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Jennifer Knight‐Madden

Biographic Data

ID6807233
NAMEJennifer Knight‐Madden
GIVEN NAMESJennifer
FAMILY NAMEKnight‐Madden
SIGNATUREMADDEN J K
AFFILIATIONSUniversity of the West Indies System
ORCID0000-0002-0939-1648
VERIFIEDYes
TOTAL WORKS4
TOTAL CITATIONS0
WORKS AS AUTHOR4
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2010
LATEST PUBLICATION YEAR2021
H-INDEX0
  • How Free Is Free Health Care? An Assessment of Universal Health Coverage Among Jamaicans with Sickle Cell Disease

    Open Access•Zachary J A Ramsay, Zachary Ramsay et al.•ARTICLE•Health Equity•2021

    Purpose: In an effort to transition toward universal health coverage (UHC), Jamaica abolished user fees at all public health facilities in 2008. We aimed to determine the extent of out-of-pocket payments (OPPs) and the other cost barriers to UHC among patients with sickle cell disease (SCD). Methods: Patients presenting to the Sickle Cell Unit in Kingston, Jamaica, for routine care between October 2019 and August 2020 were consecutively recruited…

  • Utility of paediatric quality of life and revised illness perception questionnaires in adolescents with sickle cell disease

    Monika Asnani, Antoinette Barton‐Gooden et al.•ARTICLE•Vulnerable Children and Youth…•2016

    Quality of life (QOL) and illness perceptions are important considerations when managing adolescents with sickle cell disease (SCD). This study aims to assess the psychometric properties of the SCD-specific paediatric quality of life (PedsQLTM-SCD) and the revised illness perception questionnaires (IPQ-R) in Jamaican adolescents with SCD. One hundred and fifty Jamaican adolescents (M: 74, F: 76; mean age 16.1 ± 1.9 years, range: 13–19 years) comp…

  • Carest—Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia

    Jennifer Knight-Madden, Jennifer Knight‐Madden et al.•ARTICLE•American Journal of Public Health•2016•References: 8

    Sickle cell disease (SCD) is a significant problem in the Caribbean, where many individuals have African and Asian forebears. However, reliable prevalence data and specific health care programs for SCD are often missing in this region. Closer collaboration between Caribbean territories initiated in 2006 to set up strategies to promote better equity in the health care system for SCD patients led to the formation of CAREST: the Caribbean Network of…

  • Prevalence of the metabolic syndrome and its components in relation to socioeconomic status among Jamaican young adults

    Open Access•Trevor S Ferguson, Marshall K Tulloch-Reid et al.•ARTICLE•BMC Public Health•2010

    Prevalence of the metabolic syndrome is low, but central obesity and low HDL are present in 16% and 47% of Jamaican youth, respectively. Central obesity is inversely associated with occupation and education in females

No prominent works on this page.

  • Prevalence of the metabolic syndrome and its components in relation to socioeconomic status among Jamaican young adults

    Open Access•Trevor S Ferguson, Marshall K Tulloch-Reid et al.•ARTICLE•BMC Public Health•2010

    Prevalence of the metabolic syndrome is low, but central obesity and low HDL are present in 16% and 47% of Jamaican youth, respectively. Central obesity is inversely associated with occupation and education in females

  • Utility of paediatric quality of life and revised illness perception questionnaires in adolescents with sickle cell disease

    Monika Asnani, Antoinette Barton‐Gooden et al.•ARTICLE•Vulnerable Children and Youth…•2016

    Quality of life (QOL) and illness perceptions are important considerations when managing adolescents with sickle cell disease (SCD). This study aims to assess the psychometric properties of the SCD-specific paediatric quality of life (PedsQLTM-SCD) and the revised illness perception questionnaires (IPQ-R) in Jamaican adolescents with SCD. One hundred and fifty Jamaican adolescents (M: 74, F: 76; mean age 16.1 ± 1.9 years, range: 13–19 years) comp…

  • Carest—Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia

    Jennifer Knight-Madden, Jennifer Knight‐Madden et al.•ARTICLE•American Journal of Public Health•2016•References: 8

    Sickle cell disease (SCD) is a significant problem in the Caribbean, where many individuals have African and Asian forebears. However, reliable prevalence data and specific health care programs for SCD are often missing in this region. Closer collaboration between Caribbean territories initiated in 2006 to set up strategies to promote better equity in the health care system for SCD patients led to the formation of CAREST: the Caribbean Network of…

  • How Free Is Free Health Care? An Assessment of Universal Health Coverage Among Jamaicans with Sickle Cell Disease

    Open Access•Zachary J A Ramsay, Zachary Ramsay et al.•ARTICLE•Health Equity•2021

    Purpose: In an effort to transition toward universal health coverage (UHC), Jamaica abolished user fees at all public health facilities in 2008. We aimed to determine the extent of out-of-pocket payments (OPPs) and the other cost barriers to UHC among patients with sickle cell disease (SCD). Methods: Patients presenting to the Sickle Cell Unit in Kingston, Jamaica, for routine care between October 2019 and August 2020 were consecutively recruited…

Medicine (4 works) · Disease (3 works) · Environmental health (3 works) · Gerontology (3 works) · Internal Medicine (3 works) · Family medicine (2 works) · Food Security and Health in Diverse Populations (2 works) · Health care (2 works) · Hemoglobinopathies and Related Disorders (2 works) · Nursing (2 works)

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