Skip to main content
Cureus logoLink to Cureus
. 2023 Oct 26;15(10):e47745. doi: 10.7759/cureus.47745

Prevalence of Selective Serotonin Reuptake Inhibitor Use Among Pregnant Women From 2017 to 2020 in King Abdulaziz Medical City, Jeddah, Saudi Arabia: A Retrospective Study

Alqassem Y Hakami 1,2,, Rami Ghazi Ahmad 2,3, Mustafa M Bukhari 1, Mohammed Assaf Almalki 1, Mamdoh M Ahmed 1, Mohammed M Alghamdi 1, Mulham A Kalantan 1, Khalil M Alsulami 1
Editors: Alexander Muacevic, John R Adler
PMCID: PMC10676232  PMID: 38021702

Abstract

Background: Perinatal depression is a mental health disorder that is associated with feelings of hopelessness, despair, and lack of motivation. Its effects on pregnant women are not limited to hemorrhage and hypertension and may lead to maternal mortality. As a result, maternal antidepressant usage during pregnancy has rapidly increased in the United States. Selective serotonin reuptake inhibitors (SSRIs) are considered one of the most prescribed antidepressants. Thus, this study aims to measure the prevalence of SSRI use during pregnancy.

Methods: A retrospective cross-sectional study was carried out in King Abdulaziz Medical City, Jeddah (KAMC-J), Saudi Arabia. The population consisted of all pregnant women aged 18 or older from the period of January 2017 to December 2020 (N=13484). The sampling technique was non-probability consecutive sampling.

Results: The study included 13,484 pregnant women, and further analysis revealed that 62 (0.459%) were exposed to at least one type of antidepressant during pregnancy. Of these, 12 (19.35%) had used more than one class of antidepressants. The majority of the sample, comprising 39 (62.90%) women, were between 34 and 44 years old. Furthermore, SSRIs were found to be the most commonly used antidepressant (41, 66.13%). In addition, fluoxetine was the most frequently prescribed antidepressant, with 23 (37.10%) patients receiving this medication. The dosage did not exceed 20 mg for the majority of the patients on SSRIs.

Conclusion: This study measured the prevalence and patterns of SSRIs and use of different antidepressant classes during pregnancy. After calculating the prevalence of each class of antidepressants among 62 pregnant women exposed to antidepressants, the analysis concluded that SSRIs are the most prescribed antidepressant during pregnancy. This study contributes to the growing body of literature on the use of antidepressants during pregnancy and highlights the need for ongoing research in this area.

Keywords: selective serotonin reuptake inhibitor (ssri), depression, antidepressant, pregnant, serotonin

Introduction

The global prevalence of prenatal anxiety and depression disorders in women is estimated to be 20% and 15%, respectively [1,2]. Studies have produced varying estimates of the prevalence of prenatal depression and anxiety based on countries’ income. The incidence of depression during pregnancy is estimated to be between 7% and 20% in high-income countries [3-8]. Meanwhile, rates of 20% or more have been documented in low- and middle-income countries, although less research has been conducted in these areas [9-12]. Furthermore, several studies have investigated the prevalence of anxiety and depression with respect to the specific trimesters during which they manifest. A meta-analysis by Dennis et al. showed that prenatal anxiety was more common in the third trimester followed by the second trimester and least common in the first trimester [2]. In addition, a systematic review by Okagbue et al. revealed that prenatal depression was more frequent in the third trimester and least frequent in the second trimester [13].

Prenatal depression, defined as depression that occurs during pregnancy, is a contributing factor to postpartum depression, which has been shown to have severe consequences on infants' and mothers' mental health [14]. Unrecognized and/or untreated prenatal depression may have an impact on both infants and mothers. Prenatal depression was shown to elevate the risk of premature birth, surgical delivery, and low birth weight [15,16]. Low birth weight and premature delivery are the major causes of infant deaths [17]. A study reported the association between maternal depression and significant pregnancy complications, such as reduced uterine artery blood flow, pre-eclampsia, pregnancy-induced hypertension, and antepartum hemorrhage [18]. As a result, screening for depression and its causes among pregnant women is highly recommended. Moreover, prevalence studies reported that selective serotonin reuptake inhibitors (SSRIs) are considered the most common antidepressants used during pregnancy [19]. Serotonin influences some of the activities in the adult brain, such as learning, memory, mood management, anxiety, fear, social, reproductive behavior, and higher mental functions [20]. Therefore, inhibiting the reuptake of this monoamine can alleviate the manifestations of mild to severe depression [21].

The management of depression in pregnancy is challenging and complicated. A "black box" warning was issued by the U.S. Food and Drug Administration (FDA) in 2004 regarding the use of SSRIs. The warning was issued due to the increased risk of suicidal ideation and behaviors in adolescents treated with SSRIs for major depressive disorder (MDD) [22]. Some studies reported an association between SSRIs and persistent pulmonary hypertension (PPHN) [23,24]. However, a study found no relation between SSRI use in pregnancy and PPHN [25]. Moreover, women who received SSRIs late in pregnancy had a higher chance of delivering small-for-gestational-age infants (SGA infants) [26]. In addition, several studies have shown an association between first-trimester exposure to SSRIs and some congenital disabilities [27-29]. The risk of preterm birth (PTB), identified as delivery before 37 weeks of gestation, is elevated with SSRI use and depression [30]. Several studies reported a higher prevalence of preterm birth in depressed pregnant women treated with SSRIs than in a control group [30-32].

Several studies that evaluated the prevalence of SSRI use among pregnant women showed similar outcomes. A study from New Zealand reported a decrease in antidepressant use in pregnant women from 2.7% to 2.6% following the first trimester [33]. Similarly, a previous cohort study found a reduction in antidepressant use over pregnancy from 23.9 per 1000 in the first trimester to 10.4 and 8.4 per 1000 pregnancies in the second and third trimesters, respectively [34]. Moreover, research published in Denmark investigated the prevalence of antidepressant exposure among pregnant women between 1997 and 2010. This latter study revealed an increase in exposure from 0.2% to 3.2% and a reduction in antidepressant exposure associated with pregnancy recognition [35]. In addition, a project in Nordic countries that explored the utilization of SSRIs among pregnant women reported a percentage of 3.3% out of 1,162,470 pregnant women who had been exposed to SSRIs. Moreover, in this study, due to concerns regarding the possible risk to the fetus, a high percentage of pregnant women quit using antidepressant medications upon the recognition of pregnancy [36]. Furthermore, a study in the United States discovered that 6% of 1,895,519 pregnant women were exposed to SSRIs. In addition, SSRI usage decreased in the later stages of pregnancy compared to the first term of pregnancy and before pregnancy [37].

Despite these studies, up to the authors' knowledge, there is a lack of information regarding the prevalence of antidepressant consumption among pregnant women in Saudi Arabia. Therefore, this study aims to address this research gap by identifying patterns and measuring the prevalence of SSRI use during pregnancy in a cross-sectional retrospective manner, including all pregnancies between January 2017 and December 2020 in King Abdulaziz Medical City in Jeddah (KAMC-J), Saudi Arabia.

Materials and methods

Design and setting

A retrospective cross-sectional study was carried out in KAMC-J, Saudi Arabia. The study population consisted of all pregnant women at KAMC-J from January 2017 to December 2020 (N=13484). The study used a non-probability consecutive sampling technique. To ensure data accuracy, a list of all pregnant women who visited the psychiatry department at KAMC-J was provided and filtered by the medical record department to include pregnant women with psychiatric disorders and depressive disorders and those over 18 years old. Following that, the authors utilized the filtered list to select participants who met the inclusion criteria, which required participants to be pregnant women aged 18 or older who had been exposed to at least one antidepressant during pregnancy. The data was extracted from the BESTCare system (patient data system) by the authors, who recorded variables, such as age, diagnosis of depression, type of antidepressant medication, dosage, and frequency of use during pregnancy on the data collection sheet. Pregnant women under the age of 18, pregnant women who had not been exposed to an antidepressant, and pregnant women without depressive and psychiatric disorders were excluded from the study. The required sample size was calculated using the Raosoft website with a 95% confidence interval (CI), a 50% response distribution, and a 5% margin of error. The minimal sample size required was calculated to be 377.

Statistical analysis

The study used IBM SPSS Statistics for Windows (released 2020; IBM Corp., Armonk, New York, United States) for data analysis. The number of pregnant women who filled at least one prescription or were actively using an antidepressant during pregnancy in the study group was used to calculate the prevalence of antidepressant usage during pregnancy. Patients were divided according to their age into the following groups: 24 and below, 25-34, 35-44, and 45 and above. Furthermore, antidepressants were divided into groups based on single or multiple drugs used by the patients. To describe categorical data, frequency and percentages were used, which were the drug groups, age, dosage, frequency, and each drug individually (i.e., SSRIs, serotonin and norepinephrine reuptake inhibitors (SNRIs), atypical antidepressants, and tricyclic antidepressants (TCAs)). Moreover, Fisher's exact test was used to compare categorical data, and p-value of <0.05 was considered statistically significant.

Ethical consideration

The patients’ data were presented using serial code numbers, and no personal information or any patient identifiers were reported. The researchers were the only ones with access to the collected data, and the Principal Investigator (PI) ensured the privacy and confidentiality of the subjects. All data, both electronic and hard copies, were stored within the premises of National Guard Health Affairs (NGHA) and accessible only by the PI. Approval was granted by the King Abdullah International Medical Research Center (KAIMRC) Institutional Review Board (study number: SP21J-107-03).

Results

The study included 13,484 women, and only 62 (0.459%) were exposed to at least one type of antidepressant during pregnancy; 19.35% used more than one class of antidepressants. Upon dividing patients according to age, 6.45% were at the age of 24 years and below, 25.81% were between the ages of 25 and 34 years, 62.90% were between the ages of 35 and 44 years, and 4.84% were at the age of 45 years and above (Table 1). However, there was no variation between age groups and the consumption of antidepressants. Furthermore, Fisher's exact test revealed no significant association between all age groups and different types of antidepressants, with a p-value >0.05.

Table 1. Prevalence of antidepressant use among age groups.

Age N N(%) P-value
35-44 39 62.90%   P-value > 0.05    
25-34 16 25.81%
24 and below 4 6.45%
45 and above 3 4.84%

Drug groups

Among the 62 pregnant women included in the study, 66.13% used SSRIs, such as fluoxetine and citalopram, while 8.06% used TCAs (amitriptyline), 4.84% used atypical antidepressants (mirtazapine), and 1.61% used SNRIs (venlafaxine). A proportion (19.36%) of the pregnant women were on multiple classes of antidepressants, 14.52% of which used a combination of SSRIs and atypical antidepressants; 3.23% of which used a combination of SSRIs, TCAs, and atypical antidepressants; and 1.61% of which used a combination of SSRIs and TCAs (Figure 1). In total, 77.42% of the pregnant women used only one medication. Moreover, 37.10% used fluoxetine, 20.97% used citalopram, 8.06% used amitriptyline, 4.84% used mirtazapine, 3.23% used escitalopram, 1.61% used fluvoxamine, and 1.61% used venlafaxine (Figure 1, Table 2). Among the patients who used different classes of antidepressants, 8.06% combined fluoxetine and mirtazapine; 6.45% combined citalopram and mirtazapine; 3.23% combined citalopram, amitriptyline, and mirtazapine; and 1.61% combined fluoxetine and amitriptyline. Some patients (3.23%) combined two types of SSRIs, with 1.61% using fluoxetine and citalopram and the other 1.61% using fluoxetine and paroxetine (Table 2).

Table 2. Prevalence of antidepressants.

Drug N N(%)
Fluoxetine 23 37.10%
Citalopram 13 20.97%
Amitriptyline 5 8.06%
Fluoxetine and mirtazapine 5 8.06%
Citalopram and mirtazapine 4 6.45%
Mirtazapine 3 4.84%
Citalopram, amitriptyline, and mirtazapine 2 3.23%
Escitalopram 2 3.23%
Fluoxetine and amitriptyline 1 1.61%
Fluoxetine and citalopram 1 1.61%
Fluoxetine and paroxetine 1 1.61%
Fluvoxamine 1 1.61%
Venlafaxine 1 1.61%

Figure 1. Prevalence of antidepressant drug usage during pregnancy.

Figure 1

The majority of pregnant women on antidepressants used SSRIs, followed by TCAs and atypical antidepressants.

Frequency and dosage of antidepressants

Regarding the dosage of antidepressant medications, 77.42% of the patients who used fluoxetine were on 20 mg dosage, 12.90% patients were on 40 mg, 6.45% were on 60 mg, and 3.23% patient’s dosage was missing. A large percentage (87.10%) of the patients used fluoxetine daily, and 12.90% patients’ frequencies were missing. Patients using citalopram (65%) were on 20 mg, 25% were on 10 mg, 5% was on 20 mg, and 5% was on 40 mg. Moreover, 85% of the patients used citalopram daily, while 15% patients' frequencies were missing. A proportion (78.57%) of the patients using mirtazapine used 15 mg, 7.14% was on 7.5 mg, 7.14% was on 30 mg, and 7.14% patient's dosage was missing. Meanwhile, 57.14% patients used mirtazapine daily, and 42.86% patients' frequencies were missing. A percentage (37.50%) of the patients who used amitriptyline were on 10 mg, 37.50% were on 50 mg, 12.50% was on 75 mg, and 12.50% were on 25 mg. All patients who used amitriptyline used it daily. One-hundred percent of escitalopram users were on 10 mg daily. The only patient using fluvoxamine was on 50 mg daily. The only patient using paroxetine was on 20 mg daily. The only patient using venlafaxine was on 150 mg daily (Table 3 and Table 4).

Table 3. Frequency of drug usage.

Drug Daily Missing
Fluoxetine 27 (87.10%) 4 (12.90%)
Citalopram 17 (85%) 3 (15%)
Mirtazapine 8 (57.14%) 6 (42.86%)
Amitriptyline 8 (100%) 0
Escitalopram 2 (100%) 0
Fluvoxamine 1 (100%) 0
Paroxetine 1 (100%) 0
Venlafaxine 1 (100%) 0

Table 4. Dosage of antidepressants during pregnancy.

Drug Dose N N(%)
Fluoxetine 20 mg 24 77.42%
  40 mg 4 12.90%
  60 mg 2 6.45%
  Missing (dose) 1 3.23%
Citalopram 20 mg 13 65%
  10 mg 5 25%
  30 mg 1 5%
  40 mg 1 5%
Mirtazapine 15 mg 11 78.57%
  30 mg 1 7.14%
  7.5 mg 1 7.14%
  Missing (dose) 1 7.14%
Amitriptyline 10 mg 3 37.50%
  50 mg 3 37.50%
  75 mg 1 12.50%
  25 mg 1 12.50%
Escitalopram 10 mg 2 100%
Fluvoxamine 50 mg 1 100%
Paroxetine 20 mg 1 100%
Venlafaxine 150 mg 1 100%

Discussion

A study conducted in the United States demonstrated that the effects of depression on pregnant women may exceed the impact of hemorrhage and hypertension and could lead to maternal mortality [38]. Moreover, the prevalence of maternal antidepressant usage during pregnancy have grown globally over the last 10 years, and the most prescribed antidepressants are SSRIs [39]. To the best of our knowledge, there is a lack of studies regarding the prevalence of antidepressant use among pregnant women in Saudi Arabia. This research aimed to calculate the prevalence of SSRI exposure during pregnancy in a cross-sectional retrospective manner, including pregnant women between January 2017 and December 2020 in KAMC-J, Saudi Arabia. This study indicates that the most prevalent class of antidepressants during pregnancy is SSRIs.

The statistical analysis confirms that among 62 women who used antidepressants during their pregnancy, 66.13% used at least one SSRI drug. The two most used medications were fluoxetine and citalopram, prescribed for around 50% and 32.3% of the sample, respectively. The observed results in this study regarding the SSRI usage during pregnancy were in line to the results in a study conducted by Zoega et al. in which SSRIs, citalopram, fluoxetine, and escitalopram were among the most commonly used antidepressants during pregnancy [36]. Another study done in the United States by Andrade et al. in 2016 reported that citalopram and fluoxetine as one of the most utilized antidepressants in pregnancy [37]. Moreover, data in this research found that there was no association between age groups and the use of antidepressants during pregnancy. A report by Zoega et al. found that antidepressants were mainly used in younger pregnant women aged 34 and less [36]. Conversely, some studies found that older women were more likely to use an antidepressant during pregnancy [40-42]. The similarity of results of this research with previous research might be due to the similarity of guidelines used in treating depressed pregnant patients. For example, the report on the management of depression during pregnancy by Yonkers et al. stated that SSRIs are the most prescribed class by physicians, while TCAs were among the least prescribed [43].

Furthermore, the safety of antidepressants played an important role in determining the percentages in data. The results in this research demonstrated that fluoxetine was the most used antidepressant. Several studies showed that fluoxetine use early in pregnancy has no significant association with major congenital malformations [44,45]. Another study from Australia showed that the use of fluoxetine early in pregnancy had higher chances of gastrointestinal tract malformations and malformations of the neck, ear, and face [46]. Moreover, fluoxetine showed higher chances of omphalocele, anencephaly, and craniosynostosis in infants compared to the control group [27]. Several cohort studies revealed that fluoxetine use early in pregnancy was associated with cardiac malformations [47-49]. Citalopram was the second most used antidepressant according to this research. Maternal use of citalopram in the early phases of pregnancy was associated with anomalies of the urinary system [46,48,50], gastrointestinal system [48,50], neural tube defects [51], omphalocele, anencephaly, and craniosynostosis [27]. In addition, citalopram usage in the first phases of pregnancy showed a higher risk of congenital heart defects [48,52,53].

By contrast, multiple studies demonstrated that in-utero exposure to SSRIs had no increased chance of major or specific cardiac malformations [27,28,51,54]. However, paroxetine was linked to a higher chance of cardiac malformations [54-56]. In addition, several studies attempted to study the association of fluoxetine and citalopram with miscarriages, and there was insignificant evidence of the association [44,57-63]. However, one study demonstrated that the underlying maternal depression played a significant role in miscarriage as the pregnant women had discontinued the use of antidepressants three to 12 months before the pregnancy [60]. Furthermore, this research showed that the majority of medications were prescribed at low doses; this could be attributed to antidepressant use guidelines, as physicians should start from the lowest dose possible to avoid side effects [64]. For example, it was reported that a high dose of venlafaxine (70 mg/kg) caused mild maternal intoxication [65,66]. Regardless of the risk-benefit assessment made at the start of the pregnancy, the best treatment options for pregnant women with depressive symptoms should be extensively reassessed.

The hospital's database system can provide accurate details on the types, doses, and names of antidepressants used by pregnant women; this results in obtaining accurate information under ethical standards that are not affected by recall bias. However, the study has some potential limitations. Compared to other studies, the sample size appears to be smaller because it is limited to women who gave birth in King Abdulaziz Medical City in Jeddah. Some of the pregnant mothers might be from rural areas, which could result in their deliveries and follow-ups occurring in other hospitals. Moreover, data regarding the complications of antidepressants on mothers and infants were unavailable due to discontinuation of follow-ups. Furthermore, some of the dosages and frequencies were missing from the database. Despite these limitations, the results of this study can serve as preliminary data for identifying the prevalence of antidepressant use among pregnant women. In addition, it highlights the need for psychiatrists and obstetricians-gynecologists to collaborate in the screening for depression in pregnant women and ensuring that they receive appropriate care and monitoring to minimize risks to both mothers and fetuses. The study also emphasizes the importance of educating pregnant women about the potential risks and benefits of antidepressants use during pregnancy and encourage them to discuss their medication use with their healthcare providers.

Conclusions

This study aimed to identify patterns and measure the prevalence of SSRIs and different antidepressant classes during pregnancy. The statistical analysis confirms that among 62 women who used antidepressants during their pregnancy, SSRIs are the most used drugs. The two most prescribed medications are fluoxetine and citalopram. Moreover, future studies are warranted to measure the prevalence of SSRI use among pregnant women over a 10-year period to obtain a larger sample size. Nevertheless, these results indicate the need for future research focusing on the side effects of SSRIs and other antidepressants on pregnant women due to the sensitivity of the population and the lack of local studies on the prevalence and complications.

Acknowledgments

The authors wish to thank the Research Office at King Abdullah International Medical Research Center (KAIMRC) and King Abdulaziz Medical City, Jeddah (KAMC-J) for its support.

The authors have declared that no competing interests exist.

Human Ethics

Consent was obtained or waived by all participants in this study. King Abdullah International Medical Research Center issued approval SP21J/107/03

Animal Ethics

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

References

  • 1.Identifying the women at risk of antenatal anxiety and depression: a systematic review. Biaggi A, Conroy S, Pawlby S, Pariante CM. https://pubmed.ncbi.nlm.nih.gov/26650969. J Affect Disord. 2016;191:62–77. doi: 10.1016/j.jad.2015.11.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Prevalence of antenatal and postnatal anxiety: systematic review and meta-analysis. Dennis CL, Falah-Hassani K, Shiri R. Br J Psychiatry. 2017;210:315–323. doi: 10.1192/bjp.bp.116.187179. [DOI] [PubMed] [Google Scholar]
  • 3.Point prevalence of psychiatric disorders during the second trimester of pregnancy: a population-based study. Andersson L, Sundström-Poromaa I, Bixo M, Wulff M, Bondestam K, åStröm M. Am J Obstet Gynecol. 2003;189:148–154. doi: 10.1067/mob.2003.336. [DOI] [PubMed] [Google Scholar]
  • 4.Cohort study of depressed mood during pregnancy and after childbirth. Evans J, Heron J, Francomb H, Oke S, Golding J. BMJ. 2001;323:257–260. doi: 10.1136/bmj.323.7307.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Perinatal depression: a systematic review of prevalence and incidence. Gavin NI, Gaynes BN, Lohr KN, Meltzer-Brody S, Gartlehner G, Swinson T. Obstet Gynecol. 2005;106:1071–1083. doi: 10.1097/01.AOG.0000183597.31630.db. [DOI] [PubMed] [Google Scholar]
  • 6.Prevalence, course, and risk factors for antenatal anxiety and depression. Lee AM, Lam SK, Sze Mun Lau SM, Chong CS, Chui HW, Fong DY. Obstet Gynecol. 2007;110:1102–1112. doi: 10.1097/01.AOG.0000287065.59491.70. [DOI] [PubMed] [Google Scholar]
  • 7.Depressive symptoms among pregnant women screened in obstetrics settings. Marcus SM, Flynn HA, Blow FC, Barry KL. J Womens Health (Larchmt) 2003;12:373–380. doi: 10.1089/154099903765448880. [DOI] [PubMed] [Google Scholar]
  • 8.Depressive disorders during pregnancy: prevalence and risk factors in a large urban sample. Melville JL, Gavin A, Guo Y, Fan MY, Katon WJ. Obstet Gynecol. 2010;116:1064–1070. doi: 10.1097/AOG.0b013e3181f60b0a. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Common mental disorders during pregnancy: prevalence and associated factors among low-income women in São Paulo, Brazil: depression and anxiety during pregnancy. Faisal-Cury A, Menezes P, Araya R, Zugaib M. Arch Womens Ment Health. 2009;12:335–343. doi: 10.1007/s00737-009-0081-6. [DOI] [PubMed] [Google Scholar]
  • 10.Prevalence and correlates of depression in pregnancy among Turkish women. Golbasi Z, Kelleci M, Kisacik G, Cetin A. Matern Child Health J. 2010;14:485–491. doi: 10.1007/s10995-009-0459-0. [DOI] [PubMed] [Google Scholar]
  • 11.Social stress and depression during pregnancy and in the postnatal period in British Pakistani mothers: a cohort study. Husain N, Cruickshank K, Husain M, Khan S, Tomenson B, Rahman A. J Affect Disord. 2012;140:268–276. doi: 10.1016/j.jad.2012.02.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Prevalence and psychosocial correlates of perinatal depression: a cohort study from urban Pakistan. Husain N, Parveen A, Husain M, et al. Arch Womens Ment Health. 2011;14:395–403. doi: 10.1007/s00737-011-0233-3. [DOI] [PubMed] [Google Scholar]
  • 13.Systematic review of prevalence of antepartum depression during the trimesters of pregnancy. Okagbue HI, Adamu PI, Bishop SA, Oguntunde PE, Opanuga AA, Akhmetshin EM. Open Access Maced J Med Sci. 2019;7:1555–1560. doi: 10.3889/oamjms.2019.270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Outcome of prenatal depression and risk factors associated with persistence in the first postnatal year: prospective study from Rawalpindi, Pakistan. Rahman A, Creed F. https://pubmed.ncbi.nlm.nih.gov/17098291. J Affect Disord. 2007;100:115–121. doi: 10.1016/j.jad.2006.10.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Antepartum depressive symptomatology is associated with adverse obstetric and neonatal outcomes. Chung T, Lau T, Yip A, Chiu H, Lee D. https://journals.lww.com/psychosomaticmedicine/Fulltext/2001/09000/Antepartum_Depressive_Symptomatology_Is_Associated.17.aspx. Psychosom Med. 2001;63:830–834. doi: 10.1097/00006842-200109000-00017. [DOI] [PubMed] [Google Scholar]
  • 16.Role of anxiety and depression in the onset of spontaneous preterm labor. Dayan J, Creveuil C, Herlicoviez M, Herbel C, Baranger E, Savoye C, Thouin A. https://doi.org/10.1093/aje/155. Am J Epidemiol. 2002;155:293–301. doi: 10.1093/aje/155.4.293. [DOI] [PubMed] [Google Scholar]
  • 17.Epidemiology and causes of preterm birth. Goldenberg RL, Culhane JF, Iams JD, Romero R. https://pubmed.ncbi.nlm.nih.gov/18177778. Lancet. 2008;371:75–84. doi: 10.1016/S0140-6736(08)60074-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.In utero exposure to selective serotonin reuptake inhibitors: evidence for poor neonatal adaptation. Moulsdale W, Hermann S. https://www.sciencedirect.com/science/article/pii/S1527336908000809 Newborn Infant Nurs Rev. 2008;8:123–130. [Google Scholar]
  • 19.The international prevalence of antidepressant use before, during, and after pregnancy: a systematic review and meta-analysis of timing, type of prescriptions and geographical variability. Molenaar NM, Bais B, Lambregtse-van den Berg MP, et al. J Affect Disord. 2020;264:82–89. doi: 10.1016/j.jad.2019.12.014. [DOI] [PubMed] [Google Scholar]
  • 20.Risks of using SSRI / SNRI antidepressants during pregnancy and lactation. Dubovicky M, Belovicova K, Csatlosova K, Bogi E. https://pubmed.ncbi.nlm.nih.gov/30123033. Interdiscip Toxicol. 2017;10:30–34. doi: 10.1515/intox-2017-0004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Chu A, Wadhwa R. StatPearls [Internet] Treasure Island (FL): StatPearls Publishing; 2023. Selective serotonin reuptake inhibitors. [PubMed] [Google Scholar]
  • 22.Antidepressants and the FDA's black-box warning: determining a rational public policy in the absence of sufficient evidence. Ho D. Virtual Mentor. 2012;14:483–488. doi: 10.1001/virtualmentor.2012.14.6.pfor2-1206. [DOI] [PubMed] [Google Scholar]
  • 23.Selective serotonin-reuptake inhibitors and risk of persistent pulmonary hypertension of the newborn. Chambers CD, Hernandez-Diaz S, Van Marter LJ, Werler MM, Louik C, Jones KL, Mitchell AA. N Engl J Med. 2006;354:579–587. doi: 10.1056/NEJMoa052744. [DOI] [PubMed] [Google Scholar]
  • 24.Maternal use of selective serotonin re-uptake inhibitors and persistent pulmonary hypertension of the newborn. Källén B, Olausson PO. Pharmacoepidemiol Drug Saf. 2008;17:801–806. doi: 10.1002/pds.1570. [DOI] [PubMed] [Google Scholar]
  • 25.Antidepressant medication use and risk of persistent pulmonary hypertension of the newborn. Andrade SE, McPhillips H, Loren D, et al. Pharmacoepidemiol Drug Saf. 2009;18:246–252. doi: 10.1002/pds.1710. [DOI] [PubMed] [Google Scholar]
  • 26.Antidepressant use during pregnancy and the risk of preterm delivery and fetal growth restriction. Toh S, Mitchell AA, Louik C, Werler MM, Chambers CD, Hernández-Díaz S. J Clin Psychopharmacol. 2009;29:555–560. doi: 10.1097/JCP.0b013e3181bf344c. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Use of selective serotonin-reuptake inhibitors in pregnancy and the risk of birth defects. Alwan S, Reefhuis J, Rasmussen SA, Olney RS, Friedman JM. N Engl J Med. 2007;356:2684–2692. doi: 10.1056/NEJMoa066584. [DOI] [PubMed] [Google Scholar]
  • 28.First-trimester use of selective serotonin-reuptake inhibitors and the risk of birth defects. Louik C, Lin AE, Werler MM, Hernández-Díaz S, Mitchell AA. N Engl J Med. 2007;356:2675–2683. doi: 10.1056/NEJMoa067407. [DOI] [PubMed] [Google Scholar]
  • 29.Maternal use of selective serotonin reuptake inhibitors and risk of congenital malformations. Wogelius P, Nørgaard M, Gislum M, et al. Epidemiology. 2006;17:701–704. doi: 10.1097/01.ede.0000239581.76793.ae. [DOI] [PubMed] [Google Scholar]
  • 30.Antidepressant use in depressed women during pregnancy and the risk of preterm birth: a systematic review and meta-analysis of 23 cohort studies. Chang Q, Ma XY, Xu XR, Su H, Wu QJ, Zhao YH. Front Pharmacol. 2020;11:659. doi: 10.3389/fphar.2020.00659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Selective serotonin reuptake inhibitor (SSRI) use during pregnancy and risk of preterm birth: a systematic review and meta-analysis. Eke AC, Saccone G, Berghella V. BJOG. 2016;123:1900–1907. doi: 10.1111/1471-0528.14144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Is the risk of preterm birth and low birth weight affected by the use of antidepressant agents during pregnancy? A population-based investigation. Cantarutti A, Merlino L, Monzani E, Giaquinto C, Corrao G. PLoS One. 2016;11:0. doi: 10.1371/journal.pone.0168115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Antidepressant dispensing before, during, and after pregnancy in New Zealand, 2005-2014. Donald S, Sharples K, Barson D, Horsburgh S, Parkin L. https://doi.org/10.1111/ajo.13352. Aust N Z J Obstet Gynaecol. 2021;61:837–845. doi: 10.1111/ajo.13352. [DOI] [PubMed] [Google Scholar]
  • 34.Patterns of antidepressant use during pregnancy: a nationwide population-based cohort study. Bénard-Laribière A, Pambrun E, Sutter-Dallay AL, et al. Br J Clin Pharmacol. 2018;84:1764–1775. doi: 10.1111/bcp.13608. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Prevalence of antidepressant use during pregnancy in Denmark, a nation-wide cohort study. Jimenez-Solem E, Andersen JT, Petersen M, Broedbaek K, Andersen NL, Torp-Pedersen C, Poulsen HE. PLoS One. 2013;8:0. doi: 10.1371/journal.pone.0063034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Use of SSRI and SNRI antidepressants during pregnancy: a population-based study from Denmark, Iceland, Norway, and Sweden. Zoega H, Kieler H, Nørgaard M, Furu K, Valdimarsdottir U, Brandt L, Haglund B. PLoS One. 2015;10:0. doi: 10.1371/journal.pone.0144474. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Use of selective serotonin reuptake inhibitors (SSRIs) in women delivering liveborn infants and other women of child-bearing age within the U.S. Food and Drug Administration's Mini-Sentinel program. Andrade SE, Reichman ME, Mott K, et al. Arch Womens Ment Health. 2016;19:969–977. doi: 10.1007/s00737-016-0637-1. [DOI] [PubMed] [Google Scholar]
  • 38.Homicide and suicide during the perinatal period: findings from the National Violent Death Reporting System. Palladino CL, Singh V, Campbell J, Flynn H, Gold KJ. Obstet Gynecol. 2011;118:1056–1063. doi: 10.1097/AOG.0b013e31823294da. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Analysis of shared heritability in common disorders of the brain. Anttila V, Bulik-Sullivan B, Finucane HK, et al. Science. 2018;360 doi: 10.1126/science.aap8757. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.National trends in antidepressant medication treatment among publicly insured pregnant women. Huybrechts KF, Palmsten K, Mogun H, Kowal M, Avorn J, Setoguchi-Iwata S, Hernández-Díaz S. https://doi.org/10.1016/J.GENHOSPPSYCH.2012.12.010. Gen Hosp Psychiatry. 2013;35:265–271. doi: 10.1016/j.genhosppsych.2012.12.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Increasing use of antidepressants in pregnancy. Cooper WO, Willy ME, Pont SJ, Ray WA. https://doi.org/10.1016/j.ajog.2007.01.033. Am J Obstet Gynecol. 2007;196:544–545. doi: 10.1016/j.ajog.2007.01.033. [DOI] [PubMed] [Google Scholar]
  • 42.Prevalence and patterns of antidepressant drug use during pregnancy. Ververs T, Kaasenbrood H, Visser G, Schobben F, de Jong-van den Berg L, Egberts T. https://doi.org/10.1007/s00228-006-0177-0. Eur J Clin Pharmacol. 2006;62:863–870. doi: 10.1007/s00228-006-0177-0. [DOI] [PubMed] [Google Scholar]
  • 43.The management of depression during pregnancy: a report from the American Psychiatric Association and the American College of Obstetricians and Gynecologists. Yonkers KA, Wisner KL, Stewart DE, et al. Gen Hosp Psychiatry. 2009;31:403–413. doi: 10.1016/j.genhosppsych.2009.04.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Birth outcomes in pregnant women taking fluoxetine. Chambers CD, Johnson KA, Dick LM, Felix RJ, Jones KL. N Engl J Med. 1996;335:1010–1015. doi: 10.1056/NEJM199610033351402. [DOI] [PubMed] [Google Scholar]
  • 45.Incidence of major malformations in infants following antidepressant exposure in pregnancy: results of a large prospective cohort study. Einarson A, Choi J, Einarson TR, Koren G. Can J Psychiatry. 2009;54:242–246. doi: 10.1177/070674370905400405. [DOI] [PubMed] [Google Scholar]
  • 46.Dispensing patterns and pregnancy outcomes for women dispensed selective serotonin reuptake inhibitors in pregnancy. Colvin L, Slack-Smith L, Stanley FJ, Bower C. Birth Defects Res A Clin Mol Teratol. 2011;91:142–152. doi: 10.1002/bdra.20773. [DOI] [PubMed] [Google Scholar]
  • 47.Selective serotonin reuptake inhibitors and risk for major congenital anomalies. Malm H, Artama M, Gissler M, Ritvanen A. Obstet Gynecol. 2011;118:111–120. doi: 10.1097/AOG.0b013e318220edcc. [DOI] [PubMed] [Google Scholar]
  • 48.Exposure to selective serotonin reuptake inhibitors and the risk of congenital malformations: a nationwide cohort study. Jimenez-Solem E, Andersen JT, Petersen M, et al. BMJ Open. 2012;2 doi: 10.1136/bmjopen-2012-001148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Paroxetine and fluoxetine in pregnancy: a prospective, multicentre, controlled, observational study. Diav-Citrin O, Shechtman S, Weinbaum D, et al. Br J Clin Pharmacol. 2008;66:695–705. doi: 10.1111/j.1365-2125.2008.03261.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Maternal depression, antidepressant prescriptions, and congenital anomaly risk in offspring: a population-based cohort study. Ban L, Gibson JE, West J, et al. BJOG. 2014;121:1471–1481. doi: 10.1111/1471-0528.12682. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Risks associated with selective serotonin reuptake inhibitors in pregnancy. Malm H, Klaukka T, Neuvonen PJ. Obstet Gynecol. 2005;106:1289–1296. doi: 10.1097/01.AOG.0000187302.61812.53. [DOI] [PubMed] [Google Scholar]
  • 52.Major congenital malformations following prenatal exposure to serotonin reuptake inhibitors and benzodiazepines using population-based health data. Oberlander TF, Warburton W, Misri S, Riggs W, Aghajanian J, Hertzman C. Birth Defects Res B Dev Reprod Toxicol. 2008;83:68–76. doi: 10.1002/bdrb.20144. [DOI] [PubMed] [Google Scholar]
  • 53.Selective serotonin reuptake inhibitors in pregnancy and congenital malformations: population based cohort study. Pedersen LH, Henriksen TB, Vestergaard M, Olsen J, Bech BH. BMJ. 2009;339:0. doi: 10.1136/bmj.b3569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Maternal use of selective serotonin re-uptake inhibitors in early pregnancy and infant congenital malformations. Källén BA, Otterblad Olausson P. Birth Defects Res A Clin Mol Teratol. 2007;79:301–308. doi: 10.1002/bdra.20327. [DOI] [PubMed] [Google Scholar]
  • 55.Antidepressant drugs during pregnancy and infant congenital heart defect. Källén B, Otterblad Olausson P. Reprod Toxicol. 2006;21:221–222. doi: 10.1016/j.reprotox.2005.11.006. [DOI] [PubMed] [Google Scholar]
  • 56.Bupropion in pregnancy and the prevalence of congenital malformations. Cole JA, Modell JG, Haight BR, Cosmatos IS, Stoler JM, Walker AM. Pharmacoepidemiol Drug Saf. 2007;16:474–484. doi: 10.1002/pds.1296. [DOI] [PubMed] [Google Scholar]
  • 57.Pregnancy outcome following maternal use of the new selective serotonin reuptake inhibitors: a prospective controlled multicenter study. Kulin NA, Pastuszak A, Sage SR, et al. JAMA. 1998;279:609–610. doi: 10.1001/jama.279.8.609. [DOI] [PubMed] [Google Scholar]
  • 58.Pregnancy outcomes following use of escitalopram: a prospective comparative cohort study. Klieger-Grossmann C, Weitzner B, Panchaud A, Pistelli A, Einarson T, Koren G, Einarson A. J Clin Pharmacol. 2012;52:766–770. doi: 10.1177/0091270011405524. [DOI] [PubMed] [Google Scholar]
  • 59.Prenatal antidepressant exposure and risk of spontaneous abortion - a population-based study. Kjaersgaard MI, Parner ET, Vestergaard M, et al. PLoS One. 2013;8:0. doi: 10.1371/journal.pone.0072095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Exposure to selective serotonin reuptake inhibitors in early pregnancy and the risk of miscarriage. Andersen JT, Andersen NL, Horwitz H, Poulsen HE, Jimenez-Solem E. Obstet Gynecol. 2014;124:655–661. doi: 10.1097/AOG.0000000000000447. [DOI] [PubMed] [Google Scholar]
  • 61.Use of antidepressants during pregnancy and the risk of spontaneous abortion. Nakhai-Pour HR, Broy P, Bérard A. CMAJ. 2010;182:1031–1037. doi: 10.1503/cmaj.091208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Pregnancy outcome following first-trimester exposure to fluoxetine (Prozac) Pastuszak A, Schick-Boschetto B, Zuber C, et al. https://pubmed.ncbi.nlm.nih.gov/8474204/ JAMA. 1993;269:2246–2248. [PubMed] [Google Scholar]
  • 63.Gestational exposure to antidepressants and the risk of spontaneous abortion: a review. Broy P, Bérard A. Curr Drug Deliv. 2010;7:76–92. doi: 10.2174/156720110790396508. [DOI] [PubMed] [Google Scholar]
  • 64.Benefit of small dose antidepressants for functional dyspepsia: experience from a tertiary center in eastern China. Luo L, Du L, Shen J, Cen M, Dai N. https://pubmed.ncbi.nlm.nih.gov/31593119. Medicine (Baltimore) 2019;98:0. doi: 10.1097/MD.0000000000017501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.The effect of venlafaxine on behaviour, body weight, and striatal monoamine levels on sleep-deprived female rats. De Oliveira RA, Cunha GMA, M. Borges KD, et al. https://www.sciencedirect.com/science/article/pii/S0091305704002795. Pharmacol Biochem Behav. 2004;79:499–506. doi: 10.1016/j.pbb.2004.09.001. [DOI] [PubMed] [Google Scholar]
  • 66.Effect of prenatal administration of venlafaxine on postnatal development of rat offspring. Dubovický M, Császárová E, Brnoliaková Z, Ujházy E, Navarová J, Mach M. Interdiscip Toxicol. 2012;5:92–97. doi: 10.2478/v10102-012-0016-3. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Cureus are provided here courtesy of Cureus Inc.

RESOURCES