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Article

Prevalence and Risk Factors of Depression and Anxiety among Women in the Last Trimester of Pregnancy: A Cross-Sectional Study

by
Anca Ioana Cristea Răchită
1,
Gabriela Elena Strete
2,3,*,
Andreea Sălcudean
4,*,
Dana Valentina Ghiga
5,
Flavia Rădulescu
6,
Mihai Călinescu
7,
Andreea Georgiana Nan
8,
Andreea Bianca Sasu
8,
Laura Mihaela Suciu
9 and
Claudiu Mărginean
9
1
Doctoral School, “George Emil Palade” University of Medicine, Pharmacy, Science and Technology from Târgu Mureș, 540139 Târgu Mureș, Romania
2
Department of Psychiatry, “George Emil Palade” University of Medicine, Pharmacy, Science and Technology from Târgu Mureș, 540136 Târgu Mureș, Romania
3
Mental Health Center, Mureș County Clinical Hospital, 540072 Târgu Mureș, Romania
4
Department of Ethics and Social Sciences, “George Emil Palade” University of Medicine, Pharmacy, Science and Technology from Târgu Mureș, 540136 Târgu Mureș, Romania
5
Department of Medical Scientific Research Methodology, “George Emil Palade” University of Medicine, Pharmacy, Science and Technology from Târgu Mureș, 540136 Târgu Mureș, Romania
6
Department of Endocrinology, “George Emil Palade” University of Medicine, Pharmacy, Science and Technology from Târgu Mureș, 540136 Târgu Mureș, Romania
7
Graduate of Cluj School of Public Health, Babes-Bolyai University Cluj Napoca, 400347 Cluj-Napoca, Romania
8
First Department of Psychiatry, Clinical County Hospital, 540139 Târgu Mureș, Romania
9
Department of Obstetrics and Gynecology Clinic II, “George Emil Palade” University of Medicine, Pharmacy, Science and Technology from Târgu Mureș, 540136 Târgu Mureș, Romania
*
Authors to whom correspondence should be addressed.
Medicina 2023, 59(6), 1009; https://doi.org/10.3390/medicina59061009
Submission received: 20 March 2023 / Revised: 16 May 2023 / Accepted: 22 May 2023 / Published: 24 May 2023
(This article belongs to the Section Psychiatry)

Abstract

:
Pregnancy represents a psychologically and emotionally vulnerable period, and research indicates that pregnant women have a higher prevalence of symptoms of anxiety and depression, debunking the myth that hormonal changes associated with pregnancy protect the mother. In recent years, several researchers have focused on the study of prenatal anxiety/depression—emotional disorders manifested by mood lability and low interest in activities—with a high prevalence. The main objective of this research was to conduct an antenatal screening in a cohort of pregnant women hospitalized for delivery in order to assess the prevalence of anxiety and depression. The secondary objective was to identify the risk factors associated with depression and anxiety in women in the third trimester of pregnancy. We carried out a prospective study in which we evaluated 215 pregnant women in the third trimester of pregnancy hospitalized for childbirth at the Obstetrics and Gynecology Clinic of the Târgu-Mureș County Clinical Hospital. The research was carried out between December 2019 and December 2021. The results showed that age and the environment of origin are the strongest predictors of mental health during pregnancy (OR = 0.904, 95%CI: 0.826–0.991; p = 0.029). For women from urban areas, there is an increased probability of falling at a higher level on the dependent variable (moderate depression) (OR = 2.454, 95%CI: 1.086–5.545; p = 0.032). In terms of health behaviors, none of the variables were statistically significant predictors of the outcome variable. The study highlights the importance of monitoring mental health during pregnancy and identifying relevant risk factors to provide appropriate care to pregnant women and the need for interventions to support the mental health of pregnant women. Especially in Romania, where there is no antenatal or postnatal screening for depression or other mental health conditions, these results could be used to encourage the implementation of such screening programs and appropriate interventions.

1. Introduction

Pregnancy represents a psychologically and emotionally vulnerable period, and research indicates that pregnant women have a higher prevalence of symptoms of anxiety and depression, debunking the myth that hormonal changes associated with pregnancy protect the mother. Pregnancy and the postpartum period are accepted by the scientific community as periods of increased circumstantial vulnerability to developing psychological distress [1].
Depression and anxiety are prevalent mental health conditions that can affect women during pregnancy, particularly in the last trimester. Several contributing factors have been identified that may increase the likelihood of experiencing these conditions during pregnancy. These can include a history of mental health disorders, personal or family history of depression or anxiety, previous traumatic life experiences, high levels of stress, lack of social support, and financial difficulties [2].
In recent years, there has been a growing interest among researchers in studying prenatal anxiety and depression, which are emotional disorders characterized by mood instability and decreased interest in activities. The prevalence of these disorders during pregnancy has been reported to range from 10 to 29.6% [3,4]. For perinatal depression, the global prevalence is estimated at 19.2% [5], with meta-analysis showing that the prevalence tends to be higher in the second and third trimesters (12.4%) than in the first trimester (7.4%) [6].
As such, prenatal anxiety and depression represent significant mental health concerns for pregnant women and their offspring. Identifying the risk factors, causes, and consequences of these disorders is critical for developing effective interventions to mitigate their negative impact.
Mothers from resource-limited environments may be particularly vulnerable to perinatal depression, with the prevalence of this condition potentially even higher in this group [7]. This could be attributed to various factors, such as low income and inadequate healthcare systems, which can act as risk factors for maternal psychopathology. Importantly, it should be noted that women who exhibit symptoms of depression and anxiety both before and during pregnancy may have an elevated risk of postnatal depression [8], which can adversely impact the child’s development. Therefore, it is crucial to identify and address these mental health conditions among pregnant women, especially in resource-limited settings where they may be more prevalent and have more significant consequences. Adequate healthcare access and appropriate interventions can help mitigate the risks of perinatal depression and its sequelae for both the mother and child [6]. According to a recent review, prenatal depression emerges as the most potent predictor of postnatal depression [9]. Non-psychotic depression is associated with sadness, hopelessness, sleep disturbances, fatigue, loss of appetite, feelings of worthlessness, lack of concentration, low self-esteem, and numerous neurotic-phobic symptoms [9].
Several studies have posited that the activation of the maternal stress response and alterations in the maternal endocrine and inflammatory systems have a significant role in the etiology of the effects on pregnancy and child development [10,11,12,13,14]. To date, a substantial body of literature has shown that stress during pregnancy can have an adverse impact on both pregnancy outcomes and the physiological development and behavior of offspring [10,15,16,17].
Notably, in most Eastern nations, prenatal check-ups primarily prioritize the physical health of pregnant women, with comparatively lesser emphasis placed on their emotional and mental health conditions. The prevalence of perinatal depression in Central and Eastern Europe is poorly known [18,19].
In Romania, there is no antenatal screening for depression or other mental health conditions, nor is there any screening in the postpartum period [20,21].

Objectives

The main objective of this research was to conduct an antenatal screening in a cohort of pregnant women hospitalized for delivery, in order to assess the prevalence of anxiety and depression.
The secondary objective was to identify the risk factors associated with depression and anxiety in women in the third trimester of pregnancy.
It is important to understand the prevalence of perinatal depression and find a screening method that is quick and easy to administer so that it can be used in prenatal and postnatal family care. Early identification of perinatal depression is essential to ensure proper care for both mother and child, as this condition can have serious consequences if left untreated. However, perinatal depression is a treatable condition and there is evidence that treatment can be beneficial for both mother and child. Therefore, it is important to act accordingly to prevent and treat it.

2. Materials and Methods

2.1. Study Design

We carried out a prospective study in which we evaluated 215 pregnant women in the third trimester of pregnancy, hospitalized for childbirth, at the Obstetrics and Gynecology Clinic of the Târgu-Mureș County Clinical Hospital. The research was carried out between December 2019 and December 2021.
The research was conducted following the guidelines outlined in the Declaration of Helsinki and was approved by the Ethics Committee of the “George Emil Palade” University of Medicine, Pharmacy, Science, and Technology in Târgu Mureș. (No. 199/14/06/2019).

2.2. Participants and Procedure

A total of 215 patients expressed their desire to participate in the study, selected based on the following inclusion criteria: age ≥ or equal to 16 years, with a minimum level of education (be able to read and understand a text), third trimester of pregnancy (week 28–40), the patient’s consent.
The demographic questionnaire developed by us included 11 items, including demographic and health data (age of patients ≥ 16 years, the environment of origin, marital status, educational status, social statute, pregnancy type, gestational age, the number of pregnancies, complications arising in the third trimester of pregnancy, tobacco use, alcohol consumption).
Trained and qualified staff members distributed all questionnaires to participants, and each patient was provided with information about the importance and implications of the study, as well as their rights to data protection. Informed consent was obtained from all participants prior to their inclusion in the study. This ethical approach ensured that participants were fully informed and empowered to make an informed decision about their participation in the study and that their privacy and confidentiality were protected throughout the research process.
As exclusion criteria, we considered the following aspects: patients who did not fill in the full questionnaire, and patients with a history of mental disorders (patients with a past history of mental disorders may be considered as potential risk factors for the development of antenatal depression).
Because anxiety and depression are frequently associated disorders, almost impossible to distinguish from each other, they are assessed using scales. We opted for the following scales: HADS and EDPS for screening, and the Hamilton scale (anxiety/depression) for severity assessment.

2.3. Measures

Due to the fact that the patients were hospitalized for childbirth, we used the Hospital Anxiety and Depression Scale (HADS), developed by Zigmond and Snaith in 1983 [22], for screening depression and anxiety.
The Romanian version of the HADS scale presents adequate reliability and validity and was first created by Dr. Radu Teodorescu and published in Sinapse magazine (1996). In Romania, the validity of HADS has been confirmed both among adult psychiatric and medical patients, and validation studies have shown the high internal consistency of both subscales: HADS-A (Cronbach’s α ranges from 0.68 to 0.93) and HADS-D (Cronbach’s α ranges from 0.67 to 0.90). The scale was validated in the Romanian psychiatric population by Dr. Maria Ladea [23] in her doctoral thesis and includes 14 items regarding the intensity of anxiety and depression feelings. Each item is evaluated on a 4-point Likert scale, from 0 = never to 3 = always. A score between 0 and 7 indicates the absence of depression/anxiety, a score between 8 and 10 indicates mild symptoms, while a score above 11 indicates the presence of a case that requires additional attention. For patients who scored above 11, it was necessary to differentiate anxiety from depression, using the additional Hamilton Anxiety Scale (HAMA) and Hamilton Depression Rating Scale (HDRS). As reference values, we consider that a score below 6 indicates a non-clinical case, while a score above 6 indicates a clinical case.
For the assessment of depression severity, we utilized the Hamilton Depression Rating Scale (HAMD), also known as the Hamilton Depression Rating Scale [24]. This scale quantifies the severity of depression in patients who have already received a diagnosis of depression. In clinical practice, the 17-item version is commonly used as Hamilton himself recommended that the last four items (diurnal variation, depersonalization/derealization, paranoid symptoms, and obsessive-compulsive symptoms) not be included in the total score, as these symptoms are not reflective of the overall severity of depression [25] Hamilton constructed the scale to quantify information from the patient, taken by an experienced clinician based on an unstructured interview (without specifying questions or evidence). The total score represents the following: 0–7 absence, 8–16 mild, 17–22 moderate, ≥23 severe.
Although some items on the scale are rated on a scale of 0 to 8, while others are rated on a scale of 0 to 4, the total score of the 17 items has a strong correlation of 0.93 with the first-factor score. This demonstrates that the scale is effective in providing a straightforward method for measuring the severity of a patient’s condition and tracking changes in their condition over time [26].
The Hamilton Anxiety Scale (HAMA) [27] was employed to gauge the severity of anxiety. The scale consists of a semi-structured interview with 14 items that assess both cognitive and somatic symptoms of anxiety, and the maximum score is 56. The examiner assigns scores from 0 to 4 to each item. The scores represent the following: 0—absent, indicating that the subject has never experienced these symptoms; 1—weak, indicating that symptoms occur irregularly and for brief periods; 2—moderate, indicating that symptoms manifest consistently for certain periods, requiring the subject’s effort to deal with them; 3—severe, indicating that symptoms are continuous and dominate the subject’s life; and 4—very severe, indicating that symptoms are disabling and impede the subject’s activities. The total score represents the following: 0–4 normal, 5–10 mild, 11–16 moderate, ≥17 severe. The scale permits a comprehensive evaluation of both psychological (e.g., mental stress, anxiety state) and somatic (e.g., associated biophysiological changes) symptoms of anxiety. Through factor analysis, items were determined that correspond to the mental and somatic aspects of anxiety. Expert studies have revealed that individuals diagnosed with generalized anxiety disorder or panic attacks tend to receive high scores (above 20) on the HAMA, whereas those without a clinical diagnosis tend to receive significantly lower scores [28].
The EPDS was originally developed to help identify possible depressive symptoms in the postnatal period. In addition to the HAM-D17, we employed the Edinburgh Postnatal Depression Scale (EDPS), a self-report questionnaire consisting of 10 items and originally designed for research purposes, to facilitate the identification of perinatal depression. This tool has been available for over three decades and is widely used for detecting symptoms of depression during and after pregnancy [29].
The study utilized the Edinburgh Postnatal Depression Scale (EPDS) as a self-report questionnaire to detect depressive symptoms during the antenatal period with adequate sensitivity and specificity. Responses on the EPDS are scored on a 4-point scale (0–3), with higher scores indicating a greater endorsement of each symptom. Participants with a total score of 12 or more on the EPDS were classified as having a high possibility of depression, while a score of 9–11 indicated a possible risk of depression. The study employed the Romanian version of the EPDS (EPDS-R) [30], which has been validated for use in the Romanian population. The mean EPDS-R score was 10.1 (SD: 6.5), with scores ranging from 0 to 29.
The study also utilized the Center for Epidemiologic Studies Depression Scale (CES-D) as a self-report questionnaire to assess depression. The Romanian version of the CES-D (CES-D(R)) was used. The mean EPDS-R score was 10.1 (SD: 6.5), with scores ranging from 0 to 29. The mean CESD(R) score was 24.7 (SD: 13.1), with scores ranging from 7 to 60. As indicated by Cronbach’s α, reliability (internal consistency) for both EPDS-R and CES-D(R) scores were robust (α = 0.88 and 0.93, respectively) in this study sample.
The Romanian version of the Edinburgh Postnatal Depression Scale (EPDS-R) has been validated for use in detecting depressive symptoms in pregnant women in Romania. In this version, a score of >12 was identified as the optimal reference point for prenatal screening, with a correct classification rate of 81.1%. Using this cutoff point, the prevalence rate of depressive symptoms in the study sample was found to be 33.7%.
The EPDS-R demonstrated robust psychometric properties in the population and is recommended as a valid, reliable, and easy-to-administer tool for detecting depression in pregnant women in Romania. The reference values for the EPDS-R in this study were nonclinical (<10), subclinical (10–11), and clinical (≥12), as defined by the original EPDS [31].
Symptom severity was based on cutoff scores and ranked (EPDS, 1 = no depression, 2 = possible depression, 3 = high possibility of depression, and 4 = depressed; GAD, 1 = minimal anxiety, 2 = mild anxiety, 3 = moderate anxiety and 4 = severe anxiety).

2.4. Statistical Analysis

The statistical analysis included both descriptive (frequency, percentage) and inferential statistics. We applied the Chi-square test and the Fisher test to determine the association of qualitative variables. To quantify the relationship between multiple predictor variables and the outcome variable, we performed binary logistic regression and ordinal regression for ordinal dependent variables. For each independent variable included, the estimated coefficient (estimate) associated with each independent variable, the 95% confidence interval around the respective estimate, the exponential coefficient (Exp (B)), the Wald 95% confidence interval around the exponential coefficient, and the p-value associated with that independent variable were calculated. The p-value represents the statistical significance of the relationship between each independent variable and the dependent variable. The significance threshold was chosen for a p-value of 0.05. Microsoft Excel 2016 (Microsoft® Corp., Redmond, WA, USA) was used for data entry and analyzes were analyzed using IBM SPSS Statistics [30,32].

3. Results

A total of 215 pregnant women in the third trimester were included in the study after applying the exclusion criteria. The age range of participants was 16 to 40 (mean = 26.35). The majority (55.35%) were between 25 and 34 years old, with an average of the groups of women ≤ 35 years old of between 21.22472–28.14286, while in the ≥35-years-old group, the average was 37.42857. The majority of subjects (53.49%) were from urban areas. Regarding marital status, the majority (85.12%) were single/divorced, and 91.63% had no higher education. Regarding social status, the majority (67.91%) were employed. In terms of pregnancy planning, 87.44% were unplanned, while in terms of the number of previous pregnancies, 62.79% were multiparous. In terms of nicotine and alcohol consumption, almost half of the women (49.77%) reported smoking, while one-quarter (22.79%) reported alcohol consumption (Table 1).
The characteristics in Table 1 represent the frequency and percentage of pregnant women included in the study according to socio-demographic variables and information related to their health.
The presence of depression, anxiety is demonstrated in Table 2, which shows that 1/3 (31.63%) of the participants scored in the clinical range for depression on the EDPS scale, while 55.35% scored in the nonclinical range and 13.02% scored in the subclinical range.
Anxiety measured on the HADS A scale highlights a majority (88.37%) with scores in the clinical range and a small proportion (11.63%) in the non-clinical range.
Regarding depression measured on the HADS D scale, approximately the same majority (84.65%) scored in the clinical range, and a small proportion (15.35%) in the nonclinical range.
We established associations between depression scores (EDPS, HADS A, and HADS D) and various socio-demographic and health factors. To take into account the complexity and to have more ordered levels in the dependent variables, we used ordinal regression, allowing the interaction of these variables with one or more independent variables.
Table 3, Table 4, Table 5, Table 6 and Table 7 show the results of the logistic regression analysis with the variables EDPS (a measure of depression or psychological distress), HADS A, HADS D, and several predictor variables including age, background, marital status, level of education, employment status, pregnancy characteristics, and health behaviors (smoking, alcohol consumption). For each independent variable, the estimated coefficient (estimate) associated with each independent variable, the 95% confidence interval around the respective estimate, the exponential coefficient (Exp (B)), the Wald 95% confidence interval around the exponential coefficient, and the p-value associated with that independent variable were included. The p-value represents the statistical significance of the relationship between each independent variable and the dependent variable.
Based on the p-values, for EDPS (Table 3), none of the variables is a statistically significant predictor of the outcome variable.
Based on the p-values, for HAMD (Table 4), age and background are statistically significant predictors of the outcome variable. As age increases there is a decreased probability of falling at a higher level on the dependent variable (moderate depression) (OR = 0.904, 95%CI: 0.826–0.991; p = 0.029). For women from urban areas, there is an increased probability of falling at a higher level on the dependent variable (moderate depression) (OR = 2.454, 95%CI: 1.086–5.545; p = 0.032).
Based on the p-values, for HAMA (Table 5), the environment of origin is a statistically significant predictor of the outcome variable. For women from urban areas, there is an increased probability of falling to a higher level on the dependent variable (moderate depression), (OR = 1.845, 95%CI: 1.004–3.391), statistically significant (p = 0.046).
Based on the p values, for HADS D and HADS A (Table 6 and Table 7), none of the variables are statistically significant predictors of the outcome variable.

4. Discussion

We tried to assess how widespread antenatal anxiety and depression are in a sample of pregnant women in the last trimester of pregnancy using the following scales: EDPS, HADS A, HADS D, HAMA, and HAMD. The study was carried out on a small sample of pregnant women in the third trimester of pregnancy hospitalized for childbirth from a geographical area limited to a single Mures county, (with the particularity: according to the data of the National Institute of Statistics (INNS), in Romania, in 2019 the number of divorces increased by 1.7 compared to the previous year, the number of registered marriages was decreasing, and last but not least, there was an increase in the number of teenage mothers (16–20 years old), which may limit the generalization of the results to the Romanian population [33].
The study found a prevalence of prenatal depression of 31.63% (Table 2), which is similar to what has been reported in other studies.
Studies conducted in Turkey, Canada, India, and Nepal have also reported a significant prevalence of depressive symptoms in pregnant women [34,35,36,37]. For example, a Canadian study [35] with 1987 participants reported a prevalence of depressive symptoms in 37% of women and anxiety symptoms in 56.6%. Similarly, Sanchana et al. [35] reported a prevalence of 40.5% and Sapkota et al. [36] found that 37.5% of participants had some level of depressive symptoms. In a recent study by Umuziga [37], it was found that 37.6% of women in their third trimester of pregnancy had suggestive depression symptoms (EPDS ≥ 10). These findings suggest that prenatal depression is a significant health issue affecting a substantial proportion of pregnant women worldwide.
In this study, the prevalence of anxiety symptoms in pregnant women was found to be high, with 88.37% (Table 2) of participants presenting scores in the clinical range on the HADS A scale. A score below 6 indicating a nonclinical case was used as a reference, with a score above 6 indicating a clinical case; therefore, the values obtained were high (Table 2). This finding is consistent with previous studies in the literature that have reported high prevalence rates of anxiety in pregnant women worldwide. For example, Leach et al. (2014) [38] found that prevalence rates of anxiety symptoms in pregnant women in Australia ranged from 6.8% to 59.5%. Similarly, studies in Canada (Dennis et al., 2017; Fawcett et al., 2019) [38,39] and the United Kingdom (Nielsen-Scott et al., 2019) [40] have also reported high prevalence rates of anxiety in pregnant women. It should be noted that differences in prevalence rates may be due to various factors, including the assessment tools and cutoff points we used, as well as cultural differences in the perception of mental health.
We also examined the influence of socio-demographic variables and mental health status (Table 1).
The study found that depressive symptoms during pregnancy, as measured by the HAMD scale, are associated with factors such as age and environment. Additionally, the results showed that younger maternal age is statistically associated with higher levels of prenatal depressive symptoms on the HAMD scale. However, there is inconsistency in the literature regarding this association, as some studies have found that younger maternal age increases the likelihood of depression during pregnancy. This is not surprising given that other similar studies have also shown that younger women are more likely to develop prenatal depression [41,42,43].
The association between age and antenatal depression is a topic of interest for researchers, and findings have been inconsistent. We found that the age range of participants was 16 to 40 (mean = 26.35), with the majority (55.35%) being between 25 and 34 years old. Some studies suggest that younger age is associated with a higher risk of depression during pregnancy, particularly for women under 25 years old [44], under 20 years old [45], or between 15 and 20 years old [46]. This may be due to factors such as incomplete education, unstable economic situations with lower income and job instability, and unemployment [46]. Conversely, other studies have found that older maternal age is associated with a higher risk of antenatal depression, particularly for women over 35 years old or over 30 years old [47,48].
Research suggests that environment may be a significant factor in the development of prenatal depressive symptoms, but findings are inconclusive in many studies. Regarding our study, we confirmed that women from urban areas have a statistically increased risk of developing prenatal depressive symptoms and anxiety. In contrast, other studies suggest that women in rural areas are at increased risk of risk factors for antenatal depression, such as obesity and diabetes [49,50,51,52].
Nidey et al. [53], mention that women from a rural environment have an increased risk of perinatal depression compared to women from an urban environment. This suggests that women from a rural environment may experience unique health barriers that may increase the risk of depression. The results highlight the importance of identifying and prioritizing women at risk of perinatal depression and anxiety and ensuring access to appropriate interventions and support.
Civil status was not found to be a risk factor for depression and anxiety, despite 85.12% being divorced/unmarried (Table 1). This can be explained by the evolution of Romanian society and the changing role of women in it: the change in values and social perceptions about family and marriage, the increase in women’s financial independence, more young women choosing to have children before getting married compared to previous generations, a desire to avoid potential relationship problems, and some may consider marriage as an outdated social convention and not a priority in their lives.
Other studies have shown that partner absence, including being single, divorced, separated, or in polygamous marriages, is associated with higher rates of depression during pregnancy [54].
In contrast, our results did not find a significant association between a low educational level and depression and anxiety during pregnancy, but previous research has consistently shown a link between lower educational levels and antenatal depression [55,56,57,58,59,60].
In our research, we also analyzed the social status factor in relation to depression and anxiety during pregnancy, but we did not identify any association between them. However, various studies have shown that poor socioeconomic status is often associated with the occurrence of prenatal depression [61,62,63,64]. This is often due to the economic difficulties encountered in such situations, which can form a vicious circle for antenatal depression.
The mental well-being of pregnant women is of utmost importance, which is why researchers need to consider obstetric factors when studying the risk of antenatal depression [65,66,67]. Unplanned pregnancy has been found in several studies to be a risk factor for antenatal depression, while planned pregnancy has been associated with lower levels of depression. In terms of the type of pregnancy, our study did not find significant associations with depression and anxiety, but other researchers have consistently shown that women who did not plan their pregnancy are more prone to depression [49,68]. The relationship between the number of pregnancies and antenatal depression is still unclear, with conflicting results in different studies. While some studies found that nulliparity is associated with an increased risk of depression during pregnancy [47], most studies suggest that multiparity is linked to higher levels of antenatal depression [47,67,68,69].
Another obstetric factor studied in relation to depression and anxiety was gestational age. In our study, gestational age was not a predictive factor for depression or anxiety. However, studies such as the one by Rezaee R. and Framarzi M. demonstrated a positive correlation between gestational age and anxiety (F = 1.903, p = 0.006) and depression (F = 2.101, p = 0.003) in a proportion of 68.1% [70].
Smoking and alcohol consumption during pregnancy may increase the risk of depression and the relationship may be mediated by oxidative stress. In terms of nicotine and alcohol consumption, almost half of the women (49.77%) reported smoking, while one-quarter (22.79%) reported alcohol consumption (Table 1). From the point of view of health behaviors (smoking, alcohol consumption) we calculated the estimated coefficient associated with each independent variable, but none of the variables was a statistically significant predictor of the outcome variable (Table 3). Other authors [71] identified interaction effects between tobacco use and childbirth anxiety (p < 0.001), and interaction between tobacco use and pregnancy depression (p = 0.032), demonstrating that there are different types of interaction effects between tobacco use and anxiety or depression. In addition, the study of Wubetu et al. [72] suggests that alcohol consumption during pregnancy may increase the risk of depression and that this relationship may be mediated by a number of factors, such as social support, anxiety, and stress. Considering the negative impact of alcohol and tobacco consumption during pregnancy, more importance should be given to primary prevention. It is very important to carry out periodic assessments throughout pregnancy, as they can help identify health problems or early intervention in situations that require medical attention.

Limits of the Study

This study conducted on pregnant women in the third trimester was limited by: a small sample size, the inclusion of only women hospitalized for childbirth, and a limited geographic area, which restricts the generalizability of the findings to the general population. Furthermore, the study did not consider the impact of stressful life events, such as the COVID-19 pandemic, and other psychosocial risk factors, such as social support, couple relationships, a family history of mental disorders, and personality traits. These factors could have affected the accuracy and comprehensiveness of the study’s results.
It is important to acknowledge these limitations when interpreting the study’s findings and to exercise caution when extrapolating them to other populations or contexts. Future research with larger and more diverse samples, and a broader range of factors considered, could provide a more complete understanding of the relationship between pregnancy and mental health.

5. Conclusions

The study underscores the significance of monitoring mental health throughout pregnancy, as well as identifying pertinent risk factors in order to deliver appropriate care to expectant mothers.
The manifestation of both anxiety and depression during pregnancy is often linked to several factors. Recognizing these associated factors can facilitate the early implementation of mental health monitoring measures throughout pregnancy.
Demographic and health-related factors are closely interrelated and can have a significant impact on the maternal psycho-affective state. Upon examining the associated risk factors, it was revealed that younger maternal age is associated with prenatal depressive symptoms. Anxiety was also found to be a common occurrence during pregnancy.
The results obtained showed that age and the environment of origin are the strongest predictors of mental health during pregnancy.
The introduction of a screening program that also provides psychological counseling in prenatal care can be very helpful for women who are experiencing stress and anxiety or who are in disadvantaged social situations. This program could be implemented at the level of the health system, and medical staff could be trained in providing appropriate counseling and support to these women.
Moreover, the findings emphasize the necessity for implementing interventions aimed at supporting the mental well-being of pregnant women.

Author Contributions

Conceptualization, A.I.C.R.; methodology, A.I.C.R. and G.E.S.; formal analysis, D.V.G., F.R. and M.C.; validation, D.V.G.; investigation, A.I.C.R.; resources, A.I.C.R., L.M.S. and C.M.; data curation, A.I.C.R., M.C., A.G.N. and A.B.S.; writing, A.I.C.R.; original draft preparation, A.I.C.R.; writing review and editing, A.I.C.R.; supervision, C.M., A.S. and G.E.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethics Committee of “George Emil Palade” University of Medicine, Pharmacy, Science and Technology from Târgu Mureș (No. 199, 14/06/2019).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Data is unavailable due to privacy and ethical restrictions.

Conflicts of Interest

The authors declare that there is no conflict of interest.

References

  1. Dunkel Schetter, C.; Tanner, L. Anxiety, depression and stress in pregnancy: Implications for mothers, children, research, and practice. Curr. Opin. Psychiatry 2012, 25, 141–148. [Google Scholar] [CrossRef]
  2. Lancaster, C.A.; Gold, K.J.; Flynn, H.A.; Yoo, H.; Marcus, S.M.; Davis, M.M. Risk factors for depressive symptoms during pregnancy: A systematic review. Am. J. Obstet. Gynecol. 2010, 202, 5–14. [Google Scholar] [CrossRef] [PubMed]
  3. Winter, C.; Van Acker, F.; Bonduelle, M.; Van Berkel, K.; Belva, F.; Liebaers, I.; Nekkebroeck, J. Depression, pregnancy-related anxiety and parental-antenatal attachment in couples using preimplantation genetic diagnosis. Hum. Reprod. 2016, 31, 1288–1299. [Google Scholar] [CrossRef] [PubMed]
  4. Chen, J.; Cross, W.M.; Plummer, V.; Lam, L.; Sun, M.; Qin, C.; Tang, S. The risk factors of antenatal depression: A cross-sectional survey. J. Clin. Nurs. 2019, 28, 3599–3609. [Google Scholar] [CrossRef] [PubMed]
  5. Woody, C.A.; Ferrari, A.J.; Siskind, D.J.; Whiteford, H.A.; Harris, M.G. A systematic review and meta-regression of the prevalence and incidence of perinatal depression. J. Affect. Disord. 2017, 219, 86–92. [Google Scholar] [CrossRef]
  6. Bennett, H.A.; Einarson, A.; Taddio, A.; Koren, G.; Einarson, T.R. Prevalence of depression during pregnancy: Systematic review. Obs. Gynecol. 2004, 3, 698–709. [Google Scholar] [CrossRef]
  7. Parsons, C.E.; Young, K.S.; Rochat, T.S.; Kringelbach, M.L.; Stein, A. Postnatal depression and its effects on child development: A review of evidence from low- and middle-income countries. Br. Med. Bull. 2012, 10, 57–79. [Google Scholar] [CrossRef]
  8. Milgrom, J.; Gemmill, A.W.; Bilszta, J.L.; Hayes, B.; Barnett, B.; Brooks, J.; Ericksen, J.; Ellwood, D.; Buist, A. Antenatal risk factors for postnatal depression: A large prospective study. J. Affect. Disord. 2008, 108, 147–157. [Google Scholar] [CrossRef]
  9. Mumtaz, S.; Akram, B. Management of anxiety among pregnant women with serious medical conditions: A multicentre study. J. Pak. Med. Assoc. 2020, 70, 1966–1969. [Google Scholar] [CrossRef]
  10. Davis, E.P.; Glynn, L.M.; Waffarn, F.; Sandman, C.A. Prenatal maternal stress programs infant stress regulation. J. Child Psychol. Psychiatry 2011, 52, 119. [Google Scholar] [CrossRef]
  11. Stewart, D.E.; Vigod, S.N. Postpartum Depression: Pathophysiology, Treatment, and Emerging Therapeutics. Annu. Rev. Med. 2019, 70, 183–196. [Google Scholar] [CrossRef]
  12. Abdollahi, F.; Zarghami, M. Effect of Postpartum Depression on Women’s Mental and Physical Health Four Years after Childbirth. East Mediterr. Health J. 2018, 24, 1002–1009. [Google Scholar] [CrossRef] [PubMed]
  13. Tissera, H.; Auger, E.; Séguin, L.; Kramer, M.S.; Lydon, J.E. Happy Prenatal Relationships, Healthy Postpartum Mothers: A Prospective Study of Relationship Satisfaction, Postpartum Stress, and Health. Psychol. Health 2021, 36, 461–477. [Google Scholar] [CrossRef]
  14. Van den Bergh, B.R.; Dahnke, R.; Mennes, M. Prenatal stress and the developing brain: Risks for neurodevelopmental disorders. Dev. Psychopathol. 2018, 30, 743–762. [Google Scholar] [CrossRef] [PubMed]
  15. Coussons-Read, M.E. Effects of prenatal stress on pregnancy and human development: Mechanisms and pathways. Obstet. Med. 2013, 6, 52–57. [Google Scholar] [CrossRef]
  16. Grigoriadis, S.; Graves, L.; Peer, M.; Mamisashvili, L.; Tomlinson, G.; Dennis, C.L.; Steiner, M.; Brown, C.; Cheung, A.; Dawson, H. Maternal Anxiety During Pregnancy and the Association with Adverse Perinatal Outcomes: Systematic Review and Meta-Analysis. J. Clin. Psychiatry 2018, 95, 813. [Google Scholar] [CrossRef] [PubMed]
  17. Lobel, M.; Cannella, D.L.; Graham, J.E.; DeVincent, C.; Schneider, J.; Meyer, B.A. Pregnancy-specific stress, prenatal health behaviors, and birth outcomes. Health Psychol. 2008, 27, 604–615. [Google Scholar] [CrossRef]
  18. Høivik, M.S.; Eberhard-Gran, M.; Elisabeth, C.; Wang, A.; Dørheim, S.K. Perinatal mental health around the world: Priorities for research and service development in Norway. Bjpsych Int. 2021, 18, 102–105. [Google Scholar] [CrossRef]
  19. Wickberg, B.; Bendix, M.; Blomdahl Wetterholm, M.; Skalkidou, A. Perinatal mental health around the world: Priorities for research and service development in Sweden. Bjpsych Int. 2020, 17, 6–8. [Google Scholar] [CrossRef]
  20. Brînzaniuc, A. Prevalence and determinants of prenatal depression symptoms in a Romanian sample of pregnant women: A comparative analysis across socioeconomic groups. Eur. J. Public Health 2013, 23, 89–91. [Google Scholar] [CrossRef]
  21. Enatescu, V.R.; Bernad, E.; Gluhovschi, A.; Papava, I.; Romosan, R.; Palicsak, A.; Munteanu, R.; Craina, M.; Enatescu, I. Perinatal characteristics and mother’s personality profile associated with increased likelihood of postpartum depression occurrence in a Romanian outpatient sample. J. Ment. Health 2017, 26, 212–219. [Google Scholar] [CrossRef] [PubMed]
  22. Zigmond, A.S.; Snaith, R.P. The Hospital Anxiety and Depression Scale. Acta Psychiatry Scand. 1983, 67, 361–370. [Google Scholar] [CrossRef] [PubMed]
  23. Ladea, M. Validarea Scalei de Anxietate Si Depresie (HADS) Pe o Populatie de Pacienti Psihiatrici Din Tara Noastra. 2003. Available online: http://www.romjpsychiat.ro/article/validarea-scalei-de-anxietate-si-depresie-had38s-pe-opopulatie-de-pacienti-psihiatrici-dintara-noastr-maria-ladea (accessed on 15 February 2019).
  24. Hamilton, M. A rating scale for depression. J. Neurol. Neurosurg. Psychiatry 1960, 23, 56–62. [Google Scholar] [CrossRef] [PubMed]
  25. Clark Haley, M. Concussion and Mental Health: Case Series. Master’s Thesis, Northern Michigan University, Marquette, MI, USA, 2022; p. 719. [Google Scholar]
  26. Hamilton, M. Development of a Rating Scale for Primary Depressive Illness. Brit. J. Soc. Clin. Psychol. 1967, 6, 278–296. [Google Scholar] [CrossRef]
  27. Hamilton, M. The Assessment of Anxiety States by Rating. Br. J. Med. Psychol. 1959, 32, 50–55. [Google Scholar] [CrossRef]
  28. Schutte, N.S.; Malouff, J.M. Sourcebook of Adult Assessment Strategies; Springer: New York, NY, USA, 1995; pp. 127–134. [Google Scholar]
  29. Cox, J.L.; Holden, J.M.; Sagovsky, R. Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale. Br. J. Psychiatry 1987, 150, 782–786. [Google Scholar] [CrossRef]
  30. Available online: https://real-statistics.com/ordinal-regression (accessed on 15 December 2022).
  31. Wallis, A.B.; Fernandez, R.; Oprescu, F.; Cherecheş, R.; Zlati, A.; Dungy, C. Validation of a Romanian scale to detect antenatal depression. Cent. Eur. J. Med. 2012, 7, 216–223. [Google Scholar] [CrossRef]
  32. Available online: https://real-statistics.com/free-download/real-statistics-resource-pack/ (accessed on 15 December 2022).
  33. Available online: https://insse.ro/cms/sites/default/files/field/publicatii/evenimente_demografice_in_anul_2019.pdf (accessed on 15 December 2022).
  34. Lebel, C.; MacKinnon, A.; Bagshawe, M.; Tomfohr-Madsen, L.; Giesbrecht, G. Elevated depression and anxiety symptoms among pregnant individuals during the COVID-19 pandemic. J. Affect. Disord. 2020, 277, 5–13. [Google Scholar] [CrossRef]
  35. Sanchana, D.A.; Ethirajan, D.S.; Selvamani, D.I.; Rohini, D.G. Assessment of the prevalence of depression, anxiety and stress symptoms in term antenatal women- a tertiary care center experience during the COVID-19 pandemic. Ann. Trop. Med. Public Health 2021, 23, SP232372. [Google Scholar] [CrossRef]
  36. Sapkota, B.; Mali, N.S.; Singh, R.D.; Yogi, I.; Maharjan, D.; Maharjan, M. Prenatal anxiety among pregnant women visiting in antenatal care outpatient department at Paropakar Maternity and Women’s hospital. Int. J. Health Sci. Res. 2019, 9, 173–181. [Google Scholar]
  37. Umuziga, M.P.; Oluyinka Adejumo, O.; Hynie, M. A cross-sectional study of the prevalence and factors associated with symptoms of perinatal depression and anxiety in Rwanda. BMC Pregnancy Childbirth 2020, 20, 68. [Google Scholar]
  38. Fawcett, E.J.; Fairbrother, N.; Cox, M.L.; White, I.R.; Fawcett, J.M. The Prevalence of Anxiety Disorders During Pregnancy and the Postpartum Period: A Multivariate Bayesian Meta-Analysis. J. Clin. Psychiatry 2019, 80, 18r12527. [Google Scholar] [CrossRef]
  39. Dennis, C.L.; Falah-Hassani, K.; Shiri, R. Prevalence of antenatal and postnatal anxiety: Systematic review and meta-analysis. Br. J. Psychiatry 2017, 210, 315–323. [Google Scholar] [CrossRef]
  40. Nielsen-Scott, M.; Fellmeth, G.; Opondo, C.; Alderdice, F. Prevalence of perinatal anxiety in low- and middle-income countries: A systematic review and meta-analysis. J. Affect. Disord. 2022, 306, 71–79. [Google Scholar] [CrossRef]
  41. Adina, J.; Morawska, A.; Mitchell, A.E.; Haslam, D.; Ayuku, D. Depression and anxiety in second and third trimesters among pregnant women in Kenya. J. Affect. Disord. Rep. 2022, 10, 100447. [Google Scholar] [CrossRef]
  42. Lee, A.M.; Lam, S.K.; Sze Mun Lau, S.M.; Chong, C.S.; Chui, H.W.; Fong, D.Y. Prevalence, course, and risk factors for antenatal anxiety and depression. Obs. Gynecol. 2007, 110, 1102–1112. [Google Scholar] [CrossRef] [PubMed]
  43. Marchesi, C.; Bertoni, S.; Maggini, C. Major and minor depression in pregnancy. Obs. Gynecol. 2009, 113, 1292–1298. [Google Scholar] [CrossRef]
  44. Kheirabadi, G.R.; Maracy, M.R. Perinatal depression in a cohort study on Iranian women. J. Res. Med. Sci. 2010, 15, 41–49. [Google Scholar]
  45. Bödecs, T.; Szilágyi, E.; Cholnoky, P.; Sándor, J.; Gonda, X.; Rihmer, Z.; Horváth, B. Prevalence and psychosocial background of anxiety and depression emerging during the first trimester of pregnancy: Data from a Hungarian population-based sample. Psychiatr. Danub. 2013, 25, 352–358. [Google Scholar]
  46. Thompson, O.; Ajayi, I. Prevalence of antenatal depression and associated risk factors among pregnant women attending antenatal clinics in Abeokuta North Local Government Area, Nigeria. Depress. Res. Treat. 2016, 2016, 4518979. [Google Scholar] [CrossRef] [PubMed]
  47. Coll, C.V.N.; da Silveira, M.F.; Bassani, D.G.; Netsi, E.; Wehrmeister, F.C.; Barros, F.C.; Stein, A. Antenatal depressive symptoms among pregnant women: Evidence from a Southern Brazilian population-based cohort study. J. Affect. Disord. 2017, 209, 140–146. [Google Scholar] [CrossRef]
  48. Weobong, B.; Soremekun, S.; Ten Asbroek, A.H.; Amenga-Etego, S.; Danso, S.; Owusu-Agyei, S.; Prince, M.; Kirkwood, B.R. Prevalence and determinants of antenatal depression among pregnant women in a predominantly rural population in Ghana: The DON population-based study. J. Affect. Disord. 2014, 165, 1–7. [Google Scholar] [CrossRef] [PubMed]
  49. Tittman, S.M.; Harteau, C.; Beyer, K.M. The effects of geographic isolation and social support on the health of Wisconsin women. WMJ 2016, 115, 65–69. [Google Scholar]
  50. Hutto, H.F.; Kim-Godwin, Y.; Pollard, D.; Kemppainen, J. Postpartum depression among White, African American, and Hispanic low-income mothers in rural southeastern North Carolina. J. Community Health Nurs. 2011, 28, 41–53. [Google Scholar] [CrossRef]
  51. Bloom, T.L.; Bullock, L.F.; Parsons, L. Rural pregnant women’s stressors and priorities for stress reduction. Issues Ment. Health Nurs. 2012, 33, 813–819. [Google Scholar] [CrossRef]
  52. Trivedi, T.; Liu, J.; Probst, J.; Merchant, A.; Jhones, S.; Martin, A.B. Obesity and obesity-related behaviors among rural and urban adults in the USA. Rural Remote Health 2015, 15, 3267. [Google Scholar] [CrossRef] [PubMed]
  53. Nichole Nidey. Perinatal Depression Risk and Rural Women. J. Rural Health 2020, 36, 9–16. [Google Scholar] [CrossRef] [PubMed]
  54. Tewodros, W.; Dibaba, Y.; Abdisa, E.D. Prevalence of antenatal depression and associated factors among pregnant women attending antenatal care in Addis Ababa, Ethiopia. Arch. Women Ment. Health 2020, 23, 855–863. [Google Scholar]
  55. Adewuya, A.O.; Ola, B.A.; Aloba, O.O.; Dada, A.O.; Fasoto, O.O. Prevalence and correlates of depression in late pregnancy among Nigerian women. Depress. Anxiety 2007, 24, 15–21. [Google Scholar] [CrossRef]
  56. Jonsdottir, S.S.; Thome, M.; Steingrimsdottir, T.; Lydsdottir, L.B.; Sigurdsson, J.F.; Olafsdottir, H.; Swahnberg, K. Partner relationship, social support and perinatal distress among pregnant Icelandic women. Women Birth 2017, 30, e46–e55. [Google Scholar] [CrossRef]
  57. Woldetensay, Y.K.; Belachew, T.; Biesalski, H.K.; Ghosh, S.; Lacruz, M.E.; Scherbaum, V. The role of nutrition, intimate partner violence and social support in prenatal depressive symptoms in rural Ethiopia: Community based birth cohort study 11 Medical and Health Sciences 1117 Public Health and Health Services. BMC Pregnancy Childbirth 2018, 18, 374. [Google Scholar]
  58. Ramohlola, M. Prevalence and Factors Associated with Depression amongst Pregnant Women at Helene Franz Hospital of the Limpopo Province, South Africa. Available online: http://hdl.handle.net/10386/3612 (accessed on 24 August 2022).
  59. Shrestha, S.; Pun, K.D. Anxiety on primigravid women attending antenatal care: A hospital based cross-sectional study. Kathmandu Univ. Med. J. KUMJ 2018, 16, 23–27. [Google Scholar] [PubMed]
  60. Akinsulore, A.; Temidayo, A.M.; Oloniniyi, I.O.; Olalekan, B.O.; Yetunde, O.B. Pregnancy-related anxiety symptoms and associated factors amongst pregnant women attending a tertiary hospital in south-west Nigeria. S. Afr. J. Psychiatry 2021, 27, 1616. [Google Scholar] [CrossRef]
  61. Grote, N.K.; Bridge, J.A.; Gavin, A.R.; Melville, J.L.; Iyengar, S.; Katon, W.J. A meta-analysis of depression during pregnancy and the risk of preterm birth, low birth weight, and intrauterine growth restriction. Arch. Gen. Psychiatry 2010, 67, 1012–1024. [Google Scholar] [CrossRef]
  62. Baron, E.; Hanlon, C.; Mall, S.; Honikman, S.; Breuer, E.; Kathree, T. Mental health in primary care in five low- and middle-income countries: A situtational analysis. BMC Health Serv. Res. 2016, 16, 53. [Google Scholar] [CrossRef] [PubMed]
  63. Tang, X.; Lu, Z.; Hu, D.; Zhong, X. Influencing factors for prenatal stress, anxiety and depression in early pregnancy among women in Chongqing, China. J. Affect. Disord. 2019, 253, 292–302. [Google Scholar] [CrossRef]
  64. Lilliecreutz, C.; Larén, J.; Sydsjö, G.; Josefsson, A. Effect of maternal stress during pregnancy on the risk for preterm birth. BMC Pregnancy Childbirth 2016, 16, 5. [Google Scholar] [CrossRef]
  65. Weng, S.C.; Huang, J.P.; Huang, Y.L.; Lee, T.S.; Chen, Y.H. Effects of tobacco exposure on perinatal suicidal ideation, depression, and anxiety. BMC Public Health 2016, 16, 623. [Google Scholar] [CrossRef]
  66. Al-Azri, M.; Al-Lawati, I.; Al-Kamyani, R.; Al-Kiyumi, M.; Al-Rawahi, A.; Davidson, R.; Al-Maniri, A. Prevalence and risk factors of antenatal depression among Omani women in a Primary Care Setting: Cross-sectional study. Sultan Qaboos Univ. Med. J. 2016, 16, e35–e41. [Google Scholar] [CrossRef]
  67. González-Mesa, E.; Kabukcuoglu, K.; Körükcü, O.; Blasco, M.; Ibrahim, N.; Kavas, T. Cultural factors influencing antenatal depression: A cross-sectional study in a cohort of Turkish and Spanish women at the beginning of the pregnancy. J. Affect. Disord. 2018, 238, 256–260. [Google Scholar] [CrossRef]
  68. Duko, B.; Ayano, G.; Bedaso, A. Depression among pregnant women and associated factors in Hawassa city, Ethiopia: An institution-based cross-sectional study. Reprod. Health 2019, 16, 25. [Google Scholar] [CrossRef] [PubMed]
  69. Couto, T.; Cardoso, M.N.; Brancaglion, M.Y.; Faria, G.C.; Garcia, F.D.; Nicolato, R.; de Miranda, D.M.; Corrêa, H. Antenatal depression: Prevalence and risk factor patterns across the gestational period. J. Affect. Disord. 2016, 192, 70–75. [Google Scholar] [CrossRef] [PubMed]
  70. Rezaee, R.; Framarzi, M. Mental health and pregnancy. Iran. J. Nurs. Midwifery Res. Spec. Issue Health Wellbeing 2014, 19, S45–S49. [Google Scholar]
  71. Pereira, B.; Figueiredo, B.; Pinto, T.M.; Míguez, M.C. Effects of Tobacco Consumption and Anxiety or Depression during Pregnancy on Maternal and Neonatal Health. Int. J. Environ. Res. Public Health 2020, 17, 8138. [Google Scholar] [CrossRef]
  72. Wubetu, A.D.; Habte, S.; Dagne, K. Prevalence of risky alcohol use behavior and associated factors in pregnant antenatal care attendees in Debre Berhan, Ethiopia. BMC Psychiatry 2019, 19, 250. [Google Scholar] [CrossRef] [PubMed]
Table 1. Frequency according to socio-demographic variables and health-related information (N = 215).
Table 1. Frequency according to socio-demographic variables and health-related information (N = 215).
CharacteristicsFrequency (n)%
Socio-demographic
Age category<258941.40%
25–3411955.35%
≥3573.26%
EnvironmentRural10046.51%
Urban11553.49%
Marital statusMarried3214.88%
Unmarried/Divorced18385.12%
Educational statusNo higher education19791.63%
With higher education188.37%
Social statusEmployed14667.91%
Housewife6932.09%
Health information
Pregnancy typeUnplanned18887.44%
Planned2712.56%
Gestational age29–332813.02%
≥3418786.98%
Number of pregnanciesMultiparous13562.79%
Nulliparous8037.21%
SmokingNonsmoking10850.23%
Smoking10749.77%
Alcohol consumptionNo alcohol consumption16677.21%
With alcohol consumption4922.79%
Total215100.00%
Legend: n = number; %—percentage.
Table 2. Proportion of participants with nonclinical, clinical, and subclinical depression/anxiety (Chi-square test).
Table 2. Proportion of participants with nonclinical, clinical, and subclinical depression/anxiety (Chi-square test).
EDPSFrequency (n)%
Clinical6831.63%
Nonclinical11955.35%
Subclinical2813.02%
Total215100.00%
HADS AFrequency (n)%
Clinical19088.37%
Nonclinical2511.63%
Total215100.00%
HADS DFrequency (n)%
Clinical18284.65%
Nonclinical3315.35%
Total215100.00%
Legend: n = number; %—percentage; EDPS (Edinburgh Postnatal Depression Scale): Nonclinical < 10, Subclinical, 10–11, Clinical ≥ 12; HADS A (Hospital Anxiety and Depression Scale): No anxiety under 6 (nonclinical), anxiety over 6 (clinical); HADS D (Hospital Anxiety and Depression Scale) No depression under 6 (nonclinical), depression over 6 (clinical).
Table 3. Association of depressive symptoms (EDPS) with socio-demographic and health factors (ordinal logistic regression) [32].
Table 3. Association of depressive symptoms (EDPS) with socio-demographic and health factors (ordinal logistic regression) [32].
EDPSEstimate95% C.I.Exp (B)95% Wald C.I. for Exp (B)Value p
Lower Upper LowerUpper
PredictorsAge−0.021−0.0920.050.980.9111.0530.569
Environment0.314−0.3160.9441.3690.7262.5800.329
Marital status−0.295−1.0730.4820.7440.3391.6360.457
Educational Status−0.356−1.3350.6230.7010.2621.8710.476
Social Status−0.277−0.9290.3750.7580.3911.4690.405
Pregnancy type0.049−0.8170.9141.0500.442.5040.912
Pregnancy age0.268−0.5731.1081.3070.5593.0590.532
No. of pregnancies−0.084−0.7150.5480.920.4841.7470.795
Smoker−0.386−0.9250.1530.680.3971.1630.161
Alcohol consumption0.122−0.5390.7831.1300.5842.1860.717
Legend: 95% C.I.—confidence interval; Exp (B)—exponential coefficient; EDPS (Edinburgh Postnatal Depression Scale): Nonclinical < 10, Subclinical, 10–11, Clinical ≥ 12; Obs. No predicted change in the probability of being in a higher category as the values of the independent variables increase.
Table 4. Association of depressive symptoms (HAMD) with socio-demographic and health factors (ordinal logistic regression) [32].
Table 4. Association of depressive symptoms (HAMD) with socio-demographic and health factors (ordinal logistic regression) [32].
HAMDEstimate95% C.I.Exp (B)95% Wald C.I. for Exp (B)Value p
LowerUpperLowerUpper
PredictorsAge−0.101−0.191−0.010.9040.8260.9910.029
Environment0.8980.0781.7172.4541.0865.5450.032
Marital status−0.641−1.6780.3960.5270.1841.5050.225
Educational Status−0.948−2.2340.3380.3880.1091.3830.149
Social Status−0.039−0.8620.7850.9620.422.2020.927
Pregnancy type0.284−0.8171.3861.3290.4493.9310.613
Pregnancy age0.776−0.2381.7902.1730.7895.9880.134
No. of pregnancies0.783−0.0261.5922.1880.9724.9250.058
Smoker−0.327−1.0190.3650.7210.3611.4380.354
Alcohol consumption0.329−0.5361.1941.3900.593.2740.456
Legend: 95% C.I.—confidence interval; Exp (B)—exponential coefficient; HAMD (Hamilton Depression Rating Scale): 0–7 absence, 8–16 mild, 17–22 moderate, ≥23 severe.
Table 5. Association of depressive symptoms (HAMA) with socio-demographic and health factors (ordinal logistic regression) [32].
Table 5. Association of depressive symptoms (HAMA) with socio-demographic and health factors (ordinal logistic regression) [32].
HAMAEstimate95% C.I.Exp (B)95% Wald C.I. for Exp (B)Value p
LowerUpperLowerUpper
PredictorsAge0.009−0.060.0771.0090.9441.0780.803
Environment0.6130.011.2151.8451.0043.3910.046
Marital status0.236−0.5130.9861.2670.6152.6100.537
Educational Status0.239−0.7211.1981.2700.4813.3540.626
Social Status−0.158−0.7840.4670.8540.4541.6040.620
Pregnancy type0.028−0.8010.8581.0290.4512.3470.947
Pregnancy age0.134−0.6480.9161.1430.5292.4710.737
No. of pregnancies0.424−0.1861.0331.5270.8292.8130.173
Smoker−0.365−0.8840.1550.6950.4131.1690.169
Alcohol consumption−0.236−0.8710.40.790.4141.5070.468
Legend: 95% C.I.—confidence interval; Exp (B)—exponential coefficient; HAMA (Hamilton Anxiety Rating Scale): 0–4 normal, 5–10 mild, 11–16 moderate, ≥17 severe.
Table 6. Association of depressive symptoms (HADS D) with socio-demographic and health factors (ordinal logistic regression) [32].
Table 6. Association of depressive symptoms (HADS D) with socio-demographic and health factors (ordinal logistic regression) [32].
HADS-DExp (B)95% C.I. for Exp (B)Value p
LowerUpper
PredictorsAge1.0280.9221.1450.620
Environment0.5820.2331.4500.245
Marital status1.0130.3023.4000.983
Educational Status1.2130.3054.8320.784
Social Status1.3510.5323.4320.527
Pregnancy type2.1480.7186.4280.172
Pregnancy age1.6540.5924.6230.337
No. of pregnancies1.1680.4732.8850.737
Smoker0.9070.4151.9820.807
Alcohol consumption1.5830.5834.2970.367
Legend: Exp (B)—exponential coefficient; 95% C.I.—confidence interval; HADS-D (Hospital Anxiety and Depression Scale): Nonclinical under 6, Clinical over 6.
Table 7. Association of depressive symptoms (HADS A) with socio-demographic and health factors (Ordinal logistic regression) [32].
Table 7. Association of depressive symptoms (HADS A) with socio-demographic and health factors (Ordinal logistic regression) [32].
HADSAExp (B)95% C.I. for Exp (B)Value p
LowerUpper
PredictorsAge1.0350.9141.1710.590
Environment2.4090.856.8250.098
Marital status1.0910.3143.7900.891
Educational Status1.6980.3169.1260.537
Social Status1.1490.4163.1730.789
Pregnancy type0.7430.1962.8130.661
Pregnancy age1.1340.3233.9790.844
No. of pregnancies1.1570.4213.1740.778
Smoker0.6960.2871.6890.423
Alcohol consumption0.4720.1791.2410.128
Legend: Exp (B)—exponential coefficient; 95% C.I.—confidence interval; HADS A (Hospital Anxiety and Depression Scale): Nonclinical under 6, Clinical over 6.
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Răchită, A.I.C.; Strete, G.E.; Sălcudean, A.; Ghiga, D.V.; Rădulescu, F.; Călinescu, M.; Nan, A.G.; Sasu, A.B.; Suciu, L.M.; Mărginean, C. Prevalence and Risk Factors of Depression and Anxiety among Women in the Last Trimester of Pregnancy: A Cross-Sectional Study. Medicina 2023, 59, 1009. https://doi.org/10.3390/medicina59061009

AMA Style

Răchită AIC, Strete GE, Sălcudean A, Ghiga DV, Rădulescu F, Călinescu M, Nan AG, Sasu AB, Suciu LM, Mărginean C. Prevalence and Risk Factors of Depression and Anxiety among Women in the Last Trimester of Pregnancy: A Cross-Sectional Study. Medicina. 2023; 59(6):1009. https://doi.org/10.3390/medicina59061009

Chicago/Turabian Style

Răchită, Anca Ioana Cristea, Gabriela Elena Strete, Andreea Sălcudean, Dana Valentina Ghiga, Flavia Rădulescu, Mihai Călinescu, Andreea Georgiana Nan, Andreea Bianca Sasu, Laura Mihaela Suciu, and Claudiu Mărginean. 2023. "Prevalence and Risk Factors of Depression and Anxiety among Women in the Last Trimester of Pregnancy: A Cross-Sectional Study" Medicina 59, no. 6: 1009. https://doi.org/10.3390/medicina59061009

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