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Implementation of a wake-up and unknown symptom onset stroke protocol 唤醒和未知症状发作中风方案的实施
Pub Date : 2022-10-19 DOI: 10.5430/cns.v10n1p32
B. Jennings, E. Creel, D. Lee, G. Vidal
Background: Establishing a symptom onset timeline for stroke patients is one of the essential aspects of thrombolytic therapy. Implementing an MRI protocol can potentially increase the rate of thrombolytic therapy and expand treatment to patients who would otherwise be excluded.Objective: This project aimed to increase the rate of thrombolytic therapy by incorporating an additional layer of evaluation within the established acute stroke code process for patients with wake-up stroke (WUS) or unknown symptom onset stroke.Methods: Patients 18 years of age and older who presented as WUS eligible for thrombolytic therapy underwent acute MRI. Patients with a diffusion weighted image and fluid attenuated inversion recovery mismatch (DWI-FLAIR Mismatch) on MRI were treated with thrombolytic therapy.Results: Chi-square test of independence showed patients who underwent the MRI protocol (N = 35) had a higher proportion of alteplase (tissue plasminogen activator,tPA) treatment when compared to a similar sample (N = 44) from 2019 acute stoke logs; ꭓ2 (1, N = 79) = 8.16, p = .006. Six patients received thrombolytic. Safety showed no symptomatic intracerebral hemorrhage (sICH) or deaths.
背景:为脑卒中患者建立症状发作时间表是溶栓治疗的重要方面之一。实施核磁共振成像方案可以潜在地提高溶栓治疗的率,并扩大治疗范围,否则将被排除在外的患者。目的:本项目旨在通过在已建立的急性卒中编码过程中对醒脑(WUS)或未知症状发作的卒中患者纳入额外的评估层来提高溶栓治疗的率。方法:18岁及以上的WUS符合溶栓治疗条件的患者进行急性MRI检查。在MRI上出现扩散加权图像和液体衰减反转恢复失配(DWI-FLAIR失配)的患者接受溶栓治疗。结果:独立性卡方检验显示,与2019年急性卒中日志中的类似样本(N = 44)相比,接受MRI方案的患者(N = 35)接受阿替普酶(组织纤溶酶原激活剂,tPA)治疗的比例更高;ꭓ2 (1,N = 79) = 8.16, p = 0.006。6例患者接受溶栓治疗。安全性显示无症状性脑出血(sICH)或死亡。
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引用次数: 0
Pandemic-related pregnancy stress among a group of Egyptian women during COVID-19 pandemic COVID-19大流行期间一群埃及妇女与大流行相关的妊娠压力
Pub Date : 2022-09-28 DOI: 10.5430/cns.v10n1p22
Dina Mohamed Abuelkheir, A. El-Nemer
Objective: Prenatal maternal stress is a known risk factor for preterm birth, low birth weight, and infant health problems and may have long-term impacts on the offspring. The study aimed to assess pandemic-related pregnancy stress among a group of Egyptian women during COVID-19 pandemic.Methods: The study used a descriptive cross-sectional design on 100 pregnant women who were selected using the purposive sample technique. The study was conducted at antenatal clinics of the Obstetrics and Gynecology Department at Mansoura University Hospitals, Mansoura city, Dakahlia governorate, Egypt. Two tools were utilized for gathering data; a structured interviewing questionnaire was used to assess the socio-demographic and reproductive characteristics of the studied pregnant women and the Pandemic-Related Pregnancy Stress scale was used to assess pandemic-related pregnancy stress among the studied pregnant women.Results: The study findings revealed that less than half of pregnant women during the COVID-19 pandemic reported elevated levels of stress related to feeling unprepared for childbirth and around three-quarters experienced high stress related to perinatal infection.Conclusions: The study concluded that the studied pregnant women during the COVID-19 pandemic had high levels of stress related to inadequate preparation for childbirth and stress related to the potential for perinatal infection. In addition, infection stress was more prevalent than preparedness stress among the studied pregnant women. It is recommended to provide prenatal educational programs related to coping strategies during the pandemic.
目的:产前母亲压力是早产、低出生体重和婴儿健康问题的一个已知风险因素,并可能对后代产生长期影响。该研究旨在评估新冠肺炎大流行期间一组埃及妇女与流行病相关的妊娠压力。方法:本研究采用描述性横断面设计,对100名孕妇进行了研究,这些孕妇是通过有目的的抽样技术选择的。这项研究是在埃及达卡利亚省曼苏拉市曼苏拉大学医院妇产科的产前诊所进行的。使用了两个工具来收集数据;使用结构化访谈问卷评估研究孕妇的社会人口统计学和生殖特征,并使用流行病相关妊娠压力量表评估研究孕妇中与流行病相关的妊娠压力。结果:研究结果显示,在新冠肺炎大流行期间,不到一半的孕妇报告称,与对分娩毫无准备有关的压力水平升高,约四分之三的孕妇经历了与围产期感染有关的高压力。结论:研究得出的结论是,新冠肺炎大流行期间,受试孕妇的压力水平较高,与分娩准备不足有关,而压力与围产期感染的可能性有关。此外,在所研究的孕妇中,感染压力比准备压力更普遍。建议在疫情期间提供与应对策略相关的产前教育计划。
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引用次数: 0
Patients’ perspective on early discharge with drain in situ after breast cancer surgery 乳腺癌术后原位引流早期出院患者的看法
Pub Date : 2022-05-23 DOI: 10.5430/cns.v10n1p14
Laila Al-Balushi, Suad Al-Kharosui
Due to the increasing number of breast cancer (BC) cases in Oman and the impact of the novel coronavirus disease 2019 (COVID-19) on bed situation in the hospital, a policy of early discharge (ED) with drain after BC surgery was initiated at one of the tertiary hospitals in Oman. The uniqueness of this policy is no home visit follow-up conducted after discharge and the main mode of communication was through social media account (Instagram media). This policy then was evaluated by conducting a quasi-experimental study using a survey with ten open and closed-ended questions, five questions to explore patient experience using a five-point Likert scale. A total of 41 female patients responded to the survey. Almost 96% of the participants stated being well informed about drain care pre- and post-surgery at home. 9% of the participants developed early sign of infection and was managed at out-patient clinics. Participants with bilateral drains expressed more pain than those with single drain. 90% stated satisfied being discharged with breast drain whereas 10% preferred to stay in the hospital until the drains were removed. This study found that the policy of ED with a drain after breast cancer (BC) surgery is practical and well-accepted by most patients. The role of breast nurse and presence of family and institutional support enhanced the success of the policy implementation. To optimize patient care, conducting a training program by breast nurse for nurses at local health centres about care management of patients with drain could improve care and enhance patient satisfaction.
由于阿曼乳腺癌(BC)病例不断增加,以及2019年新型冠状病毒病(COVID-19)对医院床位状况的影响,阿曼一家三级医院启动了BC手术后提前出院(ED)并引流的政策。该政策的独特之处在于出院后不进行家访随访,主要沟通方式是通过社交媒体账号(Instagram媒体)。然后,通过进行一项准实验研究来评估这一政策,该研究使用了一个带有十个开放式和封闭式问题的调查,五个问题使用五点李克特量表来探索患者体验。共有41名女性患者参与了调查。几乎96%的参与者表示对术前和术后在家引流护理有充分的了解。9%的参与者出现了感染的早期迹象,并在门诊进行了治疗。双侧引流的参与者比单侧引流的参与者表现出更多的疼痛。90%的人表示对乳房引流管出院感到满意,而10%的人更愿意留在医院直到引流管被清除。本研究发现,在乳腺癌(BC)手术后进行ED引流是可行的,并为大多数患者所接受。母乳护理人员的作用以及家庭和机构支持的存在促进了政策执行的成功。为优化患者护理,开展母乳护理人员对地方保健中心护士的护理管理培训,可以改善护理,提高患者满意度。
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引用次数: 0
Weaning success among COPD patients following ventilator care bundle application 应用呼吸机护理捆绑包治疗COPD患者的断奶成功率
Pub Date : 2022-03-01 DOI: 10.5430/cns.v10n1p1
E. Hammouda, H. Ahmed, Amro Moawad, Nahed Kandeel
Objective: Several studies evaluated the effectiveness of the ventilator care bundle in reducing the occurrence of ventilatorassociated pneumonia. The ventilator care bundle efficacy in early mechanical ventilation weaning has not been adequately assessed. The study aimed to investigate the weaning success among chronic obstructive pulmonary disease (COPD) patients following ventilator care bundle application.Methods: This study is quasi-experimental, recruiting 80 mechanically ventilated COPD patients (40 patients for each bundle and control group). It was conducted at the respiratory intensive care units (ICUs) at Mansoura University Hospital, Egypt. Data were collected using a mechanically ventilated patient (MVP) assessment tool, a ventilator care bundle compliance checklist, and MVP evaluation tools based on the Burns’ Wean Assessment Program (BWAP) checklist and the patient’s ventilation indicators.Results: The results revealed that almost 75% of the bundle group was successfully weaned from invasive mechanical ventilation at the first attempt of the spontaneous breathing trial compared with 32.5% of the control group. The ventilation duration and length of ICU stay were reduced in the bundle compared with the control group.Conclusions: The bundle group demonstrated higher weaning scores than the control group. Therefore, we recommend the integration of the ventilator care bundle in the weaning trial of MVPs to accelerate weaning and reduce the duration of mechanical ventilation.
目的:几项研究评估了呼吸机护理包在减少呼吸机相关性肺炎发生方面的有效性。呼吸机护理包在早期机械通气脱机中的效果尚未得到充分评估。本研究旨在探讨慢性阻塞性肺疾病(COPD)患者应用呼吸机护理捆绑包后的脱机成功率。方法:本研究采用准实验模式,招募机械通气COPD患者80例(每组40例,对照组40例)。它是在埃及曼苏拉大学医院的呼吸重症监护病房进行的。使用机械通气患者(MVP)评估工具、呼吸机护理包依从性检查表和基于烧伤断奶评估程序(BWAP)检查表和患者通气指标的MVP评估工具收集数据。结果:结果显示,与对照组的32.5%相比,捆绑组在首次尝试自主呼吸试验时成功脱离有创机械通气的比例接近75%。与对照组相比,治疗组通气时间和ICU住院时间均有所减少。结论:捆绑组断奶评分高于对照组。因此,我们建议在mvp的脱机试验中整合呼吸机护理包,以加速脱机并减少机械通气的持续时间。
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引用次数: 0
Converting threats from COVID-19 in long term care into opportunities for improvement 将COVID-19对长期护理的威胁转化为改善的机会
Pub Date : 2022-01-05 DOI: 10.5430/cns.v9n2p36
Leona Konieczny
The effects of the COVID-19 pandemic on long term care (LTC) have been published in the literature and experienced by residents, their support persons and nursing staff. The morbidity and mortality, as well as the threats of isolation and psychosocial distress continue. Both LTC residents and staff experience physiological and psychological impacts. Nurses can use the current threats produced by the pandemic to advocate for alternate models of care and reduced isolation for residents. The pandemic is an opportunity for nursing advocacy in LTC for shared governance and empowerment, involvement in policy development, and oversight in policy implementation. Nurses are presented with the opportunities for advocacy related to resources and reshaping the paradigm of residential care for older adults.
新冠肺炎大流行对长期护理(LTC)的影响已发表在文献中,居民、其支持人员和护理人员也经历过这种影响。发病率和死亡率以及孤立和心理痛苦的威胁仍在继续。LTC居民和工作人员都会经历生理和心理影响。护士可以利用当前疫情带来的威胁,倡导替代护理模式,减少对居民的隔离。疫情为LTC的护理宣传提供了一个机会,以实现共同治理和赋权、参与政策制定和监督政策实施。护士们有机会进行与资源相关的宣传,并重塑老年人住院护理的模式。
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引用次数: 0
Perceptions, beliefs and societal factors impacting on exclusive breastfeeding of primiparous mothers: An exploratory study 初产妇纯母乳喂养的认知、信仰和社会因素影响:一项探索性研究
Pub Date : 2021-10-31 DOI: 10.5430/cns.v9n2p30
Fahima Al Harthy, Asma Al Zaabi, Najat Al Ajmi, Afaf Elshiekh, Kamila Al Alawi, Lamia Mahmoud, Mudhar Al Adawi
This study aims to explore the perceptions of Omani primiparous mothers towards exclusive breastfeeding. A qualitative exploratory study was conducted at Royal Hospital between March and November 2020. Purposive sampling was applied to recruit newly delivered mothers and face to face interview was done for data collection. Interview protocol along with prompts was used to guide researchers during the interview. Specific questions were administered to assess mothers’ knowledge of exclusive breastfeeding, sources of information, influencing factors toward exclusive breastfeeding and intention to exclusively breastfeeding. Thematic analysis revealed six themes, namely: the effects of lack of knowledge on the mother perception towards exclusive BF, family members influencing the decision-making process regarding BF, impact of social life on BF practices, the effect of mother’s beliefs on exclusive BF, factor that affect BF practice in early days, mother’s concern regarding emotional support for successful exclusive BF. This study revealed a lack of basic knowledge on exclusive breastfeeding among mothers. Moreover, grandmothers and husbands were found to be the most influential family members on the decision regarding exclusive breastfeeding. Mothers had major concerns regarding milk adequacy in the first few days after delivery and emotional support plays a major role in encouraging exclusive breastfeeding.
本研究旨在探讨阿曼初产妇对纯母乳喂养的看法。2020年3月至11月在皇家医院进行了一项定性探索性研究。采用有目的抽样的方法招募新分娩母亲,并采用面对面访谈的方式收集数据。在访谈过程中,使用访谈协议和提示来指导研究人员。通过具体的问题来评估母亲对纯母乳喂养的知识、信息来源、纯母乳喂养的影响因素和纯母乳喂养的意图。主题分析揭示了六个主题,分别是:知识缺乏对母亲对专任男朋友认知的影响、家庭成员对专任男朋友决策过程的影响、社会生活对专任男朋友实践的影响、母亲信仰对专任男朋友实践的影响、早期影响专任男朋友实践的因素、母亲对专任男朋友成功的情感支持的关注。这项研究表明,母亲缺乏纯母乳喂养的基本知识。此外,祖母和丈夫被认为是决定纯母乳喂养的最具影响力的家庭成员。在分娩后的最初几天,母亲们主要担心母乳是否充足,而情感支持在鼓励纯母乳喂养方面发挥着重要作用。
{"title":"Perceptions, beliefs and societal factors impacting on exclusive breastfeeding of primiparous mothers: An exploratory study","authors":"Fahima Al Harthy, Asma Al Zaabi, Najat Al Ajmi, Afaf Elshiekh, Kamila Al Alawi, Lamia Mahmoud, Mudhar Al Adawi","doi":"10.5430/cns.v9n2p30","DOIUrl":"https://doi.org/10.5430/cns.v9n2p30","url":null,"abstract":"This study aims to explore the perceptions of Omani primiparous mothers towards exclusive breastfeeding. A qualitative exploratory study was conducted at Royal Hospital between March and November 2020. Purposive sampling was applied to recruit newly delivered mothers and face to face interview was done for data collection. Interview protocol along with prompts was used to guide researchers during the interview. Specific questions were administered to assess mothers’ knowledge of exclusive breastfeeding, sources of information, influencing factors toward exclusive breastfeeding and intention to exclusively breastfeeding. Thematic analysis revealed six themes, namely: the effects of lack of knowledge on the mother perception towards exclusive BF, family members influencing the decision-making process regarding BF, impact of social life on BF practices, the effect of mother’s beliefs on exclusive BF, factor that affect BF practice in early days, mother’s concern regarding emotional support for successful exclusive BF. This study revealed a lack of basic knowledge on exclusive breastfeeding among mothers. Moreover, grandmothers and husbands were found to be the most influential family members on the decision regarding exclusive breastfeeding. Mothers had major concerns regarding milk adequacy in the first few days after delivery and emotional support plays a major role in encouraging exclusive breastfeeding.","PeriodicalId":72616,"journal":{"name":"Clinical nursing studies","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46031565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of implementing epilepsy educational guidelines on nurses’ performance and patients’ outcomes 实施癫痫教育指导方针对护士工作表现和患者预后的影响
Pub Date : 2021-10-17 DOI: 10.5430/cns.v9n2p20
Walaa Zahran, W. Sherif, H. Mohamed
Objective: Epilepsy is considered one of the most common neurological diseases affecting 65 people worldwide. People with epilepsy are more likely to get injured and die prematurely than the general population. Nurses must acquire professional knowledge related to epilepsy and should strengthen patients to play a more active role in their care to improve their understanding of their diseases. The study aimed to evaluate implementing epilepsy educational guidelines on nurses’ performance and patients’ outcomes.Methods: A quasi-experimental research design was conducted at the Neurology department in Mansoura University Hospital. This study sample is a convenient sample of 28 nurses and a purposive sample of 60 adult patients with epilepsy who attend the neurological department in Mansoura University Hospital.Results: The results indicate a significant improvement in nurses’ knowledge and practice regarding epilepsy. Also, it helped to improve patients’ knowledge and thus promoted epilepsy self-management behaviors in the study group.Conclusions: The designed nursing guidelines have achieved their objectives by improving nurses’ knowledge and practice regarding epileptic patient care, in addition to improving patients’ knowledge and epilepsy self-management scale for the study group compared with the control group.
目的:癫痫被认为是最常见的神经系统疾病之一,影响全世界65人。癫痫患者比一般人群更容易受伤和过早死亡。护士必须掌握癫痫相关的专业知识,加强患者在护理中发挥更积极的作用,提高对疾病的认识。本研究旨在评估实施癫痫教育指南对护士绩效和患者预后的影响。方法:在曼苏拉大学附属医院神经内科进行准实验研究设计。本研究样本是曼苏拉大学医院神经内科的28名护士的方便样本和60名成年癫痫患者的目的样本。结果:结果表明护士对癫痫的知识和实践有了明显的提高。也有助于提高患者的知识,从而促进研究组的癫痫自我管理行为。结论:与对照组相比,研究组患者知识水平和癫痫自我管理量表均有所提高,研究组护士癫痫病人护理知识和实践水平均有所提高,达到了设计护理指南的目的。
{"title":"Effect of implementing epilepsy educational guidelines on nurses’ performance and patients’ outcomes","authors":"Walaa Zahran, W. Sherif, H. Mohamed","doi":"10.5430/cns.v9n2p20","DOIUrl":"https://doi.org/10.5430/cns.v9n2p20","url":null,"abstract":"Objective: Epilepsy is considered one of the most common neurological diseases affecting 65 people worldwide. People with epilepsy are more likely to get injured and die prematurely than the general population. Nurses must acquire professional knowledge related to epilepsy and should strengthen patients to play a more active role in their care to improve their understanding of their diseases. The study aimed to evaluate implementing epilepsy educational guidelines on nurses’ performance and patients’ outcomes.Methods: A quasi-experimental research design was conducted at the Neurology department in Mansoura University Hospital. This study sample is a convenient sample of 28 nurses and a purposive sample of 60 adult patients with epilepsy who attend the neurological department in Mansoura University Hospital.Results: The results indicate a significant improvement in nurses’ knowledge and practice regarding epilepsy. Also, it helped to improve patients’ knowledge and thus promoted epilepsy self-management behaviors in the study group.Conclusions: The designed nursing guidelines have achieved their objectives by improving nurses’ knowledge and practice regarding epileptic patient care, in addition to improving patients’ knowledge and epilepsy self-management scale for the study group compared with the control group.","PeriodicalId":72616,"journal":{"name":"Clinical nursing studies","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45341613","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nursing and medical students’ perceptions of interprofessional education and social interactions: A qualitative study 护理和医学生对跨专业教育和社会互动的认知:一项定性研究
Pub Date : 2021-07-05 DOI: 10.5430/CNS.V9N2P12
Maryam Alaradi, Maryam Abdulsalam, Khalifa Albenjasim, Omar Ahmed Alwahoush, Salwa Abdulmalek, Wadha Alsherooqi
Objective: Interprofessional education (IPE) is becoming increasingly popular and highly recommended for inclusion in curricula for healthcare professionals. Implementing IPE may improve students’ knowledge, skills, and attitudes toward collaborative teamwork, thereby improving health services and health outcomes for patients. This work aimed to explore nursing and medical students’ perceptions of IPE and social interactions.Methods: A qualitative study was conducted using a purposive sample of eight nursing and medical students. Data were collected via two semi-structured focus-group sessions and were analyzed using inductive thematic analysis.Results: Five main themes and seven subthemes emerged. The main themes were (1) IPE meaning, (2) IPE barriers, (3) IPE facilitators, (4) social interactions, and (5) bridging gaps in students’ perspectives. We found that students from both schools had a clear understanding of the definition and importance of IPE. Students reported that lack of interaction is an issue that they have never attempted to address. Students highlighted that IPE enhances IP collaboration and teamwork.Conclusions: Teaching students about IP communication and professional roles and involving students in joint sessions prepare them for a promising future of high-quality patient care.
目的:跨专业教育(IPE)正变得越来越流行,强烈建议将其纳入医疗保健专业人员的课程。实施IPE可以提高学生的知识、技能和对合作团队的态度,从而改善医疗服务和患者的健康结果。本研究旨在探讨护医学生对IPE与社会互动的认知。方法:对8名护理医科学生进行定性研究。通过两次半结构化焦点小组会议收集数据,并使用归纳主题分析进行分析。结果:出现5个主旋律和7个副旋律。主题为:(1)国际政治经济学的意义;(2)国际政治经济学的障碍;(3)国际政治经济学的促进者;(4)社会互动;(5)弥合学生视角上的差距。我们发现,两所学校的学生对国际政治经济学的定义和重要性都有清晰的认识。学生们报告说,缺乏互动是一个他们从未试图解决的问题。学生们强调,国际政治教育促进了知识产权合作和团队合作。结论:向学生讲授IP通信和专业角色,并让学生参与联合会议,为他们提供高质量患者护理的美好未来做好准备。
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引用次数: 0
Empowerment perception and health-related quality of life among schizophrenic patients 精神分裂症患者赋权感知与健康相关生活质量
Pub Date : 2021-01-27 DOI: 10.5430/CNS.V9N1P45
H. Chiu, Hui-Man Huang
Objective: The study aims to explore the perception of empowerment, HRQoL and their relationship in schizophrenia patients in rehabilitation ward. Methods: Cross-sectional correlational design and convenience sampling were used to recruit 102 subjects from rehabilitation wards of a psychiatric hospital in southern Taiwan. Three instruments were used: the Brief Psychiatric Rating Scale, the Empowerment Scale (subscales: self-esteem and self-efficacy, power-powerlessness, righteous anger, and community autonomy), and the Taiwanese version of the World Health Organization Quality of Life Questionnaire (WHOQOL-BREF) with four domains (physical health, psychological, social relationship, and environment). Results: (1) Overall empowerment perception and overall HRQoL were at a moderate and above level in patients with schizophrenia in rehabilitation ward. (2) Older patients having a lower empowerment perception with power-powerlessness than youngers; the more severe the psychiatric symptoms, the lower the righteous anger. (3) Male patients scored higher than female patients on overall HRQoL and “environment” domain. The duration of mental illness also influenced at “environment” domain, 6-10 years group scored higher than ≤ 5 years group. (4) Actively participate in rehabilitation activities correlated positively; psychiatric symptoms correlated negatively with overall HRQoL and with each individual domain. (5) Empowerment perception correlated positively with overall HRQoL and with each individual domain. Conclusions: Mental health workers should assist chronic schizophrenic patients in coping with their psychiatric symptoms, allow patients to express negative emotions, and provide opportunities for patients to make their own decisions and exercise their own rights.
目的:探讨康复病房精神分裂症患者的授权感、HRQoL及其关系。方法:采用交叉相关设计和方便抽样方法,从台湾南部某精神病院的康复病房招募102名受试者。使用了三种工具:简要精神病评定量表、授权量表(分量表:自尊和自我效能、权力无能为力、义愤和社区自治),以及台湾版的世界卫生组织生活质量问卷(WHOQOL-BREF),包括四个领域(身体健康、心理、社会关系和环境)。结果:(1)康复病房精神分裂症患者的整体赋权感知和整体HRQoL均处于中等及以上水平。(2) 与年轻人相比,老年患者对权力无能为力的授权认知较低;精神症状越严重,正义的愤怒就越低。(3) 男性患者在整体HRQoL和“环境”领域的得分高于女性患者。精神疾病的持续时间也在“环境”领域受到影响,6-10岁组的得分高于≤5岁组。(4) 积极参与康复活动呈正相关;精神症状与整体HRQoL和每个个体领域呈负相关。(5) 授权感知与整体HRQoL和每个个体领域呈正相关。结论:精神卫生工作者应协助慢性精神分裂症患者应对其精神症状,允许患者表达负面情绪,并为患者提供自主决策和行使权利的机会。
{"title":"Empowerment perception and health-related quality of life among schizophrenic patients","authors":"H. Chiu, Hui-Man Huang","doi":"10.5430/CNS.V9N1P45","DOIUrl":"https://doi.org/10.5430/CNS.V9N1P45","url":null,"abstract":"Objective: The study aims to explore the perception of empowerment, HRQoL and their relationship in schizophrenia patients in rehabilitation ward. Methods: Cross-sectional correlational design and convenience sampling were used to recruit 102 subjects from rehabilitation wards of a psychiatric hospital in southern Taiwan. Three instruments were used: the Brief Psychiatric Rating Scale, the Empowerment Scale (subscales: self-esteem and self-efficacy, power-powerlessness, righteous anger, and community autonomy), and the Taiwanese version of the World Health Organization Quality of Life Questionnaire (WHOQOL-BREF) with four domains (physical health, psychological, social relationship, and environment). Results: (1) Overall empowerment perception and overall HRQoL were at a moderate and above level in patients with schizophrenia in rehabilitation ward. (2) Older patients having a lower empowerment perception with power-powerlessness than youngers; the more severe the psychiatric symptoms, the lower the righteous anger. (3) Male patients scored higher than female patients on overall HRQoL and “environment” domain. The duration of mental illness also influenced at “environment” domain, 6-10 years group scored higher than ≤ 5 years group. (4) Actively participate in rehabilitation activities correlated positively; psychiatric symptoms correlated negatively with overall HRQoL and with each individual domain. (5) Empowerment perception correlated positively with overall HRQoL and with each individual domain. Conclusions: Mental health workers should assist chronic schizophrenic patients in coping with their psychiatric symptoms, allow patients to express negative emotions, and provide opportunities for patients to make their own decisions and exercise their own rights.","PeriodicalId":72616,"journal":{"name":"Clinical nursing studies","volume":"9 1","pages":"45"},"PeriodicalIF":0.0,"publicationDate":"2021-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48460730","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Quality of life in patients with mild acute brain injury and their carers’ needs in Greece 希腊轻度急性脑损伤患者的生活质量及其护理人员的需求
Pub Date : 2021-01-18 DOI: 10.5430/CNS.V9N1P39
Evgenia Stasinopoulou, M. Giannakopoulou, G. Fildisis, M. Kalafati, C. Lemonidou
Background: Investigating quality of life (QoL) is of crucial importance for the scientific community as it could function not only as an indicator of prognosis and post-traumatic clinical and psychological changes in patients who have suffered from acute brain injury (ABI), but also as an indicator of the effectiveness of their treatment and social rehabilitation. In addition, it can highlight changes in the carer’s health, social life and well-being. This study examined the QoL of patients following ABI and the needs of their carers. Material and methodology: This study was conducted in patients suffering from ABI, who were admitted to the General Hospital of Attica “KAT” and to the National Rehabilitation Center and on their carers. Data collection including demographics and Quality of Life After Brain Injury Questionnaire (QOLIBRI) and the Family Needs Questionnaire (FNQ) was performed during patients’ rehabilitation, while six months after release, a follow-up survey was conducted using the same questionnaires. Statistical analysis of data was performed using SPSS. Results: We analysed 50 patients with mild ABI (GCS ≥ of 13/15) during rehabilitation and six months after release and found that their QoL improves and is positively related to improvement of health status (i.e. in terms of thinking ability, QoL improves from r = 2.33, p < .01 to r = 3.37, p < .001). We also found that “Age” has the greatest impact on the patient’s progress for recovery and the general QoL after ABI ( r = -0.423, p < .01). In addition, it was found that carers of patients with ABI are confronted with the burden of care, while they record both fulfilled and unmet needs regarding their individual needs (i.e. only for 30% of the sample the need for help in preparing them for the worst is met). Conclusions: Our study confirms previous findings that underline that ABI has a major impact on QoL of both patients and their carers providing them with long-term daily care. Although it has been found that over time there is an improvement in the QoL of patients with ABI, the absence of an official support network for carers from public health system, hospitals and rehabilitation centers may adversely affect the QoL of patients and their carers. Therefore, more structured, long-term family-wide monitoring and support is needed, focusing on identifying those at risk of social isolation and incomplete social networking.
背景:研究生活质量(QoL)对科学界至关重要,因为它不仅可以作为急性脑损伤(ABI)患者预后和创伤后临床和心理变化的指标,还可以作为他们治疗和社会康复有效性的指标。此外,它还可以突出护理人员的健康、社会生活和幸福感的变化。本研究调查了ABI患者的生活质量及其护理人员的需求。材料和方法:这项研究是在阿提卡综合医院和国家康复中心的ABI患者及其护理人员中进行的。在患者康复期间进行了数据收集,包括人口统计和脑损伤后生活质量问卷(QOLIBRI)和家庭需求问卷(FNQ),而在出院六个月后,使用相同的问卷进行了随访调查。使用SPSS对数据进行统计分析。结果:我们分析了50名轻度ABI(GCS≥13/15)患者在康复期间和出院后6个月的生活质量,发现他们的生活质量得到改善,并与健康状况的改善呈正相关(即在思维能力方面,生活质量从r=2.33,p<.01提高到r=3.37,p<.001)。我们还发现,“年龄”对患者的康复进展影响最大以及ABI后的总体生活质量(r=-0.423,p<0.01)。此外,研究发现,ABI患者的护理人员面临着护理负担,同时他们记录了关于个人需求的满足和未满足需求(即,只有30%的样本满足了帮助他们做好最坏准备的需求)。结论:我们的研究证实了先前的研究结果,即ABI对患者及其护理人员的生活质量有重大影响,为他们提供长期的日常护理。尽管已经发现,随着时间的推移,ABI患者的生活质量有所改善,但公共卫生系统、医院和康复中心缺乏官方的护理人员支持网络,可能会对患者及其护理人员的生活质量产生不利影响。因此,需要更结构化、更长期的全家庭监测和支持,重点是识别那些有社交孤立和社交网络不完整风险的人。
{"title":"Quality of life in patients with mild acute brain injury and their carers’ needs in Greece","authors":"Evgenia Stasinopoulou, M. Giannakopoulou, G. Fildisis, M. Kalafati, C. Lemonidou","doi":"10.5430/CNS.V9N1P39","DOIUrl":"https://doi.org/10.5430/CNS.V9N1P39","url":null,"abstract":"Background: Investigating quality of life (QoL) is of crucial importance for the scientific community as it could function not only as an indicator of prognosis and post-traumatic clinical and psychological changes in patients who have suffered from acute brain injury (ABI), but also as an indicator of the effectiveness of their treatment and social rehabilitation. In addition, it can highlight changes in the carer’s health, social life and well-being. This study examined the QoL of patients following ABI and the needs of their carers. Material and methodology: This study was conducted in patients suffering from ABI, who were admitted to the General Hospital of Attica “KAT” and to the National Rehabilitation Center and on their carers. Data collection including demographics and Quality of Life After Brain Injury Questionnaire (QOLIBRI) and the Family Needs Questionnaire (FNQ) was performed during patients’ rehabilitation, while six months after release, a follow-up survey was conducted using the same questionnaires. Statistical analysis of data was performed using SPSS. Results: We analysed 50 patients with mild ABI (GCS ≥ of 13/15) during rehabilitation and six months after release and found that their QoL improves and is positively related to improvement of health status (i.e. in terms of thinking ability, QoL improves from r = 2.33, p < .01 to r = 3.37, p < .001). We also found that “Age” has the greatest impact on the patient’s progress for recovery and the general QoL after ABI ( r = -0.423, p < .01). In addition, it was found that carers of patients with ABI are confronted with the burden of care, while they record both fulfilled and unmet needs regarding their individual needs (i.e. only for 30% of the sample the need for help in preparing them for the worst is met). Conclusions: Our study confirms previous findings that underline that ABI has a major impact on QoL of both patients and their carers providing them with long-term daily care. Although it has been found that over time there is an improvement in the QoL of patients with ABI, the absence of an official support network for carers from public health system, hospitals and rehabilitation centers may adversely affect the QoL of patients and their carers. Therefore, more structured, long-term family-wide monitoring and support is needed, focusing on identifying those at risk of social isolation and incomplete social networking.","PeriodicalId":72616,"journal":{"name":"Clinical nursing studies","volume":"9 1","pages":"39"},"PeriodicalIF":0.0,"publicationDate":"2021-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45531277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Clinical nursing studies
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