Diana L. Connor
University of Pittsburgh
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Featured researches published by Diana L. Connor.
PLOS Neglected Tropical Diseases | 2010
Bruce Y. Lee; Kristina M. Bacon; Diana L. Connor; Alyssa M. Willig; Rachel R. Bailey
Background Chagas disease, caused by the parasite Trypanosoma cruzi (T. cruzi), is the leading etiology of non-ischemic heart disease worldwide, with Latin America bearing the majority of the burden. This substantial burden and the limitations of current interventions have motivated efforts to develop a vaccine against T. cruzi. Methodology/Principal Findings We constructed a decision analytic Markov computer simulation model to assess the potential economic value of a T. cruzi vaccine in Latin America from the societal perspective. Each simulation run calculated the incremental cost-effectiveness ratio (ICER), or the cost per disability-adjusted life year (DALY) avoided, of vaccination. Sensitivity analyses evaluated the impact of varying key model parameters such as vaccine cost (range:
Vaccine | 2012
Bruce Y. Lee; Brigid E. Cakouros; Tina Marie Assi; Diana L. Connor; Joel S. Welling; Souleymane Kone; Ali Djibo; Angela R. Wateska; Lionel Pierre; Shawn T. Brown
0.50–
BMC Public Health | 2011
Tina Marie Assi; Shawn T. Brown; Ali Djibo; Bryan A. Norman; Jayant Rajgopal; Joel S. Welling; Sheng I. Chen; Rachel R. Bailey; Souleymane Kone; Hailu Kenea; Diana L. Connor; Angela R. Wateska; Anirban Jana; Stephen R. Wisniewski; Willem G. van Panhuis; Donald S. Burke; Bruce Y. Lee
200), vaccine efficacy (range: 25%–75%), the cost of acute-phase drug treatment (range:
American Journal of Tropical Medicine and Hygiene | 2012
Bruce Y. Lee; Kristina M. Bacon; Mirat Shah; Sarah Beth Kitchen; Diana L. Connor; Rachel B. Slayton
10–
American Journal of Tropical Medicine and Hygiene | 2011
Bruce Y. Lee; Diana L. Connor; Sarah Beth Kitchen; Kristina M. Bacon; Mirat Shah; Shawn T. Brown; Rachel R. Bailey; Yongjua Laosiritaworn; Donald S. Burke; Derek A. T. Cummings
150 to account for variations in acute-phase treatment regimens), and risk of infection (range: 1%–20%). Additional analyses determined the incremental cost of vaccinating an individual and the cost per averted congestive heart failure case. Vaccination was considered highly cost-effective when the ICER was ≤1 times the GDP/capita, still cost-effective when the ICER was between 1 and 3 times the GDP/capita, and not cost-effective when the ICER was >3 times the GDP/capita. Our results showed vaccination to be very cost-effective and often economically dominant (i.e., saving costs as well providing health benefits) for a wide range of scenarios, e.g., even when risk of infection was as low as 1% and vaccine efficacy was as low as 25%. Vaccinating an individual could likely provide net cost savings that rise substantially as risk of infection or vaccine efficacy increase. Conclusions/Significance Results indicate that a T. cruzi vaccine could provide substantial economic benefit, depending on the cost of the vaccine, and support continued efforts to develop a human vaccine.
Vaccine | 2014
Shawn T. Brown; Benjamin Schreiber; Brigid E. Cakouros; Angela R. Wateska; Hamadou M. Dicko; Diana L. Connor; Mercy Mvundura; Bryan A. Norman; Carol Levin; Jayant Rajgopal; Mélanie Avella; Caroline Lebrun; Erin Claypool; Proma Paul; Bruce Y. Lee
OBJECTIVE Determine the effects on the vaccine cold chain of making different types of World Health Organization (WHO) Expanded Program on Immunizations (EPI) vaccines thermostable. METHODS Utilizing a detailed computational, discrete-event simulation model of the Niger vaccine supply chain, we simulated the impact of making different combinations of the six current EPI vaccines thermostable. FINDINGS Making any EPI vaccine thermostable relieved existing supply chain bottlenecks (especially at the lowest levels), increased vaccine availability of all EPI vaccines, and decreased cold storage and transport capacity utilization. By far, the most substantial impact came from making the pentavalent vaccine thermostable, increasing its own vaccine availability from 87% to 97% and the vaccine availabilities of all other remaining non-thermostable EPI vaccines to over 93%. By contrast, making each of the other vaccines thermostable had considerably less effect on the remaining vaccines, failing to increase the vaccine availabilities of other vaccines to more than 89%. Making tetanus toxoid vaccine along with the pentavalent thermostable further increased the vaccine availability of all EPI vaccines by at least 1-2%. CONCLUSION Our study shows the potential benefits of making any of Nigers EPI vaccines thermostable and therefore supports further development of thermostable vaccines. Eliminating the need for refrigerators and freezers should not necessarily be the only benefit and goal of vaccine thermostability. Rather, making even a single vaccine (or some subset of the vaccines) thermostable could free up significant cold storage space for other vaccines, and thereby help alleviate supply chain bottlenecks that occur throughout the world.
American Journal of Public Health | 2012
Bruce Y. Lee; Tina Marie Assi; Jayant Rajgopal; Bryan A. Norman; Sheng I. Chen; Shawn T. Brown; Rachel B. Slayton; Souleymane Kone; Hailu Kenea; Joel S. Welling; Diana L. Connor; Angela R. Wateska; Anirban Jana; Ann E. Wiringa; Willem G. van Panhuis; Donald S. Burke
BackgroundMany countries, such as Niger, are considering changing their vaccine vial size presentation and may want to evaluate the subsequent impact on their supply chains, the series of steps required to get vaccines from their manufacturers to patients. The measles vaccine is particularly important in Niger, a country prone to measles outbreaks.MethodsWe developed a detailed discrete event simulation model of the vaccine supply chain representing every vaccine, storage location, refrigerator, freezer, and transport device (e.g., cold trucks, 4 × 4 trucks, and vaccine carriers) in the Niger Expanded Programme on Immunization (EPI). Experiments simulated the impact of replacing the 10-dose measles vial size with 5-dose, 2-dose and 1-dose vial sizes.ResultsSwitching from the 10-dose to the 5-dose, 2-dose and 1-dose vial sizes decreased the average availability of EPI vaccines for arriving patients from 83% to 82%, 81% and 78%, respectively for a 100% target population size. The switches also changed transport vehicles utilization from a mean of 58% (range: 4-164%) to means of 59% (range: 4-164%), 62% (range: 4-175%), and 67% (range: 5-192%), respectively, between the regional and district stores, and from a mean of 160% (range: 83-300%) to means of 161% (range: 82-322%), 175% (range: 78-344%), and 198% (range: 88-402%), respectively, between the district to integrated health centres (IHC). The switch also changed district level storage utilization from a mean of 65% to means of 64%, 66% and 68% (range for all scenarios: 3-100%). Finally, accounting for vaccine administration, wastage, and disposal, replacing the 10-dose vial with the 5 or 1-dose vials would increase the cost per immunized patient from
Vaccine | 2013
Tina Marie Assi; Shawn T. Brown; Souleymane Kone; Bryan A. Norman; Ali Djibo; Diana L. Connor; Angela R. Wateska; Jayant Rajgopal; Rachel B. Slayton; Bruce Y. Lee
0.47US to
PLOS ONE | 2013
Leila A. Haidari; Diana L. Connor; Angela R. Wateska; Shawn T. Brown; Leslie E. Mueller; Bryan A. Norman; Michelle M. Schmitz; Proma Paul; Jayant Rajgopal; Joel S. Welling; Jim Leonard; Sheng I. Chen; Bruce Y. Lee
0.71US and
Vaccine | 2016
Leila A. Haidari; Shawn T. Brown; Marie Ferguson; Emily Bancroft; Marie L. Spiker; Allen Wilcox; Ramya Ambikapathi; Vidya Sampath; Diana L. Connor; Bruce Y. Lee
1.26US, respectively.ConclusionsThe switch from the 10-dose measles vaccines to smaller vial sizes could overwhelm the capacities of many storage facilities and transport vehicles as well as increase the cost per vaccinated child.