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The epocakir package makes clinical coding of patients with kidney disease using clinical practice guidelines easy. The guidelines used are the evidence-based KDIGO guidelines. This package covers acute kidney injury (AKI), anemia, and chronic liver disease(CKD).
aki_staging()
: Classification of AKI staging (aki_stages
) with automatic selection of:
aki_bCr()
: AKI based on baseline creatinineaki_SCr()
: AKI based on changes in serum creatinineaki_UO()
: AKI based on urine outputanemia()
: Classification of anemia
Classification of albuminuria (Albuminuria_stages
)
Albuminuria_staging_ACR()
: Albuminuria based on Albumin excretion rateAlbuminuria_staging_AER()
: Albuminuria based on Albumin-to-creatinine ratioeGFR()
: Estimation of glomerular filtration rate with automatic selection of:
eGFR_adult_SCr()
: eGFR based on the 2009 CKD-EPI creatinine equationeGFR_adult_SCysC()
: eGFR based on the 2012 CKD-EPI cystatin C equationeGFR_adult_SCr_SCysC()
: eGFR based on the 2012 CKD-EPI creatinine-cystatin C equationeGFR_child_SCr()
: eGFR based on the pediatric creatinine-based equationeGFR_child_SCr_BUN()
: eGFR based on the pediatric creatinine-BUN equationeGFR_child_SCysC()
: eGFR based on the pediatric cystatin C-based equationGFR_staging()
: Staging of GFR (GFR_stages
)
Multiple utility functions including:
conversion_factors
: Conversion factors used throughout the KDIGO guidelinesas_metric()
: Conversion of a measured value into metric unitsdob2age()
: Calculation of age from a date of birthbinary2factor()
: Conversion of binary data into factors based on a column namecombine_date_time_cols()
: Combining separate date and time columns into a single date and time columncombn_changes
: Generating changes between measurementsAutomatic conversion of units class objects
Tidy output allowing seamless integration with functions from the tidyverse
Tidyeval via programming with dplyr
Comprehensive tests and coverage
library(epocakir)
library(dplyr)
library(units)
Often clinical data must be cleansed and tidied before analysis can begin. To assist in this, several utility functions have been included. To explore these, consider a sample clinical dataset clinical_obvs
:
# Example workflow: clinical_obvs <- read.csv("cohort.csv")
glimpse(clinical_obvs)
#> Rows: 3
#> Columns: 9
#> $ `Patient Number` <chr> "p10001", "p10002", "p10003"
#> $ `Admission Date` <chr> "2020-03-05", "2020-03-06", "2020-03-17"
#> $ `Admission Time` <chr> "14:01:00", "09:10:00", "12:48:00"
#> $ Discharge_date <chr> "2020-03-10", "2020-03-16", "2020-03-18"
#> $ Discharge_time <chr> "16:34:00", "18:51:00", "09:12:00"
#> $ `Date of Birth` <chr> "1956-01-09", "1997-12-04", "1973-05-28"
#> $ Male <lgl> TRUE, FALSE, TRUE
#> $ Height <dbl> 182, 161, 168
#> $ Surgery <lgl> FALSE, FALSE, TRUE
clinical_obvs %>%
tidy_obvs <- combine_date_time_cols() %>%
mutate(
Age = dob2age(`Date of Birth`),
Height = as_metric(height = set_units(as.numeric(Height), "cm"))
%>%
) binary2factor(Male, Surgery)
glimpse(tidy_obvs)
#> Rows: 3
#> Columns: 8
#> $ `Patient Number` <chr> "p10001", "p10002", "p10003"
#> $ `Admission DateTime` <dttm> 2020-03-05 14:01:00, 2020-03-06 09:10:00, 2020-03…
#> $ Discharge_DateTime <dttm> 2020-03-10 16:34:00, 2020-03-16 18:51:00, 2020-0…
#> $ `Date of Birth` <chr> "1956-01-09", "1997-12-04", "1973-05-28"
#> $ Male <ord> Male, Not_Male, Male
#> $ Height [m] 1.82 [m], 1.61 [m], 1.68 [m]
#> $ Surgery <ord> Not_Surgery, Not_Surgery, Surgery
#> $ Age <Duration> 2114121600s (~66.99 years), 791769600s (~25.09 y…
Make sure to use set_units()
from the units
package to convert all measurements into unit objects for automatic unit conversion in epocakir.
Next consider the sample aki_pt_data
dataset. It is possible to use aki_staging()
to automatically classify the presence and staging of AKI. If a particular method is required, it is possible to classify AKI using aki_bCr()
, aki_SCr()
or aki_UO().
# Example workflow: aki_pt_data <- read.csv("aki.csv")
head(aki_pt_data)
#> # A tibble: 6 × 7
#> SCr_ bCr_ pt_id_ dttm_ UO_ aki_staging_type aki_
#> [mg/dl] [mg/dl] <chr> <dttm> [ml/kg] <chr> <ord>
#> 1 2 1.5 <NA> NA NA aki_bCr No AKI
#> 2 2.5 1.5 <NA> NA NA aki_bCr AKI Stage 1
#> 3 3 1.5 <NA> NA NA aki_bCr AKI Stage 2
#> 4 3.5 1.5 <NA> NA NA aki_bCr AKI Stage 2
#> 5 4 1.5 <NA> NA NA aki_bCr AKI Stage 3
#> 6 4.5 1.5 <NA> NA NA aki_bCr AKI Stage 3
aki_staging(aki_pt_data,
SCr = "SCr_", bCr = "bCr_", UO = "UO_",
dttm = "dttm_", pt_id = "pt_id_"
)#> [1] No AKI AKI Stage 1 AKI Stage 2 AKI Stage 2 AKI Stage 3 AKI Stage 3
#> [7] No AKI No AKI AKI Stage 1 No AKI No AKI AKI Stage 1
#> [13] No AKI No AKI No AKI AKI Stage 1 No AKI AKI Stage 2
#> [19] AKI Stage 3 AKI Stage 1 AKI Stage 3 AKI Stage 2 No AKI AKI Stage 1
#> [25] AKI Stage 3 AKI Stage 3 No AKI
#> Levels: No AKI < AKI Stage 1 < AKI Stage 2 < AKI Stage 3
%>%
aki_pt_data mutate(aki = aki_staging(
SCr = SCr_, bCr = bCr_, UO = UO_,
dttm = dttm_, pt_id = pt_id_
%>%
)) select(pt_id_, SCr_:dttm_, aki)
#> # A tibble: 27 × 5
#> pt_id_ SCr_ bCr_ dttm_ aki
#> <chr> [mg/dl] [mg/dl] <dttm> <ord>
#> 1 <NA> 2 1.5 NA No AKI
#> 2 <NA> 2.5 1.5 NA AKI Stage 1
#> 3 <NA> 3 1.5 NA AKI Stage 2
#> 4 <NA> 3.5 1.5 NA AKI Stage 2
#> 5 <NA> 4 1.5 NA AKI Stage 3
#> 6 <NA> 4.5 1.5 NA AKI Stage 3
#> 7 pt1 3.4 NA 2020-10-23 09:00:00 No AKI
#> 8 pt1 3.9 NA 2020-10-25 21:00:00 No AKI
#> 9 pt1 3 NA 2020-10-20 09:00:00 AKI Stage 1
#> 10 pt2 3.4 NA 2020-10-18 22:00:00 No AKI
#> # … with 17 more rows
%>%
aki_pt_data mutate(aki = aki_SCr(
SCr = SCr_, dttm = dttm_, pt_id = pt_id_
%>%
)) select(pt_id_, SCr_:dttm_, aki)
#> # A tibble: 27 × 5
#> pt_id_ SCr_ bCr_ dttm_ aki
#> <chr> [mg/dl] [mg/dl] <dttm> <ord>
#> 1 <NA> 2 1.5 NA No AKI
#> 2 <NA> 2.5 1.5 NA No AKI
#> 3 <NA> 3 1.5 NA No AKI
#> 4 <NA> 3.5 1.5 NA No AKI
#> 5 <NA> 4 1.5 NA No AKI
#> 6 <NA> 4.5 1.5 NA No AKI
#> 7 pt1 3.4 NA 2020-10-23 09:00:00 No AKI
#> 8 pt1 3.9 NA 2020-10-25 21:00:00 No AKI
#> 9 pt1 3 NA 2020-10-20 09:00:00 AKI Stage 1
#> 10 pt2 3.4 NA 2020-10-18 22:00:00 No AKI
#> # … with 17 more rows
Similarly, eGFR()
offers the ability to automatically select the appropriate formula to estimate the glomerular filtration rate. If a particular formula is required, then eGFR_adult_SCr
, eGFR_adult_SCysC
, eGFR_adult_SCr_SCysC
, eGFR_child_SCr
, eGFR_child_SCr_BUN
, or eGFR_child_SCysC
can be used.
# Example workflow: aki_pt_data <- read.csv("aki.csv")
head(eGFR_pt_data)
#> # A tibble: 6 × 10
#> SCr_ SCysC_ Age_ male_ black_ height_ BUN_ eGFR_calc_…¹ eGFR_ pedia…²
#> [mg/dl] [mg/L] [years] <lgl> <lgl> [m] [mg/dl] <chr> [mL/… <lgl>
#> 1 0.5 NA 20 FALSE FALSE NA NA eGFR_adult_… 139. FALSE
#> 2 NA 0.4 20 FALSE FALSE NA NA eGFR_adult_… 162. FALSE
#> 3 0.5 0.4 20 FALSE FALSE NA NA eGFR_adult_… 167. FALSE
#> 4 0.5 NA 30 FALSE TRUE NA NA eGFR_adult_… 150. FALSE
#> 5 NA 0.4 30 FALSE TRUE NA NA eGFR_adult_… 155. FALSE
#> 6 0.5 0.4 30 FALSE TRUE NA NA eGFR_adult_… 171. FALSE
#> # … with abbreviated variable names ¹eGFR_calc_type_, ²pediatric_
eGFR(eGFR_pt_data,
SCr = "SCr_", SCysC = "SCysC_",
Age = "Age_", height = "height_", BUN = "BUN_",
male = "male_", black = "black_", pediatric = "pediatric_"
)#> Units: [mL/1.73m2/min]
#> [1] 139.32466 161.68446 166.81886 150.52336 155.33226 171.35616 139.32466
#> [8] 66.77365 96.41798 150.52336 64.15027 99.04045 49.63420 161.68446
#> [15] 97.06854 53.62373 155.33226 99.70870 49.63420 66.77365 56.10368
#> [22] 53.62373 64.15027 57.62964 155.99874 173.48118 178.86404 168.53768
#> [29] 166.66552 183.72895 155.99874 71.64555 103.37985 168.53768 68.83077
#> [36] 106.19167 66.06766 173.48118 116.50660 71.37808 166.66552 119.67546
#> [43] 66.06766 71.64555 67.33849 71.37808 68.83077 69.17003 99.12000
#> [50] 148.21219 165.89761
%>%
eGFR_pt_data dplyr::mutate(eGFR = eGFR(
SCr = SCr_, SCysC = SCysC_,
Age = Age_, height = height_, BUN = BUN_,
male = male_, black = black_, pediatric = pediatric_
%>%
)) select(SCr_:pediatric_, eGFR)
#> # A tibble: 51 × 11
#> SCr_ SCysC_ Age_ male_ black_ height_ BUN_ eGFR_…¹ eGFR_ pedia…² eGFR
#> [mg/dl] [mg/L] [years] <lgl> <lgl> [m] [mg/… <chr> [mL/… <lgl> [mL/…
#> 1 0.5 NA 20 FALSE FALSE NA NA eGFR_a… 139. FALSE 139.
#> 2 NA 0.4 20 FALSE FALSE NA NA eGFR_a… 162. FALSE 162.
#> 3 0.5 0.4 20 FALSE FALSE NA NA eGFR_a… 167. FALSE 167.
#> 4 0.5 NA 30 FALSE TRUE NA NA eGFR_a… 150. FALSE 151.
#> 5 NA 0.4 30 FALSE TRUE NA NA eGFR_a… 155. FALSE 155.
#> 6 0.5 0.4 30 FALSE TRUE NA NA eGFR_a… 171. FALSE 171.
#> 7 0.5 NA 20 FALSE FALSE NA NA eGFR_a… 139. FALSE 139.
#> 8 NA 1.2 20 FALSE FALSE NA NA eGFR_a… 66.8 FALSE 66.8
#> 9 0.5 1.2 20 FALSE FALSE NA NA eGFR_a… 96.4 FALSE 96.4
#> 10 0.5 NA 30 FALSE TRUE NA NA eGFR_a… 150. FALSE 151.
#> # … with 41 more rows, and abbreviated variable names ¹eGFR_calc_type_,
#> # ²pediatric_
%>%
eGFR_pt_data dplyr::mutate(eGFR = eGFR_adult_SCr(
SCr = SCr_, Age = Age_, male = male_, black = black_
%>%
)) select(SCr_:pediatric_, eGFR)
#> # A tibble: 51 × 11
#> SCr_ SCysC_ Age_ male_ black_ height_ BUN_ eGFR_…¹ eGFR_ pedia…² eGFR
#> [mg/dl] [mg/L] [years] <lgl> <lgl> [m] [mg/… <chr> [mL/… <lgl> [mL/…
#> 1 0.5 NA 20 FALSE FALSE NA NA eGFR_a… 139. FALSE 139.
#> 2 NA 0.4 20 FALSE FALSE NA NA eGFR_a… 162. FALSE NA
#> 3 0.5 0.4 20 FALSE FALSE NA NA eGFR_a… 167. FALSE 139.
#> 4 0.5 NA 30 FALSE TRUE NA NA eGFR_a… 150. FALSE 151.
#> 5 NA 0.4 30 FALSE TRUE NA NA eGFR_a… 155. FALSE NA
#> 6 0.5 0.4 30 FALSE TRUE NA NA eGFR_a… 171. FALSE 151.
#> 7 0.5 NA 20 FALSE FALSE NA NA eGFR_a… 139. FALSE 139.
#> 8 NA 1.2 20 FALSE FALSE NA NA eGFR_a… 66.8 FALSE NA
#> 9 0.5 1.2 20 FALSE FALSE NA NA eGFR_a… 96.4 FALSE 139.
#> 10 0.5 NA 30 FALSE TRUE NA NA eGFR_a… 150. FALSE 151.
#> # … with 41 more rows, and abbreviated variable names ¹eGFR_calc_type_,
#> # ²pediatric_
See https://alwinw.github.io/epocakir/reference/index.html for more usage details and package reference.
See https://kdigo.org/guidelines/ for full KDIGO guidelines.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.