《三种抗阳性菌药物比较》由会员分享，可在线阅读，更多相关《三种抗阳性菌药物比较（31页珍藏版）》请在金锄头文库上搜索。
1、Vancocinpro20091218稳可信VS替考拉宁及利奈唑胺（药物的三大特性比较）l有效性l安全性l经济性Vancocinpro20091218稳可信的有效性l作用机制l耐药及敏感率lMIC：万古MIC“飘逸”而非“漂移”l临床疗效l指南推荐Vancocinpro20091218重杀菌机制相对于人工合成抗生素的单一抑菌机制万古霉素让葡萄球菌更无从抵抗1. 影响细菌细胞膜的通透性2. 抑制细菌细胞壁的合成3. 抑制细菌浆内RNA合成123MDRSP=多药耐药菌株,MRSH=溶血性葡萄球菌实用抗感染治疗学第一版汪复、张婴元主编，第九章多肽类抗生素：pp281,pp284.Vancocinpr
2、o20091218稳可信上市 年全球仅出现 株耐药1997年日本首先报告了对万古霉素中度敏感的金黄色葡萄球菌(VISA)12002年07年在北美地区先后共确定9株耐药的金黄色葡萄球菌(VRSA)2我国尚无报道1,ChemotherJA,HiramatsuK,JanakiH.Methicillin-resistantStaphylococcusaureusclinicalstrainwithreducedvancomycinsusceptibility.1997,40:135-1362,FinksJ,WellsE,DykeTL,etal.VancomycinResistantStaphyloco
3、ccusaureus,MichiganUSA,2007.EmergingInfectiuosDiseases2009,15(6):943-945.Vancocinpro20091216重杀菌机制赋予万古霉素持久不变的敏感率1.SanchesIS,MatoR,LencastreHD,etal.PatternsofmultidrugresistanceamongMethicillinResistantHospitalIsolatesofCoagulase-PositiveandCoagulase-NegativeStaphylococciColletedintheInternationalMuti
4、centerStudyRESISTin1997and1998.MicrobialDrugResistance2000,6(3):199-211.2.实用抗感染治疗学第一版汪复、张婴元主编,第九章多肽类抗生素：pp281,pp284.Vancocinpro20091218作用于核糖体单一抑菌机制的利奈唑胺的耐药1999年12000年2001年22005年3三期临床时出现2株LRE利奈唑胺上市出现3株LRSA美国匹兹堡大学医疗中心ICU出现74株LRCNSLRE=耐利奈唑胺肠球菌,LRSA=耐利奈唑胺金葡菌,LRCNS=耐利奈唑胺凝固酶阴性葡萄球菌1.VenikataG,GoldHS.Antimi
5、crobialresistancetoLinezolid.ClinicalInfectiousDiseases2004,39:1010-1015.2.TsiodrasS,GoldHS,SakoulasG,etal.LinezolidresistanceinaclinicalisolateofStaphylococcusaureus.Lancet2001,358:207-208.3.PoloskiBA,AdamsJ,ClarkeL,etal.EpidemiologicalProfileofLinezolid-ResistantCoagulase-NegativeStaphylocucci.Cli
6、nicalInfectiousDiseases2006,43:165-171.本套幻灯仅供内部学习，团销时按实际情况重组本套幻灯仅供内部学习，团销时按实际情况重组所有金葡菌对万古霉素仍保持100%敏感率2007年ZAAPS细菌耐药性监测结果JonesRN,KohnoS,OnoY,etal.ZAAPSInternationalSurveillanceProgram(2007)forLinezolidresistance:resultsfrom5591Gram-Positiveclinicalisolatesin23countries.DiagnosticMicrobiologyandInfect
7、iousDisease2009,64:191-201.敏感率%Vancocinpro20091218国内葡萄球菌对万古霉素保持 敏感率2008年中国CHINET细菌耐药性监测结果(n=3525)(n=2313)耐药金葡菌敏感率(%)汪复,朱德妹,胡付品等.2008年中国CHINET细菌耐药性监测.中国感染与化疗杂志2009,9(5):321-329.Vancocinpro20091218国内葡萄球菌对万古霉素保持 敏感率全国主要抗生素对葡萄球菌属敏感率监测(Mohnarin)2008(n=10409)(n=5981)肖永红，王 进，赵彩云等，20062007年Mohnarin细菌耐药监测,中华
8、医院感染学杂志2008,18(8):1051-1056Vancocinpro20091218利奈唑胺目前的MIC分布情况图220004008001200160020000.120.250.51248利奈唑胺MIC(g/ml)株数(N)6株4株2007年ZAAPS细菌耐药性监测结果1万古霉素对于金葡菌的MIC90仅为1mg/LJonesRN,KohnoS,OnoY,etal.ZAAPSInternationalSurveillanceProgram(2007)forLinezolidresistance:resultsfrom5591Gram-Positiveclinicalisolatesin
9、23countries.DiagnosticMicrobiologyandInfectiousDisease2009,64:191-201.Vancocinpro2009121811欧洲43家医院监测结果Bacteria Year Strain NoVancomycin Teicoplanin MICrMIC90MICrMIC90S. aureus20053370.25-210.12-8220062200.5-210.25-4120071310.5-210.25-412008690.25-210.25-41CoNS2005933282007810.5-220.25-842008910.25-2
10、20.12-84S. pyogenes 2005410.250.25NtNt 2006-20071460.12-0.50.250.03-40.032008540.12-0.250.250.03-112820.25-1280.25ECCMID 2009, p1620Vancocinpro20091218ECCMID 2009, 1637Vancocinpro2009121813万古霉素和利奈唑胺治疗院内肺炎疗效相当在利奈唑胺提交给FDA的临床报告中详细描述了治疗医院内肺炎的临床研究.该研究用万古霉素和利奈唑胺进行对照显示万古霉素可评价临床疗效为60%，利奈唑胺可评价临床疗效57%，二者疗效相当，
11、利奈唑胺疗效并未超越万古霉素。0 01010202030304040505060利奈唑胺利奈唑胺万古霉素万古霉素利奈唑胺利奈唑胺万古霉素万古霉素ZYVOX 产品说明书信息 Distributed by Pfizer Pharmacia&Upjohn Company Divison of Pfizer Inc,NY,NY10017 LAB-0319-16.0 %Vancocinpro20091218 linezolid versus Vancomycin or Teicoplanin for Nosocomial Pneumonia: A Meta-Analysis AC. KALIL, M.
12、H. MURTHY , E. HERMSEN , et al.Methods: Prospective, randomized trials which tested linezolid vs. vancomycin or teicoplanin for treatment of NP were included. Heterogeneity was analyzed by I2 and Q statistics. Relative Risks (RR) were based on the Mantel-Haenszel method. Outcomes analyzed included c
13、linical cure (CC), microbiologic eradication (ME), and side effects. Results: 8 linezolid trials (6 vancomycin, 2 teicoplanin) were included (N=853). The linezolid vs glycopeptide analysis shows: CC RR=1.01(95% CI 0.93,1.10, p=0.80; I2=0%; N=853); ME RR=1.10 (CI 0.97,1.23; p=0.11; I2=0%; N=597); and
14、 MRSA population RR=1.14 (CI 0.82,1.58; p=0.44; I2=47%; N=191). If linezolid is compared to vancomycin only, the CC RR remains 1.01(CI 0.90,1.12), and ME and MRSA RRs are: 1.06 (CI 0.88,1.28) and 1.04 (CI 0.73,1.47), respectively. The risk of thrombocytopenia (RR=1.92 CI 1.29,2.86; p=0.001) and GI e
15、vents (RR=1.90 CI 1.04,3.48; p=0.03) were significantly higher with linezolid, but no differences were seen for renal dysfunction (RR=0.82 CI 0.52,1.27; p=0.37), or all-cause deaths (RR=0.95 CI 0.76,1.18; p=0.63). 2008 ICAAC K-5332008 ICAAC K-533Conclusions: Meta-analysis did not detect clinical sup
16、eriority of linezolid vs. glycopeptides for treatment of NP. Compared to linezolid, vancomycin was not associated with more renal dysfunction. linezolid showed a significant increase in the risk of thrombocytopenia and GI events. Available data does not support the claim that linezolid is superior t
17、o vancomycin for the treatment of NP.Vancocinpro20091218万古霉素治疗MRSA感染疗效未被超越包括菌血症、肺炎以及皮肤软组织感染万古霉素1g/次，每天2次7-28天(n=220),利奈唑胺600mg/次，每天2次7-28天(n=240)StevensDL,HerrD,LampirisH,etal.LinezolidversusVancomycinfortheTreatmentofMethicillin ResistantStaphylococcusaureusInfections.ClinicalInfectiousDiseases2002
18、,34:1481-1490.Vancocinpro20091218万古霉素治疗MRSA起效时间未被超越万古霉素1gq12h，7-21天(n=61),利奈唑胺600mgq12h，7-21天(n=57),*退热定义为体温完全恢复正常时间(天)P=0.2057P=0.1760P=0.6149Http:/www.clinicalstudyresults.org/documents/company-study_1864_0.pdfVancocinpro20091218稳可信：众多权威指南推荐l桑福德-抗微生物治疗指南2009-2010版l美国胸科协会(ATS)-关于医院获得性、呼吸机相关及医疗相关肺炎治
19、疗指南l美国抗感染协会(IDSA)-关于导管相关感染治疗指南lHAP亚洲工作组-关于HAP组首次共识l欧洲心脏协会(ESC)-关于感染性心内膜炎的预防、诊断及治疗指南l英国抗菌化疗协会(BSAC)-关于MRSA感染预防和治疗指南万古霉素治疗MRS感染的首选Vancocinpro20091218稳可信的安全性l适应症比较l副作用比较Vancocinpro20091218患者，疗效安全看得见！稳可信：拥有广泛的适应症适应症万古霉素1利奈唑胺2替考拉宁3肺炎皮肤软组织感染导管相关血流感染FDA警告？感染性心内膜炎X？脑膜炎X肺脓肿X脓胸X腹膜炎X骨髓炎X关节炎X 1.万古霉素产品说明书,2.利奈唑胺
20、产品说明书,3.替考拉宁产品说明书Vancocinpro20091218利奈唑胺受到美国FDA的警告1利奈唑胺已被FDA批准的适应证包括： 用于治疗耐万古霉素的屎肠球菌感染、医源性肺炎、社区获得性肺炎、非复杂性的皮肤及软组织感染、复杂性的皮肤和软组织感染（包括未并发骨髓炎的糖尿病足部感染）。2007年FDA提醒医务工作者： 利奈唑胺未获批准用于导管相关性血流感染、导管 接触部位感染。相关报导：FDA-利奈唑胺适应证外用药增加死亡风险SFDA网站相关报导检索关键词：利奈唑胺1,WilcoxMH,TackKJ,BouzaE,etal.Complicatedskinandskinstructurei
21、nfectionsandCatheterRelatedBloodstreamInfectionsNoninferiorityofLinezolidinPhase3Sutdy.ClinicalInfectiousDisease2009,48:203-212.2,FDAAlert3/18/2007.Vancocinpro20091218万古霉素纯度提高，肾毒性发生率大大减少 1.RybakM,LomaestoB,RotschaferJC,etal.Therapeuticmonitoryofvancomycininadultpatients:AconsensusreviewoftheASHP,IDS
22、AandtheSIDP.AmJHealth-SystPharm2009,66:82-98.2.林东昉、吴菊芳、张婴元等。利奈唑胺与万古霉素治疗革兰阳性菌感染的随机、双盲、对照、多中心临床试验。中国感染与化疗杂志2009,9(1):10-173.Stevens D.L. Herr D, Lampiris H,et al.Linezolid versus Vancomycin for the Treatment of Methicillin-Resistant Staphylococcus aureus Infections. Clinical Infectious Diseases 2002,
23、34:1481904.Abad F, CalboF, Zapater P,et al. Comparative pharmacoeconomic study of vancomycin and teicoplanin in intensive care patients.International Journal of Antimicrobial Agents ,2000,15:65715.Downs NJ, Robert E. Neihart, MD, Jeanette M. Dolezal,et al.Mild Nephrotoxicity Associated With Vancomyc
24、in Use.6.Sorrell TC, Collignon PJ.A prospective study of adverse reactions associated with vancomycin therapy.J Antimicrob Chemother. 1985 Aug,16(2):235-41.7.Farbert BF,Moellering RC,Retrospective Study of the Toxicity of Preparations of Vancomycin from 1974 to 1981, Antimicrobial agents and chemoth
25、erapy. 1983,23(1):138-1418.Levine DP. Vancomycin:A History. Clinical Infectious Diseases 2006, 42:S5-12Vancocinpro20091218稳可信稀释后静脉滴注稳可信稀释后静脉滴注药物浓度不超过药物浓度不超过 5 5毫克毫克/ /毫升毫升每次滴注时间应该超过每次滴注时间应该超过 60 60分钟分钟肾功能损害及年长患者应调整剂量肾功能损害及年长患者应调整剂量必要时监测血药浓度必要时监测血药浓度经常改变输注部位经常改变输注部位稳可信应用准则Vancocinpro2009121823肾功能异常病人
26、剂量调整方法肌酐值以肌酐值以mol/L表示时，表示时，K=0.814本公式应用于女性值，求得值需乘以本公式应用于女性值，求得值需乘以0.85首次负荷剂量首次负荷剂量:15mg/kg()血清肌酐值年龄）肌酐清除率（-=Kkgml140min/Vancocinpro2009121824剂量调整例子某男性病人65岁，体重为70kg,血肌酐值为160mol/L该病人每日稳可信的给药总量为9.370=651mg()6 . 0160814. 065140kmin/=-=）肌酐清除率（gmlVancocinpro20091218万古霉素与替考拉宁安全性比较万古霉素(n=252)替考拉宁(n=275)肾毒性意
27、大利大样本临床对照试验1血小板减少美国大样本临床对照试验2发生率(%)发生率(%)P=0.68P=0.003万古霉素(n=417)替考拉宁(n=406)MenichetitiF,MartinoB,BucaneveG,etal.EffectsofTeicoplaninandThoseofVancomycininInitialEmpericalAntibioticRegimenforFebrileNeutropenicPatientswithHeamatologicMalignancies.Anitmicrobialagentsandchemotherapy,1994,38(9):2041-204
28、6.WilsonAPR,CompativesafetyofTeicoplaninandVancomycin.InternationalJournalofAntimicrobialAgents,1998,10:143-152Vancocinpro20091218万古霉素治疗MRSA感染副反应发生率与利奈唑胺比较发生率(%)P=0.006P=0.037P=0.139无统计学差异万古霉素1g/次，每天2次7-28天(n=220),利奈唑胺600mg/次，每天2次7-28天(n=240)StevensDL,HerrD,LampirisH,etal.LinezolidversusVancomycinfo
29、rtheTreatmentofMethicillin ResistantStaphylococcusaureusInfections.ClinicalInfectiousDiseases2002,34:1481-1490.Vancocinpro2009121827 万古霉素和利奈唑胺安全性的比较由于万古霉素制剂的纯度显著提高，目前临床大量应用万古霉素，证实其肾毒性很少见,包括调整剂量后用于肾功能受损的病人，同时万古霉素的肾毒性具有可逆性28。而有数据表明，利奈唑胺引起的严重不良反应血小板减少的病例高达35%,在肾功能损伤的病人应用利奈唑胺引起的血小板减少达到65%,29。高纯度的万古霉素具有良
30、好的安全性28 Wakefield DS, Pfaller M, Massanari RM, Hammons GT. Variation in methicillin-resistant Staphylococcus aureus occurrence by geographic location and hospital characteristics. Infect Control. 1987;8(4):151-729 Yen-Hung Lin, Vin-Cent Wu High frequency of linezolid-associated thrombocytopenia Amon
31、g patients with renal insufficiency. International Journal of Antimicrobial Agent 28(2006)345-351 Vancocinpro20091218 linezolid versus Vancomycin or Teicoplanin for Nosocomial Pneumonia: A Meta-Analysis AC. KALIL, M. H. MURTHY , E. HERMSEN , et al.Methods: Prospective, randomized trials which tested
32、 linezolid vs. vancomycin or teicoplanin for treatment of NP were included. Heterogeneity was analyzed by I2 and Q statistics. Relative Risks (RR) were based on the Mantel-Haenszel method. Outcomes analyzed included clinical cure (CC), microbiologic eradication (ME), and side effects. Results: 8 lin
33、ezolid trials (6 vancomycin, 2 teicoplanin) were included (N=853). The linezolid vs glycopeptide analysis shows: CC RR=1.01(95% CI 0.93,1.10, p=0.80; I2=0%; N=853); ME RR=1.10 (CI 0.97,1.23; p=0.11; I2=0%; N=597); and MRSA population RR=1.14 (CI 0.82,1.58; p=0.44; I2=47%; N=191). If linezolid is com
34、pared to vancomycin only, the CC RR remains 1.01(CI 0.90,1.12), and ME and MRSA RRs are: 1.06 (CI 0.88,1.28) and 1.04 (CI 0.73,1.47), respectively. The risk of thrombocytopenia (RR=1.92 CI 1.29,2.86; p=0.001) and GI events (RR=1.90 CI 1.04,3.48; p=0.03) were significantly higher with linezolid, but
35、no differences were seen for renal dysfunction (RR=0.82 CI 0.52,1.27; p=0.37), or all-cause deaths (RR=0.95 CI 0.76,1.18; p=0.63). 2008 ICAAC K-5332008 ICAAC K-533Conclusions: Meta-analysis did not detect clinical superiority of linezolid vs. glycopeptides for treatment of NP. Compared to linezolid,
36、 vancomycin was not associated with more renal dysfunction. linezolid showed a significant increase in the risk of thrombocytopenia and GI events. Available data does not support the claim that linezolid is superior to vancomycin for the treatment of NP.Vancocinpro20091218利萘唑胺引起的血小板减少的问题l利萘唑胺关于引起血小板
37、减少的原因可能是： 通过抑制线粒体呼吸、促使成熟血小板减少； 作用于血小板生成素受体，导致血小板生成减少l 利萘唑胺引起血小板减少的危害利萘唑胺引起血小板的发生率高（可达47%）,程度严重（可下降到基础值的30%-79%），近半数患者需要停药，影响预期治疗血小板下降到30%的患者的死亡率是血小板正常患者的1.54倍Vancocinpro20091218稳可信的经济性 进口抗耐药革兰阳性菌药物中价格最低！Vancocinpro20091218抗耐药阳性菌药物经济性比较药物用法用量单价(元/支)日治疗费用(元)稳可信1.0g/bid154元（0.5g/支）154*4支=616替考拉宁首日0.4g/bid维持0.4g/qd343元（0.2g/支）首日4支1372元维持343*2支=686利奈唑胺0.6g/bid482元（0.6g/袋）482*2袋=964
