Jennifer L. Rakeman
New York City Department of Health and Mental Hygiene
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Emerging Infectious Diseases | 2015
Molly M. Kratz; Don Weiss; Alison Ridpath; Jane R. Zucker; Anita Geevarughese; Jennifer L. Rakeman; Jay K. Varma
Questions about how to protect this at-risk population deserve careful consideration.
Clinical Infectious Diseases | 2016
Leena N. Patel; Robert J. Arciuolo; Jie Fu; Francesca R. Giancotti; Jane R. Zucker; Jennifer L. Rakeman; Jennifer B. Rosen
Background On 14 January 2014, a vaccinated student presented with parotitis. Mumps immunoglobulin M (IgM) testing was negative and reverse-transcription polymerase chain reaction (RT-PCR) testing was not performed, resulting in a missed diagnosis and the start of an outbreak at a New York City (NYC) university. Methods Mumps case investigations included patient interviews, medical records review, and laboratory testing including mumps serology and RT-PCR. Case patients were considered linked to the outbreak if they attended or had epidemiologic linkage to the university. Epidemiologic, clinical, and laboratory data for outbreak cases residing in NYC were analyzed. Results Fifty-six NYC residents with mumps were identified with onset between 12 January and 30 April 2014. Fifty-three cases (95%) were university students, 1 (2%) was a staff member, and 2 (4%) had epidemiologic links to the university. The median age was 20 years (range 18-37 years). All cases had parotitis. Three cases were hospitalized, including 1 of 2 cases with orchitis. Fifty-four (96%) cases had received ≥1 mumps-containing vaccine, 1 (2%) was unvaccinated due to religious exemption, and 1 (2%) had unknown vaccination status. Two of the 44 (5%) cases tested by serology were mumps IgM positive, and 27 of the 40 (68%) tested by RT-PCR were positive. Conclusions Mumps outbreaks can occur in highly vaccinated populations. Mumps should be considered in patients with parotitis regardless of vaccination status. RT-PCR is the preferred testing method; providers should not rely on IgM testing alone. High vaccination coverage and control measures likely limited the extent of the outbreak.
Emerging Infectious Diseases | 2017
Pascal Lapierre; Elizabeth J. Nazarian; Yan Zhu; Danielle Wroblewski; Amy Saylors; Teresa Passaretti; Scott Hughes; Anthony Tran; Ying Lin; John Kornblum; Shatavia S. Morrison; Jeffrey W. Mercante; Robert Fitzhenry; Don Weiss; Brian H. Raphael; Jay K. Varma; Howard A. Zucker; Jennifer L. Rakeman; Kimberlee A. Musser
During the summer of 2015, New York, New York, USA, had one of the largest and deadliest outbreaks of Legionnaires’ disease in the history of the United States. A total of 138 cases and 16 deaths were linked to a single cooling tower in the South Bronx. Analysis of environmental samples and clinical isolates showed that sporadic cases of legionellosis before, during, and after the outbreak could be traced to a slowly evolving, single-ancestor strain. Detection of an ostensibly virulent Legionella strain endemic to the Bronx community suggests potential risk for future cases of legionellosis in the area. The genetic homogeneity of the Legionella population in this area might complicate investigations and interpretations of future outbreaks of Legionnaires’ disease.
Emerging Infectious Diseases | 2017
Kenya Murray; Vasudha Reddy; John Kornblum; HaeNa Waechter; Ludwin F. Chicaiza; Inessa Rubinstein; Sharon Balter; Sharon K. Greene; Sarah L. Braunstein; Jennifer L. Rakeman; Catherine M. Dentinger
Approximately 20% of Shigella isolates tested in New York City, New York, USA, during 2013–2015 displayed decreased azithromycin susceptibility. Case-patients were older and more frequently male and HIV infected than those with azithromycin-susceptible Shigella infection; 90% identified as men who have sex with men. Clinical interpretation guidelines for azithromycin resistance and outcome studies are needed.
Clinical Infectious Diseases | 2017
Christopher T. Lee; Sally Slavinski; Corinne Schiff; Mario Merlino; Demetre Daskalakis; Dakai Liu; Jennifer L. Rakeman; Mark Misener; Corinne Thompson; Yin Ling Leung; Jay K. Varma; Alicia M. Fry; Fiona Havers; Todd Davis; Sandra Newbury; Marcelle Layton; Bisrat Abraham; Joel Ackelsberg; Mike Antwi; Sharon Balter; Alexander Davidson; Paula Del Rosso; Katelynn Devinney; Marie Dorsinville; Anne D. Fine; Bruce Gutelius; Lucretia Jones; Ellen Lee; Kristen Lee; Natasha McIntosh
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.
Diagnostic Microbiology and Infectious Disease | 2015
Arianne Ramautar; Tanya A. Halse; Lola Arakaki; Mike Antwi; Paula Del Rosso; Marie Dorsinville; Elizabeth J. Nazarian; Linda Steiner-Sichel; Lillian V. Lee; Michelle Dickinson; Danielle Wroblewski; Nellie B. Dumas; Kimberlee A. Musser; Beth M. Isaac; Jennifer L. Rakeman; Don Weiss
Confirmed and probable cases of invasive Neisseria meningitidis (Nm) infection are reportable in New York City. We conducted a study to identify Nm among culture-negative reports of bacterial and viral meningitis. During the study period, 262 reports of suspected meningitis were eligible. Cerebrospinal fluid (CSF) specimens from 138 patients were obtained for testing. No Nm cases were detected. Results from real-time polymerase chain reaction and 16S on CSF specimens were concordant with hospital microbiology findings in 80%; however, other pathogenic organisms were detected in 14 culture-negative specimens. New York Citys surveillance system appears to be effective at capturing cases of Nm meningitis. Nucleic acid testing is useful for detecting the presence of bacterial DNA when antibiotic therapy precedes lumbar puncture or bacterial cultures are negative. It remains unanswered whether culture-negative cases of Nm bacteremia are being missed by reportable disease surveillance.
Mbio | 2018
Nischay Mishra; Adrian Caciula; Adam R. Price; Riddhi K. Thakkar; James P. Ng; Lokendra V. Chauhan; Komal Jain; Xiaoyu Che; Diego A. Espinosa; Magelda Montoya Cruz; Angel Balmaseda; Eric Sullivan; Jigar Patel; Richard G. Jarman; Jennifer L. Rakeman; Christina Egan; Chantal Reusken; Marion Koopmans; Eva Harris; Rafal Tokarz; Thomas Briese; W. Ian Lipkin
ABSTRACT Zika virus (ZIKV) is implicated in fetal stillbirth, microcephaly, intracranial calcifications, and ocular anomalies following vertical transmission from infected mothers. In adults, infection may trigger autoimmune inflammatory polyneuropathy. Transmission most commonly follows the bite of infected Aedes mosquitoes but may also occur through sexual intercourse or receipt of blood products. Definitive diagnosis through detection of viral RNA is possible in serum or plasma within 10 days of disease onset, in whole blood within 3 weeks of onset, and in semen for up to 3 months. Serological diagnosis is nonetheless critical because few patients have access to molecular diagnostics during the acute phase of infection and infection may be associated with only mild or inapparent disease that does not prompt molecular testing. Serological diagnosis is confounded by cross-reactivity of immune sera with other flaviviruses endemic in the areas where ZIKV has recently emerged. Accordingly, we built a high-density microarray comprising nonredundant 12-mer peptides that tile, with one-residue overlap, the proteomes of Zika, dengue, yellow fever, West Nile, Ilheus, Oropouche, and chikungunya viruses. Serological analysis enabled discovery of a ZIKV NS2B 20-residue peptide that had high sensitivity (96.0%) and specificity (95.9%) versus natural infection with or vaccination against dengue, chikungunya, yellow fever, West Nile, tick-borne encephalitis, or Japanese encephalitis virus in a microarray assay and an enzyme-linked immunosorbent assay (ELISA) of early-convalescent-phase sera (2 to 3 weeks after onset of symptomatic infection). IMPORTANCE The emergence of Zika virus (ZIKV) as a teratogen is a profound challenge to global public health. Molecular diagnosis of infection is straightforward during the 3-week period when patients are viremic. However, serological diagnosis thereafter of historical exposure has been confounded by cross-reactivity. Using high-density peptide arrays that tile the proteomes of a selection of flaviviruses to identify a ZIKV-specific peptide, we established two assays that enable sensitive and specific diagnosis of exposure to ZIKV. These assays may be useful in guiding clinical management of mothers at risk for potential exposure to ZIKV and enable insights into the epidemiology of ZIKV infections. The emergence of Zika virus (ZIKV) as a teratogen is a profound challenge to global public health. Molecular diagnosis of infection is straightforward during the 3-week period when patients are viremic. However, serological diagnosis thereafter of historical exposure has been confounded by cross-reactivity. Using high-density peptide arrays that tile the proteomes of a selection of flaviviruses to identify a ZIKV-specific peptide, we established two assays that enable sensitive and specific diagnosis of exposure to ZIKV. These assays may be useful in guiding clinical management of mothers at risk for potential exposure to ZIKV and enable insights into the epidemiology of ZIKV infections.
Emerging Infectious Diseases | 2018
Amanda Wahnich; Sandhya Clark; Danielle Bloch; Hannah Kubinson; Gili Hrusa; Dakai Liu; Jennifer L. Rakeman; Bisram Deocharan; Lucretia Jones; Sally Slavinski; Alaina Stoute; Robert Mathes; Don Weiss; Erin E. Conners
Sentinel, enhanced passive, and syndromic surveillance in 2016 did not identify any evidence of transmission.
Disaster Medicine and Public Health Preparedness | 2018
Syra S. Madad; Anna Tate; Maytal Rand; Celia Quinn; Neil M. Vora; Machelle Allen; Nicholas V. Cagliuso; Jennifer L. Rakeman; Sean Studer; Joseph Masci; Jay K. Varma; Ross Wilson
ABSTRACTThe Zika virus was largely unknown to many health care systems before the outbreak of 2015. The unique public health threat posed by the Zika virus and the evolving understanding of its pathology required continuous communication between a health care delivery system and a local public health department. By leveraging an existing relationship, NYC Health+Hospitals worked closely with New York City Department of Health and Mental Hygiene to ensure that Zika-related processes and procedures within NYC Health+Hospitals facilities aligned with the most current Zika virus guidance. Support given by the public health department included prenatal clinical and laboratory support and the sharing of data on NYC Health+Hospitals Zika virus screening and testing rates, thus enabling this health care delivery system to make informed decisions and practices. The close coordination, collaboration, and communication between the health care delivery system and the local public health department examined in this article demonstrate the importance of working together to combat a complex public health emergency and how this relationship can serve as a guide for other jurisdictions to optimize collaboration between external partners during major outbreaks, emerging threats, and disasters that affect public health. (Disaster Med Public Health Preparedness. 2018;12:689-691).
Disaster Medicine and Public Health Preparedness | 2017
Jay K. Varma; David J. Prezant; Ross Wilson; Celia Quinn; Glenn Asaeda; Nicholas V. Cagliuso; Jennifer L. Rakeman; Marisa Raphael
The worlds largest outbreak of Ebola virus disease began in West Africa in 2014. Although few cases were identified in the United States, the possibility of imported cases led US public health systems and health care facilities to focus on preparing the health care system to quickly and safely identify and respond to emerging infectious diseases. In New York City, early, coordinated planning among city and state agencies and the health care delivery system led to a successful response to a single case diagnosed in a returned health care worker. In this article we describe public health and health care system preparedness efforts in New York City to respond to Ebola and conclude that coordinated public health emergency response relies on joint planning and sustained resources for public health emergency response, epidemiology and laboratory capacity, and health care emergency management. (Disaster Med Public Health Preparedness. 2017;11:370-374).