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1.
Ig Sanita Pubbl ; 68(4): 565-88, 2012.
Article in Italian | MEDLINE | ID: mdl-23073376

ABSTRACT

The communication is strategic in Public Health because it is at the heart of who we are as human beings. It is our way of exchanging information and it also ensures the effectiveness of empowerment strategies. In this semantic context, the effective communication/education/information can be a Patient Safety tool because can reduce the adverse events by failure of information or education. In the multicultural collectivity, the risk of miscommunication and unsafe care is very high. This paper describes the design of a multilingual information/education tools to reduce the information failure in vaccination and the related adverse events by information failure or deficiency of adherence in the paediatric vaccination.


Subject(s)
Communication , Patient Safety , Vaccination , Humans
2.
Acta Paediatr ; 92(6): 734-6, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12856987

ABSTRACT

AIM: Efforts are currently made to detect vesicoureteric reflux (VUR) early after urinary infections in order to limit secondary renal damage. This study investigated the extent to which recommendations for the detection of VUR are put into practice, and their influence on the age at diagnosis. METHODS: The age at diagnosis of VUR after urinary tract infections was analysed in 126 patients (48M, 78F) referred to a tertiary centre in Milan between 1976 and 1999. RESULTS: The median age at diagnosis was 34 mo in subjects born before and 8 mo (p < 0.001) in those born after 1988. The difference was statistically significant in female but not in male subjects. The figures from Milan were compared with those for 102 patients (35M, 65F) born between 1946 and 1970, treated in Melbourne and reported in 1976. In Melbourne the median age at diagnosis was 1-2 y for boys and 5-6 y for girls; in Milan, the corresponding figures were <1 y and 1-2 y. The difference between Melbourne and Milan was statistically significant for both genders. CONCLUSION: In Milan VUR is now detected earlier than in the past. This trend is more marked in females than in males, but reflux is still detected earlier in boys.


Subject(s)
Urinary Tract Infections/complications , Vesico-Ureteral Reflux/etiology , Age Factors , Australia , Child , Child, Preschool , Female , Humans , Infant , Italy/epidemiology , Male , Sex Factors , Vesico-Ureteral Reflux/diagnosis , Vesico-Ureteral Reflux/therapy
3.
G Ital Nefrol ; 20(2): 120-6, 2003.
Article in Italian | MEDLINE | ID: mdl-12746796

ABSTRACT

The wide association between urinary tract malformations and dysplastic kidneys, known as CAKUT (Congenital Anomalies of the Kidney and Urinary Tract), could be caused by a single disorder of the embryonic development of the kidney and urinary tract. These complex patterns of development are under genetic control. A positive family history strongly suggests a genetic origin of these conditions. Linkage studies show an extreme genetic heterogenicity and an important phenotypic and clinical variability of the same mutation. Some urinary tract malformations have been investigated in the context of clinical syndromes. The renal-coloboma syndrome is an autosomal dominant human disease, secondary to mutation of the PAX2 transcription factor, characterized by optic nerve coloboma, renal anomalies and vesicoureteral reflux. However, most of the urinary tract anomalies can occur in isolation. Studies have shown the association of hereditary hydronephrosis with HLA antigens on chromosome 6 and the association of VUR with the mutations in a locus of chromosome 1. The higher frequency and severity of some uropathies in the male gender may be explained by a linkage-disequilibrium phenomenon or a X-linked transmission pattern. For example, the mutations in the AGTR2 gene on chromosome X were observed in animal models but not yet confirmed in human subjects. Finally, the ACE gene polymorphism is associated with a higher incidence of congenital hypo-dysplastic kidneys and represents a significant risk factor for the development of progressive renal damage.


Subject(s)
Kidney/pathology , Urinary Tract/abnormalities , Abnormalities, Multiple/genetics , Animals , Chromosomes, Human, Pair 1/genetics , Coloboma/genetics , Congenital Abnormalities/genetics , DNA-Binding Proteins/chemistry , DNA-Binding Proteins/genetics , DNA-Binding Proteins/physiology , Disease Models, Animal , Female , Gene Expression Regulation, Developmental , Genetic Linkage , Humans , Kidney/embryology , Male , Mice , Models, Molecular , Multigene Family , Optic Nerve/abnormalities , PAX2 Transcription Factor , Peptidyl-Dipeptidase A/genetics , Protein Conformation , Receptor, Angiotensin, Type 2 , Receptors, Angiotensin/genetics , Transcription Factors/chemistry , Transcription Factors/genetics , Transcription Factors/physiology , Urinary Tract/embryology , Vesico-Ureteral Reflux/genetics , X Chromosome
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