1.Knowledge, Attitude, and Practice Towards Safety and Health Risks Among Food Manufacturing Workers in Malaysia
Nur Shahida Murad ; Nor Ashikin Sopian ; Nurud Suria Suhaimi ; Indah Lutfiya ; Wan Zaiton Wan Sulaiman
International Journal of Public Health Research 2026;16(1):2457-2467
Knowledge, Attitude, and Practice Towards Safety ; Health Risks ; Food Manufacturing
Introduction
Food manufacturing in Malaysia exposes workers to numerous potential hazards and health risks throughout the work process. This study aimed to determine the level of knowledge, attitude, and practice (KAP) towards safety and health risks among food manufacturing workers and to examine the relationship between these domains.
Methods
A cross-sectional study was performed involving 80 workers from three food manufacturing factories in Negeri Sembilan. KAP was assessed through a validated questionnaire adapted from a previous study.
Results
All workers (100%) demonstrated a positive attitude, 98.7% show good practice, and 93.8% exhibit a good level of knowledge towards safety and health risks. The correlation study showed significant positive correlations between gender and attitude, and between education level and attitude, indicating that these sociodemographic factors influence safety attitudes. Work experience is significantly associated with knowledge, suggesting that work experience enhances knowledge. The study also reveals weak positive correlations among knowledge, attitude, and practice (KAP) regarding safety and health risk, but a significant correlation is observed between knowledge and practice.
Conclusions
These findings suggest that fostering practical knowledge is essential for ensuring safe work behaviors. Prioritizing hands-on safety training can help bridge the gap between theoretical attitude and daily operational safety, ultimately reducing occupational health risks among food manufacturing workers.
2.Two heartbeats, one tumor: Non-functioning adrenocortical tumor in pregnancy
Nur Nisrina Yahya ; Noor Rafhati Adyani Abdullah
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):21-
Introduction:
Adrenocortical carcinoma (ACC) is a rare and aggressive
malignancy, with an incidence of 1–2 cases per million
annually. Its occurrence during pregnancy is exceptionally uncommon, presenting significant diagnostic and management challenges due to overlapping physiological changes
and concerns for both maternal and fetal outcomes. While
most cases are hormonally functional, non-functioning
ACC during pregnancy is particularly rare and may result
in delayed diagnosis.
Case:
A 35-year-old Malay female was referred following ultrasonography for persistent back and left flank pain, which
revealed a left adrenal incidentaloma and a concurrent
10-week intrauterine pregnancy. There were no clinical
signs of hormone excess. Physical examination revealed a
normotensive patient with a large, palpable left abdominal
mass, without Cushingoid or virilizing features.
Magnetic resonance imaging (MRI) demonstrated a 12.1
× 10.3 × 12.8 cm heterogeneous left adrenal mass with
cystic and necrotic components, displacing adjacent
structures. Hormonal evaluation was within normal limits:
24-hour urinary cortisol 320.2 nmol/24 hours (reference
range [RR] 11.8–350), midnight salivary cortisol <3 and
4.2 nmol/L (RR <11.3), plasma metanephrine <0.2 nmol/L
(RR <0.5), normetanephrine 0.6 nmol/L (RR <0.9), and
17-hydroxyprogesterone 223 ng/dL (RR <285), consistent
with a non-functioning tumor.
Following multidisciplinary consultation, the patient
underwent open left adrenalectomy at 16 weeks’ gestation.
Histopathological analysis confirmed ACC (Weiss score
8/9) without extra-adrenal extension. Surveillance MRI at
32 weeks demonstrated no recurrence or residual mass.
At 40 weeks’ gestation, she delivered a healthy infant, and
both mother and child remain well on follow-up.
Conclusion
Non-functioning ACC during pregnancy is rare and
poses significant diagnostic challenges. Early imaging,
comprehensive hormonal assessment, and timely surgical
intervention during the second trimester are essential.
Multidisciplinary management is crucial to optimizing
maternal and fetal outcomes.
Female
;
Pregnancy
;
Heart Rate
;
Neoplasms
3.Prevalence of Diabetic Peripheral Neuropathy and Its Association With Serum Neuron-Specific Enolase Among Type 2 Diabetes Mellitus Patients
Siti Kaamilah Mohd Zin ; Fatimah Zaherah Mohamed Shah ; Nor Amelia Mohd Fauzi ; Rohana Abdul Ghani ; Nur &lsquo ; Aini Eddy Warman
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):33-
Introduction:
Diabetic peripheral neuropathy (DPN) is a common
complication of type 2 diabetes mellitus (T2DM), with
nerve conduction studies recognized as the diagnostic
gold standard. Serum neuron-specific enolase (NSE) has
been linked with DPN. This study aims to determine the
prevalence of DPN among T2DM patients, evaluate clinical
characteristics, and explore the relationship between NSE
and DPN.
Methodology:
A cross-sectional study was conducted at Universiti
Teknologi MARA Specialist Centre Sungai Buloh and
Hospital Al-Sultan Abdullah, involving patients aged 18–60
years, diagnosed with T2DM for more than 5 years (n = 132).
All participants underwent anthropometric measurement,
completed the Michigan Neuropathy Screening Instrument
evaluation, and biochemical parameters, including lipid
profile, hemoglobin A1c, and serum creatine and NSE.
The diagnosis of DPN was made based on positive NCS
findings. Logistic regression was used to identify factors
associated with DPN.
Results:
The study population had a mean age of 60.16 ± 10.28 years
and a mean duration of diabetes of 14.82 ± 6.66 years. The
prevalence of DPN was 51.5% (n = 68). Serum NSE levels
were significantly higher (p = 0.003) and independently
associated with the presence of DPN (adjusted odds ratio
[OR] 1.033, 95% confidence interval [CI] 1.009–1.058, p =
0.006). Participants with DPN were also more likely to be
on insulin therapy (p = 0.040). In addition, retinopathy
(adjusted OR 3.567, 95% CI 1.528–8.329, p = 0.013) and
elevated Urine Albumin-to-Creatinine Ratio levels
indicating albuminuria (adjusted OR 1.031, 95% CI 1.002–
1.061, p = 0.037) were significantly associated with DPN.
Conclusion
More than half of the study population had DPN, which
was significantly associated with both retinopathy and
nephropathy, as well as with elevated serum NSE.
This emphasizes the importance of early screening and
highlights the role of NSE as a surrogate marker for
neuropathy in diabetes.
Humans
;
Diabetes Mellitus, Type 2
;
Diabetic Neuropathies
;
Prevalence
;
Phosphopyruvate Hydratase
4.The Rotated Bipedicled Tram Flap: Maximising Breast Projection but Minimising Donor Morbidity - A Case Report
Norlia Abdullah ; Saiyidah Adila Mohd Adib ; Nur Fa&rsquo ; izah Ab Muin ; Nordashima Abd Shukor ; Suria Hayati Md Pauzi
Journal of Surgical Academia 2026;16(1):19-23
The Rotated Bipedicled Tram Flap: Maximising Breast Projection but Minimising Donor Morbidity - A Case Report
Autologous breast reconstruction using the transverse rectus abdominis myocutaneous (TRAM) flap remains a cornerstone of breast reconstructive surgery. However, with the classical TRAM flap, it is challenging to close a large post mastectomy defect in nulliparous and/or slim women. The resultant reconstructed breast also lacks projection. This case reported a novel modified TRAM flap technique performed in a nullipara. She had previously undergone a hysterectomy and oophorectomy for endometrial carcinoma via a pfannenstiel incision. She presented with a large left breast invasive micropapillary carcinoma (ER/PR negative HER2 3+) with only marginal response to neoadjuvant chemotherapy. She underwent a left mastectomy with axillary dissection and immediate breast reconstruction. The rotated bipedicled TRAM Flap was used to close the large defect, maximising breast projection while minimising donor site morbidity.
5.Global Diagnostic Criteria for Gestational Diabetes Mellitus: A Scoping Review Protocol to Inform Policy in Malaysia
Siti Sarah Hamzah ; Shazana Rifham Abdullah ; Nur Zati Iwani Ahmad Kamil ; Liyana Ahmad Zamri ; Nur Azlin Zainal Abidin ; Sharifah Nortasya Sayed ; Muhamad Kamarudin
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):47-48
Introduction:
Gestational diabetes mellitus (GDM) is a common pregnancy complication associated with adverse maternal and
neonatal outcomes, including hypertensive disorders,
caesarean delivery, macrosomia, and increased lifetime
risk of type 2 diabetes. Despite its clinical importance,
considerable international variation exists in GDM
screening and diagnostic criteria. Multiple frameworks are currently used, including those from the World Health
Organization (WHO), International Association of Diabetes
and Pregnancy Study Groups, Carpenter and Coustan, and
the National Diabetes Data Group. Differences in glucose
thresholds, testing protocols (one-step versus two-step),
and universal versus risk-based screening contribute
to heterogeneity in reported prevalence and healthcare
burden. In multi-ethnic, middle-income settings such as
Malaysia, identifying an evidence-informed and contextappropriate diagnostic approach is critical.
Methodology:
This scoping review follows the Joanna Briggs Institute
methodology and will be reported in accordance with the
PRISMA Extension for Scoping Reviews (PRISMA-ScR).
PubMed, Scopus, and ScienceDirect will be searched for
English-language studies, reviews, guidelines, and consensus statements reporting GDM diagnostic criteria. Two
reviewers will independently screen and select studies.
Results:
Data will be charted on country, study type, diagnostic
criteria, gestational age at screening, and reported
challenges. Findings will be synthesized descriptively and
presented in tables and figures. No formal risk-of-bias
assessment will be conducted.
Conclusion
This review will provide a comprehensive overview of
global diagnostic practices, highlight variations and gaps,
and support evidence-based selection of a suitable GDM
screening and diagnostic strategy for Malaysia.
Diabetes, Gestational
;
Malaysia
;
Policy
;
Review Literature as Topic
6.Determinants of Polycystic Ovarian Syndrome Among Adolescents with Overweight and Obesity: A Case-Control Study Protocol
Shazana Rifham Abdullah ; Nur Zati Iwani Ahmad Kamil ; Siti Sarah Hamzah ; Norhashimah Abu Seman ; Farah Huda Mohkiar ; Nur Azlin Zainal Abidin ; Ezarul Faradianna Lokman ; Azahadi Omar ; Liyana Ahmad Zamri ; Fatin Saparuddin ; Syarifah Nortasya Sayed Muhamad Kamarudin ; Puteri Sofia Nadira Megat Kamaruddin ; B. Vimala A/P R.M.T. Balasubramaniam ; Fazliana Mansor ; Nur Azurah Abdul Ghani ; Abqariyah Yahya ; Rahima Dahlan @Mohd Shafie ; Ahmad Ali Zainuddin ; Kimberly Yuin Y&rsquo ; ng Wong ; Janet Yeow Hua Hong ; Nik Sumayyah Nik Mhd Nor ; Mohd Fairulnizal Md Noh ; Muhammad Yazid Jalaludin
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):61-
Introduction:
Polycystic ovarian syndrome (PCOS) is a complex
endocrine disorder that significantly affects adolescent
girls, particularly those with overweight or obesity.
However, data examining the determinants and metabolic
profiles of PCOS among adolescents with overweight
and obesity remain limited, especially in Malaysia. This
protocol describes a case-control study investigating the
cardiometabolic, dietary, and psychosocial determinants of
PCOS among adolescents with overweight and obesity.
Methodology:
This study is designed as a case-control study involving
adolescent girls aged 13–16 years with a body mass
index z-score >+1 standard deviation. Cases are defined as adolescent girls with a confirmed diagnosis of PCOS
based on the recommendations of the 2017 International
Consortium of Paediatric Endocrinology (ICPE), while
controls are those who do not meet the diagnostic criteria
for PCOS. A total sample size of 440 participants is required.
Participants will be recruited from 22 secondary schools
selected from a list of schools in Kuala Lumpur. Data on
sociodemographic characteristics, psychosocial health,
physical activity, and dietary intake will be collected using
structured questionnaires. Blood samples will be obtained
and analyzed for diagnostic testing (free testosterone),
exclusion tests (thyroid-stimulating hormone, folliclestimulating hormone, luteinizing hormone, estradiol,
prolactin, and dehydroepiandrosterone sulfate), and
biochemical parameters (liver function tests, lipid profile,
hemoglobin A1c, fasting glucose, fasting insulin, and
inflammatory markers).
Results:
The study is expected to generate comprehensive data on
the cardiometabolic, dietary, and psychosocial determinants of PCOS among adolescents with overweight and
obesity. The findings will inform early screening strategies
and targeted interventions aimed at reducing long-term
reproductive and cardiometabolic complications.
Conclusion
This protocol outlines a structured approach to investigating PCOS in adolescence and addresses current gaps
in early identification and risk stratification among highrisk populations.
Adolescent
;
Humans
;
Case-Control Studies
;
Overweight
;
Polycystic Ovary Syndrome
;
Obesity
7.Steroid-Responsive Encephalopathy Associated With Thyroiditis
Chua Chong Yee ; Nur Haziqah Baharum ; Fadzliana Hanum Jalal ; Gunavathy Muthusamy
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):107-
Introduction:
Steroid-responsive encephalopathy associated with
thyroiditis (STREAT) is a rare clinical entity. Clinical
presentations of STREAT can range from a strokelike presentation to psychiatric symptoms. STREAT is
diagnosed based on four major criteria which include
altered cognitive function, new or worsening psychiatric
symptoms, elevated antithyroid antibodies, and exclusion
of infectious, toxic, metabolic, or neoplastic causes. Corticosteroids are the cornerstone of treatment, with reported
excellent response in neurocognitive symptoms resolution.
Case:
This was a case of a 48-year-old male with Graves’s disease
who underwent radioiodine therapy 4 months earlier
and was started on levothyroxine 100 mcg 2 weeks prior
to presentation. He presented with 4 days of behavioral
symptoms, irritable mood with auditory and visual
hallucinations. There was no history of fever, headache, limb
weakness, or seizure. On general appearance, the patient
was agitated, talking incoherently, and disorientated with
normal vitals. There was no delayed relaxation of the reflex. The examination of the cranial nerve, motor, sensory, and
cerebellar system was normal. A lumbar puncture showed
normal opening pressure with a high protein CSF content
of 1,596 mg/L. The thyroid-stimulating hormone (TSH) was
elevated at 72.7 uIU/mL and T4 at 9.56 pmol/L. Serum antithyroid peroxidase was elevated at 877.42 IU/mL, and antiTSH receptor antibody at 21.30 IU/L. CSF oligonal band,
serum aquaporin-4, and viral screening were negative; noncontrasted computed tomography brain revealed normal
findings. Based on the clinical history and examination,
a diagnosis of STREAT was made at the emergency
department. The patient was initiated on hydrocortisone
100 mg three times a day. Within 24–48 hours of steroid
therapy, marked improvement and subsequent resolution
of the mental status and behavioral symptoms were seen.
Conclusion
Hashimoto’s thyroiditis can rarely lead to STREAT, a
condition with diverse neurological manifestations, where
early recognition and prompt corticosteroid therapy are
essential for favorable outcomes.
Brain Diseases
;
Thyroiditis
;
Steroids
8.Thyrotoxicosis Associated with Guillain–Barré Syndrome: A Rare Autoimmune Overlap
Nur Asmak Abdullah ; Rabeah Md Zuki ; Mohamed Azlam Micdhadhu
Journal of the ASEAN Federation of Endocrine Societies 2026;41(S1):117-118
Introduction:
The coexistence of thyroid storm and Guillain–Barré
syndrome (GBS) is rare, with few reported cases. A shared
autoimmune mechanism has been suggested, although
the exact pathophysiology remains unclear. In severe
thyrotoxicosis, new neurological symptoms may be overlooked or attributed to metabolic causes, delaying diagnosis
and posing a diagnostic and therapeutic challenge. We
report a case of a 43-year-old female with Graves’ disease
complicated by thyroid storm and Acute Motor Axonal
Neuropathy (AMAN), a variant of GBS, highlighting the
importance of early recognition and multidisciplinary
management.
Case:
A 43-year-old female with no prior medical illness
presented with fever, generalized weakness, fine tremors,
and 10 kg weight loss over 5 months. On arrival, she was
lethargic, febrile (40.2°C), and tachycardic (148 bpm),
consistent with thyroid storm by Burch–Wartofsky
criteria. She denied preceding diarrheal illness or upper
respiratory tract symptoms. The thyroid function test
showed markedly elevated free thyroxine 4 (>64.35 pmol/L)
and suppressed thyroid-stimulating hormone (TSH)
(<0.008 mIU/L). Subsequent testing revealed elevated TSH
receptor antibodies (>40 IU/L), confirming Graves’ disease.
Her course was complicated by anaphylactic shock with
transient cardiac arrest, followed by acute kidney injury and
respiratory failure requiring intensive care unit admission
and mechanical ventilation. Following extubation,
symmetrical limb weakness with generalized areflexia and
bilateral foot drop was observed. Nerve conduction studies
demonstrated a symmetrical axonal motor-predominant
polyneuropathy consistent with AMAN.
She received five sessions of plasma exchange and showed
marked neurological improvement, while thyroid and
renal function normalized at discharge.
Conclusion
This case highlights a rare and potentially life-threatening
association of thyroid storm and AMAN. Severe
thyrotoxicosis can precipitate atypical autoimmune
complications, underscoring the need for vigilance.
Clinicians should consider neurological evaluation in
patients with severe thyrotoxicosis presenting with newonset motor weakness.
Thyrotoxicosis
9.The prognostic significance of the fibrosis-5 index in patients with acute decompensated heart failure.
Sefa TATAR ; Yunus Emre YAVUZ ; Hilal Nur GEDIK ; Abdullah IÇLI ; Hakan AKILLI
Journal of Geriatric Cardiology 2025;22(6):587-595
BACKGROUND:
Acute decompensated heart failure (ADHF) is one of the leading causes of mortality, highlighting the importance of early identification of high-risk patients. The fibrosis-5 (FIB-5) index, traditionally used to evaluate hepatic fibrosis, may hold prognostic value in ADHF patients by reflecting systemic congestion, inflammation, and organ dysfunction. The hypothesis of this study is that the FIB-5 index is an independent predictor of 1-month mortality in patients with ADHF.
METHODS:
This retrospective study included 155 patients diagnosed with ADHF between 2020 and 2024. Patients were divided into two groups based on their left ventricular ejection fraction (LVEF ≤ 40% or LVEF > 50%). Survival was monitored for one month, and clinical, biochemical, and echocardiographic parameters were compared between survivors and death. Logistic regression and receiver operating characteristic curve analyses were performed to assess the prognostic value of the FIB-5 index.
RESULTS:
During the 1-month follow-up, 66 patients (42.6%) died. The mean FIB-5 index was significantly lower in non-survivors (-10.46 ± 6.93) compared to survivors (-8.10 ± 6.67) (P = 0.03). Multivariate regression analysis identified the FIB-5 index as an independent predictor of 1-month mortality (OR = 1.089, 95% CI: 1.022-1.160, P = 0.009). The receiver operating characteristic curve analysis demonstrated an area under the curve of 0.609 (95% CI: 0.51-0.699) with sensitivity of 59.6% and specificity of 63.4%. Kaplan-Meier survival analysis revealed significantly higher mortality rates among patients with lower FIB-5 values (log-rank: 7.887, P = 0.005).
CONCLUSIONS
The FIB-5 index is an independent predictor of 1-month mortality in ADHF patients. Its low cost, non-invasive nature, and ability to reflect systemic inflammation and congestion make it a promising tool for risk stratification. Prospective studies are needed to validate its utility in clinical practice and evaluate its role in guiding therapeutic decisions.


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