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1.
Acta Cardiol ; 55(4): 261-3, 2000 Aug.
Article in English | MEDLINE | ID: mdl-11041125

ABSTRACT

An unusual case is reported of thromboembolus in the right atrium associated with cardiogenic shock and multiple pulmonary micro-embolisms. Two-dimensional echocardiograpy demonstrated a large irregular mass in the right atrium floating freely, prolapsing through the tricuspid valve into the right ventricle during diastole, and leading to inflow and outflow obstruction. An emergency operation was performed and the thromboembolic material was successfully extracted from the right atrium without using cardiopulmonary bypass. This exemplary case highlights the benefit of surgical intervention rather than more conservative approaches such as anticoagulation and/or thrombolysis.


Subject(s)
Cardiac Surgical Procedures , Heart Diseases/surgery , Shock, Cardiogenic/surgery , Thrombosis/surgery , Adult , Echocardiography , Electrocardiography , Follow-Up Studies , Heart Diseases/diagnosis , Humans , Male , Shock, Cardiogenic/etiology , Thrombosis/complications , Thrombosis/diagnosis , Time Factors
2.
Res Exp Med (Berl) ; 200(1): 43-51, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11197921

ABSTRACT

The neuroprotective effect of trimetazidine (TMZ) was tested prospectively in a rabbit spinal cord ischemia model. Ischemia was induced by clamping the aorta just distal to the left renal artery and proximal aortic bifurcation for 20 min. Twenty-five male New Zealand white rabbits were randomized as follows: TMZ group (n=100) receiving 3 mg/kg trimetazidine intravenously before the occlusion of the aorta; control group undergoing occlusion but receiving no pharmacologic intervention (n=10); sham-operation group (n=5) subjected to operative dissections without aortic occlusion. Physiological parameters and somatosensory evoked potentials (SEP) were monitored in animals before the ischemia, during the ischemia and in the 1st, 15th and 60th min of reperfusion. Neurologic status was assessed 24 and 48 h after the operation. The spinal cord, abdominal aorta, and its branches were processed for histopathologic examinations 48 h after the operation. At the end of the ischemic period, the average N1-P1 amplitude was reduced to 22% of the baseline in all ischemic animals. This was followed by a gradual return to 90+/-2% of the initial amplitude in the TMZ group and 81+/-2% in the control group (P<0.05) after 60 min of reperfusion. The average motor function score was significantly higher in the TMZ group than the control group (3.7+/-0.5 vs 3.1+/-0.6 at 24 and 3.5+/-0.7 vs 2.9+/-0.6 at 48 h; P<0.05). Histologic observations were clearly correlated with the neurologic findings. The results suggest that trimetazidine reduces spinal cord injury during thoracoabdominal aortic operations and may have therapeutic utility during high risk operations.


Subject(s)
Neuroprotective Agents/pharmacology , Spinal Cord Ischemia/prevention & control , Trimetazidine/pharmacology , Animals , Disease Models, Animal , Evoked Potentials, Somatosensory , Humans , Male , Rabbits , Spinal Cord Ischemia/pathology , Spinal Cord Ischemia/physiopathology
3.
Eur J Cardiothorac Surg ; 10(5): 339-46, 1996.
Article in English | MEDLINE | ID: mdl-8737690

ABSTRACT

Cardiopulmonary bypass (CPB) produces an inflammatory response due to the interaction of blood with a foreign body surface. The lungs are most affected by this inflammatory response. Pentoxifylline (PTX), a phosphodiesterase inhibitor and an inhibitor of leukocyte activation, is used to minimize damage in lungs where leukocytes play an important role. Twenty patients with mitral valve stenosis with planned mitral valve surgery were included in the study. The ten patients receiving pentoxifylline (PTX group) were administered 400 mg PTX orally TID for 3 days preoperatively and, following anesthetic induction, a 300 mg PTX infusion was given. The ten patients receiving no PTX were the control group (CT). Platelet and leukocyte counts, mean pulmonary arterial pressure (mPAP), pulmonary capillary wedge pressure (PCWP), cardiac index (CI), pulmonary vascular resistance (PVR), alveolar-arterial PO2 gradient (AaDO2) were measured just before and after CPB, and 2 h postoperatively. The number of the leukocytes increased in the blood samples drawn 15 min after CPB in both groups and 2 h postoperatively showed no statistical change. The number of platelets had decreased significantly at the end of the CPB in both groups and, 2 h postoperatively, there was a further decrease in the blood count in the control group (P < 0.05). There was no significant difference in either the preoperative or postoperative PAP, PAWP, and CI. Pulmonary vascular resistance increased in both groups following the CPB (CT, before: 136 +/- 44, after: 177 +/- 94 dyne. sec.cm-5; PTX, before: 151 +/- 82, after 182 +/- 43 dynes.sec.cm-5). Two hours postoperatively, a considerable increase continued in the control group (CT 219 +/- 170 dynes.sec. cm-5), while there was an insignificant increase in the PTX group (PTX 193 +/- 51 dynes.sec.cm-5) (P < 0.05). The alveolar-arterial PO2 gradient increased after the CPB in both groups but a moderate decrease was observed 2 h postoperatively. In lung biopsy specimens taken before and after the CPB, there was marked leukocyte sequestration in the control group, whereas the number of leukocytes was seen to be insignificant in the PTX group (P < 0.005). This dosage regimen of PTX inhibits the postoperative increase in PVR and greatly minimized leukocyte sequestration in the lung due to CPB.


Subject(s)
Cardiopulmonary Bypass , Foreign-Body Reaction/prevention & control , Mitral Valve Stenosis/surgery , Pentoxifylline/administration & dosage , Phosphodiesterase Inhibitors/administration & dosage , Systemic Inflammatory Response Syndrome/prevention & control , Adult , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Foreign-Body Reaction/immunology , Hemodynamics/drug effects , Humans , Leukocyte Count/drug effects , Lung/blood supply , Male , Middle Aged , Mitral Valve Stenosis/immunology , Neutrophils/drug effects , Neutrophils/immunology , Platelet Count/drug effects , Premedication , Pulmonary Alveoli/immunology , Systemic Inflammatory Response Syndrome/immunology , Vascular Resistance/drug effects , Vascular Resistance/immunology
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