Cardioplegic arrest represented one of the most important (probably the greatest) achievement of cardiac surgery in the last 40 years because it allowed, on one hand, the feasibility of treating all heart pathologies with a stopped and bloodless heart and then to ensure, at the same time, myocardial protection during the ischemic period. Cardioplegic solutions usually used can be crystalloid or blood based. Custodiol® solution, also called histidine-tryptophan-ketoglutarate (HTK) or Bretschneider’s solution, is a particular kind of long-acting intracellular crystalloid cardioplegia (CCP) that differs from other extracellular cardioplegic solutions because of its low sodium and potassium content that induce the diastolic cardiac arrest through an hyperpolarization of the myocyte plasma membrane. A low sodium solution seems to effect the lowest energy turnover compared with high potassium cardioplegia (1), histidine acts as buffer of anaerobic metabolites produced during the ischaemic period, ketoglutarate is used as precursor for ATP production, tryptophan as membrane-stabilizator and mannitol to reduce cellular oedema and for its radical scavenger properties. Custodiol®, moreover, for its attractive capacity to provide a long myocardial protection with a single infusion is widely used in complex cardiac surgery and for organ preservation in allowing performance of complex procedures without interruption. On the other hand, blood-based cardioplegic solutions (like Calafiore-cardioplegia) are characterized by high potassium levels as depolarisation factor inducing cardiac arrest in diastole (2). This kind of cardioplegia, that can be administered with continuous or intermittent flow and at body or low temperature, seems to provide a “more physiologic” cardiac arrest because blood could reduce the damaging effects of prolonged ischemia (3,4). According to other, high-potassium cardioplegia “era” seems to come to an end due to discover of harmful effects onto ischemic myocardium (5).
In the last years, a lot of studies analyzed pros and cons of these two types of cardioplegic solutions in the different areas of cardiac surgery (6), both in adults and in pediatrics (7,8), in order to find unique and shared indications but today the debate is still open especially in valve surgery. In fact, while literature swarms of clinical investigations about use of cardioplegic strategies in coronary artery bypass (CAB) surgery (9), there are few and conflicting studies comparing their use in valve surgery.
The most recent review about this topic belong to Hoyer et al., where it was analyzed a single-centre experience on 7,263 patients undergone isolated aortic valve surgery with the aim of compare cold blood cardioplegia (BCP) and cold CCP (10). Among patients that received one of the two types of cardioplegia, exploratory analysis revealed that group treated with cold BCP had an high percentage of associated comorbidities such as diabetes, peripheral vascular disease (PVD) or chronic obstructive pulmonary disease (COPD). Furthermore, the main indications for the use of BCP seemed to have been an impaired cardiac function (LVEF <30%, NYHA ≥III) or prior cardiac surgery probably for the widespread opinion that intermittently BCP provides higher myocardial preservation due to its more physiological properties and oxygen-carrying capacity (4,11). This seems to be in accordance also with Braathen et coll. where percentage of patients with LVEF >50% were higher, even if statistically not significant, in the group treated with CCP (12) but not with Viana et al. that, on the other hand, reported a lower percentage of patients with impaired cardiac function (Severe LV dysfunction or NYHA > II) in CCP group compared with BCP group (13).
A really important factor that influence distribution and effectiveness of a cardioplegic solution, beyond the chemical composition, is the anatomical state of the coronary tree and the myocardium; infact, although in isolated aortic valve surgical patients coronary arteries are usually free of haemodynamic significant stenosis, the distribution of cardioplegia can be hampered by microcirculatory dysfunctions that are typically present in hypertrofied hearts (14). In the cases, a good option to prevent poor distribution of cardioplegia could be the BCP that, for its features, allow an intermittent antegrade/retrograde administration even if Ascione et al. demonstrated that also only antegrade intermittent administration of cold BCP can be useful for patients with hypertrophied hearts undergoing aortic valve surgery (15). Hoyer et al., in this regard, reported a statistically significant difference in the percentage of patients that received anterograde/retrograde cardioplegia between two group that was higher among BCP patients (10). According to others, it seems even that warm BCP gives an higher myocardial protection in aortic valve repair (AVR) surgery compared to cold BCP (16). Øvrum et al., on the contrary, showed that retrograde cold BCP was not superior to retrograde cold CCP for patients undergoing AVR (17).
As previously mentioned, it’s clearly evident of how there are a lot of contradictory results about comparison between crystalloid or blood cardioplegic solution in cardiac surgery especially because populations or outcome variables are generally various among the different works.
In the study of Hoyer et al., the author analyzed retrospectively 825 matched patients in order to avoid as much as possible selection biases. Patients undergone isolated AVR and treated with HTK solution or Calafiore Cardioplegia were retrospectively included; CCP were readministered if aortic cross-clamp exceeded 90 min while BCP, in contrast with the original protocol (2), was infused by cooling to 15 °C. Outcomes analyzed were mainly clinic: in fact, operative mortality (OM, death within 30 days of surgery), re-exploration for bleeding, low cardiac output syndrome (LCOS), intra-aortic balloon pump (IABP) implantation, extracorporeal membrane oxygenation (ECMO) implantation, onset of myocardial infarction or cardiac arrhythmias were studied as indirect indicators of myocardial damage without considering cardiac enzymes release, as often done by other authors. OM, of about 2%, was the same between the two groups as well as for the other outcome variables; only cardiac arrhythmias were slightly more frequently observed among BCP patients. On these bases, authors concluded that it seems that are no difference in myocardial protection using cold blood or crystalloid cardioplegia in mitral valve surgery, in accordance with other reports found in the literature. Braathen et al. demonstrated that HTK in elective mitral surgery protects the myocardium equally well compared to repetitive antegrade cold BCP according to post operative serum levels of myocardial enzymes (12); he found only a significant increase in spontaneous ventricular fibrillation after the cross-clamp removal in patients receiving HTK that, however, did not influence the release of myocardial enzymes compared with BCP. In contrast with the observations there is the work of Sakata et al. (18): he reported more adequate myocardial protection in mitral valve surgery provided by HTK solutions compared to BCP because there were more spontaneous defibrillation and a lower requirement of inotropic in CCP group. Gaudino et al., on the other hand, concluded that HTK solution offers inferior RV protection compared with warm BCP, mainly in the hearts with depressed pre-operative RV function, in patients undergone mitral valve surgery (19). Fannelop et al. found the same results (11) for what concerns LV protection in the pig.
In conclusion, as resulted from the analysis of the literature, the debate about effectiveness of Custodiol and BCP in myocardial protection and on mid or long-term clinical outcome in aortic valve surgery is still open even if there are some points of agreements. Custodiol®, in this regard, seems to be attractive for its capacity to give long myocardial protection and a bloodless and motionless operative field after single-dose application; this is very important for open-heart procedures like AVR or in all minimally invasive approaches where a clear and unobstructed view is of particular importance and where a repetitive application of BCP is non really suitable (20). In this regard, in our center experience Custodiol® is routinely used, even in congenital heart surgery, for all procedure performed with a thoracotomy approach as minimally invasive aortic valve replacement. On the other hand, the use of cold BCP seems to be the preferred approach in patients with impaired cardiac functions; in fact, while the heart remains completely ischaemic during the long arrest obtained with Custodiol®, intermittent administration of blood-based cardioplegic solution seems to provide a better myocardial protection especially for it high oxygen and metabolites-carrying capacity. This results are shared also by Hoyer et al. that found superior long-term survival when BCP was used intraoperatively in patients with low LVEF undergone AVR. Similarly, Jin et al. reported that in these patients, post-operative catecholamine infusion can be avoided when myocardial protection is achieved with cold BCP (21).
In summary, CCP seems to produce good operative and post-operative results as BCP both in myocardial protection and in peri-OM and post-operative complications so each case have to be individually evaluated. The best cardioplegic solution, in fact, remains surely still unknown, especially for aortic valve surgery, but further investigations about patients with a lot of comorbidities, like impaired cardiac function that might significantly influence the susceptibility of the myocardium to ischaemia-reperfusion injury, are maybe necessary.
Acknowledgements
None.
Provenance: This is an Invited Editorial commissioned by Section Editor Dr. Raffaele Giordano (Department of Advanced Biomedical Sciences, Adult and Pediatric Cardiac Surgery, University of Naples Federico II, Naples, Italy).
Conflicts of Interest: The authors have no conflicts of interest to declare.
References
- 1.Preusse CJ. Custodiol Cardioplegia: A Single-Dose Hyperpolarizing Solution. J Extra Corpor Technol 2016;48:P15-20. [PMC free article] [PubMed] [Google Scholar]
- 2.Calafiore AM, Teodori G, Mezzetti A, et al. Intermittent antegrade warm blood cardioplegia. Ann Thorac Surg 1995;59:398-402. 10.1016/0003-4975(94)00843-V [DOI] [PubMed] [Google Scholar]
- 3.Salerno TA. Continuous blood cardioplegia: option for the future or return to the past? J Mol Cell Cardiol 1990;22:49. 10.1016/0022-2828(90)90270-C2157853 [DOI] [Google Scholar]
- 4.Follette DM, Mulder DG, Maloney JV, et al. Advantages of blood cardioplegia over continuous coronary perfusion or intermittent ischemia. Experimental and clinical study. J Thorac Cardiovasc Surg 1978;76:604-19. [PubMed] [Google Scholar]
- 5.Dobson GP, Faggian G, Onorati F, et al. Hyperkalemic cardioplegia for adult and pediatric surgery: end of an era? Front Physiol 2013;4:228. 10.3389/fphys.2013.00228 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Edelman JJ, Seco M, Dunne B, et al. Custodiol for myocardial protection and preservation: a systematic review. Ann Cardiothorac Surg 2013;2:717-28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Giordano R, Arcieri L, Cantinotti M, et al. Custodiol Solution and Cold Blood Cardioplegia in Arterial Switch Operation: Retrospective Analysis in a Single Center. Thorac Cardiovasc Surg 2016;64:53-8. [DOI] [PubMed] [Google Scholar]
- 8.Giordano R, Cantinotti M, Arcieri L, et al. Arterial Switch Operation and Plasma Biomarkers: Analysis and Correlation with Early Postoperative Outcomes. Pediatr Cardiol 2017;38:1071-6. 10.1007/s00246-017-1621-x [DOI] [PubMed] [Google Scholar]
- 9.Guru V, Omura J, Alghamdi AA, et al. Is blood superior to crystalloid cardioplegia? A meta-analysis of randomized clinical trials. Circulation 2006;114:I331-8. 10.1161/CIRCULATIONAHA.105.001644 [DOI] [PubMed] [Google Scholar]
- 10.Hoyer A, Lehmann S, Mende M, et al. Custodiol versus cold Calafiore for elective cardiac arrest in isolated aortic valve replacement: a propensity-matched analysis of 7263 patients. Eur J Cardiothorac Surg 2017;52:303-9. 10.1093/ejcts/ezx052 [DOI] [PubMed] [Google Scholar]
- 11.Fannelop T, Dahle GO, Salminen PR, et al. Multidose cold oxygenated blood is superior to a single dose of Bretschneider HTK-cardioplegia in the pig. Ann Thorac Surg 2009;87:1205-13. 10.1016/j.athoracsur.2009.01.041 [DOI] [PubMed] [Google Scholar]
- 12.Braathen B, Jeppsson A, Scherstén H, et al. One single dose of histidine-tryptophan-ketoglutarate solution gives equally good myocardial protection in elective mitral valve surgery as repetitive cold blood cardioplegia: a prospective randomized study. J Thorac Cardiovasc Surg 2011;141:995-1001. 10.1016/j.jtcvs.2010.07.011 [DOI] [PubMed] [Google Scholar]
- 13.Viana FF, Shi WY, Hayward PA, et al. Custodiol versus blood cardioplegia in complex cardiac operations: an Australian experience. Eur J Cardiothorac Surg 2013;43:526-31. 10.1093/ejcts/ezs319 [DOI] [PubMed] [Google Scholar]
- 14.Rajappan K, Rimoldi OE, Dutka DP, et al. Mechanisms of coronary microcirculatory dysfunction in patients with aortic stenosis and angiographically normal coronary arteries. Circulation 2002;105:470-76. 10.1161/hc0402.102931 [DOI] [PubMed] [Google Scholar]
- 15.Ascione R, Caputo M, Gomes WJ, et al. Myocardial injury in hypertrophic hearts of patients undergoing aortic valve surgery using cold or warm blood cardioplegia. Eur J Cardiothorac Surg 2002;21:440-6. 10.1016/S1010-7940(01)01168-X [DOI] [PubMed] [Google Scholar]
- 16.Calafiore AM, Teodori G, Bosco G, et al. Intermittent antegrade warm blood cardioplegia in aortic valve replacement. J Card Surg 1996;11:348-54. 10.1111/j.1540-8191.1996.tb00061.x [DOI] [PubMed] [Google Scholar]
- 17.Øvrum E, Tangen G, Tølløfsrud S, et al. Cold blood versus cold crystalloid cardioplegia: a prospective randomised study of 345 aortic valve patients. Eur J Cardiothorac Surg 2010;38:745-9. 10.1016/j.ejcts.2010.03.052 [DOI] [PubMed] [Google Scholar]
- 18.Sakata J, Morishita K, Ito T, et al. Comparison of clinical outcome between histidine-triptophan-ketoglutalate solution and cold blood cardioplegic solution in mitral valve replacement. J Card Surg 1998;13:43-7. 10.1111/j.1540-8191.1998.tb01053.x [DOI] [PubMed] [Google Scholar]
- 19.Gaudino M, Pragliola C, Anselmi A, et al. Randomized trial of HTK versus warm blood cardioplegia for right ventricular protection in mitral surgery. Scand Cardiovasc J 2013;47:359-67. 10.3109/14017431.2013.836241 [DOI] [PubMed] [Google Scholar]
- 20.Garbade J, Davierwala P, Seeburger J, et al. Myocardial protection during minimally invasive mitral valve surgery: strategies and cardioplegic solutions. Ann Cardiothorac Surg 2013;2:803-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Jin XY, Gibson DG, Pepper JR. Early changes in regional and global left ventricular function after aortic valve replacement. Comparison of crystalloid, cold blood, and warm blood cardioplegias. Circulation 1995;92:II155-62. 10.1161/01.CIR.92.9.155 [DOI] [PubMed] [Google Scholar]