Suzanne M. Marks
Centers for Disease Control and Prevention
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Publication
Featured researches published by Suzanne M. Marks.
Emerging Infectious Diseases | 2014
Suzanne M. Marks; Jennifer Flood; Barbara J. Seaworth; Yael Hirsch-Moverman; Lori R. Armstrong; Sundari Mase; Katya Salcedo; Peter Oh; Edward A. Graviss; Paul W. Colson; Lisa Armitige; Manuel Revuelta; Kathryn Sheeran
Drug resistance was extensive and care was complex; nevertheless, high rates of treatment completion were achieved albeit at considerable cost.
International Journal of Tuberculosis and Lung Disease | 2013
D. Shepardson; Suzanne M. Marks; H. Chesson; Amy Kerrigan; David P. Holland; Nigel A. Scott; X. Tian; Andrey S. Borisov; Nong Shang; Charles M. Heilig; Timothy R. Sterling; Margarita E. Villarino; W. R. Mac Kenzie
SETTING A large randomized controlled trial recently showed that for treating latent tuberculous infection (LTBI) in persons at high risk of progression to tuberculosis (TB) disease, a 12-dose regimen of weekly rifapentine plus isoniazid (3HP) administered as directly observed treatment (DOT) can be as effective as 9 months of daily self-administered isoniazid (9H). OBJECTIVES To assess the cost-effectiveness of 3HP compared to 9H. DESIGN A computational model was designed to simulate individuals with LTBI treated with 9H or 3HP. Costs and health outcomes were estimated to determine the incremental costs per active TB case prevented and per quality-adjusted life year (QALY) gained by 3HP compared to 9H. RESULTS Over a 20-year period, treatment of LTBI with 3HP rather than 9H resulted in 5.2 fewer cases of TB and 25 fewer lost QALYs per 1000 individuals treated. From the health system and societal perspectives, 3HP would cost respectively US
American Journal of Public Health | 2000
Suzanne M. Marks; Zachary Taylor; Nilka Ríos Burrows; Mohamed G. Qayad; Bess Miller
21,525 and
Clinical Infectious Diseases | 2013
Suzanne M. Marks; Wendy A. Cronin; Thara Venkatappa; Gina Maltas; Sandy Chon; Sharon Sharnprapai; Mary Gaeddert; Jane Tapia; Susan E. Dorman; Sue Etkind; Claud Crosby; Henry M. Blumberg; John Bernardo
4294 more per TB case prevented, and respectively
Journal of Public Health Management and Practice | 2002
Maureen Wilce; Robin Shrestha-Kuwahara; Zachary Taylor; Noreen Qualls; Suzanne M. Marks
4565 and
Clinical Infectious Diseases | 2017
Suzanne M. Marks; Sundari Mase; Sapna Morris
911 more per QALY gained. CONCLUSIONS 3HP may be a cost-effective alternative to 9H, particularly if the cost of rifapentine decreases, the effectiveness of 3HP can be maintained without DOT, and 3HP treatment is limited to those with a high risk of progression to TB disease.
International Journal of Tuberculosis and Lung Disease | 2016
Suzanne M. Marks; Yael Hirsch-Moverman; Katya Salcedo; Edward A. Graviss; Peter Oh; Barbara Seaworth; Jennifer Flood; Lori R. Armstrong; L. Armitige; Sundari Mase
OBJECTIVES This study assessed whether homeless patients are hospitalized for tuberculosis (TB) more frequently and longer than other patients and possible reasons for this. METHODS We prospectively studied hospitalizations of a cohort of TB patients. RESULTS HIV-infected homeless patients were hospitalized more frequently than other patients, while homeless patients who had no insurance or whose insurance status was unknown were hospitalized longer. Hospitalization cost
Clinical Infectious Diseases | 2017
Amy L. Sandul; Nwabunie Nwana; J Mike Holcombe; Mark N. Lobato; Suzanne M. Marks; Risa M. Webb; Shu-Hua Wang; Brock Stewart; Phil Griffin; Garrett Hunt; Neha Shah; Asween Marco; Naveen Patil; Leonard Mukasa; Ruth N. Moro; John A. Jereb; Sundari Mase; Terence Chorba; Sapna Bamrah-Morris; Christine Ho
2000 more per homeless patient than for other patients. The public sector paid nearly all costs. CONCLUSIONS Homeless people may be hospitalized less if given access to medical care that provides early detection and treatment of TB infection and disease and HIV infection. Providing housing and social services may also reduce hospital utilization and increase therapy completion rates.
Public Health Reports | 2015
Victor Balaban; Suzanne M. Marks; Sue Etkind; Dolly Katz; Julie Higashi; Jennifer Flood; Ann Cronin; Christine Ho; Awal Khan; Terence Chorba
BACKGROUND The utility of Mycobacterium tuberculosis direct nucleic acid amplification testing (MTD) for pulmonary tuberculosis disease diagnosis in the United States has not been well described. METHODS We analyzed a retrospective cohort of reported patients with suspected active pulmonary tuberculosis in 2008-2010 from Georgia, Hawaii, Maryland, and Massachusetts to assess MTD use, effectiveness, health-system benefits, and cost-effectiveness. RESULTS Among 2140 patients in whom pulmonary tuberculosis was suspected, 799 (37%) were M. tuberculosis-culture-positive. Eighty percent (680/848) of patients having acid-fast-bacilli-smear-positive specimens had MTD performed; MTD positive-predictive value (PPV) was 98% and negative-predictive value (NPV) was 94%. Nineteen percent (240/1292) of patients having smear-negative specimens had MTD; MTD PPV was 90% and NPV was 88%. Among patients suspected of tuberculosis but not having MTD, smear PPV for lab-confirmed tuberculosis was 77% and NPV 78%. Compared with no MTD, MTD significantly decreased time to diagnosis in patients with smear-positive/MTD-positive specimens, decreased respiratory isolation for patients having smear-positive/MTD-negative/culture-negative specimens, decreased outpatient days of unnecessary tuberculosis medications, and reduced resources expended on contact investigation. While MTD generally cost more than no MTD, incremental cost savings occurred in patients with human immunodeficiency virus (HIV) or homelessness to diagnose or to exclude tuberculosis, and in patients with substance abuse having smear-negative specimens to exclude tuberculosis. CONCLUSIONS MTD improved diagnostic accuracy and timeliness and reduced unnecessary respiratory isolation, treatment, and contact investigations. It was cost saving in patients with HIV, homelessness, or substance abuse, but not in others.
Travel Medicine and Infectious Disease | 2014
Margaret S. Coleman; Karen J. Marienau; Nina Marano; Suzanne M. Marks; Martin S. Cetron
To describe the policies and procedures used by 11 urban tuberculosis control programs to conduct contact investigations, written policies were reviewed and semistructured interviews were conducted with program managers and staff. Qualitative analysis showed that contact investigation policies and procedures vary widely. Most policies address risk factor assessment and contact prioritization; however, none of the policies provide comprehensive guidance for the entire process. Staffing patterns vary, but, overall, staff receive little formal training; informal monitoring practices predominate. Comprehensive guidelines and programmatic support are needed to improve the quality of contact investigation processes.