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The beneficial effects of conservative treatment with biofeedback and electrostimulation on pelvic floor disorders 生物反馈和电刺激保守治疗盆底疾病的有益效果
Q2 Medicine Pub Date : 2023-09-22 DOI: 10.4103/tcmj.tcmj_174_23
Mei-Chen Chen, Pei-Hsuan Lai, Dah-Ching Ding
A BSTRACT Objectives: Pelvic floor disorders (PFDs) such as stress urinary incontinence (SUI) and pelvic organ prolapse (POP) can be managed through conservative treatments, such as conservative management involving biofeedback (BF) and electrostimulation. This study aimed to investigate the therapeutic effects of conservative treatments on PFDs. Materials and Methods: A retrospective cohort study was conducted. Women with PFD who underwent 1–3 months of BF and electrostimulation between January 1, 2020, and January 31, 2021, were included in the study. BF treatment was administered using three sensors to monitor pelvic floor muscle activity, providing patients with immediate feedback and guidance on muscle exercises. One session lasted for 5–10 min. Electrostimulation treatment utilized a specially made pelvic belt with electrode sheets to stimulate and contract pelvic floor muscles passively. One session lasted for 15 min. Six therapies in 1 month were prescribed. Pre- and post-treatment Pelvic Floor Distress Inventory (PFDI-20) scores, including POP distress inventory 6 (POPDI-6), colorectal-anal distress inventory (CRAD-8), and urinary distress inventory 6 (UDI-6) scores, were compared. Subgroup analysis by age, menopause, body mass index (BMI), and child delivery mode was performed. Results: The study included 51 women with PFDs (SUI, POP, frequency or urgency or nocturia, and pain) treated with BF and electrostimulation, with a mean age of 49.94 ± 13.63 years. Sixteen patients (37.1%) were menopausal, with a mean menopause age of 50 ± 5.20 years. Twenty-six patients (68.4%) had a history of normal vaginal delivery. The mean PFDI-20 scores before and after treatment were 32.67 (standard deviation [SD] 10.05) and 25.99 (SD 9.61), respectively ( P < 0.001). This decrease in scores reflected an improvement in subjective perceptions of symptoms and quality of life. The POPDI-6, CRAD-8, and UDI-6 scores significantly decreased after treatment. Subgroup analysis of scores change regarding age, menopause, BMI, and child delivery mode was not statistically significant. Conclusions: The study demonstrated the effectiveness of BF and electrostimulation for treating women with PFDs. The findings contributed to the understanding of treatment duration, patient characteristics, and the potential benefits of a multimodal approach. Moreover, the study’s diverse participant population and the use of validated outcome measures enhance the generalizability and scientific rigor of the findings.
目的:盆底疾病(PFDs)如压力性尿失禁(SUI)和盆腔器官脱垂(POP)可以通过保守治疗来治疗,如生物反馈(BF)和电刺激等保守治疗。本研究旨在探讨保守治疗PFDs的疗效。材料和方法:进行回顾性队列研究。在2020年1月1日至2021年1月31日期间接受了1 - 3个月BF和电刺激的PFD女性被纳入研究。BF治疗采用三个传感器监测骨盆底肌肉活动,为患者提供肌肉锻炼的即时反馈和指导。一个疗程持续5-10分钟。电刺激治疗使用特制的带电极片的骨盆带被动刺激和收缩骨盆底肌肉。每次治疗15分钟,1个月内进行6次治疗。比较治疗前后盆底窘迫量表(PFDI-20)评分,包括POP窘迫量表6 (POPDI-6)、结直肠-肛门窘迫量表(CRAD-8)和尿窘迫量表6 (UDI-6)评分。按年龄、绝经期、体重指数(BMI)和分娩方式进行亚组分析。结果:本研究纳入了51例经BF和电刺激治疗的PFDs (SUI、POP、尿频或尿急或夜尿、疼痛)患者,平均年龄49.94±13.63岁。绝经16例(37.1%),平均绝经年龄50±5.20岁。26例(68.4%)有正常阴道分娩史。治疗前后PFDI-20平均评分分别为32.67分(标准差[SD] 10.05)和25.99分(SD 9.61) (P <0.001)。这种分数的下降反映了对症状和生活质量的主观认知的改善。治疗后POPDI-6、CRAD-8、UDI-6评分均显著降低。亚组分析中年龄、绝经期、BMI和分娩方式的评分变化无统计学意义。结论:该研究证明了BF和电刺激治疗女性PFDs的有效性。研究结果有助于了解治疗时间、患者特征和多模式方法的潜在益处。此外,该研究的多样化的参与者群体和有效的结果测量方法的使用增强了研究结果的普遍性和科学严谨性。
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引用次数: 0
Current insights into the interplay between gut microbiota-derived metabolites and metabolic-associated fatty liver disease. 肠道菌群衍生代谢物与代谢相关脂肪肝疾病之间相互作用的最新见解
IF 1.5 Q2 Medicine Pub Date : 2023-09-07 eCollection Date: 2023-10-01 DOI: 10.4103/tcmj.tcmj_122_23
Rachmad Anres Dongoran, Fang-Cen Tu, Chin-Hung Liu

Metabolic dysfunction-associated fatty liver disease (MAFLD) is a prevalent and challenging disease associated with a significant health and economic burden. MAFLD has been subjected to and widely investigated in many studies; however, the underlying pathogenesis and its progression have yet to understand fully. Furthermore, precise biomarkers for diagnosing and specific drugs for treatment are yet to be discovered. Increasing evidence has proven gut microbiota as the neglected endocrine organ that regulates homeostasis and immune response. Targeting gut microbiota is an essential strategy for metabolic diseases, including MAFLD. Gut microbiota in the gut-liver axis is connected through tight bidirectional links through the biliary tract, portal vein, and systemic circulation, producing gut microbiota metabolites. This review focuses on the specific correlation between gut microbiota metabolites and MAFLD. Gut microbiota metabolites are biologically active in the host and, through subsequent changes and biological activities, provide implications for MAFLD. Based on the review studies, gut-liver axis related-metabolites including short-chain fatty acids, bile acids (BAs), lipopolysaccharide, choline and its metabolites, indole and its derivates, branched-chain amino acids, and methionine cycle derivates was associated with MAFLD and could be promising MAFLD diagnosis biomarkers, as well as the targets for MAFLD new drug discovery.

代谢功能障碍相关脂肪性肝病(MAFLD)是一种流行且具有挑战性的疾病,与重大的健康和经济负担相关。许多研究都对mald进行了广泛的研究;然而,其潜在的发病机制及其进展尚未完全了解。此外,用于诊断的精确生物标志物和用于治疗的特异性药物尚未被发现。越来越多的证据表明,肠道微生物群是被忽视的调节体内平衡和免疫反应的内分泌器官。针对肠道微生物群是治疗代谢性疾病(包括MAFLD)的重要策略。肠肝轴上的肠道菌群通过胆道、门静脉、体循环等紧密双向连接,产生肠道菌群代谢物。本文综述了肠道菌群代谢物与MAFLD之间的具体关系。肠道微生物代谢物在宿主体内具有生物活性,并通过随后的变化和生物活性,为MAFLD提供了启示。综述发现,肝肠轴相关代谢产物包括短链脂肪酸、胆汁酸、脂多糖、胆碱及其代谢物、吲哚及其衍生物、支链氨基酸、蛋氨酸循环衍生物等与MAFLD相关,可能是MAFLD诊断的重要生物标志物,也是MAFLD新药开发的靶点。
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引用次数: 0
Restraint stress-associated gastrointestinal injury and implications from the Evans blue-fed restraint stress mouse model. 束缚应激相关胃肠道损伤及伊文思蓝喂养束缚应激小鼠模型的启示
IF 1.5 Q2 Medicine Pub Date : 2023-09-07 eCollection Date: 2024-01-01 DOI: 10.4103/tcmj.tcmj_101_23
Der-Shan Sun, Te-Sheng Lien, Hsin-Hou Chang

The association between stress and gastrointestinal (GI) tract diseases is well established, while the exact mechanism remains elusive. As a result, it is urgent to establish mouse models to investigate restraint stress-associated GI leakage, but current models have their limitations. A new Evans blue-fed restraint mouse model has recently been developed that allows researchers to study restraint stress-associated GI leakage in live animals. This review article will focus on this model, including its mechanisms, clinical implications, and applications for studying restraint stress-associated GI injury. Recent findings from studies using this model will also be highlighted, along with their potential for diagnosis and treatment. The article aims to discuss about current research and provide recommendations for further study, ultimately improving our understanding of the link between stress and GI injury and improving patient outcomes.

压力与胃肠道(GI)疾病之间的关系已得到公认,但其确切的机制却仍然难以捉摸。因此,迫切需要建立小鼠模型来研究束缚应激相关的胃肠道渗漏,但目前的模型有其局限性。最近开发出了一种新的伊文思蓝喂约束小鼠模型,研究人员可利用这种模型在活体动物中研究约束应激相关的胃肠道渗漏。本综述文章将重点介绍该模型,包括其机制、临床意义以及在研究束缚应激相关消化道损伤中的应用。文章还将重点介绍使用该模型进行研究的最新发现及其在诊断和治疗方面的潜力。文章旨在讨论当前的研究,并为进一步研究提供建议,最终提高我们对压力与消化道损伤之间联系的认识,改善患者的预后。
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引用次数: 0
Treating overactive bladder symptoms after transurethral prostatic surgery for benign prostatic hyperplasia - Which medication to choose? 治疗良性前列腺增生经尿道前列腺手术后膀胱过度活动症状-选择哪种药物?
IF 1.5 Q2 Medicine Pub Date : 2023-08-22 eCollection Date: 2023-10-01 DOI: 10.4103/tcmj.tcmj_123_23
Cheng-Ling Lee, Hann-Chorng Kuo

Objectives: Overactive bladder (OAB) symptoms are often encountered in patients after transurethral resection of the prostate (TUR-P) or transurethral incision of the prostate (TUI-P) for benign prostatic obstruction (BPO). Either antimuscarinics or β-3 agonist has been found effective in relieving OAB symptoms. However, urologists usually do not prescribe such medication immediately after TUR-P or TUI-P to avoid an increase in postvoid residual and risk of urinary tract infection. If OAB medication can be used and adverse events (AEs) can be reduced to minimum, patients' quality of life after bladder outlet obstruction surgery could be improved. This study compared the safety and efficacy between solifenacin and mirabegron in men undergoing TUR-P or TUI-P.

Materials and methods: This prospective, randomized trial compared the safety and efficacy of OAB medication on the reduction in Urgency Severity Score (USS), OAB Symptoms Score (OABSS), International Prostate Symptom Score, and urgency urinary incontinence episodes in men with BPO undergoing surgical intervention. All patients could void smoothly after catheter removal and were randomly received daily solifenacin 5 mg, mirabegron 50 mg, or no interventions for 4 weeks. At 2 and 4 weeks postoperatively, participants' OAB symptoms and AEs were evaluated.

Results: A total of 57 men were enrolled in this study with a mean age of 70.8 ± 6.1 years. At 2 weeks postoperatively, USS (1.56 ± 1.72 vs. 2.39 ± 1.72 vs. 2.26 ± 1.73, P < 0.011) and OABSS (5.33 ± 3.65 vs. 7.67 ± 4.19 vs. 8.58 ± 4.31, P < 0.000) were significantly reduced in patients taking solifenacin, mirabegron, or control, respectively. Two patients in the solifenacin group developed urinary retention. However, the changes of variables at 4 weeks postoperatively were insignificant among the three groups.

Conclusion: Solifenacin and mirabegron are two different drug classes both equally effective in treating immediate OAB symptoms after TUR-P or TUI-P. However, OAB symptoms could be relieved at 4 weeks without any medication. Considering AEs, β-3 agonist has a more favorable safety profile than antimuscarinics.

目的:膀胱过动(OAB)症状是经尿道前列腺切除术(turp)或经尿道前列腺切开(TUI-P)治疗良性前列腺梗阻(BPO)后常见的症状。抗毒蕈素或β-3激动剂均可有效缓解OAB症状。然而,泌尿科医生通常不会在turp或TUI-P后立即开这种药,以避免增加尿后残留和尿路感染的风险。如果能够使用OAB药物,并将不良事件(ae)降低到最低,则可以改善膀胱出口梗阻手术后患者的生活质量。本研究比较了索利那新和米拉贝龙在turp或TUI-P患者中的安全性和有效性。材料和方法:这项前瞻性随机试验比较了OAB药物对外科手术治疗的BPO患者急症严重程度评分(USS)、OAB症状评分(OABSS)、国际前列腺症状评分(International Prostate Symptom Score)和急症尿失禁发作降低的安全性和有效性。所有患者拔除导管后均能顺利排空,随机给予每日索利那新5 mg、米拉比格隆50 mg,或不干预4周。在术后2周和4周,评估参与者的OAB症状和ae。结果:共有57名男性入组,平均年龄70.8±6.1岁。术后2周,索利那新、米拉比格龙和对照组的USS(1.56±1.72∶2.39±1.72∶2.26±1.73,P < 0.011)和OABSS(5.33±3.65∶7.67±4.19∶8.58±4.31,P < 0.000)分别显著降低。索利那新组2例患者出现尿潴留。但三组术后4周各项指标变化均不显著。结论:索利那新与mirabegron是治疗turp或TUI-P术后即刻OAB症状的两种不同药物类别。然而,在没有任何药物的情况下,OAB症状可以在4周后缓解。考虑到ae, β-3激动剂比抗毒蕈素具有更有利的安全性。
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引用次数: 0
Diagnosis and treatment of female alopecia: Focusing on the iron deficiency-related alopecia. 女性脱发的诊断与治疗:以缺铁性脱发为重点。
IF 1.5 Q2 Medicine Pub Date : 2023-08-22 eCollection Date: 2023-10-01 DOI: 10.4103/tcmj.tcmj_95_23
Chia-Shuen Lin, Li-Yi Chan, Jen-Hung Wang, Chung-Hsing Chang

Objectives: Alopecia is a soft but meaningful complaint affecting women's physical and psychological health. Female alopecia (FA) has diverse etiologies. Nonetheless, FA is stereotyped as female pattern hair loss, also known as female androgenetic alopecia, and has not been thoroughly investigated. This study aimed to identify the etiologies of FA at a tertiary medical center in Eastern Taiwan.

Materials and methods: This retrospective study enrolled female patients with hair loss who visited the dermatology department of (blinded information). A complete history taking was obtained, including the onset and duration of alopecia, menstruation, gynecologic diseases, psychological stress, underlying diseases, vaccination, and dietary habits, etc., Blood tests were performed, including hemoglobin (Hb), ferritin, Zn, autoimmune and thyroid profiles, etc., Iron deficiency (ID) was defined as serum ferritin level <60 ng/mL. The hair condition, ferritin, and Hb levels were monitored every 3 months after supplementation.

Results: A total of 155 patients were recruited. The etiologies of FA were diverse; the top five etiologies were nutrient deficiencies (83.9%), autoimmune (14.8%) and thyroid (7.7%) diseases, psychological stress (12.3%), and coronavirus disease 2019 (COVID-19) vaccination (6.5%). ID accounted for 70.3% of cases. The disease duration was an important prognostic factor for the improvement of serum ferritin. Patients with subjective improvement of hair regrowth also had more increase of ferritin levels after iron supplementation. The corresponding ferritin level for female anemia (Hb: 12.0 g/dL) was 5.1 ng/mL, lower than the adequate level for hair growth (40-60 ng/mL), the corresponding Hb level of which was 13.1-13.8 g/dL.

Conclusion: The causes of FA varied, including nutrient deficiencies, autoimmune diseases, psychological stress, thyroid diseases, and COVID-19 vaccination, etc., Therefore, a complete survey before treatment is essential. Seventy percentage of FA cases were ID-FA. We suggest to redefine the serum ferritin level ≥60 ng/mL, with the corresponding Hb ≥13.0 g/dL as the normal range for early diagnosis. Initiation of iron supplementation within 6 months would result in a better prognosis.

目的:脱发是一种影响女性身心健康的软而有意义的主诉。女性脱发(FA)有多种病因。尽管如此,FA被定型为女性型脱发,也被称为女性雄激素性脱发,并没有得到彻底的研究。本研究旨在了解台湾东部某三级医疗中心的FA病因。材料与方法:本研究采用回顾性研究方法,招募了就诊于(盲法资料)皮肤科的女性脱发患者。收集完整的病史,包括脱发的发病和持续时间、月经、妇科疾病、心理应激、基础疾病、疫苗接种、饮食习惯等,进行血液检查,包括血红蛋白(Hb)、铁蛋白、锌、自身免疫和甲状腺等,将铁蛋白缺乏症(ID)定义为血清铁蛋白水平。FA的病因多种多样;排在前五位的病因分别是营养缺乏(83.9%)、自身免疫性疾病(14.8%)和甲状腺疾病(7.7%)、心理应激(12.3%)和2019冠状病毒病(COVID-19)疫苗接种(6.5%)。身份证占70.3%。病程是影响血清铁蛋白改善的重要预后因素。主观头发再生改善的患者在补铁后铁蛋白水平也有更多的提高。女性贫血对应的铁蛋白水平(Hb: 12.0 g/dL)为5.1 ng/mL,低于毛发生长所需的铁蛋白水平(40 ~ 60 ng/mL),而毛发生长所需的铁蛋白水平为13.1 ~ 13.8 g/dL。结论:FA的病因多种多样,包括营养缺乏、自身免疫性疾病、心理应激、甲状腺疾病、COVID-19疫苗接种等,治疗前进行全面调查是必要的。70%的FA病例为ID-FA。我们建议重新定义血清铁蛋白水平≥60 ng/mL,相应的Hb≥13.0 g/dL作为早期诊断的正常范围。6个月内开始补铁可获得较好的预后。
{"title":"Diagnosis and treatment of female alopecia: Focusing on the iron deficiency-related alopecia.","authors":"Chia-Shuen Lin, Li-Yi Chan, Jen-Hung Wang, Chung-Hsing Chang","doi":"10.4103/tcmj.tcmj_95_23","DOIUrl":"10.4103/tcmj.tcmj_95_23","url":null,"abstract":"<p><strong>Objectives: </strong>Alopecia is a soft but meaningful complaint affecting women's physical and psychological health. Female alopecia (FA) has diverse etiologies. Nonetheless, FA is stereotyped as female pattern hair loss, also known as female androgenetic alopecia, and has not been thoroughly investigated. This study aimed to identify the etiologies of FA at a tertiary medical center in Eastern Taiwan.</p><p><strong>Materials and methods: </strong>This retrospective study enrolled female patients with hair loss who visited the dermatology department of (blinded information). A complete history taking was obtained, including the onset and duration of alopecia, menstruation, gynecologic diseases, psychological stress, underlying diseases, vaccination, and dietary habits, etc., Blood tests were performed, including hemoglobin (Hb), ferritin, Zn, autoimmune and thyroid profiles, etc., Iron deficiency (ID) was defined as serum ferritin level <60 ng/mL. The hair condition, ferritin, and Hb levels were monitored every 3 months after supplementation.</p><p><strong>Results: </strong>A total of 155 patients were recruited. The etiologies of FA were diverse; the top five etiologies were nutrient deficiencies (83.9%), autoimmune (14.8%) and thyroid (7.7%) diseases, psychological stress (12.3%), and coronavirus disease 2019 (COVID-19) vaccination (6.5%). ID accounted for 70.3% of cases. The disease duration was an important prognostic factor for the improvement of serum ferritin. Patients with subjective improvement of hair regrowth also had more increase of ferritin levels after iron supplementation. The corresponding ferritin level for female anemia (Hb: 12.0 g/dL) was 5.1 ng/mL, lower than the adequate level for hair growth (40-60 ng/mL), the corresponding Hb level of which was 13.1-13.8 g/dL.</p><p><strong>Conclusion: </strong>The causes of FA varied, including nutrient deficiencies, autoimmune diseases, psychological stress, thyroid diseases, and COVID-19 vaccination, etc., Therefore, a complete survey before treatment is essential. Seventy percentage of FA cases were ID-FA. We suggest to redefine the serum ferritin level ≥60 ng/mL, with the corresponding Hb ≥13.0 g/dL as the normal range for early diagnosis. Initiation of iron supplementation within 6 months would result in a better prognosis.</p>","PeriodicalId":45873,"journal":{"name":"Tzu Chi Medical Journal","volume":null,"pages":null},"PeriodicalIF":1.5,"publicationDate":"2023-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10683524/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76997267","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cystoscopic characteristic findings of interstitial cystitis and clinical implications. 间质性膀胱炎的膀胱镜特征性发现及其临床意义。
IF 1.5 Q2 Medicine Pub Date : 2023-08-22 eCollection Date: 2024-01-01 DOI: 10.4103/tcmj.tcmj_172_23
Wan-Ru Yu, Yuan-Hong Jiang, Jia-Fong Jhang, Hann-Chorng Kuo

Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic inflammatory bladder disease of unknown etiology, characterized by bladder pain and frequency urgency symptoms. Based on the cystoscopic findings after hydrodistention under anesthesia, the phenotype of IC/BPS includes no glamerulation, characteristic glomerulation, and with Hunner's lesion. IC is specifically defined if there are characteristic Hunner's lesion appeared in cystoscopy or after hydrodistention. If there are glomerulations without Hunner's lesion, BPS should be considered. The definition of Hunner's lesion and glomerulations differs based on different definition and observations. Currently, there has been no clear description and grading of the glomerulations and Hunner's lesion. Because the classification of IC/BPS has an impact on the treatment strategy and associated with therapeutic outcome, it is unmet to have a clear definition and consensus on the characteristic cystoscopic findings of IC/BPS. This article reviews the literature and presents the figures of Hunner's lesions and description of different mucosal lesions after cystoscopic hydrodistention.

间质性膀胱炎/膀胱疼痛综合征(IC/BPS)是一种病因不明的慢性膀胱炎性疾病,以膀胱疼痛和尿频尿急症状为特征。根据麻醉下膀胱水肿术后的膀胱镜检查结果,IC/BPS 的表型包括无肾盂积水、特征性肾盂积水和伴有 Hunner 病变。如果膀胱镜检查或肾积水后出现特征性的 Hunner 病变,则明确定义为 IC。如果有肾小球但无 Hunner 病变,则应考虑 BPS。根据不同的定义和观察结果,Hunner 病变和肾小球的定义也有所不同。目前,对肾小球和 Hunner 病变还没有明确的描述和分级。由于 IC/BPS 的分级对治疗策略有影响,并与治疗效果相关,因此对 IC/BPS 的特征性膀胱镜检查结果有一个明确的定义并达成共识仍是一个未知数。本文回顾了相关文献,介绍了膀胱镜水滞留术后 Hunner 病变的图像和不同粘膜病变的描述。
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引用次数: 0
Intrabony defect management with a bone graft (hydroxyapatite and β-tricalcium phosphate) alone and in combination with a diode laser: A randomized control trial. 骨移植(羟基磷灰石和β-磷酸三钙)单独和联合二极管激光治疗骨内缺损:一项随机对照试验。
IF 1.5 Q2 Medicine Pub Date : 2023-07-12 eCollection Date: 2023-10-01 DOI: 10.4103/tcmj.tcmj_316_22
K C Vinaya, Vaibhav Awinashe, Dipak Baliram Patil, Prashant Babaji, Nazargi Mahabob, B Kaushik Shetty, Anuj Singh Parihar

Objectives: The current research was conducted to evaluate the use of a diode laser and a bone graft (hydroxyapatite [HA] + β-tricalcium phosphate [β-TCP]) in healing of intrabony defects.

Materials and methods: In this split-mouth evaluation, 40 patients with bilateral intrabony defects were treated with, Group I (control) - bone graft alone (HA + β-TCP) and Group II, (test) - bone graft with a diode laser. The clinical and radiologic parameters of all patients, such as plaque index (PI), probing depth (PD), gingival index (GI), gingival recession (GR), and relative clinical attachment level (RCAL) were recorded at baseline, after 3 months and after 6 months.

Results: Reductions in PI, PD, GI, GR, and RCAL were found after 6 months. Furthermore, significant differences were displayed in the intra-group comparison while those of the inter-group evaluation (P > 0.05) were insignificant.

Conclusion: In both groups, considerable decrease in intrabony pockets was discovered; however, the inter-group comparison was insignificant in relation to GR and RCAL.

目的:本研究旨在评价二极管激光和骨移植物(羟基磷灰石[HA] + β-磷酸三钙[β-TCP])在骨内缺损愈合中的应用。材料与方法:本实验选取40例双侧骨内缺损患者,分别采用ⅰ组(对照组)-单纯骨移植(HA + β-TCP)和ⅱ组(试验组)-二极管激光骨移植治疗。记录所有患者的临床和影像学参数,如牙菌斑指数(PI)、探诊深度(PD)、牙龈指数(GI)、牙龈退行度(GR)和相对临床附着水平(RCAL),分别在基线、3个月和6个月后。结果:6个月后PI、PD、GI、GR、RCAL均有所下降。组内比较差异有统计学意义,组间比较差异无统计学意义(P > 0.05)。结论:两组患者骨内囊明显减少;而GR和RCAL组间比较不显著。
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引用次数: 0
Application of transcranial brain stimulation in dementia. 经颅脑刺激在痴呆中的应用。
IF 1.5 Q2 Medicine Pub Date : 2023-07-12 eCollection Date: 2023-10-01 DOI: 10.4103/tcmj.tcmj_91_23
Yuncin Luo, Feng-Yi Yang, Raymond Y Lo

The number of patients with dementia grows rapidly as the global population ages, which posits tremendous health-care burden to the society. Only cholinesterase inhibitors and a N-methyl-D-aspartate receptor antagonist have been approved for treating patients with Alzheimer's disease (AD), and their clinical effects remained limited. Medical devices serve as an alternative therapeutic approach to modulating neural activities and enhancing cognitive function. Four major brain stimulation technologies including deep brain stimulation (DBS), transcranial magnetic stimulation (TMS), transcranial direct current stimulation (tDCS), and transcranial ultrasound stimulation (TUS) have been applied to AD in a clinical trial setting. DBS allows electrical stimulation at the specified nucleus but remains resource-demanding, and after all, an invasive surgery; whereas TMS and tDCS are widely available and affordable but less ideal with respect to localization. The unique physical property of TUS, on the other hand, allows both thermal and mechanical energy to be transduced and focused for neuromodulation. In the context of dementia, using focused ultrasound to induce blood-brain barrier opening for delivering drugs and metabolizing amyloid protein has drawn great attention in recent years. Furthermore, low-intensity pulsed ultrasound has demonstrated its neuroprotective effects in both in vitro and in vivo studies, leading to ongoing clinical trials for AD. The potential and limitation of transcranial brain stimulation for treating patients with dementia would be discussed in this review.

随着全球人口老龄化,痴呆症患者数量迅速增长,给社会带来了巨大的医疗负担。只有胆碱酯酶抑制剂和n -甲基- d -天冬氨酸受体拮抗剂已被批准用于治疗阿尔茨海默病(AD)患者,其临床效果仍然有限。医疗器械是调节神经活动和增强认知功能的一种替代治疗方法。脑深部电刺激(DBS)、经颅磁刺激(TMS)、经颅直流电刺激(tDCS)和经颅超声刺激(TUS)四种主要的脑刺激技术已经在临床试验中应用于AD。DBS允许对特定的核进行电刺激,但仍然需要资源,毕竟是一种侵入性手术;而TMS和tDCS广泛可用且价格合理,但在本地化方面不太理想。另一方面,TUS独特的物理性质允许热能和机械能被转导并集中用于神经调节。在痴呆的背景下,利用聚焦超声诱导血脑屏障打开以传递药物和代谢淀粉样蛋白近年来备受关注。此外,低强度脉冲超声在体外和体内研究中都证明了其神经保护作用,因此正在进行阿尔茨海默病的临床试验。本综述将讨论经颅脑刺激治疗痴呆患者的潜力和局限性。
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引用次数: 0
Roles of gut microbes in metabolic-associated fatty liver disease. 肠道微生物在代谢相关脂肪肝疾病中的作用
IF 1.5 Q2 Medicine Pub Date : 2023-07-11 eCollection Date: 2023-10-01 DOI: 10.4103/tcmj.tcmj_86_23
Chun-Yao Chen, Han-Chen Ho

Metabolic-associated fatty liver disease (MAFLD) is the most common chronic liver disease. Gut dysbiosis is considered a significant contributing factor in disease development. Increased intestinal permeability can be induced by gut dysbiosis, followed by the entry of lipopolysaccharide into circulation to reach peripheral tissue and result in chronic inflammation. We reviewed how microbial metabolites push host physiology toward MAFLD, including short-chain fatty acids (SCFAs), bile acids, and tryptophan metabolites. The effects of SCFAs are generally reported as anti-inflammatory and can improve intestinal barrier function and restore gut microbiota. Gut microbes can influence intestinal barrier function through SCFAs produced by fermentative bacteria, especially butyrate and propionate producers. This is achieved through the activation of free fatty acid sensing receptors. Bile is directly involved in lipid absorption. Gut microbes can alter bile acid composition by bile salt hydrolase-producing bacteria and bacterial hydroxysteroid dehydrogenase-producing bacteria. These bile acids can affect host physiology by activating farnesoid X receptor Takeda G protein-coupled receptor 5. Gut microbes can also induce MAFLD-associated symptoms by producing tryptophan metabolites kynurenine, serotonin, and indole-3-propionate. A summary of bacterial genera involved in SCFAs production, bile acid transformation, and tryptophan metabolism is provided. Many bacteria have demonstrated efficacy in alleviating MAFLD in animal models and are potential therapeutic candidates for MAFLD.

代谢性脂肪性肝病(MAFLD)是最常见的慢性肝病。肠道生态失调被认为是疾病发展的重要因素。肠道生态失调可引起肠通透性增加,随后脂多糖进入循环到达外周组织,导致慢性炎症。我们综述了微生物代谢物如何推动宿主生理向MAFLD发展,包括短链脂肪酸(SCFAs)、胆汁酸和色氨酸代谢物。SCFAs的作用通常被报道为抗炎,可以改善肠道屏障功能和恢复肠道微生物群。肠道微生物可以通过发酵菌,尤其是丁酸和丙酸菌产生的SCFAs影响肠道屏障功能。这是通过激活游离脂肪酸感应受体实现的。胆汁直接参与脂质吸收。肠道微生物可以通过胆盐水解酶产生菌和细菌羟基类固醇脱氢酶产生菌改变胆汁酸组成。这些胆汁酸可以通过激活法脂类X受体Takeda G蛋白偶联受体5来影响宿主生理。肠道微生物也可以通过产生色氨酸代谢物犬尿氨酸、血清素和吲哚-3-丙酸来诱导mafld相关症状。综述了参与SCFAs生产、胆汁酸转化和色氨酸代谢的细菌属。许多细菌已经在动物模型中证明了减轻MAFLD的功效,并且是潜在的MAFLD治疗候选者。
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引用次数: 0
Reliability and validity of the Taiwanese version of the collaborative practice assessment tool: A pilot study. 台湾版合作实践评估工具的信度与效度:初步研究。
IF 1.5 Q2 Medicine Pub Date : 2023-07-01 DOI: 10.4103/tcmj.tcmj_200_22
Chen-Pei Ho, Hsiu-Chen Yeh, Ming-Shinn Lee, Wei-Chun Cheng

Objectives: To promote teamwork communication and collaboration between health-care professionals, educators emphasized proper training programs to develop interprofessional collaborative practice (IPCP) among postgraduate (PG) trainees. A literature review indicated that the faculty necessarily measured the competency in IPCP with structured and applicable assessment tools in collocation to training programs domestically. A cross-sectional psychometric study was conducted to construct a reliable assessment tool for measuring PG learning outcome in Taiwan through a bidirectional translation. The study aimed to assess the interprofessional team behavior of trainees using the Taiwanese version of the collaborative practice assessment tool (T-CPAT).

Materials and methods: The study recruited 43 participants to undergo a PG training program in a single institute and to complete T-CPAT. Data were analyzed using SPSS 22.0 software. We employed descriptive analysis of demographic variables. The validity of T-CPAT was analyzed by experts in different specialties and its availability was assessed by item-level analysis. Furthermore, the T-CPAT reliability was tested using Cronbach's α.

Results: The average score was 305.2 (standard deviation = 38.08), and the expert validity of the T-CPAT was 0.96. In the item-level analysis, there were no failure items in T-CAPT. Cronbach's α reached 0.94 (95% confidence interval = 0.90-0.96).

Conclusion: The study demonstrated good reliability and validity for the T-CPAT. Thus, the T-CPAT can be used to accurately measure and assess the competence of IPCP in PG trainees in general medicine in Taiwan. The results were deemed sufficient to provide faculties with related arrangements for future teaching plans.

目的:为了促进卫生保健专业人员之间的团队沟通和协作,教育工作者强调了适当的培训计划,以培养研究生(PG)学员的跨专业协作实践(IPCP)。文献综述表明,在国内的培训项目中,教师必须使用结构化和适用的评估工具来衡量IPCP的能力。本研究以横断面心理测量学为研究对象,透过双向翻译,建构一个可靠的评估工具来测量台湾地区PG学习效果。本研究旨在运用台湾版合作实践评估工具(T-CPAT)评估实习生的跨专业团队行为。材料和方法:本研究招募了43名参与者在一个机构接受PG培训计划并完成T-CPAT。数据分析采用SPSS 22.0软件。我们采用人口统计变量的描述性分析。采用不同专业的专家分析T-CPAT的效度,采用项目水平分析评估其有效性。采用Cronbach’s α检验T-CPAT信度。结果:T-CPAT的平均得分为305.2分(标准差为38.08),专家效度为0.96。在项目层面分析中,T-CAPT不存在不合格项目。Cronbach’s α达到0.94(95%置信区间= 0.90-0.96)。结论:T-CPAT具有良好的信度和效度。因此,T-CPAT可以准确地衡量和评估台湾全科医学PG学员的IPCP能力。研究结果足以为院系未来的教学计划作出相关安排。
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Tzu Chi Medical Journal
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