studies were extracted and an overall 3651 samples from 2825 patients and 145 controls were used for our qualitative analysis. Most studies reported ddPCR was more accurate than RT-qPCR in detecting and quantifying SARS-CoV-2 levels, especially in patients with low viral loads. ddPCR was also found highly effective in quantifying SARS-CoV-2 RNAemia levels in hospitalized patients, monitoring their disease course, and predicting their response to therapy. These findings suggest ddPCR could serve as a complement or alternative SARS-CoV-2 tool with emerging diagnostic, prognostic, and therapeutic value, especially in hospital settings. Additional research is still needed to standardize its laboratory protocols, also to accurately assess its role in monitoring COVID-19 therapy response and in identifying SARS-CoV-2 emerging variants.


Introduction
The coronavirus disease 2019 (COVID-19)-first emerging in Wuhan, China, and rapidly spreading worldwide since then-was declared a global pandemic in 2020 by the World Health Organization (WHO) [1]. COVID-19 is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Prompt and accurate SARS-CoV-2 detection is the first step towards efficiently controlling this pandemic [2]. Policymakers also rely on accurate SARS-CoV-2 diagnosis to shape the appropriate response to the COVID-19 pandemic [3]. In addition, evidence suggests SARS-CoV-2 viral loads fluctuate through a patient's hospital course [4], while higher SARS-CoV-2 levels have been linked to increased disease severity and mortality [5]. Furthermore, the levels of SARS-CoV-2 viral load have strongly been associated with its transmission rate in both vaccinated and unvaccinated individuals [6]. Notably, viral load levels can be used to predict the response to treatment in hospitalized COVID-19 patients [7]. This highlights the need for tools that can both accurately diagnose COVID-19, besides quantifying its levels to assess prognosis and monitor therapy response.
Nucleic acid amplification testing (NAAT) by quantitative reverse transcription PCR (RT-qPCR) is considered the reference standard for the detection of SARS-CoV-2, as recommended by the WHO and Centers for Disease Control and Prevention (CDC) [8,9]. However, RT-qPCR testing does have its limitations, including suboptimal sensitivity in low viral concentration samples, susceptibility to PCR inhibitors, false-positive results due to the background DNA/RNA contamination, and the need for a standard curve to quantify the results [10,11]. Of interest, it could even be initially negative in patients with clinical or radiologic suspicion of pneumonia, while being able to detect the viral RNA some days later [12]. Finally, RT-qPCR's sensitivity varies widely according to the type of samples used [13]. Consequently, there is an emerging need for a more accurate tool to detect SARS-CoV-2 and quantify its levels.
Except RT-qPCR, other approved diagnostic tests include antigen and antibody testing, using flow type (LFA) or enzyme-linked immunoassays (ELISA) [14]. There is also a variety of novel diagnostic techniques, such as clustered regularly interspaced short palindromic repeats (CRISPR), loop mediated isothermal amplification (LAMP), next generation sequencing (NGS), and digital PCR [15]. The latter is an innovative technology able to detect and quantify nucleic acids without needing a standard curve [16,17]. Digital PCR could be either chip-based or more often droplet-based (droplet digital PCR; ddPCR) [18]. There is evidence that ddPCR can play an important role in diagnosing various fungal, bacterial, and viral pathogens with high sensitivity and precision [17]. Studies have shown that ddPCR accurately detects and quantifies SARS-CoV-2, even in low viral load samples; it is also more tolerant to inhibition compared to RT-qPCR [10,19]. This is because PCR inhibitors are diluted following the compartmentalization of the initial PCR reaction mixture into multiple reactions before the amplification step [16,17].
The aim of this systematic review was to collect all available literature and qualitatively evaluate ddPCR's diagnostic, prognostic, and therapeutic value in COVID-19 patients. Our hypothesis was that ddPCR exhibits an enhanced ability to detect the SARS-CoV-2 RNA than traditional testing such as RT-qPCR, while its accurate RNA quantification could have significant prognostic and therapeutic value. To our knowledge, this is the first systematic review that jointly assesses the diagnostic and prognostic role of ddPCR in COVID-19 disease.

Literature Search
The initial electronic database search identified 184 studies (108 from PubMed and 76 from Scopus), of which 69 were duplicates. The updated search on 21 October identified another 25 articles from PubMed, giving us a total of 209 studies. A total of 140 titles and abstracts were screened after duplicates were removed, out of which 45 were considered eligible for full text screening. Six studies were further excluded; five of them did not report on the outcomes of interest and one had no full text available. A total of 39 studies were included in the final qualitative analysis. The flow and screening process are described in detail in Figure 1.
The sources of samples were heterogenous among the included studies. The most used source was the nasopharyngeal swabs. Other commonly used sources were the blood, plasma, saliva, oropharyngeal, sputum, and respiratory excretions. Some studies also reported the use of rectal, urine, and bronchoalveolar lavage (BAL) samples [30,44,45]. One study reported using colostrum samples [55]. Tables 1 and 2 summarize the characteristics and main findings of the articles included. The sources of samples were heterogenous among the included studies. The most used source was the nasopharyngeal swabs. Other commonly used sources were the blood, plasma, saliva, oropharyngeal, sputum, and respiratory excretions. Some studies also reported the use of rectal, urine, and bronchoalveolar lavage (BAL) samples [30,44,45]. One study reported using colostrum samples [55]. Tables 1 and 2 summarize the characteristics and main findings of the articles included. • ddPCR's detection ability was at least equivalent to RT-qPCR's; yet, unlike RT-qPCR, ddPCR's performance was not affected by the primer-probe sets' sequences.

Diagnostic Performance of Digital PCR
Evidence suggests that ddPCR assays exhibit an enhanced analytical sensitivity, as assessed by measuring their limit of detection (LOD). Abasiyanik [32,48]. Two other groups designed their ddPCR assays targeting the ORF1ab and N genes; Dong et al. measured LODs of 2 copies/reaction for both genes, whereas Nyaruaba et al. 1.42 and 2.75 copies/reaction for the ORF1ab and N genes, respectively [22,27]. Of interest, another study targeted the E, N, RdRP, N2, and N3 genes, reporting LODs ranging from 7 to 24.3 copies/reaction [42]. Notably, the LODs of ddPCR assays were found to be lower than those of RT-qPCR, meaning that ddPCR showed a higher analytical sensitivity. Zhang [41], while Alteri et al. found a LOD of 2.9 copies/reaction (95% CI: 2.0-11.5), which was 5 to 10 times lower that the LODs of the comparison RT-qPCR assays used [34]. Of interest, one study found striking differences among the LODs reported between the ddPCR and reference RT-qPCR assays tested, while targeting the ORF1ab and N genes. Whereas the LODs of ddPCR for the two genes were 2.1 (95% CI: 1.5-4.2) and 1.8 (95% CI: 1.4-3.3) copies/reaction, they were 1039 (95% CI: 763.2-1862) and 873.2 (95% CI: 639.8-1633.2) copies/reaction for RT-qPCR, translating to an approximate 500 times higher analytical sensitivity of ddPCR [12].
Besides its enhanced analytical performance, all included studies revealed that ddPCR had at least a comparable clinical performance with RT-qPCR, while most reported that ddPCR exhibited a superior detection ability. The main findings are summarized in Table 1. Several studies showed that ddPCR was able to detect the SARS-CoV-2 virus in samples found negative with RT-qPCR, especially when the viral load copy number was low. For instance, a study performed by Alteri et al. showed that ddPCR was able to detect 19 positive cases with low viral load initially testing negative with RT-qPCR [34]. Cassinari et al. also compared the diagnostic performance of ddPCR with RT-qPCR in saliva and nasopharyngeal swab samples. RT-qPCR was able to detect SARS-CoV-2 in 8/13 saliva samples from patients testing positive with RT-qPCR assay in nasopharyngeal samples, resulting in a sensitivity of 62% [35]. On the other hand, ddPCR was able to detect the SARS-CoV-2 virus in 11/13 of the saliva samples tested, yielding a sensitivity of 85% [35]. Both assays reported concordant results while testing nasopharyngeal swab samples [35]. Moreover, Kim et al. reported that ddPCR was able to detect 63 samples with low copy number of SARS-CoV-2 that were reported as negative by RT-qPCR, of which 55% were from symptomatic patients [32]. The improved detection ability of ddPCR was tested in different populations and samples. A study by Ramirez-Rosas et al. showed that ddPCR detected more positive SARS-CoV-2 samples compared with RT-qPCR in nasopharyngeal samples from mothers (41/133 compared to 16/133, respectively) and neonates (24/131 compared to 11/131, respectively), also in colostrum samples (20/140 compared to 3/140, respectively) [55].
Of interest, a study conducted by Dong et al. reported that the true positive rate of detection was drastically improved from 28.2% to 87.4% upon testing with ddPCR compared to digital PCR in patients with fever [22]. Moreover, digital PCR was able to resolve a few ambiguous RT-qPCR results, detecting the SARS-CoV-2 virus in 17 cases of SARS-CoV-2 reported as equivocal (16/17) or negative (1/17) from 29 close contacts [22]. Marchio et al. also demonstrated the ability of ddPCR to clarify RT-qPCR ambiguous cases, reporting as positive 2/8 equivocal samples [40].
A reason why ddPCR exhibits an enhanced SARS-CoV-2 detection ability compared to RT-qPCR was shown in a study by Szwebel et al.; the authors reported that ddPCR displayed increased tolerance to PCR inhibitors, in contrast to RT-qPCR, and revealed its emerging potential for viral diagnostics [45].
Whereas most studies contrasted the performance of ddPCR with RT-qPCR, a few used a different comparison tool. For instance, a study compared ddPCR with LumiraDx rapid antigen testing, with the former showing superior diagnostic accuracy by detecting false-negative results of the latter [36].

Prognostic and Therapeutic Value of Digital PCR
Accumulating evidence suggests that the dynamic monitoring of the SARS-CoV2 RNA plasma levels correlate with the disease status (progression or remission) and response to therapy. Although most eligible studies of this systematic review evaluated the diagnostic performance of ddPCR compared to RT-qPCR, we also extracted data from 10 studies assessing the prognostic performance of ddPCR and their main findings are summarized in Table 2. Four of them showed that ddPCR can accurately quantify SARS-CoV-2 RNA levels, especially in immunocompromised patients and hospitalized patients with severe COVID-19 infections [23,37,46,49]. Furthermore, a study conducted by Ram-Mohan et al. showed that ddPCR, compared to traditional RT-qPCR, was superior for detecting and quantifying SARS-CoV-2 RNAemia in hospitalized patients over a course of 30 days [52]. ddPCR was still able to detect RNAemia in 6.8% of patients at seven days, whereas RT-qPCR could not detect any RNAemia after three days [52]. Notably, this study showed that the higher levels of SARS-CoV-2 RNA in the patients' plasma were correlated with a higher probability of developing severe disease [52].
A study by Szwebel et al. revealed that ddPCR was able to predict the clinical deterioration of a patient by detecting elevated SARS-CoV-2 RNA plasma levels [45]. Similarly, the virus clearance from the plasma was associated with the patient's clinical recovery [45]. This indicates that ddPCR may be used to monitor the course of COVID-19 disease. A study by Veyer et al. further corroborated these findings, showing that ddPCR was able to detect SARS-CoV RNAemia in 74% of the hospitalized pneumonia patients tested, while the presence of RNAemia at presentation was associated with disease severity, longer hospital length, progression, and extrapulmonary complications [47].
A few studies have also highlighted the role of ddPCR in predicting response to COVID-19 therapy [30,43]. Sabbatinelli et al. revealed that low serum miR-146a-5p levels, detected with ddPCR, were associated with resistance to treatment with the anti-IL-6 receptor tocilizumab (TCZ) and poor overall survival [43]. Lastly, Yu et al. found that the viral load was markedly higher in early and progressive stages of the disease compared with the recovery stage-thus, higher viral loads may indicate disease progression-suggesting that an accurate quantification via ddPCR at different time points may be the key to monitor the disease course and evaluate response to therapy [30].

Discussion
This systematic review suggests ddPCR is a high-performance modality of potential diagnostic, prognostic, and therapeutic value in COVID-19 patients (Figure 2). ddPCR's enhanced diagnostic potential was shown in a recent meta-analysis, exhibiting a higher sensitivity than RT-qPCR and LAMP in detecting SARS-CoV-2; this particular study extracted and analyzed ddPCR data from seven studies [57]. Our findings also indicate that the diagnostic performance of ddPCR was at least comparable with RT-qPCR, with the vast majority of the included studies showing that ddPCR was superior in detecting and quantifying the SARS-CoV-2 RNA levels. Notably, when the COVID-19 diagnosis is already established, ddPCR's superb quantifying ability could be used to dynamically monitor the disease course-as high viral RNA levels in plasma imply disease severity or progression, whereas low levels imply remission-in addition to the response to therapy. Our study demonstrates that ddPCR could aid in decreasing the false-negative or ambiguous results reported with other assays, such as RT-qPCR or rapid antigen tests, especially in samples with low viral loads. Of interest, ddPCR is an end-point system, where the droplets are simply counted as positive (fluorescent) or negative (non-fluorescent). In contrast to RT-qPCR, it provides absolute target quantification (which is based on the amount of positive and negative droplets), without requiring an external calibration curve or keeping the reference material needed to construct it [58,59]. RT-qPCR is susceptible to amplification inhibitors; however, ddPCR is more tolerant to them-due to its nature that involves partitioning of the initial mixture before amplification into multiple reactions, a process that dilutes the inhibitors and enhances the signal/noise proportion-resulting in higher SARS-CoV-2 detection rates and enhanced reproducibility [45]. As a result, it has a much lower LOD [56,60]. For instance, one study conducted by Martin et al. measured the LODs of RT-PCR and ddPCR, revealing that ddPCR's LOD was 8 copies/reaction, in contrast to RT-PCR's 34 copies/reaction [41]. RT-qPCR's lower analytical sensitivity could explain its higher false negative reports [21,61].
Because of its excellent detection ability, ddPCR could be a valuable assay to complement, or even replace RT-qPCR under specific scenarios. For instance, it could be the primary testing method in the hospital setting, especially in samples of low or fluctuating viral loads, or when the clinical suspicion is high. Furthermore, ddPCR could aid in resolving the undetermined results reported by RT-qPCR or in confirming negative results of patients before their discharge, leading to improved surveillance and control and reduction of false-negative interpretations [40]. In the community setting, ddPCR could be useful for the early detection of SARS-CoV-2, especially when RT-qPCR testing is negative in individuals at risk of carrying the virus, shortening the window period. Of interest, Our study demonstrates that ddPCR could aid in decreasing the false-negative or ambiguous results reported with other assays, such as RT-qPCR or rapid antigen tests, especially in samples with low viral loads. Of interest, ddPCR is an end-point system, where the droplets are simply counted as positive (fluorescent) or negative (non-fluorescent). In contrast to RT-qPCR, it provides absolute target quantification (which is based on the amount of positive and negative droplets), without requiring an external calibration curve or keeping the reference material needed to construct it [58,59]. RT-qPCR is susceptible to amplification inhibitors; however, ddPCR is more tolerant to them-due to its nature that involves partitioning of the initial mixture before amplification into multiple reactions, a process that dilutes the inhibitors and enhances the signal/noise proportion-resulting in higher SARS-CoV-2 detection rates and enhanced reproducibility [45]. As a result, it has a much lower LOD [56,60]. For instance, one study conducted by Martin et al. measured the LODs of RT-PCR and ddPCR, revealing that ddPCR's LOD was 8 copies/reaction, in contrast to RT-PCR's 34 copies/reaction [41]. RT-qPCR's lower analytical sensitivity could explain its higher false negative reports [21,61].
Because of its excellent detection ability, ddPCR could be a valuable assay to complement, or even replace RT-qPCR under specific scenarios. For instance, it could be the primary testing method in the hospital setting, especially in samples of low or fluctuating viral loads, or when the clinical suspicion is high. Furthermore, ddPCR could aid in resolving the undetermined results reported by RT-qPCR or in confirming negative results of patients before their discharge, leading to improved surveillance and control and reduction of false-negative interpretations [40]. In the community setting, ddPCR could be useful for the early detection of SARS-CoV-2, especially when RT-qPCR testing is negative in individuals at risk of carrying the virus, shortening the window period. Of interest, there is evidence that the SARS-CoV-2 virus appears in the saliva in the early course of the infection [53]. A study conducted by Cassinari et al. showed that ddPCR had superior sensitivity compared to RT-qPCR (85% versus 62%) when testing saliva samples from patients positive for SARS-CoV-2 with nasopharyngeal sampling [35].
As mentioned before, ddPCR has several advantages over other commercial tests used for COVID-19 diagnostics, such as RT-qPCR. However, because of certain disadvantagessuch as its limited availability, higher cost, relatively low throughput, and longer turnaround times compared to RT-qPCR-it could be unfeasible to regularly perform ddPCR in the community setting, instead of rapid antigen or RT-qPCR testing [34,40]. Some of these disadvantages can yet be overcome. For instance, Yin et al. designed a rapid digital PCR providing robust results in less than 15 min [29]. Similar to other assays used for SARS-CoV-2 detection, another drawback of ddPCR includes the generation of false positive results, caused by the inaccurate interpretation of negative droplets as positive [58]. The presence of false positive droplets could even appear while testing no-template controls [58]. To deal with this issue, a few of the included studies focused their investigation on symptomatic patients, for example during their hospitalization [21,22,34,48]. This helped confirm their clinical suspicion and our findings indicate the ddPCR outperformed RT-qPCR in such clinical scenarios. One way to deal with potential false positive results in asymptomatic patients could be to retest a sample using the same or a different assay. Notably, a study by Yin et al. showed that RT-qPCR required more undetermined samples to be retested, when compared to ddPCR [29].
Multiple parameters need to be adjusted, as they could impact the sensitivity of ddPCR. These include the amount of input genetic material, the concentration of the primers used in the reaction, the cycling conditions (e.g., duration of denaturation, annealing, and extension; number of cycles; temperature during annealing and extension), also determining the fluorescence threshold and LOD [62]. Of interest, a study showed that undigested fragments could fail packaging into droplets, compromising the performance of the assay [63]. Even if less likely than RT-qPCR, ddPCR detection ability could also be impacted by inhibitors or non-target genetic material. Thus, optimization of the ddPCR assay and strict quality control measures are needed to achieve accurate and reproducible results [58,62]. Improved artificial intelligence algorithms could also help towards this direction [64].
Apart from its enhanced diagnostic performance, ddPCR could play a key role in stratifying disease severity, assessing prognosis, and monitoring response to therapy in COVID-19 patients. Although evidence is still preliminary, ddPCR may have the potential to become an ancillary tool or the primary modality in these settings. One study reported elevated SARS-CoV-2 RNA concentration in plasma was associated with severe illness in COVID-19 patients [49]. Furthermore, a higher viral load in the plasma was associated with increased mortality or ICU admission [46,49]. ddPCR was also accurate in detecting and quantifying SARS-CoV-2 RNA plasma levels in immunocompromised and ICU patients, a finding with potential clinical significance [23,37,46,49]. Indeed, ddPCR could serve as the emerging diagnostic modality of choice to monitor patients under such settings. In addition, evidence has shown that, through quantifying the SARS-CoV-2 RNA plasma levels, ddPCR could monitor COVID-19 patients' disease course and response to therapy [30]. Besides targeting the SARS-CoV-2 genome, ddPCR was further able to assess response to therapy by detecting the levels of serum-miR-146a-5p after treatment with TCZ [43].
Our study mainly compared the diagnostic accuracy of ddPCR with RT-qPCR. Except these two, other NAATs have been used for SARS-CoV-2 detection, for example LAMP. In contrast to PCR-based assays that run in thermal cyclers, the latter operates on a constant temperature (60-65 • C), and its results can be assessed with simple visual detection, without needing a machine [65,66]. LAMP is a fast and economical modality that holds promise in COVID-19 diagnostics. However, its sensitivity has been found to be lower than that of ddPCR [57]. Similar to ddPCR, NGS has also been reported to have diagnostic, prognostic, and therapeutic value in COVID-19 patients, while it has also shown to be robust in identifying coinfections in such patients. NGS comes though with expensive infrastructure and needs highly trained laboratory personnel, including bioinformatics support [67].
This systematic review is not without its limitations. Firstly, there was heterogeneity among the ddPCR and/or RT-qPCR laboratory protocols used in the included studies. There was also a variety of sample sources used, potentially affecting the diagnostic accuracy of ddPCR. A recent study reported that ddPCR's sensitivity varied among different sources of samples, with the highest positive detection rate being in nasopharyngeal swabs [67], yet further evidence focusing on the diagnostic performance of ddPCR across diverse samples would be desirable. Both protocol and sample source diversity prohibited us from conducting a quantitative analysis. Most of the eligible studies in this review assessed the diagnostic accuracy of ddPCR, especially in comparison to RT-qPCR; in contrast, there were fewer studies that discussed the prognostic value of ddPCR or evaluated its role in monitoring COVID-19 therapy response, further necessitating the need for additional future research. Lastly, limited evidence suggests the distinct SARS-CoV-2 variants do not have a significant impact on the diagnostic performance of NAAT assays and that ddPCR should be effective in detecting them [68,69]. Notably, a study by Perchetti et al. suggested that ddPCR is superior to RT-qPCR for detecting and differentiating COVID-19 variants [70], yet it is clear that more studies are needed to unravel ddPCR's potential in this scenario.

Search Strategy
This systematic review was conducted according to the standards set by the Preferred Reporting Item for Systematic Review and Meta-Analysis (PRISMA) Statement [71]. Two electronic databases (PubMed and Scopus) were comprehensively searched until 13 July 2021. An additional search was performed on 21 October on the PubMed database. The following search strategy was employed to identity all articles reporting on the diagnostic, prognostic, and therapeutic value of digital PCR in COVID-19 patients: ("digital PCR" OR ddPCR) AND (COVID-19 OR SARSCoV2). No specific filters were used, like publication date or article type.

Study Selection
Articles written in English were considered eligible if they studied or compared the use of digital PCR with other diagnostic techniques in samples derived from humans with a suspected or established COVID-19 diagnosis. There were no restrictions on the type of clinical samples studied (e.g., nasopharyngeal swabs, saliva, and blood) or the phase of COVID-19 infection. Articles were excluded if they studied solely non-human (e.g., cell lines, animal models, environmental) or post-mortem tissue samples. Editorials, reviews, and conference abstracts were also excluded. Duplicates were removed by using the Paperpile reference manager (https://paperpile.com/app, accessed on 13 July 2021).
Two authors (M.M.A. and A.I.) independently performed an initial title and abstract screening using the Rayyan software [72]. This was followed by a full-text screening. Any disagreements were resolved by a third author (I.P.N.). Bibliography lists of all relevant articles were reviewed to identify any studies missed by the database search, using a snowball approach [73].

Data Extraction
Relevant data were extracted independently by two authors (A.I. and M.M.A.) on an Excel ® spreadsheet. Any disagreements were resolved by a third author (I.P.N.). The following data were extracted: first author, year, number of samples, number of patients and/or controls, source of samples, diagnostic performance of ddPCR and/or comparison methodology, and main ddPCR findings of potential prognostic and therapeutic value.

Study Outcomes
This study aimed to assess the diagnostic, prognostic, and therapeutic value of ddPCR in COVID-19 patients, regardless of the sample type. It also aimed to compare the diagnostic performance of ddPCR with other diagnostic tools such as RT-qPCR and rapid antigen testing.

Conclusions
Current evidence suggests that ddPCR may improve SARS-CoV-2 detection, besides monitoring the disease course and treatment response of COVID-19 patients. This review indicates that ddPCR diagnostic ability could be superior to that of other diagnostic methods, including RT-qPCR and rapid antigen testing. Additionally, our findings suggest that ddPCR is a robust prognostic tool in COVID-19 patients, as it can effectively quantify and monitor the SARS-CoV-2 viral load levels throughout the course of the disease. Thus, it could serve as the modality of choice in selected clinical scenarios, such as in monitoring hospitalized patients and confirming their negative results before discharge, also in resolving indeterminate RT-qPCRs. However, further research-especially in the form of prospective studies and randomized clinical trials-is needed to standardize its validity and clinical utility and fully decipher its value.