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1.
J Occup Environ Med ; 2024 Jun 24.
Article in English | MEDLINE | ID: mdl-38913827

ABSTRACT

OBJECTIVE: This paper aims to review the risks associated with using lentiviral and retroviral vectors in research and clinical settings and to propose an update to an effective treatment plan. METHODS: Risks of exposure were evaluated based on vector design, safety features, viral tropism, transgene, and means and modes of transmission. These risks were weighed against the potential risks and benefits of current HIV medications. RESULTS: We recommend the following post-exposure prophylactic treatment for significant lentiviral vector exposures: 1) dolutegravir 50 mg. taken once a day for 7 days; and 2) tenofovir disoproxil fumarate 300 mg. taken once a day for 7 days (28 days of both medications for replication-competent vectors). CONCLUSIONS: Due to the highly efficient delivery of transgenes by modern lentiviral and retroviral vectors, post-exposure prophylaxis is indicated to prevent vector integration and oncogenic risks.

2.
Clin Infect Dis ; 76(3): e319-e326, 2023 02 08.
Article in English | MEDLINE | ID: mdl-35666508

ABSTRACT

BACKGROUND: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant has spread rapidly throughout the world since being identified in South Africa in November 2021. Few studies have assessed primary series and booster vaccine effectiveness against Omicron among US healthcare workers. METHODS: We conducted a test-negative case-control design to estimate BNT162b2 and mRNA1273 primary vaccination and booster effectiveness against SARS-CoV-2 infection and symptomatic coronavirus disease 2019 during an Omicron surge among employees of the University of Pennsylvania Health System. The study period was between 1 July 2021 and 5 April 2022. We defined the Delta period as 1 July to 12 December 2021 and the Omicron period as beginning 12 December 21. RESULTS: Our sample included 14 520 tests (2776 [19%] positive)-7422 (506 [7%] positive) during Delta and 7098 (2270 [32%] positive) during Omicron. Benchmarked against Delta, the vaccine effectiveness of 2 vaccine doses was lower during Omicron, with no significant protection against infection. Booster doses added significant protection, although they also showed reduced effectiveness during Omicron. Compared with findings in employees who had received 2 vaccine doses, 3 doses of BNT162b2 had a relative effectiveness of 50% (95% confidence interval, 42%-56%) during Omicron, relative to 78% (63%-87%) during Delta; 3 doses of mRNA1273 had a relative effectiveness of 56% (45%-65%) during Omicron, relative to 96% (82%-99%) during Delta. Restricting the sample to symptomatic tests yielded similar results to our primary analysis. After initial waning in BNT162b2 booster protection against infection, it remained largely stable for ≥16 weeks after vaccination. CONCLUSIONS: Our findings provide a strong rationale for boosters among healthcare workers in the Omicron era.


Subject(s)
COVID-19 , Vaccines , Humans , BNT162 Vaccine , SARS-CoV-2 , COVID-19/prevention & control , Health Personnel , 2019-nCoV Vaccine mRNA-1273 , RNA , RNA, Messenger
3.
Appl Biosaf ; 27(3): 169-190, 2022 Sep 01.
Article in English | MEDLINE | ID: mdl-36196095

ABSTRACT

Introduction: Field work with bats is an important contribution to many areas of research in environmental biology and ecology, as well as microbiology. Work with bats poses hazards such as bites and scratches, and the potential for exposure to infectious pathogens such as rabies virus. It also exposes researchers to many other potential hazards inherent to field work, such as environmental conditions, delayed emergency responses, or challenging work conditions. Methods: This article discusses the considerations for a thorough risk assessment process around field work with bats, pre- and post-occupational health considerations, and delves into specific considerations for areas related to biosafety concerns-training, personal protective equipment, safety consideration in field methods, decontamination, and waste. It also touches on related legal and ethical issues that sit outside the realm of biosafety, but which must be addressed during the planning process. Discussion: Although the focal point of this article is bat field work located in northern and central America, the principles and practices discussed here are applicable to bat work elsewhere, as well as to field work with other animal species, and should promote careful considerations of how to safely conduct field work to protect both researchers and animals.

5.
J Occup Environ Med ; 62(7): e355-e369, 2020 07.
Article in English | MEDLINE | ID: mdl-32730040

ABSTRACT

: On May 17, 2019, the US Centers for Disease Control and Prevention and National Tuberculosis Controllers Association issued new Recommendations for Tuberculosis Screening, Testing, and Treatment of Health Care Personnel, United States, 2019, updating the health care personnel-related sections of the Guidelines for Preventing the Transmission of Mycobacterium tuberculosis in Health-Care Settings, 2005. This companion document offers the collective effort and experience of occupational health, infectious disease, and public health experts from major academic and public health institutions across the United States and expands on each section of the 2019 recommendations to provide clarifications, explanations, and considerations that go beyond the 2019 recommendations to answer questions that may arise and to offer strategies for implementation.


Subject(s)
Disease Transmission, Infectious/prevention & control , Health Personnel/standards , Tuberculosis/diagnosis , Tuberculosis/therapy , Advisory Committees/organization & administration , Advisory Committees/standards , Centers for Disease Control and Prevention, U.S./standards , Humans , Infection Control/standards , Latent Tuberculosis/diagnosis , Latent Tuberculosis/prevention & control , Latent Tuberculosis/therapy , Latent Tuberculosis/transmission , Mass Screening/standards , Mycobacterium tuberculosis/isolation & purification , Occupational Health/standards , Risk Assessment , Societies, Medical/standards , Tuberculosis/prevention & control , Tuberculosis/transmission , United States
6.
Mayo Clin Proc ; 94(10): 2127-2141, 2019 10.
Article in English | MEDLINE | ID: mdl-31515104

ABSTRACT

Medical Center Occupational Health (MCOH) programs must protect health care personnel (HCP) against the occupational risk of vaccine-preventable diseases. This thematic review outlines the rationale for the use of recommended vaccines in HCP; summarizes the available evidence regarding vaccine effectiveness, administration, and assessment of immunity; and provides guidance for MCOH programs navigating challenging situations.


Subject(s)
Health Personnel , Occupational Diseases/prevention & control , Occupational Health , Vaccination , Vaccines , Humans , Occupational Diseases/microbiology
10.
J Clin Virol ; 57(2): 109-14, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23434396

ABSTRACT

BACKGROUND: Nosocomial spread of varicella-zoster virus (VZV) infection can cause severe disease among vulnerable patient-populations and healthcare personnel (HCP). Limited data are available on duration of varicella vaccine-induced protection among adults and to what extent cell-mediated immunity (CMI) and antibody avidity contribute to protection. OBJECTIVE: Evaluate humoral and cell-mediated immune responses of HCP who received a 2-dose regimen of varicella vaccine, and observe the responses to a 3rd vaccine dose among HCP who were seronegative after vaccination. STUDY DESIGN: A convenience sample of HCP with documented 2 doses of varicella vaccine was used to assess acquired VZV immune parameters (cytokine production, IgG avidity). HCP seronegative after 2 doses of vaccine were offered a third dose and evaluated further. Vaccine recipients' immune responses were compared with responses from persons with history of wild-type VZV infection. RESULTS: The convenience sample consisted of 101 HCP with documented 2 doses of varicella vaccine; 12 (11.9%) were seronegative post-vaccination. 11.5% of 61 seropositive 2-dose recipients produced low avidity antibody, suggesting suboptimal response to vaccine. Seven 2-dose vaccinees who were VZV seronegative seroconverted after a third dose; however, 3/7 (42.9%) produced low avidity IgG. 142 persons with a history of varicella were all VZV IgG seropositive, and all had moderate to high avidity IgG. CONCLUSIONS: Measurements of serum IgG titers alone may not accurately reflect vaccine protection. Varicella vaccination of HCP remains important but further studies are needed to evaluate CMI and antibody avidity responses in HCP vaccinated with two doses of varicella vaccine.


Subject(s)
Chickenpox Vaccine/administration & dosage , Chickenpox Vaccine/immunology , Chickenpox/immunology , Health Personnel/statistics & numerical data , Herpesvirus 3, Human/immunology , Vaccination/statistics & numerical data , Adolescent , Adult , Aged , Antibodies, Viral/blood , Antibodies, Viral/immunology , Antibody Affinity , Chickenpox/prevention & control , Chickenpox/virology , Cross Infection/immunology , Cytokines/metabolism , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Humans , Immunity, Cellular , Male , Middle Aged , Young Adult
11.
Infect Control Hosp Epidemiol ; 33(12): 1262-5, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23143368

ABSTRACT

We surveyed physicians in a national occupational medicine society regarding diagnosis of latent tuberculosis infection in healthcare workers. Most respondents used a combination of skin testing and interferon gamma release assays. Respondents integrating interferon gamma release assays into screening placed greater importance on employee acceptability and convenience.


Subject(s)
Attitude of Health Personnel , Latent Tuberculosis/diagnosis , Latent Tuberculosis/drug therapy , Occupational Medicine , Practice Patterns, Physicians' , Health Facilities , Humans , Interferon-gamma Release Tests , Patient Acceptance of Health Care , Statistics, Nonparametric , Surveys and Questionnaires , Tuberculin Test
13.
Vaccine ; 28(13): 2517-21, 2010 Mar 16.
Article in English | MEDLINE | ID: mdl-20117259

ABSTRACT

AIM: We surveyed physicians' opinions and acceptance of influenza immunization. SCOPE: A web-based survey was sent to all physicians in two academic departments during spring 2009. RESULTS: 227 (40.5%) physicians responded. Physicians who frequently cared for high-risk patients self-reported higher immunization rates than physicians with infrequent contact (P=0.0002). There were no significant differences in immunization rates between emergency medicine (EM) and internal medicine (IM), between those with and without children at home, nor by age group. A majority (84.6%) supported mandatory vaccination. IM physicians were more supportive of mandates than EM physicians (P<0.0001). CONCLUSION: Self-reported immunization rates were high among study physicians. Acceptance of mandatory vaccination was substantial, but varied by specialty.


Subject(s)
Attitude of Health Personnel , Immunization/statistics & numerical data , Influenza Vaccines/immunology , Influenza, Human/prevention & control , Patient Acceptance of Health Care/statistics & numerical data , Physicians , Adult , Female , Humans , Influenza, Human/transmission , Male , Middle Aged
14.
Clin Infect Dis ; 46 Suppl 3: S195-203, 2008 Mar 15.
Article in English | MEDLINE | ID: mdl-18284359

ABSTRACT

After the 2001 anthrax bioterror attacks, the Centers for Disease Control and Prevention developed an algorithm to evaluate patients rapidly for suspected smallpox. A prospective, multicenter study examined the performance of this algorithm in assessing patients with an acute, generalized vesicular or pustular rash (AGVPR) admitted to emergency departments and inpatient units of 12 acute-care hospitals in 6 states. Of 26,747 patients (3.5% of all admissions) with rashlike conditions screened, 89 (1.2 patients per 10,000 admissions) had an AGVPR. Physicians or study staff classified none of 73 enrolled patients as being at high risk for having smallpox; 72 (99%) were classified as being at low risk, and 1 was classified as being at moderate risk. The discharge diagnosis for 55 (75%) of these 73 participants was varicella illness. Use of the algorithm did not result in misclassification of AGVPR as high risk for smallpox. The algorithm is a highly specific tool for clinical evaluation of suspected smallpox disease.


Subject(s)
Algorithms , Disaster Planning , Disease Outbreaks/prevention & control , Exanthema/virology , Smallpox/diagnosis , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Diagnosis, Differential , Exanthema/etiology , Female , Humans , Infant , Male , Medical Audit , Middle Aged , Prospective Studies , United States
16.
Infect Control Hosp Epidemiol ; 24(3): 202-6, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12683513

ABSTRACT

BACKGROUND: Five cases of primary varicella zoster virus (VZV) we re diagnosed among hospital healthcare workers (HCWs). All had complied with a pre-employment VZV screening program and had been considered immune. OBJECTIVES: To summarize the investigation of VZV among un-immunized HCWs and to provide recommendations for avoiding false-positive serologic tests. DESIGN: Risk of transmission of VZV to susceptible HCWs is minimized through serologic screening. Varicella vaccine is recommended for susceptible HCWs. A commercially available latex bead agglutination assay (LA) is widely used because it is rapid and easy to perform. LA was compared with the whole-cell varicella ELISA standardized in the Centers for Disease Control and Prevention (CDC) National Herpes Laboratory. SETTING/POPULATION: Large inner-city, tertiary-employee population. RESULTS: In a year, 5 HCWs presented with laboratory-confirmed primary varicella infection. Four had VZV exposures 2 weeks prior to presentation. All had documented positive VZV titers by LA performed at hire. None were offered VZV vaccination. The original LAs were judged false-positives. INTERVENTION/FOLLOW-UP INVESTIGATION: Fifty-three consecutive VZV LA samples from the hospital laboratory were retested at the CDC. Forty-four samples concurred. Of the remaining 9, 4 were positive by hospital LA but negative by CDC IgG ELISA. Four were equivocal by hospital LA but negative by CDC IgG ELISA and LA. One was positive by hospital LA but negative by LA and equivocal by ELISA at the CDC. CONCLUSION: LA may be prone to false-positive results and inappropriate for screening hospital HCWs.


Subject(s)
Chickenpox/etiology , Disease Outbreaks , Herpesvirus 3, Human/pathogenicity , Infectious Disease Transmission, Professional-to-Patient , Personnel, Hospital , Adult , Chickenpox/diagnosis , Chickenpox/transmission , Enzyme-Linked Immunosorbent Assay , False Positive Reactions , Female , Herpesvirus 3, Human/immunology , Hospitals, Urban , Humans , Immunoglobulin G/analysis , Male , Middle Aged , Pregnancy , Risk Assessment , Serologic Tests
17.
J Occup Environ Med ; 44(12): 1100-5, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12500451

ABSTRACT

The effect of both a cost control and health care management initiative (HCMI) on Workers' Compensation costs at a self-insured University Hospital was assessed. Seven cohorts of injured workers were studied. Cost control measures started in 1993 included early return to work and injury prevention programs, internal administration of legal cases, and utilization of modified duty assignments. The health care management initiative fully in place in 1997 included aggressive case management and preferred provider panel utilization. Workers' Compensation indemnity costs and lost workdays incurred by each cohort were compared. A 41 to 59% reduction in indemnity payments and 46 to 67% reduction in lost time cases were realized after the health care management initiative was fully in place. During this time, accepted claims were reduced by 10 to 15%. The quality of the provider panel, as measured by academic credentials, experience and board certification, did not change. Cost control measures, without comprehensive case management, did not decrease these parameters significantly. The health care management initiative realized reductions in lost time cases and Workers' Compensation indemnity costs.


Subject(s)
Delivery of Health Care/economics , Managed Care Programs/economics , Workers' Compensation/economics , Costs and Cost Analysis , Humans , Pennsylvania
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