ライフサイエンスコーパス: blood cardioplegia

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1 mp CABG (with or without valve surgery) with blood cardioplegia.

2 anced in the coronary microcirculation after blood cardioplegia.

3 ulmonary bypass and randomized to either all-blood cardioplegia (AB group) or dilute blood cardiopleg

4 nutes of 10 degrees C antegrade intermittent blood cardioplegia and 30 minutes of reperfusion.

5 In this study, the effects of blood cardioplegia and brief reperfusion on vascular rea

6 Blood cardioplegia and combined antegrade and retrograde

7 Both all-blood cardioplegia and dilute cardioplegia have disadvan

8 s C) antegrade potassium all-blood or dilute blood cardioplegia and maintained with tepid retrograde

9 vested from patients (n=15) before and after blood cardioplegia and short-term reperfusion under cond

10 this, early death (6% crystalloid versus 4% blood cardioplegia) and late death (24% crystalloid vers

11 L)-supplemented blood (RSR13-BC) to standard blood cardioplegia (BC).

12 of ONOO(-) may exist between crystalloid and blood cardioplegia (BCP) environments.

13 tested the hypothesis that ADO-supplemented blood cardioplegia (BCP) or ADO administered during repe

14 of the intraoperative administration of cold blood cardioplegia, blood cardioplegia containing 500 mi

15 Cardioplegic arrest (CA) using cold blood cardioplegia (CBC) has been reported to reduce isc

16 oplegia containing 500 microM adenosine, and blood cardioplegia containing 2 mM adenosine.

17 e administration of cold blood cardioplegia, blood cardioplegia containing 500 microM adenosine, and

18 all-blood cardioplegia (AB group) or dilute blood cardioplegia (Dil group).

19 ditioning activation adjuvant to hypothermic blood cardioplegia enhances postischemic contractile rec

20 loid cardioplegia (iC-CCP; n=8) or with cold blood cardioplegia (iC-BCP; n=6) administered intermitte

21 ety and tolerance of adenosine when added to blood cardioplegia in increasing doses to enhance myocar

22 The advantages of blood cardioplegia include the oxygen-carrying capacity,

23 oid cardioplegia (iW-CCP) (n=8) or with warm blood cardioplegia (iW-BCP) (n=8) administered intermitt

24 atrial segment exposed to cold, hyperkalemic blood cardioplegia (mean, 60 minutes) and a brief period

25 o determine the effect, if any, of adenosine blood cardioplegia on blood component usage after heart

26 During hypothermic blood cardioplegia, oxygen delivery to myocytes is minim

27 ) and late death (24% crystalloid versus 21% blood cardioplegia) statistics were not significantly di

28 stalloid cardioplegia versus those receiving blood cardioplegia were found to have significantly more

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