TY - JOUR
T1 - Incidence and prevalence rate estimation of GH treatment exposure in Piedmont pediatric population in the years 2002-2004
T2 - Data from the GH registry
AU - Migliaretti, Giuseppe
AU - Aimaretti, G.
AU - Borraccino, A.
AU - Bellone, J.
AU - Vannelli, S.
AU - Angeli, A.
AU - Benso, L.
AU - Bona, G.
AU - Camanni, F.
AU - de Sanctis, C.
AU - Ravaglia, A.
AU - Cavallo, F.
PY - 2006/5
Y1 - 2006/5
N2 - Objective: The aim of this study is to estimate the annual incidence and prevalence rate of the GH treatment exposure in patients under the age of 18 treated for hypopituitarism or isolated GH deficiency (GHD) in Piedmont, during the period January 1, 2002 to December 31, 2004. Methods: The selection criteria for recombinant human GH (rhGH) treatment in childhood were approved by the Ministry of Health in Italy in the yr 1998. The present analysis is based on data from the Registry of subjects receiving GH therapy (GH Registry) made up of the 918 pediatric patients (age <18 yr) with a diagnosis of GHD (excluding Prader-Willi and Turner syndromes and other conditions), diagnosed in the period January 1, 2002 - December 31, 2004. The case series has been described as regards the number of cases per year of diagnosis; the prevalence and incidence rates, calculated per 10,000 (‰) inhabitants, are given for each year of the study period. Results: The prevalence rate increases slightly from 8.62‰ in 2002 to 9.44‰ in 2004 and the incidence rates estimated were 2.49‰, 1.86‰ and 1.97‰ in the yr 2002, 2003 and 2004, respectively. Conclusion: The Pie dmont GH Registry represents the first database available in Italy and could set an example for the other Italian regions as well.
AB - Objective: The aim of this study is to estimate the annual incidence and prevalence rate of the GH treatment exposure in patients under the age of 18 treated for hypopituitarism or isolated GH deficiency (GHD) in Piedmont, during the period January 1, 2002 to December 31, 2004. Methods: The selection criteria for recombinant human GH (rhGH) treatment in childhood were approved by the Ministry of Health in Italy in the yr 1998. The present analysis is based on data from the Registry of subjects receiving GH therapy (GH Registry) made up of the 918 pediatric patients (age <18 yr) with a diagnosis of GHD (excluding Prader-Willi and Turner syndromes and other conditions), diagnosed in the period January 1, 2002 - December 31, 2004. The case series has been described as regards the number of cases per year of diagnosis; the prevalence and incidence rates, calculated per 10,000 (‰) inhabitants, are given for each year of the study period. Results: The prevalence rate increases slightly from 8.62‰ in 2002 to 9.44‰ in 2004 and the incidence rates estimated were 2.49‰, 1.86‰ and 1.97‰ in the yr 2002, 2003 and 2004, respectively. Conclusion: The Pie dmont GH Registry represents the first database available in Italy and could set an example for the other Italian regions as well.
KW - Epidemiology
KW - GH deficiency
KW - Incidence
KW - Prevalence
UR - http://www.scopus.com/inward/record.url?scp=33745889002&partnerID=8YFLogxK
U2 - 10.1007/BF03344127
DO - 10.1007/BF03344127
M3 - Article
SN - 0391-4097
VL - 29
SP - 438
EP - 442
JO - Journal of Endocrinological Investigation
JF - Journal of Endocrinological Investigation
IS - 5
ER -