ライフサイエンスコーパス: non-Q wave MI

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1 events consisted of 3 deaths, 2 acute MIs, 1 non-Q-wave MI, and 3 cases of CHF.

2 yocardial infarction (MI); positive group, 4 non-Q-wave MIs and 12 myocardial revascularizations; non

3 There were 28 patients (16%) who had a non-Q-wave MI.

4 routine evaluation were defined as having a non-Q-wave MI.

5 time, and there is no specific ECG sign of a non-Q-wave MI.

6 7 women and 976 men with unstable angina and non-Q wave MI at the time of enrollment were compared.

7 The proportion of unstable angina and non-Q wave MI for women was similar in the trial and Reg

8 n compared with men with unstable angina and non-Q wave MI have not been extensively studied.

9 2) The outcome with unstable angina and non-Q wave MI is related to severity of illness and not

10 th revascularization for unstable angina and non-Q wave MI was similar for women and men.

11 evaluating patients with unstable angina and non-Q wave MI, little prospective information is availab

12 ower incidence of peri-procedural Q-wave and non-Q-wave MI.

13 myocardial infarction [MI] through 30 days; non-Q-wave MI through 24 h; and ipsilateral stroke or ne

14 ial infarction [MI]) in patients who evolved non-Q-wave MI (NQMI) following thrombolytic therapy.

15 r, proportionately more men in the trial had non-Q wave MI than men in the Registry.

16 osite end point of death, postprocedural MI, non-Q-wave MI after PCI hospitalization, or urgent targe

17 ttributable mainly to a greater frequency of non-Q-wave MI with acolysis (19.6% versus 7.9%, P=0.03).

18 with a significant reduction in the risk of non-Q-wave MI (unadjusted odds ratio 0.18, 95% confidenc

19 tted to the hospital with unstable angina or non-Q wave MI.

20 l of 8676 admissions with unstable angina or non-Q-wave MI were enumerated and, of these, 3318 patien

21 .1% vs. 0.06%, p = 0.009) and periprocedural non-Q wave MI (8.7% vs. 4.2%, p = 0.003) were more frequ

22 re was a higher prevalence of periprocedural non-Q wave MI (28% vs. 16%, p = 0.009) in the multiple S

23 ificantly higher frequency of periprocedural non-Q-wave MIs, and 3) equivalent repeat revascularizati

24 acteristics, (2) a higher rate of procedural non-Q-wave MI, and (3) similar TLR and overall major car

25 associated with a reduced risk of procedural non-Q-wave MIs.

26 with a lower incidence of procedure-related non-Q-wave MIs (duration of pretreatment <1 day, 29% had

27 ery useful in risk stratifying patients with non-Q wave MI.

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