Preventing Transmission of Chagas Disease in the U.S. Blood Supply: A Cost Effectiveness Analysis of Testing the Blood Bank Donations Danielle Doughman.

Slides:



Advertisements
Similar presentations
TB and poverty agenda in WPR WHO/WPRO Stop TB. World Health Organization Percentage of population living below US$1 a day.
Advertisements

WHO comparative evaluation of serologic assays for Chagas disease Journal Club April 2, 2009.
1 Sixty-Four-Slice Computed Tomography of the Coronary Arteries: Cost-Effectiveness Analysis of Patients Presenting to the ED with Low Risk Chest Pain.
HIV in the United Kingdom: 2013 HIV and AIDS Reporting Section Centre for Infectious Disease Surveillance and Control (CIDSC) Public Health England London,
Chagas Disease Tabitha Martel Epidemiology November 15, 2007.
W: Supported by Epidemiology of sub-patent Plasmodium falciparum infection: implications for detection of hotspots.
Teenage conceptions in Wales The challenge of intervention and evaluation.
Dengue Transfusion Risk Model Lyle R. Petersen, MD, MPH Brad Biggerstaff, PhD Division of Vector-Borne Diseases Centers for Disease Control and Prevention.
The influence of endemic infections on cattle culling and movement David Carslake, Laura Green, Habtu Weldegebriel and Graham Medley University of Warwick,
1 Risks and Benefits of Home-Use HIV Test Kits Richard Forshee, Ph.D. U.S. Food and Drug Administration Center for Biologics Evaluation and Research Office.
Cost-effectiveness of different starting criteria of antiretroviral therapy in Mexico. Caro Y., Colchero A., Valencia A., Bautista-Arredondo S., Sierra.
Dengue Virus and Its Risk to the U.S. Blood Supply
1 Babesia BPAC: FDA Perspective Sanjai Kumar, PhD Division of Emerging and Transfusion- Transmitted Diseases Office of Blood Research and Review CBER,
Screening for HBsAg and Anti-HBc in North American Blood Donors John Saldanha, Roche Molecular Systems SoGAT XXI, May, 2009, Brussels, Belgium.
Workshop Summary FDA Workshop on Testing for malarial Infections in Blood Donors Sanjai Kumar, Ph.D. Center for Biologics Evaluation and Research Food.
Chronic diseases 1.Chronic diseases have long and variable preclinical phases. 2.The preclinical phase is that portion of the disease natural history during.
Hepatitis C for the General Practitioner Morris Sherman MB BCh PhD FRCP(C) University of Toronto January 2013.
21 August 2015 Samreen Ijaz Virus Reference Department Health Protection Agency Indigenous HEV infection in the UK: a hazard for blood donation?
FDA Guidance for Industry: Use of Serological Tests to Reduce the Risk of Transmission of Trypanosoma cruzi Infection in Whole Blood and Blood Components.
H.I.V./ A.I.Ds ..
Sexually Transmitted Diseases
DAREDEVILS: Prajwal Acharya, Cristina Johnson, Julie David, Jen Masciovecchio, Yen Phan.
Hepatitis C Education & Awareness. Women In Government Women In Government Foundation, Inc. is a national, non-profit, non-partisan organization of women.
Adult Viral Hepatitis Update Roxanne Ereth, MPH, BS Hepatitis C Program Manager Adult Viral Hepatitis Prevention Coordinator.
Lesson 4 Treatment for HIV / AIDS
© 2005, Johns Hopkins University. All rights reserved. Department of Health, Behavior & Society David Holtgrave, PhD, Professor & Chair.
Analysis of Infection of Trypanosoma cruzi, Causative Agent of Chagas Disease, in Triatomine Insects from Southern Arizona Acknowledgements: Teresa Gregory,
Washington D.C., USA, July 2012www.aids2012.org Estimating the Costs and Impacts of HIV/AIDS Programs for Botswana Examples of the ART Program and.
Knowing what you get for what you pay An introduction to cost effectiveness FETP India.
Effect of Hypertension and Dyslipidemia on glycemic control among Type 2 Diabetes patients in Thailand Dr. Mya Thandar Dr.PH. Batch 5 1.
T. cruzi Incidence Study in Blood Donors and its Implications for One-time Testing of Blood Donors Robert Duncan, Ph.D. DETTD, CBER, FDA Blood Products.
1 Blood Systems Trypanosoma cruzi and Chagas Disease Studies and Potential Strategies for Targeted Testing of Donors Blood Products Advisory Committee.
Monthly Journal article review: Vimmi Kang PGY 2
Current Status of Issues Related to West Nile virus testing and donor screening Hira Nakhasi, Ph.D. Director, DETTD/OBRR CBER, FDA.
Jamie Bartram With adaptations by Mark Sobsey, UNC- Chapel Hill Water, Sanitation and Health: the Millennium Development Goals and Reducing the Global.
Lower Hudson Valley Perinatal Network Serving Dutchess, Putnam, Rockland & Westchester Counties Presented at the Quarterly Education & Networking Conference.
Effect of Hypertension and Dyslipidemia on glycemic control among Type 2 Diabetes patients in Thailand Dr. Mya Thandar DrPH Batch 5 1.
Glucose Control and Monitoring
Household Infestation Rates of Chagas Disease Vectors and Trypanosoma cruzi Prevalence in Southern Ecuador Stanton Jasicki Dr. Daniel Herman Dr. Mario.
Cost-effectiveness of Screening Tests Mark Hlatky, MD Stanford University.
Eastern European Alliance for Reproductive Choice REPRODUCTIVE CHOICE FOR HIV- INFECTED WOMEN Prof. POSOKHOVA S.P. UKRAINE УКРАЇНАУКРАЇНА.
Pompe Disease Evidence Evaluation Michael Watson, PhD, on behalf of Piero Rinaldo, MD, PhD, and the Decision-Making Workgroup October 1, 2008.
Issues Related to Implementation of Blood Donor Screening for Infection with Trypanosoma cruzi Presentation to BPAC April 26, 2007 Robert Duncan, PhD.
Hepatitis B The Basics David Wong University of Toronto March 2005.
RISK COMMUNICATION APPROACH TSEAC 15 December 2006 Mark Weinstein, Ph.D. FDA, Center for Biologics Evaluation and Research.
CURRENT HEALTH PROBLEMS IN STUDENT'S HOME SOUNTRIES HEPATITIS B IN MALAYSIA MOHD ZHARIF ABD HAMID AMINUDDIN BAKI AMRAN.
Public health impacts of donor screening for T. cruzi infection Susan P. Montgomery, DVM MPH Division of Parasitic Diseases Centers for Disease Control.
Vaccines & Biologicals (V&B) Cost-effectiveness of safe injection policies: Study rationale and proposed methodology Ulla Kou, WHO SIGN meeting in New.
1 Update on Study to Further Define the Incidence of T. cruzi Infection in the US Blood Donor Population Susan L. Stramer, PhD American Red Cross BPAC.
Appendix 2 Comparison of screening from age 20 and age 25 Table of harms and benefits.
A Cost-Effectiveness Analysis of Maternal Genotyping to Guide Treatment in Postnatal Patients.
Universal Opt-Out Screening for HIV in Health Care Settings, Cost Effectiveness in Action Douglas K. Owens, MD, MS VA Palo Alto Health Care System and.
Methods Background Abstract Probability Parameters Selected References Genetic testing for BRCA mutations in high-risk women is cost-effective under base-
Cost-effectiveness of initiating and monitoring HAART based on WHO versus US DHHS guidelines in the developing world Peter Mazonson, MD, MBA Arthi Vijayaraghavan,
Chapter 7: Epidemiology of Chronic Diseases. “The Change You Like to See….” (1 of 3) Chronic diseases result from prolongation of acute illness. – With.
00002-E-1 – 1 December 2001 THE HIV/AIDS PANDEMIC Focus on Africa By Dr. David Elkins HIV/AIDS Prevention and Care Project Nairobi, Kenya September 2002.
Provider Initiated HIV Counseling and Testing Unit 1: Introduction to HIV/AIDS.
CBER Current Considerations for Blood Donor Screening for West Nile Virus Pradip N. Akolkar, Ph.D. Maria Rios, Ph.D. DETTD, OBRR Blood Products Advisory.
HIV\AIDS Statistics Advanced Humanities Adkins. HIV HIV stands for human immunodeficiency virus. This is the virus that causes AIDS. HIV is different.
Treatment for HIV and AIDS
Lesson 4 Treatment for HIV / AIDS
Contents Global impact 2.Service cascade 3. Policies and WHO support.
INTRODUCTION: CERVICAL CANCER SCREENING
How dangerous are Donor Travels?
Copyright © 2017 American Academy of Pediatrics.
Relationship between CMV & PU disease
Lesson 4 Treatment for HIV / AIDS
Influenza Vaccine Effectiveness Against Pediatric Deaths:
Chagas Disease Ashleigh Dixon.
Contents Global impact 2.Service cascade 3. Policies and WHO support.
Presentation transcript:

Preventing Transmission of Chagas Disease in the U.S. Blood Supply: A Cost Effectiveness Analysis of Testing the Blood Bank Donations Danielle Doughman Health Policy and Management, Gillings School of Global Public Health, University of North Carolina at Chapel Hill Chagas disease is a parasitic infection common in rural areas of the Americas with substandard housing Precise prevalence figures difficult to ascertain due to lack of detection as nearly half of all cases remain asymptomatic. Chagas not endemic in the U.S., but between 3,000 and 1 Million cases estimated in the US, especially along US- Mexico border, Appalachia, and Mississippi Delta regions Only 7 known cases of Chagas disease transmission via blood transfusion in the US and Canada. FDA does not require blood banks to test blood for Chagas disease, and the disease prevalence is not tracked by the CDC, though 65% of blood banks voluntarily test With heightened attention to immigration from Latin America to the U.S., there have been concerns about Chagas in the U.S. blood supply. Those with symptoms develop life-long gastrointestinal or cardiac complications, sometimes leading to death. In December 2006, the FDA approved a Chagas screening assay for blood called the Ortho T. cruzi ELISA Test System (enzyme-linked immune sorbent assay) Background Results Limitations Conclusions Background: Chagas Disease is a parasitic infection that affects people living in poor, rural areas of the Americas. Though Chagas is not endemic to the U.S., increased attention on immigration from Latin America to the U.S. coupled with the availability of a highly effective assay highlight the need for testing of blood donations for Chagas, which may be transmitted through transfusion. Currently, blood banks are not required to test for Chagas, although 65% voluntarily do so. Objective: To estimate incremental cost-effectiveness of blood bank testing and screening strategies for Chagas. Design: Cost-effectiveness analysis with a decision tree model. Data Sources: Peer-reviewed literature. Target Population: U.S. adult blood donors and transfusion recipients ages Time Horizon: 20 years. Perspective: Societal. Interventions: 1) the ELISA test for all blood donations, 2) verbal screen with ELISA testing for those with a positive screen, and 3) testing new donors only. Outcome Measures: Costs (in 2008 U.S. dollars), cases averted, and incremental cost per case averted. Results of Base-Case Analysis: Testing All averts 20 additional cases over Screen and Test, but at a cost of $3.6 million per additional case averted. Test New Donors resulted in worse outcomes (increase of 14 cases) but lower costs than the standard (Screen and Test). Results of Sensitivity Analysis: The analysis is most sensitive to whether or not a negative verbal screen was obtained. The model results were relatively insensitive to all other variables. Conclusions: Testing All averts the most cases, however, it is cost-prohibitive at a threshold of $100,000 per case averted. ABSTRACT Assumptions Data Methods Acknowledgements Assume same transmission risk for both red blood cell and platelet transfusion For a person with Chagas becomes symptomatic, the disease outcomes have been collapsed into two categories: 1) Cardiac abnormalities, and 2) gastrointestinal disease. Cases of Chagas disease due to reactivation have been excluded The model assumes testing requires only one ELISA test, and does not include costs associated with notification and appropriate follow-up with infected individuals and their families. Blood donation losses due to other screening and expiration not included and assumed to be consistent across the three alternatives All donors positive for Chagas will present in the chronic stage and not require the treatment appropriate for those with newly acquired. Assuming 100% cure of those with acute disease when rate is only about 85% No costs assumed for tracking of established donors’ Chagas status. This study used a cost-effectiveness analysis with a decision tree model to estimate the costs and outcomes for three tsting alternatives over a 20 year period for a cohort of 15 million U.S. adults ages 18 to 65 (the average number of blood donations in the U.S. each year, rounded to the nearest million). Blood Banks decide to either 1) Verbally Screen each donor, and test the blood donations of those at high risk, 2) Test all blood donations, or 3) Test only new donors. Blood found to be infected is discarded, donors with Chagas are deferred, and blood believed to be uninfected is given to transfusion recipients. If a person is given infected blood, they may be treated successfully in the first two months, or will progress to chronic disease. Of those, about half will develop gastrointestinal or cardiac symptoms, some requiring surgery or leading to death. Thanks to Andrea Biddle, Stephanie Wheeler, Rebecca Garr, Cheri Poss, and Elizabeth Walker for their valuable suggestions. This study does not consider deaths averted so the high costs of Chagas care in the last year of life may make testing seem less cost-effective. Prevalence rates of Chagas are very difficult ot ascertain with any certainty since many cases go undiagnosed and the disease is not tracked in the U.S. Base-Case Analysis: DeterministicIncremental CostsTotal Cases Costs Cases Averted CE Ratio Screen &Test $55,579, Test All$129,178,677-25$73,599,63920 $3,621,824 Test New Donors$27,247, $28,331, $1,963,019 With the given probabilities, assumptions and costs, testing more frequently for Chagas disease in the blood supply is not cost effective. These results contradict the analysis conducted by Wilson in 2008, which found both Testing All and Test and Screen cost- effective alternatives to No Testing. Sensitivity analysis demonstrates that the decision is most sensitive to whether or not a person has a negative verbal screen, so a more precise screen that limits the need for tests may help bring costs down, but probably not nearly enough for any alternative to be cost-effective any where near $100,000 per case. If costs in the last year of life due to Chagas were taken into account, the intervention would become most cost effective, but, again, not at the $100,000 threshold. Only the variable Negative Verbal Screen for Chagas Risk demonstrated caused significant variability in model results. At typical rates of $100,000 per case averted, no alternative is cost-effective. At $2,000,000 per case averted, Screen and Test and Testing New Donors cross, indicating equalibrium in cost-effectiveness Testing New Donors is cheapest, but results in the most cases of disease. Testing only new donors is the cheapest option but still costs nearly $2 million per case averted, and increases the total number of disease cases over Screen and Test Testing All is most effective in reducing the total number of cases, but costs an additional $73.6 million for only 20 additional cases averted over the standard.