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ORIGINAL CONTRIBUTION |
| Department of Cardiovascular Surgery, University Hospital of Vaud, Rue de Bugnon 46, Lausanne CH-1011, Switzerland |
First, the background to the utilization of aprotinin has been adequately reported by the authors in both the scientific and clinical aspects. Second, the treatment of all patients strictly followed the preoperatively determined rules, particularly with regard to the decision of utilizing blood or blood products during or after the operation. This goal is difficult to achieve, particularly in a pro-spective study with pediatric patients. Furthermore, the authors were able to demonstrate the advantages of aprotinin by comparison with a control group not receiving aprotinin, even if we do not know if the control group is a historical group of matched patients or another prospective study with blinded random allocation. All the arguments in favor of increased coagulation disturbances in cyanotic children are well put in this manuscript, but the clinical comparison with a matched group of non-cyanotic children could provide clear evidence of the clinical consequences of cyanosis versus non-cyanosis on the effects of aprotinin.
Lastly, the authors reported the current knowledge of the antiinflammatory properties of aprotinin, but they did not provide any information regarding the evaluation of this property in their experience, since they did not report any clinical parameter reflecting the inflammatory response. Furthermore, they did not use "controlled reoxygenation" at the beginning of cardiopulmonary bypass, known to be a potential method of reducing the negative effects of uncontrolled acute reoxygenation after a period of chronic hypoxia. This paper will definitely stimulate all readers who are involved in the care of pediatric patients under-going cardiopulmonary bypass for repair of cyanotic congenital heart defects to further extend the current knowledge on control of postoperative coagulation disorders.
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