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951.
目的探讨电脑控温毯对重症手足口病患儿体温的控制效果。方法将2011年6月至2012年1月儿科重症监护室收治的68例重症手足口病患儿按照随机数字表法分为研究组和对照组各34例,对照组在体温〉39℃时使用布洛芬混悬滴剂降温;研究组在体温〉39℃时使用布洛芬混悬滴剂联合电脑控温毯降温。观察两组患儿在采用降温措施后1、2、3、4、6h的体温变化及全天呼吸、心率的波动幅度,高热持续时间。结果研究组的降温效果明显优于对照组(P〈0.01);研究组全天呼吸、心率波动幅度明显小于对照组(P〈0.01),高热持续时间较对照组明显缩短(P〈0.01)。结论使用电脑控温毯能有效控制重症手足口病患儿的体温,缩短病程,有效防止并发症。 相似文献
952.
Li Zhan Xie Xinfang Zhang Xue Shi Sufang Liu Lijun Chen Pei Sui Guili Lyu Jicheng Zhang Hong 《中华肾脏病杂志》2019,35(2):81-87
Objective To establish the measurement of IgA1 O-glycan-specific antiglycan autoantibodies in patients with IgA nephropathy (IgAN), and evaluate their role in the development and progression of IgAN. Methods In the IgAN regular follow-up cohort of Peking University Institute of Nephrology from January 2006 to December 2015, 170 patients drawn by stratified randomization were enrolled in this study. Enzyme-linked immunosorbent assay (ELISA) was used to determine the levels of plasma galactose-deficient IgA1 (Gd-IgA1) and antiglycan autoantibody (IgG and IgA1). The correlation between antiglycan autoantibodies and clinicopathological parameters was analyzed by linear correlation and multiple linear regression analysis. The receiver operating characteristic curve (ROC) was used to evaluate the value of plasma anti glycide antibodies in the diagnosis of IgAN. Results IgG and IgA1 antiglycan autoantibodies that specifically recognized Fab-hinge region (Fab-HR) antigens could be detected in both IgAN and healthy control group. Agglutinin inhibition test showed that the specific antigen epitope was N-acetylgalactosamine (GalNAc) residue exposed to galactose deficiency in IgA1 hinged region. There was no significant difference in the absolute levels of plasma IgG antiglycan autoantibodies between IgAN and healthy controls (P=0.963). After adjustment of the plasma level of IgG, the normalized antiglycan autoantibody (ln[IgG antiglycan antibody/IgG]) in patients with IgAN was significantly higher than that in healthy controls (0.58±0.31 vs 0.37±0.11, P﹤0.01). The normalized level of IgG antiglycan autoantibody in IgAN patients was positively correlated with 24 h urine protein level during renal biopsy (Spearman r=0.183, P﹤0.05), and was also significantly correlated with 24 h urinary protein level after adjusting for baseline clinical and pathological factors (β=0.713, 95%CI 0.323-1.102, P﹤0.01). The area under ROC curve (AUC) of normalized IgG antiglycan autoantibody in the diagnosis of IgAN was 0.764 (95% CI 0.682-0.845, P﹤0.05). Using the cut-off value of 0.396, the sensitivity and specificity of normalized IgG antiglycan autoantibody for IgAN were 0.729 and 0.700 respectively. There was no significant difference in the absolute or normalized levels of IgA1 antiglycan autoantibodies between IgAN patients and healthy controls. Conclusions Gd-IgA1-specific antiglycan autoantibodies can be detected both in IgAN patients and healthy controls. They are elevated in some patients with IgAN and possibly involved in the development of IgAN. 相似文献
953.
Yushu Wang Xiuli Shi Rongsheng Du Yucheng Chen Qing Zhang 《Internal and emergency medicine》2018,13(2):231-241
The impact of red blood cell transfusion on outcomes in patients with acute coronary syndrome is controversial. Pubmed, EMBASE, and Cochrane Library were searched for studies of red blood cell transfusion and acute coronary syndrome that were published in any language, from January 1, 1966, to April 1, 2016. We analyzed 17 observational studies, of 2,525,550 subjects. We conducted a systematic review with meta-analysis of studies assessing the association between blood transfusion and the risk for all-cause mortality and reinfarction. The search yielded 17 observational studies, of 2,525,550 subjects, during a study follow-up period, ranging from 30 days to 5 years. Red blood cell transfusion compared with no blood transfusion is associated with higher short- and long-term all-cause mortality as well as reinfarction rates (adjusted RR 2.23; 95% CI 1.47–3.39; HR 1.93; 95% CI 1.12–3.34; RR 2.61; 95% CI 2.17–3.14, respectively). In hemoglobin-stratified analyses, a graded association between red blood cell transfusion and mortality was observed, transfusion and risk of all-cause mortality was borderline significant at hemoglobin levels below 8.0 g/dL (RR 0.52; 95% CI 0.25–1.06), and was associated with an increased risk of mortality at a hemoglobin above 10 g/dL (RR 3.34; 95% CI 2.25–4.97). Red blood cell transfusion was associated with an increased risk of short- and long-term mortality as well as myocardial reinfarction. However, transfusion appeared to have beneficial or neutral effects on mortality at hemoglobin levels below 8.0 g/dL, and harmful effects above 10 g/dL. A large definitive randomized controlled trial addressing this issue is urgently required. 相似文献
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史子千 《国际医药卫生导报》2017,23(17)
目的 探讨齐拉西酮与奥氮平治疗早期精神分裂症的效果及安全性.方法 将本院收治100例早期精神分裂症患者随机分为对照组与实验组,各50例.对照组给予奥氮平治疗,试验组给予齐拉西酮治疗.比较两组临床疗效、自我管理能力等差异.结果 试验组总有效率为92.0%,高于对照组的88.0%,差异无统计学意义(P>0.05).治疗后,试验组自我管理能力为(73.68±5.31)分,高于对照组的(60.66±4.37)分;试验组不良反应率为4.0%,低于对照组的20.0%;差异均具有统计学意义(均P<0.05).结论 齐拉西酮较奥氮平治疗早期精神分裂症效果佳,值得临床选择. 相似文献
959.
Guanheng Yang Wansheng Shi Xingyin Hu Jingzhi Zhang Zhijuan Gong Xinbing Guo Zhaorui Ren Fanyi Zeng 《Haematologica》2014,99(8):1304-1311
Although β-thalassemia is one of the most common human genetic diseases, there is still no effective treatment other than bone marrow transplantation. Induced pluripotent stem cells have been considered good candidates for the future repair or replacement of malfunctioning organs. As a basis for developing transgenic induced pluripotent stem cell therapies for thalassemia, β654 induced pluripotent stem cells from a β654 -thalassemia mouse transduced with the normal human β-globin gene, and the induced pluripotent stem cells with an erythroid-expressing reporter GFP were used to produce chimeric mice. Using these chimera models, we investigated changes in various pathological indices including hematologic parameters and tissue pathology. Our data showed that when the chimerism of β654 induced pluripotent stem cells with the normal human β-globin gene in β654 mice is over 30%, the pathology of anemia appeared to be reversed, while chimerism ranging from 8% to 16% provided little improvement in the typical β-thalassemia phenotype. Effective alleviation of thalassemia-related phenotypes was observed when chimerism with the induced pluripotent stem cells owning the erythroid-expressing reporter GFP in β654 mouse was greater than 10%. Thus, 10% or more expression of the exogenous normal β-globin gene reduces the degree of anemia in our β-thalassemia mouse model, whereas treatment with β654 induced pluripotent stem cells which had the normal human β-globin gene had stable therapeutic effects but in a more dose-dependent manner. 相似文献
960.