心血管康复医学杂志
心血管康複醫學雜誌
심혈관강복의학잡지
JOURNAL OF CARDIOVASCULAR REHABILITATION MEDICINE
2015年
2期
175-179
,共5页
刘英%杨勇%刘惠亮%韩玮
劉英%楊勇%劉惠亮%韓瑋
류영%양용%류혜량%한위
急性冠状动脉综合征%血管成形术,气囊,冠状动脉%C反应蛋白质%阿托伐他汀
急性冠狀動脈綜閤徵%血管成形術,氣囊,冠狀動脈%C反應蛋白質%阿託伐他汀
급성관상동맥종합정%혈관성형술,기낭,관상동맥%C반응단백질%아탁벌타정
Acute coronary syndrome%Angioplasty,balloon,coronary%C-reactive protein%Atorvastatin
目的:观察急性冠脉综合征(ACS )行PCI患者使用阿托伐他汀序贯治疗6个月的疗效以及安全性。方法:连续入选280例ACS患者,随机均分为序贯治疗组(术前2d给予阿托伐他汀80mg ,术后给予40mg/d ,1月后改为20mg/d)及常规治疗组(术前未服用阿托伐他汀,术后及维持量均予20mg/d),观察6个月,比较两组患者的疗效及安全性。结果:两组术后18h~24h肌酸激酶同工酶(CK‐MB)、心肌肌钙蛋白I (cTnI)水平均明显高于治疗前,序贯治疗组的水平明显低于常规治疗组[CK‐MB :(2.72±0.52)μg/L 比(6.04±0.51)μg/L ,cTnI :(0.28±0.13)μg/L比(0.42±0.16)μg/L , P均<0.01];术后2d ,序贯治疗组高敏C反应蛋白(hsCRP)水平即显著低于常规治疗组,一直维持到术后6月[(1.49±0.78) mg/L比(2.34±0.51) mg/L , P=0.001],序贯治疗组血脂水平(除高密度脂蛋白水平显著升高外)较常规治疗组显著降低( P均<0.01);两组转氨酶大于3倍以上比例、主要不良心血管事件(MACE)发生率无明显差异(P均>0.05)。结论:急性冠脉综合征患者PCI术前80mg阿托伐他汀联合术后40mg阿托伐他汀治疗,可明显降低炎症反应,改善血脂;与常规剂量比较,未明显增加药物不良反应,安全有效。
目的:觀察急性冠脈綜閤徵(ACS )行PCI患者使用阿託伐他汀序貫治療6箇月的療效以及安全性。方法:連續入選280例ACS患者,隨機均分為序貫治療組(術前2d給予阿託伐他汀80mg ,術後給予40mg/d ,1月後改為20mg/d)及常規治療組(術前未服用阿託伐他汀,術後及維持量均予20mg/d),觀察6箇月,比較兩組患者的療效及安全性。結果:兩組術後18h~24h肌痠激酶同工酶(CK‐MB)、心肌肌鈣蛋白I (cTnI)水平均明顯高于治療前,序貫治療組的水平明顯低于常規治療組[CK‐MB :(2.72±0.52)μg/L 比(6.04±0.51)μg/L ,cTnI :(0.28±0.13)μg/L比(0.42±0.16)μg/L , P均<0.01];術後2d ,序貫治療組高敏C反應蛋白(hsCRP)水平即顯著低于常規治療組,一直維持到術後6月[(1.49±0.78) mg/L比(2.34±0.51) mg/L , P=0.001],序貫治療組血脂水平(除高密度脂蛋白水平顯著升高外)較常規治療組顯著降低( P均<0.01);兩組轉氨酶大于3倍以上比例、主要不良心血管事件(MACE)髮生率無明顯差異(P均>0.05)。結論:急性冠脈綜閤徵患者PCI術前80mg阿託伐他汀聯閤術後40mg阿託伐他汀治療,可明顯降低炎癥反應,改善血脂;與常規劑量比較,未明顯增加藥物不良反應,安全有效。
목적:관찰급성관맥종합정(ACS )행PCI환자사용아탁벌타정서관치료6개월적료효이급안전성。방법:련속입선280례ACS환자,수궤균분위서관치료조(술전2d급여아탁벌타정80mg ,술후급여40mg/d ,1월후개위20mg/d)급상규치료조(술전미복용아탁벌타정,술후급유지량균여20mg/d),관찰6개월,비교량조환자적료효급안전성。결과:량조술후18h~24h기산격매동공매(CK‐MB)、심기기개단백I (cTnI)수평균명현고우치료전,서관치료조적수평명현저우상규치료조[CK‐MB :(2.72±0.52)μg/L 비(6.04±0.51)μg/L ,cTnI :(0.28±0.13)μg/L비(0.42±0.16)μg/L , P균<0.01];술후2d ,서관치료조고민C반응단백(hsCRP)수평즉현저저우상규치료조,일직유지도술후6월[(1.49±0.78) mg/L비(2.34±0.51) mg/L , P=0.001],서관치료조혈지수평(제고밀도지단백수평현저승고외)교상규치료조현저강저( P균<0.01);량조전안매대우3배이상비례、주요불양심혈관사건(MACE)발생솔무명현차이(P균>0.05)。결론:급성관맥종합정환자PCI술전80mg아탁벌타정연합술후40mg아탁벌타정치료,가명현강저염증반응,개선혈지;여상규제량비교,미명현증가약물불량반응,안전유효。
Objective:To observe therapeutic effect and safety of six‐month atrovastatin sequential treatment on pa‐tients with acute coronary syndrome (ACS) undergoing PCI .Methods :A total of 280 ACS patients were consecu‐tively enrolled ,randomly and equally divided into sequential treatment group (received atorvastatin 80mg 2d before PCI operation ,then 40mg/d after operation ,20mg/d a month later ) and routine treatment group (no taking atorv‐astatin before PCI operation ,then 20mg/d after operation and as a maintenance dose ) .Both groups were observed for six months ,therapeutic effect and safety were compared between two groups .Results:Compared with before PCI ,there were significant rise in levels of creatine kinase isoenzyme (CK‐MB) and cardiac troponin I (cTnI) after PCI 18h~24h in two groups ,and those of sequential treatment group were significantly lower than those in routine treatment group [CK‐MB:(2.72 ± 0.52) μg/L vs .(6.04 ± 0.51) μg/L ,cTnI : (0.28 ± 0.13) μg/L vs .(0.42 ± 0.16) μg/L , P < 0.01 both ];Compared with routine treatment group , the high sensitive C reactive protein (hsCRP) level significantly reduced in sequential treatment group after PCI 2d ,and continued until post‐operation six months [ (2.34 ± 0.51) mg/L vs .(1.49 ± 0.78) mg/L ,P=0.001];the blood lipids levels (except level of high density lipoprotein cholesterol significantly rose ) in sequential treatment group were significant lower than those of routine treatment group , P<0.01 all;there were no significant difference in percentage of transaminase level high‐er than normal three times and incidence rates of major adverse cardiovascular events (MACE) between two groups , P>0.05 all .Conclusion:Preoperative 80mg atrovastatin combined postoperative 40mg atrovastatin treatment can significantly reduce inflammatory reaction ,improve blood lipids ;compared with routine dose ,it doesn't significant‐ly increase adverse drug reactions ,so it's safe and effective .