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Enhanced cognitive behaviour therapy for adolescents with eating disorders: development, effectiveness, and future challenges. 针对进食障碍青少年的强化认知行为疗法:发展、有效性和未来挑战。
IF 2.3 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-09-04 DOI: 10.1186/s13030-024-00315-7
Riccardo Dalle Grave, Simona Calugi

Eating disorders can significantly impact the psychosocial functioning and physical health of adolescents. Early and effective treatment is crucial to prevent long-lasting and potentially devastating adverse effects. The National Institute for Health and Care Excellence has recommended cognitive behaviour therapy (CBT) for eating disorders in adolescents when family therapy is unacceptable, contraindicated, or ineffective. This recommendation was primarily based on the review of promising results from the enhanced version of CBT (CBT-E) adapted for adolescents with eating disorders aged between 12 and 19 years. A non-randomized effectiveness trial has also shown that CBT-E achieved a similar outcome to family-based treatment (FBT) at 6- and 12-months. CBT-E has several advantages. It is acceptable to young people, and its collaborative nature suits ambivalent young patients who may be particularly concerned about control issues. The transdiagnostic scope of the treatment is an advantage as it can treat the full range of disorders that occur in adolescent patients. It is an individual one-on-one treatment that does not necessitate the full involvement of the family. This approach is particularly beneficial for families that can only provide limited support. Future challenges include clarifying the relative efficacy of CBT-E and family therapy for the treatment of adolescent patients with eating disorders in a randomized control trial and increasing its effectiveness, identifying the reasons for the lack of response, and modifying the treatment accordingly.

饮食失调会严重影响青少年的社会心理功能和身体健康。早期有效的治疗对于防止长期的、潜在的破坏性不良影响至关重要。美国国家健康与护理卓越研究所(National Institute for Health and Care Excellence)建议,当家庭治疗不可接受、有禁忌或无效时,可采用认知行为疗法(CBT)治疗青少年进食障碍。这一建议主要是基于对针对 12 至 19 岁进食障碍青少年的认知行为疗法增强版(CBT-E)的审查结果。一项非随机有效性试验也表明,CBT-E 在 6 个月和 12 个月后的疗效与基于家庭的治疗(FBT)相似。CBT-E 有几个优点。它为年轻人所接受,其合作性质适合可能特别关注控制问题的矛盾的年轻患者。该疗法的跨诊断范围也是其优点之一,因为它可以治疗青少年患者出现的各种障碍。这是一种一对一的个人治疗,不需要家庭的全面参与。对于只能提供有限支持的家庭来说,这种方法尤其有益。未来的挑战包括在随机对照试验中明确 CBT-E 和家庭疗法治疗青少年饮食失调症患者的相对疗效,并提高其有效性,找出缺乏反应的原因,并相应地修改治疗方法。
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引用次数: 0
A qualitative study on the experiences of family caregivers of children with End Stage Kidney Disease (ESKD). 关于终末期肾病(ESKD)患儿家庭照顾者经历的定性研究。
IF 2.3 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-08-16 DOI: 10.1186/s13030-024-00314-8
Edward Appiah Boateng, Mabel Baaba Bisiw, Rosemary Agyapomah, Isaac Enyemadze, Joana Kyei-Dompim, Samuel Peprah Kumi, Dorothy Serwaa Boakye

Background: Family caregivers, mostly parents, are greatly involved in the care of their children with end stage kidney disease (ESKD) globally. Yet, the experiences of these caregivers and the demands placed on them by the caregiving role have not been explored or documented in Ghana. This study explored how caregiving affects the psychological, physical, social, and spiritual well-being of family caregivers of children with end stage kidney disease (ESKD) in Ghana.

Methods: A phenomenological approach with the purposive sampling technique was used to gather data from 12 family caregivers of children with ESKD at a pediatric renal unit in Ghana. A semi-structured interview guide was constructed based on the constructs of the City of Hope Quality of Life (QoL) Family Caregiver Model and the research objectives. Colaizzi's thematic analysis approach was utilized to analyze data for this study. Themes were organized under the domains of the chosen model, and a new theme outside these domains was also generated.

Results: The majority of the family caregivers experienced anxiety, fear, uncertainty, and hopelessness in response to the children's diagnosis and care. The thought of the possibility of the children dying was deeply traumatizing for our participants. Most participants reported bodily pains and physical ailments because of lifting and caring for the children. Financial constraint was also a key issue for all the family caregivers. Most of them received diverse support from their families and loved ones. Due to the demanding nature of the care, most family caregivers had to change or quit their jobs. They coped with the challenges through prayers, participating in religious activities, and being hopeful in God for healing.

Conclusion: All the family caregivers had their psychological well-being compromised as a result of the challenges they encountered physically, socially, and spiritually. Continuous psychosocial support, funding support, and review of policies on leave for civil workers with children diagnosed with ESKD are urgently required.

背景:在全球范围内,家庭照顾者(主要是父母)在很大程度上参与了对患有终末期肾病(ESKD)的儿童的照顾。然而,加纳尚未探讨或记录这些照顾者的经历以及照顾角色对他们提出的要求。本研究探讨了照料如何影响加纳终末期肾病(ESKD)患儿家庭照料者的心理、生理、社会和精神福祉:方法:采用现象学方法和目的性抽样技术,从加纳一家儿科肾脏病医院的 12 名 ESKD 患儿家庭照顾者那里收集数据。根据 "希望之城 "生活质量(QoL)家庭照顾者模型的结构和研究目标,制定了半结构式访谈指南。本研究采用科莱兹主题分析法对数据进行分析。在所选模式的领域下组织主题,并在这些领域之外产生一个新的主题:结果:大多数家庭照顾者对儿童的诊断和护理都感到焦虑、恐惧、不确定和绝望。一想到孩子可能会死亡,我们的参与者就深受创伤。大多数参与者都报告说,由于抬举和照顾患儿,他们的身体出现了疼痛和病痛。经济拮据也是所有家庭照顾者面临的一个关键问题。他们中的大多数人都得到了家人和亲人的不同支持。由于护理工作要求苛刻,大多数家庭照顾者不得不更换或辞去工作。他们通过祈祷、参加宗教活动和对上帝的治愈充满希望来应对挑战:所有家庭照顾者的心理健康都因他们在身体、社会和精神上遇到的挑战而受到损害。当务之急是提供持续的社会心理支持、资金支持,并对有确诊 ESKD 患儿的公务员的休假政策进行审查。
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引用次数: 0
Effects of a video-viewing intervention with positive word stimulation on the depressive symptoms of older patients with cardiac disease and subthreshold depression: a pilot randomized controlled trial protocol. 带有正面词语刺激的视频观看干预对患有心脏病和阈下抑郁症的老年患者抑郁症状的影响:随机对照试验方案。
IF 2.3 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-07-16 DOI: 10.1186/s13030-024-00312-w
Masataka Sakimoto, Takumi Igusa, Takuya Kobayashi, Hiroyuki Uchida, Aya Fukazawa, Chihaya Machida, Hirokuni Fujii, Keisuke Sekine, Minori Kurosaki, Kenji Tsuchiya, Senichiro Kikuchi, Kazuki Hirao

Background: Intervention for older patients with cardiac disease and subthreshold depression (StD) may be an effective strategy to prevent the development of major depressive disorder. The subliminal priming with supraliminal reward stimulation (SPSRS) website developed by us is an advanced intervention that can improve depressive symptoms in individuals with StD by presenting positive word stimuli in videos. However, its efficacy for treating depressive symptoms in older patients with cardiac disease and StD has not been investigated. Here, we present a pilot randomized controlled trial protocol to investigate the preliminary efficacy of an intervention for older patients with cardiac disease with StD.

Methods: The study was designed as a single-center, open-label, pilot, randomized, parallel-group trial. The participants will include 30 older patients with cardiac disease and StD who are hospitalized in acute wards. The Experimental group received the SPSRS intervention (video viewing with positive word stimuli; n = 15) and the Control group will receive the YouTube intervention (video viewing without positive word stimuli; n = 15). In both groups, the intervention will be administered for 10 min per day, five times per week for 1 week. The primary outcome will be the change in the scores on the Japanese version of the Beck Depression Inventory-II at 1 week after the baseline assessment. The secondary outcomes will be the changes in the Specific Activity Scale, New York Heart Association functional classification, as well as grip strength at 1 week after the baseline assessment.

Discussion: This pilot randomized controlled trial will be the first to evaluate the SPSRS intervention for depressive symptoms in older patients with cardiac disease and StD who are admitted to acute wards. The results will provide tentative indications regarding the impact of the intervention on depressive symptoms among older patients with cardiac disease and StD who are admitted to acute wards, and will contribute to the planning of a full-scale study.

Trial registration: UMIN, UMIN000052155. Registered September 8, 2023, https://center6.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000059526 . This study was registered with the University Hospital Medical Information Network (UMIN) (UMIN000052155) in Japan.

背景:对患有心脏病和阈下抑郁症(StD)的老年患者进行干预可能是预防重度抑郁症发展的有效策略。我们开发的 "潜意识引物与阈上奖赏刺激(SPSRS)"网站是一种先进的干预方法,通过在视频中呈现积极的词语刺激,可改善阈下抑郁症患者的抑郁症状。然而,该疗法对患有心脏病和 StD 的老年患者抑郁症状的治疗效果尚未进行研究。在此,我们提出了一个试验性随机对照试验方案,以研究对患有心脏病并伴有 StD 的老年患者进行干预的初步疗效:研究设计为单中心、开放标签、试验性、随机、平行组试验。参与者包括 30 名在急症病房住院的患有心脏病和 StD 的老年患者。实验组接受 SPSRS 干预(观看有正面词语刺激的视频;n = 15),对照组接受 YouTube 干预(观看无正面词语刺激的视频;n = 15)。两组的干预时间均为每天 10 分钟,每周 5 次,持续 1 周。主要结果是在基线评估后 1 周,日文版贝克抑郁量表-II 分数的变化。次要结果是基线评估一周后特定活动量表、纽约心脏协会功能分类以及握力的变化:这项随机对照试验将首次评估 SPSRS 对急性病房收治的患有心脏病和 StD 的老年患者抑郁症状的干预效果。试验结果将初步表明该干预措施对急性病房收治的老年心脏病和 StD 患者抑郁症状的影响,并将有助于全面研究的规划:试验注册:UMIN,UMIN000052155。注册日期:2023 年 9 月 8 日,https://center6.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000059526 。本研究已在日本大学医院医疗信息网(UMIN)注册(UMIN000052155)。
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引用次数: 0
Proof of mechanism investigation of Transcutaneous auricular vagus nerve stimulation through simultaneous measurement of autonomic functions: a randomized controlled trial protocol. 通过同时测量自律神经功能对经皮耳模迷走神经刺激进行机制验证研究:随机对照试验方案。
IF 2.1 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-06-18 DOI: 10.1186/s13030-024-00311-x
Ruri Katsunuma, Tsunehiko Takamura, Mitsuhiko Yamada, Atsushi Sekiguchi

Background: The autonomic nervous system plays a vital role in regulating physiological functions. Transcutaneous auricular vagus nerve stimulation (taVNS) is a method that provides insights into autonomic nerve modulation. This paper presents a research protocol investigating proof of mechanism for the impact of taVNS on autonomic functions and aims to both deepen theoretical understanding and pave the way for clinically relevant applications.

Methods: This protocol employs a single-blind, randomized cross-over design involving 10 healthy male participants. Simultaneous assessment of both the afferent and efferent aspects of the vagus nerve will be performed by integrating physiological measures, magnetic resonance imaging, and a questionnaire survey. Electrocardiogram will be measured to assess changes in heart rate, as a primary outcome, and heart rate variability. Active taVNS and sham stimulation will be compared, which ensures precision and blinding. Electrical stimulation will be applied to the left concha cymba and the left lobule for the active and sham conditions, respectively. The specific parameters of taVNS involve a pulse width of 250 µs, a frequency of 25 Hz, and a current adjusted to the perception threshold (0.1 mA ≤ 5 mA), delivered in cycles of 32 s on and 28 s off.

Conclusions: This research investigates proof of mechanism for taVNS to elucidate its modulatory effects on the central and peripheral components of the autonomic nervous system. Beyond theoretical insights, the findings will provide a foundation for designing targeted neuromodulation strategies, potentially benefiting diverse patient populations experiencing autonomic dysregulation. By elucidating the neural mechanisms, this study contributes to the evolution of personalized and effective clinical interventions in the field of neuromodulation.

Trial registration: JRCT, jRCTs032220332, Registered 13 September 2022; https://jrct.niph.go.jp/latest-detail/jRCTs032220332 .

背景:自律神经系统在调节生理功能方面发挥着重要作用。经皮耳廓迷走神经刺激(taVNS)是一种能深入了解自律神经调节的方法。本文介绍了一项研究方案,调查taVNS对自律神经功能影响的机制证明,旨在加深理论理解并为临床相关应用铺平道路:该方案采用单盲、随机交叉设计,涉及 10 名健康男性参与者。将通过综合生理测量、磁共振成像和问卷调查对迷走神经的传入和传出进行同步评估。将测量心电图以评估心率变化(作为主要结果)和心率变异性。将对活性 taVNS 和假刺激进行比较,以确保精确性和盲法。电刺激将分别作用于主动和假性条件下的左侧冠状动脉和左侧小叶。taVNS的具体参数包括250微秒的脉冲宽度、25赫兹的频率以及根据感知阈值调整的电流(0.1毫安≤5毫安),以32秒开28秒关为周期进行刺激:本研究调查了 taVNS 的机制证明,以阐明其对自律神经系统中枢和外周组成部分的调节作用。除理论见解外,研究结果还将为设计有针对性的神经调控策略奠定基础,从而使自主神经失调的不同患者群体从中受益。通过阐明神经机制,这项研究有助于神经调控领域个性化和有效临床干预措施的发展:JRCT,jRCTs032220332,2022年9月13日注册;https://jrct.niph.go.jp/latest-detail/jRCTs032220332 。
{"title":"Proof of mechanism investigation of Transcutaneous auricular vagus nerve stimulation through simultaneous measurement of autonomic functions: a randomized controlled trial protocol.","authors":"Ruri Katsunuma, Tsunehiko Takamura, Mitsuhiko Yamada, Atsushi Sekiguchi","doi":"10.1186/s13030-024-00311-x","DOIUrl":"10.1186/s13030-024-00311-x","url":null,"abstract":"<p><strong>Background: </strong>The autonomic nervous system plays a vital role in regulating physiological functions. Transcutaneous auricular vagus nerve stimulation (taVNS) is a method that provides insights into autonomic nerve modulation. This paper presents a research protocol investigating proof of mechanism for the impact of taVNS on autonomic functions and aims to both deepen theoretical understanding and pave the way for clinically relevant applications.</p><p><strong>Methods: </strong>This protocol employs a single-blind, randomized cross-over design involving 10 healthy male participants. Simultaneous assessment of both the afferent and efferent aspects of the vagus nerve will be performed by integrating physiological measures, magnetic resonance imaging, and a questionnaire survey. Electrocardiogram will be measured to assess changes in heart rate, as a primary outcome, and heart rate variability. Active taVNS and sham stimulation will be compared, which ensures precision and blinding. Electrical stimulation will be applied to the left concha cymba and the left lobule for the active and sham conditions, respectively. The specific parameters of taVNS involve a pulse width of 250 µs, a frequency of 25 Hz, and a current adjusted to the perception threshold (0.1 mA ≤ 5 mA), delivered in cycles of 32 s on and 28 s off.</p><p><strong>Conclusions: </strong>This research investigates proof of mechanism for taVNS to elucidate its modulatory effects on the central and peripheral components of the autonomic nervous system. Beyond theoretical insights, the findings will provide a foundation for designing targeted neuromodulation strategies, potentially benefiting diverse patient populations experiencing autonomic dysregulation. By elucidating the neural mechanisms, this study contributes to the evolution of personalized and effective clinical interventions in the field of neuromodulation.</p><p><strong>Trial registration: </strong>JRCT, jRCTs032220332, Registered 13 September 2022; https://jrct.niph.go.jp/latest-detail/jRCTs032220332 .</p>","PeriodicalId":9027,"journal":{"name":"BioPsychoSocial Medicine","volume":"18 1","pages":"15"},"PeriodicalIF":2.1,"publicationDate":"2024-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11184723/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141417613","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The reliability and validity of a developed anxiety scale specific to primary focal hyperhidrosis symptoms. 针对原发性局灶性多汗症症状开发的焦虑量表的可靠性和有效性。
IF 2.1 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-06-04 DOI: 10.1186/s13030-024-00310-y
Sayaka Ogawa, Jun Tayama, Hiroyuki Murota, Masakazu Kobayashi, Hirohisa Kinoshita, Seiko Nakamichi

Background: Patients with primary focal hyperhidrosis (hyperhidrosis) are known to have higher levels of anxiety induced by sweating than those who do not. However, in hyperhidrosis, no scale has been developed to measure anxiety specific to hyperhidrosis symptoms. Therefore, this study aimed to develop an anxiety scale specific to hyperhidrosis symptoms (ASSHS) and to verify its reliability and validity.

Methods: Based on previous studies on hyperhidrosis and a preliminary survey conducted with 26 university students who met the diagnostic criteria for hyperhidrosis, 40 items that adequately reflected anxiety specific to hyperhidrosis symptoms were obtained. A survey was done to examine the internal consistency and validity of the our developed ASSHS. In total, 1,207 participants (680 male and 527 female; mean age ± standard deviation 18.7 ± 0.9 years) were included. A second survey (re-survey) was conducted three weeks later to verify the reliability. It included 201 participants (85 male and 116 female; mean age ± standard deviation 18.6 ± 0.7 years). The survey items included (1) the diagnostic criteria for hyperhidrosis, (2) our anxiety scale developed for primary focal hyperhidrosis symptoms (ASSHS), (3) Hyperhidrosis Disease Severity Scale (HDSS), (4) State-Trait Anxiety Inventory (STAI), (5) Hospital Anxiety and Depression Scale (HADS), (6) Dermatology Life Quality Index (DLQI), and (7) presence of anxiety induced by sweating.

Results: The results of the factor analysis revealed 10 items with one factor, "anxiety specific to hyperhidrosis symptoms." The alpha coefficient of the ASSHS was α = 0.94. The correlation coefficient between the scores at re-test was r = 0.75. A moderate positive correlation was found between the ASSHS, HDSS (r = 0.53), and anxiety induced by sweating (r = 0.47) (all p < 0.001). Additionally, participants with hyperhidrosis symptoms had significantly higher ASSHS scores than did those without hyperhidrosis symptoms (p < 0.001). Those with mild/moderate hyperhidrosis and those with severe hyperhidrosis had significantly higher the ASSHS scores than did those without hyperhidrosis (p < 0.001).

Conclusions: This scale has sufficient reliability and validity as an instrument to measure anxiety specific to hyperhidrosis symptoms.

背景:众所周知,原发性局灶性多汗症(多汗症)患者因出汗而产生的焦虑程度高于非多汗症患者。然而,在多汗症患者中,尚未开发出专门针对多汗症症状的焦虑量表。因此,本研究旨在开发一种专门针对多汗症症状的焦虑量表(ASSHS),并验证其可靠性和有效性:根据以往有关多汗症的研究以及对 26 名符合多汗症诊断标准的大学生进行的初步调查,获得了 40 个能充分反映多汗症症状特有焦虑的项目。为了检验我们开发的 ASSHS 的内部一致性和有效性,我们进行了一项调查。共有 1207 名参与者(男性 680 人,女性 527 人;平均年龄(标准差)为 18.7 ± 0.9 岁)参与了调查。三周后进行了第二次调查(重新调查),以验证其可靠性。该调查包括 201 名参与者(男性 85 人,女性 116 人;平均年龄(标准差)为 18.6 ± 0.7 岁)。调查项目包括:(1)多汗症诊断标准;(2)我们针对原发性局灶性多汗症症状开发的焦虑量表(ASSHS);(3)多汗症疾病严重程度量表(HDSS);(4)状态-特质焦虑量表(STAI);(5)医院焦虑和抑郁量表(HADS);(6)皮肤科生活质量指数(DLQI);(7)出汗引起的焦虑:因子分析结果显示,10 个条目包含一个因子,即 "多汗症症状特有的焦虑"。ASSHS 的α系数为 α = 0.94。复测得分之间的相关系数为 r = 0.75。在 ASSHS、HDSS(r = 0.53)和出汗引起的焦虑(r = 0.47)之间发现了中等程度的正相关(均为 p 结论):该量表具有足够的可靠性和有效性,可用于测量多汗症症状所特有的焦虑。
{"title":"The reliability and validity of a developed anxiety scale specific to primary focal hyperhidrosis symptoms.","authors":"Sayaka Ogawa, Jun Tayama, Hiroyuki Murota, Masakazu Kobayashi, Hirohisa Kinoshita, Seiko Nakamichi","doi":"10.1186/s13030-024-00310-y","DOIUrl":"10.1186/s13030-024-00310-y","url":null,"abstract":"<p><strong>Background: </strong>Patients with primary focal hyperhidrosis (hyperhidrosis) are known to have higher levels of anxiety induced by sweating than those who do not. However, in hyperhidrosis, no scale has been developed to measure anxiety specific to hyperhidrosis symptoms. Therefore, this study aimed to develop an anxiety scale specific to hyperhidrosis symptoms (ASSHS) and to verify its reliability and validity.</p><p><strong>Methods: </strong>Based on previous studies on hyperhidrosis and a preliminary survey conducted with 26 university students who met the diagnostic criteria for hyperhidrosis, 40 items that adequately reflected anxiety specific to hyperhidrosis symptoms were obtained. A survey was done to examine the internal consistency and validity of the our developed ASSHS. In total, 1,207 participants (680 male and 527 female; mean age ± standard deviation 18.7 ± 0.9 years) were included. A second survey (re-survey) was conducted three weeks later to verify the reliability. It included 201 participants (85 male and 116 female; mean age ± standard deviation 18.6 ± 0.7 years). The survey items included (1) the diagnostic criteria for hyperhidrosis, (2) our anxiety scale developed for primary focal hyperhidrosis symptoms (ASSHS), (3) Hyperhidrosis Disease Severity Scale (HDSS), (4) State-Trait Anxiety Inventory (STAI), (5) Hospital Anxiety and Depression Scale (HADS), (6) Dermatology Life Quality Index (DLQI), and (7) presence of anxiety induced by sweating.</p><p><strong>Results: </strong>The results of the factor analysis revealed 10 items with one factor, \"anxiety specific to hyperhidrosis symptoms.\" The alpha coefficient of the ASSHS was α = 0.94. The correlation coefficient between the scores at re-test was r = 0.75. A moderate positive correlation was found between the ASSHS, HDSS (r = 0.53), and anxiety induced by sweating (r = 0.47) (all p < 0.001). Additionally, participants with hyperhidrosis symptoms had significantly higher ASSHS scores than did those without hyperhidrosis symptoms (p < 0.001). Those with mild/moderate hyperhidrosis and those with severe hyperhidrosis had significantly higher the ASSHS scores than did those without hyperhidrosis (p < 0.001).</p><p><strong>Conclusions: </strong>This scale has sufficient reliability and validity as an instrument to measure anxiety specific to hyperhidrosis symptoms.</p>","PeriodicalId":9027,"journal":{"name":"BioPsychoSocial Medicine","volume":"18 1","pages":"14"},"PeriodicalIF":2.1,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11149174/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141247453","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinico-demographic factors associated with the treatment response to cognitive behavioral therapy for insomnia. 与失眠认知行为疗法治疗反应相关的临床人口学因素。
IF 2.1 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-05-17 DOI: 10.1186/s13030-024-00308-6
Ayana Hotchi, Wataru Yamadera, Masayuki Iwashita, Tomohiro Utsumi, Misato Amagai, Sakumi Nakamura, Takako Suzuki, Masahiro Shigeta

Background: Cognitive behavioral therapy for insomnia (CBT-I) is among the recommended non-pharmacological treatments for patients with insomnia. While there are multiple reports on the effects of CBT-I treatment, few studies evaluating the factors associated with the treatment response to CBT-I have been reported. The present study aimed to confirm the effects of CBT-I in patients with insomnia and to examine the clinico-demographic factors that can predict the outcomes of CBT-I in these patients.

Methods: Overall, 62 patients were included in the present study. To confirm the effectiveness of CBT-I, we compared the pre- and post-CBT-I therapy values of several sleep parameters. Furthermore, to identify the clinico-demographic factors that could be predictive of the treatment response to CBT-I, we performed generalized linear model (GLM) analysis.

Results: The values of several sleep parameters were significantly lower after treatment than at baseline. The results of the GLM analysis revealed that sex and occupation were significantly associated with the treatment response to CBT-I.

Conclusions: The present results suggest that several clinico-demographic factors should be considered in the treatment of patients with insomnia.

背景:失眠认知行为疗法(CBT-I)是失眠患者推荐的非药物治疗方法之一。虽然有多篇关于 CBT-I 治疗效果的报道,但很少有研究评估与 CBT-I 治疗反应相关的因素。本研究旨在确认 CBT-I 对失眠症患者的疗效,并研究可预测 CBT-I 对这些患者疗效的临床人口学因素:本研究共纳入 62 名患者。为了证实 CBT-I 的有效性,我们比较了 CBT-I 治疗前后几项睡眠参数的数值。此外,为了确定可预测 CBT-I 治疗反应的临床人口学因素,我们进行了广义线性模型(GLM)分析:结果:治疗后多个睡眠参数值明显低于基线值。GLM分析结果显示,性别和职业与CBT-I的治疗反应显著相关:结论:本研究结果表明,在治疗失眠症患者时应考虑一些临床人口学因素。
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引用次数: 0
Work-related problems and the psychosocial characteristics of individuals with irritable bowel syndrome: an updated literature review. 工作相关问题与肠易激综合征患者的社会心理特征:最新文献综述。
IF 2.1 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-05-15 DOI: 10.1186/s13030-024-00309-5
Nagisa Sugaya

Background: Irritable bowel syndrome (IBS) is a common, functional gastrointestinal disorder. Because IBS often develops and worsens with stress, it requires treatment from both physical and mental perspectives. Recent years have seen increasing reports of its impact on the daily performance and productivity of workers with IBS, leading to sick leaves and lower quality of life. Therefore, this narrative review aimed to summarize the work and psychosocial characteristics of individuals with IBS.

Main body: Workers with IBS report greater occupational stressors and work productivity impairments, including presenteeism or absenteeism, in addition to suffering from psychological distress, low quality of life, and medical and economic problems, similar to those with IBS in the general population. Anxiety about abdominal symptoms, as well as the severity of IBS, is related to the degree of interference with one's work. Regarding the association between characteristics of work and IBS, shift work and job demands/discretion have been associated with IBS. Studies on specific occupations have revealed associations between IBS and various occupational stressors in healthcare workers, firefighters, and military personnel. Telecommuting, which has become increasingly popular during the coronavirus disease pandemic, has not found to improve IBS. Moreover, the effectiveness of medication, diet, and a comprehensive self-management program, including cognitive behavioral therapy, in improving the productivity of workers with IBS have been examined.

Conclusion: As mentioned above, the IBS of workers is related not only to their problematic physical and mental health but also to work-related problems; workers with IBS exhibit severe occupational stress factors and work productivity impairment. Further research is required to develop efficient and appropriate interventions for workers.

背景:肠易激综合征(IBS肠易激综合征(IBS)是一种常见的功能性胃肠道疾病。由于肠易激综合征经常在压力下发生和恶化,因此需要从生理和心理两个角度进行治疗。近年来,关于肠易激综合征对患有该病的工人的日常表现和工作效率的影响的报道越来越多,导致病假和生活质量下降。因此,本综述旨在总结肠易激综合征患者的工作和社会心理特征:与普通人群中的肠易激综合征患者相似,肠易激综合征患者除了遭受心理困扰、生活质量低下以及医疗和经济问题外,还报告了更大的职业压力和工作效率损害,包括旷工或缺勤。对腹部症状的焦虑以及肠易激综合征的严重程度与个人工作受干扰的程度有关。关于工作特点与肠易激综合征之间的关系,轮班工作和工作要求/自由裁量权与肠易激综合征有关。对特定职业的研究表明,在医护人员、消防员和军人中,肠易激综合征与各种职业压力之间存在关联。在冠状病毒疾病流行期间越来越流行的远程办公并没有改善肠易激综合征。此外,还研究了药物、饮食和综合自我管理计划(包括认知行为疗法)在提高肠易激综合征患者工作效率方面的效果:如上所述,工人的肠易激综合征不仅与他们的身心健康问题有关,还与工作相关问题有关;肠易激综合征工人表现出严重的职业压力因素和工作效率受损。需要进一步开展研究,为工人制定高效、适当的干预措施。
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引用次数: 0
The effects of loving-kindness meditation on doctors' communication anxiety, trust, calling and defensive medicine practice. 慈爱冥想对医生沟通焦虑、信任、呼叫和防御性医疗实践的影响。
IF 2.1 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-05-10 DOI: 10.1186/s13030-024-00307-7
Hao Chen, Chao Liu, Kan Wu, Chia-Yih Liu, Wen-Ko Chiou

Objective: The study investigated the effects of loving-kindness meditation (LKM) on doctors' communication anxiety, trust, calling, and defensive medicine practice.

Methods: This study recruited 94 doctors from a hospital in China, randomized them to an LKM group (n = 47), and waited for the control group (n = 47). The experimental group accepted an 8-week LKM interference while the waiting for the control group underwent no interference. Researchers measured four major variable factors (communication anxiety, trust, calling, and defensive medicine practice) before and after the LKM intervention.

Results: In the experimental group, trust, and calling were significantly higher, and communication anxiety, and defensive medicine practice were significantly lower than in the control group. In the control group, there were no noticeable differences in any of the four variables between the pre-test and post-test.

Conclusions: The results of this study demonstrate that LKM may help to improve trust, and calling, and reduce communication anxiety and defensive medicine practice. The finding of LKM's effect extends the understanding of the integrative effects of positive psychology on the decrease of defensive medicine practice.

Trial registration: ChiCTR2300074568. Registered in Chinese Clinical Trial Registry (ChiCTR), 9 August, 2023.

目的:本研究探讨了慈爱冥想(LKM)对医生沟通焦虑、信任、呼叫和防御性医疗实践的影响:本研究探讨了慈爱冥想(LKM)对医生的沟通焦虑、信任、呼叫和防御性医疗实践的影响:本研究从中国某医院招募了94名医生,将他们随机分为LKM组(47人)和对照组(47人)。实验组接受为期 8 周的兰光干扰,而等待对照组则不接受任何干扰。研究人员测量了兰光干预前后的四个主要变量因素(沟通焦虑、信任、呼叫和防御性医疗实践):结果:与对照组相比,实验组的信任度和呼叫率明显较高,而沟通焦虑和防御性医疗行为则明显较低。在对照组中,四个变量在测试前和测试后都没有明显差异:本研究的结果表明,兰考医学可以帮助提高信任度和感召力,减少沟通焦虑和防御性医疗行为。LKM效果的发现扩展了人们对积极心理学对减少防御性医疗实践的综合效果的理解:ChiCTR2300074568。注册于中国临床试验注册中心(ChiCTR),2023年8月9日。
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引用次数: 0
Time-dependent complexity characterisation of activity patterns in patients with Chronic Fatigue Syndrome 慢性疲劳综合征患者活动模式随时间变化的复杂性特征
IF 2.1 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-04-02 DOI: 10.1186/s13030-024-00305-9
Paloma Rabaey, Peter Decat, Stefan Heytens, Dirk Vogelaers, An Mariman, Thomas Demeester
Chronic Fatigue Syndrome patients suffer from symptoms that cannot be explained by a single underlying biological cause. It is sometimes claimed that these symptoms are a manifestation of a disrupted autonomic nervous system. Prior works studying this claim from the complex adaptive systems perspective, have observed a lower average complexity of physical activity patterns in chronic fatigue syndrome patients compared to healthy controls. To further study the robustness of such methods, we investigate the within-patient changes in complexity of activity over time. Furthermore, we explore how these changes might be related to changes in patient functioning. We propose an extension of the allometric aggregation method, which characterises the complexity of a physiological signal by quantifying the evolution of its fractal dimension. We use it to investigate the temporal variations in within-patient complexity. To this end, physical activity patterns of 7 patients diagnosed with chronic fatigue syndrome were recorded over a period of 3 weeks. These recordings are accompanied by physicians’ judgements in terms of the patients’ weekly functioning. We report significant within-patient variations in complexity over time. The obtained metrics are shown to depend on the range of timescales for which these are evaluated. We were unable to establish a consistent link between complexity and functioning on a week-by-week basis for the majority of the patients. The considerable within-patient variations of the fractal dimension across scales and time force us to question the utility of previous studies that characterise long-term activity signals using a single static complexity metric. The complexity of a Chronic Fatigue Syndrome patient’s physical activity signal does not suffice to characterise their high-level functioning over time and has limited potential as an objective monitoring metric by itself.
慢性疲劳综合征患者的症状无法用单一的生物学原因来解释。有时有人声称,这些症状是自律神经系统紊乱的一种表现。之前从复杂适应系统的角度研究这一说法的作品观察到,与健康对照组相比,慢性疲劳综合征患者身体活动模式的平均复杂度较低。为了进一步研究这种方法的稳健性,我们研究了患者体内活动复杂性随时间的变化。此外,我们还探讨了这些变化与患者功能变化之间的关系。我们提出了一种异速聚合法的扩展方法,该方法通过量化分形维度的演变来描述生理信号的复杂性。我们用它来研究病人内部复杂性的时间变化。为此,我们记录了 7 名被诊断为慢性疲劳综合症患者为期 3 周的身体活动模式。这些记录附有医生对患者每周功能的判断。我们报告了患者内部随着时间的推移在复杂性方面的显著变化。所获得的衡量标准取决于评估的时间范围。对于大多数患者来说,我们无法在复杂性和每周功能之间建立一致的联系。患者内部分形维度在不同尺度和时间上的巨大差异迫使我们质疑以往使用单一静态复杂性指标描述长期活动信号的研究的实用性。慢性疲劳综合症患者体力活动信号的复杂性不足以描述他们在一段时间内的高级功能,其本身作为客观监测指标的潜力有限。
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引用次数: 0
Disabling symptoms associated with increased axillary temperature in patients with functional hyperthermia. 功能性高热患者腋温升高引起的致残症状。
IF 2.1 4区 医学 Q2 PSYCHIATRY Pub Date : 2024-03-26 DOI: 10.1186/s13030-024-00306-8
Takakazu Oka

Background: I previously reported a case of functional hyperthermia (FH) in a patient with an axillary temperature just slightly above 37.0 °C who persistently requested treatment. Because the severity of her fatigue increased remarkably when her axillary temperature increased above 37.0 °C, she felt that the temperature of 37.0 °C was disabling. In the present study, I analyzed a larger number of patients with FH to investigate the incidence of disabling symptoms with increasing body temperature, the kinds of symptoms associated with increased body temperature, and the temperatures at which these symptoms became disabling.

Main body: Twenty patients with FH (7 men, 13 women; mean age ± standard deviation, 31.2 ± 10.9 years) who visited my department were asked whether they had any disabling symptoms associated with an increase in axillary temperature and, if so, at what temperature the symptoms became disabling. Sixteen of 20 patients (80.0%) responded that they had such symptoms, which included worsening of general fatigue (n = 12, 75.0%), feelings that their brain did not work properly (n = 5, 31.3%), inability to move (n = 4, 25.0%), hot flashes/feeling of heat (n = 3, 18.8%), headache (n = 2, 12.5%), dizziness (n = 2, 12.5%) and anorexia (n = 1, 6.3%). The axillary temperatures at which patients felt worsening fatigue ranged from 37.0 °C to 37.4 °C in 7 of the 12 patients (58.3%) who experienced worsening fatigue. The patients also reported that the disabling symptoms, with the exception of headache, were not alleviated by antipyretics.

Conclusions: Many patients with FH reported worsening fatigue as a disabling symptom associated with increased axillary temperature; more than half of those patients experienced worsening fatigue in the temperature range of 37.0 °C to 37.4 °C. These findings suggest that the reasons patients with FH consider 37 °C disabling and seek medical treatment are that physical symptoms such as fatigue worsen at 37 °C, although this temperature is assumed by many physicians to be within the normal range or just above the normal range of axillary temperature, and that most hyperthermia-associated symptoms are not alleviated by antipyretic drugs.

背景:我曾报告过一例功能性高热(FH)患者,其腋下温度略高于 37.0 °C,但她一直要求治疗。因为当她的腋下温度升高到 37.0 °C以上时,她的疲劳程度明显加重,因此她认为 37.0 °C的温度会使她丧失工作能力。在本研究中,我对更多的 FH 患者进行了分析,以调查体温升高时致残症状的发生率、与体温升高相关的症状类型以及这些症状致残的温度:我们询问了到我科就诊的 20 名 FH 患者(7 名男性,13 名女性;平均年龄(± 标准差):31.2± 10.9 岁)是否有与腋窝体温升高相关的致残症状,如果有,这些症状在什么温度下变得致残。20 名患者中有 16 人(80.0%)回答有此类症状,其中包括全身疲劳加重(12 人,75.0%)、感觉大脑无法正常工作(5 人,31.3%)、无法移动(4 人,25.0%)、潮热/感觉热(3 人,18.8%)、头痛(2 人,12.5%)、头晕(2 人,12.5%)和厌食(1 人,6.3%)。在出现疲劳加重症状的 12 名患者中,有 7 人(58.3%)的腋窝温度在 37.0 ℃ 至 37.4 ℃ 之间。患者还表示,除头痛外,退烧药无法缓解其他致残症状:结论:许多腋窝淋巴结肿大患者表示,疲劳加重是与腋窝体温升高相关的致残症状;其中一半以上的患者在体温 37.0 ℃ 至 37.4 ℃ 范围内出现疲劳加重。这些研究结果表明,FH患者认为37 °C的体温会使其丧失能力并寻求治疗的原因是,尽管许多医生认为37 °C的体温在正常范围内或略高于正常腋温范围,但疲劳等身体症状在37 °C时会加重,而且大多数高热相关症状不会因退烧药而减轻。
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BioPsychoSocial Medicine
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