INDUCTION IMMUNOSUPPRESSION WITH THE MONOCLONAL-ANTIBODY OKT3 AFTER CARDIAC TRANSPLANTATION

Citation
Dd. Stapleton et al., INDUCTION IMMUNOSUPPRESSION WITH THE MONOCLONAL-ANTIBODY OKT3 AFTER CARDIAC TRANSPLANTATION, The American journal of the medical sciences, 306(1), 1993, pp. 16-19
Citations number
11
Categorie Soggetti
Medicine, General & Internal
ISSN journal
00029629
Volume
306
Issue
1
Year of publication
1993
Pages
16 - 19
Database
ISI
SICI code
0002-9629(1993)306:1<16:IIWTMO>2.0.ZU;2-7
Abstract
The routine use of monoclonal induction immunosuppression with OKT3 af ter orthotopic heart transplantation remains controversial. This study examined the clinical response of prophylactic monoclonal induction i mmunosuppression versus standard triple-drug immunosuppression in 41 p atients who underwent orthotopic heart transplantation from January 19 89 to December 1990 at this institution. Of these, eight received mono clonal induction immunosuppression for a period of 10 to 14 days. All patients received identical triple-drug immunosuppression with the exc eption of cyclosporine starting on the fifth postoperative day in thos e who received OKT3. At 6 months the duration of hospitalization, free dom from rejection, incidence of infection requiring hospitalization, and serum creatinine in the monoclonal induction immunosuppression and triple-drug groups were compared. It was found that the length of hos pital stay in the OKT3 group was 14.3 +/- 4.5 days, compared with 14.7 +/- 4.7 days in the triple-drug group and that freedom from rejection was 66% in the OKT3 group compared with 75% in the triple-drug group. In addition, it was found that the incidence of infection was 36% in the OKT3 group compared with 38% in the triple-drug group and that ser um creatinine at 6 months was 1.36 +/- 0.26 mg/dl in the OKT3 group co mpared with 1.45 +/- 0.73 mg/dl in the triple-drug group. Finally, pat ient survival at 1 year for the monoclonal induction immunosuppression group was 100% compared with 91% for the triple-drug group. It was co ncluded that induction immunosuppression with monoclonal induction imm unosuppression does not reduce the duration of hospitalization or the incidence of rejection, change the incidence of infection, alter renal function, decrease the incidence of allograft coronary artery disease , or improve the survival rate as compared with standard triple-drug i mmunosuppression.