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1.
J Heart Lung Transplant ; 14(5): 963-7, 1995.
Article in English | MEDLINE | ID: mdl-8800734

ABSTRACT

BACKGROUND: To avoid the long-term side effects of corticosteroids, corticosteroid-free immunosuppression has been introduced immediately or late (more than 6 months) after heart transplantation. Late corticosteroid weaning may have a higher success rate as patients are selected on the basis of rejection history. Previous reports of HLA-DR mismatching and the long-term metabolic benefits with respect to corticosteroid weaning have been equivocal. METHODS: One hundred and one eligible heart transplant recipients receiving triple-drug immunosuppression 6 months from heart transplantation were weaned from prednisone by decreasing the daily prednisone dose by 1 mg each month. Moderate rejection episodes were recorded and after conclusion of the study, HLA-DR mismatching of recipient and donor was reviewed. Serum cholesterol level, body weight, and number of patients receiving blood pressure medications were recorded before and 1 year after corticosteroid weaning. RESULTS: Successful weaning from corticosteroids was achieved in 82% of patients. Of 31 patients with zero or one HLA-DR mismatch, 30 (97%) were successfully weaned. For those patients more than 1 year after discontinuation of corticosteroids, 67 had more weight loss and a lower serum cholesterol level than 15 patients who were unsuccessful at corticosteroid weaning and dependent on corticosteroids. CONCLUSIONS: Heart transplant recipients can safely be weaned from corticosteroids late after heart transplantation with zero or one HLA-DR mismatch conferring a higher success rate. The long-term metabolic benefits of corticosteroid weaning include a reduction in weight and serum cholesterol.


Subject(s)
Cholesterol/blood , HLA-DR Antigens/analysis , Heart Transplantation , Immunosuppressive Agents/administration & dosage , Prednisone/administration & dosage , Body Weight , Female , Graft Rejection/prevention & control , Histocompatibility , Humans , Male , Time Factors
2.
J Am Coll Cardiol ; 20(7): 1556-61, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1452930

ABSTRACT

OBJECTIVES: The objective of this study was to determine the frequency of pulmonary complications, feasibility of early hospital discharge and requirements for postoperative inotropic and chronotropic support in patients receiving amiodarone therapy before heart transplantation. BACKGROUND: Although many patients waiting for heart transplantation will die of arrhythmias before a donor heart is found, the use of amiodarone has been limited by concern about increased complications in the perioperative period. METHODS: The 29 patients receiving amiodarone at the time of heart transplantation at University of California, Los Angeles Medical Center between October 1986 and September 1990 were compared with 29 control recipients to evaluate postoperative morbidity. Patients were receiving amiodarone for recurrent ventricular tachyarrhythmias (n = 11), atrial fibrillation (n = 2) or complex ventricular ectopic activity (n = 16). The average daily dose was 360 +/- 230 mg/day for an average of 11 +/- 22 months before transplantation. Amiodarone and control groups had a similar ejection fraction (0.18 +/- 0.07 vs. 0.20 +/- 0.08), frequency of coronary disease, age and gender. There were three more status I patients in the control group. OKT3 was given to only two patients receiving amiodarone and 12 control patients at high risk for renal dysfunction. RESULTS: Postoperatively, the duration of assisted ventilation was 21 +/- 19 h after amiodarone therapy versus 26 +/- 2 h in the control group (20 +/- 18 h vs. 15 +/- 9 h after excluding patients receiving OKT3), discharge arterial oxygen saturation was > 95% in both groups. Two patients in the amiodarone group with a smoking history of > 100 pack-years developed bilateral pulmonary infiltrates of brief duration. Although patients receiving amiodarone required atrial pacing more frequently (eight vs. two patients) and had a lower heart rate at discharge (75 +/- 18 vs. 86 +/- 11 beats/min), the duration of inotropic support (2.1 +/- 1.5 vs. 3.5 +/- 2.5 days) and of hospital stay (10 +/- 3 vs. 15 +/- 10 days) was not higher in the amiodarone than in the control group. The mortality rate at 30 days was similar in the two groups (6.8% vs. 3.4%, p = NS). CONCLUSIONS: Amiodarone therapy before heart transplantation may contribute to occasional pulmonary complications but does not significantly increase perioperative morbidity or mortality with the regimens used in this retrospective study.


Subject(s)
Amiodarone/therapeutic use , Arrhythmias, Cardiac/drug therapy , Heart Transplantation , Postoperative Complications/epidemiology , Aged , Amiodarone/administration & dosage , Amiodarone/adverse effects , Arrhythmias, Cardiac/complications , Cardiac Pacing, Artificial/statistics & numerical data , Cardiotonic Agents/therapeutic use , Feasibility Studies , Forced Expiratory Volume/drug effects , Heart Rate/drug effects , Hemodynamics/drug effects , Hospitals, University , Humans , Length of Stay/statistics & numerical data , Los Angeles/epidemiology , Middle Aged , Patient Discharge/statistics & numerical data , Postoperative Complications/etiology , Postoperative Complications/mortality , Respiration, Artificial/statistics & numerical data , Retrospective Studies , Stroke Volume/drug effects , Treatment Outcome
3.
J Heart Lung Transplant ; 11(2 Pt 2): 428-30, 1992.
Article in English | MEDLINE | ID: mdl-1571341

ABSTRACT

Steroid-free maintenance immunosuppression is frequently initiated early after transplantation. There is concern that later steroid withdrawal, particularly after previous rejection, may cause more serious rejection. To determine the safety of gradual weaning from steroid maintenance, 68 patients (more than 6 months from transplantation) were weaned from 5 mg/day by decreasing the daily dose by 1 mg each month, with monthly biopsies. Asymptomatic moderate rejection occurred in 13 compliant patients. Rejection with hemodynamic compromise occurred in two patients with documented medication noncompliance, who were excluded from further analysis. Successful weaning without rejection was possible in 53 of 66 (80%) compliant patients. Compared with the rejection group, there were no differences in the number of women, previous rejection episodes, or time from transplantation. All moderate rejection episodes responded to oral steroid pulse therapy. The two serious rejections after noncompliance responded to OKT3. There were no symptoms from steroid withdrawal that required taper alteration. We conclude that regardless of previous rejection episodes, weaning from maintenance steroids can be attempted safely if guided by frequent biopsy procedures, but compliance is critical.


Subject(s)
Heart Transplantation , Immunosuppression Therapy , Immunosuppressive Agents/therapeutic use , Prednisone/adverse effects , Substance Withdrawal Syndrome , Biopsy , Graft Rejection , Humans , Muromonab-CD3/therapeutic use , Myocardium/pathology , Patient Compliance , Time Factors
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