1.The quality of life, situations and emerging concerns of parents of children with neurodevelopmental disorders in Philippine Children's Medical Center during COVID-19 pandemic.
Annelyn Fatima M. Lopez ; Ermenilda L. Avendañ ; o ; Aileen Marie O. Vargas ; Lara C. Baylon ; Rorilee Q. Angeles
The Philippine Children’s Medical Center Journal 2022;18(1):32-56
BACKGROUND:
COVID-19 resulted in a public health emergency and quarantine measures which may negatively impact vulnerable populations.
OBJECTIVES:
This study intends to determine the quality of life, situations and emerging
concerns of parents of children with neurodevelopmental disorders during the ongoing
pandemic.
METHODOLOGY:
A cross-sectional survey using a socio-demographic questionnaire, situations and emerging concerns during the coronavirus pandemic and WHOQOL-BREF (Filipino version) for parental quality of life was documented via Google Forms. Parents of patients aged 2-18 years seen at the PCMC Neurodevelopmental Pediatrics OPD during July to December 2019 were recruited.
RESULTS:
Data from 115 respondents showed a lower score in the environmental domain.
Child characteristics comparable with QoL scores include sex, severity of ID and ADHD
while parent characteristics comparable with the QoL scores include educational attainment,
monthly family income, father’s employment status and family structure (P-value <0.05).
Most respondents reported situations of physical distancing (82.61%) and curfew (80.87%).
Inability to access essential services (43.48-74.48%) were further compounded by limited
financial resources (51.30%) and public transport (60%). Government policy received
included quarantine pass (90.43%), food allowance or relief package (86.09%), disinfection
(60.87%), DSWD-SAP (42.61%) and cash distribution (41.74%).
RECOMMENDATIONS
Programs and policies should be planned accordingly to provide improvement of quality of life to parents and their child with neurodevelopmental disorder.
Neurodevelopmental Disorders
3.We got to move it, move it: The lived experiences of family carers of youth with chronic neurodevelopmental disorders as they enter into adult health care
Michelle G SY ; Maria Minerva P CALIMAG ; Rosalina Q DE SAGUN ; Maria Antonia Aurora M VALENCIA
Journal of Medicine University of Santo Tomas 2020;4(2):486-499
Background and objective :
Neurodevelopmental
disabilities in adolescents have signifi cant effects on
medical and social function. One of these challenges
is their transition into adult care. Parental involvement
is critical because these young adults may have more
diffi culties in making informed decisions independently. Thus, the transition process involves not only the
direct health care needs of the young adult, but the
needs and concerns of the parents or carers who are
instrumental in guiding that process. This study aims
to explore the expectations and experiences of family carers of youths with chronic neurodevelopmental
disorders who have undergone or are about to undergo transition into adult healthcare in a Filipino-based
health care system.
Methods:
A descriptive phenomenology was used to
gain an in-depth understanding of parents’ perceptions
and experiences of their youths’ transition process from
a pediatric to an adult health care setting. The results
were analyzed manually using Colaizzi’s method, which
involves integrating both the destructured and restructured analysis principles of phenomenology. Purposive
sampling was used to interview 13 family carers of 13
youths with various neurodevelopmental disorders using a semi-structured interview questionnaire.
Results :
Despite the lack of information on the transition process, our study found that carers did not have
a strong inclination to resist the transition event. Most
of the carers treat the health care provider as a major
decision maker in determining the timing and manner
of transition, adopting a “doctor knows best” attitude.
Several other hindrances and facilitators to successful
transition were also identifi ed and are similar to the
current literature.
Conclusion
This study provides a greater understanding of carers’ perceptions and experiences of
transition care for youths with neurodevelopmental
disorders in the local setting. They exhibited trust and confi dence in the medical profession as a whole, and
had a “doctor knows best” attitude that may enable
successful transitioning.
Transitional Care
;
Neurology
;
Neurodevelopmental Disorders
;
Caregivers
4.Progress in Modeling Neural Tube Development and Defects by Organoid Reconstruction.
Neuroscience Bulletin 2022;38(11):1409-1419
It is clear that organoids are useful for studying the structure as well as the functions of organs and tissues; they are able to simulate cell-to-cell interactions, symmetrical and asymmetric division, proliferation, and migration of different cell groups. Some progress has been made using brain organoids to elucidate the genetic basis of certain neurodevelopmental disorders. Such as Parkinson's disease and Alzheimer's disease. However, research on organoids in early neural development has received insufficient attention, especially that focusing on neural tube precursors. In this review, we focus on the recent research progress on neural tube organoids and discuss both their challenges and potential solutions.
Humans
;
Organoids
;
Neural Tube
;
Neurodevelopmental Disorders/genetics*
;
Brain
;
Alzheimer Disease
5.Advances in genetic research on autism spectrum disorders.
Kaituo HUANG ; Ye ZHANG ; Rui ZHAO ; Shanshan HU
Chinese Journal of Medical Genetics 2022;39(1):103-107
Autism spectrum disorder (ASD) is a set of neurodevelopmental disorders. Patients usually exhibit certain degree of social interaction impairment in accompany with impairment in language development as well as repetitive behaviors or interests. In recent years, ASD-related variants, genes, functional pathways, and expression patterns in the brain have been discovered, along with advance in sequencing techniques. This article reviews various aspects of genetic research in association with ASD.
Autism Spectrum Disorder/genetics*
;
Cognition
;
Genetic Research
;
Humans
;
Neurodevelopmental Disorders
6.Depression and anxiety among caregivers of children and adolescents with neurodevelopmental disorders in a government tertiary hospital during the Covid-19 pandemic
Erik Jan T. Estrada ; Ermenilda L. Avendañ ; o ; Anna Lizza S. Mañ ; alac
The Philippine Children’s Medical Center Journal 2023;19(2):17-31
Objectives:
To determine the burden of COVID-19 related mental health problems such as
anxiety and/or depression among caregivers of children and adolescents with neurodevelopmental
disorders in a government tertiary hospital.
Materials and Methods:
This is a cross-sectional study conducted at the Out-patient
Department of PCMC. Caregiver data sheet and HADS-P forms were given to eligible caregivers.
Results:
A total of 102 caregivers were included. The prevalence of significant risk for
anxiety disorder among caregivers of children and adolescents with neurodevelopmental disorders
is 34.31% (n=35), 1.96% (n=2) for depression and 3.92% (n=4) for both anxiety and depression.
Using logistic regression, marital status of common law partner and female sex have significant
association with depression and anxiety; the number of household members has a direct
association to significant risk for both anxiety and depression.
Conclusion
Female sex and common law partnership as marital status are associated with
2-3 times of having significant risk for anxiety or depression. The number of household members
is correlated with an increased significant risk of having both anxiety and depression. Screening
caregivers using appropriate tests would identify caregivers at significant risk for anxiety and
depression and further create intervention programs.
Anxiety
;
Depression
;
Caregiversl
;
Neurodevelopmental Disorders
;
COVID-19
;
Mental Health
7.Clinical Implications of Social Communication Disorder.
Journal of the Korean Academy of Child and Adolescent Psychiatry 2017;28(4):192-196
Social (pragmatic) communication disorder (SCD) is a new diagnosis included under communication disorders in the neurodevelopmental disorders section of Diagnostic and Statistical Manual of Mental Disorders-5. SCD is defined as a primary deficit in the social use of nonverbal and verbal communication. SCD has very much in common with pragmatic language impairment, which is characterized by difficulties in understanding and using language in context and following the social rules of language, despite relative strengths in word knowledge and grammar. SCD and Autism Spectrum Disorder (ASD) are similar in that they both involve deficits in social communication skills, however individuals with SCD do not demonstrate restricted interests, repetitive behaviors, insistence on sameness, or sensory abnormalities. It is essential to rule out a diagnosis of ASD by verifying the lack of these additional symptoms, current or past. The criteria for SCD are qualitatively different from those of ASD and are not equivalent to those of mild ASD. It is clinically important that SCD should be differentiated from high-functioning ASD (such as Asperger syndrome) and nonverbal learning disabilities. The ultimate goals are the refinement of the conceptualization, development and validation of assessment tools and interventions, and obtaining a comprehensive understanding of the shared and unique etiologic factors for SCD in relation to those of other neurodevelopmental disorders.
Autism Spectrum Disorder
;
Communication Disorders
;
Diagnosis
;
Learning Disorders
;
Neurodevelopmental Disorders
;
Social Communication Disorder*
8.Comparative Analysis of the WISC between Two ADHD Subgroups
Yoichiro KUBO ; Tetsufumi KANAZAWA ; Yasuo KAWABATA ; Koyuki TANAKA ; Tatsushi OKAYAMA ; Miho FUJTA ; Atsushi TSUTSUMI ; Shingo YOKOTA ; Hiroshi YONEDA
Psychiatry Investigation 2018;15(2):172-177
OBJECTIVE: The prevalence of attention deficit/hyperactivity disorder (ADHD) in school-age children is 7.2%, and ADHD is divided into clinical subtypes. METHODS: The current study explored whether specific cognitive profiles as assessed using the Wechsler Intelligence Scale for Children (WISC)-IV could be obtained for each clinical ADHD subtype (ADHD-Inattentive type and ADHD-Combined type) and investigated the correlation between WISC scores and parental age at their children’s birth or birthweight. The enrolled sample comprised 12 ADHD-I and 15 ADHD-C subjects. RESULTS: An impaired Processing Speed Index was found in ADHD-I. The age of the father at the child’s birth and birthweight positively correlated with the full scale intelligence quotient (FSIQ) score in the WISC assessment. CONCLUSION: Inattentiveness within the behaviors of the children with ADHD-I is partly due to the impaired processing speed, therefore effective support for ADHD will be conducted if educator decreases their speaking speed. Since biological basis of ADHD is still largely unknown, future studies using both psychological and biological methods will reveal the etiology of ADHD. These scientific assessments will provide information for more effective approaches in the care of children with ADHD.
Child
;
Cognitive Science
;
Fathers
;
Humans
;
Intelligence
;
Neurodevelopmental Disorders
;
Parents
;
Parturition
;
Prevalence
9.Aberrant Neural Activation Underlying Idiom Comprehension in Korean Children with High Functioning Autism Spectrum Disorder.
Namwook KIM ; Uk Su CHOI ; Sungji HA ; Seul Bee LEE ; Seung Ha SONG ; Dong Ho SONG ; Keun Ah CHEON
Yonsei Medical Journal 2018;59(7):897-903
PURPOSE: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by social communication impairments and repetitive behaviors or restricted interests. Impaired pragmatic language comprehension is a universal feature in individuals with ASD. However, the underlying neural basis of pragmatic language is poorly understood. In the present study, we examined neural activation patterns associated with impaired pragmatic language comprehension in ASD, compared to typically developing children (TDC). MATERIALS AND METHODS: Functional magnetic resonance imaging (fMRI) was applied to 15 children with ASD and 18 TDC using the Korean pragmatic language task. RESULTS: Children with ASD were less accurate than TDC at comprehending idioms, particularly when they were required to interpret idioms with mismatched images (mismatched condition). Children with ASD also showed different patterns of neural activity than TDC in all three conditions (neutral, matched, and mismatched). Specifically, children with ASD showed decreased activation in the right inferior frontal gyrus (IFG) (Brodmann area 47) in the mismatched condition, compared with TDC (IFG; t(31)=3.17, p < 0.001). CONCLUSION: These results suggest that children with ASD face difficulties in comprehending pragmatic expressions and apply different pragmatic language processes at the neural level.
Autism Spectrum Disorder*
;
Autistic Disorder*
;
Child*
;
Comprehension*
;
Humans
;
Magnetic Resonance Imaging
;
Neurodevelopmental Disorders
;
Prefrontal Cortex
10.Early Postnatal Valproic Acid Exposure Increase the Protein Level of Astrocyte Markers in Frontal Cortex of Rat.
Tamanna Jahan MONY ; Jae Won LEE ; Sung Soo KIM ; Wanjoo CHUN ; Hee Jae LEE
Clinical Psychopharmacology and Neuroscience 2018;16(2):214-217
OBJECTIVE: In our previous study, it has been reported that valproic acid (VPA) effects gliogenesis and increases the number of glial precursor cells during the early postnatal period. However there is no specific report that whether this process is going on up to the age of mature brain development and the consequence effect of this ongoing gliogenesis process. METHODS: As an ongoing study, using Immunoblotting analysis, we checked the level of glial protein and glial-derived factor markers in the frontal cortex of a rat brain at postnatal day (PND) 21. RESULTS: The finding of the study suggests that, in the VPA group (p < 0.05), early exposure elicited significantly to increase the expression level of glial protein cells at PND 21 in the frontal cortex of rat brain. CONCLUSION: Therefore we suggest that, alter gliogenesis and abnormal number of glial cells modulate the neurobiological dysfunction and induces the risk of neurodevelopmental disorders.
Animals
;
Astrocytes*
;
Brain
;
Frontal Lobe*
;
Immunoblotting
;
Neurodevelopmental Disorders
;
Neuroglia
;
Rats*
;
Valproic Acid*