首页 > 最新文献

Journal of rehabilitation medicine. Clinical communications最新文献

英文 中文
PAIN IN POST-POLIO SYNDROME: A SEPARATE PAIN ENTITY? 脊髓灰质炎后综合征的疼痛:一个单独的疼痛实体?
Pub Date : 2022-01-22 eCollection Date: 2022-01-01 DOI: 10.2340/20030711-1000077
Evert Christiaan Boshuis, Eva Melin, Kristian Borg
Background Most patients with polio recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called post-polio syndrome. Although poliovirus has been almost eliminated, 12–20 million people worldwide still have polio sequelae. The pain is described mainly as nociceptive, but some patients experience neuropathic pain. The aim of this study was to further characterize post-polio pain. Patients and methods A total of 20 patients with post-polio syndrome participated in the study. Physical examination was performed, and questionnaires containing pain drawing and visual analogue scales (VAS) for pain intensity during rest and motion and VAS for fatigue were completed. A walk test was performed to evaluate physical performance. Results Pain intensity was high (42/100 on the VAS at rest and 62/100 while moving). The pain was localized in both joints and muscles. Pain in the muscles was of “deep aching” character, included “muscle cramps” and was located mainly in polio-weakened limbs. Conclusion Muscle pain in patients with post-polio syndrome does not fulfil the criteria for either nociceptive or neuropathic pain; thus, it is suggested that the pain is termed “post-polio muscular pain”. The intensity of post-polio muscular pain is higher while moving, but does not influence physical function, and is separate from fatigue. LAY ABSTRACT Most polio patients recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called Post-Polio Syndrome. Though the poliovirus has almost been eliminated, 12-20 million people worldwide still have polio-sequelae. The pain is mainly described as nociceptive, but some patients experience neuropathic pain. This study was undertaken to further characterize post-polio pain. We examined 20 Post-polio patients and found that the pain was localised in both joints and muscles. The pain in the muscles was of ‘deep aching’ character, included ‘muscle cramps’ and was mainly located in polio-weakened limbs. The intensity of the pain is higher while moving but does not influence the physical function. To know more about the characteristics of the pain perceived gives better possibilities for treatment and rehabilitation
背景:大多数脊髓灰质炎患者从最初的感染中恢复,但在15-40年后出现肌肉无力、疼痛和疲劳,这种情况称为脊髓灰质炎后综合征。尽管脊髓灰质炎病毒几乎已被消灭,但全世界仍有1200万至2000万人患有脊髓灰质炎后遗症。疼痛主要被描述为伤害性疼痛,但也有一些患者经历神经性疼痛。本研究的目的是进一步表征脊髓灰质炎后疼痛。患者与方法:共20例脊髓灰质炎后综合征患者参与研究。进行体格检查,并完成疼痛图和视觉模拟量表(VAS)对休息和运动时的疼痛强度和疲劳的VAS评分。进行行走测试以评估身体表现。结果:疼痛强度高(静止时VAS评分为42/100,运动时为62/100)。疼痛局限于关节和肌肉。肌肉疼痛具有“深度疼痛”特征,包括“肌肉痉挛”,主要位于脊髓灰质炎削弱的肢体。结论:脊髓灰质炎后综合征患者的肌肉疼痛不符合伤害性疼痛和神经性疼痛的标准;因此,有人建议将这种疼痛称为“脊髓灰质炎后肌肉疼痛”。脊髓灰质炎后肌肉疼痛的强度在运动时更高,但不影响身体功能,与疲劳无关。
{"title":"PAIN IN POST-POLIO SYNDROME: A SEPARATE PAIN ENTITY?","authors":"Evert Christiaan Boshuis, Eva Melin, Kristian Borg","doi":"10.2340/20030711-1000077","DOIUrl":"https://doi.org/10.2340/20030711-1000077","url":null,"abstract":"Background Most patients with polio recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called post-polio syndrome. Although poliovirus has been almost eliminated, 12–20 million people worldwide still have polio sequelae. The pain is described mainly as nociceptive, but some patients experience neuropathic pain. The aim of this study was to further characterize post-polio pain. Patients and methods A total of 20 patients with post-polio syndrome participated in the study. Physical examination was performed, and questionnaires containing pain drawing and visual analogue scales (VAS) for pain intensity during rest and motion and VAS for fatigue were completed. A walk test was performed to evaluate physical performance. Results Pain intensity was high (42/100 on the VAS at rest and 62/100 while moving). The pain was localized in both joints and muscles. Pain in the muscles was of “deep aching” character, included “muscle cramps” and was located mainly in polio-weakened limbs. Conclusion Muscle pain in patients with post-polio syndrome does not fulfil the criteria for either nociceptive or neuropathic pain; thus, it is suggested that the pain is termed “post-polio muscular pain”. The intensity of post-polio muscular pain is higher while moving, but does not influence physical function, and is separate from fatigue. LAY ABSTRACT Most polio patients recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called Post-Polio Syndrome. Though the poliovirus has almost been eliminated, 12-20 million people worldwide still have polio-sequelae. The pain is mainly described as nociceptive, but some patients experience neuropathic pain. This study was undertaken to further characterize post-polio pain. We examined 20 Post-polio patients and found that the pain was localised in both joints and muscles. The pain in the muscles was of ‘deep aching’ character, included ‘muscle cramps’ and was mainly located in polio-weakened limbs. The intensity of the pain is higher while moving but does not influence the physical function. To know more about the characteristics of the pain perceived gives better possibilities for treatment and rehabilitation","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000077"},"PeriodicalIF":0.0,"publicationDate":"2022-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ed/8c/JRMCC-5-1000077.PMC8793922.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39930753","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: 1
INCLUDING EXERCISE SELF-MANAGEMENT AS PART OF INPATIENT REHABILITATION IS FEASIBLE, SAFE AND EFFECTIVE FOR PATIENTS WITH COGNITIVE IMPAIRMENT. 将运动自我管理作为认知障碍患者住院康复的一部分是可行、安全、有效的。
Pub Date : 2022-01-13 eCollection Date: 2022-01-01 DOI: 10.2340/20030711-1000076
Natasha K Brusco, Helen Kugler, Fiona Dufler, Annemarie L Lee, Brianna Walpole, Meg E Morris, Keith D Hill, Christina L Ekegren, Sara L Whittaker, Nicholas F Taylor

Objective: To test the feasibility, safety and effectiveness of the My Therapy programme for inpatients with mild-moderate cognitive impairment.

Design: Observational pilot study.

Patients: Rehabilitation inpatients with mild-moderate cognitive impairment.

Methods: During their inpatient admission, participants received My Therapy, a programme that can increase the dose of rehabilitation through independent self-practice of exercises, outside of supervised therapy. Outcomes included My Therapy participation, falls, Functional Independence Measure (FIM) and 10-m walk test. Outcomes were compared with those of participants without cognitive impairment from the original My Therapy study (n = 116) using χ 2 and independent t-tests.

Results: Eight participants with mild-moderate cognitive impairment (mean (standard deviation (SD)) age 89.6 years (4.8); 3 women) were included. All participants completed the My Therapy programme on at least one day of their admission, with no associated falls. Participants had an 8.4 s (SD 5.1) reduction in their 10-m walk test and a 21.5 point (SD 11.1) improvement on FIM scores from admission to discharge. There were no significant between-group differences in feasibility, safety or effectiveness for participants with and without cognitive impairment.

Conclusion: This pilot study has shown that including exercise self-management as part of inpatient rehabilitation is feasible, safe and effective for patients with cognitive impairment.

目的:探讨My治疗方案治疗轻中度认知功能障碍的可行性、安全性和有效性。设计:观察性先导研究。患者:康复住院的轻中度认知障碍患者。方法:在他们住院期间,参与者接受了我的治疗,这是一个可以通过独立的自我练习来增加康复剂量的项目,在监督治疗之外。结果包括我的治疗参与、跌倒、功能独立测量(FIM)和10米行走测试。使用χ 2和独立t检验比较原始My Therapy研究(n = 116)中无认知障碍的参与者的结果。结果:8例轻度至中度认知障碍患者(平均(标准差(SD))年龄89.6岁(4.8岁);包括3名女性)。所有参与者至少在入院的一天内完成了“我的治疗”项目,没有相关的跌倒。从入院到出院,参与者的10米步行测试减少了8.4秒(SD 5.1), FIM评分提高了21.5分(SD 11.1)。对于有和没有认知障碍的参与者,两组之间在可行性、安全性或有效性方面没有显著差异。结论:本初步研究表明,将运动自我管理作为认知障碍患者住院康复的一部分是可行、安全、有效的。
{"title":"INCLUDING EXERCISE SELF-MANAGEMENT AS PART OF INPATIENT REHABILITATION IS FEASIBLE, SAFE AND EFFECTIVE FOR PATIENTS WITH COGNITIVE IMPAIRMENT.","authors":"Natasha K Brusco,&nbsp;Helen Kugler,&nbsp;Fiona Dufler,&nbsp;Annemarie L Lee,&nbsp;Brianna Walpole,&nbsp;Meg E Morris,&nbsp;Keith D Hill,&nbsp;Christina L Ekegren,&nbsp;Sara L Whittaker,&nbsp;Nicholas F Taylor","doi":"10.2340/20030711-1000076","DOIUrl":"https://doi.org/10.2340/20030711-1000076","url":null,"abstract":"<p><strong>Objective: </strong>To test the feasibility, safety and effectiveness of the My Therapy programme for inpatients with mild-moderate cognitive impairment.</p><p><strong>Design: </strong>Observational pilot study.</p><p><strong>Patients: </strong>Rehabilitation inpatients with mild-moderate cognitive impairment.</p><p><strong>Methods: </strong>During their inpatient admission, participants received My Therapy, a programme that can increase the dose of rehabilitation through independent self-practice of exercises, outside of supervised therapy. Outcomes included My Therapy participation, falls, Functional Independence Measure (FIM) and 10-m walk test. Outcomes were compared with those of participants without cognitive impairment from the original My Therapy study (<i>n</i> = 116) using <i>χ</i> <sup>2</sup> and independent <i>t</i>-tests.</p><p><strong>Results: </strong>Eight participants with mild-moderate cognitive impairment (mean (standard deviation (SD)) age 89.6 years (4.8); 3 women) were included. All participants completed the My Therapy programme on at least one day of their admission, with no associated falls. Participants had an 8.4 s (SD 5.1) reduction in their 10-m walk test and a 21.5 point (SD 11.1) improvement on FIM scores from admission to discharge. There were no significant between-group differences in feasibility, safety or effectiveness for participants with and without cognitive impairment.</p><p><strong>Conclusion: </strong>This pilot study has shown that including exercise self-management as part of inpatient rehabilitation is feasible, safe and effective for patients with cognitive impairment.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000076"},"PeriodicalIF":0.0,"publicationDate":"2022-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/54/22/JRMCC-5-1000076.PMC8771766.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39611717","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
POST-COVID SYMPTOMS AND WHOLE-BODY CRYOTHERAPHY: A CASE REPORT. 新冠肺炎后症状与全身冷冻治疗1例
Pub Date : 2022-01-13 eCollection Date: 2022-01-01 DOI: 10.2340/20030711-1000075
Michele Gobbi, Giulia Trotti, Massimo Tanzi, Fatma Kasap, Paolo Piterà, Paolo Capodaglio
Missing (Case Report)
{"title":"POST-COVID SYMPTOMS AND WHOLE-BODY CRYOTHERAPHY: A CASE REPORT.","authors":"Michele Gobbi,&nbsp;Giulia Trotti,&nbsp;Massimo Tanzi,&nbsp;Fatma Kasap,&nbsp;Paolo Piterà,&nbsp;Paolo Capodaglio","doi":"10.2340/20030711-1000075","DOIUrl":"https://doi.org/10.2340/20030711-1000075","url":null,"abstract":"Missing (Case Report)","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000075"},"PeriodicalIF":0.0,"publicationDate":"2022-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/91/c3/JRMCC-5-1000075.PMC8771767.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39611716","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: 2
OSTEOCHONDROSES IN CHILDREN'S SPORTS PRACTICE - A RARE CASE OF VAN NECK-ODELBERG DISEASE. 儿童运动训练中的骨软骨病——范内克-奥德伯格病的一个罕见病例。
Pub Date : 2022-01-01 DOI: 10.2340/jrmcc.v5.4593
João P Fonseca, Pedro Figueiredo, João P Pinheiro

Background: Osteochondroses are a set of conditions concerning the ossification of the developing bone. Higher intensity in sports activities can increase its occurrence in children. There is no consensus on its etiology, with multiple factors being involved. Van Neck-Odelberg disease is a rare osteochondrosis located in ischiopubic synchondrosis. Treatment is mainly conservative, with activity suspension. Addressing and correcting the predisposing factors is crucial to these injuries.

Case report: We present a case of a 6-year-old futsal player who experienced mechanical inguinal moderate pain during sports practice. After performing physical examination, laboratory tests, and radiographic evaluation, the patient was diagnosed with Van Neck-Odelberg disease. Sports activities were suspended while a conservative treatment was performed, with subsequent follow-up over 3.5 years. No symptom recurrence was reported.

Conclusion: Increased intensity of sports activities is associated with overuse injuries in children, especially before completing the ossification process. Preventive measures must remain the primary concern in children's sports practice.

背景:骨软骨症是一组与发育中的骨骨化有关的疾病。高强度的体育活动可增加儿童的发病率。其病因尚未达成共识,涉及多种因素。Van Neck-Odelberg病是一种罕见的骨软骨病,位于坐骨耻骨软骨联合症。治疗以保守为主,暂停活动。解决和纠正诱发因素对这些损伤至关重要。病例报告:我们提出一个6岁的五人制足球运动员谁经历机械腹股沟中度疼痛在运动练习。经过体格检查、实验室检查和影像学评估,患者被诊断为Van Neck-Odelberg病。在保守治疗期间暂停体育活动,随访超过3.5年。无症状复发报告。结论:运动强度的增加与儿童的过度使用性损伤有关,特别是在完成骨化过程之前。预防措施仍然是儿童体育实践中首要关注的问题。
{"title":"OSTEOCHONDROSES IN CHILDREN'S SPORTS PRACTICE - A RARE CASE OF VAN NECK-ODELBERG DISEASE.","authors":"João P Fonseca,&nbsp;Pedro Figueiredo,&nbsp;João P Pinheiro","doi":"10.2340/jrmcc.v5.4593","DOIUrl":"https://doi.org/10.2340/jrmcc.v5.4593","url":null,"abstract":"<p><strong>Background: </strong>Osteochondroses are a set of conditions concerning the ossification of the developing bone. Higher intensity in sports activities can increase its occurrence in children. There is no consensus on its etiology, with multiple factors being involved. Van Neck-Odelberg disease is a rare osteochondrosis located in ischiopubic synchondrosis. Treatment is mainly conservative, with activity suspension. Addressing and correcting the predisposing factors is crucial to these injuries.</p><p><strong>Case report: </strong>We present a case of a 6-year-old futsal player who experienced mechanical inguinal moderate pain during sports practice. After performing physical examination, laboratory tests, and radiographic evaluation, the patient was diagnosed with Van Neck-Odelberg disease. Sports activities were suspended while a conservative treatment was performed, with subsequent follow-up over 3.5 years. No symptom recurrence was reported.</p><p><strong>Conclusion: </strong>Increased intensity of sports activities is associated with overuse injuries in children, especially before completing the ossification process. Preventive measures must remain the primary concern in children's sports practice.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":"5 ","pages":"4593"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/dc/5f/JRMCC-5-4593.PMC9772922.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10508687","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: 1
Efficacy of Electromechanically-Assisted Rehabilitation of Upper Limb Function in Post-Stroke Patients: A Randomized Controlled Study. 脑卒中后患者机电辅助上肢功能康复的疗效:一项随机对照研究。
Pub Date : 2021-11-24 eCollection Date: 2021-01-01 DOI: 10.2340/20030711-1000074
Ji-Hyun Kim, Myoung-Hwan Ko, Jin Woo Park, Ho Jun Lee, Ki Yeun Nam, Yeon-Gyo Nam, Chi-Hun Oh, Joong Hee Park, Bum Sun Kwon

Objective: To investigate the efficacy of electromechanically-assisted rehabilitation of upper limb function in post-stroke patients.

Design: Randomized controlled trial.

Subjects: Forty-eight stroke patients.

Methods: Patients were randomly assigned to control and experimental groups. The control group underwent occupational therapy training with conventional methods. The experimental group underwent electromechanically-assisted training using an end effector robot (Camillo®). Interventions were provided for 30 min per day, 5 days a week, for 4 weeks. Primary outcome was change in Fugl-Meyer Assessment (FMA) before and after training. Secondary outcomes were changes in hand function, upper limb strength, spasticity, mental status and quality of life.

Results: Mean improvement in FMA was 1.17 (standard deviation (SD) 4.18) in the control group and 2.52 (SD 5.48) in the experimental group. Although FMA in the experimental group improved significantly after training, the improvement in FMA did not differ significantly between groups. Among the secondary outcomes, the Motricity Index (MI) improved significantly after training in the experimental group, and the change in MI between groups was statistically significant.

Conclusion: Electromechanically-assisted rehabilitation using Camillo® was not more effective than conventional occupation therapy for upper arm function.

目的:探讨电机械辅助上肢功能康复对脑卒中后患者的治疗效果。设计:随机对照试验。研究对象:48例中风患者。方法:将患者随机分为对照组和实验组。对照组采用常规方法进行职业治疗训练。实验组使用末端执行器机器人(Camillo®)进行机电辅助训练。干预每天30分钟,每周5天,持续4周。主要观察指标为训练前后Fugl-Meyer评估(FMA)的变化。次要结局是手功能、上肢力量、痉挛、精神状态和生活质量的变化。结果:对照组患者FMA平均改善1.17(标准差4.18),实验组患者平均改善2.52(标准差5.48)。虽然实验组在训练后FMA有明显提高,但两组间FMA的改善无显著差异。次要指标中,实验组运动指数(moicity Index, MI)训练后明显改善,组间变化有统计学意义。结论:Camillo®机电辅助康复对上臂功能的改善并不比传统的职业治疗更有效。
{"title":"Efficacy of Electromechanically-Assisted Rehabilitation of Upper Limb Function in Post-Stroke Patients: A Randomized Controlled Study.","authors":"Ji-Hyun Kim,&nbsp;Myoung-Hwan Ko,&nbsp;Jin Woo Park,&nbsp;Ho Jun Lee,&nbsp;Ki Yeun Nam,&nbsp;Yeon-Gyo Nam,&nbsp;Chi-Hun Oh,&nbsp;Joong Hee Park,&nbsp;Bum Sun Kwon","doi":"10.2340/20030711-1000074","DOIUrl":"https://doi.org/10.2340/20030711-1000074","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the efficacy of electromechanically-assisted rehabilitation of upper limb function in post-stroke patients.</p><p><strong>Design: </strong>Randomized controlled trial.</p><p><strong>Subjects: </strong>Forty-eight stroke patients.</p><p><strong>Methods: </strong>Patients were randomly assigned to control and experimental groups. The control group underwent occupational therapy training with conventional methods. The experimental group underwent electromechanically-assisted training using an end effector robot (Camillo®). Interventions were provided for 30 min per day, 5 days a week, for 4 weeks. Primary outcome was change in Fugl-Meyer Assessment (FMA) before and after training. Secondary outcomes were changes in hand function, upper limb strength, spasticity, mental status and quality of life.</p><p><strong>Results: </strong>Mean improvement in FMA was 1.17 (standard deviation (SD) 4.18) in the control group and 2.52 (SD 5.48) in the experimental group. Although FMA in the experimental group improved significantly after training, the improvement in FMA did not differ significantly between groups. Among the secondary outcomes, the Motricity Index (MI) improved significantly after training in the experimental group, and the change in MI between groups was statistically significant.</p><p><strong>Conclusion: </strong>Electromechanically-assisted rehabilitation using Camillo® was not more effective than conventional occupation therapy for upper arm function.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000074"},"PeriodicalIF":0.0,"publicationDate":"2021-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a6/ec/JRMCC-4-1000074.PMC8628063.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39687439","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: 3
DO YOUTHS WITH NEUROMOTOR DISORDER AND THEIR THERAPISTS PREFER A MIXED OR VIRTUAL REALITY HEAD-MOUNTED DISPLAY? 患有神经运动障碍的青少年和他们的治疗师更喜欢混合现实或虚拟现实头戴式显示器吗?
Pub Date : 2021-11-08 eCollection Date: 2021-01-01 DOI: 10.2340/20030711-1000072
Corinne Ammann-Reiffer, Urs Keller, Andrina Kläy, Lea Meier, Hubertus J A VAN Hedel

Objective: To evaluate the usability of 2 head-mounted displays in youths undergoing neurorehabilitation; a mixed reality head-mounted display and a virtual reality head-mounted display.

Design: Observational cross-sectional study.

Patients: Thirteen youths (age range 7.8-16.5 years) with neuromotor disorder.

Methods: Youths wore a mixed reality or a virtual reality head-mounted display while being verbally guided through a scene with virtual objects. Differences between the 2 systems, regarding usability, user experience, and acceptability, were evaluated using standardized questions for the youths and their therapists. System preferences and symptoms of cybersickness were noted.

Results: Both head-mounted displays were easy to mount and adjust to the children's heads, but the mixed reality system was unstable in 40% of the youths. Participants stated that they could move naturally with both devices. Object appearance scored higher with the virtual reality system, while therapists rated youths' movement execution and needed additional support in favour of the mixed reality system. Most youths preferred the virtual reality device, mainly due to the more distinct appearance of objects and the objects' richer colours. Therapists' preferences were balanced. Two children reported minimal signs of cybersickness.

Conclusion: Youths and therapists accepted both systems well, with advantages regarding usability, user experience, and preference for the virtual reality, and acceptability for the mixed reality head-mounted display.

目的:评价两种头戴式显示器在青少年神经康复中的应用价值;混合现实头戴式显示器和虚拟现实头戴式显示器。设计:观察性横断面研究。患者:青少年神经运动障碍13例(年龄7.8-16.5岁)。方法:青少年戴着混合现实或虚拟现实头戴式显示器,同时通过虚拟物体的场景进行口头引导。两种系统在可用性、用户体验和可接受性方面的差异,通过对青少年及其治疗师的标准化问题进行评估。系统偏好和晕屏症状被记录下来。结果:两种头戴式显示器都易于安装和调整到儿童头部,但混合现实系统在40%的青少年中不稳定。参与者表示,他们可以用这两种设备自然地移动。物体外观在虚拟现实系统中得分更高,而治疗师对青少年的运动执行进行了评分,并且需要额外的支持来支持混合现实系统。大多数年轻人更喜欢虚拟现实设备,主要是因为物体的外观更清晰,物体的颜色更丰富。治疗师的偏好是平衡的。两名儿童报告了轻微的晕屏症状。结论:青少年和治疗师对两种系统的接受度都很好,在可用性、用户体验、虚拟现实偏好和混合现实头戴式显示器方面都有优势。
{"title":"DO YOUTHS WITH NEUROMOTOR DISORDER AND THEIR THERAPISTS PREFER A MIXED OR VIRTUAL REALITY HEAD-MOUNTED DISPLAY?","authors":"Corinne Ammann-Reiffer,&nbsp;Urs Keller,&nbsp;Andrina Kläy,&nbsp;Lea Meier,&nbsp;Hubertus J A VAN Hedel","doi":"10.2340/20030711-1000072","DOIUrl":"https://doi.org/10.2340/20030711-1000072","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the usability of 2 head-mounted displays in youths undergoing neurorehabilitation; a mixed reality head-mounted display and a virtual reality head-mounted display.</p><p><strong>Design: </strong>Observational cross-sectional study.</p><p><strong>Patients: </strong>Thirteen youths (age range 7.8-16.5 years) with neuromotor disorder.</p><p><strong>Methods: </strong>Youths wore a mixed reality or a virtual reality head-mounted display while being verbally guided through a scene with virtual objects. Differences between the 2 systems, regarding usability, user experience, and acceptability, were evaluated using standardized questions for the youths and their therapists. System preferences and symptoms of cybersickness were noted.</p><p><strong>Results: </strong>Both head-mounted displays were easy to mount and adjust to the children's heads, but the mixed reality system was unstable in 40% of the youths. Participants stated that they could move naturally with both devices. Object appearance scored higher with the virtual reality system, while therapists rated youths' movement execution and needed additional support in favour of the mixed reality system. Most youths preferred the virtual reality device, mainly due to the more distinct appearance of objects and the objects' richer colours. Therapists' preferences were balanced. Two children reported minimal signs of cybersickness.</p><p><strong>Conclusion: </strong>Youths and therapists accepted both systems well, with advantages regarding usability, user experience, and preference for the virtual reality, and acceptability for the mixed reality head-mounted display.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000072"},"PeriodicalIF":0.0,"publicationDate":"2021-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/71/7f/JRMCC-4-1000072.PMC8591301.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39755278","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: 1
SAFETY AND EFFECTIVENESS OF A STATIC WEARABLE CHAIR FOR PATIENTS REQUIRING REHABILITATION: A PRELIMINARY REPORT. 用于需要康复的患者的静态可穿戴椅子的安全性和有效性:初步报告。
Pub Date : 2021-11-08 eCollection Date: 2021-01-01 DOI: 10.2340/20030711-1000071
Yoshitaka Maeda, Kosuke Oiwa, Tameto Naoi, Mitsuya Morita, Toshiki Mimura, Joji Kitayama, Hiroshi Kawahira

Objective: To evaluate the acceptability of using a static wearable chair for patients requiring rehabilitation.

Methods: The acceptability of use of a static wearable chair during rehabilitation was assessed via static balance and subjective evaluation of 7 healthy subjects and 3 patients during standing training. Participants performed 1 standing task in free mode (in which the knee could bend freely) and 1 in support mode (in which the user could sit on the wearable chair with the knee slightly bent) for 3 min. For balance evaluation, the skeletal coordinates were measured. For subjective evaluation, a visual analogue scale questionnaire was administered before and after each task.

Results: Balance assessment revealed that patients had less head sway during support, whereas subjective evaluation showed that the device support created a positive psychological state in terms of stability, comfort, satisfaction, interest in usage, and motivation for rehabilitation. However, patients reported feeling strangeness, fear, or restraint during support.

Conclusion: The static wearable chair improved the static balance of 3 patients and created a more positive psychological state. Use of the device is considered acceptable for use with rehabilitation patients. However, patients might feel strangeness, fear, and restraint during support. Familiarization with the static wearable chair may make it more acceptable among rehabilitation patients.

目的:评价需要康复的患者使用静态可穿戴椅的可接受性。方法:通过7名健康受试者和3名患者站立训练时的静态平衡和主观评价,评估可穿戴式静态椅在康复过程中使用的可接受性。参与者在自由模式下(膝盖可以自由弯曲)和支撑模式下(用户可以坐在可穿戴式椅子上,膝盖轻微弯曲)分别进行1次站立任务,持续3分钟。为了评估平衡,测量骨骼坐标。为了进行主观评价,在每个任务之前和之后进行了视觉模拟量表问卷调查。结果:平衡评估显示患者在支持期间头部晃动较少,而主观评估显示设备支持在稳定性,舒适性,满意度,使用兴趣和康复动机方面创造了积极的心理状态。然而,患者报告在支持过程中感到陌生、恐惧或约束。结论:静态可穿戴椅改善了3例患者的静态平衡,使患者的心理状态更加积极。该装置被认为可用于康复患者。然而,患者在支持过程中可能会感到陌生、恐惧和克制。熟悉静态可穿戴椅可能会使其更容易被康复患者接受。
{"title":"SAFETY AND EFFECTIVENESS OF A STATIC WEARABLE CHAIR FOR PATIENTS REQUIRING REHABILITATION: A PRELIMINARY REPORT.","authors":"Yoshitaka Maeda,&nbsp;Kosuke Oiwa,&nbsp;Tameto Naoi,&nbsp;Mitsuya Morita,&nbsp;Toshiki Mimura,&nbsp;Joji Kitayama,&nbsp;Hiroshi Kawahira","doi":"10.2340/20030711-1000071","DOIUrl":"https://doi.org/10.2340/20030711-1000071","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the acceptability of using a static wearable chair for patients requiring rehabilitation.</p><p><strong>Methods: </strong>The acceptability of use of a static wearable chair during rehabilitation was assessed via static balance and subjective evaluation of 7 healthy subjects and 3 patients during standing training. Participants performed 1 standing task in free mode (in which the knee could bend freely) and 1 in support mode (in which the user could sit on the wearable chair with the knee slightly bent) for 3 min. For balance evaluation, the skeletal coordinates were measured. For subjective evaluation, a visual analogue scale questionnaire was administered before and after each task.</p><p><strong>Results: </strong>Balance assessment revealed that patients had less head sway during support, whereas subjective evaluation showed that the device support created a positive psychological state in terms of stability, comfort, satisfaction, interest in usage, and motivation for rehabilitation. However, patients reported feeling strangeness, fear, or restraint during support.</p><p><strong>Conclusion: </strong>The static wearable chair improved the static balance of 3 patients and created a more positive psychological state. Use of the device is considered acceptable for use with rehabilitation patients. However, patients might feel strangeness, fear, and restraint during support. Familiarization with the static wearable chair may make it more acceptable among rehabilitation patients.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000071"},"PeriodicalIF":0.0,"publicationDate":"2021-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/25/a5/JRMCC-4-1000071.PMC8591300.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39755277","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
Benefits of Outpatient Cardiac Rehabilitation in an Adult Patient with Coarctation of the Aorta and Moyamoya Disease. 成人主动脉缩窄合并烟雾病患者门诊心脏康复的益处
Pub Date : 2021-10-15 eCollection Date: 2021-01-01 DOI: 10.2340/20030711-1000069
Ruiwen Zhang, Cong Chen, Eric H K Yeung, Kai-Hang Yiu

Case report: We report the effect of a 6-week outpatient (phase II) cardiac rehabilitation in a 38-year-old man with post-stented coarctation of the aorta, moyamoya disease and hypertension. The cardiac rehabilitation programme comprised physiotherapist-guided aerobic exercises, resistance training and relaxation exercises. Clinical and functional assessment was performed before and after the cardiac rehabilitation programme.

Discussion: There is a lack of recommendations to guide cardiac rehabilitation in patients with coarctation of the aorta. This case not only had coarctation of the aorta, but also had moyamoya disease and hypertension. A cardiac rehabilitation programme after surgery provided meaningful improvements in all outcomes, including exercise capacity, clinical outcomes, quality of life and depression symptoms. Systematic cardiac rehabilitation was found to be feasible in this patient with coarctation of the aorta, and may have the potential to benefit more patients.

Conclusion: Cardiac rehabilitation resulted in significant clinical and functional improvements in this case with coarctation of the aorta following surgery. Guidelines should be implemented to provide safe and effective cardiac rehabilitation in such patients. Furthermore, large-scale studies are needed to evaluate the clinical benefits of structured cardiac rehabilitation in patients following cardiac surgery.

病例报告:我们报告了一名38岁的患有支架后主动脉缩窄、烟雾病和高血压的男性患者6周门诊(II期)心脏康复的效果。心脏康复计划包括物理治疗师指导的有氧运动、阻力训练和放松运动。在心脏康复计划前后进行临床和功能评估。讨论:缺乏指导主动脉缩窄患者心脏康复的建议。该病例不仅有主动脉缩窄,还伴有烟雾病和高血压。术后心脏康复方案对所有结果都有显著改善,包括运动能力、临床结果、生活质量和抑郁症状。系统的心脏康复治疗在这例主动脉缩窄患者中是可行的,并且有可能使更多的患者受益。结论:心脏康复治疗对主动脉缩窄患者的临床和功能有显著改善。应实施指导方针,为这类患者提供安全有效的心脏康复。此外,需要大规模的研究来评估心脏手术后患者结构化心脏康复的临床益处。
{"title":"Benefits of Outpatient Cardiac Rehabilitation in an Adult Patient with Coarctation of the Aorta and Moyamoya Disease.","authors":"Ruiwen Zhang,&nbsp;Cong Chen,&nbsp;Eric H K Yeung,&nbsp;Kai-Hang Yiu","doi":"10.2340/20030711-1000069","DOIUrl":"https://doi.org/10.2340/20030711-1000069","url":null,"abstract":"<p><strong>Case report: </strong>We report the effect of a 6-week outpatient (phase II) cardiac rehabilitation in a 38-year-old man with post-stented coarctation of the aorta, moyamoya disease and hypertension. The cardiac rehabilitation programme comprised physiotherapist-guided aerobic exercises, resistance training and relaxation exercises. Clinical and functional assessment was performed before and after the cardiac rehabilitation programme.</p><p><strong>Discussion: </strong>There is a lack of recommendations to guide cardiac rehabilitation in patients with coarctation of the aorta. This case not only had coarctation of the aorta, but also had moyamoya disease and hypertension. A cardiac rehabilitation programme after surgery provided meaningful improvements in all outcomes, including exercise capacity, clinical outcomes, quality of life and depression symptoms. Systematic cardiac rehabilitation was found to be feasible in this patient with coarctation of the aorta, and may have the potential to benefit more patients.</p><p><strong>Conclusion: </strong>Cardiac rehabilitation resulted in significant clinical and functional improvements in this case with coarctation of the aorta following surgery. Guidelines should be implemented to provide safe and effective cardiac rehabilitation in such patients. Furthermore, large-scale studies are needed to evaluate the clinical benefits of structured cardiac rehabilitation in patients following cardiac surgery.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000069"},"PeriodicalIF":0.0,"publicationDate":"2021-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/55/8a/JRMCC-4-1000069.PMC8526919.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39561285","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
Validation of the Post-Covid-19 Functional Status Scale into Mexican-Spanish. 新冠肺炎后功能状态量表在墨西哥-西班牙语中的验证
Pub Date : 2021-10-08 eCollection Date: 2021-01-01 DOI: 10.2340/20030711-1000070
Luis Antonio Moreno-Torres, Carmelita Elizabeth Ventura-Alfaro

Aim: To translate and validate the Post-COVID-19 Functional Status Scale into Mexican-Spanish.

Materials and methods: A cross-sectional study was performed for transcultural validation of the Post-COVID-19 Functional Status Scale in people over 18 years of age, using the international guidelines for validation published by Beaton and Guillemin. Diagnostic and clinimetric validity tests were applied to the scale. Statistical analysis was performed with the statistical program R.

Results: The scale was applied to 249 patients, obtaining a Cronbach's alpha of 0.84 for the structured interview, and 0.67 for the self-reported questionnaire. When comparing both tests, and considering the structured interview as the reference test, the self-reported questionnaire had a sensitivity of 86.2%, a specificity of 96.3%, and a negative predictive value of 95.8%.

Conclusion: A practical and valid scale was obtained, in concordance with that published in the original version, which can be used in daily clinical practice and rehabilitation. The scale can be used to rapidly and adequately identify post-COVID-19 patients with alterations in functionality who could benefit from rehabilitation therapy.

目的:将新冠肺炎后功能状态量表翻译成墨西哥语并进行验证。材料和方法:采用Beaton和Guillemin发布的国际验证指南,对18岁以上人群的covid -19后功能状态量表进行跨文化验证的横断面研究。对量表进行了诊断和临床效度检验。结果:该量表应用于249例患者,结构化访谈的Cronbach's alpha为0.84,自述问卷的Cronbach's alpha为0.67。比较两种测试,并考虑结构化访谈作为参考测试,自我报告问卷的敏感性为86.2%,特异性为96.3%,阴性预测值为95.8%。结论:获得了一份实用有效的量表,与原版本相符,可用于日常临床和康复。该量表可用于快速、充分地识别可从康复治疗中受益的功能改变的covid -19后患者。
{"title":"Validation of the Post-Covid-19 Functional Status Scale into Mexican-Spanish.","authors":"Luis Antonio Moreno-Torres,&nbsp;Carmelita Elizabeth Ventura-Alfaro","doi":"10.2340/20030711-1000070","DOIUrl":"https://doi.org/10.2340/20030711-1000070","url":null,"abstract":"<p><strong>Aim: </strong>To translate and validate the Post-COVID-19 Functional Status Scale into Mexican-Spanish.</p><p><strong>Materials and methods: </strong>A cross-sectional study was performed for transcultural validation of the Post-COVID-19 Functional Status Scale in people over 18 years of age, using the international guidelines for validation published by Beaton and Guillemin. Diagnostic and clinimetric validity tests were applied to the scale. Statistical analysis was performed with the statistical program R.</p><p><strong>Results: </strong>The scale was applied to 249 patients, obtaining a Cronbach's alpha of 0.84 for the structured interview, and 0.67 for the self-reported questionnaire. When comparing both tests, and considering the structured interview as the reference test, the self-reported questionnaire had a sensitivity of 86.2%, a specificity of 96.3%, and a negative predictive value of 95.8%.</p><p><strong>Conclusion: </strong>A practical and valid scale was obtained, in concordance with that published in the original version, which can be used in daily clinical practice and rehabilitation. The scale can be used to rapidly and adequately identify post-COVID-19 patients with alterations in functionality who could benefit from rehabilitation therapy.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000070"},"PeriodicalIF":0.0,"publicationDate":"2021-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/5b/5a/JRMCC-4-1000070.PMC8505751.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39525860","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: 7
Early Active Rehabilitation Treatment for a Patient with a Stable Type of Fifth Metatarsal Base Fracture: a Case Report. 稳定型第五跖骨基底骨折患者的早期积极康复治疗1例。
Pub Date : 2021-09-10 eCollection Date: 2021-01-01 DOI: 10.2340/20030711-1000068
Long Jiao, Juan Xi, Aicui Lin

In China, the stable type of fifth metatarsal base fracture is usually treated by rehabilitation methods after the limbs have been fixed for approximately 4 weeks. A 37-year-old woman fractured her fifth metatarsal base, with a stable fracture type. From the second day of the fracture onward, she agreed to participate in rehabilitative treatment that did not involve surgery or long-term fixation. Fourteen days after the fracture, the patient was able to bear 100% of her body weight and stand for 20 min in a normal posture with supportive elbow crutches. She was able to return to work with double elbow crutches after 25 days. On the 30th day after the fracture, the patient was able to walk 300 m outdoors without any walking aids and with no discomfort. Two months after the fracture, the patient went jogging and was participating in all of her normal daily activities. This case shows that, for stable type fractures of the fifth metatarsal base, rehabilitation starting on the second day after the fracture can help accelerate the patient's return to normal physical activities.

在中国,稳定型第五跖底骨折通常在四肢固定约4周后进行康复治疗。37岁女性第5跖骨基底骨折,骨折类型稳定。从骨折的第二天起,她同意参加不涉及手术或长期固定的康复治疗。骨折后14天,患者能够承受100%的体重,并在支撑肘部拐杖下以正常姿势站立20分钟。25天后,她依靠双肘拐杖重返工作岗位。在骨折后的第30天,患者能够在没有任何助行设备的情况下在室外行走300米,没有任何不适。骨折两个月后,患者开始慢跑,并参加所有正常的日常活动。本病例提示,对于第5跖底稳定型骨折,骨折后第2天开始进行康复治疗有助于加快患者恢复正常的身体活动。
{"title":"Early Active Rehabilitation Treatment for a Patient with a Stable Type of Fifth Metatarsal Base Fracture: a Case Report.","authors":"Long Jiao,&nbsp;Juan Xi,&nbsp;Aicui Lin","doi":"10.2340/20030711-1000068","DOIUrl":"https://doi.org/10.2340/20030711-1000068","url":null,"abstract":"<p><p>In China, the stable type of fifth metatarsal base fracture is usually treated by rehabilitation methods after the limbs have been fixed for approximately 4 weeks. A 37-year-old woman fractured her fifth metatarsal base, with a stable fracture type. From the second day of the fracture onward, she agreed to participate in rehabilitative treatment that did not involve surgery or long-term fixation. Fourteen days after the fracture, the patient was able to bear 100% of her body weight and stand for 20 min in a normal posture with supportive elbow crutches. She was able to return to work with double elbow crutches after 25 days. On the 30<sup>th</sup> day after the fracture, the patient was able to walk 300 m outdoors without any walking aids and with no discomfort. Two months after the fracture, the patient went jogging and was participating in all of her normal daily activities. This case shows that, for stable type fractures of the fifth metatarsal base, rehabilitation starting on the second day after the fracture can help accelerate the patient's return to normal physical activities.</p>","PeriodicalId":73929,"journal":{"name":"Journal of rehabilitation medicine. Clinical communications","volume":" ","pages":"1000068"},"PeriodicalIF":0.0,"publicationDate":"2021-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/86/9d/JRMCC-4-1000068.PMC8438790.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39430341","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
期刊
Journal of rehabilitation medicine. Clinical communications
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1