肾移植患者生存质量及影响因素分析

探讨肾移植患者的生存质量及影响因素.采用健康状况调查问卷(SF-36)调查广州地区医疗机构145例肾移植受者移植前和移植后6个月的生存质量.移植后6个月患者的生存质量评分较移植前有明显提高.文化程度、有无配偶、经济状况、肾源、健康知识掌握程度等因素对患者的生存质量影响较大.医护人员应为肾移植患者提供个性化护理,以提高患者的生存质量.     

终末期肾病患者替代治疗方法的临床决策

血液透析、腹膜透析和肾移植是终末期肾病患者替代治疗的主要方法,三种治疗方法各有优缺点。临床上应根据患者原发病因、替代治疗并发症、卫生经济学、生存质量、所在地医疗条件、非医疗因素等作出科学临床决策,最大限度延长患者生命,提高生存质量。     

终末期肾病患者替代治疗方法的临床决策

血液透析、腹膜透析和肾移植是终末期肾病患者替代治疗的主要方法,三种治疗方法各有优缺点.临床上应根据患者原发病因、替代治疗并发症、卫生经济学、生存质量、所在地医疗条件、非医疗因素等作出科学临床决策,最大限度延长患者生命,提高生存质量.     

住院放化疗肺癌患者生活质量影响因素分析

生活质量研究是近年来肿瘤治疗研究的热点之一。应用生存质量核心问卷（QLQ—C30）及卡氏功能量表,于治疗前、中、后进行问卷式调查,探讨60例经病理证实接受放、化疗的肺癌患者生活质量的影响因素,预测患者预后和远期生存状态,为住院放化疗肺癌的治疗方法提供一个较好的参考标准,对放化疗肺癌的治疗水平和改善生活质量起到了一定的推动作用。     

奥伦自理理论对充血性心力衰竭患者综合生存质量的预后影响研究

研究分析奥伦自理理论对充血性心力衰竭患者综合生存质量的预后影响。选取2012年2月~2013年5月本院收治的90例充血性心力衰竭患者为研究对象,将90例患者遵循随机分配的原则分为对照组（常规护理干预组）45例和观察组（奥伦自理理论组）45例,然后将两组患者护理干预前和护理干预后1个月、3个月的MLHFQ量表、WHOQOL-100量表及Zung量表评估结果进行统计与比较。观察组护理干预后1个月、3个月的MLHFQ量表评分均低于对照组,WHOQOL-100量表评分高于对照组,Zung量表评分与阳性率均低于对照组,P均〈0.05,两组护理干预后的评估结果差异均有统计学意义。奥伦自理理论有助于改善充血性心力衰竭患者的综合生存质量,在此类患者中的应用价值较高。     

子宫腺肌病合并肺栓塞临床特点分析及治疗方式选择

探讨子宫腺肌病合并肺栓塞的临床特点,分析两者关系。回顾性分析中国医科大学附属盛京医院2014年12月至2017年12月收治的子宫腺肌病合并肺栓塞患者6例。结果6例患者中处于经期5例,围绝经期1例,低危3例,中低危3例。发病年龄43岁～52岁[(48.33±3.83)岁],体质量指数(BMI)(29.15±2.37)kg/m2,子宫腺肌病病程12个月～24个月[(16.67±5.89)个月],肺栓塞病程为入院前16个月至入院后2天,6例患者均无明显的肺栓塞高危因素。5例患者CA125高于正常,6例患者全部贫血,肺通气灌注显像和CT肺动脉造影提示6例患者均有不同程度肺动脉栓塞,其中5例双侧肺动脉栓塞,1例右侧肺动脉栓塞。子宫腺肌病是一种"易栓症",在其病程中应时刻警惕肺栓塞形成,贫血、CA125升高可使血栓形成风险提高。     

QLQ-3O量表在乳腺癌化疗患者中的应用

应用EORTCQLQ-30核心量表调查初治乳腺癌化疗患者的生存质量。运用自身对比的队列研究方式,调查了42名乳腺癌化疗患者。结果显示化疗带来的生存质量的下降是显著但短暂的;某些因素对生存质量的影响较大,值得针对性地采取干预措施;对一些调查项目的修改,可以使EORTC QLQ-30量表更好地适应我国的国情和文化。     

Lipo PGE1在肾移植中的应用

为了探讨前列腺素E1的脂微球载体靶向制剂（Lipo PGE1）对肾移植术后移植肾功能恢复和血流动力学的影响,80例肾移植受者在术后被随机分成两组：PGE1组和对照组。PGE1组从手术当天起至术后第14天每天给予静脉注射Lipo PGE1 20μg。比较两组术后尿量、血肌酐、彩色多普勒超声下移植肾收缩期最大血流速度（PSV）和血流阻力指数（RI）以及两组肾功能恢复延迟（DGF）的发生率。应用Lipo PGE1的患者术后尿量明显高于对照组（P〈0．05）,而血肌酐、PSV、RI和肾功能恢复延迟发生率则明显低于对照组（P〈0．05）。因此,前列腺素E1有利于肾移植术后移植肾功能的恢复,对肾移植术后早期肾动脉血流动力学有促进作用。     

肾移植受者社会支持及影响因素分析

采用肖水源编制的社会支持评定量表调查广州地区医疗机构145例肾移植受者.结果显示肾移植受者社会支持与常模比较差异具有统计学意义.性别、年龄、文化程度、婚姻状况、是否重返工作或学习对患者的社会支持影响较大.医护人员应帮助患者优化并鼓励其主动利用社会支持网络.     

麻风治愈者生存质量及影响因素的研究

对668名麻风治愈者的生存质量进行调查研究,发现麻风治愈者生存质量各领域评分均低于常模,生理、心理领域和总的生存质量及健康状况评分低于家属组。住院组和畸残组各领域评分分别低于社区组和无畸残组。家庭人均收入、文化程度、生活地点、病程和畸残等因素对麻风治愈者生存质量影响较大。     

Effect of family environment and donor source on patient quality of life following renal transplantation.

The authors examined the degree to which the supportiveness of a patient's family environment predicts change in quality of life following renal transplantation. The sample consisted of 95 patients receiving renal grafts from either a living donor or a cadaveric donor. Patients were initially assessed prior to transplantation with follow-up assessment occurring an average of 5.5 months after transplantation. Among patients receiving a living-donor kidney, those reporting a more supportive family environment exhibited reduced depression, improved mobility, and improved social functioning. However, those living-donor recipients reporting less family support exhibited increased depression and diminished mobility and social functioning after transplantation. Patients receiving a kidney from a cadaveric donor showed modest improvements in quality of life regardless of the degree of family support.     

Mispredicting and misremembering: patients with renal failure overestimate improvements in quality of life after a kidney transplant

OBJECTIVE: People tend to overestimate the impact that future events will have on their quality of life. In the case of a medical treatment like kidney transplant, this should result in biased predictions--overestimates of how much the transplant will benefit quality of life. The authors surveyed kidney transplant patients, both before and after transplant, to test whether they would overestimate the benefits of a successful transplant for their quality of life. DESIGN: The authors interviewed 307 patients on a waiting list for cadaveric renal or renal-pancreatic transplant, and 195 patients one year after a successful transplant. A sub sample of patients were interviewed both before and after transplant. MAIN OUTCOME MEASURES: The survey included measures of quality of life, both in terms of an overall estimate (0-100), and across sub domains, including health, employment, and travel. RESULTS: Cross-sectional results suggested that overall quality of life improved after transplant, but the predictions of pretransplant patients overestimated the magnitude of the improvement (p < .01). In addition, patients predicted large improvements in specific life domains that did not change. These results were confirmed in longitudinal, prospective analyses. Additional analyses showed that posttransplant patients recalled their pretransplant quality of life to be much lower than what they had reported at the time. CONCLUSION: Consistent with an impact bias, patients substantially overestimated the benefits of a successful kidney transplant, both in terms of predictions of life after treatment, and in their memories of QOL before the transplant.     

The Effects of Psycho-Education on the Health-Related Quality of life on Mastalgia Patients

Mastalgia has been accepted as an issue which highly affects the daily life. Our primary purpose in this study is to research the effects of the pain in a group of women with mastalgia not depending on the organic etiology of the quality of life. The second purpose of ours is to depict whether psycho-education has an effect on the pain and the quality of life in these patients. In order to research the effect of Mastalgia on the quality of life, the data of the whole study group have been compared with the Turkey standard data of SF-36 scale. A randomized pre–post intervention study was conducted in Adana Numune Hospital General Surgical Department. The study consists of 98 mastalgia patients who do not have any organic etiology. Psycho-education was given to randomly allocated 66 patients (Psycho-Education Group: PEG) and not given to the other 32 patients (Non-Psycho-Education Group: Non-PEG). The Visual Analog Skala (VAS) and the quality of life scale (SF-36) were applied to all patients. All invantories were re-applied 2 months later. When compared SF-36 subscale data of the whole patient group with the norm results of SF-36 determined for Turkey, the difference in the quality of life of all subscales except for physical function subscale was found statistically significant. While no difference was found between the PEG and Non-PEG for the whole subscales before psycho-education, the difference in the whole subscales after psycho-education was found statistically significant. After psycho-education the difference in the VAS scores between PEG and Non-PEG was found statistically significant. Our study has shown that mastalgia has a negative effect on the quality of life. This study has also revealed that psycho-education must be considered as an effective alternative to reducing pain and increasing the quality of life on mastalgia patients.     

乳腺癌患者术后自我效能、应对方式及生活质量的相关性研究

调查乳腺癌患者术后自我效能、应对方式与生活质量,探讨三者间的相互关系.应用一般自我效能感量表、医学应对问卷和生活质量测定量表对116例乳腺癌术后患者的自我效能、应对方式和生活质量状况进行测评,并分析三者间的相互关系.乳腺癌术后患者自我效能处于较低水平,应对方式趋向于采取屈服方式,生活质量处于较高水平,自我效能、应对方式和生活质量三者之间存在一定程度的关联,可以通过提高患者的自我效能,指导患者采用积极的应对方式改善其生活质量.     

Psychological Adjustment and Knowledge About Hereditary Hemochromatosis in a Clinic-Based Sample: A Prospective Study

This study assessed psychological adjustment and quality of life relative to population-based norms and knowledge about hereditary hemochromatosis in a sample of 101 patients who attended a hemochromatosis clinic. Participants were assessed prior to their clinic visit, and two weeks and 12 months after attendance, using self-administered questionnaires. Mean Mental Health Component Scores from the Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) (45.3, 95% CI 43.2, 47.4) were as compromised as those found amongst stroke victims (45.9, 95% CI 42.8, 49.0) who had participated in a national health survey. Recall of the genetic testing result was less than optimal, in that only 69.3% of those with genetic testing results knew whether they carried one or two mutations. This study demonstrates that patients would benefit from routine assessment of psychological distress and referral to mental health professionals of those whose levels of distress suggest a need for clinical intervention. Results also show that patients may benefit from strategies aimed at improving recall of genetic testing results.     

老年膀胱癌患者术后生活质量及其影响因素的研究

调查老年膀胱癌患者术后生活质量现状及其影响因素,为护理干预和健康管理提供依据。选择我院2013年6月至2014年1月收治的老年膀胱癌患者142例作为研究对象,于患者术后3个月采用膀胱癌特异性量表（FACT-BL）,社会支持评定量表（SSRS）进行数据收集。结果老年膀胱癌患者术后FACT-BL平均得分为（94．33＆#177;8．31）分,SSRS平均得分为（33．70＆#177;4．42）分,不同手术方式躯体状况（PWB）,社会/家庭状况（FWB）,FACT-BL 得分差异具有统计学意义（P＜0．05）,老年膀胱癌患者术后生活质量与社会支持呈正相关关系（P＜0．05）。手术方式与老年膀胱癌患者术后生活质量密切相关,应结合患者的具体情况选择合适的手术方式,实时观察患者的社会支持水平。     

小组治疗对2型糖尿病患者生活质量和临床指标的影响

观察小组治疗对2型糖尿病患者生活质量及糖代谢的影响。将67名2型糖尿病患者随机分为实验组和对照组。两组均给以降糖药物治疗,实验组并给予小组干预。每位患者均于治疗前、治疗后3个月末和5个月末检测糖代谢指标,治疗前和治疗后5个月末测查健康调查简表（SF-36）。结果为实验组临床指标改善优于对照组（P〈0．05）,实验组与对照组相比生活质量明显提高（P〈0．01）。结论认为小组治疗对改善糖尿病患者生活质量和糖代谢情况有着积极作用。     

Quality of Life and Coping of Women Treated for Breast Cancer and Their Caregiver. What are the Interactions?

This longitudinal study analyzed the interactions between the quality of life and the coping strategies of 100 patients treated for breast cancer and their caregivers. Data were collected after diagnosis, at the end of treatment, and 6?months after treatment with the Quality of Life Questionnaire-C30 (QLQ-C30), Duke Health Profile and Ways of Coping Checklist for both patients and caregivers. The theoretical model was tested using a typology of patients and mixed model analyses. The quality of life of patients changed over time and no cluster effect was found. The influence of the sociodemographic characteristics, coping strategies (patients and caregivers) and the quality of life of caregivers on patient's quality of life were different according to the quality of life dimensions considered. To understand the adaptation of patients to their disease, it is therefore essential to look at whether the caregiver is capable of playing a supporting role.     

Quality of life and depression in haemodialysis patients

Chronic kidney disease is associated with a high prevalence of depression, which increases inversely with the glomerular filtration rate. This paper aims to evaluate the factors associated with a low quality of life and depression in patients on haemodialysis. Two hundred patients undergoing haemodialysis answered the Medical Outcomes Study 36 – Item Short – Form Health Survey (SF-36) and Beck Depression Inventory (BDI). Clinical and laboratory variables were analysed and correlated with these two tools. The prevalence of depression was 29%. Anaemia and hypoalbuminemia were independent risk factors for depression. All SF-36 domains showed worse results in patients with depression, and the pain domain presented the highest correlation. Our findings provide evidence that patients on haemodialysis have a low quality of life and a high prevalence of depression. A greater number of comorbidities, an excessive number of medications, diabetes mellitus, anaemia and hypoalbuminemia were associated with a reduced quality of life.