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1. Introduction
Tuberculosis (TB) is an infectious disease caused by the bacillus Mycobacterium tuberculosis (Mtb) and is a major global health problem. According to the World Health Organization (WHO), the estimated global incidence of TB was 9.87 million cases in 2020 [1]. TB is a multisystemic disease with a protean presentation. Compared to pulmonary TB (PTB), relatively less attention has been given to extrapulmonary TB (EPTB) from public health entities, likely due to the fact that most forms of EPTB do not contribute to TB transmission [2]. In fact, 16% of reported TB cases globally in 2019 were EPTB [3]. While not usually transmissible, EPTB can cause serious morbidity and mortality [4–6]. TB is transmitted when people afflicted with PTB expel TB bacteria into the air; these airborne bacilli are subsequently inhaled by another person and settle in the lungs and grow. If the immune system does not stop TB germs from growing, the TB germs begin to multiply in the body. From there they can disseminate throughout the lymphatic or hematogenous systems and subsequently infect single or multiple extrapulmonary sites, such as the pleura, lymph nodes, and meninges [7]. The mechanisms of EPTB dissemination are complicated [8].
EPTB has a wide variety of nonspecific clinical presentations according to the location of the TB lesions. In clinical practice, EPTB concurrent with other types of EPTB (concurrent EPTB) is often observed, but little information exists about the association networks of concurrent EPTB. Concurrent EPTB cases are different and more difficult to treat than a single EPTB lesion [9]. The proportion of EPTB in TB patients varies greatly in different countries [6, 10]. In addition, studies from different countries reported an increase in the proportion of EPTB [2, 10]. A possible reason for this is that economic and medical improvement enables more and more patients with EPTB to seek treatment [11]. As information pertaining to concurrent EPTB is scarce, research efforts are needed to seek and diagnose concurrent EPTB types and explore the epidemiological characteristics and association networks that exist in concurrent EPTB. In this work, we address this gap in knowledge by conducting a large-scale multicenter observational study. The results can be used to alert clinicians to the occurrence of concurrent EPTB and to optimize treatment regimens used for such cases.
2. Methods
2.1. Study Subjects
The study was performed at 21 hospitals from 15 provinces in China, most of which were specialized TB hospitals. All the consecutive adult inpatients (≥ 15 years) with confirmed EPTB diagnoses from Jan 1, 2011, to Dec 31, 2017, were included in the study (not including cases of EPTB with concurrent PTB). TB was primarily categorized by the lesion site. The diagnosis of TB was based on WHO guidelines [12] and the TB clinical diagnosis standards issued by the Chinese Medical Association [13]. In general, TB was diagnosed using both traditional and modern methods based on clinical symptoms and physical signs together with results obtained by bacteriological methods (including sputum smear microscopy, bacterial culture, and molecular diagnostic methods), X-ray/CT findings, pathology, and treatment outcomes after a course of anti-TB chemotherapy.
2.2. Data Management and Statistical Analysis
Measures taken to guarantee data quality included both the implementation of a standardized study protocol and standardized training of research staff. Clinical characteristics of TB-afflicted inpatients (e.g., age, gender, and site of disease) were obtained from medical records. Descriptive statistical analysis included frequencies and proportions for categorical variables. Multivariable logistic regression analysis was used to examine the associations of gender/age groups and determinations of odds ratios were conducted for concurrent EPTB. Primary analyses were based on tests for trends, modeling the ordered age categories as linear terms. A
Association rule analysis, a technique used to discover the relationships hidden in large databases, has been used in a variety of other fields [14, 15]. The Apriori algorithm makes it possible to apply a set of association rules to data mining. The principle of Apriori is based on two steps: the first step searches for item sets that exceed the minimum support threshold value while the second step generates association rules and filters them by selecting “confidence” item sets (based on a threshold) from item sets found in the first step [16, 17]. For the association rule of A concurrent with B, support, confidence, and lift were defined as follows: Support = P(A), Confidence = P(B|A), and Lift = P(A∩B)/[P(A) ∗ P(B)], whereby A is antecedent and B is consequent. Lift was used to evaluate the magnitude of association rules whereby a lift > 1 indicated a positive association rule and a lift ≥ 3 indicated a strong association rule. Association rules for concurrent EPTB were analyzed using the Apriori algorithm by setting the minimum support degree and the minimum confidence degree.
All data were collected in MS Office Excel datasheets (Microsoft, Redmond, WA, USA), and all analyses were conducted using SPSS software for Windows Version 23 and SPSS Modeler Version 14.1(IBM Corp, Armonk, NY, USA). The association network graph was made by UCINET 6.212 (Analytic Technologies, Lexington, KY, USA).
2.3. Ethical Approval and Consent to Participate
This was a retrospective observational analysis of de-identified medical records. Individual informed consent was not obtained. Given that the medical information of inpatients was recorded anonymously by case history and would not bring any risk to the participants, the ethics committee of the Beijing Chest Hospital, Capital Medical University, approved this study, with a waiver of informed consent from the patients.
3. Results
3.1. EPTB Patient Characteristics
A total of 75,993 adult EPTB patients (not including cases of EPTB concurrent with PTB) were included. The characteristics for our patient cohort are shown in Table 1. The ratio of male:female was 1.32. The proportions of 15–24 years and 25–34 years of age EPTB patients were the most. A total of 80 types of EPTB diseases were found. The most common types of EPTB lesions were tuberculous pleurisy (46.47%), followed by tuberculous lymphadenitis of the neck (10.49%), and tuberculous meningitis (7.22%). Approximately 13% of EPTB patients had at least two EPTB lesions.
Table 1
The characteristics of EPTB inpatients.
Variables | N (75,993) | Proportion (%) |
Gender | ||
Female | 32,738 | 43.08 |
Male | 43,255 | 56.92 |
Age group | ||
15–24 years | 15,822 | 20.82 |
25–34 years | 15,763 | 20.74 |
35–44 years | 11,326 | 14.90 |
45–54 years | 11,517 | 15.16 |
55–64 years | 10,111 | 13.31 |
≥ 65 years | 11,454 | 15.07 |
EPTB types | ||
Exclusively EPTB | 66,249 | 87.18 |
Concurrent EPTB | 9744 | 12.82 |
Note: Exclusively EPTB: only one EPTB lesion; concurrent EPTB: at least two EPTB lesions.
3.2. The Concurrent EPTB in Different Gender and Age Groups
The concurrent EPTB in different gender and age groups is shown in Figure 1. Among all the age groups, the percent of concurrent EPTB in females was greater than the corresponding percent of male cases.
[figure(s) omitted; refer to PDF]
In the fully adjusted multivariable logistic regression models, it was found that female EPTB patients (aOR = 1.129, 95% CI: 1.081–1.178) were more likely to have concurrent EPTB. Notably, as age increased, the risk of concurrent EPTB decreased (aOR < 1, p value for trend < 0.001). When the ≥ 65 years age group was set as the reference, the 15–24 years group (aOR = 1.319, 95% CI: 1.225–1.421), 25–34 years group (aOR = 1.313, 95% CI: 1.219–1.414), 35–44 years group (aOR = 1.269, 95% CI: 1.172–1.375), and 45–54 years group (aOR = 1.154, 95% CI: 1.064–1.251) were more likely to have concurrent EPTB (Table 2).
Table 2
Association between gender, age group, and concurrent EPTB in multivariable analysis.
Variables | No. of concurrent EPTB (%) | aOR (95% CI) | |
Gender | |||
Female | 4466 (13.6) | 1.129 (1.081–1.178) | < 0.001 |
Male | 5278 (12.2) | Reference | |
Age group (years) | |||
15–24 | 2184 (13.8) | 1.319 (1.225–1.421) | < 0.001 |
25–34 | 2188 (13.9) | 1.313 (1.219–1.414) | < 0.001 |
35–44 | 1527 (13.5) | 1.269 (1.172–1.375) | < 0.001 |
45–54 | 1424 (12.4) | 1.154 (1.064–1.251) | 0.001 |
55–64 | 1181 (11.7) | 1.086 (0.998–1.182) | 0.057 |
≥ 65 | 1240 (10.8) | Reference | |
Trend test | — | 0.945 (0.933–0.957) | < 0.001 |
3.3. The Association Network of Concurrent EPTB in EPTB Patients
EPTB manifested as exclusively EPTB or concurrent EPTB. It was found that many types of EPTB disease may have concurrence with other EPTB. The proportions of concurrent EPTB in different EPTB diseases were different. Some EPTB diseases existed mainly in concurrence with other types of EPTB. EPTB diseases (≥ 100 cases) with a proportion of concurrent EPTB > 50% are shown in Table 3, sorted by the proportion of concurrent EPTB. The proportion of concurrent with other types of EPTB in ureteric TB, sacral TB, and tuberculous abscess of the psoas major was more than 70%.
Table 3
The proportion of concurrent EPTB > 50% in EPTB disease (≥ 100 cases).
EPTB types | n | Concurrent EPTB proportion (%) |
Ureteric tuberculosis | 194 | 78.87 |
Sacral tuberculosis | 229 | 78.60 |
Tuberculous abscess of psoas major | 349 | 70.77 |
Vesical tuberculosis | 165 | 69.70 |
Hepatic tuberculosis | 148 | 63.51 |
Tuberculosis of abdominal lymph nodes | 211 | 58.77 |
Tuberculosis of mediastinal lymph nodes | 687 | 55.75 |
Tuberculous pericarditis | 2409 | 54.67 |
Oviduct tuberculosis | 167 | 52.69 |
Brain tuberculoma | 104 | 50.96 |
Note: n-the case of EPTB disease. Concurrent EPTB proportion − (concurrent EPTB)/(concurrent EPTB + exclusively EPTB).
The association network graph of concurrent types of EPTB in EPTB diseases is shown in Figure 2. A line connecting two types of EPTB diseases indicates that they were concurrent. For example, the connected line between tuberculous pleurisy and tuberculous peritonitis means tuberculous peritonitis is concurrent with tuberculous pleurisy. The association network graph showed that almost all the EPTB diseases may be concurrent with other types of EPTB. A bigger EPTB disease node indicates a greater number of concurrent EPTB types. For example, the node of tuberculous pleurisy was the biggest, indicating that tuberculous pleurisy has the most concurrence with other types of EPTB. EPTB diseases (≥ 100 cases) with ≥ 40 other concurrent types of EPTB disease are shown in Table 4, sorted by the concurrent types. Tuberculous pleurisy (concurrent types = 66) and tuberculous lymphadenitis of the neck (concurrent types = 64) were concurrent with more than 60 other types of EPTB disease.
[figure(s) omitted; refer to PDF]
Table 4
The concurrent types (≥ 40) in EPTB disease (≥ 100 cases).
EPTB types | n (%) | No. of concurrent other types of EPTB (%) |
Tuberculous pleurisy | 35,316 (46.47) | 66 (82.50%) |
Tuberculous lymphadenitis of the neck | 7974 (10.49) | 64 (80.00%) |
Lumbar vertebra tuberculosis | 4504 (5.93) | 59 (73.75%) |
Tuberculous meningitis | 5485 (7.22) | 53 (66.25%) |
Thoracic vertebra tuberculosis | 2786 (3.67) | 51 (63.75%) |
Tuberculous peritonitis | 4157 (5.47) | 48 (60.00%) |
Chest wall tuberculosis | 2343 (3.08) | 48 (60.00%) |
Renal tuberculosis | 1579 (2.08) | 48 (60.00%) |
Tuberculous empyema | 3475 (4.57) | 46 (57.50%) |
Cutaneous tuberculosis | 467 (0.61) | 44 (55.00%) |
Tuberculosis of mediastinal lymph nodes | 687 (0.90) | 43 (53.75%) |
Intestinal tuberculosis | 1278 (1.68) | 41 (51.25%) |
Tuberculous pericarditis | 2409 (3.17) | 40 (50.00%) |
Knee joint tuberculosis | 667 (0.88) | 40 (50.00%) |
Note: Concurrent types—one type of EPTB concurrent with the number of other types of EPTB. n% = n/75993
The most common concurrent EPTB types (≥ 100 cases) are listed in Table 5, sorted by cases. The case numbers of tuberculous peritonitis concurrent with tuberculous pleurisy (1.64%), tuberculous pericarditis concurrent with tuberculous pleurisy (1.48%), and thoracic vertebra TB concurrent with lumbar vertebra TB (0.70%) were greater than other types of concurrent EPTB cases.
Table 5
The cases of concurrent EPTB types (cases ≥ 100).
Concurrent EPTB types | n | Proportion (%) |
Tuberculous peritonitis concurrent with tuberculous pleurisy | 1249 | 1.64 |
Tuberculous pericarditis concurrent with tuberculous pleurisy | 1124 | 1.48 |
Thoracic vertebra tuberculosis concurrent with lumbar vertebra tuberculosis | 533 | 0.70 |
Tuberculous meningitis concurrent with tuberculous pleurisy | 444 | 0.58 |
Tuberculous lymphadenitis of neck concurrent with tuberculous pleurisy | 406 | 0.53 |
Bronchial tuberculosis concurrent with tuberculous pleurisy | 384 | 0.51 |
Intestinal tuberculosis concurrent with tuberculous peritonitis | 314 | 0.41 |
Chest wall tuberculosis concurrent with tuberculous pleurisy | 279 | 0.37 |
Pelvic tuberculosis concurrent with tuberculous peritonitis | 276 | 0.36 |
Thoracic vertebra tuberculosis concurrent with tuberculous pleurisy | 274 | 0.36 |
Chest wall tuberculosis concurrent with tuberculous empyema | 253 | 0.33 |
Tuberculous empyema concurrent with tuberculous pleurisy | 207 | 0.27 |
Lumbar vertebra tuberculosis concurrent with tuberculous pleurisy | 184 | 0.24 |
Tuberculosis of axillary lymph nodes concurrent with tuberculous lymphadenitis of neck | 175 | 0.23 |
Bronchial tuberculosis concurrent with tuberculous lymphadenitis of neck | 172 | 0.23 |
Sacral tuberculosis concurrent with lumbar vertebra tuberculosis | 157 | 0.21 |
Lumbar vertebra tuberculosis concurrent with tuberculous abscess of psoas major | 153 | 0.20 |
Tuberculous peritonitis concurrent with tuberculous pericarditis | 145 | 0.19 |
Tuberculosis of mediastinal lymph nodes concurrent with tuberculous lymphadenitis of neck | 142 | 0.19 |
Intestinal tuberculosis concurrent with tuberculous pleurisy | 136 | 0.18 |
Lumbar vertebra tuberculosis concurrent with tuberculous meningitis | 136 | 0.18 |
Pelvic tuberculosis concurrent with tuberculous meningitis | 115 | 0.15 |
Note: Proportion = n
3.4. Association Rule Analysis of Concurrent EPTB
In order to find most of the possible association rules of concurrent EPTB, the parameters were set as follows: minimum instances were set to 100 cases, the minimum confidence degree was set to 20.00%, and lift was ≥ 1. After executing the association rule analysis, 17 association rules were obtained. The association rules are shown in Table 6 and are sorted by confidence. The first rule row(ID=1) in Table 6 was interpreted a total of 229 sacral tuberculosis cases (Instances), sacral tuberculosis accounted for 0.30% of all the EPTB cases (Support), while sacral tuberculosis concurrent with lumbar vertebra tuberculosis accounted for 68.56% of sacral tuberculosis cases (Confidence). The confidence value for ureteric TB with concurrent renal TB cases was the second highest (50.52%), followed by tuberculous pericarditis with concurrent tuberculous pleurisy (46.66%). The strongest association rule was found for vesical TB with concurrent ureteric TB (lift = 166.18), ureteric TB with concurrent vesical TB (lift = 166.18), and in TB of the hilar lymph nodes concurrent with TB of the mediastinal lymph nodes (lift = 24.82), whereby the lift value of ≥ 3 indicated that ureteric TB was positively associated with vesical TB, vesical TB was positively associated with ureteric TB, and TB of mediastinal lymph nodes was positively associated with TB of hilar lymph nodes.
Table 6
The association rules of concurrent EPTB (mininstances = 100, minconfidence = 20%, and lift ≥ 1).
Consequent | Antecedent | ID | Instances | Support (%) | Confidence (%) | Lift |
Lumbar vertebra tuberculosis | Sacral tuberculosis | 1 | 229 | 0.30 | 68.56 | 11.57 |
Renal tuberculosis | Ureteric tuberculosis | 2 | 194 | 0.26 | 50.52 | 24.31 |
Tuberculous pleurisy | Tuberculous pericarditis | 3 | 2409 | 3.17 | 46.66 | 1.01 |
Renal tuberculosis | Vesical tuberculosis | 4 | 165 | 0.22 | 45.45 | 21.88 |
Lumbar vertebra tuberculosis | Tuberculous abscess of psoas major | 5 | 349 | 0.46 | 43.84 | 7.40 |
Ureteric tuberculosis | Vesical tuberculosis | 6 | 165 | 0.22 | 42.42 | 166.18 |
Vesical tuberculosis | Ureteric tuberculosis | 7 | 194 | 0.26 | 36.08 | 166.18 |
Tuberculous meningitis | Brain tuberculoma | 8 | 104 | 0.14 | 30.77 | 4.26 |
Tuberculous peritonitis | Pelvic tuberculosis | 9 | 1039 | 1.37 | 26.56 | 4.86 |
Tuberculous lymphadenitis of neck | Inguinal lymph node tuberculosis | 10 | 245 | 0.32 | 26.53 | 2.53 |
Pelvic tuberculosis | Oviduct tuberculosis | 11 | 167 | 0.22 | 26.34 | 19.27 |
Tuberculous lymphadenitis of neck | Tuberculosis of axillary lymph nodes | 12 | 703 | 0.93 | 24.89 | 2.37 |
Tuberculous peritonitis | Intestinal tuberculosis | 13 | 1278 | 1.68 | 24.57 | 4.49 |
Pelvic tuberculosis | Endometrial tuberculosis | 14 | 185 | 0.24 | 23.24 | 17.00 |
Tuberculosis of mediastinal lymph nodes | Tuberculosis of hilar lymph nodes | 15 | 205 | 0.27 | 22.44 | 24.82 |
Tuberculous lymphadenitis of neck | Tuberculosis of mediastinal lymph nodes | 16 | 687 | 0.90 | 20.67 | 1.97 |
Tuberculous peritonitis | Hepatic tuberculosis | 17 | 148 | 0.19 | 20.27 | 3.71 |
Note: ID displays the sequence of the association rules. Instances display the cases of EPTB lesion. Mininstances: the lowest of instance. Minconfidence: the lowest of confidence.
4. Discussion
TB has many forms of extrapulmonary manifestations, affecting almost every organ of the body. It has been reported that there are significant differences in the susceptibility to EPTB in different parts of the body by age, race/ethnicity, sex, and country of origin [2, 10, 18]. The age-gender percent-bar-graph of concurrent EPTB showed that among all the age groups, the percent of concurrent EPTB in females was greater than the corresponding percent of male cases in Figure 1. But the results of 25–34 years (
It was found that females have a higher risk of developing EPTB through epidemiological studies conducted in industrialized countries and resource-limited countries with high burdens of TB [10, 21]. According to the data of this study, females with EPTB (aOR = 1.129, 95% CI: 1.081–1.178) were also more likely to have concurrent EPTB. Consistent with studies in the United States [10], Germany [18], Denmark [22], the European Union [2], and India [23], an association between female gender and EPTB is observed. In many studies, females tended to be more likely to have EPTB than males [24, 25]. In this study, it was found that female EPTB patients were more likely to have concurrent EPTB. An explanation for this finding remains elusive, but it suggests that female gender might play a role such as genetic and endocrine factors.
The proportions of concurrent EPTB in different EPTB diseases were different. Some EPTB diseases existed mainly in concurrence with other types of EPTB. Urogenital TB is a type of common extrapulmonary presentation of TB [26]. Ureteral TB generally does not occur alone and is normally concurrent with renal TB. It was reported that about 50% patients with renal TB have ureteric involvement [27, 28]. Our results showed that ureteral TB concurrent with other types of EPTB accounted for 78.87% of ureteral TB disease. The reason for this may be that Mtb from renal medullary lesions spread downstream with the urine to the ureters, the ureterovesical junction, and into the bladder [29–32]. Starting from primary PTB, bacillemia is responsible for bacillus distribution in parenchymatous organs, with possible colonization of the kidneys and prostate. Renal lesions are then initially bilateral, cortical, glomerular, and pericapillary, initiating hematogenous dissemination, and are concomitant with other hematogenic foci in the prostate and other organs outside the urogenital system [33]. Furthermore, involvement of the contralateral ureter occurs through retrograde ascending dissemination secondary to contracted bladder and vesicoureteral reflux [34]. Moreover, Mtb is introduced to the ureter via the bloodstream and lymphatic system, leading to ureteric TB [35–37]. Finally, the bacilli enter the periglomerular capillaries of the kidney, causing abscess formation, and gradually involve the ureter, bladder, prostate, seminal vesicle, epididymis, testes, or extra urinary organs, such as the lymph nodes, spleen, liver, and vertebrae [38, 39]. Therefore, ureteral TB often occurs simultaneously with renal TB.
Additionally, TB in the sacroiliac joint is not a rare finding [40]. It is reported that sacroiliac involvement is associated with 8%–10% of the cases of spinal TB [41]. Spinal TB usually follows hematogenous spread from the lung or genitourinary tract [42]. It is also possible that lymphatic drainage of the pleura or kidney may involve the para-aortic lymph nodes which may secondarily involve the vertebrae [43]. Usually, two or more contiguous vertebrae are involved in spinal TB, owing to hematogenous spread through one intervertebral artery feeding two adjacent vertebrae [44]. Once a vertebra has been sufficiently eroded by the process, the infection spreads gradually into the adjacent vertebrae via vascular and subligamentous routes [45]. Involvement of the sacrum is usually secondary to the lumbar spine and mainly caused by direct spread of infection [46]. Therefore, sacral TB is often accompanied by lumbar TB. The proportion of sacral TB concurrent with other TB is as high as 78.60% in this study. The psoas muscle lies in close proximity to a number of structures, including the diaphragm, pancreas, large and small intestines, kidney, ureter, spinal column, hip, and neighboring muscles (quadratus lumborum, erector spinae, and iliacus) [47–49]. Tuberculous abscess of the psoas major is more common in clinic settings [50, 51]. The psoas major abscess is not the primary lesion but often is caused by pus from the intervertebral space of lumbar or thoracic TB [50, 51]. The psoas major abscess is generally distributed from top to bottom. However, it is important to note that some psoas major abscesses may spread both upward and downward [51]. The abscess may rupture into the peritoneal cavity [52]. Therefore, tuberculous abscess of the psoas major concurrent with other TB accounts for a high proportion of EPTB cases; in this study, the proportion of tuberculous abscess of the psoas major concurrent with other types of EPTB was 70.77%.
The association network diagram of EPTB diseases concurrent with other types of EPTB shows that almost all the EPTB diseases may be concurrent with other types of EPTB. Tuberculous pleurisy, tuberculous lymphadenitis of the neck, and lumbar vertebra TB ranked among the top three kinds of EPTB concurrent with a number of other types of EPTB disease. Tuberculous pleurisy is the most common EPTB [53]. It is believed that delayed hypersensitivity plays a large role in the pathogenesis of tuberculous pleural effusion [54]. Fluid that enters the pleural space can originate in the pleural capillaries, the interstitial spaces of the lung, the intrathoracic lymphatics, the intrathoracic blood vessels, the peritoneal cavity [55], or the pericardial cavity [56]. The TB bacillus invades the pleural space after the rupture of a pulmonary caseous focus (Ghon focus) in the subpleural region, by contiguity of the pulmonary lesion, by rupture of a mediastinal lymph node, or via hematogenous dissemination [57–59]. Tuberculous pleurisy may cause other types of EPTB via lymphatic or hematogenous dissemination. Pleural lesions can affect not only the abdominal cavity and the subdiaphragmatic organs such as the liver [60] but also the chest wall and even ribs or sternum. Therefore, tuberculous pleurisy is prone to concurrence with other types of EPTB.
Peripheral lymph node TB is one of the most common manifestations of EPTB and one of the most common diseases affecting peripheral lymph nodes [61–63]. The pathogenesis of peripheral mycobacterial lymphadenitis is incompletely understood. Most cases in adults may be the result of the reactivation of lymph node disease sown during lymphatic transmission from a primary respiratory infection [63, 64]. Tuberculous lymphadenitis of the neck may be spread not only by the lymphatic route but also by the hematogenous route from a focus in the lung, genitourinary tract, the skeletal system, or elsewhere [64]. Tuberculous lymphadenitis of the neck may also affect the surrounding skin and soft tissue and can also affect most organs in the head and neck region, such as the lymph nodes, larynx, middle ear, oral cavity, and pharynx [65]. Tuberculous lymphadenitis of the neck may invade the lymphatic system (known as lymphatic metastasis), causing lymph node TB in other parts and distant EPTB through hematogenous metastasis [64]. For the above reasons, tuberculous lymphadenitis of the neck is also more likely to be concurrent with other EPTB.
The proportion of lumbar TB reported in the literature ranges from 22.8% to 45% among all the patients with spinal TB [66, 67]. Lumbar TB concurrent with other types of EPTB is related to the following factors. Firstly, Mtb spreads to the lumbar spine through the blood system, causing lumbar vertebra TB. This disease is not only transmitted through arteries [68], but some investigators favor the possibility that spread of lumbar vertebra TB occurs via Batson’s valveless venous vertebral plexus [69, 70]. Secondly, lumbar vertebra TB may originate from adjacent vertebrae bodies and directly invade the lower thoracic vertebrae. Lumbar vertebra TB can cause paraspinal abscess, sacral vertebra TB [71], abdominal cavity viscera TB, and surrounding soft tissue TB. Finally, lumbar vertebra TB may result in the formation of cold abscesses, which release bacteria into the blood that spread via the hematogenous route to remote organs or tissues, leading to distant EPTB [72, 73].
Our study found that about 13% EPTB patients had at least two EPTB lesions. The most common types of EPTB concurrent with other types of EPTB were tuberculous peritonitis concurrent with tuberculous pleurisy (1.64%), tuberculous pericarditis concurrent with tuberculous pleurisy (1.48%), and thoracic vertebra TB concurrent with lumbar TB (0.70%). Abdominal TB may occur directly or indirectly via spread from the primary lesion which generally affects the following organs: lymph nodes, peritoneum, ileocecal junction, colon, liver, spleen, and adrenal glands; solid viscera are affected to a greater extent than the gastrointestinal tract [74]. Tuberculous peritonitis concurrent with tuberculous pleurisy may be caused by lymphatic spread or hematogenous dissemination due to low immunity. Pericardial involvement is caused by the retrograde lymphatic spread of Mtb from peritracheal, peribronchial, or mediastinal lymph nodes or from the hematogenous spread of primary TB infection [75]. The diffusion of Mtb to the pericardium occurs mainly through the rupture of adjacent mediastinal lymph nodes [76]. Tuberculous pericarditis develops secondary to contiguous spread from the mediastinal nodes, lungs, spine, or sternum or during miliary dissemination [77]. The mediastinal pleura and pericardium are adjacent to one another. Tuberculous pericarditis can directly invade the mediastinal pleura, resulting in tuberculous pleurisy. Moreover, it may spread through the blood when the patient’s immunity is low, resulting in their concurrence. Approximately 1%–3% of the patients with TB involve infection of the skeletal system, and the spine is the most common target of osteoarticular TB, especially the thoracolumbar spine [78]. There are two possible reasons for thoracic TB concurrence with lumbar TB: firstly, spinal TB occurs through hematogenous dissemination, which can be transmitted from the lungs or via activation of a dormant infection in the bone or joint post trauma [79]. Secondly, the thoracic vertebrae and lumbar vertebrae are adjacent to one another and can be directly invaded [80].
The association rules (confidence and lift) were different between concurrent EPTB. Our study found that sacral TB with concurrent lumbar vertebra TB accounted for 68.56% of sacral TB cases. The confidence value for ureteric TB concurrent with renal TB cases was the second highest (50.52%). Sacral involvement is usually secondary to the lumbar spine and is mainly caused by the direct spread of infection [81]. Urogenital TB accounts for 30%–40% of all extrapulmonary cases [82]. Renal lesions, initially bilateral, cortical, glomerular, and pericapillary, are typically hematogenously spread, accompanied by other hematogenous lesions from other organs aside from the prostate and urogenital system [83]. Starting with a pulmonary focus, 2%–20% of patients developed urogenital TB through hematogenous spread to the kidney, prostate, and epididymis. The spread continued through the descending collection system to the ureter, bladder, and urethra and finally through the ejaculatory duct to the genital organs [84]. Ureteral TB and vesical TB are secondary to downward infection through the collection system. In ureteral TB, multiple strictures develop throughout the ureter; these are mainly anatomical strictures such as vesicoureteral junctions, followed by ureterorenal junctions and strictures at the midureter [85, 86].
4.1. Strengths and Limitations
This study had several strengths, including its large-scale multicenter representative sample, its detailed analysis of diagnostic types of concurrent EPTB, and its novel determinations of confidence/lift values of concurrent EPTB. However, the study also had several limitations. First, it may have been subject to Berkson’s bias since the study population was all hospitalized TB patients of which concurrent EPTB cases had a high likelihood of being hospitalized, causing the subsequent overestimation of their proportions within the general population. Secondly, most hospitals in our study were TB-specialized hospitals; thus, our findings may not represent the general TB patient population or apply to settings elsewhere in the country. Thirdly, the analysis did not consider low-frequency disease complications and comorbidities in China (e.g., HIV) and other factors such as initial treatment or retreatment, income, and smoking. We did not collect the information of immunocompromised conditions. Fourthly, we could not determine the order of concurrent EPTB for the observational study.
5. Conclusions
In conclusion, the present study revealed the association network occurrence of concurrent EPTB types and analyzed the association rules among EPTB for the first time in a large sample population. It was found that almost all the EPTB diseases may be concurrent with other types of EPTB. The number of cases of tuberculous peritonitis concurrent with tuberculous pleurisy, tuberculous pericarditis concurrent with tuberculous pleurisy, and thoracic vertebra TB concurrent with lumbar TB was greater than other types of EPTB. Clinicians should be alert to the incidence of concurrent EPTB and that these patients require administration of customized treatment regimens in order to achieve the best outcomes.
Ethics Statement
The research was studied on the data archived in our institute and ethics approval and consent was given by the medical ethics committee of Beijing Chest Hospital, Capital Medical University. The need for informed consent was waived because this was an observational retrospective study and all patient data were analyzed anonymously and approved by Medical ethics committee of Beijing Chest Hospital, Capital Medical University. The following reference number is (2018.4.16).
Consent
Please see the Ethics Statement.
Disclosure
A preprint has previously been published [87].
Author Contributions
All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising, or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work. Jiajia Yu, Yunqing Chang, Chen Liang, and Shengsheng Liu contributed equally.
Funding
This work was supported by “Beijing Key Clinical Specialty Project” and Tongzhou District Development Support Plan for High-Level Talent (No. YHLD2019035), by National Key R&D Program of China (2022YFC2304802).
[1] World Health Organization, Global Tuberculosis Report 2021, 2021.
[2] A. Sandgren, V. Hollo, M. J. van der Werf, "Extrapulmonary Tuberculosis in the European Union and European Economic Area, 2002 to 2011," Euro Surveillance, vol. 18 no. 12,DOI: 10.2807/ese.18.12.20431-en, 2013.
[3] World Health Organization, Global Tuberculosis Report 2020, 2020.
[4] F. Hammami, M. Koubaa, A. Chakroun, "Omparative Analysis between Tuberculous Meningitis and Other Forms of Extrapulmonary Tuberculosis," Germs, vol. 11 no. 1, pp. 23-31, DOI: 10.18683/germs.2021.1237, 2021.
[5] A. Sbayi, A. Arfaoui, H. Janah, S. E. Koraichi, A. Quyou, "Epidemiological Characteristics and Some Risk Factors of Extrapulmonary Tuberculosis in Larache, Morocco," Pan African Medical Journal, vol. 36,DOI: 10.11604/pamj.2020.36.381.24870, 2020.
[6] I. K. Holden, T. Lillebaek, P. H. Andersen, S. Bjerrum, C. Wejse, I. S. Johansen, "Extrapulmonary Tuberculosis in Denmark From 2009 to 2014; Characteristics and Predictors for Treatment Outcome," Open Forum Infectious Diseases, vol. 6 no. 10,DOI: 10.1093/ofid/ofz388, 2019.
[7] V. D. Mathiasen, P. H. Andersen, I. S. Johansen, T. Lillebaek, C. Wejse, "Clinical Features of Tuberculous Lymphadenitis in a Low-Incidence Country," International Journal of Infectious Diseases, vol. 98, pp. 366-371, DOI: 10.1016/j.ijid.2020.07.011, 2020.
[8] X. Qian, D. T. Nguyen, J. Lyu, A. E. Albers, X. Bi, E. A. Graviss, "Risk Factors for Extrapulmonary Dissemination of Tuberculosis and Associated Mortality During Treatment for Extrapulmonary Tuberculosis," Emerging Microbes and Infections, vol. 7 no. 1,DOI: 10.1038/s41426-018-0106-1, 2018.
[9] National Health Commission of the People’s Republic of China, "Technical Specifications for Tuberculosis Prevention and Control in China," 2020. https://tb.chinacdc.cn/ggl/202004/P020200414515703939844.pdf
[10] H. M. Peto, R. H. Pratt, T. A. Harrington, P. A. LoBue, L. R. Armstrong, "Epidemiology of Extrapulmonary Tuberculosis in the United States, 1993–2006," Clinical Infectious Diseases, vol. 49 no. 9, pp. 1350-1357, DOI: 10.1086/605559, 2009.
[11] Y. Liu, Z. Jiang, H. Chen, "Description of Demographic and Clinical Characteristics of Extrapulmonary Tuberculosis in Shandong, China," Hippokratia, vol. 24 no. 1, pp. 27-32, 2020.
[12] WHO, "Tuberculosis(TB)," . https://www.who.int/tb/areas-of-work/laboratory/en/
[13] Chinese Medical Association, Clinical Diagnosis Standard of TB for Clinical Technology Operation (TB Volumes), 2005.
[14] G. Sarıyer, C. Öcal Taşar, "Highlighting the Rules Between Diagnosis Types and Laboratory Diagnostic Tests for Patients of an Emergency Department: Use of Association Rule Mining," Health Informatics Journal, vol. 26 no. 2, pp. 1177-1193, DOI: 10.1177/1460458219871135, 2020.
[15] O. Pattanaprateep, M. McEvoy, J. Attia, A. Thakkinstian, "Evaluation of Rational Nonsteroidal Anti-inflammatory Drugs and Gastro-Protective Agents Use; Association Rule Data Mining Using Outpatient Prescription Patterns," BMC Medical Informatics and Decision Making, vol. 17 no. 1,DOI: 10.1186/s12911-017-0496-3, 2017.
[16] H. Ibrahim, A. Saad, A. Abdo, A. Sharaf Eldin, "Mining Association Patterns of Drug-Interactions Using Post Marketing FDA’s Spontaneous Reporting Data," Journal of Biomedical Informatics, vol. 60, pp. 294-308, DOI: 10.1016/j.jbi.2016.02.009, 2016.
[17] Available from: https://www.ibm.com/support/knowledgecenter/en/SS3RA7_15.0.0/com.ibm
[18] M. Forssbohm, M. Zwahlen, R. Loddenkemper, H. L. Rieder, "Demographic Characteristics of Patients With Extrapulmonary Tuberculosis in Germany," European Respiratory Journal, vol. 31 no. 1, pp. 99-105, DOI: 10.1183/09031936.00020607, 2008.
[19] T. Jo, N. Kuse, M. Inomata, "Efficacy and Safety of Semi-Flexible Thoracoscopiccryobiopsy in the Diagnosis of Elderly Tuberculous Pleurisy," Respiratory Medicine Case Reports, vol. 29,DOI: 10.1016/j.rmcr.2020.101008, 2020.
[20] H. Ryan, J. Yoo, P. Darsini, "Corticosteroids for Tuberculous Pleurisy," Cochrane Database of Systematic Reviews, vol. 3 no. 3,DOI: 10.1002/14651858.CD001876.pub3, 2017.
[21] C. T. Sreeramareddy, K. V. Panduru, S. C. Verma, H. S. Joshi, M. N. Bates, "Comparison of Pulmonary and Extrapulmonary Tuberculosis in Nepal: A Hospital-Based Retrospective Study," BMC Infectious Diseases, vol. 8 no. 1,DOI: 10.1186/1471-2334-8-8, 2008.
[22] X. Zhang, A. B. Andersen, T. Lillebaek, "Effect of Sex, Age, and Race on the Clinical Presentation of Tuberculosis: a 15-Year Population-Based Study," The American Society of Tropical Medicine and Hygiene, vol. 85 no. 2, pp. 285-290, DOI: 10.4269/ajtmh.2011.10-0630, 2011.
[23] V. K. Arora, R. Gupta, "Trends of Extra-Pulmonary Tuberculosis Under Revised National Tuberculosis Control Programme: A Study From South Delhi," Indian Journal of Tuberculosis, vol. 53, pp. 77-83, 2006.
[24] M. Di Nuzzo, A. Trentini, A. Grilli, "Extrapulmonary Tuberculosis Among Immigrants in a Low-TB Burden and High Immigrant Receiving City of Northern Italy," The Journal of Infection in Developing Countries, vol. 12 no. 02, pp. 73-79, DOI: 10.3855/jidc.10167, 2018.
[25] B. Musellim, S. Erturan, E. Sonmez Duman, G. Ongen, "Comparison of Extra-Pulmonary and Pulmonary Tuberculosis Cases: Factors Influencing the Site of Reactivation," International Journal of Tuberculosis and Lung Disease, vol. 9 no. 11, pp. 1220-1223, 2005.
[26] G. J. Wise, V. K. Marella, "Genitourinary Manifestations of Tuberculosis," Urologic Clinics of North America, vol. 30 no. 1, pp. 111-121, DOI: 10.1016/s0094-0143(02)00123-4, 2003.
[27] A. A. Figueiredo, A. M. Lucon, "Urogenital Tuberculosis: Update and Review of 8961 Cases from the World Literature," Reviews in Urology, vol. 10 no. 3, pp. 207-217, 2008.
[28] J. G. Gow, S. Barbosa, "Genitourinary Tuberculosis. A Study of 1117 Cases over a Period of 34 Years," British Journal of Urology, vol. 56 no. 5, pp. 449-455, 1984.
[29] E. Kulchavenya, K. Naber, T. E. Bjerklund Johansen, "Urogenital Tuberculosis: Classification, Diagnosis, and Treatment," European Urology Supplements, vol. 15 no. 4, pp. 112-121, DOI: 10.1016/j.eursup.2016.04.001, 2016.
[30] S. Adhikari, B. Basnyat, "Extrapulmonary Tuberculosis: A Debilitating and Often Neglected Public Health Problem," BMJ Case Reports, vol. 11 no. 1,DOI: 10.1136/bcr-2018-226098, 2018.
[31] A. Abbara, R. N. Davidson, "Etiology and Management of Genitourinary Tuberculosis," Nature Reviews Urology, vol. 8 no. 12, pp. 678-688, DOI: 10.1038/nrurol.2011.172, 2011.
[32] J. B. Eastwood, C. M. Corbishley, J. M. Grange, "Tuberculosis and the Kidney," Journal of the American Society of Nephrology, vol. 12 no. 6, pp. 1307-1314, DOI: 10.1681/asn.v1261307, 2001.
[33] E. M. Medlar, D. M. Spain, R. W. Holliday, "Post-Mortem Compared With Clinical Diagnosis of Genito-Urinary Tuberculosis in Adult Males," The Journal of Urology, vol. 61 no. 6, pp. 1078-1088, DOI: 10.1016/s0022-5347(17)69186-9, 1949.
[34] A. A. de Figueiredo, A. M. Lucon, M. Srougi, "Bladder Augmentation for the Treatment of Chronic Tuberculous Cystitis. Clinical and Urodynamic Evaluation of 25 Patients after Long Term Follow-Up," Neurourology and Urodynamics, vol. 25 no. 5, pp. 433-440, DOI: 10.1002/nau.20264, 2006.
[35] J. Furin, H. Cox, M. Pai, "Tuberculosis," The Lancet, vol. 393 no. 10181, pp. 1642-1656, DOI: 10.1016/s0140-6736(19)30308-3, 2019.
[36] U. Jayarajah, M. Gunawardene, M. Willaraarachchi, "Clinical Characteristics and Outcome of Genitourinary Tuberculosis in Sri Lanka: An Observational Study," BMC Infectious Diseases, vol. 21 no. 1,DOI: 10.1186/s12879-021-06990-z, 2021.
[37] M. R. Altiparmak, S. Trabulus, I. I. Balkan, "Urinary Tuberculosis: A Cohort of 79 Adult Cases," Renal Failure, vol. 37 no. 7, pp. 1157-1163, DOI: 10.3109/0886022x.2015.1057460, 2015.
[38] K. Nakane, M. Yasuda, T. Deguchi, "Nationwide Survey of Urogenital Tuberculosis in Japan," International Journal of Urology, vol. 21 no. 11, pp. 1171-1177, DOI: 10.1111/iju.12549, 2014.
[39] A. K. Hemal, N. P. Gupta, T. P. Rajeev, R. Kumar, L. Dar, P. Seth, "Polymerase Chain Reaction in Clinically Suspected Genitourinary Tuberculosis: Comparison With Intravenous Urography, Bladder Biopsy, and Urine Acid Fast Bacilli Culture," Urology, vol. 56 no. 4, pp. 570-574, DOI: 10.1016/s0090-4295(00)00668-3, 2000.
[40] R. C. Cabot, R. E. Scully, E. J. Mark, "Case 5-1988: A 34-Year-Old Man With a Destructive Sacral Lesion and a Left Gluteal Mass," New England Journal of Medicine, vol. 318 no. 5, pp. 306-312, DOI: 10.1056/nejm198802043180508, 1988.
[41] J. Pouchot, P. Vinceneux, J. Barge, "Tuberculosis of the Sacroiliac Joint: Clinical Features, Outcome, and Evaluation of Closed Needle Biopsy in 11 Consecutive Cases," The American Journal of Medicine, vol. 84 no. 3, pp. 622-628, DOI: 10.1016/0002-9343(88)90146-5, 1988.
[42] J. Ahmadi, A. Bajaj, S. Destian, H. D. Segall, C. S. Zee, "Spinal Tuberculosis: Atypical Observations at MR Imaging," Radiology, vol. 189 no. 2, pp. 489-493, DOI: 10.1148/radiology.189.2.8210378, 1993.
[43] D. C. Yao, D. J. Sartoris, "Musculoskeletal Tuberculosis," Radiologic Clinics of North America, vol. 33 no. 4, pp. 679-689, DOI: 10.1016/s0033-8389(22)00612-1, 1995.
[44] A. Kulali, S. Cobanoğlu, F. Ozyilmaz, "Spinal Tuberculosis With Circumferential Involvement of Two Noncontiguous Isolated Vertebral Levels: Case Report," Neurosurgery, vol. 35 no. 6, pp. 1154-1158, DOI: 10.1097/00006123-199412000-00022, 1994.
[45] T. Patankar, A. Krishnan, D. Patkar, "Imaging in Isolated Sacral Tuberculosis: A Review of 15 Cases," Skeletal Radiology, vol. 29 no. 7, pp. 392-396, DOI: 10.1007/s002560000229, 2000.
[46] R. Sament, V. Bachhal, N. R. Gopinathan, R. K. Sen, "Isolated Tuberculosis of Sacrum With Monoparesis: An Atypical Presentation," Asian Spine Journal, vol. 7 no. 4, pp. 351-354, DOI: 10.4184/asj.2013.7.4.351, 2013.
[47] B. Goldberg, J. R. Hedges, D. W. Stewart, "Psoas Abscess," Journal of Emergency Medicine, vol. 1 no. 6, pp. 533-537, DOI: 10.1016/0736-4679(84)90007-6, 1984.
[48] F. Gordin, C. Stamler, J. Mills, "Pyogenic Psoas Abscesses: Noninvasive Diagnostic Techniques and Review of the Literature," Clinical Infectious Diseases, vol. 5 no. 6, pp. 1003-1011, DOI: 10.1093/clinids/5.6.1003, 1983.
[49] I. Gruenwald, J. Abrahamson, O. Cohen, "Psoas Abscess: Case Report and Review of the Literature," The Journal of Urology, vol. 147 no. 6, pp. 1624-1626, DOI: 10.1016/s0022-5347(17)37650-4, 1992.
[50] R. A. Harrigan, F. H. Kauffman, M. B. Love, "Tuberculous Psoas Abscess," Journal of Emergency Medicine, vol. 13 no. 4, pp. 493-498, DOI: 10.1016/0736-4679(95)80006-9, 1995.
[51] Z. Li, M. He, X. Chen, X. Yang, S. Zhang, G. Jin, "Single-Stage Posterior Resection of the Transversal Process Combined With an Intervertebral Foraminal Approach for Debridement, Interbody Fusion, Internal Fixation for the Treatment of Lumbar Tuberculosis and Psoas Major Abscess," International Orthopaedics, vol. 46 no. 2, pp. 331-339, DOI: 10.1007/s00264-021-05244-6, 2022.
[52] G. Singh, H. S. Shukla, "Acute Abdominal Complications of Tuberculous Psoas Abscesses," Tubercle, vol. 72 no. 4,DOI: 10.1016/0041-3879(91)90066-2, 1991.
[53] J. A. Shaw, C. F. N. Koegelenberg, "Pleural Tuberculosis," Clinics in Chest Medicine, vol. 42 no. 4, pp. 649-666, DOI: 10.1016/j.ccm.2021.08.002, 2021.
[54] R. W. Light, "Update on Tuberculous Pleural Effusion," Respirology, vol. 15 no. 3, pp. 451-458, DOI: 10.1111/j.1440-1843.2010.01723.x, 2010.
[55] L. Yang, Y. J. Hu, F. G. Li, X. J. Chang, T. H. Zhang, Z. T. Wang, "Analysis of Cytokine Levers in Pleural Effusions of Tuberculous Pleurisy and Tuberculous Empyema," Mediators of Inflammation, vol. 2016,DOI: 10.1155/2016/3068103, 2016.
[56] N. O. Fowler, "Tuberculous Pericarditis," JAMA, vol. 266 no. 1, pp. 99-103, DOI: 10.1001/jama.1991.03470010103039, 1991.
[57] A. A. Lazarus, S. McKay, R. Gilbert, "Pleural Tuberculosis," Disease-a-Month, vol. 53 no. 1, pp. 16-21, DOI: 10.1016/j.disamonth.2006.10.002, 2007.
[58] A. Gopi, S. M. Madhavan, S. K. Sharma, S. A. Sahn, "Diagnosis and Treatment of Tuberculous Pleural Effusion in 2006," Chest, vol. 131 no. 3, pp. 880-889, DOI: 10.1378/chest.06-2063, 2007.
[59] J. M. Porcel, "Tuberculous Pleural Effusion," Lung, vol. 187 no. 5, pp. 263-270, DOI: 10.1007/s00408-009-9165-3, 2009.
[60] S. Bandyopadhyay, P. K. Maity, "Hepatobiliary Tuberculosis," Journal of the Association of Physicians of India, vol. 61 no. 6, pp. 404-407, 2013.
[61] J. M. Fontanilla, A. Barnes, C. F. von Reyn, "Current Diagnosis and Management of Peripheral Tuberculous Lymphadenitis," Clinical Infectious Diseases, vol. 53 no. 6, pp. 555-562, DOI: 10.1093/cid/cir454, 2011.
[62] U. Handa, I. Mundi, S. Mohan, "Nodal Tuberculosis Revisited: A Review," J Infect Dev Ctries, vol. 6 no. 01,DOI: 10.3855/jidc.2090, 2011.
[63] A. W. Artenstein, J. H. Kim, W. J. Williams, R. C. Chung, "Isolated Peripheral Tuberculous Lymphadenitis in Adults: Current Clinical and Diagnostic Issues," Clinical Infectious Diseases, vol. 20 no. 4, pp. 876-882, DOI: 10.1093/clinids/20.4.876, 1995.
[64] F. J. Miller, J. M. Cashman, "Origin of Peripheral Tuberculous Lymphadenitis in Childhood," The Lancet, vol. 271 no. 7015, pp. 286-289, DOI: 10.1016/s0140-6736(58)91030-4, 1958.
[65] S. Das, D. Das, U. T. Bhuyan, N. Saikia, "Head and Neck Tuberculosis: Scenario in a Tertiary Care Hospital of North Eastern India," Journal of Clinical and Diagnostic Research, vol. 10 no. 1, pp. MC04-MC7, DOI: 10.7860/JCDR/2016/17171.7076, 2016.
[66] H. Wang, C. Li, J. Wang, Z. Zhang, Y. Zhou, "Characteristics of Patients With Spinal Tuberculosis: Seven-Year Experience of a Teaching Hospital in Southwest China," International Orthopaedics, vol. 36 no. 7, pp. 1429-1434, DOI: 10.1007/s00264-012-1511-z, 2012.
[67] Y. Yao, H. Zhang, H. Liu, Z. Zhang, Y. Tang, Y. Zhou, "Prognostic Factors for Recovery After Anterior Debridement/Bone Grafting and Posterior Instrumentation for Lumbar Spinal Tuberculosis," World Neurosurgery, vol. 104, pp. 660-667, DOI: 10.1016/j.wneu.2017.05.076, 2017.
[68] A. D. Gouliamos, D. T. Kehagias, S. Lahanis, "MR Imaging of Tuberculous Vertebral Osteomyelitis: Pictorial Review," European Radiology, vol. 11 no. 4, pp. 575-579, DOI: 10.1007/s003300000631, 2001.
[69] O. V. Batson, "The Vertebral Vein System. Caldwell Lecture, 1956," American Journal of Roentgenology, Radium Therapy and Nuclear Medicine, vol. 78 no. 2, pp. 195-212, 1957.
[70] S. S. Desai, "Early Diagnosis of Spinal Tuberculosis by MRI," Journal of Bone and Joint Surgery British Volume, vol. 76 no. 6, pp. 863-869, DOI: 10.1302/0301-620x.76b6.7983108, 1994.
[71] T. Rathod, A. Sathe, S. Kolur, "Multidrug-Resistant Tuberculosis of Lumbosacral Spine Producing Extensive Destruction With Lumbosacral Kyphosis," BMJ Case Reports, vol. 13 no. 5,DOI: 10.1136/bcr-2020-234246, 2020.
[72] E. Bozzola, M. Bozzola, A. Magistrelli, "Paediatric Tubercular Spinal Abscess Involving the Dorsal, Lumbar and Sacral Regions and Causing Spinal Cord Compression," Informe Medico, vol. 21 no. 3, pp. 220-223, 2013.
[73] T. Jiang, J. Zhao, M. He, K. Wang, M. Fowdur, Y. Wu, "Outcomes and Treatment of Lumbosacral Spinal Tuberculosis: A Retrospective Study of 53 Patients," PLoS One, vol. 10 no. 6,DOI: 10.1371/journal.pone.0130185, 2015.
[74] S. Gambhir, M. Ravina, K. Rangan, "Imaging in Extrapulmonary Tuberculosis," International Journal of Infectious Diseases, vol. 56, pp. 237-247, DOI: 10.1016/j.ijid.2016.11.003, 2017.
[75] D. W. Ortbals, L. V. Avioli, "Tuberculous Pericarditis," Archives of Internal Medicine, vol. 139 no. 2, pp. 231-234, DOI: 10.1001/archinte.1979.03630390083028, 1979.
[76] G. Cherian, "Diagnosis of Tuberculous Aetiology in Pericardial Effusions," Postgraduate Medical Journal, vol. 80 no. 943, pp. 262-266, DOI: 10.1136/pgmj.2003.013664, 2004.
[77] M. P. Golden, H. R. Vikram, "Extrapulmonary Tuberculosis: An Overview," American Family Physician, vol. 72 no. 9, pp. 1761-1768, 2005.
[78] D. Mulleman, S. Mammou, I. Griffoul, A. Avimadje, P. Goupille, J. P. Valat, "Characteristics of Patients With Spinal Tuberculosis in a French Teaching Hospital," Joint Bone Spine, vol. 73 no. 4, pp. 424-427, DOI: 10.1016/j.jbspin.2005.10.013, 2006.
[79] S. Andronikou, M. Bindapersad, N. Govender, "Musculoskeletal Tuberculosis-Imaging Using Low-End and Advanced Modalities for Developing and Developed Countries," Acta Radiologica, vol. 52 no. 4, pp. 430-441, DOI: 10.1258/ar.2011.100444, 2011.
[80] Y. Tang, W. J. Wu, S. Yang, "Surgical Treatment of Thoracolumbar Spinal Tuberculosis-A Multicentre, Retrospective, Case-Control Study," Journal of Orthopaedic Surgery and Research, vol. 14 no. 1,DOI: 10.1186/s13018-019-1252-4, 2019.
[81] R. Sament, V. Bachhal, N. R. Gopinathan, R. K. Sen, "Isolated Tuberculosis of Sacrum With Monoparesis: An Atypical Presentation," Asian Spine Journal, vol. 7 no. 4, pp. 351-354, DOI: 10.4184/asj.2013.7.4.351, 2013.
[82] R. Ramanathan, A. Kumar, R. Kapoor, M. Bhandari, "Relief of Urinary Tract Obstruction in Tuberculosis to Improve Renal Function. Analysis of Predictive Factors," British Journal of Urology, vol. 81 no. 2, pp. 199-205, DOI: 10.1046/j.1464-410x.1998.00500.x, 1998.
[83] A. S. Narayana, "Overview of Renal Tuberculosis," Urology, vol. 19 no. 3, pp. 231-237, DOI: 10.1016/0090-4295(82)90490-3, 1982.
[84] A. A. Figueiredo, A. M. Lucon, M. Srougi, "Urogenital Tuberculosis," Microbiology Spectrum, vol. 5 no. 1,DOI: 10.1128/microbiolspec.tnmi7-0015-2016, 2017.
[85] W. K. Kerr, G. L. Gale, K. S. S. Peterson, "Reconstructive Surgery for Genitourinary Tuberculosis," The Journal of Urology, vol. 101 no. 3, pp. 254-266, DOI: 10.1016/s0022-5347(17)62324-3, 1969.
[86] P. Carl, L. Stark, "Indications for Surgical Management of Genitourinary Tuberculosis," World Journal of Surgery, vol. 21 no. 5, pp. 505-510, DOI: 10.1007/pl00012277, 1997.
[87] W. Kang, J. Yu, L. Cheng, "Study on the Association Network of Tuberculosis Lesions in Adult Extrapulmonary Tuberculosis in China: A Large-Scale Multi-Center Observational Study," ,DOI: 10.21203/rs.3.rs-2710384/v1, 2023.
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Abstract
Background: Extrapulmonary tuberculosis (EPTB) is a significant health problem which can lead to severe morbidity and mortality. In clinical practice, EPTB can have a variety of nonspecific clinical manifestations and can be concurrent with other types of EPTB. As information pertaining to concurrent EPTB is scarce, research efforts are needed to find concurrent EPTB types and to explore the association networks and rules of concurrent EPTB.
Materials and Methods: An observational multicenter study was carried out at 21 hospitals from 15 provinces in China from Jan 1, 2011, to Dec 31, 2017. All the adult EPTB inpatients (≥ 15 years) were included. Multivariable logistic regression analysis was used to examine the associations of gender and age group for concurrent EPTB. The association network and rules for concurrent EPTB were analyzed by the Apriori algorithm.
Results: A total of 75,993 adult EPTB inpatients (not including EPTB concurrent with PTB) were included. The ratio of male:female was 1.32. The most common types of EPTB lesions were tuberculous pleurisy (46.47%). In the fully adjusted multivariable logistic regression models, it was found that female EPTB patients (aOR = 1.129, 95% CI: 1.081–1.178) were more likely to have concurrent EPTB. As age increased, the risk of concurrent EPTB decreased (aOR < 1, p value for trend < 0.001). The association network graph showed that almost all the EPTB diseases may be concurrent with other types of EPTB. Ureteric tuberculosis and sacral tuberculosis diseases existed mainly in concurrence with other types of EPTB (about 80%). Tuberculous pleurisy and tuberculous lymphadenitis of the neck could be concurrent with more than 60 other types of EPTB disease. The most common concurrent EPTB types were tuberculous peritonitis concurrent with tuberculous pleurisy (1.64%). Sacral tuberculosis concurrentwith lumbar vertebra tuberculosis had the highest confidence value (68.56%). The strongest association rule was found for vesical tuberculosis concurrent with ureteric tuberculosis (lift = 166.18) and ureteric tuberculosis concurrent with vesical tuberculosis (lift = 166.18).
Conclusion: The present study revealed the occurrence of concurrent EPTB types and analyzed the association network and rules among adult EPTB for the first time in a large sample population. Clinicians should be alert to the incidence of concurrent EPTB and that these patients require administration of customized treatment regimens in order to achieve the best outcomes.
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1 Department of Infectious Diseases and Clinical Microbiology Beijing Chao-Yang Hospital Capital Medical University Beijing China; Beijing Chest Hospital Capital Medical University Beijing Tuberculosis and Thoracic Tumor Research Institute Beijing China
2 Department of Infectious Diseases Shanxi Bethune Hospital Shanxi Academy of Medical Sciences Tongji Shanxi Hospital Third Hospital of Shanxi Medical University Taiyuan Shanxi Province, China
3 Department of Infectious Diseases Beijing Tsinghua Changgung Hospital School of Clinical Medicine Tsinghua University Beijing China
4 Department of Tuberculosis Anhui Chest Hospital/Anhui Provincial Institute for Tuberculosis Prevention and Treatment Hefei China
5 Beijing Chest Hospital Capital Medical University Beijing Tuberculosis and Thoracic Tumor Research Institute Beijing China
6 Shenyang Chest Hospital No. 11 Beihai Street, Dadong District, Shenyang China
7 Guangzhou Chest Hospital No. 62, Heng Zhi Gang Road, Yuexiu District, Guangzhou Guangdong, China
8 Chest Hospital of Xinjiang No. 106 Yan’An Road, Tianshan District, Urumqi Xinjiang, China
9 The Third People’s Hospital of Kunming No. 319 Wujing Road, Kunming City Yunnan Province, China
10 Shandong Provincial Chest Hospital No. 12 Lieshishandong Road, Licheng District, Jinan Shandong, China
11 Jiangxi Chest (Third People) Hospital No. 346 Dieshan Road, Donghu District, Nanchang City Jiangxi Province, China
12 Chang Chun Infectious Diseases Hospital No. 2699, Sandao Section, Changji South Line, Erdao District, Changchun City Jilin Province, China
13 Chongqing Public Health Medical Center No. 109, Baoyu Road, Geleshan Town, Shapingba District, Chongqing China
14 Fuzhou Pulmonary Hospital of Fujian No. 2, Lakeside, Cangshan District, Fuzhou China
15 Taiyuan Fourth People’s Hospital Number 231, Xikuang Street, WanBailin District, Taiyuan City Shanxi Province, China
16 Tianjin Haihe Hospital Number 890, Shuanggang Zhen Jingu Road, Jinnan District, Tianjin China
17 Third People’s Hospital of Shenzhen 29 Bulan Road, District Longgang, Shenzhen China
18 The First Affiliated Hospital of Chongqing Medical University No. 1 Youyi Road, Yuzhong District, Chongqing China
19 Weifang No.2 People’s Hospital No. 7th Yuanxiao Street Kuiwen District, Weifang China
20 The Fifth People’s Hospital of Suzhou No. 10 Guangqian Road, Suzhou City Jiangsu Province, China
21 Affiliated Hospital of Zunyi Medical College No. 149 Delian Road, Zunyi Guizhou, China
22 The Fifth People’s Hospital of Wuxi No.1215, GuangRui Road, Wuxi China
23 TB Hospital of Siping City No. 10 Dongshan Road, Tiedong District, Siping City Jilin Province, China
24 Baoding Hospital for Infectious Disease No. 608 Dongfeng East Road, Lianchi District, Baoding City Hebei Province, China
25 The First Affiliated of XiaMen University Zhenhai Roud, Siming District, Xiamen City Fujian Province, China