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Research Article| Volume 17, ISSUE 4, P749-769, July 1995

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Two approaches to comparing hospital charges between cadaveric renal transplant patients who received Orthoclone OKT® 3 sterile solution or Atgam® sterile solution for induction therapy

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      Abstract

      The objectives of this study were: (1) to compare total hospital charges for a sample of cadaveric renal transplant patients categorized according to the type of induction therapy used (Orthoclone OKT®3 Sterile Solution or Atgam® Sterile Solution); (2) to compare specific charge categories between the two groups; and (3) to examine the relationship between charges and a set of independent variables. A retrospective review was conducted of hospital charges associated with a sample of renal transplant patients. The overall sample for this study comprised 510 patient discharges from 22 hospitals in the United States. Comparisons between the OKT3 and Atgam groups were made for total and specific charge categories using two different approaches to help control variations in charges that were not related to the type of induction therapy used. The first approach consisted of t test or chi-square comparisons between the groups for subsets of observations that had been identified in a stepwise fashion. These judgment samples were defined to remove sources of variation in charges other than those resulting from the type of induction therapy selected. The second approach used multiple linear regression analysis to help statistically control variation in charges from other sources. The results showed that higher drug charges in the Atgam group were offset by lower charges in other categories (P < 0.05). These findings suggest that hospital formulatory committees should consider all relevant costs, not just drug acquisition costs, when selecting products. However, further investigation is warranted to explore differences in charges due to: (1) between-hospital variation; (2) patients' severity of illness before receiving induction therapy; and (3) differences in side-effect profiles for the two induction therapies.
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      References

        • Frampton JE
        • Faulds D
        Cyclosporin—A pharmacoeconomic evaluation of its use in renal transplantation.
        PharmacoEconomics. 1993; 4: 366-395
        • Karlix J
        Solid organ transplantation.
        Am Pharm. 1994; NS34: 59-69
        • Barry JM
        Immunosuppressive drugs in renal transplantation.
        Drugs. 1992; 44: 554-566
        • Norman DJ
        • Kahana L
        • Stuart FP
        • et al.
        A randomized clinical trial of induction therapy with OKT3 in kidney transplantation.
        Transplantation. 1993; 55: 44-50
        • Suthanthiran M
        • Strom TB
        Renal transplantation.
        NEJM. 1994; 331: 365-376
      1. Cyclosporin in renal transplantation: Pharmacoeconomic data support clinical practice but many questions remain.
        Drug Ther Perspect. 1994; 4 (Anonymous): 1-4
        • Segal R
        • Oh T
        • Ben-Joseph R
        • et al.
        A pharmacoeconomic analysis of IV H2-receptor antagonist use in 40 hospitals.
        Hosp Formul. 1994; 29: 379-391
        • Batluk TD
        • Bennett WM
        • Norman DJ
        Cytokine nephropathy during antilymphocyte therapy.
        Transplant Proc. 1993; 25 (Suppl 1): 27-30
        • Büsing M
        • Mellert J
        • Greger B
        • et al.
        Acute pulmonary insufficiency due to OKT3 therapy.
        Transplant Proc. 1990; 22: 1779-1781
        • Cockfield SM
        • Preiksaitis J
        • Harvey C
        • et al.
        Is sequential use of ALG and OKT3 in renal transplants associated with an increased incidence of fulminant posttransplant lymphoproliferative disorder?.
        Transplant Proc. 1991; 23: 1106-1107
        • Kehinde EO
        • Veitch PS
        • Scriven K
        • et al.
        Complications of using OKT3 for induction of immunosuppression in recipients of kidneys from non-heart beating donors.
        Transplant Proc. 1994; 26: 3123-3125
        • Kreis H
        Adverse events associated with OKT3 immunosuppression in the prevention or treatment of allograft rejection.
        Clin Transplant. 1993; 7: 431-446
        • Raasveld MHM
        • Bemelman FJ
        • Schellekens PT
        • et al.
        Complement activation during OKT3 treatment: A possible explanation for respiratory side effects.
        Kidney Int. 1993; 43: 1140-1149
        • Blumberg MS
        Potentials and limitations of database research illustrated by the QMMP AMI Medicare Mortality Study.
        Stat Med. 1991; 10: 637-646
        • Lewis NJW
        • Patwell JT
        • Briesacher BA
        The role of insurance claims databases in drug therapy outcomes research.
        PharmacoEconomics. 1993; 4: 323-330
        • Mendenhall W
        • Sincich T
        2nd ed. A Second Course in Business Statistics: Regression Analysis. Dellen Publishing Company, San Francisco1986: 5-83
        • Mason CH
        • Perreault WD
        Collinearity, power, and interpretation of multiple regression analysis.
        J Market Res. 1991; 28: 268-280