Volume 21, Issue 3 (10-2024)                   J Res Dev Nurs Midw 2024, 21(3): 21-25 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Zeidabadi B, Iranpour A, Alavi-Arjas F, Baneshi M R, Shamsadini Moghadam S, Moqaddasi Amiri M et al . Maternal stress in the fetal anomaly screening process: A prospective cohort study. J Res Dev Nurs Midw 2024; 21 (3) :21-25
URL: http://nmj.goums.ac.ir/article-1-1770-en.html
1- Department of Health Education and Promotion, Sirjan School of Medical Sciences, Sirjan, Iran
2- Department of Health Education and Promotion, Faculty of Public Health, Kerman University of Medical Sciences, Kerman, Iran
3- Department of Midwifery, Sirjan School of Medical Sciences, Sirjan, Iran , f.alaviarjas@gmail.com
4- Australian Women and Girls’ Health Research (AWaGHR) Centre, School of Public Health, The University of Queensland, Brisbane, Australia
5- Department of Public Health, Sirjan School of Medical Sciences, Sirjan, Iran
6- Department of Midwifery and Reproductive Health, School of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Full-Text [PDF 494 kb]   (419 Downloads)     |   Abstract (HTML)  (680 Views)
Full-Text:   (124 Views)
Introduction
A growing body of literature indicated that psychosocial, cultural and environmental stressors experienced during gestation can be detrimental to maternal and fetal health. Moreover, prenatal stress can influence the physiological, behavioral, and cognitive development of offspring (1-6). The prevalence of prenatal stress is 16.5-74% in various societies, ranging from 16.5 to 74% in Iran (7).
Pregnant women often experience significant levels of anxiety and stress due to the fear of developing fetal abnormalities (8, 9). Approximately one-quarter of miscarriages and 4% of stillbirths are attributed to trisomies. Trisomy 21 is most commonly non-lethal and hence has been the main focus of genetic screening programs. Amniocentesis is a prenatal test that can diagnose genetic disorders (Such as Down syndrome and spina bifida) and other health issues in a fetus (10).
Screening in the first trimester of pregnancy helps determine the risk of the fetus having certain birth defects (11). A nuchal translucency (NT) test is an optional ultrasound performed in the first trimester of pregnancy that serves as an effective screening tool for high-risk pregnancies and fetal abnormalities. An increase in NT (Accumulation of fluid in the back of the fetus's neck) implies a higher likelihood of fetal chromosomal disorders and diseases, such as cardiac issues and genetic syndromes is revealed (12). NT ultrasound, with its minimal complications, is the preferred approach for screening fetal anomalies during the first trimester of pregnancy (13). The possibility of Down and Turner syndromes can be established by measuring NT between the 11th and 14th week of gestation and evaluating the major risk factors (14,15). It has been revealed that even in fetuses with normal standard karyotype, increasing NT is associated with cardiac problems or anomalies, pathogenic or potentially pathogenic genetic variations identified through whole exome sequencing (16). Pregnant women are subjected to a significant degree of stress while awaiting the results of non-invasive anomaly screening tests.
In addition to NT measurement, other ultrasound parameters, such as the fetal nasal bone, tricuspid valve flow, and maternal serum markers, are also used for fetal anomaly screening process (17). First-trimester combined testing has yielded detection rates of 90% for Down syndrome, 97% for Edward syndrome, and 92% for Patau syndrome, accompanied by a false positive rate of 4%. This accuracy is realized through the amalgamation of various biomarkers, which include maternal free beta-human chorionic gonadotropin (β-hCG), pregnancy-associated plasma protein (PAPP-A), NT, and maternal age (18).
Considering the ability of non-invasive screening tests to detect fetal abnormalities in the first trimester, pregnant women often experience significant anxiety and stress before the tests and while waiting for the results. In the following steps, at-risk or high-risk mothers are subjected to invasive diagnostic tests (19).
As an invasive diagnostic test, amniocentesis is a prenatal test usually performed during the second or third trimester of pregnancy. It can diagnose certain chromosomal conditions (Such as Down syndrome) or genetic conditions (Such as cystic fibrosis) (20). In addition to being extremely expensive, invasive tests like chorionic villus sampling (CVS) and amniocentesis carry a risk of miscarriage (21). For this reason, some high-risk pregnant women refuse to undertake invasive diagnostic testing, and they experience high levels of tension and worry until the conclusion of their pregnancy (22). Although prenatal genetic screening tests help couples decide whether to proceed with a possible pregnancy, many pregnant women fear the procedure because they think it will hurt them. They are also worried about adverse effects and fetal harm during the sample procedure (23). As a result, they may experience substantial mental and emotional stress (22). Although it has gotten less attention, the psychological impact of prenatal anomaly screening methods is important.  It is also worth pointing out that most studies conducted so far have looked at the association between prenatal stress and outcomes like preterm delivery, birth weight, and other variables (24). Nevertheless, there have been few studies on the relationship between fetal anomaly screening and maternal stress.
The current study explored the background factors influencing maternal stress. Furthermore, the study compared the level of prenatal stress experienced by pregnant mothers with/without the results of fetal abnormalities prior to, during, and after the fetal anomaly tests. The results indicate those who require additional help in coping with stress and provide an answer to the question of whether screening for fetal anomalies reduces a mother's stress. Initially, the study identified the fundamental variables influencing maternal stress and then, the stress levels of women with and without fetal anomalies were compared before, during, and after the fetal anomaly screening tests.

Methods
Study design and participants
This prospective cohort study was conducted at the public health center of Sirjan, Iran, from March 2022 to January 2023 using the convenience sampling process to measure the mean score of perceived stress. Referring to analogous research (25), a sample size calculation was conducted with an alpha level (α) of 0.05, a power of 90%, and a precision of 2%. Accounting for a potential 30% decline in response rates, the study required a minimum of 228 participants.
To be eligible for inclusion in the study, participants had to be in their 6th-10th week of a singleton pregnancy, consent to undergo fetal anomaly screening tests, including serological and ultrasonographic tests, and have no complication with the current pregnancy (e.g., preeclampsia, spotting, an incomplete mole, an ovarian cyst or myoma), have no history of or current known mental illness, have no known medical anomalies, as well as have no current chorionic diseases (e.g., diabetes mellitus, hypertension, hypothyroidism, etc.). The study neither included mothers who had previous children with any type of congenital anomaly, nor those who had a positive history of diagnostic or screening fetal anomaly tests in the previous or current pregnancy.
Exclusion criteria were unwillingness to continue the study, refusal to carry out diagnostic tests following abnormal results from screening tests, the presence of any maternal disease or an unusual occurrence in a normal pregnancy course (High blood pressure, gestational diabetes, thyroid disorders, etc.), and finally detection of any unusual results in the course of pregnancy, including bleeding, spotting, early rupturing of the membranes, miscarriage, mole, ectopic pregnancy. After explaining research objectives and procedure, written informed consent was obtained from eligible participants.
Data collection
The Perceived Stress Scale (PSS) developed by Cohen, Kamarck (26) was applied for data accumulation. Additionally, the individual would provide background details, including age, level of education, occupation, economic status, number of children, number of pregnancies, family history, and type of pregnancy (Wanted or unwanted pregnancy). For illiterate subjects, it would be completed by a midwife or a health expert.
Instrument
Perceived Stress Scale (PSS)
The PSS-14 is comprised of 14 items intended to measure how unpredictable, uncontrollable, and overloaded individuals find their life circumstances. It was developed by Cohen et al. (1983) (26). Each item is rated on a 5-point Likert scale, ranging from 0 = 'never' to 4 = 'very often'. Scores range from 0-56, with higher scores indicating greater perceived stress. Respondents’ scores on the PSS-14 are intended to be compared to the larger sample. Scores are obtained by reverse scoring the positively stated items (items number 4, 5, 6, 7, 9, 10, and 13) and then summing the scores across all 14 items. A score of 0 to 18 indicates a low level of stress, 18 to 36 indicates moderate stress, and above 36 indicates a high level of stress. This questionnaire's validity was established through the use of a correlation coefficient of 0.63, a value that is statistically significant at p <0.05 level. Also, Bastani et al. applied PSS-14 in Iranian population and confirmed its reliability (Cronbach’s alpha = 0.74) (27).  Maroufizadeh et al. proved the validity of the Persian version of the 10-item PSS in adult asthmatic patients (28).
Procedure
Initially, background variables were measured by a researcher-made questionnaire. Then, and all participants filled out the PSS-14 questionnaire at 6-10 weeks of pregnancy.
Maternal serum fetal anomaly screening (Free- β-hCG and PAPP-A) and NT ultrasonography were required of all individuals at comprehensive health centers between weeks 11 and 14. Based on the likelihood that the fetus would have trisomy 13, 18, or 21 syndromes, the test was conducted using a maternal serum sample, and the findings showed low-risk, at-risk, or high-risk conditions. Additionally, NT ultrasound was conducted using the fetus's Crown-rump length (CRL) and the clear, bright space behind its neck as measurements. An abnormally high NT level was associated with a higher chance of trisomy 21 and fetal cardiac problems. Ultimately, the laboratory assessed the outcomes of maternal serum test and NT measurement to classify the mothers as belonging to either the low-risk or high-risk category.
After the first-trimester screening test (Weeks 11-14), a second stage of evaluation was carried out and the participants were divided into three groups: low-risk, at-risk, or high-risk. When they had all been given their screening results, the subjects completed the PSS questionnaire. Without additional help, the low-risk group keeps their pregnancy going. It is recommended that the at-risk group get screening tests during the second trimester of pregnancy. The high-risk group was referred to a gynecologist or perinatologist for invasive diagnostic testing (Amniocentesis or CVS) to determine whether to terminate the pregnancy.
The last assessment of perceived stress was performed in the third stage of evaluation, in the 15-20 weeks of pregnancy, as follows: in the Low-risk group, the perceived stress was evaluated while completing standard pregnancy care at the health facility.
Following the results of screening tests (15-20 weeks), at-risk group participants were assigned to low-risk or high-risk groups, and the perceived stress in the groups (Low-risk or high-risk) was assessed. After obtaining the findings of invasive amniocentesis or CVS test, perceived stress was measured in the high-risk group. Finally, changes in pregnant mothers' perceived stress were assessed.
Statistical methods
The Kolmogorov-Smirnov test was employed to analyze the normality of the stress score of expectant women in aggregate and in each demographic subgroup. In addition, the Freidman test and linear regression were used to compare the stress levels of background variables across two or more states. Friedman test was used for measuring the association between maternal stress and fetal abnormality test results. Data were analyzed with Statistical Package for the Social Sciences (SPSS) software version 26 at a significance level of 0.05.

Results
In total, 228 women completed all three surveys (Response rate 79.21%). The results revealed that 86.4% (197) were 35 and younger, 88.6% (202) were housewives, and 26.3% (60) were in marriages with relatives. Also, 31.6% (72) had no children and 8.8% (20) had unwanted pregnancies (Table 1).
The findings demonstrated that education had a positive effect on the participants' initial stress levels, with university-graduated women reporting lower stress levels than those with a diploma degree or less (P=0.05, β=1.74). Also, there was a significant difference (P=0.016, β=2.27) between the group with previous live child and the group without. This implies those having at least one child were less stressed. Table 2 summarizes the variations for all subjects with/without typical NT ultrasound. The level of stress measured in all pregnant women indicated that the perceived stress on the first attempt was higher than on the second (P=0.0001) and the third times (p <0.0001).
Figure 1 depicts the trend of stress changes in all three groups (All participating pregnant women, pregnant women with abnormal NT ultrasound, and pregnant women with normal NT ultrasound).

Table 1. The demographic characteristics of pregnant mothers and analysis of maternal perceived stress in subgroups
Table 2. Stress changes trend in pregnant women at three stages before (6-10 weeks), during (11-14 weeks) and after (15-20 weeks) fetal anomaly screening

Figure 1. Level of perceived stress in pregnant women participating in the study
As illustrated in Figure 1, the perceived stress of the pregnant women in the study was 47 in the initial phase, 45 in the second phase, and 44 in the third phase. There was an increase in stress before the screening test, but it was reduced following the tests. Besides, the initial measurement of perceived stress in pregnant women with abnormal NT ultrasound was 48, whereas dropped in the second and third levels.

Discussion
Our findings revealed that the mean perceived stress levels during weeks 6-10 were significantly higher than those observed in weeks 15-20. These are in agreement with other studies conducted on healthy singleton pregnant women that demonstrate a decrease in maternal stress over time (29,30). The researchers identified that the primary sources of stress during pregnancy stem from concerns about abortion, fetal development, prenatal results, and physical changes associated with pregnancy (31,32). By utilizing sonography to track fetal growth and surpass the high-risk abortion period in the first trimester, women can adapt to the changes of pregnancy more effectively, leading to a reduction in maternal stress over time.
The abnormal outcome of maternal serum screening test or NT in the ultrasound suggested a high likelihood of fetal anomaly, thus requiring an invasive diagnostic test (Amniocentesis or CVS). The findings of the present research indicated that despite the use of these highly precise diagnostic tests, maternal stress did not decrease. Other investigations have evidenced the impact of fetal abnormalities diagnosis on the psychological well-being of mothers and the amount of perceived stress they endure (33,34).
The prevalence of fetal abnormalities in each nation has an extensive effect on the health of mothers. Previous studies have established a prevalence of 2.3% (35) and 2.6% in Iran (36). In the present study, six women received abnormal NT ultrasounds, which is consistent with other Iranian studies. Furthermore, this study aimed to explore the association between sociodemographic characteristics and maternal-reported stress. The results highlighted the important role of educational level and having at least one live child in decreasing basic maternal stress. Educational attainment plays a pivotal role in mental health (37). There is a growing amount of evidence exhibiting the positive influence of educational level on women's stress during pregnancy, delivery, and postpartum (38-40).
Low educational level as a principal social determinant may be a harbinger of a lower quality of life and a rise in maternal stress. Pregnant women of higher educational levels may be more likely to seek information about their concerns on scientific websites, discuss their fears with healthcare providers, understand the explanations provided, and grasp the accuracy of screening tests.
Although our study found no significant relationship between the number of children and maternal stress, having at least one previous live birth was associated with a decrease in pregnancy-specific stress. Previous studies demonstrated a substantial effect of the number of existing live births on stress during pregnancy (41-43). Based on previous experiences and challenges that resulted in a positive outcome, the mother's self-assurance was reinforced during the subsequent pregnancy. Although pregnancy is a novel experience for all mothers, previous pregnancies can alleviate the anxiety of facing unfamiliar and unforeseen pregnancy difficulties. Though maternal stress has multiple sources, our research did not identify any additional factors that correlated with maternal stress levels. A larger sample size may have uncovered additional factors that could influence stress levels.
Overall, the mean perceived stress was 47 during weeks 6-10, with any score in above 36 considered a high amount of stress according to PSS. According to the PSS employed in other studies in Iran, the average stress score of healthy pregnant women was found to vary between 24 and 28 (44-46).
Zareipour et al. showed that 17.7% of pregnant women experienced high levels of stress (47). All of these articles showed a high level of maternal stress; however, the perceived stress score in our results was evidently higher than in previous studies (Approximately 47 compared to 24-28 in healthy women). The stress level in our study was even higher than perceived stress in mothers undergoing amniocentesis. It appears that confounding factors, such as the COVID-19 pandemic and the subsequent vaccination campaigns have led to this significant increase.
This study coincided with the outbreak of COVID-19 in Iran, and this unprecedented event might have affected maternal stress. Additionally, before our study began, a nationwide program for vaccinations was initiated against COVID-19 during pregnancy period, raising serious apprehensions about the potential for fetal mortality or morbidity in the wider population due to the use of the novel vaccine during pregnancy. Consistent with our results, other studies reported that pregnant women experienced a significant level of stress during the COVID-19 pandemic (48-50).
This study was conducted during a new wave of mass COVID infections and the introduction of a vaccination program for pregnant women, creating a challenging environment that resulted in serious mental and emotional problems. Designing a study under less stressful conditions with a higher sample size would provide more precise data.

Conclusion
The findings of this study demonstrated that pregnant women experience significant stress, especially those who are in the first pregnancy and those with unusual ultrasound results. In addition, women with a university degree and a normal ultrasound who had a second or subsequent pregnancy experienced significantly less stress than other women. For women with normal screening results, maternal stress levels decreased over time, while for those with abnormal NT sonography results, the stress level remained unchanged.

Acknowledgement
We would like to thank all pregnant women who participated in this study and all midwives of government health centers who helped us in this research.

Funding sources
This study was financially supported by Sirjan School of Medical Sciences (Grant No. 400000014).

Ethical statement
The ethical committee of Sirjan School of Medical Sciences approved this research (Ethics code: R.SIRUMS.REC.1400.018). Written informed consent was obtained from all participants. The participants' data were gathered and examined confidentiality, and the participants joined the study with full awareness and the liberty to withdraw from the research at any time.

Conflicts of interest
The authors have no competing interests to declare.

Author contributions
FA-A and BZ designed the study and carried out the necessary steps before starting the study. Coordination with health centers and data collection were done by MT and data analysis was done by MRB and M MA, F A-A, BZ, AI and S SM wrote the main manuscript text. All authors read and approved the final manuscript.
Type of study: Original Article | Subject: Midwifery

References
1. Traylor CS, Johnson JD, Kimmel MC, Manuck TA. Effects of psychological stress on adverse pregnancy outcomes and nonpharmacologic approaches for reduction: an expert review. Am J Obstet Gynecol MFM. 2020;2(4):100229. [View at Publisher] [DOI] [PMID] [Google Scholar]
2. Gokoel AR, Abdoel Wahid F, Zijlmans WCWR, Shankar A, Hindori-Mohangoo AD, Covert HH, et al. Influence of perceived stress on prenatal depression in Surinamese women enrolled in the CCREOH study. Reprod Health. 2021;18(1):136. [View at Publisher] [DOI] [PMID] [Google Scholar]
3. Stylianou-Riga P, Kouis P, Kinni P, Rigas A, Papadouri T, Yiallouros PK, et al. Maternal socioeconomic factors and the risk of premature birth and low birth weight in Cyprus: a case-control study. Reprod Health. 2018;15(1):157. [View at Publisher] [DOI] [PMID] [Google Scholar]
4. Van den Bergh BR, van den Heuvel MI, Lahti M, Braeken M, de Rooij SR, Entringer S, et al. Prenatal developmental origins of behavior and mental health: The influence of maternal stress in pregnancy. Neurosci Biobehav Rev. 2020;117:26-64. [View at Publisher] [DOI] [PMID] [Google Scholar]
5. Gaml-Sørensen A, Brix N, Henriksen TB, Ramlau-Hansen CH. Maternal stress in pregnancy and pubertal timing in girls and boys: A cohort study. Fertil Steril. 2024;122(4):715-26. [View at Publisher] [DOI] [PMID] [Google Scholar]
6. Ramos BA, Formiga CKMR, Oliveira NRGd, Marçal PGE, Ferreira RG, Saidah TK, et al. Relationship between Maternal Stress and Neurobehavioral Indicators of Preterm Infants in the Neonatal Intensive Care Unit. Children. 2024;11(8):889. [View at Publisher] [DOI] [PMID] [Google Scholar]
7. Miltoft CB, Rode L, Ekelund CK, Sundberg K, Kjærgaard S, Zingenberg H, et al. Contingent first‐trimester screening for aneuploidies with cell‐free DNA in a Danish clinical setting. Ultrasound Obstet Gynecol. 2018;51(4):470-9. [View at Publisher] [DOI] [PMID] [Google Scholar]
8. Bekkhus M, Oftedal A, Braithwaite E, Haugen G, Kaasen A. Paternal psychological stress after detection of fetal anomaly during pregnancy. A prospective longitudinal observational study. Front Psychol. 2020;11:1848. [View at Publisher] [DOI] [PMID] [Google Scholar]
9. Khakbazan Z, Farnam F, Abdollahi P, Arjmandifar M. Women's Concerns and Experiences of Fetal Anomaly Screening Process: A Qualitative Study. Int J Community Based Nurs Midwifery. 2023;11(1):44-56. [View at Publisher] [DOI] [PMID] [Google Scholar]
10. Howie C. Down's syndrome screening and reproductive politics: care, choice and disability in the prenatal clinic. J Reprod Infant Psychol. 2019;37(5):566-7. [View at Publisher] [DOI] [Google Scholar]
11. Viotti M. Preimplantation genetic testing for chromosomal abnormalities: aneuploidy, mosaicism, and structural rearrangements. Genes. 2020;11(6):602. [View at Publisher] [DOI] [Google Scholar]
12. Ozyuncu O, Tanacan A, Fadiloglu E, Unal C, Ziyadova G, Deren O. Impact of increased nuchal translucency values on pregnancy outcomes: a tertiary center experience. Fetal Pediatr Pathol. 2021;40(3):189-97. [View at Publisher] [DOI] [PMID] [Google Scholar]
13. Tekesin I. Pregnancy outcome in foetuses with increased nuchal translucency-10-years' experience in a prenatal medical practice. J Obstet Gynaecol. 2020;40(4):455-60. [View at Publisher] [DOI] [PMID] [Google Scholar]
14. Reimers R, High F, Kremen J, Wilkins‐Haug L. Prenatal diagnosis of sex chromosome aneuploidy-What do we tell the prospective parents? Prenat Diagn. 2023;43(2):250-60. [View at Publisher] [DOI] [PMID] [Google Scholar]
15. Arjunan S, Thomas MC. A review of ultrasound imaging techniques for the detection of down syndrome. IRBM. 2020;41(2):115-23. [View at Publisher] [DOI] [Google Scholar]
16. Di Girolamo R, Rizzo G, Khalil A, Alameddine S, Lisi G, Liberati M, et al. Whole exome sequencing in fetuses with isolated increased nuchal translucency: a systematic review and meta-analysis. J Matern Fetal Neonatal Med. 2023;36(1):2193285. [View at Publisher] [DOI] [PMID] [Google Scholar]
17. Kagan KO, Sonek J, Kozlowski P. Antenatal screening for chromosomal abnormalities. Arch Gynecol Obstet. 2022;305(4):825-35. [View at Publisher] [DOI] [PMID] [Google Scholar]
18. Santorum M, Wright D, Syngelaki A, Karagioti N, Nicolaides KH. Accuracy of first‐trimester combined test in screening for trisomies 21, 18 and 13. Ultrasound Obstet Gynecol. 2017;49(6):714-20. [View at Publisher] [DOI] [PMID] [Google Scholar]
19. Okoror CEM, Arora S. Prenatal diagnosis after high chance non-invasive prenatal testing for trisomies 21, 18 and 13, chorionic villus sampling or amniocentesis?-Experience at a district general hospital in the United Kingdom. Eur J Obstet Gynecol Reprod Biol X. 2023;19:100211. [View at Publisher] [DOI] [PMID] [Google Scholar]
20. Graf WD, Cohen BH, Kalsner L, Pearl PL, Sarnat HB, Epstein LG, et al. Fetal anomaly diagnosis and termination of pregnancy. Dev Med Child Neurol. 2023;65(7):900-7. [View at Publisher] [DOI] [PMID] [Google Scholar]
21. Di Mascio D, Khalil A, Rizzo G, Buca D, Liberati M, Martellucci CA, et al. Risk of fetal loss following amniocentesis or chorionic villus sampling in twin pregnancy: systematic review and meta‐analysis. Ultrasound Obstet Gynecol. 2020;56(5):647-55. [View at Publisher] [DOI] [PMID] [Google Scholar]
22. Monni G, Corda V, Iuculano A, Afshar Y. The decline of amniocentesis and the increase of chorionic villus sampling in modern perinatal medicine. Journal of Perinatal Medicine. 2020;48(4):307-12. [View at Publisher] [DOI] [PMID] [Google Scholar]
23. Marc-Aurele KL. Decisions parents make when faced with potentially life-limiting fetal diagnoses and the importance of perinatal palliative care. Front Pediatr. 2020;8:574556. [View at Publisher] [DOI] [PMID] [Google Scholar]
24. Jeličić L, Veselinović A, Ćirović M, Jakovljević V, Raičević S, Subotić M. Maternal Distress during Pregnancy and the Postpartum Period: Underlying Mechanisms and Child's Developmental Outcomes-A Narrative Review. Int J Mol Sci. 2022;23(22):13932. [View at Publisher] [DOI] [PMID] [Google Scholar]
25. Karimi N, Bahadori F, Khalkhali HR, Rabiepoor S. Evaluation of anxiety and perceived stress in mothers undergoing amniocentesis. Nursing And Midwifery Journal. 2017;15(4):292-300. [View at Publisher] [Google Scholar]
26. Cohen S, Kamarck T, Mermelstein R. A global measure of perceived stress. J Health Soc Behav. 1983;24(4):385-96. [View at Publisher] [DOI] [PMID] [Google Scholar]
27. Bastani F, Hidarnia A, Kazemnejad A, Vafaei M, Kashanian M. A randomized controlled trial of the effects of applied relaxation training on reducing anxiety and perceived stress in pregnant women. J Midwifery Womens Health. 2005;50(4):e36-40. [View at Publisher] [DOI] [PMID] [Google Scholar]
28. Maroufizadeh S, Zareiyan A, Sigari N. Reliability and validity of Persian version of perceived stress scale (PSS-10) in adults with asthma. Arch Iran Med. 2014;17(5):361-5. [View at Publisher] [PMID] [Google Scholar]
29. Racine N, Plamondon A, Hentges R, Tough S, Madigan S. Dynamic and bidirectional associations between maternal stress, anxiety, and social support: The critical role of partner and family support. J Affect Disord. 2019;252:19-24. [View at Publisher] [DOI] [PMID] [Google Scholar]
30. Preis H, Somers J, Mahaffey B, Lobel M. When pregnancy and pandemic coincide: changes in stress and anxiety over the course of pregnancy. J Reprod Infant Psychol. 2024;42(3):395-409. [View at Publisher] [DOI] [PMID] [Google Scholar]
31. Cortes Hidalgo AP, Neumann A, Bakermans‐Kranenburg MJ, Jaddoe VW, Rijlaarsdam J, Verhulst FC, et al. Prenatal maternal stress and child IQ. Child Dev. 2020;91(2):347-65. [View at Publisher] [DOI] [PMID] [Google Scholar]
32. 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. [View at Publisher] [DOI] [PMID] [Google Scholar]
33. Kaasen A, Helbig A, Malt UF, Næs T, Skari H, Haugen G. Maternal psychological responses during pregnancy after ultrasonographic detection of structural fetal anomalies: A prospective longitudinal observational study. PLoS One. 2017;12(3):e0174412. [View at Publisher] [DOI] [PMID] [Google Scholar]
34. Harris JM, Franck L, Michie S. Assessing the psychological effects of prenatal screening tests for maternal and foetal conditions: a systematic review. J Reprod Infant Psychol. 2012;30(3):222-46. [View at Publisher] [DOI] [Google Scholar]
35. Vatankhah S, Jalilvand M, Sarkhosh S, Azarmi M, Mohseni M. Prevalence of Congenital Anomalies in Iran: A Review Article. Iran J Public Health. 2017;46(6):733-43. [View at Publisher] [PMID] [Google Scholar]
36. Irani M, Khadivzadeh T, Asghari Nekah SM, Ebrahimipour H, Tara F. The prevalence of congenital anomalies in Iran: A Systematic Review and Meta-analysis. The Iranian Journal of Obstetrics, Gynecology and Infertility. 2018;21(Supple):29-41. [View at Publisher] [DOI] [Google Scholar]
37. Lund C, Brooke-Sumner C, Baingana F, Baron EC, Breuer E, Chandra P, et al. Social determinants of mental disorders and the Sustainable Development Goals: a systematic review of reviews. Lancet Psychiatry. 2018;5(4):357-69. [View at Publisher] [DOI] [PMID] [Google Scholar]
38. Wang W, Wen L, Zhang Y, Wang L, Wang L, Chen Z, et al. Maternal prenatal stress and its effects on primary pregnancy outcomes in twin pregnancies. J Psychosom Obstet Gynaecol. 2020;41(3):198-204. [View at Publisher] [DOI] [PMID] [Google Scholar]
39. Tanhae Reshvanloo F, Tavasoli Z, Talepasand S. The role of mothers' awareness about infants care in stress and anxiety during pregnancy: an invariance based on educational level. Zanko J Med Sci. 2018;18(59):80-91. [View at Publisher] [Google Scholar]
40. Mokhtari Zanjani P, Tehranian N, Changizi N, Mohammadi E, Farzinrad B, Kazemnejad A. Maternal mental health concerns during the COVID-19 pandemic in Iran: a content analysis study. Reprod Health. 2023;20(1):102. [View at Publisher] [DOI] [PMID] [Google Scholar]
41. Kim Y, Chung CW. Development of the Korean pregnancy stress scale. Jpn J Nurs Sci. 2018;15(2):113-24. [View at Publisher] [DOI] [PMID] [Google Scholar]
42. Shapiro GD, Séguin JR, Muckle G, Monnier P, Fraser WD. Previous pregnancy outcomes and subsequent pregnancy anxiety in a Quebec prospective cohort. J Psychosom Obstet Gynaecol. 2017;38(2):121-32. [View at Publisher] [DOI] [PMID] [Google Scholar]
43. Riquelme-Gallego B, Martínez-Vázquez S, Caparros-Gonzalez RA. Pandemic-related stress in pregnant women during the first COVID-19 lockdown and neonatal development. J Reprod Infant Psychol. 2023:1-16. [View at Publisher] [DOI] [PMID] [Google Scholar]
44. Kashanian M, Faghankhani M, YousefzadehRoshan M, EhsaniPour M, Sheikhansari N. Woman's perceived stress during pregnancy; stressors and pregnancy adverse outcomes. J Matern Fetal Neonatal Med. 2021;34(2):207-15. [View at Publisher] [DOI] [PMID] [Google Scholar]
45. Rabipoor S, Abedi M. Perceived Stress and Prenatal Distress during Pregnancy and its Related Factors. J Res Dev Nurs Midw. 2020;17(1):67-80. [View at Publisher] [DOI] [Google Scholar]
46. Bani S, Hasanpour S, Farzadi L, Mirghafourvand M, Golshani F, Ranjbar M. Self-Care Performance of Pregnant Women in Preventing COVID-19 Infection and Its Relationship with Perceived Stress. Iran J Psychiatry. 2023;18(1):26-34. [View at Publisher] [DOI] [PMID] [Google Scholar]
47. Zareipour M, Sadeghianifar A, Amirzehni J, Parsnezhad M, Ayuoghi Rahnema V. Exploring of depression, anxiety and stress in pregnant women referred to health centers of Urmia. Rahavard Salamat Journal. 2017;3(2):19-30. [View at Publisher] [Google Scholar]
48. Rastegari L, Mossayebnezhad R, Hosseinkhani A, Arsang-Jang S. Perceived Stress and Social Support in Pregnant Women during the COVID-19 Pandemic. Nursing and Midwifery Studies. 2023;12(1):42-7. [View at Publisher] [DOI] [Google Scholar]
49. Wheeler JM, Misra DP, Giurgescu C. Stress and coping among pregnant black women during the COVID‐19 pandemic. Public Health Nursing. 2021;38(4):596-602. [View at Publisher] [DOI] [PMID] [Google Scholar]
50. Otu A, Yaya S. Uncovering the collateral impacts of COVID-19 on maternal mental health. Reprod Health. 2022;19(1):115. [View at Publisher] [DOI] [PMID] [Google Scholar]

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2025 CC BY-NC 4.0 | Journal of Research Development in Nursing and Midwifery

Designed & Developed by : Yektaweb