38 results on '"Slavinski S"'
Search Results
2. Birth Defects Among Fetuses and Infants of US Women With Evidence of Possible Zika Virus Infection During Pregnancy
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Honein, M.A., Dawson, A.L., Petersen, E.E., Jones, A.M., Lee, E.H., Yazdy, M.M., Ahmad, N., Macdonald, J., Evert, N., Bingham, A., Ellington, S.R., Shapiro-Mendoza, C.K., Oduyebo, T., Fine, A.D., Brown, C.M., Sommer, J.N., Gupta, J., Cavicchia, P., Slavinski, S., White, J.L., Owen, S.M., Petersen, L.R., Boyle, C., Meaney-Delman, D., and Jamieson, D.J.
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- 2017
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3. Vital Signs: Update on Zika Virus–Associated Birth Defects and Evaluation of All U.S. Infants with Congenital Zika Virus Exposure — U.S. Zika Pregnancy Registry, 2016
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Reynolds, M. R., Jones, A. M., Petersen, E. E., Lee, E. H., Rice, M. E., Bingham, A., Ellington, S. R., Evert, N., Reagan-Steiner, S., Oduyebo, T., Brown, C. M., Martin, S., Ahmad, N., Bhatnagar, J., Macdonald, J., Gould, C., Fine, A. D., Polen, K. D., Lake-Burger, H., Hillard, C. L., Hall, N., Mahsa Yazdy, Slaughter, K., Sommer, J. N., Adamski, A., Raycraft, M., Fleck-Derderian, S., Gupta, J., Newsome, K., Baez-Santiago, M., Slavinski, S., White, J. L., Moore, C. A., Shapiro-Mendoza, C. K., Petersen, L., Boyle, C., Jamieson, D. J., Meaney-Delman, D., Honein, M. A., Adair, J., Ruberto, I., Haselow, D. T., Im, L., Jilek, W., Lehmann, M. S., Olney, R., Porse, C. C., Ramstrom, K. C., Sowunmi, S., Marzec, N. S., Davis, K., Esponda-Morrison, B., Zachariah Fraser, M., O’connor, C. A., Chung, W., Richardson, F., Sexton, T., Stocks, M. E., Woldai, S., Bundek, A. M., Zambri, J., Goldberg, C., Eisenstein, L., Jackson, J., Kopit, R., Logue, T., Mendoza, R., Feldpausch, A., Graham, T., Mann, S., Park, S. Y., Carter, K. K., Potts, E. J., Stevens, T., Simonson, S., Tonzel, J. L., Davis, S., Robinson, S., Hyun, J. K., Jenkins, E. M., Piccardi, M., Reid, L. D., Dunn, J. E., Higgins, C. A., Lin, A. E., Munshi, G. S., Sandhu, K., Scotland, S. J., Soliva, S., Copeland, G., Signs, K. A., Schiffman, E., Byers, P., Hand, S., Mulgrew, C. L., Hamik, J., Koirala, S., Ludwig, L. A., Fredette, C. R., Garafalo, K., Worthington, K., Ropri, A., Ade, J. N., Alaali, Z. S., Blog, D., Brunt, S. J., Bryant, P., Burns, A. E., Carson, K., Dupuis, A. P., Sullivan-Frohm, A., Griffin, J., Hidalgo, C., Lance, L. A., Many, P. S., Naizby, B. E., Polfleit, M. J., Rahman, T., Rem, T., Robbins, A. E., Rowlands, J. V., Seaver, C., Seward, K. A., Smith, L., Sohi, I., Wester, R. E., Bush, S., Dean, A. B., Demarest, V., Dufort, E. M., Furuya, A. M., Fuschino, M., Kulas, K. E., Lamson, D. M., Lee, W. T., Limberger, R., Marchewka, M. J., Popowich, M., St George, K., Wong, S. J., Zeng, L., Glaze, V. H., Souto, M. I., Ackelsberg, J., Alex, B., Ballen, V., Baumgartner, J., Bloch, D., Clark, S., Conners, E., Cooper, H., Davidson, A., Dentinger, C., Deocharan, B., Vito, A., Fu, J., Hrusa, G., Iqbal, M., Iwamoto, M., Jones, L., Kubinson, H., Lash, M., Layton, M., Lee, C. T., Liu, D., Mcgibbon, E., Moy, M., Ngai, S., Parton, H. B., Peterson, E., Poy, J., Rakeman, J., Stoute, A., Thompson, C., Weiss, D., Westheimer, E., Winters, A., Younis, M., Chan, R. L., Cronquist, L. J., Caton, L., Lind, L., Nalluswami, K., Perella, D., Brady, D. S., Gosciminski, M., Mcauley, P., Drociuk, D., Leedom, V., Witrick, B., Bollock, J., Hartel, M. B., Lucinski, L. S., Mcdonald, M., Miller, A. M., Ponson, T. A., Price, L., Nance, A. E., Peterson, D., Cook, S., Martin, B., Oltean, H., Neary, J., Baker, M. A., Cummons, K., Bryan, K., Arnold, K. E., Arth, A. C., Bollweg, B. C., Cragan, J. D., Dawson, A. L., Denison, A. M., Dziuban, E. J., Estetter, L., Silva-Flannery, L., Free, R. J., Galang, R. R., Gary, J., Goldsmith, C. S., Green, C., Hale, G. L., Hayes, H. M., Igbinosa, I., Kelly Keating, M., Khan, S., Kim, S. Y., Lampe, M., Lewis, A., Mai, C., Martines, R. B., Miers, B., Moore, J., Muehlenbachs, A., Nahabedian, J., Panella, A., Parihar, V., Patel, M. M., Brett Rabeneck, D., Rasmussen, S. A., Ritter, J. M., Rollin, D. C., Sanders, J. H., Shieh, W. -J, Simeone, R. M., Simon, E. L., Sims, J. R., Spivey, P. J., Talley-Mcrae, H., Tshiwala, A. K., Maldeghem, K., Viens, L., Wainscott-Sargent, A., Williams, T., and Zaki, S.
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0301 basic medicine ,Gerontology ,medicine.medical_specialty ,Microcephaly ,Health (social science) ,Epidemiology ,Health, Toxicology and Mutagenesis ,Vital signs ,Congenital Abnormalities ,Zika virus ,03 medical and health sciences ,Fetus ,0302 clinical medicine ,Health Information Management ,Central Nervous System Diseases ,Pregnancy ,Humans ,Medicine ,Eye Abnormalities ,Neural Tube Defects ,Registries ,030212 general & internal medicine ,Pregnancy Complications, Infectious ,Pregnancy registry ,biology ,Vital Signs ,Zika Virus Infection ,business.industry ,Obstetrics ,Public health ,Infant, Newborn ,Brain ,Infant ,Gestational age ,Zika Virus ,General Medicine ,biology.organism_classification ,medicine.disease ,United States ,030104 developmental biology ,Female ,business - Abstract
Background In collaboration with state, tribal, local, and territorial health departments, CDC established the U.S. Zika Pregnancy Registry (USZPR) in early 2016 to monitor pregnant women with laboratory evidence of possible recent Zika virus infection and their infants. Methods This report includes an analysis of completed pregnancies (which include live births and pregnancy losses, regardless of gestational age) in the 50 U.S. states and the District of Columbia (DC) with laboratory evidence of possible recent Zika virus infection reported to the USZPR from January 15 to December 27, 2016. Birth defects potentially associated with Zika virus infection during pregnancy include brain abnormalities and/or microcephaly, eye abnormalities, other consequences of central nervous system dysfunction, and neural tube defects and other early brain malformations. Results During the analysis period, 1,297 pregnant women in 44 states were reported to the USZPR. Zika virus-associated birth defects were reported for 51 (5%) of the 972 fetuses/infants from completed pregnancies with laboratory evidence of possible recent Zika virus infection (95% confidence interval [CI] = 4%-7%); the proportion was higher when restricted to pregnancies with laboratory-confirmed Zika virus infection (24/250 completed pregnancies [10%, 95% CI = 7%-14%]). Birth defects were reported in 15% (95% CI = 8%-26%) of fetuses/infants of completed pregnancies with confirmed Zika virus infection in the first trimester. Among 895 liveborn infants from pregnancies with possible recent Zika virus infection, postnatal neuroimaging was reported for 221 (25%), and Zika virus testing of at least one infant specimen was reported for 585 (65%). Conclusions and implications for public health practice These findings highlight why pregnant women should avoid Zika virus exposure. Because the full clinical spectrum of congenital Zika virus infection is not yet known, all infants born to women with laboratory evidence of possible recent Zika virus infection during pregnancy should receive postnatal neuroimaging and Zika virus testing in addition to a comprehensive newborn physical exam and hearing screen. Identification and follow-up care of infants born to women with laboratory evidence of possible recent Zika virus infection during pregnancy and infants with possible congenital Zika virus infection can ensure that appropriate clinical services are available.
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- 2017
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4. The severity of pandemic H1N1 influenza in the United States, from April to July 2009: a Bayesian analysis
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Medina, W, Michelangelo, D, Milhofer, J, Milyavskaya, I, Misener, M, Mizrahi, J, Moskin, L, Motherwell, M, Myers, C, Nair, HP, Nguyen, T, Nilsen, D, Nival, J, Norton, J, Oleszko, W, Olson, C, Paladini, M, Palumbo, L, Papadopoulos, P, Parton, H, Paternostro, J, Paynter, L, Perkins, K, Perlman, S, Persaud, H, Peters, C, Pfeiffer, M, Platt, R, Pool, L, Punsalang, A, Rasul, Z, Rawlins, V, Reddy, V, Rinchiuso, A, Rodriguez, T, Rosal, R, Ryan, M, Sanderson, M, Scaccia, A, Seligson, AL, Seupersad, J, SevereDildy, J, Siddiqi, A, Siemetzki, U, Glaser, M, Girdharrie, L, Singh, T, Slavinski, S, Slopen, M, Snuggs, T, Starr, D, Stayton, C, Fung, L, Fu, J, Friedman, S, Frieden, T, France, AM, Stoute, A, Terlonge, J, Ternier, A, Thorpe, L, Travers, C, Tsoi, B, Turner, K, Tzou, J, Vines, S, Waddell, EN, Walker, D, Warner, C, Weisfuse, I, Weiss, D, WilliamsAkita, A, Wilson, E, Fitzgerald, K, Harper, S, Hasnain, Q, Hedge, S, Heller, M, Hendrickson, D, Herskovitz, A, Hinterland, K, Holmes, R, Hom, J, Hon, J, Hopke, T, Hsieh, J, Hughes, S, Immerwahr, S, Incalicchio, AM, Jasek, J, Jimenez, J, Johns, M, Jones, L, Jordan, H, Kambili, C, Kang, J, Kapell, D, Karpati, A, Kerker, B, Konty, K, Kornblum, J, Krigsman, G, Laraque, F, Layton, M, Lee, E, Lee, L, Lee, S, Lim, S, Marx, M, McGibbon, E, Mahoney, K, Marin, G, Matte, T, McAnanama, R, McKay, R, McKay, C, McVeigh, K, Medina, E, Fireteanu, AM, Fine, A, FilsAime, C, Fernandez, M, Feliciano, R, Farley, S, Evans, M, Eisenhower, D, Egger, J, Edwin, B, Edghill, Z, Wong, M, Wu, C, Yang, D, Younis, M, Yusuff, S, Zimmerman, C, Zucker, J, Eavey, J, Durrah, J, Duquaine, D, DiGrande, L, DiCaprio, K, Diaz, L, Deocharan, B, Del Cid, O, DeGrechie, S, DeGrasse, A, Darkins, B, Daniels, A, Da Costa, CA, Crouch, B, Coyle, C, Costarella, R, Corey, C, Cook, D, Cook, H, Cone, J, Cimini, D, Chamany, S, Camurati, L, Campbell, M, Cajigal, A, Cai, L, Butts, B, Burke, M, Bregman, B, Bornschlegel, K, Blank, S, Betz, J, Berger, M, Berg, D, Bell, G, Begier, E, Beaudry, G, Beatrice, ST, Barbot, O, Balter, S, Backman, P, Atamian, J, Aston, C, AgborTabi, E, Adman, G, Adamski, A, Ackelsberg, J, Lipsitch, M, Biedrzycki, P, Finelli, L, Cooper, BS, Riley, S, Reed, C, Hagy, A, De Angelis, D, Presanis, AM, Goranson, C, Griffing, F, Gupta, L, Hamilton, C, Hanson, H, HartmanO'Connell, I, and Team, The New York City Swine Flu Investigation
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medicine.medical_specialty ,Pediatrics ,Hospitalization - statistics and numerical data ,medicine.medical_treatment ,Population ,Public Health and Epidemiology/Infectious Diseases ,Influenza, Human - classification - epidemiology ,Disease Outbreaks ,03 medical and health sciences ,0302 clinical medicine ,Influenza A Virus, H1N1 Subtype ,Epidemiology ,Pandemic ,Severity of illness ,Infectious Diseases/Viral Infections ,medicine ,Credible interval ,030212 general & internal medicine ,Young adult ,education ,Mechanical ventilation ,0303 health sciences ,education.field_of_study ,030306 microbiology ,business.industry ,Incidence (epidemiology) ,virus diseases ,Bayes Theorem ,General Medicine ,3. Good health ,Medicine ,business ,Research Article - Abstract
Marc Lipsitch and colleagues use complementary data from two US cities, Milwaukee and New York City, to assess the severity of pandemic (H1N1) 2009 influenza in the United States., Background Accurate measures of the severity of pandemic (H1N1) 2009 influenza (pH1N1) are needed to assess the likely impact of an anticipated resurgence in the autumn in the Northern Hemisphere. Severity has been difficult to measure because jurisdictions with large numbers of deaths and other severe outcomes have had too many cases to assess the total number with confidence. Also, detection of severe cases may be more likely, resulting in overestimation of the severity of an average case. We sought to estimate the probabilities that symptomatic infection would lead to hospitalization, ICU admission, and death by combining data from multiple sources. Methods and Findings We used complementary data from two US cities: Milwaukee attempted to identify cases of medically attended infection whether or not they required hospitalization, while New York City focused on the identification of hospitalizations, intensive care admission or mechanical ventilation (hereafter, ICU), and deaths. New York data were used to estimate numerators for ICU and death, and two sources of data—medically attended cases in Milwaukee or self-reported influenza-like illness (ILI) in New York—were used to estimate ratios of symptomatic cases to hospitalizations. Combining these data with estimates of the fraction detected for each level of severity, we estimated the proportion of symptomatic patients who died (symptomatic case-fatality ratio, sCFR), required ICU (sCIR), and required hospitalization (sCHR), overall and by age category. Evidence, prior information, and associated uncertainty were analyzed in a Bayesian evidence synthesis framework. Using medically attended cases and estimates of the proportion of symptomatic cases medically attended, we estimated an sCFR of 0.048% (95% credible interval [CI] 0.026%–0.096%), sCIR of 0.239% (0.134%–0.458%), and sCHR of 1.44% (0.83%–2.64%). Using self-reported ILI, we obtained estimates approximately 7–9× lower. sCFR and sCIR appear to be highest in persons aged 18 y and older, and lowest in children aged 5–17 y. sCHR appears to be lowest in persons aged 5–17; our data were too sparse to allow us to determine the group in which it was the highest. Conclusions These estimates suggest that an autumn–winter pandemic wave of pH1N1 with comparable severity per case could lead to a number of deaths in the range from considerably below that associated with seasonal influenza to slightly higher, but with the greatest impact in children aged 0–4 and adults 18–64. These estimates of impact depend on assumptions about total incidence of infection and would be larger if incidence of symptomatic infection were higher or shifted toward adults, if viral virulence increased, or if suboptimal treatment resulted from stress on the health care system; numbers would decrease if the total proportion of the population symptomatically infected were lower than assumed. Please see later in the article for the Editors' Summary, Editors' Summary Background Every winter, millions of people catch influenza—a viral infection of the airways—and about half a million people die as a result. In the US alone, an average of 36,000 people are thought to die from influenza-related causes every year. These seasonal epidemics occur because small but frequent changes in the virus mean that an immune response produced one year provides only partial protection against influenza the next year. Occasionally, influenza viruses emerge that are very different and to which human populations have virtually no immunity. These viruses can start global epidemics (pandemics) that kill millions of people. Experts have been warning for some time that an influenza pandemic is long overdue and in, March 2009, the first cases of influenza caused by a new virus called pandemic (H1N1) 2009 (pH1N1; swine flu) occurred in Mexico. The virus spread rapidly and on 11 June 2009, the World Health Organization declared that a global pandemic of pH1N1 influenza was underway. By the beginning of November 2009, more than 6,000 people had died from pH1N1 influenza. Why Was This Study Done? With the onset of autumn—drier weather and the return of children to school help the influenza virus to spread—pH1N1 cases, hospitalizations, and deaths in the Northern Hemisphere have greatly increased. Although public-health officials have been preparing for this resurgence of infection, they cannot be sure of its impact on human health without knowing more about the severity of pH1N1 infections. The severity of an infection can be expressed as a case-fatality ratio (CFR; the proportion of cases that result in death), as a case-hospitalization ratio (CHR; the proportion of cases that result in hospitalization), and as a case-intensive care ratio (CIR; the proportion of cases that require treatment in an intensive care unit). Because so many people have been infected with pH1N1 since it emerged, the numbers of cases and deaths caused by pH1N1 infection are not known accurately so these ratios cannot be easily calculated. In this study, the researchers estimate the severity of pH1N1 influenza in the US between April and July 2009 by combining data on pH1N1 infections from several sources using a statistical approach known as Bayesian evidence synthesis. What Did the Researchers Do and Find? By using data on medically attended and hospitalized cases of pH1N1 infection in Milwaukee and information from New York City on hospitalizations, intensive care use, and deaths, the researchers estimate that the proportion of US cases with symptoms that died (the sCFR) during summer 2009 was 0.048%. That is, about 1 in 2,000 people who had symptoms of pH1N1 infection died. The “credible interval” for this sCFR, the range of values between which the “true” sCFR is likely to lie, they report, is 0.026%–0.096% (between 1 in 4,000 and 1 in 1,000 deaths for every symptomatic case). About 1 in 400 symptomatic cases required treatment in intensive care, they estimate, and about 1 in 70 symptomatic cases required hospital admission. When the researchers used a different approach to estimate the total number of symptomatic cases—based on New Yorkers' self-reported incidence of influenza-like-illness from a telephone survey—their estimates of pH1N1 infection severity were 7- to 9-fold lower. Finally, they report that the sCFR and the sCIR were highest in people aged 18 or older and lowest in children aged 5–17 years. What Do These Findings Mean? Many uncertainties (for example, imperfect detection and reporting) can affect estimates of influenza severity. Even so, the findings of this study suggest that an autumn–winter pandemic wave of pH1N1 will have a death toll only slightly higher than or considerably lower than that caused by seasonal influenza in an average year, provided pH1N1 continues to behave as it did during the summer. Similarly, the estimated burden on hospitals and intensive care facilities ranges from somewhat higher than in a normal influenza season to considerably lower. The findings of this study also suggest that, unlike seasonal influenza, which kills mainly elderly adults, a high proportion of deaths from pH1N1infection will occur in nonelderly adults, a shift in age distribution that has been seen in previous pandemics. With these estimates in hand and with continued close monitoring of the pandemic, public-health officials should now be in a better position to plan effective strategies to deal with the pH1N1 pandemic. Additional Information Please access these Web sites via the online version of this summary at http://dx.doi.org/10.1371/journal.pmed.1000207. The US Centers for Disease Control and Prevention provides information about influenza for patients and professionals, including specific information on pandemic H1N1 (2009) influenza Flu.gov, a US government Web site, provides access to information on H1N1, avian and pandemic influenza The World Health Organization provides information on seasonal influenza and has detailed information on pandemic H1N1 (2009) influenza (in several languages) The UK Health Protection Agency provides information on pandemic influenza and on pandemic H1N1 (2009) influenza More information for patients about H1N1 influenza is available through Choices, an information resource provided by the UK National Health Service
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- 2016
5. HumanBrucella canisInfection and Subsequent Laboratory Exposures Associated with a Puppy, New York City, 2012
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Dentinger, C. M., primary, Jacob, K., additional, Lee, L. V., additional, Mendez, H. A., additional, Chotikanatis, K., additional, McDonough, P. L., additional, Chico, D. M., additional, De, B. K., additional, Tiller, R. V., additional, Traxler, R. M., additional, Campagnolo, E. R., additional, Schmitt, D., additional, Guerra, M. A., additional, and Slavinski, S. A., additional
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- 2014
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6. Human Brucella canis Infection and Subsequent Laboratory Exposures Associated with a Puppy, New York City, 2012.
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Dentinger, C. M., Jacob, K., Lee, L. V., Mendez, H. A., Chotikanatis, K., McDonough, P. L., Chico, D. M., De, B. K., Tiller, R. V., Traxler, R. M., Campagnolo, E. R., Schmitt, D., Guerra, M. A., and Slavinski, S. A.
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CANIS ,BRUCELLA ,MEDICAL microbiology ,PUBLIC health ,HEALTH education ,PREVENTIVE medicine ,PUBLIC health research - Abstract
Human Brucella canis infection incidence is unknown. Most identified cases are associated with pet dogs. Laboratory-acquired infections can occur following contact with Brucella spp. We identified a paediatric B. canis case, the source and other exposed persons. A 3-year-old New York City child with fever and dyspnoea was hospitalized for 48 h for bronchiolitis. After her admission, blood culture grew B. canis, she was prescribed anti-microbials and recovered. B. canis was also isolated from blood of the child's pet dog; these isolates were genetically similar. The dog originated from an Iowa breeding facility which was quarantined after identification of the dog's infection. Additionally, 31 laboratory workers were exposed and subsequently monitored for symptoms; 15 completed postexposure prophylaxis. To our knowledge, this is the first report strongly suggesting B. canis zoonotic transmission to a child in the United States, and highlights the need for coordinated control policies to minimize human illness. [ABSTRACT FROM AUTHOR]
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- 2015
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7. Inhalation anthrax associated with dried animal hides--Pennsylvania and New York City, 2006
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Walsh, J., Fraser, G., Hunt, E., Husband, B., Nalluswami, K., Pollard, K., Reynolds, S., Urdaneta, V., Aston, C., Balter, S., Beatrice, S., Beaudry, G., Berg, D., Clark, N., Frieden, T., Karpati, A., Layton, M., Lee, L., Leighton, J., Moskin, L., Mullin, S., Phillips, M., Paykin, A, Prud'homme, J., Slavinski, S., Tucker, A., Weisfuse, I., Weiss, D., Wolsk, G., Bacon, C., Glasgow, E., Gomez, T., Swartz, W., Baden, D., Clark, T., Dauphin, L.A., Diaz, P., Dykewicz, C.A., Fleischauer, A., Frank, M., Gee, J.E., Hoffmaster, A., Kim, H., Marston, C., Meyer, R., McQuiston, J., Newton, B., Papagiotas, S., Pesik, N., Piester, T., Quinn, C., Reagan, S., Rotz, L., Rosenberg, P., Rosenstein, N., Shadomy, S., Semanova, V., Treadwell, T., Wilkins, P., Winchell, J., Burr, G., Dowell, C., Hornsby-Myers, J., Kiefer, M., King, B., Nguyen, T.Q., Arboleda, N., and Tsoi, B.
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Diagnosis ,Reports ,Health aspects ,Anthrax -- Reports -- Diagnosis ,Hides -- Health aspects -- Reports ,Hides and skins -- Health aspects -- Reports - Abstract
On February 21, 2006, the Pennsylvania Department of Health (PDOH) reported to CDC and the New York City (NYC) Department of Health and Mental Hygiene (DOHMH) a case of inhalation [...]
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- 2006
8. Evaluation of placental and fetal tissue specimens for Zika virus infection — 50 states and district of Columbia, January-December, 2016
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Reagan-Steiner, S., Simeone, R., Simon, E., Bhatnagar, J., Oduyebo, T., Free, R., Denison, A. M., Rabeneck, D. B., Ellington, S., Petersen, E., Gary, J., Hale, G., Keating, M. K., Martines, R. B., Muehlenbachs, A., Ritter, J., Lee, E., Davidson, A., Conners, E., Scotland, S., Sandhu, K., Bingham, A., Kassens, E., Smith, L., St George, K., Ahmad, N., Tanner, M., Beavers, S., Miers, B., Maldeghem, K., Khan, S., Rabe, I., Gould, C., Meaney-Delman, D., Honein, M. A., Shieh, W. -J, Jamieson, D. J., Fischer, M., Zaki, S. R., Kretschmer, M., Tarter, K., Yaglom, H., Alhajmohammad, S., Chhabra, D., Jilek, W., Madala, M., Messenger, S., Porse, C. C., Salas, M., Singh, D., Skallet, S., Sowunmi, S., Marzec, N. S., Davis, K., Esponda-Morrison, B., Fraser, M. Z., O’connor, C. A., Chung, W. M., Richardson, F., Stocks, M. E., Bundek, A. M., Zambri, M. L., Allen, A., Etienne, M. K., Jackson, J., Landis, V., Logue, T., Muse, N., Prieto, J., Rojas, M., Feldpausch, A., Graham, T., Mann, S., Park, S. Y., Freeman, D., Potts, E. J., Stevens, T., Simonson, S., Tonzel, J. L., Davis, S., Robinson, S., Hyun, J. K., Jenkins, E. M., Brown, C., Soliva, S., Schiffman, E., Byers, P., Hand, S., Mulgrew, C. L., Hamik, J., Koirala, S., Ludwig, E., Fredette, C. R., Mathewson, A. A., Garafalo, K., Worthington, K., Ropri, A., Bloch, D., Clark, S., Cooper, H., Fine, A. D., Hrusa, G., Iwamoto, M., Kubinson, H., Lee, C. T., Slavinski, S., Wilson, E., Winters, A., Yang, D. Y., Ade, J. N., Alaali, Z., Alvarez, K., Backenson, P. B., Blog, D., Dean, A., Dufort, E., Furuya, A. M., Fuschino, M., Hull, R., Kleabonas, M., Kulas, K., Kurpiel, P., Lance, L. A., Leak, E., Limberger, R. J., Ostrowski, S., Polfleit, M., Robbins, A., Rowlands, J. V., Sohi, I., Sommer, J. N., White, J., Wiley, D., Zeng, L., Chan, R. L., Macfarquhar, J., Cronquist, L., Lind, L., Nalluswami, K., Perella, D., Brady, D. S., Gosciminski, M., Mcauley, P., Teevan, B. E., Drociuk, D., Leedom, V., Witrick, B., Bollock, J., Kightlinger, L., Hartel, M. B., Lucinski, L. S., Mcdonald, M., Miller, A. M., Ponson, T. A., Price, L., Broussard, K., Nance, A. E., Peterson, D., Martin, B., Browne, S., Griffin-Thomas, L. A., Macdonald, J. O., Neary, J., Oltean, H., Adamski, A., Baez-Santiago, M., Bollweg, B. C., Cragan, J. D., Ermias, Y., Estetter, L. B. C., Fleck-Derderian, S., Goldsmith, C. S., Groenewold, M. R., Hayes, H., Igbinosa, I., Jenkinson, T. G., Jones, A. M., Lewis, A., Moore, C. A., Newsome, K. B., Parihar, V., Patel, M. M., Paulino, A., Rasmussen, S. A., Raycraft, M., Reynolds, M. R., Rollin, D. C., Sanders, J. H., Shapiro-Mendoza, C., Silva-Flannery, L., Spivey, P., Tshiwala, A. K., Williams, T. R., Bower, W. A., Davlantes, E., Forward, T. R., Fukunaga, R., Hines, J., Hu, S. S., Leung, J., Lewis, L., Martin, S., Mcnamara, L., Omura, J. D., Robinson, C. L., Schmit, K., Self, J. L., Shah, M., Straily, A., Dyne, E. A., Vu, M., and Williams, C.
9. Knowledge and practices related to louse- and flea-borne diseases among staff providing services to people experiencing homelessness in the United States.
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Rich SN, Carpenter A, Dell B, Henderson R, Adams S, Bestul N, Grano C, Sprague B, Leopold J, Schiffman EK, Lomeli A, Zadeh H, Alarcón J, Halai UA, Nam YS, Seifu L, Slavinski S, Crum D, Mosites E, Salzer JS, Hinckley AF, McCormick DW, and Marx GE
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- Humans, Animals, United States epidemiology, Lice Infestations epidemiology, Lice Infestations prevention & control, Flea Infestations epidemiology, Flea Infestations veterinary, Siphonaptera microbiology, Surveys and Questionnaires, Female, Insect Vectors microbiology, Insect Vectors parasitology, Male, Adult, Ill-Housed Persons, Health Knowledge, Attitudes, Practice
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Background and Aims: Louse-borne Bartonella quintana infection and flea-borne murine typhus are two potentially serious vector-borne diseases that have led to periodic outbreaks among people experiencing homelessness in the United States. Little is known about louse- and flea-borne disease awareness and prevention among staff who provide services to the population. We surveyed staff in seven US states to identify gaps in knowledge and prevention practices for these diseases., Methods and Results: Surveys were administered to 333 staff at 89 homeless shelters and outreach teams in California, Colorado, Georgia, Maryland, Minnesota, New York and Washington from August 2022 to April 2023. Most participants (>68%) agreed that body lice and fleas are a problem for people experiencing homelessness. About half were aware that diseases could be transmitted by these vectors; however, most could not accurately identify which diseases. Less than a quarter of staff could describe an appropriate protocol for managing body lice or fleas. Misconceptions included that clients must isolate or be denied services until they are medically cleared., Conclusions: Our findings reveal significant knowledge gaps among staff who provide services to people experiencing homelessness in the prevention and control of louse- and flea-borne diseases. This demonstrates an urgent need for staff training to both reduce disease and prevent unnecessary restrictions on services and housing., (© 2024 Wiley‐VCH GmbH. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.)
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- 2024
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10. Notes from the Field: Illnesses After Administration of Presumed Counterfeit Botulinum Toxin in Nonmedical Settings - Tennessee and New York City, March 2024.
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Thomas CM, McElroy R, Yackley J, Fill MA, Goonewardene D, Mackley C, Roth E, Ackelsberg J, Slavinski S, Habrun C, Hodge B, Rush C, Brown CM, Waltenburg MA, Bertling LH, McGorty M, Johnson R, Schaffner W, Jones TF, and Dunn JR
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- Humans, Tennessee, New York City epidemiology, Adult, Female, Middle Aged, Male, Counterfeit Drugs, Botulinum Toxins analysis, Botulinum Toxins administration & dosage
- Abstract
Competing Interests: All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Roisin McElroy reports payment from St. Joseph’s Health Centre/Unity Health Toronto, Toronto, Canada for provision of emergency medical clinical services. Mary-Margaret A. Fill reports receipt of travel funding from the Council of State and Territorial Epidemiologists (CSTE) for travel to CSTE Executive Board meetings and CSTE conference and unpaid service as member-at-large of CSTE’s Executive Board and the University of Tennessee’s One Health Committee. Catherine M. Brown reports receipt of travel support from CSTE for attendance at the CSTE annual conference and unpaid service as a CSTE Executive Board member. No other potential conflicts of interest were disclosed.
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- 2024
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11. Notes from the Field: Severe Bartonella quintana Infections Among Persons Experiencing Unsheltered Homelessness - New York City, January 2020-December 2022.
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Rich SN, Beeson A, Seifu L, Mitchell K, Wroblewski D, Juretschko S, Keller M, Gnanaprakasam R, Agladze M, Kodama R, Kupferman T, Bhatnagar J, Martines RB, Reagan-Steiner S, Slavinski S, Kuehnert MJ, Bergeron-Parent C, Corvese G, Marx GE, and Ackelsberg J
- Subjects
- Humans, New York City epidemiology, Trench Fever, Ill-Housed Persons
- Abstract
Competing Interests: All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Kara Mitchell reports the following relationships with the Association of Public Health Laboratories: consultant for a public health–related doctorate program to develop molecular course content, funded travel to national meetings, and a leadership or fiduciary role with the Laboratory Systems and Standards Committee. No other potential conflicts of interest were disclosed.
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- 2023
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12. Notes from the Field: Clinical and Epidemiologic Characteristics of Mpox Cases from the Initial Phase of the Outbreak - New York City, May 19-July 15, 2022.
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Kyaw NTT, Kipperman N, Alroy KA, Baumgartner J, Crawley A, Peterson E, Ross A, Fowler RC, Ruiz VE, Leelawong M, Hughes S, Juste-Tranquille M, Lovingood K, Joe CD, Chase M, Shinall A, Ackelsberg J, Bergeron-Parent C, Badenhop B, Slavinski S, Reddy V, and Lee EH
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- Humans, New York City epidemiology, Disease Outbreaks, Mpox, Monkeypox epidemiology
- Abstract
Competing Interests: All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. No potential conflicts of interest were disclosed.
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- 2022
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13. Rabies in a Dog Imported from Azerbaijan - Pennsylvania, 2021.
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Whitehill F, Bonaparte S, Hartloge C, Greenberg L, Satheshkumar PS, Orciari L, Niezgoda M, Yager PA, Pieracci EG, McCullough J, Evenson A, Brown CM, Schnitzler H, Lipton B, Signs K, Stobierski MG, Austin C, Slager S, Ernst M, Kerins J, Simeone A, Singh A, Hale S, Stanek D, Shehee P, Slavinski S, McDermott D, Zinna PA, Campagna R, and Wallace RM
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- Animals, Azerbaijan, Dogs, Humans, Pennsylvania, Prospective Studies, United States, Vaccination veterinary, Dog Diseases prevention & control, Rabies epidemiology, Rabies prevention & control, Rabies veterinary, Rabies Vaccines, Rabies virus
- Abstract
On June 16, 2021, rabies virus infection was confirmed in a dog included in a shipment of rescue animals imported into the United States from Azerbaijan. A multistate investigation was conducted to prevent secondary rabies cases, avoid reintroduction of a dog-maintained rabies virus variant (DMRVV), identify persons who might have been exposed and would be recommended to receive rabies postexposure prophylaxis, and investigate the cause of importation control failures. Results of a prospective serologic monitoring (PSM) protocol suggested that seven of 32 (22%) animals from the same shipment as the dog with confirmed rabies virus infection and who had available titer results after rabies vaccine booster had not been adequately vaccinated against rabies before importation. A requirement for rabies vaccination certificates alone will not adequately identify improper vaccination practices or fraudulent paperwork and are insufficient as a stand-alone rabies importation prevention measure. Serologic titers before importation would mitigate the risk for importing DMRVV., Competing Interests: All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Patricia A. Zinna reports that she is the New Jersey State Representative for the Humane Society Veterinary Medical Association. No other potential conflicts of interest were disclosed.
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- 2022
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14. Determining the role of natural SARS-CoV-2 infection in the death of domestic pets: 10 cases (2020-2021).
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Carpenter A, Ghai RR, Gary J, Ritter JM, Carvallo FR, Diel DG, Martins M, Murphy J, Schroeder B, Brightbill K, Tewari D, Boger L, Gabel J, Cobb R, Hennebelle J, Stanton JB, McCullough K, Mosley YC, Naikare HK, Radcliffe R, Parr B, Balsamo G, Robbins B, Smith D, Slavinski S, Williams C, Meckes D, Jones D, Frazier T, Steury K, Rooney J, Torchetti M, Wendling N, Currie D, Behravesh CB, and Wallace RM
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- Animals, Cats, Dogs, Pets, SARS-CoV-2, COVID-19 veterinary, Cat Diseases diagnosis, Cat Diseases epidemiology, Dog Diseases diagnosis, Dog Diseases epidemiology
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Objective: To establish a pathoepidemiological model to evaluate the role of SARS-CoV-2 infection in the first 10 companion animals that died while infected with SARS-CoV-2 in the US., Animals: 10 cats and dogs that tested positive for SARS-CoV-2 and died or were euthanized in the US between March 2020 and January 2021., Procedures: A standardized algorithm was developed to direct case investigations, determine the necessity of certain diagnostic procedures, and evaluate the role, if any, that SARS-CoV-2 infection played in the animals' course of disease and death. Using clinical and diagnostic information collected by state animal health officials, state public health veterinarians, and other state and local partners, this algorithm was applied to each animal case., Results: SARS-CoV-2 was an incidental finding in 8 animals, was suspected to have contributed to the severity of clinical signs leading to euthanasia in 1 dog, and was the primary reason for death for 1 cat., Conclusions and Clinical Relevance: This report provides the global community with a standardized process for directing case investigations, determining the necessity of certain diagnostic procedures, and determining the clinical significance of SARS-CoV-2 infections in animals with fatal outcomes and provides evidence that SARS-CoV-2 can, in rare circumstances, cause or contribute to death in pets.
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- 2021
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15. Evaluating Surveillance for and Estimating Administration of Rabies Postexposure Prophylaxis in the United States, 2012-2018.
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Whitehouse ER, Person MK, Brown CM, Slavinski S, Rao AK, and Blanton JD
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- Animals, Antibodies, Viral administration & dosage, Humans, Rabies epidemiology, Rabies virology, Rabies Vaccines administration & dosage, Rabies virus immunology, Rabies virus physiology, Sentinel Surveillance, United States epidemiology, Post-Exposure Prophylaxis statistics & numerical data, Rabies prevention & control, Rabies veterinary
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Background: An evaluation of postexposure prophylaxis (PEP) surveillance has not been conducted in over 10 years in the United States. An accurate assessment would be important to understand current rabies trends and inform public health preparedness and response to human rabies., Methodology/principle Findings: To understand PEP surveillance, we sent a survey to public health leads for rabies in 50 U.S. states, Puerto Rico, Washington DC, Philadelphia, and New York City. Of leads from 54 jurisdictions, 39 (72%) responded to the survey; 12 reported having PEP-specific surveillance, five had animal bite surveillance that included data about PEP, four had animal bite surveillance without data about PEP, and 18 (46%) had neither. Although 12 jurisdictions provided data about PEP use, poor data quality and lack of national representativeness prevented use of this data to derive a national-level PEP estimate. We used national-level and state specific data from the Healthcare Cost & Utilization Project (HCUP) to estimate the number of people who received PEP based on emergency department (ED) visits. The estimated annual average of initial ED visits for PEP administration during 2012-2017 in the United States was 46,814 (SE: 1,697), costing upwards of 165 million USD. State-level ED data for initial visits for administration of PEP for rabies exposure using HCUP data was compared to state-level surveillance data from Maryland, Vermont, and Georgia between 2012-2017. In all states, state-level surveillance data was consistently lower than estimates of initial ED visits, suggesting even states with robust PEP surveillance may not adequately capture individuals who receive PEP., Conclusions: Our findings suggest that making PEP a nationally reportable condition may not be feasible. Other methods of tracking administration of PEP such as syndromic surveillance or identification of sentinel states should be considered to obtain an accurate assessment., Competing Interests: The authors have declared that no competing interests exist.
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- 2021
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16. A fatal case report of antibody-dependent enhancement of dengue virus type 1 following remote Zika virus infection.
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Bonheur AN, Thomas S, Soshnick SH, McGibbon E, Dupuis AP 2nd, Hull R, Slavinski S, Del Rosso PE, Weiss D, Hunt DT, McCabe ME, Dean AB, Folkerth R, Laib AM, and Wong SJ
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- Antibodies, Viral, Antibody-Dependent Enhancement, Child, Cross Reactions, Humans, Travel, Dengue, Dengue Virus, Zika Virus, Zika Virus Infection diagnosis
- Abstract
Background: Dengue virus (DENV) is endemic in many parts of the world. Antibody dependent enhancement (ADE) in DENV infections occurs when a person with primary immunity is infected by a second, different DENV strain. Antibodies to Zika virus (ZIKV), which emerged in the Western Hemisphere in 2015, are cross reactive with DENV and theoretically could provoke ADE in a DENV naïve individual., Case Presentation: DENV infection was suspected in a child who had recently returned from a one-month stay in the Dominican Republic. The child presented with fever, vomiting, abdominal pain, and in hypovolemic shock. Volume and pressor resuscitation were unsuccessful, and the child died less than 24 h after hospitalization. Laboratory results suggested an early acute first DENV infection since serum, plasma, and spinal fluid had DENV1 detected by polymerase chain reaction (PCR), yet the serum lacked IgG antibodies to DENV nonstructural protein 1 (NS1) of all four DENV serotypes. This acute DENV infection occurred in the presence of a remote ZIKV infection as determined by antibodies to ZIKV NS1 envelope by multiplex microsphere immunoassay and an exceptionally high plaque reduction neutralization titer to ZIKV. ZIKV IgG avidity index was high, confirming a past infection. DENV1 RNA was detected in all ten organs and tissues examined by PCR. The severe and fatal complications reported here suggest that a remote ZIKV infection may provoke an exaggerated immune response leading to hypovolemic shock when primarily infected by DENV1., Conclusion: We report the first known patient in the United States with a rapidly progressive and fatal case of travel-associated DENV in which prior exposure to ZIKV likely played a role in triggering an ADE phenomenon. This association of prior ZIKV immunity and subsequent new dengue infection is a worrisome phenomenon and an important contribution to the body of knowledge on immunity to flaviviruses., (© 2021. The Author(s).)
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- 2021
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17. From People to Panthera : Natural SARS-CoV-2 Infection in Tigers and Lions at the Bronx Zoo.
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McAloose D, Laverack M, Wang L, Killian ML, Caserta LC, Yuan F, Mitchell PK, Queen K, Mauldin MR, Cronk BD, Bartlett SL, Sykes JM, Zec S, Stokol T, Ingerman K, Delaney MA, Fredrickson R, Ivančić M, Jenkins-Moore M, Mozingo K, Franzen K, Bergeson NH, Goodman L, Wang H, Fang Y, Olmstead C, McCann C, Thomas P, Goodrich E, Elvinger F, Smith DC, Tong S, Slavinski S, Calle PP, Terio K, Torchetti MK, and Diel DG
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- Animals, Betacoronavirus classification, Betacoronavirus genetics, Betacoronavirus isolation & purification, COVID-19, Coronavirus Infections diagnosis, Coronavirus Infections virology, Genome, Viral genetics, Haplotypes, Humans, New York City epidemiology, One Health, Phylogeny, Pneumonia, Viral diagnosis, Pneumonia, Viral virology, SARS-CoV-2, Zoonoses epidemiology, Zoonoses transmission, Zoonoses virology, Animals, Zoo virology, Betacoronavirus physiology, Coronavirus Infections transmission, Coronavirus Infections veterinary, Pandemics veterinary, Panthera virology, Pneumonia, Viral transmission, Pneumonia, Viral veterinary
- Abstract
Despite numerous barriers to transmission, zoonoses are the major cause of emerging infectious diseases in humans. Among these, severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), and ebolaviruses have killed thousands; the human immunodeficiency virus (HIV) has killed millions. Zoonoses and human-to-animal cross-species transmission are driven by human actions and have important management, conservation, and public health implications. The current SARS-CoV-2 pandemic, which presumably originated from an animal reservoir, has killed more than half a million people around the world and cases continue to rise. In March 2020, New York City was a global epicenter for SARS-CoV-2 infections. During this time, four tigers and three lions at the Bronx Zoo, NY, developed mild, abnormal respiratory signs. We detected SARS-CoV-2 RNA in respiratory secretions and/or feces from all seven animals, live virus in three, and colocalized viral RNA with cellular damage in one. We produced nine whole SARS-CoV-2 genomes from the animals and keepers and identified different SARS-CoV-2 genotypes in the tigers and lions. Epidemiologic and genomic data indicated human-to-tiger transmission. These were the first confirmed cases of natural SARS-CoV-2 animal infections in the United States and the first in nondomestic species in the world. We highlight disease transmission at a nontraditional interface and provide information that contributes to understanding SARS-CoV-2 transmission across species. IMPORTANCE The human-animal-environment interface of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an important aspect of the coronavirus disease 2019 (COVID-19) pandemic that requires robust One Health-based investigations. Despite this, few reports describe natural infections in animals or directly link them to human infections using genomic data. In the present study, we describe the first cases of natural SARS-CoV-2 infection in tigers and lions in the United States and provide epidemiological and genetic evidence for human-to-animal transmission of the virus. Our data show that tigers and lions were infected with different genotypes of SARS-CoV-2, indicating two independent transmission events to the animals. Importantly, infected animals shed infectious virus in respiratory secretions and feces. A better understanding of the susceptibility of animal species to SARS-CoV-2 may help to elucidate transmission mechanisms and identify potential reservoirs and sources of infection that are important in both animal and human health., (Copyright © 2020 McAloose et al.)
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- 2020
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18. First 12 Months of Life for Infants in New York City, New York, With Possible Congenital Zika Virus Exposure.
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Lee EH, Cooper H, Iwamoto M, Lash M, Conners EE, Bloch D, Clark S, Hrusa G, Kubinson H, Paladini M, McGibbon E, Rakeman JL, Fine AD, Limberger RJ, Liu D, and Slavinski S
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- Antibodies, Viral blood, Developmental Disabilities etiology, Female, Humans, Immunoglobulin M blood, Infant, Infant, Newborn, Infectious Disease Transmission, Vertical, Male, New York City, Pregnancy, Zika Virus Infection complications, Zika Virus Infection diagnosis, Microcephaly etiology, Pregnancy Complications, Infectious, Zika Virus immunology, Zika Virus Infection congenital
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Background: Our goal was to characterize the epidemiology and clinical significance of congenital Zika virus (ZIKV) exposure by prospectively following a cohort of infants with possible congenital exposure through their first year of life., Methods: We included infants born in New York City between 2016 and 2017 who had or were born to a woman who had laboratory evidence of ZIKV infection during pregnancy. We conducted provider/patient interviews and reviewed medical records to collect information about the pregnant women and, for infants, clinical and neurodevelopmental status at birth and 2, 6, and 12 months of age., Results: Of the 404 infants who met inclusion criteria, most (385 [95.3%]) appeared well, whereas 19 (4.7%) had a possible ZIKV-associated birth defect. Seven had congenital ZIKV syndrome, and 12 were microcephalic without other abnormalities. Although infants with congenital ZIKV syndrome manifested clinical and neurodevelopmental sequelae during their first year of life, all 12 infants with isolated microcephaly were normocephalic and appeared well by 2 months of age. Laboratory evidence of ZIKV was detected for 22 of the infants, including 7 (31.8%) with a birth defect. Among 148 infants without a birth defect and negative/no laboratory results on ZIKV testing, and for whom information was available at 1 year, 4 presented with a developmental delay., Conclusions: Among infants with possible congenital ZIKV exposure, a small proportion had possible ZIKV-associated findings at birth or at follow-up, or laboratory evidence of ZIKV. Identifying and monitoring infants with possible ZIKV exposure requires extensive efforts by providers and public health departments. Longitudinal studies using standardized clinical and developmental assessments are needed for infants after possible congenital ZIKV exposure., (© The Author(s) 2019. Published by Oxford University Press on behalf of The Journal of the Pediatric Infectious Diseases Society.)
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- 2020
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19. Development and validation of a portable, point-of-care canine distemper virus qPCR test.
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Tomaszewicz Brown A, McAloose D, Calle PP, Auer A, Posautz A, Slavinski S, Brennan R, Walzer C, and Seimon TA
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- Animals, Animals, Wild, Austria, Distemper Virus, Canine immunology, Freezing, Hair virology, Nose virology, Point-of-Care Systems, RNA, Viral isolation & purification, Raccoons virology, Reproducibility of Results, Sensitivity and Specificity, Skin virology, United States, Vaccines, Attenuated, Distemper virology, Distemper Virus, Canine genetics, Real-Time Polymerase Chain Reaction instrumentation, Real-Time Polymerase Chain Reaction methods
- Abstract
Canine distemper virus (CDV) is a multi-host pathogen that can cause significant mortality in domestic, wild terrestrial and marine mammals. It is a major conservation threat in some endangered species. Infection can result in severe respiratory disease and fatal encephalitis. Diagnosis and disease monitoring in wildlife, and differentiation of CDV from rabies (a life-threatening zoonotic disease that can produce similar neurologic signs), would benefit from the availability of a portable, point-of-care (POC) diagnostic test. We therefore developed a quantitative RT-PCR assay for CDV using shelf-stable, lyophilized reagents and target-specific primers and probes for use with the handheld Biomeme two3™ qPCR thermocycler. Biomeme's extraction methodology, lyophilized reagents, and thermocycler were compared to our standard laboratory-based methods to assess sensitivity, efficiency and overall test performance. Results using a positive control plasmid for CDV showed comparable sensitivity (detection of 50 copies) and PCR efficiency between the two platforms, and CDV detection was similar between platforms when tested using a modified live CDV vaccine. Significantly higher Ct values (average Ct = 5.1 cycles) were observed using the Biomeme platform on known CDV positive animal samples. CDV detection using the Biomeme platform was similar in 25 of 26 samples from suspect CDV cases when compared to standard virology laboratory testing. One false positive was observed that was negative upon retest. The Biomeme methodology can be adapted for detection of specific targets, and this portable technology saves time by eliminating the need for local or international sample transport for laboratory-based diagnostics. However, results of our testing suggest that decreased diagnostic sensitivity (higher Ct values) relative to laboratory-based methods was observed using animal samples, so careful validation and optimization are essential. Portable qPCR platforms can empower biologists and wildlife health professionals in remote and low-resource settings, which will greatly improve our understanding of CDV disease ecology and associated conservation threats in wildlife., Competing Interests: The authors have declared that no competing interests exist.
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- 2020
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20. Maternal Zika Virus Infection: Association With Small-for-Gestational-Age Neonates and Preterm Birth.
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Cooper HJ, Iwamoto M, Lash M, Conners EE, Paladini M, Slavinski S, Fine AD, Kennedy J, Heinke D, Ciaranello A, Seage GR 3rd, and Lee EH
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- Adult, Cohort Studies, Female, Humans, Infant, Newborn, New York City epidemiology, Pregnancy, Premature Birth etiology, Prenatal Care, Retrospective Studies, Young Adult, Infant, Small for Gestational Age, Pregnancy Complications, Infectious, Premature Birth epidemiology, Zika Virus Infection
- Abstract
Objective: To evaluate whether antenatal Zika virus infection is associated with risk of having a small-for-gestational-age (SGA) neonate, risk of preterm birth, and lower mean birth weight of term neonates., Methods: For this retrospective observational study, we linked birth record data for women who delivered liveborn singleton neonates in New York City in 2016 to data for pregnant women with Zika virus infection reported to the New York City Health Department. We restricted the analysis to nonsmoking, nonwhite women and adjusted for maternal characteristics. Among women with antenatal Zika virus infection, we used modified Poisson regression to assess risks of having an SGA neonate and of delivering preterm, and linear regression to assess the association of infection with mean birth weight of term neonates., Results: Of 116,034 deliveries of singleton neonates in New York City in 2016, 251 (0.2%) were to women with antenatal Zika virus infection. A higher percentage of women with Zika virus infection delivered an SGA neonate compared with those without (11.2% vs 5.8%; adjusted relative risk [RR] 1.8; 95% CI 1.3-2.6). There was no difference in preterm birth prevalence for women with and without Zika virus infection (adjusted RR 1.0; 95% CI 0.69-1.6). Mean birth weight of term neonates born to women with Zika virus infection was 47 g less (95% CI -105 to 11 g); this difference was not statistically significant in crude or adjusted analyses., Conclusion: For a cohort of New York City women, antenatal Zika virus infection was associated with an increased risk of having an SGA neonate, but not preterm birth or lower mean birth weight of term neonates. This supports a putative association between Zika virus infection during pregnancy and SGA.
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- 2019
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21. Public Health Management of Persons Under Investigation for Ebola Virus Disease in New York City, 2014-2016.
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Winters A, Iqbal M, Benowitz I, Baumgartner J, Vora NM, Evans L, Link N, Munjal I, Ostrowsky B, Ackelsberg J, Balter S, Dentinger C, Fine AD, Harper S, Landman K, Laraque F, Layton M, Slavinski S, Weiss D, Rakeman JL, Hughes S, Varma JK, and Lee EH
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- Adolescent, Adult, Child, Child, Preschool, Female, Hemorrhagic Fever, Ebola diagnosis, Hemorrhagic Fever, Ebola physiopathology, Humans, Infant, Male, Middle Aged, New York City epidemiology, Population Surveillance, Risk Assessment, Young Adult, Disease Outbreaks, Hemorrhagic Fever, Ebola epidemiology, Public Health Administration
- Abstract
During 2014-2016, the largest outbreak of Ebola virus disease (EVD) in history occurred in West Africa. The New York City Department of Health and Mental Hygiene (DOHMH) worked with health care providers to prepare for persons under investigation (PUIs) for EVD in New York City. From July 1, 2014, through December 29, 2015, we classified as a PUI a person with EVD-compatible signs or symptoms and an epidemiologic risk factor within 21 days before illness onset. Of 112 persons who met PUI criteria, 74 (66%) sought medical care and 49 (44%) were hospitalized. The remaining 38 (34%) were isolated at home with daily contact by DOHMH staff members. Thirty-two (29%) PUIs received a diagnosis of malaria. Of 10 PUIs tested, 1 received a diagnosis of EVD. Home isolation minimized unnecessary hospitalization. This case study highlights the importance of developing competency among clinical and public health staff managing persons suspected to be infected with a high-consequence pathogen.
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- 2019
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22. Detection of Avian Influenza A(H7N2) Virus Infection Among Animal Shelter Workers Using a Novel Serological Approach-New York City, 2016-2017.
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Poirot E, Levine MZ, Russell K, Stewart RJ, Pompey JM, Chiu S, Fry AM, Gross L, Havers FP, Li ZN, Liu F, Crossa A, Lee CT, Boshuizen V, Rakeman JL, Slavinski S, Harper S, and Gould LH
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- Adult, Aged, Animals, Birds, Cats, Cross Reactions, Female, Humans, Influenza A Virus, H7N2 Subtype isolation & purification, Influenza, Human transmission, Male, Middle Aged, New York City epidemiology, Orthomyxoviridae Infections epidemiology, Orthomyxoviridae Infections virology, Seroepidemiologic Studies, Zoonoses, Antibodies, Viral blood, Disease Outbreaks veterinary, Influenza A Virus, H7N2 Subtype immunology, Influenza in Birds virology, Influenza, Human virology, Orthomyxoviridae Infections veterinary
- Abstract
Background: In 2016, an influenza A(H7N2) virus outbreak occurred in cats in New York City's municipal animal shelters. One human infection was initially detected., Methods: We conducted a serological survey using a novel approach to rule out cross-reactive antibodies to other seasonal influenza viruses to determine whether additional A(H7N2) human infections had occurred and to assess exposure risk., Results: Of 121 shelter workers, one had serological evidence of A(H7N2) infection, corresponding to a seroprevalence of 0.8% (95% confidence interval, .02%-4.5%). Five persons exhibited low positive titers to A(H7N2) virus, indicating possible infection; however, we could not exclude cross-reactive antibody responses to seasonal influenza viruses. The remaining 115 persons were seronegative. The seropositive person reported multiple direct cat exposures without using personal protective equipment and mild illness with subjective fever, runny nose, and sore throat., Conclusions: We identified a second case of A(H7N2) infection from this outbreak, providing further evidence of cat-to-human transmission of A(H7N2) virus., (Published by Oxford University Press for the Infectious Diseases Society of America 2018.)
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- 2019
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23. Zika Virus Infection Among Pregnant Women and Their Neonates in New York City, January 2016-June 2017.
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Conners EE, Lee EH, Thompson CN, McGibbon E, Rakeman JL, Iwamoto M, Cooper H, Vora NM, Limberger RJ, Fine AD, Liu D, and Slavinski S
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- Adult, Female, Humans, Infant, Newborn, Infectious Disease Transmission, Vertical statistics & numerical data, New York City epidemiology, Pregnancy, Pregnancy Complications, Infectious etiology, Pregnancy Complications, Infectious virology, Retrospective Studies, Risk Factors, Zika Virus Infection diagnosis, Zika Virus Infection etiology, Zika Virus Infection transmission, Pregnancy Complications, Infectious epidemiology, Travel-Related Illness, Zika Virus Infection epidemiology
- Abstract
Objective: To describe and compare differences in the epidemiologic, clinical, and laboratory characteristics of pregnant women with confirmed or probable Zika virus infection and to compare the risk of having a neonate with laboratory evidence of Zika virus infection with that of having a neonate without evidence of Zika virus infection by maternal characteristics., Methods: We conducted a retrospective cohort study of women with Zika virus infection who completed pregnancy in New York City from January 1, 2016 to June 30, 2017. Confirmed Zika virus infection was defined as 1) nucleic acid amplification test-detected Zika virus, or 2) a nonnegative enzyme-linked immunosorbent assay test result and a plaque-reduction neutralization test result positive for Zika virus but negative for dengue virus, or 3) delivery of a neonate with laboratory evidence of Zika virus infection. Probable infection was defined as a nonnegative enzyme-linked immunosorbent assay test result and a positive plaque-reduction neutralization test result for Zika virus and dengue virus., Results: We identified 390 women with confirmed (28%) or probable (72%) Zika virus infection. Fever, rash, arthralgia, or conjunctivitis was reported by 31% of women and were more common among women with confirmed than with probable infection (43% vs 26%, P=.001). Of 366 neonates born to these women, 295 (81%) were tested for Zika virus and 22 (7%) had laboratory-diagnosed congenital Zika virus infection. The relative risk (RR) for having a neonate with laboratory evidence of Zika virus infection was greater among women with fever (RR 4.8, 95% CI 2.1-10.7), tingling (RR 4.8, CI 1.7-13.7), or numbness (RR 6.9, CI 2.6-18.2) during pregnancy or the periconception period. However, the RR did not differ whether the mother had confirmed or probable Zika virus infection (RR 1.6, CI 0.7-4.1)., Conclusion: In New York City, a greater proportion of women had probable Zika virus infection than confirmed infection. Women with some symptoms during pregnancy or periconceptionally were more likely to have a neonate with laboratory evidence of Zika virus infection. Neonates born to women with confirmed or probable Zika virus infection should be tested for Zika virus infection.
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- 2018
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24. Death from Transfusion-Transmitted Anaplasmosis, New York, USA, 2017.
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Goel R, Westblade LF, Kessler DA, Sfeir M, Slavinski S, Backenson B, Gebhardt L, Kane K, Laurence J, Scherr D, Bussel J, Dumler JS, and Cushing MM
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- Aged, Anaplasma phagocytophilum genetics, Anaplasma phagocytophilum pathogenicity, Anaplasmosis diagnosis, Anaplasmosis microbiology, Anaplasmosis pathology, Anemia pathology, Anemia therapy, Factor XI Deficiency pathology, Factor XI Deficiency therapy, Fatal Outcome, Humans, Male, Perioperative Period, Shock, Septic diagnosis, Shock, Septic microbiology, Shock, Septic pathology, Urinary Bladder Neoplasms blood supply, Urinary Bladder Neoplasms pathology, Urinary Bladder Neoplasms surgery, Urinary Bladder Neoplasms therapy, Anaplasma phagocytophilum isolation & purification, Anaplasmosis etiology, Erythrocyte Transfusion adverse effects, Shock, Septic etiology
- Abstract
We report a death from transfusion-transmitted anaplasmosis in a 78-year-old man. The patient died of septic shock 2 weeks after a perioperative transfusion with erythrocytes harboring Anaplasma phagocytophilum. The patient's blood specimens were positive for A. phagocytophilum DNA beginning 7 days after transfusion; serologic testing remained negative until death.
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- 2018
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25. Epidemiological Characteristics and Laboratory Findings of Zika Virus Cases in New York City, January 1, 2016-June 30, 2017.
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McGibbon E, Moy M, Vora NM, Dupuis A, Fine A, Kulas K, Limberger R, Liu D, Rakeman J, St George K, and Slavinski S
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- Adolescent, Adult, Animals, Antibodies, Viral, Child, Child, Preschool, Female, Humans, Immunoglobulin M blood, Infant, Male, Middle Aged, New York City epidemiology, Pregnancy, Pregnancy Complications, Infectious pathology, RNA, Viral genetics, RNA, Viral isolation & purification, Young Adult, Zika Virus genetics, Zika Virus Infection pathology, Zika Virus Infection virology, Pregnancy Complications, Infectious epidemiology, Pregnancy Complications, Infectious virology, Zika Virus isolation & purification, Zika Virus Infection epidemiology
- Abstract
Background: An outbreak of Zika virus (ZIKV) began in May 2015 in Brazil and rapidly spread throughout the Americas; New York City (NYC) has a diverse population with ∼1.8 million residents who were born in ZIKV-affected areas. Before July 24, 2017, the Centers for Disease Control and Prevention (CDC) ZIKV testing recommendations included nucleic acid amplification-based tests for serum and urine specimens collected ≤14 days of illness onset or last potential exposure, and ZIKV immunoglobulin M (IgM) assay when ZIKV RNA is not detected or for specimens collected within 2-12 weeks of illness onset or last potential exposure, followed by a plaque reduction neutralization test (PRNT). However, the New York public health laboratories and commercial laboratories tested specimens collected beyond these time frames., Methods: We analyzed 1080 noncongenital ZIKV cases in NYC residents who met the Council for State and Territorial Epidemiologist's ZIKV case definitions., Results: Among cases, 98% were travel associated, 1% were sexually transmitted, and 1% had unknown exposures; 412 (38%) cases were pregnant women. Of 672 patients with ZIKV RNA detected in serum or urine specimens, 48 (7%) tested positive >14 days after either symptom onset or last potential exposure date (range 15-99 days). Of 390 patients diagnosed based on serology alone (i.e., not tested or not detectable for ZIKV RNA), 60 (15%) had a positive ZIKV IgM and PRNT >12 weeks after symptom onset or last potential exposure date (range 85-273 days)., Conclusion: Our findings correspond with CDC's updated guidance to test symptomatic pregnant women up to 12 weeks past onset of symptoms. ZIKV IgM antibody testing may also be warranted for pregnant women regardless of symptoms if their exposure occurred during their pregnancy or periconception period. Providers should understand the scope of diagnostic testing and its limitations to appropriately counsel patients, especially pregnant women.
- Published
- 2018
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26. Surveillance for Mosquitoborne Transmission of Zika Virus, New York City, NY, USA, 2016.
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Wahnich A, Clark S, Bloch D, Kubinson H, Hrusa G, Liu D, Rakeman JL, Deocharan B, Jones L, Slavinski S, Stoute A, Mathes R, Weiss D, and Conners EE
- Subjects
- Adolescent, Adult, Animals, Child, Female, Humans, Male, Middle Aged, New York City epidemiology, Pregnancy, Young Adult, Culicidae virology, Sentinel Surveillance, Zika Virus isolation & purification, Zika Virus Infection diagnosis, Zika Virus Infection epidemiology
- Abstract
A large number of imported cases of Zika virus infection and the potential for transmission by Aedes albopictus mosquitoes prompted the New York City Department of Health and Mental Hygiene to conduct sentinel, enhanced passive, and syndromic surveillance for locally acquired mosquitoborne Zika virus infections in New York City, NY, USA, during June-October 2016. Suspected case-patients were those >5 years of age without a travel history or sexual exposure who had >3 compatible signs/symptoms (arthralgia, fever, conjunctivitis, or rash). We identified 15 suspected cases and tested urine samples for Zika virus by using real-time reverse transcription PCR; all results were negative. We identified 308 emergency department visits for Zika-like illness, 40,073 visits for fever, and 17 unique spatiotemporal clusters of visits for fever. We identified no evidence of local transmission. Our experience offers possible surveillance tools for jurisdictions concerned about local mosquitoborne Zika virus or other arboviral transmission.
- Published
- 2018
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27. Outbreak of Influenza A(H7N2) Among Cats in an Animal Shelter With Cat-to-Human Transmission-New York City, 2016.
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Lee CT, Slavinski S, Schiff C, Merlino M, Daskalakis D, Liu D, Rakeman JL, Misener M, Thompson C, Leung YL, Varma JK, Fry A, Havers F, Davis T, Newbury S, and Layton M
- Subjects
- Animals, Antibodies, Viral blood, Cats, Humans, Influenza A Virus, H7N2 Subtype genetics, Influenza A virus immunology, Influenza, Human epidemiology, Influenza, Human virology, New York City epidemiology, Orthomyxoviridae Infections epidemiology, Orthomyxoviridae Infections virology, Polymerase Chain Reaction, Disease Outbreaks veterinary, Influenza A Virus, H7N2 Subtype isolation & purification, Influenza, Human transmission, Orthomyxoviridae Infections veterinary
- Abstract
We describe the first case of cat-to-human transmission of influenza A(H7N2), an avian-lineage influenza A virus, that occurred during an outbreak among cats in New York City animal shelters. We describe the public health response and investigation., (© The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.)
- Published
- 2017
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28. HEALTH SURVEY OF FREE-RANGING RACCOONS (PROCYON LOTOR) IN CENTRAL PARK, NEW YORK, NEW YORK, USA: IMPLICATIONS FOR HUMAN AND DOMESTIC ANIMAL HEALTH.
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Rainwater KL, Marchese K, Slavinski S, Humberg LA, Dubovi EJ, Jarvis JA, McAloose D, and Calle PP
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- Animals, Animals, Domestic, Health Surveys, Humans, Lead blood, New York, Animal Diseases, Raccoons parasitology, Raccoons physiology
- Abstract
We conducted health assessments on 113 free-ranging raccoons ( Procyon lotor ) in Central Park, New York City, US, in February 2010, September 2010, and November 2011 in conjunction with a trap-vaccinate-release program to control a raccoon rabies epizootic. Five individuals were sampled at two time points for 118 raccoon examinations in total. We tested 13 of 13 and 8 of 13 euthanized raccoons for rabies and canine distemper virus (CDV), respectively, by antigen testing on brain tissue; all were negative for both viruses. Endoparasitism was the most common necropsy finding, with definitive identification of Baylisascaris procyonis in six of eight (75%) necropsied raccoons. Multiple intestinal parasites were detected in feces of living raccoons, including ascarid-type ova in 25 of 80 (31%) raccoons, with B. procyonis confirmed in one sample. Median blood lead level was 7.3 μg/dL (n=104). Rabies virus neutralizing antibody titer was ≥0.5 IU/mL in 9 of 88 (10%) raccoons naive to rabies vaccination and in 13 of 20 (65%) previously vaccinated raccoons. The majority of raccoons we tested were seropositive for canine parvovirus-2 (54/59, 92%) and Toxoplasma gondii (39/60, 65%). Fewer were seropositive for Rickettsia rickettsii (3/30, 10%). None were seropositive for CDV (n=108), canine adenovirus-1 (n=60), or Borrelia burgdorferi (n=30). Ectoparasites found during 16 of 118 (13.6%) physical examinations included Ixodes texanus ticks (15/118, 12.7%) and Trichodectes octomaculatus lice (1/118, 0.8%). We detected Campylobacter jejuni in 5 of 79 (6%) fecal samples. We detected 11 Salmonella enterica serotypes in 70 of 111 (63.1%) enteric cultures, the most common of which were Salmonella Newport (20/70, 29%) and Salmonella Oranienburg (20/70, 29%). These results indicate that raccoons in Central Park likely are involved in the environmental occurrence and potential disease transmission of a variety of infectious and noninfectious diseases of concern for human, wildlife, and domestic animal health.
- Published
- 2017
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29. Birth Defects Among Fetuses and Infants of US Women With Evidence of Possible Zika Virus Infection During Pregnancy.
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Honein MA, Dawson AL, Petersen EE, Jones AM, Lee EH, Yazdy MM, Ahmad N, Macdonald J, Evert N, Bingham A, Ellington SR, Shapiro-Mendoza CK, Oduyebo T, Fine AD, Brown CM, Sommer JN, Gupta J, Cavicchia P, Slavinski S, White JL, Owen SM, Petersen LR, Boyle C, Meaney-Delman D, and Jamieson DJ
- Subjects
- Adolescent, Adult, Brain virology, Congenital Abnormalities epidemiology, Female, Humans, Infant, Microcephaly epidemiology, Microcephaly virology, Middle Aged, Neural Tube Defects epidemiology, Neuroimaging, Pregnancy, Pregnancy Complications, Infectious virology, United States, Young Adult, Zika Virus, Brain abnormalities, Congenital Abnormalities virology, Eye Abnormalities virology, Fetus virology, Neural Tube Defects virology, Zika Virus Infection epidemiology
- Abstract
Importance: Understanding the risk of birth defects associated with Zika virus infection during pregnancy may help guide communication, prevention, and planning efforts. In the absence of Zika virus, microcephaly occurs in approximately 7 per 10 000 live births., Objective: To estimate the preliminary proportion of fetuses or infants with birth defects after maternal Zika virus infection by trimester of infection and maternal symptoms., Design, Setting, and Participants: Completed pregnancies with maternal, fetal, or infant laboratory evidence of possible recent Zika virus infection and outcomes reported in the continental United States and Hawaii from January 15 to September 22, 2016, in the US Zika Pregnancy Registry, a collaboration between the CDC and state and local health departments., Exposures: Laboratory evidence of possible recent Zika virus infection in a maternal, placental, fetal, or infant sample., Main Outcomes and Measures: Birth defects potentially Zika associated: brain abnormalities with or without microcephaly, neural tube defects and other early brain malformations, eye abnormalities, and other central nervous system consequences., Results: Among 442 completed pregnancies in women (median age, 28 years; range, 15-50 years) with laboratory evidence of possible recent Zika virus infection, birth defects potentially related to Zika virus were identified in 26 (6%; 95% CI, 4%-8%) fetuses or infants. There were 21 infants with birth defects among 395 live births and 5 fetuses with birth defects among 47 pregnancy losses. Birth defects were reported for 16 of 271 (6%; 95% CI, 4%-9%) pregnant asymptomatic women and 10 of 167 (6%; 95% CI, 3%-11%) symptomatic pregnant women. Of the 26 affected fetuses or infants, 4 had microcephaly and no reported neuroimaging, 14 had microcephaly and brain abnormalities, and 4 had brain abnormalities without microcephaly; reported brain abnormalities included intracranial calcifications, corpus callosum abnormalities, abnormal cortical formation, cerebral atrophy, ventriculomegaly, hydrocephaly, and cerebellar abnormalities. Infants with microcephaly (18/442) represent 4% of completed pregnancies. Birth defects were reported in 9 of 85 (11%; 95% CI, 6%-19%) completed pregnancies with maternal symptoms or exposure exclusively in the first trimester (or first trimester and periconceptional period), with no reports of birth defects among fetuses or infants with prenatal exposure to Zika virus infection only in the second or third trimesters., Conclusions and Relevance: Among pregnant women in the United States with completed pregnancies and laboratory evidence of possible recent Zika infection, 6% of fetuses or infants had evidence of Zika-associated birth defects, primarily brain abnormalities and microcephaly, whereas among women with first-trimester Zika infection, 11% of fetuses or infants had evidence of Zika-associated birth defects. These findings support the importance of screening pregnant women for Zika virus exposure.
- Published
- 2017
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30. Suspected Female-to-Male Sexual Transmission of Zika Virus - New York City, 2016.
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Davidson A, Slavinski S, Komoto K, Rakeman J, and Weiss D
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- Adult, Female, Humans, Male, New York City, RNA, Viral blood, RNA, Viral isolation & purification, RNA, Viral urine, Travel, Sexually Transmitted Diseases, Viral, Zika Virus isolation & purification, Zika Virus Infection diagnosis, Zika Virus Infection transmission
- Abstract
A routine investigation by the New York City (NYC) Department of Health and Mental Hygiene (DOHMH) identified a nonpregnant woman in her twenties who reported she had engaged in a single event of condomless vaginal intercourse with a male partner the day she returned to NYC (day 0) from travel to an area with ongoing Zika virus transmission. She had headache and abdominal cramping while in the airport awaiting return to NYC. The following day (day 1) she developed fever, fatigue, a maculopapular rash, myalgia, arthralgia, back pain, swelling of the extremities, and numbness and tingling in her hands and feet. In addition, on day 1, the woman began menses that she described as heavier than usual. On day 3 she visited her primary care provider who obtained blood and urine specimens. Zika virus RNA was detected in both serum and urine by real-time reverse transcription-polymerase chain reaction (rRT-PCR) performed at the DOHMH Public Health Laboratory using a test based on an assay developed at CDC (1). The results of serum testing for anti-Zika virus immunoglobulin M (IgM) antibody performed by the New York State Department of Health Wadsworth Center laboratory was negative using the CDC Zika IgM antibody capture enzyme-linked immunosorbent assay (Zika MAC-ELISA) (2).
- Published
- 2016
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31. Zika Virus Surveillance and Preparedness - New York City, 2015-2016.
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Lee CT, Vora NM, Bajwa W, Boyd L, Harper S, Kass D, Langston A, McGibbon E, Merlino M, Rakeman JL, Raphael M, Slavinski S, Tran A, Wong R, and Varma JK
- Abstract
Zika virus has rapidly spread through the World Health Organization's Region of the Americas since being identified in Brazil in early 2015. Transmitted primarily through the bite of infected Aedes species mosquitoes, Zika virus infection during pregnancy can cause spontaneous abortion and birth defects, including microcephaly (1,2). New York City (NYC) is home to a large number of persons who travel frequently to areas with active Zika virus transmission, including immigrants from these areas. In November 2015, the NYC Department of Health and Mental Hygiene (DOHMH) began developing and implementing plans for managing Zika virus and on February 1, 2016, activated its Incident Command System. During January 1-June 17, 2016, DOHMH coordinated diagnostic laboratory testing for 3,605 persons with travel-associated exposure, 182 (5.0%) of whom had confirmed Zika virus infection. Twenty (11.0%) confirmed patients were pregnant at the time of diagnosis. In addition, two cases of Zika virus-associated Guillain-Barré syndrome were diagnosed. DOHMH's response has focused on 1) identifying and diagnosing suspected cases; 2) educating the public and medical providers about Zika virus risks, transmission, and prevention strategies, particularly in areas with large populations of immigrants from areas with ongoing Zika virus transmission; 3) monitoring pregnant women with Zika virus infection and their fetuses and infants; 4) detecting local mosquito-borne transmission through both human and mosquito surveillance; and 5) modifying existing Culex mosquito control measures by targeting Aedes species of mosquitoes through the use of larvicides and adulticides.
- Published
- 2016
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32. Compendium of Animal Rabies Prevention and Control, 2016.
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Brown CM, Slavinski S, Ettestad P, Sidwa TJ, and Sorhage FE
- Subjects
- Animals, Rabies prevention & control, Rabies veterinary
- Published
- 2016
- Full Text
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33. Rabies in a Dog Imported from Egypt with a Falsified Rabies Vaccination Certificate--Virginia, 2015.
- Author
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Sinclair JR, Wallace RM, Gruszynski K, Freeman MB, Campbell C, Semple S, Innes K, Slavinski S, Palumbo G, Bair-Brake H, Orciari L, Condori RE, Langer A, Carroll DS, and Murphy J
- Subjects
- Animals, Cats, Dog Diseases prevention & control, Dogs, Egypt, Female, Humans, Public Health, Rabies diagnosis, Rabies prevention & control, Records standards, Rescue Work, Travel, Virginia, Dog Diseases diagnosis, Fraud, Rabies veterinary, Rabies Vaccines administration & dosage, Records veterinary, Vaccination veterinary
- Abstract
Canine rabies virus variant has been eliminated in the United States and multiple other countries. Globally, however, dogs remain the principal source for human rabies infections. The World Health Organization recommends that when dogs cross international borders, national importing authorities should require an international veterinary certificate attesting that the animal did not show signs of rabies at the time of shipment, was permanently identified, vaccinated, or revaccinated, and had been subjected to a serologic test for rabies before shipment. On June 8, 2015, an adult female dog that had recently been picked up from the streets of Cairo, Egypt, and shipped by a U.S. animal rescue organization to the United States was confirmed to have rabies by the Virginia Department of General Services Division of Consolidated Laboratory Services (DCLS). This dog was part of a large shipment of dogs and cats from Egypt that rescue organizations had distributed to multiple states for adoption. During the investigation, public health officials learned that the rabies vaccination certificate used for entry of the rabid dog into the United States had intentionally been falsified to avoid exclusion of the dog from entry under CDC's current dog importation regulations. This report underscores the ongoing risk posed by U.S. importation of domestic animals that have not been adequately vaccinated against rabies.
- Published
- 2015
- Full Text
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34. Trap-vaccinate-release program to control raccoon rabies, New York, USA.
- Author
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Slavinski S, Humberg L, Lowney M, Simon R, Calvanese N, Bregman B, Kass D, and Oleszko W
- Subjects
- Animals, New York City, Program Evaluation, Rabies epidemiology, Rabies virology, Treatment Outcome, Animals, Wild virology, Communicable Disease Control methods, Disease Outbreaks, Rabies prevention & control, Rabies Vaccines administration & dosage, Raccoons virology, Vaccination veterinary
- Abstract
In 2009, an outbreak of raccoon rabies in Central Park in New York City, New York, USA, infected 133 raccoons. Five persons and 2 dogs were exposed but did not become infected. A trap-vaccinate-release program vaccinated ≈ 500 raccoons and contributed to the end of the epizootic.
- Published
- 2012
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35. Using emergency department data to conduct dog and animal bite surveillance in New York City, 2003-2006.
- Author
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Bregman B and Slavinski S
- Subjects
- Adolescent, Adult, Aged, Animals, Cats, Child, Child, Preschool, Dogs, Emergency Service, Hospital trends, Female, Humans, Infant, Male, Mice, Middle Aged, New York City epidemiology, Rats, Retrospective Studies, Seasons, Sex Factors, Young Adult, Bites and Stings epidemiology, Emergency Service, Hospital statistics & numerical data, Population Surveillance methods
- Abstract
Objectives: Most animal bites in the United States are due to dogs, with approximately 4.7 million reports per year. Surveillance for dog and other animal bites requires a substantial investment of time and resources, and underreporting is common. We described the use and findings of electronic hospital emergency department (ED) chief complaint data to characterize patients and summarize trends in people treated for dog and other animal bites in New York City (NYC) EDs between 2003 and 2006., Methods: Retrospective data were obtained from the syndromic surveillance system at the NYC Department of Health and Mental Hygiene. We used a statistical program to identify chief complaint free-text fields as one of four categories of animal bites. We evaluated descriptive statistics and univariate associations on the available demographic data. The findings were also compared with data collected through the existing passive reporting animal bite surveillance system., Results: During the study period, more than 6,000 animal bite patient visits were recorded per year. The proportion of visits for animal bites did not appear to change over time. Dog bites accounted for more than 70% and cat bites accounted for 13% of animal bite patient visits. Demographic characteristics of patients were similar to those identified in NYC's passive surveillance system., Conclusions: Our findings suggest that the use of ED data offers a simple, less resource-intensive, and sustainable way of conducting animal bite surveillance and a novel use of syndromic surveillance data. However, it cannot replace traditional surveillance used to manage individual patients for potential rabies exposures.
- Published
- 2012
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36. Public health and environmental response to the first case of naturally acquired inhalational anthrax in the United States in 30 years: infection of a new york city resident who worked with dried animal hides.
- Author
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Nguyen TQ, Clark N, Karpati A, Goldberg A, Paykin A, Tucker A, Baker A, Almiroudis A, Fine A, Tsoi B, Aston C, Berg D, Weiss D, Connelly E, Beaudry G, Weisfuse I, Durrah JC, Prudhomme J, Leighton J, Ackelsberg J, Mahoney K, Van Vynck L, Lee L, Moskin L, Layton M, Wong M, Raphael M, Robinson M, Phillips M, Jones M, Jeffery N, Nieves R, Slavinski S, Mullin S, Beatrice ST, Balter S, Blank S, Frieden T, Keifer M, Rosenstein N, Diaz P, Clark T, Compton H, Daloia J, Cardarelli J, Norrell N, Horn E, Jackling S, Bacon C, Glasgow E, Gomez T, Baltzersen RA, Kammerdener C, Margo-Zavazky D, Colgan J, and Pulaski P
- Subjects
- Anthrax diagnosis, Bacillus anthracis isolation & purification, Case-Control Studies, Community-Acquired Infections epidemiology, Humans, New York City epidemiology, Spores, Bacterial, Anthrax transmission, Inhalation Exposure, Occupational Exposure, Tanning
- Abstract
In Pennsylvania on February 16, 2006, a New York City resident collapsed with rigors and was hospitalized. On February 21, the Centers for Disease Control and Prevention and the New York City Department of Health and Mental Hygiene were notified that Bacillus anthracis had been identified in the patient's blood. Although the patient's history of working with dried animal hides to make African drums indicated the likelihood of a natural exposure to aerosolized anthrax spores, bioterrorism had to be ruled out first. Ultimately, this case proved to be the first case of naturally occurring inhalational anthrax in 30 years. This article describes the epidemiologic and environmental investigation to identify other cases and persons at risk and to determine the source of exposure and scope of contamination. Because stricter regulation of the importation of animal hides from areas where anthrax is enzootic is difficult, public healthcare officials should consider the possibility of future naturally occurring anthrax cases caused by contaminated hides. Federal protocols are needed to assist in the local response, which should be tempered by our growing understanding of the epidemiology of naturally acquired anthrax. These protocols should include recommended methods for reliable and efficient environmental sample collection and laboratory testing, and environmental risk assessments and remediation.
- Published
- 2010
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37. Lymphocytic choriomeningitis virus meningitis, New York, NY, USA, 2009.
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Asnis DS, Muana O, Kim DG, Garcia M, Rollin PE, and Slavinski S
- Subjects
- Humans, Lymphocytic Choriomeningitis cerebrospinal fluid, Male, Middle Aged, New York City, Serologic Tests, Lymphocytic Choriomeningitis diagnosis
- Abstract
We describe a case of lymphocytic choriomeningitis virus (LCMV) meningitis in a New York, NY, resident who had no apparent risk factors. Clues leading to the diagnosis included aseptic meningitis during winter and the finding of hypoglycorrachia and lymphocytosis in the cerebrospinal fluid. LCMV continues to be an underdiagnosed zoonotic disease.
- Published
- 2010
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38. Child care-associated outbreak of Escherichia coli O157:H7 and hemolytic uremic syndrome.
- Author
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Raffaelli RM, Paladini M, Hanson H, Kornstein L, Agasan A, Slavinski S, Weiss D, Fennelly GJ, and Flynn JT
- Subjects
- Child, Preschool, Diarrhea complications, Diarrhea epidemiology, Diarrhea microbiology, Escherichia coli Infections microbiology, Feces microbiology, Female, Humans, Infant, Male, Shiga Toxins analysis, Disease Outbreaks, Escherichia coli Infections complications, Escherichia coli Infections epidemiology, Escherichia coli O157 isolation & purification, Hemolytic-Uremic Syndrome epidemiology, Hemolytic-Uremic Syndrome microbiology
- Abstract
We present an outbreak of E. coli O157:H7 diarrhea in an urban child care center. Eleven of 45 attendees with diarrhea had positive tests (stool culture or shiga-like toxin assay) for E. coli O157:H7. Two of these 11 (18%) progressed to hemolytic uremic syndrome. Diarrheal illness in child care centers should be considered a public health risk. Staff education, hand washing, and cohorting or exclusion of attendees with diarrhea must be performed to help control infectious outbreaks.
- Published
- 2007
- Full Text
- View/download PDF
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