2021
DOI: 10.1186/s12879-021-06719-y
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Efficacy and safety of polymyxin B in carbapenem-resistant gram-negative organisms infections

Abstract: Objective To investigate how to use polymyxin B rationally in order to produce the best efficacy and safety in patients with carbapenem-resistant gram-negative organisms (CRO) infection. Methods The clinical characteristics and microbiological results of 181 patients caused by CRO infection treated with polymyxin B in the First Affiliated Hospital from July 2018 to May 2020 were retrospectively analyzed. The bacterial clearance rate, clinical effic… Show more

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Cited by 7 publications
(7 citation statements)
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“…The duration of treatment for PES was strongly associated with effectiveness. Similar to the study of Xia et al on PBS ( 42 ) and consistent with the consensus recommended duration, the treatment groups with durations of 8–14 days and more than 14 days exhibited significantly greater efficacy than those with durations of 7 days or less. Longer treatment duration and greater cumulative doses of medication, while boosting efficacy, can increase the risk of adverse effects in patients, whereas in this trial there was no differences in the prevalence of AKI between efficacy groups.…”
Section: Discussionsupporting
confidence: 81%
“…The duration of treatment for PES was strongly associated with effectiveness. Similar to the study of Xia et al on PBS ( 42 ) and consistent with the consensus recommended duration, the treatment groups with durations of 8–14 days and more than 14 days exhibited significantly greater efficacy than those with durations of 7 days or less. Longer treatment duration and greater cumulative doses of medication, while boosting efficacy, can increase the risk of adverse effects in patients, whereas in this trial there was no differences in the prevalence of AKI between efficacy groups.…”
Section: Discussionsupporting
confidence: 81%
“…It is also possible that the renal impairment of patients in our study may have been complicated by other factors, such as other nephrotoxic drug use, multiple organ dysfunction syndrome, and septic shock. Multiple studies have shown that polymyxin B has dosedependent nephrotoxicity (27,35,36). Nelson et al found a dose of ≥250 mg per day was associated with a higher incidence of AKI (37).…”
Section: Discussionmentioning
confidence: 99%
“…Multiple studies have shown that polymyxin B has dose-dependent nephrotoxicity ( 27 , 35 , 36 ). Nelson et al found a dose of ≥250 mg per day was associated with a higher incidence of AKI ( 37 ).…”
Section: Discussionmentioning
confidence: 99%
“…No serious toxicity was observed in the group of patients who received a long-term intravenous colistin sulfate treatment (24). Xia et al found that approximately 10% of patients treated with polymyxin B for CRO infections developed acute kidney injury, but 23.5% recovered after discontinuation colistin sulfate treatment (14). However, a safety study of PMB in Chinese patients, excluding those receiving renal replacement therapy, found that 38.7% developed nephrotoxicity, and the daily dose of PMB was a risk factor for nephrotoxicity (P=0.026) (25).…”
Section: Independent Factors Associated With Mortalitymentioning
confidence: 99%
“…Polymyxins are polypeptide antibiotics, and mainly include polymyxin B (PMB), colistin sulfate, and colistimethate sodium (CMS). Currently, several studies have investigated the clinical efficacy and safety of polymyxin B and CMS in the treatment of CRO infections, including CRPA, CRAB, and CRKP infections (12)(13)(14)(15). The colistin sulfate is available late.…”
Section: Introductionmentioning
confidence: 99%