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Preoperative Anxiety and Information Needs Among Patients in the Preoperative Holding Area.
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-21 DOI: 10.1016/j.jopan.2024.10.001
Wuxing Li, Qifen He, Li Hu, Ning An, Huiping Wang, Qing Zeng

Purpose: This study aims to evaluate the current state of preoperative anxiety and the informational needs of patients undergoing surgery in a preoperative holding area.

Design: Descriptive and Pre post study.

Methods: A total of 655 elective surgery patients awaiting surgery were selected from November 2021 to March 2022. Multiple linear regression analyses were conducted to examine the factors associated with preoperative anxiety and informational needs in patients exhibiting shadow responses.

Findings: The patients' mean anxiety scores were 10.33 ± 3.25. Among them, 51 patients had mean anxiety scores greater than or equal to 12, indicating a state of anxiety. The mean informational needs scores were 7.81 ± 2.66. A total of 71 patients had mean informational needs scores greater than or equal to 5, reflecting a moderate or higher level of informational needs. Multiple linear regression analysis identified gender, age, surgical table, type of surgery, quality of sleep before surgery, surgical experience, and anesthesia experience as the primary factors influencing preoperative anxiety in patients awaiting surgery. Age, surgical experience, and anesthesia experience were identified as the main factors affecting informational needs in the preoperative holding area.

Conclusions: Patients undergoing surgery in the preoperative holding area exhibit heightened levels of anxiety and informational needs. Nurses must provide enhanced psychological support interventions for these patients, particularly focusing on those who are older, female, undergoing repeated operations, gynecological surgeries, experiencing poor sleep quality before surgery, or have had distressing surgical or anesthesia experiences.

{"title":"Preoperative Anxiety and Information Needs Among Patients in the Preoperative Holding Area.","authors":"Wuxing Li, Qifen He, Li Hu, Ning An, Huiping Wang, Qing Zeng","doi":"10.1016/j.jopan.2024.10.001","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.10.001","url":null,"abstract":"<p><strong>Purpose: </strong>This study aims to evaluate the current state of preoperative anxiety and the informational needs of patients undergoing surgery in a preoperative holding area.</p><p><strong>Design: </strong>Descriptive and Pre post study.</p><p><strong>Methods: </strong>A total of 655 elective surgery patients awaiting surgery were selected from November 2021 to March 2022. Multiple linear regression analyses were conducted to examine the factors associated with preoperative anxiety and informational needs in patients exhibiting shadow responses.</p><p><strong>Findings: </strong>The patients' mean anxiety scores were 10.33 ± 3.25. Among them, 51 patients had mean anxiety scores greater than or equal to 12, indicating a state of anxiety. The mean informational needs scores were 7.81 ± 2.66. A total of 71 patients had mean informational needs scores greater than or equal to 5, reflecting a moderate or higher level of informational needs. Multiple linear regression analysis identified gender, age, surgical table, type of surgery, quality of sleep before surgery, surgical experience, and anesthesia experience as the primary factors influencing preoperative anxiety in patients awaiting surgery. Age, surgical experience, and anesthesia experience were identified as the main factors affecting informational needs in the preoperative holding area.</p><p><strong>Conclusions: </strong>Patients undergoing surgery in the preoperative holding area exhibit heightened levels of anxiety and informational needs. Nurses must provide enhanced psychological support interventions for these patients, particularly focusing on those who are older, female, undergoing repeated operations, gynecological surgeries, experiencing poor sleep quality before surgery, or have had distressing surgical or anesthesia experiences.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-02-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143477226","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Implementation of an Evidence-based Protocol to Increase the Use of Goal-directed Hemodynamic Therapy.
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-20 DOI: 10.1016/j.jopan.2024.09.014
Cole Davis, Kelly Lindsay, Kelsey Jacks, Kendall Lowery, Jamie Nichols, Amy Yerdon

Purpose: This quality improvement project aimed to increase goal-directed hemodynamic therapy (GHDT) utilization in adult patients undergoing coronary artery bypass grafts (CABG) by implementing an evidence-based intraoperative GDHT protocol.

Design: A quality improvement project.

Methods: The team implemented a training bundle to raise awareness of complications associated with IOH, educate providers about GDHT benefits, and explain how to incorporate the protocol to guide intraoperative hemodynamic management. The team performed retrospective chart reviews to determine baseline and post-implementation GDHT protocol utilization and IOH incidence.

Findings: After receiving the education and protocol implementation, anesthesia providers began using the GDHT monitors on 100% of CABG procedures at this facility. A total of 60 patient charts were reviewed. Average cumulative hypotensive time decreased by 16.8%, from 26.37 minutes to 21.93 minutes (P = .375, 95% CI [-5.49, 13.35]).

Conclusions: Although there was no significant reduction in IOH, the training bundle and team support increased anesthesia providers' interest in using GDHT monitors. This led to a significant rise in its utilization. A future project is planned to expand the GDHT monitors and protocol to the entire operating room. Post-anesthesia care and intensive care units desiring to increase GDHT use may benefit from similar projects.

{"title":"Implementation of an Evidence-based Protocol to Increase the Use of Goal-directed Hemodynamic Therapy.","authors":"Cole Davis, Kelly Lindsay, Kelsey Jacks, Kendall Lowery, Jamie Nichols, Amy Yerdon","doi":"10.1016/j.jopan.2024.09.014","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.014","url":null,"abstract":"<p><strong>Purpose: </strong>This quality improvement project aimed to increase goal-directed hemodynamic therapy (GHDT) utilization in adult patients undergoing coronary artery bypass grafts (CABG) by implementing an evidence-based intraoperative GDHT protocol.</p><p><strong>Design: </strong>A quality improvement project.</p><p><strong>Methods: </strong>The team implemented a training bundle to raise awareness of complications associated with IOH, educate providers about GDHT benefits, and explain how to incorporate the protocol to guide intraoperative hemodynamic management. The team performed retrospective chart reviews to determine baseline and post-implementation GDHT protocol utilization and IOH incidence.</p><p><strong>Findings: </strong>After receiving the education and protocol implementation, anesthesia providers began using the GDHT monitors on 100% of CABG procedures at this facility. A total of 60 patient charts were reviewed. Average cumulative hypotensive time decreased by 16.8%, from 26.37 minutes to 21.93 minutes (P = .375, 95% CI [-5.49, 13.35]).</p><p><strong>Conclusions: </strong>Although there was no significant reduction in IOH, the training bundle and team support increased anesthesia providers' interest in using GDHT monitors. This led to a significant rise in its utilization. A future project is planned to expand the GDHT monitors and protocol to the entire operating room. Post-anesthesia care and intensive care units desiring to increase GDHT use may benefit from similar projects.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143477224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Implementation of Perioperative Anesthesia Considerations for Military Veterans Who Consume Cannabis: A Quality Improvement Project.
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-19 DOI: 10.1016/j.jopan.2024.10.006
Emily Sullivan, Cynthia L Foronda, Nicole A Gonzaga Gomez, Karina A Gattamorta, Denise C Vidot

Purpose: As no widely accepted recommendations or guidelines on perioperative management for the cannabis-consuming patient exist, this quality improvement project aimed to identify and implement evidence-based recommendations for cannabis-consuming patients throughout the perioperative period. The objectives of this project were (1) to improve anesthesia providers' knowledge on how to care for cannabis-consuming patients, (2) to increase anesthesia providers' self-efficacy in caring for cannabis-consuming patients, and (3) to assess the frequency of utilization of the given evidence-based recommendation.

Design: This quality improvement project incorporated a pretest-posttest design.

Methods: Nurse anesthetists, resident nurse anesthetists, and nurse practitioners (staff) in an urban veteran's hospital participated in the project. Following the Johns Hopkins Evidence-based Practice Model, a literature review was conducted via PubMed, Cochrane Library, and Cumulative Index to Nursing & Allied Health Literature to determine anesthetic considerations for cannabis consumers. Evidence was synthesized and translated into a live educational seminar that was evaluated via an electronic questionnaire before and after (pretest-postest) the seminar. Frequency of education utilization was measured via sticker poster system. Normality tests were conducted using Jamovi computer software. Wilcoxon signed-rank tests were pursued due to the skewed data distribution.

Findings: Results from 22 articles informed content for the live educational seminar; 26 staff participated in the pretest-posttest. Specific preoperative, intraoperative, and postoperative considerations were extracted from the evidence. Questionnaire results showed a 60% increase in self-efficacy (P = .001), a 44% increase in knowledge (P = .001), and a 92% utilization rate (26/28 cannabis-consuming patients) of the recommendations in the clinical setting.

Conclusions: With nearly 20% of veterans indicating use of cannabis, perianesthesia nurses should be aware of the unique preoperative, intraoperative, and postoperative considerations for the cannabis-consuming patient.

{"title":"Implementation of Perioperative Anesthesia Considerations for Military Veterans Who Consume Cannabis: A Quality Improvement Project.","authors":"Emily Sullivan, Cynthia L Foronda, Nicole A Gonzaga Gomez, Karina A Gattamorta, Denise C Vidot","doi":"10.1016/j.jopan.2024.10.006","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.10.006","url":null,"abstract":"<p><strong>Purpose: </strong>As no widely accepted recommendations or guidelines on perioperative management for the cannabis-consuming patient exist, this quality improvement project aimed to identify and implement evidence-based recommendations for cannabis-consuming patients throughout the perioperative period. The objectives of this project were (1) to improve anesthesia providers' knowledge on how to care for cannabis-consuming patients, (2) to increase anesthesia providers' self-efficacy in caring for cannabis-consuming patients, and (3) to assess the frequency of utilization of the given evidence-based recommendation.</p><p><strong>Design: </strong>This quality improvement project incorporated a pretest-posttest design.</p><p><strong>Methods: </strong>Nurse anesthetists, resident nurse anesthetists, and nurse practitioners (staff) in an urban veteran's hospital participated in the project. Following the Johns Hopkins Evidence-based Practice Model, a literature review was conducted via PubMed, Cochrane Library, and Cumulative Index to Nursing & Allied Health Literature to determine anesthetic considerations for cannabis consumers. Evidence was synthesized and translated into a live educational seminar that was evaluated via an electronic questionnaire before and after (pretest-postest) the seminar. Frequency of education utilization was measured via sticker poster system. Normality tests were conducted using Jamovi computer software. Wilcoxon signed-rank tests were pursued due to the skewed data distribution.</p><p><strong>Findings: </strong>Results from 22 articles informed content for the live educational seminar; 26 staff participated in the pretest-posttest. Specific preoperative, intraoperative, and postoperative considerations were extracted from the evidence. Questionnaire results showed a 60% increase in self-efficacy (P = .001), a 44% increase in knowledge (P = .001), and a 92% utilization rate (26/28 cannabis-consuming patients) of the recommendations in the clinical setting.</p><p><strong>Conclusions: </strong>With nearly 20% of veterans indicating use of cannabis, perianesthesia nurses should be aware of the unique preoperative, intraoperative, and postoperative considerations for the cannabis-consuming patient.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143477225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Postoperative Thirst in Surgical Patients: A Bibliometric Study.
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-12 DOI: 10.1016/j.jopan.2024.10.020
Hatice Özsoy, Askeri Çankaya, Esra Özkan, Meryem Yavuz van Giersbergen

Purpose: Thirst during surgical intervention is an important parameter that may affect the clinical course of patients. In this context, although there is a large body of knowledge in the existing literature on thirst during the surgical period, the lack of bibliometric analysis on this subject is striking. This study aims to systematically evaluate scientific publications on thirst during the surgical period, to fill the gaps in the literature, and to provide new perspectives that can guide clinical practice.

Design: Descriptive and bibliometric analyses were used.

Methods: The study universe consisted of 256 articles on postoperative thirst in the SCOPUS database. The study data were analyzed with Excel and they were visualized with VOSviewer and Bibliometrix Package in R software.

Findings: In the study, it was determined that the 256 articles identified were published in 181 different sources between 1969 and 2024, with a total of 1,194 authors contributing to these articles. In this research area, the top 3 publishing countries, China (111) has the highest productivity, followed by the United States (67) and Brazil (52). Most of the articles were published in "Journal of Perianesthesia Nursing," "British Journal of Anesthesia," and "Acta Anaesthesiologica Scandinavica."

Conclusions: The year and forecast analysis show that the number of studies on thirst, which is an important problem among surgical patients, has increased and will increase in the coming years. The increasing interest in thirst as an important problem among surgical patients shows that the interest and demand for research in this field are increasing.

{"title":"Postoperative Thirst in Surgical Patients: A Bibliometric Study.","authors":"Hatice Özsoy, Askeri Çankaya, Esra Özkan, Meryem Yavuz van Giersbergen","doi":"10.1016/j.jopan.2024.10.020","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.10.020","url":null,"abstract":"<p><strong>Purpose: </strong>Thirst during surgical intervention is an important parameter that may affect the clinical course of patients. In this context, although there is a large body of knowledge in the existing literature on thirst during the surgical period, the lack of bibliometric analysis on this subject is striking. This study aims to systematically evaluate scientific publications on thirst during the surgical period, to fill the gaps in the literature, and to provide new perspectives that can guide clinical practice.</p><p><strong>Design: </strong>Descriptive and bibliometric analyses were used.</p><p><strong>Methods: </strong>The study universe consisted of 256 articles on postoperative thirst in the SCOPUS database. The study data were analyzed with Excel and they were visualized with VOSviewer and Bibliometrix Package in R software.</p><p><strong>Findings: </strong>In the study, it was determined that the 256 articles identified were published in 181 different sources between 1969 and 2024, with a total of 1,194 authors contributing to these articles. In this research area, the top 3 publishing countries, China (111) has the highest productivity, followed by the United States (67) and Brazil (52). Most of the articles were published in \"Journal of Perianesthesia Nursing,\" \"British Journal of Anesthesia,\" and \"Acta Anaesthesiologica Scandinavica.\"</p><p><strong>Conclusions: </strong>The year and forecast analysis show that the number of studies on thirst, which is an important problem among surgical patients, has increased and will increase in the coming years. The increasing interest in thirst as an important problem among surgical patients shows that the interest and demand for research in this field are increasing.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143411344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of Magnetic Ball Pressing Combined With TEAS on Postoperative Nausea, Pain, Comfort, and Satisfaction in Patients Undergoing Gynecological Laparoscopic Surgery: A Randomized Controlled Trial.
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-12 DOI: 10.1016/j.jopan.2024.11.001
Mingming Wang, HongShuang Tong, Qingqing Liu, Lu Luo, Fanglong Ning, Fei Yu, Guocai Li

Purpose: The objective of this study was to evaluate the effects of magnetic ball press combined with transcutaneous electrical acupoint stimulation not only on the incidence of postoperative nausea and vomiting (PONV), but also on postoperative pain, comfort, and patient satisfaction in patients undergoing laparoscopic gynecological surgery.

Design: A randomized controlled trial comprising 120 patients undergoing elective gynecological surgery was conducted. These patients were randomly allocated into 3 groups, each consisting of 40 cases.

Methods: The magnetic-electricity-combined group received magnetic ball paste pressure combined with transcutaneous acupoint electrical stimulation, along with standard care. The acupoint pressure group received preoperative acupoint pressure, in addition to conventional care. The no-intervention group received only conventional care. The incidence of PONV, as well as postoperative pain, comfort, and satisfaction, were assessed within the initial 24 hours post surgery using the Visual Analog Scale (VAS) for PONV and pain, the Numerical Rating Scale for pain, the comfort scale, and a patient satisfaction scale.

Findings: The incidence of PONV within 24 hours post surgery was significantly lower in the magneto-electric combination group than in the acupressure and no-intervention groups (5% vs 57.5% vs 57.5%, P < .05). The postoperative pain score (VAS) was significantly lower in the magneto-electric combination group compared with the acupressure and no-intervention groups. The percentage of patients experiencing moderate pain was 12.5% in the magneto-electric group, 77.5% in the acupressure group, and 82.5% in the no-intervention group (P < .05). Furthermore, the magneto-electric combination group exhibited significantly higher comfort scores than the other 2 groups (105.15 ± 5.24 vs 94.65 ± 4.25 vs 91.40 ± 5.29, P < .05). Similarly, the magneto-electric combination group demonstrated significantly higher patient satisfaction scores than the other 2 groups (2.00 ± 0.00 vs 1.57 ± 0.50 vs 1.55 ± 0.50, P < .05).

Conclusions: The combination of magnetic ball compression with transcutaneous electrical stimulation of acupoints significantly reduces the incidence of PONV in patients undergoing gynecological laparoscopic surgery. Furthermore, it mitigates postoperative pain and improves patient comfort and satisfaction, thereby presenting a viable and efficacious approach for postoperative nursing interventions.

{"title":"Effect of Magnetic Ball Pressing Combined With TEAS on Postoperative Nausea, Pain, Comfort, and Satisfaction in Patients Undergoing Gynecological Laparoscopic Surgery: A Randomized Controlled Trial.","authors":"Mingming Wang, HongShuang Tong, Qingqing Liu, Lu Luo, Fanglong Ning, Fei Yu, Guocai Li","doi":"10.1016/j.jopan.2024.11.001","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.11.001","url":null,"abstract":"<p><strong>Purpose: </strong>The objective of this study was to evaluate the effects of magnetic ball press combined with transcutaneous electrical acupoint stimulation not only on the incidence of postoperative nausea and vomiting (PONV), but also on postoperative pain, comfort, and patient satisfaction in patients undergoing laparoscopic gynecological surgery.</p><p><strong>Design: </strong>A randomized controlled trial comprising 120 patients undergoing elective gynecological surgery was conducted. These patients were randomly allocated into 3 groups, each consisting of 40 cases.</p><p><strong>Methods: </strong>The magnetic-electricity-combined group received magnetic ball paste pressure combined with transcutaneous acupoint electrical stimulation, along with standard care. The acupoint pressure group received preoperative acupoint pressure, in addition to conventional care. The no-intervention group received only conventional care. The incidence of PONV, as well as postoperative pain, comfort, and satisfaction, were assessed within the initial 24 hours post surgery using the Visual Analog Scale (VAS) for PONV and pain, the Numerical Rating Scale for pain, the comfort scale, and a patient satisfaction scale.</p><p><strong>Findings: </strong>The incidence of PONV within 24 hours post surgery was significantly lower in the magneto-electric combination group than in the acupressure and no-intervention groups (5% vs 57.5% vs 57.5%, P < .05). The postoperative pain score (VAS) was significantly lower in the magneto-electric combination group compared with the acupressure and no-intervention groups. The percentage of patients experiencing moderate pain was 12.5% in the magneto-electric group, 77.5% in the acupressure group, and 82.5% in the no-intervention group (P < .05). Furthermore, the magneto-electric combination group exhibited significantly higher comfort scores than the other 2 groups (105.15 ± 5.24 vs 94.65 ± 4.25 vs 91.40 ± 5.29, P < .05). Similarly, the magneto-electric combination group demonstrated significantly higher patient satisfaction scores than the other 2 groups (2.00 ± 0.00 vs 1.57 ± 0.50 vs 1.55 ± 0.50, P < .05).</p><p><strong>Conclusions: </strong>The combination of magnetic ball compression with transcutaneous electrical stimulation of acupoints significantly reduces the incidence of PONV in patients undergoing gynecological laparoscopic surgery. Furthermore, it mitigates postoperative pain and improves patient comfort and satisfaction, thereby presenting a viable and efficacious approach for postoperative nursing interventions.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143411342","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Optimization of a Push Notification System to Improve First-case Delays: A Quality Improvement Project. 优化推送通知系统,改善首例延误:质量改进项目。
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-04 DOI: 10.1016/j.jopan.2024.11.012
Chelsea Secondino, Samantha Tortora, Kerry A Milner

Purpose: To increase first-case on-time start (FCOTS) rates at a large New England hospital by optimizing the use of a preoperative (pre-op) push notification system to reduce delays and improve operating room efficiency.

Design: The project employed a quality improvement approach guided by the Model for Improvement from the Institute for Healthcare Improvement.

Methods: A push notification system integrated into the electronic health record was used to enhance communication between surgeons and pre-op nurses across three surgical pavilions. Mandatory education sessions were provided for all enrolled staff, and Plan-Do-Study-Act cycles were conducted to refine processes and monitor outcomes. Data on notification usage and FCOTS rates were tracked from pre implementation (August 2023) through the implementation phase (December 2023).

Findings: Training resulted in 87% (n = 60) of nurses completing the push notification education, and 31% (n = 28) of surgeons confirmed reviewing training materials. Initial implementation increased push notification use among nurses from 26% to a peak of 51% in October 2023, though this later declined to 39% by year-end with net gain of 17%. Among surgeons, push notification usage peaked at 18%, with a net gain of 2% over the baseline. The East pavilion maintained relatively high FCOTS rates, decreasing slightly from 82% in October to 78% by year-end. In the North and South pavilions, increased push notification usage by nurses aligned with gradual FCOTS improvements: the North pavilion rose from 63% to 65%, while the South pavilion experienced fluctuations, ultimately achieving a 12% increase from baseline to reach 57% in December.

Conclusions: These findings suggest that while increased push notification use among nurses helped improve FCOTS in some pavilions, limited surgeon participation may have hindered the overall impact on reducing delays. Future strategies should focus on increasing engagement from all staff, improving workflow integration, and implementing ongoing performance tracking to optimize surgical efficiency across all pavilions. Enhancing FCOTS not only improves the patient experience by reducing wait times and increasing satisfaction, but also benefits staff by streamlining workflows and reducing stress. Ultimately, these improvements support organizational goals for greater efficiency and cost-effectiveness in perioperative care.

{"title":"Optimization of a Push Notification System to Improve First-case Delays: A Quality Improvement Project.","authors":"Chelsea Secondino, Samantha Tortora, Kerry A Milner","doi":"10.1016/j.jopan.2024.11.012","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.11.012","url":null,"abstract":"<p><strong>Purpose: </strong>To increase first-case on-time start (FCOTS) rates at a large New England hospital by optimizing the use of a preoperative (pre-op) push notification system to reduce delays and improve operating room efficiency.</p><p><strong>Design: </strong>The project employed a quality improvement approach guided by the Model for Improvement from the Institute for Healthcare Improvement.</p><p><strong>Methods: </strong>A push notification system integrated into the electronic health record was used to enhance communication between surgeons and pre-op nurses across three surgical pavilions. Mandatory education sessions were provided for all enrolled staff, and Plan-Do-Study-Act cycles were conducted to refine processes and monitor outcomes. Data on notification usage and FCOTS rates were tracked from pre implementation (August 2023) through the implementation phase (December 2023).</p><p><strong>Findings: </strong>Training resulted in 87% (n = 60) of nurses completing the push notification education, and 31% (n = 28) of surgeons confirmed reviewing training materials. Initial implementation increased push notification use among nurses from 26% to a peak of 51% in October 2023, though this later declined to 39% by year-end with net gain of 17%. Among surgeons, push notification usage peaked at 18%, with a net gain of 2% over the baseline. The East pavilion maintained relatively high FCOTS rates, decreasing slightly from 82% in October to 78% by year-end. In the North and South pavilions, increased push notification usage by nurses aligned with gradual FCOTS improvements: the North pavilion rose from 63% to 65%, while the South pavilion experienced fluctuations, ultimately achieving a 12% increase from baseline to reach 57% in December.</p><p><strong>Conclusions: </strong>These findings suggest that while increased push notification use among nurses helped improve FCOTS in some pavilions, limited surgeon participation may have hindered the overall impact on reducing delays. Future strategies should focus on increasing engagement from all staff, improving workflow integration, and implementing ongoing performance tracking to optimize surgical efficiency across all pavilions. Enhancing FCOTS not only improves the patient experience by reducing wait times and increasing satisfaction, but also benefits staff by streamlining workflows and reducing stress. Ultimately, these improvements support organizational goals for greater efficiency and cost-effectiveness in perioperative care.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2025-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143191052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of Sevoflurane and Propofol on Perioperative Respiratory Adverse Events in Pediatrics: A Systematic Review and Meta-analysis 七氟醚和丙泊酚对儿科围手术期呼吸系统不良事件的影响:系统回顾与元分析》。
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.jopan.2024.03.006
Caiping Li BD , Yongmei Zhu BD

Purpose

Perioperative respiratory adverse events continue to pose significant challenges in pediatric anesthesia. Research has hinted at a lower incidence of these complications in children anesthetized with propofol than sevoflurane. This study aimed to assess and compare respiratory complications in children undergoing general anesthesia with either sevoflurane or propofol during surgery.

Design

Systematic review and meta-analysis.

Methods

We conducted comprehensive searches of the PubMed, Embase, and Cochrane Library databases and manual searches to identify pertinent randomized controlled trials (RCTs) published up to August 19, 2023. The Cochrane risk assessment tool was employed to evaluate the risk of bias in the selected studies. The pooled analysis of relevant data compared respiratory complications, vomiting, agitation, anesthesia duration, extubation time, and recovery time in pediatric patients undergoing anesthesia with sevoflurane and propofol.

Findings

A total of 17 RCTs, containing 1,758 pediatric participants, were included and analyzed. Respiratory adverse events were examined, encompassing laryngospasm, apnea, cough, and SpO2. In comparison to sevoflurane, children subjected to propofol anesthesia demonstrated a significant reduction in the risk of laryngospasm (P = .001), vomiting (P < .001), and agitation (P = .029). Especially in patients receiving laryngeal mask airway, propofol anesthesia significantly reduced the incidence of laryngospasm (P = .003) and agitation (P < .001). At the same time, they exhibited an increased risk of apnea (P = .039). Notably, no statistically significant disparities were observed between sevoflurane and propofol concerning cough, SpO2 < 95%, anesthesia time, extubation time, and recovery time. Administration of propofol following sevoflurane anesthesia did not significantly impact the occurrence of vomiting or the recovery time.

Conclusions

While propofol presents an elevated risk of apnea, it concurrently yields a significant reduction in laryngospasm, vomiting, and agitation. Consequently, propofol emerges as a favorable anesthetic option for pediatric patients.
目的:围术期呼吸系统不良事件仍然是儿科麻醉的重大挑战。研究表明,与七氟醚相比,使用异丙酚麻醉的儿童发生这些并发症的几率更低。本研究旨在评估和比较在手术中使用七氟醚或异丙酚进行全身麻醉的儿童的呼吸系统并发症:系统综述和荟萃分析:我们对PubMed、Embase和Cochrane图书馆数据库进行了全面检索和人工检索,以确定截至2023年8月19日发表的相关随机对照试验(RCT)。采用 Cochrane 风险评估工具来评估所选研究的偏倚风险。对相关数据进行汇总分析,比较了接受七氟醚和丙泊酚麻醉的儿科患者的呼吸系统并发症、呕吐、躁动、麻醉持续时间、拔管时间和恢复时间:研究结果:共纳入并分析了 17 项 RCT,其中包括 1,758 名儿科参与者。对呼吸系统不良事件进行了研究,包括喉痉挛、呼吸暂停、咳嗽和SpO2。与七氟醚相比,使用异丙酚麻醉的儿童发生喉痉挛(P = .001)、呕吐(P 结论:异丙酚麻醉可显著降低呼吸道不良事件的风险:虽然异丙酚导致呼吸暂停的风险升高,但它同时显著减少了喉痉挛、呕吐和躁动。因此,异丙酚成为儿科患者的一种有利麻醉选择。
{"title":"Impact of Sevoflurane and Propofol on Perioperative Respiratory Adverse Events in Pediatrics: A Systematic Review and Meta-analysis","authors":"Caiping Li BD ,&nbsp;Yongmei Zhu BD","doi":"10.1016/j.jopan.2024.03.006","DOIUrl":"10.1016/j.jopan.2024.03.006","url":null,"abstract":"<div><h3>Purpose</h3><div>Perioperative respiratory adverse events continue to pose significant challenges in pediatric anesthesia. Research has hinted at a lower incidence of these complications in children anesthetized with propofol than sevoflurane. This study aimed to assess and compare respiratory complications in children undergoing general anesthesia with either sevoflurane or propofol during surgery.</div></div><div><h3>Design</h3><div>Systematic review and meta-analysis.</div></div><div><h3>Methods</h3><div>We conducted comprehensive searches of the PubMed, Embase, and Cochrane Library databases and manual searches to identify pertinent randomized controlled trials (RCTs) published up to August 19, 2023. The Cochrane risk assessment tool was employed to evaluate the risk of bias in the selected studies. The pooled analysis of relevant data compared respiratory complications, vomiting, agitation, anesthesia duration, extubation time, and recovery time in pediatric patients undergoing anesthesia with sevoflurane and propofol.</div></div><div><h3>Findings</h3><div>A total of 17 RCTs, containing 1,758 pediatric participants, were included and analyzed. Respiratory adverse events were examined, encompassing laryngospasm, apnea, cough, and SpO2. In comparison to sevoflurane, children subjected to propofol anesthesia demonstrated a significant reduction in the risk of laryngospasm (<em>P</em> = .001), vomiting (<em>P</em> &lt; .001), and agitation (<em>P</em> = .029). Especially in patients receiving laryngeal mask airway, propofol anesthesia significantly reduced the incidence of laryngospasm (<em>P</em> = .003) and agitation (<em>P</em> &lt; .001). At the same time, they exhibited an increased risk of apnea (<em>P</em> = .039). Notably, no statistically significant disparities were observed between sevoflurane and propofol concerning cough, SpO2 &lt; 95%, anesthesia time, extubation time, and recovery time. Administration of propofol following sevoflurane anesthesia did not significantly impact the occurrence of vomiting or the recovery time.</div></div><div><h3>Conclusions</h3><div>While propofol presents an elevated risk of apnea, it concurrently yields a significant reduction in laryngospasm, vomiting, and agitation. Consequently, propofol emerges as a favorable anesthetic option for pediatric patients.</div></div>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":"40 1","pages":"Pages 158-168"},"PeriodicalIF":1.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142299336","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mary Hanna Memorial Journalism Award
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-01 DOI: 10.1016/S1089-9472(25)00021-8
{"title":"Mary Hanna Memorial Journalism Award","authors":"","doi":"10.1016/S1089-9472(25)00021-8","DOIUrl":"10.1016/S1089-9472(25)00021-8","url":null,"abstract":"","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":"40 1","pages":"Page 4"},"PeriodicalIF":1.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143129640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of Short-term Deep Breathing Exercises on Perioperative Anxiety and Pain in Pediatric Orthopedic Patients: A Randomized Controlled Trial 短期深呼吸练习对小儿骨科患者围手术期焦虑和疼痛的影响:随机对照试验
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.jopan.2024.03.009
Lingling Hu BSN , Yanxiao Hua BSN, RN , Lingling Wang BSN , Ziwen Mao BMed , Xiaofei Jia BSN , Zhen Lei BSN , Danshao Chang BSN , Weyland Cheng PhD

Purpose

There are currently no pediatric studies examining the effects of deep breathing on perioperative pain and anxiety. This study sought to determine the effect of short-term deep breathing exercises on perioperative anxiety and pain in pediatric patients and their parents.

Design

A randomized controlled trial was conducted in the Department of Orthopaedic Surgery where pediatric patients about to undergo surgery were allocated to a control group or a deep breathing group. In the intervention group, patients and their main guardian were guided to practice 10 minutes of deep breathing exercises twice a day for 3 to 4 days prior to surgery. Perioperative anxiety and pain were measured for both the children and parents as outcome indicators.

Methods

Perioperative anxiety was measured using the modified Yale Preoperative Anxiety Scale-Short Form (mYPAS-SF) and state anxiety was measured using the State-Trait Anxiety Inventory (STAI). Patients reported their pain levels daily using the Wong-Baker FACES Pain Rating Scale. The following cutoffs were determined as high levels of anxiety: STAI (adult) > 44, STAI (child) > 36, and mYPAS-SF ≥ 30.

Findings

No significant differences were found in the STAI, mYPAS-SF, and Wong-Baker FACES Pain Rating Scale scores of the patients between the intervention and control group. Overall statistics showed that parents had significantly higher postoperative state anxiety levels toward female children (44.93 ± 9.01) compared to male children (40.18 ± 9.89). Preoperative and postoperative parental state anxiety levels were correlated with the child’s postoperative anxiety. Furthermore, children’s postoperative state anxiety was slightly correlated with postoperative pain.

Conclusions

Short-term use of our deep breathing exercises was ineffective in reducing incidences of perioperative pain and anxiety in pediatric orthopedic patients. A longer period of deep breathing administration may be required for the intervention to be effective. Parental anxiety may have an effect on anxiety levels in children, and postoperative parental anxiety may be affected by the gender of the child.
目的:目前还没有儿科研究探讨深呼吸对围术期疼痛和焦虑的影响。本研究旨在确定短期深呼吸练习对小儿患者及其家长围手术期焦虑和疼痛的影响:设计:在骨科手术部进行了一项随机对照试验,即将接受手术的小儿患者被分配到对照组或深呼吸组。在干预组中,指导患者及其主要监护人在手术前 3 到 4 天进行深呼吸练习,每天两次,每次 10 分钟。围术期焦虑和疼痛是衡量儿童和家长的结果指标:围手术期焦虑使用改良的耶鲁大学术前焦虑量表-简表(mYPAS-SF)进行测量,状态焦虑使用状态-特质焦虑量表(STAI)进行测量。患者每天使用 Wong-Baker FACES 疼痛评分量表报告其疼痛程度。以下分界点被确定为高度焦虑:STAI(成人)> 44,STAI(儿童)> 36,mYPAS-SF≥ 30:干预组和对照组患者的 STAI、mYPAS-SF 和 Wong-Baker FACES 疼痛评分量表得分无明显差异。总体统计结果显示,与男性患儿(40.18 ± 9.89)相比,女性患儿家长的术后状态焦虑水平(44.93 ± 9.01)明显更高。术前和术后家长的状态焦虑水平与儿童的术后焦虑水平相关。此外,儿童的术后状态焦虑与术后疼痛略有相关:结论:短期使用我们的深呼吸练习无法有效降低小儿骨科患者围手术期疼痛和焦虑的发生率。可能需要更长时间的深呼吸练习才能使干预有效。父母的焦虑可能会影响儿童的焦虑水平,术后父母的焦虑可能会受到儿童性别的影响。
{"title":"Effect of Short-term Deep Breathing Exercises on Perioperative Anxiety and Pain in Pediatric Orthopedic Patients: A Randomized Controlled Trial","authors":"Lingling Hu BSN ,&nbsp;Yanxiao Hua BSN, RN ,&nbsp;Lingling Wang BSN ,&nbsp;Ziwen Mao BMed ,&nbsp;Xiaofei Jia BSN ,&nbsp;Zhen Lei BSN ,&nbsp;Danshao Chang BSN ,&nbsp;Weyland Cheng PhD","doi":"10.1016/j.jopan.2024.03.009","DOIUrl":"10.1016/j.jopan.2024.03.009","url":null,"abstract":"<div><h3>Purpose</h3><div>There are currently no pediatric studies examining the effects of deep breathing on perioperative pain and anxiety. This study sought to determine the effect of short-term deep breathing exercises on perioperative anxiety and pain in pediatric patients and their parents.</div></div><div><h3>Design</h3><div>A randomized controlled trial was conducted in the Department of Orthopaedic Surgery where pediatric patients about to undergo surgery were allocated to a control group or a deep breathing group. In the intervention group, patients and their main guardian were guided to practice 10 minutes of deep breathing exercises twice a day for 3 to 4 days prior to surgery. Perioperative anxiety and pain were measured for both the children and parents as outcome indicators.</div></div><div><h3>Methods</h3><div>Perioperative anxiety was measured using the modified Yale Preoperative Anxiety Scale-Short Form (mYPAS-SF) and state anxiety was measured using the State-Trait Anxiety Inventory (STAI). Patients reported their pain levels daily using the Wong-Baker FACES Pain Rating Scale. The following cutoffs were determined as high levels of anxiety: STAI (adult) &gt; 44, STAI (child) &gt; 36, and mYPAS-SF ≥ 30.</div></div><div><h3>Findings</h3><div>No significant differences were found in the STAI, mYPAS-SF, and Wong-Baker FACES Pain Rating Scale scores of the patients between the intervention and control group. Overall statistics showed that parents had significantly higher postoperative state anxiety levels toward female children (44.93 ± 9.01) compared to male children (40.18 ± 9.89). Preoperative and postoperative parental state anxiety levels were correlated with the child’s postoperative anxiety. Furthermore, children’s postoperative state anxiety was slightly correlated with postoperative pain.</div></div><div><h3>Conclusions</h3><div>Short-term use of our deep breathing exercises was ineffective in reducing incidences of perioperative pain and anxiety in pediatric orthopedic patients. A longer period of deep breathing administration may be required for the intervention to be effective. Parental anxiety may have an effect on anxiety levels in children, and postoperative parental anxiety may be affected by the gender of the child.</div></div>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":"40 1","pages":"Pages 69-75"},"PeriodicalIF":1.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141560106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of Remifentanil Pretreatment on Sufentanil-induced Cough Suppression During the Induction of General Anesthesia 瑞芬太尼预处理对全身麻醉诱导过程中苏芬太尼诱发的咳嗽抑制的影响
IF 1.6 4区 医学 Q2 NURSING Pub Date : 2025-02-01 DOI: 10.1016/j.jopan.2024.03.015
Jinjin Zhang PhD , Daying Zhang MD , Yuhan Liu PhD , Wenjun Yu MD , Yue Lin MD , Fuzhou Hua PhD , Jun Ying MD

Purpose

The aim of this study was to evaluate the effect of remifentanil pretreatment on sufentanil-induced cough during general anesthesia induction.

Design

This experimental research was conducted as a single-center, randomized, parallel-group trial.

Methods

A total of 120 patients scheduled for elective surgery were equally randomized into two groups (remifentanil and control). The incidence and severity of coughing in both groups were recorded after sufentanil administration during general anesthesia induction. The mean arterial pressure, heart rate, and pulse oxygen saturation were recorded at T1 (before the injection of remifentanil or normal saline), T2 (1 minute after remifentanil administration), T3 (before intubation), and T4 (1 minute after intubation). Additionally, the incidences of adverse events, including dizziness, nausea, apnea, truncal rigidity, bradycardia, or other adverse effects were also recorded.

Findings

The incidence of sufentanil-induced cough in the remifentanil group was significantly decreased when compared with the control group (5.0% vs 35.0%, respectively; P < .001). No statistical differences were found in mean arterial pressure, heart rate, pulse oxygen saturation, and the incidences of other side effects between the two groups at T1, T2, T3, and T4 (P > .05).

Conclusions

Pretreatment with remifentanil at a dose of 0.5 mcg/kg can effectively and safely suppress the incidence and severity of sufentanil-induced coughing, providing a reference for medication during general anesthesia induction.
目的:本研究旨在评估瑞芬太尼预处理对全身麻醉诱导期间舒芬太尼引起的咳嗽的影响:设计:本实验研究为单中心、随机、平行组试验:方法:将 120 名择期手术患者平均随机分为两组(瑞芬太尼组和对照组)。在全身麻醉诱导过程中给予舒芬太尼后,记录两组患者咳嗽的发生率和严重程度。分别在 T1(注射瑞芬太尼或生理盐水前)、T2(注射瑞芬太尼后 1 分钟)、T3(插管前)和 T4(插管后 1 分钟)记录平均动脉压、心率和脉搏氧饱和度。此外,还记录了不良事件的发生率,包括头晕、恶心、呼吸暂停、躯干僵硬、心动过缓或其他不良反应:结果:与对照组相比,瑞芬太尼组舒芬太尼引起的咳嗽发生率明显降低(分别为 5.0% vs 35.0%;P 1、T2、T3 和 T4(P > .05)):结论:0.5 mcg/kg 剂量的瑞芬太尼预处理可有效、安全地抑制舒芬太尼诱发咳嗽的发生率和严重程度,为全身麻醉诱导期间的用药提供了参考。
{"title":"Effects of Remifentanil Pretreatment on Sufentanil-induced Cough Suppression During the Induction of General Anesthesia","authors":"Jinjin Zhang PhD ,&nbsp;Daying Zhang MD ,&nbsp;Yuhan Liu PhD ,&nbsp;Wenjun Yu MD ,&nbsp;Yue Lin MD ,&nbsp;Fuzhou Hua PhD ,&nbsp;Jun Ying MD","doi":"10.1016/j.jopan.2024.03.015","DOIUrl":"10.1016/j.jopan.2024.03.015","url":null,"abstract":"<div><h3>Purpose</h3><div>The aim of this study was to evaluate the effect of remifentanil pretreatment on sufentanil-induced cough during general anesthesia induction.</div></div><div><h3>Design</h3><div>This experimental research was conducted as a single-center, randomized, parallel-group trial.</div></div><div><h3>Methods</h3><div>A total of 120 patients scheduled for elective surgery were equally randomized into two groups (remifentanil and control). The incidence and severity of coughing in both groups were recorded after sufentanil administration during general anesthesia induction. The mean arterial pressure, heart rate, and pulse oxygen saturation were recorded at T<sub>1</sub> (before the injection of remifentanil or normal saline), T<sub>2</sub> (1 minute after remifentanil administration), T<sub>3</sub> (before intubation), and T<sub>4</sub> (1 minute after intubation). Additionally, the incidences of adverse events, including dizziness, nausea, apnea, truncal rigidity, bradycardia, or other adverse effects were also recorded.</div></div><div><h3>Findings</h3><div>The incidence of sufentanil-induced cough in the remifentanil group was significantly decreased when compared with the control group (5.0% vs 35.0%, respectively; <em>P</em> &lt; .001). No statistical differences were found in mean arterial pressure, heart rate, pulse oxygen saturation, and the incidences of other side effects between the two groups at T<sub>1</sub>, T<sub>2</sub>, T<sub>3</sub>, and T<sub>4</sub> (<em>P</em> &gt; .05).</div></div><div><h3>Conclusions</h3><div>Pretreatment with remifentanil at a dose of 0.5 mcg/kg can effectively and safely suppress the incidence and severity of sufentanil-induced coughing, providing a reference for medication during general anesthesia induction.</div></div>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":"40 1","pages":"Pages 90-94"},"PeriodicalIF":1.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Perianesthesia Nursing
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