Pub Date : 2024-03-01DOI: 10.1016/j.aimed.2024.03.003
Chester Yan Jie Ng, Wen Min Ng, Yan Zhao, Linda LD Zhong
Introduction
This study aims to evaluate the clinical efficacy of different modes of acupuncture for obesity treatment in adult females. Auricular Acupuncture (AA), Electroacupuncture (EA), and Manual Acupuncture (MA) were the acupuncture methods evaluated. This was accomplished through a systematic review and meta-analysis.
Methods
Seven electronic databases were searched from inception to May 2022 to source for Randomized Control Trials (RCTs). Acupuncture's effect on obesity in adult females was measured using body mass index (BMI), waist circumference (WC), and body weight (BW). To assess the quality of the RCTs, the Cochrane Collaboration's Risk of Bias Tool was used. Pooled analysis was done using the Review Manager software and the random-effects model was used to account for heterogeneity of the included studies. The differences between treatment groups were reported as mean differences (MD).
Results
12 RCTs were selected through screening of results from electronic databases. The acupuncture and control groups each had 375 and 376 participants, respectively. Body parameters such as BMI, WC, and BW were found to be reduced by AA, EA, and MA. BMI had a MD of −0.81 kg/m² (95% CI= −1.26 to −0.37, P=0.0003), WC had a MD of −1.10 cm (95% CI= −2.08 to −0.12, P=0.03), and BW had a MD of −1.37 kg (95% CI= −2.17 to −0.58, P=0.0007).
Conclusion
Acupuncture showed potential benefits to improve BMI, BW, and WC in obese adult females, indicating its efficacy in treatment. However, these findings must be confirmed by higher-quality RCTs in the future.
引言 本研究旨在评估不同针灸方法治疗成年女性肥胖症的临床疗效。针灸方法包括耳针(AA)、电针(EA)和手针(MA)。方法检索了从开始到 2022 年 5 月的七个电子数据库,以查找随机对照试验(RCT)。针灸对成年女性肥胖症的影响通过体重指数(BMI)、腰围(WC)和体重(BW)进行测量。为了评估 RCT 的质量,使用了 Cochrane 协作的偏倚风险工具。使用 "综述管理器 "软件进行汇总分析,并使用随机效应模型来考虑纳入研究的异质性。治疗组之间的差异以平均差(MD)报告。针灸组和对照组分别有 375 名和 376 名参与者。发现 AA、EA 和 MA 均可降低体重指数(BMI)、腹围(WC)和体重(BW)等身体参数。BMI的MD值为-0.81 kg/m² (95% CI= -1.26 to -0.37, P=0.0003),WC的MD值为-1.10 cm (95% CI= -2.08 to -0.12, P=0.03),BW的MD值为-1.37 kg (95% CI= -2.17 to -0.58, P=0.0007)。针灸对肥胖成年女性的体重指数、体重和腹围有潜在的改善作用,这表明针灸具有治疗效果,但这些研究结果还需在未来进行更高质量的 RCT 研究来证实。
{"title":"The effectiveness of different modes of acupuncture for mature adult females with obesity: A systematic review and meta-analysis","authors":"Chester Yan Jie Ng, Wen Min Ng, Yan Zhao, Linda LD Zhong","doi":"10.1016/j.aimed.2024.03.003","DOIUrl":"10.1016/j.aimed.2024.03.003","url":null,"abstract":"<div><h3>Introduction</h3><p>This study aims to evaluate the clinical efficacy of different modes of acupuncture for obesity treatment in adult females. Auricular Acupuncture (AA), Electroacupuncture (EA), and Manual Acupuncture (MA) were the acupuncture methods evaluated. This was accomplished through a systematic review and meta-analysis.</p></div><div><h3>Methods</h3><p>Seven electronic databases were searched from inception to May 2022 to source for Randomized Control Trials (RCTs). Acupuncture's effect on obesity in adult females was measured using body mass index (BMI), waist circumference (WC), and body weight (BW). To assess the quality of the RCTs, the Cochrane Collaboration's Risk of Bias Tool was used. Pooled analysis was done using the Review Manager software and the random-effects model was used to account for heterogeneity of the included studies. The differences between treatment groups were reported as mean differences (MD).</p></div><div><h3>Results</h3><p>12 RCTs were selected through screening of results from electronic databases. The acupuncture and control groups each had 375 and 376 participants, respectively. Body parameters such as BMI, WC, and BW were found to be reduced by AA, EA, and MA. BMI had a MD of −0.81 kg/m² (95% CI= −1.26 to −0.37, P=0.0003), WC had a MD of −1.10 cm (95% CI= −2.08 to −0.12, P=0.03), and BW had a MD of −1.37 kg (95% CI= −2.17 to −0.58, P=0.0007).</p></div><div><h3>Conclusion</h3><p>Acupuncture showed potential benefits to improve BMI, BW, and WC in obese adult females, indicating its efficacy in treatment. However, these findings must be confirmed by higher-quality RCTs in the future.</p></div>","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"11 1","pages":"Pages 24-31"},"PeriodicalIF":1.7,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140406825","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-01DOI: 10.1016/j.aimed.2024.03.004
Mitali Jaideep Naik,, Purusotham Chippala,
Objective
To evaluate the short-term effect of Tai Chi on cognitive function in breast cancer patients undergoing radiotherapy compared to the control group receiving moderate intensity walking.
Design
Parallel, single blinded, randomized controlled trial.
Setting
Mangaluru, Karnataka, India.
Participants
44 female post-surgery Breast cancer patients undergoing radiotherapy.
Interventions
Based on the inclusion criteria patients were randomly assigned into two groups of 22 each. Group A received the Taichi intervention and Group B received the moderate-intensity walking for 30 min,5 times per week for 3 weeks.
Outcome measure
Functional Assessment of Cancer Therapy Cognitive scale version 3 (FACT-Cog 3)
Randomisation
Each random number was concealed separately within a small opaque envelope (SNOSE) and the subjects were equally allocated into two groups with an allocation of 1:1.
Statistical analysis
Independent sample t-test for between the group comparison and paired t-test for within the group comparison.
Results
There were no statistically significant results found between the groups (p-value > 0.05).
Conclusion
The present randomized controlled trial showed that Tai Chi did not improve the cancer-related cognitive Impairment in Breast cancer patients compared to moderate intensity walking. Clinical Trial Registration number: CTRI/2021/08/036012.
{"title":"Effect of Taichi on cognitive function in Breast cancer patients undergoing radiotherapy: A randomized controlled trial","authors":"Mitali Jaideep Naik,, Purusotham Chippala,","doi":"10.1016/j.aimed.2024.03.004","DOIUrl":"https://doi.org/10.1016/j.aimed.2024.03.004","url":null,"abstract":"<div><h3>Objective</h3><p>To evaluate the short-term effect of Tai Chi on cognitive function in breast cancer patients undergoing radiotherapy compared to the control group receiving moderate intensity walking.</p></div><div><h3>Design</h3><p>Parallel, single blinded, randomized controlled trial.</p></div><div><h3>Setting</h3><p>Mangaluru, Karnataka, India.</p></div><div><h3>Participants</h3><p>44 female post-surgery Breast cancer patients undergoing radiotherapy.</p></div><div><h3>Interventions</h3><p>Based on the inclusion criteria patients were randomly assigned into two groups of 22 each. Group A received the Taichi intervention and Group B received the moderate-intensity walking for 30 min,5 times per week for 3 weeks.</p></div><div><h3>Outcome measure</h3><p>Functional Assessment of Cancer Therapy Cognitive scale version 3 (FACT-Cog 3)</p></div><div><h3>Randomisation</h3><p>Each random number was concealed separately within a small opaque envelope (SNOSE) and the subjects were equally allocated into two groups with an allocation of 1:1.</p></div><div><h3>Statistical analysis</h3><p>Independent sample t-test for between the group comparison and paired t-test for within the group comparison.</p></div><div><h3>Results</h3><p>There were no statistically significant results found between the groups (p-value > 0.05).</p></div><div><h3>Conclusion</h3><p>The present randomized controlled trial showed that Tai Chi did not improve the cancer-related cognitive Impairment in Breast cancer patients compared to moderate intensity walking. Clinical Trial Registration number: CTRI/2021/08/036012.</p></div>","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"11 1","pages":"Pages 32-37"},"PeriodicalIF":1.7,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140894600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hot flashes and night sweats are among the most common and disruptive symptoms in menopausal women. The present study aimed to assess the effects of Viola odorata syrup on hot flashes and night sweats in menopausal women. V. odorata contain flavonoids, saponins, mucilage, alkaloid, vitamin C, magnesium and melatonin.
Methods
This triple-blind, Randomized Controlled Trial was conducted on 84 menopausal women aged 40–65 years referring to the healthcare centers in Mashhad, Iran. Eligible menopausal women received the V. odorata syrup (5 ml) or placebo twice daily for one month. Data were collected before, during, and after the intervention using valid and reliable daily hot flash checklists. Data analysis was performed in SPSS using independent t-test, Mann-Whitney U test, Friedman test, and Chi-square at the significance level of 0.05.
Results
In the first week (before the intervention), the intervention group (V. odorata syrup) and placebo group (control) were homogenous in terms of the frequency and intensity of hot flashes and night sweats. The Mann-Whitney U test indicated a significant difference in the duration of hot flashes between the two groups. In addition, significant differences were observed between the V. odorata syrup and placebo groups between the mean duration of hot flashes in the second (P = 0.044), third (P = 0.031), fourth (P < 0.001), and fifth weeks (P<0.001), mean frequency of hot flashes in the third, fourth, and fifth weeks (P < 0.001), and mean intensity of hot flashes in the third (P = 0.003), fourth, and fifth weeks (P < 0.001), as well as night sweats in the second week, the mean values of which were significantly lower in the V. odorata group compared to the control group.
Conclusion
V. odorata syrup could reduce the frequency, intensity, and duration of hot flashes since the second week of the treatment. Therefore, the use of this plant is recommended for the reduction of hot flashes and night sweats in menopausal women.
背景潮热和盗汗是更年期妇女最常见、最具干扰性的症状之一。本研究旨在评估臭紫苏糖浆对更年期妇女潮热和盗汗的影响。方法这项三盲随机对照试验的对象是在伊朗马什哈德市医疗保健中心就诊的 84 名 40-65 岁绝经妇女。符合条件的更年期妇女每天两次服用 V. odorata 糖浆(5 毫升)或安慰剂,为期一个月。在干预前、干预期间和干预后,使用有效可靠的每日热潮红检查表收集数据。在 SPSS 中使用独立 t 检验、Mann-Whitney U 检验、Friedman 检验和 Chi-square 进行数据分析,显著性水平为 0.05。曼-惠特尼 U 检验表明,两组在潮热持续时间上存在显著差异。此外,在第二周(P = 0.044)、第三周(P = 0.031)、第四周(P <0.001)和第五周(P<0.001)潮热的平均持续时间,第三周、第四周和第五周潮热的平均频率(P <0.001),第三周(P = 0.003)、第四周和第五周(P <0.001)潮热的平均强度,以及第二周的盗汗,与对照组相比,V. odorata 组的平均值显著降低。因此,建议使用这种植物来减少更年期妇女的潮热和盗汗。
{"title":"Effects of Viola odorata syrup on hot flashes and night sweats in menopausal women: A randomized, triple-blind, controlled trial","authors":"Fatemeh Zahra Karimi , Nahid Nazari , Fatemeh Lotfi , Seyed Reza Mazloom , Mahdi Yousefi , Hassan Rakhshandeh","doi":"10.1016/j.aimed.2024.04.001","DOIUrl":"https://doi.org/10.1016/j.aimed.2024.04.001","url":null,"abstract":"<div><h3>Background</h3><p>Hot flashes and night sweats are among the most common and disruptive symptoms in menopausal women. The present study aimed to assess the effects of <em>Viola odorata</em> syrup on hot flashes and night sweats in menopausal women. V. odorata contain flavonoids, saponins, mucilage, alkaloid, vitamin C, magnesium and melatonin.</p></div><div><h3>Methods</h3><p>This triple-blind, Randomized Controlled Trial was conducted on 84 menopausal women aged 40–65 years referring to the healthcare centers in Mashhad, Iran. Eligible menopausal women received the <em>V. odorata</em> syrup (5 ml) or placebo twice daily for one month. Data were collected before, during, and after the intervention using valid and reliable daily hot flash checklists. Data analysis was performed in SPSS using independent t-test, Mann-Whitney U test, Friedman test, and Chi-square at the significance level of 0.05.</p></div><div><h3>Results</h3><p>In the first week (before the intervention), the intervention group (<em>V. odorata</em> syrup) and placebo group (control) were homogenous in terms of the frequency and intensity of hot flashes and night sweats. The Mann-Whitney U test indicated a significant difference in the duration of hot flashes between the two groups. In addition, significant differences were observed between the <em>V. odorata</em> syrup and placebo groups between the mean duration of hot flashes in the second (P = 0.044), third (P = 0.031), fourth (P < 0.001), and fifth weeks (P<0.001), mean frequency of hot flashes in the third, fourth, and fifth weeks (P < 0.001), and mean intensity of hot flashes in the third (P = 0.003), fourth, and fifth weeks (P < 0.001), as well as night sweats in the second week, the mean values of which were significantly lower in the <em>V. odorata</em> group compared to the control group.</p></div><div><h3>Conclusion</h3><p><em>V. odorata</em> syrup could reduce the frequency, intensity, and duration of hot flashes since the second week of the treatment. Therefore, the use of this plant is recommended for the reduction of hot flashes and night sweats in menopausal women.</p></div>","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"11 1","pages":"Pages 38-44"},"PeriodicalIF":1.7,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140894602","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-01DOI: 10.1016/j.aimed.2024.03.005
Susan Arentz
{"title":"The healthcare workforce, working to ‘full-scope of practice’","authors":"Susan Arentz","doi":"10.1016/j.aimed.2024.03.005","DOIUrl":"10.1016/j.aimed.2024.03.005","url":null,"abstract":"","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"11 1","pages":"Page 1"},"PeriodicalIF":1.7,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140402576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
This study aimed to assess the effect of Curcumin and/or Nigella sativa on bone density parameters (primary outcome) and quality of life (secondary outcome) in postmenopausal women with primary osteoporosis or osteopenia.
Design
Randomized controlled trial with factorial design.
Methods
120 postmenopausal women aged 50–65 years with primary osteoporosis or osteopenia were equally randomized into four groups receiving daily capsules for six months; 1) nanomicellar Curcumin 80 mg, 2) Nigella sativa oil 1000 mg, 3) both, 4) placebo. All groups also received conventional treatments. In addition to the baseline assessment, bone mineral density (BMD), T-score, and Z-score were assessed at six months and quality of life (using the menopause-specific quality of life questionnaire) at two, four, and six months of the interventions.
Results
Five cases were lost to follow-up. No serious side events were reported. After the interventions, significant increases were observed in the femoral neck-BMD within all groups (p<0.01) as well as in the lumbar spine-BMD within the Nigella sativa and nanomicellar Curcumin-Nigella sativa groups (p<0.05). However, there was no statistically significant difference between the groups in terms of bone density parameters and overall quality of life score. In the Curcumin group, vasomotor dimension (adjusted difference −0.90, 95% CI: −1.62 to −0.18) and in the Nigella, sativa group vasomotor (-0.76, −1.50 to −0.03) and physical (-0.61, −1.09 to −0.14) dimensions of quality of life score were significantly better than the placebo group.
Conclusions
The addition of Curcumin, Nigella sativa oil, or their combination does not significantly improve bone density parameters and overall quality of life of postmenopausal women with primary osteoporosis or osteopenia compared to routine treatment, but it can improve vasomotor function of quality of life. We suggest conducting long-term interventions based on the results.
{"title":"Effect of Curcumin and/or Nigella sativa on bone density and quality of life in postmenopausal women with osteoporosis or osteopenia","authors":"Farzaneh Usefian , Azizeh Farshbaf- Khalili , Mojgan Mirghafourvand , Majid Mobasseri , Sakineh Mohammad-Alizadeh-Charandabi","doi":"10.1016/j.aimed.2024.03.002","DOIUrl":"10.1016/j.aimed.2024.03.002","url":null,"abstract":"<div><h3>Objectives</h3><p>This study aimed to assess the effect of Curcumin and/or Nigella sativa on bone density parameters (primary outcome) and quality of life (secondary outcome) in postmenopausal women with primary osteoporosis or osteopenia.</p></div><div><h3>Design</h3><p>Randomized controlled trial with factorial design.</p></div><div><h3>Methods</h3><p>120 postmenopausal women aged 50–65 years with primary osteoporosis or osteopenia were equally randomized into four groups receiving daily capsules for six months; 1) nanomicellar Curcumin 80 mg, 2) Nigella sativa oil 1000 mg, 3) both, 4) placebo. All groups also received conventional treatments. In addition to the baseline assessment, bone mineral density (BMD), T-score, and Z-score were assessed at six months and quality of life (using the menopause-specific quality of life questionnaire) at two, four, and six months of the interventions.</p></div><div><h3>Results</h3><p>Five cases were lost to follow-up. No serious side events were reported. After the interventions, significant increases were observed in the femoral neck-BMD within all groups (p<0.01) as well as in the lumbar spine-BMD within the Nigella sativa and nanomicellar Curcumin-Nigella sativa groups (p<0.05). However, there was no statistically significant difference between the groups in terms of bone density parameters and overall quality of life score. In the Curcumin group, vasomotor dimension (adjusted difference −0.90, 95% CI: −1.62 to −0.18) and in the Nigella, sativa group vasomotor (-0.76, −1.50 to −0.03) and physical (-0.61, −1.09 to −0.14) dimensions of quality of life score were significantly better than the placebo group.</p></div><div><h3>Conclusions</h3><p>The addition of Curcumin, Nigella sativa oil, or their combination does not significantly improve bone density parameters and overall quality of life of postmenopausal women with primary osteoporosis or osteopenia compared to routine treatment, but it can improve vasomotor function of quality of life. We suggest conducting long-term interventions based on the results.</p></div>","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"11 1","pages":"Pages 17-23"},"PeriodicalIF":1.7,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140273968","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-01DOI: 10.1016/j.aimed.2023.10.006
Ramin Gooruee , Naseh Pahlavani , Vahid Hadi , Saeid Hadi
Background
The aim of the present study was to evaluation the impacts of kefir intake, as a popular traditional probiotic product on the immune response and the recovery process of COVID-19 patients admitted to the hospital.
Methods
We conducted a double-blind randomized controlled trial on 100 COVID-19 patients selected from Emam Reza Hospital between February 9, 2022, and March 9, 2022. In the intervention group, participants received kefir grains (2–10 %) to milk twice a day (250 ccs each time) for two weeks. Clinical outcomes such as fever, pain, gastrointestinal symptoms, and dyspnea were collected at the beginning and end of the study using a checklist prepared by the research team. Also, each group measured inflammatory indices (ESR & CRP) and hematological factors before and after the intervention.
Results
The mean age of participants was 47.06 ± 8.90 years. WBC before (p = 0.001), neutrophil before (p = 0.001), lymphocyte before (p = 0.000) and after (p = 0.001) the intervention, hemoglobin before (p = 0.001) and after (p = 0.001) the intervention, CRP before (0.001), ESR after (p = 0.011), and oxygen saturation after (p = 0.001) the intervention had statistically significant differences between the intervention and control groups (p < 0.05).
Conclusion
Overall, two weeks of kefir intakes in COVID-19 patients had beneficial effects on ESR, WBC count, and Oxygen saturation levels. However, this probiotic product did not influence other evaluated indices including CRP and Hemoglobin in COVID-19 patients. More studies are required to clarify this topic.
{"title":"Evaluation of the effect of kefir supplementation on inflammatory markers and clinical and hematological indices in COVID-19 patients; a randomized double-blined clinical trial","authors":"Ramin Gooruee , Naseh Pahlavani , Vahid Hadi , Saeid Hadi","doi":"10.1016/j.aimed.2023.10.006","DOIUrl":"10.1016/j.aimed.2023.10.006","url":null,"abstract":"<div><h3>Background</h3><p><span>The aim of the present study was to evaluation the impacts of kefir intake, as a popular traditional </span>probiotic product on the immune response and the recovery process of COVID-19 patients admitted to the hospital.</p></div><div><h3>Methods</h3><p>We conducted a double-blind randomized controlled trial<span> on 100 COVID-19 patients selected from Emam Reza Hospital between February 9, 2022, and March 9, 2022. In the intervention group, participants received kefir grains (2–10 %) to milk twice a day (250 ccs each time) for two weeks. Clinical outcomes such as fever, pain, gastrointestinal symptoms, and dyspnea were collected at the beginning and end of the study using a checklist prepared by the research team. Also, each group measured inflammatory indices (ESR & CRP) and hematological factors before and after the intervention.</span></p></div><div><h3>Results</h3><p>The mean age of participants was 47.06 ± 8.90 years. WBC before (p = 0.001), neutrophil<span> before (p = 0.001), lymphocyte before (p = 0.000) and after (p = 0.001) the intervention, hemoglobin before (p = 0.001) and after (p = 0.001) the intervention, CRP before (0.001), ESR after (p = 0.011), and oxygen saturation after (p = 0.001) the intervention had statistically significant differences between the intervention and control groups (p < 0.05).</span></p></div><div><h3>Conclusion</h3><p>Overall, two weeks of kefir intakes in COVID-19 patients had beneficial effects on ESR, WBC count, and Oxygen saturation levels. However, this probiotic product did not influence other evaluated indices including CRP and Hemoglobin in COVID-19 patients. More studies are required to clarify this topic.</p></div>","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"11 1","pages":"Pages 10-16"},"PeriodicalIF":1.7,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136128454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hydrogen molecules, which have excellent antioxidant and anti-inflammatory effects, are absorbed through the skin and spread hematogenously throughout the body. Hydrogen-water bathing (HWB) is expected to be effective against atopic dermatitis (AD); however, its usefulness remains controversial in humans.
Objective
This study aimed to determine whether HWB has the potential to have a therapeutic effect in a pilot study conducted on six patients with AD.
Methods
AD severity was assessed based on the itching intensity per the visual analog scales (VAS) and the transepidermal water loss (TEWL) values of the lesions, in addition to macroscopic observations.
Results
HWB for eight weeks ameliorated the severity of rashes and increased TEWL levels in the trunk/limb areas that could be completely immersed in the bathwater, resulting in ameliorations in severe itching. The specificity of its therapeutic effect was further investigated in one patient who first underwent HWB for four weeks, discontinued it for two weeks, and resumed it for another four weeks. The rashes on the trunk/limb areas visibly improved after four weeks of HWB but worsened again after it was stopped for two weeks, only to improve again after the resumption of HWB for four weeks. The VAS and TEWL values also showed changes that reflected the skin condition.
Conclusion
These results suggest that HWB may be useful in the treatment of AD. To conclude the effectiveness of HWB for AD, it needs to be supported by randomized controlled trials with larger sample sizes and longer study durations in the future.
{"title":"A pilot study to evaluate the potential therapeutic effect of hydrogen-water bathing on atopic dermatitis in humans","authors":"Ailing Hu , Takuji Yamaguchi , Masahiro Tabuchi , Yasushi Ikarashi , Akio Mizushima , Hiroyuki Kobayashi","doi":"10.1016/j.aimed.2023.10.003","DOIUrl":"10.1016/j.aimed.2023.10.003","url":null,"abstract":"<div><h3>Background</h3><p>Hydrogen molecules, which have excellent antioxidant and anti-inflammatory effects, are absorbed through the skin and spread hematogenously throughout the body. Hydrogen-water bathing (HWB) is expected to be effective against atopic dermatitis (AD); however, its usefulness remains controversial in humans.</p></div><div><h3>Objective</h3><p>This study aimed to determine whether HWB has the potential to have a therapeutic effect in a pilot study conducted on six patients with AD.</p></div><div><h3>Methods</h3><p>AD severity was assessed based on the itching intensity per the visual analog scales (VAS) and the transepidermal water loss (TEWL) values of the lesions, in addition to macroscopic observations.</p></div><div><h3>Results</h3><p>HWB for eight weeks ameliorated the severity of rashes and increased TEWL levels in the trunk/limb areas that could be completely immersed in the bathwater, resulting in ameliorations in severe itching. The specificity of its therapeutic effect was further investigated in one patient who first underwent HWB for four weeks, discontinued it for two weeks, and resumed it for another four weeks. The rashes on the trunk/limb areas visibly improved after four weeks of HWB but worsened again after it was stopped for two weeks, only to improve again after the resumption of HWB for four weeks. The VAS and TEWL values also showed changes that reflected the skin condition.</p></div><div><h3>Conclusion</h3><p>These results suggest that HWB may be useful in the treatment of AD. To conclude the effectiveness of HWB for AD, it needs to be supported by randomized controlled trials with larger sample sizes and longer study durations in the future.</p></div>","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"11 1","pages":"Pages 2-9"},"PeriodicalIF":1.7,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2212958823000848/pdfft?md5=d5161a2a63237d383d64aaf5008a0a5d&pid=1-s2.0-S2212958823000848-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135411318","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}
Pub Date : 2024-01-01DOI: 10.1016/j.aimed.2024.01.001
Katherine Cheng, Joanna Harnett, Sharon Davis, Lorraine Smith
{"title":"Conversations about cannabis: the supply process in Australia","authors":"Katherine Cheng, Joanna Harnett, Sharon Davis, Lorraine Smith","doi":"10.1016/j.aimed.2024.01.001","DOIUrl":"https://doi.org/10.1016/j.aimed.2024.01.001","url":null,"abstract":"","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"35 15","pages":""},"PeriodicalIF":1.7,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139457547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-01DOI: 10.1016/j.aimed.2023.10.001
Xiang Gao, Yan Cheng, Fangyuan Liu, Xiaozhen Han, Chuanliang Liu
{"title":"The clinical efficacy and safety of Ginkgo biloba in vertigo patients: A meta-analysis","authors":"Xiang Gao, Yan Cheng, Fangyuan Liu, Xiaozhen Han, Chuanliang Liu","doi":"10.1016/j.aimed.2023.10.001","DOIUrl":"https://doi.org/10.1016/j.aimed.2023.10.001","url":null,"abstract":"","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"37 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136159601","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-10-01DOI: 10.1016/j.aimed.2023.10.002
Anwesa Chatterjee
The utilization of certain forms of complementary and alternative medicine (CAM) is prevalent among adults in the United States. While researchers have extensively studied the factors influencing CAM use in Western countries, significant barriers to its adoption remain. This paper draws attention to the obstacles faced by individuals in their journey to using CAM. Qualitative interviews were conducted with 21 patients who had turned to CAM for managing a chronic illness/condition. These in-depth, face-to-face interviews occurred in Miami, USA, during 2014-15. The sampling, data collection, and analysis processes of this study adhered to the principles outlined in Charmaz’s constructivist grounded theory approach. From the data, three central barriers to CAM utilization in the US emerged: 1) Financial barriers: A significant portion of CAM treatments is not covered by insurance, making them cost-prohibitive for many. 2) Skepticism and discouragement: Both conventional medical practitioners and a segment of the public exhibited a noticeable trend towards discouraging CAM use. 3) Evaluation challenges: Patients expressed difficulty in assessing the efficacy and benefits of various CAM treatments compared to their costs. Despite the widespread interest in and use of CAM in the US, numerous barriers hinder its broader integration into mainstream healthcare. These obstacles not only restrict healthcare choices for the general public but also appear to favor a select demographic, potentially based on income and availability of information.
{"title":"Evaluating the Barriers to the Utilization of Complementary and Alternative Medicine (CAM) in the United States: An Exploratory Study","authors":"Anwesa Chatterjee","doi":"10.1016/j.aimed.2023.10.002","DOIUrl":"https://doi.org/10.1016/j.aimed.2023.10.002","url":null,"abstract":"The utilization of certain forms of complementary and alternative medicine (CAM) is prevalent among adults in the United States. While researchers have extensively studied the factors influencing CAM use in Western countries, significant barriers to its adoption remain. This paper draws attention to the obstacles faced by individuals in their journey to using CAM. Qualitative interviews were conducted with 21 patients who had turned to CAM for managing a chronic illness/condition. These in-depth, face-to-face interviews occurred in Miami, USA, during 2014-15. The sampling, data collection, and analysis processes of this study adhered to the principles outlined in Charmaz’s constructivist grounded theory approach. From the data, three central barriers to CAM utilization in the US emerged: 1) Financial barriers: A significant portion of CAM treatments is not covered by insurance, making them cost-prohibitive for many. 2) Skepticism and discouragement: Both conventional medical practitioners and a segment of the public exhibited a noticeable trend towards discouraging CAM use. 3) Evaluation challenges: Patients expressed difficulty in assessing the efficacy and benefits of various CAM treatments compared to their costs. Despite the widespread interest in and use of CAM in the US, numerous barriers hinder its broader integration into mainstream healthcare. These obstacles not only restrict healthcare choices for the general public but also appear to favor a select demographic, potentially based on income and availability of information.","PeriodicalId":7343,"journal":{"name":"Advances in integrative medicine","volume":"62 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136093688","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}