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Application of Early Enteral Nutrition in Critically Ill Children 被引量:1
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作者 Musheng Li lini chen 《Open Journal of Pediatrics》 2021年第4期543-550,共8页
<strong>Objective:</strong> <span style="font-family:Verdana;">T</span><span style="font-family:Verdana;">he </span><span style="font-family:Verdana;&quo... <strong>Objective:</strong> <span style="font-family:Verdana;">T</span><span style="font-family:Verdana;">he </span><span style="font-family:Verdana;">o</span><span style="font-family:Verdana;">bjective is to</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> investigate the incidence of moderate and severe malnutrition in children in intensive care units, and to analyze the safety and clinical efficacy of early enteral nutrition therapy in critically ill children. </span><b><span style="font-family:Verdana;">Methods: </span></b><span style="font-family:Verdana;">A total of 80 children hospitalized in the pediatric care unit meeting the inclusion criteria were selected and general data were collected, including 48 in the early enteral nutrition (EEN) group and 32 in the late EN group. The two groups were compared in the incidence of moderate to severe malnutrition, feeding tolerance, length of stay in ICU, total length of stay, changes in blood routine and biochemical indicators.</span><b><span style="font-family:Verdana;"> Results: </span></b><span style="font-family:Verdana;">After 1 week in ICU, the feeding tolerance of the treatment group was better than that of the control group (P < 0.05). The average length of stay in ICU and total length of stay in the treatment group were shorter than those in the control group (P < 0.05). After 1 week of comprehensive treatment (anti-infection and EEN), the total number of WBC, absolute value of neutrophil and C-reactive protein in peripheral blood of the treatment group were decreased (P < 0.01), which was significantly lower than that of the control group with bacterial infection (P < </span><span style="font-family:Verdana;">0.01). After 1 week of treatment in ICU, serum prealbumin in treatment</span><span style="font-family:Verdana;"> group </span><span style="font-family:Verdana;">was significantly higher than that in control group (P < 0.05), but serum </span><span style="font-family:Verdana;">albumin was not significantly higher (P > 0.05). The rate of moderate to severe malnutrition at discharge was lower in the treatment group than at admission to the ICU (17 cases vs. 20 cases, 35.4% vs. 41.7%), but higher in the control group (19 cases vs. 16 cases, 59.4% vs. 50.0%). </span><b><span style="font-family:Verdana;">Conclusion: </span></b><span style="font-family:Verdana;">Malnutrition is prevalent in children treated in pediatric intensive care units. Early enteral nutrition therapy for critically ill children is safe and effective, that can significantly improve the nutritional status of critically ill children, reduce inflammatory response, and shorten the hospital stay.</span></span> 展开更多
关键词 Early Enteral Nutrition CHILDHOOD Critical Care Intensive Care Unit
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实验室指标在早期鉴别诊断脓毒症和川崎病中的应用 被引量:3
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作者 陈丽妮 乔莉娜 《中华妇幼临床医学杂志(电子版)》 CAS 2022年第4期460-467,共8页
目的探讨早期鉴别诊断脓毒症与川崎病的生物标志物。方法选择2017年1月1日至2018年2月28日,于四川大学华西第二医院出院时确诊为脓毒症及川崎病的患儿为研究对象,并分别纳入脓毒症组(n=286)和川崎病组(n=326)。采用Mann-Whitney U秩和... 目的探讨早期鉴别诊断脓毒症与川崎病的生物标志物。方法选择2017年1月1日至2018年2月28日,于四川大学华西第二医院出院时确诊为脓毒症及川崎病的患儿为研究对象,并分别纳入脓毒症组(n=286)和川崎病组(n=326)。采用Mann-Whitney U秩和检验对2组患儿的白细胞计数(WBC)、中性粒细胞百分比、中性粒细胞绝对计数(ANC)、C反应蛋白(CRP)、血小板计数(PLT)、血红蛋白(Hb),红细胞沉降率(ESR)、降钙素原(PCT)、血小板平均体积(MPV)、凝血酶原时间(PT)、活化部分凝血活酶时间(APTT),天冬氨酸氨基转移酶(AST)、丙氨酸转移酶(ALT)、乳酸脱氢酶(LDH)、白蛋白、血尿素氮(BUN)、血清肌酐(SCr)、D-二聚体(DD)、纤维蛋白原降解物(FDP)、国际正常化比率(INR)、肌钙蛋白I(cTnI)、肌红蛋白(Mb)、N端脑钠肽(NTBNP)、纤维蛋白原(Fg),动脉血氧分压(PaO2)、吸入氧气分数(FiO_(2))、Na^(+)、K^(+)、Ca^(2+)、Cl^(-)等指标进行统计学分析。采用χ2检验或连续性校正χ2检验对2组患儿病死率、冠状动脉扩张发生率等进行统计学分析。2组患儿的性别构成比比较,差异无统计学意义(P>0.05)。本研究遵循的程序符合2013年修订的《世界医学协会赫尔辛基宣言》的要求。结果①脓毒症组患儿年龄小于川崎病组,入院前发热时间短于川崎病组,2组比较,差异均有统计学意义(P<0.05)。②脓毒症组患儿PCT水平高于川崎病组,而中性粒细胞百分比、ANC和ESR水平低于川崎病组,2组分别比较,差异均有统计学意义(P<0.05)。此外,脓毒症组患儿PCT值>0.5 ng/mL及PCT值>2 ng/mL者占比,均高于川崎病组,而CRP水平>30 mg/L、ESR>40 mm/h者占比,均低于川崎病组,2组分别比较,差异均有统计学意义(P<0.05)。③脓毒症组患儿的MPV、AST、LDH、BUN、SCr、Cl^(-)、DD、FDP、cTnI、Mb水平,均高于川崎病组,而Hb、PLT、ALT、Fg水平,均低于川崎病组,并且差异亦均有统计学意义(P<0.05)。④2组患儿呼吸系统功能损伤、循环系统功能损伤、消化系统功能损伤、泌尿系统功能损伤、凝血功能异常、血电解质异常、贫血及血小板增多者所占比例比较,差异均有统计学意义(P<0.05)。⑤脓毒症组与川崎病组住院期间患儿死亡率分别为5.2%(15例)与0,并且差异有统计学意义(χ2=17.527,P<0.001)。结论儿童脓毒症和川崎病在早期难以鉴别,易被误诊和漏诊。二者虽然很多实验室检查结果类似,但亦有部分实验室结果存在差异。脓毒症患儿的脏器损伤更严重、预后更差。 展开更多
关键词 脓毒症 黏膜皮肤淋巴结综合征 生物标记 诊断 鉴别 超声检查 多普勒 彩色 儿童
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Cancer-associated fibroblasts in breast cancer:Challenges and opportunities 被引量:18
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作者 Dengdi Hu Zhaoqing Li +9 位作者 Bin Zheng Xixi Lin Yuehong Pan Peirong Gong Wenying Zhuo Yujie Hu Cong chen lini chen Jichun Zhou Linbo Wang 《Cancer Communications》 SCIE 2022年第5期401-434,共34页
The tumor microenvironment is proposed to contribute substantially to the progression of cancers,including breast cancer.Cancer-associated fibroblasts(CAFs)are the most abundant components of the tumor microenvironmen... The tumor microenvironment is proposed to contribute substantially to the progression of cancers,including breast cancer.Cancer-associated fibroblasts(CAFs)are the most abundant components of the tumor microenvironment.Studies have revealed that CAFs in breast cancer originate from several types of cells and promote breast cancer malignancy by secreting factors,generating exosomes,releasing nutrients,reshaping the extracellular matrix,and suppressing the function of immune cells.CAFs are also becoming therapeutic targets for breast cancer due to their specific distribution in tumors and their unique biomarkers.Agents interrupting the effect of CAFs on surrounding cells have been developed and applied in clinical trials.Here,we reviewed studies examining the heterogeneity of CAFs in breast cancer and expression patterns of CAF markers in different subtypes of breast cancer.We hope that summarizing CAFrelated studies from a historical perspective will help to accelerate the development of CAF-targeted therapeutic strategies for breast cancer. 展开更多
关键词 Cancer-associated fibroblasts breast cancer therapeutic target tumor microenvironment BIOMARKER tumor heterogeneity
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