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Empirical cefepime+vancomycin versus ceftazidime+vancomycin versus meropenem+vancomycin in the treatment of healthcare-associated meningitis: results of the multicenter ephesus study
Herein, we analyzed the efficacy of main antibiotic therapy regimens in the treatment of healthcare-associated meningitis (HCAM). This retrospective cohort study was conducted in 18 tertiary-care academic hospitals Turkey, India, Egypt and Romania. We extracted data and outcomes of all patients with...
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Published in: | BMC Infectious Diseases 2023, Vol.23 (1) |
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creator | Sipahi, Oguz Resat Akyol, Deniz Ormen, Bahar Cicek-Senturk, Gonul Mermer, Sinan Onal, Ugur Amer, Fatma Saed, Maysaa Abdallah Ozdemir, Kevser Tukenmez-Tigen, Elif Oztoprak, Nefise Altin, Ummugulsum Kurtaran, Behice Popescu, Corneliu Petru Sakci, Mustafa Suntur, Bedia Mutay Gautam, Vikas Sharma, Megha Kaya, Safak Akcil, Eren Fatma Kaya, Selcuk Turunc, Tuba Ergen, Pinar Kandemir, Ozlem Cesur, Salih Bardak-Ozcem, Selin Ozgiray, Erkin Yurtseven, Taskin Erdem, Huseyin Aytac Sipahi, Hilal Arda, Bilgin Pullukcu, Hüsnü Tasbakan, Meltem Yamazhan, Tansu Aydemir, Sohret Ulusoy, Sercan |
description | Herein, we analyzed the efficacy of main antibiotic therapy regimens in the treatment of healthcare-associated meningitis (HCAM). This retrospective cohort study was conducted in 18 tertiary-care academic hospitals Turkey, India, Egypt and Romania. We extracted data and outcomes of all patients with post-neurosurgical meningitis cases fulfilling the study inclusion criteria and treated with empirical therapy between December 2006-September 2018. Twenty patients in the cefepime + vancomycin-(CV) group, 31 patients in the ceftazidime + vancomycin-(CFV) group, and 119 patients in the meropenem + vancomycin-(MV) group met the inclusion criteria. The MV subgroup had a significantly higher mean Glasgow Coma Score, a higher rate of admission to the intensive care unit within the previous month, and a higher rate of antibiot herapy within the previous month before the meningitis episode (p < 0.05). Microbiological success on Day 3-5, end of treatment (EOT) clinical success (80% vs. 54.8%% vs 57.9%), and overall success (EOT success followed by one-month survival without relapse or reinfection 65% vs. 51.6% vs. 45.3%), EOT all cause mortality (ACM) and day 30 ACM (15% vs. 22.6% vs. 26%) did not differ significantly (p > 0.05) among the three cohorts. No regimen was effective against carbapenem-resistant bacteria, and vancomycin resulted in an EOT clinical success rate of 60.6% in the methicillin-resistant staphylococci or ampicillin-resistant enterococci subgroup (n = 34). Our study showed no significant difference in terms of clinical success and mortality among the three treatment options. All regimens were ineffective against carbapenem-resistant bacteria. Vancomycin was unsuccessful in approximately 40% of cases involving methicillin-resistant staphylococci or ampicillin-resistant enterococci. |
doi_str_mv | 10.1186/s12879-023-08596-z |
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This retrospective cohort study was conducted in 18 tertiary-care academic hospitals Turkey, India, Egypt and Romania. We extracted data and outcomes of all patients with post-neurosurgical meningitis cases fulfilling the study inclusion criteria and treated with empirical therapy between December 2006-September 2018. Twenty patients in the cefepime + vancomycin-(CV) group, 31 patients in the ceftazidime + vancomycin-(CFV) group, and 119 patients in the meropenem + vancomycin-(MV) group met the inclusion criteria. The MV subgroup had a significantly higher mean Glasgow Coma Score, a higher rate of admission to the intensive care unit within the previous month, and a higher rate of antibiot herapy within the previous month before the meningitis episode (p < 0.05). Microbiological success on Day 3-5, end of treatment (EOT) clinical success (80% vs. 54.8%% vs 57.9%), and overall success (EOT success followed by one-month survival without relapse or reinfection 65% vs. 51.6% vs. 45.3%), EOT all cause mortality (ACM) and day 30 ACM (15% vs. 22.6% vs. 26%) did not differ significantly (p > 0.05) among the three cohorts. No regimen was effective against carbapenem-resistant bacteria, and vancomycin resulted in an EOT clinical success rate of 60.6% in the methicillin-resistant staphylococci or ampicillin-resistant enterococci subgroup (n = 34). Our study showed no significant difference in terms of clinical success and mortality among the three treatment options. All regimens were ineffective against carbapenem-resistant bacteria. Vancomycin was unsuccessful in approximately 40% of cases involving methicillin-resistant staphylococci or ampicillin-resistant enterococci.</description><identifier>ISSN: 1471-2334</identifier><identifier>EISSN: 1471-2334</identifier><identifier>DOI: 10.1186/s12879-023-08596-z</identifier><language>eng</language><publisher>BioMed Central Ltd</publisher><subject>Antibacterial agents ; Complications and side effects ; Cross infection ; Dosage and administration ; Drug therapy ; Meningitis ; Nosocomial infections ; Patient outcomes ; Prevention ; Risk factors ; Staphylococcal infections</subject><ispartof>BMC Infectious Diseases, 2023, Vol.23 (1)</ispartof><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27901</link.rule.ids></links><search><creatorcontrib>Sipahi, Oguz Resat</creatorcontrib><creatorcontrib>Akyol, Deniz</creatorcontrib><creatorcontrib>Ormen, Bahar</creatorcontrib><creatorcontrib>Cicek-Senturk, Gonul</creatorcontrib><creatorcontrib>Mermer, Sinan</creatorcontrib><creatorcontrib>Onal, Ugur</creatorcontrib><creatorcontrib>Amer, Fatma</creatorcontrib><creatorcontrib>Saed, Maysaa Abdallah</creatorcontrib><creatorcontrib>Ozdemir, Kevser</creatorcontrib><creatorcontrib>Tukenmez-Tigen, Elif</creatorcontrib><creatorcontrib>Oztoprak, Nefise</creatorcontrib><creatorcontrib>Altin, Ummugulsum</creatorcontrib><creatorcontrib>Kurtaran, Behice</creatorcontrib><creatorcontrib>Popescu, Corneliu Petru</creatorcontrib><creatorcontrib>Sakci, Mustafa</creatorcontrib><creatorcontrib>Suntur, Bedia Mutay</creatorcontrib><creatorcontrib>Gautam, Vikas</creatorcontrib><creatorcontrib>Sharma, Megha</creatorcontrib><creatorcontrib>Kaya, Safak</creatorcontrib><creatorcontrib>Akcil, Eren Fatma</creatorcontrib><creatorcontrib>Kaya, Selcuk</creatorcontrib><creatorcontrib>Turunc, Tuba</creatorcontrib><creatorcontrib>Ergen, Pinar</creatorcontrib><creatorcontrib>Kandemir, Ozlem</creatorcontrib><creatorcontrib>Cesur, Salih</creatorcontrib><creatorcontrib>Bardak-Ozcem, Selin</creatorcontrib><creatorcontrib>Ozgiray, Erkin</creatorcontrib><creatorcontrib>Yurtseven, Taskin</creatorcontrib><creatorcontrib>Erdem, Huseyin Aytac</creatorcontrib><creatorcontrib>Sipahi, Hilal</creatorcontrib><creatorcontrib>Arda, Bilgin</creatorcontrib><creatorcontrib>Pullukcu, Hüsnü</creatorcontrib><creatorcontrib>Tasbakan, Meltem</creatorcontrib><creatorcontrib>Yamazhan, Tansu</creatorcontrib><creatorcontrib>Aydemir, Sohret</creatorcontrib><creatorcontrib>Ulusoy, Sercan</creatorcontrib><title>Empirical cefepime+vancomycin versus ceftazidime+vancomycin versus meropenem+vancomycin in the treatment of healthcare-associated meningitis: results of the multicenter ephesus study</title><title>BMC Infectious Diseases</title><description>Herein, we analyzed the efficacy of main antibiotic therapy regimens in the treatment of healthcare-associated meningitis (HCAM). This retrospective cohort study was conducted in 18 tertiary-care academic hospitals Turkey, India, Egypt and Romania. We extracted data and outcomes of all patients with post-neurosurgical meningitis cases fulfilling the study inclusion criteria and treated with empirical therapy between December 2006-September 2018. Twenty patients in the cefepime + vancomycin-(CV) group, 31 patients in the ceftazidime + vancomycin-(CFV) group, and 119 patients in the meropenem + vancomycin-(MV) group met the inclusion criteria. The MV subgroup had a significantly higher mean Glasgow Coma Score, a higher rate of admission to the intensive care unit within the previous month, and a higher rate of antibiot herapy within the previous month before the meningitis episode (p < 0.05). Microbiological success on Day 3-5, end of treatment (EOT) clinical success (80% vs. 54.8%% vs 57.9%), and overall success (EOT success followed by one-month survival without relapse or reinfection 65% vs. 51.6% vs. 45.3%), EOT all cause mortality (ACM) and day 30 ACM (15% vs. 22.6% vs. 26%) did not differ significantly (p > 0.05) among the three cohorts. No regimen was effective against carbapenem-resistant bacteria, and vancomycin resulted in an EOT clinical success rate of 60.6% in the methicillin-resistant staphylococci or ampicillin-resistant enterococci subgroup (n = 34). Our study showed no significant difference in terms of clinical success and mortality among the three treatment options. All regimens were ineffective against carbapenem-resistant bacteria. Vancomycin was unsuccessful in approximately 40% of cases involving methicillin-resistant staphylococci or ampicillin-resistant enterococci.</description><subject>Antibacterial agents</subject><subject>Complications and side effects</subject><subject>Cross infection</subject><subject>Dosage and administration</subject><subject>Drug therapy</subject><subject>Meningitis</subject><subject>Nosocomial infections</subject><subject>Patient outcomes</subject><subject>Prevention</subject><subject>Risk factors</subject><subject>Staphylococcal infections</subject><issn>1471-2334</issn><issn>1471-2334</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2023</creationdate><recordtype>report</recordtype><recordid>eNqVjs9KxDAQh4MouK6-gKdcRaJJW_vHm8iKnrwsXktIp-1Ik5ZMurj7YD6fKXjYgxdhYGb4fh8zjF0readUmd-TSsqiEjJJhSwfqlwcTthKZYUSSZpmp0fzObsg-pRSFWVSrdj3xk7o0eiBG2hhQgu3O-3MaPcGHd-Bp5kWFPQBm7-pBT9O4MAes1ihBx486GDBBT62vAc9hN5oD0ITjQZ1gCbqDl2HAemRe6B5CLSEF9vGBU20wXOYeliuUZib_SU7a_VAcPXb1-zmZbN9fhWdHqDG-EV0vkKnZ6L67f2jfiryQsoyybP0P9kfT7xy9w</recordid><startdate>20230928</startdate><enddate>20230928</enddate><creator>Sipahi, Oguz Resat</creator><creator>Akyol, Deniz</creator><creator>Ormen, Bahar</creator><creator>Cicek-Senturk, Gonul</creator><creator>Mermer, Sinan</creator><creator>Onal, Ugur</creator><creator>Amer, Fatma</creator><creator>Saed, Maysaa Abdallah</creator><creator>Ozdemir, Kevser</creator><creator>Tukenmez-Tigen, Elif</creator><creator>Oztoprak, Nefise</creator><creator>Altin, Ummugulsum</creator><creator>Kurtaran, Behice</creator><creator>Popescu, Corneliu Petru</creator><creator>Sakci, Mustafa</creator><creator>Suntur, Bedia Mutay</creator><creator>Gautam, Vikas</creator><creator>Sharma, Megha</creator><creator>Kaya, Safak</creator><creator>Akcil, Eren Fatma</creator><creator>Kaya, Selcuk</creator><creator>Turunc, Tuba</creator><creator>Ergen, Pinar</creator><creator>Kandemir, Ozlem</creator><creator>Cesur, Salih</creator><creator>Bardak-Ozcem, Selin</creator><creator>Ozgiray, Erkin</creator><creator>Yurtseven, Taskin</creator><creator>Erdem, Huseyin Aytac</creator><creator>Sipahi, Hilal</creator><creator>Arda, Bilgin</creator><creator>Pullukcu, Hüsnü</creator><creator>Tasbakan, Meltem</creator><creator>Yamazhan, Tansu</creator><creator>Aydemir, Sohret</creator><creator>Ulusoy, Sercan</creator><general>BioMed Central Ltd</general><scope>IOV</scope></search><sort><creationdate>20230928</creationdate><title>Empirical cefepime+vancomycin versus ceftazidime+vancomycin versus meropenem+vancomycin in the treatment of healthcare-associated meningitis: results of the multicenter ephesus study</title><author>Sipahi, Oguz Resat ; Akyol, Deniz ; Ormen, Bahar ; Cicek-Senturk, Gonul ; Mermer, Sinan ; Onal, Ugur ; Amer, Fatma ; Saed, Maysaa Abdallah ; Ozdemir, Kevser ; Tukenmez-Tigen, Elif ; Oztoprak, Nefise ; Altin, Ummugulsum ; Kurtaran, Behice ; Popescu, Corneliu Petru ; Sakci, Mustafa ; Suntur, Bedia Mutay ; Gautam, Vikas ; Sharma, Megha ; Kaya, Safak ; Akcil, Eren Fatma ; Kaya, Selcuk ; Turunc, Tuba ; Ergen, Pinar ; Kandemir, Ozlem ; Cesur, Salih ; Bardak-Ozcem, Selin ; Ozgiray, Erkin ; Yurtseven, Taskin ; Erdem, Huseyin Aytac ; Sipahi, Hilal ; Arda, Bilgin ; Pullukcu, Hüsnü ; Tasbakan, Meltem ; Yamazhan, Tansu ; Aydemir, Sohret ; Ulusoy, Sercan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-gale_incontextgauss_IOV_A7670082643</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antibacterial agents</topic><topic>Complications and side effects</topic><topic>Cross infection</topic><topic>Dosage and administration</topic><topic>Drug therapy</topic><topic>Meningitis</topic><topic>Nosocomial infections</topic><topic>Patient outcomes</topic><topic>Prevention</topic><topic>Risk factors</topic><topic>Staphylococcal infections</topic><toplevel>online_resources</toplevel><creatorcontrib>Sipahi, Oguz Resat</creatorcontrib><creatorcontrib>Akyol, Deniz</creatorcontrib><creatorcontrib>Ormen, Bahar</creatorcontrib><creatorcontrib>Cicek-Senturk, Gonul</creatorcontrib><creatorcontrib>Mermer, Sinan</creatorcontrib><creatorcontrib>Onal, Ugur</creatorcontrib><creatorcontrib>Amer, Fatma</creatorcontrib><creatorcontrib>Saed, Maysaa Abdallah</creatorcontrib><creatorcontrib>Ozdemir, Kevser</creatorcontrib><creatorcontrib>Tukenmez-Tigen, Elif</creatorcontrib><creatorcontrib>Oztoprak, Nefise</creatorcontrib><creatorcontrib>Altin, Ummugulsum</creatorcontrib><creatorcontrib>Kurtaran, Behice</creatorcontrib><creatorcontrib>Popescu, Corneliu Petru</creatorcontrib><creatorcontrib>Sakci, Mustafa</creatorcontrib><creatorcontrib>Suntur, Bedia Mutay</creatorcontrib><creatorcontrib>Gautam, Vikas</creatorcontrib><creatorcontrib>Sharma, Megha</creatorcontrib><creatorcontrib>Kaya, Safak</creatorcontrib><creatorcontrib>Akcil, Eren Fatma</creatorcontrib><creatorcontrib>Kaya, Selcuk</creatorcontrib><creatorcontrib>Turunc, Tuba</creatorcontrib><creatorcontrib>Ergen, Pinar</creatorcontrib><creatorcontrib>Kandemir, Ozlem</creatorcontrib><creatorcontrib>Cesur, Salih</creatorcontrib><creatorcontrib>Bardak-Ozcem, Selin</creatorcontrib><creatorcontrib>Ozgiray, Erkin</creatorcontrib><creatorcontrib>Yurtseven, Taskin</creatorcontrib><creatorcontrib>Erdem, Huseyin Aytac</creatorcontrib><creatorcontrib>Sipahi, Hilal</creatorcontrib><creatorcontrib>Arda, Bilgin</creatorcontrib><creatorcontrib>Pullukcu, Hüsnü</creatorcontrib><creatorcontrib>Tasbakan, Meltem</creatorcontrib><creatorcontrib>Yamazhan, Tansu</creatorcontrib><creatorcontrib>Aydemir, Sohret</creatorcontrib><creatorcontrib>Ulusoy, Sercan</creatorcontrib><collection>Gale In Context: Opposing Viewpoints</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sipahi, Oguz Resat</au><au>Akyol, Deniz</au><au>Ormen, Bahar</au><au>Cicek-Senturk, Gonul</au><au>Mermer, Sinan</au><au>Onal, Ugur</au><au>Amer, Fatma</au><au>Saed, Maysaa Abdallah</au><au>Ozdemir, Kevser</au><au>Tukenmez-Tigen, Elif</au><au>Oztoprak, Nefise</au><au>Altin, Ummugulsum</au><au>Kurtaran, Behice</au><au>Popescu, Corneliu Petru</au><au>Sakci, Mustafa</au><au>Suntur, Bedia Mutay</au><au>Gautam, Vikas</au><au>Sharma, Megha</au><au>Kaya, Safak</au><au>Akcil, Eren Fatma</au><au>Kaya, Selcuk</au><au>Turunc, Tuba</au><au>Ergen, Pinar</au><au>Kandemir, Ozlem</au><au>Cesur, Salih</au><au>Bardak-Ozcem, Selin</au><au>Ozgiray, Erkin</au><au>Yurtseven, Taskin</au><au>Erdem, Huseyin Aytac</au><au>Sipahi, Hilal</au><au>Arda, Bilgin</au><au>Pullukcu, Hüsnü</au><au>Tasbakan, Meltem</au><au>Yamazhan, Tansu</au><au>Aydemir, Sohret</au><au>Ulusoy, Sercan</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Empirical cefepime+vancomycin versus ceftazidime+vancomycin versus meropenem+vancomycin in the treatment of healthcare-associated meningitis: results of the multicenter ephesus study</atitle><jtitle>BMC Infectious Diseases</jtitle><date>2023-09-28</date><risdate>2023</risdate><volume>23</volume><issue>1</issue><issn>1471-2334</issn><eissn>1471-2334</eissn><abstract>Herein, we analyzed the efficacy of main antibiotic therapy regimens in the treatment of healthcare-associated meningitis (HCAM). This retrospective cohort study was conducted in 18 tertiary-care academic hospitals Turkey, India, Egypt and Romania. We extracted data and outcomes of all patients with post-neurosurgical meningitis cases fulfilling the study inclusion criteria and treated with empirical therapy between December 2006-September 2018. Twenty patients in the cefepime + vancomycin-(CV) group, 31 patients in the ceftazidime + vancomycin-(CFV) group, and 119 patients in the meropenem + vancomycin-(MV) group met the inclusion criteria. The MV subgroup had a significantly higher mean Glasgow Coma Score, a higher rate of admission to the intensive care unit within the previous month, and a higher rate of antibiot herapy within the previous month before the meningitis episode (p < 0.05). Microbiological success on Day 3-5, end of treatment (EOT) clinical success (80% vs. 54.8%% vs 57.9%), and overall success (EOT success followed by one-month survival without relapse or reinfection 65% vs. 51.6% vs. 45.3%), EOT all cause mortality (ACM) and day 30 ACM (15% vs. 22.6% vs. 26%) did not differ significantly (p > 0.05) among the three cohorts. No regimen was effective against carbapenem-resistant bacteria, and vancomycin resulted in an EOT clinical success rate of 60.6% in the methicillin-resistant staphylococci or ampicillin-resistant enterococci subgroup (n = 34). Our study showed no significant difference in terms of clinical success and mortality among the three treatment options. All regimens were ineffective against carbapenem-resistant bacteria. Vancomycin was unsuccessful in approximately 40% of cases involving methicillin-resistant staphylococci or ampicillin-resistant enterococci.</abstract><pub>BioMed Central Ltd</pub><doi>10.1186/s12879-023-08596-z</doi></addata></record> |
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subjects | Antibacterial agents Complications and side effects Cross infection Dosage and administration Drug therapy Meningitis Nosocomial infections Patient outcomes Prevention Risk factors Staphylococcal infections |
title | Empirical cefepime+vancomycin versus ceftazidime+vancomycin versus meropenem+vancomycin in the treatment of healthcare-associated meningitis: results of the multicenter ephesus study |
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