Diagnostic performance of the Xpert MTB/RIF assay in BAL fluid samples from patients under clinical suspicion of pulmonary tuberculosis: a tertiary care experience in a high-tuberculosis-burden area

ABSTRACT

Objective:

To assess the diagnostic performance of the Xpert MTB/RIF assay, a rapid molecular test for tuberculosis, comparing it with that of AFB staining and culture, in BAL fluid (BALF) samples from patients with clinically suspected pulmonary tuberculosis (PTB) who are sputum smear-negative or produce sputum samples of insufficient quantity.

Methods:

This was a retrospective study of 140 cases of suspected PTB in patients who were smear-negative or produced insufficient sputum samples and were evaluated at a tertiary teaching hospital in the city of Rio de Janeiro, Brazil. All of the patients underwent fiberoptic bronchoscopy with BAL. The BALF specimens were evaluated by AFB staining, mycobacterial culture, and the Xpert MTB/RIF assay.

Results:

Among the 140 patients, results for all three microbiological examinations were available for 73 (52.1%), of whom 22 tested positive on culture, 17 tested positive on AFB staining, and 20 tested positive on the Xpert MTB/RIF assay. The sensitivity, specificity, positive predictive value, negative predictive value, and overall accuracy for AFB staining were 68.1%, 96.1%, 88.2%, 87.5%, and 87.6%, respectively, compared with 81.8%, 96.1%, 90.0%, 92.4%, and 91.8%, respectively, for the Xpert MTB/RIF assay. The agreement between AFB staining and culture was 82.3% (kappa = 0.46; p < 0.0001), whereas that between the Xpert MTB/RIF assay and culture was 91.8% (kappa = 0.8; p < 0.0001).

Conclusions:

In BALF samples, the Xpert MTB/RIF assay performs better than do traditional methods, providing a reliable alternative to sputum analysis in suspected cases of PTB. However, the rate of discordant results merits careful consideration.

Keywords:
Tuberculosis; Molecular diagnostic techniques; Bronchoscopy; Bronchoalveolar lavage fluid; Mycobacterium tuberculosis

RESUMO

Objetivo:

Avaliar o desempenho diagnóstico do teste Xpert MTB/RIF - teste molecular rápido para tuberculose, comparando-o com o da pesquisa de BAAR e da cultura, em amostras de LBA de pacientes com suspeita clínica de tuberculose pulmonar (TBP) que apresentam baciloscopia de escarro negativa ou produzem amostras com quantidade insuficiente de escarro.

Métodos:

Estudo retrospectivo de 140 casos suspeitos de TBP em pacientes que apresentaram baciloscopia negativa ou produziram amostras de escarro insuficientes e foram avaliados em um hospital-escola terciário na cidade do Rio de Janeiro (RJ). Todos os pacientes foram submetidos à fibrobroncoscopia com LBA. Os espécimes de LBA foram avaliados por meio da realização de pesquisa de BAAR, cultura para micobactérias e teste Xpert MTB/RIF.

Resultados:

Entre os 140 pacientes, resultados de todos os três exames microbiológicos estavam disponíveis para 73 (52,1%), dos quais 22 apresentaram cultura positiva, 17, pesquisa de BAAR positiva, e 20, teste Xpert MTB/RIF positivo. A sensibilidade, especificidade, valor preditivo positivo, valor preditivo negativo e precisão global da pesquisa de BAAR foram de 68,1%, 96,1%, 88,2%, 87,5% e 87,6%, respectivamente, contra 81,8%, 96,1%, 90,0%, 92,4% e 91,8%, respectivamente, do teste Xpert MTB/RIF. A concordância entre a pesquisa de BAAR e a cultura foi de 82,3% (kappa = 0,46; p < 0,0001), enquanto a concordância entre o teste Xpert MTB/RIF e a cultura foi de 91,8% (kappa = 0,8; p < 0,0001).

Conclusões:

Em amostras de LBA, o teste Xpert MTB/RIF tem melhor desempenho do que os métodos tradicionais, fornecendo uma alternativa confiável à análise do escarro em casos suspeitos de TBP. No entanto, a taxa de resultados discordantes merece uma reflexão cuidadosa.

Descritores:
Tuberculose; Técnicas de diagnóstico molecular; Broncoscopia; Líquido da lavagem broncoalveolar; Mycobacterium tuberculosis

INTRODUCTION

Tuberculosis, a disease caused by infection with Mycobacterium tuberculosis, continues to be an alarming public health problem, with high rates of morbidity and mortality worldwide. It has been estimated that there were approximately 10.0 million new cases of tuberculosis in 2019, a year in which 1.2 million and 208,000 tuberculosis-related deaths occurred among non-HIV-infected and HIV-infected individuals, respectively. Although the efforts made have saved millions of lives worldwide, reducing tuberculosis mortality by 42% since 2000, an annual decrease of approximately 4-5%, rather than the current 2%, would be needed in order to reach the End TB Strategy target of a 95% reduction by 2035. In Brazil, which is one of the 30 countries with the highest tuberculosis burden,¹ the estimated number of new cases of tuberculosis in 2019 was more than 90,000.²

One major concern regarding the management of cases of tuberculosis is that microbiological confirmation is achieved in only 40-60% of patients with pulmonary tuberculosis (PTB), the main clinical manifestation and the type of tuberculosis that is the most relevant in the chain of transmission. In addition, approximately half of all patients with PTB are sputum smear-negative for AFB or are unable to produce sputum samples of sufficient quantity,^1,3 making the diagnosis quite challenging. In such patients, fiberoptic bronchoscopy with BAL is a reliable, rapid method of collecting useful specimens for the diagnosis of PTB.^3-6 However, conventional methods, such as Ziehl-Neelsen staining, which detects AFB, and mycobacterial cultures, have poor diagnostic yields. Sputum smear microscopy for AFB is limited by its low sensitivity (approximately 40%), whereas mycobacterial culture, which is considered the gold standard, performs better (with a sensitivity of approximately 86%), although the latter is time consuming, requiring 6-8 weeks to produce a diagnosis.^7,8 Therefore, new methods have been proposed and in some cases implemented to improve diagnostic accuracy, which would allow the appropriate treatment to be instituted early, thus avoiding the spread of tuberculosis and minimizing the associated deaths. The Xpert MTB/RIF assay (GeneXpert; Cepheid, Sunnyvale, CA, USA), an automated cartridge-based assay that uses quantitative heminested real-time PCR, is a rapid (≤ 2 h) molecular test for the detection of M. tuberculosis and of resistance to rifampin.^9,10 The Xpert MTB/RIF assay has proven to have high sensitivity and specificity, as well as being a test of low complexity that is safe and cost-effective for the diagnosis and management of suspected cases of tuberculosis.^11-13 Currently, a range of clinical specimens other than spontaneous or induced sputum, such as pleural fluid, urine, cerebrospinal fluid, tracheal aspirate, and BAL fluid (BALF), have been shown to be suitable for analysis with the Xpert MTB/RIF assay.^14,15 However, there are few data in the literature regarding the analysis of BALF samples by the Xpert MTB/RIF assay for the diagnosis of PTB, especially at tertiary care facilities, as well as regarding its comparison with conventional microbiological methods. Therefore, the present study aimed to assess the performance of Xpert MTB/RIF assays of BALF samples from patients with suspected PTB who are sputum smear-negative or produce insufficient sputum samples. To that end, we evaluated such patients at a university hospital in the city of Rio de Janeiro, which ranks second among Brazilian cities in terms of tuberculosis burden.² We also evaluated the Xpert MTB/RIF assay in comparison with AFB staining, processing the BALF samples in parallel and using mycobacterial culture as the reference.

METHODS

Ethical aspects

The study was approved by the Research Ethics Committee of Pedro Ernesto University Hospital of the State University of Rio de Janeiro (Reference no. 2.013.455). All participating patients gave written informed consent.

Study design and participants

This was a retrospective analytical study of 149 patients who were sputum smear-negative, despite clinical and radiological findings suggestive of PTB. The patients were evaluated at Pedro Ernesto University Hospital, a tertiary care referral center in the city of Rio de Janeiro, Brazil, between November of 2015 and October of 2017. All of the patients underwent fiberoptic bronchoscopy. The BALF samples collected were evaluated by AFB staining, mycobacterial culture, and Xpert MTB/RIF assay. The following inclusion criteria were applied: being suspected of having PTB on the basis of clinical, physical, and radiological findings; being sputum smear-negative, producing insufficient sputum samples, or testing negative for M. tuberculosis on sputum culture; and having been referred for fiberoptic bronchoscopy. Patients who tested positive for M. tuberculosis in sputum samples (by smear microscopy or culture) were excluded, as were those with malignancy, those with fungal infection, those who were on antituberculosis regimens for more than 2 weeks, and those with a confirmed diagnosis of infection with nontuberculous mycobacteria (NTM). A confirmed diagnosis of PTB was defined as M. tuberculosis growth on mycobacterial culture of a BALF sample, which was considered the reference method. A probable diagnosis of PTB was defined as not meeting the criteria for a confirmed diagnosis of PTB but having clinical and radiological findings suggestive of tuberculosis, as well as showing a clinical response to antituberculosis treatment. Sociodemographic and clinical characteristics, such as gender, age, smoking status, history of tuberculosis, HIV status, and the presence of cavitary disease, were collected from hospital records. Smokers were defined as individuals who had smoked at least 100 cigarettes (or the equivalent) in their lifetime, and former smokers were defined as those who had quit smoking more than 12 months prior.

Patient evaluation and sample collection

In patients under intravenous sedation, clinical investigators used a flexible fiberoptic bronchoscope to perform transnasal bronchoscopy, during which there was continuous monitoring of heart rate, blood pressure, and SpO₂. In brief, after the bronchial tree had been inspected, BAL was performed by instilling sterile saline (0.9%) in serial 20-mL aliquots (up to a maximum of 200 mL). At least 50% of the total volume of the aspirate was returned, then being divided into three parts and sent to the laboratory for Ziehl-Neelsen (AFB) staining, mycobacterial culture, and Xpert MTB/RIF assay.

Smear microscopy

The BALF specimens collected from all patients were centrifuged at 3,000 × g for 15 min, after which they were submitted to microbiological tests according to Brazilian Health Regulatory Agency guidelines.¹⁶ The supernatant was carefully removed, after which it was processed in parallel for each subsequent test. For the AFB staining, a BALF sample was smeared on a glass microscope slide and allowed to dry, after which the staining was performed. After staining, a minimum of 100 fields were examined with a ×100 oil immersion objective and the smear was scanned systematically. The observation of at least one AFB was considered a positive result.

Solid culture

The BALF samples were decontaminated by using sodium hydroxide in a final concentration of 4%. After centrifugation, the supernatant was discarded and the precipitate was inoculated into tubes containing Löwenstein-Jensen solid medium. Cultures were incubated at 37°C for 60 days, being examined weekly for up to 8 weeks or until growth was observed. The growth of M. tuberculosis was identified by using a rapid immunochromatographic MPT64 antigen testing kit (SD Bioline TB Ag MPT64 Rapid test; Standard Diagnostics Inc., Yongin-si, South Korea), according to the manufacturer’s instructions.

Xpert MTB/RIF assay

Sediment from the BALF samples was processed with a DNA/RNA extraction protocol, after which the Xpert MTB/RIF platform was employed according to the manufacturer’s instructions. In brief, the samples were diluted with the sample reagent provided by the manufacturer. The clinical specimens and reagent mixture were shaken in the vortex mixer for at least 10 s and left to settle at room temperature for 15 min. As recommended, all of the solutions were then transferred to the Xpert cartridge and loaded onto the GeneXpert equipment for analysis.

Statistical analysis

In the comparison of sociodemographic, clinical, and biochemical features between the two groups (culture-confirmed PTB and non-culture-confirmed PTB), we tested the hypothesis that the different samples in the comparison were drawn from the same distribution or distributions with the same median by using Mann-Whitney U tests for continuous variables. Fisher’s exact tests were used in order to evaluate frequencies between the two groups, testing the hypothesis of independence between the groups and the categorical variables. The kappa statistic was used in analyses of agreement among mycobacterial culture, the Xpert MTB/RIF assay, and AFB staining. For the detection of M. tuberculosis in BALF samples, the performance of the Xpert MTB/RIF assay and AFB staining, as well as combinations of the two, in comparison with the gold-standard (mycobacterial culture), was estimated. We used leave-one-out cross-validation to determine their accuracy, sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV), as well as determining their rates of false-positive and false-negative results, together with the corresponding 95% confidence intervals. All statistical analyses were performed with the program R, version 3.5.2 (The R Foundation for Statistical Computing, Vienna, Austria).

RESULTS

Study design and patient characteristics

As depicted in the flow chart in Figure 1, we enrolled 149 patients who presented with clinical and radiological findings suggestive of PTB, who were sputum smear-negative or who produced sputum samples of insufficient quantity, and who underwent fiberoptic bronchoscopy. After the BALF samples had been processed and evaluated, 9 patients were excluded for receiving a final diagnosis of NTM infection. Therefore, the final study population comprised 140 patients for whom BALF test results were available. Mycobacterial culture results were available for 140 patients, M. tuberculosis being identified in 22 (15.7%) of those patients, compared with 31 (23.8%) of the 130 patients for whom AFB staining results were available and 20 (24.4%) of the 82 patients for whom Xpert MTB/RIF assay results were available. Results for all three examinations were available for 73 patients, of whom 22 (30.1%) tested positive on culture, 17 (23.2%) tested positive on AFB staining, and 20 (27.4%) tested positive on the Xpert MTB/RIF assay. None of the strains isolated were found to be resistant to rifampin.

Figure 1
Flow chart of the study design and yield of the tuberculosis diagnostic tests performed in BAL fluid samples. *Performed in only 130 of the 140 patients. ^†Performed in only 82 of the 140 patients.

Table 1 shows the demographic and clinical features of the study population, by outcome of the mycobacterial culture of the BALF samples. The median age of the patients was 56 years (IQR = 28.25 years). Seventy-eight patients (55.7%) were male, and there were no significant differences between the two groups in terms of gender distribution. All of the patients had at least one symptom suggestive of tuberculosis, the most common symptoms being weight loss (in 59.3%; p = 0.008), cough (in 57.1%), and dyspnea (in 53.6%). Cavitary disease was observed in 25 patients (17.9%). Of the 140 patients in the study population, 31 (22.1%) had previously had tuberculosis: 28 in the negative BALF culture group and 3 in the positive BALF culture group.

Table 1
Sociodemographic and clinical characteristics of the study population, by the results of mycobacterial culture of BAL fluid samples.^a

Characteristic	Result of BALF culture		Total	p
	Negative	Positive
	(n = 118)	(n = 22)	(N = 140)
Gender
Male	69 (49.3)	9 (6.4)	78 (55.7)	0.162
Female	49 (35.0)	13 (9.3)	62 (44.3)
Age in years, median (IQR)	56 (26.25)	50 (30.00)	56 (28.25)	0.6002
Smoking status
Never smoker	60 (42.9)	16 (11.4)	76 (54.3)	0.2018
Former smoker	33 (23.6)	4 (2.9)	37 (26.4)
Current smoker	25 (17.9)	2 (1.4)	27 (19.3)
Clinical features
HIV-infected	7 (5.0)	4 (2.9)	11 (7.9)	0.0718
Previous tuberculosis	28 (20.0)	3 (2.1)	31 (22.1)	0.406
Symptoms
Chest pain	46 (32.9)	8 (5.7)	54 (38.6)	1.00
Dyspnea	66 (47.1)	9 (6.4)	75 (53.6)	0.246
Fever	45 (32.1)	6 (4.3)	51 (36.4)	0.4698
Hemoptysis	49 (35.0)	4 (2.9)	53 (37.9)	0.054
Cough	67 (47.9)	13 (9.3)	80 (57.1)	1.00
Weight loss	76 (54.3)	7 (5.0)	83 (59.3)	0.0081
Cavitary diseaseb
Yes	19 (13.6)	6 (4.3)	25 (17.9)	0.229
No	99 (70.7)	16 (11.4)	115 (82.1)

• BALF: BAL fluid. ^aValues expressed as n (%), except where otherwise indicated. ^bDetermined by chest X-ray examination.

Performance of AFB staining and the Xpert MTB/RIF assay in BALF samples

Among the patients in the study population, the three methods for M. tuberculosis detection were used heterogeneously (Figure 1). Primarily, the test results were analyzed in different combinations (pairs) to evaluate the overall agreement among the Xpert MTB/RIF assay, AFB staining, and mycobacterial culture of BALF samples in suspected cases of PTB. As shown in Table 2, the Xpert MTB/RIF assay showed 91.78% agreement with culture (kappa = 0.8; p < 0.0001), compared with 82.31% for AFB staining (kappa = 0.46; p < 0.0001), regardless of whether we analyzed the sample as a whole (n = 140) or only those patients for whom results from all three examinations were available (n = 73). The agreement between the Xpert MTB/RIF assay and AFB staining was 82.2% (kappa = 0.53; p < 0.0001).

Table 2
Agreement among the results of the Xpert MTB/RIF assay, AFB staining, and mycobacterial culture in BAL fluid samples.^a

Comparison methods	Results of the comparison methods	Comparator method and results		Agreement	kappa	p
		Culture
		Negative	Positive
		118 (84.3)	22 (15.7)
Xpert MTB/RIF assay	Negative	49 (35.0)	4 (2.9)	91.78%	0.79963	< 0.0001
	Positive	2 (1.4)	18 (12.9)
AFB staining	Negative	92 (65.7)	7 (5.0)	82.31%	0.45892	< 0.0001
	Positive	16 (11.4)	15 (10.7)
		AFB staining
		Negative	Positive
		99 (70.7)	31 (22.1)
Culture	Negative	92 (65.7)	16 (11.4)	82.31%	0.45892	< 0.0001
	Positive	7 (5.0)	15 (10.7)
Xpert MTB/RIF assay	Negative	48 (34.3)	5 (3.6)	82.19%	0.53043	< 0.0001
	Positive	8 (5.7)	12 (8.6)
		Xpert MTB/RIF assay
		Negative	Positive
		53 (37.9)	20 (14.3)
Culture	Negative	49 (35.0)	2 (1.4)	91.78%	0.79963	< 0.0001
	Positive	4 (2.9)	18 (12.9)
AFB staining	Negative	48 (34.3)	8 (5.7)	82.19%	0.53043	< 0.0001
	Positive	5 (3.6)	12 (8.6)

• ^a
  Test results are presented as n (%).

When we compared the Xpert MTB/RIF assay and AFB staining in terms of their individual diagnostic performance in BALF samples, using mycobacterial culture as the reference, we found that the Xpert MTB/RIF assay had an overall accuracy of 92%, a sensitivity of 81%, a PPV of 90%, and an NPV of 92%, compared with only 87%, 68%, 88%, and 87%, respectively, for AFB staining. Two different conditions (“OR” and “AND”) were also analyzed. When the two methods were used in combination (Xpert MTB/RIF assay AND AFB staining) the specificity and PPV increased to 100%. However, the false-positive rate was higher when one or the other method was used (Xpert MTB/RIF assay OR AFB staining) than when the two were used in combination (Table 3).

Table 3
Diagnostic performance of the Xpert MTB/RIF assay and AFB staining in BAL fluid samples, in comparison with the reference method (mycobacterial culture).

Measure	Xpert MTB/RIF	AFB staining	Xpert MTB/RIF OR AFB staining	Xpert MTB/RIF AND AFB staining
	% (95% CI)	% (95% CI)	% (95% CI)	% (95% CI)
Accuracy	91.78 (87.35 to 96.21)	87.67 (82.37 to 92.97)	93.15 (89.08 to 97.22)	86.3 (80.76 to 91.85)
Sensitivity	81.82 (70.11 to 93.52)	68.18 (54.05 to 82.32)	95.45 (89.13 to 101.78)	54.55 (39.43 to 69.66)
Specificity	96.08 (92.31 to 99.85)	96.08 (92.31 to 99.85)	92.16 (86.94 to 97.37)	100.00 (100.00 to 100.00)
PPV	90.00 (80.4 to 99.6)	88.24 (76.95 to 99.52)	84.00 (73.62 to 94.38)	100.00 (100.00 to 100.00)
NPV	92.45 (87.43 to 97.48)	87.50 (81.39 to 93.61)	97.92 (95.06 to 100.78)	83.61 (77.06 to 90.16)
FPR	3.92 (0.15 to 7.69)	3.92 (0.15 to 7.69)	7.84 (2.63 to 13.06)	0.00 (0.00 to 0.00)
FNR	18.18 (6.48 to 29.89)	31.82 (17.68 to 45.95)	4.55 (−1.78 to 10.87)	45.45 (30.34 to 60.57)

• PPV: positive predictive value; NPV: negative predictive value; FPR: false-positive rate; and FNR: false-negative rate.

To promote better identification and visualization of the overall performance of the methods evaluated, we created a Venn diagram to illustrate the outcomes of the BAL Xpert MTB/RIF assay, AFB staining, and mycobacterial culture of BALF samples in the 73 patients for whom results from all three examinations were available (Figure 2). The distribution of positive (⁺) and negative (⁻) results was as follows: Xpert MTB/RIF assay⁺/culture⁺/AFB staining⁺ = 12 patients; Xpert MTB/RIF assay⁻/culture⁺/AFB staining⁻ = 1 patient; Xpert MTB/RIF assay⁺/culture⁺/AFB staining⁻ = 6 patients; Xpert MTB/RIF assay⁺/culture⁻/AFB staining⁻ = 2 patients; Xpert MTB/RIF assay⁻/culture⁺/AFB staining⁺ = 3 patients; Xpert MTB/RIF assay⁻/culture⁻/AFB staining⁺ = 2 patients. Altogether, the Xpert MTB/RIF assay identified three more cases than did AFB staining.

Figure 2
Venn diagram of the positive results of the tuberculosis diagnostic tests performed in BAL fluid samples: Xpert MTB/RIF assay (green), AFB staining (blue), and mycobacterial culture (pink). Note: numerals indicate the number of cases in which Mycobacterium tuberculosis was identified.

DISCUSSION

As previously mentioned, even though mycobacterial culture has long been considered the gold standard method for the diagnosis of PTB, 40-50% of cases are not detected by microbiological methods.¹ Sputum smear microscopy has low sensitivity and limited specificity, the latter evidenced by its incapacity to differentiate between M. tuberculosis and NTM species. In addition, some patients do not produce significant quantities of spontaneous or induced sputum,^1,3 which makes it difficult to obtain sufficient clinical specimens for microbiological analysis. In this scenario, empirical antituberculosis treatment emerges as a possible strategy to interrupt the spread of the disease and minimize the associated mortality. In the present study, we found that the Xpert MTB/RIF assay-a rapid molecular test for tuberculosis-performed better than did AFB staining in BALF samples from patients with suspected PTB who were sputum smear-negative or produced sputum samples of insufficient quantity, in a high-tuberculosis-burden area.

Recently, the Brazilian National Ministry of Health has recommended the use of the Xpert MTB/RIF assay in clinical specimens other than sputum, such as BALF, which is obtained by fiberoptic bronchoscopy, as an alternative way to investigate suspected cases of tuberculosis.² The Xpert MTB/RIF assay offers many advantages, such as providing results within 2 h, thus allowing antituberculosis treatment to be initiated sooner; high sensitivity, specificity, and overall accuracy; detecting rifampin-resistant M. tuberculosis strains; and high sensitivity and specificity for the detection of tuberculosis in HIV-infected patients.^11,13,17 Despite its limitations, which include a high false-positive rate and the high costs of equipment maintenance and reagents/components, the Xpert MTB/RIF assay has made an essential contribution in clinical practice as a rule-in or rule-out test for the diagnosis of tuberculosis.^18,19

The performance of the Xpert MTB/RIF assay in sputum samples has been well documented,^13,20,21 as has the value of BALF samples in the diagnosis of tuberculosis, especially in patients who are sputum smear-negative or unable to produce sufficient sputum samples^4,22-24; however, there have been few studies analyzing and validating the utility of molecular tests for the diagnosis of tuberculosis in BALF specimens. Khalil & Butt²⁵ demonstrated that, in comparison with mycobacterial culture, the Xpert MTB/RIF assay was superior for detecting M. tuberculosis and rifampin resistance showing high sensitivity (91.86%) and PPV (97.53%) in patients with PTB who were sputum smear-negative or unable to produce sufficient sputum samples. In a retrospective study, Agrawal et al.²⁶ also showed that the Xpert MTB/RIF assay performed better in respiratory samples (sputum and BALF) than did AFB staining. Finally, a recent study conducted at a tertiary care facility in India compared BAL the Xpert MTB/RIF assay, AFB staining, and mycobacterial culture in BALF samples from suspected cases of PTB, in a manner similar to that of the present study. Bashir et al.²⁷ observed that, although the Xpert MTB/RIF assay and AFB staining had similar overall specificity, the sensitivity of the Xpert MTB/RIF assay was much higher than was that of smear microscopy in BALF samples (97.1% vs. 36.7%). Together with all of that evidence, our data support the use of the Xpert MTB/RIF assay in BALF samples as an interesting and suitable tool to improve the diagnosis of tuberculosis.

In the present study, there were some discordant results among the outcomes of the Xpert MTB/RIF assay, AFB staining, and mycobacterial culture, particularly among the 73 patients for whom results from all three examinations were available. There were two patients in whom the BALF samples tested positive on the Xpert MTB/RIF assay, despite testing negative on AFB staining and culture. It is noteworthy that those samples had higher cycle threshold values (26.6-30.9; probes A-E), which implies low concentrations of M. tuberculosis DNA.²⁸ That could explain the negative results obtained with mycobacterial culture and AFB staining. In two other patients, M. tuberculosis was identified only by AFB staining; one of those patients, a female, was HIV-infected. Immunosuppression can favor coinfection with other pathogens, such as NTM.^29,30 However, in that case, there was no growth in mycobacterial culture, which delayed the diagnosis. In addition, there was one case in which M. tuberculosis was identified only in culture. None of those 5 patients reported having had tuberculosis previously. Therefore, on the basis of clinical and radiological criteria, they were treated with an antituberculosis regimen. After six months, all of them showed improvement in the signs and symptoms. All of these discrepancies should be interpreted with caution, the limitations of each method and the clinical status of the patients being taken into consideration.

Our study has some limitations. First, it was a single-center study, which limits the generalizability of the data. Second, because it was a retrospective study, the clinical data were limited to those available in the medical records. Third, there was a relatively small number of cases in which results were available from all three of the methods evaluated. However, the study was performed at a specialized, tertiary, referral teaching hospital in a high-tuberculosis-burden area, where numerous tools are available for the investigation and accurate diagnosis of cases of tuberculosis. In addition, mycobacterial culture results were available for all cases, and we excluded cases of NTM infection in order to avoid bias.

In summary, in BALF samples, the Xpert MTB/RIF assay performed better than did AFB staining for the diagnosis of cases of PTB in patients who were sputum smear-negative or were unable to produce sputum specimens of sufficient quantity. That could have a significant impact on clinical practice and on the management of such cases, particularly those in which the diagnosis is challenging. When the Xpert MTB/RIF assay produces results that are discordant with those of other diagnostic tools, those discrepancies must be carefully analyzed, given that tuberculosis continues to be a significant public health problem worldwide.

ACKNOWLEDGMENTS

The authors would like to thank the administration, staff, residents, and patients of the Pedro Ernesto University Hospital for participating in this study.

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• 1
  Study carried out in the Disciplina de Pneumologia e Tisiologia, Hospital Universitário Pedro Ernesto, Universidade do Estado do Rio de Janeiro - UERJ - Rio de Janeiro (RJ) Brasil.

• Financial support:

  None:

Publication Dates

• Publication in this collection
  17 May 2021
• Date of issue
  2021

History

• Received
  21 Nov 2020
• Accepted
  08 Mar 2021