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1.
Am J Hypertens ; 35(11): 955-963, 2022 11 02.
Article in English | MEDLINE | ID: mdl-36001697

ABSTRACT

BACKGROUND: Health professionals' commitment is needed to address disparities in hypertension control by ancestry, but their perceptions regarding these disparities are understudied. METHODS: Cross-sectional mixed methods study in a universal healthcare setting in the Netherlands. Snowball sampling was used to include professionals practicing in a large multicity conglomerate including the capital city. Online surveys were collected, and survey participants were randomly selected for in-depth interviews. We used quantitative and qualitative methods to analyze health professionals' awareness, beliefs, and possible interventions regarding these disparities. RESULTS: We analyzed questionnaire data of 77 health professionals (medical doctors n = 70, nurses = 7), whereas 13 were interviewed. Most professionals were women (59%), general practitioners (81%); and White-European (77%), with 79% caring for patients of diverse ancestry. Disparities in hypertension control by ancestry were perceived to exist nationally (83% [95% CI, 75;91]), but less so in health professionals' own clinics (62% [52;73]), or among their own patients (56% [45;67]). Survey respondents emphasized patient rather than provider-level factors as mediators of poor hypertension control by ancestry. The collection of data on patients' ancestry, updating guidelines, and professional training were considered helpful to reduce disparities. Interviewees further emphasized patient-level factors, but also the need to better educate health professionals and increase their awareness. CONCLUSIONS: This explorative study finds that health professionals predominantly attribute disparities in hypertension control to patient-level factors. Awareness of disparities was lower for more proximate healthcare settings. These data emphasize the need to consider health professionals' perceptions when addressing disparities in hypertension control.


Subject(s)
Attitude of Health Personnel , Hypertension , Humans , Female , Male , Cross-Sectional Studies , Health Personnel , Surveys and Questionnaires
2.
Front Public Health ; 9: 698030, 2021.
Article in English | MEDLINE | ID: mdl-34631643

ABSTRACT

Nepal is a country in south Asia with a high burden of cardiometabolic diseases (CMDs). Strengthening primary healthcare (PHC) is a key strategy to mitigate this increasing burden and achieve universal health coverage. While previous studies in Nepal have assessed PHC use among the elderly, none have specifically explored PHC use among people with CMDs. Therefore, this mixed-methods study aimed to assess the use and perception of PHC services in Nepal among people living with CMDs for primary and secondary prevention of cardiovascular disease. We used a quantitative survey followed-up by semi-structured qualitative interviews. The sampling frame comprised five PHC facilities in Sindhuli district (rural; eastern Nepal) and five in Kailali district (urban; western Nepal), with participants selected from each facility via convenience sampling. 114 people (mean age: 54.5 ± 14.7, sex ratio 1.04) with CMDs participated in the survey. Survey data showed general dissatisfaction with PHC services. Medicine cost was rated "too expensive" by 52 and 63% of rural and urban participants, respectively. Interview data showed that perceived poor bedside manner was tied to negative perceptions of PHC quality, and vice versa. Lack of resources and excessive barriers to care was mentioned by every interviewee. In conclusion, PHC use was high but overall satisfaction relatively low. Our results suggest that bedside manner is a practical target for future research. Additionally, we identified several barriers to care, and, based on existing literature, we suggest electronic-health interventions may have potential to mitigate these challenges.


Subject(s)
Cardiovascular Diseases , Primary Health Care , Adult , Aged , Ambulatory Care Facilities , Cardiovascular Diseases/epidemiology , Humans , Middle Aged , Nepal/epidemiology , Perception
3.
Health Aff (Millwood) ; 36(8): 1461-1468, 2017 08 01.
Article in English | MEDLINE | ID: mdl-28784739

ABSTRACT

Many in the scientific community are concerned about the potential increase in prevalence of insect-borne diseases such as Chagas disease, Chikungunya, dengue fever, malaria, and Zika in the United States and around the world. Beyond vaccines and drugs to prevent and treat these diseases, a comprehensive approach to fighting these diseases should include control of disease-carrying vectors, such as mosquitoes. Vector-control methods, such as using insecticides to treat bed nets and spray the walls of homes, have prevented millions of deaths from malaria. However, mosquitoes are becoming resistant to insecticides, and no new class of insecticides for vector control has been introduced in decades. We recommend the creation of a new type of incentive for the development and commercialization of safe new insecticides: a Vector Expedited Review Voucher, to be awarded to a sponsor that introduces a novel insecticide for public health use. The voucher could be redeemed to expedite registration of a second, more profitable, product by the US Environmental Protection Agency.


Subject(s)
Disease Vectors , Insecticides , Malaria/prevention & control , Pest Control/methods , Zika Virus Infection/prevention & control , Animals , Global Health , Humans , Insecticide Resistance , Insecticides/supply & distribution , Zika Virus
4.
J Opioid Manag ; 11(1): 82-8, 2015.
Article in English | MEDLINE | ID: mdl-25750169

ABSTRACT

In 2012, Duke University initiated a research project, funded by an unrestricted research grant from Millennium Laboratories, a drug testing company. The project focused on assessing the frequency and nature of questionable, unethical, and illegal business practices in the clinical drug testing industry and assessing the potential for establishing a business code of ethics. Laboratory leaders, clinicians, industry attorneys, ethicists, and consultants participated in the survey, were interviewed, and attended two face-to-face meetings to discuss a way forward. The study demonstrated broad acknowledgment of variations in the legal and regulatory environment, resulting in inconsistent enforcement of industry practices. Study participants expressed agreement that overtly illegal practices sometimes exist, particularly when laboratory representatives and clinicians discuss reimbursement, extent of testing, and potential business incentives with medical practitioners. Most respondents reported directly observing probable violations involving marketing materials, contracts, or, in the case of some individuals, directly soliciting people with offers of clinical supplies and other "freebies." While many study respondents were skeptical that voluntary standards alone would eliminate questionable business practices, most viewed ethics codes and credentialing as an important first step that could potentially mitigate uneven enforcement, while improving quality of care and facilitating preferred payment options for credentialed parties. Many were willing to participate in future discussions and industry-wide initiatives to improve the environment.


Subject(s)
Drug Monitoring/ethics , Laboratories/ethics , Medication Adherence , Substance Abuse Detection/ethics , Substance-Related Disorders/diagnosis , Accreditation , Certification , Commerce/ethics , Conflict of Interest , Drug Monitoring/standards , Fraud/ethics , Fraud/prevention & control , Government Regulation , Guideline Adherence , Guidelines as Topic , Health Care Surveys , Humans , Laboratories/legislation & jurisprudence , Laboratories/standards , Marketing of Health Services/ethics , North Carolina , Predictive Value of Tests , Program Development , Program Evaluation , Reproducibility of Results , Substance Abuse Detection/standards , Substance-Related Disorders/prevention & control , Surveys and Questionnaires
6.
Cancer Prev Res (Phila) ; 1(2): 84-90, 2008 Jul.
Article in English | MEDLINE | ID: mdl-19138940

ABSTRACT

Chemoprevention agents are an emerging new scientific area that holds out the promise of delaying or avoiding a number of common cancers. These new agents face significant scientific, regulatory, and economic barriers, however, which have limited investment in their research and development (R&D). These barriers include above-average clinical trial scales, lengthy time frames between discovery and Food and Drug Administration approval, liability risks (because they are given to healthy individuals), and a growing funding gap for early-stage candidates. The longer time frames and risks associated with chemoprevention also cause exclusivity time on core patents to be limited or subject to significant uncertainties. We conclude that chemoprevention uniquely challenges the structure of incentives embodied in the economic, regulatory, and patent policies for the biopharmaceutical industry. Many of these policy issues are illustrated by the recently Food and Drug Administration-approved preventive agents Gardasil and raloxifene. Our recommendations to increase R&D investment in chemoprevention agents include (a) increased data exclusivity times on new biological and chemical drugs to compensate for longer gestation periods and increasing R&D costs; chemoprevention is at the far end of the distribution in this regard; (b) policies such as early-stage research grants and clinical development tax credits targeted specifically to chemoprevention agents (these are policies that have been very successful in increasing R&D investment for orphan drugs); and (c) a no-fault liability insurance program like that currently in place for children's vaccines.


Subject(s)
Antineoplastic Agents/therapeutic use , Chemoprevention , Drug Discovery/economics , Drug Discovery/legislation & jurisprudence , Neoplasms/prevention & control , Patents as Topic/legislation & jurisprudence , Antineoplastic Agents/economics , Biomedical Research/economics , Biomedical Research/legislation & jurisprudence , Chemoprevention/economics , Drug Industry/economics , Drug Industry/legislation & jurisprudence , Humans , Intellectual Property , Liability, Legal , Neoplasms/economics , Orphan Drug Production/economics , Orphan Drug Production/legislation & jurisprudence , Raloxifene Hydrochloride/economics , Raloxifene Hydrochloride/therapeutic use
7.
Global Health ; 3: 11, 2007 Nov 16.
Article in English | MEDLINE | ID: mdl-18021412

ABSTRACT

BACKGROUND: Following the demise of Jordan's King Hussein bin Talal to cancer in 1999, the country's Al-Amal Center was transformed from a poorly perceived and ineffectual cancer care institution into a Western-style comprehensive cancer center. Renamed King Hussein Cancer Center (KHCC), it achieved improved levels of quality, expanded cancer care services and achieved Joint Commission International accreditation under new leadership over a three-year period (2002-2005). METHODS: An exploratory case research method was used to explain the rapid change to international standards. Sources including personal interviews, document review and on-site observations were combined to conduct a robust examination of KHCC's rapid changes. RESULTS: The changes which occurred at the KHCC during its formation and leading up to its Joint Commission International (JCI) accreditation can be understood within the conceptual frame of the transformational leadership model. Interviewees and other sources for the case study suggest the use of inspirational motivation, idealized influence, individualized consideration and intellectual stimulation, four factors in the transformational leadership model, had significant impact upon the attitudes and motivation of staff within KHCC. Changes in the institution were achieved through increased motivation and positive attitudes toward the use of JCI continuous improvement processes as well as increased professional training. The case study suggests the role of culture and political sensitivity needs re-definition and expansion within the transformational leadership model to adequately explain leadership in the context of globalizing health care services, specifically when governments are involved in the change initiative. CONCLUSION: The KHCC case underscores the utility of the transformational leadership model in an international health care context. To understand leadership in globalizing health care services, KHCC suggests culture is broader than organizational or societal culture to include an informal global network of medical professionals and Western technologies which facilitate global interaction. Additionally, political competencies among leaders may be particularly relevant in globalizing health care services where the goal is achieving international standards of care. Western communication technologies facilitate cross-border interaction, but social and political capital possessed by the leaders may be necessary for transactions across national borders to occur thus gaining access to specialized information and global thought leaders in a medical sub-specialty such as oncology.

8.
Health Aff (Millwood) ; 25(2): 313-24, 2006.
Article in English | MEDLINE | ID: mdl-16522573

ABSTRACT

Infectious and parasitic diseases create enormous health burdens, but because most of the people suffering from these diseases are poor, little is invested in developing treatments. We propose that developers of treatments for neglected diseases receive a "priority review voucher." The voucher could save an average of one year of U.S. Food and Drug Administration (FDA) review and be sold by the developer to the manufacturer of a blockbuster drug. In a well-functioning market, the voucher would speed access to highly valued treatments. Thus, the voucher could benefit consumers in both developing and developed countries at relatively low cost to the taxpayer.


Subject(s)
Developing Countries , Drug Approval/legislation & jurisprudence , Drug Industry/economics , Orphan Drug Production/economics , Anti-Infective Agents/economics , Anti-Infective Agents/supply & distribution , Antiparasitic Agents/economics , Antiparasitic Agents/supply & distribution , Drug Approval/economics , Health Services Accessibility/economics , Humans , Legislation, Drug , Marketing , Patents as Topic , Program Development , Reimbursement, Incentive , United States , United States Food and Drug Administration
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