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Pediatric Finger Warts Treated Using Taeeumjowi-tang: a case report. 使用太阴九味汤治疗小儿手指疣:病例报告。
IF 1.2 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-06-30 DOI: 10.3831/KPI.2024.27.2.172
Yeon-Kyoung Pak, Sang-Won Shin

Warts caused by the human papillomavirus (HPV) are generally treated with cryotherapy, CO2 laser ablation, interferon injections, and bleomycin injections. However, it is sometimes difficult to treat children because the treatment can be painful. In addition, recurrence may occur after treatment. In this study, warts completely disappeared following the administration of herbal medicine in two children, with warts in multiple parts of the hands and around the nails. Two pediatric patients visited the hospital for treatment of warts around their fingers and nails. Both patients received Taeeumjowi-tang (TJT) as a decoction for 60 days. TJT was performed twice per day for the 11-year-old patient and once per day for the 7-year-old patient. Patient progress was observed monthly, and the visual condition of the warts was photographed during the visits. After approximately two months of treatment, the warts disappeared from the fingers and nails of both patients. This case study suggests that the oral administration of TJT may be effective for pediatric patients with warts. Further studies are required to determine the efficacy and safety of these therapies.

由人类乳头瘤病毒(HPV)引起的疣一般采用冷冻疗法、二氧化碳激光消融术、干扰素注射和博莱霉素注射进行治疗。但是,由于治疗过程可能很痛苦,因此有时很难对儿童进行治疗。此外,治疗后还可能复发。在这项研究中,有两名儿童在服用中药后疣完全消失,他们的疣分布在手部多个部位和指甲周围。两名儿童患者因手指和指甲周围长有疣而到医院就诊。两名患者均接受了为期 60 天的太阴九味汤(Taeeumjowi-tang,TJT)煎剂治疗。11 岁的患者每天服用两次,7 岁的患者每天服用一次。每月观察患者的病情进展,并在就诊时拍摄疣体的外观状况。经过大约两个月的治疗,两名患者的手指和指甲上的疣都消失了。本病例研究表明,口服 TJT 对儿童尖锐湿疣患者可能有效。要确定这些疗法的疗效和安全性,还需要进一步的研究。
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引用次数: 0
Toxicity Assessment of a No-Pain Pharmacopuncture Extract Using a Standard Battery of In Vitro Chromosome Aberration Tests. 使用标准体外染色体畸变测试组合评估无痛药刺提取物的毒性
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-31 DOI: 10.3831/KPI.2024.27.1.38
Ji Hye Hwang

Objectives: Genotoxicity is evaluated through a chromosomal aberration test using cultured mammalian cells to determine the toxicity of no-pain pharmacopuncture (NPP), which has recently been used to treat musculoskeletal pain disorders in Korean medical clinical practice.

Methods: An initial test was performed to determine the dosage range of the NPP, followed by the main test. In this study, NPP doses of 10.0, 5.0, and 2.5%, and negative and positive controls were tested. An in vitro chromosome aberration test was performed using Chinese hamster lung cells under short-term treatment with or without metabolic activation and under continuous treatment without metabolic activation.

Results: Compared with the saline negative control group, NPP did not significantly increase the frequency of chromosomal abnormalities in Chinese hamster lung cells, regardless of the presence or absence of metabolic activation. Additionally, the number of cells with structural chromosomal abnormalities was significantly higher in the positive control group than that in the negative control group that received saline.

Conclusion: Based on the above results, the chromosomal abnormality-producing effect of NPP was determined to be negative under these test conditions.

目的:通过使用培养的哺乳动物细胞进行染色体畸变试验评估遗传毒性,以确定无痛药刺(NPP)的毒性:方法:先进行初步试验,确定 NPP 的剂量范围,然后进行主要试验。本研究测试了 10.0%、5.0%、2.5% 的 NPP 剂量以及阴性和阳性对照。使用中国仓鼠肺细胞进行了体外染色体畸变试验,试验条件为短期处理(含或不含代谢活化)和连续处理(不含代谢活化):结果:与生理盐水阴性对照组相比,无论有无代谢活化,NPP 都不会显著增加中国仓鼠肺细胞染色体异常的频率。此外,阳性对照组中染色体结构异常的细胞数量明显高于接受生理盐水的阴性对照组:根据上述结果,在这些试验条件下,NPP 的染色体异常产生效应被确定为阴性。
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引用次数: 0
Enhanced Drug Carriage Efficiency of Curcumin-Loaded PLGA Nanoparticles in Combating Diabetic Nephropathy via Mitigation of Renal Apoptosis. 通过缓解肾脏凋亡提高姜黄素载体聚乳酸(PLGA)纳米颗粒在防治糖尿病肾病中的载药效率
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-31 DOI: 10.3831/KPI.2024.27.1.1
Asmita Samadder, Banani Bhattacharjee, Sudatta Dey, Arnob Chakrovorty, Rishita Dey, Priyanka Sow, Debojyoti Tarafdar, Maharaj Biswas, Sisir Nandi

Objectives: The Curcuma-derived diferuloylmethane compound CUR, loaded on Poly (lactide-co-glycolic) acid (PLGA) nanoparticles was utilized to combat DN-induced renal apoptosis by selectively targeting and modulating Bcl2.

Methods: Upon in silico molecular docking and screening study CUR was selected as the core phytocompound for nanoparticle formulation. PLGA-nano-encapsulated-curcumin (NCUR) were synthesized following standard solvent displacement method. The NCUR were characterized for shape, size and other physico-chemical properties by Atomic Force Microscopy (AFM), Dynamic Light Scattering (DLS) and Fourier-Transform Infrared (FTIR) Spectroscopy studies. For in vivo validation of nephro-protective effects, Mus musculus were pre-treated with CUR at a dose of 50 mg/kg b.w. and NCUR at a dose of 25 mg/kg b.w. (dose 1), 12.5 mg/kg b.w (dose 2) followed by alloxan administration (100 mg/kg b.w) and serum glucose levels, histopathology and immunofluorescence study were conducted.

Results: The in silico study revealed a strong affinity of CUR towards Bcl2 (dock score -10.94 Kcal/mol). The synthesized NCUR were of even shape, devoid of cracks and holes with mean size of ~80 nm having -7.53 mV zeta potential. Dose 1 efficiently improved serum glucose levels, tissue-specific expression of Bcl2 and reduced glomerular space and glomerular sclerosis in comparison to hyperglycaemic group.

Conclusion: This study essentially validates the potential of NCUR to inhibit DN by reducing blood glucose level and mitigating glomerular apoptosis by selectively promoting Bcl2 protein expression in kidney tissue.

研究目的通过选择性靶向和调节 Bcl2,将莪术提取的二硬脂酰甲烷化合物 CUR 添加到聚乳酸(PLGA)纳米颗粒上,用于对抗 DN 诱导的肾脏凋亡:方法:经过硅学分子对接和筛选研究,CUR被选为纳米颗粒配方的核心植物化合物。采用标准溶剂置换法合成了 PLGA 纳米包囊姜黄素(NCUR)。通过原子力显微镜(AFM)、动态光散射(DLS)和傅立叶变换红外光谱(FTIR)研究,对 NCUR 的形状、大小和其他物理化学特性进行了表征。为了在体内验证肾脏保护作用,预先用 50 毫克/千克体重剂量的 CUR 和 25 毫克/千克体重剂量(剂量 1)、12.5 毫克/千克体重剂量(剂量 2)的 NCUR 处理麝鼠,然后给予阿脲(100 毫克/千克体重),并进行血糖水平、组织病理学和免疫荧光研究:硅学研究表明,CUR 对 Bcl2 有很强的亲和力(对接得分 -10.94 Kcal/mol)。合成的 NCUR 形状均匀,没有裂缝和孔洞,平均大小约为 80 nm,zeta 电位为 -7.53 mV。与高血糖组相比,剂量 1 能有效改善血清葡萄糖水平、Bcl2 的组织特异性表达、减少肾小球空间和肾小球硬化:本研究从本质上验证了 NCUR 通过降低血糖水平抑制 DN 的潜力,并通过选择性促进肾组织中 Bcl2 蛋白的表达来减轻肾小球凋亡。
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引用次数: 0
A Case Report of Prolonged Hemorrhage Following Traditional Phlebotomy (Fasd). 传统抽血术(Fasd)后出血时间延长的病例报告。
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-31 DOI: 10.3831/KPI.2024.27.1.47
Sajjad Sadeghi

Phlebotomy, a therapeutic method of bloodletting typically performed using a needle, has a traditional technique known as "Fasd." In this method, blood is extracted by creating a longitudinal incision on a vein (3-5 mm) with a surgical scalpel blade, usually blade No. 11. Due to the incision in the vessel wall, establishing hemostasis is more challenging compared to conventional methods. Hemostasis is usually achieved within minutes after Fasd. We present a case highlighting an uncommon yet significant complication of traditional phlebotomy. A 55-year-old man with no prior medical conditions underwent traditional phlebotomy at an academic traditional medicine clinic. Senior MD-PhD students in Iranian Traditional Medicine, under professor supervision, performed Fasd. A sterile scalpel blade No. 11 was used to create a longitudinal incision of approximately 4 mm on the patient's median basilic vein in the right hand. After removing 400 cc of blood, a pressure dressing was applied to the incision site. Despite attempts such as hand elevation, ice pack application, prolonged direct pressure, and tight elastic bandaging, bleeding from the incision persisted. After an hour of supportive therapy, hemostasis was eventually achieved within a few minutes using burnt cotton dressing (a traditional method for blood hemostasis). Following intravenous hydration, the patient was discharged in stable condition and reported no issues during the one-month follow-up. The traditional phlebotomy (Fasd) carries the risk of serious complications, including uncontrolled and prolonged bleeding. Further research on the efficacy and safety of burnt cotton dressing for controlling hemostasis is recommended.

抽血术是一种通常使用针头进行放血的治疗方法,其传统技术称为 "Fasd"。在这种方法中,用外科手术刀片(通常是 11 号刀片)在静脉上切开一个纵向切口(3-5 毫米)来抽取血液。由于切口在血管壁上,止血的难度比传统方法更大。通常在 Fasd 术后几分钟内就能止血。我们介绍了一个病例,该病例强调了传统抽血术中一种不常见但却很重要的并发症。一名 55 岁的男性在一家传统医学学术诊所接受了传统抽血术。伊朗传统医学的医学博士高年级学生在教授的指导下进行了 Fasd 抽血。使用 11 号无菌手术刀在患者右手正中基底静脉上切开一个约 4 毫米的纵向切口。抽出 400 毫升血液后,在切口部位进行了加压包扎。尽管尝试了抬高手部、使用冰袋、长时间直接加压和紧绷弹力绷带等方法,但切口处的出血仍在持续。经过一个小时的支持治疗,最终在几分钟内用烧焦的棉花敷料(一种传统的止血方法)止住了血。静脉补液后,患者病情稳定出院,并在一个月的随访中未报告任何问题。传统的抽血术(Fasd)存在严重并发症的风险,包括无法控制的长时间出血。建议进一步研究烧灼棉敷料控制止血的有效性和安全性。
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引用次数: 0
A Case Study of Stress-Induced Alopecia Areata Treated with Hominis Placenta Pharmacopunture. 使用人胎素药剂治疗压力引起的脱发病例研究。
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-31 DOI: 10.3831/KPI.2024.27.1.53
Yeon Woo Song, Seo Young Kang, Chae Won Kang, Seok Hee Kim, Kyung Jin Lee, Yeon Ju Kim, Jong Uk Kim, Tae Han Yook

The purpose of this study is to report the clinical application of Hominis Placenta Pharmacopunture for Alopecia areata. Patient was diagnosed as stress-induced Alopecia areata 1 years ago. To reduce symptom, we treated a patient 8 times using Hominis Placenta Pharmacopunture. Hominis Placenta was injected subcutaneously into the lesion of head scalp alopecia. According to photographs, the lesion had been replaced with new terminal hair and the size of the lesion had decreased. This case has shown that stress-induced Alopecia areata patient could be treated by Hominis Placenta Pharmacopunture.

本研究的目的是报告Hominis Placenta Pharmacopunture在治疗脱发症方面的临床应用。患者于1年前被诊断为压力性脱发。为了减轻症状,我们使用人胎素药物疗法对患者进行了8次治疗。我们将胎盘素皮下注射到头部头皮脱发的病变部位。根据照片显示,病变部位已被新的顶发取代,病变部位的面积也有所缩小。该病例表明,压力引起的脱发症患者可以通过人胎盘素药物疗法进行治疗。
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引用次数: 0
Pharmacoacupuncture for the Treatment of Frozen Shoulder: protocol for a systematic review and meta-analysis. 药物针灸治疗肩周炎:系统综述和荟萃分析方案。
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-31 DOI: 10.3831/KPI.2024.27.1.14
Ji-Ho Lee, Hyeon-Sun Park, Sang-Hyeon Park, Dong-Ho Keum, Seo-Hyun Park

Objectives: Frozen shoulder (FS) is one of the most challenging shoulder disorders for patients and clinicians. Its symptoms mainly include any combination of stiffness, nocturnal pain, and limitation of active and passive glenohumeral joint movement. Conventional treatment options for FS are physical therapy, nonsteroidal anti-inflammatory drugs, injection therapy, and arthroscopic capsular release, but adverse and limited effects continue to present problems. As a result, pharmacoacupuncture (PA) is getting attention as an alternative therapy for patients with FS. PA is a new form of acupuncture treatment in traditional Korean medicine (TKM) that is mainly used for musculoskeletal diseases. It has similarity and specificity compared to corticosteroid injection and hydrodilatation, making it a potential alternative injection therapy for FS. However, no systematic reviews investigating the utilization of PA for FS have been published. Therefore, this review aims to standardize the clinical use of PA for FS and validate its therapeutic effect.

Methods: The protocol was registered in Prospero (CRD42023445708) on 18 July 2023. Until Aug. 31, 2023, seven electronic databases will be searched for randomized controlled trials of PA for FS. Authors will be contacted, and manual searches will also be performed. Two reviewers will independently screen and collect data from retrieved articles according to predefined criteria. The primary outcome will be pain intensity, and secondary outcomes will be effective rate, Constant-Murley Score, Shoulder Pain and Disability Index, range of motion, quality of life, and adverse events. Bias and quality of the included trials will be assessed using the Cochrane handbook's risk-of-bias tool for randomized trials. Meta analyses will be conducted using Review Manager V.5.3 software. GRADE will be used to evaluate the level of evidence for each outcome.

Results: This systematic review and meta-analysis will be conducted following PRISMA statement. The results will be published in a peer-reviewed journal.

Conclusion: This review will provide scientific evidence to support health insurance policy as well as the standardization of PA in clinical practice.

目的:肩周炎(FS)是对患者和临床医生最具挑战性的肩部疾病之一。其症状主要包括僵硬、夜间疼痛、主动和被动盂肱关节活动受限。FS的传统治疗方法包括物理疗法、非甾体抗炎药物、注射疗法和关节镜关节囊松解术,但其不良反应和有限的疗效仍是问题所在。因此,作为FS患者的替代疗法,药物针灸(PA)受到了关注。药针是韩国传统医学(TKM)中的一种新型针灸疗法,主要用于治疗肌肉骨骼疾病。与皮质类固醇注射和水动力扩张相比,PA具有相似性和特异性,因此有可能成为FS的替代注射疗法。然而,目前还没有关于 PA 用于 FS 的系统性综述。因此,本综述旨在规范 PA 在 FS 中的临床应用,并验证其治疗效果:该方案于 2023 年 7 月 18 日在 Prospero(CRD42023445708)注册。在 2023 年 8 月 31 日之前,将在 7 个电子数据库中搜索 PA 治疗 FS 的随机对照试验。将与作者联系,并进行人工检索。两名审稿人将根据预先确定的标准独立筛选和收集检索到的文章数据。主要结果为疼痛强度,次要结果为有效率、Constant-Murley 评分、肩痛与残疾指数、活动范围、生活质量和不良事件。将使用 Cochrane 手册中的随机试验偏倚风险工具对纳入试验的偏倚和质量进行评估。将使用 Review Manager V.5.3 软件进行元分析。将使用 GRADE 评估每个结果的证据水平:本系统综述和荟萃分析将按照 PRISMA 声明进行。结果将发表在同行评审期刊上:本综述将为医疗保险政策以及临床实践中的PA标准化提供科学依据。
{"title":"Pharmacoacupuncture for the Treatment of Frozen Shoulder: protocol for a systematic review and meta-analysis.","authors":"Ji-Ho Lee, Hyeon-Sun Park, Sang-Hyeon Park, Dong-Ho Keum, Seo-Hyun Park","doi":"10.3831/KPI.2024.27.1.14","DOIUrl":"10.3831/KPI.2024.27.1.14","url":null,"abstract":"<p><strong>Objectives: </strong>Frozen shoulder (FS) is one of the most challenging shoulder disorders for patients and clinicians. Its symptoms mainly include any combination of stiffness, nocturnal pain, and limitation of active and passive glenohumeral joint movement. Conventional treatment options for FS are physical therapy, nonsteroidal anti-inflammatory drugs, injection therapy, and arthroscopic capsular release, but adverse and limited effects continue to present problems. As a result, pharmacoacupuncture (PA) is getting attention as an alternative therapy for patients with FS. PA is a new form of acupuncture treatment in traditional Korean medicine (TKM) that is mainly used for musculoskeletal diseases. It has similarity and specificity compared to corticosteroid injection and hydrodilatation, making it a potential alternative injection therapy for FS. However, no systematic reviews investigating the utilization of PA for FS have been published. Therefore, this review aims to standardize the clinical use of PA for FS and validate its therapeutic effect.</p><p><strong>Methods: </strong>The protocol was registered in Prospero (CRD42023445708) on 18 July 2023. Until Aug. 31, 2023, seven electronic databases will be searched for randomized controlled trials of PA for FS. Authors will be contacted, and manual searches will also be performed. Two reviewers will independently screen and collect data from retrieved articles according to predefined criteria. The primary outcome will be pain intensity, and secondary outcomes will be effective rate, Constant-Murley Score, Shoulder Pain and Disability Index, range of motion, quality of life, and adverse events. Bias and quality of the included trials will be assessed using the Cochrane handbook's risk-of-bias tool for randomized trials. Meta analyses will be conducted using Review Manager V.5.3 software. GRADE will be used to evaluate the level of evidence for each outcome.</p><p><strong>Results: </strong>This systematic review and meta-analysis will be conducted following PRISMA statement. The results will be published in a peer-reviewed journal.</p><p><strong>Conclusion: </strong>This review will provide scientific evidence to support health insurance policy as well as the standardization of PA in clinical practice.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"27 1","pages":"14-20"},"PeriodicalIF":1.4,"publicationDate":"2024-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10978440/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140336077","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
Feasibility of Emotional Freedom Techniques in Patients with Posttraumatic Stress Disorder: a pilot study. 创伤后应激障碍患者情绪自由技术的可行性:一项试点研究。
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-31 DOI: 10.3831/KPI.2024.27.1.27
Yujin Choi, Yunna Kim, Do-Hyung Kwon, Sunyoung Choi, Young-Eun Choi, Eun Kyoung Ahn, Seung-Hun Cho, Hyungjun Kim

Objectives: Posttraumatic stress disorder (PTSD) is a prevalent mental health condition, and techniques using sensory stimulation in processing traumatic memories have gained attention. The Emotional Freedom Techniques (EFT) is a psychotherapy that combines tapping on acupoints with exposure to cognitive reframing. This pilot study aimed to assess the feasibility of EFT as a treatment for PTSD by answering the following research questions 1) What is the compliance and completion rate of patients with PTSD with regard to EFT protocol? Is the dropout rate reasonable? 2) Is the effect size of EFT protocol for PTSD sufficient to justify a future trial?

Methods: Thirty participants diagnosed with PTSD were recruited. They received weekly EFT sessions for five weeks, in which they repeated a statement acknowledging the problem and accepting themselves while tapping the SI3 acupoint on the side of their hand. PTSD symptoms were evaluated using the PTSD Checklist for DSM-5 (PCL-5) before and after the intervention.

Results: Of the 30 PTSD patients (mean age 34.1 ± 9.1, 80% female), 96.7% showed over 80% compliance to the EFT sessions, and 86.7% completed the entire study process. The mean PCL-5 total score decreased significantly after the intervention, with a large effect size (change from baseline -14.33 [95% CI -19.79, -8.86], p < 0.0001, d = 1.06).

Conclusion: The study suggests that EFT is a feasible treatment for PTSD, with high session compliance and low dropout rates. The effect size observed in this study supports the need for a larger trial in the future to further investigate EFT as a treatment for PTSD. However, the lack of a control group and the use of a self-rated questionnaire for PTSD symptoms are limitations of this study. The findings of this pilot study can be used to plan a future trial.

目的:创伤后应激障碍(PTSD)是一种普遍存在的心理健康问题,利用感官刺激处理创伤记忆的技术受到人们的关注。情绪自由技术(EFT)是一种心理疗法,它将敲打穴位与接触认知重构相结合。本试验研究旨在通过回答以下研究问题,评估 EFT 作为创伤后应激障碍治疗方法的可行性 1) 创伤后应激障碍患者对 EFT 治疗方案的依从性和完成率如何?辍学率是否合理?2)EFT疗法治疗创伤后应激障碍的效果大小是否足以证明未来试验的合理性?招募了30名被诊断为创伤后应激障碍的参与者。他们每周接受一次 EFT 训练,为期五周,在训练过程中,他们在轻敲手侧 SI3 穴位的同时,重复一句承认问题并接纳自己的话。干预前后使用 DSM-5 创伤后应激障碍核对表(PCL-5)对创伤后应激障碍症状进行评估:30名创伤后应激障碍患者(平均年龄为34.1 ± 9.1岁,80%为女性)中,96.7%的患者对EFT疗程的依从性超过80%,86.7%的患者完成了整个研究过程。干预后,PCL-5总分的平均值显著下降,且效果显著(与基线相比的变化为-14.33 [95% CI -19.79, -8.86],P < 0.0001,d = 1.06):研究表明,EFT 是治疗创伤后应激障碍的可行方法,疗程依从性高,辍学率低。本研究中观察到的效应大小证明,未来有必要进行更大规模的试验,以进一步研究 EFT 作为创伤后应激障碍治疗方法的可行性。然而,缺乏对照组和使用创伤后应激障碍症状自评问卷是本研究的局限性。本试验研究的结果可用于规划未来的试验。
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引用次数: 0
Suggestion for Objective Evaluation of Comparative Pulse Diagnosis. 对比较脉诊进行客观评价的建议。
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-03-31 DOI: 10.3831/KPI.2024.27.1.21
Jun-Sang Yu

Objectives: Pulse is a method of Korean medicine diagnosis and is an important clue to detect the organs, nature, and progress of the disease. Pulse examination is included in the basic examination of Korean medicine doctors, but there is no standardized method for diagnosing pulse although the types and methods of the pulse taking are briefly described in the literature, making it difficult to spread the examination method. In this regard, I would like to propose an objective evaluation method.

Methods: Although the importance of pulse examination and the method of pulse examination are known in the literature, it is difficult for undergraduate students or inexperienced Korean medicine doctors to access it, so in this paper a method of marking the size of the pulse power in the blank space for objective evaluation was devised and presented.

Results: The size of the pulse power should be indicated using the 1-cell, 3-cell, or 5-cell method according to the left and right wrists and the cun, guan and chi on both sides.

Conclusion: The method of pulse diagnosis is an important diagnostic method as a verification process for making a Korean medical diagnosis. The remaining Korean medicine diagnostic methods, including pulse diagnosis, also need to undergo objectification. It is believed that the objectification of these diagnostic methods will lead to an improvement in the treatment rate of Korean medicine.

目的:脉象是韩医学诊断的一种方法,是检测疾病的器官、性质和进展的重要线索。脉象检查是韩医的基本检查项目之一,但文献中对脉象的种类和方法虽有简述,却没有统一的脉象诊断方法,导致检查方法难以推广。为此,笔者想提出一种客观的评价方法:方法:虽然脉象检查的重要性和脉象检查的方法在文献中都有介绍,但对于本科生或缺乏经验的韩医来说很难接触到,因此本文设计并提出了一种在空白处标注脉搏力量大小的方法,以进行客观评价:结果:应根据左右手腕和两侧的存、关、气,用 1 格、3 格或 5 格的方法标示脉力的大小:结论:脉诊法是一种重要的诊断方法,是韩医诊断的验证过程。包括脉诊在内的其他韩医诊断方法也需要经过对象化的过程。相信这些诊断方法的客观化将提高韩医学的治疗率。
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引用次数: 0
Comparison of Effectiveness of Manual Therapy for Infant Crying: systematic review and meta-analysis of randomized controlled trials. 婴儿哭闹手法治疗效果比较:随机对照试验的系统回顾和荟萃分析。
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-12-31 DOI: 10.3831/KPI.2023.26.4.285
Ui Jin Park, Hye In Jeong, Kyeong Han Kim

Objectives: The aim of this systematic review and meta-analysis is to assess and compare the effectiveness of manual therapy in alleviating infant crying, a common symptom of nocturnal crying (NC) and infantile colic (IC).

Methods: Total effective rate, crying time and adverse events were used as outcome indicators. To assess the quality, the risk of bias was determined for each study by two authors, using the Cochrane Collaboration's risk of bias tool. RevMan 5.0 was used for data analysis. A total of 98 articles were identified from 6 electronic databases.

Results: Among them, twenty-seven studies which included 13 NC and 14 IC were included. Meta-analysis showed favorable effects tuina therapy on total effective rate (TER) of NC (RR 1.20 [95% CI 1.05 to 1.37], p = 0.007), chiropractic therapy on crying time change of IC (SMD -0.83 [95% CI -1.61 to -0.06], p = 0.04) and massage on total crying time of IC (SMD -0.86 [95% CI -1.09 to -0.63], p < 0.00001). This systematic review compares different manual therapies for the treatment of NC and IC. While tuina, chiropractic, and massage show results in alleviating symptoms, the overall evidence remains limited due to the low quality and heterogeneity of the included studies.

Conclusion: Therefore, further high-quality research with unified control groups is needed to establish manual therapy as a recommended treatment option for NC and IC. Protocol registration number is CRD42022348143 01/08/2022.

目的:本系统综述和荟萃分析旨在评估和比较人工疗法在缓解婴儿哭闹(夜间哭闹(NC)和婴儿肠绞痛(IC)的常见症状)方面的有效性:方法:将总有效率、哭闹时间和不良事件作为结果指标。为了评估研究质量,两位作者使用 Cochrane 协作组织的偏倚风险工具对每项研究进行了偏倚风险评估。数据分析使用 RevMan 5.0。共从 6 个电子数据库中找到 98 篇文章:其中,27 项研究包括 13 项 NC 和 14 项 IC。元分析显示推拿疗法对NC总有效率(TER)(RR 1.20 [95% CI 1.05 to 1.37],P = 0.007)、整脊疗法对IC哭闹时间变化(SMD -0.83 [95% CI -1.61 to -0.06],P = 0.04)和按摩对IC总哭闹时间(SMD -0.86 [95% CI -1.09 to -0.63],P < 0.00001)均有良好效果。本系统综述比较了治疗NC和IC的不同手法疗法。虽然推拿、捏脊和按摩在缓解症状方面显示出效果,但由于所纳入研究的低质量和异质性,总体证据仍然有限:因此,要将手法治疗确定为NC和IC的推荐治疗方案,还需要进一步开展具有统一对照组的高质量研究。协议注册号为 CRD42022348143 01/08/2022.
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引用次数: 0
Inhibition of Glycation End Products Formation and Antioxidant Activities of Ilex paraguariensis: comparative study of fruit and leaves extracts. Ilex paraguariensis 的糖化终产物形成抑制和抗氧化活性:果实和叶片提取物的比较研究。
IF 1.4 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2023-12-31 DOI: 10.3831/KPI.2023.26.4.338
Laura Cogoi, Carla Marrassini, Elina Malen Saint Martin, María Rosario Alonso, Rosana Filip, Claudia Anesini

Objectives: Ilex paraguariensis (Aquifoleaceae) is cultivated to produce "yerba mate". Due to its nutritional, energizing, hypoglycemic and antioxidant effects, it is used in the elaboration of food, pharmaceuticals, and cosmetics. The oxidative stress related to protein glycation and production of advanced glycation end products (AGEs) leads to the development of several diseases. The objective of this work was to compare the antioxidant and anti-AGEs activity of a decoction of fruits (F) and leaves (L).

Methods: The antioxidant activity was assayed by the DPPH assay and the inhibition of egg yolk lipid peroxidation (ILP), and anti-AGEs activity, through the inhibition of the formation of fructosamine (IF), β-amyloid (Iβ), protein carbonylation (IC) and AGEs (IA). Polyphenols were quantified by HPLC.

Results: Maximum response ± SEM For F 0.01 µg/mL IF = 42 ± 4%, IC = 17 ± 2% and for 10 µg/mL IA = 38 ± 4%, Iβ = 67 ± 7%. For L 0.1 µg/mL IF = 35 ± 2%, IC = 19 ± 2% and for 100 µg/mL IA = 26 ± 3%, Iβ = 63.04 ± 2%. The DPPH IC50 = 134.8 ± 14 µg/mL for F and 34.67 ± 3 µg/mL for L. The ILP IC50 = 512.86 ± 50 µg/mL for F and 154.8 ± 15 µg/mL for L. By HPLC L presented the highest amounts of flavonoids and caffeoylquinic acids. F and L showed strong anti-AGEs activity, affecting the early stages of glycation at low concentrations and the late stages of glycation at high concentrations. The highest activity for both F and L was seen in the IF and Iβ. F presented the highest anti-AGEs potency. L presented the highest antioxidant potency, which was related to the highest content of polyphenols.

Conclusion: The fruits of I. paraguariensis could be a source of antioxidant and anti-AGEs compounds to be used with medicinal purposes or as functional food.

目的:Ilex paraguariensis(水生植物科)被种植用来生产 "耶尔巴马黛茶"。由于其营养、提神、降血糖和抗氧化作用,它被用于制作食品、药品和化妆品。与蛋白质糖化和产生高级糖化终产物(AGEs)有关的氧化应激会导致多种疾病的发生。这项工作的目的是比较果实(F)和叶片(L)煎剂的抗氧化和抗 AGEs 活性:抗氧化活性通过 DPPH 试验和抑制蛋黄脂质过氧化(ILP)进行检测,抗 AGEs 活性通过抑制果糖胺(IF)、β-淀粉样蛋白(Iβ)、蛋白质羰基化(IC)和 AGEs(IA)的形成进行检测。多酚通过高效液相色谱法进行定量:F 0.01 µg/mL IF = 42 ± 4%,IC = 17 ± 2%;10 µg/mL IA = 38 ± 4%,Iβ = 67 ± 7%。对于 L 0.1 µg/mL IF = 35 ± 2%,IC = 19 ± 2%,对于 100 µg/mL IA = 26 ± 3%,Iβ = 63.04 ± 2%。DPPH IC50 = 134.8 ± 14 µg/mL (F)和 34.67 ± 3 µg/mL (L);ILP IC50 = 512.86 ± 50 µg/mL (F)和 154.8 ± 15 µg/mL (L)。F 和 L 具有很强的抗糖化活性,低浓度时可影响糖化的早期阶段,高浓度时可影响糖化的晚期阶段。F 和 L 在 IF 和 Iβ 中的活性最高。F 的抗糖化酶活性最高。L 的抗氧化能力最强,这与多酚含量最高有关:结论:I. paraguariensis 的果实可以作为抗氧化剂和抗老年斑化合物的来源,可用于药用或作为功能性食品。
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Journal of Pharmacopuncture
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