Some studies have suggested a correlation between posaconazole (PSCZ) concentration and efficacy in preventing fungal infections; the international guidelines recommend therapeutic drug monitoring. However, few studies have investigated the association between PSCZ concentration and its representative adverse effect of hypokalemia. This study aimed to measure serum PSCZ concentrations and investigate the relationship between this parameter and hypokalemia.
Methods
This study was conducted at Aichi Medical University Hospital. All patients in the hematology department who orally received PSCZ were included, wherein their trough serum concentrations (Cmins) of PSCZ were measured using high-performance liquid chromatography. Serum potassium levels were monitored for 60 days following PSCZ initiation. Hypokalemia was defined as serum potassium levels of <3.0 mEq/L and ≥10.0 % decreases from baseline following PSCZ administration.
Results
A total of 24 patients were included. The incidence of hypokalemia was 41.7 %. The median PSCZ concentrations were comparable between patients who developed hypokalemia and those who did not (2.5 μg/mL vs 2.4 μg/mL, p = 0.98). In both groups, approximately 80 % of the patients (80.0 % vs. 78.6 %, p = 0.98) showed PSCZ concentrations below 4.0 μg/mL. No significant correlations were found between PSCZ Cmin and the rate of serum potassium level reduction (γ = −0.21, p = 0.32) or minimum potassium level (γ = −0.03, p = 0.88).
Conclusions
PSCZ might cause hypokalemia regardless of Cmin; clinicians in hematology should remain vigilant.
背景:一些研究表明泊沙康唑(PSCZ)浓度与预防真菌感染的效果相关;国际指南建议对治疗性药物进行监测。然而,很少有研究调查PSCZ浓度与其代表性的低钾血症不良反应之间的关系。本研究旨在测定血清PSCZ浓度,并探讨该参数与低钾血症的关系。方法:本研究在爱知医科大学附属医院进行。纳入血液科所有口服PSCZ的患者,采用高效液相色谱法测定其PSCZ谷血清浓度(Cmins)。在PSCZ开始后的60天内监测血清钾水平。低钾血症定义为血清钾水平。结果:共纳入24例患者。低钾血症发生率为41.7%。低钾血症患者和非低钾血症患者的中位PSCZ浓度相当(2.5μg/mL vs 2.4μg/mL, p = 0.98)。在两组中,约80%的患者(80.0%比78.6%,p = 0.98) PSCZ浓度低于4.0μg/mL。PSCZ Cmin与血清钾水平降低率(γ = -0.21, p = 0.32)或最低钾水平(γ = -0.03, p = 0.88)无显著相关。结论:与Cmin无关,PSCZ可引起低钾血症;血液学临床医生应保持警惕。
{"title":"Relationship between blood posaconazole concentration and serum potassium levels","authors":"Yuichi Shibata , Nobuhiro Asai , Mao Hagihara , Hiroshige Mikamo","doi":"10.1016/j.jiac.2025.102868","DOIUrl":"10.1016/j.jiac.2025.102868","url":null,"abstract":"<div><h3>Background</h3><div>Some studies have suggested a correlation between posaconazole (PSCZ) concentration and efficacy in preventing fungal infections; the international guidelines recommend therapeutic drug monitoring. However, few studies have investigated the association between PSCZ concentration and its representative adverse effect of hypokalemia. This study aimed to measure serum PSCZ concentrations and investigate the relationship between this parameter and hypokalemia.</div></div><div><h3>Methods</h3><div>This study was conducted at Aichi Medical University Hospital. All patients in the hematology department who orally received PSCZ were included, wherein their trough serum concentrations (Cmins) of PSCZ were measured using high-performance liquid chromatography. Serum potassium levels were monitored for 60 days following PSCZ initiation. Hypokalemia was defined as serum potassium levels of <3.0 mEq/L and ≥10.0 % decreases from baseline following PSCZ administration.</div></div><div><h3>Results</h3><div>A total of 24 patients were included. The incidence of hypokalemia was 41.7 %. The median PSCZ concentrations were comparable between patients who developed hypokalemia and those who did not (2.5 μg/mL vs 2.4 μg/mL, <em>p</em> = 0.98). In both groups, approximately 80 % of the patients (80.0 % vs. 78.6 %, <em>p</em> = 0.98) showed PSCZ concentrations below 4.0 μg/mL. No significant correlations were found between PSCZ Cmin and the rate of serum potassium level reduction (γ = −0.21, <em>p</em> = 0.32) or minimum potassium level (γ = −0.03, <em>p</em> = 0.88).</div></div><div><h3>Conclusions</h3><div>PSCZ might cause hypokalemia regardless of Cmin; clinicians in hematology should remain vigilant.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"32 1","pages":"Article 102868"},"PeriodicalIF":1.5,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145557080","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In patients with pulmonary Mycobacterium avium complex disease, the barrier function of the airway epithelium is reduced. In this study, we focused on the host defense responses of alveolar epithelial cells to M. avium.
Methods and results
Clinical isolates of M. avium were used to infect murine alveolar type 1 epithelial cells (AT1s). Administration of N-acetylcysteine suppressed bacterial growth in the infected cells. Expression of the autophagosome marker microtubule-associated protein 1 light chain 3 was decreased in M. avium-infected cells and appeared to be restored by N-acetylcysteine administration. M. avium infection negatively affected the autophagic pathway, specifically mTORC1 signaling and its upstream factor, SLC37A4, which was partially restored by N-acetylcysteine administration. Autophagy inhibition by bafilomycin attenuated the NAC-associated reduction in bacterial load, suggesting involvement of autophagy-related pathways.
Conclusions
Our results suggest that M. avium infection is associated with suppressed autophagy-related responses in AT1s. NAC may function as an immunomodulatory agent by modulating autophagy-associated pathways and reducing intracellular bacterial burden.
目的:肺鸟分枝杆菌复合体患者气道上皮屏障功能降低。在本研究中,我们重点研究了肺泡上皮细胞对鸟分枝杆菌的宿主防御反应。方法与结果:采用临床分离的鸟分枝杆菌感染小鼠肺泡1型上皮细胞(AT1s)。n -乙酰半胱氨酸抑制了感染细胞中的细菌生长。自噬体标志物微管相关蛋白1轻链3的表达在鸟分枝杆菌感染的细胞中下降,并在给予n -乙酰半胱氨酸后恢复。M. avium感染对自噬通路产生负面影响,特别是mTORC1信号及其上游因子SLC37A4, n -乙酰半胱氨酸可部分恢复自噬通路。巴非霉素对自噬的抑制减弱了nac相关的细菌负荷的减少,这表明与自噬相关的途径有关。结论:我们的研究结果表明,鸟分枝杆菌感染与at15细胞自噬相关反应的抑制有关。NAC可能作为一种免疫调节剂,通过调节自噬相关途径和减少细胞内细菌负担。
{"title":"N-acetylcysteine is associated with restoration of autophagy-related signaling and reduced intracellular Mycobacterium avium in alveolar type 1 epithelial cells","authors":"Ayako Shiozawa , Chiaki Kajiwara , Yoshikazu Ishii , Kazuhiro Tateda","doi":"10.1016/j.jiac.2025.102864","DOIUrl":"10.1016/j.jiac.2025.102864","url":null,"abstract":"<div><h3>Purpose</h3><div>In patients with pulmonary <em>Mycobacterium avium</em> complex disease, the barrier function of the airway epithelium is reduced. In this study, we focused on the host defense responses of alveolar epithelial cells to <em>M</em>. <em>avium</em>.</div></div><div><h3>Methods and results</h3><div>Clinical isolates of <em>M. avium</em> were used to infect murine alveolar type 1 epithelial cells (AT1s). Administration of N-acetylcysteine suppressed bacterial growth in the infected cells. Expression of the autophagosome marker microtubule-associated protein 1 light chain 3 was decreased in <em>M. avium</em>-infected cells and appeared to be restored by N-acetylcysteine administration. <em>M. avium</em> infection negatively affected the autophagic pathway, specifically mTORC1 signaling and its upstream factor, SLC37A4, which was partially restored by N-acetylcysteine administration. Autophagy inhibition by bafilomycin attenuated the NAC-associated reduction in bacterial load, suggesting involvement of autophagy-related pathways.</div></div><div><h3>Conclusions</h3><div>Our results suggest that <em>M. avium</em> infection is associated with suppressed autophagy-related responses in AT1s. NAC may function as an immunomodulatory agent by modulating autophagy-associated pathways and reducing intracellular bacterial burden.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102864"},"PeriodicalIF":1.5,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
We aimed to identify high-risk factors for syphilis infection in metropolitan areas, specifically Tokyo, to guide effective strategy development against syphilis epidemics.
Methods
From July 20, 2023, to January 26, 2024, a REDCap survey was administered to individuals tested for syphilis at three Tokyo clinics. Consent was obtained through an agreement option at initiation of the questionnaire permitting individuals to decline participation. By selecting the consent option and completing the survey, individuals agreed to participate in the study. This research was supported by a Ministry of Health, Labor and Welfare research grant (JPMH23HA2011) and approved by the Kochi University School of Medicine Ethics Committee (Approval No. 2023–44).
Results
A total of 215 participants were analyzed after excluding 13 from the initial cohort. Of these, 48.4 % tested positive for syphilis. Positive cases were more frequently individuals with a history of sexually transmitted infections (STIs) undergoing their first syphilis test. Symptoms strongly correlated with syphilis positivity (60.5 % among symptomatic participants). Multivariate analysis identified casual sexual relationships and a history of STIs as significant risk factors for syphilis positivity. The presence of symptoms was also significantly associated with syphilis positivity. Engagement in sex work and anal intercourse trended toward increased risk. Age, men having sex with men, and use of matchmaking apps exhibited no significant association.
Conclusion
This study identified risks related to sexual partners, sex industry involvement, and sexual activities. Promoting preventive measures among sex industry workers and patrons is crucial. Increased syphilis testing opportunities may aid in reducing disease prevalence.
{"title":"Identification of key risk factors for syphilis among high-risk populations in urban areas of Japan","authors":"Yuka Yamagishi , Marina Minami , Natsuko Nakamura , Yasuhiko Onoe , Yoshitomo Kobori , Ichiro Itoda , Hiroshige Mikamo","doi":"10.1016/j.jiac.2025.102863","DOIUrl":"10.1016/j.jiac.2025.102863","url":null,"abstract":"<div><h3>Introduction</h3><div>We aimed to identify high-risk factors for syphilis infection in metropolitan areas, specifically Tokyo, to guide effective strategy development against syphilis epidemics.</div></div><div><h3>Methods</h3><div>From July 20, 2023, to January 26, 2024, a REDCap survey was administered to individuals tested for syphilis at three Tokyo clinics. Consent was obtained through an agreement option at initiation of the questionnaire permitting individuals to decline participation. By selecting the consent option and completing the survey, individuals agreed to participate in the study. This research was supported by a Ministry of Health, Labor and Welfare research grant (JPMH23HA2011) and approved by the Kochi University School of Medicine Ethics Committee (Approval No. 2023–44).</div></div><div><h3>Results</h3><div>A total of 215 participants were analyzed after excluding 13 from the initial cohort. Of these, 48.4 % tested positive for syphilis. Positive cases were more frequently individuals with a history of sexually transmitted infections (STIs) undergoing their first syphilis test. Symptoms strongly correlated with syphilis positivity (60.5 % among symptomatic participants). Multivariate analysis identified casual sexual relationships and a history of STIs as significant risk factors for syphilis positivity. The presence of symptoms was also significantly associated with syphilis positivity. Engagement in sex work and anal intercourse trended toward increased risk. Age, men having sex with men, and use of matchmaking apps exhibited no significant association.</div></div><div><h3>Conclusion</h3><div>This study identified risks related to sexual partners, sex industry involvement, and sexual activities. Promoting preventive measures among sex industry workers and patrons is crucial. Increased syphilis testing opportunities may aid in reducing disease prevalence.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102863"},"PeriodicalIF":1.5,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Campylobacter fetus is a rare but serious pathogen, mainly affecting immunocompromised patients. Central nervous system infections, particularly meningitis, are uncommon; only one case has been reported after liver transplantation and none after splenectomy.
Case presentation
We report meningitis and bacteremia caused by C. fetus subsp. fetus (Cff) in a 70-year-old man with liver transplantation and splenectomy for hepatitis C virus-related cirrhosis, on long-term immunosuppression. He presented with intermittent fever; blood cultures grew C. fetus, and cerebrospinal fluid (CSF) cultures confirmed it. Therapy was changed from cefmetazole to meropenem and vancomycin, then de-escalated to high-dose ampicillin. After 23 days of antibiotics, he fully recovered without sequelae.
Literature review
The literature review included 36 adult cases identified through a PubMed search and our own case. Seventy-eight percent were male, with a median age of 49 years. Sixteen percent were immunocompromised, while 41 % were otherwise healthy. Exposure risks were reported in 43 %, though absent in 54 %. Of 38 isolates, 24 were subspeciated: Cff was most frequent (18/24, 75 %), followed by C. fetus subsp. intestinalis and venerealis (2 each), and single isolates of jejuni and Spirillum serpens. Relapse occurred in 22 %, and mortality was 5 %.
Conclusion
C. fetus meningitis is rare and diagnostically challenging but should be considered in immunocompromised patients, including those with post-transplantation or post-splenectomy status. Infection may occur even without clear exposure. Both blood and CSF cultures are essential, with blood cultures often positive earlier. Prompt diagnosis and targeted therapy are crucial for favorable outcomes, and long-term follow-up is recommended due to relapse risk.
{"title":"Campylobacter fetus meningitis and bacteremia: A case report in a post–liver transplant and post–splenectomy patient and a restructured literature review","authors":"Shiori Kitaya , Hatsumi Otani , Masahiro Yanagi , Taketo Kubo , Ryosuke Issiki , Yoshinori Takahashi , Megumi Oshima , Hajime Kanamori","doi":"10.1016/j.jiac.2025.102862","DOIUrl":"10.1016/j.jiac.2025.102862","url":null,"abstract":"<div><h3>Background</h3><div><em>Campylobacter fetus</em> is a rare but serious pathogen, mainly affecting immunocompromised patients. Central nervous system infections, particularly meningitis, are uncommon; only one case has been reported after liver transplantation and none after splenectomy.</div></div><div><h3>Case presentation</h3><div>We report meningitis and bacteremia caused by <em>C. fetus</em> subsp. <em>fetus</em> (Cff) in a 70-year-old man with liver transplantation and splenectomy for hepatitis C virus-related cirrhosis, on long-term immunosuppression. He presented with intermittent fever; blood cultures grew <em>C. fetus</em>, and cerebrospinal fluid (CSF) cultures confirmed it. Therapy was changed from cefmetazole to meropenem and vancomycin, then de-escalated to high-dose ampicillin. After 23 days of antibiotics, he fully recovered without sequelae.</div></div><div><h3>Literature review</h3><div>The literature review included 36 adult cases identified through a PubMed search and our own case. Seventy-eight percent were male, with a median age of 49 years. Sixteen percent were immunocompromised, while 41 % were otherwise healthy. Exposure risks were reported in 43 %, though absent in 54 %. Of 38 isolates, 24 were subspeciated: Cff was most frequent (18/24, 75 %), followed by <em>C. fetus</em> subsp. <em>intestinalis</em> and <em>venerealis</em> (2 each), and single isolates of <em>jejuni</em> and <em>Spirillum serpens</em>. Relapse occurred in 22 %, and mortality was 5 %.</div></div><div><h3>Conclusion</h3><div><em>C. fetus</em> meningitis is rare and diagnostically challenging but should be considered in immunocompromised patients, including those with post-transplantation or post-splenectomy status. Infection may occur even without clear exposure. Both blood and CSF cultures are essential, with blood cultures often positive earlier. Prompt diagnosis and targeted therapy are crucial for favorable outcomes, and long-term follow-up is recommended due to relapse risk.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102862"},"PeriodicalIF":1.5,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145530548","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lymphoproliferative disorders associated with human herpes virus 8 (HHV8) include Kaposi's sarcoma-associated herpesvirus (KSHV)/HHV8-positive multicentric Castleman disease (MCD), primary effusion lymphoma (PEL)/extracavitary PEL (EC-PEL), and KSHV/HHV8-positive diffuse large B-cell lymphoma (DLBCL). These lymphoproliferative disorders occur primarily in patients with HIV infection and immunodeficiency. HIV-negative KSHV/HHV8-positive MCD is extremely rare in Japan. We encountered a patient with KSHV/HHV8-positive large B-cell lymphoma with a history of HIV-negative, KSHV/HHV8-positive MCD. Although the KSHV/HHV8-positive MCD was in long-term remission with rituximab treatment, the patient developed refractory KSHV/HHV8-positive large B-cell lymphoma four years after the onset of MCD. The KSHV/HHV8-positive large B-cell lymphoma was refractory to chemotherapy, and the patient died. The course of this case suggests that HIV-negative KSHV/HHV-8-positive MCD may eventually lead to refractory KSHV/HHV8-positive large B-cell lymphoma, even after long-term remission with rituximab therapy.
{"title":"A case of KSHV/HHV8-positive large B-cell lymphoma in a background of HIV-negative KSHV/HHV8-positive Multicentric Castleman disease","authors":"Takafumi Tsushima , Shiho Konno , Akihiro Shoji , Chiharu Kimeda , Kosuke Matsuo , Rena Matsumoto , Sonoko Shimoji , Yoshikazu Utsu , Shin-Ichi Masuda , Kengo Takeuchi , Nobuyuki Aotsuka","doi":"10.1016/j.jiac.2025.102861","DOIUrl":"10.1016/j.jiac.2025.102861","url":null,"abstract":"<div><div>Lymphoproliferative disorders associated with human herpes virus 8 (HHV8) include Kaposi's sarcoma-associated herpesvirus (KSHV)/HHV8-positive multicentric Castleman disease (MCD), primary effusion lymphoma (PEL)/extracavitary PEL (EC-PEL), and KSHV/HHV8-positive diffuse large B-cell lymphoma (DLBCL). These lymphoproliferative disorders occur primarily in patients with HIV infection and immunodeficiency. HIV-negative KSHV/HHV8-positive MCD is extremely rare in Japan. We encountered a patient with KSHV/HHV8-positive large B-cell lymphoma with a history of HIV-negative, KSHV/HHV8-positive MCD. Although the KSHV/HHV8-positive MCD was in long-term remission with rituximab treatment, the patient developed refractory KSHV/HHV8-positive large B-cell lymphoma four years after the onset of MCD. The KSHV/HHV8-positive large B-cell lymphoma was refractory to chemotherapy, and the patient died. The course of this case suggests that HIV-negative KSHV/HHV-8-positive MCD may eventually lead to refractory KSHV/HHV8-positive large B-cell lymphoma, even after long-term remission with rituximab therapy.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102861"},"PeriodicalIF":1.5,"publicationDate":"2025-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145517684","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pseudomonas aeruginosa is a causative pathogen of nosocomial catheter-associated urinary tract infections (CAUTI), but prostate involvement, including prostatitis and prostatic abscess, is rare. The clinical characteristics of P. aeruginosa-associated CAUTI with prostatic lesions, as well as the contribution of genetic backgrounds remain unclear. We describe four cases of urinary catheter-associated prostatic infection caused by P. aeruginosa following postoperative catheterization. All patients developed fever within 10 days after surgery, and three of the four patients developed bacteremia. Three patients were diagnosed with prostatic abscess by contrast-enhanced computed tomography or magnetic resonance imaging, while one case presented with prostatitis without abscess formation. Prostate-specific antigen levels were elevated over 20 ng/mL in all three measured cases. All patients were treated successfully with prolonged antibiotic therapy (28–39 days) without surgical drainage. Notably, all three abscess cases were successfully managed with fluoroquinolone-based combination therapy, highlighting its potential role in the management of prostatic abscesses. Three of four isolates were submitted for molecular investigations. All isolates harbored exoT and exoY, whereas exoU was absent. Biofilm-associated genes were detected in two cases, but not in the remaining case. Our findings suggested that P. aeruginosa strains carrying T3SS genes (exoT and exoY) potentially develop prostatic infections, independent of biofilm-associated genes. Host and iatrogenic factors, such as catheter manipulation, may play more critical roles in the development of prostatic pathology than strain-specific determinants. Assessment of prostate-specific antigen levels and early imaging may facilitate appropriate diagnosis and effective management when P. aeruginosa is detected as a cause of CAUTI.
{"title":"Clinical and molecular characteristics of urinary catheter-associated Pseudomonas aeruginosa prostatic infection: A case series of four postoperative nosocomial infections","authors":"Shinnosuke Fukushima , Takayuki Sano , Takashige Kashimoto , Hideharu Hagiya","doi":"10.1016/j.jiac.2025.102853","DOIUrl":"10.1016/j.jiac.2025.102853","url":null,"abstract":"<div><div><em>Pseudomonas aeruginosa</em> is a causative pathogen of nosocomial catheter-associated urinary tract infections (CAUTI), but prostate involvement, including prostatitis and prostatic abscess, is rare. The clinical characteristics of <em>P. aeruginosa</em>-associated CAUTI with prostatic lesions, as well as the contribution of genetic backgrounds remain unclear. We describe four cases of urinary catheter-associated prostatic infection caused by <em>P. aeruginosa</em> following postoperative catheterization. All patients developed fever within 10 days after surgery, and three of the four patients developed bacteremia. Three patients were diagnosed with prostatic abscess by contrast-enhanced computed tomography or magnetic resonance imaging, while one case presented with prostatitis without abscess formation. Prostate-specific antigen levels were elevated over 20 ng/mL in all three measured cases. All patients were treated successfully with prolonged antibiotic therapy (28–39 days) without surgical drainage. Notably, all three abscess cases were successfully managed with fluoroquinolone-based combination therapy, highlighting its potential role in the management of prostatic abscesses. Three of four isolates were submitted for molecular investigations. All isolates harbored <em>exoT</em> and <em>exoY</em>, whereas <em>exoU</em> was absent. Biofilm-associated genes were detected in two cases, but not in the remaining case. Our findings suggested that <em>P. aeruginosa</em> strains carrying T3SS genes (<em>exoT</em> and <em>exoY</em>) potentially develop prostatic infections, independent of biofilm-associated genes. Host and iatrogenic factors, such as catheter manipulation, may play more critical roles in the development of prostatic pathology than strain-specific determinants. Assessment of prostate-specific antigen levels and early imaging may facilitate appropriate diagnosis and effective management when <em>P. aeruginosa</em> is detected as a cause of CAUTI.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102853"},"PeriodicalIF":1.5,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145505065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Reports on serum acyclovir (ACV) concentrations in patients undergoing continuous hemodiafiltration (CHDF) remain limited. We present a case describing the impact of CHDF on serum ACV levels in a patient with encephalopathy. A Japanese woman in her 70s was prescribed oral valacyclovir (VACV) at a dose of 1000 mg three times daily for herpes zoster ophthalmicus. After 7 days of treatment, she was admitted to a local hospital with fever, dysarthria, altered consciousness, hallucinations, and headache. Her serum creatinine level was elevated at 4.02 mg/dL. Intravenous ACV was initiated under the clinical suspicion of varicella zoster virus (VZV) encephalitis. However, after 3 days of treatment without improvement in consciousness, she was transferred to our hospital. Her serum ACV concentration upon admission was 14.1 μg/mL. Suspecting ACV-induced encephalopathy and renal dysfunction, CHDF was promptly initiated. Following CHDF therapy, serum ACV levels declined rapidly, accompanied by a gradual improvement in consciousness. This case suggests that CHDF may be an effective therapeutic option for managing ACV-associated nephropathy and encephalopathy.
{"title":"Impact of continuous hemodiafiltration on serum acyclovir concentrations in a patient with encephalopathy","authors":"Takahiro Ito , Kotaro Itohara , Sachi Hirata , Takeshi Kimura , Yumi Kitahiro , Tomohiro Omura , Joji Kotani , Ikuko Yano","doi":"10.1016/j.jiac.2025.102859","DOIUrl":"10.1016/j.jiac.2025.102859","url":null,"abstract":"<div><div>Reports on serum acyclovir (ACV) concentrations in patients undergoing continuous hemodiafiltration (CHDF) remain limited. We present a case describing the impact of CHDF on serum ACV levels in a patient with encephalopathy. A Japanese woman in her 70s was prescribed oral valacyclovir (VACV) at a dose of 1000 mg three times daily for herpes zoster ophthalmicus. After 7 days of treatment, she was admitted to a local hospital with fever, dysarthria, altered consciousness, hallucinations, and headache. Her serum creatinine level was elevated at 4.02 mg/dL. Intravenous ACV was initiated under the clinical suspicion of varicella zoster virus (VZV) encephalitis. However, after 3 days of treatment without improvement in consciousness, she was transferred to our hospital. Her serum ACV concentration upon admission was 14.1 μg/mL. Suspecting ACV-induced encephalopathy and renal dysfunction, CHDF was promptly initiated. Following CHDF therapy, serum ACV levels declined rapidly, accompanied by a gradual improvement in consciousness. This case suggests that CHDF may be an effective therapeutic option for managing ACV-associated nephropathy and encephalopathy.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102859"},"PeriodicalIF":1.5,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145505077","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lelliottia amnigena is a facultative anaerobe that is generally considered to show low pathogenicity, and few reports have described human infection. We describe herein a case of bacteremia due to L. amnigena in a patient with sigmoid colon cancer and schizophrenia. A 64-year-old Japanese man with schizophrenia was transferred to our hospital from a psychiatric hospital after experiencing several weeks of bloody bowel discharge and fever. He presented with hypotension, an elevated white blood cell count, raised levels of C-reactive protein, and decreased hemoglobin levels. Blood culture on transfer to our hospital detected Gram-negative rods, identified as L. amnigena by matrix-assisted laser desorption/ionization mass spectrometry and 16S rRNA gene sequencing. Antimicrobial therapy was initiated with piperacillin/tazobactam, which was later de-escalated to ampicillin/sulbactam according to the results of antimicrobial susceptibility testing, resulting in a total of 14 days of antimicrobial treatment. Computed tomography and colonoscopy revealed that the patient had sigmoid colon cancer, which was subsequently surgically resected. The sigmoid colon cancer was considered to represent the gateway for L. amnigena entry into the bloodstream. The course of treatment was favorable and the patient was transferred back to the original hospital 98 days after admission. L. amnigena bacteremia has rarely been reported, and the present case appears to represent the first detailed description. L. amnigena can cause bacteremia and sometimes lead to serious conditions in patients.
{"title":"Lelliottia amnigena bacteremia in a patient with sigmoid colon cancer and schizophrenia: a case report","authors":"Hiroshi Umemura , Yumiko Tanimichi , Ayami Karita , Hirokazu Kobayashi , Masaki Nakajima , Sachio Tsuchida , Fumitaka Ihara , Yuta Kojima , Suguru Nakajima , Kou Nagai , Tadashi Kanamori , Masahiro Suzuki , Kiyofumi Ohkusu , Tomohiro Nakayama","doi":"10.1016/j.jiac.2025.102858","DOIUrl":"10.1016/j.jiac.2025.102858","url":null,"abstract":"<div><div><em>Lelliottia amnigena</em> is a facultative anaerobe that is generally considered to show low pathogenicity, and few reports have described human infection. We describe herein a case of bacteremia due to <em>L. amnigena</em> in a patient with sigmoid colon cancer and schizophrenia. A 64-year-old Japanese man with schizophrenia was transferred to our hospital from a psychiatric hospital after experiencing several weeks of bloody bowel discharge and fever. He presented with hypotension, an elevated white blood cell count, raised levels of C-reactive protein, and decreased hemoglobin levels. Blood culture on transfer to our hospital detected Gram-negative rods, identified as <em>L. amnigena</em> by matrix-assisted laser desorption/ionization mass spectrometry and 16S rRNA gene sequencing. Antimicrobial therapy was initiated with piperacillin/tazobactam, which was later de-escalated to ampicillin/sulbactam according to the results of antimicrobial susceptibility testing, resulting in a total of 14 days of antimicrobial treatment. Computed tomography and colonoscopy revealed that the patient had sigmoid colon cancer, which was subsequently surgically resected. The sigmoid colon cancer was considered to represent the gateway for <em>L. amnigena</em> entry into the bloodstream. The course of treatment was favorable and the patient was transferred back to the original hospital 98 days after admission. <em>L. amnigena</em> bacteremia has rarely been reported, and the present case appears to represent the first detailed description. <em>L. amnigena</em> can cause bacteremia and sometimes lead to serious conditions in patients.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102858"},"PeriodicalIF":1.5,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145505038","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-08DOI: 10.1016/j.jiac.2025.102854
Yayoi Miyamatsu, Ryutaro Tanizaki
Intrathecal antibiotics are occasionally employed in the management of central nervous system infections; however, standard treatment regimens have not been clearly established, particularly for primary pyogenic ventriculitis in patients without an intraventricular drain. We report the first documented case of successful intralumbar administration of vancomycin, in combination with systemic antibiotics, for the treatment of primary pyogenic ventriculitis caused by Streptococcus dysgalactiae in a 65-year-old Japaneses woman. Despite receiving appropriate systemic antibiotic therapy, her level of consciousness showed no significant improvement, indicating that systemic therapy alone was insufficient to control the infection. Due to her advanced breast cancer, poor general condition, and limited prognosis, the neurosurgical team deemed intraventricular drainage inappropriate. As an alternative, intralumbar vancomycin therapy was initiated. Serial intrathecal vancomycin concentrations were measured during intralumbar vancomycin therapy, providing valuable pharmacokinetic data. This case highlights that intralumbar vancomycin may represent a feasible therapeutic alternative when systemic antibiotic therapy alone is insufficient. Further studies are warranted to elucidate the pharmacokinetics, efficacy, and safety of this therapeutic approach.
{"title":"Primary pyogenic ventriculitis due to Streptococcus dysgalactiae treated with intralumbar vancomycin administration: A case report","authors":"Yayoi Miyamatsu, Ryutaro Tanizaki","doi":"10.1016/j.jiac.2025.102854","DOIUrl":"10.1016/j.jiac.2025.102854","url":null,"abstract":"<div><div>Intrathecal antibiotics are occasionally employed in the management of central nervous system infections; however, standard treatment regimens have not been clearly established, particularly for primary pyogenic ventriculitis in patients without an intraventricular drain. We report the first documented case of successful intralumbar administration of vancomycin, in combination with systemic antibiotics, for the treatment of primary pyogenic ventriculitis caused by <em>Streptococcus dysgalactiae</em> in a 65-year-old Japaneses woman. Despite receiving appropriate systemic antibiotic therapy, her level of consciousness showed no significant improvement, indicating that systemic therapy alone was insufficient to control the infection. Due to her advanced breast cancer, poor general condition, and limited prognosis, the neurosurgical team deemed intraventricular drainage inappropriate. As an alternative, intralumbar vancomycin therapy was initiated. Serial intrathecal vancomycin concentrations were measured during intralumbar vancomycin therapy, providing valuable pharmacokinetic data. This case highlights that intralumbar vancomycin may represent a feasible therapeutic alternative when systemic antibiotic therapy alone is insufficient. Further studies are warranted to elucidate the pharmacokinetics, efficacy, and safety of this therapeutic approach.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102854"},"PeriodicalIF":1.5,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145488851","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Echinocandin-resistant Candida albicans (C. albicans) is a rare but increasing global concern. In Japan, at least three cases had been confirmed by the end of 2015. Mutations in FKS cause echinocandin resistance in Candida species, which is primarily driven by previous echinocandin antifungal use. C. albicans resistance to echinocandins is raising clinicians' concerns globally and could pose a threat to Japan in the near future. The fungus is also an antimicrobial-resistant pathogen, raising awareness of the risk of resistance to prophylactic antifungals. Herein, we report a case of echinocandin-resistant C. albicans at our hospital. Mutations in the FKS gene that cause echinocandin resistance in Candida species have been detected.
{"title":"Echinocandin-resistant Candida albicans: A case report from Japan","authors":"Sayaka Hikida , Yutaro Akiyama , Masahiro Ishikane , Hiroshi Shimazu , Ryo Nasu , Takayuki Shinohara , Minoru Nagi , Rei Shirai , Makiko Onakado , Nobuko Nakayama , Yoshitsugu Miyazaki , Akira Hangaishi , Norio Ohmagari","doi":"10.1016/j.jiac.2025.102856","DOIUrl":"10.1016/j.jiac.2025.102856","url":null,"abstract":"<div><div>Echinocandin-resistant Candida albicans (<em>C. albicans</em>) is a rare but increasing global concern. In Japan, at least three cases had been confirmed by the end of 2015. Mutations in FKS cause echinocandin resistance in <em>Candida</em> species, which is primarily driven by previous echinocandin antifungal use. <em>C. albicans</em> resistance to echinocandins is raising clinicians' concerns globally and could pose a threat to Japan in the near future. The fungus is also an antimicrobial-resistant pathogen, raising awareness of the risk of resistance to prophylactic antifungals. Herein, we report a case of echinocandin-resistant <em>C. albicans</em> at our hospital. Mutations in the FKS gene that cause echinocandin resistance in <em>Candida</em> species have been detected.</div></div>","PeriodicalId":16103,"journal":{"name":"Journal of Infection and Chemotherapy","volume":"31 12","pages":"Article 102856"},"PeriodicalIF":1.5,"publicationDate":"2025-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145481878","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}