李姝雅,王伊龍,王擁軍
心房顫動(dòng)(atrial fibrillation,AF)是最常見的室上性心動(dòng)過(guò)速,人群總體患病率為0.4%~1.0%[1-2]。一些心房顫動(dòng)患者缺乏明顯的、特征性的臨床表現(xiàn),許多患者直到出現(xiàn)嚴(yán)重并發(fā)癥時(shí)才被檢出心房顫動(dòng)。心房顫動(dòng)是缺血性卒中的一個(gè)重要的獨(dú)立危險(xiǎn)因素,約每6例卒中患者中有1例是心房顫動(dòng)患者[3]。伴心房顫動(dòng)的缺血性卒中患者復(fù)發(fā)率高、預(yù)后差,給社會(huì)和家庭造成沉重的負(fù)擔(dān)[4-9]。合理應(yīng)用抗凝治療可降低心房顫動(dòng)患者的卒中風(fēng)險(xiǎn)[10-11],過(guò)度抗凝治療增加患者出血風(fēng)險(xiǎn)[12-13]。由于目前醫(yī)療水平的限制及循證醫(yī)學(xué)資料的匱乏,對(duì)于心房顫動(dòng)患者的檢出和管理仍缺乏有效的、一致的意見,探索卒中合并心房顫動(dòng)患者管理規(guī)范尤為重要。
抗凝治療可以降低心房顫動(dòng)患者卒中發(fā)生率,但因出血風(fēng)險(xiǎn)而限制其臨床應(yīng)用。鑒于抗凝的利弊,評(píng)估心房顫動(dòng)患者卒中發(fā)生風(fēng)險(xiǎn)和出血風(fēng)險(xiǎn),平衡利弊,顯得極為重要。20世紀(jì)90年代初,學(xué)者們就致力于建立一個(gè)有效的心房顫動(dòng)患者卒中危險(xiǎn)評(píng)分工具(表1)[14-21],經(jīng)過(guò)20年的不斷發(fā)展,最新的卒中危險(xiǎn)分層工具是CHADS2評(píng)分(Congestiveheart failure,Hypertension,Age>75 yrs,Diabetes mellitus,prior Stroke and TIA)[22]和CHA2DS2_VASc評(píng)分[Congestive heart failure,Hypertension,Age≥75(Doubled),Diabetes,Stroke(doubled),Vascular disease,Age 65~74,and Sex category(female)][23](表2)。CHADS2評(píng)分和CHA2DS2_VASc評(píng)分已在歐洲、日本、韓國(guó)等多個(gè)地區(qū)心房顫動(dòng)人群中進(jìn)行驗(yàn)證,得到其預(yù)測(cè)1年心源性卒中風(fēng)險(xiǎn)的曲線下面積(area under curve,AUC)(C值)在0.60~0.63[24-26]。2001年問(wèn)世的CHADS2評(píng)分是基于專家共識(shí)產(chǎn)生的總分為6分的經(jīng)典危險(xiǎn)分層工具,在其產(chǎn)生隊(duì)列中顯示出良好的效度(C=0.82)。該評(píng)分因操作簡(jiǎn)單,效度良好,一經(jīng)問(wèn)世即在臨床上廣泛應(yīng)用,隨著臨床試驗(yàn)的不斷檢驗(yàn),Lip等[27]根據(jù)臨床實(shí)踐修訂了CHADS2的危險(xiǎn)分層標(biāo)準(zhǔn)。Gage等[28]將更改了分層方法的CHADS2評(píng)分在“心房顫動(dòng)患者應(yīng)用口服凝血酶抑制劑預(yù)防卒中研究”(Stroke Prevention using an ORal Thrombin Inhibitor in atrial Fibrillation,SPORTIF)中進(jìn)行驗(yàn)證,約60%的患者被分為中?;颊?,指南中對(duì)于中?;颊呖顾ㄋ幬镞x擇沒(méi)有明確推薦,限制了CHADS2評(píng)分對(duì)抗栓藥物應(yīng)用的指導(dǎo)意義。2010年CHA2DS2_VASc評(píng)分是一種以危險(xiǎn)因素為基礎(chǔ)評(píng)價(jià)非瓣膜性心房顫動(dòng)患者的方法,改進(jìn)了心房顫動(dòng)患者發(fā)生卒中的危險(xiǎn)分層。這一評(píng)分方法將CHADS2評(píng)分得到的中危人群比例降低到原來(lái)的1/4,進(jìn)一步增強(qiáng)了評(píng)分工具對(duì)抗凝治療的指導(dǎo)意義[23]。根據(jù)上述評(píng)分標(biāo)準(zhǔn),對(duì)于伴心房顫動(dòng)的缺血性卒中患者,屬于存在既往卒中病史的心房顫動(dòng)患者,至少得到2分,屬高危分層,需抗凝治療。
表1 心房顫動(dòng)患者卒中風(fēng)險(xiǎn)評(píng)分工具
表2 CHADS2和CHA2DS2_VASc評(píng)分
卒中等血栓栓塞性并發(fā)癥是心房顫動(dòng)患者致死、致殘的主要原因,合理的抗凝治療對(duì)于改善心房顫動(dòng)患者生活質(zhì)量和遠(yuǎn)期預(yù)后具有重要意義。雖然國(guó)內(nèi)外相關(guān)指南均建議給予高危心房顫動(dòng)患者血栓預(yù)防治療,但迄今多數(shù)患者并未得到相應(yīng)處理,這與口服抗凝藥物的選擇限制密切相關(guān)[29-30]。目前成熟的口服抗凝藥物只有維生素K拮抗劑華法林。華法林應(yīng)用時(shí)需根據(jù)凝血酶原國(guó)際標(biāo)準(zhǔn)化比值(international normalized ratio,INR)調(diào)整劑量,且其抗凝效果受食物影響大,出院患者自行用藥風(fēng)險(xiǎn)極大。新型口服抗凝劑凝血因子Ⅹa抑制劑克服了上述困難,具備高效、安全、固定劑量、無(wú)需監(jiān)測(cè)INR的特點(diǎn),未來(lái)將占據(jù)口服抗凝藥物的市場(chǎng),為抗凝治療帶來(lái)新的時(shí)代。達(dá)比加群酯(Pradaxa)、利伐沙班(rivaroxaban)和阿哌沙班(apixaban)是目前批準(zhǔn)上市的新型抗凝藥物。這三類新型抗凝藥物都經(jīng)過(guò)了大型臨床試驗(yàn)的證實(shí),在抗凝療效和出血風(fēng)險(xiǎn)方面不同程度地優(yōu)于阿司匹林和華法林,這就意味著在心房顫動(dòng)相關(guān)卒中預(yù)防中新型抗凝劑時(shí)代已經(jīng)到來(lái)[22,31-35]。
伴心房顫動(dòng)的缺血性卒中患者的抗凝治療是一把雙刃劍,在對(duì)心房顫動(dòng)患者進(jìn)行抗凝治療的同時(shí)應(yīng)當(dāng)評(píng)估其出血風(fēng)險(xiǎn)(表3)。出血風(fēng)險(xiǎn)的研究略晚于心房顫動(dòng)患者的卒中風(fēng)險(xiǎn),最早的出血風(fēng)險(xiǎn)評(píng)分工具誕生于1998年[36],以年齡、2周內(nèi)胃腸道出血、卒中史及并發(fā)癥為危險(xiǎn)因素,根據(jù)得分判斷出血風(fēng)險(xiǎn),其用C值代表的預(yù)測(cè)大出血的效度為0.78。1年后,Kuijer等[37]提出了以年齡、性別和癌癥三種危險(xiǎn)因素組成的抗凝治療出血風(fēng)險(xiǎn)預(yù)測(cè)評(píng)分,在其驗(yàn)證隊(duì)列中,用C值代表的評(píng)分對(duì)大出血的預(yù)測(cè)效度為0.82[95%可信區(qū)間(confidence interval,CI):0.66~0.98]。因出血風(fēng)險(xiǎn)與年齡呈正相關(guān),Shireman等[38]提出了一個(gè)適用于年齡>65歲心房顫動(dòng)患者的評(píng)分工具,其低、中、高?;颊叩某鲅史謩e為0.9%、2.0%和5.4%。2006年,Gage等[39]發(fā)表了出血危險(xiǎn)的預(yù)測(cè)量表模型:肝臟或腎臟疾病、酗酒、惡性腫瘤、高齡、血小板計(jì)數(shù)或功能降低、再次出血、高血壓、貧血、基因因素、容易摔倒危險(xiǎn)和卒中(Hepatic or renal disease,Ethanol abuse,Malignancy,Older age,Reduced platelet count or function,Re-bleeding,Hypertension,Anemia,Genetic factors,Excessive fall risk and Stroke;HEMORR2HAGES)評(píng)分工具,該評(píng)分方法較為繁瑣,但心房顫動(dòng)患者抗凝治療的出血風(fēng)險(xiǎn)隨著得分的增加而增高。2010年P(guān)isters等[40]提出的另一個(gè)預(yù)測(cè)模型:高血壓、肝/腎功能異常、卒中、出血史或易于出血因素、不穩(wěn)定國(guó)際標(biāo)準(zhǔn)化比值、老年人、藥物/酒精(Hypertension,Abnormal renal/liver function,Stroke,Bleeding history or predisposition,Labile international normalized ratio,Elderly,Drugs/alcohol,HAS-BLED)評(píng)分量表因操作簡(jiǎn)單,對(duì)單純抗血小板治療及非抗栓治療組出血風(fēng)險(xiǎn)的預(yù)測(cè)能力則強(qiáng)于其他評(píng)分系統(tǒng)(C值分別為0.91和0.80),成為歐洲心臟病協(xié)會(huì)(European Society of Cardiology,ESC)心房顫動(dòng)管理指南對(duì)出血風(fēng)險(xiǎn)定量分析的推薦工具(表4)。該量表總分為9分,規(guī)定HAS-BLED評(píng)分≥3分為高危人群,1~2分為中危人群,0分為低危人群,對(duì)于高危人群,在應(yīng)用抗凝藥物或阿司匹林時(shí)需密切注意全身出血傾向。
表3 心房顫動(dòng)患者抗凝治療出血風(fēng)險(xiǎn)評(píng)分
表4 HAS-BLED評(píng)分
HAS-BLED評(píng)分指導(dǎo)抗凝治療需與心房顫動(dòng)患者卒中風(fēng)險(xiǎn)評(píng)分工具合用。在心房顫動(dòng)患者中同時(shí)應(yīng)用CHADS2和HAS-BLED評(píng)分將會(huì)減少12%接受抗凝治療而出血的人數(shù)。當(dāng)CHADS2評(píng)分≥2時(shí),患者存在卒中高風(fēng)險(xiǎn),推薦抗凝治療,若此時(shí)HAS-BLED評(píng)分大于CHADS2評(píng)分,則出血風(fēng)險(xiǎn)超過(guò)抗凝獲益。對(duì)于CHADS2評(píng)分=1分的患者,HAS-BLED評(píng)分與CHADS2評(píng)分相差不超過(guò)2分時(shí),抗凝獲益大于出血風(fēng)險(xiǎn)[41]。
上述5種抗凝治療出血風(fēng)險(xiǎn)預(yù)測(cè)工具均是在未接受抗凝治療的研究隊(duì)列中產(chǎn)生和驗(yàn)證,為進(jìn)一步預(yù)測(cè)接受抗凝治療的患者自發(fā)性腦出血風(fēng)險(xiǎn),F(xiàn)ang等[42]提出了基于心房顫動(dòng)抗凝和危險(xiǎn)因素的研究(Anticoagulation and Risk Factors in Atrial Fibrillation,ATRIA)評(píng)分。該研究在基于社區(qū)的大規(guī)模心房顫動(dòng)患者隊(duì)列中建立了評(píng)估華法林相關(guān)出血風(fēng)險(xiǎn)評(píng)估的有效方法,在最終風(fēng)險(xiǎn)模型中識(shí)別出5個(gè)獨(dú)立變量,包括貧血、腎臟疾?。I小球?yàn)V過(guò)率<30 ml/min或接受透析)、年齡≥75歲、曾因出血住院和高血壓。效度分析得到的C統(tǒng)計(jì)值為0.74。評(píng)分劃分低危(0~3分)、中危(4分)和高危(5~10分)患者的主要出血事件發(fā)生率分別為0.8%、2.6%和5.8%。ATRIA評(píng)分產(chǎn)生后,Lip等[43]將HEMORR2HAGES評(píng)分,HAS-BLED評(píng)分和ATRIA評(píng)分的預(yù)測(cè)能力進(jìn)行了比較。效度分析(relative operating characteristic,ROC分析)顯示HAS-BLED評(píng)分預(yù)測(cè)任何臨床相關(guān)出血方面最佳,但三者對(duì)出血風(fēng)險(xiǎn)均有較保守的預(yù)測(cè)能力(C值均<0.7)。在改善分析(net reclassification index,NRI)中,HASBLED評(píng)分被證實(shí)相對(duì)于HEMORR2HAGES及ATRIA評(píng)分可以分別改善10.3%和13%。使用決定曲線分析(detrended correspondence analysis,DCA)顯示,HAS-BLED評(píng)分在臨床相關(guān)出血事件任何界值水平方面優(yōu)于ATRIA和HEMORR2HAGES評(píng)分。另外,顱內(nèi)出血是抗凝治療中最危險(xiǎn)的并發(fā)癥,只有HAS-BLED評(píng)分對(duì)顱內(nèi)出血具有預(yù)測(cè)價(jià)值。因此,HAS-BLED評(píng)分可能成為指南推薦工具。Lip教授[44]評(píng)論:“HAS-BLED高評(píng)分不能被認(rèn)為是停止抗凝治療的指標(biāo),而是促使臨床醫(yī)師關(guān)注這類需要特別留意與隨訪的高?;颊?。HAS-BLED評(píng)分使臨床醫(yī)師考慮潛在的可糾正的出血風(fēng)險(xiǎn)因素,比如未控制的血壓,不穩(wěn)定的INR值,以及合并用藥中的阿司匹林及非甾體抗炎藥。”來(lái)自中國(guó)臺(tái)灣[45]和西班牙[46]的數(shù)據(jù)同樣證實(shí)了HAS-BLED評(píng)分的優(yōu)勢(shì)。目前,HAS-BLED評(píng)分是唯一國(guó)際指南推薦的抗凝治療風(fēng)險(xiǎn)預(yù)測(cè)評(píng)分[47-49]。
陣發(fā)性和無(wú)癥狀性心房顫動(dòng)難以檢出,因此隱源性卒中和短暫性腦缺血發(fā)作患者可能存在未診斷的心房顫動(dòng),心房顫動(dòng)的檢出在卒中二級(jí)預(yù)防中處于關(guān)鍵優(yōu)先地位。我國(guó)心源性卒中的整體出院診斷率為6%~7%,這與國(guó)外報(bào)道的20%比例相距甚遠(yuǎn)[22,49],從一個(gè)側(cè)面說(shuō)明了我國(guó)心源性卒中的診斷率較低。研究證實(shí)通過(guò)新技術(shù)延長(zhǎng)心電監(jiān)測(cè)時(shí)間可提高心房顫動(dòng)檢出率,但其成本效益存在爭(zhēng)議[50-54]。美國(guó)的一項(xiàng)研究對(duì)卒中患者心房顫動(dòng)檢出(Score for the Targeting of Atrial Fibrillation,STAF)評(píng)分≥5分的患者進(jìn)行連續(xù)21 d心電監(jiān)測(cè),心源性卒中的診斷率提高到13%,這比當(dāng)時(shí)的總體診斷率提高了6%[51]。另一研究提出,通過(guò)延長(zhǎng)心電監(jiān)測(cè)時(shí)間每多診斷一位心源性卒中患者需要耗費(fèi)的成本為44 000美元[52]。對(duì)患者進(jìn)行心房顫動(dòng)風(fēng)險(xiǎn)評(píng)估,針對(duì)高?;颊哐娱L(zhǎng)心電監(jiān)測(cè)時(shí)間,提高心房顫動(dòng)檢出率,是符合成本效益的卒中二級(jí)預(yù)防內(nèi)容。2010年Suissa等[55]提出了STAF評(píng)分系統(tǒng),從4個(gè)方面對(duì)卒中患者進(jìn)行評(píng)分,總分為8分(表5)。根據(jù)相應(yīng)的受試者工作特征(receiver operating characteristic,ROC)曲線得出總得分<5分,心源性卒中的可能性<10%;如果總分≥5分,心源性卒中的可能性則可以達(dá)到90%,建議進(jìn)一步延長(zhǎng)心電監(jiān)測(cè)時(shí)間。該評(píng)分識(shí)別心房顫動(dòng)患者的敏感性為89%,特異性為88%。陣發(fā)性心房顫動(dòng)和短陣心房顫動(dòng)是提高心房顫動(dòng)檢出率的關(guān)鍵。Suissa等[56]提出,STAF評(píng)分≥5分對(duì)于陣發(fā)性心房顫動(dòng)和持續(xù)性心房顫動(dòng)的作用無(wú)顯著性差異,兩者的C值分別為0.907和0.911,其識(shí)別陣發(fā)性心房顫動(dòng)的敏感性為91%,特異性為77%。德國(guó)的一項(xiàng)研究進(jìn)一步探討了STAF評(píng)分對(duì)于陣發(fā)性心房顫動(dòng)的預(yù)測(cè)能力[57]。效度分析結(jié)果提示C值為0.84,STAF評(píng)分≥5分對(duì)于識(shí)別陣發(fā)性心房顫動(dòng)的敏感性為79%,特異性為74%。繼STAF評(píng)分之后,Malik等[58]提出了用于卒中患者心房顫動(dòng)風(fēng)險(xiǎn)預(yù)測(cè)的LADS評(píng)分(Left atrial diameter,Age,Diagnosis of stroke or TIA,and Smoking status)(表5)。該評(píng)分總分為6分,規(guī)定≥4分為心房顫動(dòng)高風(fēng)險(xiǎn)患者,其識(shí)別心房顫動(dòng)患者的敏感性為85.5%,特異性為53.1%。經(jīng)過(guò)LADS評(píng)分的分類,可減少47%的卒中或TIA患者接受長(zhǎng)時(shí)間心電監(jiān)測(cè)。由于LADS評(píng)分的預(yù)測(cè)能力略低于STAF評(píng)分,目前尚無(wú)對(duì)LADS評(píng)分進(jìn)一步驗(yàn)證的相關(guān)研究。
STAF評(píng)分篩選出卒中患者中伴發(fā)心房顫動(dòng)的高危人群,高危人群需延長(zhǎng)心電監(jiān)測(cè)時(shí)間進(jìn)一步檢出心房顫動(dòng),目前相關(guān)指南尚未對(duì)心電監(jiān)測(cè)時(shí)長(zhǎng)給予建議,研究建議對(duì)卒中患者早期實(shí)施心房顫動(dòng)篩查有助于提高心房顫動(dòng)的檢出率,最短監(jiān)測(cè)時(shí)間為4 d[59]。可插入心臟監(jiān)測(cè)器這一新技術(shù)不僅較7 d的連續(xù)心電監(jiān)測(cè)提高心房顫動(dòng)的檢出率,且對(duì)患者而言更易耐受,無(wú)不良反應(yīng),將成為提高心房顫動(dòng)檢出率的新方向[55,60]。
表5 STAF和LADS評(píng)分
目前,尚無(wú)單純用于伴心房顫動(dòng)的缺血性卒中患者的不良預(yù)后量表。用于心房顫動(dòng)患者卒中危險(xiǎn)分層的CHADS2和CHA2DS2_VASc評(píng)分,其組成元素均為卒中復(fù)發(fā)和卒中后死亡的獨(dú)立危險(xiǎn)因素。由此推測(cè),兩種評(píng)分工具可能對(duì)于發(fā)生缺血性卒中的心房顫動(dòng)患者卒中復(fù)發(fā)和不良預(yù)后方面有一定的預(yù)測(cè)價(jià)值。既往研究將CHADS2和CHA2DS2_VASc評(píng)分應(yīng)用于伴非瓣膜性心房顫動(dòng)的缺血性卒中患者預(yù)后結(jié)局的預(yù)測(cè),發(fā)現(xiàn)這兩種評(píng)分工具是不良預(yù)后和死亡的獨(dú)立危險(xiǎn)因素[61-63]。希臘的一項(xiàng)研究將CHA2DS2_VASc評(píng)分應(yīng)用于非心房顫動(dòng)患者,中、高危分層患者的5年死亡率,卒中復(fù)發(fā)率和聯(lián)合心血管事件明顯高于低危分層的患者[64]。
心房顫動(dòng)或不伴心房顫動(dòng)患者的不良預(yù)后危險(xiǎn)因素基本一致是CHA2DS2_VASc評(píng)分可用于不伴心房顫動(dòng)患者預(yù)后評(píng)價(jià)的基礎(chǔ)。隨著大型高質(zhì)量隊(duì)列研究的逐漸發(fā)展和完善,研究者們提出了多個(gè)不良預(yù)后風(fēng)險(xiǎn)預(yù)測(cè)模型(表6)。這些風(fēng)險(xiǎn)預(yù)測(cè)模型未將伴心房顫動(dòng)的缺血性卒中排除在外,可初步作為心房顫動(dòng)相關(guān)卒中的預(yù)后評(píng)估工具。
表6 缺血性卒中死亡和不良預(yù)后評(píng)估量表
iScore評(píng)分[65]是基于加拿大卒中登記的一項(xiàng)較早的預(yù)測(cè)模型,預(yù)測(cè)急性缺血性卒中患者30 d和1年的死亡風(fēng)險(xiǎn)。預(yù)測(cè)模型在建模隊(duì)列(30 d死亡,C=0.85;1年死亡,C=0.823)、內(nèi)部驗(yàn)證隊(duì)列(30 d死亡,C=0.851;1年死亡,C=0.84)和外部驗(yàn)證隊(duì)列(30 d死亡,C=0.79;1年死亡,C=0.782)中均得到較好的預(yù)測(cè)效度。隨后,iScore評(píng)分分別用于不良預(yù)后風(fēng)險(xiǎn)預(yù)測(cè),溶栓患者出血風(fēng)險(xiǎn)及預(yù)后轉(zhuǎn)歸預(yù)測(cè),均得到理想結(jié)果[66-68]。PLAN評(píng)分[69]預(yù)測(cè)模型來(lái)源于另一個(gè)加拿大卒中登記,用于預(yù)測(cè)缺血性卒中患者出院30 d、1年的死亡率和出院時(shí)改良Rankin量表(modified Rankin Scale,mRS)評(píng)分5~6分。預(yù)測(cè)模型包括9項(xiàng)臨床指標(biāo),操作相對(duì)簡(jiǎn)單,可以準(zhǔn)確預(yù)測(cè)急性缺血性卒中患者30 d死亡(C=0.87),出院時(shí)死亡或嚴(yán)重致殘(C=0.88)、1年死亡(C=0.84)。同時(shí)也可以預(yù)測(cè)出院時(shí)的良好結(jié)局(mRS 0~2)(C=0.80)。美國(guó)心臟協(xié)會(huì)在其協(xié)作醫(yī)院的冠狀動(dòng)脈疾病單元中推行的跟著指南走(Get-with-the-Guideline)建立了在院死亡模型[70],其包括美國(guó)國(guó)立衛(wèi)生研究院卒中量表(National Institutes of Health Stroke Scale,NIHSS)評(píng)分的預(yù)測(cè)模型對(duì)于院死亡的預(yù)測(cè)效度為0.85(0.84~0.86)。
洛桑卒中登記(The Acute STroke Registry and Analysis of Lausanne,ASTRAL)評(píng)分預(yù)測(cè)模型[71]主要預(yù)測(cè)不良預(yù)后風(fēng)險(xiǎn),不良預(yù)后定義為mRS評(píng)分>2分。在建模隊(duì)列中預(yù)測(cè)3個(gè)月不良預(yù)后風(fēng)險(xiǎn)的C值為0.86,在兩個(gè)其他隊(duì)列研究中進(jìn)行外部驗(yàn)證,C值分別為0.937和0.771,預(yù)測(cè)效度良好。博洛尼亞研究(the Bologna Outcome Algorithm for Stroke,BOAS)模型[72]是意大利博洛尼亞市登記隊(duì)列推出的用于預(yù)測(cè)9個(gè)月不良預(yù)后的模型,包括NIHSS評(píng)分、年齡、上肢永久癱瘓、吸氧和導(dǎo)尿5個(gè)危險(xiǎn)因素,每個(gè)危險(xiǎn)因素1分,總分為5分。0~1分為低危分組,2~5分為高危分組。該評(píng)分在建模隊(duì)列(C=0.891,95%CI 0.848~0.934)和驗(yàn)證隊(duì)列(C=0.845,95%CI 0.770~0.920)中均表現(xiàn)出良好的預(yù)測(cè)能力。美國(guó)弗明漢心臟登記研究建立了用于心臟病一級(jí)預(yù)防的(Framingham Cardiovascular Risk Score,F(xiàn)CRS)模型[73],將FCRS模型用于卒中二級(jí)預(yù)防出院時(shí)不良預(yù)后風(fēng)險(xiǎn)預(yù)測(cè)和出院去向預(yù)測(cè),得到FCRS模型對(duì)于出院時(shí)mRS≥2分的比值比(odds ratio,OR)為4.9(95%CI 0.98~24.1),出院回家的OR=0.18(95%CI 0.04~0.86),F(xiàn)CRS模型是對(duì)缺血性卒中患者出院回家的保護(hù)性因素。
上述預(yù)測(cè)模型適用于缺血性卒中患者,缺血性卒中患者發(fā)病機(jī)制及病理生理特點(diǎn)異質(zhì)性較強(qiáng),建立針對(duì)伴心房顫動(dòng)的缺血卒中患者的預(yù)測(cè)模型仍有待進(jìn)一步研究。
美國(guó)心臟協(xié)會(huì)/美國(guó)卒中學(xué)會(huì)(American Heart Association/American Stroke Association,AHA/ASA)評(píng)選出2011年全球腦血管病最重要的十大研究進(jìn)展中,與心房顫動(dòng)相關(guān)的卒中占了三席,包括心房顫動(dòng)的危險(xiǎn)因素[74]、心房顫動(dòng)患者的降壓藥物選擇[75]及新型口服抗凝藥物[31-36],成為2011年卒中研究領(lǐng)域最搶眼的熱點(diǎn)。大約有1/5的卒中是由心房顫動(dòng)所致,未被診斷的心房顫動(dòng)即無(wú)癥狀性心房顫動(dòng)很可能是原因不明卒中的病因。心房顫動(dòng)所致的卒中相對(duì)嚴(yán)重,會(huì)導(dǎo)致長(zhǎng)期的殘疾或死亡。心房顫動(dòng)作為心源性卒中最常見的原因,提高其檢出率,指導(dǎo)一級(jí)預(yù)防、二級(jí)預(yù)防及預(yù)后評(píng)估對(duì)于卒中醫(yī)療質(zhì)量改進(jìn)及提高患者生活質(zhì)量意義重大,任重而道遠(yuǎn)。
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【點(diǎn)睛】
本文介紹了心房顫動(dòng)患者卒中風(fēng)險(xiǎn)、出血風(fēng)險(xiǎn)、預(yù)后等方面預(yù)測(cè)模型和評(píng)分系統(tǒng)的發(fā)展和現(xiàn)狀。