📄 pkcross.hlp
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{smcl}
{* 20jan2005}{...}
{cmd:help pkcross}{right:dialog: {bf:{dialog pkcross}}}
{hline}
{title:Title}
{p2colset 5 20 22 2}{...}
{p2col :{hi:[R] pkcross} {hline 2}}Analyze crossover experiments{p_end}
{p2colreset}{...}
{title:Syntax}
{p 8 17 2}
{cmd:pkcross} {it:outcome} {ifin} [{cmd:,} {it:options}]
{synoptset 22 tabbed}{...}
{synopthdr}
{synoptline}
{syntab :Model}
{synopt :{opth seq:uence(varname)}}sequence variable; default is
{cmd:sequence(sequence)}{p_end}
{synopt :{opth tr:eatment(varname)}}treatment variable; default is
{cmd:treatment(treat)}{p_end}
{synopt :{opth per:iod(varname)}}period variable; default is
{cmd:period(period)}{p_end}
{synopt :{opth id(varname)}}ID variable{p_end}
{synopt :{opth car:ryover(varname)}}name of carryover variable; default is
{cmd:carryover(carry)}{p_end}
{synopt :{opt car:ryover}{cmd:(none)}}omit carryover effects from model;
default is {cmd:carryover(carry)}{p_end}
{synopt :{opt m:odel(string)}}specify the model to fit{p_end}
{synopt :{opt se:quential}}estimate sequential instead of partial sums of
squares{p_end}
{syntab :Parameterization}
{synopt :{opt p:aram}{cmd:(3)}}estimate mean and the period, treatment, and
sequence effects; assume no carryover effects exist; the default{p_end}
{synopt :{opt p:aram}{cmd:(1)}}estimate mean and the period, treatment, and
carryover effects; assume no sequence effects exist{p_end}
{synopt :{opt p:aram}{cmd:(2)}}estimate mean, period, treatment, and
period-by-treatment interaction; assume no sequence or carryover effects
exist{p_end}
{synopt :{opt p:aram}{cmd:(4)}}estimate mean, period, treatment, and
period-by-treatment interaction; assume no period or crossover effects
exist{p_end}
{synoptline}
{p2colreset}{...}
{title:Description}
{pstd}
{cmd:pkcross} analyzes data from a crossover design experiment. When
analyzing pharmaceutical trial data, if the treatment, carryover, and sequence
variables are known, the omnibus test for separability of the treatment and
carryover effects is calculated.
{pstd}
{cmd:pkcross} is one of the pk commands. Please read {helpb pk} before reading
this entry.
{title:Options}
{dlgtab:Model}
{phang}
{opth sequence(varname)} specifies the variable that contains the sequence in
which the treatment was administered. If this option is not specified,
{cmd:sequence(sequence)} is assumed.
{phang}
{opth treatment(varname)} specifies the variable that contains the treatment
information. If this option is not specified, {cmd:treatment(treat)} is
assumed.
{phang}
{opth period(varname)} specifies the variable that contains the period
information. If this option is not specified, {cmd:period(period)} is
assumed.
{phang}
{opth id(varname)} specifies the variable that contains the subject
identifiers. If this option is not specified, {cmd:id(id)} is assumed.
{phang}
{opt carryover}{cmd:(}{varname}{c |}{cmd:none}{cmd:)} specifies the variable
that contains the carryover information. If {cmd:carry(none)} is specified,
the carryover effects are omitted from the model. If this option is not
specified, {cmd:carryover(carry)} is assumed.
{phang}
{opt model(string)} specifies the model to be fitted. For higher-order
crossover designs, this can be useful if you want to fit a model other than
the default. However, {helpb anova} can also be used to fit a crossover
model. The default model for higher-order crossover designs is outcome
predicted by sequence, period, treatment, and carryover effects. By default,
the model statement is {cmd:model(sequence period treat carry)}.
{phang}
{opt sequential} specifies that sequential sums of squares be estimated.
{dlgtab:Parameterization}
{phang}
{opt param(#)} specifies which of the four parameterizations to use for the
analysis of a 2*2 crossover experiment. This option is ignored with
higher-order crossover designs. The default is {cmd:param(3)}.
{pmore}
{cmd:param(1)} estimates the overall mean, the period effects, the
treatment effects, and the carryover effects, assuming that no sequence
effects exist.
{pmore}
{cmd:param(2)} estimates the overall mean, the period effects, the treatment
effects, and the period-by-treatment interaction, assuming that no sequence
or carryover effects exist.
{pmore}
{cmd:param(3)} estimates the overall mean, the period effects, the treatment
effects, and the sequence effects, assuming that no carryover effects exist.
This is the default parameterization.
{pmore}
{cmd:param(4)} estimates the overall mean, the sequence effects, the treatment
effects, and the sequence-by-treatment interaction, assuming that no period or
crossover effects exist. When the sequence by treatment is equivalent to the
period effect, this reduces to the third parameterization.
{title:Remarks}
{pstd}
{cmd:pkcross} is designed to analyze crossover experiments. Use
{helpb pkshape} first to reshape your data. {cmd:pkcross} assumes that the
data were reshaped by {cmd:pkshape} or are organized in the same manner as
produced with {cmd:pkshape}. Washout periods are indicated by the number 0.
{title:Examples}
{phang}{cmd: . pkcross outcome}{p_end}
{phang}{cmd: . pkcross outcome, carryover(none)}{p_end}
{phang}{cmd: . pkcross outcome, param(2)}
{title:Also see}
{psee}
Manual: {bf:[R] pkcross}
{psee}
Online: {helpb pk}, {helpb pkcollapse}, {helpb pkequiv}, {helpb pkexamine},
{helpb pkshape}, {helpb pksumm}, {helpb statsby}
{p_end}
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