中华实验和临床感染病杂志(电子版)
中華實驗和臨床感染病雜誌(電子版)
중화실험화림상감염병잡지(전자판)
CHINESE JOURNAL OF EXPERIMENTAL AND CLINICAL INFECTIOUS DISEASES(ELECTRONIC VERSION)
2014年
4期
517-521
,共5页
冯铁柱%岑枝梅%张琼%范海清%邓雪梅%刘琰%李建明
馮鐵柱%岑枝梅%張瓊%範海清%鄧雪梅%劉琰%李建明
풍철주%잠지매%장경%범해청%산설매%류염%리건명
重型肝炎%静脉注射人免疫球蛋白%临床治疗
重型肝炎%靜脈註射人免疫毬蛋白%臨床治療
중형간염%정맥주사인면역구단백%림상치료
Severe hepatitis%Human intravenous immunoglobulin%Clinical treatment
目的:探讨治疗重型肝炎(SH)的有效药物,研究静脉注射人免疫球蛋白(IVIG)治疗SH的临床价值,评估其安全性。方法62例SH患者分为治疗组(30例)和对照组(32例)。对照组给予卧床休息、能量补充、调节水电解质平衡、保肝、血浆蛋白支持等综合治疗。治疗组在此基础上给予IVIG静脉注射,5 g/次,1次/d,共5 d。治疗前和治疗后分别检测两组患者的血常规、尿常规、便常规,应用全自动生化分析仪检测肝肾功能、心肌酶、血生化;应用普利生全自动血凝仪检测凝血4项指标(PT、APTT、TT和FIB)。观察时间最长6周,对生存病例随访3个月。结果治疗后两组患者在血生化学方面(TBil、PT、PA和CHE),经比较后差异具有统计学意义(P均<0.05)。治疗组30例患者中有效24例,有效率为80.00%;对照组32例患者中有效12例,有效率为37.50%,两组差异具有统计学意义(P <0.01)。不良反应:治疗组出现1例胸闷、轻度气短不适,经对症处理后症状消失,不良反应发生率为3.33%。结论应用IVIG治疗多种原因引起的SH,可以有效改善SH患者的血生化指标,显著提高SH患者的存活率,降低其病死率,且不良反应轻微,是SH安全、有效的治疗手段。
目的:探討治療重型肝炎(SH)的有效藥物,研究靜脈註射人免疫毬蛋白(IVIG)治療SH的臨床價值,評估其安全性。方法62例SH患者分為治療組(30例)和對照組(32例)。對照組給予臥床休息、能量補充、調節水電解質平衡、保肝、血漿蛋白支持等綜閤治療。治療組在此基礎上給予IVIG靜脈註射,5 g/次,1次/d,共5 d。治療前和治療後分彆檢測兩組患者的血常規、尿常規、便常規,應用全自動生化分析儀檢測肝腎功能、心肌酶、血生化;應用普利生全自動血凝儀檢測凝血4項指標(PT、APTT、TT和FIB)。觀察時間最長6週,對生存病例隨訪3箇月。結果治療後兩組患者在血生化學方麵(TBil、PT、PA和CHE),經比較後差異具有統計學意義(P均<0.05)。治療組30例患者中有效24例,有效率為80.00%;對照組32例患者中有效12例,有效率為37.50%,兩組差異具有統計學意義(P <0.01)。不良反應:治療組齣現1例胸悶、輕度氣短不適,經對癥處理後癥狀消失,不良反應髮生率為3.33%。結論應用IVIG治療多種原因引起的SH,可以有效改善SH患者的血生化指標,顯著提高SH患者的存活率,降低其病死率,且不良反應輕微,是SH安全、有效的治療手段。
목적:탐토치료중형간염(SH)적유효약물,연구정맥주사인면역구단백(IVIG)치료SH적림상개치,평고기안전성。방법62례SH환자분위치료조(30례)화대조조(32례)。대조조급여와상휴식、능량보충、조절수전해질평형、보간、혈장단백지지등종합치료。치료조재차기출상급여IVIG정맥주사,5 g/차,1차/d,공5 d。치료전화치료후분별검측량조환자적혈상규、뇨상규、편상규,응용전자동생화분석의검측간신공능、심기매、혈생화;응용보리생전자동혈응의검측응혈4항지표(PT、APTT、TT화FIB)。관찰시간최장6주,대생존병례수방3개월。결과치료후량조환자재혈생화학방면(TBil、PT、PA화CHE),경비교후차이구유통계학의의(P균<0.05)。치료조30례환자중유효24례,유효솔위80.00%;대조조32례환자중유효12례,유효솔위37.50%,량조차이구유통계학의의(P <0.01)。불량반응:치료조출현1례흉민、경도기단불괄,경대증처리후증상소실,불량반응발생솔위3.33%。결론응용IVIG치료다충원인인기적SH,가이유효개선SH환자적혈생화지표,현저제고SH환자적존활솔,강저기병사솔,차불량반응경미,시SH안전、유효적치료수단。
Objective To investigate the effective drug for the treatment of various reasons severe hepatitis and study the clinical value of human intravenous immunoglobulin (IVIG) in the treatment of severe hepatitis, assess security of IVIG drug. Methods Among 62 patients with severe hepatitis, the treatment group and the control group were composed by 30 and 32 patients, respectively. The control group was treated with rest, energy supplement, regulate water electrolyte and acid-base balance, the hepatoprotective, plasma, protein, comprehensive treatment. The treatment group was given IVIG intravenous on the basis of the control group, each 5 g, once a day for ifve times. Before and after treatment, the routine of blood, urine and stool were tested. The liver and kidney function, cardiac enzymes, blood biochemistry were detected by automatic biochemical analyzer. The cruor four kinds of projects (PT, APTT, TT and FIB) were detected by automatic coagulation analyzer. The above indicators observation time was six weeks. Survived cases were followed up for 3 months. Results After treatment, the two groups were with signiifcant differences at blood biochemistry (TBil, PT, PA and CHE) (P all<0.05). In treatment group, there were 24 cases were effective, with the efficiency of 80.00%. In control group, there were 12 cases were effective, with the efficiency of 37.50%. The efficiency in the two groups was with significant differences (P < 0.01). The improvement rate of the treatment group signiifcantly higher than that of control group. Adverse reactions:in treatment group there was one case with chest tightness, mild shortness of breath, symptoms disappeared after symptomatic treatment, accounting for 3.33%. Conclusions IVIG treatment of various reasons severe hepatitis is effective, a variety of biochemical indicators of severe hepatitis patients can improve. Followed up for 3 months, IVIG signiifcantly improved healing rate of patients with severe hepatitis. Adverse reactions are rare and mild. IVIG is effective and security drug for the treatment of severe hepatitis.