What does this package do?
The osdc (Open Source Diabetes Classifier) package classifies individuals as having type 1 diabetes (T1D) or type 2 diabetes (T2D) based on Danish register data. You provide the register data, and the package returns a data table of individuals identified as having diabetes, along with their diabetes type (T1D or T2D) and the date of the classification.
This package serves two overarching purposes:
- To provide an open-source, code-based algorithm to classify type 1 and type 2 diabetes using Danish registers as data sources.
- To inspire discussions within the Danish register-based research space on the openness and ease of use on the existing tooling and registers, and on the need for an official process for updating or contributing to existing data sources.
For a detailed description of the algorithm, see vignette("algorithm"). For the motivations and rationale behind this package, see vignette("rationale"). For a full list of required register variables, see vignette("data-sources").
Step-by-step usage
This section walks through the full workflow: loading the package, preparing data, running the classification, as well as understanding and saving the output. We use simulated data here, but the same or similar steps apply to real register data. For more information on using osdc on real register data, see Section 3.
Step 1: Install and load the package
First, you need to install and load the package:
Step 2: Check which registers are needed
The algorithm requires data from multiple Danish registers. The names of these registers can be seen below:
| Register abbreviation | Register name |
|---|---|
| bef | CPR-registerets befolkningstabel |
| lmdb | Laegemiddelstatistikregisteret |
| lpr_adm | Landspatientregisterets administrationstabel (LPR2) |
| lpr_diag | Landspatientregisterets diagnosetabel (LPR2) |
| lpr3a_kontakt | Landspatientregisterets kontakttabel (LPR3A) |
| lpr3a_diagnose | Landspatientregisterets diagnosetabel (LPR3A) |
| lpr3f_kontakter | Landspatientregisterets kontakttabel (LPR3F) |
| lpr3f_diagnoser | Landspatientregisterets diagnosetabel (LPR3F) |
| sysi | Sygesikringsregisteret |
| sssy | Sygesikringsregisteret |
| lab_forsker | Laboratoriedatabasens forskertabel |
For a table showing the specific variables needed from each register, see vignette("data-sources").
Important
To use the osdc algorithm, you need to have all the variables described in
vignette("data-sources"), so please ensure that you have the required variables before continuing.
Step 3: Prepare the data
The package requires data to be in DuckDB format, which is a high-performance database format that can handle the large volumes of data without loading everything into memory at once. See vignette("design") for more on why we use DuckDB.
For this example, we generate simulated register data using simulate_registers() and then convert it to DuckDB format:
register_data <- registers() |>
names() |>
simulate_registers() |>
purrr::map(duckplyr::as_duckdb_tibble) |>
# Convert to a DuckDB connection, as duckplyr is still
# in early development, while the DBI-DuckDB connection
# is more stable.
purrr::map(duckplyr::as_tbl)The result is a named list where each element is one register as a DuckDB table. The LPR data spans multiple versions (LPR2 and LPR3) that need to be prepared and joined into a single table before being used as input for classify_diabetes(). The same goes for the health service registers (SSSY, and SYSI). osdc provides helper functions for this:
lpr <- list(
prepare_lpr2(register_data$lpr_adm, register_data$lpr_diag),
prepare_lpr3f(register_data$lpr3f_kontakter, register_data$lpr3f_diagnoser),
prepare_lpr3a(register_data$lpr3a_kontakt, register_data$lpr3a_diagnose)
) |>
join_registers()
hsr <- list(register_data$sssy, register_data$sysi) |> join_registers()The remaining registers are extracted from the register_data list, so they are ready to be passed as arguments to classify_diabetes():
bef <- register_data$bef
lmdb <- register_data$lmdb
lab_forsker <- register_data$lab_forskerStep 4: Run the classification
Now, we’re ready to run the classification algorithm. Pass each register to classify_diabetes():
classified_diabetes <- classify_diabetes(
lpr = lpr,
hsr = hsr,
lab_forsker = lab_forsker,
bef = bef,
lmdb = lmdb
)
classified_diabetes
#> # Source: SQL [?? x 5]
#> # Database: DuckDB 1.5.2 [unknown@Linux 6.17.0-1010-azure:R 4.6.0//tmp/RtmpTmHGGW/duckplyr/duckplyr1d1a328b8a19.duckdb]
#> pnr stable_inclusion_date raw_inclusion_date has_t1d has_t2d
#> <chr> <date> <date> <lgl> <lgl>
#> 1 706974528463 2011-06-20 2011-06-20 FALSE TRUE
#> 2 504469234683 2022-03-23 2022-03-23 FALSE TRUE
#> 3 409442575549 2005-09-26 2005-09-26 FALSE TRUE
#> 4 240771768588 2018-03-19 2018-03-19 FALSE TRUE
#> 5 506644859723 2023-05-08 2023-05-08 FALSE TRUE
#> 6 298944792608 2005-09-12 2005-09-12 FALSE TRUE
#> 7 498989088479 2014-11-09 2014-11-09 FALSE TRUE
#> 8 732715981647 2016-12-19 2016-12-19 FALSE TRUE
#> 9 673530226814 2021-01-22 2021-01-22 FALSE TRUEAs seen above, this returns a DuckDB table with the individuals classified as having either T1D or T2D along with the date of the classification. Each of the columns in the output is explained in Section 2.5.1 below.
Step 5 (optional): Collect the results into R
Because the data is stored in DuckDB, the result above is a lazy reference to a database query, i.e., the data has not been loaded into R’s memory. To bring the results into R as a regular data frame, use dplyr::collect():
classified_diabetes <- classified_diabetes |>
dplyr::collect()
classified_diabetes
#> # A tibble: 9 × 5
#> pnr stable_inclusion_date raw_inclusion_date has_t1d has_t2d
#> <chr> <date> <date> <lgl> <lgl>
#> 1 732715981647 2016-12-19 2016-12-19 FALSE TRUE
#> 2 506644859723 2023-05-08 2023-05-08 FALSE TRUE
#> 3 673530226814 2021-01-22 2021-01-22 FALSE TRUE
#> 4 298944792608 2005-09-12 2005-09-12 FALSE TRUE
#> 5 498989088479 2014-11-09 2014-11-09 FALSE TRUE
#> 6 706974528463 2011-06-20 2011-06-20 FALSE TRUE
#> 7 409442575549 2005-09-26 2005-09-26 FALSE TRUE
#> 8 240771768588 2018-03-19 2018-03-19 FALSE TRUE
#> 9 504469234683 2022-03-23 2022-03-23 FALSE TRUENow, we can see that with the simulated data, 9 individuals are classified as having diabetes.
Understanding the output
The output is a table with one row per classified individual and five columns:
| Column | Description |
|---|---|
pnr |
The pseudonymised personal identification number. |
stable_inclusion_date |
The date of the second inclusion event, if on or after stable_inclusion_start_date (default: 1998). NA for earlier dates. |
raw_inclusion_date |
The date of the second inclusion event without setting NA for date earlier than the stable_inclusion_start_date. |
has_t1d |
TRUE if classified as type 1 diabetes, FALSE otherwise. |
has_t2d |
TRUE if classified as type 2 diabetes, FALSE otherwise. |
About
stable_inclusion_datevsraw_inclusion_dateThe
raw_inclusion_dateis simply the date of the second qualifying event. However, for events before 1998, the register data may not have sufficient coverage to reliably distinguish new (incident) cases from existing (prevalent) ones. Thestable_inclusion_datecolumn is set toNAfor these earlier dates to flag this uncertainty.The
classify_diabetes()function includes astable_inclusion_start_dateparameter that is01-01-1988by default. This means that you can change the date for when the classification is considered stable
For more information about the output, see the Interface section under vignette("design").
Step 6: Saving the results
Once you have the classification results, you can save them as a Parquet file for yourself or your collaborators on your DST project:
classified_diabetes |>
duckplyr::as_duckdb_tibble() |>
duckplyr::compute_parquet(
"classified_diabetes.parquet"
)Working with real register data
In a real-world scenario, the register data is too large to read into memory all at once. We recommend converting your register files into Parquet format on disk, with each register in its own folder (e.g., all lmdb files in one folder, all lab_forsker files in another, etc.).
Tip
To convert SAS (
.sas7bdat) files to Parquet, you can use thefastregpackage.
If you’re working on Statistics Denmark’s (DST) server, be aware that the pre-installed R packages can be quite old (for example, at the time of writing, library(duckplyr) loads version 0.4 of the duckplyr package from 2024, whereas the latest version on CRAN is >1.1 from 2026). These old versions don’t support the dplyr operations necessary for osdc to work.
Installing osdc with install.packages("osdc") should force the necessary updates of package dependencies. Otherwise, the latest version of any given package can be installed from DST’s local CRAN mirror by using install.packages(). The downside of this approach is that you have to repeat the package installations frequently (whenever you log on to a new virtual machine, or after the servers weekly reset).
After making sure that you have the newest version of osdc installed (which should install/update any necessary dependencies), you can load each register directly from its Parquet folder and convert it to DuckDB, as shown below.
Currently, the conversion to DuckDB requires that the user specifies some connection parameters first:
- the maximum amount of memory to be allocated for DuckDB data, e.g. 128GB which is stable and should be more than enough to hold the inputs to osdc in DuckDB
- where to temporarily store any DuckDB data that exceeds this threshold.
ddb_driver <- duckdb::duckdb(config = list(
memory = "128GB",
temp_dir = "path/to/temp/dir"
))
ddb_con <- DBI::dbConnect(ddb_driver)If you’re working with very large data sets, it’s good practice to filter the data on the Arrow side before converting to DuckDB to reduce computation and memory use. Conveniently, most of dplyr’s filtering and selection operations are supported by the arrow package. If you need to rename variables or convert their types to match the inputs expected by osdc, you can do that too:
lpr3f_diagnoser <- "path/to/lpr3f_diagnoser_parquet_folder" |>
arrow::open_dataset(unify_schemas = TRUE) |>
# Insert dplyr filtering and variable selection/renaming steps here, e.g.:
# dplyr::select(...) |>
# dplyr::mutate(...) |>
# dplyr::filter(...) |>
arrow::to_duckdb(con = ddb_con) |>
dplyr::compute()If your data (or parts of it) is already in R (e.g., as a data.frame), you can convert it to a DuckDB table with:
Important
Important notes on using
lpr3adata!A:
lpr3acontains duplicates of contacts in 2017 & 2018 that are also contained inlpr2. These rows must be filtered out before being input to osdc’sprepare_lpr3a()function.B: The
kont_starttidspunktvariable inlpr3ais adatetimetype, and must be converted to adatebefore being input toprepare_lpr3a().
The duplicate rows in lpr3a_kontakt can be removed during processing by filtering to indberetningssystem == "LPR3" Similarly, the kont_starttidspunkt variable in lpr3a can be converted to a date in a single call to dplyr::mutate() during pre-processing in Arrow. e.g.:
lpr3a_kontakt <- "path/to/lpr3a_kontakt_parquet_folder" |>
arrow::open_dataset(unify_schemas = TRUE) |>
# dplyr::select(...) |>
dplyr::mutate(kont_starttidspunkt = as.Date(kont_starttidspunkt)) |>
dplyr::filter(indberetningssystem == "LPR3") |>
arrow::to_duckdb(con = ddb_con) |>
dplyr::compute()This can be used as input to prepare_lpr3a():
lpr <- list(
prepare_lpr2(lpr_adm, lpr_diag),
prepare_lpr3f(lpr3f_kontakter, lpr3f_diagnoser),
prepare_lpr3a(lpr3a_kontakt, lpr3a_diagnose)
) |>
join_registers()Most inputs will work in the Arrow/DuckDB equivalent of their type in the original SAS file. Unless the SAS-to-Arrow conversion introduced unexpected types, you should should not need to do any further type conversion.
Once you’re done using DuckDB, you should close the driver and connection like so:
duckdb::duckdb_shutdown(ddb_driver)
DBI::dbDisconnect(ddb_con)Getting help
If you encounter a bug or have a question about how to use osdc, please open an issue on the GitHub repository. When reporting a bug, include a minimal example that reproduces the problem along to help us understand and investigate the problem.
