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Individualized homeopathic medicines in the treatment of premenstrual syndrome: A double-blind, randomized, placebo-controlled trial 治疗经前综合征的个性化顺势疗法药物:双盲、随机、安慰剂对照试验
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-08-17 DOI: 10.1016/j.explore.2024.103039
Sanjib Sahoo , Chintamani Nayak , Prasanta Rath , Soumya Bhattacharya , Suranjana Mukherjee , Abhijit Dutta

Introduction

Background: Premenstrual syndrome (PMS) is a common disorder among female population that adversely affects their physical and emotional well-being. Conventional treatments for PMS may have limitations and side effects, prompting a need for complementary therapeutic approaches. This double-blind, randomized, placebo-controlled trial aimed to investigate the efficacy of individualized Homeopathic medicines (IH) in treating PMS symptoms in comparison to placebo (PL).

Methods

This study recruited female participants of reproductive age who had been experiencing premenstrual syndrome (PMS) for >3 months, from the Outpatient Department. The participants were randomly assigned to receive either IH or PL. The measured outcomes included the Shortened Premenstrual Assessment Form (SPAF) questionnaire as the primary outcome, and the Premenstrual Tension Syndrome Visual Analogue Scale (PMTS-VAS) and the Premenstrual Tension Syndrome Observer Rating Scale – Revised (PMTS-OR) as secondary outcomes. These measures were assessed at baseline and every month for 3 months.

Results

The results showed a statistically significant reduction in total SPAF scores for the IH group compared to the placebo group (F = 11.340; P < 0.001) at month 2 (-5.5 ± 1.8, P = 0.003), and month 3 (-6.6 ± 2.0, P = 0.002). Additionally, there were significant reductions in PMTS-VAS and PMTS-OR scores in the IH compared to placebo group. Natrum muriaticum (n = 4/30, 13.3 %) was the most frequently indicated medicines in the study. Four adverse events (13.33 %) occurred in the IH group, and six adverse events (16.67 %) in the Placebo group, with no serious events reported, and no additional medicinal treatment was required for participants during the study period.

Conclusions

Individualized Homeopathic medicines were found to be significantly effective, compared to placebo in reducing PMS symptoms. Further independent replication is warranted to validate and corroborate these findings, as well as to identify the most effective Homeopathic medicines for treating PMS symptoms. Until then, clinicians may consider these findings when exploring personalized and holistic therapeutic strategies for managing PMS.

Trial Registration

CTRI/2020/11/028,796, dt. 02/11/2020

导言背景:经前期综合征(PMS)是女性人群中常见的一种疾病,对她们的身心健康造成了不利影响。经前期综合征的传统治疗方法可能存在局限性和副作用,因此需要辅助治疗方法。这项双盲、随机、安慰剂对照试验旨在研究个体化顺势疗法药物(IH)与安慰剂(PL)相比在治疗经前综合征症状方面的疗效。参与者被随机分配接受 IH 或 PL 治疗。测量结果包括作为主要结果的经前期评估简表(SPAF)问卷,以及作为次要结果的经前期紧张综合征视觉模拟量表(PMTS-VAS)和经前期紧张综合征观察者评定量表-修订版(PMTS-OR)。结果表明,与安慰剂组相比,IH 组 SPAF 总分在第 2 个月(-5.5 ± 1.8,P = 0.003)和第 3 个月(-6.6 ± 2.0,P = 0.002)显著降低(F = 11.340; P < 0.001)。此外,与安慰剂组相比,IH组的PMTS-VAS和PMTS-OR评分明显降低。本研究中最常使用的药物是硝酸甘油(4/30,13.3%)。IH组发生了4起不良事件(13.33%),安慰剂组发生了6起不良事件(16.67%),没有严重事件报告,参与者在研究期间不需要额外的药物治疗。为了验证和证实这些研究结果,并确定治疗经前综合征症状最有效的顺势疗法药物,有必要进一步进行独立复制。在此之前,临床医生在探索经前综合征的个性化整体治疗策略时,可以考虑这些研究结果。试验注册CTRI/2020/11/028,796, dt.02/11/2020
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引用次数: 0
Liberation from extracorporeal membrane oxygenation in a patient with severe COVID-19-associated acute respiratory distress syndrome using traditional Chinese medicine: A case report 用中药使一名重度 COVID-19 相关急性呼吸窘迫综合征患者摆脱体外膜氧合:病例报告
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-08-10 DOI: 10.1016/j.explore.2024.103038
Hsuan-Ting Tang , Sheng-Teng Huang , Shi-Chen Ou

Introduction

Due to the continued threat to public health posed by SARS-CoV-2 and the ongoing emergence of novel variants, the integration of traditional Chinese medicine (TCM) with Western medicine provides a novel alternative management for critically ill patients.

Case presentation

This case report describes a 54-year-old male with severe COVID-19-associated acute respiratory distress syndrome (ARDS) who required extracorporeal membrane oxygenation (ECMO) support. Despite standard treatment, ECMO liberation was unsuccessful, and complications such as pneumothorax and hemothorax ensued. However, upon initiating combined TCM therapy on the 19th day of ECMO support, the patient exhibited gradual improvements in oxygenation and ventilation, leading to successful ECMO liberation on the 31st day.

Conclusion

This case underscores the potential of integrating TCM with conventional therapies for severe COVID-19 cases, offering a valuable treatment option amidst the evolving landscape of SARS-CoV-2 variants.

导言由于 SARS-CoV-2 对公众健康的持续威胁以及新型变种的不断出现,传统中医药(TCM)与西医的结合为危重病人提供了一种新的替代治疗方法。本病例报告描述了一名 54 岁男性患者,他患有严重的 COVID-19 相关急性呼吸窘迫综合征(ARDS),需要体外膜氧合(ECMO)支持。尽管进行了规范治疗,但 ECMO 解痉治疗仍不成功,随后出现了气胸和血胸等并发症。然而,在 ECMO 支持的第 19 天开始联合中医治疗后,患者的氧合和通气情况逐渐改善,最终在第 31 天成功脱离 ECMO。
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引用次数: 0
Effects of mindfulness-based stress reduction therapy for sleep quality and perceived stress in patients with spinal cord injury 正念减压疗法对脊髓损伤患者睡眠质量和感知压力的影响
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-08-08 DOI: 10.1016/j.explore.2024.103037
Yan Cao, Huihong Wu, Sujuan Shi, Dan Xie

Objective

To explore the effect of the mindfulness-based stress reduction (MBSR) practice on sleep quality and perceived stress in patients with spinal cord injury (SCI).

Method

A total of 104 patients with SCI (diagnosed via imaging and clinical symptoms) admitted to our hospital between January 2020 and December 2022 were selected as the study participants. The patients were randomly divided into two groups: the MBSR (observation) group and the control group. The observation group received MBSR therapy and routine nursing, and the control group received music training therapy and routine nursing. The Pittsburgh Sleep Quality Index (PSQI) was used to evaluate sleep quality, and the perceived stress score was used to evaluate stress experienced by the patients at three timepoints: before intervention, 4 weeks and 8weeks after intervention.

Results

Compared with before intervention, the PSQI scores of both the control group and intervention group participants significantly decreased after intervention(P < 0.01). Compared with the 4 weeks after intervention, the PSQI scores of both groups of participants decreased in the 8 weeks after intervention(P < 0.01). There was a significant difference in PSQI scores between the two groups of participants at 4 and 8 weeks after intervention(P < 0.01). Compared with before intervention, the average perceived stress score of both the control group and intervention group participants significantly decreased after intervention(P < 0.05). Compared with the 4 weeks after intervention, the average perceived stress score of both groups of participants decreased in the 8 weeks after intervention(P < 0.01). There was a significant difference in average perceived stress score between the two groups of participants at 4(P < 0.05) and 8 weeks(P < 0.01) after intervention(P < 0.01).

Conclusion

The use of MBSR therapy could effectively improve patient sleep quality and reduce perceived stress.

方法 选取2020年1月至2022年12月期间我院收治的104例脊髓损伤(SCI)患者(通过影像学和临床症状确诊)作为研究对象。患者被随机分为两组:MBSR(观察)组和对照组。观察组接受 MBSR 治疗和常规护理,对照组接受音乐训练治疗和常规护理。采用匹兹堡睡眠质量指数(PSQI)评估睡眠质量,采用感知压力评分评估患者在干预前、干预后4周和干预后8周三个时间点的压力体验。结果与干预前相比,干预后对照组和干预组参与者的PSQI评分均显著下降(P< 0.01)。与干预后 4 周相比,干预后 8 周两组受试者的 PSQI 均有所下降(P < 0.01)。两组受试者在干预后 4 周和 8 周的 PSQI 分数有明显差异(P < 0.01)。与干预前相比,干预后对照组和干预组参与者的平均感知压力得分均明显下降(P <0.05)。与干预后 4 周相比,干预后 8 周两组参与者的平均感知压力得分均有所下降(P < 0.01)。两组受试者在干预后4周(P <0.05)和8周(P <0.01)的平均感知压力得分有明显差异(P <0.01)。
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引用次数: 0
Near-death experience: memory recovery during hypnosis 濒死体验催眠过程中的记忆恢复
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-07-24 DOI: 10.1016/j.explore.2024.103036
Marjorie Woollacott

Increasing numbers of research studies have offered evidence regarding awareness of verified events during near-death experiences (NDEs) occurring during cardiac arrest and severely impaired brain function. The prevalence of patients reporting core NDEs under these conditions is reported as 10–12 %. One question that is often asked is why this percentage is low. Though it may be hypothesized that NDEs are limited to this low percentage of patients, it is also possible that more patients experience an NDE, but that memory is impaired sufficiently such that the NDE is not recalled. In this article I present a detailed and extensively verified case study of a woman, Stephanie Arnold, who experienced an NDE during the birth of her second child when she was 41 years old. The data provide evidence that supports the hypotheses 1) that during cardiac arrest an NDE may occur, but not be remembered until hypnotic regression therapy reveals extensive details of the events that could not have been perceived with the five senses, both in the operating room and elsewhere during resuscitation. 2) that there may also be pre-cognition of the events leading to the cardiac arrest, reported in clear detail, and 3) that NDEs lead to a fundamental transformation in an individual's understanding of the nature of consciousness, their quest for meaning and purpose, their concern for others, and their appreciation of life.

越来越多的研究提供了证据,证明在心脏骤停和脑功能严重受损的濒死体验(NDE)过程中,患者能够意识到已证实的事件。据报道,在这些情况下报告核心濒死体验的患者比例为 10-12%。人们经常问的一个问题是,为什么这个比例很低。虽然可以假设 NDE 仅限于这一低比例的患者,但也有可能有更多的患者经历过 NDE,但由于记忆力受损而无法回忆起 NDE。在这篇文章中,我介绍了一个详细且经过广泛验证的案例研究,研究对象是一位名叫斯蒂芬妮-阿诺德的女性,她在 41 岁时生第二个孩子时经历了一次 NDE。这些数据提供了支持以下假设的证据:1)在心脏骤停期间,可能会发生 NDE,但直到催眠回归疗法揭示了在手术室和复苏期间五官无法感知的事件的大量细节后,才会被记起。2) 对导致心脏骤停的事件也可能有预先认知,并有清晰的细节报告;以及 3) NDE 会导致个人对意识本质的理解、对意义和目的的追求、对他人的关心以及对生命的珍惜发生根本性转变。
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引用次数: 0
The effect of acupressure and halogen light stimulation on nonstress testing and antenatal anxiety: A randomized controlled trial 穴位按摩和卤素灯刺激对非压力测试和产前焦虑的影响:随机对照试验
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-07-17 DOI: 10.1016/j.explore.2024.103035
Yasemin Sökmen , Ayten Taşpınar

Context

Acupressure and halogen light stimulation, are used to reduce false non-reactive nonstress test results related to fetal sleep.

Objective

This study was conducted to determine the effect of acupressure and halogen light stimulation on nonstress testing and anxiety during pregnancy.

Design

Randomized controlled experimental study.

Setting

The population of the study consisted of pregnant women who were requested to have a nonstress test.

Participants

The sample of the study included 132 pregnant women (acupressure group:44; halogen light group:45, and control group:43).

Methods

The acupressure group was applied acupressure on the Zhiyin acupuncture point three times, the halogen light group was applied halogen light stimulation twice on the fetal head from the mother's abdomen. In the interpretation of the results, the level of statistical significance was taken as P < 0.05.

Main outcome participants

In our study, there was no difference between the acupressure and halogen light groups in terms of the mean number of fetal movements, the number of accelerations, the time to the first acceleration, and the time to reach the reactive result in the nonstress test (P > 0.05), while the mean number of fetal movements and accelerations of these two groups were higher, and the mean time to the first acceleration and the mean time to reach the reactive result in the nonstress test were shorter than those of the control group (P < 0.05). In addition, no statistically significant difference was found between the groups in terms of mean state anxiety inventory scores (P > 0.05).

Results

Acupressure and halogen light stimulation increased the rates of reactive nonstress tests.

穴位按摩和卤素灯刺激可用于减少与胎儿睡眠有关的非反应性非应激测试的错误结果。本研究旨在确定穴位按摩和卤素灯刺激对非应激测试和孕期焦虑的影响。随机对照实验研究。研究对象包括被要求进行非应激测试的孕妇。研究样本包括 132 名孕妇(穴位按摩组:44 人;卤素灯组:45 人;对照组:43 人)。穴位按摩组对知音穴进行三次穴位按摩,卤素灯组从母亲腹部对胎儿头部进行两次卤素灯刺激。在解释结果时,统计显著性水平取 <0.05。在我们的研究中,穴位按摩组和卤素灯组在非应激试验中的平均胎动次数、加速次数、首次加速时间和达到反应性结果的时间方面没有差异(> 0.05),而这两组在非应激试验中的平均胎动次数和加速次数均高于对照组,首次加速时间和达到反应性结果的时间均短于对照组(< 0.05)。此外,在状态焦虑量表的平均得分方面,组间差异无统计学意义(> 0.05)。穴位按摩和卤素灯刺激提高了反应性非应激测试的比率。
{"title":"The effect of acupressure and halogen light stimulation on nonstress testing and antenatal anxiety: A randomized controlled trial","authors":"Yasemin Sökmen ,&nbsp;Ayten Taşpınar","doi":"10.1016/j.explore.2024.103035","DOIUrl":"10.1016/j.explore.2024.103035","url":null,"abstract":"<div><h3>Context</h3><p>Acupressure and halogen light stimulation, are used to reduce false non-reactive nonstress test results related to fetal sleep.</p></div><div><h3>Objective</h3><p>This study was conducted to determine the effect of acupressure and halogen light stimulation on nonstress testing and anxiety during pregnancy.</p></div><div><h3>Design</h3><p>Randomized controlled experimental study.</p></div><div><h3>Setting</h3><p>The population of the study consisted of pregnant women who were requested to have a nonstress test.</p></div><div><h3>Participants</h3><p>The sample of the study included 132 pregnant women (acupressure group:44; halogen light group:45, and control group:43).</p></div><div><h3>Methods</h3><p>The acupressure group was applied acupressure on the Zhiyin acupuncture point three times, the halogen light group was applied halogen light stimulation twice on the fetal head from the mother's abdomen. In the interpretation of the results, the level of statistical significance was taken as <em>P</em> &lt; 0.05.</p></div><div><h3>Main outcome participants</h3><p>In our study, there was no difference between the acupressure and halogen light groups in terms of the mean number of fetal movements, the number of accelerations, the time to the first acceleration, and the time to reach the reactive result in the nonstress test (<em>P</em> &gt; 0.05), while the mean number of fetal movements and accelerations of these two groups were higher, and the mean time to the first acceleration and the mean time to reach the reactive result in the nonstress test were shorter than those of the control group (<em>P</em> &lt; 0.05). In addition, no statistically significant difference was found between the groups in terms of mean state anxiety inventory scores (<em>P</em> &gt; 0.05).</p></div><div><h3>Results</h3><p>Acupressure and halogen light stimulation increased the rates of reactive nonstress tests.</p></div>","PeriodicalId":50459,"journal":{"name":"Explore-The Journal of Science and Healing","volume":"20 5","pages":"Article 103035"},"PeriodicalIF":1.9,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141784669","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}
引用次数: 0
Can a six-week Swedish massage reduce mood disorders and enhance the quality of life in individuals with Multiple Sclerosis? A randomized control clinical trial 为期六周的瑞典式按摩能否减轻多发性硬化症患者的情绪障碍并提高其生活质量?随机对照临床试验
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-07-14 DOI: 10.1016/j.explore.2024.103032
Aynollah Naderi , Mohammad Hossein Rezvani , Atefeh Aminian‐Far , Salimeh Hamood-Ahvazi

Introduction

There is a limited amount of research specifically focusing on the effects of Swedish massage on mood disorders and the quality of life (QOL) among individuals with MS, emphasizing the need for further investigation. Therefore, this study aimed to assess the effects of a 6-week Swedish massage on the quality of life, stress, anxiety, depression, pain, fatigue, spasticity, and sleep quality in MS patients.

Methods

This randomized controlled trial involved 70 MS patients who were divided into two groups. The massage group underwent two 50-minute sessions of whole-body Swedish massage per week for six weeks, while the usual treatment group maintained their regular medical care routine. Outcomes were Short Form-36 (SF-36) and the Depression, Anxiety, and Stress Scale (DASS), Visual Analog Scale (VAS), Fatigue Severity Scale (FSS), Pittsburgh Sleep Quality Index (PSQI-P), and Modified Ashworth Scale (MAS). These measurements were taken before and after the massage intervention.

Results

The massage group demonstrated significant improvements in QOL and its components compared to the usual treatment group (Hedge's g = 0.53 for QOL, ranging from 0.31 to 0.58 for QOL components; p < 0.001). Participants in the massage group also reported significantly lower levels of stress (Hedge's g = 0. 80), anxiety (Hedge's g = 0.47), and depression (Hedge's g = 0.70) than those in the usual treatment group (p < 0.001). Additionally, the massage group had lower levels of pain, fatigue, and spasticity, and better sleep quality compared to the usual treatment group (p < 0.05).

Conclusion

Swedish massage can be considered a valuable complementary and alternative treatment alongside conventional medicine for individuals with MS.

导言:专门针对瑞典式按摩对多发性硬化症患者的情绪障碍和生活质量(QOL)影响的研究数量有限,强调了进一步调查的必要性。因此,本研究旨在评估为期 6 周的瑞典式按摩对多发性硬化症患者的生活质量、压力、焦虑、抑郁、疼痛、疲劳、痉挛和睡眠质量的影响。按摩组每周进行两次为期 50 分钟的全身瑞典式按摩,为期六周;常规治疗组保持常规医疗护理。研究结果包括简表-36(SF-36)、抑郁、焦虑和压力量表(DASS)、视觉模拟量表(VAS)、疲劳严重程度量表(FSS)、匹兹堡睡眠质量指数(PSQI-P)和改良阿什沃斯量表(MAS)。结果与常规治疗组相比,按摩组的 QOL 及其组成部分均有显著改善(QOL 的 Hedge's g = 0.53,QOL 组成部分的 Hedge's g 为 0.31 至 0.58;p < 0.001)。按摩组参与者的压力(Hedge's g = 0.80)、焦虑(Hedge's g = 0.47)和抑郁(Hedge's g = 0.70)水平也明显低于常规治疗组(p < 0.001)。此外,与常规治疗组相比,按摩组的疼痛、疲劳和痉挛程度更低,睡眠质量更高(p < 0.05)。
{"title":"Can a six-week Swedish massage reduce mood disorders and enhance the quality of life in individuals with Multiple Sclerosis? A randomized control clinical trial","authors":"Aynollah Naderi ,&nbsp;Mohammad Hossein Rezvani ,&nbsp;Atefeh Aminian‐Far ,&nbsp;Salimeh Hamood-Ahvazi","doi":"10.1016/j.explore.2024.103032","DOIUrl":"10.1016/j.explore.2024.103032","url":null,"abstract":"<div><h3>Introduction</h3><p>There is a limited amount of research specifically focusing on the effects of Swedish massage on mood disorders and the quality of life (QOL) among individuals with MS, emphasizing the need for further investigation. Therefore, this study aimed to assess the effects of a 6-week Swedish massage on the quality of life, stress, anxiety, depression, pain, fatigue, spasticity, and sleep quality in MS patients.</p></div><div><h3>Methods</h3><p>This randomized controlled trial involved 70 MS patients who were divided into two groups. The massage group underwent two 50-minute sessions of whole-body Swedish massage per week for six weeks, while the usual treatment group maintained their regular medical care routine. Outcomes were Short Form-36 (SF-36) and the Depression, Anxiety, and Stress Scale (DASS), Visual Analog Scale (VAS), Fatigue Severity Scale (FSS), Pittsburgh Sleep Quality Index (PSQI-P), and Modified Ashworth Scale (MAS). These measurements were taken before and after the massage intervention.</p></div><div><h3>Results</h3><p>The massage group demonstrated significant improvements in QOL and its components compared to the usual treatment group (Hedge's <em>g</em> = 0.53 for QOL, ranging from 0.31 to 0.58 for QOL components; <em>p</em> &lt; 0.001). Participants in the massage group also reported significantly lower levels of stress (Hedge's <em>g</em> = 0. 80), anxiety (Hedge's <em>g</em> = 0.47), and depression (Hedge's <em>g</em> = 0.70) than those in the usual treatment group (<em>p</em> &lt; 0.001). Additionally, the massage group had lower levels of pain, fatigue, and spasticity, and better sleep quality compared to the usual treatment group (<em>p</em> &lt; 0.05).</p></div><div><h3>Conclusion</h3><p>Swedish massage can be considered a valuable complementary and alternative treatment alongside conventional medicine for individuals with MS.</p></div>","PeriodicalId":50459,"journal":{"name":"Explore-The Journal of Science and Healing","volume":"20 5","pages":"Article 103032"},"PeriodicalIF":1.9,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141622777","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}
引用次数: 0
The effect of lavender and rosemary aromatherapy application on cognitive functions, anxiety, and sleep quality in the elderly with diabetes 薰衣草和迷迭香芳香疗法对老年糖尿病患者认知功能、焦虑和睡眠质量的影响
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-07-11 DOI: 10.1016/j.explore.2024.103033
Sati Can , Yasemin Yildirim Usta , Sedat Yildiz , Kanat Tayfun

Objective

This study aimed to determine the effects of aromatherapy use on cognitive function, anxiety, and sleep quality in the elderly with diabetes.

Methods

The study was conducted with 63 participants aged 65 and over. Participants were randomly divided into three groups: lavender, rosemary and control groups. The intervention continued for four weeks. Data was collected using the Blessed Orientation Concentration Test, State-Trait Anxiety Scale, and Pittsburgh Sleep Quality Scale. Data were analyzed using One-Way ANOVA, Mann-Whitney U/Kruskal-Wallis, Wilcoxon and Friedman tests.

Results

In both intervention groups, the 4th week scores of cognitive functions, anxiety, and sleep quality after aromatherapy were significant compared to the baseline scores. In the control group, state anxiety scores were significantly higher in the 2nd and 4th weeks compared to the initial scores.

Conclusions

Inhaling lavender and rosemary has been observed to improve cognitive function and sleep quality and reduce anxiety levels. The effects of the essential oils used in the research were evaluated over four weeks. It is thought that studying for a longer period and with more samples would be beneficial. There is a need for studies examining its effects, especially in the elderly with diabetes.

目的 本研究旨在确定使用芳香疗法对患有糖尿病的老年人的认知功能、焦虑和睡眠质量的影响。 方法 本研究有 63 名 65 岁及以上的参与者参加。参与者被随机分为三组:薰衣草组、迷迭香组和对照组。干预持续四周。数据收集采用祝福定向集中测试、状态-特质焦虑量表和匹兹堡睡眠质量量表。采用单向方差分析、Mann-Whitney U/Kruskal-Wallis、Wilcoxon 和 Friedman 检验对数据进行了分析。结论据观察,吸入薰衣草和迷迭香能改善认知功能和睡眠质量,降低焦虑水平。研究中使用的精油的效果是在四周内进行评估的。我们认为,进行更长时间和更多样本的研究将是有益的。有必要对其效果进行研究,尤其是对患有糖尿病的老年人。
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引用次数: 0
Effect of neroli-flavored chewing gum on anxiety 橙花味口香糖对焦虑的影响
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-07-10 DOI: 10.1016/j.explore.2024.103028
Mozhgan Esmaeelian , Elahe Esmaeelian

The aim of this study was to assess the effectiveness of neroli-flavored chewing gum in reducing anxiety. A single-blind, two-group study was conducted on 72 university students. Participants were randomly assigned to either the commercial neroli-flavored chewing gum (CNC) group or the natural hydro-distilled neroli-flavored chewing gum (NNC) group. The research instrument used was Spielberger's State-Anxiety questionnaire. While there was no significant difference in anxiety scores between the CNC and NNC groups before the intervention, a significant difference was observed in anxiety scores 20 min after the intervention. Within-group comparisons indicated statistically significant differences between pre-test and post-test values of anxiety in the NNC group. The results of this study suggest that natural hydro-distilled neroli-flavored chewing gum can reduce anxiety in university students.

本研究旨在评估橙花味口香糖在减轻焦虑方面的效果。研究对 72 名大学生进行了单盲两组研究。参与者被随机分配到商业橙花味口香糖(CNC)组或天然氢蒸馏橙花味口香糖(NNC)组。使用的研究工具是斯皮尔伯格焦虑状态问卷。在干预前,CNC 组和 NNC 组的焦虑评分没有明显差异,但在干预 20 分钟后,焦虑评分出现了明显差异。组内比较表明,NNC 组的焦虑值在测试前和测试后有显著的统计学差异。本研究结果表明,天然水蒸馏橙花味口香糖可以减轻大学生的焦虑。
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引用次数: 0
Efficacy of aromatherapy with Lavandula angustifolia oil on postoperative pain after cardiac surgery: A randomized clinical trial 薰衣草精油芳香疗法对心脏手术后疼痛的疗效:随机临床试验
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-07-09 DOI: 10.1016/j.explore.2024.103034
Louise Constancia de Melo Alves Silva , Kauanny Vitoria Gurgel dos Santos , José Joandson de Souza dos Santos , Roberta Paolli de Paiva Oliveira Arruda Camara , Sandy Yasmine Bezerra e Silva , Hylarina Maria Montenegro Diniz Silva , Kátia Regina Barros Ribeiro , Daniele Vieira Dantas , Rodrigo Assis Neves Dantas

Objective

To evaluate the effect of aromatherapy through inhalation of Lavandula angustifolia essential oil in relieving pain during the immediate postoperative period of patients undergoing cardiac surgery.

Methods

A single-blind, randomized and controlled clinical trial, with 52 patients in the immediate postoperative period of cardiac surgery were randomly distributed into experimental (n = 26) and control (n = 26) groups. The primary outcome was whether or not pain was relieved and secondary outcomes included changes in vital signs, sleep and facial relaxation. The control group received industry standard care and application of an essential oil-free ceramic diffuser necklace. The experimental group received the inhalation intervention with pure Lavandula angustifolia essential oil, with a drop of the oil on a ceramic diffuser necklace at a distance of 15-20 cm from the patient's nose for 30 min. Pain was measured using the Numerical Visual Scale, and vital signs using the multiparametric monitor before the intervention, 10 minutes after its start and 30 minutes after the total end of inhalation. Face relaxation was assessed before and after the intervention and sleep was assessed at the end of inhalation.

Results

There was a decrease in pain levels (p < 0.001) 30 min after the end of inhalation in the Experimental Group, with a decrease in the measurements of Mean Blood Pressure (p= 0.008) and Respiratory Rate (p = 0.011). Furthermore, facial relaxation and sleep had a large effect size of 2.54 and 1.28, respectively.

Conclusion

Lavandula angustifolia essential oil was effective in relieving pain, causing sleep and relaxation, proving to be a low-cost and easy-to-use tool that the nursing team can use in their care.

方法 单盲、随机对照临床试验,将 52 名心脏手术术后患者随机分为实验组(26 人)和对照组(26 人)。主要结果是疼痛是否缓解,次要结果包括生命体征、睡眠和面部放松的变化。对照组接受行业标准护理,使用不含精油的陶瓷扩香项链。实验组接受纯薰衣草精油吸入干预,将精油滴在陶瓷扩散器项链上,距离患者鼻子 15-20 厘米,持续 30 分钟。在干预前、干预开始后 10 分钟和吸入完全结束后 30 分钟,使用数字视觉量表测量疼痛程度,并使用多参数监护仪测量生命体征。结果实验组在吸入结束 30 分钟后疼痛程度有所减轻(p < 0.001),平均血压(p= 0.008)和呼吸频率(p = 0.011)也有所下降。此外,面部放松和睡眠的效应大小较大,分别为 2.54 和 1.28。结论薰衣草精油在缓解疼痛、促进睡眠和放松方面效果显著,证明是一种低成本、易于使用的工具,护理团队可在护理工作中使用。
{"title":"Efficacy of aromatherapy with Lavandula angustifolia oil on postoperative pain after cardiac surgery: A randomized clinical trial","authors":"Louise Constancia de Melo Alves Silva ,&nbsp;Kauanny Vitoria Gurgel dos Santos ,&nbsp;José Joandson de Souza dos Santos ,&nbsp;Roberta Paolli de Paiva Oliveira Arruda Camara ,&nbsp;Sandy Yasmine Bezerra e Silva ,&nbsp;Hylarina Maria Montenegro Diniz Silva ,&nbsp;Kátia Regina Barros Ribeiro ,&nbsp;Daniele Vieira Dantas ,&nbsp;Rodrigo Assis Neves Dantas","doi":"10.1016/j.explore.2024.103034","DOIUrl":"10.1016/j.explore.2024.103034","url":null,"abstract":"<div><h3>Objective</h3><p>To evaluate the effect of aromatherapy through inhalation of <em>Lavandula angustifolia</em> essential oil in relieving pain during the immediate postoperative period of patients undergoing cardiac surgery.</p></div><div><h3>Methods</h3><p>A single-blind, randomized and controlled clinical trial, with 52 patients in the immediate postoperative period of cardiac surgery were randomly distributed into experimental (n = 26) and control (n = 26) groups. The primary outcome was whether or not pain was relieved and secondary outcomes included changes in vital signs, sleep and facial relaxation. The control group received industry standard care and application of an essential oil-free ceramic diffuser necklace. The experimental group received the inhalation intervention with pure <em>Lavandula angustifolia</em> essential oil, with a drop of the oil on a ceramic diffuser necklace at a distance of 15-20 cm from the patient's nose for 30 min. Pain was measured using the Numerical Visual Scale, and vital signs using the multiparametric monitor before the intervention, 10 minutes after its start and 30 minutes after the total end of inhalation. Face relaxation was assessed before and after the intervention and sleep was assessed at the end of inhalation.</p></div><div><h3>Results</h3><p>There was a decrease in pain levels (p &lt; 0.001) 30 min after the end of inhalation in the Experimental Group, with a decrease in the measurements of Mean Blood Pressure (p= 0.008) and Respiratory Rate (p = 0.011). Furthermore, facial relaxation and sleep had a large effect size of 2.54 and 1.28, respectively.</p></div><div><h3>Conclusion</h3><p><em>Lavandula angustifolia</em> essential oil was effective in relieving pain, causing sleep and relaxation, proving to be a low-cost and easy-to-use tool that the nursing team can use in their care.</p></div>","PeriodicalId":50459,"journal":{"name":"Explore-The Journal of Science and Healing","volume":"20 6","pages":"Article 103034"},"PeriodicalIF":1.9,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1550830724001411/pdfft?md5=685e0678ac1d6ef608c4191e3c611176&pid=1-s2.0-S1550830724001411-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141693933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Moxibustion combined with guasha therapy for recurrent neutropenia following multiple cycles of chemotherapy of ovarian cancer: A case report 艾灸结合刮痧治疗卵巢癌多周期化疗后复发性中性粒细胞减少症:病例报告。
IF 1.9 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-07-06 DOI: 10.1016/j.explore.2024.103031
Weina Zhang, Jingnan Xu, Yuxiang Wan, Ming Yang, Jinchang Huang

Neutropenia, a common side effect of chemotherapy for ovarian cancer, was observed in a 47-year-old female patient undergoing a six-cycle chemotherapy regimen. She experienced recurrent neutropenia and leukopenia but refused granulocyte colony-stimulating factor (G-CSF) due to severe bone pain and high costs. Moxibustion combined with guasha therapy (MGT) was administered each time neutropenia occurred. The treatment involved guasha therapy on the bladder meridian (BL) and the governor vessel (GV), followed by moxibustion at Zhongwan (CV 12), Guanyuan (CV 4), and Shenzhu (GV 12) points over 2–3 days. This approach led to the recovery of neutrophil and leukocyte counts, enabling the patient to complete six chemotherapy cycles without G-CSF. These findings suggest that MGT may enhance neutrophil and leukocyte counts in patients with chemotherapy-induced myelosuppression, presenting a potential alternative for those intolerant to G-CSF. However, further high-quality research is needed to confirm its efficacy.

中性粒细胞减少症是卵巢癌化疗的常见副作用,一名 47 岁的女性患者接受了六周期化疗。她反复出现中性粒细胞减少症和白细胞减少症,但由于严重的骨痛和高昂的费用,她拒绝使用粒细胞集落刺激因子(G-CSF)。每次出现中性粒细胞减少时,她都会进行艾灸结合刮痧疗法(MGT)。治疗方法包括在膀胱经(BL)和督脉(GV)上进行刮痧治疗,然后在中脘(CV 12)、关元(CV 4)和神阙(GV 12)穴位上艾灸 2-3 天。这种方法使患者的中性粒细胞和白细胞数量得到恢复,使其能够在不使用 G-CSF 的情况下完成六个化疗周期。这些研究结果表明,MGT 可以提高化疗引起的骨髓抑制患者的中性粒细胞和白细胞数量,为那些对 G-CSF 不耐受的患者提供了一种潜在的替代疗法。不过,还需要进一步的高质量研究来证实其疗效。
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Explore-The Journal of Science and Healing
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