Sharon Sharnprapai
Massachusetts Department of Public Health
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Publication
Featured researches published by Sharon Sharnprapai.
Emerging Infectious Diseases | 1999
Deborah S. Yokoe; Girish S. Subramanyan; Edward A. Nardell; Sharon Sharnprapai; Eugene McCray; Richard Platt
Data collected by health maintenance organizations (HMOs), which provide care for an increasing number of persons with tuberculosis (TB), may be used to complement traditional TB surveillance. We evaluated the ability of HMO-based surveillance to contribute to overall TB reporting through the use of routinely collected automated data for approximately 350,000 HMO members. During approximately 1.5 million person-years, 45 incident cases were identified in either HMO or public health department records. Eight (18%) confirmed cases had not been identified by the public health department. The most useful screening criterion (sensitivity of 89% and predictive value positive of 30%) was dispensing of two or more TB drugs. Pharmacy dispensing information routinely collected by many HMOs appears to be a useful adjunct to traditional TB surveillance, particularly for identifying cases without positive microbiologic results that may be missed by traditional public health surveillance methods.
Emerging Infectious Diseases | 2002
Jill Northrup; Ann C. Miller; Edward A. Nardell; Sharon Sharnprapai; Sue Etkind; Jeffrey Driscoll; Michael McGarry; Harry W. Taber; Paul Elvin; Noreen Qualls; Christopher R. Braden
We estimated direct medical and nonmedical costs associated with a false diagnosis of tuberculosis (TB) caused by laboratory cross-contamination of Mycobacterium tuberculosis cultures in Massachusetts in 1998 and 1999. For three patients who received misdiagnoses of active TB disease on the basis of laboratory cross-contamination, the costs totaled U.S.
Emerging Infectious Diseases | 2002
Sharon Sharnprapai; Ann C. Miller; Robert Suruki; Edward Corkren; Sue Etkind; Jeffrey Driscoll; Michael McGarry; Edward A. Nardell
32,618. Of the total, 97% was attributed to the public sector (local and state health departments, public health hospital and laboratory, and county and state correctional facilities); 3% to the private sector (physicians, hospitals, and laboratories); and <1% to the patient. Hospitalizations and inpatient tests, procedures, and TB medications accounted for 69% of costs, and outpatient TB medications accounted for 18%. The average cost per patient was
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
10,873 (range,
Emerging Infectious Diseases | 2002
Ann C. Miller; Sharon Sharnprapai; Robert Suruki; Edward Corkren; Edward A. Nardell; Jeffrey Driscoll; Michael McGarry; Harry W. Taber; Sue Etkind
1,033-
Emerging Infectious Diseases | 1999
Girish S. Subramanyan; Deborah S. Yokoe; Sharon Sharnprapai; Edward A. Nardell; Eugene McCray; Richard Platt
21,306). Reducing laboratory cross-contamination and quickly identifying patients with cross-contaminated cultures can prevent unnecessary and potentially dangerous treatment regimens and anguish for the patient and financial burden to the health-care system.
Journal of Public Health Management and Practice | 2006
Lilia Ponce Manangan; Marisa Moore; Michelle Macaraig; Jessica R. MacNeil; Gail Shevick; Jill Northrup; Robert Pratt; Lisa V. Adams; Janice Boutotte; Sharon Sharnprapai; Noreen Qualls
We used molecular genotyping to further understand the epidemiology and transmission patterns of tuberculosis (TB) in Massachusetts. The study population included 983 TB patients whose cases were verified by the Massachusetts Department of Public Health between July 1, 1996, and December 31, 2000, and for whom genotyping results and information on country of origin were available. Two hundred seventy-two (28%) of TB patients were in genetic clusters, and isolates from U.S-born were twice as likely to cluster as those of foreign-born (odds ratio [OR] 2.29, 95% confidence interval [CI] 1.69, 3.12). Our results suggest that restriction fragment length polymorphism analysis has limited capacity to differentiate TB strains when the isolate contains six or fewer copies of IS6110, even with spoligotyping. Clusters of TB patients with more than six copies of IS6110 were more likely to have epidemiologic connections than were clusters of TB patients with isolates with few copies of IS6110 (OR 8.01, 95%; CI 3.45,18.93).
Journal of Infection | 2007
Armen Parsyan; Jussi Saukkonen; M. Anita Barry; Sharon Sharnprapai; C. Robert Horsburgh
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.
Chest | 2007
Shalini Patel; Armen Parsyan; J. E. Gunn; M. Anita Barry; Carrie Reed; Sharon Sharnprapai; C. Robert Horsburgh
Massachusetts was one of seven sentinel surveillance sites in the National Tuberculosis Genotyping and Surveillance Network. From 1996 through 2000, isolates from new patients with tuberculosis (TB) underwent genotyping. We describe the impact that genotyping had on public health practice in Massachusetts and some limitations of the technique. Through genotyping, we explored the dynamics of TB outbreaks, investigated laboratory cross-contamination, and identified Mycobacterium tuberculosis strains, transmission sites, and accurate epidemiologic links. Genotyping should be used with epidemiologic follow-up to identify how resources can best be allocated to investigate genotypic findings.
Public Health Reports | 1999
Girish S. Subramanyan; Deborah S. Yokoe; Sharon Sharnprapai; Yuren Tang; Richard Platt
We used automated pharmacy dispensing data to characterize tuberculosis (TB) management for 45 health maintenance organization (HMO) members. Pharmacy records distinguished patients treated in HMOs from those treated elsewhere. For cases treated in HMOs, they provided useful information about appropriateness of prescribed regimens and adherence to therapy.