Scott Royal
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Featured researches published by Scott Royal.
Haemophilia | 2002
Scott Royal; W. Schramm; Erik Berntorp; Paul Giangrande; A. Gringeri; Christopher A. Ludlam; Barbara L. Kroner; T Szucs
The European Study on the Clinical Outcomes and Resource Utilization associated with Haemophilia Care was designed to compare various health outcomes associated with on‐demand and prophylactic factor substitution methods in European haemophilia patients. While the primary objective of this research is to conduct an economic analysis, an important component of this study is to evaluate quality‐of‐life differences that may exist between patients who utilize these two styles of therapy. Quality‐of‐life research has emerged as a primary measure of health outcomes because it allows the augmentation of traditional clinical indicators of health with data gathered from the patients perspective. A total of 1033 haemophilia patients from 16 European haemophilia treatment centres were enrolled in this study. The SF‐36, a multidimensional quality‐of‐life instrument, was administered to all participants. This instrument measures eight health‐related quality‐of‐life dimensions: physical functioning, physical role limitations, bodily pain, general health, vitality, social functioning, emotional role limitations, and mental health. All haemophilia subjects enrolled in the study scored significantly lower than the population normative means in the three physical dimensions and in the general health dimension. HIV‐negative haemophiliac subjects differed significantly by factor substitution type in a multivariate analysis examining all eight health dimensions. Univariate analyses testing each dimension separately indicated that patients treated prophylactically reported significantly less bodily pain, better general health, and scored significantly higher in the physical functioning, mental health, and social functioning dimensions. While these results suggest that health‐related quality‐of‐life may be better for haemophilia patients treated prophylactically, future prospective studies that gather periodic quality‐of‐life data over time should be conducted.
Haemophilia | 2002
W. Schramm; Scott Royal; Barbara L. Kroner; Erik Berntorp; Paul Giangrande; Christopher A. Ludlam; A. Gringeri; K Berger; T Szucs
We conducted a multicentre, cross‐ sectional study of 1042 haemophilia subjects across Europe to compare various health outcomes associated with on‐demand vs. prophylactic factor‐substitution therapy. Demographic, medical history, and healthcare resource utilization data were analysed along with the number of bleeding events over the past 6 months. Treatment‐cost data were also examined to provide preliminary information for future economic studies. A logistic regression analysis, controlling for other statistically significant covariates, showed that patients treated on demand were 3.4 times more likely to have had a joint bleed over the previous 6 months than those treated with prophylaxis. Multiple regression analyses further confirmed these findings, because on‐demand subjects had, on average, 5.15 more joint bleeds over the reporting period than patients treated with prophylaxis. Notably, these findings were even more dramatic for younger haemophilia patients when our study sample was stratified by age. Due to the high cost of factor replacement, healthcare costs were significantly higher for subjects treated prophylactically. While hospital costs for prophylaxis subjects were, on average, lower, statistically significant cost savings for prophylactic subjects were not noted. These results suggest that clinicians and health policy decision‐makers should consider the advantages of prophylactic therapy for haemophilia patients in formulating treatment protocols and allocating health resources.
Aids Care-psychological and Socio-medical Aspects of Aids\/hiv | 2009
Scott Royal; Daniel P. Kidder; Satyendra Patrabansh; Richard J. Wolitski; David R. Holtgrave; Angela Aidala; Sherri L. Pals; Ron Stall
Abstract The aim of this study is to investigate adherence to highly active antiretroviral therapy (HAART) in persons living with HIV/AIDS (PLWHA) who are homeless or unstably housed. We evaluated homeless or unstably housed PLWHA (n=644) in three US cities were enrolled in the Housing and Health Study. Using baseline data and controlling for gender, race, age, and education, we examined associations between self-reported two- and Seven-day adherence and access to healthcare, mental health, substance use, and attitudes toward HIV medical therapy. Of the 644 participants, 358 (55%) were currently on HAART. For two-day adherence, 280 (78%) reported missing no prescribed doses (100% adherence), and for seven-day adherence, 291 (81%) reported ≥90% adherence. Logistic regression analyses indicated being younger, not having health insurance, and drug use were associated with missing ≥1 dose over the past two days. Scoring lower on SF-36 mental component summary scale and having greater risk of depression (CES-D) and stress (Perceived Stress Scale) were associated with poorer adherence for both two- and seven-day outcomes. Negative attitudes toward HIV treatment were also associated with lower adherence. Adherence to HIV medications in this population is similar to other groups. Coexisting problems of access to healthcare, higher risk of mental health problems, along with poorer attitudes toward treatment are associated with increased likelihood of missing doses. Comprehensive models of HIV care that include a continuum of medical and social services are essential for treating this population.
Aids Care-psychological and Socio-medical Aspects of Aids\/hiv | 2009
Mark S. Friedman; Michael P. Marshal; Ron Stall; Daniel P. Kidder; Kirk D. Henny; Cari Courtenay-Quirk; Angela Aidala; Scott Royal; David R. Holtgrave
Abstract Prior research suggests that the interconnections between substance use, HIV risk and lack of adherence to HIV medications are especially strong among homeless individuals. Thus, study of these interconnections warrants public health attention. The objectives of this paper are to describe patterns of alcohol and drug use, associations between substance use and participation in high-risk sex, and associations between substance use and adherence to HIV treatment regimens among a sample of 602 homeless or unstably housed HIV-seropositive individuals who are part of a housing-based intervention – the Housing and Health Study. Participants experienced high levels of substance use. Significant associations were found between substance use and adherence to HIV treatment medications, and between substance use and high-risk sexual practices within the entire group. Group analyses by sexual orientation/gender show that the association between substance use and treatment adherence is found primarily among heterosexual males whereas the relationship between several drugs and high-risk sexual practices is strongest among gay and bisexual men. Health professionals working with HIV-seropositive individuals should routinely ascertain housing status and screen for substance use and risky sex.
Aids and Behavior | 2007
David R. Holtgrave; Kate Briddell; Eugene R Little; Arturo Valdivia Bendixen; Myrna Hooper; Daniel P. Kidder; Richard J. Wolitski; David Harre; Scott Royal; Angela Aidala
The Housing and Health study examines the effects of permanent supportive housing for homeless and unstably housed persons living with HIV. While promising as an HIV prevention intervention, providing housing may be more expensive to deliver than some other HIV prevention services. Economic evaluation is needed to determine if investment in permanent supportive housing would be cost-saving or cost-effective. Here we ask––what is the per client cost of delivering the intervention, and how many HIV transmissions have to be averted in order to exceed the threshold needed to claim cost-savings or cost-effectiveness to society? Standard methods of cost and threshold analysis were employed. Payor perspective costs range from
Aids and Behavior | 2003
Maria I Fernandez; George S Bowen; Tatiana Perrino; Scott Royal; Tiffany R. Mattson; Kristopher L. Arheart; Sylvia Cohn
9,256 to
Aids Care-psychological and Socio-medical Aspects of Aids\/hiv | 2002
Maria I Fernandez; Tatiana Perrino; Scott Royal; David Ghany; George S Bowen
11,651 per client per year; societal perspective costs range from
Aids and Behavior | 2013
David R. Holtgrave; Richard J. Wolitski; Sherri L. Pals; Angela Aidala; Daniel P. Kidder; David Vos; Scott Royal; Nkemdiri Iruka; Kate Briddell; Ron Stall; Arturo Valdivia Bendixen
10,048 to
Aids Care-psychological and Socio-medical Aspects of Aids\/hiv | 2014
Chanza Baytop; Scott Royal; Donna Hubbard McCree; Ron Simmons; Rebecca Tregerman; Carolyn Robinson; Wayne D. Johnson; Mike McLaughlin; Cristofer Price
14,032 per client per year. Considering that averting a new case of HIV saves an estimated
Aids and Behavior | 2010
Richard J. Wolitski; Daniel P. Kidder; Sherri L. Pals; Scott Royal; Angela Aidala; Ron Stall; David R. Holtgrave; David Harre; Cari Courtenay-Quirk
221,365 in treatment costs, the average cost-saving threshold across the three study cities is 0.0555. Expressed another way, if just one out of every 19 Housing & Health intervention clients avoided HIV transmission to an HIV seronegative partner the intervention would be cost-saving. The intervention would be cost-effective if it prevented just one HIV transmission for every 64 clients served.