Abstract
Coronavirus disease 2019 (COVID-19) has become a pandemic. As the first city struck by the COVID-19 outbreak, Wuhan had implemented unprecedented public health interventions. The mental health of pregnant women during these anti-epidemic controls remains unknown. A total of 274 pregnant women living in Wuhan during the COVID-19 outbreak took part in our investigation online. The data on mental health conditions were evaluated using Edinburgh Postnatal Depression Scale (EPDS), Self-Rating Anxiety Scale (SAS), Chinese Perceived Stress Scale (CPSS), and Pittsburgh Sleep Quality Index (PSQI). We also collected the information on physical health status and precautionary measures against COVID-19. The prevalence of depression, anxiety, stress, and poor sleep quality was 16.1%, 13.9%, 42.7%, 37.6%, respectively. Comparing to SAS, PSQI score in pregnant women who participated in the survey after April 8 (date of Wuhan reopening), those data collected before April 8 were significantly higher. High levels of stress, severe health concerns over the fetus, and poor hygienic practices were negatively associated with mental health conditions. In conclusion, a large proportion of pregnant women reported psychological symptoms during the epidemic, which negatively related to the severe health concerns over fetus and poor hygienic practices. More psychological support during the epidemic would promote maternal mental well-being.
Keywords: Antenatal anxiety, Antenatal depression, Stress, Sleep
1. Introduction
Coronavirus disease 2019 (COVID-19) is infectious viral pneumonia caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which was first revealed in Wuhan, China (Pan et al., 2020; Bai et al., 2020). The disease's spread was declared a Public Health Emergency of International Concern and a pandemic by WHO (WHO, 2020). The virus has infected more than 142 million individuals, with over 3.0 million deaths as of April 20, 2021 (Johns Hopkins Coronavirus Resource Center, 2021). As the first city struck by the COVID-19 outbreak, citizens in Wuhan have witnessed the rapid spread of the virus and severe shortage of healthcare resources in the early stage of the epidemic, together with fears and (mis)information overload in social media. They also experienced unprecedented public health interventions, including a 76-day city lockdown, strict social distancing measures, and home isolation. (Pan et al., 2020; Gao et al., 2020).
The epidemic has created enormous disruptions to daily life and could also affect people's mental well-being in the disease-struck regions. For example, Gao (Gao et al., 2020) has reported increased depression, anxiety, and a combination of depression and anxiety (CDA) in the general Chinese population during the COVID-19 outbreak. The elderly suicide rate in Hong Kong has also shown a sharp increase amid the epidemic of the Severe Acute Respiratory Syndrome (SARS) in 2003 (Chan et al., 2006), which was linked to social disengagement, stress, anxiety, and disease-related fears (Yip et al., 2010).
Females are predisposed to more severe anxiety and PTSD in epidemic outbreaks (Wang et al., 2020; Yali and Lobel, 1999), especially for pregnant women who undergo physiological, social, and emotional changes (Ding et al., 2014). Hence, the mental health of pregnant women may be more vulnerable to public health interventions such as city lockdown and home quarantine than the general population during the outbreak of COVID-19 (Yang et al., 2021). A meta-analysis has demonstrated that, compared to the non-pandemic period, the State-Trait Anxiety Inventory (STAI) scores on the maternal anxiety scale during pregnancy and postpartum period were significantly higher during the COVID-19 pandemic (Hessami et al., 2020). The aggravated ill mental state of pregnant women could further lead to adverse outcomes of their offspring(Stein et al., 2014), such as preterm birth, low birth weight, and negative affectivity in early childhood, internalizing behavior in school-age, high risk of depression, and low social competence in adolescent (Barker et al., 2011; Megan et al., 2011; Korhonen et al., 2012; Susan et al., 2009). Therefore, the psychological impact of COVID-19 on pregnant women cannot be ignored. One recent study demonstrated a significantly increased prevalence of anxiety and depressive symptoms in pregnant women (Wu et al., 2020), which was conducted in ten provinces across China without Wuhan. We conducted a survey focusing on maternal mental health in Wuhan, the epicenter of the COVID-19 outbreak, to establish the prevalence of psychological symptoms and the severity and identify related factors in the pregnant population during the outbreak.
2. Methods
2.1. Study design and participants
This questionnaire-based cross-sectional survey was conducted via an online crowdsourcing platform (https://www.wjx.cn/) from February 27 to May 8, 2020. Pregnant women living in Wuhan during the COVID-19 outbreak were all candidates for the survey. The participants were reached through any of the following approaches: 1) the Maternal and Child Health Hospital (MCH) in Jianghan District introduced the study in its WeChat (the Chinese version of Facebook) public platform with the link of the questionnaire shared; 2) some community healthcare personnel in the District shared the link of the questionnaire to pregnant women in their registers; and 3) the nurses in the MCH hospital guided pregnant women during their prenatal visit after the restoration of their post lockdown medical services. Jianghan District is the most affected area in Wuhan. A total of 274 women were included in the final analysis.
Our study protocol was approved by the Ethics Committee of Tongji Medical College, Huazhong University of Science and Technology, before the initiation of this survey (2020-S052). The informed consent was obtained from the participants prior to questionnaire filling, and the investigation was carried out under the Declaration of Helsinki.
2.2. Data collection
Our study focused on the symptoms of depression, anxiety, stress, and sleep quality, using self-evaluation as the outcome variables. The Edinburgh Postnatal Depression Scale (EPDS) is the most widely used measure for postpartum depressive symptoms and prenatal depressive symptoms (Cox et al., 1987; Felice et al., 2006). It contains 10 items with a score≥10 representing depressive symptoms (Guo et al., 2009). The Self-Rating Anxiety Scale (SAS), a four-rating scale with 20 items, was used to measure the level of anxiety in the past month (Wang and Chi, 1984). The total score ranges from 25 to 100, with≥50 represents anxiety symptoms. Chinese Perceived Stress Scale (CPSS), a self-reported scale of 14 items, was applied to measure the extent of perceived stress during the past month (Chu, 2005). The total score ranges from 0 to 56, with scores higher than 25 indicating a high perceived stress level (Cohen et al., 1983). Pittsburgh Sleep Quality Index (PSQI) is an 18-item self-report scale for evaluating adult sleep quality and sleep disturbances. Participants whose score >5 were characterized as having poor sleep quality (Liu et al., 1996; Smyth, 2000). All the adopted Chinese versions of measurement tools were validated, showing satisfactory reliability and validity (Guo et al., 2009; Wang and Chi, 1984; Chu, 2005; Liu et al., 1996).
Other health related information in the current study are: 1) demographic data, including age, educational level, residential location during the COVID-19 outbreak, family members living together; 2) history of maternity, including gravidity and parity, gestational age, pregnancy disorders, high-risk pregnancy (yes, no); 3) health conditions during epidemic of COVID-19, including symptoms related to COVID-19 (fever, fatigue, dry cough, sore throat, headache, anhelation, dyspnea, inappetence, nausea, diarrhea, stomachache), concern of themselves being infected (no/little, mild, moderate, severe), concern of fetus being affected by the outbreak (no/little, mild, moderate, severe); 4) hands hygienic measures including the hands hygienic practices (avoiding touching eyes, mouth and nose with hands, washing hands before eating and after using toilet, and avoiding directly touching objects in public place) with hygienic practice score calculated (1 point for each practice, the total score ranges from 0 to 3); 5) information on prenatal care included the cancelation of prenatal examination during the epidemic (yes, no) and related causes, remote counselling services provided by healthcare staff (yes, no), and counselling services seeking behaviors (yes, no).
2.3. Statistical analysis
The normally distributed variables, such as age, gestational age, were described as mean with standard deviation (SD), whereas the skewed variables, such as the total score of SAS, EPDS, CPSS, and PSQI were presented as medians and interquartile ranges (IQRs). The categorical variables, like educational level and pregnancy disorders, were presented as the frequency with proportion. Chi-square test and Mann-Whitney U test were used to compare the proportions of the positive outcomes between two groups. We compared the participants’ mental well-being investigated before and after April 8, 2020 (date of Wuhan reopening) by a generalized linear model. Multivariable logistic regression was applied to identify the related factors of the mental health outcomes. All statistical analyses and graphing were performed using SPSS statistical software version 26.0 and Graphpad version 8.0. P values were 2-tailed with statistical significance set at 0.05.
3. Results
3.1. Characteristics of pregnant women
The analyses included 274 participants with a mean (SD) age of 30.4 (3.8) years and 87.2% < 35 years old (n = 239). Over half were first pregnancy (n = 141, 51.5%), with college education (n = 203, 74.1%), living with their husband (n = 246, 89.8%). The mean (SD) gestational age was 21.4 (7.5) weeks, with the majority in the second trimester (n = 216, 78.8%). Around half (n = 135, 49.3%) were enrolled in communities or hospitals. The proportions of pregnancy comorbidities and high-risk pregnancies were 23.4% and 10.6%, respectively. Only 1.5% (n = 4) had any contact history with COVID-19 patients but no one infected. Twelve percent (n = 33) reported serve concern of fetus being affected during epidemic, 13.1% (n = 36) moderate concern, 40.5% (n = 111) mild concern, and 34.3% (n = 94) no/little concern. Regarding the prenatal check-up, the cancelation was up to 67.2% during the outbreak, with the top three reasons being the concern of being infected in hospitals (82.6%), hospitals stopped the provision of related service (37.0%), hospitals were designated for COVID-19 treatment (27.7%). Around 40% received remote services from healthcare staff, and 26.3% have actively sought prenatal counseling services (Table 1 ).
Table 1.
Description of the basic data.
Variables | n(%)a | Variables | n(%)a |
---|---|---|---|
Age, years | 30.4 ± 3.8b | The canceled prenatal check-ups | |
<35 | 239(87.2) | Regular prenatal carec | 70(38.0) |
≥35 | 35(12.8) | Blood glucose test | 28(15.2) |
Gestational age, weeks | 21.4 ± 7.5b | Toxoplasma test | 17(9.2) |
Avoiding touching eyes, mouth and nose with hands | Down's Syndrome screening | 48(26.1) | |
Yes | 219(79.9) | B-ultrasonography examination | 60(32.6) |
No | 55(20.1) | Others | 41(22.3) |
Washing hands before eating and after using toilet | Healthcare personnel provided the counselling services | ||
Yes | 261(95.3) | Medical personnel of towns or maternal and child health county hospitals | 9(8.3) |
No | 13(4.7) | Community healthcare workers | 54(49.5) |
Avoiding directly touching objects in public area | Medical personnel in Maternal and Child Health hospital at district, city and provincial levels | 19(17.4) | |
Yes | 246(89.8) | Medical staff at the general hospitals | 24(22.0) |
No | 28(10.2) | Others | 17(15.6) |
Feeling the epidemic is serious | Services mode of remote services | ||
Not serious | 38(13.9) | Telephone counseling | 82(75.2) |
Mild serious | 153(55.8) | WeChat /QQ consulting | 35(32.1) |
Moderate serious | 59(21.5) | Provision of prenatal care booklet | 12(11.0) |
Severe serious | 24(8.8) | Text-message query | 13(11.9) |
Others | 5(4.6) |
Data were presented as n(%) unless otherwise indicated.
Data were presented as mean±standard deviation.
Regular prenatal care includes abdominal circumference, blood pressure, etc.
3.2. Mental health status
The median (IQR) scores of EPDS, SAS, CPSS, PSQI were 5.0(2.0–8.0),41.0(33.0–46.0),24.0(16.0–28.0),4.0(3.0–7.0). The prevalence of depression (n = 44,16.1%), anxiety (n = 38,13.9%), stress (n = 117,42.7%), and poor sleep quality (n = 103,37.6%). A total of 62.4% developed at least one of the four symptoms. The scores of EPDS, SAS, CPSS, and PSQI were 5.77±4.54, 40.68±9.09, 21.67±8.52, and 5.02±2.90 (mean ± standard deviation), respectively. All the measurement tools showed satisfactory reliability (Cronbach's α) in our study (EPDS, 0.85; SAS, 0.80; CPSS, 0.80; PSQI, 0.84).
Both depressive and anxiety symptoms were found closely associated with the concern of being infected (depression: Z=−3.9, P<0.001; anxiety: Z=−3.9, P<0.001), the concern of fetus being affected (depression: Z=−4.6, P<0.001; anxiety: Z=−4.4, P<0.001), subjective sleep quality (depression: Z=−2.5,P = 0.01; anxiety: Z=−4.1, P = 0.02) and hygienic practice score (depression: Z=−2.3, P = 0.02; anxiety: Z=−2.3, P = 0.02). Among the pregnant women with high perceived stress or poor sleep quality, proportions of no/little concern of being infected (stress: Z=−2.5, P = 0.01; sleep: Z=−2.4, P = 0.02) and the fetus being affected (stress: Z=−3.4, P<0.001; sleep: Z=−4.0, P<0.001), good subjective sleep quality (stress: Z=−3.4, P<0.001; sleep: Z=−9.4, P<0.001) were significantly lower than the control. Gestational age was also associated with symptoms of depression and sleep quality (depression: χ2 = 18.14, P<0.001; sleep:χ2 = 6.29, P = 0.04) (Table 2 ).
Table 2.
The distributions of the four mental health conditions by covariates.
EPDS Scorea,b |
SAS Score |
CPSS Scorec |
PSQI Scored |
|||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
<10 | ≥10 | P | <50 | ≥50 | P | ≤25 | >25 | P | ≤5 | >5 | P | |
Variables | N(%) | N(%) | value | N(%) | N(%) | value | N(%) | N(%) | value | N(%) | N(%) | value |
Gestational agee | 0.0001 | 0.051 | 0.094 | 0.043 | ||||||||
The first trimester | 8(3.5) | 8(18.2) | 11(4.7) | 5(13.2) | 5(3.2) | 11(9.6) | 8(4.7) | 8(7.8) | ||||
The second trimester | 190(82.6) | 26(59.1) | 191(80.9) | 25(65.8) | 127(80.9) | 89(76.1) | 143(83.6) | 73(70.9) | ||||
The third trimester | 32(13.9) | 10(22.7) | 34(14.4) | 8(21.1) | 25(15.9) | 17(14.5) | 20(11.7) | 22(21.4) | ||||
Pregnancy comorbiditiese | 0.066 | 0.197 | 0.178 | 0.145 | ||||||||
Yes | 49(21.3) | 15(34.1) | 52(22.0) | 12(31.6) | 32(20.4) | 32(27.4) | 35(20.5) | 29(28.2) | ||||
No | 181(78.7) | 29(65.9) | 184(78.0) | 26(68.4) | 125(79.6) | 85(72.6) | 136(79.5) | 74(71.8) | ||||
Concern of themselves being infectedh | <0.0001 | <0.0001 | 0.013 | 0.018 | ||||||||
No concern | 124(53.9) | 14(31.8) | 126(53.4) | 12(31.6) | 87(55.4) | 51(43.6) | 93(54.4) | 45(43.7) | ||||
Mild concern | 88(38.3) | 14(31.8) | 92(39.0) | 10(26.3) | 58(36.9) | 44(37.6) | 65(38.0) | 37(35.9) | ||||
Moderate concern | 12(5.2) | 10(22.7) | 10(4.2) | 12(31.6) | 8(5.1) | 14(12.0) | 7(4.1) | 15(14.6) | ||||
Severe concern | 6(2.6) | 6(13.6) | 8(3.4) | 4(10.5) | 4(2.5) | 8(6.8) | 6(3.5) | 6(5.8) | ||||
Concern of fetus being affectedh | <0.0001 | <0.0001 | 0.001 | <0.0001 | ||||||||
No concern | 88(38.3) | 6(13.6) | 88(37.3) | 6(15.8) | 63(40.1) | 31(26.5) | 71(41.5) | 23(22.3) | ||||
Mild concern | 96(41.7) | 15(34.1) | 101(42.8) | 10(26.3) | 67(42.7) | 44(37.6) | 68(39.8) | 43(41.7) | ||||
Moderate concern | 27(11.7) | 9(20.5) | 26(11.0) | 10(26.3) | 15(9.6) | 21(17.9) | 20(11.7) | 16(15.5) | ||||
Severe concern | 19(8.3) | 14(31.8) | 21(8.9) | 12(31.6) | 12(7.6) | 21(17.9) | 12(7.0) | 21(20.4) | ||||
Subjective sleep qualityg | 0.012 | <0.0001 | 0.001 | <0.0001 | ||||||||
Great | 46(20.0) | 4(9.1) | 49(20.8) | 1(2.6) | 38(24.2) | 12(10.3) | 48(28.1) | 2(1.9) | ||||
Good | 144(62.6) | 26(59.1) | 149(63.1) | 21(55.3) | 96(61.1) | 74(63.2) | 119(69.6) | 51(49.5) | ||||
Bad | 40(17.4) | 14(31.8) | 38(16.1) | 16(42.1) | 23(14.6) | 31(26.5) | 4(2.3) | 50(48.5) | ||||
Hygienic practices scoreg,h, | 0.020 | 0.023 | 0.076 | 0.169 | ||||||||
0 | 3(1.3) | 4(9.1) | 5(2.1) | 2(5.3) | 2(1.3) | 5(4.3) | 4(2.3) | 3(2.9) | ||||
1 | 13(5.7) | 1(2.3) | 11(4.7) | 3(7.9) | 7(4.5) | 7(6.0) | 6(3.5) | 8(7.8) | ||||
2 | 35(15.2) | 12(27.3) | 37(15.7) | 10(26.3) | 24(15.3) | 23(19.7) | 28(16.4) | 19(18.4) | ||||
3 | 179(77.8) | 27(61.4) | 183(77.5) | 23(60.5) | 124(79.0) | 82(70.1) | 133(77.8) | 73(70.9) |
EPDS Score >10 represents depressive symptoms.
SAS Score ≥50 represents anxiety symptoms.
CPSS Score >25 represents high level of perceived stress.
PSQI Score >5 represents poor sleep quality.
P values were calculated with a Chi-Square test unless otherwise indicated
fP values were calculated with a Fisher exact test.
P values were calculated with a Mann-Whitney U test.
Hygienic practices score: hand hygienic practices include avoiding touching eyes, mouth and nose with hands, washing hands before eating and after using toilet, avoiding directly touching objects in public place; 1 point for one practice, total score ranges from 0 to 3.
Fig. 1 presents the comparisons of outcome scores between the two stages (before and after April 8). The scores of SAS (β=0.059, 95%CI, 0.0068–0.11), PSQI (β= 0.146, 95%CI, 0.0054–0.29) in the city lockdown stage were significantly higher than that of the city reopening stage, adjusting for age, gestational age, and proportion of high-risk pregnancies. Besides, the scores of sleep disturbance (β= 0.808, 95%CI, 0.21–1.41) of PSQI, were also statistically different in the two stages. There was no statistical difference in the total score of CPSS and EPDS, and all dimensions of the PSQI, except sleep disturbance in the two stages.
Fig. 1.
Comparison of scores of EPDS, SAS and PSQI before and after April 8
Adjusted for age, gestational age and proportion of high-risk pregnancy using Generalized Linear Models. The scale score in the figure is the raw data.
A: Before and after April 8; B: After April 8;
a: P value were derived from GLM (Gamma distribution); b: P value were derived from GLM (Tweedie distribution); c: P value were derived from GLM (Multinomial distribution).
3.3. Related factors for maternal mental health outcomes
Logistic regression analysis showed that, compared with little/no concern of fetus being affected, severe concern was highly associated with the four mental health symptoms, i.e., depression (OR=6.64, 95%CI, 1.70–25.92), anxiety (OR=4.30, 95%CI, 1.16–15.96), stress (OR=4.10, 95%CI, 1.62–10.41) and poor sleep quality (OR=3.94, 95%CI, 1.54–10.10). Moderate concern was also related to all the symptoms except sleep (depression: OR=4.17, 95%CI, 1.12–15.58; anxiety: OR=4.32, 95%CI, 1.22–15.26; stress: OR=2.91, 95%CI, 1.28–6.61). Moreover, high stress in the pregnant population during the COIVD-19 outbreak was related to all the other symptoms (depression: OR=13.01, 95%CI, 4.63–36.57; anxiety: OR=11.86, 95%CI, 3.90–36.05; sleep: OR=1.86, 95%CI, 1.08–3.19). Compared with those in the second or the third trimester, women in the first trimester had a higher risk of having depressive symptoms (second trimester: OR=0.15, 95%CI, 0.03–0.72) and being stressed (last trimester: OR=0.24, 95%CI, 0.06–0.94). The adjusted odds ratio of depressive symptoms were greater among those with postgraduate education or above (OR=7.36, 95%CI, 1.32–40.95) than those with high school or below, lower among those with a higher score in hygienic practices than those with 0 scores (1 score: OR=0.02, 95%CI, 0.00–0.57; 3 score: OR=0.09, 95%CI, 0.01–0.83) (Table 3 ).
Table 3.
Logistic regression analysis of the associated factors of the four mental health conditions.
OR (95% CI) |
||||
---|---|---|---|---|
Variables | EPDS, depressive symptom | SAS, anxiety symptom | CPSS, stress symptom | PSQI, sleep quality |
Educational level (ref-high school or below) | ||||
College education | 1.69(0.45–6.26) | 1.71(0.49–6.00) | 0.98(0.46–2.08) | 1.27(0.57–2.84) |
Postgraduate education or above | 7.36(1.32–40.95)* | 1.05(0.15–7.59) | 0.51(0.17–1.50) | 1.49(0.50–4.43) |
Living with their husband (ref-Yes) | 0.91(0.22–3.74) | 1.59(0.40–6.25) | 0.72(0.29–1.77) | 1.54(0.63–3.79) |
Gestational age (ref-the first trimester) | ||||
The second trimester | 0.15(0.03–0.72)* | 0.61(0.14–2.70) | 0.42(0.13–1.39) | 0.83(0.26–2.64) |
The third trimester | 0.27(0.05–1.56) | 0.61(0.11–3.30) | 0.24(0.06–0.94)* | 1.13(0.30–4.23) |
Pregnancy comorbidities (ref-no) | 1.63(0.65–4.09) | 1.55(0.62–3.87) | 1.36(0.74–2.51) | 1.26(0.68–2.35) |
Symptoms related to COVID-19 (ref-no) | 2.77(0.80–9.61) | 2.02(0.58–7.00) | 1.26(0.53–3.00) | 1.86(0.77–4.52) |
Cancelling prenatal examination (ref-no) | 2.33(0.84–6.47) | 1.66(0.64–4.32) | 1.21(0.69–2.12) | 0.96(0.54–1.72) |
Concern of fetus being affected (ref- no) | ||||
Mild concern | 2.20(0.68–7.07) | 1.24(0.39–3.79) | 1.39(0.75–2.55) | 1.79(0.94–3.40) |
Moderate concern | 4.17(1.12–15.58)* | 4.32(1.22–15.26)* | 2.91(1.28–6.61)* | 2.10(0.89–4.93) |
Severe concern | 6.64(1.70–25.92)** | 4.30(1.16–15.96)* | 4.10(1.62–10.41)** | 3.94(1.54–10.10)** |
Hygienic practices score (ref −0) | ||||
1 | 0.02(0.00–0.57)* | 0.92(0.07–11.55) | 0.38(0.05–2.89) | 2.34(0.31–17.67) |
2 | 0.15(0.01–1.54) | 0.98(0.11–8.49) | 0.29(0.05–1.82) | 1.07(0.18–6.31) |
3 | 0.09(0.01–0.83)* | 0.52(0.07–4.20) | 0.24(0.04–1.39) | 1.00(0.18–5.52) |
Hight stress (ref - normal) | 13.01(4.63–36.57)*** | 11.86(3.90–36.05)*** | —— | 1.86(1.08–3.19)* |
Abbreviation: CI, confidence interval; OR, odds ratio.
*P<0.05; **P<0.01; ***P<0.001.
4. Discussion
Our study showed a large proportion of pregnant women in Wuhan reported mental health symptoms during the COIVD-19 epidemic, including depression, anxiety, high stress, and poor sleep quality. Over 60% of participants scored above the threshold for at least one of the psychological indices. 16.1%, 13.9%, 42.7%, and 37.6% of our participants were likely to have depression, anxiety, high stress, poor sleep quality, respectively. A majority had to cancel their prenatal check-ups, with a tiny proportion received some remote counseling services. High-level pressure, severe health concerns over the fetus, early pregnancy, and high educational levels were identified as risk factors of mental health status.
Our study demonstrated that high perceived stress was an independent risk factor for depression, anxiety, and sleep quality in the pregnancy population. This finding is consistent with the previous findings suggesting a close association between antenatal depressive symptoms and stressful experiences during pregnancy (Lancaster et al., 2010; Shakeel et al., 2015). An earlier report also indicated high perceived stress was a common predictor of chronic anxiety symptoms in pregnancy (Bayrampour et al., 2015). The perceived stress stem from the emerging infectious disease outbreak, health-related concerns, home confinement, and shortage of medical resources (Stein et al., 2014; Xie et al., 2020; Fu et al., 2020) may result in poor sleep condition, including difficulty in falling asleep and short sleep duration in some pregnant women (Alan et al., 2020; Lin et al., 2021).
In our study, participants with moderate-severe concerns about their fetuses tended to develop symptoms of depression, anxiety, and stress, which was consistent with previous studies (Mortazavi et al., 2021; Rief et al., 2012; Mohammadi et al., 2019; Mortazavi et al., 2016). In our study, approximately 25% of participants reported moderate-severe concerns about their fetuses being affected by the outbreak. However, only a small proportion of them reported any contact history (1.5%) or symptoms of COVID-19 (5.1%). Therefore, some participants seemed to have exaggerated concerns relative to their actual infection risk. Some anxiety symptoms, also known as health anxiety, may arise from inappropriate or exaggerated concerns about one's health status and dysfunctional beliefs about health and illness (Rief et al., 2012). It is a high possibility for individuals to expose to health anxiety in infectious disease outbreaks (Blakey and Abramowitz, 2017; Blakey et al., 2015). Over half of the pregnant women reported health anxiety in Ireland during the COVID-19 outbreak (Corbett et al., 2020). These findings demonstrated that more effort should be made for the public to better understand of the diseases, avoid somatosensory amplification and reduce the over-concern of the health conditions. In addition, during the outbreak, a series of restrictive measures had greatly interfered the access to routine health services, including prenatal health checks, which might further intensify pregnant women's concerns about their fetus's health, affecting their sleep condition and mental well-being (Dong et al., 2020; Lin et al., 2021).
Participants with depressive symptoms were less likely to take vigilant hygienic practices. The previous studies reported the higher depressive symptoms were related to the more inferior health practices, including hygiene-related practices (Walker et al., 1999; Ranasinghe et al., 2016). Although the specific mechanisms remain unclear, the unhealthy behaviors might serve as a means of coping with depressive symptoms or could be regarded as the symptoms of depression (Zuckerman et al., 1989). Therefore, the efforts to change pregnant women's health practices might require considering their mental health status (Leung et al., 2003).
Our study also revealed that pregnant women with high educational levels tended to develop depressive symptoms, consistent with some previous findings. (Liu et al., 2021; Moghanibashi-Mansourieh., 2020; Wang et al., 2021). People with higher education levels usually engage more in work, however, the home quarantine during the outbreak directed their attention to some other aspects, such as family health, safety, and financial security, leading to more worries(Wang et al., 2021). However, some studies contradict our results, suggesting that low education is a risk factor for depression (Khademian et al., 2021; Antiporta et al., 2021; Necho et al., 2020). It is still unclear about the association between education and antenatal depression. More studies are needed to understand the complex relationship between education and antenatal depression and the underlying mechanism in such public health emergencies.
We found that depressive symptoms and high stress were more likely to occur in the first trimester of pregnancy. We assumed this might partially relate to unplanned or unwanted pregnancies, although related information was not available in our study (Bunevicius et al., 2009). Nevertheless, our results indicate pregnant women's mental state, especially in the early stage of pregnancy, might require special attention during such public health emergencies.
After adjusting for maternal age, gestational age, and proportion of high-risk pregnancy, participants’ anxiety situation and sleep quality investigated after April 8 (city reopening stage) were significantly better than those participated during the city lockdown stage. A longitudinal study has demonstrated a decreasing temporal trend of anxiety levels in a general population during and after the SARS outbreak (Leung et al., 2005). Although our findings were based on a cross-sectional design, it might also imply that anxiety symptoms and poor sleep quality could be buffered by effective epidemic control and restoration of social and life order.
Our study found no statistical significance in depression and stress levels between those investigated before and after April 8. The depressive symptoms and high stress among the pregnant women may persist long after the ‘peak’ of the epidemic due to their concern on the potential infection risk resulting from restored population mobility after reopening.
Over 60% of participants scored above the threshold for at least one of the psychological indices. The assessment and intervention for perinatal mental status should be a priority in public health emergencies. Particular attention should be given to pregnant women in the first trimester, with high-level education, high stress, and severe health concerns. Under the circumstance of home quarantine and short of medial supply, online machine learning-driven intervention platforms, online clinical consultation, and psychological hotlines applied in maternal health care are warranted (Jaroszewski et al., 2019). Regarding long-term health impacts, we should focus on depression and anxiety triggered by persistent high pressure in the post-COVID-19 period and their children's development status and mental health. Determination of whether these children have developmental delays or behavior problems is an important question for future research.
Several limitations are also worth mentioning. First, due to the data collection challenge in Wuhan during the COVID-19 outbreak, relatively few participants took part in our study. Second, there is no data available to compare the pregnant women's psychological conditions in Wuhan with those in other unaffected areas. Third, due to the nature of the online survey, we did not have control over who does and does not respond to the survey, which could have led non-respondent bias. Our conclusion might be more representative to pregnant women with higher educational levels. Fourth, women with pre-existing mental health conditions, like depression and insomnia, might be more likely to report elevated psychiatric symptoms during the outbreak. However, we did not have relevant information to exclude them from the study, which might have resulted in a biased prevalence of mental symptoms in our study. Fifth, although our study compared the participants’ mental well-being investigated before and after April 8, the schedule of city reopening was announced on March 24. Therefore, the actual difference in anxiety and fear of residents between the lockdown and post-lockdown periods could be more tremendious.
In summary, a large proportion of pregnant women reported psychological symptoms during the epidemic. The women of early pregnancy, high educational level, and severe health concern over the fetus, and high stress were at risk of developing mental health symptoms. Furthermore, the anxiety level and sleep quality could be buffered by effective epidemic control and work resumption. Our findings suggested more psychological support for pregnant women during the epidemic to relieve psychological pressures and serious health-related concerns to promote perinatal mental well-being .
Contributors
Ke Xu: Writing-Original Draft, Writing-Review & Editing, Investigation; Ya Zhang: Investigation, Formal analysis; Yuanyuan Zhang: Formal analysis; Qiao Xu: Investigation; Lan Lv: Investigation; Jianduan Zhang: Methodology, Writing-Review & Editing, Supervision.
Declaration of competing interest
No conflict of interest was declared by the authors.
Acknowledgments
Acknowledgments
We wish to thank all the participants, nurses in MCH and the healthcare staff in the community, for making this critical study possible, and Minghong Zhang for his assistance with questionnaire preparation.
Role of the funding source
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
References
- Alan S., Vurgec B.A., Cevik A. The Effects of COVID-19 Pandemic on Pregnant Women: perceived Stress, Social Support and Sleep Quality. Yonago Acta Med. 2020;63(4):360–367. doi: 10.33160/yam.2020.11.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Antiporta D.A., Cutipé Y.L., Mendoza M., et al. Depressive symptoms among Peruvian adult residents amidst a National Lockdown during the COVID-19 pandemic. BMC Psychiatry. 2021;21:111. doi: 10.1186/s12888-021-03107-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bai Y., Yao L., Wei T., et al. Presumed Asymptomatic Carrier Transmission of COVID-19. JAMA. 2020;323:1406–1407. doi: 10.1001/jama.2020.2565. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barker E.D., Jaffee S.R., Uher R., et al. The contribution of prenatal and postnatal maternal anxiety and depression to child maladjustment. Depress Anxiety. 2011;28(8):696–702. doi: 10.1002/da.20856. [DOI] [PubMed] [Google Scholar]
- Bayrampour H., McDonald S., Tough S. Risk factors of transient and persistent anxiety during pregnancy. Midwifery. 2015;31:582–589. doi: 10.1016/j.midw.2015.02.009. [DOI] [PubMed] [Google Scholar]
- Blakey S.M., Abramowitz J.S. Psychological Predictors of Health Anxiety in Response to the Zika Virus. J. Clin. Psychol. Med. Settings. 2017;24:270–278. doi: 10.1007/s10880-017-9514-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blakey S.M., Reuman L., Jacoby R.J. Abramowitz JS. Tracing “Fearbola”: psychological predictors of anxious responding to the threat of Ebola. Cogn. Ther. Res. 2015;39:816–825. doi: 10.1007/s10608-015-9701-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bunevicius R., Kusminskas L., Bunevicius A., et al. Psychosocial risk factors for depression during pregnancy. Acta Obstet. Gynecol. Scand. 2009;88:599–605. doi: 10.1080/00016340902846049. [DOI] [PubMed] [Google Scholar]
- Chan S.M., Chiu F.K., Lam C.W., Leung P.Y.V., Conwell Y. Elderly suicide and the 2003 SARS epidemic in Hong Kong. Int. J. Geriatr. Psychiatr. 2006;21:113–118. doi: 10.1002/gps.1432. [DOI] [PubMed] [Google Scholar]
- Chu L.C. Chinese Version of Perceived Stress Scale. Chin. J. Physiol. 2005;47:157–179. Chinese. [Google Scholar]
- Cohen S., Kamarck T., Mermelstein R. A gobal measure of perceived stress. J. Health Soc. Behav. 1983;24:385–396. [PubMed] [Google Scholar]
- Corbett G.A., Milne S.J., Hehir M.P., et al. Health anxiety and behavioural changes of pregnant women during the COVID-19 pandemic. Eur J Obstet Gynecol Reprod Biol. 2020:30190–30191. doi: 10.1016/j.ejogrb.2020.04.022. S0301-2115. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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. doi: 10.1192/bjp.150.6.782. [DOI] [PubMed] [Google Scholar]
- Dong H., Hu R., Lu C., et al. Investigation on the mental health status of pregnant women in China during the Pandemic of COVID-19. Arch Gynecol Obstet. 2020;303(2):463–469. doi: 10.1007/s00404-020-05805-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ding X.X., Wu Y.L., Xu S.J., et al. Maternal anxiety during pregnancy and adverse birth outcomes: a systematic review and meta-analysis of prospective cohort studies. J. Affect. Disord. 2014;159:103–110. doi: 10.1016/j.jad.2014.02.027. [DOI] [PubMed] [Google Scholar]
- Felice E., Saliba J., Grech V., Cox J. Validation of the Maltese version of the Edinburgh Postnatal Depression Scale. Arch. Womens Ment. Health. 2006;9:75–80. doi: 10.1007/s00737-005-0099-3. [DOI] [PubMed] [Google Scholar]
- Fu W., Wang C., Zou L., et al. Psychological health, sleep quality, and coping styles to stress facing the COVID-19 in Wuhan. China. Transl Psychiatry. 2020;10(1):225. doi: 10.1038/s41398-020-00913-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gao J, Zheng P., Jia Y., et al. Mental health problems and social media exposure during COVID-19 outbreak. PLoS One. 2020;15 doi: 10.1371/journal.pone.0231924. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guo X.J., Wang Y.Q., Liu Y., Chen J., Pu X.F. Study on the optimal critical value of the Edinburgh Postnatal Depression Scale in the screening of antenatal depression. Chin J Nurs. 2009;44:808–810. In Chinese. [Google Scholar]
- Hessami K., Romanelli C., Chiurazzi M., et al. COVID-19 pandemic and maternal mental health: a systematic review and meta-analysis. J Matern Fetal Neonatal Med. Nov. 2020;1:1–8. doi: 10.1080/14767058.2020.1843155. [DOI] [PubMed] [Google Scholar]
- Jaroszewski A.C., Morris R.R., Nock M.K. Randomized controlled trial of an online machine learning-driven risk assessment and intervention platform for increasing the use of crisis services. J. Consult. Clin. Psychol. 2019;87:370–379. doi: 10.1037/ccp0000389. [DOI] [PubMed] [Google Scholar]
- Johns Hopkins Coronavirus Resource Center, 2021. COVID-19 Map. https://coronavirus.jhu.edu/map.html. (accessed Mar 2, 2021).
- Korhonen M., Luoma I., Salmelin R., et al. A longitudinal study of maternal prenatal, postnatal and concurrent depressive symptoms and adolescent well-being. J Affect Disord. 2012;136(3):680–692. doi: 10.1016/j.jad.2011.10.007. [DOI] [PubMed] [Google Scholar]
- Khademian F., Delavari S., Koohjani Z., et al. An investigation of depression, anxiety, and stress and its relating factors during COVID-19 pandemic in Iran. BMC Public Health. 2021;21:275. doi: 10.1186/s12889-021-10329-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lancaster C.A., Gold K.J., Flynn H.A., et al. Risk factors for depressive symptoms during pregnancy: a systematic review. Am. J. Obstet. Gynecol. 2010;202:5–14. doi: 10.1016/j.ajog.2009.09.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leung G.M., Lai-Ming H., Chan S.K.K., et al. Longitudinal assessment of community psychobehavioral responses during and after the 2003 outbreak of severe acute respiratory syndrome in Hong Kong. Clin. Infect. Dis. 2005;40:1713–1720. doi: 10.1086/429923. [DOI] [PubMed] [Google Scholar]
- Leung G.M., Lam T.H., Ho L.M., et al. The impact of community psychological responses on outbreak control for severe acute respiratory syndrome in Hong Kong. J. Epidemiol. Community Health. 2003;57:857–863. doi: 10.1136/jech.57.11.857. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lin W., Wu B., Chen B., et al. Sleep Conditions Associate with Anxiety and Depression Symptoms among Pregnant Women during the Epidemic of COVID-19 in Shenzhen. J Affect Disord. 2021;281:567–573. doi: 10.1016/j.jad.2020.11.114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liu C., Liu D., Huang N., et al. The Combined Impact of Gender and Age on Post-traumatic Stress Symptoms, Depression, and Insomnia During COVID-19 Outbreak in China. Front Public Health. 2021;8 doi: 10.3389/fpubh.2020.620023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liu X.C., Tang M.Q., Hu L., et al. Reliability and validity of the Pittsburgh Sleep Quality Index. Chin. J. Physiol. 1996;29:103–107. In Chinese. [Google Scholar]
- Megan M., Blair L.M.G., Curta S., Elysia P.D. Prenatal maternal anxiety and early childhood temperament. Depress Anxiety. 2011;6(14):644–651. doi: 10.3109/10253890.2011.594121. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moghanibashi-Mansourieh A. Assessing the anxiety level of Iranian general population during COVID-19 outbreak. Asian J Psychiatr. 2020;51 doi: 10.1016/j.ajp.2020.102076. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mohammadi E., Nourizadeh R., Simbar M., et al. DEVELOPMENT AND PSYCHOMETRIC TESTING OF AN INSTRUMENT TO MEASURE WOMEN'S PERCEPTIONS OF UNPLANNED PREGNANCY. J Biosoc Sci. 2019;51:394–402. doi: 10.1017/S0021932018000251. [DOI] [PubMed] [Google Scholar]
- Mortazavi F., Akaberi A. Worries of Pregnant Women: testing the Farsi Cambridge Worry Scale. Scientifica (Cairo) 2016 doi: 10.1155/2016/5791560. 2016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mortazavi F., Mehrabadi M., KiaeeTabar R., et al. Pregnant women's wellbeing and worry during the COVID-19 pandemic: a cross-sectional study. BMC Pregnancy Childbirth. 2021;21:59. doi: 10.1186/s12884-021-03548-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Necho M., Birkie M., Gelaye H., et al. Depression, anxiety symptoms, Insomnia, and coping during the COVID-19 pandemic period among individuals living with disabilities in Ethiopia. PLoS ONE. 2020;15 doi: 10.1371/journal.pone.0244530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pan A., Liu L., Wang C., et al. Association of Public Health Interventions With the Epidemiology of the COVID-19 Outbreak in Wuhan, China. JAMA. 2020 doi: 10.1001/jama.2020.6130. [published online ahead of print, 2020 Apr 10] [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ranasinghe S., Ramesh S., Jacobsen K.H. Hygiene and mental health among middle school students in India and 11 other countries. J. Infect. Public Health. 2016;9:429–435. doi: 10.1016/j.jiph.2015.11.007. [DOI] [PubMed] [Google Scholar]
- Rief W., Glaesmer H., Baehr V., et al. The relationship of modern health worries to depression, symptom reporting and quality of life in a general population survey. J. Psychosomat. Res. 2012;72:318–320. doi: 10.1016/j.jpsychores.2011.11.017. [DOI] [PubMed] [Google Scholar]
- Shakeel N., Eberhard-Gran M., Sletner L., et al. A prospective cohort study of depression in pregnancy, prevalence and risk factors in a multi-ethnic population. BMC Pregnancy Childbirth. 2015;15:5. doi: 10.1186/s12884-014-0420-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smyth C. The Pittsburgh Sleep Quality Index (PSQI) Insight. 2000;25:97–98. doi: 10.1067/min.2000.107649. [DOI] [PubMed] [Google Scholar]
- Stein A., Pearson R.M., Goodman S.H., et al. Effects of perinatal mental disorders on the fetus and child. The Lancet. 2014;384:1800–1819. doi: 10.1016/S0140-6736(14)61277-0. [DOI] [PubMed] [Google Scholar]
- Susan D.F.H., Deborah S., Cerith S.W., Veronica O. Antenatal depression predicts depression in adolescent offspring:prospective longitudinal community-based study. J Affect Disord. 2009;(113):236–243. doi: 10.1016/j.jad.2008.05.018. [DOI] [PubMed] [Google Scholar]
- Walker L.O., Cooney A.T., Riggs M.W. Psychosocial and Demographic Factors Related to Health Behaviors in the 1st Trimester. JOGNN. 1999;28:606–614. doi: 10.1111/j.1552-6909.1999.tb02169.x. [DOI] [PubMed] [Google Scholar]
- Wang C., Pan R., Wan X., et al. Immediate Psychological Responses and Associated Factors during the Initial Stage of the 2019 Coronavirus Disease (COVID-19) Epidemic among the General Population in China. Int. J. Environ. Res. Public Health. 2020;17:1729. doi: 10.3390/ijerph17051729. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wang Y., Di Y., Ye J., et al. Study on the public psychological states and its related factors during the outbreak of coronavirus disease 2019 (COVID-19) in some regions of China. Psychol Health Med. 2021;26:13–22. doi: 10.1080/13548506.2020.1746817. [DOI] [PubMed] [Google Scholar]
- Wang Z.Y., Chi Y.F. Self-rating anxiety scale (SAS) Shanghai Archives of Psychiatry. 1984;2:73–74. (In Chinese) [Google Scholar]
- WHO, 2020. WHO Director-General's opening remarks at the media briefing on COVID-19-11 March 2020. https://www.who.int/dg/speeches/detail/who-director-general-s-opening-remarks-at-the-media-briefing-on-covid-19—11-march-2020. (accessed May 28, 2020).
- Wu Y., Zhang C., Liu H., et al. Perinatal depressive and anxiety symptoms of pregnant women along with COVID-19 outbreak in China. Am. J. Obstet. Gynecol. 2020 doi: 10.1016/j.ajog.2020.05.009. S0002-9378:30534-2[published online ahead of print, 2020 May 10] [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xie, X., Xue, Q., Zhou, Y., et al., 2020. Mental Health Status Among Children in Home Confinement During the Coronavirus Disease 2019 Outbreak in Hubei Province, China. JAMA pediatrics. e201619. [published online ahead of print, 2020 Apr 24]. [DOI] [PMC free article] [PubMed]
- Yali A.M., Lobel M. Coping and distress in pregnancy: an investigation of medically high risk women. J. Psychosomat. Obstet. Gynecol. 1999;20:39–52. doi: 10.3109/01674829909075575. [DOI] [PubMed] [Google Scholar]
- Yang X., Song B., Wu A., et al. Social, Cognitive, and eHealth Mechanisms of COVID-19-Related Lockdown and Mandatory Quarantine That Potentially Affect the Mental Health of Pregnant Women in China: cross-Sectional Survey Study. J Med Internet Res. 2021;22(1):e24495. doi: 10.2196/24495. 23. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yip P.S., Cheung Y.T., Chau P.H., Law Y.W. The impact of epidemic outbreak: the case of severe acute respiratory syndrome (SARS) and suicide among older adults in Hong Kong. Crisis. 2010;31:86–92. doi: 10.1027/0227-5910/a000015. [DOI] [PubMed] [Google Scholar]
- Zuckerman B., Amaro H., Bauchner H., et al. Depressive symptoms during pregnancy: relationship to poor health behaviors. Am. J. Obstet. Gynecol. 1989;160:1107–1111. doi: 10.1016/0002-9378(89)90170-1. [DOI] [PubMed] [Google Scholar]