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Featured researches published by Lynnette Brammer.


Influenza and Other Respiratory Viruses | 2009

Estimates of US influenza-associated deaths made using four different methods.

William Thompson; Praveen Dhankhar; Po-Yung Cheng; Lynnette Brammer; Martin I. Meltzer; Joseph S. Bresee; David K. Shay

Backgroundu2002 A wide range of methods have been used for estimating influenza‐associated deaths in temperate countries. Direct comparisons of estimates produced by using different models with US mortality data have not been published.


Clinical Infectious Diseases | 2011

Detecting 2009 Pandemic Influenza A (H1N1) Virus Infection: Availability of Diagnostic Testing Led to Rapid Pandemic Response

Daniel B. Jernigan; Stephen Lindstrom; J .R. Johnson; J.D. Miller; M. Hoelscher; R. Humes; R. Shively; Lynnette Brammer; S. A. Burke; J. M. Villanueva; A. Balish; Timothy M. Uyeki; Desiree Mustaquim; Amber Bishop; J. H. Handsfield; R. Astles; Xiyan Xu; Alexander Klimov; Nancy J. Cox; Michael Shaw

Diagnostic tests for detecting emerging influenza virus strains with pandemic potential are critical for directing global influenza prevention and control activities. In 2008, the Centers for Disease Control and Prevention received US Food and Drug Administration approval for a highly sensitive influenza polymerase chain reaction (PCR) assay. Devices were deployed to public health laboratories in the United States and globally. Within 2 weeks of the first recognition of 2009 pandemic influenza H1N1, the Centers for Disease Control and Prevention developed and began distributing a new approved pandemic influenza H1N1 PCR assay, which used the previously deployed device platform to meet a >8-fold increase in specimen submissions. Rapid antigen tests were widely used by clinicians at the point of care; however, test sensitivity was low (40%-69%). Many clinical laboratories developed their own pandemic influenza H1N1 PCR assays to meet clinician demand. Future planning efforts should identify ways to improve availability of reliable testing to manage patient care and approaches for optimal use of molecular testing for detecting and controlling emerging influenza virus strains.


Clinical Infectious Diseases | 2013

Human Infections With Influenza A(H3N2) Variant Virus in the United States, 2011–2012

Scott Epperson; Michael A. Jhung; Shawn Richards; Patricia Quinlisk; Lauren Ball; Mària Moll; Rachelle Boulton; Loretta Haddy; Matthew Biggerstaff; Lynnette Brammer; Susan Trock; Erin Burns; Thomas M. Gomez; Karen K. Wong; Jackie Katz; Stephen Lindstrom; Alexander Klimov; Joseph S. Bresee; Daniel B. Jernigan; Nancy J. Cox; Lyn Finelli

BACKGROUND.u2003During August 2011-April 2012, 13 human infections with influenza A(H3N2) variant (H3N2v) virus were identified in the United States; 8 occurred in the prior 2 years. This virus differs from previous variant influenza viruses in that it contains the matrix (M) gene from the Influenza A(H1N1)pdm09 pandemic influenza virus. METHODS.u2003A case was defined as a person with laboratory-confirmed H3N2v virus infection. Cases and contacts were interviewed to determine exposure to swine and other animals and to assess potential person-to-person transmission. RESULTS.u2003Median age of cases was 4 years, and 12 of 13 (92%) were children. Pig exposure was identified in 7 (54%) cases. Six of 7 cases with swine exposure (86%) touched pigs, and 1 (14%) was close to pigs without known direct contact. Six cases had no swine exposure, including 2 clusters of suspected person-to-person transmission. All cases had fever; 12 (92%) had respiratory symptoms, and 3 (23%) were hospitalized for influenza. All 13 cases recovered. CONCLUSIONS.u2003H3N2v virus infections were identified at a high rate from August 2011 to April 2012, and cases without swine exposure were identified in influenza-like illness outbreaks, indicating that limited person-to-person transmission likely occurred. Variant influenza viruses rarely result in sustained person-to-person transmission; however, the potential for this H3N2v virus to transmit efficiently is of concern. With minimal preexisting immunity in children and the limited cross-protective effect from seasonal influenza vaccine, the majority of children are susceptible to infection with this novel influenza virus.


Clinical Infectious Diseases | 2011

Surveillance for Influenza during the 2009 Influenza A (H1N1) Pandemic–United States, April 2009–March 2010

Lynnette Brammer; Lenee Blanton; Scott Epperson; Desiree Mustaquim; Amber Bishop; Krista Kniss; Rosaline Dhara; Mackenzie Nowell; Laurie Kamimoto; Lyn Finelli

The emergence in April 2009 and subsequent spread of the 2009 pandemic influenza A (H1N1) virus resulted in the first pandemic of the 21st century. This historic event was associated with unusual patterns of influenza activity in terms of the timing and persons affected in the United States throughout the summer and fall months of 2009 and the winter of 2010. The US Influenza Surveillance System identified 2 distinct waves of pandemic influenza H1N1 activity--the first peaking in June 2009, followed by a second peak in October 2009. All influenza surveillance components showed levels of influenza activity above that typically seen during late summer and early fall. During this period, influenza activity reached its highest level during the week ending 24 October 2009. This report summarizes US influenza surveillance data from 12 April 2009 through 27 March 2010.


Influenza and Other Respiratory Viruses | 2013

Estimating influenza incidence and rates of influenza-like illness in the outpatient setting.

Ashley Fowlkes; Sharoda Dasgupta; Edward Chao; Jennifer Lemmings; Kate Goodin; Meghan Harris; Karen Martin; Michelle Feist; Winfred Wu; Rachelle Boulton; Jonathan L. Temte; Lynnette Brammer; Lyn Finelli

Please cite this paper as: Fowlkes et al. (2012) Estimating influenza incidence and rates of influenza‐like illness in the outpatient setting. Influenza and Other Respiratory Viruses DOI: 10.1111/irv.12014.


Influenza and Other Respiratory Viruses | 2012

Influenza viruses in Thailand: 7 years of sentinel surveillance data, 2004–2010

Malinee Chittaganpitch; Krongkaew Supawat; Sonja J. Olsen; Sunthareeya Waicharoen; Sirima Patthamadilok; Thitipong Yingyong; Lynnette Brammer; Scott Epperson; Pathom Sawanpanyalert

Please cite this paper as: Chittaganpitch et al. (2012) Influenza viruses in Thailand: 7u2003years of sentinel surveillance data, 2004–2010. Influenza and Other Respiratory Viruses 6(4), 276–283.


Influenza and Other Respiratory Viruses | 2009

Seasonal and pandemic influenza surveillance considerations for constructing multicomponent systems.

Lynnette Brammer; Alicia Budd; Nancy J. Cox

Abstractu2002 Surveillance for influenza is essential for the selection of influenza vaccine components and detection of human infections with novel influenza A viruses that may signal the start of a pandemic. Virologic surveillance provides the foundation from which this information can be obtained. However, morbidity and mortality data are needed to better understand the burden of disease, which, in turn, can provide useful information for policy makers relevant to the allocation of resources for prevention and control efforts. Data on the impact of influenza can be used to identify groups at increased risk for severe influenza‐related complications, develop prevention and control policies, and monitor the effect of these policies. Influenza surveillance systems frequently monitor outpatient illness, hospitalizations, and deaths, but selection of influenza surveillance components should be based on the surveillance goals and objectives of the jurisdiction.


Morbidity and Mortality Weekly Report | 2017

Update: Influenza Activity — United States, October 2, 2016–February 4, 2017

Lenee Blanton; Desiree Mustaquim; Noreen Alabi; Krista Kniss; Natalie Kramer; Alicia Budd; Shikha Garg; Charisse N. Cummings; Alicia M. Fry; Joseph S. Bresee; Wendy Sessions; Rebecca Garten; Xiyan Xu; Anwar Isa Abd Elal; Larisa V. Gubareva; John Barnes; David E. Wentworth; Erin Burns; Jacqueline M. Katz; Daniel B. Jernigan; Lynnette Brammer

Influenza activity in the United States began to increase in early November 2017 and rose sharply from December through February 3, 2018; elevated influenza activity is expected to continue for several more weeks. Influenza A viruses have been most commonly identified, with influenza A(H3N2) viruses predominating, but influenza A(H1N1)pdm09 and influenza B viruses were also reported. This report summarizes U.S. influenza activity* during October 1, 2017-February 3, 2018,† and updates the previous summary (1).


Morbidity and Mortality Weekly Report | 2015

Update: Influenza Activity - United States.

Smith S; Lenee Blanton; Krista Kniss; Desiree Mustaquim; Steffens C; Carrie Reed; Bramley A; Brendan Flannery; Alicia M. Fry; Lisa A. Grohskopf; Joseph S. Bresee; Teresa R. Wallis; Rebecca Garten; Xiyan Xu; Elal Ai; Larisa V. Gubareva; John Barnes; David E. Wentworth; Erin Burns; Jacqueline M. Katz; Daniel B. Jernigan; Lynnette Brammer

CDC collects, compiles, and analyzes data on influenza activity year-round in the United States. The influenza season generally begins in the fall and continues through the winter and spring months; however, the timing and severity of circulating influenza viruses can vary by geographic location and season. Influenza activity in the United States remained low through October and November in 2015. Influenza A viruses have been most frequently identified, with influenza A (H3) viruses predominating. This report summarizes U.S. influenza activity for the period October 4-November 28, 2015.


Clinical Infectious Diseases | 2011

Timely Assessment of the Severity of the 2009 H1N1 Influenza Pandemic

Gregory L. Armstrong; Lynnette Brammer; Lyn Finelli

During the 2009 influenza pandemic, weekly mortality data were analyzed to estimate excess mortality above a seasonally adjusted baseline modeled from prior years data. Between the 1962-1963 and 2008-2009 seasons, among persons ≥ 25 years old, excess mortality had been substantially higher during influenza A(H3N2)-dominant years than during A(H1N1)-dominant years. Among persons ≥ 15 years of age, excess mortality was higher in the 1968-1969 influenza pandemic season than during any other season. During the 2009-2010 pandemic, among all age groups <65 years old, excess mortality increased earlier than during any of the previous 47 seasons, eventually exceeding mortality in any prior non-pandemic season. In the ≥ 65-year-old age group, excess mortality remained relatively low, at rates typical of seasonal influenza A(H1N1) seasons. The model provided a timely assessment of severity during the 2009-2010 influenza pandemic, showing that, compared with prior seasons, mortality was relatively high among persons <65 years old and relatively low among those ≥ 65 years old.

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Joseph S. Bresee

Centers for Disease Control and Prevention

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Lyn Finelli

National Center for Immunization and Respiratory Diseases

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Alexander Klimov

Centers for Disease Control and Prevention

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Lenee Blanton

National Center for Immunization and Respiratory Diseases

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Nancy J. Cox

Centers for Disease Control and Prevention

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Daniel B. Jernigan

National Center for Immunization and Respiratory Diseases

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Larisa V. Gubareva

National Center for Immunization and Respiratory Diseases

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Teresa R. Wallis

Centers for Disease Control and Prevention

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Desiree Mustaquim

National Center for Immunization and Respiratory Diseases

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Erin Burns

National Center for Immunization and Respiratory Diseases

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