Ulinastatin treatment and renal injury in patients undergoing aortic valve replacement with cardiopulmonary bypass. A note of aution

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Korean J Anesthesiol. 2013;64(1):91-92
Publication date (electronic) : 2013 January 21
doi : https://doi.org/10.4097/kjae.2013.64.1.91
Division of Anesthesiology, Pontificia Universidad Católica de Chile, Santiago, Chile.
Corresponding author: Guillermo Lema. Division of Anesthesiology, Pontificia Universidad Católica de Chile, Marcoleta 367, Santiago, Chile. glema@med.puc.cl

To the Editor

I have read with great interest the manuscript by Oh et al. [1], presenting the use of ulinastatin as a possible method to protect the kidney during surgery with cardiopulmonary baypass (CPB).

The authors use ulinastatin, a protease inhibitor which may supress inflammatory reactions as well as the noxious effects that free radical elimination may produce in the cells of the kidney.

I would like to add some comments to the discussion:

The damage imposed to the kidneys during cardiac surgery is multifactorial in its origin. Of course CPB has been blamed as the main factor, but there are others whose relevance is as important as the CPB itself: changes in hematocrit and temperature, use of vasoactive and nephrotoxic drugs, hemodynamic changes, low cardiac output, just to mention a few. It seems interesting then some groups have reported that the incidence of renal damage during coronary surgery off pump is at least similar to those cases performed with CPB [2].

So, specific damage to the kidneys by CPB remains to be elucidated.

Renal dysfunction following cardiac surgery with CPB has a relatively low incidence in patients with normal preoperative dysfunction. This is the case for this study. The numbers of patients in each group is too small to obtain a difference, if it exists.

There are two groups of patients at the highest risk for developing renal dysfunction after cardiac surgery: those whohave preoperative abnormal renal function (plasma creatinine level 1.5 or higher) or those with hemodynamic instability; recent myocardial infarction, use of preoperative vasoactive drugs (those with alpha effects), low cardiac output, use of intra-aortic balloon pump, sepsis among others. These are the groups that should be chosen to be studied. Unfortunately those groups are quite difficult to study due to the inherent conditions of their clinical state.

In my point of view, the study with patients with normal preoperative renal function is a dead end.

Different groups have worked for many years trying to find a therapy that may protect the kidney against insults during cardiac and non-cardiac surgery: dopamine, furosemide, fenoldopan, atrial natriuretic factor, sodium bicarbonate, n-acetyl cysteine, enoximone, dexmedetomidine, high or low hematocrit, high or low temperatures, among others. To my knowledge that therapy has not been found as of today [3].

When we talk about "renal protection", is this phrase the same as "brain protection" or "heart protection"? It is my fear that we are trying to find techniques that may keep the kidney working well during the insult, rather than looking for something that may reduce oxygen compsumption during the damage.

Just a thought.

In the meantime, results of this study should be analyzed very carefully.

References

1. Oh SY, Kim JC, Choi YS, Lee WK, Lee YK, Kwak YL. Effects of ulinastatin treatment onmyocardial and renal injury in patients undergoing aortic valve replacement with cardiopulmonary bypass. Korean J Anesthesiol 2012;62:148–153. 22379570.
2. Elmistekawy E, Chan V, Bourke ME, Dupui JY, Rubens FD, Mesana TG, et al. Off-pump coronary artery bypass grafting does not preserve renal function better than on-pump coronary artery bypass grafting: results of a case-matched study. J Thorac Cardiovasc Surg 2012;143:85–92. 22036259.
3. Bove T, Landoni G, Calabro MG, Aletti G, Marino G, Cerchierini E, et al. Renoprotective action of fenoldopam in high-risk patients undergoing cardiac surgery. Circulation 2005;111:3230–3235. 15967861.

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