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1.
Rev. bras. cir. cardiovasc ; 32(4): 312-317, July-Aug. 2017. tab, graf
Article in English | LILACS | ID: biblio-897929

ABSTRACT

Abstract Introduction: Multiple organ failure syndrome (MOFS) is a pathology associated to unspecified and severe trauma, characterized by elevated morbidity and mortality. The complex inflammatory MOFS-related reactions generate important ischemia-reperfusion responses in the induction of this syndrome. Nitric oxide elevation, through the activation of cyclic guanosine monophosphate (cGMP), has the potential of counteracting the typical systemic vasoconstriction, and platelet-induced hypercoagulation. Tadalafil would possibly act protectively by reducing cGMP degradation with consequent diffuse vasodilatation, besides reduction of platelet-induced hypercoagulation, thus, preventing multiple organ failure syndrome development. Methods: The experimental protocol was previously approved by an institution animal research committee. Experimental MOFS was induced through the stereotaxic micro-neurosurgical bilateral anterior hypothalamic lesions model. Groups of 10 Wistar rats were divided into: a) Non-operated control; b) Operated control group; c) 2 hours after tadalafil-treated operated group; d) 4 hours after tadalafil-treated operated group; e) 8 hours after post-treated operated group. The animals were sacrificed 24 hours after the neurosurgical procedure and submitted to histopathologic examination of five organs: brain, lungs, stomach, kidneys, and liver. Results: The electrolytic hypothalamic lesions resulted in a full picture of MOFS with disseminated multiple-organs lesions, provoked primarily by diffusely spread micro-thrombi. The treatment with tadalafil 2 hours after the micro-neurosurgical lesions reduced the experimental MOFS lesions development, in a highly significant level (P<0.01) of 58.75%. The treatment with tadalafil, 4 hours after the micro-neurosurgically-induced MOFS lesions, also reduced in 49.71%, in a highly significant level (P<0.01). Finally, the treatment with tadalafil 8 hours after the neurosurgical procedure resulted in a statistically significant reduction of 30.50% (P<0.05) of the experimentally-induced MOFS gravity scores. Conclusion: The phosphodiesterase 5 inhibitor, tadalafil, in the doses and timing utilized, showed to protect against the experimentally-induced MOFS.


Subject(s)
Animals , Male , Protective Agents/therapeutic use , Phosphodiesterase 5 Inhibitors/therapeutic use , Tadalafil/therapeutic use , Multiple Organ Failure/prevention & control , Thrombosis/chemically induced , Thrombosis/rehabilitation , Hypothalamus, Anterior/injuries , Stereotaxic Techniques , Rats, Wistar , Disease Progression , Protective Agents/administration & dosage , Disease Models, Animal , Preoperative Period , Phosphodiesterase 5 Inhibitors/administration & dosage , Tadalafil/administration & dosage , Multiple Organ Failure/classification , Multiple Organ Failure/etiology
2.
Rev. bras. cir. cardiovasc ; 20(1): 88-90, Jan.-Mar. 2005.
Article in Portuguese | LILACS | ID: lil-413214

ABSTRACT

Um homem de 64 anos recebeu uma prótese mecânica CarboMedics de 31 mm para refluxo mitral grave. Após quatro dias, o paciente apresentou-se com fadiga e dispnéia em repouso. Estudo do Doppler ecocardiografia transtorácica e transesofágica confirmaram uma disfunção na mobilidade do folheto da válvula protética devido à trombose e uma operação de emergência foi feita. O pós operatório transcorreu sem intercorrências. Este é um caso incomum de disfunção grave devido à trombose de uma prótese mitral mecânica em um paciente tomando anticoagulantes orais e calciparina


Subject(s)
Humans , Male , Aged , Echocardiography/instrumentation , Thrombosis/surgery , Thrombosis/physiopathology , Thrombosis/rehabilitation , Mitral Valve/abnormalities , Mitral Valve/surgery , Mitral Valve Insufficiency/physiopathology
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