宫腔粘连的危害及影响因素

宫腔粘连指因宫腔操作以及感染等因素影响,造成子宫内膜基底层受损,内膜修复过程中形成的宫腔内和(或)宫颈处粘连、闭塞等。患者可出现月经量少、痛经、不孕及反复妊娠丢失等临床症状,孕期有流产、早产、胎盘植入等风险。本文就发生宫腔粘连的影响因素,该疾病对于患者生理、心理和妊娠的影响,以及相关治疗效果的影响因素三方面加以综述。旨在引起同行对宫腔粘连的重视,加强宫腔粘连的预防。     

新型驱动基因融合阳性非小细胞肺癌脑转移的研究进展北大核心

肺癌是我国最常见且死亡率最高的恶性肿瘤之一,随着表皮生长因子受体(EGFR)、间变性淋巴瘤激酶(ALK)及活性氧1(ROS1)等驱动基因及其相应分子靶向药物的出现,晚期非小细胞肺癌的治疗和预后发生了革命性变化。此外,一些少见新型驱动基因融合,包括神经调节蛋白1(NRG1)、神经营养酪氨酸受体激酶(NTRK)和转染重排因子(RET),正逐渐发展成为全身性治疗选择。然而,这些罕见新型融合驱动基因在NSCLC脑转移中的作用机制,以及优化控制和预防脑转移的意义人们所知甚少。因此,本文就近几年罕见驱动基因融合在NSCLC脑转移中的研究进行综述。     

儿童外周静脉血标本采集的循证护理实践

目的:将儿童外周静脉血标本采集的最佳证据应用于临床实践。方法:于2020年12月至2021年3月基于复旦大学循证护理中心证据的持续质量改进模式图的标准程序,将外周静脉血标本采集的最佳证据应用于临床。证据应用前、后分别以北京市某三级甲等儿童专科医院风湿免疫科的26名护士和208例次(证据应用前)、289例次(证据应用后)患儿为研究对象开展质量审查和效果评价,使用调查问卷调查护士对最佳证据的知晓情况,采用现场观察法评估护士对最佳证据实施的依从性,由检验中心反馈血标本合格率。结果:证据应用后护士对患儿握拳时机、双人固定及站位、压脉带的使用、血标本采集顺序这4个方面共计5个指标的知晓率提升,护士执行患儿身份确认、手卫生、压脉带使用、血标本采集顺序、佩戴一次性手套这5个方面共计7个指标的依从性提升,血标本合格率提高,差异均有统计学意义(P<0.01);证据应用前、后静脉采血穿刺成功率比较,差异无统计学意义(P>0.05)。结论:儿童外周静脉血标本采集最佳证据的应用可以提升护士对证据相关知识的知晓率和依从性,提高临床护理质量,提高血标本合格率,为患儿诊断治疗提供可靠依据,不影响穿刺成功率,不增加患儿痛苦。     

实习护生情绪智力、临床实习环境与病人安全感知能力的中介效应

目的:了解实习护生情绪智力、临床实习环境与病人安全感知能力现状并探讨三者关系。方法:采用情绪智力量表、临床实习环境量表和卫生职业教育病人安全感知量表对492名实习护生进行调查。结果:实习护生情绪智力总分为(123.81±18.69)分,临床实习环境总分为(119.48±22.16)分,病人安全感知能力总分为(67.16±12.06)分,情绪智力、临床实习环境与病人安全感知能力呈正相关(r值分别为0.723和0.720,P<0.01);情绪智力在临床实习环境和病人安全感知能力间起部分中介效应,中介效应估计值为0.286(28.6%)。结论:学校要举办人文课程活动以培养情绪智力;医院应制订计划增加学习机会,选拔给予护生充分支持的带教老师,改善临床实习环境。     

Hepatotoxicity of cantharidin is associated with the altered bile acid metabolism

Cantharidin (CTD) is an effective antitumor agent. However, it exhibits significant hepatotoxicity, the mechanism of which remains unclear. In this study, biochemical and histopathological analyses complemented with ultra-high-performance liquid chromatography–tandem mass spectrometry (UHPLC-MS/MS)-based targeted metabolomic analysis of bile acids (BAs) were employed to investigate CTD-induced hepatotoxicity in rats. Sixteen male and female Sprague–Dawley rats were randomly divided into two groups: control and CTD (1.0 mg/kg) groups. Serum and liver samples were collected after 28 days of intervention. Biochemical, histopathological, and BA metabolomic analyses were performed for all samples. Further, the key biomarkers of CTD-induced hepatotoxicity were identified via multivariate and metabolic pathway analyses. In addition, metabolite–gene–enzyme network and Kyoto Encyclopedia of Genes and Genomes pathway analyses were used to identify the signaling pathways related to CTD-induced hepatotoxicity. The results revealed significantly increased levels of biochemical indices (alanine aminotransferase, aspartate aminotransferase, and total bile acid). Histopathological analysis revealed that the hepatocytes were damaged. Further, 20 endogenous BAs were quantitated via UHPLC-MS/MS, and multivariate and metabolic pathway analyses of BAs revealed that hyocholic acid, cholic acid, and chenodeoxycholic acid were the key biomarkers of CTD-induced hepatotoxicity. Meanwhile, primary and secondary BA biosynthesis and taurine and hypotaurine metabolism were found to be associated with the mechanism by which CTD induced hepatotoxicity in rats. This study provides useful insights for research on the mechanism of CTD-induced hepatotoxicity.