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Moriah J. Brier Rhonda M. Williams Aaron P. Turner Alison W. Henderson Ann Marie Roepke Daniel C. Norvell Helene Henson Joseph M. Czerniecki 《Archives of physical medicine and rehabilitation》2018,99(3):452-458
Objective
To describe the relationship between caregiver-specific support and conflict, and psychosocial outcomes among individuals experiencing their first dysvascular lower extremity amputation (LEA).Design
Cross-sectional cohort study using self-report surveys.Setting
Department of Veterans Affairs, academic medical center, and level I trauma center.Participants
Individuals undergoing their first major LEA because of complications of peripheral arterial disease (PAD) or diabetes who have a caregiver and completed measures of caregiver support and conflict (N=137; 94.9% men).Interventions
Not applicable.Main Outcome Measures
The Patient Health Questionnaire-9 to assess depression and the Satisfaction With Life Scale to assess life satisfaction.Results
In multiple regression analyses, controlling for global levels of perceived support, self-rated health, age, and mobility, caregiver-specific support was found to be associated with higher levels of life satisfaction and caregiver-specific conflict was found to be associated with lower levels of life satisfaction and higher levels of depressive symptoms.Conclusions
The specific relationship between individuals with limb loss and their caregivers may be an important determinant of well-being. Conflict with caregivers, which has received little attention thus far in the limb loss literature, appears to play a particularly important role. Individuals with limb loss may benefit from interventions with their caregivers that both enhance support and reduce conflict. 相似文献43.
Stephanie Rigot Lynn Worobey Michael L. Boninger 《Archives of physical medicine and rehabilitation》2018,99(8):1591-1598
Objectives
To investigate the relation of gait training (GT) during inpatient rehabilitation (IPR) to outcomes of people with traumatic spinal cord injury (SCI).Design
Prospective observational study using the SCIRehab database.Setting
Six IPR facilities.Participants
Patients with new SCI (N=1376) receiving initial rehabilitation.Interventions
Patients were divided into groups consisting of those who did and did not receive GT. Patients were further subdivided based on their primary mode of mobility as measured by the FIM.Main Outcome Measures
Pain rating scales, Patient Health Questionnaire Mood Subscale, Satisfaction With Life Scale, and Craig Handicap Assessment and Reporting Technique (CHART).Results
Nearly 58% of all patients received GT, including 33.3% of patients who were primarily using a wheelchair 1 year after discharge from IPR. Those who used a wheelchair and received GT, received significantly less transfer and wheeled mobility training (P<.001). CHART physical independence (P=.002), mobility (P=.024), and occupation (P=.003) scores were significantly worse in patients who used a wheelchair at 1 year and received GT, compared with those who used a wheelchair and did not receive GT in IPR. Older age was also a significant predictor of worse participation as measured by the CHART.Conclusions
A significant percentage of individuals who are not likely to become functional ambulators are spending portions of their IPR stays performing GT, which is associated with less time allotted for other functional interventions. GT in IPR was also associated with participation deficits at 1 year for those who used a wheelchair, implying the potential consequences of opportunity costs, pain, and psychological difficulties of receiving unsuccessful GT. Clinicians should consider these data when deciding to implement GT during initial IPR. 相似文献44.
Shelley A. Wiechman Kara McMullen Gretchen J. Carrougher Jame A. Fauerbach Colleen M. Ryan David N. Herndon Radha Holavanahalli Nicole S. Gibran Kimberly Roaten 《Archives of physical medicine and rehabilitation》2018,99(7):1311-1317
Objective
To identify important sources of distress among burn survivors at discharge and 6, 12, and 24 months postinjury, and to examine if the distress related to these sources changed over time.Design
Exploratory.Setting
Outpatient burn clinics in 4 sites across the country.Participants
Participants who met preestablished criteria for having a major burn injury (N=1009) were enrolled in this multisite study.Interventions
Participants were given a previously developed list of 12 sources of distress among burn survivors and asked to rate on a 10-point Likert-type scale (0=no distress to 10=high distress) how much distress each of the 12 issues was causing them at the time of each follow-up.Main Outcomes Measures
The Medical Outcomes Study 12-Item Short-Form Health Survey was administered at each time point as a measure of health-related quality of life. The Satisfaction With Appearance Scale was used to understand the relation between sources of distress and body image. Finally, whether a person returned to work was used to determine the effect of sources of distress on returning to employment.Results
It was encouraging that no symptoms were worsening at 2 years. However, financial concerns and long recovery time are 2 of the highest means at all time points. Pain and sleep disturbance had the biggest effect on ability to return to work.Conclusions
These findings can be used to inform burn-specific interventions and to give survivors an understanding of the temporal trajectory for various causes of distress. In particular, it appears that interventions targeted at sleep disturbance and high pain levels can potentially effect distress over financial concerns by allowing a person to return to work more quickly. 相似文献45.
B. Abu Sheikh RN MSc D.H. Arabiat RN PhD S.L. Holmes RN PhD CHPE CNE Y. Khader BDS ScD D. Hiyasat MD D. Collyer MA DPSN S. Abu‐Shiekh RN 《International nursing review》2018,65(1):114-121
Aim
To examine the impact of patient characteristics, anthropometric measurement and patient clinical variables on their appraisal of treatment satisfaction and well‐being.Background
Treatment satisfaction and well‐being are instrumental in achieving diabetes care goals. Nursing practices and healthcare policies may inform interventions in these areas.Introduction
The prevalence of diabetes is high in the Middle East. An understanding of relationships between clinical and socio‐demographic variables and well‐being and treatment satisfaction is needed to improve care and patient outcomes.Methods
A total of 1002 patients completed tools measuring well‐being, treatment satisfaction and socio‐demographic characteristics. A series of bivariate and multivariate analysis were conducted to identify factors associated with well‐being and treatment satisfaction.Results
Males reported better treatment satisfaction and well‐being than females. Older participants, those who were compliant to diet, with controlled diabetes, and no neuropathy reported higher treatment satisfaction scores and well‐being scores. Insulin therapy was associated with better treatment satisfaction.Discussion
Females, participants who were not prescribed diabetic diets and those with complications were more likely to be negatively impacted by diabetes. Individuals with diabetes who were treated with insulin had higher treatment satisfaction than those who used oral hypoglycaemic agents.Conclusion and implication for nursing and health policy
These findings are important in assisting nurses and other healthcare professionals in identifying patients with diabetes with low treatment satisfaction who may present a greater risk for poor well‐being. Additionally, they lend support to developing policies for frequent screenings and special therapeutic interventions that are needed to maximize patients’ treatment satisfaction and well‐being in the Middle East and elsewhere. 相似文献46.
47.
48.
目的:探讨护理干预联合左卡尼丁在维持性血液透析患者中的应用效果。方法:2017年9月至2019年10月,将86例维持性血液透析患者作为研究目标,按照随机数表法分为对照组43例(常规护理);观察组43例(系统化护理)。对比两组的护理满意度、心理健康状态以及各项炎症指标。结果:两组患者护理满意度分别为74.42%、95.35%(P<0.05)。对照组、观察组患者心理健康状况评分差异显著(P<0.05)。对照组、观察组患者白细胞介素6、肿瘤坏死因子α、C反应蛋白水平差异显著(P<0.05)。结论:通过对维持性血液透析患者采用护理干预联合左卡尼丁治疗,能够有效改善其心理健康状态、恢复各项炎症指标,疗效显著,临床应用价值较高。 相似文献
49.
目的:为满足解放军总医院第五医学中心(以下简称“我院”)住院药房实际工作的需要,优化药学部药学服务质量,提高药学服务满意度。方法:采取随机抽样的方法,收集我院28个临床科室工作人员关于药学服务满意度的调查问卷。采用利克特量表,设置态度分值,通过Microsoft Excel软件对评分进行统计分析。结果:收集有效问卷226份,满意度平均得分>4.3分;病区对住院药房的药学服务基本满意,用药咨询评分最低,仅为(4.38±0.49)分,发药准确度[(4.44±0.89)分]和有效沟通[(4.84±0.39)分]方面有待提高。结论:我院各科室对住院药房的药学服务基本满意,问题主要体现在用药咨询和发药准确度等方面,整体药学服务质量还有一定的上升空间。 相似文献
50.
目的 了解肾移植受者手术决策参与满意度现状并分析其影响因素。 方法 2020年11月—2021年1月,采用便利抽样法选取成都市某三级甲等综合医院器官移植门诊随访的272例肾移植受者进行调查。采用肾移植受者一般资料调查表、决策期待量表、患者家属手术决策参与程度调查表、患者对医疗决策知情程度调查表、患者对医疗决策参与的满意度调查问卷,对肾移植受者进行调查。 结果 肾移植受者手术决策参与满意度总分为（78.84±11.47）分,其中,信息维度得分为（70.70±17.14）分,交流协商维度得分为（79.69±13.75）分,决策维度得分为（80.73±12.47）分,总满意度及信心维度得分为（84.25±12.67）分。年龄、家属参与手术决策的程度、医疗费用支付方式以及患者对于手术决策知情程度等对肾移植受者手术决策参与满意度有影响（均P<0.05）。多元线性回归分析显示,患者对于手术决策知情程度是肾移植受者手术决策参与满意度的独立影响因素（P<0.001）。 结论 肾移植受者手术决策参与满意度水平有待提高,对手术决策的知情程度是影响其参与满意度的主要因素。医护人员应结合肾移植受者年龄和家属参与程度,对其手术决策知情情况进行综合评估,制订个体化决策辅助干预措施。 相似文献