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Yousra H. AL JAZAIRY Hassan Suliman HALAWANY Nawaf AL HUSSAINAN Nassr AL MAFLEHI Nimmi Biju ABRAHAM Vimal JACOB 《Industrial health》2014,52(4):324-333
A disparity exists in the educational qualifications of dental assistants working in
various public and private institutions in Riyadh, Saudi Arabia. The aim of this study was
to assess the influence of professional and personal characteristics on job satisfaction
among dental assistants. A cross-sectional survey was performed among dental assistants
using a 24-item self-administered questionnaire. Multinomial logistic regression was used
to assess the relationship between overall job satisfaction and other variables. The
overall response rate was 72.1%. Factor analysis suggested that five underlying factors
were related to job satisfaction. The mean score for overall job satisfaction was 3.86
(satisfied) out of 5. Among the work environment factors, the highest mean score, 4.26
(satisfied), was obtained for quality of service, and the lowest mean score, 2.78
(neutral), was obtained for the perception of income. The income and general prospects of
the profession was significantly associated with overall job satisfaction. This study
suggests that for dental assistants, professional and personal life, quality of service,
perception of income and prestige and self-respect are important factors for job
satisfaction. Despite differences in professional formation standards, in general, the
study participants were considerably satisfied with their jobs. 相似文献
73.
Iman Amy Betawi Sinaria Kamil Abdel Jabbar Mohammad. A. AL Jabery Haidar Ibrahim Zaza Muhannad Al-Shboul 《Early child development and care》2014,184(12):1992-2003
This study examined fathers' perceptions regarding their home-based activities (HBA) and the influence of fathers' demographic characteristics on their perceptions and practices at home. A total of 396 fathers completed a survey questionnaire describing their demographic information, perceptions and their practices regarding their involvement in HBA. Results indicated that fathers have moderate level of practice concerning their HBA, yet they have low perception of their actual practice at HBA. In addition, there was a statistical significance in HBA due to fathers' age, educational level and specialisation which had an influence on their perceptions as well. Recommendations and implications of future research were discussed. 相似文献
74.
Danielle Carpenter Carmen Taype Jon Goulding Mike Levin Brian Eley Suzanne Anderson Marie-Anne Shaw John AL Armour 《BMC medical genetics》2014,15(1):1-8
Background
22q11.2 deletion syndrome (22q11.2DS) is a common microdeletion syndrome, which occurs in approximately 1:4000 births. Familial autosomal dominant recurrence of the syndrome is detected in about 8-28% of the cases. Aim of this study is to evaluate the intergenerational and intrafamilial phenotypic variability in a cohort of familial cases carrying a 22q11.2 deletion.Methods
Thirty-two 22q11.2DS subjects among 26 families were enrolled.Results
Second generation subjects showed a significantly higher number of features than their transmitting parents (212 vs 129, P?=?0.0015). Congenital heart defect, calcium-phosphorus metabolism abnormalities, developmental and speech delay were more represented in the second generation (P?<?0.05). Ocular disorders were more frequent in the parent group. No significant difference was observed for the other clinical variables. Intrafamilial phenotypic heterogeneity was identified in the pedigrees. In 23/32 families, a higher number of features were found in individuals from the second generation and a more severe phenotype was observed in almost all of them, indicating the worsening of the phenotype over generations. Both genetic and epigenetic mechanisms may be involved in the phenotypic variability.Conclusions
Second generation subjects showed a more complex phenotype in comparison to those from the first generation. Both ascertainment bias related to patient selection or to the low rate of reproductive fitness of adults with a more severe phenotype, and several not well defined molecular mechanism, could explain intergenerational and intrafamilial phenotypic variability in this syndrome. 相似文献75.
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AL Naik A Savlania A Gupta P Rastogi A Singh 《Annals of the Royal College of Surgeons of England》2021,103(3):e94
Behçet’s disease is a rare disease characterised by recurrent oral ulcers, with systemic manifestations including genital ulcers, ocular disease, skin lesions, gastrointestinal disease, neurologic disease, vascular disease and arthritis. Most clinical manifestations of Behçet’s disease are believed to be due to vasculitis. The heterogeneous clinical spectrum is influenced by sex, ethnicity and country of residence. Vascular manifestation in the form of isolated large brachial artery aneurysm is rare in children. Treatment involves aneurysmorrhaphy to avoid rupture or ischaemic sequelae in addition to lifelong medical management to control vasculitis. 相似文献
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