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用于冠状动脉疾病二级预防的阿司匹林治疗的个体化分配

Personalized allocation of acetylsalicylic acid therapy for secondary prevention of coronary artery disease.

作者信息

Hegde Nischal N, Mathew Navin, Thachathodiyl Rajesh, Menon Jaideep C

机构信息

Department of Cardiology, Amrita Institute of Medical Sciences, Kochi, India.

出版信息

Front Cardiovasc Med. 2022 Sep 27;9:1004473. doi: 10.3389/fcvm.2022.1004473. eCollection 2022.

Abstract

BACKGROUND

A single-daily dose of 75 mg of acetylsalicylic acid inhibits 100% of thromboxane-B2 synthesis within 30-60 min. Thromboxane-B2 synthesis then recovers slowly as new platelets are released from the bone marrow. Normally, only 10% of the platelets are replaced daily by new platelets entering circulation. Hence, 24 h after a dose of acetylsalicylic acid, thromboxane-B2 synthesis is still suppressed by more than 90%. Hence, there is an adequate anti-platelet effect even after 24 h of acetylsalicylic acid intake. However, some patients treated with once-daily acetylsalicylic acid may have an incomplete 24-h suppression of thromboxane-B2 synthesis due to increased platelet turnover. The response could be improved in such patients by twice-daily acetylsalicylic acid administration. This study aimed to identify such a group of patients who would benefit from a twice-daily dose of acetylsalicylic acid.

MATERIALS AND METHODS

Serum thromboxane-B2 levels were measured in 79 patients with coronary artery disease receiving 75 mg of acetylsalicylic acid for secondary prophylaxis. Serum levels of thromboxane-B2 were measured after 4 and 24 h of acetylsalicylic acid intake. Patients were then classified into three groups: steady suppression group (serum thromboxane B2 is adequately suppressed at 4 and 24 h), i.e., adequate response to acetylsalicylic acid; fast recovery group (more than 10% rise in serum thromboxane-B2 levels at 24-h when compared to at 4-h) and non-responders (serum thromboxane-B2 levels of >3,100 pg/ml after 4 h of acetylsalicylic acid intake). Patients in the fast recovery group were given twice-daily acetylsalicylic acid and thromboxane-B2 levels were re-measured.

RESULTS

A total of 20 patients (24.3%) had steady suppression of thromboxane-B2 and 11 patients (13.9%) belonged to the fast recovery group, i.e., thromboxane-B2 levels were adequately suppressed at 4 h but had recovered by more than 10% at 24 h; which was adequately suppressed by twice-daily acetylsalicylic acid (p 0.004). A total of 48 patients (60.8%) were non-responders.

CONCLUSION

Twice-daily acetylsalicylic acid may be beneficial if serum thromboxane-B2 levels at 4 h are <3,100 and >3,100 pg/ml at 24 h. If thromboxane-B2 levels at 4 and 24 h is <3100 pg/ml but if there is a >10% rise in serum thromboxane B2 at 24 h as compared to that at 4 h, then twice-daily acetylsalicylic acid should be considered. However, if thromboxane-B2 at 4 and 24 h is >3,100 pg/ml consider switching over to a P2Y12 inhibitor.

摘要

背景

每日单次服用75毫克阿司匹林可在30 - 60分钟内抑制100%的血栓素B2合成。随着骨髓释放新的血小板,血栓素B2合成随后缓慢恢复。正常情况下,每天仅有10%的血小板被进入循环的新血小板替代。因此,服用阿司匹林24小时后,血栓素B2合成仍被抑制超过90%。所以,即使在摄入阿司匹林24小时后仍有足够的抗血小板作用。然而,一些接受每日一次阿司匹林治疗的患者可能由于血小板更新增加而对血栓素B2合成的24小时抑制不完全。通过每日两次服用阿司匹林,这类患者的反应可能会得到改善。本研究旨在确定这样一组能从每日两次服用阿司匹林中获益的患者。

材料与方法

对79例接受75毫克阿司匹林进行二级预防的冠心病患者测定血清血栓素B2水平。在摄入阿司匹林4小时和24小时后测定血清血栓素B2水平。然后将患者分为三组:稳定抑制组(血清血栓素B2在4小时和24小时均得到充分抑制),即对阿司匹林反应良好;快速恢复组(与4小时相比,24小时血清血栓素B2水平升高超过10%)和无反应者(摄入阿司匹林4小时后血清血栓素B2水平>3100皮克/毫升)。对快速恢复组患者给予每日两次阿司匹林,并重新测定血栓素B2水平。

结果

共有20例患者(24.3%)血栓素B2得到稳定抑制,11例患者(13.9%)属于快速恢复组,即血栓素B2水平在4小时得到充分抑制,但在24小时恢复超过10%;每日两次服用阿司匹林可充分抑制(p<0.004)。共有48例患者(60.8%)为无反应者。

结论

如果4小时时血清血栓素B2水平<3100皮克/毫升且24小时时>3100皮克/毫升,每日两次服用阿司匹林可能有益。如果4小时和24小时时血栓素B2水平<3100皮克/毫升,但与4小时相比24小时血清血栓素B2升高>10%,则应考虑每日两次服用阿司匹林。然而,如果4小时和24小时时血栓素B2水平>3100皮克/毫升,则考虑换用P2Y12抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9611/9551163/35631e50fbc6/fcvm-09-1004473-g001.jpg

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