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感染病患者多重耐藥菌感染風(fēng)險(xiǎn)診斷演示文稿當(dāng)前第1頁\共有49頁\編于星期五\9點(diǎn)(優(yōu)選)感染病患者多重耐藥菌感染風(fēng)險(xiǎn)診斷當(dāng)前第2頁\共有49頁\編于星期五\9點(diǎn)DiscoveryofAntibacterialAgentsCycloserineErythromycinEthionamideIsoniazidMetronidazolePyrazinamideRifamycinTrimethoprimVancomycinVirginiamycinImipenem19301940
195019601970198019902000PenicillinProntosilCephalosporinCEthambutolFusidicacidMupirocinNalidixicacidOxazolidinonesCecropinFluoroquinolonesNeweraminoglycosidesSemi-syntheticpenicillins&cephalosporinsNewercarbapenemsTrinemsSyntheticapproachesEmpiric
screeningNewermacrolides&ketolidesRifampicinRifapentineSemi-syntheticglycopeptidesSemi-syntheticstreptograminsNeomycinPolymixinStreptomycinThiacetazoneChlortetracyclineGlycylcyclinesMinocyclineChloramphenicol當(dāng)前第3頁\共有49頁\編于星期五\9點(diǎn)臨床關(guān)注的耐藥問題
ResistancesofClinicalConcerns革蘭陽性細(xì)菌金匍菌–
MRSA,VISA,VRSAVRE(地理上差別)肺炎鏈球菌
–青霉素和大環(huán)內(nèi)酯耐藥
革蘭陰性細(xì)菌腸桿菌科ESBLs-喹諾酮,頭孢菌素,青霉素類,氨基糖苷類碳青霉烯酶(KPC,NDM-1?)-碳青酶烯耐藥在中國出現(xiàn)和蔓延非發(fā)酵菌(假單孢菌/不動(dòng)桿菌)喹諾酮,頭孢菌素,青霉素類,氨基糖苷,碳青霉烯類當(dāng)前第4頁\共有49頁\編于星期五\9點(diǎn)InfectionControlAntibioticstewardshipVREMRSAABESBLK.pneumoniaeAntibioticControlandInfectionControl:TheTwoSidesoftheResistance“Coin”RekhaMurthy.ImplementationofStrategiestoControlAntimicrobialResistanceChest2001;119;405-411ControlofAntibioticResistance當(dāng)前第5頁\共有49頁\編于星期五\9點(diǎn)經(jīng)驗(yàn)性抗感染治療的基本原則耐藥背景下的個(gè)體化治療理性回歸/責(zé)任所在當(dāng)前第6頁\共有49頁\編于星期五\9點(diǎn)慢性咳嗽和黃痰-原因哮喘后鼻腔鼻漏病毒感染后氣道高反應(yīng)性胃酸返流吸煙相關(guān)的慢性支氣管炎支氣管擴(kuò)張癥彌漫性泛細(xì)支氣管炎肺泡蛋白沉積癥急性發(fā)熱
-WBC不高/淋巴增高(無感染灶)-病毒!
-WBC增高/中性粒增高/核左移-可能細(xì)菌?。课?病原體?-原發(fā)性菌血癥?慢性發(fā)熱
-IE、布病、慢性感染灶?結(jié)核病?-非感染性發(fā)熱藥物熱、風(fēng)濕病、惡性腫瘤正確診斷是正確治療的前提發(fā)熱的診斷與鑒別診斷當(dāng)前第7頁\共有49頁\編于星期五\9點(diǎn)27-year-oldmanwithacutelymphocyticleukemia.51-year-oldmanwithchronicmyelogenousleukemia.22-year-oldwomanwithadultT-cellleukemia.67-year-oldwomanwithadultT-cellleukemia.61-year-oldmanwithinterstitialfibrosis;patientwasreceivingchlorambucilforchroniclymphocyticleukemia.COP當(dāng)前第8頁\共有49頁\編于星期五\9點(diǎn)RapidtestsWhenavailable.Gramstain!!!Startadequateantibioticcoverage(within1hour?)TillouAetal.AmSurg2004;70:841-4DrainpurulentcollectionSamplingIncludinginvasiveprocedureswhenneeded(BAL…)
合格標(biāo)本進(jìn)行微生物學(xué)檢查開始經(jīng)驗(yàn)性抗感染治療
目標(biāo)治療經(jīng)驗(yàn)性治療和目標(biāo)治療的統(tǒng)一當(dāng)前第9頁\共有49頁\編于星期五\9點(diǎn)選擇哪種抗菌藥物
感染部位的常見病原學(xué)選擇能夠覆蓋病原體的抗感染藥物
-抗菌譜/組織穿透性/耐藥性/安全性/費(fèi)用考慮藥代動(dòng)力學(xué)/藥效動(dòng)力學(xué)考慮病人生理和病理生理狀態(tài)
高齡/兒童/孕婦/哺乳腎功不全/肝功不全/肝腎功能聯(lián)合不全其它因素
殺菌和抑菌/單藥和聯(lián)合/靜脈和口服/療程
經(jīng)驗(yàn)性抗感染治療-合理選擇藥物
-considerationsinchoosingantibioticforempirictherapy
評(píng)估病原體
-有的而放矢!評(píng)估耐藥性
-到位不越位!病情嚴(yán)重性評(píng)估+當(dāng)前第10頁\共有49頁\編于星期五\9點(diǎn)-個(gè)體化評(píng)估-特殊修正因子
先期抗菌藥物對(duì)細(xì)菌學(xué)及其耐藥性影響
不同部位感染-病原體的流行病學(xué)從病原學(xué)認(rèn)識(shí)感染性疾病SSSSPCP當(dāng)前第11頁\共有49頁\編于星期五\9點(diǎn)抗菌譜(coverage)組織穿透性(tissuepenetration)耐藥性(resistance,specificallylocalresistance)-參考代表性資料/依靠當(dāng)?shù)刭Y料安全性(safetyprofile)
-藥物本身/制劑/工藝/雜質(zhì)費(fèi)用/效益(cost/effectiveness)-失敗或副作用致再治療費(fèi)用更高經(jīng)驗(yàn)性抗感染治療-藥物選擇的基本原則當(dāng)前第12頁\共有49頁\編于星期五\9點(diǎn)評(píng)價(jià)病原體耐藥可能?
是否耐藥菌?
-了解耐藥病原體流行狀況
參考代表性治療/依靠當(dāng)?shù)刭Y料-個(gè)體化用藥-合理用藥的精髓病人來源:社區(qū)、養(yǎng)老院、醫(yī)院高齡、基礎(chǔ)疾病、近期抗菌藥物、近期住院、侵襲性操作、晚發(fā)醫(yī)院感染
當(dāng)前第13頁\共有49頁\編于星期五\9點(diǎn)S.aureusPenicillin[1944]Penicillin-resistantS.aureus金黃色葡萄球菌耐藥的發(fā)生發(fā)展過程Methicillin[1962]Methicillin-resistantS.aureus(MRSA)Vancomycin-resistantenterococci(VRE)Vancomycin[1990s][1997]VancomycinintermediateS.aureus(VISA)[2002]Vancomycin-resistantS.aureusCDC,MMWR2002;51(26):565-567[1960]當(dāng)前第14頁\共有49頁\編于星期五\9點(diǎn)評(píng)價(jià)病原體耐藥可能?
是否耐藥菌?
-了解耐藥病原體流行狀況
參考代表性治療/依靠當(dāng)?shù)刭Y料-個(gè)體化用藥-合理用藥的精髓病人來源:社區(qū)、養(yǎng)老院、醫(yī)院高齡、基礎(chǔ)疾病、近期抗菌藥物、近期住院、侵襲性操作、晚發(fā)醫(yī)院感染
當(dāng)前第15頁\共有49頁\編于星期五\9點(diǎn)中國大陸ESBL的發(fā)生率%
WangH,ChenM.DiagnosMicrobiolInfectDis,2005,51,201-208CMSS/SEANIR/CARES.year細(xì)菌耐藥監(jiān)測結(jié)果如何解讀?當(dāng)前第16頁\共有49頁\編于星期五\9點(diǎn)實(shí)驗(yàn)室藥物敏感性監(jiān)測的解讀意義-反映了耐藥趨勢/告誡要謹(jǐn)慎使用抗菌藥物
-影響選擇藥物/考慮耐藥性對(duì)療效的影響不足
-實(shí)驗(yàn)室收集菌株/大型教學(xué)醫(yī)院/ICU
抗生素選擇壓力導(dǎo)致耐藥性高估!-沒有臨床背景資料/不能用于指導(dǎo)個(gè)體化用藥
(年齡、基礎(chǔ)疾病、社區(qū)/醫(yī)院感染、前期抗菌藥物使用情況)
當(dāng)前第17頁\共有49頁\編于星期五\9點(diǎn)NoRiskFactors
forMDROsRiskFactors
forMDREnterobacteriaceaeaRiskFactorsfor
MDRPseudomonasHealthcare
contact
NoYes!(eg,recenthospitaladmission,nursinghome,dialysis)withoutinvasiveprocedureYes,Longhospitalizationand/orinfectionfollowinginvasiveprocedures(>5days)RecentAbx
NoYes!(≥14daysinpast90days)Yes!
(≥14daysinpast90days)對(duì)Patient
characteristics
Youngfewcomorbidities≥65yrscomorbiditiessuchasTPNorrenalinsufficiencyco-morbiditiessuchasCF,structurallungdisease,advancedAIDS,neutropenia,orothersevereimmunodeficiencyDrugsofchoiceAmoxi/calvAmpicillin/sulb2ndor3rdGFQsPip/tazoCefaperazone/sulbactamertapenemCeftazidinecefepimePip/tazoCefperazone/sulbactamImipenemmeropenemaExceptnonfermenters/non-Pseudomonasspecies.AdaptedfromCarmeliY.Predictivefactorsformultidrug-resistantorganisms.In:RoleofErtapenemintheEraofAntimicrobialResistance[newsletter].Availableat:www.invanz.co.il/secure/downloads/IVZ_Carmeli_NL_2006_W-226364-NL.pdf.Accessed7April2008;DimopoulosG,FalagasME.EurInfect
Dis.2007;49–51;Ben-AmiR,etal.ClinInfectDis.2006;42(7):925–934;Pop-VicasAE,D’AgataEMC.ClinInfectDis.2005;40(12):1792–1798;ShahPM.ClinMicrobiolInfect.2008;14(suppl1):175–180.StratificationforRiskforMDRGram-NegativePathogens當(dāng)前第18頁\共有49頁\編于星期五\9點(diǎn)重癥感染≠耐藥菌感染!重癥感染≠革蘭陰性腸桿菌科細(xì)菌感染!肺炎鏈球菌、化膿性鏈球菌、軍團(tuán)菌、肺孢子菌等均可致重癥感染PCPLD對(duì)于選擇抗菌藥物-耐藥性
VS
嚴(yán)重性哪個(gè)更重要?當(dāng)前第19頁\共有49頁\編于星期五\9點(diǎn)PCPLD耐藥菌感染
VS
嚴(yán)重感染-PCP和LD告訴我們什么?觀點(diǎn):
-耐藥性判斷對(duì)于合理選擇抗菌藥物更重要!
[包括重癥感染]-即使重癥感染,抗感染治療方案仍需根據(jù)病原體及其耐藥性評(píng)估來制定當(dāng)前第20頁\共有49頁\編于星期五\9點(diǎn)經(jīng)驗(yàn)性抗感染治療的基本原則耐藥背景下的個(gè)體化治療以CAP/HAP為例當(dāng)前第21頁\共有49頁\編于星期五\9點(diǎn)22CravenDE.CurrOpinInfectDis.2006;19:153-160.TheChangingSpectrumofPneumonia
CAP,HCAP,HAP"Healthcare-associatedpneumoniaisarelativelynewclinicalentitythatincludesaspectrumofadultptswhohaveacloseassociationwithacute-carehospitalsorresideinchronic-caresettingsthatincreasetheirriskforpneumoniacausedbyMDRpathogens."PneumoniaCAPaHCAPbHAPc/VAPdMorbidity&MortalityRiskofMDRPathogensa.CAP=community-acquiredpneumoniab.HCAP=healthcare-associatedpneumoniac.HAP=hospital-acquiredpneumoniad.VAP=ventilator-associatedpneumonia當(dāng)前第22頁\共有49頁\編于星期五\9點(diǎn)H.influenzaeK.pneumoniaeS.pneumoniaeM.pneumoniaeL.pneumophila
C.pneumoniae當(dāng)前第23頁\共有49頁\編于星期五\9點(diǎn)Community-acquiredpneumoniainEurope*病原體社區(qū)治療入院治療ICU發(fā)表的研究數(shù)量92313肺炎鏈球菌19,325,921,7流感嗜血桿菌3,34,05,1軍團(tuán)菌1,94,97,9金匍菌0,21,47,6GNB0,42,77,5肺炎支原體11,17,52鸚鵡熱衣原體1,51,91,3病毒11,710,95,1病原學(xué)不明49,843,841,5*WoodheadM.EurRespJ2002;20:Suppl.36,20-27病原體排序肺鏈
Spneumoniae非典型病原體
atypicals
流感嗜血桿菌
Hinfuenzae卡他莫拉菌
Mcatarrhalis金葡菌
Saureus革蘭陰性腸桿菌
GNB……流感流行后/壞死性肺炎MRSA?√√√√??當(dāng)前第24頁\共有49頁\編于星期五\9點(diǎn)HistoryofMRSAinU.S.‘59青霉素上市第一個(gè)MRSA菌株出現(xiàn)HealthcareassociatedMRSACA-MRSACA-MRSA爆發(fā)于不同人群兒童中出現(xiàn)沒有“經(jīng)典”危險(xiǎn)因素的MRS感染‘98MMWR報(bào)告4例健康兒童死于MRSA感染‘99CA-MRSA成為SSTI的主要原因‘04‘05在美國侵襲性MRSA導(dǎo)致18,650死亡
當(dāng)前第25頁\共有49頁\編于星期五\9點(diǎn)Community–AcquiredMRSAIncontrasttotheriseinnosocomialMRSAfrom1990tothepresent,growingawarenessofcommunity-acquiredMRSAhasoccurredthroughpublishedreportsofMRSAoutbreaksforwhichtraditionalriskfactorswerenotidentified.Necrotizingpneumonia,UnitedStatesandEurope1980OutbreakinDetroit,Mich2/3ofpatientswereIVDUMid1990sChildrenw/oidentifiableriskfactorsLate1990s
1998-Athletes/sportsteams1999-NativeAmericans2000
Prisonandjailpopulations2003IVDU=intravenousdrugusers.GroomAVetal.JAMA.2001;286:1201-1205.HeroldBCetal.JAMA.1998;279:593-598.CDC.MorbMortalWklyRep.2001;50:919-922.NaimiTSetal.JAMA.2003;290:2976-2984.ZetolaNetal.LancetInfectDis.2005;5:275-286.LevineDPetal.AnnInternMed.1982;97:330-338.CDC.MorbMortalWklyRep.2003;52:793-795.GilletYetal.Lancet.2002;359:753-759.CDC.MorbMortalWklyRep.1999;48:707-710.當(dāng)前第26頁\共有49頁\編于星期五\9點(diǎn)RemainsanuncommoncauseofCAP
-CDCsurveillancestudyofinvasiveMRSA1-~0.74/100,000-EMERGEncyIDNETStudyGroup(12U.S.ERs)2
MRSAaccountedfor2.4%ofallCAP;5%ofICUCAPButhasemergedasacauseofsevereCAP
Comparedtonon-MRSACAP,patientswere2:Moreill(morelikelytobecomatose,requireintubation,pressorsanddieintheER)MoreCXRabnormalities(multipleinfiltrates,cavitation)Mortalityrate14%(upto50%insomestudies)EpidemiologyofMRSACommunity-AcquiredPneumonia(CAP)1KlevensJAMA2007;298:1763-1771;2MoranCID2012;54:1126-33當(dāng)前第27頁\共有49頁\編于星期五\9點(diǎn)ApproachtoEmpiricTherapy:CAPEmpirictreatmentforMRSAisrecommendedforsevereCAPdefinedby:ICUadmissionNecrotizingorcavitaryinfiltratesEmpyemaDiscontinueempiricRxifculturesdonotgrowMRSA
LiuCID2011;52;285-322中國社區(qū)MRSA流行病學(xué)?我們?cè)趺崔k?ValentiniAnnofClinMicro2008當(dāng)前第28頁\共有49頁\編于星期五\9點(diǎn)CharacterizationofCA-MRSAAssociatedwithSkinandSoftTissueInfectioninBeijing:HighPrevalenceofPVL+ST398AprospectivecohortofadultswithSSTIbetween2009.01~2010.08at4hospitalsinBeijing501SSTIpatientswereenrolled-Cutaneousabscess(40.7%);impetigo(6.8%);cellulitis(4.8%)S.aureusaccountedfor32.7%(164/501)-5isolates(5/164,3.0%)wereCA-MRSA-mostdominantSTwasST398(17.6%)-prevalenceofPVLgenewas41.5%(66/159)inMSSA.王輝
PLoSONE,2012;7(6):e38577.到目前為止CA-MRSA所致CAP尚無報(bào)告當(dāng)前第29頁\共有49頁\編于星期五\9點(diǎn)EpidemiologyofMRSAH-MRSAReservoires-hospitals-LTCFs5geneticbackgroudsH-MRSAincommunity-patientswithriskfactors-contactwithpatientswithriskfactorsTruecommunity-MRSA-nohealthcare-associatedriskfactors-withPVLgeneshealthcarecommunityAcquiredOnsetH-MRSA感染危險(xiǎn)因素:年齡>65歲,嚴(yán)重基礎(chǔ)疾病,傷口廣譜抗生素使用,住院時(shí)間延長,多次住院侵襲性操作(氣管插管、切開/植入血管導(dǎo)管)合理使用抗MRSA藥物糖肽類/利奈唑胺當(dāng)前第30頁\共有49頁\編于星期五\9點(diǎn)PredictionofMRSAinPatientswithNon-NosocomialpneumoniaBMCInfectiousDiseases2013,13:370doi:10.1186/1471-2334-13-370RetrospectivestudyfromJanuary2008toDecember2011.943culture-positiveMRSAandnon-MRSApneumoniaoutsidethehospitalIdentifiedriskfactorsassociatedwithMRSApneumonia.當(dāng)前第31頁\共有49頁\編于星期五\9點(diǎn)Community-acquiredpneumoniainEurope*病原體社區(qū)治療入院治療ICU發(fā)表的研究數(shù)量92313肺炎鏈球菌19,325,921,7流感嗜血桿菌3,34,05,1軍團(tuán)菌1,94,97,9金匍菌0,21,47,6GNB0,42,77,5肺炎支原體11,17,52鸚鵡熱衣原體1,51,91,3病毒11,710,95,1病原學(xué)不明49,843,841,5*WoodheadM.EurRespJ2002;20:Suppl.36,20-27病原體排序肺鏈
Spneumoniae非典型病原體
atypicals
流感嗜血桿菌
Hinfuenzae卡他莫拉菌
Mcatarrhalis金葡菌
Saureus革蘭陰性腸桿菌
GNB……√√√√??當(dāng)前第32頁\共有49頁\編于星期五\9點(diǎn)CAPduetoGNBANSORP,2002-2004,912CAP93(10.1%)werecausedbyGNB腸桿菌科-K.pneumoniae(59),Enterobacterspp.(7),S.marcescens(1)非發(fā)酵菌-P.aeruginosa(25),A.baumannii(1),Highermorbidityandco-morbiddiseasesSepticshock,malignancy,CVdisease,smoking,hypoNa,dyspneaHighermortality
18.3%vs6.1%(p<0.001)(Kangetal.EurJClinMicrobiolInfectDis2008;27:657)當(dāng)前第33頁\共有49頁\編于星期五\9點(diǎn)PrevalenceofESBL+EnterobacteriaceaeinCAP?+=102/1052=9.7%Invitroactivitiesofertapenemagainstdrug-resistantSpneumoniaeandotherrespiratorypathogensfrom12AsiancountriesDiagnosticMicrobiologyandInfectiousDisease56(2006)445–450.11/102=13%91/102=87%當(dāng)前第34頁\共有49頁\編于星期五\9點(diǎn)高齡Advancedage誤吸Aspiration護(hù)理院Nursinghomeresident(nowHCAP)基礎(chǔ)心肺疾病Underlyingcardiopulmonarydisorders
-不包括結(jié)構(gòu)性肺疾病近期抗生素暴露RecentAbx疾病嚴(yán)重性(hintforG–ve/legionella)CAP-革蘭陰性桿菌及耐藥評(píng)估CID2005當(dāng)前第35頁\共有49頁\編于星期五\9點(diǎn)CAP-銅綠假單胞菌及耐藥性評(píng)估-嚴(yán)重結(jié)構(gòu)性肺疾病
severestructurallungdisease,(bronchiectasis,severeCOPD)-近期抗生素暴露
recentantibiotictherapy
-近期住院特別是入住ICU機(jī)械通氣recentstayinhospital(especiallyintheICUforMV)AdaptedfromMandellLA,etal.ClinInfectDis.2003;37:1405–1433.-易患因素:誤吸風(fēng)險(xiǎn)-老年、腦血管病等-臨床綜合征:吸入性肺炎、壞死性肺炎、肺膿腫、膿胸CAP-厭氧菌評(píng)估當(dāng)前第36頁\共有49頁\編于星期五\9點(diǎn)氟喹諾酮類的地位?
-左氧氟沙星、莫西沙星、環(huán)丙沙星?-內(nèi)酰胺類+新大環(huán)內(nèi)酯類
-肺炎鏈球菌對(duì)大環(huán)內(nèi)酯耐藥并不影響其在聯(lián)合治療中的地位!
-如何選擇?-內(nèi)酰胺?
CAP經(jīng)驗(yàn)性治療中的兩個(gè)方案的實(shí)踐當(dāng)前第37頁\共有49頁\編于星期五\9點(diǎn)喹諾酮在CAP治療中具有重要地位呼吸喹諾酮(RespiratoryFQs)
多重耐藥肺鏈(MDRSP)
非典型病原體
ESBL陰性腸桿菌科細(xì)菌
MSSA環(huán)丙沙星/大劑量左氧氟沙星
用于銅綠假單胞菌的聯(lián)合治療√√√√當(dāng)前第38頁\共有49頁\編于星期五\9點(diǎn)氟喹諾酮類的地位?-內(nèi)酰胺類+新大環(huán)內(nèi)酯類(如何選擇?-內(nèi)酰胺?)-沒有PRSP危險(xiǎn)因素-青霉素類(!?)
-無需覆蓋耐藥腸桿菌科、銅綠:
抗肺鏈為主-酶抑制劑復(fù)合制劑-氨芐西林/舒巴坦、阿莫西林/棒酸
頭孢菌素呋辛、曲松、噻肟而非哌酮、他啶抗腸桿菌科-優(yōu)選他啶哌酮然后噻肟、曲松-需覆蓋耐藥腸桿菌科、銅綠
頭孢哌酮/舒巴坦、哌拉西林/他唑巴坦、頭孢他啶(銅綠)碳青霉烯(腸桿菌科優(yōu)選厄他培南、非發(fā)酵菌選亞胺培南和美洛培南)當(dāng)前第39頁\共有49頁\編于星期五\9點(diǎn)懷疑HAP、VAP或HCAP晚發(fā)(>5days)HAP或
MDR病原體的危險(xiǎn)因素否是窄譜抗菌藥物廣譜抗菌藥物-針對(duì)MDR病原體HAP初始經(jīng)驗(yàn)性抗菌藥物選擇的流程圖ATS.AmJRespirCritCareMed2005;171:388-416既往90天內(nèi)曾經(jīng)使用過抗菌藥物住院時(shí)間為5天或更長在社區(qū)或其他醫(yī)療機(jī)構(gòu)抗生素耐藥出現(xiàn)的頻率高存在HCAP相關(guān)危險(xiǎn)因素90天內(nèi)住急性病院兩天及以上家庭內(nèi)輸液治療(含抗生素)30天內(nèi)有過持續(xù)透析家庭外傷治療家庭成員有耐多藥病原體感染免疫抑制性疾病和/或免疫抑制劑治療陰性預(yù)計(jì)值的價(jià)值更大當(dāng)前第40頁\共有49頁\編于星期五\9點(diǎn)StratificationofHAPPatientsatRiskforMDROrganismsThedifferencesnotfirmlysettledAvailabledataindicateinspontaneouslybreathingpts-potentiallydrugresistantmicroorganismsmayplayaminorrole-GNEB(abxsusceptible),Saureus(MSSA)andSpneumoniaeasleadingpathogens-spontaneouslybreathingVSventilatedEwigS,TorresA,etal.(1999)Bacterialcolonizationpatternsinmechanicallyventilatedpatientswithtraumaticandmedicalheadinjury.Incidence,riskfactors,andassociationwithVAP.AmJRespirCritCareMed159:188–198RelloJ,TorresA(1996)MicrobialcausesofVAP.SeminRespirInfect11:24–31當(dāng)前第41頁\共有49頁\編于星期五\9點(diǎn)MechanicalVentilationIsAssociatedWithaSignificantlyIncreasedIncidenceofRespiratoryTractMRSAInfectionPujolMetal.EurJClinMicrobiolInfectDis.1998;17:622-628.AprospectivecohortstudyconductedtodefinetheclinicalandepidemiologicalcharacteristicsofMRSAVAPacquiredduringa
large-scaleoutbreakofMRSA當(dāng)前第42頁\共有49頁\編于星期五\9點(diǎn)TimefromHospitalization(days)TimefromIntubation(days)Late-onsetHAPEarly-onsetVAPLate-onsetVAPEarly-onsetHAP0123456701234567(AmericanThoracicSociety.AmJRespirCritCareMed2005;171:388-416)StratificationofPatientsatRiskforMDROrganisms-earlyonsetVSlate-onset當(dāng)前第43頁\共有49頁\編于星期五\9點(diǎn)Early-onset Late-onsetpneumonia pneumonia Othersbasedon(<5days) (>5days)specificrisksS.pneumoniae P.aeruginosa AnaerobicbacteriaH.influenzae
Enterobacterspp. LegionellapneumophilaS.aureus
Acinetobacterspp.
InfluenzaAandB
Enterobacteriaceae K.pneumoniae RSV
S.marcescens Fungi E.coli
OtherGNB
S.aureus(MRSA)
GNB,Gram-negativebacilli;MRSA,methicillin-resistantS.aureusAdaptedfromAmJRespirCritCareMed.2005;171:388–416.StratificationofHAPPatientsatRiskforMDROrganisms-earlyonsetVSlate-onset當(dāng)前第44頁\共有49頁\編于星期五\9點(diǎn)-RecentAntibioticTherapyandPseudomonalResistanceTrouilletJLetal.ClinInfectDis.2002;34:1047-1054.P.aeruginosaVAP:34isolatespiperacillinandmulti-drugresistant;101sensitiveUseofantibiotics(imipenem,thirdgenerationcephalosporinandquinolone)within15daysofVAPincreasedPAresistancetothesameagent-patient-specificabxrotationaP=.0009 bP=.003
cP=.001 dP=.05ResistanceofPaeruginosaStrainsToImipenem,Ceftazidime,orCiprofloxacin,Accordingto
PreviousTherapyWithImipenem,a3rd-generationCephalosporin,oraFluoroquinoloneNo.(%)ofpatients,bypreviousdrugtherapyreceivedImipenemThird-generationcephalosporinFluoroquinoloneStrainresistanceNo(n=114)Yes(n=21)No(n=73)Yes(n=62)No(n=100)Yes(n=35)Toimipenem
19(16.7)
11(52.4) a
12(16.4)
18(29.0)
18(18)
12(34.3) dToceftazidime
17(14.9)
7(33.3)
6(8.2)
18(29.0) b
14(
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