Pub Date : 2024-04-06DOI: 10.1016/j.pcorm.2024.100388
Marzoq Ali Odhah , Abdulnasser Ahmed Haza'a , Saddam Ahmed Al-Ahdal , Muhammad Sadeq Al-Awar , Abdulfatah Saleh Al-Jaradi , Bandar Al-haguri , Mohammed M Al-Jabri , Taha Mohammed Alashwal
Background
Medication errors (MEs) frequently occur during the execution and administration of anesthesia and are influenced by several factors, such as the experience of the anesthesia staff, the severity of comorbidities, and the technique used. Without pharmacy approval or referral to other staff, anesthesia staff prepare, administer, and monitor powerful anesthetic drugs. This study aimed to evaluate medication errors made by anesthesia staff members working in government hospitals in Sana'a City, Yemen. Methods: A total of 102 anesthesia staff members in government hospitals participated in a descriptive cross-sectional study consistent with the STROBE guidelines was used. The data were collected through a self-administered questionnaire administered during a previous study from March 26th to April 9th, 2022.
Results
A total of 83.3% of the participants were males. A total of 37.3% were aged 25–30 years, 58.8% had 1–5 years of experience, 52.0% had a diploma, and 80.4% were anesthesia technology specialists. In relation to medication errors, 56.9% of them experienced administration errors in their anesthesia practice. There were statistically significant differences in the opinions of preventive measures between anesthesiologists and anesthesia technology specialists.
Conclusion
There was a high occurrence of anesthetic medication errors in Sana'a government hospitals. Syringe labeling practices need to be standardized by policymakers, and future studies should concentrate on the factors that encourage reporting errors in nonpunitive cultures.
{"title":"Assessment of Medication Errors among Anesthesia Staff in Government Hospitals in Sana'a City, Yemen","authors":"Marzoq Ali Odhah , Abdulnasser Ahmed Haza'a , Saddam Ahmed Al-Ahdal , Muhammad Sadeq Al-Awar , Abdulfatah Saleh Al-Jaradi , Bandar Al-haguri , Mohammed M Al-Jabri , Taha Mohammed Alashwal","doi":"10.1016/j.pcorm.2024.100388","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100388","url":null,"abstract":"<div><h3>Background</h3><p>Medication errors (MEs) frequently occur during the execution and administration of anesthesia and are influenced by several factors, such as the experience of the anesthesia staff, the severity of comorbidities, and the technique used. Without pharmacy approval or referral to other staff, anesthesia staff prepare, administer, and monitor powerful anesthetic drugs. This study aimed to evaluate medication errors made by anesthesia staff members working in government hospitals in Sana'a City, Yemen. Methods: A total of 102 anesthesia staff members in government hospitals participated in a descriptive cross-sectional study consistent with the STROBE guidelines was used. The data were collected through a self-administered questionnaire administered during a previous study from March 26th to April 9th, 2022.</p></div><div><h3>Results</h3><p>A total of 83.3% of the participants were males. A total of 37.3% were aged 25–30 years, 58.8% had 1–5 years of experience, 52.0% had a diploma, and 80.4% were anesthesia technology specialists. In relation to medication errors, 56.9% of them experienced administration errors in their anesthesia practice. There were statistically significant differences in the opinions of preventive measures between anesthesiologists and anesthesia technology specialists.</p></div><div><h3>Conclusion</h3><p>There was a high occurrence of anesthetic medication errors in Sana'a government hospitals. Syringe labeling practices need to be standardized by policymakers, and future studies should concentrate on the factors that encourage reporting errors in nonpunitive cultures.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100388"},"PeriodicalIF":0.0,"publicationDate":"2024-04-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140549416","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}
Since the hospital stay of patients after ambulatory surgery is short, it is important to determine the factors that may cause problems in the early postoperative period. Among these factors, the effects of which are not fully known are active smoking and secondhand smoke exposure. This study aimed to elucidate how active smoking and secondhand smoke exposure effect early outcomes of ambulatory surgery.
Methods
A prospective observational study was conducted with 124 patients (42 active smokers, 40 nonsmokers exposed to secondhand smoke and 42 nonsmokers) who underwent ambulatory general surgery. Patients were closely monitored for cardiac and respiratory complications, as well as pain, opioid use, and nausea and vomiting until discharge from the hospital.
Results
Postoperative complications were observed in 50.8 % of the patients. Hypotension was more common in active smokers compared with nonsmokers and nonsmokers exposed to secondhand smoke. Smokers were more likely to require postoperative supplemental oxygen therapy. Pain intensity at 1st and 4th hours after surgery was significantly higher in smokers (p < 0.005). In addition, nonsmokers exposed to secondhand smoke exhibited more severe pain than nonsmokers (p = 0.001). There were no statistically significant differences between the groups with regard to opioid consumption.
Conclusion
Although smoking and secondhand smoke exposure are not associated with serious complications after ambulatory surgery, patients' comfort and the success of ambulatory surgery may be negatively affected due to severe pain associated with smoking and secondhand smoke exposure.
{"title":"The effect of active smoking and secondhand smoke exposure on early outcomes of ambulatory surgery: A prospective observational study","authors":"Betül Güven , Cemile Karaaslan Sevinç , Birgül Ödül Özkaya , Okan Soyhan","doi":"10.1016/j.pcorm.2024.100387","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100387","url":null,"abstract":"<div><h3>Purpose</h3><p>Since the hospital stay of patients after ambulatory surgery is short, it is important to determine the factors that may cause problems in the early postoperative period. Among these factors, the effects of which are not fully known are active smoking and secondhand smoke exposure. This study aimed to elucidate how active smoking and secondhand smoke exposure effect early outcomes of ambulatory surgery.</p></div><div><h3>Methods</h3><p>A prospective observational study was conducted with 124 patients (42 active smokers, 40 nonsmokers exposed to secondhand smoke and 42 nonsmokers) who underwent ambulatory general surgery. Patients were closely monitored for cardiac and respiratory complications, as well as pain, opioid use, and nausea and vomiting until discharge from the hospital.</p></div><div><h3>Results</h3><p>Postoperative complications were observed in 50.8 % of the patients. Hypotension was more common in active smokers compared with nonsmokers and nonsmokers exposed to secondhand smoke. Smokers were more likely to require postoperative supplemental oxygen therapy. Pain intensity at 1st and 4th hours after surgery was significantly higher in smokers (<em>p</em> < 0.005). In addition, nonsmokers exposed to secondhand smoke exhibited more severe pain than nonsmokers (<em>p</em> = 0.001). There were no statistically significant differences between the groups with regard to opioid consumption.</p></div><div><h3>Conclusion</h3><p>Although smoking and secondhand smoke exposure are not associated with serious complications after ambulatory surgery, patients' comfort and the success of ambulatory surgery may be negatively affected due to severe pain associated with smoking and secondhand smoke exposure.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100387"},"PeriodicalIF":0.0,"publicationDate":"2024-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140339365","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}
Pub Date : 2024-03-27DOI: 10.1016/j.pcorm.2024.100386
Seham M. Moeen, Mohammed Yasser Y. Makhlouf, Mohamed H. Bakri
Objectives
The subcostal transversus abdominis plane (STAP) block has recently been included in the enhanced recovery after surgery (ERAS) protocol for laparoscopic cholecystectomy (LC). In our study on STAP for LC, we compared the effectiveness of adding low-dose magnesium sulphate (MgSO4) to bupivacaine versus using bupivacaine alone. MgSO4 was hypothesized to enhance the analgesic effects of bupivacaine and therefore aid in the recovery process.
Methods
Sixty patients, aged 18–65 years, ASA I–II, undergoing LC, were randomly assigned to receive bilateral STAP 15 min before skin incision with 20 ml bupivacaine 0.25 % and either 150 mg MgSO4 (BM group) or 1.5 ml normal saline (B group). Pain scores, time to initial analgesic demand, overall analgesic requirement, sedation, emetic episodes, time to get out of bed, and patient satisfaction were recorded for the first 24 h following surgery. The Mann-Whitney U test was used to analyze the non-normally distributed data between groups, while the Chi-square test or Fisher’s exact test was used to test categorical data.
Results
The BM group had statistically significant but clinically insignificant lower pain scores at rest and during coughing in the post-anesthesia care unit (PACU) (P = 0.005 and P = 0.003), at 1 h (P = 0.005 and P = 0.015), 6 h (P = 0.009 and P = 0.003), 12 h (P = 0.017 and P = 0.001), and 24 h (P = 0.001 and P = 0.001) after surgery compared to the B group. Kaplan–Meier curves for times to the first paracetamol and morphine doses showed significant differences (log-rank test) between the groups (P = 0.001 and P = 0.003, respectively). Additionally, the total doses of paracetamol (P = 0.001) and morphine (P = 0.001) in the BM group were significantly lower than those in the B group during the first 24 h after surgery. Sedation and emetic episodes were identical between the groups. The Patient in the BM group ambulated faster (P = 0.001) and were more satisfied (P = 0.026) than those in the B group.
Conclusions
Adding a low-dose (150 mg) of MgSO4 to bupivacaine in the STAP block for LC was associated with improved analgesic outcomes in the first 24 h after surgery.
Ethical approval
Medical Ethics Committee of Faculty of Medicine, IRB no: 17,100,622 on November 15, 2016.
Trial registration
ClinicalTrials.gov (NCT03612947) on August 2, 2018.
{"title":"Impact of a transversus abdominis plane block with low-dose magnesium sulphate coupled to bupivacaine on postoperative pain after laparoscopic cholecystectomy: A randomized trial","authors":"Seham M. Moeen, Mohammed Yasser Y. Makhlouf, Mohamed H. Bakri","doi":"10.1016/j.pcorm.2024.100386","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100386","url":null,"abstract":"<div><h3>Objectives</h3><p>The subcostal transversus abdominis plane (STAP) block has recently been included in the enhanced recovery after surgery (ERAS) protocol for laparoscopic cholecystectomy (LC). In our study on STAP for LC, we compared the effectiveness of adding low-dose magnesium sulphate (MgSO<sub>4</sub>) to bupivacaine versus using bupivacaine alone. MgSO<sub>4</sub> was hypothesized to enhance the analgesic effects of bupivacaine and therefore aid in the recovery process.</p></div><div><h3>Methods</h3><p>Sixty patients, aged 18–65 years, ASA I–II, undergoing LC, were randomly assigned to receive bilateral STAP 15 min before skin incision with 20 ml bupivacaine 0.25 % and either 150 mg MgSO<sub>4</sub> (BM group) or 1.5 ml normal saline (B group). Pain scores, time to initial analgesic demand, overall analgesic requirement, sedation, emetic episodes, time to get out of bed, and patient satisfaction were recorded for the first 24 h following surgery. The Mann-Whitney <em>U</em> test was used to analyze the non-normally distributed data between groups, while the Chi-square test or Fisher<sup>’</sup>s exact test was used to test categorical data.</p></div><div><h3>Results</h3><p>The BM group had statistically significant but clinically insignificant lower pain scores at rest and during coughing in the post-anesthesia care unit (PACU) (<em>P</em> = 0.005 and <em>P</em> = 0.003), at 1 h (<em>P</em> = 0.005 and <em>P</em> = 0.015), 6 h (<em>P</em> = 0.009 and <em>P</em> = 0.003), 12 h (<em>P</em> = 0.017 and <em>P</em> = 0.001), and 24 h (<em>P</em> = 0.001 and <em>P</em> = 0.001) after surgery compared to the B group. Kaplan–Meier curves for times to the first paracetamol and morphine doses showed significant differences (log-rank test) between the groups (<em>P</em> = 0.001 and <em>P</em> = 0.003, respectively). Additionally, the total doses of paracetamol (<em>P</em> = 0.001) and morphine (<em>P</em> = 0.001) in the BM group were significantly lower than those in the B group during the first 24 h after surgery. Sedation and emetic episodes were identical between the groups. The Patient in the BM group ambulated faster (<em>P</em> = 0.001) and were more satisfied (<em>P</em> = 0.026) than those in the B group.</p></div><div><h3>Conclusions</h3><p>Adding a low-dose (150 mg) of MgSO<sub>4</sub> to bupivacaine in the STAP block for LC was associated with improved analgesic outcomes in the first 24 h after surgery.</p></div><div><h3>Ethical approval</h3><p>Medical Ethics Committee of Faculty of Medicine, IRB no: 17,100,622 on November 15, 2016.</p></div><div><h3>Trial registration</h3><p>ClinicalTrials.gov (NCT03612947) on August 2, 2018.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100386"},"PeriodicalIF":0.0,"publicationDate":"2024-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140327648","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}
Pub Date : 2024-03-23DOI: 10.1016/j.pcorm.2024.100384
Cory James WILLIAMS , Leanna WOODS , Chloe TANNAGAN , Jed DUFF
Objective
This scoping review aimed to identify and synthesise existing literature on patient-facing e-health interventions to support self-management and preparation for or recovery from surgery for adult patients.
Introduction
Patients waiting for surgery often experience distress and uncertainty, which can lead to suboptimal surgical preparation and recovery. E-health interventions may provide new models of care to address these issues and maximise value-based healthcare.
Inclusion criteria
Studies were included if adult patients utilised an e-health intervention to support self-management in preparation for and recovery from their surgery, with interventions targeting any perioperative phase.
Methods
The review followed Joanna Briggs Institute methodology and included sources from 2010 onwards in MEDLINE, Embase, PubMed, Cumulative Index for Nursing and Allied Health Literature, Google Scholar and ProQuest. Four reviewers undertook screening and data was presented in tabular and diagrammatic form with a narrative summary.
Results
From 2293 records, 48 papers with a total of 41 unique studies from 15 countries were included. Most interventions supported patients in the postoperative phase only for bowel/colorectal cancer surgery and total hip arthroplasty Quality was generally good to average, with limitations including small sample sizes, single-centre studies, and a failure to include a comparison group. Just 35 % of interventions were codesigned with input from patients during the development process. Development and evaluation methods were workshops (17 %) and unvalidated attitudinal studies (65 %), respectively. E-health interventions showed positive impacts on clinical outcomes (54 %), user satisfaction (65 %), utilisation of the interventions (46 %), and health system outcomes (24 %).
Conclusions
E-health interventions for self-management of surgery preparation and recovery were prevalent in 15 countries, but mostly focused on postoperative support and lacked input from end-users during development. Future studies should address these limitations by creating applications that support patients from all surgical specialities and involving patients and families in the development process.
本范围综述旨在识别和综合现有文献,这些文献涉及面向患者的电子健康干预措施,以支持成年患者的自我管理以及手术准备或术后恢复。电子健康干预措施可提供新的护理模式来解决这些问题,并最大限度地提高基于价值的医疗保健。纳入标准如果成年患者利用电子健康干预措施来支持手术准备和术后恢复过程中的自我管理,且干预措施针对任何围手术期阶段,则纳入该研究。方法该综述遵循 Joanna Briggs 研究所的方法,纳入了 2010 年以来 MEDLINE、Embase、PubMed、Cumulative Index for Nursing and Allied Health Literature、Google Scholar 和 ProQuest 中的资料来源。结果从 2293 条记录中,共纳入了来自 15 个国家的 48 篇论文和 41 项独特的研究。大多数干预措施仅在肠癌/结直肠癌手术和全髋关节置换术的术后阶段为患者提供支持 质量总体良好或一般,不足之处包括样本量小、单中心研究以及未纳入对比组。仅有 35% 的干预措施在制定过程中听取了患者的意见。开发和评估方法分别为研讨会(17%)和未经验证的态度研究(65%)。电子健康干预措施对临床结果(54%)、用户满意度(65%)、干预措施的利用率(46%)和医疗系统结果(24%)产生了积极影响。未来的研究应通过开发支持所有外科专科患者的应用程序以及让患者和家属参与开发过程来解决这些局限性。
{"title":"Patient-facing e-health interventions to promote self-management in adult surgical patients: A scoping review","authors":"Cory James WILLIAMS , Leanna WOODS , Chloe TANNAGAN , Jed DUFF","doi":"10.1016/j.pcorm.2024.100384","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100384","url":null,"abstract":"<div><h3>Objective</h3><p>This scoping review aimed to identify and synthesise existing literature on patient-facing e-health interventions to support self-management and preparation for or recovery from surgery for adult patients.</p></div><div><h3>Introduction</h3><p>Patients waiting for surgery often experience distress and uncertainty, which can lead to suboptimal surgical preparation and recovery. E-health interventions may provide new models of care to address these issues and maximise value-based healthcare.</p></div><div><h3>Inclusion criteria</h3><p>Studies were included if adult patients utilised an e-health intervention to support self-management in preparation for and recovery from their surgery, with interventions targeting any perioperative phase.</p></div><div><h3>Methods</h3><p>The review followed Joanna Briggs Institute methodology and included sources from 2010 onwards in MEDLINE, Embase, PubMed, Cumulative Index for Nursing and Allied Health Literature, Google Scholar and ProQuest. Four reviewers undertook screening and data was presented in tabular and diagrammatic form with a narrative summary.</p></div><div><h3>Results</h3><p>From 2293 records, 48 papers with a total of 41 unique studies from 15 countries were included. Most interventions supported patients in the postoperative phase only for bowel/colorectal cancer surgery and total hip arthroplasty Quality was generally good to average, with limitations including small sample sizes, single-centre studies, and a failure to include a comparison group. Just 35 % of interventions were codesigned with input from patients during the development process. Development and evaluation methods were workshops (17 %) and unvalidated attitudinal studies (65 %), respectively. E-health interventions showed positive impacts on clinical outcomes (54 %), user satisfaction (65 %), utilisation of the interventions (46 %), and health system outcomes (24 %).</p></div><div><h3>Conclusions</h3><p>E-health interventions for self-management of surgery preparation and recovery were prevalent in 15 countries, but mostly focused on postoperative support and lacked input from end-users during development. Future studies should address these limitations by creating applications that support patients from all surgical specialities and involving patients and families in the development process.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100384"},"PeriodicalIF":0.0,"publicationDate":"2024-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2405603024000189/pdfft?md5=1c5f9e28ff2faeaeb6a96c607173b89b&pid=1-s2.0-S2405603024000189-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140346831","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}
Pub Date : 2024-03-19DOI: 10.1016/j.pcorm.2024.100385
Gemma Echarri , Matilda Lafuente , José M. Domínguez-Roldán , Agustín Díaz , Gonzalo Tamayo
Elaboration of a consensus document to address perioperative blood pressure (BP) in neurocritical patients, made with anesthesia and resuscitation, and intensive medicine specialists in Spain, by means of a modified Delphi methodology in two rounds with a questionnaire answered by 65 panelists. Consensus was reached in 126 (74.6 %) of 169 statements, with 113 agreements (66.9 %). Consensus was obtained for the use of clevidipine, urapidil, and beta-blockers for acute hypertension in head trauma patients and for brain tumor surgery, among others. The experts considered that the existing clinical studies evaluating the optimal perioperative therapy in neurocritical patients with altered BP are insufficient and that most recommendations are based on clinical experience. Therefore, treatment must be individualized regardless of absolute BP target value and based on occurrence/absence of acute organ damage and the coexistence of other diseases.
{"title":"Perioperative management of blood pressure in neurocritical patients: Consensus reached through the Delphi method","authors":"Gemma Echarri , Matilda Lafuente , José M. Domínguez-Roldán , Agustín Díaz , Gonzalo Tamayo","doi":"10.1016/j.pcorm.2024.100385","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100385","url":null,"abstract":"<div><p>Elaboration of a consensus document to address perioperative blood pressure (BP) in neurocritical patients, made with anesthesia and resuscitation, and intensive medicine specialists in Spain, by means of a modified Delphi methodology in two rounds with a questionnaire answered by 65 panelists. Consensus was reached in 126 (74.6 %) of 169 statements, with 113 agreements (66.9 %). Consensus was obtained for the use of clevidipine, urapidil, and beta-blockers for acute hypertension in head trauma patients and for brain tumor surgery, among others. The experts considered that the existing clinical studies evaluating the optimal perioperative therapy in neurocritical patients with altered BP are insufficient and that most recommendations are based on clinical experience. Therefore, treatment must be individualized regardless of absolute BP target value and based on occurrence/absence of acute organ damage and the coexistence of other diseases.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100385"},"PeriodicalIF":0.0,"publicationDate":"2024-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140195799","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}
Pub Date : 2024-03-14DOI: 10.1016/j.pcorm.2024.100383
Oluwafemi P. Owodunni , Eduardo Biala Jr. , Luxey Sirisegaram , Dianne Bettick , Susan L Gearhart , April L. Ehrlich
Background
Frailty is common in geriatric emergency surgery and associated with increased risk for poor postoperative outcomes. Frailty screening is challenging in emergency settings. The Edmonton Frail Scale (EFS) is a valid tool to screen for patients at high risk for poor postoperative outcomes. Recently, the EFS was modified to decrease dependence on staff to perform physical measures. This modification, the EFS-Acute Care (EFS-AC), has not been validated. We wish to assess the agreement between the EFS and the EFS-AC.
Study design
We performed a prospective cohort study from 10/2021 – 10/2022 screening 688 patients ≥ 65 years with both the EFS and EFS-AC preoperatively. We assessed the ability of the EFS-AC to discriminate frailty identified by the EFS and compared the association of both scales with loss of independence (LOI), hospital length of stay (LOS), ICU admissions, and ICU LOS. Receiver Operator Curves were used to estimate the discriminatory thresholds for LOI.
Results
688 patients with a median age 73 (IQR 68, 77) were enrolled. The EFS-AC was able to discriminate individuals’ frailty status by the EFS with excellent agreement (AUC 0.971 [0.958, 0.983]). An EFS-AC threshold score of ≥ 6 points lead to 93.60 % of individuals being correctly identified (77.87 % sensitivity and 97.00 % specificity). Both EFS and EFS-AC ≥ 6 were similarly associated with a higher risk for all clinical outcomes assessed and demonstrated similar ability to predict LOI.
Conclusions
The EFS-AC is a valid preoperative frailty screen, and due to its self-reported nature, can be administered in the acute care setting, during virtual visits, or through digital health apps. Real-time screening can assist with better understanding patient needs and lead to interventions to prevent poor hospital outcomes.
{"title":"Validation of the self-reported Edmonton frail scale - Acute care in patients ≥ 65 years undergoing surgery","authors":"Oluwafemi P. Owodunni , Eduardo Biala Jr. , Luxey Sirisegaram , Dianne Bettick , Susan L Gearhart , April L. Ehrlich","doi":"10.1016/j.pcorm.2024.100383","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100383","url":null,"abstract":"<div><h3>Background</h3><p>Frailty is common in geriatric emergency surgery and associated with increased risk for poor postoperative outcomes. Frailty screening is challenging in emergency settings. The Edmonton Frail Scale (EFS) is a valid tool to screen for patients at high risk for poor postoperative outcomes. Recently, the EFS was modified to decrease dependence on staff to perform physical measures. This modification, the EFS-Acute Care (EFS-AC), has not been validated. We wish to assess the agreement between the EFS and the EFS-AC.</p></div><div><h3>Study design</h3><p>We performed a prospective cohort study from 10/2021 – 10/2022 screening 688 patients ≥ 65 years with both the EFS and EFS-AC preoperatively. We assessed the ability of the EFS-AC to discriminate frailty identified by the EFS and compared the association of both scales with loss of independence (LOI), hospital length of stay (LOS), ICU admissions, and ICU LOS. Receiver Operator Curves were used to estimate the discriminatory thresholds for LOI.</p></div><div><h3>Results</h3><p>688 patients with a median age 73 (IQR 68, 77) were enrolled. The EFS-AC was able to discriminate individuals’ frailty status by the EFS with excellent agreement (AUC 0.971 [0.958, 0.983]). An EFS-AC threshold score of ≥ 6 points lead to 93.60 % of individuals being correctly identified (77.87 % sensitivity and 97.00 % specificity). Both EFS and EFS-AC ≥ 6 were similarly associated with a higher risk for all clinical outcomes assessed and demonstrated similar ability to predict LOI.</p></div><div><h3>Conclusions</h3><p>The EFS-AC is a valid preoperative frailty screen, and due to its self-reported nature, can be administered in the acute care setting, during virtual visits, or through digital health apps. Real-time screening can assist with better understanding patient needs and lead to interventions to prevent poor hospital outcomes.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100383"},"PeriodicalIF":0.0,"publicationDate":"2024-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140188024","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}
The sterilization of instruments is a critical process to perform the activity in the operating rooms and ensure the safety of patients. The best approach to improve the performance of the sterilization is the risk management. Nevertheless, improving the performance in sterilization units in developing countries presents a real challenge.
Purpose
Designing an effective risk management project in health sector, specifically in sterilization units, adaptable to the context of developing countries (DC).
Methods
This study uses Failure Modes and Effects Analysis (FMEA) to manage risks in healthcare in DC. Modifications to the implementation of the recommended tool mode. A case study of the sterilization unit of a tertiary Moroccan national reference university hospital was conducted to verify the effectiveness of the model.
Findings
The present study demonstrated that the proposed model is adaptable to the DC context. This model was implemented with minimal resources and was highly efficient.
Conclusions
The increase of risks in healthcare is a challenge for managers in DC. This study highlights the first successful experience of risk management in Moroccan healthcare sector.
{"title":"Health management risks in developing countries: Case of a sterilization unit in a Moroccan public hospital","authors":"Amine En-Naaoui , Mohammed Kaicer , Wahid Chaouki , Mohsine Mimouni , Aicha Aguezzoul","doi":"10.1016/j.pcorm.2024.100382","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100382","url":null,"abstract":"<div><h3>Background</h3><p>The sterilization of instruments is a critical process to perform the activity in the operating rooms and ensure the safety of patients. The best approach to improve the performance of the sterilization is the risk management. Nevertheless, improving the performance in sterilization units in developing countries presents a real challenge.</p></div><div><h3>Purpose</h3><p>Designing an effective risk management project in health sector, specifically in sterilization units, adaptable to the context of developing countries (DC).</p></div><div><h3>Methods</h3><p>This study uses Failure Modes and Effects Analysis (FMEA) to manage risks in healthcare in DC. Modifications to the implementation of the recommended tool mode. A case study of the sterilization unit of a tertiary Moroccan national reference university hospital was conducted to verify the effectiveness of the model.</p></div><div><h3>Findings</h3><p>The present study demonstrated that the proposed model is adaptable to the DC context. This model was implemented with minimal resources and was highly efficient.</p></div><div><h3>Conclusions</h3><p>The increase of risks in healthcare is a challenge for managers in DC. This study highlights the first successful experience of risk management in Moroccan healthcare sector.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100382"},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140139013","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}
Pub Date : 2024-03-11DOI: 10.1016/j.pcorm.2024.100381
Zachary G. Freedman , Kevin L. Xu , Mary E. McAlevy , Joseph Y. Clark
Uvular necrosis is a known risk factor following general anesthesia due to compression of blood flow to the uvula. We report a case of uvular necrosis followed by uvular deviation in a male patient after undergoing two surgeries in four days. He had a sore throat and experienced a foreign body sensation in his throat following the second surgery. He was treated conservatively, but his uvula remained deviated four years later at follow up. Although uvular injury is a known complication of general anesthesia, it is important to understand the risk factors, recognize the conditions, and have a high index of suspicion when evaluating patients with sore throats after anesthesia.
{"title":"Uvula Trauma and Damage: If You Don't Look, You Won't Find It: A Case Report","authors":"Zachary G. Freedman , Kevin L. Xu , Mary E. McAlevy , Joseph Y. Clark","doi":"10.1016/j.pcorm.2024.100381","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100381","url":null,"abstract":"<div><p>Uvular necrosis is a known risk factor following general anesthesia due to compression of blood flow to the uvula. We report a case of uvular necrosis followed by uvular deviation in a male patient after undergoing two surgeries in four days. He had a sore throat and experienced a foreign body sensation in his throat following the second surgery. He was treated conservatively, but his uvula remained deviated four years later at follow up. Although uvular injury is a known complication of general anesthesia, it is important to understand the risk factors, recognize the conditions, and have a high index of suspicion when evaluating patients with sore throats after anesthesia.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100381"},"PeriodicalIF":0.0,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140122549","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}
Pub Date : 2024-03-06DOI: 10.1016/j.pcorm.2024.100380
Raja Ahmad Anzari, Rudi Kurniadi Kadarsah, Iwan Abdul Rachman
Endotracheal intubation is the gold standard for airway management. Direct laryngoscopy is a difficult procedure with a high failure rate. A 3D printed video laryngoscope can be used as a more affordable replacement for a laryngoscope. The aim of this study was to evaluate the success rate and time of endotracheal intubation in manikins using the Alba 3D printed video laryngoscope, the C-MAC video laryngoscope and the Macintosh operated by medical students. This study was conducted using a cross sectional randomised study method involving 36 medical students. This study found that the mean endotracheal intubation time using Alba 3D Print was significantly shorter than using Macintosh, but not better than C-MAC (VL3D-25 vs LDM-50.5 vs VLC-21.5 s) with a p-value of <0.001. The success rate of endotracheal intubation using Alba 3D moulds was significantly better than using Macintosh, but not statistically significant when compared to C-MAC (VL3D-91.7% vs LDM-97.2% vs VLC-75%) with p-value <0.05). This study concluded that the use of Alba 3D prints has a better success rate and time compared to Macinctosh and can be an affordable alternative to commercial video laryngoscopes such as C-MAC for educational purposes.
气管插管是气道管理的黄金标准。直接喉镜检查是一项困难的手术,失败率很高。3D 打印视频喉镜可作为喉镜的替代品,价格更实惠。本研究的目的是评估医科学生使用 Alba 3D 打印视频喉镜、C-MAC 视频喉镜和 Macintosh 操作模拟人进行气管插管的成功率和时间。这项研究采用横断面随机研究方法进行,共有 36 名医科学生参与。研究发现,使用 Alba 3D Print 的平均气管插管时间明显短于使用 Macintosh,但不优于 C-MAC(VL3D-25 vs LDM-50.5 vs VLC-21.5秒),P 值为 <0.001。使用阿尔巴三维模具进行气管插管的成功率明显优于使用 Macintosh,但与 C-MAC 相比无统计学意义(VL3D-91.7% vs LDM-97.2% vs VLC-75%,p 值为 <0.05)。这项研究得出结论,与 Macinctosh 相比,使用 Alba 3D 打印机的成功率更高、时间更短,可以成为 C-MAC 等商用视频喉镜的经济型替代品,用于教学目的。
{"title":"Comparing Alba 3D printed video laryngoscope vs. video laryngoscope C-MAC® vs. direct macintosh laryngoscope operated by medical students: A randomized, crossover, manikin study","authors":"Raja Ahmad Anzari, Rudi Kurniadi Kadarsah, Iwan Abdul Rachman","doi":"10.1016/j.pcorm.2024.100380","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100380","url":null,"abstract":"<div><p>Endotracheal intubation is the gold standard for airway management. Direct laryngoscopy is a difficult procedure with a high failure rate. A 3D printed video laryngoscope can be used as a more affordable replacement for a laryngoscope. The aim of this study was to evaluate the success rate and time of endotracheal intubation in manikins using the Alba 3D printed video laryngoscope, the C-MAC video laryngoscope and the Macintosh operated by medical students. This study was conducted using a cross sectional randomised study method involving 36 medical students. This study found that the mean endotracheal intubation time using Alba 3D Print was significantly shorter than using Macintosh, but not better than C-MAC (VL3D-25 vs LDM-50.5 vs VLC-21.5 s) with a p-value of <0.001. The success rate of endotracheal intubation using Alba 3D moulds was significantly better than using Macintosh, but not statistically significant when compared to C-MAC (VL3D-91.7% vs LDM-97.2% vs VLC-75%) with p-value <0.05). This study concluded that the use of Alba 3D prints has a better success rate and time compared to Macinctosh and can be an affordable alternative to commercial video laryngoscopes such as C-MAC for educational purposes.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100380"},"PeriodicalIF":0.0,"publicationDate":"2024-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140160933","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}
Pub Date : 2024-03-05DOI: 10.1016/j.pcorm.2024.100379
Franklin Dexter , Richard H. Epstein
When operating room (OR) allocated times are calculated, reports ideally are accompanied with attachment or link to an article describing the specific optimization method used. In addition, many stakeholders (e.g., managers and committee members) also need a background source. Our review supplies in one downloadable publication such an article. Our review covers the fundamental knowledge sufficient to read the thousands of articles on OR staffing and case scheduling, including references describing the specific method implemented, and to understand relevant studies of implementation (e.g., behavioral operations and managerial epidemiology). Inappropriate OR allocation and case scheduling can be mitigated by ensuring that when there is a case waiting to start, to be done today, the number of ORs in use for each such service is at least the number that maximizes the efficiency of use of OR time. Implementation means performing mathematical calculations using hospital data or anesthesia billing information. Physician leadership ensures that the statistical methods used are appropriate and applied for case scheduling. When done properly, there are opportunities to reduce turnover times and late first case of the day starts targeted toward reducing over-utilized time. These actions facilitate growth in surgical practices, increase OR productivity, and help prevent surgical teams from working late because of poor staffing and staff scheduling.
{"title":"Fundamentals of operating room allocation and case scheduling to minimize the inefficiency of use of the time","authors":"Franklin Dexter , Richard H. Epstein","doi":"10.1016/j.pcorm.2024.100379","DOIUrl":"https://doi.org/10.1016/j.pcorm.2024.100379","url":null,"abstract":"<div><p>When operating room (OR) allocated times are calculated, reports ideally are accompanied with attachment or link to an article describing the specific optimization method used. In addition, many stakeholders (e.g., managers and committee members) also need a background source. Our review supplies in one downloadable publication such an article. Our review covers the fundamental knowledge sufficient to read the thousands of articles on OR staffing and case scheduling, including references describing the specific method implemented, and to understand relevant studies of implementation (e.g., behavioral operations and managerial epidemiology). Inappropriate OR allocation and case scheduling can be mitigated by ensuring that when there is a case waiting to start, to be done today, the number of ORs in use for each such service is at least the number that maximizes the efficiency of use of OR time. Implementation means performing mathematical calculations using hospital data or anesthesia billing information. Physician leadership ensures that the statistical methods used are appropriate and applied for case scheduling. When done properly, there are opportunities to reduce turnover times and late first case of the day starts targeted toward reducing over-utilized time. These actions facilitate growth in surgical practices, increase OR productivity, and help prevent surgical teams from working late because of poor staffing and staff scheduling.</p></div>","PeriodicalId":53468,"journal":{"name":"Perioperative Care and Operating Room Management","volume":"35 ","pages":"Article 100379"},"PeriodicalIF":0.0,"publicationDate":"2024-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140296478","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}