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CO-DESIGN OF AN INTERVENTION TO INCREASE LEISURE PARTICIPATION FOR ADOLESCENTS WITH CEREBRAL PALSY GMFCS LEVELS IV AND V 共同设计一项干预措施,以增加脑性麻痹青少年的休闲参与 GMFCS IV 级和 V 级
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100671
Caline Cristine de Araújo Ferreira Jesus , Ângela Cristina Dornelas da Silva , Beatriz Helena Brugnaro , Sandreane Maria dos Santos Moura , Karolinne Souza Monteiro , Egmar Longo
<div><h3>Background</h3><p>Adolescents with cerebral palsy (CP) experience restrictions in leisure activities participation, which can impact their socialization, self-determination, and quality of life. Patient and Public Involvement (PPI) is a crucial strategy for successful interventions where the target audience participates in the research stages. Strategies such as co-design, where healthcare professionals, patients, and families collaboratively discuss preferences, priorities, and necessary ingredients, can be crucial for intervention success.</p></div><div><h3>Objectives</h3><p>To co-design an intervention aimed at improving leisure activities participation of adolescents with CP in partnership with adolescents, families, and rehabilitation professionals.</p></div><div><h3>Methods</h3><p>The study was based on Participatory Action Research and was conducted through remote discussion groups with 5 adolescents aged 12-17 years with CP, 3 classified as level IV and 2 as level V on the Gross Motor Function Classification System, their families, 3 physiotherapists, and 2 occupational therapists. The Brazilian version of the Involvement Matrix (IM) was used to manage the participants' involvement in co-designing the intervention. The IM allows research participants to know different involvement roles in the research (Listener, Co-thinker, Advisor, Partner, and Decision-maker). The Participation and Environment Measure for Children and Youth (PEM-CY), community section, was used to assess the adolescents' participation profile.</p></div><div><h3>Results</h3><p>The preparation phase included 6 group meetings. In the first meeting, the IM was presented, and participants chose their roles for the study. Three chose the role of Decision-maker (1 professional, 1 adolescent with CP, and 1 mother), and 12 chose the role of Partner (4 professionals, 4 adolescents, and 4 mothers). Partners contributed suggestions, while decision-makers planned the participation groups. The second and third meetings included adolescents/families and rehabilitation professionals separately, where the concept of participation was discussed. The results of the PEM-CY were discussed in the fourth and fifth meetings. The last meeting of this phase included all participants, who discussed barriers and facilitators of participation and identified the necessary ingredients for the intervention. In this meeting, a model of intervention to increase the participation of adolescents with disabilities was presented as a strategy to facilitate the co-construction of the intervention proposal. The Co-design phase included three meetings with all participants; in the first two, co-construction of the intervention was conducted, and in the last, the co-constructed intervention was presented, and the intervention proposal was validated by all participants.</p></div><div><h3>Conclusion</h3><p>This study presents an innovative proposal that uses PPI for co-designing an intervention aimed at
背景患有脑性瘫痪(CP)的青少年在参与休闲活动时会受到限制,这可能会影响他们的社交、自决和生活质量。患者和公众参与(PPI)是成功干预的关键策略,目标受众可参与研究阶段。该研究以参与式行动研究为基础,通过远程讨论小组与 5 名 12-17 岁的脊髓灰质炎青少年(其中 3 名在粗大运动功能分类系统中被划分为 IV 级,2 名被划分为 V 级)、他们的家人、3 名物理治疗师和 2 名职业治疗师进行了讨论。巴西版的参与矩阵(IM)用于管理参与者参与共同设计干预措施的情况。参与矩阵允许研究参与者了解自己在研究中的不同参与角色(倾听者、共同思考者、顾问、合作伙伴和决策者)。儿童与青少年参与和环境测量(PEM-CY)的社区部分用于评估青少年的参与情况。在第一次会议上,介绍了 IM,参与者选择了自己在研究中的角色。3 人选择了决策者的角色(1 名专业人员、1 名患有先天性心脏病的青少年和 1 名母亲),12 人选择了合作伙伴的角色(4 名专业人员、4 名青少年和 4 名母亲)。合作伙伴提出建议,而决策者则对参与小组进行规划。在第二和第三次会议上,青少年/家庭和康复专业人员分别讨论了参与的概念。第四和第五次会议讨论了 PEM-CY 的结果。这一阶段的最后一次会议包括所有参与者,他们讨论了参与的障碍和促进因素,并确定了干预的必要成分。在这次会议上,提出了一个提高残疾青少年参与度的干预模式,作为促进共同构建干预方案的策略。共同设计阶段包括与所有参与者举行的三次会议;在前两次会议上,进行了干预措施的共同构建,在最后一次会议上,介绍了共同构建的干预措施,所有参与者对干预建议进行了验证。下一步将测试与目标受众共同设计的干预措施的可行性,由于考虑到了所研究人群的实际需求,因此可以取得更好的结果。
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引用次数: 0
ELECTROMYOGRAPHIC PROFILE OF THE WRIST AND ELBOW FLEXORS DURING PNF MOTOR IRRADIATION PNF 运动照射时手腕和肘部屈肌的肌电图特征
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100677
Carlos Henrique R Horsczaruk , José Vicente P Martins , Claudia Vargas , Laura A.S Oliveira , Thiago C Lemos

Background

Proprioceptive Neuromuscular Facilitation (PNF) is a concept that has been applied to treating numerous disabling disorders. Among the basic PNF procedures, there is motor irradiation, in which resistance is applied to a body segment to generate muscle activation in another segment and thus obtain improvement in muscle strength. The generated muscular activation can be analyzed in several ways, one of them being Electromyography (EMG). Electromyographic analysis has suggested that target muscles of irradiation demonstrate electromyographic activity during irradiation in healthy individuals and in those with neurological disorders. Despite this, the neuromuscular activation profile (amplitude and temporality) resulting from the different stimuli and positions used in PNF has not yet been investigated.

Objectives

To analyze the neuromuscular activation profile of upper limb muscles in healthy individuals during the application of different PNF irradiation protocols.

Methods

This is a cross-sectional study in which 32 healthy individuals of both sexes, aged between 18 and 45 years. After signing the consent form, the handedness of a subject in activities of daily living, level of physical activity, and sociodemographic characteristics will be identified. First, the EMG signals of the upper limb muscles (biceps brachii, brachioradialis, flexor carpi radialis, and triceps) will be collected during a maximum voluntary contraction (3 repetitions held for 3s with an interval of 30s between contractions). Then, the EMG signal of these muscles of the non-preferential limb will be collected, during 4 PNF irradiation techniques in a randomized order for each participant. Each irradiation will be applied 3 times, maintaining the contraction for 5s, with a 10s interval between them. After each irradiation will be checked the perceived exertion.

Results

The study is in the data collection phase.

Conclusion

It is expected through this study to verify if the applied irradiation techniques activate the musculatures described anecdotally in the clinical literature.

Implications

The study can generate an understanding of motor irradiation and the use of the technique to improve the strength of a body segment.

背景先觉神经肌肉刺激(PNF)是一种概念,已被用于治疗多种致残性疾病。在 PNF 的基本程序中,有一种是运动辐照,即在身体的某一部位施加阻力,使另一部位的肌肉激活,从而改善肌肉力量。产生的肌肉激活可以通过多种方式进行分析,肌电图(EMG)就是其中之一。肌电图分析表明,健康人和患有神经系统疾病的人在接受照射时,照射目标肌肉会表现出肌电图活动。目标分析健康人在使用不同的 PNF 照射方案时上肢肌肉的神经肌肉激活情况。方法这是一项横断面研究,32 名健康人参加了研究,男女均有,年龄在 18 至 45 岁之间。在签署同意书后,将确定受试者在日常生活活动中的用手情况、体力活动水平和社会人口学特征。首先,采集受试者上肢肌肉(肱二头肌、肱肌、桡侧屈肌和肱三头肌)在最大自主收缩时的肌电信号(重复 3 次,每次 3 秒,收缩间隔 30 秒)。然后,在对每位受试者进行 4 次随机顺序的 PNF 照射时,收集非偏爱肢体这些肌肉的肌电信号。每次照射 3 次,保持收缩 5 秒钟,每次间隔 10 秒钟。结论通过这项研究,有望验证所应用的照射技术是否能激活临床文献中传闻的肌肉组织。
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引用次数: 0
ANTICIPATORY SYNERGY ADJUSTMENTS: A NARRATIVE REVIEW OF STUDIES USING THE UNCONTROLLED MANIFOLD APPROACH IN INDIVIDUALS WITH NEUROLOGICAL DYSFUNCTIONS 预期协同调整:对在神经功能障碍患者中使用不可控流形方法的研究的叙述性回顾
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100604
Alice Brochado Campolina , Valéria Andrade Pinto , Daniela Virgínia Vaz

Background

According to the Uncontrolled Manifold (UCM) approach, motor synergies allow motor flexibility while ensuring stable task performance. The stronger the motor synergies, the greater performance stabilization. Thus, just before the start of a new motor task, the synergies need to be attenuated to facilitate the initiation or change of movement. This reduction in synergy during the preparation for movement initiation is called Anticipatory Synergy Adjustments (ASAs). In individuals with neurological deficits, changes in the timing or magnitude of ASAs can result in reduced movement agility or greater difficulty initiating a new task. Additionally, altered ASAs can serve as preclinical markers of neurological dysfunctions such as Parkinson's disease or multiple sclerosis.

Objectives

The aim of this study was to characterize the behavior of ASAs in populations with neurological dysfunctions and analyze their clinical implications.

Methods

A narrative review of studies that used the UCM approach to quantify ASAs in individuals with neurological dysfunctions was conducted.

Results

The review resulted in the inclusion of 9 exploratory studies. The study samples consisted of individuals with Parkinson's disease (PD), olivopontocerebellar atrophy (OA), stroke, multiple sclerosis (MS), and cerebral palsy (CP). The motor tasks analyzed in the studies were divided into manual tasks and standing postural control tasks. In individuals with PD, MS, and OA, delayed and smaller magnitude of ASAs were observed when compared to healthy individuals. In individuals with CP and stroke, ASAs in manual tasks differed from healthy individuals in small magnitudes.

Conclusion

In general, the observed changes in ASAs in the study lead to reduced agility during task execution and greater difficulty initiating new movements.

Implications

The use of the UCM method and the analysis of ASAs appears to be sensitive for the early detection of some neurological conditions and tracking disease progression and intervention effects, especially in individuals with subcortical disorders. However, using UCM to evaluate patients in the clinical context is still challenging. Its application requires specific technology and knowledge, which limits its use to the search environment. It would be interesting if future studies investigated the relationship between the behavior of ASAs and performance in commonly used functional instruments/questionnaires in clinical practice so that the understanding and application of the UCM method in the clinical context can be optimized.

背景根据 "不可控整体"(UCM)方法,运动协同作用在确保任务表现稳定的同时,还能提高运动灵活性。运动协同作用越强,任务表现的稳定性就越高。因此,在新的运动任务开始之前,需要减弱协同作用,以促进运动的开始或改变。这种在运动开始前的准备过程中减弱协同作用的现象被称为 "预期协同调整"(ASA)。对于有神经系统缺陷的人来说,ASA 的时间或幅度的变化可能会导致运动灵活性降低或启动新任务更加困难。此外,ASA 的改变可作为神经功能障碍(如帕金森病或多发性硬化症)的临床前标志物。研究目的:本研究旨在描述神经功能障碍人群中 ASA 的行为特征,并分析其临床意义。研究样本包括帕金森病 (PD)、橄榄小脑萎缩 (OA)、中风、多发性硬化症 (MS) 和脑瘫 (CP) 患者。研究分析的运动任务分为手动任务和站立姿势控制任务。与健康人相比,在帕金森病、多发性硬化症和开放性脊柱炎患者中观察到的 ASA 延迟且幅度较小。一般来说,研究中观察到的 ASA 变化会导致任务执行过程中的灵活性降低,启动新动作的难度增加。然而,在临床环境中使用 UCM 评估患者仍具有挑战性。其应用需要特定的技术和知识,这就限制了其在搜索环境中的使用。如果未来的研究能调查 ASA 的行为与临床实践中常用的功能性工具/问卷的表现之间的关系,从而优化 UCM 方法在临床中的理解和应用,那将会非常有趣。
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引用次数: 0
TELEREHABILITATION VERSUS A DIGITAL BOOKLET FOR PATIENTS WITH CHRONIC NON-SPECIFIC NECK PAIN: STUDY PROTOCOL OF A RANDOMIZED CONTROLLED TRIAL 针对慢性非特异性颈部疼痛患者的远程康复与数字手册:随机对照试验的研究方案
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100667
Juliene Corrêa Barbosa , Bruna Vale da Luz , Breno Felipe Portal da Silva , Maurício Oliveira Magalhães

Background

Neck pain is a common disabling condition that directly affects the performance of daily life activities and participation in professional, social and sports activities, being one of the main causes of functional disability in the world. Telerehabilitation-based treatments have demonstrated their importance due to their ease of use, low cost, and tendency to improve clinical outcomes. However, in the current scientific evidence, there is a lack of studies that exemplify telerehabilitation protocols in individuals with chronic non-specific neck pain.

Objectives

The study was to verify the effect of a telerehabilitation protocol versus an online self-care booklet in individuals with non-specific chronic neck pain.

Methods

This is a blinded, randomized, controlled clinical trial that compares a telerehabilitation program for neck pain with a control group that will receive an online self-care booklet. Seventy patients will be recruited. Assessments and measures will perform before treatment, after 6 weeks and at 3 months after randomization. For this purpose, assessments and follow-ups will be carried out completely remotely, through online platforms (Google Meet, smartphone messages, email) and telephone calls. The primary outcome will be functional disability measured by the Neck Disability Index questionnaire consisting of 10 items. Secondary outcomes will be pain intensity measured using the numeric rating scale, perceived global effect measured using the perceived global exertion scale, patient self-efficacy using the Pain Self Efficacy Questionnaire, quality of life using the SF-12, and kinesiophobia through the Scale of Kinesiophobia. This clinical trial was approved by the Research Ethics Committee (no. 5.458.454) and was registered in the Brazilian Registry of Clinical Trials (no. RBR-10h7khvk).

Results

No results so far.

Conclusion

This study will examine whether the telerehabilitation treatment approach is superior to the self-care booklet in patients with chronic neck pain, functional disability, pain intensity, perceived global effect, patient self-efficacy, quality of life and kinesiophobia.

Implications

The study will impact clinical practice because telerehabilitation is a treatment option that aims to promote improvements in the functional disability and pain intensity of individuals with nonspecific chronic neck pain. This form of treatment appears as an alternative to ease the logistical and organizational conditions promoted by face-to-face care.

背景颈部疼痛是一种常见的致残性疾病,直接影响日常生活活动的进行以及职业、社会和体育活动的参与,是世界上功能性残疾的主要原因之一。基于远程康复的治疗方法因其使用方便、成本低廉、易于改善临床效果而显示出其重要性。本研究旨在验证远程康复方案与在线自我护理手册对非特异性慢性颈部疼痛患者的治疗效果。将招募 70 名患者。将在治疗前、6 周后和随机分配后 3 个月进行评估和测量。为此,评估和随访将通过在线平台(Google Meet、智能手机信息、电子邮件)和电话完全远程进行。主要结果是颈部残疾指数(Neck Disability Index)调查问卷中 10 个项目的功能残疾程度。次要结果是使用数字评分量表测量疼痛强度、使用感知总体用力量表测量感知总体效果、使用疼痛自我效能问卷测量患者自我效能、使用 SF-12 测量生活质量,以及使用运动恐惧症量表测量运动恐惧症。本临床试验已获得研究伦理委员会批准(编号:5.458.454),并在巴西临床试验登记处登记(编号:RBR-10h7khvk)。结果目前尚无结果。结论本研究将考察远程康复治疗方法在慢性颈痛患者的功能障碍、疼痛强度、感知的总体效果、患者自我效能、生活质量和运动恐惧症方面是否优于自我护理手册。研究意义这项研究将对临床实践产生影响,因为远程康复是一种旨在改善非特异性慢性颈痛患者功能障碍和疼痛强度的治疗方法。这种治疗方式可以缓解面对面治疗所带来的后勤和组织方面的问题。
{"title":"TELEREHABILITATION VERSUS A DIGITAL BOOKLET FOR PATIENTS WITH CHRONIC NON-SPECIFIC NECK PAIN: STUDY PROTOCOL OF A RANDOMIZED CONTROLLED TRIAL","authors":"Juliene Corrêa Barbosa ,&nbsp;Bruna Vale da Luz ,&nbsp;Breno Felipe Portal da Silva ,&nbsp;Maurício Oliveira Magalhães","doi":"10.1016/j.bjpt.2024.100667","DOIUrl":"https://doi.org/10.1016/j.bjpt.2024.100667","url":null,"abstract":"<div><h3>Background</h3><p>Neck pain is a common disabling condition that directly affects the performance of daily life activities and participation in professional, social and sports activities, being one of the main causes of functional disability in the world. Telerehabilitation-based treatments have demonstrated their importance due to their ease of use, low cost, and tendency to improve clinical outcomes. However, in the current scientific evidence, there is a lack of studies that exemplify telerehabilitation protocols in individuals with chronic non-specific neck pain.</p></div><div><h3>Objectives</h3><p>The study was to verify the effect of a telerehabilitation protocol versus an online self-care booklet in individuals with non-specific chronic neck pain.</p></div><div><h3>Methods</h3><p>This is a blinded, randomized, controlled clinical trial that compares a telerehabilitation program for neck pain with a control group that will receive an online self-care booklet. Seventy patients will be recruited. Assessments and measures will perform before treatment, after 6 weeks and at 3 months after randomization. For this purpose, assessments and follow-ups will be carried out completely remotely, through online platforms (Google Meet, smartphone messages, email) and telephone calls. The primary outcome will be functional disability measured by the Neck Disability Index questionnaire consisting of 10 items. Secondary outcomes will be pain intensity measured using the numeric rating scale, perceived global effect measured using the perceived global exertion scale, patient self-efficacy using the Pain Self Efficacy Questionnaire, quality of life using the SF-12, and kinesiophobia through the Scale of Kinesiophobia. This clinical trial was approved by the Research Ethics Committee (no. 5.458.454) and was registered in the Brazilian Registry of Clinical Trials (no. RBR-10h7khvk).</p></div><div><h3>Results</h3><p>No results so far.</p></div><div><h3>Conclusion</h3><p>This study will examine whether the telerehabilitation treatment approach is superior to the self-care booklet in patients with chronic neck pain, functional disability, pain intensity, perceived global effect, patient self-efficacy, quality of life and kinesiophobia.</p></div><div><h3>Implications</h3><p>The study will impact clinical practice because telerehabilitation is a treatment option that aims to promote improvements in the functional disability and pain intensity of individuals with nonspecific chronic neck pain. This form of treatment appears as an alternative to ease the logistical and organizational conditions promoted by face-to-face care.</p></div>","PeriodicalId":49621,"journal":{"name":"Brazilian Journal of Physical Therapy","volume":"28 ","pages":"Article 100667"},"PeriodicalIF":3.4,"publicationDate":"2024-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140179652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
OVERVIEW OF THE ECONOMIC BURDEN OF MUSCULOSKELETAL PAIN IN CHILDREN AND ADOLESCENTS: A SYSTEMATIC REVIEW WITH META-ANALYSIS 儿童和青少年肌肉骨骼疼痛的经济负担概述:系统回顾与荟萃分析
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100670
Caique de Melo do Espírito Santo , Verônica Souza Santos , Steven J. Kamper , Christopher M. Williams , Gisela Cristiane Miyamoto , Tiê Parma Yamato
<div><h3>Background</h3><p>Some studies suggest a high economic burden among children and adolescents with musculoskeletal pain. However, there is no summary in the literature to understand the scenario of the economic burden of musculoskeletal pain in this population.</p></div><div><h3>Objectives</h3><p>This study aimed to synthesize the economic burden of musculoskeletal pain in children and adolescents.</p></div><div><h3>Methods</h3><p>We conducted electronic searches on MEDLINE, EMBASE, CINAHL, EconLit, NHS-EED, and HTA databases from inception to July/2022. We included cost-of-illness studies that estimated healthcare, patient/family, lost productivity, and/or societal costs in children and adolescents (up to 24 years old) with musculoskeletal pain. The primary outcome was cost, and the results were grouped by the same cost categories (i.e., healthcare, patient/family, lost productivity, societal), conditions, time horizon, and cost range for musculoskeletal pain. All costs were inflated to the same reference year (2021) and converted to American Dollars ($). The risk of bias the included studies was assessed using a checklist based on the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) statement.</p></div><div><h3>Results</h3><p>We included 45 cost-of-illness studies (n=665,623). Thirty-eight studies (84.4%) were conducted in high-income countries, six (13.3%) in upper-middle-income countries, and one (2.2%) in lower-middle-income countries. Regarding the risk of bias assessment, 75.5% (n=34 studies) clearly presented the unit costs, and 69% (n=31 studies) presented the expenditure data transparently. In contrast, more than half of the studies did not include productivity costs or sensitivity analysis. The annual healthcare costs ranged from $143 to $41,379 per child/adolescent (n=22 studies). The annual patient/family costs ranged from $287 to $27,972 per child/adolescent (n=9 studies). The annual lost productivity costs ranged from $124 to $4,671 per child/adolescent (n=7 studies). The annual societal costs ranged from $1,095 to $69,351 per child/adolescent (n=9 studies). Children and adolescents with juvenile idiopathic arthritis and musculoskeletal pain had higher annual incremental healthcare costs than children and adolescents without these conditions (mean difference: $3,800, 95% confidence interval [CI]: 50 to 7,550; mean difference: $740, 95% CI: 470 to 1,010, respectively).</p></div><div><h3>Conclusion</h3><p>The annual economic burden of musculoskeletal pain per child and adolescent ranged from $124 to $69,351.</p></div><div><h3>Implications</h3><p>This systematic review summarizes the evidence of the economic burden of musculoskeletal pain in children and adolescents. The results of this study showed that the musculoskeletal pain in children and adolescents seems to represent an important part of the economic burden in children's health. However, our estimates span a large range for all cost categories, maki
背景一些研究表明,患有肌肉骨骼疼痛的儿童和青少年的经济负担很重。本研究旨在总结儿童和青少年肌肉骨骼疼痛的经济负担。方法我们在 MEDLINE、EMBASE、CINAHL、EconLit、NHS-EED 和 HTA 数据库中进行了电子检索,检索时间从开始到 2022 年 7 月。我们纳入了对患有肌肉骨骼疼痛的儿童和青少年(24 岁以下)的医疗保健、患者/家庭、生产力损失和/或社会成本进行估算的疾病成本研究。主要结果是成本,研究结果按相同的成本类别(即医疗保健、患者/家庭、生产力损失、社会)、条件、时间范围和肌肉骨骼疼痛的成本范围进行分组。所有成本均膨胀至同一参考年(2021 年),并换算成美元($)。纳入研究的偏倚风险采用基于《卫生经济评估综合报告标准》(CHEERS)声明的核对表进行评估。结果我们纳入了 45 项疾病成本研究(n=665,623)。其中 38 项研究(84.4%)在高收入国家进行,6 项研究(13.3%)在中上收入国家进行,1 项研究(2.2%)在中低收入国家进行。在偏倚风险评估方面,75.5%(34 项研究)清楚地列出了单位成本,69%(31 项研究)透明地列出了支出数据。相比之下,半数以上的研究未包含生产成本或敏感性分析。每名儿童/青少年的年度医疗成本从 143 美元到 41 379 美元不等(22 项研究)。每名儿童/青少年每年的患者/家庭成本从 287 美元到 27,972 美元不等(9 项研究)。每名儿童/青少年每年损失的生产力成本从 124 美元到 4,671 美元不等(7 项研究)。每名儿童/青少年每年的社会成本从 1,095 美元到 69,351 美元不等(9 项研究)。患有幼年特发性关节炎和肌肉骨骼疼痛的儿童和青少年的年度增量医疗成本高于没有这些病症的儿童和青少年(平均差异:3,800 美元,95% 置信区间 [CI]:50 至 7,550;平均差异:2,000 美元,95% 置信区间 [CI]:50 至 7,550):本系统综述总结了儿童和青少年肌肉骨骼疼痛经济负担的证据。研究结果表明,儿童和青少年肌肉骨骼疼痛似乎是儿童健康经济负担的重要组成部分。然而,我们对所有费用类别的估算范围都很大,因此很难解释这一人群的经济负担。
{"title":"OVERVIEW OF THE ECONOMIC BURDEN OF MUSCULOSKELETAL PAIN IN CHILDREN AND ADOLESCENTS: A SYSTEMATIC REVIEW WITH META-ANALYSIS","authors":"Caique de Melo do Espírito Santo ,&nbsp;Verônica Souza Santos ,&nbsp;Steven J. Kamper ,&nbsp;Christopher M. Williams ,&nbsp;Gisela Cristiane Miyamoto ,&nbsp;Tiê Parma Yamato","doi":"10.1016/j.bjpt.2024.100670","DOIUrl":"https://doi.org/10.1016/j.bjpt.2024.100670","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;p&gt;Some studies suggest a high economic burden among children and adolescents with musculoskeletal pain. However, there is no summary in the literature to understand the scenario of the economic burden of musculoskeletal pain in this population.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objectives&lt;/h3&gt;&lt;p&gt;This study aimed to synthesize the economic burden of musculoskeletal pain in children and adolescents.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;p&gt;We conducted electronic searches on MEDLINE, EMBASE, CINAHL, EconLit, NHS-EED, and HTA databases from inception to July/2022. We included cost-of-illness studies that estimated healthcare, patient/family, lost productivity, and/or societal costs in children and adolescents (up to 24 years old) with musculoskeletal pain. The primary outcome was cost, and the results were grouped by the same cost categories (i.e., healthcare, patient/family, lost productivity, societal), conditions, time horizon, and cost range for musculoskeletal pain. All costs were inflated to the same reference year (2021) and converted to American Dollars ($). The risk of bias the included studies was assessed using a checklist based on the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) statement.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;p&gt;We included 45 cost-of-illness studies (n=665,623). Thirty-eight studies (84.4%) were conducted in high-income countries, six (13.3%) in upper-middle-income countries, and one (2.2%) in lower-middle-income countries. Regarding the risk of bias assessment, 75.5% (n=34 studies) clearly presented the unit costs, and 69% (n=31 studies) presented the expenditure data transparently. In contrast, more than half of the studies did not include productivity costs or sensitivity analysis. The annual healthcare costs ranged from $143 to $41,379 per child/adolescent (n=22 studies). The annual patient/family costs ranged from $287 to $27,972 per child/adolescent (n=9 studies). The annual lost productivity costs ranged from $124 to $4,671 per child/adolescent (n=7 studies). The annual societal costs ranged from $1,095 to $69,351 per child/adolescent (n=9 studies). Children and adolescents with juvenile idiopathic arthritis and musculoskeletal pain had higher annual incremental healthcare costs than children and adolescents without these conditions (mean difference: $3,800, 95% confidence interval [CI]: 50 to 7,550; mean difference: $740, 95% CI: 470 to 1,010, respectively).&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;p&gt;The annual economic burden of musculoskeletal pain per child and adolescent ranged from $124 to $69,351.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Implications&lt;/h3&gt;&lt;p&gt;This systematic review summarizes the evidence of the economic burden of musculoskeletal pain in children and adolescents. The results of this study showed that the musculoskeletal pain in children and adolescents seems to represent an important part of the economic burden in children's health. However, our estimates span a large range for all cost categories, maki","PeriodicalId":49621,"journal":{"name":"Brazilian Journal of Physical Therapy","volume":"28 ","pages":"Article 100670"},"PeriodicalIF":3.4,"publicationDate":"2024-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140179655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
EFFICACY OF PHARMACOLOGICAL AND NON-PHARMACOLOGICAL THERAPIES ON PAIN AND DISABILITY IN PLANTAR FASCIITIS: A SYSTEMATIC REVIEW AND META-ANALYSIS 药物和非药物疗法对足底筋膜炎疼痛和残疾的疗效:系统回顾和荟萃分析
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100656
Bianca Martins Lourenço , Mariana Gabrich Moraes Campos , Laísa Braga Maia , Brenda Katrovyevysky Costa Castro , Renato Guilherme Trede , Vinicius Cunha Oliveira
<div><h3>Background</h3><p>Plantar fasciitis (PF) is one of the most common musculoskeletal conditions of the foot. Estimates of lifetime prevalence are up to 34.7% of the general population. Most of the time, PF is self-limited, but the time for complete resolution of symptoms can take up to a year, impairing the quality of life of patients. Non-pharmacological therapies are the first-choice management option for PF, such as biomechanical support, stretching, and extracorporeal shock wave therapy [ESWT]. In addition, other pharmacologic options are commonly prescribed (e.g., nonsteroidal anti-inflammatory drugs [NSAIDs], botulinum toxin, platelet-rich plasma injections, corticosteroid injections). However, there is no consensus on the decision-making process because they are limited in scope and methodology. Current evidence also needs to be updated with the aim of providing reliable evidence for the management of PF, taking into account that some new types of pharmacological and non-pharmacological therapies are being investigated (e.g., orthoses, shoes).</p></div><div><h3>Objective</h3><p>To investigate the effects of pharmacological and non-pharmacological therapies on pain and disability in PF.</p></div><div><h3>Methods</h3><p>Systematic review of randomized controlled trials (RCTs). Data sources: AMED, MEDLINE, PEDro, COCHRANE, SPORTDISCUSS, CINAHL, EMBASE, and PsycINFO without language or date restrictions until February 3<sup>rd</sup>, 2023. RCTs that evaluated the efficacy of any pharmacological and non-pharmacological therapies in comparison with control (placebo, sham, waiting list, or no intervention) on pain intensity and disability in people with PF were the eligibility criteria. Two reviewers independently screened eligible studies, extracted data, assessed the methodological quality of included studies, and assessed certainty of evidence using the Recommendations, Assessment, Development, and Reviews (GRADE) grading framework.</p></div><div><h3>Results</h3><p>Seventeen different therapies investigated in 28 studies were included in the quantitative analysis. Moderate certainty evidence showed short-term effects of custom orthoses on pain intensity when compared with control (MD, -12.0 [95% CI: -17.1 to -7.0) and that orthoses did not reduce long-term pain intensity (MD, -5.9 [95% CI: -21.2 to 9.5]). Low-certainty evidence showed short-term effects in favor of taping (MD, -21.3 [95% CI: -38.6 to 4.0]) on pain intensity. For disability, low-certainty evidence showed that high-quality studies are needed.</p></div><div><h3>Conclusions</h3><p>The results of this meta-analysis should be evaluated by clinicians, stakeholders, and researchers, taking into account that most investigated interventions currently have low or very low certainty. Our findings expose the need to develop new larger studies with high methodological quality. Clinical</p></div><div><h3>Implications</h3><p>Current evidence supports customized orthoses and taping on s
背景足底筋膜炎(PF)是足部最常见的肌肉骨骼疾病之一。据估计,其终生患病率高达总人口的 34.7%。大多数情况下,足背痛是自限性的,但症状完全缓解可能需要长达一年的时间,从而影响患者的生活质量。非药物疗法是治疗 PF 的首选方案,如生物力学支持、拉伸和体外冲击波疗法 [ESWT]。此外,其他药物疗法也是常用的治疗方法(如非甾体抗炎药、肉毒杆菌毒素、富血小板血浆注射、皮质类固醇注射等)。然而,由于这些研究的范围和方法有限,因此在决策过程方面尚未达成共识。考虑到一些新型药物疗法和非药物疗法(如矫形器、鞋)正在接受研究,目前的证据也需要更新,以便为治疗 PF 提供可靠的证据。数据来源AMED、MEDLINE、PEDro、COCHRANE、SPORTDISCUSS、CINAHL、EMBASE 和 PsycINFO,无语言和日期限制,直至 2023 年 2 月 3 日。符合资格的标准是评估任何药物和非药物疗法与对照组(安慰剂、假、等待名单或无干预)相比对 PF 患者疼痛强度和残疾的疗效的 RCT。两名审稿人独立筛选符合条件的研究、提取数据、评估纳入研究的方法学质量,并使用建议、评估、发展和评论(GRADE)分级框架评估证据的确定性。结果28项研究中的17种不同疗法被纳入定量分析。中度确定性证据显示,与对照组相比,定制矫形器对疼痛强度有短期影响(MD,-12.0 [95% CI:-17.1 至 -7.0]),矫形器不会降低长期疼痛强度(MD,-5.9 [95% CI:-21.2 至 9.5])。低确定性证据显示,短期效果有利于绑带(MD,-21.3 [95% CI:-38.6 至 4.0])对疼痛强度的影响。结论临床医生、利益相关者和研究人员应评估本荟萃分析的结果,同时考虑到目前大多数调查干预措施的确定性较低或非常低。我们的研究结果表明,有必要开展新的、规模更大、方法质量更高的研究。临床启示目前有证据表明,与对照组相比,定制矫形器和绑带能减轻短期疼痛强度,但确定性证据分别为中度和低度。prospero:(CRD42021224416)。
{"title":"EFFICACY OF PHARMACOLOGICAL AND NON-PHARMACOLOGICAL THERAPIES ON PAIN AND DISABILITY IN PLANTAR FASCIITIS: A SYSTEMATIC REVIEW AND META-ANALYSIS","authors":"Bianca Martins Lourenço ,&nbsp;Mariana Gabrich Moraes Campos ,&nbsp;Laísa Braga Maia ,&nbsp;Brenda Katrovyevysky Costa Castro ,&nbsp;Renato Guilherme Trede ,&nbsp;Vinicius Cunha Oliveira","doi":"10.1016/j.bjpt.2024.100656","DOIUrl":"https://doi.org/10.1016/j.bjpt.2024.100656","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;p&gt;Plantar fasciitis (PF) is one of the most common musculoskeletal conditions of the foot. Estimates of lifetime prevalence are up to 34.7% of the general population. Most of the time, PF is self-limited, but the time for complete resolution of symptoms can take up to a year, impairing the quality of life of patients. Non-pharmacological therapies are the first-choice management option for PF, such as biomechanical support, stretching, and extracorporeal shock wave therapy [ESWT]. In addition, other pharmacologic options are commonly prescribed (e.g., nonsteroidal anti-inflammatory drugs [NSAIDs], botulinum toxin, platelet-rich plasma injections, corticosteroid injections). However, there is no consensus on the decision-making process because they are limited in scope and methodology. Current evidence also needs to be updated with the aim of providing reliable evidence for the management of PF, taking into account that some new types of pharmacological and non-pharmacological therapies are being investigated (e.g., orthoses, shoes).&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objective&lt;/h3&gt;&lt;p&gt;To investigate the effects of pharmacological and non-pharmacological therapies on pain and disability in PF.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;p&gt;Systematic review of randomized controlled trials (RCTs). Data sources: AMED, MEDLINE, PEDro, COCHRANE, SPORTDISCUSS, CINAHL, EMBASE, and PsycINFO without language or date restrictions until February 3&lt;sup&gt;rd&lt;/sup&gt;, 2023. RCTs that evaluated the efficacy of any pharmacological and non-pharmacological therapies in comparison with control (placebo, sham, waiting list, or no intervention) on pain intensity and disability in people with PF were the eligibility criteria. Two reviewers independently screened eligible studies, extracted data, assessed the methodological quality of included studies, and assessed certainty of evidence using the Recommendations, Assessment, Development, and Reviews (GRADE) grading framework.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;p&gt;Seventeen different therapies investigated in 28 studies were included in the quantitative analysis. Moderate certainty evidence showed short-term effects of custom orthoses on pain intensity when compared with control (MD, -12.0 [95% CI: -17.1 to -7.0) and that orthoses did not reduce long-term pain intensity (MD, -5.9 [95% CI: -21.2 to 9.5]). Low-certainty evidence showed short-term effects in favor of taping (MD, -21.3 [95% CI: -38.6 to 4.0]) on pain intensity. For disability, low-certainty evidence showed that high-quality studies are needed.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusions&lt;/h3&gt;&lt;p&gt;The results of this meta-analysis should be evaluated by clinicians, stakeholders, and researchers, taking into account that most investigated interventions currently have low or very low certainty. Our findings expose the need to develop new larger studies with high methodological quality. Clinical&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Implications&lt;/h3&gt;&lt;p&gt;Current evidence supports customized orthoses and taping on s","PeriodicalId":49621,"journal":{"name":"Brazilian Journal of Physical Therapy","volume":"28 ","pages":"Article 100656"},"PeriodicalIF":3.4,"publicationDate":"2024-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140179691","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
INCREASED MORTALITY RISK DUE TO THE COMBINATION OF DEPRESSION AND 25(OH)D DEFICIENCY IN ENGLISH OLDER ADULTS 英国老年人因同时患有抑郁症和缺乏 25(oh)d 而增加了死亡风险
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100662
Bruna Daniel Rabelo , Ione Jayce Ceola Schneider
<div><h3>Background</h3><p>Depression is one of the most disabling diseases. It affects approximately 5.7% of older adults. In parallel, there is a high prevalence of vitamin D deficiency in this population, and it advantages the development of depressive symptoms. There are few studies about the influence of the association of depression and vitamin D deficiency on mortality.</p></div><div><h3>Objectives</h3><p>To investigate whether the combination of depression and vitamin D deficiency increases the mortality risk in older adults.</p></div><div><h3>Methods</h3><p>It is a cohort study with data from wave 6 (2012-3) of the English Longitudinal Study of Ageing, a population-based study with adults aged 50 years and over, living in England. Depression was measured by the Center for Epidemiologic Studies – Depression (CES-D-8) with a cut-off point of ≥4 symptoms, and deficiency of vitamin D (<25 nmol/L) was estimated by the blood levels of 25-hydroxyvitamin D [25(OH)D]. Thus, four groups were formed: depression/25(OH)D deficiency, no depression/no 25(OH)D deficiency, depression/without 25(OH)D deficiency, and no depression/with 25(OH)D deficiency. Follow-up time was the interval between the wave 6 interview and the last contact (wave 7 or wave 8) or death, and the maximum was 60 months. Stata 14.0 was used to perform Kaplan-Meier curves and Cox regression. The adjustments were by age group, sex, wealth, physical exercise, smoking, alcohol consumption, body mass index, basic and instrumental activities of daily living, and chronic and circulatory diseases.</p></div><div><h3>Results</h3><p>Of the 5,050 participants, 22.5% had depression, and 15.1% had 25(OH)D deficiency. When combining the outcomes, 4.85% had depression/25(OH)D deficiency and 67.2% had no depression/25(OH)D deficiency. The combination depression/25(OH)D deficiency was more prevalent in women, lower wealth quintile, sedentary, smokers, obese, with difficulties in activities of daily living, and with chronic and circulatory diseases. At the end of the follow-up, the survival rate was 19.1% (95%CI:3.3–44.8) in those with depression/25(OH)D deficiency and 50.4% (95%CI:36.0–63.1) in the opposite group. In the adjusted analysis, the risk of death was 78% (95%CI:1.17–2.70) higher in the depression/25(OH)D deficiency group compared to the no depression/without 25(OH)D deficiency group. The other groups (depression/no 25(OH)D deficiency, no depression/ with 25(OH)D deficiency) had no significantly increased risk of death. Sensitivity analysis confirms the importance of grouping because depression alone is a risk factor for mortality (HR:1.33; 95%CI:1.02–1.73), while 25(OH)D deficiency alone is not (HR:1.26; 95%CI:0.95–1.68).</p></div><div><h3>Conclusion</h3><p>The grouping of depression and 25(OH)D deficiency is an independent mortality risk in older adults. The maintenance of adequate levels of 25(OH)D in this population is a challenge because there is a reduction in its metabolism in the
背景抑郁症是致残率最高的疾病之一。约有 5.7% 的老年人患有抑郁症。与此同时,维生素 D 缺乏症在这一人群中的发病率也很高,这有利于抑郁症状的发展。方法 这是一项队列研究,数据来自英国老龄化纵向研究的第 6 波(2012-3 年),这是一项基于人口的研究,研究对象为居住在英国的 50 岁及以上的成年人。抑郁症由流行病学研究中心-抑郁症(CES-D-8)测量,截断点为症状≥4,维生素 D 缺乏症(<25 nmol/L)由血液中 25- 羟基维生素 D [25(OH)D]水平估算。因此,共分为四组:抑郁症/25(OH)D 缺乏组、无抑郁症/无 25(OH)D 缺乏组、抑郁症/无 25(OH)D 缺乏组、无抑郁症/有 25(OH)D 缺乏组。随访时间是指从第 6 波访谈到最后一次联系(第 7 波或第 8 波)或死亡之间的时间间隔,最长为 60 个月。使用Stata 14.0进行卡普兰-梅耶曲线和Cox回归。结果 在 5050 名参与者中,22.5% 的人患有抑郁症,15.1% 的人缺乏 25(OH)D。将这两项结果合并后,4.85%的人患有抑郁症/25(OH)D 缺乏症,67.2%的人没有抑郁症/25(OH)D 缺乏症。女性、财富五分位数较低、久坐不动、吸烟、肥胖、日常生活有困难、患有慢性病和循环系统疾病者更容易合并抑郁/25(OH)D 缺乏症。在随访结束时,抑郁/25(OH)D缺乏症患者的存活率为19.1%(95%CI:3.3-44.8),相反组别的存活率为50.4%(95%CI:36.0-63.1)。在调整分析中,抑郁/25(OH)D 缺乏组的死亡风险比无抑郁/无 25(OH)D 缺乏组高 78% (95%CI:1.17-2.70)。其他组别(抑郁/无25(OH)D缺乏症、无抑郁/有25(OH)D缺乏症)的死亡风险没有显著增加。敏感性分析证实了分组的重要性,因为单独抑郁是一个死亡风险因素(HR:1.33;95%CI:1.02-1.73),而单独 25(OH)D 缺乏则不是(HR:1.26;95%CI:0.95-1.68)。由于 25(OH)D 在皮肤中的代谢减少,且难以摄入来源食物,因此在这一人群中保持足够的 25(OH)D 水平是一项挑战。因此,必须重视抑郁症状和 25(OH)D 缺乏症的筛查。意义 重要的是要识别、干预和治疗维生素 D 缺乏症或抑郁症状加重的患者,以减少这些风险因素,提高老年人的生存率。
{"title":"INCREASED MORTALITY RISK DUE TO THE COMBINATION OF DEPRESSION AND 25(OH)D DEFICIENCY IN ENGLISH OLDER ADULTS","authors":"Bruna Daniel Rabelo ,&nbsp;Ione Jayce Ceola Schneider","doi":"10.1016/j.bjpt.2024.100662","DOIUrl":"https://doi.org/10.1016/j.bjpt.2024.100662","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Background&lt;/h3&gt;&lt;p&gt;Depression is one of the most disabling diseases. It affects approximately 5.7% of older adults. In parallel, there is a high prevalence of vitamin D deficiency in this population, and it advantages the development of depressive symptoms. There are few studies about the influence of the association of depression and vitamin D deficiency on mortality.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objectives&lt;/h3&gt;&lt;p&gt;To investigate whether the combination of depression and vitamin D deficiency increases the mortality risk in older adults.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Methods&lt;/h3&gt;&lt;p&gt;It is a cohort study with data from wave 6 (2012-3) of the English Longitudinal Study of Ageing, a population-based study with adults aged 50 years and over, living in England. Depression was measured by the Center for Epidemiologic Studies – Depression (CES-D-8) with a cut-off point of ≥4 symptoms, and deficiency of vitamin D (&lt;25 nmol/L) was estimated by the blood levels of 25-hydroxyvitamin D [25(OH)D]. Thus, four groups were formed: depression/25(OH)D deficiency, no depression/no 25(OH)D deficiency, depression/without 25(OH)D deficiency, and no depression/with 25(OH)D deficiency. Follow-up time was the interval between the wave 6 interview and the last contact (wave 7 or wave 8) or death, and the maximum was 60 months. Stata 14.0 was used to perform Kaplan-Meier curves and Cox regression. The adjustments were by age group, sex, wealth, physical exercise, smoking, alcohol consumption, body mass index, basic and instrumental activities of daily living, and chronic and circulatory diseases.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;p&gt;Of the 5,050 participants, 22.5% had depression, and 15.1% had 25(OH)D deficiency. When combining the outcomes, 4.85% had depression/25(OH)D deficiency and 67.2% had no depression/25(OH)D deficiency. The combination depression/25(OH)D deficiency was more prevalent in women, lower wealth quintile, sedentary, smokers, obese, with difficulties in activities of daily living, and with chronic and circulatory diseases. At the end of the follow-up, the survival rate was 19.1% (95%CI:3.3–44.8) in those with depression/25(OH)D deficiency and 50.4% (95%CI:36.0–63.1) in the opposite group. In the adjusted analysis, the risk of death was 78% (95%CI:1.17–2.70) higher in the depression/25(OH)D deficiency group compared to the no depression/without 25(OH)D deficiency group. The other groups (depression/no 25(OH)D deficiency, no depression/ with 25(OH)D deficiency) had no significantly increased risk of death. Sensitivity analysis confirms the importance of grouping because depression alone is a risk factor for mortality (HR:1.33; 95%CI:1.02–1.73), while 25(OH)D deficiency alone is not (HR:1.26; 95%CI:0.95–1.68).&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;p&gt;The grouping of depression and 25(OH)D deficiency is an independent mortality risk in older adults. The maintenance of adequate levels of 25(OH)D in this population is a challenge because there is a reduction in its metabolism in the","PeriodicalId":49621,"journal":{"name":"Brazilian Journal of Physical Therapy","volume":"28 ","pages":"Article 100662"},"PeriodicalIF":3.4,"publicationDate":"2024-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140179697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
CLINICAL-EPIDEMIOLOGICAL PROFILE OF HOSPITALIZED CHILDREN IN PEDIATRIC INTENSIVE CARE UNIT WITH PHYSIOTHERAPY 儿科重症监护室住院儿童接受物理治疗的临床流行病学概况
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100617
Ana Cristina de Medeiros Garcia Maciel , Mariana Beatriz de Souza Santos Fonseca Ginane , Anderson Santana de Morais , Vitória Jéssica Teixeira Dantas Brito , Ruth Batista Bezerra Fagundes , Jessica Fernandes de Medeiros

Background

The Pediatric Intensive Care Unit of philanthropic public hospitals belonging to the Unified Health System serves children with the most varied pathologies, clinical and surgical, being a reference for many services in the metropolitan region. Technological advances in health and the improvement of public policies in the prevention, control, and fight against child injuries gradually contribute to reducing infant mortality rates.

Objectives

To identify the epidemiological profile and clinical evolution of children and adolescents hospitalized in the Pediatric Intensive Care Unit of a reference hospital in Natal/RN in physiotherapeutic follow-up.

Methods

Descriptive and retrospective study carried out at the Pediatric Intensive Care Unit of the Hospital Infantil Varela Santiago (reference in Neurosurgical and Oncological care), Natal/RN, through quantitative analysis of data from medical records of children between 0 and 15 years old in physiotherapeutic follow-up in the first quarter of 2023 (January to March). Age, sex, evolution to discharge/death, length of hospital stays, need for mechanical ventilation, and duration of mechanical ventilation were obtained by descriptive and retrospective analysis of medical records, with categorical variables expressed in absolute frequencies and percentages and continuous variables, presented as averages and standard deviation.

Results

Sixty-three (63) children were admitted to Physiotherapy, 34 boys (53.96%) with a mean age of 3.77±4.29 years. The length of stay in the ICU was 14.3 ± 22.8 days; 21 children (33.33%) required invasive mechanical ventilation, with a mean IMV time of 14.8±17.3 days. As an outcome, 15 children (23.80%) were transferred to other services or discharged straight home, 39 (61.90%) were discharged to the ward, 6 (9.52%) died, and 3 (4.76%) remained hospitalized.

Conclusion

We observed a predominance of male children in this Intensive Care Unit, with an average age of 3.7 years. The length of stay can be correlated with the complexity of the Unit in question (neurosurgical and oncology children), with a mortality rate below 10%.

Implications

Knowledge of the profile of this Unit implies improvement in care, optimization of treatment, reduction of expenses, and length of stay during hospitalization.

背景隶属于联合卫生系统的慈善公立医院儿科重症监护室为患有各种临床和外科病症的儿童提供服务,是首都地区许多服务的参照。健康领域的技术进步以及预防、控制和抗击儿童伤害方面公共政策的完善,逐渐促进了婴儿死亡率的降低。 目的 确定在纳塔尔/尼泊尔参考医院儿科重症监护室住院的儿童和青少年的流行病学概况和临床演变情况,并对其进行物理治疗跟踪。方法通过对 2023 年第一季度(1 月至 3 月)理疗随访的 0 至 15 岁儿童的病历数据进行定量分析,在纳塔尔省圣地亚哥瓦雷拉婴儿医院(神经外科和肿瘤科参考医院)儿科重症监护室开展描述性和回顾性研究。通过对医疗记录进行描述性和回顾性分析,获得了年龄、性别、出院/死亡演变情况、住院时间、机械通气需求和机械通气持续时间,分类变量以绝对频率和百分比表示,连续变量以平均值和标准偏差表示。结果63名儿童接受了物理治疗,其中34名男孩(53.96%),平均年龄为(3.77±4.29)岁。在重症监护室的住院时间为(14.3±22.8)天;21 名患儿(33.33%)需要进行有创机械通气,平均通气时间为(14.8±17.3)天。结果,15 名患儿(23.80%)转到其他服务机构或直接出院回家,39 名患儿(61.90%)出院回到病房,6 名患儿(9.52%)死亡,3 名患儿(4.76%)继续住院治疗。住院时间的长短与该重症监护室的复杂程度(神经外科和肿瘤科患儿)有关,死亡率低于 10%。意义了解该重症监护室的情况有助于改善护理、优化治疗、减少费用和缩短住院时间。
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引用次数: 0
CAN MUSCLE POWER TRAINING AID THE BIOMECHANICAL AND PHYSIOLOGICAL ADAPTATIONS IN ENDURANCE RUNNERS? 肌肉力量训练是否有助于耐力跑运动员的生物力学和生理适应?
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100694
Danilo Fonseca Leonel , Jonatas Ferreira Silva Santos , Alysson Afonso Nadalin Enes , Gustavo Oneda , Walter Luiz Arcanjo Júnior , Fernando Joaquim Gripp Lopes
<div><h3>Background</h3><p>The performance of long-distance runners is predicted by the interaction between physical variables, and plyometric and endurance training can change the interaction between these variables. In this way, it becomes necessary to investigate these promoted adaptations and how their transfer to performance occurs.</p></div><div><h3>Objectives</h3><p>The study aimed to verify the combined effect of plyometric and endurance training on performance variables in long-distance runners.</p></div><div><h3>Methods</h3><p>The sample consisted of 23 male runners between 18 and 50 years old, athletes of 10km races and divided into two experimental groups: combined training (CT; Plyometric + endurance training; n = 11) and isolated training (ET; endurance training only; n = 12). The volunteers were submitted to two moments of evaluation, performed before and after the experimental protocol, consisting of anthropometric evaluations, muscle power, running economy, biomechanical test, maximum progressive test, and 10-km performance. For the experimental protocol, the volunteers were divided into pairs into the ET or CT groups according to the result obtained in the 10-kilometer test performed before the start of training. At the end of the experimental protocol (8 weeks), the athletes were reassessed, and the tests used were the same as those used in the initial assessment.</p></div><div><h3>Results</h3><p>In muscle power tests, a significant increase in jumps (CMJ and SJ) was reported at the end of training, regardless of the evaluated group. In the biomechanical variables, an increase in contact time with the ground and vertical oscillation was found, in addition to a decrease in stride frequency and leg stiffness at the end of the training protocol, in both analyzed groups. Regarding the physiological variables, an increase in running economy, respiratory compensation points and peak velocity on treadmill was found, but VO<sub>2</sub>max remained stable after the experimental protocol. Finally, the final performance in the 10km did not show a significant effect, but the race strategy (initial phase) and peak velocity increased in both groups.</p></div><div><h3>Conclusion</h3><p>CT (endurance + plyometrics) elicited similar changes in muscle power, biomechanical, physiological and performance variables, when compared to runners who performed ET.</p></div><div><h3>Implications</h3><p>Even with the lowest volume of running in the CT group, the effects were similar to the group that only performed ET, a relevant finding when considering that a high volume of running training can lead to injuries due to stress or repetition. Based on our findings, it is recommended to include neuromuscular training in weekly training routines, with the insertion of activities aimed at improving contact with the ground, technical efficiency and energy use of the muscle stretching-shortening cycle. It is also suggested that the neuromuscular training load is
背景长跑运动员的成绩是通过身体变量之间的相互作用来预测的,而负重和耐力训练可以改变这些变量之间的相互作用。方法样本由 23 名年龄在 18 至 50 岁之间的男性长跑运动员组成,他们都是 10 公里比赛的运动员,分为两个实验组:联合训练组(CT;负重负重训练+耐力训练;n = 11)和孤立训练组(ET;仅耐力训练;n = 12)。志愿者在实验方案前后接受了两次评估,包括人体测量评估、肌肉力量、跑步经济性、生物力学测试、最大进步测试和 10 公里成绩。在实验方案中,根据训练开始前进行的 10 公里测试结果,志愿者被分成两对,一组为 ET 组,另一组为 CT 组。在实验方案结束时(8 周),对运动员进行了重新评估,所使用的测试与最初评估时使用的测试相同。在生物力学变量方面,两个分析组都发现,训练结束时,除了步频和腿部僵硬度下降外,与地面的接触时间和垂直摆动也增加了。在生理变量方面,发现跑步经济性、呼吸补偿点和跑步机上的峰值速度都有所增加,但最大氧饱和度在实验方案结束后保持稳定。结论与进行 ET 的跑步者相比,CT(耐力 + 负重)在肌肉力量、生物力学、生理和成绩变量方面引起了相似的变化。意义即使 CT 组的跑步量最小,其效果也与只进行 ET 的组相似,考虑到大运动量的跑步训练可能会因压力或重复而导致受伤,这是一个相关的发现。根据我们的研究结果,建议将神经肌肉训练纳入每周的例行训练中,并加入旨在改善与地面接触、技术效率和肌肉拉伸-缩短周期能量利用的活动。此外,还建议根据周期确定神经肌肉训练负荷,并经常从纵跳的最佳高度进行控制。最后,应在日常训练的特定时段进行负重活动,其主要目的是提高肌肉力量。
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引用次数: 0
WORK ABILITY PREDICTS OCCUPATIONAL HEALTH-RELATED ABSENTEEISM IN PROFESSIONAL DRIVERS: A 1-YEAR LONGITUDINAL STUDY 工作能力预测职业司机与职业健康有关的缺勤:一项为期 1 年的纵向研究
IF 3.4 3区 医学 Q1 ORTHOPEDICS Pub Date : 2024-03-21 DOI: 10.1016/j.bjpt.2024.100690
Cynthia Mara Zilli Casagrande , Arthur de Sá Ferreira

Background

Work ability (WA) is considered the result of the interaction of personal, social, and other factors related to the work environment. To what extent WA can predict absenteeism at work due to occupational health in professional drivers remains poorly investigated.

Objectives

To analyze the association between work ability and occupational health-related absenteeism at work in professional drivers.

Methods

From 2020 to 2021, 449 professional drivers were assessed for sociodemographic information, lifestyle (Baecke questionnaire, Work Stress Scale), and work ability (Work Ability Index, WAI) in Curitiba, Paraná (Brazil). Follow-up assessments were conducted at 6 and 12 months by telephone to answer 3 questions that aimed at information about professional performance, situations of occupational absenteeism, and accidents at work.

Results

After 12 months of the initial interview, 270/449 drivers (60%) remained as research participants and the others did not remain active in the profession (n=29/449, 7%) or did not respond to telephone contact (n= 53/449, 12%). WAI was inversely associated (β=-0.119 CI 95% -0.233 to -0.006, P=0.039) with general absenteeism at 12 months, explaining better WAI variability and showing a better fit of the latter model (AIC=137, R²= 0.028, P=0.074 vs. R² = 0.050, AIC = 92, P=0.039). Separating the reasons for absenteeism between occupational health and accidents at work, we concluded that WAI was inversely associated with absenteeism due to occupational health at 6 months ((β=-0.096 CI95% -0.187 to -0.006, P=0.037) and accidents at work at 12 months (β=-0.189 95% CI -0.331 to -0.047, P=0.009).

Conclusion

Work ability can predict 1-year absenteeism due to occupational health in professional drivers.

Implications

Absenteeism due to occupational health can be detected using current work ability information in professional drivers. Further studies are required to test whether ergonomic interventions can promote occupational health and decrease absenteeism in this population.

背景工作能力(WA)被认为是与工作环境相关的个人、社会和其他因素相互作用的结果。方法从 2020 年到 2021 年,在巴西巴拉那州库里提巴对 449 名职业司机进行了社会人口学信息、生活方式(Baecke 问卷、工作压力量表)和工作能力(工作能力指数,WAI)的评估。在6个月和12个月时通过电话进行了后续评估,回答了3个问题,这些问题的目的是了解职业表现、职业缺勤情况和工作事故。在 12 个月时,WAI 与一般缺勤成反比(β=-0.119 CI 95% -0.233 to -0.006,P=0.039),更好地解释了 WAI 的变化,并显示出后一模型的拟合度更高(AIC=137,R²= 0.028,P=0.074 vs. R²= 0.050,AIC=92,P=0.039)。将缺勤原因分为职业健康和工伤事故两种,我们得出结论,WAI 与 6 个月时因职业健康造成的缺勤成反比(β=-0.096 CI95% -0.187 to -0.006,P=0.037),与 12 个月时因工伤事故造成的缺勤成反比(β=-0.189 95% CI -0.331 to -0.047,P=0.009)。结论工作能力可以预测职业驾驶员因职业健康而导致的 1 年旷工。需要进一步开展研究,以检验人体工程学干预措施是否能促进职业健康并减少该人群的缺勤率。
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引用次数: 0
期刊
Brazilian Journal of Physical Therapy
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