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Distinguishing clinical characteristics of central nervous system tuberculosis in immunodeficient and non-immunodeficient individuals: a 12-year retrospective study
Central nervous system tuberculosis (CNS TB) is a severe Mycobacterium tuberculosis (MTB) infection. It is unclear whether a patient's immune status alters the clinical manifestations and treatment outcomes of CNS TB. Between January 2007-December 2018, chart reviews of CNS TB, including tuberc...
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Published in: | Annals of clinical microbiology and antimicrobials 2023-08, Vol.22 (1), p.69-69, Article 69 |
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description | Central nervous system tuberculosis (CNS TB) is a severe Mycobacterium tuberculosis (MTB) infection. It is unclear whether a patient's immune status alters the clinical manifestations and treatment outcomes of CNS TB.
Between January 2007-December 2018, chart reviews of CNS TB, including tuberculous meningitis (TBM), tuberculoma/abscess, and TB myelitis, were made. Subjects were categorized as immunodeficient (ID) and non-immunodeficient (NID).
Of 310 subjects, 160 (51.6%) were in the ID group-132 (42.6%) had HIV and 28 (9.0%) had another ID, and 150 (48.4%) were in the NID group. The mean age was 43.64 ± 16.76 years, and 188 (60.6%) were male. There were 285 (91.9%) TBM, 16 (5.2%) tuberculoma/abscess, and 9 (2.9%) myelitis cases. The TBM characteristics in the ID group were younger age (p = 0.003), deep subcortical location of tuberculoma (p = 0.030), lower hemoglobin level (p |
doi_str_mv | 10.1186/s12941-023-00615-w |
format | article |
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Between January 2007-December 2018, chart reviews of CNS TB, including tuberculous meningitis (TBM), tuberculoma/abscess, and TB myelitis, were made. Subjects were categorized as immunodeficient (ID) and non-immunodeficient (NID).
Of 310 subjects, 160 (51.6%) were in the ID group-132 (42.6%) had HIV and 28 (9.0%) had another ID, and 150 (48.4%) were in the NID group. The mean age was 43.64 ± 16.76 years, and 188 (60.6%) were male. There were 285 (91.9%) TBM, 16 (5.2%) tuberculoma/abscess, and 9 (2.9%) myelitis cases. The TBM characteristics in the ID group were younger age (p = 0.003), deep subcortical location of tuberculoma (p = 0.030), lower hemoglobin level (p < 0.001), and lower peripheral white blood cell count (p < 0.001). Only HIV individuals with TBM had an infection by multidrug-resistant MTB (p = 0.013). TBM mortality was varied by immune status -HIV 22.8%, other ID 29.6%, and NID 14.8% (p < 0.001). Factors significantly associated with unfavorable outcomes in TBM also differed between the HIV and NID groups.
TBM is the most significant proportion of CNS TB. Some of the clinical characteristics of TBM, such as age, radiographic findings, hematological derangement, and mortality, including factors associated with unfavorable outcomes, differed between ID and non-ID patients.</description><identifier>ISSN: 1476-0711</identifier><identifier>EISSN: 1476-0711</identifier><identifier>DOI: 10.1186/s12941-023-00615-w</identifier><identifier>PMID: 37550721</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Abscess ; Abscesses ; Acids ; Adult ; Age ; Blood cell count ; Care and treatment ; Central nervous system ; Cerebrospinal fluid ; Clinical outcomes ; Complications and side effects ; Demographic aspects ; Diagnosis ; Female ; Health aspects ; Hemoglobin ; HIV ; HIV Infections - complications ; Human immunodeficiency virus ; Humans ; Immune status ; Immunodeficiency ; Infections ; Leukocytes ; Male ; Meningitis ; Middle Aged ; Mortality ; Multidrug resistance ; Mycobacterium tuberculosis ; Myelitis ; Nervous system ; Patients ; Pulmonary tuberculosis ; Radiography ; Retrospective Studies ; Sample size ; Spinal cord ; Tuberculoma ; Tuberculoma - complications ; Tuberculosis ; Tuberculosis, Central Nervous System - complications ; Tuberculosis, Central Nervous System - diagnosis ; Tuberculosis, Central Nervous System - drug therapy ; Tuberculosis, Meningeal - complications ; Tuberculosis, Meningeal - diagnosis ; Tuberculosis, Meningeal - drug therapy</subject><ispartof>Annals of clinical microbiology and antimicrobials, 2023-08, Vol.22 (1), p.69-69, Article 69</ispartof><rights>2023. BioMed Central Ltd., part of Springer Nature.</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>BioMed Central Ltd., part of Springer Nature 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-e7a160cc66c3748b05e9d8bb0b5dcbe10c5b5b2d74fbfee5fe4d89a3481811733</citedby><cites>FETCH-LOGICAL-c564t-e7a160cc66c3748b05e9d8bb0b5dcbe10c5b5b2d74fbfee5fe4d89a3481811733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10408106/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2852188433?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37550721$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saifon, Woraseth</creatorcontrib><creatorcontrib>Karaketklang, Khemajira</creatorcontrib><creatorcontrib>Jitmuang, Anupop</creatorcontrib><title>Distinguishing clinical characteristics of central nervous system tuberculosis in immunodeficient and non-immunodeficient individuals: a 12-year retrospective study</title><title>Annals of clinical microbiology and antimicrobials</title><addtitle>Ann Clin Microbiol Antimicrob</addtitle><description>Central nervous system tuberculosis (CNS TB) is a severe Mycobacterium tuberculosis (MTB) infection. It is unclear whether a patient's immune status alters the clinical manifestations and treatment outcomes of CNS TB.
Between January 2007-December 2018, chart reviews of CNS TB, including tuberculous meningitis (TBM), tuberculoma/abscess, and TB myelitis, were made. Subjects were categorized as immunodeficient (ID) and non-immunodeficient (NID).
Of 310 subjects, 160 (51.6%) were in the ID group-132 (42.6%) had HIV and 28 (9.0%) had another ID, and 150 (48.4%) were in the NID group. The mean age was 43.64 ± 16.76 years, and 188 (60.6%) were male. There were 285 (91.9%) TBM, 16 (5.2%) tuberculoma/abscess, and 9 (2.9%) myelitis cases. The TBM characteristics in the ID group were younger age (p = 0.003), deep subcortical location of tuberculoma (p = 0.030), lower hemoglobin level (p < 0.001), and lower peripheral white blood cell count (p < 0.001). Only HIV individuals with TBM had an infection by multidrug-resistant MTB (p = 0.013). TBM mortality was varied by immune status -HIV 22.8%, other ID 29.6%, and NID 14.8% (p < 0.001). Factors significantly associated with unfavorable outcomes in TBM also differed between the HIV and NID groups.
TBM is the most significant proportion of CNS TB. Some of the clinical characteristics of TBM, such as age, radiographic findings, hematological derangement, and mortality, including factors associated with unfavorable outcomes, differed between ID and non-ID patients.</description><subject>Abscess</subject><subject>Abscesses</subject><subject>Acids</subject><subject>Adult</subject><subject>Age</subject><subject>Blood cell count</subject><subject>Care and treatment</subject><subject>Central nervous system</subject><subject>Cerebrospinal fluid</subject><subject>Clinical outcomes</subject><subject>Complications and side effects</subject><subject>Demographic aspects</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Health aspects</subject><subject>Hemoglobin</subject><subject>HIV</subject><subject>HIV Infections - complications</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immune status</subject><subject>Immunodeficiency</subject><subject>Infections</subject><subject>Leukocytes</subject><subject>Male</subject><subject>Meningitis</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Multidrug resistance</subject><subject>Mycobacterium tuberculosis</subject><subject>Myelitis</subject><subject>Nervous system</subject><subject>Patients</subject><subject>Pulmonary tuberculosis</subject><subject>Radiography</subject><subject>Retrospective Studies</subject><subject>Sample size</subject><subject>Spinal cord</subject><subject>Tuberculoma</subject><subject>Tuberculoma - complications</subject><subject>Tuberculosis</subject><subject>Tuberculosis, Central Nervous System - complications</subject><subject>Tuberculosis, Central Nervous System - diagnosis</subject><subject>Tuberculosis, Central Nervous System - drug therapy</subject><subject>Tuberculosis, Meningeal - complications</subject><subject>Tuberculosis, Meningeal - diagnosis</subject><subject>Tuberculosis, Meningeal - drug therapy</subject><issn>1476-0711</issn><issn>1476-0711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUstuFDEQHCEQCYEf4IAsceEywZ7xY5YLisIrUiQucLb86Nn1asYO9sxG-z98KL3ZJWQj5ENb3VVldbmq6jWj54x18n1hzYKzmjZtTalkor59Up0yrmRNFWNPH9xPqhelrCltEKeeVyetEoKqhp1Wvz-FMoW4nENZYSFuCDE4MxC3Mtm4CfJu7gpJPXEQp4yjCHmT5kLKtkwwkmm2kN08pBIKCZGEcZxj8tAHF5BBTPQkplg_7ofowyb42QzlAzGENfUWTCYZppzKDbgpbICUafbbl9WzHlHw6lDPqp9fPv-4_FZff_96dXlxXTsh-VSDMkxS56R0reKdpQIWvrOWWuGdBUadsMI2XvHe9gCiB-67hWl5xzrGVNueVVd7XZ_MWt_kMJq81ckEfddIealNRjcG0Asjoe8YNa0F3hm-oKCkUBbNVqqHBWp93GvdzHYEf_DuSPR4EsNKL9NGM8opCktUeHdQyOnXDGXSYygOhsFEQPt103GluOScIvTtI-g6zTmiV4gSDes63rb_UEuDG4TYJ3zY7UT1hZKYjlYwjqjz_6DweBiDSxH_D_tHhGZPcPhvJUN_vySjehdUvQ-qRry-C6q-RdKbh_bcU_4ms_0Ds-PoNA</recordid><startdate>20230807</startdate><enddate>20230807</enddate><creator>Saifon, Woraseth</creator><creator>Karaketklang, Khemajira</creator><creator>Jitmuang, Anupop</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230807</creationdate><title>Distinguishing clinical characteristics of central nervous system tuberculosis in immunodeficient and non-immunodeficient individuals: a 12-year retrospective study</title><author>Saifon, Woraseth ; Karaketklang, Khemajira ; Jitmuang, Anupop</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-e7a160cc66c3748b05e9d8bb0b5dcbe10c5b5b2d74fbfee5fe4d89a3481811733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abscess</topic><topic>Abscesses</topic><topic>Acids</topic><topic>Adult</topic><topic>Age</topic><topic>Blood cell count</topic><topic>Care and treatment</topic><topic>Central nervous system</topic><topic>Cerebrospinal fluid</topic><topic>Clinical outcomes</topic><topic>Complications and side effects</topic><topic>Demographic aspects</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Health aspects</topic><topic>Hemoglobin</topic><topic>HIV</topic><topic>HIV Infections - complications</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immune status</topic><topic>Immunodeficiency</topic><topic>Infections</topic><topic>Leukocytes</topic><topic>Male</topic><topic>Meningitis</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Multidrug resistance</topic><topic>Mycobacterium tuberculosis</topic><topic>Myelitis</topic><topic>Nervous system</topic><topic>Patients</topic><topic>Pulmonary tuberculosis</topic><topic>Radiography</topic><topic>Retrospective Studies</topic><topic>Sample size</topic><topic>Spinal cord</topic><topic>Tuberculoma</topic><topic>Tuberculoma - complications</topic><topic>Tuberculosis</topic><topic>Tuberculosis, Central Nervous System - complications</topic><topic>Tuberculosis, Central Nervous System - diagnosis</topic><topic>Tuberculosis, Central Nervous System - drug therapy</topic><topic>Tuberculosis, Meningeal - complications</topic><topic>Tuberculosis, Meningeal - diagnosis</topic><topic>Tuberculosis, Meningeal - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saifon, Woraseth</creatorcontrib><creatorcontrib>Karaketklang, Khemajira</creatorcontrib><creatorcontrib>Jitmuang, Anupop</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Proquest Health and Medical Complete</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Annals of clinical microbiology and antimicrobials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saifon, Woraseth</au><au>Karaketklang, Khemajira</au><au>Jitmuang, Anupop</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinguishing clinical characteristics of central nervous system tuberculosis in immunodeficient and non-immunodeficient individuals: a 12-year retrospective study</atitle><jtitle>Annals of clinical microbiology and antimicrobials</jtitle><addtitle>Ann Clin Microbiol Antimicrob</addtitle><date>2023-08-07</date><risdate>2023</risdate><volume>22</volume><issue>1</issue><spage>69</spage><epage>69</epage><pages>69-69</pages><artnum>69</artnum><issn>1476-0711</issn><eissn>1476-0711</eissn><abstract>Central nervous system tuberculosis (CNS TB) is a severe Mycobacterium tuberculosis (MTB) infection. It is unclear whether a patient's immune status alters the clinical manifestations and treatment outcomes of CNS TB.
Between January 2007-December 2018, chart reviews of CNS TB, including tuberculous meningitis (TBM), tuberculoma/abscess, and TB myelitis, were made. Subjects were categorized as immunodeficient (ID) and non-immunodeficient (NID).
Of 310 subjects, 160 (51.6%) were in the ID group-132 (42.6%) had HIV and 28 (9.0%) had another ID, and 150 (48.4%) were in the NID group. The mean age was 43.64 ± 16.76 years, and 188 (60.6%) were male. There were 285 (91.9%) TBM, 16 (5.2%) tuberculoma/abscess, and 9 (2.9%) myelitis cases. The TBM characteristics in the ID group were younger age (p = 0.003), deep subcortical location of tuberculoma (p = 0.030), lower hemoglobin level (p < 0.001), and lower peripheral white blood cell count (p < 0.001). Only HIV individuals with TBM had an infection by multidrug-resistant MTB (p = 0.013). TBM mortality was varied by immune status -HIV 22.8%, other ID 29.6%, and NID 14.8% (p < 0.001). Factors significantly associated with unfavorable outcomes in TBM also differed between the HIV and NID groups.
TBM is the most significant proportion of CNS TB. Some of the clinical characteristics of TBM, such as age, radiographic findings, hematological derangement, and mortality, including factors associated with unfavorable outcomes, differed between ID and non-ID patients.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37550721</pmid><doi>10.1186/s12941-023-00615-w</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abscess Abscesses Acids Adult Age Blood cell count Care and treatment Central nervous system Cerebrospinal fluid Clinical outcomes Complications and side effects Demographic aspects Diagnosis Female Health aspects Hemoglobin HIV HIV Infections - complications Human immunodeficiency virus Humans Immune status Immunodeficiency Infections Leukocytes Male Meningitis Middle Aged Mortality Multidrug resistance Mycobacterium tuberculosis Myelitis Nervous system Patients Pulmonary tuberculosis Radiography Retrospective Studies Sample size Spinal cord Tuberculoma Tuberculoma - complications Tuberculosis Tuberculosis, Central Nervous System - complications Tuberculosis, Central Nervous System - diagnosis Tuberculosis, Central Nervous System - drug therapy Tuberculosis, Meningeal - complications Tuberculosis, Meningeal - diagnosis Tuberculosis, Meningeal - drug therapy |
title | Distinguishing clinical characteristics of central nervous system tuberculosis in immunodeficient and non-immunodeficient individuals: a 12-year retrospective study |
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