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Singh et al.                                                                                                                                                         Myocardial protection in cardiac transplantation

           the 2 groups. There was however a higher inotropic   mortality (46% vs. 42%, P = 0.7) and cause of death
           score in the HTK group at 24 h (P = 0.03). Multivariate   (chronic rejection: 50% vs. 50%; neoplasia: 33% vs.
           analysis revealed a significantly reduced bypasstime in   25%, P = 0.8). Survival at 12 years was 50 ± 12% vs.
           the HTK group (P = 0.002). They concluded that HTK   52 ± 11% (P = 0.9). Follow-up echocardiogram showed
           was superior due to the reduced pumping time albeit   similar mean left ventricular ejection fraction (LVEF; 47
           with a higher post-operative inotrope score. A single   ± 12% vs. 49 ± 11%, P = 0.7) and prevalence of LVEF <
           dose  of  HTK  provided  similar  myocardial  protection   35% (21% vs. 18%, P = 0.8). The prevalence of chronic
           as repeated doses of CBC solution in donated hearts.   rejection was similar in both groups (42% vs. 32%, P
           Minami  et  al. [26]   noted  an  increment  in  troponin  and   =  0.1),  but  severe allograft  vasculopathy  was  more
           CK-MB levels if the ischaemic times were > 4 h using   prevalent in the St Thomas cardioplegia group (64%
           HTK  solution  but  concluded  that  it  was  still  within   vs.  17%,  P = 0.04). There were no other between-
           acceptable limits when compared to other crystalloid   group differences [31] .
           cardioplegias CK-MB 25 IU and troponin I 21 pg/mL,
           with ischaemic time of 263 min).                   Eurocollins
                                                              Collins  et al. [32]  designed an “intracellular” organ
           HTK is an intracellular type of cardioplegic solution. It   preservation solution and is credited to being one
           lowers concentrations of sodium and calcium thereby   of  the  first  solutions  to  attempt  the  advancement  of
           inducing cardiac arrest by deprivation of extracellular   organ preservation based on changes that occur
           sodium thus preventing depolarisation of the action   during cell hypothermia.  The predecessor to the
           potential. Calcium channels open leading to increased   Eurocollins solution, Collins solution, provided reliable
           cytosolic  calcium  and  potentially  aggravating  cellular   preservation and was the organ preservation fluid of
           injury, indirectly reducing the calcium concentration.   choice in abdominal organ transplantation especially
           Histidine in the HTK solution, acts as a buffer enhancing   renal preservation.
           the efficiency of anaerobic glycolysis. This has been
           quoted by several sources to be its primary advantage,   Collins solution has a high potassium content alongside
           with its buffering capacity allowing effective myocardial   a glucose osmotic barrier. Despite achieving relatively
           preservation.  The  Ketoglutarate  (α-KG)  component   long storage times for abdominal organs, hearts were
           serves as a high energy ATP provider during reperfusion.   more susceptible to ischaemic  injury and the low
           Tryptophan stabilises the cell membranes. Mannitol, an   protective properties  of  glucose  compounded by the
           osmotic diuretic is added to reduce cellular oedema as   acidotic conditions resulting from glucose conversion
           it has free radical scavenging properties thus reducing   to lactate resulted in the addition of mannitol or sucrose
           the extent of ischaemic injury [27] .              instead of glucose as the impermeant [33] . Euro-Collins
                                                              solution however fell out of favour due to the variability
           St Thomas’s solution                               of recovery of hearts at non-uniform temperatures [34] .
           St Thomas’s solution (StH) is an extracellular type of
           cardioplegic solution that induces rapid cardiac arrest   University of Wisconsin (Belzer UW/Viaspan)
           by high potassium and magnesium concentrations     University of Wisconsin Solution (UW) was formulated
           alongside the membrane stabilising effect of       by James et al. [35]  in the late 1980s as the preservation
           procaine [28] .  Addition of  a buffer  and reduction of   fluid of choice for pancreas preservation. Prior to its
           calcium concentrations resulted in the formation of   introduction,  abdominal organs preserved in Collins
           No. 2 (Plegisol, Abbott Laboratories, North Chicago,   solution would have limited ischaemic tolerance of
           III.). In a rat model, Plegisol was shown to be superior   about 8 h. Belzer and Southard developed UW solution
           to its predecessor with lower rates of post-operative   initially to prolong liver and pancreas preservation.
           ventricular  fibrillation,  increased  left  ventricular   Their initial experiments of canine pancreases were
           pressure  and  recovery  of  aortic  flow [29] . Addition of   encouraging and used it  for liver and kidneys with
           procaine in this solution reduces the incidence of post-  similarly encouraging results [36-38] .
           declamping ventricular fibrillation. Luciani et al. [30]  group
           performed a prospective single blinded randomised   UW solution became the “gold standard” of preservation
           control trial comparing cold blood cardioplegia to StH   fluids  as  it  first  highlighted  the  lack  of  equilibrium
           (crystalloid cardioplegia). Spontaneous sinus rhythm   achieved by Na /K  ratios during cold preservation [39] .
                                                                              +
                                                                            +
           was  significantly  higher  in  the  blood  cardioplegia   It  contains  lactobionate  and  raffinose,  which  are
           group (11% vs. 40%) (P = 0.02) with a higher creatine   metabolically inert, making  it suitable for multiorgan
           kinase (P = 0.01) and CK-MB (144 ± 90 IU vs. 102 ±   usage.  Both  these  substances  which  are  osmotically
           59 IU) (P = 0.06). They performed a follow up study   active prevent organ oedema. Addition of adenosine
           12 years later and revealed no difference in terms of   provides precursor of an energy source (ATP).

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