临床荟萃 ›› 2022, Vol. 37 ›› Issue (1): 5-13.doi: 10.3969/j.issn.1004-583X.2022.01.001
• 循证研究 • 下一篇
收稿日期:
2020-12-05
出版日期:
2022-01-20
发布日期:
2022-01-20
通讯作者:
李树生
E-mail:shushengli16@sina.com
基金资助:
Xiao Liuniu, Zhong Yanxia, Li Shusheng()
Received:
2020-12-05
Online:
2022-01-20
Published:
2022-01-20
Contact:
Li Shusheng
E-mail:shushengli16@sina.com
摘要:
目的 系统评价体外血液净化技术(extracorporeal hemopurification, EH)对脓毒症患者临床预后的影响,并探讨相关细胞因子水平变化与临床预后的关联。方法 检索Pubmed, Web of Science, Cochrane Library, 中国知网数据库,纳入从2010年1月至2020年1月所有符合标准的,有关EH对脓毒症患者影响的相关文献,使用Review Manager 5.3进行森林图分析,探讨EH与脓毒症患者的住院病死率(in-hospital mortality, IHM)和重症监护室住院时长的关联,并进一步分析细胞因子水平的改变与临床预后关联。结果 共28篇文献纳入研究,累计2 587例患者,Meta分析结果显示EH(血液灌注、血液滤过、血液吸附、细胞因子吸附等)可显著降低脓毒症患者的IHM(OR=0.83, P=0.04),但并不影响患者的重症监护室住院时长(OR=-0.50, P=0.69)。亚组分析提示:高容量血液滤过或多黏菌素B血液灌注,并不能降低脓毒症患者的IHM(P=0.22;P=0.87);同样EH不能改善烧伤性脓毒症以及脓毒症性急性肾衰竭患者的IHM(P=0.08;P=0.77)。针对EH带来相关细胞因子水平降低的脓毒症患者,虽然IHM没有显著下降(P=0.48), 但是重症监护室的住院时长明显缩短(OR=-17.58,P=0.04)。结论 脓毒症患者,若无相关禁忌证,建议行体外血液净化作为辅助治疗。在治疗过程中,对相关细胞因子水平的调控,是有效缩短重症监护室住院时长的关键。
中图分类号:
肖刘牛, 钟燕霞, 李树生. 体外血液净化技术对脓毒症临床预后及细胞因子影响的Meta分析[J]. 临床荟萃, 2022, 37(1): 5-13.
Xiao Liuniu, Zhong Yanxia, Li Shusheng. Effect of extracorporeal hemopurification for clinical prognosis and cytokine levels of septic: A meta-analysis[J]. Clinical Focus, 2022, 37(1): 5-13.
纳入研究 | 患者 数量 | 平均 年龄(岁) | 性别 | 体外血液净化技术 | 治疗方法(例) | 死亡(例) | 炎症因子下降(例) | ICU住院时间(d) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
男 | 女 | 血液净化 | 传统治疗 | 血液净化 | 传统治疗 | 血液净化 | 传统治疗 | 血液净化 | 传统治疗 | ||||||||
Hassan[ | 23 | 61.64 | 16 | 7 | 偶联血浆滤过吸附 | 11 | 12 | 5 | 10 | - | - | 10.27 | 8.75 | ||||
Maynar[ | 21 | 74.35 | 9 | 12 | 多黏菌素B血液灌注 | 14 | 7 | 3 | 3 | - | - | 5 | 6 | ||||
Quenot[ | 60 | 66.6 | 42 | 18 | 高容量血液滤过 | 29 | 31 | 6 | 10 | - | - | 21 | 20 | ||||
Quinto[ | 64 | 63.2 | 43 | 21 | 血液滤过 | 64 | 10 | 54 | 3 | 33 | - | - | |||||
Schädler[ | 97 | 65.5 | 70 | 27 | 血液吸附 | 47 | 50 | 6 | 5 | - | - | - | - | ||||
Guo[ | 22 | 54.3 | 15 | 7 | 高容量血液滤过 | 11 | 11 | 4 | 6 | - | - | - | - | ||||
Huang[ | 44 | 74.8 | 24 | 20 | 血液灌注 | 24 | 20 | 11 | 11 | - | - | 27.9 | 29.4 | ||||
Kim[ | 40 | 67.25 | 24 | 16 | 多黏菌素B血液灌注 | 20 | 20 | 10 | 10 | - | - | 10.9 | 14.6 | ||||
Friesecke[ | 20 | 60.3 | 16 | 4 | 细胞因子吸附 | 20 | 18 | 2 | 8 | 1 | 31.2 | 67.2 | |||||
Servillo[ | 13 | 58.07 | 7 | 6 | 血液滤过 | 13 | 3 | 10 | 2 | 5 | 3 | 4 | |||||
Joannes-Boyau[ | 137 | 69 | 83 | 54 | 高容量血液滤过 | 66 | 71 | 25 | 29 | - | - | 29 | 30 | ||||
Chung[ | 37 | 48.5 | 26 | 11 | 高容量血液滤过 | 23 | 14 | 5 | 5 | - | - | 67 | 57 | ||||
Park[ | 212 | 62.1 | 138 | 74 | 高容量血液滤过 | 105 | 107 | 69 | 69 | - | - | 18.2 | 11.5 | ||||
Friesecke[ | 198 | 60.12 | - | - | 细胞因子吸附 | 135 | 63 | 88 | 48 | - | - | 16.77 | 34.9 | ||||
Hawchar[ | 20 | 65.6 | 13 | 7 | 细胞因子吸附 | 10 | 10 | 1 | 3 | - | - | 10.2 | 10.0 | ||||
Xu[ | 22 | 31.25 | 19 | 3 | 血液透析 | 11 | 11 | 1 | 4 | 6 | 8 | - | - | ||||
Livigni[ | 184 | 65.25 | 121 | 63 | 偶联血浆滤过吸附 | 91 | 93 | 41 | 44 | - | - | 6.2 | 6.5 | ||||
Tamme[ | 19 | 65 | 12 | 7 | 高容量血液滤过 | 19 | 9 | 10 | 8 | 8 | 11.5 | 34.5 | |||||
Wu[ | 43 | 46.5 | 31 | 12 | 血液滤过 | 43 | 6 | 27 | 4 | 10 | 12.0 | 20.5 | |||||
Kade[ | 28 | 60.29 | - | - | 高容量血液滤过 | 28 | 18 | 10 | 5 | 7 | - | - | |||||
Zhang[ | 280 | 58.29 | 172 | 108 | 高容量血液滤过 | 141 | 139 | 81 | 81 | - | 21.9 | 25.9 | |||||
Dellinger[ | 450 | 59.85 | 273 | 177 | 多黏菌素B血液灌注 | 224 | 226 | 78 | 85 | - | - | - | - | ||||
Payen[ | 232 | 71.75 | 134 | 98 | 多黏菌素B血液灌注 | 119 | 113 | 33 | 22 | - | - | - | - | ||||
You[ | 82 | 40.95 | 65 | 17 | 高容量血液滤过 | 41 | 41 | 9 | 13 | - | - | 34.5 | 28.5 | ||||
Miao[ | 155 | 56 | 110 | 45 | 高容量血液滤过 | 93 | 62 | 26 | 21 | - | - | 11.7 | 15.4 | ||||
Zuccrai[ | 9 | - | 5 | 4 | 细胞因子吸附 | 9 | 5 | 4 | 1 | 1 | - | - | |||||
Shum[ | 15 | 74.25 | - | - | 血液吸附 | 7 | 8 | 1 | 3 | - | - | 12.5 | 5.3 | ||||
Peng[ | 60 | - | - | - | 血液灌注 | 30 | 30 | 14 | 23 | 20 | 10 | 8 | 4 |
表1 研究对象临床特点
纳入研究 | 患者 数量 | 平均 年龄(岁) | 性别 | 体外血液净化技术 | 治疗方法(例) | 死亡(例) | 炎症因子下降(例) | ICU住院时间(d) | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
男 | 女 | 血液净化 | 传统治疗 | 血液净化 | 传统治疗 | 血液净化 | 传统治疗 | 血液净化 | 传统治疗 | ||||||||
Hassan[ | 23 | 61.64 | 16 | 7 | 偶联血浆滤过吸附 | 11 | 12 | 5 | 10 | - | - | 10.27 | 8.75 | ||||
Maynar[ | 21 | 74.35 | 9 | 12 | 多黏菌素B血液灌注 | 14 | 7 | 3 | 3 | - | - | 5 | 6 | ||||
Quenot[ | 60 | 66.6 | 42 | 18 | 高容量血液滤过 | 29 | 31 | 6 | 10 | - | - | 21 | 20 | ||||
Quinto[ | 64 | 63.2 | 43 | 21 | 血液滤过 | 64 | 10 | 54 | 3 | 33 | - | - | |||||
Schädler[ | 97 | 65.5 | 70 | 27 | 血液吸附 | 47 | 50 | 6 | 5 | - | - | - | - | ||||
Guo[ | 22 | 54.3 | 15 | 7 | 高容量血液滤过 | 11 | 11 | 4 | 6 | - | - | - | - | ||||
Huang[ | 44 | 74.8 | 24 | 20 | 血液灌注 | 24 | 20 | 11 | 11 | - | - | 27.9 | 29.4 | ||||
Kim[ | 40 | 67.25 | 24 | 16 | 多黏菌素B血液灌注 | 20 | 20 | 10 | 10 | - | - | 10.9 | 14.6 | ||||
Friesecke[ | 20 | 60.3 | 16 | 4 | 细胞因子吸附 | 20 | 18 | 2 | 8 | 1 | 31.2 | 67.2 | |||||
Servillo[ | 13 | 58.07 | 7 | 6 | 血液滤过 | 13 | 3 | 10 | 2 | 5 | 3 | 4 | |||||
Joannes-Boyau[ | 137 | 69 | 83 | 54 | 高容量血液滤过 | 66 | 71 | 25 | 29 | - | - | 29 | 30 | ||||
Chung[ | 37 | 48.5 | 26 | 11 | 高容量血液滤过 | 23 | 14 | 5 | 5 | - | - | 67 | 57 | ||||
Park[ | 212 | 62.1 | 138 | 74 | 高容量血液滤过 | 105 | 107 | 69 | 69 | - | - | 18.2 | 11.5 | ||||
Friesecke[ | 198 | 60.12 | - | - | 细胞因子吸附 | 135 | 63 | 88 | 48 | - | - | 16.77 | 34.9 | ||||
Hawchar[ | 20 | 65.6 | 13 | 7 | 细胞因子吸附 | 10 | 10 | 1 | 3 | - | - | 10.2 | 10.0 | ||||
Xu[ | 22 | 31.25 | 19 | 3 | 血液透析 | 11 | 11 | 1 | 4 | 6 | 8 | - | - | ||||
Livigni[ | 184 | 65.25 | 121 | 63 | 偶联血浆滤过吸附 | 91 | 93 | 41 | 44 | - | - | 6.2 | 6.5 | ||||
Tamme[ | 19 | 65 | 12 | 7 | 高容量血液滤过 | 19 | 9 | 10 | 8 | 8 | 11.5 | 34.5 | |||||
Wu[ | 43 | 46.5 | 31 | 12 | 血液滤过 | 43 | 6 | 27 | 4 | 10 | 12.0 | 20.5 | |||||
Kade[ | 28 | 60.29 | - | - | 高容量血液滤过 | 28 | 18 | 10 | 5 | 7 | - | - | |||||
Zhang[ | 280 | 58.29 | 172 | 108 | 高容量血液滤过 | 141 | 139 | 81 | 81 | - | 21.9 | 25.9 | |||||
Dellinger[ | 450 | 59.85 | 273 | 177 | 多黏菌素B血液灌注 | 224 | 226 | 78 | 85 | - | - | - | - | ||||
Payen[ | 232 | 71.75 | 134 | 98 | 多黏菌素B血液灌注 | 119 | 113 | 33 | 22 | - | - | - | - | ||||
You[ | 82 | 40.95 | 65 | 17 | 高容量血液滤过 | 41 | 41 | 9 | 13 | - | - | 34.5 | 28.5 | ||||
Miao[ | 155 | 56 | 110 | 45 | 高容量血液滤过 | 93 | 62 | 26 | 21 | - | - | 11.7 | 15.4 | ||||
Zuccrai[ | 9 | - | 5 | 4 | 细胞因子吸附 | 9 | 5 | 4 | 1 | 1 | - | - | |||||
Shum[ | 15 | 74.25 | - | - | 血液吸附 | 7 | 8 | 1 | 3 | - | - | 12.5 | 5.3 | ||||
Peng[ | 60 | - | - | - | 血液灌注 | 30 | 30 | 14 | 23 | 20 | 10 | 8 | 4 |
[1] |
Rimmele T, Kellum JA. Clinical review: Blood purification for sepsis[J]. Critical Care, 2011, 15(1):205.
doi: 10.1186/cc9411 URL |
[2] |
Putzu A, Schorer R, Lopez-Delgado JC, et al. Blood purification and mortality in sepsis and septic shock[J]. Anesthesiology, 2019, 131(3):580-593.
doi: 10.1097/ALN.0000000000002820 URL |
[3] |
Zhou F, Peng Z, Murugan R, et al. Blood purification and mortality in sepsis[J]. Crit Care Med, 2013, 41(9):2209-2220.
doi: 10.1097/CCM.0b013e31828cf412 URL |
[4] | Steltzer H, Grieb A, Mostafa K, et al. Use of Cytosorb in traumatic amputation of the forearm and severe septic shock[J]. Case Rep Crit Care, 2017, 2017:8747616. |
[5] |
Kade G, Literacki S, Rzeszotarska A, et al. Removal of procalcitonin and selected cytokines during continuous veno-venous hemodialysis using high cutoff hemofilters in patients with sepsis and acute kidney injury[J]. Blood Purif, 2018, 46(2):153-159.
doi: 10.1159/000488929 URL |
[6] |
Chihara S, Masuda Y, Tatsumi H, et al. Evaluation of pre-and post-dilution continuous veno-venous hemofiltration on leukocyte and platelet function in patients with sepsis[J]. Int J Artif Organs, 2019, 42(1):9-16.
doi: 10.1177/0391398818801292 pmid: 30278811 |
[7] |
Oudemans-Van Straaten HM, Elbers PW. How to explain and exploit the beneficial effects of high-volume hemofiltration on hemodynamics and strong ion gap[J]. Intensive Care Med, 2013, 39(6):1140-1142.
doi: 10.1007/s00134-013-2820-4 pmid: 23361626 |
[8] |
Hassan J, Cader RA, Kong NC, et al. Original article: Coupled plasma filtration adsorption (CPFA) plus continuous veno-venous haemofiltration (CVVH) versus CVVH alone as an adjunctive therapy in the treatment of sepsis[J]. EXCLI J, 2013, 12:681-692.
pmid: 26600735 |
[9] | Maynar J, Martínez-Sagasti F, Herrera-Gutiérrez M, et al. Direct hemoperfusion with polymyxin B-immobilized cartridge in severe sepsis due to intestinal perforation: hemodynamic findings and clinical considerations in anticoagulation therapy[J]. Rev Esp Quimioter, 2013, 26(2):151-158. |
[10] |
Quenot JP, Binquet C, Vinsonneau C, et al. Very high volume hemofiltration with the Cascade system in septic shock patients[J]. Intensive Care Med, 2015, 41(12):2111-2120.
doi: 10.1007/s00134-015-4056-y URL |
[11] |
Quinto BM, Iizuka IJ, Monte JC, et al. TNF-α depuration is a predictor of mortality in critically ill patients under continuous veno-venous hemodiafiltration treatment[J]. Cytokine, 2015, 71(2):255-260.
doi: 10.1016/j.cyto.2014.10.024 pmid: 25461406 |
[12] | Schädler D, Pausch C, Heise D, et al. The effect of a novel extracorporeal cytokine hemoadsorption device on IL-6 elimination in septic patients: A randomized controlled trial[J]. PLoS One, 2017, 12(10):e187015. |
[13] |
Guo J, Tao W, Tang D, et al. Th17/Regulatory T cell imbalance in sepsis patients with multiple organ dysfunction syndrome: Attenuated by high-volume hemofiltration[J]. Int J Artif Organs, 2017, 40(11):607-614.
doi: 10.5301/ijao.5000625 URL |
[14] |
Huang Z, Wang SR, Su W, et al. Removal of humoral mediators and the effect on the survival of septic patients by hemoperfusion with neutral microporous resin column[J]. Ther Apher Dial, 2010, 14(6):596-602.
doi: 10.1111/tap.2010.14.issue-6 URL |
[15] |
Kim JJ, Park YJ, Moon KY, et al. Polymyxin B hemoperfusion as a feasible therapy after source control in abdominal septic shock[J]. World J Gastrointest Surg, 2019, 11(12):422-432.
doi: 10.4240/wjgs.v11.i12.422 URL |
[16] |
Friesecke S, Träger K, Schittek GA, et al. International registry on the use of the CytoSorb® adsorber in ICU patients: Study protocol and preliminary results[J]. Med Klin Intensivmed Notfmed, 2019, 114(8):699-707.
doi: 10.1007/s00063-017-0342-5 pmid: 28871441 |
[17] | Servillo G, Vargas M, Pastore A, et al. Immunomodulatory effect of continuous venovenous hemofiltration during sepsis: Preliminary data[J]. Biomed Res Int, 2013, 2013:108951. |
[18] |
Joannes-Boyau O, Honoré PM, Perez P, et al. High-volume versus standard-volume haemofiltration for septic shock patients with acute kidney injury (IVOIRE study): A multicentre randomized controlled trial[J]. Intensive Care Med, 2013, 39(9):1535-1546.
doi: 10.1007/s00134-013-2967-z pmid: 23740278 |
[19] |
Chung KK, Coates EC, Smith DJ Jr, et al. High-volume hemofiltration in adult burn patients with septic shock and acute kidney injury: A multicenter randomized controlled trial[J]. Crit Care, 2017, 21(1):89.
doi: 10.1186/s13054-017-1678-1 URL |
[20] |
Park JT, Lee H, Kee YK, et al. High-dose versus conventional-dose continuous venovenous hemodiafiltration and patient and kidney survival and cytokine removal in sepsis-associated acute kidney injury: A randomized controlled trial[J]. Am J Kidney Dis, 2016, 68(4):599-608.
doi: 10.1053/j.ajkd.2016.02.049 URL |
[21] |
Friesecke S, Stecher SS, Gross S, et al. Extracorporeal cytokine elimination as rescue therapy in refractory septic shock: A prospective single-center study[J]. J Artif Organs, 2017, 20(3):252-259.
doi: 10.1007/s10047-017-0967-4 pmid: 28589286 |
[22] |
Hawchar F, László I, Öveges N, et al. Extracorporeal cytokine adsorption in septic shock: A proof of concept randomized, controlled pilot study[J]. J Crit Care, 2019, 49:172-178.
doi: S0883-9441(18)30777-9 pmid: 30448517 |
[23] |
Xu C, Fan K, Xie L, et al. Evaluation of optimized continuous venovenous hemodiafiltration therapy efficiency in severe burn patients with sepsis[J]. Burns Trauma, 2014, 2(3):125-129.
doi: 10.4103/2321-3868.137604 URL |
[24] | Livigni S, Bertolini G, Rossi C, et al. Efficacy of coupled plasma filtration adsorption (CPFA) in patients with septic shock: A multicenter randomised controlled clinical trial[J]. BMJ Open, 2014, 4(1):e003536. |
[25] | Tamme K, Maddison L, Kruusat R, et al. Effects of high volume haemodiafiltration on inflammatory response profile and microcirculation in patients with septic shock[J]. Biomed Res Int, 2015, 2015:125615. |
[26] |
Wu J, Ren J, Liu Q, et al. Effects of changes in the levels of damage-associated molecular patterns following continuous veno-venous hemofiltration therapy on outcomes in acute kidney injury patients with sepsis[J]. Front Immunol, 2019, 9:3052.
doi: 10.3389/fimmu.2018.03052 URL |
[27] |
Kade G, Lubas A, Rzeszotarska A, et al. Effectiveness of high cut-off hemofilters in the removal of selected cytokines in patients during septic shock accompanied by acute kidney injury-preliminary study[J]. Med Sci Monit, 2016, 22:4338-4344.
doi: 10.12659/MSM.896819 URL |
[28] |
Zhang P, Yang Y, Lv R, et al. Effect of the intensity of continuous renal replacement therapy in patients with sepsis and acute kidney injury: A single-center randomized clinical trial[J]. Nephrol Dial Transplant, 2012, 27(3):967-973.
doi: 10.1093/ndt/gfr486 URL |
[29] |
Dellinger RP, Bagshaw SM, Antonelli M, et al. Effect of targeted polymyxin B hemoperfusion on 28-day mortality in patients with septic shock and elevated endotoxin level[J]. JAMA, 2018, 320(14):1455-1463.
doi: 10.1001/jama.2018.14618 pmid: 30304428 |
[30] |
Payen DM, Guilhot J, Launey Y, et al. Early use of polymyxin B hemoperfusion in patients with septic shock due to peritonitis: A multicenter randomized control trial[J]. Intensive Care Med, 2015, 41(6):975-984.
doi: 10.1007/s00134-015-3751-z URL |
[31] |
You B, Zhang YL, Luo GX, et al. Early application of continuous high-volume haemofiltration can reduce sepsis and improve the prognosis of patients with severe burns[J]. Crit Care, 2018, 22(1):173.
doi: 10.1186/s13054-018-2095-9 URL |
[32] |
Miao H, Wang F, Xiong X, et al. Clinical benefits of high-volume hemofiltration in critically Ill pediatric patients with severe sepsis: A retrospective cohort study[J]. Blood Purif, 2018, 45(1-3):18-27.
doi: 10.1159/000481249 URL |
[33] |
Zuccari S, Damiani E, Domizi R, et al. Changes in cytokines, haemodynamics and microcirculation in patients with sepsis/septic shock undergoing continuous renal replacement therapy and blood purification with cytosorb[J]. Blood Purif, 2020, 49(1-2):107-113.
doi: 10.1159/000502540 URL |
[34] |
Shum HP, Leung YW, Lam SM, et al. Alteco endotoxin hemoadsorption in gram-negative septic shock patients[J]. Indian J Crit Care Med, 2014, 18(12):783-788.
doi: 10.4103/0972-5229.146305 URL |
[35] |
Peng ZY, Wang HZ, Carter MJ, et al. Acute removal of common sepsis mediators does not explain the effects of extracorporeal blood purification in experimental sepsis[J]. Kidney Int, 2012, 81(4):363-369.
doi: 10.1038/ki.2011.320 URL |
[1] | 崔兰丹, 杨春燕. 脓毒症患者甲状腺激素的变化特点及研究进展[J]. 临床荟萃, 2024, 39(1): 70-74. |
[2] | 黄赛虎, 龙中洁, 董兴强, 孟祥营, 吴水燕, 柏振江. 血液肿瘤患儿合并脓毒血症的病原学特点及临床特征[J]. 临床荟萃, 2024, 39(1): 38-42. |
[3] | 唐爱军, 汪丽韡. 脓毒症患者入院时血小板计数及凝血指标对28天生存状况的预测价值[J]. 临床荟萃, 2023, 38(3): 250-254. |
[4] | 周利娟, 诸彭伟, 曹梅, 程真梅, 吴峤微, 李勇. 铁蛋白、红细胞参数及血浆D-二聚体与儿童脓毒症的相关性[J]. 临床荟萃, 2023, 38(1): 60-63. |
[5] | 周彬, 曾词正, 黄宇戈, 钟娩玲, 吴家园. pSOFA评分联合C-反应蛋白、降钙素原在脓毒症患儿预后评估中的作用[J]. 临床荟萃, 2022, 37(7): 616-622. |
[6] | 张孟媛, 朱勇. 降钙素原清除率及序贯器官衰竭估计评分对脓毒症患者预后的预测价值[J]. 临床荟萃, 2022, 37(3): 225-229. |
[7] | 侯伟, 张丽君, 张曼, 王亚坤, 贾美轩, 田利远. 外周血白细胞不高的脓毒症患儿84例临床分析[J]. 临床荟萃, 2021, 36(9): 799-802. |
[8] | Eamran Hossain, 田亚, 陈源, 张少丹, 张会丰. IPEX综合征并发肠源性脓毒症1例并文献复习[J]. 临床荟萃, 2021, 36(5): 453-457. |
[9] | 高其庆, 李卓虹, 周浩, 彭劼. 脓毒症相关性血小板减少[J]. 临床荟萃, 2021, 36(10): 946-950. |
[10] | 晁彦公,中国重症超声研究组. 脓毒症急性肾损伤时血管活性药物的选择[J]. 临床荟萃, 2019, 34(7): 599-603. |
[11] | 刘丽霞1, 王小亭2, 晁彦公3, 张宏民2, 武钧4,尹万红5, 张丽娜6, 何伟7, 朱然8, 丁欣2, 张倩1, 胡振杰1, 中国重症超声研究组. 脓毒症急性肾损伤:一种微循环疾病[J]. 临床荟萃, 2019, 34(7): 595-598. |
[12] | 冯钧帅,傅彩虹,马茹,周倩倩,周慧茹,张金周,高军龙,王贤东. 血浆滤过透析治疗肝衰竭合并脓毒症的疗效[J]. 临床荟萃, 2019, 34(4): 330-333. |
[13] | 徐瑞山a,张晓莉b. 重症脓毒症患者外周血免疫因子的表达及临床意义[J]. 临床荟萃, 2018, 33(7): 579-582,586. |
[14] | 张延威, 赵麦良, 张圣, 周奎龙, 高辉,王军辉,赵星,李超. 血必净联合乌司他丁治疗脓毒症诱导急性呼吸窘迫综合征的效果观察#br#[J]. 临床荟萃, 2018, 33(7): 575-578. |
[15] | 宋中海1a,高辉1a,卢纯1b,董士民2. 血清降钙素原联合T淋巴细胞亚群及中性粒细胞CD64对脓毒症病情程度与预后的评估价值[J]. 临床荟萃, 2018, 33(7): 568-574. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||