37 research outputs found

    Mass Vaccination Campaign Following Community Outbreak of Meningococcal Disease

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    During December 12–29, 1998, seven patients ages 2–18 years were diagnosed with serogroup C meningococcal disease in two neighboring Florida towns with 33,000 residents. We evaluated a mass vaccination campaign implemented to control the outbreak. We maintained vaccination logs and recorded the resources used in the campaign that targeted 2- to 22-year-old residents of the two towns. A total of 13,148 persons received the vaccinations in 3 days. Vaccination coverage in the target population was estimated to be 86% to 99%. Five additional cases of serogroup C meningococcal disease occurred in the community during the year after the campaign began, four in patients who had not received the vaccine. The cost of control efforts was approximately $370,000. Although cases continued to occur, the vaccination campaign appeared to control the outbreak. Rapid implementation, a targeted approach, and high coverage were important to the campaign's success

    SARS-CoV-2 Antibody Prevalence Among Healthcare Workers and First Responders, Florida, May-June, 2020

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    Background: The SARS-CoV-2 virus responsible for severe respiratory infection associated with coronavirus disease 2019 (COVID-19) was first confirmed in Florida on March 1, 2020. Responding to the pandemic, multi-agency collaborative partnerships put in place actions integrating point-of-care antibody testing at established large-scale COVID-19 testing sites where the baseline seropositivity of COVID-19 in health care workers and first responders in Florida at the start of the pandemic was established. Purpose: Determine the seropositivity of healthcare workers and first responders at five drive thru testing sites using a rapid SARS-CoV-2 antibody test in Florida from May 6 through June 3, 2020. Methods: The first drive-thru SARS-CoV-2 antibody test site was opened at Miami Hard Rock Stadium, May 6, 2020. Testing expanded to three additional sites on May 9, 2020: Jacksonville, Orlando, and Palm Beach. The fifth and final site, Miami Beach, began testing on May 21, 2020. Healthcare workers and first responder’s self-seeking SARS-CoV-2 testing were designated for antibody testing and completed a laboratory collection form on-site for the point-of-care test. All testing was performed on whole blood specimens (obtained by venipuncture) using the Cellex Inc. qSARS-CoV-2 IgG/IgM Rapid Test. Seropositivity was assessed by univariate analysis and by logistic regression including the covariates age, sex, race/ethnicity, and testing location. Results and Discussion: As of June 3, 2020, of 5,779 healthcare workers and first responders tested, 4.1% were seropositive (range 2.6–8.2%). SARS-COV-2 antibody tests had higher odds of being positive for persons testing at the Miami Hard Rock Stadium (aOR 2.24 [95% C.I. 1.48-3.39]), persons of Haitian/Creole ethnicity (aOR 3.28 [95% C.I. 1.23-8.72]), Hispanic/Latino(a) ethnicity (aOR 2.17 [95% C.I. 1.50-3.13], and Black non-Hispanic persons (aOR 1.63 [95% C.I. 1.08-2.46]). SARS-COV-2 antibody prevalence among first responders and healthcare workers in five sites in Florida varied by race and ethnicity and by testing location

    Convalescent plasma in patients admitted to hospital with COVID-19 (RECOVERY): a randomised controlled, open-label, platform trial

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    SummaryBackground Azithromycin has been proposed as a treatment for COVID-19 on the basis of its immunomodulatoryactions. We aimed to evaluate the safety and efficacy of azithromycin in patients admitted to hospital with COVID-19.Methods In this randomised, controlled, open-label, adaptive platform trial (Randomised Evaluation of COVID-19Therapy [RECOVERY]), several possible treatments were compared with usual care in patients admitted to hospitalwith COVID-19 in the UK. The trial is underway at 176 hospitals in the UK. Eligible and consenting patients wererandomly allocated to either usual standard of care alone or usual standard of care plus azithromycin 500 mg once perday by mouth or intravenously for 10 days or until discharge (or allocation to one of the other RECOVERY treatmentgroups). Patients were assigned via web-based simple (unstratified) randomisation with allocation concealment andwere twice as likely to be randomly assigned to usual care than to any of the active treatment groups. Participants andlocal study staff were not masked to the allocated treatment, but all others involved in the trial were masked to theoutcome data during the trial. The primary outcome was 28-day all-cause mortality, assessed in the intention-to-treatpopulation. The trial is registered with ISRCTN, 50189673, and ClinicalTrials.gov, NCT04381936.Findings Between April 7 and Nov 27, 2020, of 16 442 patients enrolled in the RECOVERY trial, 9433 (57%) wereeligible and 7763 were included in the assessment of azithromycin. The mean age of these study participants was65·3 years (SD 15·7) and approximately a third were women (2944 [38%] of 7763). 2582 patients were randomlyallocated to receive azithromycin and 5181 patients were randomly allocated to usual care alone. Overall,561 (22%) patients allocated to azithromycin and 1162 (22%) patients allocated to usual care died within 28 days(rate ratio 0·97, 95% CI 0·87–1·07; p=0·50). No significant difference was seen in duration of hospital stay (median10 days [IQR 5 to >28] vs 11 days [5 to >28]) or the proportion of patients discharged from hospital alive within 28 days(rate ratio 1·04, 95% CI 0·98–1·10; p=0·19). Among those not on invasive mechanical ventilation at baseline, nosignificant difference was seen in the proportion meeting the composite endpoint of invasive mechanical ventilationor death (risk ratio 0·95, 95% CI 0·87–1·03; p=0·24).Interpretation In patients admitted to hospital with COVID-19, azithromycin did not improve survival or otherprespecified clinical outcomes. Azithromycin use in patients admitted to hospital with COVID-19 should be restrictedto patients in whom there is a clear antimicrobial indication

    Utilizing Syndromic Surveillance for Hurricane Irma-Related CO Poisonings in Florida

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    ObjectiveThis study describes how Florida Poison Information Center Network (FPICN) and emergency department (ED) data accessed through Florida’s syndromic surveillance system were used to conduct near real-time carbon monoxide (CO) poisoning surveillance and active case finding in response to Hurricane Irma in Florida.IntroductionOn September 10, 2017, Hurricane Irma made landfall in Florida. Over 90% of Florida counties reported power outages as of September 11. During power outages, CO poisonings often occur due to indoor use of fuel combustion sources (e.g., cooking, heating) or generators for electricity.CO poisoning is a reportable condition in Florida; health care providers and laboratories are required to report suspected cases to the Florida Department of Health (FDOH). In Florida, approximately 202 cases of CO poisoning are reported each year (three-year average from 2014 to 2016). In addition to passive surveillance, FDOH uses the Electronic Surveillance System for the Early Notification of Community-based Epidemics (ESSENCE-FL) to find cases of CO poisoning. ESSENCE-FL provides access to ED data from 98% (255 out of 260) of EDs in Florida and all statewide FPICN call data (includes three poison control centers). ESSENCE-FL provides near real-time access to these data sets, as ED data are uploaded every 2 hours or once a day (depending on the hospital system) and FPICN data are uploaded every 10 minutes. The statewide FPICN database includes information about substance, signs and symptoms, exposure scenario, and patient identification information provided by the individual caller or clinician from a health care facility.MethodsIn addition to receipt of health care provider reports through traditional disease reporting, active case finding was conducted using ESSENCE-FL during Hurricane Irma. Exposure calls to the FPICN indicating CO exposure were extracted from the statewide database. Calls coded with the following medical outcomes were excluded: no health effect, not followed – judged as nontoxic exposure, not followed – minimal clinical effects possible, unrelated effect – the exposure was probably not responsible for the effect(s), and confirmed non-exposure. To query ESSENCE-FL ED data, a free-text query was created and executed against the concatenated chief complaint and discharge diagnosis (CCDD) field: (^carbon^,andnot,(,^retention^ ,or,^narcosis^,),),or,^monox^,or,(,^generator^,and, (,^fumes^,or,^expos^,or,^nausea^, or,^headach^,or,^exhaust^,or,^garage^,or,^inhale^,),) . Results of these queries were analyzed and sent to county and regional epidemiologists daily for investigation.Reports of CO poisoning exposures were investigated by collecting medical records and conducting interviews using an expanded risk factor questionnaire.1 Cases were classified using Florida’s reportable disease case definition2 and documented in the electronic reportable disease surveillance system, Merlin (see process flow chart). Descriptive analysis of Hurricane Irma-related CO poisoning cases reported in Merlin was conducted to characterize morbidity, mortality, and exposure scenarios.ResultsIn September 2017, FDOH investigated 666 reports of CO poisoning and identified 529 people (79.4%) who met the case definition for CO poisoning. Among 529 cases, 56.3% were reported by ED data, 5.7% by FPICN data, 29.1% from both data sets, and the remaining 8.9% by other sources (e.g., self-report, media). About 60.1% of cases were only reported by FPICN and ED data, 33.1% by health care providers and laboratories, and 6.8% by other sources. Among 15 deaths, 20% were identified through active case finding using ED and FPICN data. CO poisoning cases peaked on September 12 (within two days of hurricane landfall) and decreased by September 16, as power was restored. About 95% of cases reported CO exposures within the first week of hurricane landfall.Merlin data analysis of 529 cases identified some notable findings related to Hurricane Irma. CO poisoning rates were highest among those aged 5–14 years (4.8 per 100,000 population), and the mean age was 33.2 years (median: 31 years, range: 3 months – 89 years). Most cases were in females (55.6%), non-Hispanics (58.3%), and whites (73%). CO exposures were predominantly caused by generator use (97.5%). Among 516 generator-related exposures, 15.7% of people had a CO detector, 62.8% did not have CO detector, and it was unknown for 21.5%. Among 516 residential exposures due to generator use, 31.3% of people reported generator use inside the home, attached garage, or other attached structures, and 66% reported generator use outside the home, including covered decks and carports. Among 340 people who reported generator use outside the home, 63.5% reported having a generator within 20 feet of windows, doors, air conditioners, or air intake vents.ConclusionsEven though CO poisoning is a reportable condition in Florida, use of active surveillance was key in the public health response to Hurricane Irma-related CO poisonings. FDOH would not have identified 60% of these hurricane-related CO poisoning cases without access to FPICN and ED data. During Hurricane Irma, active case finding complemented routine disease surveillance not only in early detection of CO poisonings but also in guiding rapid public health response. Similarly, in the 2005 hurricane season, FDOH monitored FPICN data and identified an increase in CO poisonings.3 Based on near-real-time CO poisoning surveillance, FDOH produced daily situation reports, sent out a press release about the dangers of CO poisoning from generator use, prepared a YouTube video, and conducted educational outreach through social media and text alert. Other jurisdictions may benefit from use of near real-time ED and poison control center data to better understand the magnitude and characteristics of CO poisonings during power outages in their areas. Public education messages need to emphasize outdoor use of generators (at least 20 feet away from doors, windows, and air conditioners) and use of CO detectors.References1. Florida Department of Health. Carbon monoxide poisoning enhanced case report form; October 2017. Available at: www.floridahealth.gov/diseases-and-conditions/disease-reporting-and-management/disease-reporting-and-surveillance/_documents/crf-co-hurricane-irma-enhanced-surveillance.pdf2. Florida Department of Health. Carbon monoxide poisoning case definition; 2018. Available at: www.floridahealth.gov/diseases-and-conditions/disease-reporting-and-management/disease-reporting-and-surveillance/_documents/cd-carbon-monoxide.pdf3. Monitoring Poison Control Center Data to Detect Health Hazards During Hurricane Season—Florida, 2003-2005. JAMA. 2006;295(21):2469–2470.
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