Pub Date : 2024-12-30DOI: 10.1016/j.jopan.2024.09.006
Mehmet Nasır Ozbek, Ezgi Seyhan Ak
Purpose: This study aimed to investigate the effect of preoperative tele-nursing counseling on anxiety and patient satisfaction in day surgery.
Design: Randomized controlled study design was employed.
Methods: The study was conducted in a city hospital and a university hospital in Istanbul between July 2022 and May 2023 with patients who met the study criteria. The sample consisted of 160 patients in the experimental (n = 80) and control (n = 80) groups. In the first interview, the patients who came to be examined (experimental and control groups) were given the Descriptive Information Form and the Surgery-specific Anxiety Scale. The patients in the experimental group were given a training booklet and counseling with tele-nursing practice the day before the surgery, and the patients in the control group were given routine clinical follow-up and a training booklet. The patients (experimental and control) were given the Surgery-specific Anxiety Scale on the day they came for surgery before they were taken into surgery. After the surgery, the Patient's Perception of Nursing Care Scale was applied to the patients. The patients in the experimental group were also given the Tele-nursing Evaluation Form.
Findings: As a result of the study, the patients in the experimental group who received tele-nursing counseling had lower levels of surgery-specific anxiety than the control group. Patients in the experimental group were statistically significantly more satisfied with nursing care.
Conclusions: Providing preoperative tele-nursing counseling to patients scheduled for day surgery contributed to the reduction of anxiety and worry of the patients and increased the satisfaction of the patients.
{"title":"The Effect of Preoperative Tele-nursing Counseling on Anxiety and Patient Satisfaction in Day Surgery: A Randomized Controlled Trial.","authors":"Mehmet Nasır Ozbek, Ezgi Seyhan Ak","doi":"10.1016/j.jopan.2024.09.006","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.006","url":null,"abstract":"<p><strong>Purpose: </strong>This study aimed to investigate the effect of preoperative tele-nursing counseling on anxiety and patient satisfaction in day surgery.</p><p><strong>Design: </strong>Randomized controlled study design was employed.</p><p><strong>Methods: </strong>The study was conducted in a city hospital and a university hospital in Istanbul between July 2022 and May 2023 with patients who met the study criteria. The sample consisted of 160 patients in the experimental (n = 80) and control (n = 80) groups. In the first interview, the patients who came to be examined (experimental and control groups) were given the Descriptive Information Form and the Surgery-specific Anxiety Scale. The patients in the experimental group were given a training booklet and counseling with tele-nursing practice the day before the surgery, and the patients in the control group were given routine clinical follow-up and a training booklet. The patients (experimental and control) were given the Surgery-specific Anxiety Scale on the day they came for surgery before they were taken into surgery. After the surgery, the Patient's Perception of Nursing Care Scale was applied to the patients. The patients in the experimental group were also given the Tele-nursing Evaluation Form.</p><p><strong>Findings: </strong>As a result of the study, the patients in the experimental group who received tele-nursing counseling had lower levels of surgery-specific anxiety than the control group. Patients in the experimental group were statistically significantly more satisfied with nursing care.</p><p><strong>Conclusions: </strong>Providing preoperative tele-nursing counseling to patients scheduled for day surgery contributed to the reduction of anxiety and worry of the patients and increased the satisfaction of the patients.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142903842","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}
Pub Date : 2024-12-27DOI: 10.1016/j.jopan.2024.09.020
Mujgan Solak, Sinem Gecit, Turkan Ozbayir
Purpose: Health literacy is a complex issue that affects the health outcomes of surgical patients. This study aimed to determine the health literacy of general surgery patients.
Design: A descriptive cross-sectional study.
Methods: The sample of the descriptive study consisted of 420 patients who applied to the general surgery outpatient clinic of the hospital between December 2019 and April 2020. Research data were collected using the "Patient Information Form" and "Health Literacy Index" prepared by the researchers in line with the literature. The score ranges of the Health Literacy Index are a minimum of 5 and a maximum of 25. Data were analyzed by number and percentile distribution, mean, standard deviation, t test, and one-way analysis of variance.
Findings: The mean age of the participants in the study was 47.58 ± 14.92 years and 56.2% of them were women. Participants' Health Literacy Index total score average was determined as 101.33 ± 18.56. Individuals received a maximum score of 25 points in access to information and a minimum score of 7 points in understanding the information from the subindices. There was a statistically significant difference between the demographic characteristics (eg, age, marital status, gender, education level, occupation, place of residence) of the participants and their health literacy levels.
Conclusions: The health literacy levels of the participants in the research are adequate and at a good level. We recommend evaluation of health literacy levels in surgical patients to reduce complications and enable patients to participate effectively in care.
{"title":"Health Literacy of General Surgery Patients: A Cross-sectional Study.","authors":"Mujgan Solak, Sinem Gecit, Turkan Ozbayir","doi":"10.1016/j.jopan.2024.09.020","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.020","url":null,"abstract":"<p><strong>Purpose: </strong>Health literacy is a complex issue that affects the health outcomes of surgical patients. This study aimed to determine the health literacy of general surgery patients.</p><p><strong>Design: </strong>A descriptive cross-sectional study.</p><p><strong>Methods: </strong>The sample of the descriptive study consisted of 420 patients who applied to the general surgery outpatient clinic of the hospital between December 2019 and April 2020. Research data were collected using the \"Patient Information Form\" and \"Health Literacy Index\" prepared by the researchers in line with the literature. The score ranges of the Health Literacy Index are a minimum of 5 and a maximum of 25. Data were analyzed by number and percentile distribution, mean, standard deviation, t test, and one-way analysis of variance.</p><p><strong>Findings: </strong>The mean age of the participants in the study was 47.58 ± 14.92 years and 56.2% of them were women. Participants' Health Literacy Index total score average was determined as 101.33 ± 18.56. Individuals received a maximum score of 25 points in access to information and a minimum score of 7 points in understanding the information from the subindices. There was a statistically significant difference between the demographic characteristics (eg, age, marital status, gender, education level, occupation, place of residence) of the participants and their health literacy levels.</p><p><strong>Conclusions: </strong>The health literacy levels of the participants in the research are adequate and at a good level. We recommend evaluation of health literacy levels in surgical patients to reduce complications and enable patients to participate effectively in care.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142903825","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}
Pub Date : 2024-12-20DOI: 10.1016/j.jopan.2024.09.001
Özkan Sir, Ebubekir Kaplan, Tayyar Akbulut
Purpose: Cardiovascular diseases are a leading cause of morbidity and mortality worldwide. Clinically, various techniques are used to diagnose coronary artery diseases. Coronary angiography is considered the gold standard for the diagnosis of coronary artery disease. The aim of this study is to determine the effect of cold spray applied before local anesthesia on pain and anxiety during coronary angiography procedures.
Design: The study was designed as a randomized controlled trial.
Methods: The study was conducted in the angiography unit of a training and research hospital between January and March 2023. Data collection tools included a patient information form, Visual Analog Scale, and State-Trait Anxiety Inventory.
Results: When the total mean scores of the Visual Analog Scale of the individuals in the intervention and control groups were examined, a statistically significant difference was found between the mean scores of the patients in the intervention group and the control group (P < .05). A significant difference was found between the individuals in the intervention and control groups in terms of the total scores of the state anxiety scale after cold spray (P < .001), with the mean scores of the control group higher than the intervention group.
Conclusions: The application of cold spray before local anesthesia in coronary angiography significantly reduced pain and anxiety levels.
{"title":"The Effect of Cold Spray Applied Before Local Anesthesia on Anxiety and Pain in Coronary Angiography Procedure: A Randomized Controlled Study.","authors":"Özkan Sir, Ebubekir Kaplan, Tayyar Akbulut","doi":"10.1016/j.jopan.2024.09.001","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.001","url":null,"abstract":"<p><strong>Purpose: </strong>Cardiovascular diseases are a leading cause of morbidity and mortality worldwide. Clinically, various techniques are used to diagnose coronary artery diseases. Coronary angiography is considered the gold standard for the diagnosis of coronary artery disease. The aim of this study is to determine the effect of cold spray applied before local anesthesia on pain and anxiety during coronary angiography procedures.</p><p><strong>Design: </strong>The study was designed as a randomized controlled trial.</p><p><strong>Methods: </strong>The study was conducted in the angiography unit of a training and research hospital between January and March 2023. Data collection tools included a patient information form, Visual Analog Scale, and State-Trait Anxiety Inventory.</p><p><strong>Results: </strong>When the total mean scores of the Visual Analog Scale of the individuals in the intervention and control groups were examined, a statistically significant difference was found between the mean scores of the patients in the intervention group and the control group (P < .05). A significant difference was found between the individuals in the intervention and control groups in terms of the total scores of the state anxiety scale after cold spray (P < .001), with the mean scores of the control group higher than the intervention group.</p><p><strong>Conclusions: </strong>The application of cold spray before local anesthesia in coronary angiography significantly reduced pain and anxiety levels.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142873232","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}
Pub Date : 2024-12-20DOI: 10.1016/j.jopan.2024.09.010
Tito D Tubog, Terri D Kane
Purpose: Evaluate the effectiveness of various drugs in preventing postdischarge nausea and vomiting (PDNV).
Design: Systematic review.
Methods: A search for evidence was conducted in PubMed, CINAHL, Cochrane Collaboration, and Google Scholar and gray literature. Only randomized controlled trials examining a pharmacological agent to prevent PDNV were included in the study. The quality appraisal of the literature was conducted using the proposed algorithm described in the Johns Hopkins Nursing Evidence-Based Practice Evidence Level and Quality Guide.
Findings: A total of 8 randomized controlled trials involving 1,441 patients were analyzed. The efficacy of pharmacological agents, including dexamethasone, olanzapine, ondansetron, palonosetron, ramosetron, promethazine, and casopitant in the prevention of PDNV, varied. Additionally, a combination of two or more drugs is a more effective therapy than using a single drug in mitigating PDNV. The review also underscored the individual patient factors that can play a significant role in identifying appropriate prevention and treatment modalities.
Conclusions: There is limited evidence on the efficacy of pharmacological agents in preventing PDNV. The scarcity of large-scale, clinical trials specifically focusing on PDNV restricts the ability to recommend prophylactic drug therapy for reducing its incidence.
{"title":"Pharmacological Strategies for Postdischarge Nausea and Vomiting: Evidence-based Review Update.","authors":"Tito D Tubog, Terri D Kane","doi":"10.1016/j.jopan.2024.09.010","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.010","url":null,"abstract":"<p><strong>Purpose: </strong>Evaluate the effectiveness of various drugs in preventing postdischarge nausea and vomiting (PDNV).</p><p><strong>Design: </strong>Systematic review.</p><p><strong>Methods: </strong>A search for evidence was conducted in PubMed, CINAHL, Cochrane Collaboration, and Google Scholar and gray literature. Only randomized controlled trials examining a pharmacological agent to prevent PDNV were included in the study. The quality appraisal of the literature was conducted using the proposed algorithm described in the Johns Hopkins Nursing Evidence-Based Practice Evidence Level and Quality Guide.</p><p><strong>Findings: </strong>A total of 8 randomized controlled trials involving 1,441 patients were analyzed. The efficacy of pharmacological agents, including dexamethasone, olanzapine, ondansetron, palonosetron, ramosetron, promethazine, and casopitant in the prevention of PDNV, varied. Additionally, a combination of two or more drugs is a more effective therapy than using a single drug in mitigating PDNV. The review also underscored the individual patient factors that can play a significant role in identifying appropriate prevention and treatment modalities.</p><p><strong>Conclusions: </strong>There is limited evidence on the efficacy of pharmacological agents in preventing PDNV. The scarcity of large-scale, clinical trials specifically focusing on PDNV restricts the ability to recommend prophylactic drug therapy for reducing its incidence.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142873196","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}
Purpose: Laryngeal microsurgery is a challenging surgery because of the risk of airway complications. Therefore, extubation is of significant importance. We aimed to investigate the effect of magnesium sulfate on extubation quality, recovery features, and complications.
Design: A prospective, randomized, controlled clinical trial.
Methods: Ninety-eight adult patients scheduled for larynx laser microsurgery were included and randomly allocated to two groups to receive magnesium sulfate 30 mg/kg in 100 mL saline infusion (maximum 2 g) (group M) or saline 100 mL (group S) before induction of anesthesia. Anesthesia induction was performed with propofol 2 mg/kg, rocuronium 0.6 mg/kg, remifentanil 0.5 mcg/kg, and general anesthesia maintained with total intravenous anesthesia (propofol 3 to 7 mg/kg, remifentanil 0.05 to 0.1 mcg/kg/min, and O2/air 30/70 mixture). A train of four was used for neuromuscular monitoring. Extubation quality score, extubation time, postanesthesia care unit time, numerical rating scale, and complications were recorded.
Findings: Extubation quality scores were better in group M than group S (46 patients compared to 28 patients who had mild or no cough, P < .001, respectively). Extubation time was similar between groups. Postanesthesia care unit time was 15.7 ± 2.9 minutes in group M and 13.4 ± 4.6 minutes in group S, respectively (P = .01). Numerical rating scale scores were lower in group M than in group S (1 (1 to 2), 3 (2 to 3.5), respectively, P < .001).
Conclusions: Magnesium sulfate before induction of anesthesia resulted in better extubation quality scores without delayed recovery and positively affected postoperative analgesia.
{"title":"The Effect of Magnesium Sulfate on Extubation Quality Score and Recovery in Larynx Laser Microsurgery: A Prospective, Randomized, Controlled Study.","authors":"Suat Aslan, İstemihan Karakayalı, Feride Karacaer, Demet Laflı Tunay, Murat Ilgınel, Elvan Onan, Ebru Biricik","doi":"10.1016/j.jopan.2024.09.004","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.004","url":null,"abstract":"<p><strong>Purpose: </strong>Laryngeal microsurgery is a challenging surgery because of the risk of airway complications. Therefore, extubation is of significant importance. We aimed to investigate the effect of magnesium sulfate on extubation quality, recovery features, and complications.</p><p><strong>Design: </strong>A prospective, randomized, controlled clinical trial.</p><p><strong>Methods: </strong>Ninety-eight adult patients scheduled for larynx laser microsurgery were included and randomly allocated to two groups to receive magnesium sulfate 30 mg/kg in 100 mL saline infusion (maximum 2 g) (group M) or saline 100 mL (group S) before induction of anesthesia. Anesthesia induction was performed with propofol 2 mg/kg, rocuronium 0.6 mg/kg, remifentanil 0.5 mcg/kg, and general anesthesia maintained with total intravenous anesthesia (propofol 3 to 7 mg/kg, remifentanil 0.05 to 0.1 mcg/kg/min, and O<sub>2</sub>/air 30/70 mixture). A train of four was used for neuromuscular monitoring. Extubation quality score, extubation time, postanesthesia care unit time, numerical rating scale, and complications were recorded.</p><p><strong>Findings: </strong>Extubation quality scores were better in group M than group S (46 patients compared to 28 patients who had mild or no cough, P < .001, respectively). Extubation time was similar between groups. Postanesthesia care unit time was 15.7 ± 2.9 minutes in group M and 13.4 ± 4.6 minutes in group S, respectively (P = .01). Numerical rating scale scores were lower in group M than in group S (1 (1 to 2), 3 (2 to 3.5), respectively, P < .001).</p><p><strong>Conclusions: </strong>Magnesium sulfate before induction of anesthesia resulted in better extubation quality scores without delayed recovery and positively affected postoperative analgesia.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142873234","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}
Pub Date : 2024-12-19DOI: 10.1016/j.jopan.2024.08.021
Dilay Hacidursunoğlu Erbaş, Fatma Eti Aslan
Purpose: To develop the Safe Use of Technology in the Operating Room Scale (SUTORS) and evaluation of its psychometric properties.
Design: The study was a scale development study including the validity and reliability analyses.
Methods: The study was conducted in training and research hospitals located in Istanbul, Turkey. The sample population comprised all health care professionals working in the operating rooms of the relevant hospitals. A total of 54 health care professionals were recruited for the preliminary implementation, and those who participated were excluded from the final sample. The sample size consisted of 437 health care professionals. The study collected data using the Healthcare Professional Identification Form and the SUTORS. The scope, content, and language appropriateness were evaluated. The data were then analyzed using various statistical methods, including Cronbach's α, halving, principal component analysis, confirmatory factor analysis, discriminative item analysis, cumulative explained variance, and composite reliability values.
Findings: The health care professionals had an average age of 30.69 ± 6.64 years and had been working in the operating room for an average of 5.94 ± 5.86 years, and 39.6% of them were nurses. The scale draft consisted of 134 items and 3 sections in total, and a 53-item scale was constructed as a result of content and linguistic validity. On completion of the explanatory and confirmatory factor analyses, the SUTORS, consisting of 45 items and 3 separate scale sections, was finalized. The scale comprises 45 items and 3 distinct sections for general applications, surgical team, and anesthesia team. Cronbach's α values were calculated for each section, resulting in 0.928, 0.906, and 0.946, respectively.
Conclusions: All three sections of the SUTORS are valid and reliable measures that can be used to assess the safe use of technology in the operating room.
{"title":"Safe Use of Technology in the Operating Room Scale: Development and Psychometric Properties.","authors":"Dilay Hacidursunoğlu Erbaş, Fatma Eti Aslan","doi":"10.1016/j.jopan.2024.08.021","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.08.021","url":null,"abstract":"<p><strong>Purpose: </strong>To develop the Safe Use of Technology in the Operating Room Scale (SUTORS) and evaluation of its psychometric properties.</p><p><strong>Design: </strong>The study was a scale development study including the validity and reliability analyses.</p><p><strong>Methods: </strong>The study was conducted in training and research hospitals located in Istanbul, Turkey. The sample population comprised all health care professionals working in the operating rooms of the relevant hospitals. A total of 54 health care professionals were recruited for the preliminary implementation, and those who participated were excluded from the final sample. The sample size consisted of 437 health care professionals. The study collected data using the Healthcare Professional Identification Form and the SUTORS. The scope, content, and language appropriateness were evaluated. The data were then analyzed using various statistical methods, including Cronbach's α, halving, principal component analysis, confirmatory factor analysis, discriminative item analysis, cumulative explained variance, and composite reliability values.</p><p><strong>Findings: </strong>The health care professionals had an average age of 30.69 ± 6.64 years and had been working in the operating room for an average of 5.94 ± 5.86 years, and 39.6% of them were nurses. The scale draft consisted of 134 items and 3 sections in total, and a 53-item scale was constructed as a result of content and linguistic validity. On completion of the explanatory and confirmatory factor analyses, the SUTORS, consisting of 45 items and 3 separate scale sections, was finalized. The scale comprises 45 items and 3 distinct sections for general applications, surgical team, and anesthesia team. Cronbach's α values were calculated for each section, resulting in 0.928, 0.906, and 0.946, respectively.</p><p><strong>Conclusions: </strong>All three sections of the SUTORS are valid and reliable measures that can be used to assess the safe use of technology in the operating room.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142873201","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}
Pub Date : 2024-12-18DOI: 10.1016/j.jopan.2024.09.008
Özlem Doğu, Öznur Tiryaki, Emin Levent Aksoy, Mehmet Sühha Bostancı
Purpose: This study aimed to compare the effect of povidone iodine (PI) and chlorhexidine gluconate (CG) shower groups on the healing process in cesarean section operations.
Design: Randomized controlled trial.
Methods: Patients were recruited from Gynecology and Obstetrics Hospital in Turkey between February and May 2021. In total, 102 pregnant women were scheduled for elective cesareans. They were randomly divided into PI group (A), CG group (B), and CG shower group (C) operated by three gynecology and obstetrics physicians. During the data collection, a demographics form, an incision site evaluation form, a visual analog scale (VAS), and a postpartum comfort questionnaire (PPCQ) were used. Data from the in-house blinding study to avoid bias and follow-up of the women were done for 7-day duration following postnatal to assess postoperative comfort, pain, and wound complications.
Findings: The VAS, pain, erythema, warm, edema, discharge, and wound opening were statistically evaluated at the incision site with 3 measurements for each of the groups. There was a significant difference in the CG groups (2 and 3) (VAS P < .000, erythema P < .05, and edema P < .05). The mean PPCQ score was higher in the CG groups (2 and 3) and showed a significant difference compared with the PI group (P < .000).
Conclusions: Due to the antiseptic and nonirritating properties of CG, showering 6 hours before the operation contributed to the wound healing process according to the incision site evaluation form and to a corresponding increased PPCQ level of the mother in the postoperative period.
{"title":"The Effect of Using Chlorhexidine Gluconate and Povidone Iodine Solution on the Healing Process Before a Cesarean Section.","authors":"Özlem Doğu, Öznur Tiryaki, Emin Levent Aksoy, Mehmet Sühha Bostancı","doi":"10.1016/j.jopan.2024.09.008","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.008","url":null,"abstract":"<p><strong>Purpose: </strong>This study aimed to compare the effect of povidone iodine (PI) and chlorhexidine gluconate (CG) shower groups on the healing process in cesarean section operations.</p><p><strong>Design: </strong>Randomized controlled trial.</p><p><strong>Methods: </strong>Patients were recruited from Gynecology and Obstetrics Hospital in Turkey between February and May 2021. In total, 102 pregnant women were scheduled for elective cesareans. They were randomly divided into PI group (A), CG group (B), and CG shower group (C) operated by three gynecology and obstetrics physicians. During the data collection, a demographics form, an incision site evaluation form, a visual analog scale (VAS), and a postpartum comfort questionnaire (PPCQ) were used. Data from the in-house blinding study to avoid bias and follow-up of the women were done for 7-day duration following postnatal to assess postoperative comfort, pain, and wound complications.</p><p><strong>Findings: </strong>The VAS, pain, erythema, warm, edema, discharge, and wound opening were statistically evaluated at the incision site with 3 measurements for each of the groups. There was a significant difference in the CG groups (2 and 3) (VAS P < .000, erythema P < .05, and edema P < .05). The mean PPCQ score was higher in the CG groups (2 and 3) and showed a significant difference compared with the PI group (P < .000).</p><p><strong>Conclusions: </strong>Due to the antiseptic and nonirritating properties of CG, showering 6 hours before the operation contributed to the wound healing process according to the incision site evaluation form and to a corresponding increased PPCQ level of the mother in the postoperative period.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142848104","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}
Pub Date : 2024-12-06DOI: 10.1016/j.jopan.2024.08.023
Xin Liu, Ju Gao
Purpose: The purpose of this study was to systematically encapsulate the array of discomfort symptoms ensuing from sedative-administered colonoscopy, with the overarching objective of formulating screening criteria conducive to the identification of the core clinical symptoms characterizing postoperative fatigue syndrome (POFS).
Design: A single-center descriptive study.
Methods: We selected patients who had undergone a sedative-administered colonoscopy and conducted a telephone follow-up to examine the occurrence of postoperative discomfort symptoms.The Common Terminology Criteria for Adverse Events (Version 5.0) was used to determine the discomfort symptoms and preliminarily assess the severity by comparing the collected patient feedback information. Basic patient information was collected at the anesthesia clinic or at the endoscopy center. The initial telephone follow-ups were conducted 24 hours after the examination.
Findings: The analysis involved 542 patients who successfully completed the investigation, yielding a compilation of 19 postoperative discomfort symptoms, encompassing fatigue, lethargy, dizziness, and others. Following a meticulous screening process, the identified core clinical symptoms of POFS were narrowed down to fatigue, lethargy, dizziness, and headache.
Conclusions: The diagnostic criteria for POFS should encompass the presence of fatigue, lethargy, dizziness, and headache, as these symptoms constitute the core clinical manifestations.
{"title":"Examination of Core Clinical Symptoms of Postoperative Fatigue Syndrome Following Colonoscopy With Sedation.","authors":"Xin Liu, Ju Gao","doi":"10.1016/j.jopan.2024.08.023","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.08.023","url":null,"abstract":"<p><strong>Purpose: </strong>The purpose of this study was to systematically encapsulate the array of discomfort symptoms ensuing from sedative-administered colonoscopy, with the overarching objective of formulating screening criteria conducive to the identification of the core clinical symptoms characterizing postoperative fatigue syndrome (POFS).</p><p><strong>Design: </strong>A single-center descriptive study.</p><p><strong>Methods: </strong>We selected patients who had undergone a sedative-administered colonoscopy and conducted a telephone follow-up to examine the occurrence of postoperative discomfort symptoms.The Common Terminology Criteria for Adverse Events (Version 5.0) was used to determine the discomfort symptoms and preliminarily assess the severity by comparing the collected patient feedback information. Basic patient information was collected at the anesthesia clinic or at the endoscopy center. The initial telephone follow-ups were conducted 24 hours after the examination.</p><p><strong>Findings: </strong>The analysis involved 542 patients who successfully completed the investigation, yielding a compilation of 19 postoperative discomfort symptoms, encompassing fatigue, lethargy, dizziness, and others. Following a meticulous screening process, the identified core clinical symptoms of POFS were narrowed down to fatigue, lethargy, dizziness, and headache.</p><p><strong>Conclusions: </strong>The diagnostic criteria for POFS should encompass the presence of fatigue, lethargy, dizziness, and headache, as these symptoms constitute the core clinical manifestations.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142787454","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}
Pub Date : 2024-12-06DOI: 10.1016/j.jopan.2024.09.005
Yahya Agus, Gulsah Kose
Purpose: This study aimed to investigate the impact of music on preoperative fear and anxiety in patients undergoing thyroid surgery.
Design: This was a randomized controlled prospective study.
Methods: This study was conducted at the general surgery clinic of a training and research hospital from April 10, 2021 to April 1, 2022. The study included 76 patients who were scheduled for thyroid surgery and were randomized into equal-sized intervention (music) and control groups. Participants in the music group were asked to listen to music for at least 30 minutes every 3 hours until surgery. Both groups completed the Surgical Fear Questionnaire (SFQ) and Anxiety Specific to Surgery Questionnaire (ASSQ) 24 hours before surgery and 1 hour before transfer to the operating room. Descriptive statistics, χ2 tests, independent and paired sample t tests, one-way analysis of variance, and Pearson's correlation were used for data analysis.
Findings: Although the post-test scores of both the music and control groups on the SFQ and ASSQ were significantly lower than the pretest scores, there was no significant difference between the two groups. Additionally, there was no significant difference between the sociodemographic characteristics and the obtained SFQ and ASSQ scores. A moderate positive correlation was found between the SFQ and ASSQ scores.
Conclusions: The findings indicate that listening to music did not reduce preoperative fear and anxiety in patients undergoing thyroid surgery.
{"title":"The Effect of Music on Preoperative Fear and Anxiety in Patients Undergoing Thyroid Surgery: A Randomized Controlled Trial.","authors":"Yahya Agus, Gulsah Kose","doi":"10.1016/j.jopan.2024.09.005","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.09.005","url":null,"abstract":"<p><strong>Purpose: </strong>This study aimed to investigate the impact of music on preoperative fear and anxiety in patients undergoing thyroid surgery.</p><p><strong>Design: </strong>This was a randomized controlled prospective study.</p><p><strong>Methods: </strong>This study was conducted at the general surgery clinic of a training and research hospital from April 10, 2021 to April 1, 2022. The study included 76 patients who were scheduled for thyroid surgery and were randomized into equal-sized intervention (music) and control groups. Participants in the music group were asked to listen to music for at least 30 minutes every 3 hours until surgery. Both groups completed the Surgical Fear Questionnaire (SFQ) and Anxiety Specific to Surgery Questionnaire (ASSQ) 24 hours before surgery and 1 hour before transfer to the operating room. Descriptive statistics, χ<sup>2</sup> tests, independent and paired sample t tests, one-way analysis of variance, and Pearson's correlation were used for data analysis.</p><p><strong>Findings: </strong>Although the post-test scores of both the music and control groups on the SFQ and ASSQ were significantly lower than the pretest scores, there was no significant difference between the two groups. Additionally, there was no significant difference between the sociodemographic characteristics and the obtained SFQ and ASSQ scores. A moderate positive correlation was found between the SFQ and ASSQ scores.</p><p><strong>Conclusions: </strong>The findings indicate that listening to music did not reduce preoperative fear and anxiety in patients undergoing thyroid surgery.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142802960","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}
Purpose: In response to nurse concerns of the need for additional support from unit nursing assistants (NA) at the bedside, we set a goal to improve RN satisfaction with the role of the NA in the postanesthesia care unit (PACU).
Design: Prospective pre/post design.
Methods: Using LEAN methodology, the NA role was expanded to encompass their full scope of practice at the bedside, and the responsibility of performing patient transport from the PACU was reallocated to a Centralized Transport Service over a 6-month period.
Findings: The total number of transports performed by NA decreased by approximately 20%. Time spent waiting for a Centralized Transporter decreased from an average of 56 to 11 minutes. RN satisfaction increased in the 3 areas explored, with a 12.5% increase in median overall satisfaction with the NA role. Our facility's Hospital Consumer Assessment of Healthcare Providers and Systems scores also increased from previous months after this project, alluding to more effective care delivered to patients in the PACU.
Conclusions: Realignment of roles can promote efficiency and throughput. Communication fosters teamwork and can improve staff satisfaction.
{"title":"Influence of the Nursing Assistant Role in Nurse Satisfaction, Efficiency, and Patient Satisfaction in the Postanesthesia Care Unit.","authors":"Jill Setaro, Edana Ree, Jan Johrden, Allison Julian, Nicole Cruse, Jill Agostino","doi":"10.1016/j.jopan.2024.08.024","DOIUrl":"https://doi.org/10.1016/j.jopan.2024.08.024","url":null,"abstract":"<p><strong>Purpose: </strong>In response to nurse concerns of the need for additional support from unit nursing assistants (NA) at the bedside, we set a goal to improve RN satisfaction with the role of the NA in the postanesthesia care unit (PACU).</p><p><strong>Design: </strong>Prospective pre/post design.</p><p><strong>Methods: </strong>Using LEAN methodology, the NA role was expanded to encompass their full scope of practice at the bedside, and the responsibility of performing patient transport from the PACU was reallocated to a Centralized Transport Service over a 6-month period.</p><p><strong>Findings: </strong>The total number of transports performed by NA decreased by approximately 20%. Time spent waiting for a Centralized Transporter decreased from an average of 56 to 11 minutes. RN satisfaction increased in the 3 areas explored, with a 12.5% increase in median overall satisfaction with the NA role. Our facility's Hospital Consumer Assessment of Healthcare Providers and Systems scores also increased from previous months after this project, alluding to more effective care delivered to patients in the PACU.</p><p><strong>Conclusions: </strong>Realignment of roles can promote efficiency and throughput. Communication fosters teamwork and can improve staff satisfaction.</p>","PeriodicalId":49028,"journal":{"name":"Journal of Perianesthesia Nursing","volume":" ","pages":""},"PeriodicalIF":1.6,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142773852","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}