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Randomized Controlled Study on Safety and Feasibility of Transfusion Trigger Score of Emergency Operations 被引量:9
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作者 De-Xing Liu Jin Liu +3 位作者 Fan Zhang Qiu-Ying Zhang mian xie Zhao-Qiong Zhu 《Chinese Medical Journal》 SCIE CAS CSCD 2015年第13期1801-1808,共8页
Background: Due to the floating of the guideline, there is no evidence-based evaluation index on when to start the blood transfusion for patients with hemoglobin (Hb) level between 7 and 10 g/dl. As a restdt, the t... Background: Due to the floating of the guideline, there is no evidence-based evaluation index on when to start the blood transfusion for patients with hemoglobin (Hb) level between 7 and 10 g/dl. As a restdt, the trigger point of blood transtiision may be different in the emergency use of the existing transfusion guidelines. The present study was designed to evaluate whether the scheme can be safely and effectively used for emergency patients, so as to be supported by multicenter and large sample data in the future. Methods: From June 2013 to June 2014, patients were randomly divided into the experimental group (Peri-operative Transfusion Trigger Score of Emergency [POTTS-E] group) and the control group (control group). The between-group differences in the patients' demography and baseline inlbrmation, mortality and blood transfusion-related complications, heart rate, resting arterial pressure, body temperature, and Hb values were compared. The consistency of red blood cell (RBC) transiiision standards of the two groups of patients with the current blood transfusion guideline, namely the compliance of the guidelines, utilization rate, and per-capita consumption of autologous RBC were analyzed. Results: During the study period, a total of 72 patients were recorded, and 65 of them met the inclusion criteria, which included 33 males and 32 females with a mean age of(34.8 ± 14.6) years. 50 tmderwent abdomen surgery, 4 underwent chest surgery, 11 underwent arms and legs surgery. There was no statistical difference between the two groups for demography and baseline inlbrmation. There was also no statistical differences between the two groups in anesthesia time, intraoperative rehydration, staying time in postanesthetic care unit, emergency hospitalization, postoperative 72 h Acute Physiologic Assessment and Chronic Health Evaluation II scores, blood transliision-related complications and mortality. Only tile POTTS-E group on the 1st postoperative day Hb was lower than group control, P 〈 0.05. POTTS-E group was totally (100%) conlbrmed to the requirements of the transfusion guideline to RBC inliision, which was higher than that of the control group (81.25%), P 〈 0.01.There were no statistical differences in utilization rates of autologous blood of the two groups; the utilization rates ofallogeneic RBC, total allogeneic RBC and total RBC were 48.48%, 51.5%, and 75.7% in POTTS-E group, which were lower than those of the control group (84.3%, 84.3%, and 96.8%) P 〈 0.05 or P 〈 0.01. Per capita consumption of intraoperative allogeneic RBC. total allogeneic RBC and total RBC were 0 (0, 3.0), 2.0 (0, 4.0), and 3.1 (0.81, 6.0) in POTTS-E groups were all lower than those of control group (4.0 [2.0, 4.0], 4.0 [2.0, 6.0] and 5.8 [2.7, 8.2]), P 〈 0.05 or P 〈 0.00 I. Conclusions: Peri-operative Transfilsion Trigger Score-E evaluation scheme is used to guide the application of RBC. There are no differences in the recent prognosis of patients with the traditional transfusion guidelines. This scheme is sate; Compared with doctor experience-based sub iective assessment, the scoring scheme was closer to patient physiological needs lbr transfusion and more reasonable: Utilization rate and the per capita consumption of RBC are obviously declined, which has clinical significance and is feasible. Based on the abovementioned three points, POTTS-E scores scheme is safe, reasonable, and practicable and has the value tbr carrying out multicenter and large sample clinical researches. 展开更多
关键词 Emergency Operations Transfusion Guideline: Transfusion Trigger Score Red Blood Cell
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靶向炎性细胞因子的生物制剂及其临床应用 被引量:4
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作者 陈锦 谢冕 +2 位作者 李路军 刘东旭 刘梦元 《生物工程学报》 CAS CSCD 北大核心 2019年第6期1009-1020,共12页
细胞因子可介导许多生物学过程并受到机体的严格调节,其调节的失控可引发一系列疾病如自身免疫炎症和肿瘤。在过去的十几年中,一些能够有效调节细胞因子生物学作用的生物制剂如重组抗炎细胞因子、细胞因子受体以及中和性抗体等被广泛应... 细胞因子可介导许多生物学过程并受到机体的严格调节,其调节的失控可引发一系列疾病如自身免疫炎症和肿瘤。在过去的十几年中,一些能够有效调节细胞因子生物学作用的生物制剂如重组抗炎细胞因子、细胞因子受体以及中和性抗体等被广泛应用到由细胞因子失调引起的相关疾病的治疗。尤其是近年来,一些具有创新性的靶向细胞因子的新型生物制剂在不断涌现。文中对近年来国际上靶向炎症细胞因子(TNF-α、IL-1β、IL-6、IL-17)的生物制剂的研发和临床应用的相关进展进行了综述,指出其副作用和应用风险,并结合其他学者和自己的研究工作提出减少副作用和风险的途径和方法。利用现代生物技术提高抗细胞因子生物制剂针对炎症或肿瘤组织的特异性,是靶向炎性细胞因子生物制剂未来的重要发展方向。 展开更多
关键词 靶向治疗 炎性细胞因子 自身免疫 生物制剂
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