鐘 武 王 亮 陳紅生
(瀘州醫(yī)學(xué)院附屬醫(yī)院急診科,四川 瀘州 646000)
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口服抗凝劑利伐沙班與華法林預(yù)防非瓣膜性心房纖維顫動患者血栓栓塞的療效比較
鐘武王亮陳紅生
(瀘州醫(yī)學(xué)院附屬醫(yī)院急診科,四川瀘州646000)
〔摘要〕目的比較利伐沙班與華法林非瓣膜性心房纖維顫動(AF)患者的有效性和安全性。方法采用CHADS2評分法納入122例評分≥2的AF患者,隨機分為利伐沙班組和華法林組(對照組)。結(jié)果利伐沙班組主要安全性終點事件發(fā)生率與華法林組相比無顯著性差異,風(fēng)險比(OR)為3.28,95%置信區(qū)間(CI,-9.7,16.2),P=0.78。另外,利伐沙班組的總出血事件數(shù)值顯著低于華法林組,OR16.39,95%CI(1.4,31.4),P=0.03。結(jié)論利伐沙班與華法林相比,在CHADS2≥2的患者中其安全性和有效性的相似。一般而言CHADS評分≥2的患者如果被新診斷有AF,根據(jù)病患可能罹患血栓癥的可能性,給予抗凝血藥物,可以優(yōu)先選擇利伐沙班。
〔關(guān)鍵詞〕口服抗凝;腦卒中;華法林;利伐沙班;血栓;心房纖維顫動
心房纖維顫動(AF)是最常見的心律失常疾病之一〔1~3〕。若不及時消除,很快會導(dǎo)致心臟停搏,造成死亡。AF多發(fā)生于老年人〔4,5〕。由于AF發(fā)生時,失去了原本心房收縮對于心室舒張末期填充的貢獻(xiàn),加上經(jīng)常合并過快的心室速率,縮短了舒張期的心室血流量的填充時間,所以經(jīng)常成為心衰竭病人臨床癥狀突然惡化的主因〔3,6〕。當(dāng)AF合并其他各種心血管疾病時,更可加重病人死亡率達(dá)2倍之多〔7~10〕。在未發(fā)生血栓的AF病例中,腦卒中風(fēng)險升高了4~5倍,提示此類患者需要采用抗凝治療〔11,12〕。CHADS2評分是全球中的一個最簡單有效的評分系統(tǒng),該方法可以綜合評價每個腦卒中患者的危險因素〔13~15〕。盡管AF患者CHADS2評分高預(yù)示著發(fā)生血栓的高風(fēng)險,并有可能需要抗凝治療,但是他們也伴隨有出血的高風(fēng)險〔16~19〕,目前對利伐沙班和WFR之間的療效對比尚缺乏有效數(shù)據(jù)〔20,21〕。因此,本研究結(jié)合CHADS2評分方法對利伐沙班的安全性和療效華法林之間開展了比較研究。
1資料與方法
1.1入選及排除標(biāo)準(zhǔn)本研究為單中心、隨機、雙盲且平行對照臨床研究。根據(jù)美國心臟病協(xié)會的推薦,以CHADS2評分來確定AF患者發(fā)生血栓的危險程度。評分標(biāo)準(zhǔn):①心力衰竭:1分;②高血壓:1分;③大于75歲:1分;④糖尿病:1分;⑤有腦梗死或腦缺血史:2分;上面的5項評分相加就是CHADS2評分。處理:①評分在2分以上為高危險:建議口服華法林抗凝。②評分為1分為中度危險:口服阿司匹林或華法林抗凝。③評分為0分為低度危險:口服阿司匹林抗凝。若CHADS2 評分≥2,則該患者風(fēng)險足夠高,應(yīng)口服抗凝藥,納入本研究序列。若CHADS2評分0或1的患者,排除出本研究。
1.2研究對象所有122例患者按1∶1的比例隨機進(jìn)入利伐沙班組或華法林組。研究遵循赫爾辛基宣言和我國頒布的藥物臨床試驗質(zhì)量管理規(guī)范,方案經(jīng)倫理委員會討論通過后執(zhí)行。我院自2010年2月至2012年12月選擇非瓣膜性AF患者122例。對比觀察利伐沙班(德國 Bayer healthcare AG公司生產(chǎn))、華法林(齊魯制藥)這兩種藥物的臨床療效及安全性。122例例AF患者均經(jīng)臨床癥狀、檢查體征及心電圖(Cardiofax-M型號,日本光電NIHON KOHDEN公司生產(chǎn))確診,排除瓣膜性AF。非瓣膜性AF患者,在招募前30 d心電圖記錄并確診。患者前6個月無相關(guān)用藥史,并排除肌酐清除率<30 ml/min患者。采用計算機生成隨機數(shù)字表,患者根據(jù)該法隨機分為利伐沙班和華法林組。利伐沙班是口服給藥,每日1次,15 mg/d。華法林需要劑量調(diào)整,年齡>70歲給藥后控制INR為2.0~3.0,70歲或以上控制INR為1.6~2.6,預(yù)先設(shè)定的最大研究期為6個月。
1.3觀察指標(biāo)在研究結(jié)束時,統(tǒng)計分析事件發(fā)生率,風(fēng)險比(OR)等方法進(jìn)行總結(jié)。療效主要結(jié)果是通過超聲多普勒(Logiq E9型號美國GE公司生產(chǎn))或血管成像(CX50型號荷蘭飛利浦公司生產(chǎn))檢測癥狀性靜脈血栓栓塞癥(VTE)和無癥狀深靜脈血栓(DVT)。安全性指標(biāo)主要觀察出血事件的發(fā)生次數(shù)。
1.4統(tǒng)計學(xué)方法組間比較行t及χ2檢驗。
2結(jié)果
2.1兩組患者的一般情況比較兩組AF患者年齡、性別、體重等指標(biāo)均無顯著性差異(P>0.05)。見表1。
表1 兩組患者一般情況比較(n=61)
2.2兩組療效及不良反應(yīng)比較利伐沙班組與華法林組總心血管事件及總出血事件的發(fā)生率分別為9.8%(6/61),13.1%(8/61),9.8%(6/61)和23.0%(14/61),其OR分別3.28(95%CI:-9.7~16.2)和16.39(95%CI:1.4~31.4)。華法林組中的總出血事件顯著升高(P=0.03)。
3討論
通常處理AF的病人時,一般必須了解到此病的臨床表現(xiàn)采取的不同治療策略,如使用CHADS2評分策略〔22,23〕。CHADS2評分包括心力衰竭、高血壓、年齡>75歲、糖尿病和既往腦卒中或一過性腦缺血發(fā)作(TIA),前面4個危險因素各為1分,最后一個為2分〔24~27〕。本研究結(jié)果顯示,利伐沙班在療效方面不劣于華法林,但在安全性方面優(yōu)于利伐沙班。另外,雖然研究療效差異并不顯著,利伐沙班與華法林相比可以顯著降低所有原因的心血管事件。另外華法林抗凝患者一旦發(fā)生腦梗死,因INR一般大于1.4往往無法融栓〔28~30〕。因此,在更大樣本的臨床研究中可能提示利伐沙班的療效優(yōu)于華法林。
另外,本研究也有一些局限性,如這項試驗并不是設(shè)計來檢測研究藥物和CHADS2評分亞群之間的相互作用。雖然類似的人口統(tǒng)計學(xué)特征進(jìn)行了利伐沙班與華法林組之間觀察到每個CHADS2評分類別,但是各組人群數(shù)量比較小。此外,本研究結(jié)果均來自臨床試驗的人口,可能會偏離現(xiàn)實世界中的患者人群。盡管有這些限制,利伐沙班的安全性和效力和劑量調(diào)整華法林戰(zhàn)爭之間的差異??傊珹F的藥物處理,最重要的是要理清患者的基本病因,采用CHADS2評分配合新型抗凝血劑利伐沙班的使用,使得患者從藥物的選擇中得到最大的益處,最少的副作用。綜上所述,CHADS評分≥2的患者如果患者被新診斷有AF,根據(jù)病患可能罹患血栓癥的可能性,來給予抗凝血藥物,可以優(yōu)先選擇新藥利伐沙班。
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〔2014-10-11修回〕
(編輯趙慧玲/曹夢園)
〔中圖分類號〕R322.1+1
〔文獻(xiàn)標(biāo)識碼〕A
〔文章編號〕1005-9202(2016)05-1094-03;
doi:10.3969/j.issn.1005-9202.2016.05.033
通訊作者:王亮(1980-),男,醫(yī)師,主要從事血管外科研究。
第一作者:鐘武(1973-),男,碩士,副教授,主要從事血管外科疾病研究。