- Research article
- Open Access
Decreased mortality seen in rifampicin/multidrug-resistant tuberculous meningitis treated with linezolid in Shenzhen, China
BMC Infectious Diseases volume 21, Article number: 1015 (2021)
The morbidity of rifampicin/multidrug-resistant tuberculous meningitis (RR/MDR-TBM) has shown an increasing trend globally. Its mortality rate is significantly higher than that of non-rifampicin/multidrug-resistant tuberculous meningitis (NRR/MDR-TBM). This article aimed to explore risk factors related to RR/MDR-TBM, and compare therapeutic effects of linezolid (LZD)- and non-linezolid-containing regimen for RR/MDR-TB patients in Shenzhen city. Furthermore, we aimed to find a better therapy for pathogen-negative TBM with RR/MDR-TBM related risk factors.
We conducted a retrospective study enrolling 137 hospitalized cases with confirmed TBM from June 2014 to March 2020. All patients were divided into RR/MDR-TBM group (12 cases) and NRR/MDR-TBM group (125 cases) based on GeneXpert MTB/RIF and (or) phenotypic drug susceptibility test results using cerebral spinal fluid (CSF). The risk factors related to RR/MDR-TBM were investigated through comparing clinical and examination features between the two groups. The mortality rate of RR/MDR-TBM patients treated with different regimens was analyzed to compare their respective therapeutic effects. A difference of P < 0.05 was considered statistically significant.
Most patients (111/137, 81%) were from southern or southwestern China, and a large proportion (72/137, 52.55%) belonged to migrant workers. 12 cases were RR/MDR-TBM (12/137, 8.8%) while 125 cases were NRR/MDR-TBM (125/137, 91.2%). The proportion of patients having prior TB treatment history in the RR/MDR-TBM group was significantly higher than that of the NRR/MDR-TBM group (6/12 vs. 12/125, 50% vs. 10.5%, P < 0.01). No significant difference was observed on other clinical and examination features between the two groups. Mortality was significantly lower in RR/MDR-TBM patients on linezolid-containing treatment regimen than those who were not (0/7 versus 3/5, 0% versus 60%, P = 0.045).
The main related risk factor of RR/MDR-TBM is the history of anti-tuberculosis treatment. Linezolid-containing regimen appears to lower mortality rate of RR/MDR-TBM significantly in our study. We think Linezolid should be evaluated prospectively in the treatment of RR/MDR-TBM.
Tuberculous meningitis (TBM) is the most fatal form of tuberculosis, especially in children or adults co-infected with HIV. Even with the use of standardized anti-tuberculosis (TB) treatment, mortality can still reach as high as 20%–50%, and nearly half of the survivors will develop serious central nervous system sequelae [1, 2]. In recent years, an increase in the number of drug-resistant tuberculous meningitis cases had been reported. Compared to non-drug-resistant tuberculous meningitis, drug-resistant tuberculous meningitis, especially rifampicin/multidrug-resistant tuberculous meningitis (RR/MDR-TBM) is more lethal with increased medical cost for the patient [3, 4]. China is the world's second largest country with a high burden of RR/MDR-TB, the estimated number of people infected with RR/MDR-TB in 2019 was about 65,000 (about 14% of the world total). RR/MDR-TB accounted for 7.1% and 23% in newly diagnosed and previously treated tuberculosis patients respectively . As the most lethal form of tuberculosis, the incidence of TBM constituted about 1% of all tuberculosis cases worldwide , and about 7.23% of extrapulmonary tuberculosis cases in China . However, the incidence of RR/MDR-TBM and its related risk factors remains unclear. Herein, we conducted a retrospective study in which 137 confirmed TBM patients were enrolled. These patients were hospitalized in the Third People’s Hospital of Shenzhen from June 2014 to March 2020. The hospital is the only designated hospital for the treatment of TBM patients in Shenzhen city. Shenzhen is a megacity with a long-term lived population of more than 13 million, with a large floating population of migrant workers from other cities, especially the southern and southwestern provinces of China. Thus TBM cases being treated in our hospital can reflect the general situation of the disease in south and southwest China to some extent. We compared the related characteristics (including demographic, clinical and examination characteristics) between RR/MDR-TBM and non-rifampicin/multidrug-resistant tuberculous meningitis (NRR/MDR-TBM) patients to explore risk factors associated with RR/MDR-TBM. Furthermore, we compared the effects of linezolid- (LZD) and non-linezolid-containing (non-LZD) regimens on the prognosis of RR/MDR-TBM. On this basis, we discussed the empirical treatment regimen for pathogen-negative TBM with RR/MDR-TBM related risk factors. We hope it will help improve the prognosis of RR/MDR-TBM and pathogen-negative TBM in China.
Patients’ enrollment and data collection:
Enrollment process: This study adopted a retrospective method. We collected the data of 151 tuberculous meningitis patients who were hospitalized and met the diagnostic criteria for confirmed tuberculous meningitis from June 2014 to March 2020. Among them, 14 patients who did not perform GeneXpert MTB/RIF and drug susceptibility test (DST) were excluded. Finally, 137 patients were enrolled in the study (Fig. 1), including 98 males and 39 females, age ranged from 2 to 76 years, with a median age of 29 years. We collected the demographic/clinical and examination characteristics of these patients from the medical record through the hospital information system (HIS) and the hospital laboratory information system (LIS), and confirmed the survival status of discharged patients through phone and medical follow-up.
Entry criteria: Met the diagnostic criteria for definite tuberculous meningitis , that is, in addition to the clinical manifestations of TBM and abnormality of cerebrospinal fluid (CSF), the patient’s CSF examination met at least one of the following two criteria: 1. GeneXpert MTB/RIF (GeneXpert) positive nucleic acid test for Mycobacterium tuberculosis (MTB). 2. BACTEC MGIT 960 positive culture identifying as MTB, with a phenotypic drug sensitivity test (DST) performed simultaneously. Only one pathogen-positive CSF result was analyzed for each patient.
Diagnostic criteria for RR/MDR TBM cases: Met the diagnostic criteria for definite tuberculous meningitis case and fulfilled at least one of the following two criteria: 1. Positive GeneXpert test indicating resistance to rifampicin (RIF) 2. CSF MTB positive culture, and DST showing resistance to rifampicin and resistance or sensitivity to isoniazid.
We described the demographic features of TBM patients according to the results of GeneXpert and/or DST in CSF. All patients were divided into RR/MDR group and NRR/MDR group, then we compared the differences of the main clinical and examination characteristics between the two groups. On this basis, we explored the associated risk factors of RR/MDR TBM. Finally, we compared the differences in mortality between the two groups and the impact of different regimen on the prognosis of RR/MDR-TBM.
Method of obtaining CSF specimen: Lumbar puncture was performed within 24 h from admission. For patients whose CSF was acquired through lateral ventricle drainage, the pressure of CSF was measured. The CSF specimen was submitted at once after collection for tests such as white blood cell count and classification, biochemistry, acid-fast bacillus (AFB), GeneXpert, MTB culture and species identification, Cryptococcus membrane polysaccharide antigen, bacteria and fungi smears and culture. The volume of CSF used for GeneXpert and MTB culture was 1–2 ml.
Laboratory examination method:
BACTEC MGIT 960 Mycobacterium Culture Identification System for cerebrospinal fluid MTB: according to literature .
The phenotypic drug susceptibility test (DST) of MTB: absolute concentration method was adopted . The test covered a minimum of 4 drugs (isoniazid, rifampin, ethambutol, streptomycin), including low and high concentration.
Acid-fast staining, white blood cell count and classification, biochemistry of CSF and blood routine, blood biochemistry, blood tuberculosis interferon release assay (IGRA) and HIV antibody were operated in accordance with the instruction of the instrument and kit.
Anti-tuberculosis treatment regimen: Non-RR/MDR-TBM group: Anti-tuberculosis treatment regimen included: Isoniazid (10–15 mg/Kg/day, the maximum dose was 0.9 g/day, administered intravenously during hospitalization, then changed to oral administration after discharge); Rifampicin (10-15 mg/Kg/day, maximum 0.6 g/day, administered intravenously during hospitalization, and changed to oral administration after discharge); Pyrazinamide (25–30 mg/Kg/day, 1.5–2.0 g for adults, oral or nasal administration); ethambutal (15 mg/kg/day, 0.75–1.0 g for adults, oral or nasal administration). Some patients were supplemented with streptomycin injection or levofloxacin (or moxifloxacin) on top of the above. Full course of treatment for NRR/MDR-TBM is 12–18 months except in the patient’s death. RR/MDR-TBM group: 7 patients were treated with LZD-containing regimen (LZD 1200 mg/day, intravenously or orally in the first 2 weeks of hospitalization, then changed to oral administration 600 mg/day, for a course of 3 to 18 months). The regimen also included levofloxacin (or moxifloxacin) and 2–4 of the following drugs: cycloserine, pyrazinamide, high-dose isoniazid, amikacin, protionamide, in dosage in accordance with the nation’s management guideline for RR/MDR-TB). Five patients received the non-LZD-containing regimen in the early stage which included the following 4–6 drugs: levofloxacin (moxifloxacin), pyrazinamide, high-dose isoniazid, rifampicin, amikacin, protionamide, cycloserine and ethambutol. The scheduled course of treatment for RR/MDR-TBM was a minimum of 24 months except for the patient’s death. In addition to anti-tuberculosis therapy, all patients were treated with glucocorticoids for up to 3 months and other adjuvant treatments deemed necessary such as mannitol for lowering intracranial pressure. Several were performed with lateral ventricle drainage.
Treatment outcome: expressed as survival status at the end of the treatment course . In the case the course of treatment had not been finished, the survival status at 6 months of treatment was taken as treatment outcome. Treatment outcome was expressed as death or survival.
Statistical methods: qualitative data were expressed as percentages; quantitative data were expressed as mean or median ± standard deviation. Rates were compared using chi-square test or Fisher's exact probability method, and quantitative data were compared using t-test or rank-sum test. The difference was considered statistically significant when P < 0.05. The statistical software used is Prism 5.0 software package.
Birthplace and occupational distribution of the TBM patients: most of the patients came from southern and southwestern provinces of China, such as Guangdong province (18.3%) and Guangxi Zhuang Autonomous Region (9.5%). Migrant workers (72 cases, 52.55%) were the most common occupation for these patients (Table 1).
Drug resistance profile of the TBM patients: the difference of drug resistance between new cases and previously treated cases was (6/119, 5.0%) and (6/18, 33.3%) for rifampicin and (3/119, 2.5%) and (4/18, 22.2%) for multidrug respectively. Both were shown to be significant statistically (P < 0.01) (Table 2).
Comparison of clinical features and CSF examination features between RR/MDR-TBM group and NRR/MDR-TBM groups: 50% of the patients in the RR/MDR-TBM group had a history of anti-tuberculosis treatment (6/12), while only 10.5% were reported in the NRR/MDR-TBM group (6/125). The difference between the two groups was statistically significant (P < 0.01). Difference in other factors showed no statistical significance (Table 3).
Comparison of mortality between RR/MDR-TBM group and NRR/MDR-TBM group: the difference of mortality between RR/MDR-TBM group and NRR/MDR-TBM group showed no statistical significance, regardless of treatment completion and follow-up status. See Table 4.
Comparison of mortality between RR/MDR-TBM patients groups treated with different regimens: among RR/MDR-TBM patients, the mortality of patients treated with LZD-containing regimen at early treatment stage was significantly lower compared with those without (P = 0.045), see Table 5–6.
The study showed that most of the TBM patients being treated in our hospital were from the south and southwest of China, with a large proportion of them being migrant workers. RR/MDR-TBM accounted for a relatively high proportion among them. The history of anti-tuberculosis treatment was found to be one of the related risk factors for RR/MDR-TBM. Treatment regimen comprising linezolid seemed to be decreasing the mortality of RR/MDR-TBM significantly.
The incidence of TB in the south and southwest of China has been reported to be higher than other regions of the country. This was found to be consistent with the findings in our study based on patient’s demographic data. More than half of the patients in our study were migrant workers. The high incidence of TBM among them may be attributed to poor nutrition and deprivation of rest resulted from a low income and long working hours. A weak or impaired immune system fails to provide proper defense against Mycobacteria tuberculosis.
More and more RR/MDR-TBM had been reported in recent years. Some small sample size studies had shown that RR/MDR-TBM accounted for 12%–39.29% of TBM patients in western China, and the ratio of isoniazid-resistant TBM even reached as high as 64.29% [14, 15]. Even in children with first-time TB infection, MDR and XDR accounted for 7.2% . Although the sample size of these studies was small, it still indicated that RR/MDR-TBM is not a rare disease in China. Reports from other countries also suggested that RR/MDR-TBM constituted a relatively high proportion of TBM patients [3, 4, 17, 18]. Our study showed the proportion of RR/MDR-TMB patients in Shenzhen is also high (12/137, 8.8%). In terms of proportion, RR/MDR-TMB in previously treated cases is significantly higher than that of primary infection cases (33.3% vs. 5.0%, P < 0.01), which is in line with the situation of RR/MDR-PTB. This can be explained by the fact that TBM is developed from PTB. Therefore, the history of anti-tuberculosis treatment should be considered as the main risk factor for RR/MDR-TBM.
A series of literature suggested that the risk factors associated with RR/MDR pulmonary tuberculosis included previous history of anti-tuberculosis treatment, HIV infection, diabetes and other factors [4, 5, 17,18,19]. In our study, only the history of anti-TB treatment showed a significant statistical difference between the RR/MDR-TBM and NRR/MDR-TBM groups (6/12 vs. 18/119, P < 0.01), while the difference of other factors was statistically insignificant. The reason maybe partly due to the low ratio of comorbidity such as HIV and diabetes in our study. Therefore, TBM patients with prior anti-TB treatment history are more susceptible to be RR/MDR-TBM. Treatment outcomes of RR/MDR-TBM can be extremely unfavorable. For example, it was reported the mortality of RR/MDR-TBM treated with first-line anti-tuberculosis drugs could reached as high as 100% . Therefore, the early diagnosis of tuberculous meningitis and the evaluation of its drug resistance appeared critical for formulating an effective regimen. In our study, the NRR/MDR-TBM patients were treated with high dose of INH and standard dose of RIF (10 mg/kg, the maximum dose is 0.6 g), PZA, EMB according to the national tuberculosis management guideline. Some of these patients’ regimen were supplemented with another drug such as levofloxacin or moxifloxacin. Some research showed that high dose of RIF (20–35 mg/kg administered orally, and standard dose of INH) was able to improve treatment outcomes due to a higher RIF concentration in plasma and CSF, especially when RIF was administered intravenously [20, 21]. Other research did not reach the same conclusion above, though . We believe that high dose of INH is more important than high dose of RIF for the treatment of TBM. First because INH has excellent early bactericidal activity (EBA), and the genotype of N-acetyltransferase type 2 (NAT2) for the majority of Chinese are rapid acetylators. Recently, a study conducted by Jing had shown that about 36.0%, 42.7% and 21.3% Chinese population are fast, intermediate and slow acetylators respectively according to NAT2 genotype. A population pharmacokinetic (PPK) model for isoniazid among Chinese tuberculosis patients was established for the first time which suggested an approximated dosage of 800 mg/day, 500 mg/day or 300 mg/day for fast, intermediate and slow acetylators, respectively, in order to achieve effective and safe plasma concentration . Standard dose of INH for most Chinese TBM patients will only result in low drug concentration in plasma and CSF, regardless of its potent permeability through the blood brain barrier (BBB). However, a high dose of INH plus RIF will increase the incidence of hepatotoxicity easily. Thus, we chose high dose of INH and standard dose of RIF, of which RIF was administered intravenously instead of orally to increase drug level in plasma and CSF. According to the previous report, 13 mg/kg of IV RIF can achieve an equivalent of AUC0-24 h which drives rifampicin effect and a higher Cmax compared to 20 mg/kg of orally administered RIF .
Many patients in the NRR/MDR-TBM group were lost to follow-up. Reasons behind may include: an invalid contact number due to an expired calling card or the patient leaving the city to return to his/her birthplace due to loss of job. Secondly, we cannot rule out that possibility of the telephone number being cancelled was due to the patients’ death. So we assume two extreme situations, that is, patients who were lost to follow-up in this study either survived or died (the real situation should locate between these two extremes). And the results showed that in any case, the difference of mortality between the RR/MDR-TBM group and NRR/MDR-TBM group remained insignificant, indicating that after timely and proper anti-TB treatment, the mortality of RR/MDR-TBM patients was not higher than that of NRR/MDR-TBM.
Among RR/MDR-TBM patients, mortality rate in patients on treatment regimen with LZD was significantly lower than those without (see Tables 5–6). This showed that LZD may improve treatment outcome due to its strong early bactericidal activity (EBA) and excellent permeability through the blood–brain barrier (BBB). Its CSF-to-serum ratio of the areas under the curves nearly reached 1.0 . Some retrospective studies had indicated that LZD was able to manifest satisfactory effect to life-threatening TBM and improved their early outcomes for both children and adult TBM patients. In Li’s research involving 86 children with TBM, 32 (88.9%) in 36 LZD-treated hospitalized cases and 35 (70%) of 50 control group had favorable outcomes (p = 0.037). In addition, there was no significant difference in the frequency of adverse effect between the 2 groups . In another research conducted by Sun et al. 16 LZD-treated TBM patients (BMRC grade II or III) achieved a faster and higher percentage of Glasgow coma scale and temperature recovery, a higher CSF/blood glucose ratio, and lower CSF white blood cell counts than the control group did (p < 0.05) . But in these two studies, DST or fast detection of MTB nucleic acid such as Genexpert MTB/RIF had not been performed, so the proportion of RR/MDR-TBM was unclear. The addition of a single drug to a failing regimen is perilous, as it may induce further resistance. Meanwhile, the case number in Sun et al.’s study is too small to reach a good representation of evidence-based conclusion and the study only evaluated interim outcome, long term outcome was not known. Only some case reports observed favorable long term outcomes of RR/MDR-TBM patients who received LZD treatment [26, 27]. To our knowledge, our cohort study appears to be the first one to evaluate the long term outcomes of LZD-containing regimen on RR/MDR-TBM patients.
For pathogen-positive TBM cases, anti-tuberculosis treatment regimen can be formulated based on the results of drug sensitivity test. Unfortunately, only less than 40% of total non-HIV TBM cases in this study were tested pathogen-positive even with the use of assays with high sensitivity and specificity like GeneXpert RIF/MTB or GeneXpert Ultra . For pathogen-negative cases, it is advisable to initiate empirical anti-tuberculosis treatment as early as possible. The regimen consists of first-line drugs (isoniazid, rifampicin, pyrazinamide, ethambutol), which, however, has yielded unsatisfactory outcome on drug-resistant TBM, especially RR/MDR-TBM. Even when fluoroquinolones is added to the regimen and the dose of rifampicin is increased, it can only lower the mortality of isoniazid-resistant TBM but not that of RR/MDR-TBM [3, 18]. Previous literatures and our study showed that the proportion of RR/MDR-TBM in pathogen-positive TBM patients with prior TB treatment history is very high in China. We believe the same also exists in pathogen-negative TBM patients with previous TB treatment history. Treatment regimen composes of first-line anti-tuberculosis drugs alone will obviously worsen their outcome. So for pathogen-negative TBM cases treated previously, linezolid may be beneficial when it is added to an empirical treatment regimen. But this should be evaluated by large scale and prospective study. Meanwhile the regimen should contain other effective second-line drugs, such as levofloxacin (moxifloxacin) or cycloserine . The challenge, however, is whether RIF should be included in the regimen, since more than 60% of the previously treated TBM patients in our study showed sensitivity to RIF, and a large proportion of them complicated with PTB, so RIF and other first-line drugs should also be included.
There are some limitations in this study. First of all, it is unclear whether the drug resistance profile of pathogen-negative TBM patients is exactly the same as that of pathogen-positive TBM patient. Meanwhile, DST did not test sensitivity to some second line drugs such as linezolid, fluroquinolones and cycloserine. Secondly, the number of RR/MDR-TBM cases was very small, so the lower mortality was not necessarily due to LZD but maybe by chance. It is necessary to further increase case number for a prospective multicenter cohort study to evaluate the efficacy and adverse effects of LZD-containing regimens. Finally, the high proportion of lost to follow-up patients in the NRR/MDR-TBM group also made it difficult to analyze the results, although we had made appropriate assumptions.
The history of anti-tuberculosis treatment is considered to be the main related risk factor of RR/MDR-TBM. Notwithstanding our small sample size retrospective study, LZD-containing regimen seemed to lower the mortality of RR/MDR-TBM significantly. We think LZD should be evaluated prospectively in the treatment of RR/MDR TBM.
Availability of data and materials
Some of them have been provided in the manuscript, the rest was available from the corresponding author on reasonable request.
Acid fast bacilli
Blood brain barrier
The modified British Medical Research Council
Drug susceptibility test
Early bactericidal activity
Glasgow Coma Scale
Hospital information system
Human Immunodeficiency Virus
Laboratory information system
Non-rifampicin/multidrug-resistant tuberculous meningitis
Rifampicin/multidrug-resistant tuberculous meningitis
World Health Organization
Chiang SS, Khan FA, Milstein MB, Tolman AW, Benedetti A, Starke JR, et al. Treatment outcomes of childhood tuberculous meningitis: a systematic review and meta-analysis. Lancet Infect Dis. 2014;14(10):947–57. https://doi.org/10.1016/S1473-3099(14)70852-7 (Epub 2014 Aug 6).
Graham SM, Donald PR. Death and disability: the outcomes of tuberculous meningitis. Lancet Infect Dis. 2014;14(10):902–4. https://doi.org/10.1016/S1473-3099(14)70872-2 (Epub 2014 Aug 6).
Heemskerk AD, Nguyen MTH, Dang HTM, Vinh Nguyen CV, Nguyen LH, Do TDA, et al. Clinical outcomes of patients with drug-resistant tuberculous meningitis treated with an intensified antituberculosis regimen. Clin Infect Dis. 2017;65(1):20–8. https://doi.org/10.1093/cid/cix230.
Vinnard C, King L, Munsiff S, Crossa A, Iwata K, Pasipanodya J, et al. Long-term mortality of patients with tuberculous meningitis in New York city: a cohort study. Clin Infect Dis. 2017;64(4):401–7. https://doi.org/10.1093/cid/ciw763.
World Health Organization, Geneva, Switzerland: Global tuberculosis report 2020.
Phypers M, Harris T, Power C. CNS tuberculosis: a longitudinal analysis of epidemiological and clinical features. Int J Tuberc Lung Dis. 2006;10(1):99–103.
Kang W, Yu J, Du J, Yang S, Chen H, Liu J, et al. The epidemiology of extrapulmonary tuberculosis in China: a large-scale multi-center observational study. PLoS ONE. 2020;15(8): e0237753. https://doi.org/10.1371/journal.pone.0237753.
Marais S, Thwaites G, Schoeman JF, Török ME, Misra UK, Prasad K, et al. Tuberculous meningitis: a uniform case definition for use in clinical research. Lancet Infect Dis. 2010;10(11):803–12. https://doi.org/10.1016/S1473-3099(10)70138-9 (Epub 2010 Sep 6).
Jyothy A, Ratageri VH, Illalu S, Fattepur SR, Wari PK. The utility of CSF Xpert MTB/RIF in diagnosis of tubercular meningitis in children. Indian J Pediatr. 2019;86(12):1089–93. https://doi.org/10.1007/s12098-019-03032-0 (Epub 2019 Jul 19).
Nhu NT, Heemskerk D, Thu Do DA, Chau TT, Mai NT, Nghia HD, et al. Evaluation of GeneXpert MTB/RIF for diagnosis of tuberculous meningitis. J Clin Microbiol. 2014;52(1):226–33. https://doi.org/10.1128/JCM.01834-13 (Epub 2013 Nov 6).
Koh WJ, Ko Y, Kim CK, Park KS, Lee NY. Rapid diagnosis of tuberculosis and multidrug resistance using a MGIT 960 system. Ann Lab Med. 2012;32(4):264–9. https://doi.org/10.3343/alm.2012.32.4.264 (Epub 2012 Jun 20).
Kam KM, Yip CW. Surveillance of Mycobacterium tuberculosis susceptibility to second-line drugs in Hong Kong, 1995–2002, after the implementation of DOTS-plus. Int J Tuberc Lung Dis. 2004;8(6):760–6.
Jullien S, Ryan H, Modi M, Bhatia R. Six months therapy for tuberculous meningitis. Cochrane Database Syst Rev. 2016;9(9):CD012091. https://doi.org/10.1002/14651858.CD012091.pub2.
Duo L, Ying B, Song X, Lu X, Ye Y, Fan H, et al. Molecular profile of drug resistance in tuberculous meningitis from southwest china. Clin Infect Dis. 2011;53(11):1067–73. https://doi.org/10.1093/cid/cir663 (Epub 2011 Oct 21).
Wang T, Feng GD, Pang Y, Liu JY, Zhou Y, Yang YN, et al. High rate of drug resistance among tuberculous meningitis cases in Shaanxi province, China. Sci Rep. 2016;4(6):25251. https://doi.org/10.1038/srep25251.
Wang DM, Li QF, Zhu M, Wu GH, Li X, Xu YH, et al. Epidemiological, clinical characteristics and drug resistance situation of culture-confirmed children TBM in southwest of China: a 6-year retrospective study. BMC Infect Dis. 2020;20(1):318. https://doi.org/10.1186/s12879-020-05041-3.
Vinnard C, Winston CA, Wileyto EP, MacGregor RR, Bisson GP. Multidrug resistant tuberculous meningitis in the United States, 1993–2005. J Infect. 2011;63(3):240–2. https://doi.org/10.1016/j.jinf.2011.07.005 (Epub 2011 Jul 19).
Heemskerk AD, Bang ND, Mai NT, Chau TT, Phu NH, Loc PP, et al. Intensified antituberculosis therapy in adults with tuberculous meningitis. N Engl J Med. 2016;374(2):124–34. https://doi.org/10.1056/NEJMoa1507062.
Hsu AH, Lee JJ, Chiang CY, Li YH, Chen LK, Lin CB. Diabetes is associated with drug-resistant tuberculosis in Eastern Taiwan. Int J Tuberc Lung Dis. 2013;17(3):354–6. https://doi.org/10.5588/ijtld.11.0670 (Epub 2012 Dec 8).
Yunivita V, Dian S, Ganiem AR, Hayati E, Hanggono Achmad T, Purnama Dewi A, et al. Pharmacokinetics and safety/tolerability of higher oral and intravenous doses of rifampicin in adult tuberculous meningitis patients. Int J Antimicrob Agents. 2016;48(4):415–21. https://doi.org/10.1016/j.ijantimicag.2016.06.016 (Epub 2016 Jul 26).
Marais S, Cresswell FV, Hamers RL, Te Brake LHM, Ganiem AR, Imran D, et al. High dose oral rifampicin to improve survival from adult tuberculous meningitis: a randomised placebo-controlled double-blinded phase III trial (the HARVEST study). Wellcome Open Res. 2020;25(4):190. https://doi.org/10.12688/wellcomeopenres.15565.2.
Jing W, Zong Z, Tang B, Wang J, Zhang T, Wen S, et al. Population pharmacokinetic analysis of isoniazid among pulmonary tuberculosis patients from China. Antimicrob Agents Chemother. 2020;64(3):e01736-e1819. https://doi.org/10.1128/AAC.01736-19.PMID:31907179.
Nau R, Sörgel F, Eiffert H. Penetration of drugs through the blood-cerebrospinal fluid/blood-brain barrier for treatment of central nervous system infections. Clin Microbiol Rev. 2010;23(4):858–83. https://doi.org/10.1128/CMR.00007-10.
Li H, Lu J, Liu J, Zhao Y, Ni X, Zhao S. Linezolid is associated with improved early outcomes of childhood tuberculous meningitis. Pediatr Infect Dis J. 2016;35(6):607–10. https://doi.org/10.1097/INF.0000000000001114.
Sun F, Ruan Q, Wang J, Chen S, Jin J, Shao L, et al. Linezolid manifests a rapid and dramatic therapeutic effect for patients with life-threatening tuberculous meningitis. Antimicrob Agents Chemother. 2014;58(10):6297–301. https://doi.org/10.1128/AAC.02784-14 (Epub 2014 Aug 4).
Alsleben N, Garcia-Prats AJ, Hesseling AC, Willemse M, Donald PR, Schaaf HS. Successful treatment of a child with extensively drug-resistant tuberculous meningitis. J Pediatric Infect Dis Soc. 2015;4(3):e41–4. https://doi.org/10.1093/jpids/piu120 (Epub 2014 Dec 23).
Kaplan SR, Topal J, Sosa L, Malinis M, Huttner A, Malhotra A, et al. A patient with central nervous system tuberculomas and a history of disseminated multi-drug-resistant tuberculosis. J Clin Tuberc Other Mycobact Dis. 2017;10:9-16. https://doi.org/10.1016/j.jctube.2017.12.004. Erratum in: J Clin Tuberc Other Mycobact Dis. 2020;21:100177
Donovan J, Thu DDA, Phu NH, Dung VTM, Quang TP, Nghia HDT, et al. Xpert MTB/RIF Ultra versus Xpert MTB/RIF for the diagnosis of tuberculous meningitis: a prospective, randomised, diagnostic accuracy study. Lancet Infect Dis. 2020;20(3):299–307. https://doi.org/10.1016/S1473-3099(19)30649-8 (Epub 2020 Jan 7).
Wasserman S, Davis A, Wilkinson RJ, Meintjes G. Key considerations in the pharmacotherapy of tuberculous meningitis. Expert Opin Pharmacother. 2019;20(15):1791–5. https://doi.org/10.1080/14656566.2019.1638912 (Epub 2019 Jul 15).
We are sincerely grateful to Guo-Hui Liu, Sen-Lin Zhan, Jian Zeng, Hong-Mei Zhang, Wei-Jian Liu, Liang Fu, Jun-feng Zhen, Jie Tan, Yu-Xiang Wang, Tao Chen, Jian Li, Xue Ke, Zhi-Chao Liu, Zhi Liu for the provision of patient cases to the research.
This work was supported financially by Guangdong Province Science and Technology Project (2020B1111170014), and Shenzhen Fund for Guangdong Provincial High-level Clinical Key Specialties (No. SZGSP010). The funding organizations had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
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This study was approved by the ethics committee of The Third People’s Hospital of Shenzhen as part of the National Key Project for Infectious Disease and complied with the Declaration of Helsinki. Informed consent was not obtained as it is a retrospective study.
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Fang, MT., Su, YF., An, HR. et al. Decreased mortality seen in rifampicin/multidrug-resistant tuberculous meningitis treated with linezolid in Shenzhen, China. BMC Infect Dis 21, 1015 (2021). https://doi.org/10.1186/s12879-021-06705-4
- Tuberculous meningitis
- Blood–brain barrier
- Rifampicin/multidrug-resistant TBM