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多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察

OBJECTIVE: To assess the efficacy and safety of polymyxin B in neutropenic patients with hematologic disorders who had refractory gram-negative bacterial bloodstream infection. METHODS: From August 2021 to July 2022, we retrospectively analyzed neutropenic patients with refractory gram-negative bact...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450549/
https://www.ncbi.nlm.nih.gov/pubmed/37550204
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2023.06.007
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collection PubMed
description OBJECTIVE: To assess the efficacy and safety of polymyxin B in neutropenic patients with hematologic disorders who had refractory gram-negative bacterial bloodstream infection. METHODS: From August 2021 to July 2022, we retrospectively analyzed neutropenic patients with refractory gram-negative bacterial bloodstream infection who were treated with polymyxin B in the Department of Hematology of the First Affiliated Hospital of the Soochow University between August 2021 to July 2022. The cumulative response rate was then computed. RESULTS: The study included 27 neutropenic patients with refractory gram-negative bacterial bloodstream infections. Polymyxin B therapy was effective in 22 of 27 patients. The median time between the onset of fever and the delivery of polymyxin B was 3 days [interquartile range (IQR): 2–5]. The median duration of polymyxin B treatment was 7 days (IQR: 5–11). Polymyxin B therapy had a median antipyretic time of 37 h (IQR: 32–70). The incidence of acute renal dysfunction was 14.8%(four out of 27 cases), all classified as “injury” according to RIFLE criteria. The incidence of hyperpigmentation was 59.3%. CONCLUSION: Polymyxin B is a viable treatment option for granulocytopenia patients with refractory gram-negative bacterial bloodstream infections.
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spelling pubmed-104505492023-08-26 多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To assess the efficacy and safety of polymyxin B in neutropenic patients with hematologic disorders who had refractory gram-negative bacterial bloodstream infection. METHODS: From August 2021 to July 2022, we retrospectively analyzed neutropenic patients with refractory gram-negative bacterial bloodstream infection who were treated with polymyxin B in the Department of Hematology of the First Affiliated Hospital of the Soochow University between August 2021 to July 2022. The cumulative response rate was then computed. RESULTS: The study included 27 neutropenic patients with refractory gram-negative bacterial bloodstream infections. Polymyxin B therapy was effective in 22 of 27 patients. The median time between the onset of fever and the delivery of polymyxin B was 3 days [interquartile range (IQR): 2–5]. The median duration of polymyxin B treatment was 7 days (IQR: 5–11). Polymyxin B therapy had a median antipyretic time of 37 h (IQR: 32–70). The incidence of acute renal dysfunction was 14.8%(four out of 27 cases), all classified as “injury” according to RIFLE criteria. The incidence of hyperpigmentation was 59.3%. CONCLUSION: Polymyxin B is a viable treatment option for granulocytopenia patients with refractory gram-negative bacterial bloodstream infections. Editorial office of Chinese Journal of Hematology 2023-06 /pmc/articles/PMC10450549/ /pubmed/37550204 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2023.06.007 Text en 2023年版权归中华医学会所有 https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 License.
spellingShingle 论著
多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察
title 多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察
title_full 多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察
title_fullStr 多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察
title_full_unstemmed 多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察
title_short 多黏菌素B治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察
title_sort 多黏菌素b治疗粒细胞缺乏伴难治性革兰阴性菌血流感染27例临床观察
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450549/
https://www.ncbi.nlm.nih.gov/pubmed/37550204
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2023.06.007
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