基本情報
研究分野
1経歴
7-
2020年10月 - 現在
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2020年4月 - 2021年9月
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2016年4月 - 2020年3月
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2014年4月 - 2016年3月
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2013年4月 - 2014年3月
学歴
3-
2015年4月 - 2019年3月
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2000年4月 - 2006年3月
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1997年4月 - 2000年3月
論文
108-
QJM : monthly journal of the Association of Physicians 2024年10月21日
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Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2024年7月4日OBJECTIVES: We aim to assess the early use of contrast-enhanced computed tomography (CECT) of patients with severe acute pancreatitis (SAP) using the computed tomography severity index (CTSI) in prognosis prediction. The CTSI combines quantification of pancreatic and extrapancreatic inflammation with the extent of pancreatic necrosis. METHODS: Post-hoc retrospective analysis of a large, multicentric database (44 institutions) of SAP patients in Japan. The area under the curve (AUC) of the CTSI for predicting mortality and the odds ratio (OR) of the extent of pancreatic inflammation and necrosis were calculated using multivariable analysis. RESULTS: In total, 1097 patients were included. The AUC of the CTSI for mortality was 0.65 (95 % confidence interval [CI:] [0.59-0.70]; p < 0.001). In multivariable analysis, necrosis 30-50 % and >50 % in low-enhanced pancreatic parenchyma (LEPP) was independently associated with a significant increase in mortality, with OR 2.04 and 95 % CI 1.01-4.12 (P < 0.05) and OR 3.88 and 95 % CI 2.04-7.40 (P < 0.001), respectively. However, the extent of pancreatic inflammation was not associated with mortality, regardless of severity. CONCLUSIONS: The degree of necrosis in LEPP assessed using early CECT of SAP was a better predictor of mortality than the extent of pancreatic inflammation.
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Journal of critical care medicine (Universitatea de Medicina si Farmacie din Targu-Mures) 10(3) 213-221 2024年7月AIM OF THE STUDY: Peripheral intravascular catheter (PIVC) insertion is frequently performed in the emergency room (ER) and many failures of initial PIVC insertion occur. To reduce the failures, new needles were developed. This study aimed to investigate whether the use of the newly developed needle reduced the failure of initial PIVC insertion in the ER compared with the use of the existing needle. MATERIAL AND METHODS: This single-centre, prospective observational study was conducted in Japan between April 1, 2022, and February 2, 2023. We included consecutive patients who visited our hospital by ambulance as a secondary emergency on a weekday during the day shift (from 8:00 AM to 5:00 PM). The practitioners for PIVC insertion and assessors were independent. The primary and secondary outcomes were the failure of initial PIVC insertion and number of procedures, respectively. We defined the difficulty of titrating, leakage, and hematoma within 30 s after insertion as failures. To evaluate the association between the outcomes and the use of newly developed needles, we performed multivariate logistic regression and multiple regression analyses by adjusting for covariates. RESULTS: In total, 522 patients without missing data were analysed, and 81 (15.5%) patients showed failure of initial PIVC insertion. The median number of procedures (interquartile range) was 1 (1-1). Multivariate logistic regression analysis revealed no significant association between the use of newly developed PIVCs and the failure of initial PIVC insertion (odds ratio, 0.79; 95% confidence interval, [0.48-1.31]; p = 0.36). Moreover, multiple regression analysis revealed no significant association between the use of newly developed PIVCs and the number of procedures (regression coefficient, -0.0042; 95% confidence interval, [-0.065-0.056]; p = 0.89). CONCLUSIONS: Our study did not show a difference between the two types of needles with respect to the failure of initial PIVC insertion and the number of procedures.
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Journal of critical care medicine (Universitatea de Medicina si Farmacie din Targu-Mures) 10(3) 232-244 2024年7月INTRODUCTION: Early and accurate identification of high-risk patients with peripheral intravascular catheter (PIVC)-related phlebitis is vital to prevent medical device-related complications. AIM OF THE STUDY: This study aimed to develop and validate a machine learning-based model for predicting the incidence of PIVC-related phlebitis in critically ill patients. MATERIALS AND METHODS: Four machine learning models were created using data from patients ≥ 18 years with a newly inserted PIVC during intensive care unit admission. Models were developed and validated using a 7:3 split. Random survival forest (RSF) was used to create predictive models for time-to-event outcomes. Logistic regression with least absolute reduction and selection operator (LASSO), random forest (RF), and gradient boosting decision tree were used to develop predictive models that treat outcome as a binary variable. Cox proportional hazards (COX) and logistic regression (LR) were used as comparators for time-to-event and binary outcomes, respectively. RESULTS: The final cohort had 3429 PIVCs, which were divided into the development cohort (2400 PIVCs) and validation cohort (1029 PIVCs). The c-statistic (95% confidence interval) of the models in the validation cohort for discrimination were as follows: RSF, 0.689 (0.627-0.750); LASSO, 0.664 (0.610-0.717); RF, 0.699 (0.645-0.753); gradient boosting tree, 0.699 (0.647-0.750); COX, 0.516 (0.454-0.578); and LR, 0.633 (0.575-0.691). No significant difference was observed among the c-statistic of the four models for binary outcome. However, RSF had a higher c-statistic than COX. The important predictive factors in RSF included inserted site, catheter material, age, and nicardipine, whereas those in RF included catheter dwell duration, nicardipine, and age. CONCLUSIONS: The RSF model for the survival time analysis of phlebitis occurrence showed relatively high prediction performance compared with the COX model. No significant differences in prediction performance were observed among the models with phlebitis occurrence as the binary outcome.
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The American journal of emergency medicine 82 183-189 2024年6月15日BACKGROUND: Status epilepticus (SE) is potentially life-threatening, however, it is unclear which antiepileptic drugs (AEDs) should be used as second-line AEDs. OBJECTIVE: We conducted a network meta-analysis (NMA) of randomized controlled trials (RCTs) comparing multiple second-line AEDs for SE to investigate the efficacy of AEDs. METHODS: We searched MEDLINE, CENTRAL, ClinicalTrials.gov, and World Health Organization International Clinical Trials Platform Search Portal and included RCTs for patients aged ≥15 years with SE on December 31, 2023. We compared multiple second-line AEDs for SE including fosphenytoin (fPHT), lacosamide (LCM), levetiracetam (LEV), phenytoin (PHT), phenobarbital (PHB), and valproate (VPA). The primary and secondly outcomes were termination of seizures integrating the absence of seizure recurrence at 30 min and 60 min, and adverse events associated with AEDs, respectively, with expressing as relative risk (RR) with a 95% confidence interval (CI). We conducted a NMA using frequentist-based approach with multivariate random effects, and assessed the certainty based on the Grading of Recommendations, Assessment, Development, and Evaluations framework. RESULTS: Seven RCTs (n = 780) were included, and statistically significant difference was detected between VPA vs. PHB (RR, 0.67; 95% CI, 0.53-0.85; very low certainty), fPHT vs. PHB (RR, 0.66; 95% CI, 0.48-0.90; very low certainty), LCM vs. PHB (RR, 0.62; 95% CI, 0.41-0.93; very low certainty), and LEV vs. PHB (RR, 0.69; 95% CI, 0.51-0.94; very low certainty). Moreover, PHB was the highest in the ranking for termination of seizures. For adverse events, no significant reduction was observed owing to the selection of AEDs, although the ranking of PHB was the lowest. CONCLUSIONS: PHB may have been the most effective for seizure termination as second-line AEDs in adult patients with SE. However, the certainty of almost all comparisons was "very low", and careful interpretation is essential.
MISC
449-
Intensivist 9(1) 175-185 2017年1月中心静脈カテーテル留置において,内頸静脈,鎖骨下静脈,大腿静脈いずれにおいても,超音波ガイド下穿刺は成功率上昇と合併症軽減の観点から,標準的手技である。中心静脈カテーテル留置のみならず,動脈カテーテル留置や末梢静脈カテーテル留置においても,超音波ガイド下穿刺により成功率を上昇させ,合併症を軽減させることができる。超音波ガイド下穿刺での鎖骨下(腋窩)静脈穿刺は機械的合併症が少なく,カテーテル関連血流感染症のリスクが少ないことから,中心静脈カテーテル留置の第一選択となる。(著者抄録)
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Intensivist 9(1) 238-245 2017年1月
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日本集中治療医学会雑誌 24(1) 57-63 2017年1月日本集中治療医学会/日本呼吸療法医学会ARDS診療ガイドライン作成委員会は、今回、日本呼吸器学会ARDS診療ガイドライン作成委員会と合同で「ARDS診療ガイドライン2016」を作成し公開した。今回は13の診療疑問(clinical question)について、国内でもまだ取りあげられることの少ないGRADE(Grading of Recommendations Assessment、Development and Evaluation)systemを用いたシステマティックレビューとその推奨度決定の手法を取り入れた。これにより、従来に比して信頼性の高い診療ガイドラインを作成することができた。(著者抄録)
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Annals of the American Thoracic Society 14(1) 149-150 2017年1月1日
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レジデントノート 18(12) 2259-2269 2016年11月(1)重症患者における"消化器の評価"は消化管だけの評価では終わらない(2)"消化器の評価"のアプローチは症状・身体所見、既往歴、チューブ類(胃管など)、血液検査、画像検査の順であり、プロブレムリストごとのアセスメント・プランが重要である(3)重症患者においては、消化管出血のリスク、便常異常(便秘・下痢)を評価することが重要である(4)肝機能異常≠肝臓疾患であり、体系的なアプローチが必要である(著者抄録)
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人工呼吸 33(2) 113-120 2016年11月日本呼吸療法医学会/日本集中治療医学会ARDS診療ガイドライン作成委員会は、日本呼吸器学会(JRS)ARDS診療ガイドライン作成委員会と合同で「ARDS診療ガイドライン2016」を作成し公開した。今回は13の診療疑問(clinical question:CQ)について、国内でもまだ取り上げられることの少ないGRADE(Grading of Recommendations Assessment、Development and Evaluation)systemを用いたシステマティックレビューとその推奨度決定の手法を取り入れた。これにより従来に比して信頼性の高い診療ガイドラインを作成することができた。(著者抄録)
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Intensivist 8(4) 944-952 2016年10月
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Intensivist 8(3) 557-570 2016年7月気胸,血胸,膿胸の治療を決める際には,原因や分類の理解が必要不可欠である。原発性気胸は穿刺吸引を施行,続発性気胸は胸腔ドレーンを挿入,その後5〜7日経過してもエアリークが継続する場合には手術介入を考慮してよい。血胸は胸腔ドレーンで管理するのを基本とし,排液の1日量または6時間当たりの排液量,患者の血行動態を考慮したうえで手術介入を考慮すべきである。膿胸の治療にはLightの分類が非常に有用で,Class 1〜3は抗菌薬投与のみで治癒可能だが,Class 4以上では胸腔ドレナージをすべきである。(著者抄録)
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Intensivist 8(3) 700-707 2016年7月
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救急・集中治療 28(7-8) 609-616 2016年7月<point>血液培養採取時の皮膚消毒薬には、0.5%クロルヘキシジンアルコールを使う。静脈カテーテル挿入時の皮膚消毒薬には、0.5%クロルヘキシジンアルコールを使う。術創部感染予防のための皮膚消毒薬には、0.5%クロルヘキシジンアルコールを使う。クロルヘキシジンアルコールを使用する際には粘膜面への使用は禁忌であり、皮膚熱傷を防ぐためにも最後まで乾燥させる。どの消毒薬を使用する際にも消毒効果を最大限に発揮させるために、きちんと最後まで乾燥させる。(著者抄録)
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GASTROENTEROLOGY 150(4) S709-S709 2016年4月
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日本集中治療医学会学術集会(Web) 43rd(Suppl.) SY15‐5 (WEB ONLY)-248 2016年1月15日
書籍等出版物
6講演・口頭発表等
39所属学協会
5-
2012年8月 - 現在
共同研究・競争的資金等の研究課題
3-
日本学術振興会 科学研究費助成事業 基盤研究(C) 2021年4月 - 2026年3月
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日本学術振興会 科学研究費助成事業 基盤研究(C) 2019年4月 - 2024年3月
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日本学術振興会 科学研究費助成事業 2017年4月 - 2019年3月