Page 444 - Contributed Paper Session (CPS) - Volume 2
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CPS1917 Trijya S.
                  2 as initial estimates. We have also included the mean absolute percent error
                  (MAP E) of each method, which is given by
                                                 
                                                             ̂
                                               1    |( ) − ( )|
                                                       
                                                                
                                       =  ∑                 ×  100.
                                                       ( )
                                                            
                                                =1

                  This  measures  the  predictive  power  of  the  method.  The  estimates  of  the
                  asymptotic standard errors of the estimates obtained using the `nls' R package
                  are also given within parentheses in Table 1.

                  4.   Discussion and Conclusion
                      Shah  (1973)  suggested  a  regression-difference  equation  method  for
                  obtaining initial parameter estimates needed to start an iterative estimation
                  procedure in the case of a mixture of exponential distributions. However, this
                  method is of limited use since it is applicable only to equally spaced data. In
                  pharmacokinetic analysis, observations are rarely measured at equal intervals.
                  Our  proposed  methods  are  not  only  applicable  to  unequally  spaced
                  observations, but have also been shown to yield remarkably lower RSS and
                  MAPE values compared to Shah's method, as is evident from Table 1.
                      Moreover,  important  pharmacokinetic  parameters  of  interest  like  drug
                  transfer rates, volume of  a  drug in a  patient's  blood stream at time t  and
                  clearance  of  the  drug  from  the  body  are  all  functions  of  A,  B,    as
                  discussed in Appleton (1995). Hence, these parameters need to be estimated
                  with as much precision as possible. A close examination of the RSS and MAPE
                  values in Table 1 also reveals that although initial estimates obtained by all
                  methods give convergence to same optimum values, the performance of the
                  method incorporating information regarding tail behavior (that is, method 2)
                  is better. The initial estimates of parameters obtained using method 2 are, in
                  general, closer to the optimum values compared to those obtained by Shah's
                  method or method 1 and, as such, convergence is attained in a much smaller
                  number of iterations for method 2.
                      An undesirable feature which has been noticed in the findings is that the
                  fitted  values  corresponding  to  the  first  time  point  are  negative  for  Shah's
                  method and method 1. This is another reason that method 2 should be used
                  in  preference  to  method  1  or  Shah's  method  in  order  to  obtain  initial
                  estimates.








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