Oral Corticosteroids; Pregnancy; Drug Utilization
Oral corticosteroids (OCS) are used to control flares in various conditions such as allergic
diseases or autoimmune diseases in pregnant women.
1 OCS may also be considered for
pregnant women as pregnancy can change immunological responses that could potentially
aggravate pre-existing allergic conditions.
1 Additionally, beyond their approved indications,
OCS are frequently prescribed for off-label indications, such as supporting in vitro
fertilization or preventing recurrent miscarriage in early pregnancy.
2,3 OCS are therefore
drugs with a high likelihood of exposure during pregnancy, even among women who did not
have previously used OCS.
J Korean Med Sci. 2025 Jan 13;40(2):e80
https://doi.org/10.3346/jkms.2025.40.e80
eISSN 1598-6357·pISSN 1011-8934
Obstetrics & Gynecology
Real-World Utilization Patterns of Oral
Corticosteroids During Pregnancy:
A Nationwide Population-Based Study
in Korea
Brief Communication
Received: Oct 1, 2024
Accepted: Dec 16, 2024
Published online: Dec 31, 2024
Addresses for Correspondence:
Ahhyung Choi, PharmD, PhD
School of Pharmacy, Sungkyunkwan University,
2066 Seobu-ro, Jangan-gu, Suwon 16419,
Republic of Korea; Harvard-MIT Center for
Regulatory Science, Harvard Medical School,
Boston, MA 02215, USA.
Email:
[email protected]
Ju-Young Shin, PhD
School of Pharmacy, Sungkyunkwan University,
2066 Seobu-ro, Jangan-gu, Suwon 16419,
Republic of Korea.
Email:
[email protected]
* Jeongin Oh and Yongtai Cho contributed
equally to this work.
© 2025 The Korean Academy of Medical
Sciences.
This is an Open Access article distributed
under the terms of the Creative Commons
Attribution Non-Commercial License (https://
creativecommons.org/licenses/by-nc/4.0/)
which permits unrestricted non-commercial
use, distribution, and reproduction in any
medium, provided the original work is properly
cited.
Jeongin Oh ,1* Yongtai Cho ,1* Jung Yeol Han ,2 Ahhyung Choi ,1,3 and
Ju-Young Shin 1,4,5
1 School of Pharmacy, Sungkyunkwan University, Suwon, Korea
2 Korean Mothersafe Counselling Center, Department of Obstetrics and Gynecology, Inje University, Ilsan
Paik Hospital, Goyang, Korea
3 Harvard-MIT Center for Regulatory Science, Harvard Medical School, Boston, MA, USA
4 Department of Biohealth Regulatory Science, Sungkyunkwan University, Suwon, Korea
5 Department of Clinical Research Design & Evaluation, Samsung Advanced Institute for Health Sciences
and Technology (SAIHST), Sungkyunkwan University, Seoul, Korea
ORCID iDs
Jeongin Oh
https://orcid.org/0009-0000-6779-0957
Yongtai Cho
https://orcid.org/0000-0003-3303-7881
Jung Yeol Han
https://orcid.org/0000-0001-5611-2392
Ahhyung Choi
https://orcid.org/0000-0002-0101-7328
Ju-Young Shin
https://orcid.org/0000-0003-1010-7525
Funding
This research was supported by a grant (RS-
2024-00332632) from Ministry of Food and
Drug Safety in 2024–2028. The funder had
no role in the study design; in the collection,
analysis, and interpretation of data; in the
writing of the report; and in the decision to
submit the article for publication.
Disclosure
Ju-Young Shin received grants from the
Ministry of Food and Drug Safety, the
Ministry of Health and Welfare, the National
Research Foundation of South Korea, and
pharmaceutical companies, including Pfizer,
UCB, and LG Chem, outside the submitted
work.
Data Sharing Statement
No additional data are available to the public.
Author Contributions
Conceptualization: Oh J, Cho Y, Han JY, Choi
A, Shin JY; Data curation: Oh J, Cho Y; Formal
analysis: Oh J; Funding acquisition: Shin JY;
Investigation: Oh J; Methodology: Oh J, Cho Y,
Han JY, Choi A, Shin JY; Project administration:
Han JY, Choi A, Shin JY; Supervision: Choi
A, Shin JY; Validation: Choi A, Shin JY;
Visualization: Oh J, Cho Y; Writing - original
draft: Oh J, Cho Y, Choi A; Writing - review &
editing: Oh J, Cho Y, Han JY, Choi A, Shin JY.
Yet, no studies to date have evaluated the patterns of OCS usage during pregnancy including
the indications for which they are prescribed. Thus, we aimed to describe the OCS utilization
patterns in pregnant women using a large nationwide database in South Korea.
We conducted a retrospective observational study using the Health Insurance Review and
Assessment (HIRA) database of South Korea from 2009 to 2022. The HIRA database, which
covers almost the entire South Korean population, contains data on patient’s demographics
and healthcare claims record (e.g., diagnoses, prescription records, and medical procedures)
from both in- and outpatient settings. Using this nationally representative database, we
identified all pregnancies with delivery records defined based on HIRA procedure codes
(Supplementary Table 1) between January 1, 2010, and December 31, 2021. Pregnancies
resulting in non-live births were not included in the analysis. The last menstrual period
(LMP) was estimated based on the delivery date and diagnoses of preterm birth, using a
validated algorithm in administrative healthcare database.
4 Specifically, LMP was estimated
by subtracting 245 days from the delivery date if the mother had a diagnostic code for preterm
delivery (O42, O60.1, O60.3), and by subtracting 273 days for otherwise full-term delivery.
We first described the baseline characteristics of the pregnancies according to OCS exposure
during pregnancy. OCS exposed pregnancies were defined as pregnancies with ≥ 1 OCS
prescription from LMP to the day before the delivery date and unexposed pregnancies were
defined as those without OCS prescription from LMP to the day before the delivery date. In each
pregnancy, we assessed maternal age, insurance type, and obstetric conditions (e.g., nulliparity,
multifetal pregnancies) at delivery. We also evaluated the indication-related conditions (e.g.,
autoimmune inflammatory disease, skin disease, respiratory system disease), comorbidities,
and comedications from 180 days before LMP to the day before the date of delivery and
healthcare utilization within 180 days prior to LMP. Baseline characteristics are presented as
frequencies and percentages for categorical variables and as means and standard deviations for
continuous variables. Absolute standardized differences (aSD) were calculated to quantify the
differences between the OCS-exposed and unexposed pregnancies.
In addition, we described the annual prevalence of OCS exposure during pregnancy from
2010 to 2021. We further analyzed the prevalence by individual OCS. As prednisolone and
methylprednisolone accounted for majority of the OCS usage (> 90%), we grouped the OCS
as: 1) prednisolone, 2) methylprednisolone, and 3) others (dexamethasone, betamethasone,
deflazacort, hydrocortisone and triamcinolone). We also calculated the number of OCS
prescriptions during five different assessment windows: 1) pre-pregnancy period (one year
before the LMP), 2) first trimester (LMP to day 90 of gestation), 3) second trimester (day 90 to
day 180), 4) third trimester (day 180 to delivery), and 5) postpartum period (1 year after delivery).
Lastly, we evaluated the annual proportion of individual indication among OCS exposed
pregnancies. Indications were identified based on the primary International Classification of
Diseases, Tenth Revision (ICD- 10) diagnosis of OCS prescription and were categorized into
six groups: autoimmune inflammatory disease, asthma, diseases of the skin, diseases of the
respiratory system, pregnancy-associated condition, and others. Disease of the respiratory system
included all subcodes of ICD- 10 Chapter J, while pregnancy-associated conditions included in
vitro fertilization, female infertility, threatened abortion, and subcodes of ICD- 10 code “Z3,”
which are health service encounters related to reproduction. A detailed list of indications and the
corresponding diagnostic codes for each indication is provided in Supplementary Table 2. We also
assessed the proportion of each OCS indication among OCS exposed pregnancies (or women)
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during pre-pregnancy, first trimester, second trimester, third trimester and postpartum period. All
analyses were performed using SAS Enterprise Guide 7 .1 software (SAS Institute, Cary, NC, USA).
We identified a total of 4,574,294 pregnancies, of which 283,001 (6.2%) have been exposed
to OCS during pregnancy. The median (interquartile range) duration of OCS prescription
during pregnancy was 4.0 (3.0–6.0) days. Compared with unexposed pregnancies, OCS
exposed pregnancies were older, more likely to have comorbidities (e.g., gastrointestinal
diseases and hypertension), and had a higher number of diagnoses (distinct 3-digit ICD- 10
codes) recorded (6.79 vs. 4.84, aSD 0.46) (Table 1 ). As expected, the prevalence of indication-
related conditions was significantly higher in the OCS-exposed group.
During the study period, the prevalence of OCS exposure notably increased from 4.98% in
2010 to 6.65% in 2021. Among individuals younger than 35 years, the prevalence rose from
4.89% in 2010 to 5.77% in 2021. In those aged 35 years and older, the prevalence increased
from 5.48% in 2010 to 8.34% in 2021 (Supplementary Table 3). Methylprednisolone (45.2%)
and prednisolone (45.0%) accounted for the majority of OCS usage (Fig. 1A). Across the
pregnancy period, OCS prescriptions sharply declined during the first trimester and gradually
increased during the third trimester, specifically near the delivery date (Fig. 1B). Among all
pregnancies, 230,274 (5.03%) were exposed during the first trimester, followed by 37 ,861
(0.83%) in the second trimester and 35,130 (0.77%) in the third trimester.
Among OCS exposed pregnancies, respiratory (40.48%) and skin (22.17%) diseases
were the most prevalent indications (Fig. 2A). The proportion of pregnancy-associated
conditions showed a notable increase from 9.31% in 2017 to 34.87% in 2021. The proportion
of OCS usage for diseases of respiratory system increased from 12.80% in 2010 to 21.88%
in 2019, but subsequently declined, with 14.26% in 2021 (Fig. 2A). Rheumatoid arthritis
(0.72%) and systemic lupus erythematosus (0.60%) were the most prevalent indication
among autoimmune inflammatory diseases, and dermatitis (15.57%) and urticaria (5.70%)
accounted the high proportions among diseases of the skin. Acute upper respiratory tract
infections (15.74%) predominated among diseases of the respiratory system, and within
the pregnancy associated conditions, treatment of infertility (5.94%) had high proportions.
Majority of the OCS prescriptions were used for acute conditions such as skin and
respiratory diseases both during pregnancy and pre-pregnancy (Fig. 2B). The proportions of
autoimmune diseases and asthma were relatively low but increased after gestation (Fig. 2B).
In this nationwide population-based study that comprises all pregnancies with live births
from 2010 to 2021, the prevalence of OCS exposure during pregnancy was 6.2%. This
proportion was higher than that reported in previous studies conducted in the United States
and Australia.
5,6 Throughout the study period, methylprednisolone and prednisolone were
the most frequently used OCS during pregnancy, possibly due to their limited placenta
transfer.
7 We also observed a large decrease in OCS prescriptions after the time of gestation.
This finding would indicate that many women tend to discontinue OCS after recognizing that
they are pregnant, which would also be attributed to concerns on the safety of prenatal OCS
use. Of note, most of the OCS prescriptions were used for acute conditions during pregnancy
and the median duration of prescription was relatively short (4 days). In South Korea, OCS
prescriptions for infertility treatment have been covered by health insurance from 2017 ,
which coincides with the increase in OCS prescriptions for pregnancy-associated conditions
after 2017 .
8 The prevalence of OCS prescriptions during pregnancy generally increased over
the study period, with a more pronounced rise in older women. However, there was a slight
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Table 1. Characteristics of pregnancies according to OCS exposure
Characteristics No. of pregnancies (%) Absolute standardized
differenceOCS (n = 283,001) Unexposed (n = 4,291,174)
Maternal age at delivery, yr 0.10
44 356 (0.12) 3,375 (0.08)
Medical aid recipient 3,247 (1.15) 35,901 (0.84) 0.03
Comorbidities
Depression 2,158 (0.76) 17,185 (0.40) 0.05
Diabetes 6,909 (2.44) 80,159 (1.87) 0.04
Dyslipidemia 8,272 (2.92) 83,123 (1.94) 0.06
Endometriosis 2,232 (0.79) 24,783 (0.58) 0.03
Epilepsy/Seizures 4,342 (1.53) 40,451 (0.94) 0.05
Gastrointestinal diseases 96,927 (34.25) 709,403 (16.53) 0.42
Hypertension 31,749 (11.22) 325,089 (7.58) 0.13
Migraine/Headache 14,829 (5.24) 130,260 (3.04) 0.11
Polycystic ovarian syndrome 4,789 (1.69) 33,631 (0.78) 0.08
Renal disease 1,841 (0.65) 14,852 (0.35) 0.04
Thyroid disorders 37,769 (13.35) 515,058 (12.00) 0.04
Indication-related conditions
Autoimmune inflammatory disease
Ankylosing spondylitis 426 (0.15) 691 (0.02) 0.05
Inflammatory bowel disease 398 (0.14) 2,640 (0.06) 0.03
Psoriatic arthropathies 1,087 (0.38) 4,869 (0.11) 0.05
Rheumatoid arthritis 2,274 (0.80) 1,727 (0.04) 0.12
Systemic lupus erythematosus 1,847 (0.65) 1,060 (0.02) 0.11
Asthma 10,161 (3.59) 25,669 (0.60) 0.21
Diseases of the skin
Atopic dermatitis 7,070 (2.50) 27,426 (0.64) 0.15
Contact dermatitis 60,272 (21.30) 206,963 (4.82) 0.50
Urticaria 22,685 (8.02) 46,792 (1.09) 0.34
Other skin diseases 20,320 (7.18) 86,399 (2.01) 0.25
Diseases of the respiratory system
Acute upper respiratory infections 116,574 (41.19) 872,808 (20.34) 0.46
Acute lower respiratory infections 68,854 (24.33) 365,221 (8.51) 0.44
Non-infectious upper respiratory tract disease 71,878 (25.40) 350,116 (8.16) 0.47
Non-infectious bronchus disease 15,010 (5.30) 76,480 (1.78) 0.19
Pregnancy-associated conditions
Treatment of infertility 11,288 (3.99) 33,163 (0.77) 0.21
In vitro fertilization 27,016 (9.55) 279,528 (6.51) 0.11
Threatened abortion 31,071 (10.98) 393,103 (9.16) 0.06
Maternal medication use
Antidiabetics 6,749 (2.38) 62,473 (1.46) 0.07
Antihistamines 201,528 (71.21) 1,230,367 (28.67) 0.94
Fertility drug 19,359 (6.84) 116,508 (2.71) 0.19
Inhaled corticosteroids 8,555 (3.02) 22,250 (0.52) 0.19
NSAIDs 116,592 (41.20) 558,097 (13.01) 0.67
Paracetamol 160,426 (56.69) 1,423,675 (33.18) 0.49
Obstetric conditions
Nulliparity 128,482 (45.40) 2,295,582 (53.49) 0.16
Cesarean birth 141,408 (49.97) 1,795,756 (41.85) 0.16
Multifetal pregnancies 9,311 (3.29) 76,830 (1.79) 0.10
Healthcare utilization, mean ± SD
No. of distinct diagnoses 6.79 ± 4.57 4.84 ± 3.91 0.46
No. of prescription drugs other than OCS 14.15 ± 10.48 9.50 ± 8.76 0.48
No. of outpatient visits 8.19 ± 7.71 5.35 ± 5.73 0.42
No. of inpatient visits 0.11 ± 0.44 0.08 ± 0.37 0.08
Obstetric comorbidity index 0.38 ± 0.73 0.23 ± 0.57 0.22
NSAID = nonsteroidal anti-inflammatory drug, OCS = oral corticosteroids, SD = standard deviation.
decrease in 2021, likely driven by fewer prescriptions for respiratory system diseases. This
coincides with the implementation of social distancing measures during the coronavirus
disease 2019 pandemic, which resulted in reduced respiratory infection rates.
9,10
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Any oral corticosteroid Prednisolone Methylprednisolone Other OCS a
A
0
1
2
3
4
5
6
9
8
7
2010
Year
Temporal trends in OCS prescription during pregnancy
Prevalence of OCS exposed pregnancies,
per /one.LP/zero.LP/zero.LP pregnancies
2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021
B
0
160,000
140,000
120,000
100,000
80,000
60,000
40,000
20,000
/minus.cap/five.LP/two.LP
Weeks from conception
OCS exposure before, during, and after pregnancy
Pre-pregnancy /one.LPst trimester /two.LPnd trimester /three.LPrd trimester Postpartum period
No. of prescription fills per /two.LP-week period
/nine.LP/zero.LP/six.LP/six.LP/two.LP/six.LP/one.LP/two.LPConception
date (LMP)
Delivery
date
Fig. 1. Trends of OCS prescriptions in pregnant women. Temporal trends in OCS prescription during pregnancy (A) and prescription patterns before, during and
after pregnancy (B).
OCS = oral corticosteroids, LMP = last menstrual period.
aOther OCS include deflazacort, hydrocortisone and triamcinolone.
This study has several limitations. We defined the OCS usage based on prescriptions,
which may not accurately reflect actual exposure. In addition, although we identified the
indications via the primary diagnoses of OCS prescriptions, it may not align with the actual
indications. Lastly, because the HIRA database does not contain information on the start of
pregnancy or LMP, we estimated these based on delivery dates and preterm birth diagnostic
codes. While the algorithm we used has demonstrated a high positive predictive value for
determining gestational age in administrative databases, there remains some potential for
misclassification, and further validation of this algorithm is needed within the HIRA database.
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Diseases of the respiratory system Diseases of the skin Pregnancy associated condition
Asthma Autoimmune inflammatory disease Others
A
0
5
10
15
20
25
30
50
45
40
35
2010
Year
Temporal trends in proportion of OCS indications during pregnancy
Proportion of OCS indications, %
2011 2012 2013 2014 2015 2016 2017 2018 2019 2020 2021
B OCS indications before, and during pregnancy
Pre-pregnancy
n = /five.LP/eight.LP/eight.LP,/five.LP/five.LP/zero.LP
Autoimmune inflammatory disease Asthma Diseases of the skin Diseases of the respiratory system Pregnancy associated condition Others
0 10 20 30 40 50
/zero.LP./six.LP
/one.LP./five.LP
/three.LP/one.LP./seven.LP
/four.LP/five.LP./zero.LP
/two.LP./six.LP
/one.LP/eight.LP./six.LP
60
%
/one.LPst trimester
n = /two.LP/three.LP/zero.LP,/two.LP/seven.LP/four.LP
10 20 30 40 500
/one.LP./five.LP
/one.LP./five.LP
/two.LP/eight.LP./four.LP
/four.LP/one.LP./four.LP
/one.LP/zero.LP./one.LP
/one.LP/seven.LP./one.LP
60
%
/two.LPnd trimester
n = /three.LP/five.LP,/one.LP/three.LP/zero.LP
0 10 20 30 40 50
/eight.LP./three.LP
/three.LP./seven.LP
/one.LP/nine.LP./four.LP
/two.LP/seven.LP./five.LP
/two.LP/two.LP./two.LP
/one.LP/eight.LP./nine.LP
60
%
/three.LPrd trimester
n = /three.LP/seven.LP,/eight.LP/six.LP/one.LP
0 10 20 30 40 50
/seven.LP./two.LP
/three.LP./seven.LP
/one.LP/seven.LP./zero.LP
/two.LP/five.LP./three.LP
/two.LP/five.LP./two.LP
/two.LP/one.LP./five.LP
60
%
Fig. 2. Indications of OCS prescriptions in pregnant women. Temporal trends in indications of OCS during pregnancy (A) and OCS indications according to timing
of exposure (B).
OCS = oral corticosteroids.
Overall, our findings highlight the common usage of OCS during pregnancy for various
indications. Further studies should be conducted to confirm the safety of OCS use in
pregnant populations.
Ethics statement
This study was approved by the Institutional Review Board of Sungkyunkwan University (No.
2023- 12-047), and the requirement for informed patient consent was waived as our study used
deidentified claims data.
SUPPLEMENTARY MATERIALS
Supplementary Table 1
Procedure codes used to define the live birth deliveries
Supplementary Table 2
Categorization of OCS indications using ICD- 10 codes
Supplementary Table 3
Time trend of oral corticosteroid prescription during pregnancy stratified by maternal age at
delivery