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370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections

BACKGROUND: Double beta-lactams are used to treat infective endocarditis, but the incidence rate of adverse events is unclear. We aimed to compare the incidence rates of adverse events of ampicillin(ABPC) versus ABPC plus ceftriaxone(CTRX) and ABPC/MPIPC(cloxacillin). METHODS: We retrospectively inc...

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Autores principales: Ishikawa, Kazuhiro, Kobayashi, Daiki, Mori, Nobuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676930/
http://dx.doi.org/10.1093/ofid/ofad500.440
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author Ishikawa, Kazuhiro
Kobayashi, Daiki
Mori, Nobuyoshi
author_facet Ishikawa, Kazuhiro
Kobayashi, Daiki
Mori, Nobuyoshi
author_sort Ishikawa, Kazuhiro
collection PubMed
description BACKGROUND: Double beta-lactams are used to treat infective endocarditis, but the incidence rate of adverse events is unclear. We aimed to compare the incidence rates of adverse events of ampicillin(ABPC) versus ABPC plus ceftriaxone(CTRX) and ABPC/MPIPC(cloxacillin). METHODS: We retrospectively included adult bacteremia patients admitted to St. Luke's International Hospital and received ABPC, ABPC plus CTRX, and ABPC/MPIPC between 2004 and 2022. We excluded patients on hemodialysis, those with missing data, those who used more than three beta-lactam antimicrobials, and beta-lactam other than ABPC, CTRX, or ABPC/MPIPC. All statistical analysis was done using IBM SPSS. RESULTS: We included 280, 59, and 43 patients for ABPC, ABPC plus CTRX, and ABPC/MPIPC, respectively. There were significant differences in median age(70.8 [standard deviation: SD 16.6], 64.3[16.7], 56.6[17.5]), male sex(62.1%, 47.5%, 72.1%), qSOFA ≥2 (23.1%, 64.4%, 41.9%), admission in an intensive care unit(6.4%, 40.7%, 14.0%), mechanical ventilation (5.4%, 23.7%, 20.9%), use of vasopressor (10.4%, 32.2%, 23.3%), administration of vancomycin (7.5%, 27.1%, 41.9%) or clindamycin (19.6%, 23.7%, 44.2%) for more than three days, hepatic dysfunction (AST: 42.6[81.5], 120.4[493.0], 54.1[68.5], ALT: 33.1[35.9], 98.2[380.0], 46.6[67.6], anemia(Hgb: 10.8[2.1], 11.6[2.4], 11.9[2.8] and thrombocytopenia (PLT: 203.5[105.0], 154.8[115.0], 255.9[159.7]) on admission. There were significant differences in AKI (9.0%, 12.3%, 30.2%), treatment duration (13.9 [12.1] days, 9.1 [8.7] days 29.0 (19.2) days, and duration of hospitalization 34.1[31.1] days, 48.3 [50.4] days, 51.6 [32.5] days, but no difference in 30 days mortality (4.3%, 6.8%, 2.3%) and 90 days mortality (8.2%, 13.6%, 7.0%). Kaplan-Meier analysis showed no significant difference between ABPC and CTRX plus ABPC in AKI, but there was a significant difference between ABPC and ABPC/MPIPC(figure 1, 2). The hazard ratio of ABPC/MPIPC for AKI was 1.572(95% confidence interval, 1.067-2.315)(figure 3). [Figure: see text] [Figure: see text] CONCLUSION: Double beta-lactam therapy with ABPC plus CTRX may be relatively safe, but careful follow-up is needed for platelet count and hepatic function. On the other hand, ABPC/MPIPC has a significantly higher incidence of AKI compared to other antimicrobials. Factors associated with AKI [Figure: see text] Abbreviation: AKI, acute kidney injury; ABPC, ampicillin; MPIPC, cloxacillin; CI, coincidence interval DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106769302023-11-27 370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections Ishikawa, Kazuhiro Kobayashi, Daiki Mori, Nobuyoshi Open Forum Infect Dis Abstract BACKGROUND: Double beta-lactams are used to treat infective endocarditis, but the incidence rate of adverse events is unclear. We aimed to compare the incidence rates of adverse events of ampicillin(ABPC) versus ABPC plus ceftriaxone(CTRX) and ABPC/MPIPC(cloxacillin). METHODS: We retrospectively included adult bacteremia patients admitted to St. Luke's International Hospital and received ABPC, ABPC plus CTRX, and ABPC/MPIPC between 2004 and 2022. We excluded patients on hemodialysis, those with missing data, those who used more than three beta-lactam antimicrobials, and beta-lactam other than ABPC, CTRX, or ABPC/MPIPC. All statistical analysis was done using IBM SPSS. RESULTS: We included 280, 59, and 43 patients for ABPC, ABPC plus CTRX, and ABPC/MPIPC, respectively. There were significant differences in median age(70.8 [standard deviation: SD 16.6], 64.3[16.7], 56.6[17.5]), male sex(62.1%, 47.5%, 72.1%), qSOFA ≥2 (23.1%, 64.4%, 41.9%), admission in an intensive care unit(6.4%, 40.7%, 14.0%), mechanical ventilation (5.4%, 23.7%, 20.9%), use of vasopressor (10.4%, 32.2%, 23.3%), administration of vancomycin (7.5%, 27.1%, 41.9%) or clindamycin (19.6%, 23.7%, 44.2%) for more than three days, hepatic dysfunction (AST: 42.6[81.5], 120.4[493.0], 54.1[68.5], ALT: 33.1[35.9], 98.2[380.0], 46.6[67.6], anemia(Hgb: 10.8[2.1], 11.6[2.4], 11.9[2.8] and thrombocytopenia (PLT: 203.5[105.0], 154.8[115.0], 255.9[159.7]) on admission. There were significant differences in AKI (9.0%, 12.3%, 30.2%), treatment duration (13.9 [12.1] days, 9.1 [8.7] days 29.0 (19.2) days, and duration of hospitalization 34.1[31.1] days, 48.3 [50.4] days, 51.6 [32.5] days, but no difference in 30 days mortality (4.3%, 6.8%, 2.3%) and 90 days mortality (8.2%, 13.6%, 7.0%). Kaplan-Meier analysis showed no significant difference between ABPC and CTRX plus ABPC in AKI, but there was a significant difference between ABPC and ABPC/MPIPC(figure 1, 2). The hazard ratio of ABPC/MPIPC for AKI was 1.572(95% confidence interval, 1.067-2.315)(figure 3). [Figure: see text] [Figure: see text] CONCLUSION: Double beta-lactam therapy with ABPC plus CTRX may be relatively safe, but careful follow-up is needed for platelet count and hepatic function. On the other hand, ABPC/MPIPC has a significantly higher incidence of AKI compared to other antimicrobials. Factors associated with AKI [Figure: see text] Abbreviation: AKI, acute kidney injury; ABPC, ampicillin; MPIPC, cloxacillin; CI, coincidence interval DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10676930/ http://dx.doi.org/10.1093/ofid/ofad500.440 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Ishikawa, Kazuhiro
Kobayashi, Daiki
Mori, Nobuyoshi
370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections
title 370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections
title_full 370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections
title_fullStr 370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections
title_full_unstemmed 370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections
title_short 370. The comparison of adverse events in combination with double beta-lactam antimicrobials: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin with bloodstream infections
title_sort 370. the comparison of adverse events in combination with double beta-lactam antimicrobials: ampicillin plus ceftriaxone and ampicillin/cloxacillin with bloodstream infections
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10676930/
http://dx.doi.org/10.1093/ofid/ofad500.440
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