首页|替加环素致重症感染患者发生低纤维蛋白原血症的危险因素分析

替加环素致重症感染患者发生低纤维蛋白原血症的危险因素分析

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目的 分析替加环素致重症感染患者发生低纤维蛋白原血症的相关危险因素。方法 101例重症医学科接受替加环素治疗的重症感染患者,根据应用替加环素后患者是否发生低纤维蛋白原血症分为低FIB组[发生低纤维蛋白原血症,纤维蛋白原(FIB)<2。0 g/L,43 例]和对照组(未发生低纤维蛋白原血症,FIB≥2。0 g/L,58 例)。统计患者的临床资料,分析替加环素致低纤维蛋白原血症的危险因素,停用替加环素后FIB水平变化情况。结果 单因素分析结果发现,低FIB组的腹腔感染占比 41。86%、维持剂量 100 mg q。12 h。占比 30。23%高于对照组的 10。34%、12。07%,用替加环素前FIB水平(3。71±1。27)g/L低于对照组的(4。65±1。49)g/L,替加环素应用时间(8。98±2。47)d长于对照组的(7。33±2。33)d(P<0。05)。两组年龄、性别、基础疾病、既往手术史、应用替加环素前序贯器官衰竭评分(SOFA)评分、应用替加环素前急性生理学和慢性健康评估系统Ⅱ(APACHEⅡ)评分、致病菌、用替加环素前器官功能、负荷剂量 100 mg、联合应用头孢哌酮钠舒巴坦钠占比比较无统计学差异(P>0。05)。多因素分析结果显示:替加环素致低纤维蛋白原血症的的主要危险因素为腹腔感染、用替加环素前FIB水平低(P<0。05)。低FIB组患者有 24 例患者停用替加环素,其中有 19 例患者在停用替加环素后其FIB恢复至正常水平,比例为79。17%,恢复正常的时间为(5。52±2。06)d。结论 替加环素致重症感染患者发生低纤维蛋白原血症的危险因素为腹腔感染、用替加环素前FIB水平低。临床治疗中要预防腹腔感染,并且尽量缩短用药时间,注意监测患者FIB水平。
Analysis of risk factors for hypofibrinogenemia in patients with severe infection caused by tigecycline
Objective To analyze the related risk factors for hypofibrinogenemia in patients with severe infection caused by tigecycline.Methods 101 patients with severe infection in intensive care unit who received tigecycline treatment were selected.The patients were divided into low FIB group[with hypofibrinogenemia,fibrinogen(FIB)<2.0 g/L,43 cases]and control group(without hypofibrinogenemia,FIB≥2.0 g/L,58 cases)according to whether they had hypofibrinogenemia or not.The clinical data were collected and the risk factors of tigecycline-induced hypofibrinogenemia and the change of FIB level after tigacycline was discontinued were analyzed.Results Univariate analysis showed that abdominal infection accounted for 41.86%in low FIB group and maintenance dose of 100 mg q.12 h.accounted for 30.23%,which were higher than 10.34%and 12.07%in the control group;the level of FIB before tigecycline was(3.71±1.27)g/L,which was lower than(4.65±1.49)g/L in the control group;the tigecycline treatment time was(8.98±2.47)d,which was longer than(7.33±2.33)d in the control group(P<0.05).There was no significant difference between the two groups in terms of age,sex,underlying diseases,previous surgical history,sequential organ failure assessment(SOFA)score before tigecycline treatment,acute physiology and chronic health evaluationⅡ(APACHEⅡ)score before tigecycline treatment,pathogenic bacteria,organ function before tigecycline treatment,proportion of load dose 100 mg and combined use of cefoperazone and sulbactam sodium(P>0.05).Multivariate analysis showed that the main risk factors of tigacycline induced hypofibrinogenemia were abdominal infection and low FIB level before tigecycline treatment(P<0.05).In the low FIB group,there were 24 patients who stopped tigecycline,among which 19 patients recovered to normal level after stopping tigecycline,the proportion was 79.17%,and the recovery time was(5.52±2.06)d.Conclusion The risk factors of hypofibrinogenemia in patients with severe infection caused by tigecycline are abdominal infection and low FIB level before tigecycline treatment.In clinical treatment,it is necessary to prevent abdominal infection,shorten the medication time as much as possible,and pay attention to monitoring the FIB level of patients.

TigecyclineHypofibrinogenemiaSevere infectionRisk factors

许冬玲、谭永峰

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110016 辽宁省人民医院重症医学科

替加环素 低纤维蛋白原血症 重症感染 危险因素

2024

中国现代药物应用
中国水利电力医学科学技术学会

中国现代药物应用

影响因子:0.862
ISSN:1673-9523
年,卷(期):2024.18(3)
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