Study Design and Setting
This study was designed as a multicentre, prospective observational study, conducted over eight months. The three tertiary centres chosen for this study—University of Malaya Medical Centre (UMMC) in Kuala Lumpur, Hospital Sultanah Aminah (HSA) in Johor Bahru, and Hospital Raja Permaisuri Bainun (HRPB) in Ipoh—represent major referral centres with paediatric surgical units serving a broad population across urban and rural regions. These centres reflect a typical middle-income healthcare system that includes a mixture of well-resourced urban hospitals and more resource-constrained regional centres.
Participants
Mothers of neonates diagnosed with congenital abnormalities were recruited for the study if their neonates met specific inclusion criteria. These criteria included a wide range of surgical congenital abnormalities such as thoracic (congenital diaphragmatic hernia, congenital pulmonary airway malformation), abdominal (omphalocele, gastroschisis), gastrointestinal (bowel atresia, anorectal malformation), and urological (posterior urethral valve, congenital hydronephrosis) anomalies. Neonates born during the study period and referred to paediatric surgery were included if their mothers consented to participate.
Neonates had non-surgical congenital abnormalities or where the mother had pre-existing mental health conditions (such as anxiety or depression) that could independently affect the maternal anxiety scores, were excluded. Additionally, families where the mother was not the primary caregiver or unable to provide consent (e.g., due to illness or other incapacity) were also excluded. Only mothers were included in this study because they are typically the primary caregivers in the early neonatal period, especially in the context of a middle-income country like Malaysia, where mothers often bear the primary responsibility for neonatal care.
Data Collection
Data were collected from antenatal records, postnatal medical files, and by administering structured questionnaires. The primary outcome measured was the antenatal detection rate of congenital abnormalities. The timing of the diagnosis—antenatal or postnatal—was noted, along with details of any antenatal counselling provided.
To evaluate the psychological impact on mothers, the Spielberg State-Trait Anxiety Inventory (STAI) was used. The STAI consists of two scales: the Y-1 form measures state anxiety, reflecting how respondents feel “at the moment,” while the Y-2 form measures trait anxiety, indicating baseline anxiety levels. Mothers were asked to complete the STAI within the first week postpartum.
Variables and Definitions
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Antenatal Detection Rate: The proportion of neonates whose congenital abnormalities were diagnosed during pregnancy via routine antenatal care.
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Maternal Anxiety: Measured using the STAI, with higher scores indicating greater anxiety. STAI scores are categorized into low, moderate, and severe anxiety based on standardized thresholds.
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Antenatal Counselling: Defined as consultations provided to expectant mothers by paediatric surgeons, paediatricians, or obstetricians regarding the congenital abnormality diagnosed antenatally.
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Surgical Condition: Defined as a congenital abnormality that requires surgical intervention by a general paediatric surgical team during the neonatal period or early infancy. This includes conditions that involve thoracic (e.g., congenital diaphragmatic hernia), abdominal (e.g., omphalocele, gastroschisis), gastrointestinal (e.g., bowel atresia, anorectal malformation), and urological (e.g., posterior urethral valve, congenital hydronephrosis) anomalies, all of which necessitate corrective surgery for optimal outcomes.
Statistical Analysis
Data were analysed using descriptive statistics to summarize demographic and clinical variables. Mann-Whitney U tests was used to compare maternal anxiety between groups based on antenatal versus postnatal diagnosis. A two-way ANOVA was employed to assess whether antenatal consultations with paediatric surgeons had a significant effect on anxiety scores. A p-value of ≤ 0.05 was considered statistically significant.
A power calculation was not performed for this study due to the observational and exploratory nature of the research, as well as the relatively limited pool of eligible participants during the study period. The sample size was determined based on the availability of cases at the participating centres. This study was intended to provide preliminary insights into antenatal detection rates and maternal anxiety, which will inform future, larger-scale studies with appropriate sample size calculations.