| Literature DB >> 34362540 |
Erica S Shenoy1, David J Weber2.
Abstract
An effective occupational health program is a key aspect of preventing exposure to infectious agents and subsequent infection, as well as evaluation and management of postexposure prophylaxis and infections in health care personnel (HCP) by educating HCP regarding proper handling of sharps, early identification and isolation of potentially infectious patients, implementation of standard and transmission-based precautions, and offering counseling of HCP regarding nonroutine prophylaxis. Occupational health services (OHS) must also apply standardized processes for determining when exposures have occurred and providing appropriate management, and provide immediate availability of a medical evaluation following a nonprotected exposure to an infectious disease.Entities:
Keywords: Health care personnel; Immunization; Occupational health; Preexposure prophylaxis; Vaccines
Mesh:
Substances:
Year: 2021 PMID: 34362540 PMCID: PMC8331250 DOI: 10.1016/j.idc.2021.04.008
Source DB: PubMed Journal: Infect Dis Clin North Am ISSN: 0891-5520 Impact factor: 5.982
Fig. 1The hierarchy of controls. Interventions at the top of the hierarchy can potentially be more effective than those at the bottom. Elimination and substitution strategies are highly effective but can be difficult to implement. An example of an effective elimination strategy is vaccination. Engineering controls are designed to remove a hazard before the hazard comes in contact with the worker. Use of airborne infection isolation rooms for airborne diseases such as measles is an example of engineering controls. Administrative controls, such as symptom screening of visitors, patients, and HCP, can be challenging to maintain over time. Use of personal protective equipment (PPE), although highly effective when used correctly and consistently, requires effort by HCP to achieve protection.
Commonly cited references related to health care personnel occupational exposure
| Author | Title | Most Recently Updated | Link |
|---|---|---|---|
| CDC, National Center for Emerging and Zoonotic Infectious Diseases, Division of Healthcare Quality and Promotion | Infection Control in Healthcare Personnel: Infrastructure and Routine Practices for Occupational Infection Prevention and Control Services | 2019 | |
| CDC | Recommended Vaccines for Healthcare Workers | 2020 | |
| ACIP | ACIP Vaccine Recommendations and Guidelines | 2020 | |
| Society for Healthcare Epidemiology of America | Management of Healthcare Personnel Living With Hepatitis B, Hepatitis C, or Human Immunodeficiency Virus in US Healthcare Institutions | 2020 |
Abbreviation: ACIP, Advisory Committee on Immunization Practices.
Methods of showing proof of immunity of health care personnel
| Vaccine | Birth Before 1957 | Physician Diagnosis | Positive Serology | Self-Report | Documented Appropriate Vaccine Series |
|---|---|---|---|---|---|
| Mumps (MMR) | Yes | Yes | Yes | No | Yes |
| Measles (MMR) | Yes | Yes | Yes | No | Yes |
| Rubella (MMR) | Yes | No | Yes | No | Yes |
| Varicella | No | Yes | Yes | Yes | Yes |
| Hepatitis B | No | — | >10 mIU/mL | No | Yes |
| Influenza | No | No | No | No | Yes |
| SARS-CoV-2 | No | No | No | No | Yes |
“Yes” in any column is acceptable evidence of immunity.
Greater than 96% of HCP born before 1957 were shown to be immune to measles, mumps, and/or rubella.
Abbreviation: MMR, measles, mumps, rubella.
Written documentation (ie, signed by a health care provider).
Consider immunization of HCP born before 1957; recommend during an outbreak.
All HCP of child-bearing potential should be immunized.
Requires laboratory confirmation of infection.
Based on published literature: greater than 97% of HCP born before 1980 were shown to be immune to varicella in 2014.
Obtain anti–hepatitis B surface antibody (anti-HBs) titer, 1 to 2 months after the last vaccine dose; if immunization is remote and anti-HBs titer not available, see text for management.
Immunizations recommended for nonimmune health care personnel
| Vaccine | Health Care Personnel | Comments |
|---|---|---|
| Mumps | All (2 doses) | Provide as MMR |
| Measles | All (2 doses) | Provide as MMR |
| Rubella | All (1 dose) | Provide as MMR |
| Varicella | All (2 doses) | — |
| Hepatitis B | HCP with potential exposure to blood or contaminated body fluids (2 or 3 doses depending on vaccine) | — |
| Meningococcal (serogroups A, C, Y, W) | Clinical microbiologists (1 dose; booster every 5 y) | All vaccines available are now conjugate products |
| Meningococcal (serogroup B) | Clinical microbiologists (2 or 3 doses, depending on manufacturer); booster every 2–3 y | MenB-FHbp and MenB-4C are not interchangeable |
| Influenza | All (1 dose each year) | HCP who care for severely immunocompromised persons who require care in a protected environment should receive IIV or RIV; HCP who receive LAIV should avoid providing care for severely immunocompromised persons (ie, persons receiving care in protected hospital unit such as BMTU) for 7 d after immunization |
| SARS-CoV-2 | All (frequency of immunization not yet established) | |
Abbreviations: BMTU, bone marrow transplant unit; IIV, inactivated influenza vaccine; LAIV, live, attenuated influenza vaccine; RIV, recombinant influenza vaccine.
Recommended work restrictions for health care personnel colonized/exposed or infected with selected infectious agents
| Infection or Infectious Agent | Exposed or Colonized | Infected (Duration of Restrictions) |
|---|---|---|
| Conjunctivitis (adenovirus) | Exposed; no restriction unless illness develops | Restrict from patient contact and contact with the patient’s environment (until discharge ceases) |
| Cytomegalovirus | No restriction | No restriction |
| Diarrheal diseases | No restriction unless illness develops | Acute disease: exclude from duty (until >48–72 h after symptoms resolve) |
| Diphtheria | Exposed: no restriction unless illness develops | Exclude from duty (until antimicrobial therapy completed and 2 cultures obtained ≥24 h apart are negative) |
| Hepatitis A | Exposed: no restriction unless illness develops | Restrict from patient contact, contact with patient’s environment, and food handling (until 7 d after onset of jaundice) |
| Hepatitis B (chronic) | — | Restrictions based on review of only HCP who perform exposure-prone procedures by expert panel (see text) |
| Hepatitis C | — | Restrictions based on review of HCP who perform exposure-prone procedures by expert panel (see text) |
| Herpes simplex (genital) | — | No restriction |
| Herpes simplex (hands; herpetic whitlow) | — | Restrict from patient contact and contact with the patient’s environment (until lesions heal) |
| Herpes simplex (orofacial) | — | Evaluate for need to restrict from care of high-risk patients |
| HIV | — | Restrictions based on review of HCP who perform exposure-prone procedures by expert panel (see text) |
| Measles | Exposed (susceptible HCP): exclude from duty (from the fifth day after first exposure through 21st day after last exposure and/or after rash appears) | Exclude from duty (until 4 d after the rash appears) |
| Meningococcal infections | Exposed: no restriction unless illness develops | Exclude from duty (until 24 h after start of effective therapy) |
| Methicillin-resistant | Colonized: no restrictions unless or ill or epidemiologically/molecular test linked to patient infections | Allow to work provided lesions can be contained under a bandage and clothes; if lesions on exposed area (eg, hand/wrists, face/neck), exclude from duty (until lesions healed) |
| Mumps | Exposed (susceptible HCP): exclude from duty (from the 12th day after first exposure through 26th day after last exposure or after onset of parotitis) | Exclude from duty (until 9 d after onset of parotitis) |
| Pertussis | Exposure (asymptomatic): no restriction unless develops illness (PEP recommended) | Exclude from duty (from beginning of catarrhal stage through third week after onset of paroxysms or until 5 d after start of effective antimicrobial therapy) |
| Rubella | Exposed (susceptible HCP): exclude from duty (from seventh day after first exposure through 21st day after last exposure) | Exclude from duty (until 5 d after rash appears) |
| Group A | Colonized: no restrictions unless or ill or epidemiologically/molecular test linked to patient infections | Restrict from patient care, contact with patient’s environment, or food handling (until 24 h after adequate treatment started) |
| Tuberculosis | Latent tuberculous infection: no restrictions | Active pulmonary tuberculosis; exclude from duty (until proved noninfectious) |
| Varicella | Exposed (susceptible): exclude from duty from 10th day after first exposure through 21st day (27th day if varicella immune globulin provided) after last exposure | Exclude from duty (until all lesions dried and crusted) |
| Zoster | Exposed (susceptible): same as varicella | Localized, in healthy HCP: allow to work provided lesions can be contained under a bandage and clothes; if lesions on exposed area (eg, hand/wrists, face/neck), exclude from duty (until lesions dried and crusted) |
| Viral respiratory tract infections (acute) | No restrictions unless illness develops | Febrile: exclude from duty (until afebrile for >24 h) |
| SARS-CoV-2 | Detailed recommendations related to HCP restrictions after exposure to SARS-CoV-2 are available | |
Consider restrictions if HCP exposed to highly contagious disease transmitted by the respiratory route or close contact (eg, MERS-CoV [Middle East respiratory syndrome coronavirus], Ebola).
| Airborne | Bites | Blood Borne | Contact (Direct and Indirect) | Droplet |
|---|---|---|---|---|
Measles Tuberculosis (pulmonary, laryngeal) Varicella zoster virus (primary varicella or disseminated herpes zoster) | Rabies Tetanus | HBV HCV HIV | Anthrax (cutaneous)
Hepatitis A MRSA SARS-CoV-2 Varicella zoster virus (herpes zoster) Herpes simplex | Diphtheria Influenza Invasive group A streptococcus Invasive Pertussis Plague SARS-CoV-2 |
| At initial employment | Evaluation for ability to perform job functions Screen for illicit drugs Medical evaluation of selected HCP Department of transportation (required for use of certain motor vehicles) Flight physical (required of pilots) Police/security for use of weapons Review of immunity to vaccine-preventable diseases ( Evaluation for tuberculosis Symptom review for active tuberculosis Testing for latent tuberculosis (TST or IGRA; IGRA preferred) Allergy screening for common health care–associated products Latex/natural rubber, germicides (antiseptics, disinfectants) Counseling for pregnant or immunocompromised personnel (voluntary) Education Fire and electrical safety Prevention of sharps injury Appropriate hand hygiene and proper use of personal protective equipment Workplace violence Disaster planning: weather, bomb threats, biothreats, chemical spills Reporting infectious disease exposures, injuries, illnesses OSHA required (if applicable): blood-borne pathogens, tuberculosis/respiratory protection |
| Annual | Symptom evaluation for tuberculosis Review of immunity to vaccine-preventable diseases Influenza immunization |
| Miscellaneous | Hearing evaluation if part of OSHA-required hearing conservation program Test for color blindness if performing high-level disinfection |
| Education | OSHA required (if applicable): blood-borne pathogens, tuberculosis/respiratory protection Others as recommended/required by health care facility |
| When needed | Evaluation for possible communicable disease Consideration for treatment and job restriction/furlough if disease poses threat to patients or other HCP Evaluation for postexposure prophylaxis Consideration for treatment and job restriction/furlough if disease poses threat to patients or other HCP Evaluation of injured personnel (eg, strains, sprains, lacerations) Provide first aid Refer to emergency department or specialized clinic for severe injuries Provide long-term care Communicate with worker’s compensation department Return-to-work evaluation for non–work-related injuries/illnesses Fit-for-duty examination (may include drug and alcohol testing) |