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原发性血小板增多症合并冠状动脉粥样硬化性心脏病患者的临床特征分析 被引量:13
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作者 张金 郭荣 +3 位作者 李晓红 吴晓丹 徐智滔 何飞 《中国现代医学杂志》 CAS 2020年第9期75-79,共5页
目的分析原发性血小板增多症合并冠状动脉粥样硬化性心脏病(以下简称冠心病)患者的临床特征。方法收集2014年1月—2018年6月于郑州大学第一附属医院住院治疗的21例原发性血小板增多症合并冠心病患者的临床资料,分析其临床特征。结果21... 目的分析原发性血小板增多症合并冠状动脉粥样硬化性心脏病(以下简称冠心病)患者的临床特征。方法收集2014年1月—2018年6月于郑州大学第一附属医院住院治疗的21例原发性血小板增多症合并冠心病患者的临床资料,分析其临床特征。结果21例患者中,男性6例,女性15例,平均年龄(60.8±10.7)岁;合并心血管危险因素者17例;JAK2V617F基因突变阳性者16例;既往有血栓病史者6例;入院平均血小板计数为(880±360)×109/L;急性心肌梗死起病者7例,不稳定性心绞痛者9例,稳定型冠心病者5例;病变累及左前降支者17例;9例患者行支架置入治疗,共置入支架12枚;16例患者接受了阿司匹林联合氯吡格雷或替格瑞洛的双联抗血小板治疗,5例患者接受阿司匹林单抗治疗;20例患者院外长期口服羟基脲治疗,1例患者行干扰素治疗;平均随访时间(27±17)个月,随访期间平均血小板计数(395±116)×109/L,较入院时下降(P<0.05)。1例患者于治疗后发生急性心力衰竭,1例患者发生消化道出血及脑梗死,1例患者发生消化道出血及脑出血,1例患者发生脑梗死,1例患者发生肺栓塞。结论原发性血小板增多症合并冠心病患者最常累及冠状动脉的左前降支,且起病表现以急性冠状动脉综合征者多见,心血管危险因素及JAK2V617F基因突变与其发病相关,临床上需注意预防脑血管并发症及出血事件。 展开更多
关键词 血小板增多 冠状动脉粥样硬化性心脏病 临床特征
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Follow-up study on symptom distress in esophageal cancer patients undergoing repeated dilation 被引量:2
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作者 Li Liu Qian-Wen Liu +4 位作者 xiao-dan wu Shu-Yue Liu Hui-Jiao Cao Yu-Tong Hong Hui-Ying Qin 《World Journal of Clinical Cases》 SCIE 2020年第16期3503-3514,共12页
BACKGROUND Repeated endoscopic probe dilatation is the most preferred treatment for esophageal stenosis which may cause high levels of symptom distress in the patient’s home rehabilitation stage.AIM To explore the ch... BACKGROUND Repeated endoscopic probe dilatation is the most preferred treatment for esophageal stenosis which may cause high levels of symptom distress in the patient’s home rehabilitation stage.AIM To explore the changes in the symptom distress level and its correlation with the dilation effect in patients with esophageal carcinoma undergoing repeated dilations for lumen stenosis.METHODS The difference(R2-R1)between the diameter of the esophageal stenosis opening(R1)of the patients before dilation(R1)and after dilation(R2)was calculated to describe the extent and expansion of the esophageal stenosis before and after dilation.The M.D.Anderson Symptom Inventory was used to describe the symptom distress level of patients with dilation intermittence during their stay at home and to explore the correlation between the dilation effect and symptom distress level.RESULTS The diameter of the esophagus(R1)increased before each dilation in patients undergoing esophageal dilation(P<0.05).The diameter(R2)increased after dilation(P<0.05);the dilation effect(R2-R1)decreased with the number of dilations(P<0.05).The total symptom distress score significantly increased with the number of dilations(P<0.05).The symptom distress scores of the patients were negatively correlated(P<0.05)with the previous dilation effect(R2-R1)and the esophageal diameter(R2)after the previous dilation.After the 1 st to 4 th dilations,the patient’s symptom distress score was negatively correlated with the esophageal diameter(R12)before the next dilation,while there was no significant correlation(P>0.05)with the other dilations.CONCLUSION In patients who have undergone repeated dilations,better effect stands for lower symptom distress level and the increase in symptom distress has a prompt effect on the severity of the next occurrence of restenosis. 展开更多
关键词 Esophageal carcinoma Dilation of esophageal stenosis Symptom distress Dilation effect Lumen stenosis Repeated dilation
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The Minimum Local Analgesic Concentration of Epidural Lidocaine for Herpetic Neuralgia
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作者 Shao-xiong Fu Yan-qing Chen +1 位作者 Rong-guo Liu xiao-dan wu 《麻醉与监护论坛》 2013年第4期292-294,共3页
关键词 利多卡因 带状疱疹 有效浓度 神经痛 硬膜 数字减影血管造影 镇痛 EC50
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A frameshift mutation in exon 19 of MLH1 in a Chinese Lynch syndrome family: a pedigree study 被引量:1
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作者 Qiao-qi SUI wu JIANG +3 位作者 xiao-dan wu Yi-hong LING Zhi-zhong PAN Pei-rong DING 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2019年第1期105-108,共4页
Lynch syndrome (LS),an autosomal dominantly inherited disease previously known as hereditary non-polyposis coloreetal cancer (HNPCC),leads to a high risk of colorectal cancer (CRC)as well as malignancy at certain site... Lynch syndrome (LS),an autosomal dominantly inherited disease previously known as hereditary non-polyposis coloreetal cancer (HNPCC),leads to a high risk of colorectal cancer (CRC)as well as malignancy at certain sites including endometrium,ovary,stomach,and small bowel (Hampel et al.,2008;Lynch et al.,2009).Clinically,LS is considered the most common hereditary CRC-predisposing syndrome, accounting for about 3% of all CRC cases (Popat et al., 2005).LS is associated with mutations of DNA mismatch repair (MMR)genes such as MLH1,MSH2, MSH6,PMS2,and EPCAM (Ligtenberg et al.,2009;Lynch et al.,2009),which can trigger a high frequency of replication errors in both microsatellite regions and repetitive sequences in the coding regions of various cancer-related genes. 展开更多
关键词 Lync综合征 家系 DNA错配修复基因 置换 移码突变
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