L. Hannah Gould

Dr. L. Hannah Gould

orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2017 in Emerging Infectious Diseases
Verified
Journal Article
Open access
LGL. Hannah Gould
L. Hannah Gould
JKJennifer Kline
Jennifer Kline
CMCaitlin Monahan
Caitlin Monahan
KVKatherine Vierk
Katherine Vierk
The proportion of US food that is imported is increasing; most seafood and half of fruits are imported. We identified a small but increasing number of foodborne disease outbreaks associated with imported foods, most commonly fish and produce. New outbreak investigation tools and federal regulatory authority are key to maintaining food safety.

20 September 2024 in International Journal of Infectious Diseases
Verified
Journal Article
Open access
FAFrederick Angulo
Frederick Angulo
ECEmily Colby
Emily Colby
ALAnne-Mette Lebech
Anne-Mette Lebech
PLPer-Eric Lindgren
Per-Eric Lindgren
Anna Moniuszko-MalinowskaAnna Moniuszko-Malinowska
Anna Moniuszko-Malinowska
JSJames H. Stark
James H. Stark
To better understand the Lyme borreliosis (LB) burden in Europe, we aimed to estimate the incidence of symptomatic Borrelia burgdorferi sensu lato (Bbsl) infections after adjusting public health LB surveillance data for under-detection of symptomatic Bbsl infections. Data from seroprevalence studies and estimates of the symptomatic proportion and duration of antibody detection in Bbsl-infected individuals, derived from reviews of the published literature, were used to adjust public health LB surveillance data to estimate the incidence of symptomatic Bbsl infection in nine European countries from 2018-2022. The prevalence of anti-Bbsl antibodies ranged from 2.3% in Romania to 9.4% in Germany. Under-detection multipliers varied across surveillance systems; using 10-year duration of antibody detection, multipliers were 2.4-10.5 in countries reporting all LB cases and 54.6-722.2 in countries reporting only Lyme neuroborreliosis cases. The incidence of symptomatic Bbsl infection adjusted for under-detection was highest in Finland, Germany, Norway, Poland, and Switzerland, intermediate in the Czech Republic and Denmark, and lowest in Ireland and Romania. Adjustment of LB surveillance for under-detection found a high incidence of symptomatic Bbsl infection in several European countries. Differences in LB surveillance systems should be considered when comparing surveillance data between countries and when estimating LB disease burden.

24 April 2024 in Zoonoses and Public Health
Verified
Journal Article
Open access
LGL. Hannah Gould
L. Hannah Gould
AFAdam Fathalla
Adam Fathalla
JMJennifer C. Moïsi
Jennifer C. Moïsi
JSJames H. Stark
James H. Stark
Introduction: Lyme disease (LD), caused by the spirochete Borrelia burgdorferi, is the most common vector‐borne disease in the United States. Although most surveillance‐reported cases are in people who are White, data suggest worse outcomes among people from racial and ethnic minority groups.Methods: We conducted a systematic literature review to describe racial disparities in LD. We described the epidemiology of LD by race and ethnicity, including clinical presentation at diagnosis, and summarised the literature on knowledge, attitudes and practices related to LD and ticks by race and ethnicity.Results: Overall, the incidence and prevalence of LD were 1.2–3.5 times higher in White persons than in persons who identified as Asian or Pacific Islander and 4.5–6.3 times higher in White persons than in persons who identified as Black. Across multiple studies, people from racial and ethnic minority groups were more likely than White people to have disseminated manifestations of LD, including neurological manifestations and arthritis, and less likely to have erythema migrans. People from racial and ethnic minority groups were also more likely to report disease onset in the fall and less likely to report disease onset in the summer. Possible reasons for these disparities include lack of recognition of the disease in people with darker skin tones, lack of knowledge of disease risk for some groups and differences in exposure risk.Conclusions: Taken together, these results reinforce that all people residing in high‐incidence areas are at risk of LD, regardless of race or ethnicity. Future prevention measures should be broadly targeted to reach all at‐risk populations.

29 May 2019 in Epidemiology and Infection
Verified
Journal Article
Open access
PDF file
PSPaula Strassle
Paula Strassle
WGW. Gu
W. Gu
BBB. B. Bruce
B. B. Bruce
LGL. Hannah Gould
L. Hannah Gould
Sex and age differences in food preferences may be reflected in the demographics of outbreaks. Outbreaks from 1998–2015 with a single confirmed implicated food source in the Centers for Disease Control and Prevention Foodborne Disease Outbreak Surveillance System were analysed using logistic regression to assess associations between a food category, sex and age. Males were more likely to be involved in outbreaks attributed to beef, pork, game, dairy and shellfish; females were more likely to be involved in grains-beans, nuts-seeds, fruits, sprouts and vegetable row crops outbreaks. Children <5-years-old were more likely than other age groups to be involved in dairy outbreaks, children 5–19-years-old were most likely to be involved in beef and game outbreaks, adults 20–49-years-old were most likely to be involved in fish, shellfish and sprout outbreaks and adults ⩾50-years-old were most likely to be involved in turkey outbreaks. Age and sex are associated with specific food categories in outbreaks. This information may be useful in helping to identify sources of foodborne disease outbreaks.

20 September 2024 in American Journal of Epidemiology
Verified
Journal Article
Open access
PDF file
LGL. Hannah Gould
L. Hannah Gould
RFRebecca Fee
Rebecca Fee
JWJohn White
John White
NWNoah Webb
Noah Webb
MCMaureen Carlyle
Maureen Carlyle
SPSarah Pugh
Sarah Pugh
Lyme disease (LD) is the most common vector-borne disease in the United States, with 476 000 cases estimated each year. It is unclear how LD risk factors vary by residential setting. We conducted a case-control study on LD risk according to rural, urban, and suburban residential settings. Individuals from 15 high-incidence states and the District of Columbia in the Optum Research Database were identified as cases (LD medical claim) or controls (no LD medical claim, matched by county of residence and census block group population density). Participants were surveyed about LD history, outdoor activities, and residential characteristics. The final analytic data set had 750 LD cases and 965 controls. Residence in a rural setting had increased LD risk (odds ratio [OR], 1.41; 95% CI, 1.16-1.72). In multivariable analyses, activities associated with LD were hiking/walking/running or having an occupation in forests, wooded areas, or areas of tall grass (all respondents), and spending time in a yard (rural and urban residents only). Public health interventions can help prevent LD in high-incidence jurisdictions by reinforcing the near-universal LD risk for rural residents and highlighting activities that lead to increased LD risk for those in areas with less ubiquitous tick exposure like in urban and suburban settings.

31 August 2022 in Journal of Public Health Management & Practice
Verified
Journal Article
Open access
LGL. Hannah Gould
L. Hannah Gould
SFStephanie E. Farquhar
Stephanie E. Farquhar
SGSophia Greer
Sophia Greer
MTMadeline Travers
Madeline Travers
LRLisa Ramadhar
Lisa Ramadhar
AVAyanna Vasquez
Ayanna Vasquez
Objective: To develop recommendations to embed equity into data work at a local health department and a framework for antiracist data praxis. Design: A working group comprised staff from across the agency whose positions involved data collection, analysis, interpretation, or communication met during April-July 2018 to identify and discuss successes and challenges experienced by staff and to generate recommendations for achieving equitable data practices. Setting: Local health department in New York City. Results: The recommendations encompassed 6 themes: strengthening analytic skills, communication and interpretation, data collection and aggregation, community engagement, infrastructure and capacity building, and leadership and innovation. Specific projects are underway or have been completed. Conclusions: Improving equity in data requires changes to data processes and commitment to racial and intersectional justice and process change at all levels of the organization and across job functions. We developed a collaborative model for how a local health department can reform data work to embed an equity lens. This framework serves as a model for jurisdictions to build upon in their own efforts to promote equitable health outcomes and become antiracist organizations.