Key result
Multidose cardioplegia over 750mL is linked to lower peak troponin during prolonged CPB.
Why the study?
Myocardial cell ischaemic injury during cardiopulmonary bypass and aortic crossclamp limits outcomes in CABG, and factors affecting troponin I release need clarification.
Does cardioplegia volume and dosing strategy affect peak troponin I release after CABG?
Observational (n=172)
No
Does cardioplegia volume and dosing strategy affect peak troponin I release after CABG?
p-value: p=0.033
Cardiopulmonary bypass time is the most significant factor impacting myocardial cell damage during CABG, though >750mls of multidose cardioplegia offers protection for ischaemia times up to 62 minutes.
Higher-volume multidose cardioplegia may limit troponin rise with longer ischaemia; leaves open optimal dosing pending prospective trials.
Background Myocardial cell ischaemic injury during cardiopulmonary bypass and aortic crossclamp remains a key limiting factor to patient outcomes in coronary artery bypass grafting. Troponin I has been shown to be an effective indicator of myocardial ischaemic injury and achieves peak levels early post-operatively. Methods All consenting CABG patients from one centre, during a one year period, were recruited. All surgeries were performed using identical techniques besides the cardioplegia volume and number of doses. Troponin I levels were checked regularly post-operatively until a peak troponin I level was ascertained. All the patient demographics, crossclamp times, bypass times and cardioplegia dosing were analysed using multiple combinations of statistical tools. Results 172 patients were included in the study and cardiopulmonary bypass (CPB) time was found to be significant as a single variable (p=0.033). The combination of CBP time and ischaemia time (p=0.002) and the combination of CPB time and multidose cardioplegia (p=0.009), were both found to significantly effect peak troponin I levels. Another analysis was performed on the volume of cardioplegia used. While this was not significant as an individual variable it did become significant when combined with ischaemia time at a threshold total cardioplegia volume of 750mls (p=0.026). Conclusions The conclusion therefore is that using over 750mls of cardioplegia in multiple doses will safely protect against an ischaemia time of up to 62min. However there is no protection against the CPB time, which proved to have the most impact on myocardial cell damage in our practice.
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Sladden et al. (2017) conducted an observational in Coronary artery bypass grafting (CABG) (n=172). Cardiopulmonary bypass time and cardioplegia volume was evaluated on Peak troponin I levels (p=0.033). Cardiopulmonary bypass time significantly impacted peak troponin I levels (p=0.033), while using over 750mls of multidose cardioplegia protected against ischaemia times up to 62 minutes.
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