Initial empirical antibiotics of non-carbapenems for ESBL-producing E. coli and K. pneumoniae bacteremia in children: a retrospective medical record review
The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for trea...
Saved in:
Published in | BMC infectious diseases Vol. 22; no. 1; p. 866 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
21.11.2022
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia.
Data from pediatric patients aged ≤ 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children's Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables.
A total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22-4.88, and adjusted OR 0.1; 95% CI 0.01-1.56].
The empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. |
---|---|
AbstractList | BACKGROUNDThe efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia. METHODSData from pediatric patients aged ≤ 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children's Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables. RESULTSA total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22-4.88, and adjusted OR 0.1; 95% CI 0.01-1.56]. CONCLUSIONSThe empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia. Data from pediatric patients aged ≤ 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children's Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables. A total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22-4.88, and adjusted OR 0.1; 95% CI 0.01-1.56]. The empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. Abstract Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia. Methods Data from pediatric patients aged ≤ 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children’s Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables. Results A total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22–4.88, and adjusted OR 0.1; 95% CI 0.01–1.56]. Conclusions The empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum [beta]-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia. Methods Data from pediatric patients aged [less than or equai to] 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children's Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables. Results A total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22-4.88, and adjusted OR 0.1; 95% CI 0.01-1.56]. Conclusions The empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. Keywords: ESBL producers, Bacteremia, Empirical antibiotics, Carbapenem, Children Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia. Methods Data from pediatric patients aged ≤ 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children’s Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables. Results A total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22–4.88, and adjusted OR 0.1; 95% CI 0.01–1.56]. Conclusions The empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum [beta]-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia. Data from pediatric patients aged [less than or equai to] 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children's Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables. A total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22-4.88, and adjusted OR 0.1; 95% CI 0.01-1.56]. The empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. Abstract Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae bacteremia in children remains controversial. We compared clinical and microbial outcomes according to the types of empirical antibiotics for treating pediatric patients with ESBL-producing E. coli and K. pneumoniae bacteremia. Methods Data from pediatric patients aged ≤ 18 years who were hospitalized with monomicrobial ESBL-producing E. coli or K. pneumoniae bacteremia at Asan Medical Center Children’s Hospital, Seoul, Korea between January 2014 and May 2019 were analyzed retrospectively. The impact of empirical therapy was assessed as 30-day all-cause mortality and 2-day microbiological outcomes evaluated by the sterility of blood cultures collected on day 2 after empirical antibiotic administration. Logistic regression analysis was used to control for the effects of confounding variables. Results A total of 53 patients with bacteremia caused by ESBL-producing E. coli (n = 29) and K. pneumoniae (n = 24) were included in this study; the median age was 3.6 years, and all had underlying comorbidities. As empirical antibiotics, 27 patients were treated with meropenem, and non-carbapenem agents were administered to 26 patients; 84.6% (22/26) were converted to carbapenem antibiotics as the definitive antibiotic by day 2 after empirical antibiotic administration. Overall, the 30-day all-cause mortality of ESBL-producing E. coli and K. pneumoniae bacteremia was 17.0% (9/53). After adjustment, there was no statistically significant association of use of a non-carbapenem agent as an empirical antibiotic with microbiological failure on day 2 and 30-day all-cause mortality [adjusted odds ratio (OR) 1.0; 95% confidence interval (CI) 0.22–4.88, and adjusted OR 0.1; 95% CI 0.01–1.56]. Conclusions The empirical use of non-carbapenems might not be a risk factor for mortality and early microbiological outcomes in pediatric patients with ESBL-producing E. coli and K. pneumoniae BSI if early transition to appropriate antimicrobial therapy was possible. |
ArticleNumber | 866 |
Audience | Academic |
Author | Kim, Mi-Na Lee, Jina Park, Saera So, HyeJin |
Author_xml | – sequence: 1 givenname: Saera surname: Park fullname: Park, Saera organization: Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-Ro 43-Gil, Songpa-Gu, Seoul, 05505, Republic of Korea – sequence: 2 givenname: HyeJin surname: So fullname: So, HyeJin organization: Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-Ro 43-Gil, Songpa-Gu, Seoul, 05505, Republic of Korea – sequence: 3 givenname: Mi-Na surname: Kim fullname: Kim, Mi-Na organization: Department of Laboratory Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea – sequence: 4 givenname: Jina surname: Lee fullname: Lee, Jina email: entier@amc.seoul.kr organization: Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-Ro 43-Gil, Songpa-Gu, Seoul, 05505, Republic of Korea. entier@amc.seoul.kr |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36404302$$D View this record in MEDLINE/PubMed |
BookMark | eNqNks1u1DAUhSNURH_gBVggS2xgkcF27DhhgVSqAUaMVIkCW8uxb6YeJXZqJwM8Cy-LZ6aUDmKBsrBlf-dc-eScZkfOO8iypwTPCKnKV5HQStQ5pjTHoqpILh5kJ4QJktOiYEf39sfZaYxrjImoaP0oOy5KhlmB6Un2c-HsaFWHoB9ssDrtlBttY_1odUS-RWlorlVo1AAO-ohaH9D86u0yH4I3k7ZuheYzpH1nk9KgjzM0OJh676wC1Cg9QoDeKmQd0te2MwHca6RQgDH4OIAe7QZQD2Y3O4D2waRlY-Hb4-xhq7oIT27Xs-zLu_nniw_58vL94uJ8meuyIGMuFOOqUTVuOdMMc6Vq0RIOXGPTYM14VZbQiKZuQAutMOEY87JiRrdCC9DFWbbY-xqv1nIItlfhh_TKyt2BDyupQoqjA0kMUZixptUpQlGb2nBOgGFSFy1obpLXm73XMDXpURrcGFR3YHp44-y1XPmNrEshqhongxe3BsHfTBBH2duooeuUAz9FSUVRsZpSThP6_C907afgUlSJ4rzEoqT8D7VS6QHWtT7N1VtTeS6SGxWiFIma_YNKn0k_T6fetTadHwheHggSM8L3caWmGOXi6tP_s5dfD1m6Z3WqRwzQ3mVHsNzWXu5rL1Pt5a72cit6dj_1O8nvnhe_ABDJ_uo |
CitedBy_id | crossref_primary_10_3390_microorganisms11081951 crossref_primary_10_4274_jpea_2023_238 |
Cites_doi | 10.1111/j.1469-0691.2011.03570.x 10.1128/AAC.46.5.1481-1491.2002 10.1093/cid/cir790 10.2147/IDR.S276975 10.1179/146532807X170501 10.1086/599376 10.1093/cid/ciw353 10.14776/piv.2015.22.3.178 10.1128/AAC.01523-12 10.1016/j.eimc.2019.02.008 10.1080/00365540500348978 10.1128/AAC.49.2.760-766.2005 10.1186/1471-2431-10-39 10.1128/AAC.41.5.987 10.14776/piv.2021.28.e11 10.1007/s15010-009-8325-y 10.1093/jac/dkm225 10.3390/microorganisms9091914 10.1378/chest.130.3.787 10.1016/S0891-5520(05)70395-0 10.1128/JCM.43.2.745-749.2005 10.1371/journal.pone.0143729 10.1016/S1473-3099(14)70950-8 10.1136/archdischild-2015-308707 10.1016/S2214-109X(18)30278-X 10.5402/2012/508512 10.1099/jmm.0.04966-0 10.1155/2013/756209 10.1371/journal.pone.0171216 10.1001/jama.2018.12163 10.1128/AAC.01509-06 10.1086/321893 10.3390/ph6111335 10.1186/1471-2334-12-245 10.3346/jkms.2008.23.1.53 10.3201/eid0805.010204 10.1086/502477 10.1186/s13756-018-0373-6 10.1186/1756-0500-3-116 10.1016/j.scitotenv.2021.145697 |
ContentType | Journal Article |
Copyright | 2022. The Author(s). COPYRIGHT 2022 BioMed Central Ltd. 2022. 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. The Author(s) 2022 |
Copyright_xml | – notice: 2022. The Author(s). – notice: COPYRIGHT 2022 BioMed Central Ltd. – notice: 2022. 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. – notice: The Author(s) 2022 |
DBID | CGR CUY CVF ECM EIF NPM AAYXX CITATION IOV ISR 3V. 7QL 7T2 7U9 7X7 7XB 88E 8C1 8FI 8FJ 8FK ABUWG AFKRA AZQEC BENPR C1K CCPQU DWQXO FYUFA GHDGH H94 K9. M0S M1P M7N PIMPY PQEST PQQKQ PQUKI PRINS 7X8 5PM DOA |
DOI | 10.1186/s12879-022-07881-7 |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef Gale In Context: Opposing Viewpoints Gale In Context: Science ProQuest Central (Corporate) Bacteriology Abstracts (Microbiology B) Health and Safety Science Abstracts (Full archive) Virology and AIDS Abstracts Health & Medical Collection ProQuest Central (purchase pre-March 2016) Medical Database (Alumni Edition) Public Health Database Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central ProQuest Central Essentials ProQuest Central Environmental Sciences and Pollution Management ProQuest One Community College ProQuest Central Korea Health Research Premium Collection Health Research Premium Collection (Alumni) AIDS and Cancer Research Abstracts ProQuest Health & Medical Complete (Alumni) Health & Medical Collection (Alumni Edition) PML(ProQuest Medical Library) Algology Mycology and Protozoology Abstracts (Microbiology C) Publicly Available Content Database ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef Publicly Available Content Database ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest Central China Environmental Sciences and Pollution Management ProQuest Central Health Research Premium Collection Health and Medicine Complete (Alumni Edition) ProQuest Central Korea Bacteriology Abstracts (Microbiology B) Algology Mycology and Protozoology Abstracts (Microbiology C) AIDS and Cancer Research Abstracts Health & Safety Science Abstracts ProQuest Medical Library (Alumni) ProQuest Public Health Virology and AIDS Abstracts ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition ProQuest One Academic ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE CrossRef Publicly Available Content Database |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 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: 3 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 4 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Public Health |
EISSN | 1471-2334 |
EndPage | 866 |
ExternalDocumentID | oai_doaj_org_article_1d1a044bfc36479d9d551e40193fec5d A727327767 10_1186_s12879_022_07881_7 36404302 |
Genre | Journal Article |
GeographicLocations | South Korea United States--US |
GeographicLocations_xml | – name: South Korea – name: United States--US |
GroupedDBID | --- -A0 0R~ 23N 2WC 3V. 53G 5VS 6J9 6PF 7X7 88E 8C1 8FI 8FJ AAFWJ AAJSJ AAWTL ABDBF ABUWG ACGFO ACGFS ACIHN ACPRK ACRMQ ADBBV ADINQ ADRAZ ADUKV AEAQA AENEX AFKRA AFPKN AFRAH AHBYD AHMBA AHYZX ALIPV ALMA_UNASSIGNED_HOLDINGS AMKLP AMTXH AOIJS BAPOH BAWUL BCNDV BENPR BFQNJ BMC BPHCQ BVXVI C24 C6C CCPQU CGR CS3 CUY CVF DIK DU5 E3Z EAD EAP EAS EBD EBLON EBS ECM EIF EMB EMK EMOBN ESX F5P FYUFA GROUPED_DOAJ GX1 HMCUK HYE IAO IHR INH INR IOV ISR ITC KQ8 M1P M48 M~E NPM O5R O5S OK1 P2P PGMZT PIMPY PQQKQ PROAC PSQYO RBZ RNS ROL RPM RSV SMD SOJ SV3 TR2 TUS UKHRP W2D WOQ WOW XSB AAYXX CITATION AFGXO ABVAZ AFNRJ 7QL 7T2 7U9 7XB 8FK AZQEC C1K DWQXO H94 K9. M7N PQEST PQUKI PRINS 7X8 5PM |
ID | FETCH-LOGICAL-c631t-7a45aba90f54c405aa97f15e5c0db0c45866eb7b9bec7ca015005684dcf7c7ec3 |
IEDL.DBID | RPM |
ISSN | 1471-2334 |
IngestDate | Tue Oct 22 15:15:18 EDT 2024 Tue Sep 17 21:34:57 EDT 2024 Fri Oct 25 02:37:05 EDT 2024 Thu Oct 10 17:54:22 EDT 2024 Fri Feb 23 00:10:34 EST 2024 Fri Feb 02 04:17:21 EST 2024 Thu Aug 01 19:32:23 EDT 2024 Thu Aug 01 19:19:50 EDT 2024 Thu Sep 12 18:52:18 EDT 2024 Sat Sep 28 08:21:36 EDT 2024 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | Carbapenem Empirical antibiotics ESBL producers Children Bacteremia |
Language | English |
License | 2022. The Author(s). Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c631t-7a45aba90f54c405aa97f15e5c0db0c45866eb7b9bec7ca015005684dcf7c7ec3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9677890/ |
PMID | 36404302 |
PQID | 2755607625 |
PQPubID | 42582 |
PageCount | 1 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_1d1a044bfc36479d9d551e40193fec5d pubmedcentral_primary_oai_pubmedcentral_nih_gov_9677890 proquest_miscellaneous_2738492252 proquest_journals_2755607625 gale_infotracmisc_A727327767 gale_infotracacademiconefile_A727327767 gale_incontextgauss_ISR_A727327767 gale_incontextgauss_IOV_A727327767 crossref_primary_10_1186_s12879_022_07881_7 pubmed_primary_36404302 |
PublicationCentury | 2000 |
PublicationDate | 2022-11-21 |
PublicationDateYYYYMMDD | 2022-11-21 |
PublicationDate_xml | – month: 11 year: 2022 text: 2022-11-21 day: 21 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | BMC infectious diseases |
PublicationTitleAlternate | BMC Infect Dis |
PublicationYear | 2022 |
Publisher | BioMed Central Ltd BioMed Central BMC |
Publisher_xml | – name: BioMed Central Ltd – name: BioMed Central – name: BMC |
References | C-I Kang (7881_CR36) 2005; 49 R Sehgal (7881_CR42) 2007; 27 AP Magiorakos (7881_CR1) 2012; 18 DM Livermore (7881_CR33) 2002; 8 J Lee (7881_CR6) 2007; 60 PJ Stapleton (7881_CR43) 2016; 101 A Jain (7881_CR40) 2003; 52 ME Flokas (7881_CR12) 2017; 12 A Javad (7881_CR31) 2006; 38 PN Harris (7881_CR17) 2015; 15 AC Kalil (7881_CR29) 2016; 63 I Willemsen (7881_CR32) 2009; 37 7881_CR16 FNJ Frakking (7881_CR38) 2013; 57 Y-K Kim (7881_CR11) 2002; 46 LA Mermel (7881_CR23) 2009; 49 S Ryu (7881_CR34) 2018; 7 DR Linkin (7881_CR39) 2004; 25 N Vijayakanthi (7881_CR41) 2013; 2013 GA Jacoby (7881_CR8) 1997; 11 M Tumbarello (7881_CR37) 2007; 51 E Temkin (7881_CR7) 2018; 6 A Ndir (7881_CR10) 2016; 11 JR Beardsley (7881_CR27) 2006; 130 DE Ballot (7881_CR14) 2012; 2012 PNA Harris (7881_CR18) 2018; 320 VP Chaubey (7881_CR20) 2010; 3 R Nau (7881_CR30) 1997; 41 G Peralta (7881_CR19) 2012; 12 KS Ko (7881_CR5) 2008; 23 S Park (7881_CR26) 2021; 28 RR Makharita (7881_CR2) 2020; 13 I Carvalho (7881_CR3) 2021; 9 B Blomberg (7881_CR9) 2005; 43 S Kim (7881_CR13) 2015; 22 I Morrissey (7881_CR35) 2013; 6 J Rodríguez-Baño (7881_CR21) 2012; 54 SK Fridkin (7881_CR28) 2001; 33 N Kayange (7881_CR15) 2010; 10 DM Arana (7881_CR4) 2019; 37 7881_CR24 7881_CR25 7881_CR22 7881_CR44 |
References_xml | – volume: 18 start-page: 268 issue: 3 year: 2012 ident: 7881_CR1 publication-title: Clin Microbiol Infect doi: 10.1111/j.1469-0691.2011.03570.x contributor: fullname: AP Magiorakos – volume: 46 start-page: 1481 issue: 5 year: 2002 ident: 7881_CR11 publication-title: Antimicrob Agents Chemother doi: 10.1128/AAC.46.5.1481-1491.2002 contributor: fullname: Y-K Kim – volume: 54 start-page: 167 issue: 2 year: 2012 ident: 7881_CR21 publication-title: Clin Infect Dis doi: 10.1093/cid/cir790 contributor: fullname: J Rodríguez-Baño – ident: 7881_CR24 – volume: 13 start-page: 3991 year: 2020 ident: 7881_CR2 publication-title: Infect Drug Resist doi: 10.2147/IDR.S276975 contributor: fullname: RR Makharita – volume: 27 start-page: 45 issue: 1 year: 2007 ident: 7881_CR42 publication-title: Ann Trop Paediatr doi: 10.1179/146532807X170501 contributor: fullname: R Sehgal – volume: 49 start-page: 1 issue: 1 year: 2009 ident: 7881_CR23 publication-title: Clin Infect Dis doi: 10.1086/599376 contributor: fullname: LA Mermel – volume: 63 start-page: e61 issue: 5 year: 2016 ident: 7881_CR29 publication-title: Clin Infect Dis doi: 10.1093/cid/ciw353 contributor: fullname: AC Kalil – volume: 22 start-page: 178 issue: 3 year: 2015 ident: 7881_CR13 publication-title: Pediatr Infect Vaccine doi: 10.14776/piv.2015.22.3.178 contributor: fullname: S Kim – volume: 57 start-page: 3092 issue: 7 year: 2013 ident: 7881_CR38 publication-title: Antimicrob Agents Chemother doi: 10.1128/AAC.01523-12 contributor: fullname: FNJ Frakking – volume: 37 start-page: 652 issue: 10 year: 2019 ident: 7881_CR4 publication-title: Enferm Infecc Microbiol Clin doi: 10.1016/j.eimc.2019.02.008 contributor: fullname: DM Arana – volume: 38 start-page: 224 issue: 3 year: 2006 ident: 7881_CR31 publication-title: Scand J Infect Dis doi: 10.1080/00365540500348978 contributor: fullname: A Javad – volume: 49 start-page: 760 issue: 2 year: 2005 ident: 7881_CR36 publication-title: Antimicrob Agents Chemother doi: 10.1128/AAC.49.2.760-766.2005 contributor: fullname: C-I Kang – volume: 10 start-page: 39 year: 2010 ident: 7881_CR15 publication-title: BMC Pediatr doi: 10.1186/1471-2431-10-39 contributor: fullname: N Kayange – ident: 7881_CR16 – volume: 41 start-page: 987 issue: 5 year: 1997 ident: 7881_CR30 publication-title: Antimicrob Agents Chemother doi: 10.1128/AAC.41.5.987 contributor: fullname: R Nau – volume: 28 start-page: 82 issue: 2 year: 2021 ident: 7881_CR26 publication-title: Pediatric Infect Vaccine doi: 10.14776/piv.2021.28.e11 contributor: fullname: S Park – volume: 37 start-page: 432 issue: 5 year: 2009 ident: 7881_CR32 publication-title: Infection doi: 10.1007/s15010-009-8325-y contributor: fullname: I Willemsen – volume: 60 start-page: 629 issue: 3 year: 2007 ident: 7881_CR6 publication-title: J Antimicrob Chemother doi: 10.1093/jac/dkm225 contributor: fullname: J Lee – volume: 9 start-page: 1914 issue: 9 year: 2021 ident: 7881_CR3 publication-title: Microorganisms doi: 10.3390/microorganisms9091914 contributor: fullname: I Carvalho – volume: 130 start-page: 787 issue: 3 year: 2006 ident: 7881_CR27 publication-title: Chest doi: 10.1378/chest.130.3.787 contributor: fullname: JR Beardsley – volume: 11 start-page: 875 issue: 4 year: 1997 ident: 7881_CR8 publication-title: Infect Dis Clin North Am doi: 10.1016/S0891-5520(05)70395-0 contributor: fullname: GA Jacoby – volume: 43 start-page: 745 issue: 2 year: 2005 ident: 7881_CR9 publication-title: J Clin Microbiol doi: 10.1128/JCM.43.2.745-749.2005 contributor: fullname: B Blomberg – volume: 11 issue: 2 year: 2016 ident: 7881_CR10 publication-title: PLoS ONE doi: 10.1371/journal.pone.0143729 contributor: fullname: A Ndir – volume: 15 start-page: 475 issue: 4 year: 2015 ident: 7881_CR17 publication-title: Lancet Infect Dis doi: 10.1016/S1473-3099(14)70950-8 contributor: fullname: PN Harris – volume: 101 start-page: F72 issue: 1 year: 2016 ident: 7881_CR43 publication-title: Arch Dis Child Fetal Neonatal Ed doi: 10.1136/archdischild-2015-308707 contributor: fullname: PJ Stapleton – volume: 6 start-page: e969 issue: 9 year: 2018 ident: 7881_CR7 publication-title: Lancet Glob Health doi: 10.1016/S2214-109X(18)30278-X contributor: fullname: E Temkin – ident: 7881_CR25 – volume: 2012 year: 2012 ident: 7881_CR14 publication-title: ISRN Pediatr doi: 10.5402/2012/508512 contributor: fullname: DE Ballot – volume: 52 start-page: 421 issue: Pt 5 year: 2003 ident: 7881_CR40 publication-title: J Med Microbiol doi: 10.1099/jmm.0.04966-0 contributor: fullname: A Jain – volume: 2013 year: 2013 ident: 7881_CR41 publication-title: Biomed Res Int doi: 10.1155/2013/756209 contributor: fullname: N Vijayakanthi – volume: 12 start-page: e0171216 issue: 1 year: 2017 ident: 7881_CR12 publication-title: PLoS ONE doi: 10.1371/journal.pone.0171216 contributor: fullname: ME Flokas – volume: 320 start-page: 984 issue: 10 year: 2018 ident: 7881_CR18 publication-title: JAMA doi: 10.1001/jama.2018.12163 contributor: fullname: PNA Harris – volume: 51 start-page: 1987 issue: 6 year: 2007 ident: 7881_CR37 publication-title: Antimicrob Agents Chemother doi: 10.1128/AAC.01509-06 contributor: fullname: M Tumbarello – volume: 33 start-page: 324 issue: 3 year: 2001 ident: 7881_CR28 publication-title: Clin Infect Dis doi: 10.1086/321893 contributor: fullname: SK Fridkin – volume: 6 start-page: 1335 issue: 11 year: 2013 ident: 7881_CR35 publication-title: Pharmaceuticals (Basel, Switzerland) doi: 10.3390/ph6111335 contributor: fullname: I Morrissey – volume: 12 start-page: 245 year: 2012 ident: 7881_CR19 publication-title: BMC Infect Dis doi: 10.1186/1471-2334-12-245 contributor: fullname: G Peralta – ident: 7881_CR22 – volume: 23 start-page: 53 issue: 1 year: 2008 ident: 7881_CR5 publication-title: J Korean Med Sci doi: 10.3346/jkms.2008.23.1.53 contributor: fullname: KS Ko – volume: 8 start-page: 473 issue: 5 year: 2002 ident: 7881_CR33 publication-title: Emerg Infect Dis doi: 10.3201/eid0805.010204 contributor: fullname: DM Livermore – volume: 25 start-page: 781 issue: 9 year: 2004 ident: 7881_CR39 publication-title: Infect Control Hosp Epidemiol doi: 10.1086/502477 contributor: fullname: DR Linkin – volume: 7 start-page: 83 issue: 1 year: 2018 ident: 7881_CR34 publication-title: Antimicrob Resist Infect Control doi: 10.1186/s13756-018-0373-6 contributor: fullname: S Ryu – volume: 3 start-page: 116 year: 2010 ident: 7881_CR20 publication-title: BMC Res Notes doi: 10.1186/1756-0500-3-116 contributor: fullname: VP Chaubey – ident: 7881_CR44 doi: 10.1016/j.scitotenv.2021.145697 |
SSID | ssj0017829 |
Score | 2.401358 |
Snippet | The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae... Abstract Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and... The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum [beta]-lactamases (ESBL)-producing Escherichia coli and Klebsiella pneumoniae... Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum [beta]-lactamases (ESBL)-producing Escherichia coli and Klebsiella... Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella... BACKGROUNDThe efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and Klebsiella... Abstract Background The efficacy of non-carbapenems as an empirical antibiotic for extended-spectrum β-lactamases (ESBL)-producing Escherichia coli and... |
SourceID | doaj pubmedcentral proquest gale crossref pubmed |
SourceType | Open Website Open Access Repository Aggregation Database Index Database |
StartPage | 866 |
SubjectTerms | Anti-Bacterial Agents - pharmacology Anti-Bacterial Agents - therapeutic use Antibiotics Antiinfectives and antibacterials Bacteremia Bacteremia - microbiology Beta lactamases Carbapenem Carbapenems Carbapenems - therapeutic use Child Child, Preschool Children Comorbidity Complications and side effects Confidence intervals Diagnostic tests Dosage and administration Drug therapy E coli Empirical analysis Empirical antibiotics ESBL producers Escherichia coli Escherichia coli infections Health care facilities Hospitals Humans Impact analysis Klebsiella Klebsiella pneumoniae Laboratories Medical Records Meningitis Meropenem Microorganisms Mortality Pathogens Patient outcomes Patients Pediatric research Pediatrics Pneumonia Public health Regression analysis Retrospective Studies Risk analysis Risk factors Statistical analysis Sterility Urinary tract infections β Lactamase |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQD4gL4k2gIIOQOCC3edhxzK1FW7VAQaIU9Wb5WXLYZLWPX9M_25k8VhshxIXreiKtZz7PI575Qsi7qGRupfLMeOsZl14wUxjOZAlFs48RIi4OOJ9_K08v-ecrcbXzqS_sCevpgXvFHWY-MynnNjpkOldeeYjxAaoCVcTghO-8b6rGYmq4P4C4p8YRmao8XIEXloph53qK_OlMTsJQx9b_p0_eCUrThsmdCHTygNwfUkd61P_lh-ROaB6Ru-fD5fhjcnOGjUAgEeaLumP-oKC22tYtUjHTNlIo9ZnDC4YFeLj5ikLCSmcXx1_ZouN9hShGZwcUoFHDk55-OaCLJmwAqLUJ1Ha8zmFeG1o3dBwC_0gNXYb1sh1HNum8v_qh_esf2s_GPCGXJ7Ofn07Z8O0F5soiWzNpuDDWqDQK7iCpM0bJmIkgXOpt6rioyjJYaRVgQDqD700glaq4d1E6GVzxlOzBpsJzQm00wSnneZQVLzg3pUEDFpFHUeRZkZAPoyn0oqfY0F1pUpW6N5wGw-nOcFom5BittZVEeuzuBwCNHkCj_wWahLxFW2skwGiww-babFYrffb9lz7ChC5HjqO_CV38mAi9H4RiC9BwZphqgK0jsdZEcn8iCcfYTZdH3OnBjax0LoXAQ5OLhLzZLuOT2BrXhHaDMkXFFbjlPCHPephulQO7R043WJETAE-0N11p6t8dybhCZkGVvvgf6n5J7uV49rKM5dk-2VsvN-EV5HJr-7o7trdYqkha priority: 102 providerName: Directory of Open Access Journals – databaseName: ProQuest Central dbid: BENPR link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Zb9QwELZgKyEkhKBcCwUZhMQDcpvDjmNeUIu2aoEW1FLUN8vxUfKwybLZ_TX8WWZyLI0QvK7HytoznhnP8ZmQ10HJpJDKMeMKx7h0gpnUcCYzuDS7EMDiYoPzyWl2dME_XorLPuDW9GWVg05sFbWrLcbI9xIpBM5PxPvFT4avRmF2tX9C4ybZSuCmEE3I1sHs9OvZJo8A9k8NrTJ5tteANpaKYQV7hDjqTI7MUYva_7duvmacxoWT1yzR4T1yt3ch6X7H8_vkhq-2ya2TPkm-Te50oTjadRg9IL-OsUAIZvj5omwRQShsZ1mUNUI00zrQqq6YxcTDAjTfvKHgyNLZ-cFntmjxYMG60dkuBZEpYaajn3bpovJr2JHSeFq0eM9-XhpaVnRoDn9HDV361bIeWjnpvEsJ0S4sRLuemYfk4nD27cMR699kYDZL4xWThgtTGBUFwS04e8YoGWLhhY1cEVku8izzhSwUyIa0BuMp4GLl3NkgrfQ2fUQmsCj_hNAiGG-VdTzInKecm8zEnkdp4EGkSZxOyduBNXrRQW_o9sqSZ7pjpAZG6paRWk7JAXJvQ4mw2e0P9fJK96dQxy42EedFsAibr5xy4DDCN8GLDd4KNyWvkPcagTEqrLy5Muum0cdfvut9dPQSxD76F9H52YjoTU8UahAVa_puB1g6Am6NKHdGlHC87Xh4kEPdq5dG_zkMU_JyM4wzsWSu8vUaadKcK1DXyZQ87sR2szmwesR6gxE5EujR7o1HqvJHCz6uEHFQRU___7eekdsJnrI4Zkm8Qyar5do_B-9tVbzoj-hv1KtGGQ priority: 102 providerName: ProQuest – databaseName: Scholars Portal Open Access Journals dbid: M48 link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1ZbxMxELZKkRAviJuUggxC4gE57GGv10gItShVCxQkSlDfLK-PshLZTXNI8Fv4s8zsEbqi8BrPJvHMfJ7xeuYzIc-CkkkhlWPGFY5x6QQzqeFMZrBpdiFAxMUG5-OP2eGUvzsVp1ukv-6oU-Dy0q0d3ic1XXwf_zj_-QYA_7oBfJ69XMIaKxXDuvQI2dGZvEKuJhx26ljKx_-cKkA0VE23kYxZkqa8b6K59DsGgarh8_971b4QtoYllRdi1MFNcqNLLule6w23yJavbpNrx93x-R3y6whLhUDCz-Zlww1CQbFlUdZI1kzrQKu6YhaPIEAJfrakkNLSycn-BzZvmGEhztHJmILzlPCko-_HdF75NbhyaTwtGuZnPysNLSvat4m_ooYu_GpR902ddNYeDtH2BRFtu2fukunB5MvbQ9bdzsBslsYrJg0XpjAqCoJbSPuMUTLEwgsbuSKyXORZ5gtZKPASaQ2-WYFkK-fOBmmlt-k9sg2T8g8ILYLxVlnHg8x5yrnJTOx5lAYeRJrE6Yi86E2h5y0Jh242L3mmW8NpMJxuDKfliOyjtTaSSKDdfFAvznSHRx272EScF8Eigb5yykHqCL8J-WzwVrgReYq21kiRUWENzplZL5f66NNXvYcpX4IsSP8SOvk8EHreCYUaXMOaru8Bpo7UWwPJ3YEkAN0Oh3u_0z1OdCKFQFglYkSebIbxSSyeq3y9Rpk05woW7mRE7rduulEOzB5Z32BEDhx4oL3hSFV-a2jIFXIPqmjn___6IbmeIKpigFy8S7ZXi7V_BHncqnjcgPM3zA1ElA priority: 102 providerName: Scholars Portal |
Title | Initial empirical antibiotics of non-carbapenems for ESBL-producing E. coli and K. pneumoniae bacteremia in children: a retrospective medical record review |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36404302 https://www.proquest.com/docview/2755607625 https://search.proquest.com/docview/2738492252 https://pubmed.ncbi.nlm.nih.gov/PMC9677890 https://doaj.org/article/1d1a044bfc36479d9d551e40193fec5d |
Volume | 22 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Jb9QwFLbaIiEuiL0DZWQQEgeUmSx2HHPrjKZqgSnVlKIRF8triUSS0Sy_hj_Lc5ZRI8SFiw_xsxL7rbbf-4LQO8dZrBg3gTTKBIQZGshEkoClsGk2zoHH9QXO88v0_IZ8WtLlAaJdLUydtK9VPip_FaMy_1nnVq4KPe7yxMZX8yn3qGc8HB-iQxDQboveXh2Ay-NddUyWjjdggBkPfNJ66KHTA9bzQDVQ_9_m-I4_6udK3nE-Z4_QwzZqxKfN1z1GB7Z8gu7P23vxp-j3hc8BAgpbrPIa9APDiuUqrzwKM64chl1-oP3dwgqMW7HBEKvi2fXkS7CqIV_BgeHZCINU5DDS4M8jvCrtDmQ0lxarGtLZFrnEeYm7-u-PWOK13a6rrloTF82tD25OfnBTFvMM3ZzNvk3Pg_a3C4FOk2gbMEmoVJKHjhIN8ZyUnLmIWqpDo0JNaJamVjHFgf1MS39kAlFURox2TDOrk-foCCZljxFWTlrNtSGOZSQhRKYysiRMHHE0iaNkgD50rBCrBl1D1LuSLBUN4wQwTtSME2yAJp5be0qPjF0_qNa3opUPEZlIhoQopz0yPjfcQEwI74RA1VlNzQC99bwWHvui9Mk1t3K32YiLr9_FqY_lYg9v9C-i60WP6H1L5CoQDS3bggaYusfU6lGe9ChBg3W_u5M70VqQjYgZpV5fYjpAb_bdfqTPiitttfM0SUY4WOR4gF40YrpfHJi9h3ODHtYT4N7q9XtA3Wp88Va9Xv73yFfoQewVLoqCODpBR9v1zr6G2G2rhqCxSwZtNo2G6N5kdnm1GNbnINDOSQbtYvJjWGv0HzGcTU0 |
link.rule.ids | 230,315,730,783,787,867,888,2109,12068,12235,21400,24330,27936,27937,31731,31732,33278,33279,33756,33757,43322,43591,43817,53804,53806 |
linkProvider | National Library of Medicine |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Zb9QwELagSICEEJRroYBBSDwgtzmcOOYFtdVWu3RbJHqob5bjo-Rhk7DZ_TX8WWaS7NIIwWs8VmLPmfHMZ0I-eCmiXEjLtM0t48ImTMeaM5HCT7P1HjwuNjifnKaTC_71KrnqE25NX1a5tomtobaVwRz5XiSSBOdHyZf6J8Nbo_B0tb9C4za5A25fomJmh5sSjxC8n1w3ymTpXgO2WEiG9esBoqgzMXBGLWb_35b5hmsalk3e8ENHj8jDPoCk-x3HH5Nbrtwmd0_6I_Jt8qBLxNGuv-gJ-TXF8iCY4eZ10eKBUNjMIi8qBGimladlVTKDxw412L15QyGMpeOzgxmrWzRY8G10vEtBYAqYaenxLq1Lt4L9KLSjeYv27OaFpkVJ163hn6mmC7dcVOtGTjrvDoRolxSiXcfMU3JxND4_nLD-RgZm0jhcMqF5onMtA59wA6Ge1lL4MHGJCWweGJ5kaepykUuQDGE0ZlMgwMq4NV4Y4Uz8jGzBotwLQnOvnZHGci8yHnOuUx06HsSe-ySOwnhEPq1Zo-oOeEO1PyxZqjpGKmCkahmpxIgcIPc2lAia3T6oFteq10EV2lAHnOfeIGi-tNJCuAjvhBjWO5PYEXmPvFcIi1Fi3c21XjWNmn67VPsY5kWIfPQvorPvA6KPPZGvQFSM7nsdYOkItzWg3BlQgnKb4fBaDlVvXBr1RxVG5N1mGGdiwVzpqhXSxBmXYKyjEXneie1mc2D1iPQGI2Ig0IPdG46UxY8Welwi3qAMXv7_s96Se5Pzk5maTU-PX5H7EWpcGLIo3CFby8XKvYY4bpm_aZX1N6XNR3g |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Jb9QwFLagSBUX9mWggEFIHFAyWZw45taWqTq0UypKq4qL5bVEkEWzXPgr_Fmes4wmIC69xs9KbH9vsf3eF4TeWkYjSZn2hJbaI1QnnogF8WgKm2ZtLXhcV-A8O0kPz8mny-Ry41dfTdK-krlf_iz8Mv_e5FbWhRr3eWLj09k-c6xnLBjX2o5volugs0Hab9S7CwRwfKyvkcnS8QLMMGWeS10PHIG6Rwd-qKHr_9cob3ilYcbkhgs6uIu-9R_fZp788FdL6atff_E6Xmt099CdLjDFu63IfXTDlA_Q9qy7en-Ifk9dmhFImKLOG14RDIuSy7xyRM-4srisSk-564sa7GexwBAO48nZ3rFXN6yy4CPxxMcAvBx6anzk47o0K1CDXBgsG9ZoU-QC5yXuS8w_YIHnZjmv-oJQXLQXS7g9XMJt5c0jdH4w-bp_6HV_dvBUGodLjwqSCClYYBOiIGQUglEbJiZRgZaBIkmWpkZSyQBhVAl3KgOBWka0slRRo-LHaAsGZZ4iLK0wiilNLM1ITIhIRWhIEFtikzgK4xF6368zr1sCD95sfLKUt6jggAreoILTEdpzUFhLOvLt5kE1v-LdIvFQhyIgRFrlyPeZZhrCTngnxMLWqESP0BsHJO7oNUqXv3MlVosFn36-4LsuXIwcg9L_hM6-DITedUK2Atwp0dVMwNAdbddAcmcgCUZCDZt7UPPOSC14RJPEqWSUjNDrdbPr6RLvSlOtnEycEQZGPxqhJ60OrCcHRu8Y46CFDrRjMHvDFsB8Q2HeYfzZtXu-QtunHw_48fTk6Dm6HTnFDkMvCnfQ1nK-Mi8gUlzKl41N-AOTiGul |
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=Initial+empirical+antibiotics+of+non-carbapenems+for+ESBL-producing+E.+coli+and+K.+pneumoniae+bacteremia+in+children%3A+a+retrospective+medical+record+review&rft.jtitle=BMC+infectious+diseases&rft.au=Park%2C+Saera&rft.au=So%2C+HyeJin&rft.au=Kim%2C+Mi-Na&rft.au=Lee%2C+Jina&rft.date=2022-11-21&rft.pub=BioMed+Central+Ltd&rft.issn=1471-2334&rft.eissn=1471-2334&rft.volume=22&rft.issue=1&rft_id=info:doi/10.1186%2Fs12879-022-07881-7&rft.externalDocID=A727327767 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-2334&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-2334&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-2334&client=summon |