Norberto Giglio
Boston Children's Hospital
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Featured researches published by Norberto Giglio.
Pediatrics | 2008
Michael E. Pichichero; Angela Gentile; Norberto Giglio; Verónica Umido; Thomas W. Clarkson; Elsa Cernichiari; Grazyna Zareba; Carlos A. Gotelli; Mariano J. Gotelli; Lihan Yan; John J. Treanor; R. Gutierrez
OBJECTIVES. Thimerosal is a mercurial preservative that was widely used in multidose vaccine vials in the United States and Europe until 2001 and continues to be used in many countries throughout the world. We conducted a pharmacokinetic study to assess blood levels and elimination of ethyl mercury after vaccination of infants with thimerosal-containing vaccines. METHODS. Blood, stool, and urine samples were obtained before vaccination and 12 hours to 30 days after vaccination from 216 healthy children: 72 newborns (group 1), 72 infants aged 2 months (group 2), and 72 infants aged 6 months (group 3). Total mercury levels were measured by atomic absorption. Blood mercury pharmacokinetics were calculated by pooling the data on the group and were based on a 1-compartment first-order pharmacokinetics model. RESULTS. For groups 1, 2, and 3, respectively, (1) mean ± SD weights were 3.4 ± 0.4, 5.1 ± 0.6, and 7.7 ± 1.1 kg; (2) maximal mean ± SD blood mercury levels were 5.0 ± 1.3, 3.6 ± 1.5, and 2.8 ± 0.9 ng/mL occurring at 0.5 to 1 day after vaccination; (3) maximal mean ± SD stool mercury levels were 19.1 ± 11.8, 37.0 ± 27.4, and 44.3 ± 23.9 ng/g occurring on day 5 after vaccination for all groups; and (4) urine mercury levels were mostly nondetectable. The blood mercury half-life was calculated to be 3.7 days and returned to prevaccination levels by day 30. CONCLUSIONS. The blood half-life of intramuscular ethyl mercury from thimerosal in vaccines in infants is substantially shorter than that of oral methyl mercury in adults. Increased mercury levels were detected in stools after vaccination, suggesting that the gastrointestinal tract is involved in ethyl mercury elimination. Because of the differing pharmacokinetics of ethyl and methyl mercury, exposure guidelines based on oral methyl mercury in adults may not be accurate for risk assessments in children who receive thimerosal-containing vaccines.
Vaccine | 2011
Analía Urueña; Tomás Pippo; María Sol Betelu; Federico Virgilio; Norberto Giglio; Angela Gentile; Salvador García Jiménez; Barbara Jauregui; Andrew Clark; Máximo Diosque; Carla Vizzotti
OBJECTIVE Since the 10-valent pneumococcal conjugate vaccine (PCV-10) and 13-valent pneumococcal conjugate vaccine (PCV-13) were recently licensed for use in Argentina, both vaccines were evaluated to estimate the costs, health benefits and cost-effectiveness of adding a PCV to the routine child immunization schedule. METHODOLOGY The integrated TRIVAC vaccine cost-effectiveness model from Pan American Health Organizations ProVac Initiative (Version 1.0.65) was used to assess the health outcomes of 20 successive cohorts from birth to 5 years of age. PCV-10 and PCV-13 were each compared to a scenario assuming no PCV vaccination. A 3+1 (three doses+booster) schedule and a vaccination price of US
The Journal of Pediatrics | 2009
Michael E. Pichichero; Angela Gentile; Norberto Giglio; Margarita Martin Alonso; Maria Veronica Fernandez Mentaberri; Grazyna Zareba; Thomas W. Clarkson; Carlos A. Gotelli; Mariano J. Gotelli; Lihan Yan; John J. Treanor
20.75 per dose was assumed in the base case for both vaccines. RESULTS Introduction of PCV-13 rather than PCV-10 would increase the number of life years gained (LYG) by at least 10%. The number of LYG (and LYG after adjustment for DALY morbidity weights) was 56,882 (64,252) for PCV-10 compared to 65,038 (71,628) for PCV-13. From the health system perspective, the cost per DALY averted was US
Vaccine | 2010
Norberto Giglio; Alejandro Cané; Paula Micone; Angela Gentile
8973 and US
The Journal of Pediatrics | 2009
Michael E. Pichichero; Angela Gentile; Norberto Giglio; Margarita Martin Alonso; Maria Veronica Fernandez Mentaberri; Grazyna Zareba; Thomas W. Clarkson; Carlos A. Gotelli; Mariano J. Gotelli; Lihan Yan; John J. Treanor
10,948 for PCV-10 and PCV-13 respectively, and US
Human Vaccines & Immunotherapeutics | 2012
Norberto Giglio; Angela Gentile; Lydia Lees; Paula Micone; Judith Armoni; Camille Reygrobellet; Pascal Crépey
8546 and US
Vaccine | 2011
Norberto Giglio; Paula Micone; Angela Gentile
10,510 respectively, after incorporating costs saved by households. When PCV13 was compared to PCV10 directly, the additional benefits of PCV-13 was conferred at a cost of US
Journal of Global Health | 2016
Shanshan Zhang; Peter M. Sammon; Isobel King; Ana Lucia Andrade; Cristiana M. Toscano; Sheila N Araujo; Anushua Sinha; Shabir A. Madhi; Gulam Khandaker; Jiehui Kevin Yin; Robert Booy; Tanvir Huda; Qazi Sadeq-ur Rahman; Shams El Arifeen; Angela Gentile; Norberto Giglio; Mejbah Uddin Bhuiyan; Katharine Sturm–Ramirez; Bradford D. Gessner; Mardiati Nadjib; Phyllis J. Carosone–Link; Eric A. F. Simões; Jason Child; Imran Ahmed; Zulfiqar A. Bhutta; Sajid Soofi; Rumana J Khan; Harry Campbell; Harish Nair
28,147 per DALY averted. Cost-effectiveness was influenced mainly by vaccine price, serotype replacement, pneumonia mortality and discount rate. CONCLUSION Routine vaccination against S. pneumoniae in Argentina would be cost-effective with either PCV-10 or PCV-13. PCV-13, with higher coverage of local serotypes, would prevent more cases of pneumonia, invasive pneumococcal disease, sequelae and deaths with a higher number of LYG and DALYs averted, but PCV-10, due its higher impact in the prevention of AOM, would save more costs to the healthcare system.
Vaccine | 2015
Analía Urueña; Tomás Pippo; María Sol Betelu; Federico Virgilio; Laura Hernández; Norberto Giglio; Angela Gentile; Máximo Diosque; Carla Vizzotti
OBJECTIVE We conducted a population-based pharmacokinetic study to assess blood levels and elimination of mercury after vaccination of premature infants born at > or =32 and <37 weeks of gestation and with birth weight > or =2000 but <3000 g. STUDY DESIGN Blood, stool, and urine samples were obtained before vaccination and 12 hours to 30 days after vaccination from 72 premature newborn infants. Total mercury levels were measured by atomic absorption. RESULTS The mean +/- standard deviation (SD) birth weight was 2.4 +/- 0.3 kg for the study population. Maximal mean +/- SD blood mercury level was 3.6 +/- 2.1 ng/mL, occurring at 1 day after vaccination; maximal mean +/- SD stool mercury level was 35.4 +/- 38.0 ng/g, occurring on day 5 after vaccination; and urine mercury levels were mostly nondetectable. The blood mercury half-life was calculated to be 6.3 (95% CI, 3.85 to 8.77) days, and mercury levels returned to prevaccination levels by day 30. CONCLUSIONS The blood half-life of intramuscular ethyl mercury from thimerosal in vaccines given to premature infants is substantially shorter than that of oral methyl mercury in adults. Because of the differing pharmacokinetics, exposure guidelines based on oral methyl mercury in adults may not be accurate for children who receive thimerosal-containing vaccines.
Health Economics Review | 2015
Mariano Giorgi; Christian Caroli; Norberto Giglio; Paula Micone; E.C. Aiello; Cristina Vulcano; Julia Blanco; Bm Donato; Joaquin Mould Quevedo
UNLABELLED Due to the regions own conditions, universal vaccination with pneumococcal conjugate heptavalent vaccine (PCV-7) in Latin American countries is still controversial. OBJECTIVE To compare projected economic costs and health benefits associated with pneumococcal conjugate heptavalent vaccine as a routine immunization in healthy children in Argentina. DESIGN A decision analytic model of Markov simulated lifetime evolution of a birth cohort (n 696,451) was developed and compared costs and health benefits of pneumococcal disease in the presence and absence of vaccination. MAIN OUTCOME MEASURES Cost per life year (LY) gained, reduce in diseases burden and costs of vaccination. RESULTS From the societys perspective, the incremental cost per LY gained was US