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359 results on '"Matsumoto, Yuki"'

8. Whole exome and transcriptome analysis revealed the activation of ERK and Akt signaling pathway in canine histiocytic sarcoma

Author

Asada, Hajime, Tani, Akiyoshi, Sakuma, Hiroki, Hirabayashi, Miyuki, Matsumoto, Yuki, Watanabe, Kei, Tsuboi, Masaya, Yoshida, Shino, Harada, Kei, Uchikai, Takao, Goto-Koshino, Yuko, Chambers, James K., Ishihara, Genki, Kobayashi, Tetsuya, Irie, Mitsuhiro, Uchida, Kazuyuki, Ohno, Koichi, Bonkobara, Makoto, Tsujimoto, Hajime, and Tomiyasu, Hirotaka

Published
2023
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12. Analysis of gut microbiome, host genetics, and plasma metabolites reveals gut microbiome-host interactions in the Japanese population

Author

Tomofuji, Yoshihiko, Kishikawa, Toshihiro, Sonehara, Kyuto, Maeda, Yuichi, Ogawa, Kotaro, Kawabata, Shuhei, Oguro-Igashira, Eri, Okuno, Tatsusada, Nii, Takuro, Kinoshita, Makoto, Takagaki, Masatoshi, Yamamoto, Kenichi, Arase, Noriko, Yagita-Sakamaki, Mayu, Hosokawa, Akiko, Motooka, Daisuke, Matsumoto, Yuki, Matsuoka, Hidetoshi, Yoshimura, Maiko, Ohshima, Shiro, Nakamura, Shota, Fujimoto, Manabu, Inohara, Hidenori, Kishima, Haruhiko, Mochizuki, Hideki, Takeda, Kiyoshi, Kumanogoh, Atsushi, and Okada, Yukinori

Published
2023
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16. Chronic Pulmonary Disease Caused by Tsukamurella toyonakaense

Author

Kuge, Tomoki, Fukushima, Kiyoharu, Matsumoto, Yuki, Saito, Haruko, Abe, Yuko, Akiba, Eri, Haduki, Kako, Nitta, Tadayoshi, Kawano, Akira, Tanaka, Michio, Hattori, Yumi, Kawasaki, Takahiro, Matsuki, Takanori, Shiroyama, Takayuki, Motooka, Daisuke, Tsujino, Kazuyuki, Miki, Keisuke, Mori, Masahide, Kitada, Seigo, Nakamura, Shota, Iida, Tetsuya, Kumanogoh, Atsushi, and Kida, Hiroshi

Subjects
Lung diseases -- Causes of -- Case studies, Mycobacterium -- Case studies -- Identification and classification, Mycobacteria -- Case studies -- Identification and classification, Gram-positive bacterial infections -- Causes of -- Case studies, Health
Abstract

In clinical practice, unidentified Mycobacterium species are sometimes detected in respiratory specimens. Few Mycobacterium species can be identified by using methods available in clinical practice, although there are [approximately equal [...]

Published
2022
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23. Prokaryotic and viral genomes recovered from 787 Japanese gut metagenomes revealed microbial features linked to diets, populations, and diseases

Author

Tomofuji, Yoshihiko, Kishikawa, Toshihiro, Maeda, Yuichi, Ogawa, Kotaro, Otake-Kasamoto, Yuriko, Kawabata, Shuhei, Nii, Takuro, Okuno, Tatsusada, Oguro-Igashira, Eri, Kinoshita, Makoto, Takagaki, Masatoshi, Oyama, Naoki, Todo, Kenichi, Yamamoto, Kenichi, Sonehara, Kyuto, Yagita, Mayu, Hosokawa, Akiko, Motooka, Daisuke, Matsumoto, Yuki, Matsuoka, Hidetoshi, Yoshimura, Maiko, Ohshima, Shiro, Shinzaki, Shinichiro, Nakamura, Shota, Iijima, Hideki, Inohara, Hidenori, Kishima, Haruhiko, Takehara, Tetsuo, Mochizuki, Hideki, Takeda, Kiyoshi, Kumanogoh, Atsushi, and Okada, Yukinori

Published
2022
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29. Safety and efficacy of once-daily risdiplam in type 2 and non-ambulant type 3 spinal muscular atrophy (SUNFISH part 2): a phase 3, double-blind, randomised, placebo-controlled trial

Author

Volpe, Joseph J., Posner, John, Kellner, Ulrich, Quinlivan, Rosaline, Daron, Aurore, Delstanche, Stéphanie, Bruninx, Romain, Dal Farra, Fabian, Schneider, Olivier, Deconinck, Nicolas, Balikova, Irina, Delbeke, Patricia, Joniau, Inge, Tahon, Valentine, Wittevrongel, Sylvia, De Vos, Elke, Goemans, Nathalie, Casteels, Ingele, De Waele, Liesbeth, Cassiman, Catherine, Prové, Lies, Kinoo, David, Vancampenhout, Lisa, Van Den Hauwe, Marleen, Van Impe, Annelies, Prufer de Queiroz Campos Araujo, Alexandra, Chacon Pereira, Aline, Nardes, Flávia, Haefeli, Lorena, Rossetto, Julia, Ferreira Rebel, Marcos, Almeida Pereira, Jaqueline, Campbell, Craig, Sharan, Sapna, McDonald, Wendy, Scholtes, Cheryl, Mah, Jean, Sframeli, Maria, Chiu, Angela, Hagel, Jane, Oskoui, Maryam, Beneish, Raquel, Cariou-Palmer, Gaela, Pham, Connie, Toffoli, Daniela, Arpin, Stephanie, Turgeon Desilets, Sarah, Wang, Yi, Hu, Chaoping, Huan, Jianfeng, Qian, Chen, Shen, Li, Xiao, Ying, Zhou, Zhenxuan, Li, Hui, Wang, Sujuan, Xiong, Hui, Chang, Xingzhi, Dong, Hui, Liu, Ying, Sang, Tian, Wei, Cuijie, Wen, Jing, Cao, Yiwen, Ly, Xingyao, Zhao, Jingjing, Li, Wenzhu, Qin, Lun, Barisic, Nina, Galiot Delic, Martina, Ivkic, Petra Kristina, Vukojevic, Nenad, Kern, Ivana, Najdanovic, Boris, Skugor, Marin, Servais, Laurent, Boespflug-Tanguy, Odile, Gidaro, Teresa, Seferian, Andreea, De Lucia, Silvana, Barreau, Emmanuel, Mnafek, Nabila, Momtchilova, Marta Milkova, Peche, Helene, Valherie, Carole, Grange, Allison, Lilien, Charlotte, Milascevic, Darko, Tachibana, Shotaro, Ravelli, Claudia, Cardas, Ruxandra, Taytard, Jessica, Aubertin, Guillaume, Vanden Brande, Laure, Davion, Jean-Baptiste, Coopman, Stephanie, Bouacha, Ikram, Debruyne, Philippe, Defoort, Sabine, Derlyn, Gilles, Leroy, Florian, Danjoux, Loïc, Guilbaud, Julie, Desguerre, Isabelle, Barnérias, Christine, Semeraro, Michaela, Bremond-Gignac, Dominique, Bruere, Lenaic, Rateaux, Maxence, Deladrière, Élodie, Germa, Virginie, Pereon, Yann, Mercie, Sandra, Billaud, Fanny, Le Goff, Lucie, Letellier, Guy, Vuillerot, Carole, Portefaix, Aurélie, De-Montferrand, Camille, Le-Goff, Laure, Fontaine, Stephanie, Saidi, Manel, Bouzid, Nabil, Barriere, Aurélie, Tinat, Marie, Kirschner, Janbernd, Dreesbach, Michelle, Lagréze, Wolf, Michaelis, Bettina, Molnar, Fanni, Seger, Dorina, Vogt, Sibylle, Bertini, Enrico, D'Amico, Adele, Petroni, Sergio, Bonetti, Anna Maria, Carlesi, Adelina, Mizzoni, Irene, Bruno, Claudio, Priolo, Enrico, Rao, Giuseppe, Morando, Simone, Tacchetti, Paola, Zuffi, Ambra, Comi, Giacomo Pietro, Brusa, Roberta, Corti, Stefania, Daniele, Velardo, Govoni, Alessandra, Magri, Francesca, Minorini, Valeria, Osnaghi, Silvia Gabriella, Abbati, Francesca, Fassini, Federica, Foa, Michaela, Lopopolo, Amaqlia, Meneri, Megi, Zoppas, Francesca, Parente, Valeria, Baranello, Giovanni, Masson, Riccardo, Bianchi Marzoli, Stefania, Santarsiero, Diletta, Garcia Sierra, Myriam, Tremolada, Gemma, Arnoldi, Maria Teresa, Vigano, Marta, Zanin, Riccardo, Mercuri, Eugenio, Antonaci, Laura, de Sanctis, Roberto, Pane, Marika, Pera, Maria Carmela, Amorelli, Giulia Maria, Barresi, Costanza, D'Amico, Gugliemo, Orazi, Lorenzo, Coratti, Giorgia, Haginoya, Kazuhiro, Kato, Atsuko, Morishita, Yuko, Kira, Ryutaro, Akiyama, Kiyomu, Goto, Miwako, Mori, Yujiro, Okamoto, Misato, Tsutsui, Saki, Takatsuji, Yuta, Tanaka, Aya, Komaki, Hirofumi, Omori, Miina, Suzuki, Ippei, Takeuchi, Mizuki, Todoroki, Daisuke, Watanabe, Seji, Matsubayashi, Tomoko, Inakazu, Emi, Nagura, Hiroe, Suzuki, Akira, Usui, Manami, Ishikawa, Nobutsune, Harada, Yousuke, Fudeyasu, Kenishi, Hirata, Kazuhiko, Michiue, Kana, Ueda, Kazuyuki, Saito, Kayoko, Fujitani, Junko, Arakawa, Reiko, Takano, Kozue, Yashiro, Shigeko, Seki, Maiko, Sano, Nozomi, Fukuyama, Koji, Matsumoto, Yuki, Miyazaki, Hirofumi, Shibata, Minoru, Kobayashi, Kyoko, Nakamura, Yukie, Takeshima, Yasuhiro, Kuma, Moe, Kostera-Pruszczyk, Anna, Fraczek, Anna, Jedrzejowska, Maria, Lusakowska, Anna, Czeszyk-Piotrowicz, Agnieszka, Hautz, Wojciech, Rakusiewicz, Klaudia, Burlewicz, Malgorzata, Gierlak-Wojcicka, Zuzanna, Kepa, Malwina, Sikorski, Adam, Sobieraj, Marcin, Mazurkiewicz-Beldzinska, Maria, Lemska, Anna, Modrzejewska, Sandra, Koberda, Mateusz, Stodolska-Koberda, Urszula, Waskowska, Agnieszka, Kolendo, Jagoda, Sobierajska-Rek, Agnieszka, Steinborn, Barbara, Dalz, Magdalena, Grabowska, Julia, Hajduk, Wojciech, Janasiewicz-Karachitos, Justyna, Klimas, Monika, Stopa, Marcin, Gajewska, Ewa, Pusz, Beata, Vlodavets, Dmitry, Melnik, Evgenia, Leppenen, Natalya, Yupatova, Nataliya, Monakhova, Anastasya, Papina, Yulia, Shidlovsckaia, Olga, Milic Rasic, Vedrana, Brankovic, Vesna, Kosac, Ana, Djokic, Olivera, Jakšic, Vesna, Pepic, Ana, Martinovic, Jelena, Munell Casadesus, Francina, Tizzano, Eduardo, Martín Begué, Nieves, Wolley Dod, Charlotte, Subira, Olaia, Planas Pascual, Bernat, Toro Tamargo, Esther, Madruga Garrido, Marcos, Medina Romero, José David, Salinas, Marta Peña, Nascimento Osorio, Andrés, Díaz Cortés, Ana, Jiménez Gañan, Enrique, Suh, Simone Dowon, Medina Cantillo, Julita, Moya, Obdulia, Padros, Nuria, Urraca, Sandra Roca, Valdivia, Hugo Gonzalez, Pascual Pascual, Samuel, de Manuel, Sofía, Martin, Susana Noval, Burnham, Paul, Espinosa, Sandra, Moreno, Mercedes Martinez, Topaloglu, Haluk, Oncel, Ibrahim, Eroglu Ertugru, Nesibe, Konuskan, Bahadir, Eldem, Bora, Kadayifçilar, Sibel, Alemdaroglu, Ipek, Karaduman, Aynur Ayse, Yilmaz, Oznur Tunca, Bilgin, Neslihan, Sari, Seher, Chiriboga, Claudia, Lee, John J., Rome-Martin, Donnielle, Day, John W., Beres, Shannon, Duong, Tina, Gee, Richard, Dunaway Young, Sally, Fuerst-Recktenwald, Sabine, Marquet, Anne, Muelhardt, Nicoletta, Trundell, Dylan, Mazzone, Elena S, Nascimento, Andres, Gerber, Marianne, Gorni, Ksenija, Khwaja, Omar, Kletzl, Heidemarie, Scalco, Renata S, Staunton, Hannah, Yeung, Wai Yin, Martin, Carmen, Fontoura, Paulo, and Day, John W

Published
2022
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30. Humanized-Aquaporin-4-Expressing Rat Created by Gene-Editing Technology and Its Use to Clarify the Pathology of Neuromyelitis Optica Spectrum Disorder.

Author

Namatame, Chihiro, Abe, Yoichiro, Miyasaka, Yoshiki, Takai, Yoshiki, Matsumoto, Yuki, Takahashi, Toshiyuki, Mashimo, Tomoji, Misu, Tatsuro, Fujihara, Kazuo, Yasui, Masato, and Aoki, Masashi

Subjects
NEUROMYELITIS optica, LABORATORY rats, MYELIN basic protein, GENOME editing, RATS, IMMUNOGLOBULIN G, MYELIN proteins
Abstract

Conventional rodent neuromyelitis optica spectrum disorder (NMOSD) models using patient-derived immunoglobulin G (IgG) are potentially affected by the differences between the human and rodent aquaporin-4 (AQP4) extracellular domains (ECDs). We hypothesized that the humanization of AQP4 ECDs would make the rodent model lesions closer to human NMOSD pathology. Humanized-AQP4-expressing (hAQP4) rats were generated using genome-editing technology, and the human AQP4-specific monoclonal antibody (mAb) or six patient-derived IgGs were introduced intraperitoneally into hAQP4 rats and wild-type Lewis (WT) rats after immunization with myelin basic protein and complete Freund's adjuvant. Human AQP4-specific mAb induced astrocyte loss lesions specifically in hAQP4 rats. The patient-derived IgGs also induced NMOSD-like tissue-destructive lesions with AQP4 loss, demyelination, axonal swelling, complement deposition, and marked neutrophil and macrophage/microglia infiltration in hAQP4 rats; however, the difference in AQP4 loss lesion size and infiltrating cells was not significant between hAQP4 and WT rats. The patient-derived IgGs bound to both human and rat AQP4 M23, suggesting their binding to the shared region of human and rat AQP4 ECDs. Anti-AQP4 titers positively correlated with AQP4 loss lesion size and neutrophil and macrophage/microglia infiltration. Considering that patient-derived IgGs vary in binding sites and affinities and some of them may not bind to rodent AQP4, our hAQP4 rat is expected to reproduce NMOSD-like pathology more accurately than WT rats. [ABSTRACT FROM AUTHOR]

Published
2024
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38. Anxiety Levels of Children with Developmental Disorders in Japan: Based on Reports Provided by Parents

Author

Ishimoto, Yuma, Yamane, Takahiro, and Matsumoto, Yuki

Abstract

A large number of children with developmental disorders like autism spectrum disorder (ASD), learning disabilities, and attention deficit hyperactivity disorder have high anxiety. It has also been shown that the high anxiety has harmful effects on them, directly and indirectly. In this study, we conducted a survey on community samples on the level of anxiety of children with developmental disorders in Japan that had hardly been studied so far, and compared them with the anxiety in children in a general population sample in previous studies. Analysis on the 203 participants showed that children with developmental disorders have high anxiety as compared to children as in previous studies in other countries. Particularly children with ASD had a higher anxiety compared with children with developmental disorders without ASD.

Published
2019
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40. A de novo nonsense variant in the DMD gene associated with X‐linked dystrophin‐deficient muscular dystrophy in a cat.

Author

Yokoyama, Nozomu, Matsumoto, Yuki, Yamaguchi, Takahisa, Okada, Kazuki, Kinoshita, Ryohei, Shimbo, Genya, Ukawa, Hisashi, Ishii, Ryuga, Nakamura, Kensuke, Yamazaki, Jumpei, and Takiguchi, Mitsuyoshi

Subjects
*MUSCULAR dystrophy, *WHOLE genome sequencing, *CAT breeds, *GENETIC variation, *CATS, *EPICATECHIN, *Y chromosome, *FLEA control
Abstract

Background: X‐linked dystrophin‐deficient muscular dystrophy (MD) is a form of MD caused by variants in the DMD gene. It is a fatal disease characterized by progressive weakness and degeneration of skeletal muscles. Hypothesis/Objectives: Identify deleterious genetic variants in DMD by whole‐genome sequencing (WGS) using a next‐generation sequencer. Animals: One MD‐affected cat, its parents, and 354 cats from a breeding colony. Methods: We compared the WGS data of the affected cat with data available in the National Center for Biotechnology Information database and searched for candidate high‐impact variants by in silico analyses. Next, we confirmed the candidate variants by Sanger sequencing using samples from the parents and cats from the breeding colony. We used 2 genome assemblies, the standard felCat9 (from an Abyssinian cat) and the novel AnAms1.0 (from an American Shorthair cat), to evaluate genome assembly differences. Results: We found 2 novel high‐impact variants: a 1‐bp deletion in felCat9 and an identical nonsense variant in felCat9 and AnAms1.0. Whole genome and Sanger sequencing validation showed that the deletion in felCat9 was a false positive because of misassembly. Among the 357 cats, the nonsense variant was only found in the affected cat, which indicated it was a de novo variant. Conclusion and Clinical Importance: We identified a de novo variant in the affected cat and next‐generation sequencing‐based genotyping of the whole DMD gene was determined to be necessary for affected cats because the parents of the affected cat did not have the risk variant. [ABSTRACT FROM AUTHOR]

Published
2024
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41. Determination of Alzheimer's disease based on morphology and atrophy using machine learning combined with automated segmentation.

Author

Ikemitsu, Natsuki, Kanazawa, Yuki, Haga, Akihiro, Hayashi, Hiroaki, Matsumoto, Yuki, and Harada, Masafumi

Subjects
ALZHEIMER'S disease, CONVOLUTIONAL neural networks, MACHINE learning, MAGNETIC resonance imaging, CEREBRAL atrophy
Abstract

Background: To evaluate the degree of cerebral atrophy for Alzheimer's disease (AD), voxel-based morphometry has been performed with magnetic resonance imaging. Detailed morphological changes in a specific tissue area having the most evidence of atrophy were not considered by the machine-learning technique. Purpose: To develop a machine-learning system that can capture morphology features for determination of atrophy of brain tissue in early-stage AD and classification of healthy participants or patients. Material and Methods: Three-dimensional T1-weighted (3D-T1W) data were obtained from AD Neuroimaging Initiative (200 healthy controls and 200 patients with early-stage AD). Automated segmentation of 3D-T1W data was performed. Deep learning (DL) and support vector machine (SVM) were trained using 66-segmented volume values as input and AD diagnosis as output. DL was performed using 66 volume values or gray matter (GM) and white matter (WM) volume values. SVM learning was performed using 66 volume values and six regions with high variable importance. 3D convolutional neural network (3D-CNN) was trained using the segmented images. Accuracy and area under curve (AUC) were obtained. Variable importance was evaluated from logistic regression analysis. Results: DL for GM and WM volume values, accuracy 0.6; SVM for all volume values, accuracy 0.82 and AUC 0.81; DL for all volume values, accuracy 0.82 and AUC 0.8; 3D-CNN using segmental images of the whole brain, accuracy 0.5 and AUC 0.51. SVM using volume values of six regions, accuracy 0.82; image-based 3D-CNN, highest accuracy 0.69. Conclusion: Our results show that atrophic features are more considerable than morphological features in the early detection of AD. [ABSTRACT FROM AUTHOR]

Published
2024
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47. Myelin oligodendrocyte glycoprotein antibody‐associated disorders: An overview.

Author

Misu, Tatsuro, Matsumoto, Yuki, Kaneko, Kimihiko, Takahashi, Toshiyuki, Takai, Yoshiki, Ono, Hirohiko, Namatame, Chihiro, Nishiyama, Shuhei, Fujimori, Juichi, Kuroda, Hiroshi, Nakashima, Ichiro, Fujihara, Kazuo, and Aoki, Masashi

Subjects
*MYELIN oligodendrocyte glycoprotein, *POSTVACCINAL encephalitis, *ENCEPHALOMYELITIS, *OPTIC neuritis, *DEMYELINATION, *NEUROLOGICAL disorders
Abstract

In recent years, there is growing evidence of associations between antibodies against myelin oligodendrocyte glycoprotein (MOG) and several phenotypes of acute inflammatory demyelinating diseases such as acute disseminated encephalomyelitis (ADEM), optic neuritis, brainstem, and cerebral cortical encephalitis, called MOG antibody associated disorders (MOGAD). Monophasic course is known in about half of cases especially in pediatric onset ADEM and optic neuritis, mainly in cases with transient positivity of MOG antibody. Pathological features of MOGAD are considered as acute demyelinating lesions with CD4 dominant cell infiltrations, the deposition of humoral immunity, perivascular inflammation and perivenous demyelination, which is distinct from multiple sclerosis. Now the diagnosis of MOGAD is based on the international panel criteria of MOGAD launched in 2023, which the diagnostic frameworks are three parts, including MOGAD‐specific clinical features, MOG antibody positivity, and the exclusion of other diseases. The prognosis of MOGAD patients is considered relatively mild, but the problem is refractory relapsing cases. For its prevention, there are no approved drugs, but oral tapering corticosteroids, immunosuppressants such as azathioprine and mycophenolic mofetil, rituximab, and the maintenance intravenous immunoglobulin are recommended, and now there are a few clinical trials of promising biological drugs already approved in other neurological disorders. [ABSTRACT FROM AUTHOR]

Published
2024
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48. Pole Allocation Applied to Two Buildings Connected by Joint Damper.

Author

Ikeda, Yoshiki and Matsumoto, Yuki

Subjects
*FIXED point theory, *INVERSE problems
Abstract

For two adjacent buildings connected by a joint damper, an inverse problem is formulated based on the pole allocation method in control theory. The structural system is simplified as a two-degrees-of-freedom (2-DOF) lumped-mass damped shear model. The unified governing equation, which expresses the relationship between an assigned control target and the structural parameters for an earthquake-resistant building, seismically isolated building, or passively controlled building, is extended to structural control using a joint damper. The introduced equation automatically constrains the variations in the structural parameters under the assigned modal properties. The integration of the pole allocation method and fixed-point theory directly estimates the additional damping effect on the target buildings from the optimum capacity of the joint damper, which improves the trial-and-error steps at the preliminary design stage. The past fixed-point theories do not provide the additional damping effect but the optimum damping coefficient of the joint damper. The present study directly links the additional damping with the damping of the joint damper. Numerical examples are used to verify the theoretical integration using a 20-DOF building model wherein two 10-DOF models are connected by a joint damper between the top lumped masses. [ABSTRACT FROM AUTHOR]

Published
2024
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49. Relationship between teacher and student psychological well-being in a Japanese context.

Author

Takizawa, Yu, Matsumoto, Yuki, and Ishimoto, Yuma

Subjects
PSYCHOLOGICAL well-being, STUDENT well-being, JAPANESE students, SCHOOL children, PLEASURE, LIFE satisfaction, CLASSROOM environment, TEACHER-student relationships
Abstract

Psychological well-being (PWB) encompasses the positive aspects of mental health, such as hedonic wellbeing (experience of enjoyment and pleasure), eudaimonic wellbeing (experience of self-actualization), and life satisfaction (global evaluation of quality of life). Japanese teachers suffer from poor PWB with a high incidence of mental health problems. Despite the potentially significant impact of poor Japanese teachers' PWB on their students' PWB, these associations have remained largely unexplored. The present study investigated if teacher PWB has any relationship with student PWB and if teacher-student relationship, students' abilities for resilience, and classroom climate mediate the teacher and student PWB relationship, with 46 teachers and 1,256 children aged 8–12 years from Japanese schools. A multilevel mediation analysis revealed an indirect positive relationship between Japanese teacher life satisfaction and Japanese student hedonic and eudaimonic wellbeing mediated by students' abilities for resilience. There was no relationship between teacher and student hedonic and eudaimonic wellbeing. Nonetheless, the findings still imply that promoting teacher life satisfaction may contribute to the promotion of student hedonic and eudaimonic wellbeing. Future researchers could investigate if a school-based intervention targeted at both Japanese teachers and students would more effectively promote PWB among students than would such interventions aimed only at students. [ABSTRACT FROM AUTHOR]

Published
2024
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50. Urinary tract infection associated with bacteremia caused by vancomycin‐resistant enterococcus following continent urinary diversion.

Author

Morishita, Kai, Kashiwabara, Soichiro, Matsumoto, Yuki, Mizushima, Atsuhiro, Hara, Kaori, Agatsuma, Toshihiko, Mimura, Yuji, Matsumura, Hideyoshi, and Mizusawa, Hiroya

Subjects
URINARY tract infections, URINARY diversion, ENTEROCOCCAL infections, RETENTION of urine, ENTEROCOCCUS, BACTEREMIA, ACUTE kidney failure, PELVIC exenteration
Abstract

Key Clinical Message: Even in a country where vancomycin–resistant enterococcus is rare, multidrug‐resistant organism precautions are necessary when admitting patients with a history of medical exposure in other countries. On admission, screening is necessary and if infection is confirmed, a multidisciplinary approach involving different specialists is required. The patient was a 49‐year‐old Japanese female living in the United States. Total pelvic exenteration for cervical carcinoma, Miami pouch formation, and ileostomy had been performed in the United States. She returned to Japan to undergo postoperative adjuvant chemotherapy. Fever and abdominal pain occurred 42 days after surgery. She consulted the fever outpatient clinic, and a diagnosis of urinary retention‐associated acute renal failure and pyelonephritis was made. We detected vancomycin‐resistant enterococcus on urine/blood culture 5 days after admission. Infection control measures were implemented, and the ward was closed for 3 days. We administered linezolid, which was effective for pyelonephritis and bacteremia. [ABSTRACT FROM AUTHOR]

Published
2024
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