心力衰竭临床药物治疗面临的挑战-会议课件教学幻灯

单击此处编辑母版标题样式,单击此处编辑母版文本样式,第二级,第三级,第四级,第五级,*,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,*,单击此处编辑母版标题样式,单击此处编辑母版标题样式,单击此处编辑母版文本样式,第二级,第三级,第四级,第五级,Klicka hr fr att ndra formatp bakgrundsrubriken,Klicka hr fr att ndra format p bakgrundstexten,Niv tv,Niv tre,Niv fyra,Niv fem,Cliquez pour modifier les styles du texte du masque,Deuxime niveau,Troisime niveau,Quatrime niveau,Cinquime niveau,Cliquez et modifiez le titre,单击此处编辑母版标题样式,单击此处编辑母版文本样式,第二级,第三级,第四级,第五级,Click to edit Master title style,Click to edit Master text styles,Second level,Third level,Fourth level,Fifth level,单击此处编辑母版文本样式,第二级,第三级,第四级,第五级,*,单击此处编辑母版标题样式,李 勇,复旦大学华山医院心脏科,心力衰竭临床药物治疗面临的挑战,Acute Infarction(hours),Infarct Expansion(hours to days),Global Remodeling(days to months),心肌梗死后左心室重构,交感神经,RAAS,交感神经,RAAS,交感神经,RAAS,血液动力学的变化(CO、LVEDP),心力衰竭临床病症的根底,心室重塑(心室结构、,功能,的变化),心力衰竭发生开展的根底,ACEI治疗心力衰竭病死率和病残率,0,5,10,15,20,25,30,35,40,45,50,危险度降低,心衰死亡率或住院率,总死亡率,心衰死亡率,致命性/非致命性心梗,0.001,35%,0.001,23%,0.001,31%,0.04,20%,Garg R,Yusuf S.JAMA.1995;237:1450-1456.,-阻滞剂治疗心力衰竭：无可辩驳的证据,34%,Cumulative Mortality(%),Days,20,15,5,0,10,P,=.0062(adjusted),Metoprolol CR/XL,(n=1990),Placebo(n=2001),US Carvedilol Trials,1,Probability ofEvent-free Survival,Carvedilol(n=696),Placebo(n=398),Days,P,.001,0.0,0,100,200,300,400,65%,1.0,0.8,0.7,0.9,MERIT-HF,2,Survival(%of Patients),100,90,80,60,70,0,600,0,400,300,200,100,Days,Carvedilol(n=1156),Placebo(n=1133),500,600,0,400,300,200,100,500,35%,P,=.00013,COPERNICUS,4,Days,0.0,200,400,800,1.0,0.8,0.6,P,.0001,34%,Bisoprolol(n=1327),Placebo(n=1320),CIBIS-II,3,0,600,Survival,1.Packer M et al.,N Engl J Med,.1996;334:13491355.2.MERIT-HF Study Group.,Lancet.,1999;253:20012007.3.CIBIS-II Investigators.,Lancet,.1999;353:913.4.Packer M et al.,N Engl J Med,.2001;344:16511658.,0,1,2,3,年,0,10,20,30,40,50,3.5,风险比值,0.85 (95%CI 0.75-0.96),p=0.011,校正风险比值,0.85,p=0.010,483(37.9%),538(42.3%),%,NNT=23,1,年,HR 0.76,P0.001,CHARM,-,合用组：首要终点,心血管死亡或心衰住院的比例(%),抚慰剂,坎地沙坦,有危险的例数,坎地沙坦127611761063948457,抚慰剂127211361013906422,心率：心血管死亡的预测因子,Fox K et al.Lancet Online August 31,2021.,心率,70 bpm,心率,70 bpm,心血管死亡率（,%,）,P=0.0041,风险率,=1.34(1.10 1.63),时间（年）,0,0.5,1,1.5,2,0,5,10,15,Change in heart rate(bpm),Change in mortality(%),-20,-16,-12,-8,-4,0,4,8,12,-100,-80,-60,-40,-20,0,20,40,60,PROFILE,PROMISE,XAMOTEROL,VHeFT,(Prazosin),VHeFT,(HDZ/ISDN),CONSENSUS,SOLVD,US CARVEDILOL,MOCHA,CIBIS,NOR,TIMOLOL,BHAT,ANZ,*,*,GESICA,Change in Heart Rate and CHF Mortality,Kjekshus&Gullestad(1999),总死亡率,随访月,百分比,0,3,6,9,12,15,18,20,15,10,5,0,抚慰剂,美托洛尔,p=0.0096,降低危险,=44%,抚慰剂,美托洛尔,p=0.0067,降低危险,=36%,百分比,低剂量组,每3个月随访,(n=1016),高剂量组,每3个月随访,(n=2635),随访月,MERIT-HF:3个月后剂量相关的回忆性亚组分析,20,15,10,5,0,0,3,6,9,12,15,18,Wikstrand J et al.for the MERIT-HF Study Group.,4,周(41,mg),6,周(80,mg),8,周(151,mg),基线,基线,2,周(21,mg),2,周(17,mg),4,周(32,mg),6,周(64,mg),8,周与 3月(76,mg),(,次/分),美托洛尔控释片剂量,65,70,75,80,85,0,50,100,150,200,MERIT-HF:3个月后剂量相关的回忆性亚组分析,3,月(192,mg),小剂量组,大剂量组,Wikstrand J et al.for the MERIT-HF Study Group.,心率减慢,Incomplete follow-up,102 withdrew consent,3 randomisation,irregularities,Incomplete follow-up,114 withdrew consent,1 lost to follow-up,Patients and follow-up,10 917 randomised,5479 to ivabradine,5438 to placebo,Median study duration:19 months;maximum:35 months,5438 analysed,5479 analysed,12 138 screened,Study design,Ivabradine 5 mg,7.5 mg twice daily,Matching placebo,Visits,3 YEARS,Am Heart J.,2006;152:860-66,Treatment Target HR60 bpmReduce dosage or discontinue when HR40,25,55-95,78,76,75,60,68,65,年龄段,平均年龄,美国(CHS),芬兰(Helsinki),英国(Poole),丹麦.(Copen.),西班牙(Asturias),葡萄牙(EPICA),荷兰(Rotter.),瑞典(Vasteras),左心室收缩功能降低的比例,HF-PSF的比例,55,51,68,46,71,59,39,71,Petrie M,McMurray J.,Lancet,.2001;358:423-434.,Hogg K,et al,.,J Am Coll Card,.2004;43:317-327.,CHF患病率(%),0,1,2,3,4,5,6,7,8,9,10,心力衰竭患者中HF-PEF的比例,EF,50%,EF,45%,EF,50%,EF,50%,Framingham,2,(n=73),Olmstead,1,(n=137),CHS,3,(n=269),NHF Project,4,(n=19,710),1.Senni M,et al,.,Circulation,.1998;98:2282-2289,.,2.,Vasan RS,et al,.,J Am Coll Card,.1999;33:1948-1955.,3.,Gottdiener JS,et al,.,Ann Intern Med,.2002;137:631-639.,EF,50%,EF,50%,Owan,5,(n=4,596),Bhatia,6,(n=2,802),Patients(%),4.,Masoudi FA,et al,.,J Am Coll Card,.2003;41-217-223.,5.,Owan TE,et al,.,N Engl J Med,.2006;355:251-259.,6.Bhatia RS,et al,.,N Engl J Med,.2006;355:260-269,.,HF-PEF患病趋势,Owan TE,et al,.,N Engl J Med,.2006;355:251-259.,SHF,与,HF-PEF,的预后,(5,年生存率,),OWAN TE et al.N Engl J Med 2006;355:251-259,射血分数正常的患者,射血分数降低的患者,危险病例数,危险病例数,年,年,生存率,生存率,Placebo,Forced titration,Maintenance,Enrollment,Single-blind,2 weeks,W 2,W 4,W 8,M 6,M 10,M 14 to end,Every 4 months,75 mg,150 mg,300 mg,Follow-up continued until 1,440 primary endpoints occurred,N=4,128,I-PRESERVE:Study Design,Irbesartan,R,Only 1/3 pts could enter on an ACEI,Randomized,double-blind,placebo controlled trial,I-PRESERVE:,Primary Endpoint,Death or protocol specified CV hospitalization,(,Mean follow-up 49.5 months),Months from Randomization,Cumulative Incidence of Primary Events(%),40-,0-,10-,20-,30-,0,6,12,18,24,36,42,30,48,60,54,2067