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1.
J Child Psychol Psychiatry ; 54(8): 846-53, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23336424

ABSTRACT

BACKGROUND: Sensory over-responsivity (SOR) affects many individuals with autism spectrum disorders (ASD), often leading to stressful encounters during daily routines. METHODS: This study describes the associations between early SOR symptoms and the longitudinal course of restrictions in family life activities and parenting stress across three time-points in families raising a child with ASD (n = 174). Covariates were child diagnostic severity, emotional problems, and maternal affective symptoms. At time 1 mean chronological age was 28.5 months. Children were administered the Autism Diagnostic Observation Schedule (ADOS) and Mullen Scales of Early Learning (MSEL). Parents completed the Infant Toddler Sensory Profile (ITSP), Infant-Toddler Social Emotional Assessment (ITSEA), Beck Anxiety Index (BAI), and the Center for Epidemiologic Studies Depression Inventory (CES-D) at time 1; and the Parenting Stress Index (PSI) and Family Life Impairment Scale (FLIS) at the three annual time-points. RESULTS: Latent Growth Curve Models indicated that higher SOR scores on the ITSP at time 1 were associated with higher initial levels of family life impairment and parenting stress and with a smaller magnitude of change over time. These associations were independent of severity of ADOS social-communication symptoms, MSEL composite score, ITSEA externalizing and anxiety symptoms, and maternal affective symptoms as measured by the BAI and CES-D. On average FLIS and PSI did not change over time, however, there was significant individual variability. Concurrently, SOR at time 1 explained 39-45% of the variance in family stress and impairment variables. CONCLUSIONS: An evaluation of SOR should be integrated into the assessment of toddlers with ASD considering their role in family life impairment and stress.


Subject(s)
Child Development Disorders, Pervasive/psychology , Parenting/psychology , Sensation Disorders/psychology , Stress, Psychological/psychology , Adult , Child , Child Development Disorders, Pervasive/complications , Child, Preschool , Family/psychology , Female , Genetic Testing , Humans , Infant , Longitudinal Studies , Male , Psychiatric Status Rating Scales , Sensation Disorders/etiology , Stress, Psychological/etiology
2.
J Abnorm Child Psychol ; 37(5): 705-16, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19153827

ABSTRACT

Sensory over-responsivity (SOR) towards tactile and auditory input can impact children's participation in academic and social activities; however the prevalence of SOR behaviors and their relation to social-emotional problems and competence has not been rigorously studied. This study investigated SOR in a representative sample of elementary school-aged children (n = 925, 50% boys, ages 7-11 years) who were followed from infancy. Sixteen percent of parents reported that at least four tactile or auditory sensations bothered their children. Being bothered by certain sensations was common while others were relatively rare. Parents of children with versus without elevated SOR in school-age reported higher frequencies of early and co-occurring internalizing, externalizing, and dysregulation problems, and lower levels of concurrent adaptive social behaviors. Early identification of elevated SOR and assessment of concurrent social-emotional status are important to minimize their impact on social adaptive behaviors at school age.


Subject(s)
Anxiety Disorders/epidemiology , Depressive Disorder/epidemiology , Disruptive, Impulse Control, and Conduct Disorders/epidemiology , Schools , Social Alienation , Social Behavior , Adaptation, Psychological , Aggression/psychology , Anxiety Disorders/diagnosis , Anxiety Disorders/psychology , Child , Depressive Disorder/diagnosis , Depressive Disorder/psychology , Disruptive, Impulse Control, and Conduct Disorders/diagnosis , Disruptive, Impulse Control, and Conduct Disorders/psychology , Female , Follow-Up Studies , Humans , Male , Prevalence , Surveys and Questionnaires
3.
J Child Psychol Psychiatry ; 49(8): 817-25, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18498344

ABSTRACT

BACKGROUND: Individuals with autism spectrum disorders (ASDs) show variability in their sensory behaviors. In this study we identified clusters of toddlers with ASDs who shared sensory profiles and examined differences in affective symptoms across these clusters. METHOD: Using cluster analysis 170 toddlers with ASDs were grouped based on parent rating of the Infant Toddler Sensory Profile (Dunn, 2002) under-responsivity, over-responsivity, and seeking scales. Affective symptoms were evaluated with the Infant Toddler Social Emotional Assessment (Carter & Briggs-Gowan, 2005). RESULTS: Three clusters were identified: (1) low frequency of sensory symptoms (n = 44); (2) high frequency of symptoms (n = 49); and (3) mixed (n = 77); high frequency of under-and over-responsivity and low frequency of seeking). Relative to the low frequency cluster, parents rated toddlers in the high frequency and mixed clusters (both characterized by high frequencies of sensory under- and over-responsivity) as higher on negative emotionality, depression, and anxiety symptoms. Sensory and affective differences among clusters remained after co-varying severity of ASD symptoms. CONCLUSIONS: Interdisciplinary assessments are recommended for toddlers with ASDs in order to identify the interplay of sensory and affective symptoms.


Subject(s)
Autistic Disorder/diagnosis , Autistic Disorder/epidemiology , Mood Disorders/diagnosis , Mood Disorders/epidemiology , Child, Preschool , Cluster Analysis , Female , Humans , Infant , Learning , Male , Mood Disorders/psychology , Severity of Illness Index , Surveys and Questionnaires
4.
QJM ; 88(5): 333-9, 1995 May.
Article in English | MEDLINE | ID: mdl-7796088

ABSTRACT

Although full blood counts (FBC) are among the most commonly performed laboratory tests, the contribution of routine FBCs to the diagnosis of new problems is controversial. This study represents a unique linkage of a consultant haematology team, reviewing all abnormal blood counts, to an organization providing ambulatory health care to 350,000 patients. The objective was to establish the underlying clinical disorders responsible for all abnormal FBCs during a 2-month period, and to estimate the impact of the haematology team on the diagnostic work-up and management of newly identified problems. 572 (2.55%) of the 22,454 FBCs were abnormal. Of these, 357 showed microcytosis, caused by iron deficiency (58%), thalassaemia minor (35%), inflammation (6%) or chronic renal failure (1%). The most common causes of normocytic anaemia (25 patients) were disseminated malignancy and acute blood loss; of macrocytosis (27 patients), chronic liver disease and cancer; of erythrocytosis (16 patients), chronic hypoxia; of thrombocytopaenia (48 patients), chronic liver disease and ITP; of thrombocytosis (47 patients), iron deficiency and inflammation; of leukopaenia or pancytopaenia (20 patients), cirrhosis and disseminated malignancy; and of leukocytosis (26 patients), chronic leukaemias in the elderly and infection in children. Major new haematological abnormalities were encountered in 0.24% of all blood counts, representing about one new diagnosis per day. Routine blood counts do contribute to the health care of a population. Screening for haematological disease through a central clinical laboratory covering a large high-risk ambulatory population offers a cost-effective way of searching for serious clinical problems, alerting the primary physicians of their existence, and offering advice in continued evaluation and problem management.


Subject(s)
Blood Cell Count , Community Health Services , Hematologic Diseases/blood , Adolescent , Adult , Anemia, Iron-Deficiency/blood , Anemia, Iron-Deficiency/complications , Child , Child, Preschool , Female , Humans , Interprofessional Relations , Israel , Leukemia/diagnosis , Liver Diseases/diagnosis , Male , Middle Aged , Neoplasms/diagnosis , Prospective Studies , beta-Thalassemia/blood , beta-Thalassemia/complications
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