Simulate adverse event reporting in clinical trials with the goal of detecting under-reporting sites.
Monitoring of Adverse Event (AE) reporting in clinical trials is important for patient safety. We use bootstrap-based simulation to assign an AE under-reporting probability to each site in a clinical trial. The method is inspired by the ‘infer’ R package and Allen Downey’s blog article: “There is only one test!”.
install.packages("simaerep")You can install the development version from GitHub with:
# install.packages("devtools")
devtools::install_github("openpharma/simaerep")simaerep has been published as workproduct of the Inter-Company
Quality Analytics (IMPALA) consortium.
IMPALA aims to engage with Health Authorities inspectors on defining
guiding principles for the use of advanced analytics to complement,
enhance and accelerate current QA practices. simaerep has initially
been developed at Roche but is currently evaluated by other companies
across the industry to complement their quality assurance activities
(see
testimonials).
Koneswarakantha, B., Adyanthaya, R., Emerson, J. et al. An Open-Source R Package for Detection of Adverse Events Under-Reporting in Clinical Trials: Implementation and Validation by the IMPALA (Inter coMPany quALity Analytics) Consortium. Ther Innov Regul Sci 58, 591–599 (2024). https://doi.org/10.1007/s43441-024-00631-8
Koneswarakantha, B., Barmaz, Y., Ménard, T. et al. Follow-up on the Use of Advanced Analytics for Clinical Quality Assurance: Bootstrap Resampling to Enhance Detection of Adverse Event Under-Reporting. Drug Saf (2020). https://doi.org/10.1007/s40264-020-01011-5
Download as pdf in the release section generated using thevalidatoR.
Recommended Threshold: aerep$dfeval$prob_low_prob_ur: 0.95
suppressPackageStartupMessages(library(simaerep))
suppressPackageStartupMessages(library(tidyverse))
suppressPackageStartupMessages(library(knitr))
set.seed(1)
df_visit <- sim_test_data_study(
n_pat = 1000, # number of patients in study
n_sites = 100, # number of sites in study
frac_site_with_ur = 0.05, # fraction of sites under-reporting
ur_rate = 0.4, # rate of under-reporting
ae_per_visit_mean = 0.5 # mean AE per patient visit
)
df_visit$study_id <- "A"
df_visit %>%
select(study_id, site_number, patnum, visit, n_ae) %>%
head(25) %>%
knitr::kable()| study_id | site_number | patnum | visit | n_ae |
|---|---|---|---|---|
| A | S0001 | P000001 | 1 | 0 |
| A | S0001 | P000001 | 2 | 1 |
| A | S0001 | P000001 | 3 | 1 |
| A | S0001 | P000001 | 4 | 2 |
| A | S0001 | P000001 | 5 | 3 |
| A | S0001 | P000001 | 6 | 3 |
| A | S0001 | P000001 | 7 | 3 |
| A | S0001 | P000001 | 8 | 3 |
| A | S0001 | P000001 | 9 | 3 |
| A | S0001 | P000001 | 10 | 3 |
| A | S0001 | P000001 | 11 | 3 |
| A | S0001 | P000001 | 12 | 3 |
| A | S0001 | P000001 | 13 | 4 |
| A | S0001 | P000001 | 14 | 4 |
| A | S0001 | P000001 | 15 | 4 |
| A | S0001 | P000001 | 16 | 6 |
| A | S0001 | P000001 | 17 | 6 |
| A | S0001 | P000002 | 1 | 0 |
| A | S0001 | P000002 | 2 | 0 |
| A | S0001 | P000002 | 3 | 0 |
| A | S0001 | P000002 | 4 | 0 |
| A | S0001 | P000002 | 5 | 0 |
| A | S0001 | P000002 | 6 | 0 |
| A | S0001 | P000002 | 7 | 0 |
| A | S0001 | P000002 | 8 | 1 |
aerep <- simaerep(df_visit)
plot(aerep, study = "A")
Left panel shows mean AE reporting per site (lightblue and darkblue lines) against mean AE reporting of the entire study (golden line). Single sites are plotted in descending order by AE under-reporting probability on the right panel in which grey lines denote cumulative AE count of single patients. Grey dots in the left panel plot indicate sites that were picked for single plotting. AE under-reporting probability of dark blue lines crossed threshold of 95%. Numbers in the upper left corner indicate the ratio of patients that have been used for the analysis against the total number of patients. Patients that have not been on the study long enough to reach the evaluation point (visit_med75, see introduction) will be ignored.
Following the recommendation of our latest performance benchmark statistical performance can be increased by using the inframe algorithm without multiplicity correction.
Note that the plot is more noisy because no patients are excluded and only a few patients contribute to the event count at higher visits
Recommended Threshold: aerep$dfeval$prob_low_prob_ur: 0.99
aerep <- simaerep(
df_visit,
inframe = TRUE,
visit_med75 = FALSE,
mult_corr = FALSE
)
plot(aerep, study = "A")
The
inframe
algorithm uses only dbplyr compatible table operations and can be
executed within a database backend as we demonstrate here using
duckdb.
However, we need to provide a in database table that has as many rows as
the desired replications in our simulation, instead of providing an
integer for the r parameter.
con <- DBI::dbConnect(duckdb::duckdb(), dbdir = ":memory:")
df_r <- tibble(rep = seq(1, 1000))
dplyr::copy_to(con, df_visit, "visit")
dplyr::copy_to(con, df_r, "r")
tbl_visit <- tbl(con, "visit")
tbl_r <- tbl(con, "r")
aerep <- simaerep(
tbl_visit,
r = tbl_r,
inframe = TRUE,
visit_med75 = FALSE,
mult_corr = FALSE
)
plot(aerep, df_visit = tbl_visit)
#> study = NULL, defaulting to study:A
DBI::dbDisconnect(con)