The Association Between Elevated Estimated Glomerular Filtration Rate and Poor Clinical Outcomes of Pediatric Patients with Community-Acquired Bacterial Meningitis Receiving Vancomycin: A Ten-Year Retrospective Cohort Study
Introduction This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin. Methods This retrospective cohort study included children aged 1 mont...
Saved in:
Published in | Infectious diseases and therapy Vol. 14; no. 8; pp. 1899 - 1916 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cheshire
Springer Healthcare
01.08.2025
Springer Springer Nature B.V Adis, Springer Healthcare |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Introduction
This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin.
Methods
This retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children’s Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM.
Results
A total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (
P
< 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (
P
< 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR ≥ 169.21 mL/min/1.73 m
2
was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624,
P
= 0.00297; IDI 0.1057,
P
= 0.00414). Kaplan‒Meier survival analysis also revealed that an eGFR ≥ 169.21 mL/min/1.73 m
2
was associated with a greater likelihood of poor outcomes (
P
= 0.0092).
Conclusion
Elevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. |
---|---|
AbstractList | This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin.INTRODUCTIONThis study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin.This retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children's Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM.METHODSThis retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children's Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM.A total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR ≥ 169.21 mL/min/1.73 m2 was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). Kaplan‒Meier survival analysis also revealed that an eGFR ≥ 169.21 mL/min/1.73 m2 was associated with a greater likelihood of poor outcomes (P = 0.0092).RESULTSA total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR ≥ 169.21 mL/min/1.73 m2 was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). Kaplan‒Meier survival analysis also revealed that an eGFR ≥ 169.21 mL/min/1.73 m2 was associated with a greater likelihood of poor outcomes (P = 0.0092).Elevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children.CONCLUSIONElevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin. This retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children's Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM. A total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR [greater than or equal to] 169.21 mL/min/1.73 m.sup.2 was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). KaplanâMeier survival analysis also revealed that an eGFR [greater than or equal to] 169.21 mL/min/1.73 m.sup.2 was associated with a greater likelihood of poor outcomes (P = 0.0092). Elevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. Introduction This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin. Methods This retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children’s Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM. Results A total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses ( P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed ( P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR ≥ 169.21 mL/min/1.73 m 2 was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). Kaplan‒Meier survival analysis also revealed that an eGFR ≥ 169.21 mL/min/1.73 m 2 was associated with a greater likelihood of poor outcomes ( P = 0.0092). Conclusion Elevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. IntroductionThis study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin.MethodsThis retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children’s Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM.ResultsA total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR ≥ 169.21 mL/min/1.73 m2 was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). Kaplan‒Meier survival analysis also revealed that an eGFR ≥ 169.21 mL/min/1.73 m2 was associated with a greater likelihood of poor outcomes (P = 0.0092).ConclusionElevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. Introduction This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin. Methods This retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children's Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM. Results A total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR [greater than or equal to] 169.21 mL/min/1.73 m.sup.2 was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). KaplanâMeier survival analysis also revealed that an eGFR [greater than or equal to] 169.21 mL/min/1.73 m.sup.2 was associated with a greater likelihood of poor outcomes (P = 0.0092). Conclusion Elevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin. This retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children's Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM. A total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR ≥ 169.21 mL/min/1.73 m was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). Kaplan‒Meier survival analysis also revealed that an eGFR ≥ 169.21 mL/min/1.73 m was associated with a greater likelihood of poor outcomes (P = 0.0092). Elevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. Abstract Introduction This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with community-acquired bacterial meningitis (BM) receiving vancomycin. Methods This retrospective cohort study included children aged 1 month to 18 years with community-acquired BM admitted to the Department of Neurology, Children’s Hospital of Chongqing Medical University (CHCMU) from 2013 to 2023. Relevant information for all patients was collected, and clinical outcomes were assessed using the Glasgow Outcome Scale (GOS) at the time of discharge. Logistic regression analysis, receiver operating characteristic (ROC) curve analysis, integrated discrimination improvement (IDI), net reclassification improvement (NRI) indices, and survival curve analysis were employed to investigate the associations between elevated eGFR and poor clinical outcomes in pediatric patients with community-acquired BM. Results A total of 119 patients were included. Significant differences in the eGFR were observed among pediatric patients with different prognoses (P < 0.05). The initial vancomycin trough concentration in the elevated eGFR group was significantly lower than that in the normal eGFR group [5.600 (4.590; 8.060) mg/L vs. 9.205 (7.500; 12.070) mg/L]. At discharge, the GOS scores of the two groups also significantly differed (P < 0.05). In the analysis of factors influencing poor prognosis in pediatric patients with BM, an eGFR ≥ 169.21 mL/min/1.73 m2 was identified as an important factor associated with poor clinical outcomes in both univariate and multivariate analyses. Incorporating the elevated eGFR factor into the predictive model significantly improved its diagnostic performance (NRI 0.624, P = 0.00297; IDI 0.1057, P = 0.00414). Kaplan‒Meier survival analysis also revealed that an eGFR ≥ 169.21 mL/min/1.73 m2 was associated with a greater likelihood of poor outcomes (P = 0.0092). Conclusion Elevated eGFR is associated with an increased risk of poor clinical outcomes in community-acquired BM in children. |
Audience | Academic |
Author | Deng, Dongmei Hu, Xiaogang Hong, Siqi Luo, Yuanyuan He, Cuiyao Jiang, Li Lv, Fengjun Li, Tingsong Qu, Yuan Deng, Yuhua |
Author_xml | – sequence: 1 givenname: Cuiyao surname: He fullname: He, Cuiyao organization: Department of Pharmacy, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 2 givenname: Yuhua surname: Deng fullname: Deng, Yuhua organization: Department of Hepatobiliary Surgery, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 3 givenname: Tingsong surname: Li fullname: Li, Tingsong organization: Department of Rehabilitation, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 4 givenname: Dongmei surname: Deng fullname: Deng, Dongmei organization: Department of Pharmacy, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 5 givenname: Fengjun surname: Lv fullname: Lv, Fengjun organization: Department of Pharmacy, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 6 givenname: Yuan surname: Qu fullname: Qu, Yuan organization: Department of Pharmacy, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 7 givenname: Li surname: Jiang fullname: Jiang, Li organization: Department of Neurology, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 8 givenname: Siqi surname: Hong fullname: Hong, Siqi organization: Department of Neurology, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University – sequence: 9 givenname: Xiaogang surname: Hu fullname: Hu, Xiaogang email: hxgcq1987@126.com organization: Department of Pharmacy, Chongqing Jiulongpo People’s Hospital – sequence: 10 givenname: Yuanyuan surname: Luo fullname: Luo, Yuanyuan email: luoyy851225@163.com organization: Department of Neurology, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children’s Hospital of Chongqing Medical University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40679785$$D View this record in MEDLINE/PubMed |
BookMark | eNp9k89u1DAQxiNURKH0BTggS1y4pPhf4pgL2q7aUqmoVSlInCyvM9l1ldit7Wy1b8Oz8CQ8Ct5uaSlCKIc4nt_3jceZeVFsOe-gKF4RvEcwFu8ix4SSEtOqxITIuiRPiueUSFbWrKFbd-uGUrld7MZ4iXHmG06keFZsc1wLKZrqefHzYgFoEqM3VifrHdqHdAPg0EEPS52gRQcx2eF2ddT7AcLY64AObZ_CRnCeY0i7Fp15H9C0t84a3aPTMZmMR-Q7dAZtdg_WoLOsAZciurFp8eP71A_D6GxalRNzPdqQk-xrkyDY7PAJnHVzm2xE52DALvMX-qpdtl0Z696jCboAV36DfJ5zSMHHKzDJLgFN_cKHhD6nsV29LJ52uo-we_feKb4cHlxMP5Ynp0fH08lJaaqapBKk7rqmEqQTUhPRaklMRXVNhCSk4Xi2jgKVnLSY8Rk3LRcddMwwTbkAYDvF8ca39fpSXYV8Z2GlvLbqdsOHudIhWdODkpxSZnRtWM15BV0za2tooZazWnAxa7LXh43X1TgboDX5xoLuH5k-jji7UHO_VIQyJvNps8PbO4fgr0eISQ02Guh77cCPUTHKCBW4pjyjb_5CL_0YXL6rNdVUFauwfKDmOldgXedzYrM2VZOmyp1ViXqddu8fVH5aGKzJDdzZvP9I8PrPSu9L_N2gGaAbwOT_GwN09wjBaj0IajMIKg-Cuh0ERbKIbUQxw24O4aGk_6h-ATqkDrs |
Cites_doi | 10.1001/jama.2022.20521 10.1016/j.jped.2019.07.003 10.1007/s13318-019-00568-6 10.1542/peds.58.2.259 10.1086/425368 10.1159/000516647 10.1016/j.cmi.2016.01.007 10.1016/S0140-6736(75)92830-5 10.1016/j.jcrc.2013.03.003 10.1086/533448 10.1093/brain/awg113 10.3390/antibiotics10101182 10.1007/s13311-018-0651-2 10.1016/S1473-3099(09)70306-8 10.1016/j.jped.2012.10.001 10.1186/s13756-021-00895-x 10.1177/0962280215601873 10.1186/1471-2334-11-214 10.1016/j.ijid.2013.02.009 10.1016/j.ijantimicag.2017.11.013 10.1111/apa.13250 10.1007/s15010-007-6202-0 10.1007/s00431-012-1733-5 10.1056/NEJMoa1005384 10.1053/j.ackd.2017.10.002 |
ContentType | Journal Article |
Copyright | The Author(s) 2025 2025. The Author(s). COPYRIGHT 2025 Springer The Author(s) 2025. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. The Author(s) 2025 2025 |
Copyright_xml | – notice: The Author(s) 2025 – notice: 2025. The Author(s). – notice: COPYRIGHT 2025 Springer – notice: The Author(s) 2025. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: The Author(s) 2025 2025 |
DBID | C6C AAYXX CITATION NPM 3V. 7RV 7X7 7XB 8AO 8C1 8FI 8FJ 8FK ABUWG AEUYN AFKRA AZQEC BENPR CCPQU DWQXO FYUFA GHDGH K9. KB0 M0S NAPCQ PHGZM PHGZT PIMPY PJZUB PKEHL PPXIY PQEST PQQKQ PQUKI 7X8 5PM DOA |
DOI | 10.1007/s40121-025-01196-1 |
DatabaseName | Springer Nature OA Free Journals CrossRef PubMed ProQuest Central (Corporate) Nursing & Allied Health Database Health & Medical Collection ProQuest Central (purchase pre-March 2016) ProQuest Pharma Collection Public Health Database ProQuest Hospital Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest One Sustainability (subscription) ProQuest Central UK/Ireland ProQuest Central Essentials ProQuest Central (ProQuest) ProQuest One ProQuest Central Korea Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Health & Medical Complete (Alumni) Nursing & Allied Health Database (Alumni Edition) Health & Medical Collection (Alumni) Nursing & Allied Health Premium ProQuest Central Premium ProQuest One Academic ProQuest - Publicly Available Content Database ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition MEDLINE - Academic PubMed Central (Full Participant titles) Directory of Open Access Journals (DOAJ) |
DatabaseTitle | CrossRef PubMed Publicly Available Content Database ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest One Health & Nursing ProQuest Pharma Collection ProQuest Central ProQuest One Sustainability ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Health & Medical Research Collection ProQuest Central (New) ProQuest Public Health ProQuest One Academic Eastern Edition ProQuest Nursing & Allied Health Source ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Hospital Collection (Alumni) Nursing & Allied Health Premium ProQuest Health & Medical Complete ProQuest One Academic UKI Edition ProQuest Nursing & Allied Health Source (Alumni) ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic Publicly Available Content Database PubMed |
Database_xml | – sequence: 1 dbid: C6C name: Springer Nature OA Free Journals url: http://www.springeropen.com/ sourceTypes: Publisher – sequence: 2 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 3 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 4 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 2193-6382 |
EndPage | 1916 |
ExternalDocumentID | oai_doaj_org_article_94223ca6c36445ef8bd6ede69b6747b8 PMC12339840 A851285760 40679785 10_1007_s40121_025_01196_1 |
Genre | Journal Article |
GeographicLocations | China |
GeographicLocations_xml | – name: China |
GrantInformation_xml | – fundername: Chongqing Science and Health Joint Medical Scientific Research Project grantid: 2023MSXM0688 |
GroupedDBID | 0R~ 2VQ 4.4 53G 5VS 7RV 7X7 8AO 8C1 8FI 8FJ AAKKN ABDBF ABEEZ ABUWG ACACY ACGFS ACUHS ACULB ADBBV ADRAZ AEUYN AFGXO AFKRA AHBYD AHMBA AHSBF AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AOIJS BAPOH BAWUL BCNDV BENPR BKEYQ BPHCQ BVXVI C24 C6C CCPQU DIK EBS EJD ESX FYUFA GROUPED_DOAJ HMCUK HYE HZ~ IAO IHR ITC KQ8 M48 NAPCQ O9- OK1 PHGZM PHGZT PIMPY PJZUB PPXIY PQQKQ PROAC RPM SISQX SMD SOJ UKHRP ~JE AAYXX CITATION NPM PUEGO 3V. 7XB 8FK AZQEC DWQXO K9. PKEHL PQEST PQUKI 7X8 5PM |
ID | FETCH-LOGICAL-c561t-e9aff8571f79a17da91c52a617911840bff85e2941d034b4cd47fef3c3a247ee3 |
IEDL.DBID | C24 |
ISSN | 2193-8229 |
IngestDate | Wed Aug 27 01:32:23 EDT 2025 Thu Aug 21 18:26:08 EDT 2025 Fri Jul 18 18:38:13 EDT 2025 Sat Aug 23 12:48:24 EDT 2025 Wed Aug 27 16:52:25 EDT 2025 Tue Sep 02 03:57:27 EDT 2025 Fri Aug 15 02:01:18 EDT 2025 Thu Aug 14 00:04:08 EDT 2025 Tue Aug 12 01:11:13 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 8 |
Keywords | eGFR Community-acquired bacterial meningitis Vancomycin Children Outcome |
Language | English |
License | 2025. The Author(s). Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c561t-e9aff8571f79a17da91c52a617911840bff85e2941d034b4cd47fef3c3a247ee3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
OpenAccessLink | https://link.springer.com/10.1007/s40121-025-01196-1 |
PMID | 40679785 |
PQID | 3238553509 |
PQPubID | 2034749 |
PageCount | 18 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_94223ca6c36445ef8bd6ede69b6747b8 pubmedcentral_primary_oai_pubmedcentral_nih_gov_12339840 proquest_miscellaneous_3231270624 proquest_journals_3238553509 gale_infotracmisc_A851285760 gale_infotracacademiconefile_A851285760 pubmed_primary_40679785 crossref_primary_10_1007_s40121_025_01196_1 springer_journals_10_1007_s40121_025_01196_1 |
PublicationCentury | 2000 |
PublicationDate | 20250800 |
PublicationDateYYYYMMDD | 2025-08-01 |
PublicationDate_xml | – month: 8 year: 2025 text: 20250800 |
PublicationDecade | 2020 |
PublicationPlace | Cheshire |
PublicationPlace_xml | – name: Cheshire – name: New Zealand – name: Philadelphia |
PublicationTitle | Infectious diseases and therapy |
PublicationTitleAbbrev | Infect Dis Ther |
PublicationTitleAlternate | Infect Dis Ther |
PublicationYear | 2025 |
Publisher | Springer Healthcare Springer Springer Nature B.V Adis, Springer Healthcare |
Publisher_xml | – name: Springer Healthcare – name: Springer – name: Springer Nature B.V – name: Adis, Springer Healthcare |
References | DC Teixeira (1196_CR21) 2020; 96 R Hasbun (1196_CR1) 2022; 328 M Gijsen (1196_CR10) 2021; 10 CY He (1196_CR8) 2021; 65 D van de Beek (1196_CR27) 2016; 22 LY Wee (1196_CR23) 2016; 105 I Barrio (1196_CR17) 2017; 26 K Theodoridou (1196_CR22) 2013; 17 D Lepur (1196_CR3) 2007; 35 X Peng (1196_CR6) 2021; 30 S Namani (1196_CR20) 2013; 89 C He (1196_CR11) 2022; 13 VA Vasilopoulou (1196_CR25) 2011; 11 B Jennett (1196_CR16) 1975; 1 F Bargui (1196_CR4) 2012; 171 S Kastenbauer (1196_CR15) 2003; 126 WJ Tu (1196_CR18) 2019; 92 KS Kim (1196_CR2) 2010; 10 K Sridharan (1196_CR9) 2019; 44 MC Thigpen (1196_CR5) 2011; 364 GJ Schwartz (1196_CR14) 1976; 58 AS Levey (1196_CR12) 2022; 146 I Roine (1196_CR24) 2008; 46 BO Claus (1196_CR26) 2013; 28 AR Tunkel (1196_CR28) 2004; 39 C Carrié (1196_CR7) 2018; 51 WJ Tu (1196_CR19) 2018; 15 H Pottel (1196_CR13) 2018; 25 |
References_xml | – volume: 328 start-page: 2147 year: 2022 ident: 1196_CR1 publication-title: JAMA doi: 10.1001/jama.2022.20521 – volume: 96 start-page: 159 year: 2020 ident: 1196_CR21 publication-title: J Pediatr (Rio J) doi: 10.1016/j.jped.2019.07.003 – volume: 44 start-page: 807 year: 2019 ident: 1196_CR9 publication-title: Eur J Drug Metab Pharmacokinet doi: 10.1007/s13318-019-00568-6 – volume: 58 start-page: 259 year: 1976 ident: 1196_CR14 publication-title: Pediatrics doi: 10.1542/peds.58.2.259 – volume: 39 start-page: 1267 year: 2004 ident: 1196_CR28 publication-title: Clin Infect Dis doi: 10.1086/425368 – volume: 146 start-page: 302 year: 2022 ident: 1196_CR12 publication-title: Nephron doi: 10.1159/000516647 – volume: 22 start-page: S37 issue: Suppl 3 year: 2016 ident: 1196_CR27 publication-title: Clin Microbiol Infect doi: 10.1016/j.cmi.2016.01.007 – volume: 1 start-page: 480 year: 1975 ident: 1196_CR16 publication-title: Lancet doi: 10.1016/S0140-6736(75)92830-5 – volume: 28 start-page: 695 year: 2013 ident: 1196_CR26 publication-title: J Crit Care doi: 10.1016/j.jcrc.2013.03.003 – volume: 46 start-page: 1248 year: 2008 ident: 1196_CR24 publication-title: Clin Infect Dis doi: 10.1086/533448 – volume: 126 start-page: 1015 year: 2003 ident: 1196_CR15 publication-title: Brain doi: 10.1093/brain/awg113 – volume: 10 start-page: 1182 year: 2021 ident: 1196_CR10 publication-title: Antibiotics (Basel) doi: 10.3390/antibiotics10101182 – volume: 15 start-page: 1158 issue: 4 year: 2018 ident: 1196_CR19 publication-title: Neurotherapeutics doi: 10.1007/s13311-018-0651-2 – volume: 65 year: 2021 ident: 1196_CR8 publication-title: Antimicrob Agents Chemother – volume: 10 start-page: 32 year: 2010 ident: 1196_CR2 publication-title: Lancet Infect Dis doi: 10.1016/S1473-3099(09)70306-8 – volume: 89 start-page: 256 year: 2013 ident: 1196_CR20 publication-title: J Pediatr (Rio J) doi: 10.1016/j.jped.2012.10.001 – volume: 30 start-page: 24 issue: 10 year: 2021 ident: 1196_CR6 publication-title: Antimicrob Resist Infect Control doi: 10.1186/s13756-021-00895-x – volume: 13 year: 2022 ident: 1196_CR11 publication-title: Front Pharmacol – volume: 26 start-page: 2586 issue: 6 year: 2017 ident: 1196_CR17 publication-title: Stat Methods Med Res doi: 10.1177/0962280215601873 – volume: 11 start-page: 214 year: 2011 ident: 1196_CR25 publication-title: BMC Infect Dis doi: 10.1186/1471-2334-11-214 – volume: 17 start-page: e707 year: 2013 ident: 1196_CR22 publication-title: Int J Infect Dis doi: 10.1016/j.ijid.2013.02.009 – volume: 51 start-page: 443 year: 2018 ident: 1196_CR7 publication-title: Int J Antimicrob Agents doi: 10.1016/j.ijantimicag.2017.11.013 – volume: 92 start-page: e1678 issue: 15 year: 2019 ident: 1196_CR18 publication-title: Neurology – volume: 105 start-page: e22 year: 2016 ident: 1196_CR23 publication-title: Acta Paediatr doi: 10.1111/apa.13250 – volume: 35 start-page: 225 year: 2007 ident: 1196_CR3 publication-title: Infection doi: 10.1007/s15010-007-6202-0 – volume: 171 start-page: 1365 year: 2012 ident: 1196_CR4 publication-title: Eur J Pediatr doi: 10.1007/s00431-012-1733-5 – volume: 364 start-page: 2016 year: 2011 ident: 1196_CR5 publication-title: N Engl J Med doi: 10.1056/NEJMoa1005384 – volume: 25 start-page: 57 year: 2018 ident: 1196_CR13 publication-title: Adv Chronic Kidney Dis doi: 10.1053/j.ackd.2017.10.002 |
SSID | ssj0001284197 |
Score | 2.3147008 |
Snippet | Introduction
This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients... This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients with... Introduction This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients... IntroductionThis study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric patients... Abstract Introduction This study aimed to explore the association between elevated estimated glomerular filtration rate (eGFR) and poor prognosis in pediatric... |
SourceID | doaj pubmedcentral proquest gale pubmed crossref springer |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Publisher |
StartPage | 1899 |
SubjectTerms | Antibiotics Antimicrobial agents Bacterial meningitis Blood Care and treatment Children Clinical outcomes Community-acquired bacterial meningitis Creatinine Diagnosis eGFR Glomerular filtration rate Gram-positive bacteria Hydrocephalus Infectious Diseases Internal Medicine Measurement Medical prognosis Medicine Medicine & Public Health Meningitis Mortality Original Research Outcome Pathogens Pediatrics Pharmacokinetics Prediction models Regression analysis Streptococcus infections Testing Vancomycin Variables |
SummonAdditionalLinks | – databaseName: Directory of Open Access Journals (DOAJ) dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NjtMwELbQHhAXxPKbZUFGQuIAFo3jOAm3dtWyQiqs0C5aTpYTT7SV2gS16Up9G56FJ-FRmHHS0ixCXLhVtdP65xvPZ2f8DWMvkbHGRQypQO-eC2Vxu5PJMhVxqFNKCRkqS0cD04_69EJ9uIwv91J9UUxYKw_cDtzbTKEDK6wuIvTcMZRp7jQ40FmukQnn_pov-ry9zVR7upKq0GdWQYuMBKmadzdm_L05RUpmgjK5kuSZFmHPK3nx_j-X6D0fdTN-8sZLVO-bJvfY3Y5U8mHbmUN2C6r77Pa0e23-gP1EMPC9ieCjNjqLj-dwjWTT8TFa-sJ_ej-vF7Ck4FQ-mc07UV3-Gcu4rRw_q-sl78RE5_zTukHEworXJd8l_eBnrVbritMh74_v3R2UZiOGBcUd45-MWo1o_IUptCmTZiuODBZmdL7BvyAU68UGG_-OD_k5VOIrGiRWaJb19mooP6mvcOvAKRBy85BdTMbnJ6eiS-0gCiRsjYDMlmUaJ2GZZDZMnM3CIpZWk1gq7TlzKgWZqdANIpWrwqmkhDIqIitVAhA9YgdVXcETxlOXSKcTkBIiBQ4Za4YkDAa5DaVOrQvY6-3Umm-tgofZaTV7IBgEgvFAMGHARjT7u5qkvu2_QEyaDpPmX5gM2CvCjqE1AuepsN1VB2wwqW2ZIdqAxN7rQcCOezXRtot-8RZ9pltbViZClhXHETK9gL3YFdOTFC9XQb32dSikQEsVsMctWHddUnR2mKRxwNIejHt97pdUsyuvPI40J8pwegL2Zov43-36-6Ae_Y9BfcruSG-xFHx5zA6a5RqeISFs8ufe9n8BfMVdbQ priority: 102 providerName: Directory of Open Access Journals – databaseName: Health & Medical Collection dbid: 7X7 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fb9MwELZgSIgXxG8CAxkJiQewWBLHSXhBLWqZkAoT2lB5spz4wiq1yWhTpP61_CvcOW7XDMFbVbupHd_5Pp_vvmPsJSLWpEwgE2jdCyENHnfyqMpEEqqMSkKG0pBrYPJZHZ_JT9Nk6h1uKx9Wud0T3UZtm5J85G9jtC1JEqN9e3_xU1DVKLpd9SU0rrMbRF1GIV3pNN3zsWQydPVVUC9jQdzmPm_GZc9J4jMTVM-ViM-UCHu2yVH4_71R71mqq1GUV65SnYUa32G3PbTkg04W7rJrUN9jNyf-8vw--40iwfeWgw-7GC0-msMvhJyWj1DfF-7Tx3mzgCWFqPLxbO6pdflXbOOmtvykaZbcU4rO-Zd1i-8QVryp-K70Bz_pGFtXnFy93CeitBsxKCn4GP9j2BFF4wMm0NVNmq04wliYkZODf0N5bBYbHPs7PuCnUIvvqJXYoV022_xQfOw5nh84RUNuHrCz8ej0w7Hw9R1EiaitFZCbqsqSNKzS3ISpNXlYJpFRxJhKB8-CWiHKZWiPYlnI0sq0giouYxPJFCB-yA7qpobHjGc2jaxKIYoglmARtuaIxOCoMGGkMmMD9nq7svqio_HQO8JmJwca5UA7OdBhwIa0-LueRMHtvmiWP7TXaJ1LRFalUWWMkDKBKiusAgsqLxQe0YosYK9IdDRtFLhMpfH5DjhgotzSA1SECGevjgJ22OuJCl72m7fCp_0Gs9KX6hCwF7tm-iUFzdXQrF0fiitQkQzYo05Wd1OS5EBMsyRgWU-Ke3Put9Szc0c_jlgnznF5AvZmK_CX4_r3S33y_2k8Zbcip4oUW3nIDtrlGp4h3muL506p_wAOd1Nt priority: 102 providerName: ProQuest |
Title | The Association Between Elevated Estimated Glomerular Filtration Rate and Poor Clinical Outcomes of Pediatric Patients with Community-Acquired Bacterial Meningitis Receiving Vancomycin: A Ten-Year Retrospective Cohort Study |
URI | https://link.springer.com/article/10.1007/s40121-025-01196-1 https://www.ncbi.nlm.nih.gov/pubmed/40679785 https://www.proquest.com/docview/3238553509 https://www.proquest.com/docview/3231270624 https://pubmed.ncbi.nlm.nih.gov/PMC12339840 https://doaj.org/article/94223ca6c36445ef8bd6ede69b6747b8 |
Volume | 14 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3NjtMwELZgV0JcEP8ElspISBwg0iZxHIdbW7WskLpUq11UTpGTTHYrtQlqU6S-Dc_Ck_AozDhO2Cxw4BJVtZs68Tf2N_bMZ8ZeI2MNsxCUi7N76gqN7k7sF8oNPanoSEhPaFoamJ3KkwvxcREubFLYto12b7ckzUjdJbsJkh9z6fhV0imTLvo8hyH67oTrsc1xaFZWlPDMqSpojYFLiuY2W-bvt-nNSEa4_8_h-dr8dDN28sYGqpmXpvfZPUso-bBBwAN2C8qH7M7Mbpk_Yj8RCPxaJ_BRE5nFJyv4hkQz5xO08rX59GFVrWFDgal8ulxZQV1-hmVclzmfV9WGWyHRFf-0q_HFwZZXBe8O_ODzRqd1y2mB98d3m39S791hRjHH-CejRh8a7zCD5rik5ZYje4UlrW3wzwjDar3Hxr_nQ34OpfsFjREr1JuqTQvl4-oK3QZOQZD7x-xiOjkfn7j2WAc3Q7JWuxDrolBh5BVRrL0o17GXhb6WJJRK_mZKpeDHwsuPA5GKLBdRAUWQBdoXEUDwhB2UVQnPGFd55OcyAt-HQECObDVGAgbHqfZ8qXTusLdt1yZfG_WOpNNpNkBIEAiJAULiOWxEvd_VJOVt80W1uUysISexQEKVaZkFyCRDKFSaS8hBxqlEzyxVDntD2ElofMB-yrRNc8AGk9JWMkT8-_j08thhR72aaNdZv7hFX2LHlW0SIMMKwwBZnsNedcX0S4qVK6HamToUTiB94bCnDVi7RxK0bhip0GGqB-PeM_dLyuWVUR1HihPE2D0Oe9ci_ne7_v1Sn_9f9Rfsrm9sk0Isj9hBvdnBS6R9dTpgt6NFhFc19gbscDQ5nZ8NjOXTVY4HZjnlF_uCVl4 |
linkProvider | Springer Nature |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Zb9NAEF6VVAJeEDeGAosE4gFWxOv1hYRQAgktbUJUpag8LT7GNFJil8QB5U_xl_grzPhI4yJ461uU3Ti7ntm5duYbxp6ixWpHNngCtXsoVIDuji8TT9im41FLSFMFFBoYDJ3dI_Xx2D7eYr_qWhhKq6xlYiGo4yyiGPkrC3WLbVuo396efhfUNYpuV-sWGiVb7MPqJ7psizd775G-z6Ts98bvdkXVVUBEaCvkAvwgSTzbNRPXD0w3DnwzsmXgEE4nuTshjYL0lRm3LRWqKFZuAokVWYFULoCFz73EtpWFrkyLbXd7w9HhRlTHU2bR0QUlgSUITb2q1Cnq9RQhqAnqIEtQa44wG9qwaBrwt2rY0I3n8zbPXd4WOrF_nV2rjFneKbnvBtuC9Ca7PKiu62-x38iEfIMBeLfMCuO9KfxAIzfmPZQws-LTh2k2gzklxfL-ZFqB-fJDHONBGvNRls15BWI65Z-WOVINFjxL-LrZCB-VGLELTsFlXpW-5CvRiSjdGf-jW0JT4wMGUHZqmiw4Gs4wobAK_4wnIJutcO2veYePIRVfkOA4IZ9ndUUqPvYEPRZO-Zer2-zoQmh_h7XSLIV7jHuxK2PHBSnBUhCjoeyj7QftMDCl4wWxwV7UlNWnJXCIXkNEF3ygkQ90wQfaNFiXiL-eSaDfxRfZ_JuuZIj2FdpyUeBEFhqxNiReGDsQg-OHDjqFoWew58Q6mkQTkikKqgoLXDCBfOkOHj2Ju3faBttpzESREjWHa-bTlUhb6LMDaLAn62H6JaXppZAtizmUyeBIZbC7Ja-ut6QoZOl6tsG8Bhc39twcSScnBeA5WleWj-Qx2Mua4c_W9e-Xev__23jMruyOBwf6YG-4_4BdlcWxpMzOHdbK50t4iNZmHj6qjjhnXy9aqvwBftWR7g |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1bb9MwFLbGkCZeEHcCA4wE4gGsNY5zQ0KoZS0bo6NC21SejBM7rFKbjF5A_Wv8Gf4K5zhJ1wzB296q2k3tnKuPz_kOIc_AY_VT30QMrHvChILjTsyziPluEGFLSFcoDA30D4O9Y_Fh6A83yK-6FgbTKmudaBW1LlKMke94YFt83wP7tpNVaRGD3d7bs-8MO0jhTWvdTqNkkQOz_AnHt9mb_V2g9XPOe92jd3us6jDAUvAb5szEKssiP3SzMFZuqFXspj5XAWJ24tEnwVHDY-HqlicSkWoRZibzUk9xERrjwXOvkKuh57soY-EwXIvvRMK1vV1AJ3gMcdWrmh1buScQS41hL1kEXQuY27CLtn3A30ZizUpezOC8cI1rrWPvBrleubW0XfLhTbJh8ltkq19d3N8mv4Ed6Ror0E6ZH0a7Y_MD3F1Nu6BrJvbT-3ExMVNMj6W90biC9aWfYYyqXNNBUUxpBWc6pp8Wc6CfmdEio6u2I3RQosXOKIaZaVUEM1-ydoqJz_AfnRKkGh7QN2XPptGMggttRhhgoScgC8VkCWt_Tdv0yOTsC5AbJsynRV2bCo89hbMLxUzM5R1yfCmUv0s28yI39wmNdMh1EBrOjSeMBpc5Bi_QtBLl8iBS2iEva8rKsxJCRK7Aoi0fSOADaflAug7pIPFXMxH-235RTL_JSpvIWIBXl6og9cCd9U0WJTow2gRxEsDxMIkc8gJZR6KSAjKlqqq1gAUj3JdsgxBy2H3Qcsh2YyYol7Q5XDOfrJTbTJ6LokOerobxl5iwl5tiYedgTkPAhUPulby62pLA4GUY-Q6JGlzc2HNzJB-dWuhz8LO8GMjjkFc1w5-v698v9cH_t_GEbIEukR_3Dw8ekmvcSiWmeG6Tzfl0YR6B2zlPHlv5puTrZSuUP5ZTlL4 |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=The+Association+Between+Elevated+Estimated+Glomerular+Filtration+Rate+and+Poor+Clinical+Outcomes+of+Pediatric+Patients+with+Community-Acquired+Bacterial+Meningitis+Receiving+Vancomycin%3A+A+Ten-Year+Retrospective+Cohort+Study&rft.jtitle=Infectious+diseases+and+therapy&rft.au=He%2C+Cuiyao&rft.au=Deng%2C+Yuhua&rft.au=Li%2C+Tingsong&rft.au=Deng%2C+Dongmei&rft.date=2025-08-01&rft.pub=Springer&rft.issn=2193-8229&rft.volume=14&rft.issue=8&rft.spage=1899&rft_id=info:doi/10.1007%2Fs40121-025-01196-1&rft.externalDocID=A851285760 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2193-8229&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2193-8229&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2193-8229&client=summon |