20 results on '"Emma Hannay"'
Search Results
2. The inclusion of diagnostics in national health insurance schemes in Cambodia, India, Indonesia, Nepal, Pakistan, Philippines and Viet Nam
- Author
-
Madhukar Pai, Uzma Khan, Thu Anh Nguyen, Vijayashree Yellappa, Emma Hannay, Jacob Bigio, A Venkat Raman, Bachti Alisjahbana, Rishav Das, Huy Ba Huynh, Lalaine Mortera, Muhammad Aamir Safdar, Suvesh Shrestha, Sharat Chandra Verma, and Divya Srivastava
- Subjects
Medicine (General) ,R5-920 ,Infectious and parasitic diseases ,RC109-216 - Abstract
The Lancet Commission on Diagnostics highlighted a huge gap in access to diagnostic testing even for basic tests, particularly at the primary care level, and emphasised the need for countries to include diagnostics as part of their universal health coverage benefits packages. Despite the poor state of diagnostic-related services in low-income and middle-income countries (LMICs), little is known about the extent to which diagnostics are included in the health benefit packages. We conducted an analysis of seven Asian LMICs—Cambodia, India, Indonesia, Nepal, Pakistan, Philippines, Viet Nam—to understand this issue. We conducted a targeted review of relevant literature and applied a health financing framework to analyse the benefit packages available in each government-sponsored scheme. We found considerable heterogeneity in country approaches to diagnostics. Of the seven countries, only India has developed a national essential diagnostics list. No country presented a clear policy rationale on the inclusion of diagnostics in their scheme and the level of detail on the specific diagnostics which are covered under the schemes was also generally lacking. Government-sponsored insurance expansion in the eligible populations has reduced the out-of-pocket health payment burden in many of the countries but overall, there is a lack of access, availability and affordability for diagnostic-related services.
- Published
- 2023
- Full Text
- View/download PDF
3. Breaking the cycle of neglect: building on momentum from COVID-19 to drive access to diagnostic testing
- Author
-
Emma Hannay and Madhukar Pai
- Subjects
Medicine (General) ,R5-920 - Published
- 2023
- Full Text
- View/download PDF
4. COVID-19 diagnostics: preserving manufacturing capacity for future pandemics
- Author
-
Emma Hannay, Philippe Duneton, and Marta Fernández-Suárez
- Subjects
Medicine (General) ,R5-920 ,Infectious and parasitic diseases ,RC109-216 - Published
- 2022
- Full Text
- View/download PDF
5. Optimal use of COVID-19 Ag-RDT screening at border crossings to prevent community transmission: A modeling analysis.
- Author
-
Joshua M Chevalier, Karla Therese L Sy, Sarah J Girdwood, Shaukat Khan, Heidi Albert, Amy Toporowski, Emma Hannay, Sergio Carmona, and Brooke E Nichols
- Subjects
Public aspects of medicine ,RA1-1270 - Abstract
Countries around the world have implemented restrictions on mobility, especially cross-border travel to reduce or prevent SARS-CoV-2 community transmission. Rapid antigen testing (Ag-RDT), with on-site administration and rapid turnaround time may provide a valuable screening measure to ease cross-border travel while minimizing risk of local transmission. To maximize impact, we developed an optimal Ag-RDT screening algorithm for cross-border entry. Using a previously developed mathematical model, we determined the daily number of imported COVID-19 cases that would generate no more than a relative 1% increase in cases over one month for different effective reproductive numbers (Rt) and COVID-19 prevalence within the recipient country. We then developed an algorithm-for differing levels of Rt, arrivals per day, mode of travel, and SARS-CoV-2 prevalence amongst travelers-to determine the minimum proportion of people that would need Ag-RDT testing at border crossings to ensure no greater than the relative 1% community spread increase. When daily international arrivals and/or COVID-19 prevalence amongst arrivals increases, the proportion of arrivals required to test using Ag-RDT increases. At very high numbers of international arrivals/COVID-19 prevalence, Ag-RDT testing is not sufficient to prevent increased community spread, especially when recipient country prevalence and Rt are low. In these cases, Ag-RDT screening would need to be supplemented with other measures to prevent an increase in community transmission. An efficient Ag-RDT algorithm for SARS-CoV-2 testing depends strongly on the epidemic status within the recipient country, volume of travel, proportion of land and air arrivals, test sensitivity, and COVID-19 prevalence among travelers.
- Published
- 2022
- Full Text
- View/download PDF
6. Most common reasons for primary care visits in low- and middle-income countries: A systematic review.
- Author
-
Jacob Bigio, Emily MacLean, Nathaly Aguilera Vasquez, Lavanya Huria, Mikashmi Kohli, Genevieve Gore, Emma Hannay, Madhukar Pai, and Pierrick Adam
- Subjects
Public aspects of medicine ,RA1-1270 - Abstract
With the Covid-19 pandemic and the introduction of the WHO's Essential Diagnostics List (EDL), increasing global attention is focused on the crucial role of diagnostics in achieving universal health coverage. To create national EDLs and to aid health system planning, it is vital to understand the most common conditions with which people present at primary care health facilities. We undertook a systematic review of the most common reasons for primary care visits in low- and middle-income countries. Six databases were searched for articles published between January 2009 and December 2019, with the search updated on MEDLINE to January 2021. Data on the most common patient reasons for encounter (RFEs) and provider diagnoses were collected. 17 of 22,279 screened articles were included. Most studies used unvalidated diagnostic classification systems or presented provider diagnosis data grouped by organ system, rather than presenting specific diagnoses. No studies included data from low-income countries. Only four studies (from Brazil, India, Nigeria and South Africa) using the ICPC-2 classification system contained RFE and provider diagnosis data and could be pooled. The top five RFEs from the four studies were headache, fever, back or low back symptom, cough and pain general/multiple sites. The top five diagnoses were uncomplicated hypertension, upper respiratory tract infection, type 2 diabetes, malaria and health maintenance/prevention. No psychological symptoms were among the top 10 pooled RFEs. There was more variation in top diagnoses between studies than top RFEs, showing the importance of creating location-specific lists of essential diagnostics for primary care. Future studies should aim to sample primary care facilities from across their country of study and use ICPC-3 to report both patient RFEs and provider diagnoses.
- Published
- 2022
- Full Text
- View/download PDF
7. The silent and dangerous inequity around access to COVID-19 testing: A call to action
- Author
-
Carolina Batista, Peter Hotez, Yanis Ben Amor, Jerome H Kim, David Kaslow, Bhavna Lall, Onder Ergonul, J Peter Figueroa, Mayda Gursel, Mazen Hassanain, Gagandeep Kang, Heidi Larson, Denise Naniche, Timothy Sheahan, Annelies Wilder-Smith, Shmuel Shoham, Samba O Sow, Prashant Yadav, Nathalie Strub-Wourgaft, Sarah-Jane Loveday, Emma Hannay, and Maria Elena Bottazzi
- Subjects
Medicine (General) ,R5-920 - Published
- 2022
- Full Text
- View/download PDF
8. The governance of personal data for COVID-19 response: perspective from the Access to COVID-19 Tools Accelerator
- Author
-
Rigveda Kadam, Rangarajan Sampath, Ciara Staunton, Michael Johnson, Emma Hannay, and Oomen John
- Subjects
Medicine (General) ,R5-920 ,Infectious and parasitic diseases ,RC109-216 - Published
- 2021
- Full Text
- View/download PDF
9. Strategies for Using Antigen Rapid Diagnostic Tests to Reduce Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 in Low- and Middle-Income Countries: A Mathematical Modelling Study Applied to Zambia
- Author
-
Alvin X Han, Sarah J Girdwood, Shaukat Khan, Jilian A Sacks, Amy Toporowski, Naushin Huq, Emma Hannay, Colin A Russell, Brooke E Nichols, Medical Microbiology and Infection Prevention, and AII - Infectious diseases
- Subjects
Microbiology (medical) ,Infectious Diseases ,SARS-CoV-2 ,COVID-19 ,low- and middle-income countries ,diagnostic testing - Abstract
BackgroundIncreasing the availability of antigen rapid diagnostic tests (Ag-RDTs) in low- and middle-income countries (LMICs) is key to alleviating global SARS-CoV-2 testing inequity (median testing rate in December 2021–March 2022 when the Omicron variant was spreading in multiple countries: high-income countries = 600 tests/100 000 people/day; LMICs = 14 tests/100 000 people/day). However, target testing levels and effectiveness of asymptomatic community screening to impact SARS-CoV-2 transmission in LMICs are unclear.MethodsWe used Propelling Action for Testing and Treating (PATAT), an LMIC-focused agent-based model to simulate coronavirus disease 2019 (COVID-19) epidemics, varying the amount of Ag-RDTs available for symptomatic testing at healthcare facilities and asymptomatic community testing in different social settings. We assumed that testing was a function of access to healthcare facilities and availability of Ag-RDTs. We explicitly modelled symptomatic testing demand from individuals without SARS-CoV-2 and measured impact based on the number of infections averted due to test-and-isolate.ResultsTesting symptomatic individuals yields greater benefits than any asymptomatic community testing strategy until most symptomatic individuals who sought testing have been tested. Meeting symptomatic testing demand likely requires at least 200–400 tests/100 000 people/day, on average, as symptomatic testing demand is highly influenced by individuals without SARS-CoV-2. After symptomatic testing demand is satisfied, excess tests to proactively screen for asymptomatic infections among household members yield the largest additional infections averted.ConclusionsTesting strategies aimed at reducing transmission should prioritize symptomatic testing and incentivizing test-positive individuals to adhere to isolation to maximize effectiveness.
- Published
- 2022
- Full Text
- View/download PDF
10. Estimating the potential need and impact of SARS-CoV-2 test-and-treat programs with oral antivirals in low-and-middle-income countries
- Author
-
Alvin X. Han, Emma Hannay, Sergio Carmona, Bill Rodriguez, Brooke E. Nichols, and Colin A. Russell
- Abstract
Oral antivirals can potentially reduce the burden of COVID-19. However, low SARS-CoV-2 clinical testing rates in many low- and middle-income countries (LMICs) (mean Rt ≤ 1.2), increasing to 100 tests/100,000 people/day and allowing uncapped distribution of antivirals to LMICs (estimate = 26,000,000-90,000,000 courses/year for all LMICs), could avert up to 65% of severe cases, particularly in countries with older populations. For higher Rt, significant reductions in severe cases are only possible by substantially increasing testing rates or restricting clinical testing to those with higher risk of severe disease.
- Published
- 2022
- Full Text
- View/download PDF
11. SARS-CoV-2 diagnostic testing rates determine the sensitivity of genomic surveillance programs
- Author
-
Alvin X. Han, Amy Toporowski, Jilian A. Sacks, Mark D. Perkins, Sylvie Briand, Maria van Kerkhove, Emma Hannay, Sergio Carmona, Bill Rodriguez, Edyth Parker, Brooke E. Nichols, Colin A. Russell, Medical Microbiology and Infection Prevention, and AII - Infectious diseases
- Subjects
Genetics - Abstract
The first step in SARS-CoV-2 genomic surveillance is testing to identify people who are infected. However, global testing rates are falling as we emerge from the acute health emergency and remain low in many low- and middle-income countries (mean = 27 tests per 100,000 people per day). We simulated COVID-19 epidemics in a prototypical low- and middle-income country to investigate how testing rates, sampling strategies and sequencing proportions jointly impact surveillance outcomes, and showed that low testing rates and spatiotemporal biases delay time to detection of new variants by weeks to months and can lead to unreliable estimates of variant prevalence, even when the proportion of samples sequenced is increased. Accordingly, investments in wider access to diagnostics to support testing rates of approximately 100 tests per 100,000 people per day could enable more timely detection of new variants and reliable estimates of variant prevalence. The performance of global SARS-CoV-2 genomic surveillance programs is fundamentally limited by access to diagnostic testing.
- Published
- 2022
- Full Text
- View/download PDF
12. Strategies for using antigen rapid diagnostic tests to reduce transmission of SARS-CoV-2 in low- and middle-income countries: a mathematical modelling study applied to Zambia
- Author
-
Alvin X, Han, Sarah, Girdwood, Shaukat, Khan, Jilian A, Sacks, Amy, Toporowski, Naushin, Huq, Emma, Hannay, Colin A, Russell, and Brooke E, Nichols
- Abstract
Increasing the availability of antigen rapid diagnostic tests (Ag-RDTs) in low- and middle-income countries (LMICs) is key to alleviating global SARS-CoV-2 testing inequity (median testing rate in December 2021-March 2022 when the Omicron variant was spreading in multiple countries; high-income countries = 600 tests/100,000 people/day; LMICs = 14 tests/100,000 people/day). However, target testing levels and effectiveness of asymptomatic community screening to impact SARS-CoV-2 transmission in LMICs are unclear.We used PATAT, an LMIC-focused agent-based model to simulate COVID-19 epidemics, varying the amount of Ag-RDTs available for symptomatic testing at healthcare facilities and asymptomatic community testing in different social settings. We assumed that testing was a function of access to healthcare facilities and availability of Ag-RDTs. We explicitly modelled symptomatic testing demand from non-SARS-CoV-2 infected individuals and measured impact based on the number of infections averted due to test-and-isolate.Testing symptomatic individuals yields greater benefits than any asymptomatic community testing strategy until most symptomatic individuals who sought testing have been tested. Meeting symptomatic testing demand likely requires at least 200-400 tests/100,000 people/day on average as symptomatic testing demand is highly influenced by non-SARS-CoV-2 infected individuals. After symptomatic testing demand is satisfied, excess tests to proactively screen for asymptomatic infections among household members yields the largest additional infections averted.Testing strategies aimed at reducing transmission should prioritize symptomatic testing and incentivizing test-positive individuals to adhere to isolation to maximize effectiveness.
- Published
- 2022
13. Strategies for using antigen rapid diagnostic tests to reduce transmission of SARS-CoV-2 in low- and middle-income countries: a mathematical modelling study applied to Zambia
- Author
-
Alvin X. Han, Sarah Girdwood, Shaukat Khan, Jilian A. Sacks, Amy Toporowski, Naushin Huq, Emma Hannay, Colin A. Russell, and Brooke E. Nichols
- Abstract
SummaryBackgroundIncreasing the availability of antigen rapid diagnostic tests (Ag-RDTs) in low- and middle-income countries (LMICs) is key to alleviating global SARS-CoV-2 testing inequity (median testing rate in December 2021-March 2022 when the Omicron variant was spreading in multiple countries; high-income countries=600 tests/100,000 people/day; LMICs=14 tests/ 100,000 people/day). However, target testing levels and effectiveness of asymptomatic community screening to impact SARS-CoV-2 transmission in LMICs are unclear.MethodsWe used PATAT, an LMIC-focused agent-based model to simulate COVID-19 epidemics, varying the amount of Ag-RDTs available for symptomatic testing at healthcare facilities and asymptomatic community testing in different social settings. We assumed that testing was a function of access to healthcare facilities and availability of Ag-RDTs. We explicitly modelled symptomatic testing demand from non-SARS-CoV-2 infected individuals and measured impact based on the number of infections averted due to test-and-isolate.ResultsTesting symptomatic individuals yields greater benefits than any asymptomatic community testing strategy until most symptomatic individuals who sought testing have been tested.Meeting symptomatic testing demand likely requires at least 200-400 tests/100,000 people/day on average as symptomatic testing demand is highly influenced by non-SARS-CoV-2 infected individuals. After symptomatic testing demand is satisfied, excess tests to proactively screen for asymptomatic infections among household members yields the largest additional infections averted.ConclusionsTesting strategies aimed at reducing transmission should prioritize symptomatic testing and incentivizing test-positive individuals to adhere to isolation to maximize effectiveness.
- Published
- 2022
- Full Text
- View/download PDF
14. Low Testing Rates Limit the Ability of Genomic Surveillance Programs to Monitor SARS-CoV-2 Variants: A Mathematical Modelling Study
- Author
-
Alvin X. Han, Amy Toporowski, Jilian Sacks, Mark Perkins, Sylvie Briand, Maria Van Kerkhove, Emma Hannay, Sergio Carmona, Bill Rodriguez, Edyth Parker, Brooke E Nichols, and Colin Russell
- Subjects
History ,Polymers and Plastics ,Business and International Management ,Industrial and Manufacturing Engineering - Published
- 2022
- Full Text
- View/download PDF
15. Considerations for simultaneous testing of COVID-19 and tuberculosis in high-burden countries
- Author
-
Morten Ruhwald, Emma Hannay, Sanjay Sarin, Kekeletso Kao, Rajashree Sen, and Sarabjit Chadha
- Subjects
SARS-CoV-2 ,Comment ,COVID-19 ,Humans ,Tuberculosis ,General Medicine - Published
- 2022
- Full Text
- View/download PDF
16. The governance of personal data for COVID-19 response: perspective from the Access to COVID-19 Tools Accelerator
- Author
-
Emma Hannay, Ciara Staunton, Michael Johnson, Oomen John, Rangarajan Sampath, and R.M. Kadam
- Subjects
medicine.medical_specialty ,Medicine (General) ,Internet privacy ,Psychological intervention ,Stigma (botany) ,Infectious and parasitic diseases ,RC109-216 ,Global Health ,03 medical and health sciences ,0302 clinical medicine ,R5-920 ,Pandemic ,Health care ,medicine ,Global health ,Humans ,030212 general & internal medicine ,Health policy ,Digital Technology ,business.industry ,030503 health policy & services ,Health Policy ,Medical record ,Public health ,public health ,Public Health, Environmental and Occupational Health ,COVID-19 ,Privacy ,Commentary ,0305 other medical science ,business - Abstract
COVID-19 is the world’s first digital pandemic. Digital tools and technologies have been developed to track and trace the spread of the virus, screen for infection, and the pandemic has accelerated the use of digital technology in the delivery of healthcare. The continued development of these tools and technologies, the monitoring of the virus and the development of new tests, treatments and vaccines are dependent on the collection of and access to vast amounts of personal data. This includes clinical data, epidemiological data and public health data that may be collected from laboratories, medical records, wearables and smartphone apps. Previous public health emergencies (PHEs) have demonstrated the importance in making this data available, and early in the COVID-19 pandemic, there were calls for making all kinds of data, including clinical trial data, routine surveillance data, genetic sequencing, and data on the ongoing monitoring of disease control programmes, openly and rapidly available. As part of this, personal data on age, race, sex, health, ethnic group, and socioeconomic factors have been shared. This has helped led to the rapid development of COVID-19 interventions. It has also enabled the better understanding of factors contributing to difference in infection rates and effectiveness of tests, treatments, and vaccines. However, the use of this particularly sensitive data can infringe upon individual and group privacy, increase the risks of individual and group stigma and discrimination, and it may negatively impact already vulnerable, marginalised or minority populations. [...]
- Published
- 2021
17. SARS-CoV-2 testing for public health use: core principles and considerations for defined use settings
- Author
-
Emma Hannay, Catharina Boehme, and Rangarajan Sampath
- Subjects
medicine.medical_specialty ,2019-20 coronavirus outbreak ,Travel ,Coronavirus disease 2019 (COVID-19) ,business.industry ,SARS-CoV-2 ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Public health ,Comment ,COVID-19 ,General Medicine ,Data science ,COVID-19 Testing ,Core (graph theory) ,medicine ,Humans ,Prevention control ,business - Published
- 2020
18. Promoting diagnostics as a global good
- Author
-
Catharina Boehme, Emma Hannay, and Madhukar Pai
- Subjects
0301 basic medicine ,Economic growth ,2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,media_common.quotation_subject ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Outbreak ,General Medicine ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,030104 developmental biology ,0302 clinical medicine ,Promotion (rank) ,030220 oncology & carcinogenesis ,Political science ,Pandemic ,Global health ,media_common - Abstract
The COVID-19 pandemic has reasserted the central role of effective diagnostics in the response to outbreaks. But a lack of coordination still hampers widespread access to these critical tools. A diagnostics agenda for global health is urgently needed for the promotion of diagnostics as a global good and to ensure their delivery.
- Published
- 2021
- Full Text
- View/download PDF
19. We don't have more time to wait to measure how well our healthcare system is doing
- Author
-
Emma Hannay
- Subjects
Health Care Reform ,Humans ,Public Health ,Delivery of Health Care ,New Zealand ,Quality of Health Care - Published
- 2019
20. Assistive technology policy : a position paper from the first global research, innovation, and education on assistive technology (GREAT) summit
- Author
-
Malcolm MacLachlan, David Banes, Diane Bell, Johan Borg, Brian Donnelly, Michael Fembek, Ritu Ghosh, Rosemary Joan Gowran, Emma Hannay, Diana Hiscock, Evert-Jan Hoogerwerf, Tracey Howe, Friedbert Kohler, Natasha Layton, Siobhán Long, Hasheem Mannan, Gubela Mji, Thomas Odera Ongolo, Katherine Perry, Cecilia Pettersson, Jessica Power, Vinicius Delgado Ramos, Lenka Slepičková, Emma M. Smith, Kiu Tay-Teo, Priscille Geiser, and Hilary Hooks
- Subjects
Aging ,030506 rehabilitation ,Orthopedic Equipment ,Health Policy ,Rehabilitation ,Biomedical Engineering ,Physical Therapy, Sports Therapy and Rehabilitation ,Public Health, Global Health, Social Medicine and Epidemiology ,Global Health ,Self-Help Devices ,Health Services Accessibility ,03 medical and health sciences ,Speech and Hearing ,Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi ,0302 clinical medicine ,Humans ,Disabled Persons ,Orthopedics and Sports Medicine ,030212 general & internal medicine ,Power, Psychological ,Policy Making ,0305 other medical science ,Developing Countries ,Needs Assessment ,Quality of Health Care - Abstract
Increased awareness, interest and use of assistive technology (AT) presents substantial opportunities for many citizens to become, or continue being, meaningful participants in society. However, there is a significant shortfall between the need for and provision of AT, and this is patterned by a range of social, demographic and structural factors. To seize the opportunity that assistive technology offers, regional, national and sub-national assistive technology policies are urgently required. This paper was developed for and through discussion at the Global Research, Innovation and Education on Assistive Technology (GREAT) Summit; organized under the auspices of the World Health Organization's Global Collaboration on Assistive Technology (GATE) program. It outlines some of the key principles that AT polices should address and recognizes that AT policy should be tailored to the realities of the contexts and resources available. AT policy should be developed as a part of the evolution of related policy across a number of different sectors and should have clear and direct links to AT as mediators and moderators for achieving the Sustainable Development Goals. The consultation process, development and implementation of policy should be fully inclusive of AT users, and their representative organizations, be across the lifespan, and imbued with a strong systems-thinking ethos. Six barriers are identified which funnel and diminish access to AT and are addressed systematically within this paper. We illustrate an example of good practice through a case study of AT services in Norway, and we note the challenges experienced in less well-resourced settings. A number of economic factors relating to AT and economic arguments for promoting AT use are also discussed. To address policy-development the importance of active citizenship and advocacy, the need to find mechanisms to scale up good community practices to a higher level, and the importance of political engagement for the policy process, are highlighted. Policy should be evidence-informed and allowed for evidence-making; however, it is important to account for other factors within the given context in order for policy to be practical, authentic and actionable. Implications for Rehabilitation The development of policy in the area of asssitive technology is important to provide an overarching vision and outline resourcing priorities. This paper identifies some of the key themes that should be addressed when developing or revising assistive technology policy. Each country should establish a National Assistive Technology policy and develop a theory of change for its implementation.
- Published
- 2018
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.