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Social Media Influence on Surgeon Selection Among Iranian Maxillofacial Patients: Cross-Sectional Survey Study. 社交媒体对伊朗颌面患者外科医生选择的影响:横断面调查研究。
Pub Date : 2025-08-14 DOI: 10.2196/75899
Mehdi Abrishami, Milad Bayat, Elham Sheykhi Some

Background: Social media has reshaped health care decision-making; however, its influence on maxillofacial surgeon selection in non-Western contexts such as Iran remains underexplored. Understanding how patients balance digital platforms (eg, Google, Instagram) with traditional referral networks can inform trust dynamics and patient-centered care strategies.

Objective: This study aimed to evaluate the impact of social media compared to personal recommendations on maxillofacial surgeon selection among Iranian patients, assessing decision-making factors, trust perceptions, accuracy concerns, and demographic influences.

Methods: A cross-sectional survey of 384 patients at maxillofacial surgery clinics in Isfahan, Iran (September-November 2023), was conducted using structured questionnaires to collect data on demographics, surgeon selection pathways, social media use, trust, and accuracy concerns. Descriptive statistics, χ2 tests, one-sample t tests, and multiple linear regression were conducted using SPSS Version 26 to analyze platform impact and predictive variables.

Results: Personal recommendations dominated surgeon selection (239/384, 62.2%), significantly outweighing Google (75/384, 19.5%) and Instagram (11/384, 2.9%; χ²=214.3, P<.001). Google and Instagram were used by 160 (41.7%) and 119 (31.0%) patients, respectively; however, their decision-making impact was low with (mean scores: Google 2.27 (0.82), Instagram 2.14 (SD 0.79) on a 1-5 scale; t tests: P<.001). Patient-generated content drove trust, with reviews valued by 144 (37.5%) for Google and 157 (40.9%) for Instagram, and testimonials by 174 (45.3%) for Instagram. Professional credentials influenced 116 (30.2%) participants for Google. Accuracy concerns were moderate; (means values of Google 2.84 (SD 0.91), Instagram 2.85 (SD) 0.88; P<.05). Regression identified recommendations (β=.42, P<.001), credential trust (β=.19, P=.002), and review authenticity (β=.14, P=.02) as predictors, while social media use was not a significant predictor (P=.32). Participants were predominantly female (233/384, 60.7%), aged 21-30 years (117/384, 30.5%), employed (159/384, 41.4%), with moderate income (201/384, 52.3%), and no prior surgery (205/384, 53.4%). Instagram use was higher among younger patients (21-30 years: 48/117, 41.0%; χ²=12.4, P=.006).

Conclusions: Social media plays a supplementary role in the selection of maxillofacial surgeons in Iran, with traditional networks prevailing due to cultural trust and low health literacy (adequacy in 43% patients). The emphasis on credible reviews and credentials underscores the need for verified digital content. Contrasting with the digital reliance on aesthetic surgery, these findings advocate for verified profiles, patient education portals, and culturally tailored strategies to enhance trust and patient-centered care.

背景:社交媒体重塑了医疗保健决策;然而,它对非西方背景下(如伊朗)颌面外科医生选择的影响仍未得到充分探讨。了解患者如何平衡数字平台(如b谷歌、Instagram)和传统转诊网络,可以为信任动态和以患者为中心的护理策略提供信息。目的:本研究旨在评估社交媒体与个人推荐对伊朗患者颌面外科医生选择的影响,评估决策因素、信任感知、准确性关注和人口统计学影响。方法:对伊朗伊斯法罕颌面外科诊所384例患者(2023年9月至11月)进行横断面调查,采用结构化问卷收集人口统计学、外科医生选择途径、社交媒体使用、信任和准确性问题等数据。采用SPSS Version 26进行描述性统计、χ2检验、单样本t检验和多元线性回归分析平台影响及预测变量。结果:个人推荐在外科医生选择中占主导地位(239/384,62.2%),显著超过b谷歌(75/384,19.5%)和Instagram (11/384, 2.9%);结论:社交媒体在伊朗颌面外科医生的选择中起辅助作用,由于文化信任和低健康素养(43%的患者足够),传统网络占主导地位。对可信审查和证书的强调强调了对经过验证的数字内容的需求。与数字对美容手术的依赖相比,这些研究结果提倡验证档案,患者教育门户和文化定制策略,以增强信任和以患者为中心的护理。
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引用次数: 0
Evaluating Large Language Models for Preoperative Patient Education in Superior Capsular Reconstruction: Comparative Study of Claude, GPT, and Gemini. 大语言模型对上囊重建术前患者教育的评价:Claude、GPT和Gemini的比较研究。
Pub Date : 2025-06-12 DOI: 10.2196/70047
Yukang Liu, Hua Li, Jianfeng Ouyang, Zhaowen Xue, Min Wang, Hebei He, Bin Song, Xiaofei Zheng, Wenyi Gan

Background: Large language models (LLMs) are revolutionizing natural language processing, increasingly applied in clinical settings to enhance preoperative patient education.

Objective: This study aimed to evaluate the effectiveness and applicability of various LLMs in preoperative patient education by analyzing their responses to superior capsular reconstruction (SCR)-related inquiries.

Methods: In total, 10 sports medicine clinical experts formulated 11 SCR issues and developed preoperative patient education strategies during a webinar, inputting 12 text commands into Claude-3-Opus (Anthropic), GPT-4-Turbo (OpenAI), and Gemini-1.5-Pro (Google DeepMind). A total of 3 experts assessed the language models' responses for correctness, completeness, logic, potential harm, and overall satisfaction, while preoperative education documents were evaluated using DISCERN questionnaire and Patient Education Materials Assessment Tool instruments, and reviewed by 5 postoperative patients for readability and educational value; readability of all responses was also analyzed using the cntext package and py-readability-metrics.

Results: Between July 1 and August 17, 2024, sports medicine experts and patients evaluated 33 responses and 3 preoperative patient education documents generated by 3 language models regarding SCR surgery. For the 11 query responses, clinicians rated Gemini significantly higher than Claude in all categories (P<.05) and higher than GPT in completeness, risk avoidance, and overall rating (P<.05). For the 3 educational documents, Gemini's Patient Education Materials Assessment Tool score significantly exceeded Claude's (P=.03), and patients rated Gemini's materials superior in all aspects, with significant differences in educational quality versus Claude (P=.02) and overall satisfaction versus both Claude (P<.01) and GPT (P=.01). GPT had significantly higher readability than Claude on 3 R-based metrics (P<.01). Interrater agreement was high among clinicians and fair among patients.

Conclusions: Claude-3-Opus, GPT-4-Turbo, and Gemini-1.5-Pro effectively generated readable presurgical education materials but lacked citations and failed to discuss alternative treatments or the risks of forgoing SCR surgery, highlighting the need for expert oversight when using these LLMs in patient education.

背景:大型语言模型(llm)正在彻底改变自然语言处理,越来越多地应用于临床环境,以加强术前患者教育。目的:本研究旨在通过分析不同llm对上囊重建术(SCR)相关询问的反应,评价其在术前患者教育中的有效性和适用性。方法:共10名运动医学临床专家在网络研讨会上制定了11个SCR问题并制定了术前患者教育策略,并在Claude-3-Opus (Anthropic), GPT-4-Turbo (OpenAI)和Gemini-1.5-Pro(谷歌DeepMind)中输入了12个文本命令。共有3位专家对语言模型的正确性、完整性、逻辑性、潜在危害和总体满意度进行评估,术前教育文件使用DISCERN问卷和患者教育材料评估工具进行评估,并由5名术后患者对可读性和教育价值进行评价;还使用上下文包和py-可读性指标分析了所有回复的可读性。结果:在2024年7月1日至8月17日期间,运动医学专家和患者对3种语言模型生成的33份关于SCR手术的回复和3份术前患者教育文件进行了评估。在11个查询回复中,临床医生对Gemini的评分明显高于Claude的所有类别(pconclusion: Claude-3- opus, GPT-4-Turbo和Gemini-1.5- pro有效地生成了可读的手术前教育材料,但缺乏引用,未能讨论替代治疗或放弃SCR手术的风险,突出了在患者教育中使用这些法学硕士时需要专家监督。
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引用次数: 0
Use of Virtual Reality in the Pediatric Perioperative Setting and for Induction of Anesthesia: Mixed Methods Pilot Feasibility Study. 虚拟现实在儿科围手术期和麻醉诱导中的应用:混合方法试点可行性研究。
Pub Date : 2025-05-16 DOI: 10.2196/58905
Yu Tong Huang, Sofia Addab, Gianluca Bertolizio, Reggie Hamdy, Kelly Thorstad, Argerie Tsimicalis
<p><strong>Background: </strong>Children commonly experience high levels of anxiety prior to surgery. This distress is associated with postoperative maladaptive behaviors. Virtual reality (VR) is an innovative tool for reducing anxiety and pain during various medical procedures. Previous randomized controlled trials have demonstrated its efficacy in reducing children's anxiety in the preoperative waiting room or during induction.</p><p><strong>Objective: </strong>The primary aim of this study was to examine the feasibility of VR distraction throughout the perioperative period, from the waiting room until the induction of general anesthesia (GA). Secondary aims were to assess its clinical utility, tolerability, and initial clinical efficacy.</p><p><strong>Methods: </strong>A mixed methods, concurrent triangulation feasibility trial was piloted at the Shriners Hospitals for Children-Canada. Participants played an interactive VR game throughout the perioperative period, starting from the waiting room until induction. Feasibility was examined with the duration of the VR intervention, recording the number of interruptions, and taking field notes. Clinical utility was assessed using a perception questionnaire. Tolerability was evaluated by the Child Simulator Sickness Questionnaire (CSSQ). Initial clinical efficacy was assessed by the Faces Pain Scale-Revised, Faces Anxiety Scale, Graphic Rating Scale for multidimensional pain, the Induction Compliance Checklist, and the Pediatric Anesthesia Emergence Delirium scale. Quantitative data were supported with field notes and semistructured interviews with patients and parents. Quantitative and qualitative themes were compared via the triangulation protocol to produce final themes.</p><p><strong>Results: </strong>A total of 39 patients, with a mean age of 11.9 (SD 2.8) years, undergoing elective surgery under GA participated in the study. Stakeholders, including patients, parents, and health care providers, were receptive and willing to adapt to VR. Of the 39 patients, 19 (49%) continued to use VR during transportation and 6 (15%) were induced with VR. Barriers to feasibility included (1) interruptions to VR in 92% (36/39) of patients by health care professionals, (2) unpredictable surgery delays prolonging the duration of the VR intervention (mean 23.1, SD 24.4 minutes; range 5-150 minutes), and (3) discontinuation of VR before induction due to mask seal (n=3) and discomfort with supine positioning (n=2). Patients were generally satisfied with VR, deemed it acceptable and easy to use, and would recommend it to others. VR was tolerable with no self-reported simulator sickness (CSSQ: mean 0.01, SD 0.1). The mean Faces Anxiety Score was 1.5 (SD 1.1) at baseline and 0.7 (SD 0.9) during VR.</p><p><strong>Conclusions: </strong>While VR demonstrated good clinical utility and was well tolerated in the broad perioperative setting, this study highlighted important feasibility barriers in the waiting room and especial
背景:儿童在手术前通常会经历高度焦虑。这种痛苦与术后适应不良行为有关。虚拟现实(VR)是一种创新的工具,可以减少各种医疗过程中的焦虑和疼痛。以前的随机对照试验已经证明了它在术前等候室或诱导期间减少儿童焦虑的有效性。目的:本研究的主要目的是探讨从候诊室到全麻诱导(GA)整个围手术期VR牵张的可行性。次要目的是评估其临床效用、耐受性和初步临床疗效。方法:在加拿大Shriners儿童医院进行了一项混合方法,并发三角测量可行性试验。参与者在整个围手术期(从候诊室开始直到入职)都玩了一个交互式VR游戏。通过虚拟现实干预的持续时间,记录中断次数,并做现场笔记来检查可行性。临床效用评估使用感知问卷。通过儿童模拟疾病问卷(CSSQ)评估耐受性。初步临床疗效通过面部疼痛量表、面部焦虑量表、多维疼痛图形评定量表、诱导依从性检查表和小儿麻醉出现谵妄量表进行评估。定量数据由实地记录和对患者和家长的半结构化访谈支持。定量和定性主题通过三角测量协议进行比较,以产生最终主题。结果:共有39例GA下择期手术患者参与研究,平均年龄11.9 (SD 2.8)岁。包括患者、家长和医疗保健提供者在内的利益相关者都接受并愿意适应虚拟现实。39例患者中,19例(49%)在运输过程中继续使用VR, 6例(15%)被诱导使用VR。可行性的障碍包括:(1)92%(36/39)的患者被卫生保健专业人员中断VR,(2)不可预测的手术延迟延长VR干预的持续时间(平均23.1分钟,SD 24.4分钟;(3)因口罩密封(n=3)和仰卧位不适(n=2)而在诱导前停止VR。患者普遍对VR感到满意,认为其可接受且易于使用,并将其推荐给他人。VR是可以忍受的,没有自我报告的模拟器眩晕(CSSQ: mean 0.01, SD 0.1)。基线时的平均面部焦虑评分为1.5 (SD 1.1), VR期间为0.7 (SD 0.9)。结论:虽然VR显示出良好的临床实用性,并且在围手术期具有良好的耐受性,但本研究强调了在等候室,特别是在麻醉诱导过程中,在组织和技术层面上存在重要的可行性障碍。本研究强调了成功实施围手术期VR应仔细考虑的几个问题。
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引用次数: 0
Quantification of Metamorphopsia Using a Smartphone-Based Hyperacuity Test in Patients With Idiopathic Epiretinal Membranes: Prospective Observational Study. 在特发性视网膜上膜患者中使用基于智能手机的高敏度测试量化变形:前瞻性观察研究。
Pub Date : 2025-04-17 DOI: 10.2196/60959
Daria Amon, Christoph Leisser, Andreas Schlatter, Manuel Ruiss, Caroline Pilwachs, Natascha Bayer, Josef Huemer, Oliver Findl

Background: Quality of vision in patients with idiopathic epiretinal membranes (iERMs) is closely linked to distorted vision (metamorphopsia), which is often underestimated in clinical settings. Current surgical decision-making relies heavily on visual acuity and optical coherence tomography findings, which do not adequately reflect the patient's functional vision or the severity of metamorphopsia. There is a clinical need for tools that can reliably quantify this symptom to improve patient outcomes and streamline care pathways.

Objectives: This study is the first to assess the use of a novel smartphone-based hyperacuity test (SHT) in quantifying metamorphopsia before and after surgical intervention for iERMs, comparing it with a conventional printed chart.

Methods: This prospective observational study included 27 patients with iERMs with symptomatic metamorphopsia detected on the Amsler grid scheduled for vitrectomy with membrane peeling. The SHT (Alleye, Oculocare Medical Inc) and the horizontal (MH) and vertical (MV) M-chart (Inami & Co, Ltd) tests were performed 3 times before and 3 months after surgery. Pre- and postoperative metamorphopsia scores, changes in distance-corrected visual acuity, optical coherence tomography biomarkers, and subjective perception of metamorphopsia were evaluated.

Results: The mean SHT score significantly (r=0.686; P<.001) improved from 55.2 (SD 18.9) before surgery to 63.5 (SD 16.3) after surgery while the improvement of the M-chart scores were insignificant (MH r=0.37, P=.06; MV r=0.18, P=.36). Pre- and postoperative SHT scores showed very weak and insignificant correlations with the MH, MV, and MH+MV scores. Both metamorphopsia tests showed good reliability (intraclass correlation coefficients >0.75).

Conclusions: The SHT showed a significant improvement in postoperative metamorphopsia scores, indicating that it could be a valuable tool for quantifying visual distortion in patients with iERMs. While discrepancies with M-chart results were observed, both tests demonstrated good reliability. Clinically, the SHT may offer a practical solution for monitoring metamorphopsia and guiding complex surgical decision-making, particularly in telemedicine settings. Its accessibility could improve patient management, potentially enhancing preoperative triaging and reducing unnecessary visits.

背景:特发性视网膜前膜(iERMs)患者的视力质量与视力扭曲(变形)密切相关,在临床环境中经常被低估。目前的手术决策在很大程度上依赖于视力和光学相干断层扫描结果,这些结果不能充分反映患者的功能视力或变形视的严重程度。临床需要能够可靠地量化这种症状的工具,以改善患者的预后并简化护理途径。目的:本研究首次评估了一种新型的基于智能手机的超视力测试(SHT)在ierm手术干预前后量化变形的应用,并将其与传统的印刷图表进行了比较。方法:本前瞻性观察研究纳入27例在Amsler网格上检测到症状性变形的ierm患者,计划进行玻璃体切除术并剥离膜。术前和术后3个月分别进行3次SHT (Alleye, Oculocare Medical Inc .)和水平(MH)和垂直(MV) m图(Inami & Co . Ltd .)测试。评估术前和术后变形评分、距离矫正视力的变化、光学相干断层扫描生物标志物和对变形的主观感知。结果:SHT平均评分显著(r=0.686;P0.75)。结论:SHT在术后变形评分中有显著改善,表明它可以作为一种量化ierm患者视觉畸变的有价值的工具。虽然观察到与m图结果的差异,但两个测试都显示出良好的可靠性。在临床上,SHT可能为监测变形和指导复杂的手术决策提供实用的解决方案,特别是在远程医疗环境中。它的可及性可以改善患者管理,潜在地加强术前分诊和减少不必要的就诊。
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引用次数: 0
Quantification of Metamorphopsia using a Smartphone-based Hyperacuity Test in Patients with Idiopathic Epiretinal Membranes: Prospective Observational Study. 在特发性视网膜上膜患者中使用基于智能手机的超视力测试量化变形:前瞻性观察研究。
Pub Date : 2025-03-04 DOI: 10.2196/60959
Daria Amon, Chritstoph Leisser, Andreas Schlatter, Manuel Ruiss, Caroline Pilwachs, Natascha Bayer, Josef Huemer, Oliver Findl

Background: Quality of vision in patients with idiopathic epiretinal membranes (iERM) is closely linked to distorted vision (metamorphopsia), which is often underestimated in clinical settings. Current surgical decision-making relies heavily on visual acuity and OCT findings, which do not adequately reflect the patient's functional vision or the severity of metamorphopsia. There is a clinical need for tools that can reliably quantify this symptom to improve patient outcomes and streamline care pathways.

Objective: This study is the first to assess the utility of a novel smartphone-based hyperacuity test (SHT) in quantifying metamorphopsia before and after surgical intervention for iERM, comparing it to a conventional printed chart.

Methods: This prospective observational study included 27 iERM patients with symptomatic metamorphopsia detected on the Amsler grid scheduled for vitrectomy with membrane peeling. The SHT (Alleye, Oculocare medical Inc., Zurich, Switzerland) and the horizontal (MH) and vertical (MV) M-chart (Inami & Co., Ltd., Tokyo, Japan) tests were performed three times before and three months after surgery. Pre- and postoperative metamorphopsia scores, changes in distance-corrected visual acuity (DCVA), optical coherence tomography (OCT) biomarkers and subjective perception of metamorphopsia were evaluated.

Results: The mean SHT score significantly (r=.686, P<.001) improved from 55.2 ± 18.9 before surgery to 63.5 ± 16.3 after surgery while the improvement of the M-chart scores were insignificant (MH r=.37, P=.06; MV r=.18, P=.36). Pre- and postoperative SHT scores showed very weak and insignificant correlations with the MH, MV, and MH+MV scores. Both metamorphopsia tests showed good reliability (intraclass correlation coefficients >0.75).

Conclusions: The smartphone-based hyperacuity test (SHT) showed a significant improvement in postoperative metamorphopsia scores, indicating that it could be a valuable tool for quantifying visual distortion in iERM patients. While discrepancies with M-chart results were observed, both tests demonstrated good reliability. Clinically, the SHT may offer a practical solution for monitoring metamorphopsia and guiding complex surgical decision-making, particularly in telemedicine settings. Its accessibility could improve patient management, potentially enhancing pre-operative triaging and reducing unnecessary visits.

Clinicaltrial: ClinicalTrials.gov NCT05138315.

背景:特发性视网膜前膜(iERM)患者的视力质量与视力扭曲(变形)密切相关,在临床环境中经常被低估。目前的手术决策在很大程度上依赖于视力和OCT检查结果,这些结果不能充分反映患者的功能视力或变形视的严重程度。临床需要能够可靠地量化这种症状的工具,以改善患者的预后并简化护理途径。目的:本研究首次评估了一种新型基于智能手机的超视力测试(SHT)在iERM手术干预前后量化变形的实用性,并将其与传统的印刷图表进行了比较。方法:本前瞻性观察研究纳入27例在Amsler网格上检测到症状性变形的iERM患者,计划进行玻璃体切除术并剥离膜。SHT (Alleye, Oculocare medical Inc.,苏黎世,瑞士)和水平(MH)和垂直(MV) m图(Inami & Co., Ltd,东京,日本)在手术前和手术后三个月分别进行了三次测试。评估术前和术后变形评分、距离矫正视力(DCVA)、光学相干断层扫描(OCT)生物标志物的变化和变形的主观感知。结果:SHT平均评分显著(r=。686年,P0.75)。结论:基于智能手机的超视力测试(SHT)显示术后变形评分有显著改善,表明它可能是量化iERM患者视觉畸变的有价值的工具。虽然观察到与m图结果的差异,但两个测试都显示出良好的可靠性。在临床上,SHT可能为监测变形和指导复杂的手术决策提供实用的解决方案,特别是在远程医疗环境中。它的可及性可以改善患者管理,潜在地加强术前分诊和减少不必要的就诊。临床试验:ClinicalTrials.gov NCT05138315。
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引用次数: 0
Feasibility of a Comprehensive eCoach to Support Patients Undergoing Colorectal Surgery: Longitudinal Observational Study. 为结肠直肠手术患者提供综合电子辅导的可行性:纵向观察研究
Pub Date : 2025-02-25 DOI: 10.2196/67425
A Daniëlle Talen, Jobbe P L Leenen, Geert van der Sluis, Hilbrand K E Oldenhuis, Joost M Klaase, Gijsbert A Patijn

Background: The mainstay of colorectal cancer care is surgical resection, which carries a significant risk of complications. Efforts to improve outcomes have recently focused on intensive multimodal prehabilitation programs to better prepare patients for surgery, which make the perioperative process even more complex and demanding for patients. Digital applications (eCoaches) seem promising tools to guide patients during their care journey. We developed a comprehensive eCoach to support, guide, and monitor patients undergoing elective colorectal surgery through the perioperative phase of the care pathway.

Objective: The primary aim of this study was to determine its feasibility, in terms of recruitment rate, retention rate, and compliance. Also, usability and patient experience were examined.

Methods: A single-center cohort study was conducted from April to September 2023 in a tertiary teaching hospital in the Netherlands. All elective colorectal surgery patients were offered an eCoach that provided preoperative coaching of the prehabilitation protocol, guidance by giving timely information, and remote monitoring of postoperative recovery and complications. Recruitment and retention rate, as well as compliance for each part of the care pathway, were determined. Secondary, patient-reported usability measured by the Usefulness, Satisfaction, and Ease of Use questionnaire and patient experiences were reported.

Results: The recruitment rate for the eCoach was 74% (49/66). Main reasons for exclusion were digital illiteracy (n=10), not owning a smartphone (n=3), and the expected burden of use being too high (n=2). The retention rate was 80% (37/46). Median preoperative compliance with required actions in the app was 92% (IQR 87-95), and postoperative compliance was 100% (IQR 100-100). Patient-reported usability was good and patient experiences were mostly positive, although several suggestions for improvement were reported.

Conclusions: Our results demonstrate the feasibility of a comprehensive eCoach for guiding and monitoring patients undergoing colorectal surgery encompassing the entire perioperative pathway, including prehabilitation and postdischarge monitoring. Compliance was excellent for all phases of the care pathway and recruitment and retention rates were comparable with rates reported in the literature. The study findings provide valuable insights for the further development of the eCoach and highlight the potential of digital health applications in perioperative support.

背景:结直肠癌的主要治疗方法是手术切除,但手术切除有很大的并发症风险。最近,改善预后的努力集中在密集的多模式康复计划上,以更好地为患者做好手术准备,这使得围手术期过程更加复杂,对患者的要求也更高。数字应用程序(eCoaches)似乎很有希望在护理过程中指导患者。我们开发了一个全面的eCoach来支持、指导和监测接受择期结直肠手术的患者在围手术期的护理路径。目的:本研究的主要目的是在招募率、保留率和依从性方面确定其可行性。此外,还对可用性和患者体验进行了检查。方法:于2023年4月至9月在荷兰某三级教学医院进行单中心队列研究。所有择期结直肠手术患者均接受eCoach,提供术前康复方案指导,及时提供信息指导,并远程监测术后恢复和并发症。确定招募率和保留率,以及每个护理路径部分的依从性。其次,报告了患者报告的可用性,通过有用性,满意度和易用性问卷调查和患者体验来衡量。结果:eCoach的录取率为74%(49/66)。被排除在外的主要原因是数字文盲(n=10)、没有智能手机(n=3)和预期的使用负担太高(n=2)。保留率为80%(37/46)。术前对应用程序所需操作的中位依从性为92% (IQR 87-95),术后依从性为100% (IQR 100-100)。病人报告的可用性很好,病人的体验大多是积极的,尽管有一些改进的建议。结论:我们的研究结果表明,综合eCoach可用于指导和监测结直肠手术患者的整个围手术期路径,包括康复前和出院后监测。所有护理阶段的依从性都很好,招募率和保留率与文献报道的率相当。研究结果为eCoach的进一步发展提供了有价值的见解,并突出了数字健康应用在围手术期支持中的潜力。
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引用次数: 0
Implementation of Brief Submaximal Cardiopulmonary Testing in a High-Volume Presurgical Evaluation Clinic: Feasibility Cohort Study. 在大容量术前评估诊所实施简短的亚极限心肺测试:可行性研究。
Pub Date : 2025-02-17 DOI: 10.2196/65805
Zyad James Carr, Daniel Agarkov, Judy Li, Jean Charchaflieh, Andres Brenes-Bastos, Jonah Freund, Jill Zafar, Robert B Schonberger, Paul Heerdt
<p><strong>Background: </strong>Precise functional capacity assessment is a critical component for preoperative risk stratification. Brief submaximal cardiopulmonary exercise testing (smCPET) has shown diagnostic utility in various cardiopulmonary conditions.</p><p><strong>Objective: </strong>This study aims to determine if smCPET could be implemented in a high-volume presurgical evaluation clinic and, when compared to structured functional capacity surveys, if smCPET could better discriminate low functional capacity (≤4.6 metabolic equivalents [METs]).</p><p><strong>Methods: </strong>After institutional approval, 43 participants presenting for noncardiac surgery who met the following inclusion criteria were enrolled: aged 60 years and older, a Revised Cardiac Risk Index of ≤2, and self-reported METs of ≥4.6 (self-endorsed ability to climb 2 flights of stairs). Subjective METs assessments, Duke Activity Status Index (DASI) surveys, and a 6-minute smCPET trial were conducted. The primary end points were (1) operational efficiency, based on the time of the experimental session being ≤20 minutes; (2) modified Borg survey of perceived exertion, with a score of ≤7 indicating no more than moderate exertion; (3) high participant satisfaction with smCPET task execution, represented as a score of ≥8 (out of 10); and (4) high participant satisfaction with smCPET scheduling, represented as a score of ≥8 (out of 10). Student's t test was used to determine the significance of the secondary end points. Correlation between comparable structured surveys and smCPET measurements was assessed using the Pearson correlation coefficient. A Bland-Altman analysis was used to assess agreement between the methods.</p><p><strong>Results: </strong>The mean session time was 16.9 (SD 6.8) minutes. The mean posttest modified Borg survey score was 5.35 (SD 1.8). The median patient satisfaction (on a scale of 1=worst to 10=best) was 10 (IQR 10-10) for scheduling and 10 (IQR 9-10) for task execution. Subjective METs were higher when compared to smCPET equivalents (extrapolated peak METs; mean 7.6, SD 2.0 vs mean 6.7, SD 1.8; t<sub>42</sub>=2.1; P<.001). DASI-estimated peak METs were higher when compared to smCPET peak METs (mean 8.8, SD 1.2 vs mean 6.7, SD 1.8; t<sub>42</sub>=7.2; P<.001). DASI-estimated peak oxygen uptake was higher than smCPET peak oxygen uptake (mean 30.9, SD 4.3 mL kg<sup>-1</sup> min<sup>-1</sup> vs mean 23.6, SD 6.5 mL kg<sup>-1</sup> min<sup>-1</sup>; t<sub>42</sub>=7.2; P<.001).</p><p><strong>Conclusions: </strong>Implementation of smCPET in a presurgical evaluation clinic is both patient centered and clinically feasible. Brief smCPET measures, supportive of published reports regarding low sensitivity of provider-driven or structured survey measures for low functional capacity, were lower than those from structured surveys. Future studies will analyze the prediction of perioperative complications and cost-effectiveness.</p><p><strong>Trial registration: <
背景:精确的功能能力评估是术前风险分层的关键组成部分。短次最大心肺运动试验(smCPET)已显示出诊断各种心肺疾病的实用价值。目的:本研究的目的是确定smCPET是否可以在大容量的术前评估诊所中实施,并且与结构化功能能力调查相比,smCPET是否可以更好地区分低功能能力(8分)和高参与者对smCPET计划的满意度,得分为bbbb8分(10分)。方法:经机构批准,纳入43例符合以下纳入标准的非心脏手术患者:年龄0 ~ 60岁,修正心脏风险指数4.6(自我认可能爬2段楼梯)。主观METs, Duke活动状态指数(DASI)调查和6分钟smCPET试验进行。使用学生t检验来确定次要终点的显著性。使用Pearson相关系数评估可比较的结构化调查和smCPET测量之间的相关性。使用Bland-Altman分析来评估方法之间的一致性。结果:治疗时间16.9 min(±6.8)。测试后改良Borg测量为5.35(±1.8)。患者满意度中位数(IQR)[从1(最差)到10(最好)]在调度方面为10(10,10),在任务表现方面为10(9,10)。与smCPET等效(外推峰值METs)相比,主观METs更高[7.6(±2.0)vs. 6.7(±1.8),df 42, P
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引用次数: 0
Correction: A Patient-Oriented Implementation Strategy for a Perioperative mHealth Intervention: Feasibility Cohort Study. 更正:围手术期移动健康干预以患者为导向的实施策略:可行性队列研究。
Pub Date : 2025-02-12 DOI: 10.2196/71874
Daan Toben, Astrid de Wind, Eva van der Meij, Judith A F Huirne, Johannes R Anema

[This corrects the article DOI: 10.2196/58878.].

[这更正了文章DOI: 10.2196/58878]。
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引用次数: 0
Enhancing Quadruple Health Outcomes After Thoracic Surgery: Feasibility Pilot Randomized Controlled Trial Using Digital Home Monitoring. 提高胸外科手术后的四重健康结果:使用数字家庭监测的可行性试点随机对照试验。
Pub Date : 2025-02-12 DOI: 10.2196/58998
Mahesh Nagappa, Yamini Subramani, Homer Yang, Natasha Wood, Jill Querney, Lee-Anne Fochesato, Derek Nguyen, Nida Fatima, Janet Martin, Ava John-Baptiste, Rahul Nayak, Mehdi Qiabi, Richard Inculet, Dalilah Fortin, Richard Malthaner

Background: Surgical recovery after hospital discharge often presents challenges for patients and caregivers. Postoperative complications and poorly managed pain at home can lead to unexpected visits to the emergency department (ED) and readmission to the hospital. Digital home monitoring (DHM) may improve postoperative care compared to standard methods.

Objective: We conducted a feasibility study for a randomized controlled trial (RCT) to assess DHM's effectiveness following thoracic surgical procedures compared to standard care.

Methods: We conducted a 2-arm parallel-group pilot RCT at a single tertiary care center. Adult patients undergoing thoracic surgical procedures were randomized 1:1 into 2 groups: the DHM group and the standard of care (control group). We adhered to the intention-to-treat analysis principle. The primary outcome was predetermined RCT feasibility criteria. The trial would be feasible if more than 75% of trial recruitment, protocol adherence, and data collection were achieved. Secondary outcomes included 30-day ED visit rates, 30-day readmission rates, postoperative complications, length of stay, postdischarge 30-day opioid consumption, 30-day quality of recovery, patient-program satisfaction, caregiver satisfaction, health care provider satisfaction, and cost per case.

Results: All RCT feasibility criteria were met. The trial recruitment rate was 87.9% (95% CI 79.4%-93.8%). Protocol adherence and outcome data collection rates were 96.3% (95% CI 89.4%-99.2%) and 98.7% (95% CI 92.9%-99.9%), respectively. In total, 80 patients were randomized, with 40 (50%) in the DHM group and 40 (50%) in the control group. Baseline patient and clinical characteristics were comparable between the 2 groups. The DHM group had fewer unplanned ED visits (2.7% vs 20.5%; P=.02), fewer unplanned admission rates (0% vs 7.6%; P=.24), lower rates of postoperative complications (20% vs 47.5%, P=.01) shorter hospital stays (4.0 vs 6.9 days; P=.05), but more opioid consumption (111.6, SD 110.9) vs 74.3, SD 71.9 mg morphine equivalents; P=.08) compared to the control group. DHM also resulted in shorter ED visit times (130, SD 0 vs 1048, SD 1093 minutes; P=.48) and lower cost per case (CAD $12,145 [US $ 8436.34], SD CAD $8779 [US $ 6098.20] vs CAD $17,247 [US $11,980.37], SD CAD $15,313 [US $10,636.95]; P=.07). The quality of recovery scores was clinically significantly better than the controls (185.4, SD 2.6 vs 178.3, SD 3.3; P<.001). All 37 patients who completed the intervention answered the program satisfaction survey questionnaires (100%; 95% CI 90.5%-100%). Only 36 out of 80 caregivers responded to the caregiver satisfaction questionnaires at the end of the fourth week post hospital discharge (47.7%; 95% CI 35.7%-59.1%). Health care providers reported a 100% satisfaction rate.

Conclusions: This pilot RCT demonstrates the feasibility of cond

背景:出院后的手术康复对患者和护理人员来说都是一个挑战。术后并发症和家庭疼痛管理不善可能导致意外访问急诊室(ED)和再次入院。与标准方法相比,数字家庭监测(DHM)可以改善术后护理。目的:我们进行了一项随机对照试验(RCT)的可行性研究,以评估与标准治疗相比,胸外科手术后DHM的有效性。方法:我们在一个三级保健中心进行了一项两臂平行组先导随机对照试验。接受胸外科手术的成年患者按1:1随机分为两组:DHM组和标准护理组(对照组)。我们坚持意向治疗分析原则。主要结局是预先确定的RCT可行性标准。如果试验招募率、方案依从性和数据收集达到75%以上,则该试验是可行的。次要结局包括30天急诊科就诊率、30天再入院率、术后并发症、住院时间、出院后30天阿片类药物消耗量、30天康复质量、患者-项目满意度、护理人员满意度、卫生保健提供者满意度和每例费用。结果:符合所有RCT可行性标准。试验招募率为87.9% (95% CI 79.4%-93.8%)。方案依从性和结局数据收集率分别为96.3% (95% CI 89.4%-99.2%)和98.7% (95% CI 92.9%-99.9%)。共随机选取80例患者,DHM组40例(50%),对照组40例(50%)。两组患者的基线和临床特征具有可比性。DHM组计划外急诊科就诊较少(2.7% vs 20.5%;P=.02),非计划入院率较少(0% vs 7.6%;P= 0.24),术后并发症发生率较低(20% vs 47.5%, P= 0.01),住院时间较短(4.0 vs 6.9天;P= 0.05),但更多的阿片类药物消耗(111.6,SD 110.9) vs 74.3, SD 71.9 mg吗啡当量;P=.08)。DHM还缩短了ED就诊时间(130,SD 0 vs 1048, SD 1093分钟);P=.48)和更低的每例成本(12,145加元[8436.34美元],SD $8779加元[6098.20美元]vs 17,247加元[11,980.37美元],SD $15,313加元[10,636.95美元];P = . 07)。恢复评分质量显著优于对照组(185.4,SD 2.6 vs 178.3, SD 3.3;结论:该试点RCT证明了开展全面试验以评估DHM改善胸外科术后护理的有效性的可行性。DHM有望加强护理的连续性,值得进一步调查。试验注册:ClinicalTrials.gov NCT04340960;https://clinicaltrials.gov/study/NCT04340960。
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引用次数: 0
Agreement Between Provider-Completed and Patient-Completed Preoperative Frailty Screening Using the Clinical Risk Analysis Index: Cross-Sectional Questionnaire Study. 使用临床风险分析指数完成供方和患者完成术前虚弱筛查的一致性:横断面问卷研究。
Pub Date : 2025-02-10 DOI: 10.2196/66440
Mehraneh Khalighi, Amy C Thomas, Karl J Brown, Katherine C Ritchey

Background: Frailty is associated with postoperative morbidity and mortality. Preoperative screening and management of persons with frailty improves postoperative outcomes. The Clinical Risk Analysis Index (RAI-C) is a validated provider-based screening tool for assessing frailty in presurgical populations. Patient self-screening for frailty may provide an alternative to provider-based screening if resources are limited; however, the agreement between these 2 methods has not been previously explored.

Objective: The objective of our study was to examine provider-completed versus patient-completed RAI-C assessments to identify areas of disagreement between the 2 methods and inform best practices for RAI-C screening implementation.

Methods: Orthopedic physicians and physician assistants completed the RAI-C assessment on veterans aged 65 years and older undergoing elective total joint arthroplasty (eg, total hip or knee arthroplasty) and documented scores into the electronic health record during their preoperative clinic evaluation. Participants were then mailed the same RAI-C form after preoperative evaluation and returned responses to study coordinators. Agreement between provider-completed and patient-completed RAI-C assessments and differences within individual domains were compared.

Results: A total of 49 participants aged 65 years and older presenting for total joint arthroplasty underwent RAI-C assessment between November 2022 and August 2023. In total, 41% (20/49) of participants completed and returned an independent postvisit RAI-C assessment before surgery and within 180 days of their initial evaluation. There was a moderate but statistically significant correlation between provider-completed and patient-completed RAI-C assessments (r=0.62; 95% CI 0.25-0.83; P=.003). Provider-completed and patient-completed RAI-C assessments resulted in the same frailty classification in 60% (12/20) of participants, but 40% (8/20) of participants were reclassified to a more frail category based on patient-completed assessment. Agreement was the lowest between provider-completed and patient-completed screening questions regarding memory and activities of daily living.

Conclusions: RAI-C had moderate agreement when completed by providers versus the participants themselves, with more than a third of patient-completed screens resulting in a higher frailty classification. Future studies will need to explore the differences between and accuracy of RAI-C screening approaches to inform best practices for preoperative RAI-C assessment implementation.

背景:虚弱与术后发病率和死亡率相关。术前筛查和管理虚弱的人可以改善术后结果。临床风险分析指数(RAI-C)是一种有效的基于提供者的筛查工具,用于评估术前人群的脆弱性。在资源有限的情况下,患者自我虚弱筛查可以作为基于医生的筛查的替代方案;然而,这两种方法之间的一致性以前没有被探索过。目的:我们研究的目的是检查提供者完成和患者完成的rac评估,以确定两种方法之间的分歧,并为rac筛查实施提供最佳实践。方法:骨科医师和医师助理对65岁及以上接受选择性全关节置换术(如全髋关节或全膝关节置换术)的退伍军人进行RAI-C评估,并在术前临床评估时将评分记录到电子健康记录中。参与者在术前评估后邮寄相同的RAI-C表格,并将回复回复给研究协调员。比较了提供者完成的和患者完成的rac评估之间的一致性以及个别领域内的差异。结果:共有49名65岁及以上的参与者在2022年11月至2023年8月期间接受了全关节置换术的rac评估。总共有41%(20/49)的参与者在手术前和初次评估的180天内完成并返回独立的术后RAI-C评估。提供者完成的RAI-C评估与患者完成的RAI-C评估之间存在中度但有统计学意义的相关性(r=0.62;95% ci 0.25-0.83;P = .003)。提供者完成的和患者完成的RAI-C评估在60%(12/20)的参与者中导致相同的虚弱分类,但40%(8/20)的参与者根据患者完成的评估被重新分类为更虚弱的类别。在关于记忆和日常生活活动的筛查问题上,由提供者完成和患者完成的一致性最低。结论:由提供者完成的RAI-C与参与者自己完成的RAI-C有中等程度的一致性,超过三分之一的患者完成的筛查导致更高的虚弱分类。未来的研究将需要探索rac筛查方法之间的差异和准确性,以告知术前rac评估实施的最佳实践。
{"title":"Agreement Between Provider-Completed and Patient-Completed Preoperative Frailty Screening Using the Clinical Risk Analysis Index: Cross-Sectional Questionnaire Study.","authors":"Mehraneh Khalighi, Amy C Thomas, Karl J Brown, Katherine C Ritchey","doi":"10.2196/66440","DOIUrl":"10.2196/66440","url":null,"abstract":"<p><strong>Background: </strong>Frailty is associated with postoperative morbidity and mortality. Preoperative screening and management of persons with frailty improves postoperative outcomes. The Clinical Risk Analysis Index (RAI-C) is a validated provider-based screening tool for assessing frailty in presurgical populations. Patient self-screening for frailty may provide an alternative to provider-based screening if resources are limited; however, the agreement between these 2 methods has not been previously explored.</p><p><strong>Objective: </strong>The objective of our study was to examine provider-completed versus patient-completed RAI-C assessments to identify areas of disagreement between the 2 methods and inform best practices for RAI-C screening implementation.</p><p><strong>Methods: </strong>Orthopedic physicians and physician assistants completed the RAI-C assessment on veterans aged 65 years and older undergoing elective total joint arthroplasty (eg, total hip or knee arthroplasty) and documented scores into the electronic health record during their preoperative clinic evaluation. Participants were then mailed the same RAI-C form after preoperative evaluation and returned responses to study coordinators. Agreement between provider-completed and patient-completed RAI-C assessments and differences within individual domains were compared.</p><p><strong>Results: </strong>A total of 49 participants aged 65 years and older presenting for total joint arthroplasty underwent RAI-C assessment between November 2022 and August 2023. In total, 41% (20/49) of participants completed and returned an independent postvisit RAI-C assessment before surgery and within 180 days of their initial evaluation. There was a moderate but statistically significant correlation between provider-completed and patient-completed RAI-C assessments (r=0.62; 95% CI 0.25-0.83; P=.003). Provider-completed and patient-completed RAI-C assessments resulted in the same frailty classification in 60% (12/20) of participants, but 40% (8/20) of participants were reclassified to a more frail category based on patient-completed assessment. Agreement was the lowest between provider-completed and patient-completed screening questions regarding memory and activities of daily living.</p><p><strong>Conclusions: </strong>RAI-C had moderate agreement when completed by providers versus the participants themselves, with more than a third of patient-completed screens resulting in a higher frailty classification. Future studies will need to explore the differences between and accuracy of RAI-C screening approaches to inform best practices for preoperative RAI-C assessment implementation.</p>","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"8 ","pages":"e66440"},"PeriodicalIF":0.0,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11851030/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143384290","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}
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JMIR perioperative medicine
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