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Pediatr Cardiol ; 26(5): 595-600, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15690237

RESUMO

Cardiopulmonary bypass (CPB) is associated with a systemic inflammatory response. Pre-bypass steroid administration may modulate the inflammatory response, resulting in improved postoperative recovery. We performed a prospective study in the departments of cardiovascular surgery and pediatric intensive care medicine of two university hospitals that included 50 infants who underwent heart surgery. Patients received either prednisolone (30 mg/kg) added to the priming solution of the cardiopulmonary bypass circuit (steroid group) or no steroids (nonsteroid group). Clinical outcome parameters include therapy with inotropic drugs, oxygenation, blood lactate, glucose, and creatinine, and laboratory parameters of inflammation include leukocytes, C-reactive protein, and interleukin-8. Postoperative recovery (e.g., the number, dosage, and duration of inotropic drugs as well as oxygenation) was similar in patients treated with or without steroids when corrected for the type of cardiac surgery performed. After CPB, there was an inflammatory reaction, especially in patients with a long CPB time. Postoperative plasma levels of interleukin-8 were correlated with the duration of CPB time (r = 0.62, p < 0.001). Administration of steroids had no significant impact on the laboratory parameters of inflammation. Administration of prednisolone into the priming solution of the CPB circuit had no measurable influence on postoperative recovery and did not suppress the inflammatory response.


Assuntos
Anti-Inflamatórios/administração & dosagem , Ponte Cardiopulmonar/efeitos adversos , Cardiopatias Congênitas/cirurgia , Prednisolona/administração & dosagem , Síndrome de Resposta Inflamatória Sistêmica/prevenção & controle , Biomarcadores/sangue , Proteína C-Reativa/efeitos dos fármacos , Proteína C-Reativa/metabolismo , Procedimentos Cirúrgicos Cardíacos/métodos , Pré-Escolar , Creatinina/sangue , Cardiopatias Congênitas/sangue , Humanos , Lactente , Interleucina-8/sangue , Contagem de Leucócitos , Neutrófilos/efeitos dos fármacos , Neutrófilos/metabolismo , Estudos Prospectivos , Síndrome de Resposta Inflamatória Sistêmica/sangue , Síndrome de Resposta Inflamatória Sistêmica/tratamento farmacológico , Síndrome de Resposta Inflamatória Sistêmica/etiologia , Resultado do Tratamento
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