7 results on '"Yuta Ibe"'
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2. Tazobactam/ceftolozane and tobramycin combination therapy in extensively drug-resistant Pseudomonas aeruginosa infections in severe burn injury: a case report
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Yuta Ibe, Ryuichiro Kakizaki, Hirotoshi Inamura, Tomoyuki Ishigo, Yoshihiro Fujiya, Hiroyuki Inoue, Shuji Uemura, Satoshi Fujii, Satoshi Takahashi, Eichi Narimatsu, and Masahide Fukudo
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Burns injury ,Pseudomonas aeruginosa ,Tazobactam/ceftolozane ,Tobramycin ,Therapeutics. Pharmacology ,RM1-950 ,Pharmacy and materia medica ,RS1-441 - Abstract
Abstract Background Combination therapy with tazobactam/ceftolozane (TAZ/CTLZ) and high-dose aminoglycosides has been reported to be efficacious in extensively drug-resistant (XDR)-Pseudomonas aeruginosa infection. However, there are no reports of efficacy in XDR-P. aeruginosa infection for combination therapy with low-dose aminoglycosides and TAZ/CTLZ. Herein, we describe a rare case of severe burn injury patients with persistent bacteremia due to XDR-P. aeruginosa, which was successfully treated with TAZ/CTLZ and low-dose tobramycin (TOB). Case presentation A 31-year-old man was admitted to the intensive care unit with severe burn injury involving 52% of the total body surface area and a prognostic burn index of 79.5. The patient had recurrent bacterial infections since admission, and blood cultures collected on the 37th day of admission revealed the presence of P. aeruginosa strains that were resistant to all β-lactams and amikacin (AMK). The results of the antimicrobial synergistic study showed no synergistic effect of low-dose meropenem (MEPM) and AMK combination therapy. The patient had acute renal failure, and it was difficult to increase the dose of MEPM and AMK, respectively. Thus, we initiated TAZ/CTLZ 1.5 g/8 h instead of the AMK and MEPM combination therapy on the 43rd day of hospitalization. Low-dose TAZ/CTLZ was continued because of prolonged renal dysfunction and resulted in a transient clinical improvement. However, the dosage of TAZ/CTLZ could be increased as the renal function improved, but despite an increased TAZ/CTLZ dose, bacteremia persisted, and the blood cultures remained positive. Thus, TOB was added to TAZ/CTLZ at low doses for synergistic effect against Gram-negative bacteria. Blood cultures collected after initiation of combination therapy with TAZ/CTLZ and low-dose TOB were negative on two consecutive follow-up evaluations. Thereafter, although the patient had several episodes of fever and increased inflammatory response, blood cultures consistently tested negative, and all of the wounds healed. On the 93rd day, due to the good healing progress, the patient was transferred to another hospital. Conclusions TAZ/CTLZ and low-dose TOB combination therapy showed the potential for synergistic effects. Our present report suggests a novel synergistic treatment strategy for rare cases that are refractory to the treatment of infections, such as XDR-P. aeruginosa infection.
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- 2023
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3. Simulation of Vancomycin Exposure Using Trough and Peak Levels Achieves the Target Area under the Steady-State Concentration–Time Curve in ICU Patients
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Yuta Ibe, Tomoyuki Ishigo, Satoshi Fujii, Satoshi Takahashi, Masahide Fukudo, and Hideki Sato
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area under the concentration–time curve ,critically ill patients ,intensive care unit ,therapeutic drug monitoring ,vancomycin ,Therapeutics. Pharmacology ,RM1-950 - Abstract
The therapeutic drug monitoring (TDM) of vancomycin (VCM) in critically ill patients often results in the estimated area being under the concentration–time curve (AUC) values that deviate from individual observations. In this study, we investigated the factors influencing the achievement of the target AUC of VCM at steady-state in critically ill patients. We retrospectively collected data from patients treated with VCM in an intensive care unit (ICU). Multivariate analysis was used to adjust for significant factors with p < 0.05 and identify new factors affecting the achievement of the target AUC at steady-state for VCM. Among the 113 patients included in this study, 72 (64%) were in the 1-point group (trough only), whereas 41 (36%) were in the 2-point group (trough/peak). The percentage of patients achieving the target AUC at the follow-up TDM evaluation was significantly higher in the two-point group. Multivariate analysis showed that being in the 2-point group and those with a 20% or more increase (or decrease) in creatinine clearance (CCr) were both significantly associated with the success rate of achieving the target AUC at the follow-up TDM. Novel findings revealed that in patients admitted to the ICU, changes in renal function were a predictor of AUC deviation, with a 20% or more increase (or decrease) in CCr being an indicator. We believe the indicators obtained in this study are simple and can be applied clinically in many facilities. If changes in renal function are anticipated, we recommend an AUC evaluation of VCM with a two-point blood collection, close monitoring of renal function, and dose adjustment based on reanalyzing the serum concentrations of VCM.
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- 2023
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4. Delayed dexamethasone treatment at initiation of oxygen supplementation for coronavirus disease 2019 is associated with the exacerbation of clinical condition
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Yuta Ibe, Tomoyuki Ishigo, Satoshi Fujii, Yoshihiro Fujiya, Koji Kuronuma, Takeshi Tsugawa, Satoshi Takahashi, and Masahide Fukudo
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Oxygen ,Microbiology (medical) ,Infectious Diseases ,SARS-CoV-2 ,Oxygen Inhalation Therapy ,Humans ,Pharmacology (medical) ,Dexamethasone ,Retrospective Studies ,COVID-19 Drug Treatment - Abstract
Coronavirus disease 2019 (COVID-19) frequently causes inflammatory lung injury as its symptoms progress. While dexamethasone reportedly reduces inflammation and prevents progression to respiratory failure, the appropriate time to administer dexamethasone in patients with COVID-19 remains unclear.This was a single-center, retrospective cohort study, where we consecutively enrolled patients hospitalized with COVID-19 who received oxygen and oral dexamethasone (n = 85). We assessed the association between the number of days to the initiation of dexamethasone and the cumulative rate of exacerbation defined as death or initiation of mechanical ventilation within 28 days of symptom onset.The optimal cut-off value from the initiation of oxygen supplementation to that of dexamethasone administration was two days (sensitivity, 85%; specificity, 59%), whereas that from oxygen saturation (SpOIn patients with COVID-19 and hypoxemia, early administration of dexamethasone, preferably less than two days from initiation of oxygen supplementation, may be required to improve clinical outcomes.
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- 2022
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5. Effect of renal clearance on vancomycin area under the concentration–time curve deviations in critically ill patients
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Tomoyuki Ishigo, Yuta Ibe, Satoshi Fujii, Satoshi Kazuma, Tomohiro Aigami, Yuri Kashiwagi, Ryo Takada, Satoshi Takahashi, Masahide Fukudo, and Takaki Toda
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Microbiology (medical) ,Infectious Diseases ,Pharmacology (medical) - Published
- 2023
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6. Early favipiravir treatment was associated with early defervescence in non-severe COVID-19 patients
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Satoshi Fujii, Koji Kuronuma, Yuta Ibe, Hiromasa Nakata, Hirotoshi Inamura, Yusuke Kunimoto, Yoshihiro Fujiya, Satoshi Takahashi, Masahide Fukudo, and Tomoyuki Ishigo
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0301 basic medicine ,Microbiology (medical) ,Male ,medicine.medical_specialty ,Multivariate analysis ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,030106 microbiology ,Defervescence ,Favipiravir ,Antiviral Agents ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Early treatment ,Medicine ,Humans ,Pharmacology (medical) ,030212 general & internal medicine ,Retrospective Studies ,Receiver operating characteristic ,business.industry ,Proportional hazards model ,SARS-CoV-2 ,Area under the curve ,COVID-19 ,Retrospective cohort study ,Amides ,Infectious Diseases ,Treatment Outcome ,Pyrazines ,Original Article ,business - Abstract
INTRODUCTION: The antiviral drug favipiravir has been shown to have in vitro antiviral activity against severe-acute-respiratory-syndrome-coronavirus-2 (SARS-CoV-2). In this study, we investigated the clinical benefits and initiation of favipiravir treatment in patients with non-severe coronavirus-disease-2019 (COVID-19). METHODS: This study was a single-center retrospective cohort study. Receiver operating characteristic curves were drawn to calculate the area under the curve, and the optimal cut-off values for the time to initiate favipiravir treatment were calculated to predict defervescence within seven days. Univariate and multivariate Cox regression analyses were performed to identify potential influencing factors of defervescence. This was defined as a body temperature of less than 37 °C for at least 2 days. RESULTS: Data from 41 patients were used for the efficacy assessment. The days from the onset of fever to defervescence showed a positive correlation with the duration from the onset of fever to initiation of favipiravir treatment (r = 0.548, P
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- 2021
7. [Association Suvorexant and Ramelteon Use with the Risk of Falling: A Retrospective Case-control Study]
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Tomoko Kimyo, Ryo Takada, Riho Tateishi, Hiromasa Nakata, Satoshi Katano, Manabu Kitagawa, Keita Nakano, Tomoyuki Ishigo, Atsushi Miyamoto, Yuta Ibe, Akiyoshi Hashimoto, Satoshi Fujii, and Fuki Kondo
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Male ,medicine.medical_specialty ,medicine.drug_class ,Ramelteon ,Pharmaceutical Science ,Body Mass Index ,Internal medicine ,Sedative/hypnotic ,medicine ,Humans ,Hypnotics and Sedatives ,Aged ,Retrospective Studies ,Pharmacology ,Aged, 80 and over ,business.industry ,Suvorexant ,Case-control study ,Age Factors ,Odds ratio ,Azepines ,Middle Aged ,Triazoles ,Confidence interval ,Indenes ,Sedative ,Case-Control Studies ,Delirium ,Accidental Falls ,Female ,medicine.symptom ,business ,medicine.drug - Abstract
Sedative hypnotics are among the classes of drugs reported to influence falls. However, the effects of the sedative hypnotic drugs, suvorexant and ramelteon, on falls are not well known. Therefore, we conducted this retrospective case-control study to examine the association of the use of these two sedative hypnotics with the risk of falls. Conducted at the Sapporo Medical University Hospital in Japan, our study included 360 patients with fall incidents and 819 randomly selected control patients. Patients in the fall group were significantly older with a lower body mass index, and had a history of falls, disabilities in activities of daily living, cognitive impairment, and delirium. Monovariate analysis revealed that patients in the fall group frequently used ramelteon [odds ratio (OR) 2.38, 95% confidence interval (CI): 1.49-3.81, p
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- 2020
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