Count patients with marked laboratory abnormalities
Source:R/abnormal_by_marked.R
abnormal_by_marked.Rd
The analyze function count_abnormal_by_marked()
creates a layout element to count patients with marked laboratory
abnormalities for each direction of abnormality, categorized by parameter value.
This function analyzes primary analysis variable var
which indicates whether a single, replicated,
or last marked laboratory abnormality was observed. Levels of var
to include for each marked lab
abnormality (single
and last_replicated
) can be supplied via the category
parameter. Additional
analysis variables that can be supplied as a list via the variables
parameter are id
(defaults
to USUBJID
), a variable to indicate unique subject identifiers, param
(defaults to PARAM
), a
variable to indicate parameter values, and direction
(defaults to abn_dir
), a variable to indicate
abnormality directions.
For each combination of param
and direction
levels, marked lab abnormality counts are calculated
as follows:
Single, not last
&Last or replicated
: The number of patients withSingle, not last
andLast or replicated
values, respectively.Any
: The number of patients with either single or replicated marked abnormalities.
Fractions are calculated by dividing the above counts by the number of patients with at least one valid measurement recorded during the analysis.
Prior to using this function in your table layout you must use rtables::split_rows_by()
to create two
row splits, one on variable param
and one on variable direction
.
Usage
count_abnormal_by_marked(
lyt,
var,
category = list(single = "SINGLE", last_replicated = c("LAST", "REPLICATED")),
variables = list(id = "USUBJID", param = "PARAM", direction = "abn_dir"),
na_str = default_na_str(),
nested = TRUE,
...,
.stats = NULL,
.formats = NULL,
.labels = NULL,
.indent_mods = NULL
)
s_count_abnormal_by_marked(
df,
.var = "AVALCAT1",
.spl_context,
category = list(single = "SINGLE", last_replicated = c("LAST", "REPLICATED")),
variables = list(id = "USUBJID", param = "PARAM", direction = "abn_dir")
)
a_count_abnormal_by_marked(
df,
.var = "AVALCAT1",
.spl_context,
category = list(single = "SINGLE", last_replicated = c("LAST", "REPLICATED")),
variables = list(id = "USUBJID", param = "PARAM", direction = "abn_dir")
)
Arguments
- lyt
(
PreDataTableLayouts
)
layout that analyses will be added to.- category
(
list
)
a list with different marked category names for single and last or replicated.- variables
(named
list
ofstring
)
list of additional analysis variables.- na_str
(
string
)
string used to replace allNA
or empty values in the output.- nested
(
flag
)
whether this layout instruction should be applied within the existing layout structure _if possible (TRUE
, the default) or as a new top-level element (FALSE
). Ignored if it would nest a split. underneath analyses, which is not allowed.- ...
additional arguments for the lower level functions.
- .stats
-
(
character
)
statistics to select for the table.Options are:
'count_fraction', 'count_fraction_fixed_dp'
- .formats
(named
character
orlist
)
formats for the statistics. See Details inanalyze_vars
for more information on the"auto"
setting.- .labels
(named
character
)
labels for the statistics (without indent).- .indent_mods
(named
integer
)
indent modifiers for the labels. Defaults to 0, which corresponds to the unmodified default behavior. Can be negative.- df
(
data.frame
)
data set containing all analysis variables.- .var, var
(
string
)
single variable name that is passed byrtables
when requested by a statistics function.- .spl_context
(
data.frame
)
gives information about ancestor split states that is passed byrtables
.
Value
count_abnormal_by_marked()
returns a layout object suitable for passing to further layouting functions, or tortables::build_table()
. Adding this function to anrtable
layout will add formatted rows containing the statistics froms_count_abnormal_by_marked()
to the table layout.
s_count_abnormal_by_marked()
returns statisticcount_fraction
withSingle, not last
,Last or replicated
, andAny
results.
a_count_abnormal_by_marked()
returns the corresponding list with formattedrtables::CellValue()
.
Functions
count_abnormal_by_marked()
: Layout-creating function which can take statistics function arguments and additional format arguments. This function is a wrapper forrtables::analyze()
.s_count_abnormal_by_marked()
: Statistics function for patients with marked lab abnormalities.a_count_abnormal_by_marked()
: Formatted analysis function which is used asafun
incount_abnormal_by_marked()
.
Note
Single, not last
and Last or replicated
levels are mutually exclusive. If a patient has
abnormalities that meet both the Single, not last
and Last or replicated
criteria, then the
patient will be counted only under the Last or replicated
category.
Examples
library(dplyr)
df <- data.frame(
USUBJID = as.character(c(rep(1, 5), rep(2, 5), rep(1, 5), rep(2, 5))),
ARMCD = factor(c(rep("ARM A", 5), rep("ARM B", 5), rep("ARM A", 5), rep("ARM B", 5))),
ANRIND = factor(c(
"NORMAL", "HIGH", "HIGH", "HIGH HIGH", "HIGH",
"HIGH", "HIGH", "HIGH HIGH", "NORMAL", "HIGH HIGH", "NORMAL", "LOW", "LOW", "LOW LOW", "LOW",
"LOW", "LOW", "LOW LOW", "NORMAL", "LOW LOW"
)),
ONTRTFL = rep(c("", "Y", "Y", "Y", "Y", "Y", "Y", "Y", "Y", "Y"), 2),
PARAMCD = factor(c(rep("CRP", 10), rep("ALT", 10))),
AVALCAT1 = factor(rep(c("", "", "", "SINGLE", "REPLICATED", "", "", "LAST", "", "SINGLE"), 2)),
stringsAsFactors = FALSE
)
df <- df %>%
mutate(abn_dir = factor(
case_when(
ANRIND == "LOW LOW" ~ "Low",
ANRIND == "HIGH HIGH" ~ "High",
TRUE ~ ""
),
levels = c("Low", "High")
))
# Select only post-baseline records.
df <- df %>% filter(ONTRTFL == "Y")
df_crp <- df %>%
filter(PARAMCD == "CRP") %>%
droplevels()
full_parent_df <- list(df_crp, "not_needed")
cur_col_subset <- list(rep(TRUE, nrow(df_crp)), "not_needed")
spl_context <- data.frame(
split = c("PARAMCD", "GRADE_DIR"),
full_parent_df = I(full_parent_df),
cur_col_subset = I(cur_col_subset)
)
map <- unique(
df[df$abn_dir %in% c("Low", "High") & df$AVALCAT1 != "", c("PARAMCD", "abn_dir")]
) %>%
lapply(as.character) %>%
as.data.frame() %>%
arrange(PARAMCD, abn_dir)
basic_table() %>%
split_cols_by("ARMCD") %>%
split_rows_by("PARAMCD") %>%
summarize_num_patients(
var = "USUBJID",
.stats = "unique_count"
) %>%
split_rows_by(
"abn_dir",
split_fun = trim_levels_to_map(map)
) %>%
count_abnormal_by_marked(
var = "AVALCAT1",
variables = list(
id = "USUBJID",
param = "PARAMCD",
direction = "abn_dir"
)
) %>%
build_table(df = df)
#> ARM A ARM B
#> ————————————————————————————————————————————
#> ALT (n) 1 1
#> Low
#> Single, not last 1 (100%) 0
#> Last or replicated 0 1 (100%)
#> Any Abnormality 1 (100%) 1 (100%)
#> CRP (n) 1 1
#> High
#> Single, not last 1 (100%) 0
#> Last or replicated 0 1 (100%)
#> Any Abnormality 1 (100%) 1 (100%)
basic_table() %>%
split_cols_by("ARMCD") %>%
split_rows_by("PARAMCD") %>%
summarize_num_patients(
var = "USUBJID",
.stats = "unique_count"
) %>%
split_rows_by(
"abn_dir",
split_fun = trim_levels_in_group("abn_dir")
) %>%
count_abnormal_by_marked(
var = "AVALCAT1",
variables = list(
id = "USUBJID",
param = "PARAMCD",
direction = "abn_dir"
)
) %>%
build_table(df = df)
#> ARM A ARM B
#> ————————————————————————————————————————————
#> ALT (n) 1 1
#> Low
#> Single, not last 1 (100%) 0
#> Last or replicated 0 1 (100%)
#> Any Abnormality 1 (100%) 1 (100%)
#> CRP (n) 1 1
#> High
#> Single, not last 1 (100%) 0
#> Last or replicated 0 1 (100%)
#> Any Abnormality 1 (100%) 1 (100%)