唐愛 楊貴志
[摘要]目的 觀察低劑量米力農(nóng)治療≥80歲慢性心力衰竭(CHF)患者的效果。方法 選取2018年10月~2019年10月我院收治的60例≥80歲CHF患者,依據(jù)隨機(jī)數(shù)字表法分為治療組和對(duì)照組,各30例。治療組采用標(biāo)準(zhǔn)治療+低劑量米力農(nóng),對(duì)照組采用標(biāo)準(zhǔn)治療。比較兩組的治療總有效率、血壓、心率、左室射血分?jǐn)?shù)(LVEF)值、左室舒張末期內(nèi)徑(LVEDD)、左室收縮末期內(nèi)徑(LVESD)、左室收縮末期容積(LVESV)、左室舒張末期容積(LVEDV)和6 min步行試驗(yàn)距離。結(jié)果 治療組的總有效率為86.7%,顯著高于對(duì)照組的53.3%,差異有統(tǒng)計(jì)學(xué)意義(P<0.01)。治療組的LVEF[(57.2±9.3)%]、6 min步行試驗(yàn)距離[(499.5±50.2)m]明顯高于對(duì)照組[(45.7±8.8)%、(392.5±90.8)m],差異有統(tǒng)計(jì)學(xué)意義(P<0.01)。治療組的LVESV[(116.3±52.7)ml]、LVEDV[(192.6±45.4)ml]、LVESD[(47.4±6.3)mm]低于對(duì)照組[(126.2±41.5)ml、(201.9±50.2)ml、(50.2±8.6)mm],差異有統(tǒng)計(jì)學(xué)意義(P<0.05)。治療組的LVEDD為(60.6±10.1)mm,與對(duì)照組的(61.2±10.8)mm比較,差異無統(tǒng)計(jì)學(xué)意義(P>0.05)。治療組治療后的LVEF[(57.2±9.3)%]、6 min步行試驗(yàn)距離[(499.5±50.2)m]顯著高于治療前[(37.3±11.4)%、(246.6±72.2)m],差異有統(tǒng)計(jì)學(xué)意義(P<0.01)。治療組治療后的LVESV、LVEDV、LVEDD、LVESD低于治療前,差異有統(tǒng)計(jì)學(xué)意義(P<0.05);對(duì)照組治療后的LVEF、6 min步行試驗(yàn)距離高于治療前,差異有統(tǒng)計(jì)學(xué)意義(P<0.05)。對(duì)照組治療前后的LVESV、LVEDV、LVESD、LVEDD比較,差異均無統(tǒng)計(jì)學(xué)意義(P>0.05)。兩組患者治療前后的血壓、心率比較,差異無統(tǒng)計(jì)學(xué)意義(P>0.05)。結(jié)論 低劑量米力農(nóng)能明顯改善≥80歲CHF患者的心功能及運(yùn)動(dòng)耐量。
[關(guān)鍵詞]慢性心力衰竭;米力農(nóng);高齡;6 min步行試驗(yàn);超聲檢查;臨床療效
[中圖分類號(hào)] R541.6? ? ? ? ? [文獻(xiàn)標(biāo)識(shí)碼] A? ? ? ? ? [文章編號(hào)] 1674-4721(2020)8(a)-0069-04
Effect of low-dose Milrinone in the treatment of chronic heart failure patients over 80 years old
TANG Ai1? ?YANG Gui-zhi2▲
1. Department of Ultrasonography, Ji′nan Hospital of Integrated Traditional Chinese and Western Medicine, Shandong Province, Ji′nan? ?271100, China; 2. Department of Geriatrics, Ji′nan Hospital of Integrated Traditional Chinese and Western Medicine, Shandong Province, Ji′nan? ?271100, China
[Abstract] Objective To observe the effect of low-dose Milrinone in the treatment of chronic heart failure (CHF) patients over 80 years old. Methods A total of 60 patients over 80 years old with CHF were selected and divided into the treatment group and the control group by random number table method, 30 cases in each group. The treatment group was treated with standard treatment combined with low-dose Milrinone, and the control group was treated with standard treatment. The total effective rate, blood pressure, heart rate, left ventricular ejection fraction (LVEF), left ventricular end diastolic diameter (LVEDD), left ventricular end systolic diameter (LVESD), left ventricular end systolic volume (LVESV), left ventricular end diastolic volume (LVEDV) and 6-minute walking test distance were compared between the two groups. Results The total effective rate was 86.7% in the treatment group, which was significantly higher than that in the control group (53.3%), the difference was statistically significant (P<0.01). The LVEF ([57.2±9.3]%) and 6-minute walking test distance [(499.5±50.2) m] in the treatment group were higher than those in the control group ([45.7±8.8]% and [392.5±90.8] m), the differences were statistically significant (P<0.01). The LVESV ([116.3±52.7]ml), LVEDV ([192.6±45.4] ml) and LVESD ([47.4±6.3] mm) in the treatment group were lower than those in the control group ([126.2±41.5] ml, [201.9±50.2] ml and [50.2±8.6] mm), with statistical significances (P<0.05). The LVEDD in the treatment group was (60.6±10.1) mm, which in the control group was (61.2±10.8) mm, with no statistical significance (P>0.05). The LVEF ([57.2±9.3]%), 6-minute walking test distance ([499.5±50.2] m) in the treatment group after treatment were higher than those before treatment ([37.3±11.4]%, [246.6±72.2] m), the differences were statistically significant (P<0.01). The LVESD, LVEDD, LVEDV and LVESV in the treatment group after treatment were lower than those before treatment, the differences were statistically significant (P<0.05). The LVEF and 6-minute walking test distance of the control group after treatment were higher than those before treatment, the differences were statistically significant (P<0.05). There were no significant differences in LVESV, LVEDV, LVESD and LVEDD between the control group before and after treatment (P>0.05). There were no significant differences in blood pressure and heart rate between the two groups before and after treatment (P>0.05). Conclusion The low-dose Milrinone can significantly improve heart function and exercise tolerance in elderly patients over 80 years old.
[Key words] Chronic heart failure; Milrinone; Elderly; 6-minute walking test; Ultrasound; Clinical efficacy
慢性充血性心力衰竭(心衰)是心血管疾病發(fā)展的終末階段,也是患者死亡的主要因素[1-2]。本病臨床常反復(fù)急性發(fā)作,病情驟變,死亡率較高,預(yù)后較差[3-4],尤其是高齡老年的心衰患者,采取標(biāo)準(zhǔn)化的治療仍難以改善,表現(xiàn)為頑固性心衰,使得患者生活質(zhì)量嚴(yán)重下降,常多次反復(fù)住院,是臨床的一大難題[5-7]。高齡老年心衰患者合并用藥多,指南推薦的藥物對(duì)于衰弱的老年心衰患者獲益尚不確定,部分患者病程綿長,聯(lián)合應(yīng)用多種抗心衰藥物治療亦難以改善臨床癥狀。米力農(nóng)是磷酸二酯酶抑制劑,具有正性肌力作用,可以增強(qiáng)心肌收縮力,同時(shí)具有直接擴(kuò)張血管的作用,臨床常短期應(yīng)用于急性心衰和擬行心臟移植患者[8]。本研究在采用指南推薦的常規(guī)治療基礎(chǔ)上,短期聯(lián)合應(yīng)用低劑量米力農(nóng)治療≥80歲心衰患者,取得了較好的臨床效果,現(xiàn)報(bào)道如下。
1資料與方法
1.1一般資料
選取2018年10月~2019年10月我院收治的60例≥80歲心衰患者,均符合《中國心力衰竭診斷和治療指南2018》[8]診斷標(biāo)準(zhǔn),有心衰的癥狀和(或)體征,且LVEF<40%,紐約心功能(NYHA)Ⅲ~Ⅳ級(jí)者。其中NYHA心功能Ⅲ級(jí)42例,Ⅳ級(jí)18例;男38例,女22例;年齡80~95歲,平均(84.6±4.9)歲。排除標(biāo)準(zhǔn):①未糾正的瓣膜性心臟病、肥厚型心肌病;②不穩(wěn)定性心絞痛或急性心肌梗死<2個(gè)月。依據(jù)隨機(jī)數(shù)字表法將入選患者分為治療組和對(duì)照組,每組30例。兩組的性別、年齡、病因等一般資料比較,差異無統(tǒng)計(jì)學(xué)意義(P>0.05)(表1),具有可比性。本研究經(jīng)我院醫(yī)學(xué)倫理委員會(huì)審核批準(zhǔn),患者自愿參與本研究,并簽署知情同意書。
1.2方法
對(duì)照組行標(biāo)準(zhǔn)化治療[9],包括吸氧、利尿劑、血管轉(zhuǎn)換酶抑制劑(ACEI)、β受體阻滯劑、醛固酮受體拮抗劑等。治療組在CHF標(biāo)準(zhǔn)治療的基礎(chǔ)上,予以米力農(nóng)注射液(魯南貝特制藥有限公司,國藥準(zhǔn)字 H10970051,規(guī)格為5 ml:5 mg/支)10 mg入生理鹽水50 ml,微量泵6 h泵入,1次/d。連續(xù)治療7 d為1個(gè)療程。
1.3觀察指標(biāo)及療效判定標(biāo)準(zhǔn)
1.3.1觀察指標(biāo)? 采用超聲心動(dòng)圖檢測(cè)心功能指標(biāo),包括左室射血分?jǐn)?shù)(LVEF)、左室舒張末期內(nèi)徑(LVEDD)、左室收縮末期內(nèi)徑(LVESD)、左室收縮末期容積(LVESV)、左室舒張末期容積(LVEDV)。運(yùn)動(dòng)耐量檢測(cè)采用6 min步行試驗(yàn)距離,NYHA心功能Ⅳ級(jí)者除外。兩組患者治療前后均記錄血壓及心率。
1.3.2臨床療效判定標(biāo)準(zhǔn)? 顯效:LVEF提高20%或(和)NYHA心功能分級(jí)改善2級(jí)或以上;有效:LVEF提高10%~19%或(和)NYHA心功能分級(jí)改善1級(jí);無效:LVEF提高9%以下或NYHA心功能分級(jí)無改善或加重??傆行?(顯效+有效)例數(shù)/總例數(shù)×100%[10]。
1.4統(tǒng)計(jì)學(xué)方法
采用SAS 9.2軟件進(jìn)行統(tǒng)計(jì)學(xué)分析,計(jì)量資料以均數(shù)±標(biāo)準(zhǔn)差(x±s)表示,組間比較采用t檢驗(yàn);計(jì)數(shù)資料以百分率(%)表示,組間比較采用χ2檢驗(yàn),以P<0.05為差異有統(tǒng)計(jì)學(xué)意義。
2結(jié)果
2.1兩組患者治療后臨床效果的比較
治療組的總有效率為86.7%,顯著高于對(duì)照組的53.3%,差異有統(tǒng)計(jì)學(xué)意義(P<0.01)(表2)。
2.2兩組患者治療前后血壓、心率、心功能、運(yùn)動(dòng)耐量的比較
治療組治療后的LVEF、6 min步行距離明顯高于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.01);治療組治療后的LVESV、LVEDV、LVESD低于對(duì)照組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05);兩組治療后的LVEDD比較,差異無統(tǒng)計(jì)學(xué)意義(P>0.05)。治療組患者治療后的LVEF、6 min步行距離明顯高于治療前,差異有統(tǒng)計(jì)學(xué)意義(P<0.01);治療組患者治療后的LVESV、LVEDV、LVESD、LVEDD低于治療前,差異有統(tǒng)計(jì)學(xué)意義(P<0.05);對(duì)照組患者治療后的LVEF、6 min步行距離高于治療前,差異有統(tǒng)計(jì)學(xué)意義(P<0.05)。對(duì)照組治療前后的LVESV、LVEDV、LVESD、LVEDD比較,差異無統(tǒng)計(jì)學(xué)意義(P>0.05)。兩組患者治療后的血壓及心率比較,差異無統(tǒng)計(jì)學(xué)意義(P>0.05)。兩組患者治療前的心功能、運(yùn)動(dòng)耐量、血壓及心率比較,差異無統(tǒng)計(jì)學(xué)意義(P>0.05)(表3)。
3討論
我國已步入老齡化社會(huì),截至2015年,中國≥60歲的老年人口已達(dá)2.22億,其中,≥80歲的老年人占13.9%[11]。心衰的發(fā)病率和患病率隨年齡增加而增加,≥80歲人群的心衰患病率近12%。老年心衰患者容易發(fā)生心衰惡化,預(yù)后很差,住院病死率為3%,6個(gè)月的再住院率約為50%,5年病死率高達(dá)60%[12]。高齡心衰患者多病因共存,合并癥多,合并用藥多,≥80歲的心衰患者中約1/3合并癡呆,預(yù)期壽命縮短,采取的非藥物措施較少,臨床主要以藥物治療為主[13]。
米力農(nóng)是非洋地黃類正性肌力藥物,屬于磷酸二酯酶抑制劑,通過抑制環(huán)磷酸腺苷降解,升高細(xì)胞內(nèi)cAMP濃度,使Ca2+內(nèi)流增加,心肌收縮力增強(qiáng)[14];同時(shí)具有提高血管平滑肌細(xì)胞內(nèi)的cAMP水平,從而使周圍血管擴(kuò)張,降低心臟后負(fù)荷,改善心力衰竭,指南推薦其應(yīng)用于難治性心衰和伴有嚴(yán)重肺動(dòng)脈高壓心衰的短期治療[15]。研究證實(shí),長期大劑量應(yīng)用米力農(nóng)可以提高病死率[16],但小劑量短期應(yīng)用則可以提高其臨床療效,安全性較好[17]。
本研究采用米力農(nóng)低劑量(10 mg/d)短期治療高齡心衰患者,結(jié)果顯示,治療組治療7 d后的LVEF、6 min步行距離、LVESV、LVEDV、LVESD均明顯改善(P<0.05),而LVEDD差異無統(tǒng)計(jì)學(xué)意義(P>0.05),提示米力農(nóng)可明顯提高衰竭心肌的收縮功能,而對(duì)LVEDD的影響與標(biāo)準(zhǔn)化藥物治療差異無統(tǒng)計(jì)學(xué)意義。本研究結(jié)果還顯示,兩組患者治療前后的心率、血壓比較差異無統(tǒng)計(jì)學(xué)意義(P>0.05),提示米力農(nóng)對(duì)心率血壓的影響與標(biāo)準(zhǔn)藥物無異。本研究顯示,無論是臨床癥狀的改善還是心臟超聲指數(shù)的恢復(fù),治療組均明顯優(yōu)于標(biāo)準(zhǔn)治療對(duì)照組,提示低劑量米力農(nóng)短期可以顯著改善高齡心衰患者的心臟收縮功能,并能明顯改善高齡心衰患者的運(yùn)動(dòng)耐量,顯著提高6 min步行距離,且未發(fā)現(xiàn)致命性心律失常等嚴(yán)重副作用,能夠使患者安全度過急性加重期。
綜上所述,對(duì)于高齡心衰高危患者,急性加重期采用標(biāo)準(zhǔn)化方案配合低劑量米力農(nóng)短期治療控制心衰癥狀,之后只保留常規(guī)藥物穩(wěn)定病情,不失為一種值得推薦的高齡心衰患者的治療措施,臨床值得進(jìn)一步大樣本觀察。
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(收稿日期:2020-01-09)