首页 > 最新文献

JMIR perioperative medicine最新文献

英文 中文
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
{"title":"Implementation of Brief Submaximal Cardiopulmonary Testing in a High-Volume Presurgical Evaluation Clinic: Feasibility Cohort Study.","authors":"Zyad James Carr, Daniel Agarkov, Judy Li, Jean Charchaflieh, Andres Brenes-Bastos, Jonah Freund, Jill Zafar, Robert B Schonberger, Paul Heerdt","doi":"10.2196/65805","DOIUrl":"10.2196/65805","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;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]).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;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&lt;sub&gt;42&lt;/sub&gt;=2.1; P&lt;.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&lt;sub&gt;42&lt;/sub&gt;=7.2; P&lt;.001). DASI-estimated peak oxygen uptake was higher than smCPET peak oxygen uptake (mean 30.9, SD 4.3 mL kg&lt;sup&gt;-1&lt;/sup&gt; min&lt;sup&gt;-1&lt;/sup&gt; vs mean 23.6, SD 6.5 mL kg&lt;sup&gt;-1&lt;/sup&gt; min&lt;sup&gt;-1&lt;/sup&gt;; t&lt;sub&gt;42&lt;/sub&gt;=7.2; P&lt;.001).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Trial registration: &lt;","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":" ","pages":"e65805"},"PeriodicalIF":0.0,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142959816","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correction: A Patient-Oriented Implementation Strategy for a Perioperative mHealth Intervention: Feasibility Cohort Study.
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.].

{"title":"Correction: A Patient-Oriented Implementation Strategy for a Perioperative mHealth Intervention: Feasibility Cohort Study.","authors":"Daan Toben, Astrid de Wind, Eva van der Meij, Judith A F Huirne, Johannes R Anema","doi":"10.2196/71874","DOIUrl":"https://doi.org/10.2196/71874","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.2196/58878.].</p>","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"8 ","pages":"e71874"},"PeriodicalIF":0.0,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143412042","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhancing Quadruple Health Outcomes After Thoracic Surgery: Feasibility Pilot Randomized Controlled Trial Using Digital Home Monitoring.
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
<p><strong>Background: </strong>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.</p><p><strong>Objective: </strong>We conducted a feasibility study for a randomized controlled trial (RCT) to assess DHM's effectiveness following thoracic surgical procedures compared to standard care.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>This pilot RCT demonstrates the feasibility of cond
{"title":"Enhancing Quadruple Health Outcomes After Thoracic Surgery: Feasibility Pilot Randomized Controlled Trial Using Digital Home Monitoring.","authors":"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","doi":"10.2196/58998","DOIUrl":"https://doi.org/10.2196/58998","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;We conducted a feasibility study for a randomized controlled trial (RCT) to assess DHM's effectiveness following thoracic surgical procedures compared to standard care.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;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&lt;.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.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;This pilot RCT demonstrates the feasibility of cond","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"8 ","pages":"e58998"},"PeriodicalIF":0.0,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143412043","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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.
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.

{"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":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143384290","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Patient-Oriented Implementation Strategy for a Perioperative mHealth Intervention: Feasibility Cohort Study. 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 : 2025-01-14 DOI: 10.2196/58878
Daan Toben, Astrid de Wind, Eva van der Meij, Judith A F Huirne, Johannes R Anema

Background: Day surgery is being increasingly implemented across Europe, driven in part by capacity problems. Patients recovering at home could benefit from tools tailored to their new care setting to effectively manage their convalescence. The mHealth application ikHerstel is one such tool, but although it administers its functions in the home, its implementation hinges on health care professionals within the hospital.

Objective: We conducted a feasibility study of an additional patient-oriented implementation strategy for ikHerstel. This strategy aimed to empower patients to access and use ikHerstel independently, in contrast to implementation as usual, which hinges on the health care professional acting as gatekeeper. Our research question was "How well are patients able to use ikHerstel independently of their health care professional?"

Methods: We investigated the implementation strategy in terms of its recruitment, reach, dose delivered, dose received, and fidelity. Patients with a recent or prospective elective surgery were recruited using a wide array of materials to simulate patient-oriented dissemination of ikHerstel. Data were collected through web-based surveys. Descriptive analysis and open coding were used to analyze the data.

Results: Recruitment yielded 213 registrations, with 55 patients ultimately included in the study. The sample was characterized by patients undergoing abdominal surgery, with high literacy and above average digital health literacy, and included an overrepresentation of women (48/55, 87%). The implementation strategy had a reach of 81% (63/78), with 87% (55/67) of patients creating a recovery plan. Patients were satisfied with their independent use of ikHerstel, rating it an average 7.0 (SD 1.9) of 10, and 54% (29/54) of patients explicitly reported no difficulties in using it. A major concern of the implementation strategy was conflicts in recommendations between ikHerstel and the health care professionals, as well as the resulting feelings of insecurity experienced by patients.

Conclusions: In this small feasibility study, most patients were satisfied with the patient-oriented implementation strategy. However, the lack of involvement of health care professionals due to the strategy contributed to patient concerns regarding conflicting recommendations between ikHerstel and health care professionals.

背景:日间手术在欧洲越来越多地实施,部分原因是能力问题。在家康复的患者可以受益于为他们的新护理环境量身定制的工具,以有效地管理他们的康复。herstel的移动健康应用程序就是这样一个工具,但是,尽管它在家庭中管理其功能,但它的实施取决于医院内的医疗保健专业人员。目的:我们进行了一项额外的以患者为导向的ikHerstel实施策略的可行性研究。这一战略旨在使患者能够独立访问和使用ikHerstel,而不是像往常那样依靠卫生保健专业人员充当看门人。我们的研究问题是“患者独立于他们的医疗保健专业人员使用ikHerstel的能力如何?”方法:从招募、覆盖范围、给药剂量、给药剂量、保真度等方面对实施策略进行调查。近期或预期择期手术的患者被招募,使用广泛的材料来模拟以患者为导向的ikHerstel传播。数据是通过网络调查收集的。采用描述性分析和开放式编码对数据进行分析。结果:招募了213名注册患者,最终纳入了55名患者。该样本的特征是接受腹部手术的患者,具有较高的文化水平和高于平均水平的数字健康素养,并且女性的比例过高(48/55,87%)。实施策略的覆盖率为81%(63/78),87%(55/67)的患者制定了康复计划。患者对ikHerstel的独立使用感到满意,平均评分为7.0 (SD 1.9)(10分),54%(29/54)的患者明确报告使用它没有困难。实施战略的一个主要关切是,iherstel和保健专业人员之间的建议存在冲突,以及由此造成的患者的不安全感。结论:在这项小型可行性研究中,大多数患者对以患者为中心的实施策略感到满意。然而,由于该战略缺乏卫生保健专业人员的参与,导致患者担心iherstel和卫生保健专业人员之间的建议相互矛盾。
{"title":"A Patient-Oriented Implementation Strategy for a Perioperative mHealth Intervention: Feasibility Cohort Study.","authors":"Daan Toben, Astrid de Wind, Eva van der Meij, Judith A F Huirne, Johannes R Anema","doi":"10.2196/58878","DOIUrl":"10.2196/58878","url":null,"abstract":"<p><strong>Background: </strong>Day surgery is being increasingly implemented across Europe, driven in part by capacity problems. Patients recovering at home could benefit from tools tailored to their new care setting to effectively manage their convalescence. The mHealth application ikHerstel is one such tool, but although it administers its functions in the home, its implementation hinges on health care professionals within the hospital.</p><p><strong>Objective: </strong>We conducted a feasibility study of an additional patient-oriented implementation strategy for ikHerstel. This strategy aimed to empower patients to access and use ikHerstel independently, in contrast to implementation as usual, which hinges on the health care professional acting as gatekeeper. Our research question was \"How well are patients able to use ikHerstel independently of their health care professional?\"</p><p><strong>Methods: </strong>We investigated the implementation strategy in terms of its recruitment, reach, dose delivered, dose received, and fidelity. Patients with a recent or prospective elective surgery were recruited using a wide array of materials to simulate patient-oriented dissemination of ikHerstel. Data were collected through web-based surveys. Descriptive analysis and open coding were used to analyze the data.</p><p><strong>Results: </strong>Recruitment yielded 213 registrations, with 55 patients ultimately included in the study. The sample was characterized by patients undergoing abdominal surgery, with high literacy and above average digital health literacy, and included an overrepresentation of women (48/55, 87%). The implementation strategy had a reach of 81% (63/78), with 87% (55/67) of patients creating a recovery plan. Patients were satisfied with their independent use of ikHerstel, rating it an average 7.0 (SD 1.9) of 10, and 54% (29/54) of patients explicitly reported no difficulties in using it. A major concern of the implementation strategy was conflicts in recommendations between ikHerstel and the health care professionals, as well as the resulting feelings of insecurity experienced by patients.</p><p><strong>Conclusions: </strong>In this small feasibility study, most patients were satisfied with the patient-oriented implementation strategy. However, the lack of involvement of health care professionals due to the strategy contributed to patient concerns regarding conflicting recommendations between ikHerstel and health care professionals.</p>","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"8 ","pages":"e58878"},"PeriodicalIF":0.0,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11775485/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142985424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reducing Greenhouse Gas Emissions and Modifying Nitrous Oxide Delivery at Stanford: Observational, Pilot Intervention Study. 减少温室气体排放和修改一氧化二氮输送在斯坦福:观察,试点干预研究。
Pub Date : 2025-01-09 DOI: 10.2196/64921
Eric P Kraybill, David Chen, Saadat Khan, Praveen Kalra
<p><strong>Background: </strong>Inhalational anesthetic agents are a major source of potent greenhouse gases in the medical sector, and reducing their emissions is a readily addressable goal. Nitrous oxide (N<sub>2</sub>O) has a long environmental half-life relative to carbon dioxide combined with a low clinical potency, leading to relatively large amounts of N<sub>2</sub>O being stored in cryogenic tanks and H cylinders for use, increasing the chance of pollution through leaks. Building on previous findings, Stanford Health Care's (SHC's) N<sub>2</sub>O emissions were analyzed at 2 campuses and targeted for waste reduction as a precursor to system-wide reductions.</p><p><strong>Objective: </strong>We aimed to determine the extent of N<sub>2</sub>O pollution at SHC and subsequently whether using E-cylinders for N<sub>2</sub>O storage and delivery at the point of care in SHC's ambulatory surgery centers could reduce system-wide emissions.</p><p><strong>Methods: </strong>In phase 1, total SHC (Palo Alto, California) N<sub>2</sub>O purchase data for calendar year 2022 were collected and compared (volume and cost) to total Palo Alto clinical delivery data using Epic electronic health records. In phase 2, a pilot study was conducted in the 8 operating rooms of SHC campus A (Redwood City). The central N<sub>2</sub>O pipelines were disconnected, and E-cylinders were used in each operating room. E-cylinders were weighed before and after use on a weekly basis for comparison to Epic N<sub>2</sub>O delivery data over a 5-week period. In phase 3, after successful implementation, the same methodology was applied to campus B, one of 3 facilities in Palo Alto.</p><p><strong>Results: </strong>In phase 1, total N<sub>2</sub>O purchased in 2022 was 8,217,449 L (33,201.8 lbs) at a total cost of US $63,298. Of this, only 780,882.2 L (9.5%) of N<sub>2</sub>O was delivered to patients, with 7,436,566.8 L (90.5%) or US $57,285 worth lost or wasted. In phase 2, the total mass of N<sub>2</sub>O use from E-cylinders was 7.4 lbs (1 lb N<sub>2</sub>O=247.5 L) or 1831.5 L at campus A. Epic data showed that the total N<sub>2</sub>O volume delivered was 1839.3 L (7.4 lbs). In phase 3, the total mass of N<sub>2</sub>O use from E-cylinders was 10.4 lbs or 2574 L at campus B (confirming reliability within error propagation margins). Epic data showed that the total N<sub>2</sub>O volume delivered was 2840.3 L (11.5 lbs). Over phases 2 and 3, total use for campuses A and B was less than the volume of 3 E-cylinders (1 E-cylinder=1590 L).</p><p><strong>Conclusions: </strong>Converting N<sub>2</sub>O delivery from centralized storage to point-of-care E-cylinders dramatically reduced waste and expense with no detriment to patient care. Our results provide strong evidence for analyzing N<sub>2</sub>O storage in health care systems that rely on centralized storage, and consideration of E-cylinder implementation to reduce emissions. The reduction in N<sub>2</sub>O waste will help meet SHC
背景:吸入麻醉剂是医疗部门强效温室气体的主要来源,减少其排放是一个容易实现的目标。与二氧化碳相比,一氧化二氮(N2O)的环境半衰期较长,且临床效力较低,导致相对大量的一氧化二氮被储存在低温储罐和H钢瓶中使用,增加了通过泄漏造成污染的机会。在之前的研究结果的基础上,斯坦福医疗保健(SHC)的N2O排放在两个校区进行了分析,并以减少废物为目标,作为全系统减排的先驱。目的:我们旨在确定SHC的N2O污染程度,以及随后在SHC的门诊手术中心的护理点使用电子气瓶储存和输送N2O是否可以减少系统范围的排放。方法:在第一阶段,收集加州帕洛阿尔托市SHC (Palo Alto, California) 2022年N2O购买数据,并使用Epic电子健康记录将其与帕洛阿尔托市临床交付数据进行比较(数量和成本)。第二阶段,在红木城SHC a校区的8个手术室进行了试点研究。切断中央N2O管道,各手术室使用e -气瓶。电子气瓶在使用前后每周称重一次,与Epic N2O在5周内的输送数据进行比较。在第三阶段,成功实施后,同样的方法被应用到校园B,在帕洛阿尔托的三个设施之一。结果:在第一阶段,2022年购买的氧化亚氮总量为8,217,449升(33,201.8磅),总成本为63,298美元。其中,只有780882.2升(9.5%)的一氧化二氮被送到患者手中,7436566.8升(90.5%)或57285美元的一氧化二氮被丢失或浪费。在第二阶段,从e -气缸中释放的N2O总质量为7.4 lbs (1 lb N2O=247.5 L)或1831.5 L。Epic数据显示,总N2O释放量为1839.3 L (7.4 lbs)。在第三阶段,B校区的e -气缸使用的N2O总质量为10.4磅(2574升)(在误差传播范围内证实了可靠性)。Epic数据显示,N2O的总排放量为2840.3升(11.5磅)。在第二阶段和第三阶段,A校区和B校区的总使用量小于3个电子气瓶的体积(1个电子气瓶=1590 L)。结论:将N2O从集中存储转换为护理点电子气瓶显著减少了浪费和费用,且不会损害患者护理。我们的研究结果为分析依赖集中存储的卫生保健系统中的N2O存储以及考虑实施e缸以减少排放提供了强有力的证据。减少一氧化二氮废物将有助于实现SHC的目标,即在2030年之前将第1类和第2类排放量减少50%。
{"title":"Reducing Greenhouse Gas Emissions and Modifying Nitrous Oxide Delivery at Stanford: Observational, Pilot Intervention Study.","authors":"Eric P Kraybill, David Chen, Saadat Khan, Praveen Kalra","doi":"10.2196/64921","DOIUrl":"10.2196/64921","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Inhalational anesthetic agents are a major source of potent greenhouse gases in the medical sector, and reducing their emissions is a readily addressable goal. Nitrous oxide (N&lt;sub&gt;2&lt;/sub&gt;O) has a long environmental half-life relative to carbon dioxide combined with a low clinical potency, leading to relatively large amounts of N&lt;sub&gt;2&lt;/sub&gt;O being stored in cryogenic tanks and H cylinders for use, increasing the chance of pollution through leaks. Building on previous findings, Stanford Health Care's (SHC's) N&lt;sub&gt;2&lt;/sub&gt;O emissions were analyzed at 2 campuses and targeted for waste reduction as a precursor to system-wide reductions.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;We aimed to determine the extent of N&lt;sub&gt;2&lt;/sub&gt;O pollution at SHC and subsequently whether using E-cylinders for N&lt;sub&gt;2&lt;/sub&gt;O storage and delivery at the point of care in SHC's ambulatory surgery centers could reduce system-wide emissions.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;In phase 1, total SHC (Palo Alto, California) N&lt;sub&gt;2&lt;/sub&gt;O purchase data for calendar year 2022 were collected and compared (volume and cost) to total Palo Alto clinical delivery data using Epic electronic health records. In phase 2, a pilot study was conducted in the 8 operating rooms of SHC campus A (Redwood City). The central N&lt;sub&gt;2&lt;/sub&gt;O pipelines were disconnected, and E-cylinders were used in each operating room. E-cylinders were weighed before and after use on a weekly basis for comparison to Epic N&lt;sub&gt;2&lt;/sub&gt;O delivery data over a 5-week period. In phase 3, after successful implementation, the same methodology was applied to campus B, one of 3 facilities in Palo Alto.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;In phase 1, total N&lt;sub&gt;2&lt;/sub&gt;O purchased in 2022 was 8,217,449 L (33,201.8 lbs) at a total cost of US $63,298. Of this, only 780,882.2 L (9.5%) of N&lt;sub&gt;2&lt;/sub&gt;O was delivered to patients, with 7,436,566.8 L (90.5%) or US $57,285 worth lost or wasted. In phase 2, the total mass of N&lt;sub&gt;2&lt;/sub&gt;O use from E-cylinders was 7.4 lbs (1 lb N&lt;sub&gt;2&lt;/sub&gt;O=247.5 L) or 1831.5 L at campus A. Epic data showed that the total N&lt;sub&gt;2&lt;/sub&gt;O volume delivered was 1839.3 L (7.4 lbs). In phase 3, the total mass of N&lt;sub&gt;2&lt;/sub&gt;O use from E-cylinders was 10.4 lbs or 2574 L at campus B (confirming reliability within error propagation margins). Epic data showed that the total N&lt;sub&gt;2&lt;/sub&gt;O volume delivered was 2840.3 L (11.5 lbs). Over phases 2 and 3, total use for campuses A and B was less than the volume of 3 E-cylinders (1 E-cylinder=1590 L).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;Converting N&lt;sub&gt;2&lt;/sub&gt;O delivery from centralized storage to point-of-care E-cylinders dramatically reduced waste and expense with no detriment to patient care. Our results provide strong evidence for analyzing N&lt;sub&gt;2&lt;/sub&gt;O storage in health care systems that rely on centralized storage, and consideration of E-cylinder implementation to reduce emissions. The reduction in N&lt;sub&gt;2&lt;/sub&gt;O waste will help meet SHC","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"8 ","pages":"e64921"},"PeriodicalIF":0.0,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11757946/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142959826","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development and Validation of a Routine Electronic Health Record-Based Delirium Prediction Model for Surgical Patients Without Dementia: Retrospective Case-Control Study. 基于常规电子健康记录的无痴呆手术患者谵妄预测模型的开发和验证:回顾性病例对照研究。
Pub Date : 2025-01-09 DOI: 10.2196/59422
Emma Holler, Christina Ludema, Zina Ben Miled, Molly Rosenberg, Corey Kalbaugh, Malaz Boustani, Sanjay Mohanty

Background: Postoperative delirium (POD) is a common complication after major surgery and is associated with poor outcomes in older adults. Early identification of patients at high risk of POD can enable targeted prevention efforts. However, existing POD prediction models require inpatient data collected during the hospital stay, which delays predictions and limits scalability.

Objective: This study aimed to develop and externally validate a machine learning-based prediction model for POD using routine electronic health record (EHR) data.

Methods: We identified all surgical encounters from 2014 to 2021 for patients aged 50 years and older who underwent an operation requiring general anesthesia, with a length of stay of at least 1 day at 3 Indiana hospitals. Patients with preexisting dementia or mild cognitive impairment were excluded. POD was identified using Confusion Assessment Method records and delirium International Classification of Diseases (ICD) codes. Controls without delirium or nurse-documented confusion were matched to cases by age, sex, race, and year of admission. We trained logistic regression, random forest, extreme gradient boosting (XGB), and neural network models to predict POD using 143 features derived from routine EHR data available at the time of hospital admission. Separate models were developed for each hospital using surveillance periods of 3 months, 6 months, and 1 year before admission. Model performance was evaluated using the area under the receiver operating characteristic curve (AUROC). Each model was internally validated using holdout data and externally validated using data from the other 2 hospitals. Calibration was assessed using calibration curves.

Results: The study cohort included 7167 delirium cases and 7167 matched controls. XGB outperformed all other classifiers. AUROCs were highest for XGB models trained on 12 months of preadmission data. The best-performing XGB model achieved a mean AUROC of 0.79 (SD 0.01) on the holdout set, which decreased to 0.69-0.74 (SD 0.02) when externally validated on data from other hospitals.

Conclusions: Our routine EHR-based POD prediction models demonstrated good predictive ability using a limited set of preadmission and surgical variables, though their generalizability was limited. The proposed models could be used as a scalable, automated screening tool to identify patients at high risk of POD at the time of hospital admission.

背景:术后谵妄(POD)是老年人大手术后常见的并发症,与不良预后相关。早期识别出POD高危患者可以进行有针对性的预防工作。然而,现有的POD预测模型需要住院期间收集的住院患者数据,这延迟了预测并限制了可扩展性。目的:本研究旨在利用常规电子健康记录(EHR)数据开发并外部验证基于机器学习的POD预测模型。方法:我们收集了2014年至2021年期间在印第安纳州3家医院接受全麻手术且住院时间至少为1天的50岁及以上患者的所有手术经历。既往存在痴呆或轻度认知障碍的患者被排除在外。使用混淆评估法记录和谵妄国际疾病分类(ICD)代码对POD进行鉴定。没有谵妄或护士记录的精神错乱的对照组按年龄、性别、种族和入院年份与病例匹配。我们训练了逻辑回归、随机森林、极端梯度增强(XGB)和神经网络模型,利用入院时可获得的常规电子病历数据中的143个特征来预测POD。采用入院前3个月、6个月和1年的监测期,为每家医院开发了单独的模型。采用受试者工作特征曲线下面积(AUROC)评价模型性能。每个模型使用保留数据进行内部验证,使用其他2家医院的数据进行外部验证。使用校准曲线评估校准。结果:研究队列包括7167例谵妄病例和7167例匹配对照。XGB优于所有其他分类器。接受12个月入院前数据训练的XGB模型的auroc最高。表现最好的XGB模型在保留集上的平均AUROC为0.79 (SD 0.01),在其他医院的数据上进行外部验证时,平均AUROC降至0.69-0.74 (SD 0.02)。结论:我们的常规基于ehr的POD预测模型使用有限的入院前和手术变量显示出良好的预测能力,尽管其通用性有限。所提出的模型可作为一种可扩展的自动化筛选工具,用于在入院时识别POD高风险患者。
{"title":"Development and Validation of a Routine Electronic Health Record-Based Delirium Prediction Model for Surgical Patients Without Dementia: Retrospective Case-Control Study.","authors":"Emma Holler, Christina Ludema, Zina Ben Miled, Molly Rosenberg, Corey Kalbaugh, Malaz Boustani, Sanjay Mohanty","doi":"10.2196/59422","DOIUrl":"10.2196/59422","url":null,"abstract":"<p><strong>Background: </strong>Postoperative delirium (POD) is a common complication after major surgery and is associated with poor outcomes in older adults. Early identification of patients at high risk of POD can enable targeted prevention efforts. However, existing POD prediction models require inpatient data collected during the hospital stay, which delays predictions and limits scalability.</p><p><strong>Objective: </strong>This study aimed to develop and externally validate a machine learning-based prediction model for POD using routine electronic health record (EHR) data.</p><p><strong>Methods: </strong>We identified all surgical encounters from 2014 to 2021 for patients aged 50 years and older who underwent an operation requiring general anesthesia, with a length of stay of at least 1 day at 3 Indiana hospitals. Patients with preexisting dementia or mild cognitive impairment were excluded. POD was identified using Confusion Assessment Method records and delirium International Classification of Diseases (ICD) codes. Controls without delirium or nurse-documented confusion were matched to cases by age, sex, race, and year of admission. We trained logistic regression, random forest, extreme gradient boosting (XGB), and neural network models to predict POD using 143 features derived from routine EHR data available at the time of hospital admission. Separate models were developed for each hospital using surveillance periods of 3 months, 6 months, and 1 year before admission. Model performance was evaluated using the area under the receiver operating characteristic curve (AUROC). Each model was internally validated using holdout data and externally validated using data from the other 2 hospitals. Calibration was assessed using calibration curves.</p><p><strong>Results: </strong>The study cohort included 7167 delirium cases and 7167 matched controls. XGB outperformed all other classifiers. AUROCs were highest for XGB models trained on 12 months of preadmission data. The best-performing XGB model achieved a mean AUROC of 0.79 (SD 0.01) on the holdout set, which decreased to 0.69-0.74 (SD 0.02) when externally validated on data from other hospitals.</p><p><strong>Conclusions: </strong>Our routine EHR-based POD prediction models demonstrated good predictive ability using a limited set of preadmission and surgical variables, though their generalizability was limited. The proposed models could be used as a scalable, automated screening tool to identify patients at high risk of POD at the time of hospital admission.</p>","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"8 ","pages":"e59422"},"PeriodicalIF":0.0,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11757977/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142959821","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Parental Perspectives on Pediatric Surgical Recovery: Narrative Analysis of Free-Text Comments From a Postoperative Survey. 父母对儿童手术恢复的看法:术后调查中自由文本评论的叙事分析。
Pub Date : 2024-12-20 DOI: 10.2196/65198
Jessica Luo, Nicholas C West, Samantha Pang, Julie M Robillard, Patricia Page, Neil K Chadha, Heng Gan, Lynnie R Correll, Randa Ridgway, Natasha Broemling, Matthias Görges
<p><strong>Background: </strong>Qualitative experience data can inform health care providers how to best support families during pediatric postoperative recovery. Patient experience data can also provide actionable information to guide health care quality improvement; positive feedback can confirm the efficacy of current practices and systems, while negative comments can identify areas for improvement.</p><p><strong>Objective: </strong>This study aimed to understand families' perspectives regarding their children's surgical recovery using qualitative patient experience data (free-text comments) from a prospective cohort study conducted within a larger study developing a postoperative-outcome risk stratification model.</p><p><strong>Methods: </strong>Participants were parents or guardians of children aged 0-18 years who underwent surgery at a pediatric tertiary care facility; children undergoing either outpatient or inpatient procedures were eligible to be enrolled. Participants with English as a second language were offered translational services during the consent process and were included if any family member could translate the surveys into their preferred language. Participants were ineligible if they and their families could not understand English or the child had a neurodevelopmental disability. Perioperative data were collected from families using web-based surveys, including 1 preoperative survey and follow-up surveys sent on postoperative days 1, 2, 3, 7, 15, 30, and 90. Surveys were completed until the family indicated the child was fully recovered or until postoperative day 90 was reached. Follow-up surveys included opportunities to leave free-text comments on the child's surgical experience.</p><p><strong>Results: </strong>In total, 91% (453/500) of enrolled families completed at least 1 postoperative survey; 53% (242/453) provided at least 1 free-text comment and were included in the presented analysis, based on a total of 485 comments. The patient's age distribution was bimodal (modes at 2-3 and 14-15 years), with 66% (160/242) being male. Patients underwent orthopedic (60/242, 25%), urological (39/242, 16%), general (36/242,15%), otolaryngological (31/242, 13%), ophthalmological (32/242, 13%), dental (27/242, 11%), and plastic (17/242, 7%) surgeries. Largely positive comments (398/485, 82%) were made on the recovery and clinical care experience. A key theme for improvement included "communication," with subthemes highlighting parental concerns regarding the "preoperative discussions," "clarity of discharge instructions," and "continuity of care." Other themes included "length of stay" and "recovery experience." Feedback also suggested survey design amendments for future iterations of this instrument.</p><p><strong>Conclusions: </strong>Collecting parental recovery feedback is feasible and valued by families. Findings underscored the significance of enhancing communication strategies between health care providers and parents to alig
背景:定性经验数据可以告知卫生保健提供者如何在儿科术后恢复期间最好地支持家庭。患者体验数据还可以提供可操作的信息,以指导卫生保健质量的提高;积极的反馈可以确认当前实践和系统的有效性,而消极的评论可以确定需要改进的地方。目的:本研究旨在通过一项前瞻性队列研究中的定性患者体验数据(自由文本评论)来了解家庭对其儿童手术恢复的看法,该研究是在一项大型研究中进行的,该研究开发了一种术后结局风险分层模型。方法:参与者是在儿科三级医疗机构接受手术的0-18岁儿童的父母或监护人;接受门诊或住院治疗的儿童均符合入选条件。在同意过程中为英语为第二语言的参与者提供翻译服务,如果任何家庭成员可以将调查翻译成他们喜欢的语言,则包括在内。如果参与者和他们的家人不懂英语,或者孩子有神经发育障碍,那么他们就没有资格。围手术期数据通过基于网络的调查从家庭中收集,包括1次术前调查和术后1、2、3、7、15、30和90天的随访调查。直到家庭表明患儿完全康复或术后第90天完成调查。后续调查包括留下孩子手术经验的自由文本评论的机会。结果:91%(453/500)的入选家庭完成了至少1次术后调查;53%(242/453)提供了至少1条自由文本评论,并纳入了基于485条评论的分析。患者的年龄分布呈双峰分布(2-3岁和14-15岁),其中66%(160/242)为男性。患者接受骨科(60/242,25%)、泌尿外科(39/242,16%)、普通外科(36/242,15%)、耳鼻喉科(31/242,13%)、眼科(32/242,13%)、牙科(27/242,11%)和整形外科(17/242,7%)手术。大部分正面评价(398/485,82%)是关于康复和临床护理经验。改进的一个关键主题包括“沟通”,其子主题突出了家长对“术前讨论”、“出院指示的清晰度”和“护理的连续性”的关注。其他主题包括“住院时间”和“康复经验”。反馈还建议对该仪器的未来迭代进行调查设计修改。结论:收集父母康复反馈信息是可行的,受到家庭的重视。研究结果强调了加强卫生保健提供者和家长之间沟通策略的重要性,以协调期望并支持积极的以家庭为中心的护理。我们的术后调查允许家属提供可操作的建议,以改善他们的体验,这可能是他们在医院遇到时没有考虑到的。我们的纵向调查方案可以扩展,以支持持续的质量改进计划,包括近实时的患者反馈,以改善患者和家属的医疗保健体验。
{"title":"Parental Perspectives on Pediatric Surgical Recovery: Narrative Analysis of Free-Text Comments From a Postoperative Survey.","authors":"Jessica Luo, Nicholas C West, Samantha Pang, Julie M Robillard, Patricia Page, Neil K Chadha, Heng Gan, Lynnie R Correll, Randa Ridgway, Natasha Broemling, Matthias Görges","doi":"10.2196/65198","DOIUrl":"10.2196/65198","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Qualitative experience data can inform health care providers how to best support families during pediatric postoperative recovery. Patient experience data can also provide actionable information to guide health care quality improvement; positive feedback can confirm the efficacy of current practices and systems, while negative comments can identify areas for improvement.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aimed to understand families' perspectives regarding their children's surgical recovery using qualitative patient experience data (free-text comments) from a prospective cohort study conducted within a larger study developing a postoperative-outcome risk stratification model.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Participants were parents or guardians of children aged 0-18 years who underwent surgery at a pediatric tertiary care facility; children undergoing either outpatient or inpatient procedures were eligible to be enrolled. Participants with English as a second language were offered translational services during the consent process and were included if any family member could translate the surveys into their preferred language. Participants were ineligible if they and their families could not understand English or the child had a neurodevelopmental disability. Perioperative data were collected from families using web-based surveys, including 1 preoperative survey and follow-up surveys sent on postoperative days 1, 2, 3, 7, 15, 30, and 90. Surveys were completed until the family indicated the child was fully recovered or until postoperative day 90 was reached. Follow-up surveys included opportunities to leave free-text comments on the child's surgical experience.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;In total, 91% (453/500) of enrolled families completed at least 1 postoperative survey; 53% (242/453) provided at least 1 free-text comment and were included in the presented analysis, based on a total of 485 comments. The patient's age distribution was bimodal (modes at 2-3 and 14-15 years), with 66% (160/242) being male. Patients underwent orthopedic (60/242, 25%), urological (39/242, 16%), general (36/242,15%), otolaryngological (31/242, 13%), ophthalmological (32/242, 13%), dental (27/242, 11%), and plastic (17/242, 7%) surgeries. Largely positive comments (398/485, 82%) were made on the recovery and clinical care experience. A key theme for improvement included \"communication,\" with subthemes highlighting parental concerns regarding the \"preoperative discussions,\" \"clarity of discharge instructions,\" and \"continuity of care.\" Other themes included \"length of stay\" and \"recovery experience.\" Feedback also suggested survey design amendments for future iterations of this instrument.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;Collecting parental recovery feedback is feasible and valued by families. Findings underscored the significance of enhancing communication strategies between health care providers and parents to alig","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"7 ","pages":"e65198"},"PeriodicalIF":0.0,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11699487/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142869670","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Exploring the Knowledge, Attitudes, and Perceptions of Hospital Staff and Patients on Environmental Sustainability in the Operating Room: Quality Improvement Survey Study. 探索医院员工和患者对手术室环境可持续性的知识、态度和看法:质量改善调查研究。
Pub Date : 2024-11-28 DOI: 10.2196/59790
Nicole Kasia Stachura, Sukham K Brar, Jacob Davidson, Claire A Wilson, Celia Dann, Mike Apostol, John Vecchio, Shannon Bilodeau, Anna Gunz, Diana Catalina Casas-Lopez, Ruediger Noppens, Ken Leslie, Julie E Strychowsky

Background: In Canada, the health care system has been estimated to generate 33 million metric tons of greenhouse gas emissions annually. Health care systems, specifically operating rooms (ORs), are significant contributors to greenhouse gas emissions, using 3 to 6 times more energy than the hospital's average unit.

Objective: This quality improvement study aimed to investigate the knowledge, attitudes, and perceptions of staff members and patients on sustainability in the OR, as well as identify opportunities for initiatives and barriers to implementation.

Methods: A total of 2 surveys were developed, consisting of 27 questions for staff members and 22 questions for patients and caregivers. Topics included demographics, knowledge and attitudes regarding environmental sustainability, opportunities for initiatives, and perceived barriers. Multiple-choice, Likert-scale, and open-ended questions were used.

Results: A total of 174 staff members and 37 patients participated. The majority (152/174, 88%) of staff members had received no and minimal training on sustainability, while 93% (162/174) cited practicing sustainability at work as moderately to extremely important. Among patients and caregivers, 54% (20/37) often or always noticed when a hospital is being eco-friendly. Both staff members and patients agreed that improving sustainability would boost satisfaction (125/174, 71.8% and 22/37, 59.4%, respectively) and hospital reputation (22/37, 59.4% and 25/37, 69.5%, respectively). The staff members' highest-rated environmental initiatives included transitioning to reusables, education, and improved energy consumption, while patients prioritized increased nature, improved food sourcing, and education. Perceived barriers to these initiatives included cost, lack of education, and lack of incentives.

Conclusions: Staff members and patients and caregivers in a large academic health care center acknowledge the significance of environmental sustainability in the OR. While they do not perceive a direct impact on patient care, they anticipate positive effects on satisfaction and hospital reputation. Aligning initiatives with staff members and patient and caregiver preferences can help drive meaningful change within the OR and beyond.

背景:在加拿大,卫生保健系统估计每年产生3300万公吨的温室气体排放。卫生保健系统,特别是手术室(or),是温室气体排放的重要贡献者,使用的能源比医院的平均单位多3到6倍。目的:本质量改进研究旨在调查工作人员和患者对手术室可持续性的知识、态度和看法,并确定实施的机会和障碍。方法:共进行2项问卷调查,其中工作人员问卷27题,患者及护理人员问卷22题。主题包括人口统计、关于环境可持续性的知识和态度、倡议的机会以及感知到的障碍。采用多项选择题、李克特量表和开放式问题。结果:共174名工作人员参与,37名患者参与。大多数(152/ 174,88%)员工没有接受或只接受过最少的可持续发展培训,而93%(162/174)的员工认为在工作中实践可持续发展是中等至极其重要的。在患者和护理人员中,54%(20/37)经常或总是注意到医院何时是环保的。工作人员和患者都认为,改善可持续性可以提高满意度(125/174,71.8%和22/37,59.4%)和医院声誉(22/37,59.4%和25/37,69.5%)。工作人员评价最高的环保举措包括向可重复使用物品过渡、教育和改善能源消耗,而患者优先考虑的是增加自然环境、改善食物来源和教育。这些举措的障碍包括成本、缺乏教育和缺乏激励。结论:一家大型学术医疗中心的工作人员、患者和护理人员认识到手术室环境可持续性的重要性。虽然他们没有察觉到对病人护理的直接影响,但他们预计会对满意度和医院声誉产生积极影响。将计划与工作人员、患者和护理人员的偏好结合起来,可以帮助推动手术室内外有意义的变革。
{"title":"Exploring the Knowledge, Attitudes, and Perceptions of Hospital Staff and Patients on Environmental Sustainability in the Operating Room: Quality Improvement Survey Study.","authors":"Nicole Kasia Stachura, Sukham K Brar, Jacob Davidson, Claire A Wilson, Celia Dann, Mike Apostol, John Vecchio, Shannon Bilodeau, Anna Gunz, Diana Catalina Casas-Lopez, Ruediger Noppens, Ken Leslie, Julie E Strychowsky","doi":"10.2196/59790","DOIUrl":"10.2196/59790","url":null,"abstract":"<p><strong>Background: </strong>In Canada, the health care system has been estimated to generate 33 million metric tons of greenhouse gas emissions annually. Health care systems, specifically operating rooms (ORs), are significant contributors to greenhouse gas emissions, using 3 to 6 times more energy than the hospital's average unit.</p><p><strong>Objective: </strong>This quality improvement study aimed to investigate the knowledge, attitudes, and perceptions of staff members and patients on sustainability in the OR, as well as identify opportunities for initiatives and barriers to implementation.</p><p><strong>Methods: </strong>A total of 2 surveys were developed, consisting of 27 questions for staff members and 22 questions for patients and caregivers. Topics included demographics, knowledge and attitudes regarding environmental sustainability, opportunities for initiatives, and perceived barriers. Multiple-choice, Likert-scale, and open-ended questions were used.</p><p><strong>Results: </strong>A total of 174 staff members and 37 patients participated. The majority (152/174, 88%) of staff members had received no and minimal training on sustainability, while 93% (162/174) cited practicing sustainability at work as moderately to extremely important. Among patients and caregivers, 54% (20/37) often or always noticed when a hospital is being eco-friendly. Both staff members and patients agreed that improving sustainability would boost satisfaction (125/174, 71.8% and 22/37, 59.4%, respectively) and hospital reputation (22/37, 59.4% and 25/37, 69.5%, respectively). The staff members' highest-rated environmental initiatives included transitioning to reusables, education, and improved energy consumption, while patients prioritized increased nature, improved food sourcing, and education. Perceived barriers to these initiatives included cost, lack of education, and lack of incentives.</p><p><strong>Conclusions: </strong>Staff members and patients and caregivers in a large academic health care center acknowledge the significance of environmental sustainability in the OR. While they do not perceive a direct impact on patient care, they anticipate positive effects on satisfaction and hospital reputation. Aligning initiatives with staff members and patient and caregiver preferences can help drive meaningful change within the OR and beyond.</p>","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"7 ","pages":"e59790"},"PeriodicalIF":0.0,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11638685/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142752510","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of Consumer Wearables Data on Pediatric Surgery Clinicians' Management: Multi-Institutional Scenario-Based Usability Study. 消费类可穿戴设备数据对小儿外科临床医生管理的影响:基于场景的多机构可用性研究。
Pub Date : 2024-11-12 DOI: 10.2196/58663
Michela Carter, Samuel C Linton, Suhail Zeineddin, J Benjamin Pitt, Christopher De Boer, Angie Figueroa, Ankush Gosain, David Lanning, Aaron Lesher, Saleem Islam, Chethan Sathya, Jane L Holl, Hassan Mk Ghomrawi, Fizan Abdullah

Background: At present, parents lack objective methods to evaluate their child's postoperative recovery following discharge from the hospital. As a result, clinicians are dependent upon a parent's subjective assessment of the child's health status and the child's ability to communicate their symptoms. This subjective nature of home monitoring contributes to unnecessary emergency department (ED) use as well as delays in treatment. However, the integration of data remotely collected using a consumer wearable device has the potential to provide clinicians with objective metrics for postoperative patients to facilitate informed longitudinal, remote assessment.

Objective: This multi-institutional study aimed to evaluate the impact of adding actual and simulated objective recovery data that were collected remotely using a consumer wearable device to simulated postoperative telephone encounters on clinicians' management.

Methods: In total, 3 simulated telephone scenarios of patients after an appendectomy were presented to clinicians at 5 children's hospitals. Each scenario was then supplemented with wearable data concerning or reassuring against a postoperative complication. Clinicians rated their likelihood of ED referral before and after the addition of wearable data to evaluate if it changed their recommendation. Clinicians reported confidence in their decision-making.

Results: In total, 34 clinicians participated. Compared with the scenario alone, the addition of reassuring wearable data resulted in a decreased likelihood of ED referral for all 3 scenarios (P<.01). When presented with concerning wearable data, there was an increased likelihood of ED referral for 1 of 3 scenarios (P=.72, P=.17, and P<.001). At the institutional level, there was no difference between the 5 institutions in how the wearable data changed the likelihood of ED referral for all 3 scenarios. With the addition of wearable data, 76% (19/25) to 88% (21/24 and 22/25) of clinicians reported increased confidence in their recommendations.

Conclusions: The addition of wearable data to simulated telephone scenarios for postdischarge patients who underwent pediatric surgery impacted clinicians' remote patient management at 5 pediatric institutions and increased clinician confidence. Wearable devices are capable of providing real-time measures of recovery, which can be used as a postoperative monitoring tool to reduce delays in care and avoidable health care use.

背景:目前,家长缺乏客观的方法来评估孩子出院后的术后恢复情况。因此,临床医生只能依赖家长对患儿健康状况的主观评估以及患儿表达症状的能力。家庭监测的这种主观性造成了不必要的急诊室(ED)使用和治疗延误。然而,整合使用消费类可穿戴设备远程收集的数据有可能为临床医生提供术后患者的客观指标,以促进知情的纵向远程评估:这项多机构研究旨在评估在模拟术后电话会诊中加入使用消费可穿戴设备远程收集的实际和模拟客观恢复数据对临床医生管理的影响:方法:总共向 5 家儿童医院的临床医生演示了 3 个阑尾切除术后患者的模拟电话情景。然后在每个场景中加入有关术后并发症的可穿戴数据,或对术后并发症进行安慰。在添加可穿戴数据前后,临床医生对转诊到急诊室的可能性进行评分,以评估是否改变了他们的建议。临床医生报告了对其决策的信心:共有 34 名临床医生参与。与单独的场景相比,在所有 3 个场景中,增加了令人放心的可穿戴数据后,急诊室转诊的可能性都降低了(PC 结论:在模拟场景中增加可穿戴数据后,急诊室转诊的可能性降低了:在儿科手术患者出院后的模拟电话情景中加入可穿戴数据,对5家儿科机构临床医生的远程患者管理产生了影响,并增强了临床医生的信心。可穿戴设备能够提供实时恢复情况,可用作术后监测工具,减少护理延误和可避免的医疗使用。
{"title":"Impact of Consumer Wearables Data on Pediatric Surgery Clinicians' Management: Multi-Institutional Scenario-Based Usability Study.","authors":"Michela Carter, Samuel C Linton, Suhail Zeineddin, J Benjamin Pitt, Christopher De Boer, Angie Figueroa, Ankush Gosain, David Lanning, Aaron Lesher, Saleem Islam, Chethan Sathya, Jane L Holl, Hassan Mk Ghomrawi, Fizan Abdullah","doi":"10.2196/58663","DOIUrl":"10.2196/58663","url":null,"abstract":"<p><strong>Background: </strong>At present, parents lack objective methods to evaluate their child's postoperative recovery following discharge from the hospital. As a result, clinicians are dependent upon a parent's subjective assessment of the child's health status and the child's ability to communicate their symptoms. This subjective nature of home monitoring contributes to unnecessary emergency department (ED) use as well as delays in treatment. However, the integration of data remotely collected using a consumer wearable device has the potential to provide clinicians with objective metrics for postoperative patients to facilitate informed longitudinal, remote assessment.</p><p><strong>Objective: </strong>This multi-institutional study aimed to evaluate the impact of adding actual and simulated objective recovery data that were collected remotely using a consumer wearable device to simulated postoperative telephone encounters on clinicians' management.</p><p><strong>Methods: </strong>In total, 3 simulated telephone scenarios of patients after an appendectomy were presented to clinicians at 5 children's hospitals. Each scenario was then supplemented with wearable data concerning or reassuring against a postoperative complication. Clinicians rated their likelihood of ED referral before and after the addition of wearable data to evaluate if it changed their recommendation. Clinicians reported confidence in their decision-making.</p><p><strong>Results: </strong>In total, 34 clinicians participated. Compared with the scenario alone, the addition of reassuring wearable data resulted in a decreased likelihood of ED referral for all 3 scenarios (P<.01). When presented with concerning wearable data, there was an increased likelihood of ED referral for 1 of 3 scenarios (P=.72, P=.17, and P<.001). At the institutional level, there was no difference between the 5 institutions in how the wearable data changed the likelihood of ED referral for all 3 scenarios. With the addition of wearable data, 76% (19/25) to 88% (21/24 and 22/25) of clinicians reported increased confidence in their recommendations.</p><p><strong>Conclusions: </strong>The addition of wearable data to simulated telephone scenarios for postdischarge patients who underwent pediatric surgery impacted clinicians' remote patient management at 5 pediatric institutions and increased clinician confidence. Wearable devices are capable of providing real-time measures of recovery, which can be used as a postoperative monitoring tool to reduce delays in care and avoidable health care use.</p>","PeriodicalId":73557,"journal":{"name":"JMIR perioperative medicine","volume":"7 ","pages":"e58663"},"PeriodicalIF":0.0,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11599887/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142634016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
JMIR perioperative medicine
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1