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M L Foegh

Publications and source records attributed to M L Foegh.

112 records · Page 7Linked to original sources
PubMedDate not supplied

Liposomal amphotericin B for treatment of pulmonary aspergillosis in a heart transplant patient.

Pulmonary aspergillosis developed in a 52-year-old man 2 months after heart transplantation for ischemic cardiomyopathy. Conventional amphotericin B therapy caused marked deterioration of his already compromised kidney function after only 10% of the projected total dose. Conversion to liposomal encapsulated amphotericin B was associated with reversal of the kidney dysfunction and clearing of the pulmonary infiltrate. It is now 16 months since completion of therapy, and there is no evidence of recurrent infection.

Amphotericin B↗
PubMedDate not supplied

Platelet deposition in rat heart allografts and the effect of a thromboxane receptor antagonist.

The effect of a thromboxane antagonist, L640,035 on platelet deposition in heart allografts was studied. Twenty Lewis rats received heterotopic allografts from Lewis x Brown-Norway F1 hybrid. All recipients received azathioprine (5 mg/kg/day). The rats were divided into three groups. Groups II and III were also treated daily with either the vehicle for L640,035 or L640,035 respectively. Syngeneic indium-111-labeled platelet deposition was determined in the allograft and the native heart at 6, 9, and 13 days after transplantation; group III was studied on the sixth and ninth day only. A rapidly increasing platelet deposition was seen in allografts from rats given azathioprine; whereas the thromboxane antagonist prevented the increase in platelet deposition on the ninth day.

Animals↗
PubMedDate not supplied

HMG-CoA reductase inhibitors in organ transplantation.

Hydroxymethylglutaryl coenzyme A (HMG-CoA) reductase inhibitors reduces serum cholesterol in patients with high cholesterol blood levels including organ transplant recipients. HMG-CoA reductase inhibitor also inhibits a series of immune responses and thus have the potential of exerting immunosuppressive effect in patients with organ allografts. Experimentally, HMG-CoA reductase inhibitors reduces transplant arteriosclerosis. Whether this is linked to an immunosuppressive effect or not is unknown. There is little evidence that post-transplant hyperlipidemia directly increases the risk of cardiovascular diseases. Lipid lowering with HMG-CoA reductase inhibitor is not indicated for all allograft recipients but should be used if other cardiovascular risk factors are present.

Animals↗