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Abstract
Objectives To develop an algorithm to identify pregnancy episodes in women at childbearing age using SIDIAP (Information System for the Improvement of Research in Primary Care) data (Catalunya, Spain).
To describe drugs dispensed during gestation.
Design Construction of an algorithm to identify all pregnancy episodes occurred from January 2011 to June 2020 in women aged 12–50. The variables used to create the algorithm include first day of last menstrual period, reasons for pregnancy termination and diagnoses registered in the primary healthcare records. Population-based cohort study including the pregnancy episodes identified by the algorithm.
Setting Catalonia, Spain.
Participants All women aged 12–50 with at least one pregnancy episode occurred during January 2011–June 2020.
Interventions No interventions performed.
Primary and secondary outcome measures Identification of pregnancy episodes through an algorithm and description of drug exposure.
Results We identified 327 865 pregnancy episodes in 250 910 people with a mean age of 31.3 years. During the study period, 83.4% of the episodes were exposed to at least one drug. The most frequent groups dispensed were iron preparations (48% of pregnancy episodes), iodine therapy (40.2%), analgesics and antipyretics (28%), penicillins (19.8%), vitamin B12 plus folic acid (19.7%) and non-steroidal anti-inflammatory drugs (NSAIDs, 15.1%). The supplements were more frequently dispensed at least twice, and the drugs for acute conditions were mainly dispensed only once during the pregnancy episode.
Conclusions We developed an algorithm to automatically identify the pregnancy periods in SIDIAP.
We described prescription drugs used during pregnancy. The most used ones were supplements, analgesics, NSAID or antibiotics.
SIDIAP might be an efficient database to study drug safety during pregnancy and the consequences of drug use in the offspring.
Trial registration number EUPAS37675.
- Reproductive medicine
- CLINICAL PHARMACOLOGY
- PRIMARY CARE
Data availability statement
Data are available on reasonable request. All data relevant to the study are included in the article or uploaded as online supplemental information. The datasets generated and/or analysed during the current study are not publicly available due to patient privacy and data protection concerns, but they are available from the corresponding author on reasonable request. All data generated or analysed during this study are included in this published article and its supplementary information files.
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
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STRENGTHS AND LIMITATIONS OF THIS STUDY
One limitation of the algorithm development is the lack of information on women whose pregnancies are followed up in the hospital or in private settings.
Other limitation of the algorithm is that it has not been validated. Nevertheless, the number and distribution of pregnancies are in line with the previous algorithms published.
Despite these limitations, Information System for the Improvement of Research in Primary Care database might be a valid and efficient resource to study drug safety during pregnancy, as it captures clinical information of most of the Catalan population.
Introduction
Drug use during pregnancy and breast feeding has not been widely analysed due to the exclusion of pregnant and lactating people from the participation in clinical trials for ethical reasons and due to the generalised lack of investigation in women’s health.1–3 However, the use of drugs during gestation and breast feeding may entail risk of different health problems for these women and for the fetus and the newborns1 4 and also the non-use of certain drugs can lead to worsening of chronical and acute conditions in the mother or to complications for the infant, such as drugs to treat asthma,5 6 autoimmune disorders,7 8 diabetes9 10 or epilepsy.11
Deciding and planning on pharmacotherapy based on the safety profile of a drug during those periods can be challenging for prescribers. For this reason, it is necessary to assess drug safety through postapproval observational studies for drugs which cannot be discontinued during pregnancy, drugs to treat pregnancy-related conditions and drugs with preclinical evidence of risk for the offspring.12 13
Apart from birth cohorts established worldwide to gain knowledge on perinatal health,14 in the last decades, database studies are offering numerous advantages to study medicines safety in pregnant and lactating women and in their offspring, such as the large number of people included, the availability of mother–child linked data, long follow-up periods, information on consequences derived from drug use or on confounders or the possibility to design algorithms through machine learning methods.13 15–18 Algorithms are often necessary because electronic health records (EHR) lack of a unique register to unambiguously identify the gestation periods. Thus, it is usual to design algorithms to identify pregnancies with the purpose of studying drug use during gestation through database studies.17 19 20
We aimed to develop an algorithm to identify pregnancy episodes for all women aged from 12 to 50 between January 2011 and June 2020 using data from the EHR of primary healthcare (PHC) in Catalunya, Spain. With the pregnancies identified by the algorithm we aimed to describe the drugs dispensed during gestation.
Methods
Study design
First, construction of an algorithm to identify all pregnancy episodes occurred from January 2011 to June 2020 in women at childbearing age (12–50 years) in Catalonia, Spain. And second, population-based cohort study including the pregnancy episodes identified by the algorithm.
Data source
The study data source is the Information System for the Improvement of Research in Primary Care (SIDIAP),21 22 which captures clinical information of approximately 5,8 million Catalan citizens (around 80% of the Catalan population). This information is pseudonymised and it is originated from different data sources: (1) (EHR in PHC of the Catalan Health Institute); including sociodemographic characteristics, comorbidities registered as International Classification of Diseases (ICD)-10 codes,23 specialist referrals, clinical parameters, toxic habits, sickness leave, date of death, laboratory test data and drug prescriptions issued in PHC, registered as Anatomical Therapeutic Chemical (ATC) classification system codes.24 (2) Sexual and reproductive healthcare (ASSIR) records, which is the EHR module used by gynaecologists and midwives to register variables related with the sexual and reproductive health of women and follow-up of pregnancies, as date of last menstrual period (LMP), gestational week, date of delivery or pregnancy termination—based on ultrasound results—or termination outcomes. (3) Pharmacy invoice data corresponding to the PHC drug prescriptions, classified according to the ATC classification.24
We used pregnancy-related ICD-10 codes and ASSIR records to design the pregnancy algorithm.
Variables
The variables collected to describe the study population at the pregnancy start date (PSD) were: age, socioeconomic status by MEDEA (Mortalidad en áreas pequeñas Españolas y Desigualdades socioEconómicas y Ambientales) index,25 body mass index, comorbidities, smoking status and alcohol intake; for this study the latter two correspond to records of less than 12 months before PSD.
We used the pharmacy invoice dispensing data to assess the drug exposure. Pregnancy episodes were classified as exposed to drugs when there was at least one dispensing from 30 days before PSD up to 30 days after delivery date, and per pregnancy trimester as follows; first trimester: from 30 days before PSD to 120 days after PSD; second trimester: from 120 days after PSD to 210 days after PSD and third trimester: from 210 days after PSD to 30 days after delivery date. This definition of the pregnancy trimesters was done for exposure definition purposes in order to consider the particularities of the pharmacy invoice register.
We described the most dispensed pharmacological groups (ATC) in overall pregnancies and by trimester, the frequency of groups with one or more than one dispensing during the pregnancy episode, and the most frequent active principles dispensed more than once.
Algorithm development
We created a three-step sequential algorithm to identify the pregnancy episodes occurring during the study period, define their duration and the outcome of the pregnancy.
Step 1: identification of potential pregnancies
We carried out a hierarchical and mutually exclusive search in our data source of records linked to gestation. We used the specific record of LMP to identify a potential pregnancy registered in ASSIR. If LMP was not available, the algorithm searched for the following records (figure 1): positive pregnancy test, gestational week, fetal death and PHC diagnoses indicating pregnancy or abortion (ICD-10 codes). See online supplemental table 1 for full list of codes.
Supplemental material
Algorithm flow chart with selection and validation steps. The figure shows the flow chart with the algorithm steps. ASSIR, sexual and reproductive healthcare centres; ICD-10, International Classification of Diseases 10th version.
Step 2: length of pregnancy
We determined the length of pregnancy using the LMP, the pregnancy episode end date (delivery or abortion), the diagnostic codes dates suggestive of pregnancy end and the weeks of gestation registries in ASSIR. If dates were unknown, they were imputed according to the criteria established (figure 1). Pregnancy episodes shorter than 4 or longer than 43 weeks were excluded.
Step 3: outcome of pregnancy
Reasons for pregnancy termination were identified by the ASSIR end label and completed by ICD-10 diagnoses related to childbirth or the puerperium. We imputed an outcome for episodes with unknown outcome and known length: abortion for length <24 weeks and live birth if ≥24 weeks (threshold for fetal viability/feasibility).
During the development of the algorithm, pregnancy episodes were scrutinised for potential inconsistencies, such as pregnancy duration discrepancy with pregnancy outcomes, overlapping episodes, those starting or terminating out of the study period after imputation dates and finally a minimum time lapse of 4 weeks was established between the dates of the different episodes.
Study size
The study size included all pregnancy episodes identified through the algorithm in women aged 12–50 during the study period.
Statistical analysis
After identifying all women with pregnancy episodes defined by the algorithm, we described the study population and the drug exposure, using frequencies and percentages for categorical variables and mean and SD for continuous variables.
Missing values on baseline variables are reported in table 1. Missing data for PSD, end date and labels of pregnancy termination outcomes were imputed as explained in the Algorithm development.
Baseline sociodemographic and clinical characteristics of the women with pregnancy episodes included in the study
All analyses were conducted with R software (V.4.1 or superior).
Patient and public involvement statement
The Research Ethics Committee of IDIAPJGol has patient and public representation who participated in reviewing and approving the study protocol.
Results
From January 2011 to June 2020, our algorithm identified 327 865 pregnancy episodes in 2 50 910 women (1.3 episodes per woman), and a total sum of follow-up of 210,463.1 years (1.6 episodes/year). These women had a mean age of 31.3 years, and 56.8% of the episodes occurred between 30 and 39 years of age. When we analysed the data from the registry of the pregnancy episodes defined by the algorithm, 76.8% of them had complete data on the start and end of the pregnancy and the results of the episode in the EHR. Out of them, 80.6% of pregnancy episodes ended with live births, 19.2% resulted in abortion, 0.15% were stillbirths and 0.08% were ectopic or molar pregnancies (online supplemental figure).
Supplemental material
Baseline sociodemographic and clinical characteristics of pregnant women at PSD are included in table 1. Among the most frequent comorbidities at baseline, 24.5% of women had an active diagnosis of anxiety, 14.5% were obese and 9.1% had a respiratory disease. Smoking and alcohol habits had a high number of missing values at PSD.
During the period studied, 274 799 (83.4%) of the pregnancy episodes were exposed to at least one drug. The most dispensed pharmacological groups during the overall pregnancies and by trimester are shown in figure 2. Overall, the most frequent groups were iron preparations (dispensed in 48.0% of the pregnancy episodes), iodine therapy (40.2%), other analgesics and antipyretics (28.0%), penicillins (19.8%), vitamin B12 with folic acid (19.7%) and non-steroidal anti-inflammatory drugs (NSAID, 15.1%). In online supplemental table, we show the 15 most frequently dispensed groups and active principles during the overall pregnancies and by trimester.
Frequency of drug exposure during overall pregnancy episodes and by trimester. The figure includes the six most dispensed pharmacological groups during the overall pregnancy episodes and by trimester, in percentages calculated over the number of pregnancy episodes. NSAID, non-steroidal anti-inflammatory drug.
Of the most used pharmacological groups, the supplements were more frequently dispensed at least twice during the pregnancy episode (69.6% for iodine, 62.5% for iron or 50.7% for vitamin B12 and folic acid) and the drugs used for acute conditions were mainly dispensed only once during the episode (83% of NSAID dispensing, 78.4% of penicillins and 69.3% of other analgesics and antipyretics, see table 2).
Exposure to the most frequent pharmacological groups during pregnancy
The most dispensed substances from these frequent ATC groups are shown in figure 3, being the combination of iodide, vitamin B12 and folic acid (42.5% of episodes), ferrous sulfate (37.6%) and paracetamol (31.1%) the most used drugs. Other frequent drugs dispensed were antibiotics (eg, fosfomycin: 14.8%).
Most frequent drugs with more than one dispensing per pregnancy episode. The figure shows the most dispensed substances within the most frequent pharmacological groups dispensed during pregnancy, in percentages calculated over the number of pregnancy episodes.
Discussion
In the absence of a unique register to identify pregnancies in our setting, we designed the algorithm in the current research context where many algorithms have been published aiming to identify pregnancies and assess drug exposure risks during pregnancy.17 19 20 26 27 Once generated, we identified 327 865 pregnancy episodes in a cohort of women at childbearing age attended in PHC from 2011 to 2020, accounting for 1.3 episodes per woman, which matches the observed numbers in Catalonia (1.21) and Spain (1.19).28 29 The type of pregnancy end identified with our algorithm was similar to BIFAP algorithm, which identified 21.5% pregnancy losses, 0.8% ectopic pregnancies and 0.2% stillbirths.17 The first step of our algorithm consisted in searching for the LMP, which is a pregnancy-related specific date which is only registered in the ASSIR records at the pregnancy monitoring initiation, so we considered it as the highest quality registry to identify PSD.
Regarding the clinical characteristics of the population studied, it is remarkable the high number of missing records for tobacco and alcohol habits in pregnant women in our database (91.2% of smoking missing values the prior 12 months vs 22.1% of smoking missing values any time before PSD). It may be recommendable to reinforce the need to record these variables more accurately so health professionals attending pregnant people may initiate smoking cessation interventions when necessary.30
With regard to the most common comorbidities at PSD, it is noteworthy that nearly 25% of pregnant women in our study had a diagnosis of anxiety, which is frequently described in women at childbearing age with other concomitant mental disorders such as depression,31–34 which also showed a significant prevalence in our cohort (5.7%). Respiratory diseases or migraine were frequent in our cohort, these disorders have commonly been reported during pregnancy with the challenges associated to their management.5 6 35 36
Dispensation of drugs was frequent in the identified pregnancy episodes. Among the most prescribed, supplements are recommended during pregnancy.30 37 Drugs used for acute conditions, such as NSAID, analgesics or antibiotics, were also identified, as during pregnancy infectious diseases or pain conditions are also frequently reported. We need to point out that supplements or analgesics counts might be under-reported due to the availability of over the counter (OTC) medicines, not captured in our database. Other OTC drugs that can be underestimated include antacids or laxatives, which are frequently used by gestating women.19 38 39 Among the most frequent antibiotics we found fosfomycin and amoxicillin, which might have been prescribed for common infections during pregnancy such as urinary tract infections.30 40
Despite the high prevalence of anxiety disorders in our cohort, anxiolytic or antidepressant drugs were not among the most used pharmacological groups. This may be related with the absence of evidence and safety concerns on the use of psychotropic medications during pregnancy.41–43 Other studies have reported similar levels of utilisation of these drugs.44–46
One limitation of our study concerning the algorithm development is the lack of information on women whose pregnancies are followed up in the hospital or in private settings. The pregnancies referred to hospitals for follow-up include those women with chronic and autoimmune diseases which can increase the risk of complications during the pregnancy or at delivery. Although each ASSIR has different referral protocols, some of the conditions include: history of miscarriages, history of chromosomal anomalies, history of prematurity, morbid obesity, pre-eclampsia, gestational diabetes, severe anaemia, etc.30 Other limitation is the lack of a specific validation of the algorithm. Nevertheless, the number and distribution of pregnancies and the drug use during gestation are in line with previous studies,17 19 and similar to the Catalan28 and Spanish29 official data.
As pointed out, some of the drug counts in our study might be underestimated, as we are not able to capture OTC drugs, which are frequently used by pregnant women and are often not registered in EHR, being one of the usual limitations of these type of studies.18 19 47
Despite the limitations, SIDIAP database might be a valid and efficient resource to study drug safety during pregnancy, as it captures clinical information of most of the Catalan population, we have developed an algorithm to automatically identify the pregnancy periods, and an algorithm to link mother and child pairs has also been developed and can be used to study pregnancy outcomes. It is an algorithm which establishes mother and child pairs linked through national insurance number and coinsurance status.48 We have also mapped SIDIAP pregnancy data to the ConcePTION common data model, which has demonstrated its potential to address questions about utilisation, effectiveness and safety of medicines during pregnancy and lactation.49 All of this might help to fill the gap in the currently available evidence, as safety concerns on drug use during pregnancy affect not only women, but also the fetus and the newborns, and it is also applicable to the lactation period, which we are also planning to assess within our database.
Conclusions
We have developed an algorithm to automatically identify the pregnancy periods, which will allow us to study not only the drug use in pregnant people, but its consequences in these women’s health and in their offspring’s.
We have described the use of prescription drugs in a large cohort of pregnant women. The most used drugs during pregnancy were recommended supplements and drugs used for acute conditions, such as analgesics, NSAID or antibiotics.
SIDIAP database might be an efficient resource to study drug safety during pregnancy.
Data availability statement
Data are available on reasonable request. All data relevant to the study are included in the article or uploaded as online supplemental information. The datasets generated and/or analysed during the current study are not publicly available due to patient privacy and data protection concerns, but they are available from the corresponding author on reasonable request. All data generated or analysed during this study are included in this published article and its supplementary information files.
Ethics statements
Patient consent for publication
Ethics approval
This study involves human participants and the study protocol was approved by the Research Ethics Committee of IDIAPJGol. Number 19/107-P, 26 June 2019. This is a database research study which has been conducted according to the guidelines of the Declaration of Helsinki (Fortaleza, Brazil 2013) and does not require consent from the people included to participate or for publication. The need for consent was waived by the Research Ethics Committee of IDIAPJGol as it is deemed unnecessary according to European legislation (Regulation (EU) 2016/679).The need for consent was waived by the Research Ethics Committee of IDIAPJGol as it is deemed unnecessary according to European legislation (Regulation (EU0) 2016/679).
Acknowledgments
The authors want to thank María Aragón and Clara Rodríguez for the data acquisition process from SIDIAP database.
References
Supplementary materials
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Footnotes
Contributors MLV: conceptualisation, study design, data curation, writing (original draft), review and editing. AG-L: conceptualisation, study design, data curation, writing, review and editing. OP-V: study design, data curation, formal analysis and review. CVC: data curation, formal analysis, writing (original draft), review and editing. JRM: conceptualisation, study design, data curation and review. CVU: conceptualisation, study design, writing, review and editing. MG-S: conceptualisation, study design, data curation, writing (original draft), review and editing. RM: conceptualisation, data curation, study design, writing, review and editing. MG-S is responsible for the overall content as the guarantor.
Funding This study received funding from the 8th call for SIDIAP grants, 2018–2019, expedient number 4R18/188; and from Health Department of the Generalitat de Catalunya, in the call corresponding to 2021 for the granting of funding of the Strategic Plan for Research and Innovation in Health (PERIS) 2021–2024, modality Research Projects in Primary Care, expedient number SLT/21/000068.
Competing interests None declared.
Patient and public involvement Patients and/or the public were involved in the design, or conduct, or reporting, or dissemination plans of this research. Refer to the Methods section for further details.
Provenance and peer review Not commissioned; externally peer reviewed.
Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.