Cindy M. Weinbaum
Centers for Disease Control and Prevention
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Featured researches published by Cindy M. Weinbaum.
Annals of Internal Medicine | 2012
David B. Rein; Bryce D. Smith; John S. Wittenborn; Sarah B. Lesesne; Laura Danielle Wagner; Douglas W. Roblin; Nita Patel; John W. Ward; Cindy M. Weinbaum
BACKGROUND In the United States, hepatitis C virus (HCV) infection is most prevalent among adults born from 1945 through 1965, and approximately 50% to 75% of infected adults are unaware of their infection. OBJECTIVE To estimate the cost-effectiveness of birth-cohort screening. DESIGN Cost-effectiveness simulation. DATA SOURCES National Health and Nutrition Examination Survey, U.S. Census, Medicare reimbursement schedule, and published sources. TARGET POPULATION Adults born from 1945 through 1965 with 1 or more visits to a primary care provider annually. TIME HORIZON Lifetime. PERSPECTIVE Societal, health care. INTERVENTION One-time antibody test of 1945-1965 birth cohort. OUTCOME MEASURES Numbers of cases that were identified and treated and that achieved a sustained viral response; liver disease and death from HCV; medical and productivity costs; quality-adjusted life-years (QALYs); incremental cost-effectiveness ratio (ICER). RESULTS OF BASE-CASE ANALYSIS Compared with the status quo, birth-cohort screening identified 808,580 additional cases of chronic HCV infection at a screening cost of
Digestive and Liver Disease | 2011
David B. Rein; John S. Wittenborn; Cindy M. Weinbaum; Miriam Sabin; Bryce D. Smith; Sarah B. Lesesne
2874 per case identified. Assuming that birth-cohort screening was followed by pegylated interferon and ribavirin (PEG-IFN+R) for treated patients, screening increased QALYs by 348,800 and costs by
Hepatology | 2009
Cindy M. Weinbaum; Eric E. Mast; John W. Ward
5.5 billion, for an ICER of
AIDS | 2005
Cindy M. Weinbaum; Keith Sabin; Scott S. Santibanez
15,700 per QALY gained. Assuming that birth-cohort screening was followed by direct-acting antiviral plus PEG-IFN+R treatment for treated patients, screening increased QALYs by 532,200 and costs by
Clinical Infectious Diseases | 2014
Faruque Ahmed; Megan C. Lindley; Norma J. Allred; Cindy M. Weinbaum; Lisa A. Grohskopf
19.0 billion, for an ICER of
Clinical Infectious Diseases | 2011
Bryce D. Smith; Eyasu H. Teshale; Amy Jewett; Cindy M. Weinbaum; Alan Neaigus; Holly Hagan; Sam M. Jenness; Sharon K. Melville; Richard D. Burt; Hanne Thiede; Alia Al-Tayyib; Praveen R. Pannala; IIsa W. Miles; Alexa M. Oster; Amanda Smith; Teresa Finlayson; Kristina E. Bowles; Elizabeth DiNenno
35,700 per QALY saved. RESULTS OF SENSITIVITY ANALYSIS The ICER of birth-cohort screening was most sensitive to sustained viral response of antiviral therapy, the cost of therapy, the discount rate, and the QALY losses assigned to disease states. LIMITATION Empirical data on screening and direct-acting antiviral treatment in real-world clinical settings are scarce. CONCLUSION Birth-cohort screening for HCV in primary care settings was cost-effective. PRIMARY FUNDING SOURCE Division of Viral Hepatitis, Centers for Disease Control and Prevention.
Digestive and Liver Disease | 2012
Alain H. Litwin; Bryce D. Smith; Mari-Lynn Drainoni; Diane McKee; Allen L. Gifford; Elisa Koppelman; Cindy L. Christiansen; Cindy M. Weinbaum; William N. Southern
BACKGROUND Without diagnosis and antiviral therapy, many patients with chronic hepatitis C infections will develop end-stage liver disease and die from complications. AIMS To evaluate the future impacts of preventive interventions and treatment advances, this paper forecasts a baseline estimate of the future morbidity and mortality of prevalent hepatitis C when left untreated. METHODS We simulated the future disease progression and death for all Americans with prevalent hepatitis C in 2005. To validate the model, we used past seroprevalence to forecast contemporary outcomes. We used the validated model to forecast future cases of end-stage liver disease, transplants, and deaths from 2010 to 2060, and we estimated credible intervals using Monte Carlo simulation. RESULTS When programmed with past data, our model predicted current levels of hepatitis C outcomes with accuracy between ±1% and 13%. Morbidity and mortality from hepatitis C will rise from 2010 to a peak between the years 2030 and 2035. We forecasted a peak of 38,600 incident cases of end-stage liver disease; 3200 referrals for transplant; and 36,100 deaths. CONCLUSIONS Because current rates of screening and treatment are low, future morbidity and mortality from hepatitis C are likely to increase substantially without public health interventions to increase treatment.
Journal of Viral Hepatitis | 2011
William N. Southern; Mari-Lynn Drainoni; Bryce D. Smith; Cindy L. Christiansen; Diane McKee; Allen L. Gifford; Cindy M. Weinbaum; Devin Thompson; Elisa Koppelman; Stacia Maher; Alain H. Litwin
Early identification of persons with chronic HBV infection enables infected persons to receive necessary care to prevent or delay onset of liver disease, and enables the identification and vaccination of susceptible household contacts and sex partners, interrupting ongoing transmission. Testing has been recommended previously to enable primary prevention of HBV infection among close contacts for pregnant women, household contacts and sex partners of HBV‐infected persons, persons born in countries with hepatitis B surface antigen (HBsAg) prevalence of more than 8%, persons who are the source of blood or body fluid exposures that might warrant postexposure prophylaxis (e.g., needlestick injury to a healthcare worker or sexual assault), and to enable appropriate treatment for infants born to HBsAg‐positive mothers and persons infected with human immunodeficiency virus. Recently, with the increasing availability of efficacious hepatitis B treatment, the Centers for Disease Control and Prevention published new recommendations for public health evaluation and management for chronically infected persons and their contacts and extended testing recommendations to include persons born in geographic regions with HBsAg prevalence of greater than 2%, men who have sex with men, and injection drug users. Patient and provider education, developing partnerships between health departments and community organizations, and other resources will be needed to assure appropriate populations are tested and care provided for persons newly identified as HBsAg‐positive. (HEPATOLOGY 2009;49:S35–S44.)
American Journal of Public Health | 2012
Mari-Lynn Drainoni; Alain H. Litwin; Bryce D. Smith; Elisa Koppelman; M. Diane McKee; Cindy L. Christiansen; Allen L. Gifford; Cindy M. Weinbaum; William N. Southern
The 2 million persons incarcerated in US prisons and jails are disproportionately affected by hepatitis B virus (HBV), hepatitis C virus (HCV) and HIV, with prevalences of infection two to ten times higher than in the general population. Infections are largely due to sex- and drug-related risk behaviors practised outside the correctional setting, although transmission of these infections has also been documented inside jails and prisons. Public health strategies to prevent morbidity and mortality from these infections should include hepatitis B vaccination, HCV and HIV testing and counseling, medical management of infected persons, and substance abuse treatment in incarcerated populations.
Journal of Clinical Virology | 2012
Amy Jewett; Bryce D. Smith; Richard S. Garfein; J. Cuevas-Mota; Eyasu H. Teshale; Cindy M. Weinbaum
BACKGROUND Influenza vaccination of healthcare personnel (HCP) is recommended in >40 countries. However, there is controversy surrounding the evidence that HCP vaccination reduces morbidity and mortality among patients. Key factors for developing evidence-based recommendations include quality of evidence, balance of benefits and harms, and values and preferences. METHODS We conducted a systematic review of randomized trials, cohort studies, and case-control studies published through June 2012 to evaluate the effect of HCP influenza vaccination on mortality, hospitalization, and influenza cases in patients of healthcare facilities. We pooled trial results using meta-analysis and assessed evidence quality using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach. RESULTS We identified 4 cluster randomized trials and 4 observational studies conducted in long-term care or hospital settings. Pooled risk ratios across trials for all-cause mortality and influenza-like illness were 0.71 (95% confidence interval [CI], .59-.85) and 0.58 (95% CI, .46-.73), respectively; pooled estimates for all-cause hospitalization and laboratory-confirmed influenza were not statistically significant. The cohort and case-control studies indicated significant protective associations for influenza-like illness and laboratory-confirmed influenza. No studies reported harms to patients. Using GRADE, the quality of the evidence for the effect of HCP vaccination on mortality and influenza cases in patients was moderate and low, respectively. The evidence quality for the effect of HCP vaccination on patient hospitalization was low. The overall evidence quality was moderate. CONCLUSIONS The quality of evidence is higher for mortality than for other outcomes. HCP influenza vaccination can enhance patient safety.