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ObjectiveThe use of mechanical circulatory support (MCS) in lung transplantation has been steadily increasing over the prior decade, with evolving strategies for incorporating support in the preoperative, intraoperative, and postoperative settings. There is significant practice variability in the use of these techniques, however, and relatively limited data to help establish institutional protocols. The objective of the AATS Clinical Practice Standards Committee (CPSC) expert panel was to review the existing literature and establish recommendations about the use of MCS before, during, and after lung transplantation.MethodsThe AATS CPSC assembled an expert panel of 16 lung transplantation physicians who developed a consensus document of recommendations. The panel was broken into subgroups focused on preoperative, intraoperative, and postoperative support, and each subgroup performed a focused literature review. These subgroups formulated recommendation statements for each subtopic, which were evaluated by the entire group. The statements were then developed via discussion among the panel and refined until consensus was achieved on each statement.ResultsThe expert panel achieved consensus on 36 recommendations for how and when to use MCS in lung transplantation. These recommendations included the use of veno-venous extracorporeal membrane oxygenation (ECMO) as a bridging strategy in the preoperative setting, a preference for central veno-arterial ECMO over traditional cardiopulmonary bypass during the transplantation procedure, and the benefit of supporting selected patients with MCS postoperatively.ConclusionsAchieving optimal results in lung transplantation requires the use of a wide range of strategies. MCS provides an important mechanism for helping these critically ill patients through the peritransplantation period. Despite the complex nature of the decision making process in the treatment of these patients, the expert panel was able to achieve consensus on 36 recommendations. These recommendations should provide guidance for professionals involved in the care of end-stage lung disease patients considered for transplantation.  相似文献   
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背景 我国居民精神障碍死亡相关流行病学分析较少,上海作为经济发达地区,居民健康信息化较为完善,能够为深层次分析居民更小分类的疾病特征和死亡原因提供数据支撑,且分析上海市女性精神障碍死亡情况及趋势有助于了解当地女性精神障碍疾病负担。 目的 分析2005—2021年上海市浦东新区女性居民精神障碍死亡情况及其趋势。 方法 整理2005—2021年浦东新区全人口户籍居民死因监测资料,采用粗死亡率、标化死亡率、减寿年数和减寿率等指标分析当地女性居民精神障碍死亡情况,并采用Joinpont回归模型计算年度变化百分比(APC)和平均年度变化百分比(AAPC)进行趋势分析。 结果 2005—2021年上海市浦东新区女性精神障碍死亡1 165例,占同期总死亡人数的0.32%,粗死亡率为4.82/10万,标化死亡率为1.85/10万。上海市浦东新区女性精神障碍粗死亡率2005—2012年呈下降趋势(APC=-13.05%,P=0.002),2012—2021年呈上升趋势(APC=7.66%,P=0.012);标化死亡率2005—2012年呈下降趋势(APC=-16.79%,P<0.001),2005—2021年整体呈下降趋势(AAPC=-4.93%,P=0.009);减寿率2005—2012年呈下降趋势(APC=-13.79%,P<0.001),2012—2021年呈上升趋势(APC=6.93%,P=0.011)。2005—2021年上海市浦东新区女性精神障碍死亡年龄为50.8~105.8岁,死亡年龄分布以≥80岁为主(79.48%),且≥80岁女性精神障碍死亡比例整体呈上升趋势(AAPC=0.98%,P=0.027);70~79岁女性精神障碍死亡比例为16.57%,其死亡比例(AAPC=-5.13%,P=0.026)、粗死亡率(AAPC=-7.20%,P=0.003)和减寿率(AAPC=-6.89%,P=0.005)整体均呈下降趋势。 结论 2005—2021年上海市浦东新区女性精神障碍标化死亡率整体呈下降趋势,但高龄(≥80岁)女性精神障碍死亡比例整体呈上升趋势。高龄女性居民精神障碍疾病负担值得当地重点关注,促进高龄女性精神健康有益于提高当地女性健康水平。  相似文献   
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Background and aimsSkin autofluorescence (SAF) can non-invasively assess the accumulation of tissue AGEs. We investigated the association between SAF and kidney dysfunction in participants with T2D.MethodsOf 4030 participants consecutively measured SAF at baseline, 3725 participants free of end-stage kidney disease (ESKD) were included in the analyses. The association of SAF with incident ESKD or ≥30% reduction in estimated glomerular filtration rate (eGFR) was examined with Cox regression, linear mixed-effects model for the association with annual eGFR decline, and mediation analyses for the mediating roles of renal markers.ResultsDuring a median (IQR) 1.8 (1.1–3.1) years of follow-up, 411 participants developed the outcome. SAF was associated with progression of kidney disease (hazard ratio 1.15 per SD, 95% confidence interval [CI] [1.04, 1.28]) and annual decline in eGFR (β ?0.39 per SD, 95% CI [?0.71, ?0.07]) after adjustment for risk factors, including baseline eGFR and urinary albumin-creatinine ratio (UACR). Decreased eGFR (12.9%) and increased UACR (25.8%) accounted for 38.7% of the effect of SAF on renal outcome.ConclusionsSAF is independently associated with progression of kidney disease. More than half of its effect is independent of renal markers. SAF is of potential to be a prognostic marker for kidney dysfunction.  相似文献   
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Background and aimsCurrent strategies to reduce cardiovascular disease (CVD) risk in young adults are largely limited to those at extremes of risk. In cohort studies we have shown cluster analysis identified a large sub-group of adolescents with multiple risk factors. This study examined if individuals classified at ‘high-risk’ by cluster analysis could also be identified by their Framingham risk scores.Methods and resultsRaine Study data at 17- (n = 1048) and 20-years (n = 1120) identified high- and low-risk groups by cluster analysis using continuous measures of systolic BP, BMI, triglycerides and insulin resistance. We assessed:- CVD risk at 20-years using the Framingham 30 yr-risk-score in the high- and low-risk clusters, and cluster stability from adolescence to adulthood.Cluster analysis at 17- and 20-years identified a high-risk group comprising, 17.9% and 21.3%, respectively of the cohort. In contrast, only 1.2% and 3.4%, respectively, met the metabolic syndrome criteria, all of whom were within the high-risk cluster. Compared with the low-risk cluster, Framingham scores of the high-risk cluster were elevated in males (9.4%; 99%CI 8.3, 10.6 vs 6.0%; 99%CI 5.7, 6.2) and females (4.9%; 99%CI 4.4, 5.4 vs 3.2%; 99%CI 3.0, 3.3) (both P < 0.0001). A score >8 for males and >4 for females identified those at high CVD risk with 99% confidence.ConclusionCluster analysis using multiple risk factors identified ~20% of young adults at high CVD risk. Application of our Framingham 30 yr-risk cut-offs to individuals allows identification of more young people with multiple risk factors for CVD than conventional metabolic syndrome criteria.  相似文献   
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目的:回顾性分析比较心肌梗死(MI)后不同病程心力衰竭(心衰)患者应用沙库巴曲缬沙坦(Sacubitril/Valsartan,LCZ696)的 临床疗效是否存在差异。方法: 收集2018 年1 月1 日—2020 年6 月30 日在天津市第一中心医院心内科住院并首次服用 LCZ696 的MI 后心衰患者共150 例,分为并发心衰组,心衰病程≤2 年组和心衰病程>2 年组,各50 例,以治疗后3、6、12 个月 为时间节点进行为期1 年的回访,观察心脏超声指标变化和生存情况,并用Cox 回归分析影响疗效的因素。结果:3组患者左心 室射血分数(LVEF)(F=62.111,P<0.01)和舒张末期内径(LVEDD)(F=38.444,P<0.01)分别呈逐渐上升和下降趋势,其中在并发 心衰组的变化最显著,组间差异存在统计学意义。3 组间累积无终点事件生存率(90.0%、57.8%、35.3%)有统计学意义(字2= 32.754,P<0.01)。Cox 回归分析发现长心衰病程患者终点事件发生的风险大(HR=10.407,95%CI:3.957~27.371,P<0.001)。结论: MI 后心衰患者早期启用LCZ696 更有利于改善左室重构,无事件生存率更高。  相似文献   
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目的:探讨早泄的类型和年龄因素与盐酸达泊西汀临床疗效的关系。方法:选取2018年10月至2020年1月在秦皇岛市第一医院生殖医学科男科门诊治疗的96例早泄患者作为研究对象。根据早泄的类型将患者分为原发组(原发性早泄)42例、继发组(继发性早泄)54例;再根据年龄将患者分为青年组(<35岁)46例、中年组(≥35岁)50例。各组患者均于性交前1~3 h给予盐酸达泊西汀30 mg,口服;所有患者均连续治疗2个月,停药1个月后随访。观察各组患者治疗前后阴道内射精潜伏期(IELT)、早泄诊断标准量表(PEDT)评分、早泄分析表(PEP)评分、临床疗效和复发情况。结果:(1)原发组、继发组患者治疗后和随访末期IELT、PEDT评分较治疗前有显著改善,且继发组患者治疗后和随访末期的IELT显著长于原发组,PEDT评分显著低于原发组,差异均有统计学意义(P<0.05)。两组患者治疗后和随访末期的各项PEP评分与治疗前比较,均有显著改善,差异有统计学意义(P<0.05)。治疗后和随访末期,继发组患者的射精控制能力和性生活满意度评分显著高于原发组,早泄相关苦恼、早泄对伴侣关系的影响评分显著低于原发组,差异均有统计学意义(P<0.05)。(2)青年组、中年组患者治疗后和随访末期IELT、PEDT评分较治疗前有显著改善,青年组患者的IELT显著长于中年组,而PEDT评分显著低于中年组,差异均有统计学意义(P<0.05)。两组患者治疗后和随访末期的各项PEP评分与治疗前比较,均有显著改善,差异均有统计学意义(P<0.05)。治疗后,青年组患者的射精控制能力评分显著高于中年组,早泄相关苦恼及早泄对伴侣关系的影响评分显著低于中年组;随访末期,青年组患者的早泄相关苦恼及早泄对伴侣关系的影响评分显著低于中年组,差异均有统计学意义(P<0.05)。(3)原发组、继发组患者的总有效率分别为71.43%(30/42)、88.89%(48/54),复发率分别为30.95%(13/42)、9.26%(5/54),21.42%(9/42)、7.41%(4/54)组间的差异均有统计学意义(P<0.05)。青年组、中年组患者的总有效率分别为89.13%(41/46)、72.00%(36/50),组间的差异有统计学意义(P<0.05);复发率分别为17.39%(8/46)、20.00%(10/50),组间的差异无统计学意义(P>0.05)。结论:盐酸达泊西汀治疗继发性早泄的临床效果优于原发性早泄,治疗青年早泄患者的临床效果优于中年早泄患者。  相似文献   
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BackgroundPharmacy is a growing profession in the Kingdom of Saudi Arabia which has experienced tremendous changes in the past 20 years. Pharmacy practice or clinical pharmacy have an attention ever since the emerging of PharmD programs throughout the Saudi universities. As a result, the number of affiliated faculty in the pharmacy practice departments has increased dramatically in the past 20 years and thus significant changes in research output were observed.ObjectivesThe main objective is to conduct a bibliometric analysis and evaluate the research output of pharmacy practice faculty in Saudi Universities from 2000 to 2021MethodsA systematic search was conducted using Scopus database to explore the research output from pharmacy practice affiliated faculty from 2000 to 2021. The following search terms AFFILORG (“Pharmacy Practice Department” OR “Department of Pharmacy practice” OR “Clinical Pharmacy Department” OR “Department of Clinical Pharmacy” OR “Department of Pharmacy Services”) AND AFFILCOUNTRY (“Saudi Arabia” OR “KSA” OR “Kingdom of Saudi Arabia”) were used. Only original research papers were retrieved and analyzed using MS Excel (v16.0), MS Access (v16.0), Bibexcel (v2017), VOS viewer, and Biblioshiny.ResultsIn the past two decades, most publications with pharmacy practice departments affiliation were pharmacy practice research irrelevant (only 1075 out of 2809). King Saud University and King Abdulaziz University were the top performing institutes, and median of 5-year impact factor for journals was more than 3 for most of the top 10 institutes. 19% of the total retrieved articles were review publications were the rest majorly classified as cross-sectional studies.ConclusionThe research contribution of pharmacy practice departments in Saudi Arabia has been improving. Key recommendations are to promote more applied and interventional research, increase publications in top journals, and enhance national collaborations.  相似文献   
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摘要: 目的 系统评价注射用头孢哌酮钠/舒巴坦钠(商品名:舒普深)在中国治疗临床感染的有效性和安全性。 方法 系 统检索万方、中国知网、维普、SinoMed、PubMed和Cochrane Library数据库,收集1978年至2019年7月4日公开发表的关于头孢 哌酮/舒巴坦在中国治疗临床感染方面的文献,按照纳入排除标准进行筛选,使用Stata 15.0和SAS 9.4软件进行荟萃(Meta)分析。 主要结局指标包括临床有效率与痊愈率,次要结局指标包括细菌清除率(株)与不良事件发生率。 结果 最终纳入110篇文献,其 中有82篇、87篇分别纳入有效率和痊愈率的Meta分析。结果显示,头孢哌酮/舒巴坦治疗临床感染的总有效率为80.3% [95%置信 区间(CI): 77.4%~83.0%],痊愈率为50.1% (95%CI: 45.1%~55.1%)。共38项研究报告了细菌清除率,结果显示细菌清除率为81.1% (95%CI: 76.9%~84.9%)。62篇文献报告治疗中发生的不良事件例数,合计不良事件的发生率为7.4% (95%CI: 6.1%~8.9%),包括 血液系统不良事件、胃肠道不良事件、肝肾功能损害及皮肤不良事件等。与其他对照药物相比,头孢哌酮/舒巴坦治疗临床感染 的有效性和安全性良好。 结论 头孢哌酮/舒巴坦的临床应用效果较为可观,对治疗临床感染具有较高的价值,安全性好。但 临床应注意合理用药,加强对头孢哌酮/舒巴坦的不良事件监测,减少不良事件。  相似文献   
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