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1.
Biosecur Bioterror ; 6(1): 57-65, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18386973

ABSTRACT

OBJECTIVES: Public health agencies are often tasked with the development and execution of interventions, but the communication strategy and its impact on the effectiveness of an intervention is often not evaluated or incorporated by local and state health agencies. The primary objective of this study was to determine the impact of information from various sources on knowledge about an emergency preparedness public health intervention involving the mass distribution of medicine. METHODS: The study used validated written mail surveys containing 12 simple knowledge-based questions. One-way ANOVA, the Studentized Newman-Keuls (SNK) test, logistic regression, and multiple regression were used to evaluate the data. RESULTS: Reading an educational fact sheet or receiving job training were the highest predictive variables for correct responses on the survey among all groups. Commercial media were found to potentially diminish comprehension among survey respondents. There was significant variability in knowledge among different groups surveyed, ranging from an average of 15% to 74% correct responses on the survey. CONCLUSIONS: This study found that job training and fact sheets that are delivered directly to the intended recipients are very effective at enhancing knowledge among the general public and emergency responders. Conversely, we found that commercial media, such as television, may be detrimental to educating the public about important public health interventions. The internet was not widely used by the survey respondents to obtain information; this raises questions regarding the usefulness of websites for emergency preparedness education.


Subject(s)
Communication , Disaster Planning , Emergency Medical Services , Information Dissemination , Pharmaceutical Preparations/supply & distribution , Bioterrorism , Data Collection , Health Knowledge, Attitudes, Practice , Humans , Information Services , Potassium Iodide/supply & distribution , Public Health Administration , United States
2.
Clin Infect Dis ; 45(5): 527-33, 2007 Sep 01.
Article in English | MEDLINE | ID: mdl-17682984

ABSTRACT

BACKGROUND: In contrast to pharmaceutical manufacturers, compounding pharmacies adhere to different quality-control standards, which may increase the likelihood of undetected outbreaks. In 2005, the Centers for Disease Control and Prevention received reports of cases of Serratia marcescens bloodstream infection occurring in patients who underwent cardiac surgical procedures in Los Angeles, California, and in New Jersey. An investigation was initiated to determine whether there was a common underlying cause. METHODS: A matched case-control study was conducted in Los Angeles. Case record review and environmental testing were conducted in New Jersey. The Centers for Disease Control and Prevention performed a multistate case-finding investigation; isolates were compared using pulsed-field gel electrophoresis analysis. RESULTS: Nationally distributed magnesium sulfate solution (MgSO(4)) from compounding pharmacy X was the only significant risk factor for S. marcescens bloodstream infection (odds ratio, 6.4; 95% confidence interval, 1.1-38.3) among 6 Los Angeles case patients and 18 control subjects. Five New Jersey case patients received MgSO(4) from a single lot produced by compounding pharmacy X; culture of samples from open and unopened 50-mL bags in this lot yielded S. marcescens. Seven additional case patients from 3 different states were identified. Isolates from all 18 case patients and from samples of MgSO(4) demonstrated indistinguishable pulsed-field gel electrophoresis patterns. Compounding pharmacy X voluntarily recalled the product. Neither the pharmacy nor the US Food and Drug Administration could identify a source of contamination in their investigations of compounding pharmacy X. CONCLUSIONS: A multistate outbreak of S. marcescens bloodstream infection was linked to contaminated MgSO(4) distributed nationally by a compounding pharmacy. Health care personnel should take into account the different quality standards and regulation of compounded parenteral medications distributed in large quantities during investigations of outbreaks of bloodstream infection.


Subject(s)
Bacteremia/epidemiology , Cardiovascular Agents/adverse effects , Disease Outbreaks , Drug Contamination , Magnesium Sulfate/adverse effects , Serratia Infections/etiology , Serratia marcescens/pathogenicity , Adolescent , Adult , Aged , Aged, 80 and over , Bacteremia/microbiology , Cardiac Surgical Procedures , Centers for Disease Control and Prevention, U.S./statistics & numerical data , Cross Infection/epidemiology , Cross Infection/microbiology , Drug Compounding/adverse effects , Drug Compounding/standards , Female , Humans , Los Angeles/epidemiology , Male , Middle Aged , New Jersey/epidemiology , Risk Factors , Serratia Infections/epidemiology , Serratia marcescens/isolation & purification , United States
3.
Am J Public Health ; 97 Suppl 1: S100-2, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17413064

ABSTRACT

The Nuclear Regulatory Commission requires states to consider including potassium iodide as a protective measure in the unlikely event of a major release of radioactivity from a nuclear power plant. We evaluated emergency preparedness knowledge, including proper potassium iodide use, among the general public and emergency responders located around New Jersey's nuclear power plants. We found that knowledge about responder chain of command, evacuation routes, and some aspects of potassium iodide usage was incomplete among the general public and emergency responders.


Subject(s)
Health Knowledge, Attitudes, Practice , Neoplasms, Radiation-Induced/prevention & control , Potassium Iodide/administration & dosage , Power Plants , Radioactive Hazard Release , Thyroid Neoplasms/prevention & control , Air Pollutants, Radioactive , Disaster Planning , Humans , New Jersey , Surveys and Questionnaires
4.
Public Health Rep ; 122(3): 311-8, 2007.
Article in English | MEDLINE | ID: mdl-17518302

ABSTRACT

To describe state-level actions and policies during the 2004-2005 influenza vaccine shortage and determine whether these or other factors were related to vaccination coverage, we surveyed all state health departments (including the District of Columbia). We included 2004-2005 Behavioral Risk Factor Surveillance System data to examine whether state-level actions, policies, or other factors like vaccine supply were related to changes in vaccination coverage in adults aged > or = 65 years from the previous non-shortage year. We found that 96% (n = 49) of states reported adopting or recommending adherence to the initial national interim influenza vaccination recommendations. Of these, at some point during the season, 22% (n = 11) reported local public health agencies issued prioritization recommendations that differed from the state health department's guidance. Eighty percent (n = 41) initiated at least one emergency response activity and 43% (n = 22) referred to or implemented components of their pandemic influenza plans. In 35% (n = 18), emergency or executive orders were issued or legislative action occurred. In a multivariable linear regression model, the availability and use of practitioner contact lists and having a relatively high vaccine supply in early October 2004 were associated with smaller decreases in coverage for adults aged > or = 65 years from the previous non-shortage season (p = 0.003, r2 = 0.26). States over-whelmingly followed national vaccination prioritization guidelines and used a range of activities to manage the 2004-2005 vaccine shortage. The availability and use of practitioner contact lists and having a relatively high vaccine supply early in the season were associated with smaller decreases in coverage from the previous non-shortage season.


Subject(s)
Government Agencies/organization & administration , Health Policy , Influenza Vaccines/supply & distribution , Public Health Administration , State Government , Aged , Behavioral Risk Factor Surveillance System , Centers for Disease Control and Prevention, U.S. , Guidelines as Topic , Humans , United States
5.
Health Phys ; 92(2 Suppl): S18-26, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17228184

ABSTRACT

The primary objective of this study was to evaluate a joint state and local government-sponsored potassium iodide (KI) distribution program in New Jersey. This program is part of a radiological emergency response system for residents living within the Emergency Planning Zones (EPZs) of nuclear power facilities. KI pills and an informational fact sheet were distributed locally at six different public clinics in the summer of 2002. In this study, a mailed survey was developed, pilot tested, and sent to the general public to assess knowledge about KI use. The survey consisted of two groups of people, those who attended a KI distribution clinic and those that did not attend a clinic. There was a statistically significant difference in knowledge among the two groups of survey respondents regarding KI prophylaxis, with a mean of 46% of survey questions answered correctly by those who attended a clinic vs. 15% by those who did not attend. Certain questions were problematic for the public to answer correctly and included potential low compliance with government instructions for taking KI, confusion regarding where the public can obtain KI pills during an emergency, and the lack of awareness on the proper use of KI for children, pregnant women, and persons over the age of 40 y. Additional outreach in these specific areas is warranted. This study also found that there was a highly variable geographic pattern of homes that have a supply of KI pills, with some areas having 60% of the households supplied with pills from the clinic while other areas had as low as 1% of the homes supplied with KI pills.


Subject(s)
Disaster Planning , Health Education , Health Knowledge, Attitudes, Practice , Nuclear Reactors , Potassium Iodide/supply & distribution , Adult , Aged , Aged, 80 and over , Community Participation , Emergencies , Female , Humans , Male , Middle Aged , Neoplasms, Radiation-Induced/prevention & control , New Jersey , Potassium Iodide/therapeutic use , Radioactive Hazard Release , Residence Characteristics , Thyroid Neoplasms/prevention & control
6.
Expert Rev Vaccines ; 16(12): 1217-1230, 2017 12.
Article in English | MEDLINE | ID: mdl-29053937

ABSTRACT

INTRODUCTION: The active component of the herpes zoster vaccine (ZVL), licensed for people ≥50 years of age, is a live attenuated varicella-zoster virus. ZVL is contraindicated for immune compromised individuals, with limited regard to the degree of immunosuppression. Areas covered: This review evaluates phase I and II and observational studies for ZVL, and published reports of the off-label use of ZVL, for conditions and therapies for which investigators considered the risk-benefit for using ZVL to be favorable. It also discusses exploratory trials of ZVL for additional immune compromising conditions, and summarizes clinical guidelines from many countries and professional societies that are based upon recent investigations. Studies in immune compromised patients of investigational vaccines that do not contain live virus are reviewed. Expert commentary: It is likely that past and ongoing research with ZVL will define immune compromising diseases and/or therapies for which the risk-benefit for using ZVL vaccine is favorable. The main variables to consider in this assessment in immune compromised patients are safety, immunogenicity, protection against herpes zoster, and persistence of protection. Vaccination against herpes zoster prior to suppressing immunity is an important clinical strategy, although efficacy of this approach has not been evaluated in a clinical trial.


Subject(s)
Herpes Zoster Vaccine/adverse effects , Herpes Zoster Vaccine/immunology , Herpes Zoster/prevention & control , Immunocompromised Host , Clinical Trials, Phase I as Topic , Clinical Trials, Phase II as Topic , Herpes Zoster Vaccine/administration & dosage , Humans , Observational Studies as Topic , Practice Guidelines as Topic , Vaccines, Attenuated/administration & dosage , Vaccines, Attenuated/adverse effects , Vaccines, Attenuated/immunology
7.
JAMA ; 296(20): 2476-9, 2006 Nov 22.
Article in English | MEDLINE | ID: mdl-17119144

ABSTRACT

CONTEXT: Botulism is a potentially lethal paralytic disease caused primarily by toxins of the anaerobic, spore-forming bacterium Clostridium botulinum. Although botulinum toxin A is available by prescription for cosmetic and therapeutic use, no cases of botulism with detectable serum toxin have previously been attributed to cosmetic or therapeutic botulinum toxin injections. On November 27, 2004, 4 suspected botulism case-patients with a link to cosmetic botulinum toxin injections were reported to the Centers for Disease Control and Prevention. OBJECTIVE: To investigate the clinical, epidemiological, and laboratory aspects of 4 suspected cases of iatrogenic botulism. DESIGN, SETTING, AND PATIENTS: Case series on 4 botulism case-patients. MAIN OUTCOME MEASURES: Clinical characteristics of the 4 case-patients, epidemiological associations, and mouse bioassay neutralization test results from case-patient specimens and a toxin sample. RESULTS: Clinical characteristics of the 4 case-patients were consistent with those of naturally occurring botulism. All case-patients had been injected with a highly concentrated, unlicensed preparation of botulinum toxin A and may have received doses 2857 times the estimated human lethal dose by injection. Pretreatment serum toxin levels in 3 of the 4 case-patients were equivalent to 21 to 43 times the estimated human lethal dose; pretreatment serum from the fourth epidemiologically linked case-patient was not available. A 100-microg vial of toxin taken from the same manufacturer's lot as toxin administered to the case-patients contained a toxin amount sufficient to kill approximately 14,286 adults by injection if disseminated evenly. CONCLUSIONS: These laboratory-confirmed cases of botulism demonstrate that clinical use of unlicensed botulinum toxin A can result in severe, life-threatening illness. Further education and regulation are needed to prevent the inappropriate marketing, sale, and clinical use of unlicensed botulinum toxin products.


Subject(s)
Botulinum Toxins, Type A , Botulism/etiology , Cosmetic Techniques/adverse effects , Iatrogenic Disease , Botulinum Toxins, Type A/administration & dosage , Botulinum Toxins, Type A/blood , Botulinum Toxins, Type A/standards , Botulinum Toxins, Type A/supply & distribution , Botulism/blood , Botulism/diagnosis , Botulism/epidemiology , Cluster Analysis , Cosmetic Techniques/standards , Humans , Iatrogenic Disease/epidemiology , Legislation, Drug , Lethal Dose 50 , United States
8.
MD Advis ; 14(1): 15-16, 2021.
Article in English | MEDLINE | ID: mdl-35838619
9.
Chest ; 128(1): 207-15, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16002937

ABSTRACT

STUDY OBJECTIVES: Sarcoidosis is a granulomatous disorder with heterogeneous clinical manifestations, which are potentially reflective of a syndrome with different etiologies leading to similar histologic findings. We examined the relationship between environmental and occupational exposures, and the clinical phenotype of sarcoidosis. DESIGN: We performed a cross-sectional study of incident sarcoidosis cases that had been identified by A Case Control Etiologic Study of Sarcoidosis. Subjects were categorized into the following two groups: (1) pulmonary-only disease; and (2) systemic disease (with or without pulmonary involvement). Logistic regression was used to examine the associations of candidate exposures with clinical phenotype. SETTING: Ten academic medical centers across the United States. PATIENTS: The current study included 718 subjects in whom sarcoidosis had been diagnosed within 6 months of study enrollment. Patients met the following criteria prior to enrollment: (1) tissue confirmation of noncaseating granulomas on tissue biopsy on one or more organs within 6 months of study enrollment with negative stains for acid-fast bacilli and fungus; (2) clinical signs or symptoms that were consistent with sarcoidosis; (3) no other obvious explanation for the granulomatous disease; and (4) age > 18 years. MEASUREMENTS AND RESULTS: Several exposures were associated with significantly less likelihood of having extrapulmonary disease in multivariate analysis, including agricultural organic dusts and wood burning. The effects of many of these exposures were significantly different in patients of different self-defined race. CONCLUSIONS: The differentiation of sarcoidosis subjects on the basis of clinical phenotypes suggests that these subgroups may have unique environmental exposure associations. Self-defined race may play a role in the determination of the effect of certain exposures on disease phenotypes.


Subject(s)
Environmental Exposure/adverse effects , Occupational Exposure/adverse effects , Sarcoidosis/etiology , Adult , Cross-Sectional Studies , Data Interpretation, Statistical , Female , Humans , Logistic Models , Male , Phenotype , Risk Factors , Sarcoidosis/epidemiology
10.
Sarcoidosis Vasc Diffuse Lung Dis ; 22(2): 147-53, 2005 Jun.
Article in English | MEDLINE | ID: mdl-16053031

ABSTRACT

AIM: To assess lung involvement and the association of demographic and psychosocial factors with respiratory health in 736 persons with sarcoidosis at enrollment in A Case Control Etiologic Study of Sarcoidosis (ACCESS). METHODS: 736 patients with biopsy diagnosis of sarcoidosis within 6 months of enrollment were studied at 10 US centers. Lung involvement was evaluated by chest radiography, spirometry and dyspnea questionnaire. Demographics, number of involved extrathoracic organ systems, comorbidities, and health-related quality of life (HRQL) were assessed. RESULTS: 95% of patients had lung involvement. 8% were Scadding Stage 0, 40% I, 37% II, 10% III, and 5% IV 51% reported dyspnea. Increasing radiographic lung stage was associated with decreasing Forced Vital Capacity (FVC) (p < 0.01). Patients with higher stages had more airways obstruction and dyspnea. 46% of cases and 27% of controls had Center for Epidemiologic Studies Depression Scale (CES-D) scores of 9 or greater, (p < 0.001). Age > or = 40, African-American race, body mass index > or = 30kg/m2, and CES-D scores > 9 were associated with decreased FVC and greater dyspnea. Impaired spirometry and greater dyspnea were associated with poorer quality of life. CONCLUSION: A "global" approach to the sarcoidosis patient, including careful assessment of dyspnea and health related quality of life, as well as of lung function and radiographic changes, and any extrathoracic involvement, is important, not only in management of the individual patient, but should also prove beneficial in assessing outcomes in clinical trials in the future.


Subject(s)
Psychological Tests , Quality of Life , Sarcoidosis, Pulmonary , Adult , Black or African American/ethnology , Biopsy , Case-Control Studies , Depression/diagnosis , Depression/epidemiology , Depression/psychology , Dyspnea/diagnosis , Dyspnea/epidemiology , Dyspnea/psychology , Female , Humans , Incidence , Male , Predictive Value of Tests , Prognosis , Radiography, Thoracic , Sarcoidosis, Pulmonary/diagnosis , Sarcoidosis, Pulmonary/epidemiology , Sarcoidosis, Pulmonary/psychology , Severity of Illness Index , Spirometry , Surveys and Questionnaires , United States/epidemiology
11.
J Occup Environ Med ; 47(3): 226-34, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15761318

ABSTRACT

OBJECTIVES: To determine whether specific occupations and industries may be associated with sarcoidosis. METHODS: A Case Control Etiologic Study of Sarcoidosis (ACCESS) obtained occupational and environmental histories on 706 newly diagnosed sarcoidosis cases and matched controls. We used Standard Industrial Classification (SIC) and Standard Occupational Classification (SOC) to assess occupational contributions to sarcoidosis risk. RESULTS: Univariable analysis identified elevated risk of sarcoidosis for workers with industrial organic dust exposures, especially in Caucasian workers. Workers for suppliers of building materials, hardware, and gardening materials were at an increased risk of sarcoidosis as were educators. Work providing childcare was negatively associated with sarcoidosis risk. Jobs with metal dust or metal fume exposures were negatively associated with sarcoidosis risk, especially in Caucasian workers. CONCLUSIONS: In this study, we found that exposures in particular occupational settings may contribute to sarcoidosis risk.


Subject(s)
Job Description , Occupations , Sarcoidosis/etiology , Adolescent , Adult , Aged , Aged, 80 and over , Case-Control Studies , Female , Humans , Industry , Male , Middle Aged , Risk Factors , Sarcoidosis/epidemiology
13.
Infect Control Hosp Epidemiol ; 24(11): 848-52, 2003 Nov.
Article in English | MEDLINE | ID: mdl-14649774

ABSTRACT

OBJECTIVE: To characterize risk factors for invasive pneumococcal infection in a nursing home outbreak. DESIGN: Outbreak investigation, case-control study. SETTING: A 114-bed nursing home in New Jersey. PARTICIPANTS: Case-patients were nursing home residents hospitalized with febrile respiratory illness and radiographic findings consistent with pneumonia, and either sputum specimens positive for diplococci or blood cultures positive for Streptococcus pneumoniae, with illness onset during April 3-24, 2001. Control-patients were selected randomly from remaining residents without respiratory symptoms. METHODS: Chart reviews were performed for case-patients and control-patients. Serotyping and susceptibility testing were performed on S. pneumoniae isolates. Long-term-care facilities (LTCFs) were surveyed to assess compliance with a state regulation mandating pneumococcal vaccination of residents 65 years and older. RESULTS: Nine case-patients were identified, with a median age of 86 years (range, 78 to 100 years). The median age of control-patients was 86 years (range, 58 to 95 years). No case-patients versus 9 (50%) control-patients received pneumococcal vaccine before the outbreak (OR, 0; CI95, 0-0.7). Recent antibiotic use, pneumonia history, and physical functioning were not associated with illness. Illness attack rate was 16% among all unvaccinated residents versus 0 among vaccinated residents. S. pneumoniae serotype 14, included in pneumococcal vaccine, was isolated from blood cultures of 7 case-patients. Of 361 LTCFs (42%) that replied to the survey, 28 (8%) were not complying with state immunization regulations. CONCLUSIONS: This outbreak occurred in an LTCF with low vaccine coverage. Implementing standing order programs, enforcing regulations, documenting vaccinations, and providing education might increase coverage among nursing home residents.


Subject(s)
Cross Infection/epidemiology , Disease Outbreaks/prevention & control , Mandatory Programs/legislation & jurisprudence , Nursing Homes/standards , Pneumococcal Vaccines/administration & dosage , Pneumonia, Pneumococcal/epidemiology , Vaccination/statistics & numerical data , Aged , Aged, 80 and over , Case-Control Studies , Cross Infection/microbiology , Cross Infection/transmission , Female , Health Knowledge, Attitudes, Practice , Humans , Infection Control/legislation & jurisprudence , Infection Control/statistics & numerical data , Male , New Jersey/epidemiology , Nursing Homes/legislation & jurisprudence , Pneumonia, Pneumococcal/microbiology , Pneumonia, Pneumococcal/prevention & control , Risk Factors , Serotyping , Streptococcus pneumoniae/isolation & purification , Streptococcus pneumoniae/pathogenicity , Vaccination/legislation & jurisprudence
14.
Am J Prev Med ; 26(4): 311-4, 2004 May.
Article in English | MEDLINE | ID: mdl-15110058

ABSTRACT

BACKGROUND: Influenza and pneumococcal disease are major causes of vaccine-preventable death among the elderly. In an effort to raise immunization rates, New Jersey in 1999 adopted a regulation requiring hospitals to offer pneumococcal and influenza vaccinations to all inpatients aged 65 and over. This study examined the effect of implementation strategies on immunization rates within hospitals in 2000 and 2001. METHODS: Hospital infection control directors were surveyed and random chart review was conducted from a stratified sample of hospitals. The infection control director's assessment of their institution's success was a major outcome measure. RESULTS: Relatively few respondents thought their hospital has been successful in implementing new immunization protocols. Approximately 67% responded that they did not think physicians agreed with the "scope and nature" of the regulation. Physician attitudes led the list of barriers to implementation cited by respondents. Chart review revealed moderate amounts of immunization assessment performed by nurses, but virtually no evidence of physicians' orders for immunization. CONCLUSIONS: Thus far, there is little evidence that the New Jersey regulation has resulted in a meaningful change in pneumococcal or influenza vaccination practices.


Subject(s)
Influenza Vaccines , Pneumococcal Vaccines , Vaccination/legislation & jurisprudence , Aged , Hospitals , Humans , New Jersey , Practice Patterns, Physicians'
15.
Sarcoidosis Vasc Diffuse Lung Dis ; 20(3): 204-11, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14620163

ABSTRACT

A cohort of 215 sarcoidosis patients from the ACCESS study underwent a clinical evaluation at study enrollment and two years later. Approximately 80% of subjects had an improved or stable FVC, FEV1, chest radiograph determined by Scadding stage, and dyspnea scale. African-Americans had less improvement in FVC than Caucasians (p = 0.04). Patients with erythema nodosum at presentation were more likely to have improvement in the chest radiograph at two-year follow-up (p = 0.007). Patients with a lower annual family income were more likely to worsen with respect to dyspnea (p = 0.01) and more likely to have new organ involvement at two-year follow-up (p = 0.045). The development of new organ involvement over the two year follow-up period was more common in African-Americans compared to Caucasians (p = 0.002) and more likely in those with extrapulmonary involvement at study entry (p = 0.003). There was an excellent concordance between changes in FVC and FEV1 over the two-year period. However, changes in FVC alone were inadequate to describe the change in pulmonary status of the patients, as changes in chest radiographic findings or the level of dyspnea did often but not always move in the same direction as FVC. In conclusion, data from this heterogeneous United States sarcoidosis population indicate that sarcoidosis tends to improve or remain stable over two years in the majority of patients. Several factors associated with improved or worse outcome over two years were identified.


Subject(s)
Black or African American , Sarcoidosis/complications , Sarcoidosis/pathology , White People , Adult , Case-Control Studies , Cohort Studies , Disease Progression , Dyspnea/classification , Dyspnea/etiology , Female , Humans , Male , Middle Aged , Prognosis , Respiratory Function Tests , United States
16.
Public Health Rep ; 119(6): 552-6, 2004.
Article in English | MEDLINE | ID: mdl-15504446

ABSTRACT

The Smallpox Pre-Event Vaccination Program (SPVP) for public health and hospital-based health care workers began on January 24, 2003. This report summarizes efforts made by health officials in Florida, Nebraska, New Jersey, and Tennessee to facilitate the voluntary participation of acute care hospitals in the SPVP. Seven common characteristics contributed to the success of programs in these four states: (1) early planning, building on existing competencies, and state government support, (2) carrying the program forward on a planned timeline with experienced vaccination staff, (3) use of multifaceted training activities, (4) use of mock scenarios and field exercises to avoid early problems, (5) establishment and fostering of good relationships and lines of communication with stakeholders and the mass media, (6) addressing liability and workers' compensation concerns prior to initiation of the SPVP, and (7) attention to vaccination clinic logistics.


Subject(s)
Bioterrorism , Health Personnel , Immunization Programs/organization & administration , Public Health Practice/standards , Smallpox Vaccine/administration & dosage , Smallpox/prevention & control , Florida , Hospitals , Nebraska , New Jersey , Program Development , Program Evaluation , Smallpox/transmission , Tennessee , United States
17.
JAMA ; 291(16): 1994-8, 2004 Apr 28.
Article in English | MEDLINE | ID: mdl-15113818

ABSTRACT

CONTEXT: Little is known about potential long-term health effects of bioterrorism-related Bacillus anthracis infection. OBJECTIVE: To describe the relationship between anthrax infection and persistent somatic symptoms among adults surviving bioterrorism-related anthrax disease approximately 1 year after illness onset in 2001. DESIGN, SETTING, AND PARTICIPANTS: Cross-sectional study of 15 of 16 adult survivors from September through December 2002 using a clinical interview, a medical review-of-system questionnaire, 2 standardized self-administered questionnaires, and a review of available medical records. MAIN OUTCOME MEASURES: Health complaints summarized by the body system affected and by symptom categories; psychological distress measured by the Revised 90-Item Symptom Checklist; and health-related quality-of-life indices by the Medical Outcomes Study 36-Item Short-Form Health Survey (version 2). RESULTS: The anthrax survivors reported symptoms affecting multiple body systems, significantly greater overall psychological distress (P<.001), and significantly reduced health-related quality-of-life indices compared with US referent populations. Eight survivors (53%) had not returned to work since their infection. Comparing disease manifestations, inhalational survivors reported significantly lower overall physical health than cutaneous survivors (mean scores, 30 vs 41; P =.02). Available medical records could not explain the persisting health complaints. CONCLUSION: The anthrax survivors continued to report significant health problems and poor life adjustment 1 year after onset of bioterrorism-related anthrax disease.


Subject(s)
Anthrax , Bioterrorism , Quality of Life , Survivors , Absenteeism , Adult , Anthrax/physiopathology , Anthrax/psychology , Bioterrorism/psychology , Cross-Sectional Studies , Follow-Up Studies , Health Status , Health Status Indicators , Humans , Middle Aged , Respiratory Tract Infections/microbiology , Respiratory Tract Infections/physiopathology , Respiratory Tract Infections/psychology , Skin Diseases, Bacterial/microbiology , Skin Diseases, Bacterial/physiopathology , Skin Diseases, Bacterial/psychology , Stress, Psychological , Survivors/psychology , United States
18.
N J Med ; 101(9 Suppl): 45-50; quiz 50-2, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15497734

ABSTRACT

The DHSS and federal agencies have expanded their surveillance efforts to improve existing methods of reporting notifiable communicable diseases and to include additional data sources that might provide a more comprehensive view of disease activity in New Jersey. Currently, the DHSS is evaluating these efforts and recognizes several issues that need to be addressed, including: assessment of the timeliness, completeness, and accuracy of surveillance data; validation of surveillance data through comparison with hospital uniform billing data; characterization of the sensitivity of alerts through examination of reasons for identified aberrations in disease activity; evaluation of DHSS staffs and LINCS epidemiologists' follow-up efforts in response to alerts; evaluation of cumulative data trends to determine patterns in baseline disease activity (e.g., variations in disease activity attributed to seasonality); development of methods to integrate data from all surveillance efforts to provide timely, comprehensive, and coordinated summaries of disease activity and to distribute these summaries regularly to all New Jersey public health partners to better inform public health and clinical management; and development of a coordinated multi-agency response plan in conjunction with adjacent states. Though the DHSS hopes that these surveillance efforts will contribute to the early detection of sentinel events that might represent possible bioterrorist or emerging infectious disease threats, the DHSS will also need to engage the medical community more fully in surveillance activities. In previous experiences, astute clinicians were responsible for the identification of the first cases of West Nile virus, anthrax, and SARS. Therefore, to further ensure the success of its surveillance efforts, the DHSS will also need to continue educating clinicians about its surveillance activities and the importance of timely reporting of patients with illness patterns that might suggest an unusual infectious disease outbreak associated with bioterrorism or emerging infectious diseases.


Subject(s)
Communicable Disease Control/standards , Communicable Diseases/epidemiology , Disease Notification/standards , Disease Outbreaks/prevention & control , Population Surveillance/methods , Communicable Disease Control/trends , Communicable Diseases/diagnosis , Female , Humans , Incidence , Male , New Jersey/epidemiology , Public Health Practice , Risk Assessment , Risk Management
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