Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Patricia Sacco"'
Preferences for Adult Pneumococcal Vaccine Recommendations Among United States Health Care Providers
Autor:
Patricia Sacco, Kelley Myers, Christine Poulos, Carolyn Sweeney, Kelly Hollis, Vincenza Snow, Jeffrey T. Vietri
Publikováno v:
Infectious Diseases and Therapy, Vol 8, Iss 4, Pp 657-670 (2019)
Abstract Introduction In 2014, the Advisory Committee on Immunization Practices (ACIP) of the US Centers for Disease Control and Prevention (CDC) recommended 13-valent pneumococcal conjugate vaccine (PCV13) followed by 23-valent pneumococcal polysacc
Externí odkaz:
https://doaj.org/article/4a62e87914cc46a4a038a418f8e046c3
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-17 (2017)
Abstract Background Angelman syndrome (AS) is a rare disorder with a relatively well-defined phenotype. Despite this, very little is known regarding the unmet clinical needs and burden of this condition, especially with regard to some of the most pre
Externí odkaz:
https://doaj.org/article/d8ccf950f4d5401ab5fba535d9f8b1aa
Preferences for Adult Pneumococcal Vaccine Recommendations Among United States Health Care Providers
Autor:
Christine Poulos, Vincenza Snow, Jeffrey Vietri, Carolyn Sweeney, Kelley H. Myers, Patricia Sacco, Kelly Hollis
Publikováno v:
Infectious Diseases and Therapy, Vol 8, Iss 4, Pp 657-670 (2019)
Infectious Diseases and Therapy
Infectious Diseases and Therapy
Introduction In 2014, the Advisory Committee on Immunization Practices (ACIP) of the US Centers for Disease Control and Prevention (CDC) recommended 13-valent pneumococcal conjugate vaccine (PCV13) followed by 23-valent pneumococcal polysaccharide va
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-17 (2017)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Angelman syndrome (AS) is a rare disorder with a relatively well-defined phenotype. Despite this, very little is known regarding the unmet clinical needs and burden of this condition, especially with regard to some of the most prevalent cl
Publikováno v:
Journal of Intellectual Disability Research. 60:844-855
BACKGROUND: The purpose of this study was to assess the construct validity of the Aberrant Behaviour Checklist-utility index (ABC-UI) by examining the relationship between healthcare resource utilisation by patients with fragile X syndrome (FXS) as w
Autor:
Mei Sheng Duh, Patricia Sacco, Patrick Lefebvre, Elizabeth Faust, Marjolaine Gauthier-Loiselle, Francis Vekeman, Raquel Lahoz
Publikováno v:
American Journal on Intellectual and Developmental Disabilities. 120:444-459
This study evaluated the incremental healthcare costs associated with Fragile X syndrome (FXS) for patients and their caregivers. Using administrative healthcare claims data (1999-2012), subjects with ≥ 1 FXS diagnosis (ICD-9-CM: 759.83) were match
Publikováno v:
Journal of Medical Economics. 13:492-499
Pseudomonas aeruginosa (PA) is the most common airway pathogen in cystic fibrosis (CF) patients. The objective of this analysis was to determine the costs of managing PA infection in CF patients with a chronic regimen of tobramycin inhalation solutio
Publikováno v:
Current Medical Research and Opinion. 26:1957-1965
Treatment effectiveness depends upon administering medications as prescribed, and adherence is critical for Alzheimer's disease (AD) patients to receive optimal benefit from therapy. The objective of this study was to investigate factors associated w
Autor:
Bonnie B. Dean, Daniel Aguilar, Robert Maykut, David G. Tinkelman, Patricia Sacco, Brian Calimlim
Publikováno v:
Journal of Asthma. 47:539-544
To evaluate asthma symptom frequency, severity, and control among children with asthma and to evaluate the impact on social functioning and sleep impairment.Using a cross-sectional design, adult caregivers of children aged 6-12 years with moderate to
Publikováno v:
Expert Opinion on Pharmacotherapy. 9:751-766
Cystic fibrosis is the most common incurable hereditary disease in the US. Persistent respiratory infection is the leading cause of morbidity and mortality in cystic fibrosis patients.This study aimed to review the literature on economic and quality