occupational health update: extended care facilities

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Occupational Health Update: Extended Care Facilities James J. Hill III, MD MPH FACOEM Associate Professor & Program Director Department of Physical Medicine & Rehabilitation University of North Carolina School of Medicine Medical Director, Occupational Health, UNC Chapel Hill Associate Medical Director, Occupational Health, UNC Hospitals Diplomate, American Board of Physical Medicine & Rehabilitation Diplomate, American Board of Preventive Medicine/Occupational Medicine Certified Strength and Conditioning Specialist (CSCS), NSCA

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Occupational Health Update:Extended Care Facilities

James J. Hill III, MD MPH FACOEMAssociate Professor & Program Director

Department of Physical Medicine & RehabilitationUniversity of North Carolina School of Medicine

Medical Director, Occupational Health, UNC Chapel HillAssociate Medical Director, Occupational Health, UNC Hospitals

Diplomate, American Board of Physical Medicine & RehabilitationDiplomate, American Board of Preventive Medicine/Occupational Medicine

Certified Strength and Conditioning Specialist (CSCS), NSCA

Goals

• Understand occupational health services in a healthcare facility

• Understand pre-exposure evaluation and vaccine-preventable disease for healthcare personnel

• Understand post-exposure prophylaxis for occupational-acquired infectious diseases

• Understand how to manage exposure to blood or potentially infectious material

• Understand basic workplace accommodations in the setting of the ADA

Disclosures• I am actively seeking various sources of revenue

that will allow me to add substantial bias to the following information – but I have none at this time.

• The original presentation for LTC facilities/SPICE was developed by Dr. David Weber, Medical Director, Hospital Epidemiology and Occupational Health Services, UNC Hospitals

Occupational Health Services

Health care facilities• Top five hazards (OSHA 2015)

» Musculoskeletal Disorders related to patient or resident handling

» Bloodborne Pathogens

» Workplace Violence

» Tuberculosis

» Slips, Trips and Falls

Health care facilities• Infections

» Aerosol/droplet• Viral• Pertussis• Tuberculosis

» Bloodborne pathogens• HIV• HBV• HCV

» Contact• Syphilis• MRSA• Norovirus

Health care facilities• Other hazards

» Chemical• Solvents, cleaning supplies, medical gases

» Radiation• Ionizing radiation, radioisotopes, lasers

» Electrical» Workplace Violence» Stress» Shift work

Workplace Safety

• Goals» To provide a safe environment for patients

and health care personnel (HCP)» To minimize risk of injury» To minimize risk of exposure to infectious

disease• How?

» Commitment to health and safety» Formal organized program to evaluate risks in

the workplace » Formal organized program to provide

effective, efficient care to the affected patient and/or HCP

Traditional View ofWorkplace Safety

Workplace Safety

• Prevention is superior to treatment• A safe work environment reduces workplace

costs while improving patient safety• The tools that we use for reducing

occupationally acquired infections can also reduce the risk of injuries

Occupational Health• Pre-employment screening

» HCP-recommended vaccinations» Employment physical » Drugs/alcohol screening» Allergy screening (gloves)» Baseline TB testing» Fit test medical clearance » Hearing evaluation/audiogram» Fitness-for-duty

• pregnancy, immunocompromised, security-sensitive

Occupational Health• Annual

» TB screening (facility and/or regulatory dependent)

» Influenza vaccination» DOT/FMCSA drug/alcohol testing (facility

dependent)» Policy development» Education » Wellness (facility dependent)

Occupational Health• Event-driven

» Communicable disease exposures» Blood-borne pathogens» Contact investigations» Acute injury» Infection Control» Ergonomic evaluation» Indoor air quality» For cause drug/alcohol testing» ADA/FMLA/Fitness-for-Duty

OSHA

CDC/NIOSH

Legal/Administration

Worker’s Compensation

Infection Control

Workplace Safety

State/Local Health Departments

DHHS

Health Care Personnel

Centers for Medicare Services

Occupational Health

Pre-exposure prophylaxis

Vaccine Preventable Diseases• Anthrax• Diphtheria• Hepatitis A/B/D• H. influenza type• Human

papillomavirus (HPV)

• Influenza A and B• Japanese

encephalitis• Lyme disease• Measles• Monkeypox• Mumps• Rabies

• Meningococcal A,C,Y,W135

• Meningococcal B• Pertussis• Pneumococcal• Poliomyelitis• Rotavirus• Rubella• Smallpox• Tetanus• Tuberculosis• Typhoid fever• Varicella (Zoster)• Yellow fever

Why do I have to get vaccinated? • Vaccine-preventable diseases haven’t gone away.• Vaccination can mean the difference between life

and death.» In the US, vaccine-preventable infections kill

more individuals annually than HIV/AIDS, breast cancer, or traffic accidents. Approximately 50,000 adults die each year from vaccine-preventable diseases in the US.

• Vaccines are safe and effective.• When you get sick, your children, grandchildren,

and parents are at risk, too.

I’ve heard that vaccines don’t work

So, do I have to get vaccinated?• 10A NCAC 13D .2209 INFECTION CONTROL

» (a) A facility shall establish and maintain an infection control program for the purpose of providing a safe, clean and comfortable environment and preventing the transmission of diseases and infection.

I can’t get vaccinated, I’m …….• Pregnant

» Live-attenuated vaccines contraindicated (with some exceptions)

• Immunocompromised» Case-dependent, concern is vaccine efficacy as

well as patient safety• Allergic to eggs

» Vaccine-dependent (may have egg-free formulations available)

• On blood thinners» “Let me see your arm”

• Afraid of needles» “Quick, look over there”

I can’t get vaccinated, I’m …….“Not willing to get vaccinated, despite all the

things you have just told me ”

Disease Herd Immunity ThresholdDiphtheria 85%

Measles 83-94%Mumps 75-86%

Pertussis 92-94%Polio 80-86%

Rubella 80-85%Smallpox 83-85%

”Pick battles that are small enough to win, big enough to be important”

Immunization documentationVaccine Birth before

1957MD Dx + Serology Self Report Documented

Vaccination

Mumps 1 Yes3 No

Measles 1 Yes3 No

Rubella 1,2 No No

Varicella No Yes 4 No

Hepatitis B No >10 MIU/mL4 No

Pertussis No No No No

Influenza No No No No

1Consider immunization of HCP born before 1957, recommend during an outbreak; 2All HCP of childbearing potential should be immunized; 3requires lab confirmation; 4Obtain 1-6 months post last vaccine dose

Weber DJ, Schaffner W. ICHE 2011;32:912-4

Specific Vaccines

Hepatitis B

• Indications» Universal; HCP with potential blood exposure

(OSHA required OR signed refusal)• Administration

» Prior to administration do not routinely perform serologic screening for HB unless cost effective

» After 3rd dose, test for immunity (>10 mIU/mL){OSHA required}; if inadequate provide 3 more doses and test again for immunity; if inadequate test consider as “non-responder”

» If non-immune after 6 (or 3) doses, test for HBsAg

050

100150200250300350

1985 1987 1989 1991 1993 1995 1997 1999

Year

Inci

denc

e pe

r 10

0,00

0

Estimated Incidence of HBV infections among HCP and General Population,

United States, 1985-1999

OSHA mandate (1991)

Influenza vaccines• Standard IM inactivate influenza vaccine (TIV) {>

6 months}• Inhaled live-attenuated influenza vaccine (LAIV)

{ages 2-49}• Other formulations

» High titer influenza vaccine {>65 years}» Intradermal influenza vaccine {18-64 years}» Cell culture-based influenza vaccine^ {>18 years}

(egg-free)» Two 2 quadrivalent influenza (2 A, 2 B strains)

vaccines {>3}» Recombinant influenza (HA only) vaccine^ {18-49}

(egg-free)

Influenza vaccines• ACIP recommendations

» 1 annual dose for all persons > 6 months of age» Required to be offered to residents and HCP in ECFs

in NC» Immunize as soon as vaccine becomes available for

the current season

Measles, Mumps, Rubella (MMR)• Measles

» Born before 1957: Consider immune (except during outbreak): Born after 1957: 2 doses

» Immunity = Appropriate immunizations or positive serology

• Mumps» Born before 1957: Consider immune (except

during outbreak): Born after 1957: 2 doses» Immunity = Appropriate immunizations or

positive serology• Rubella

» 1 dose of MMR to susceptible women of childbearing potential

» Immunity: Positive serology or documented vaccine

Varicella

• Special consideration should be given to those who have close contact with» persons at high risk for severe disease (e.g.,

immunocompromised persons)» persons are at high risk for exposure or

transmission (e.g., teachers of young children, college students, military recruits, international travelers)

• Immunity» birth before 1980 (not HCP or pregnant

women), history of varicella or zoster by a HCP, positive serology, or laboratory evidence of infection

Zoster Vaccine

• One dose for persons > 60 years of age regardless of whether they had a prior episode of zoster» FDA approved for persons > 50 years of age -

ACIP statement to be delayed (pending resolution of vaccine shortage)

» Live attenuated vaccine; avoid in immunocompromised persons

Tetanus-diphtheria-acellularpertussis (/Tdap)

• Substitute 1 dose Tdap for all adults when Td booster due» May be use to provide tetanus PEP» Provide to all adults with exposure to young

children (no delay after Td)» Recommended for pregnant women

(preferably 2nd or 3rd trimester)» Only one dose of Tdap is required, employees

who are 10 years out from Tdap should be boosted with Td.

Meningococcal Vaccine

• Recommended for adults had high risk of disease (persistent complement deficiency, functional or anatomic asplenia, or HIV infection (adolescents))» 2-dose primary series administered 2-months apart

for persons aged 2-54 MCV4,» persons < 55 years; MPSV4 persons > 56 years

Pneumococcal Vaccines• Polysaccharide vaccine (PPSV23)

» Contains 23 different pneumococcal strains» FDA approved for all person > 50 years of age» FDA approved for high risk persons 19-64 years of age

• Conjugate vaccine (PCV13)» Contains 13 different pneumococcal strains» Conjugation with diphtheria toxin may improve

immunogenicity» FDA approved for all person > 50 years of age» When indicated only a single dose is recommended for

adults

Pneumococcal Vaccines

• Adults aged 19-64 with immunocompromising conditions or anatomical/functional asplenia» Similar to adults aged > 65, however, can give

second vaccine 8 weeks after initial vaccine» Adults aged 19-64 years who reside in nursing

home or long-term care facility: Administer PPSV23

Exposure Assessment

Exposure Disease

Dose Host

Exposure Assessment

• You have to be exposed to be at risk for the disease» ex. Blood on intact skin, limited time in patient

room

• The definition of exposure is agent-specific

Exposure Assessment

• Potentially infectious material» Contaminated fluids: blood, CSF, vaginal

secretions, semen, synovial, pleural, peritoneal, pericardial, amniotic

• Route of exposure» Percutaneous» Mucous membrane» Non-intact skin

• Risk» HIV, HBV, HCV

Exposure Assessment

• Droplet» Sneezing (velocity 50 m/s; distance 6 m)» Coughing (velocity 10 m/s; distance 2 m)» Breathing (velocity 1 m/s; distance <1 m)

• Route of exposure» Mucous membrane (hand-oral)» Non-intact skin

• Risk» Influenza, adenovirus, RSV, pertussis, N.

meningitides, group A streptococcus

Exposure Assessment

• Contact» Stool, draining wounds, uncontrolled secretions,

pressure ulcers, or presence of ostomy tubes and/or bags draining body fluids

• Route of exposure» Mucous membrane (hand-oral)» Non-intact skin

• Risk» norovirus, rotavirus, C. difficile, syphilis

Exposure Assessment

• Airborne• Route of exposure

» Respiratory» Contact with infected fluid

• Risk» TB, measles, chickenpox, disseminated zoster,

zoster in immunocompromised patient

Exposure Assessment

• Exposure is agent-specific• Ex. Tuberculosis

» Risk of TB infection is determined by duration of exposures (days to weeks, not minutes to hours)

» Household contacts have different ventilation requirements related to air exchanges per hour

» However, there is no ”safe time” to be exposed to TB

Post-exposure prophylaxis

Plague doctor(Library of Medicine/CDC)

Ebola doctor(UNC School of Medicine)

Post-exposure prophylaxis

• Pertussis» Azithromycin (regardless of vaccine status)

• Meningococcal» Ciprofloxacin

• Influenza» Antivirals (depends on sensitivities)

• Human Bite» Augmentin

• Chickenpox/Shingles» Vaccination

• Norovirus» Supportive, removal from work until

asymptomatic

Bloodborne Pathogens

Bloodborne Pathogens

• Approximately 385,000 needle sticks and other sharps-related injuries to hospital-based healthcare personnel each year.

• 88% (50/57) of the documented cases of occupational HIV transmission from 1985-2004 involved a percutaneous exposure. Of those, 45/57 involved a hollow-borne needle.

• 41% of sharp injuries occur during use; 40% after use/before disposal; 15% during/after disposal

OSHA BloodbornePathogens Standard

• Employers must establish a written exposure control plan and provide annual training

• Mandates use of universal precautions (all body fluids assumed contaminated except sweat)

• Employers must utilize engineering and work practice controls to minimize/eliminate exposure» Needleless devices, single-hand recapping,

handwashing stations, sharps containers, laundry, disposal of contaminated material

(29 CFR 1910.1013)

OSHA BloodbornePathogens Standard

• Requires offering hepatitis B vaccine to persons with the potential for exposure

• Testing of exposed employees for Hepatitis B and HIV

• Post-exposure prophylaxis must be immediately available as per CDC guidelines

(29 CFR 1910.1013)

OSHA BloodbornePathogens Standard

• All work-related needle stick injuries and cuts from sharp objects that are contaminated with another person's blood or other potentially infectious material are OSHA-reportable regardless of the source patient disease status.

Incidence of bloodborne pathogen exposures, UNC Hospitals, 1997-2011

Bloodborne Pathogens• Risk (percutaneous exposure)

» HBV• 22.0 – 30.0% (HBeAG+)• 1.0 – 6.0% (HBeAG-)

» HCV• 1.8%

» HIV• 0.3% (1 in 300)

• Risk (mucous membrane)» HBV

• Yes (rate unknown)» HCV

• Yes (rate unknown but very small)» HIV

• 0.1% (1 in 1000)• < 0.1% (non-intact skin)

CDC, 2003

RISK

Post-exposure pathway

• Test source for hepatitis B (HBsAg), hepatitis C, HIV (consider rapid test)

• Provide hepatitis B prophylaxis, if indicated • Provide follow-up for hepatitis C, if indicated• If source HIV+ or at “high risk” for HIV, offer

employee HIV prophylaxis per CDC protocol

Post-exposure pathway

• 10A NCAC 41A .0202• CONTROL MEASURES – HIV

» When the source case is known, the attending physician or occupational health provider responsible for the exposed person shall notify the healthcare provider of the source case that an exposure has occurred.

» This healthcare provider shall arrange HIV testing of the source person (unless known to be HIV+) and notify the OHS provider of the test results.

» Source patient consent is not required

Current HIV PEP

• Three-drug regiment» Tenofovir-emtricitabine (Truvada) + raltegravir

(Isentress) for 4 weeks» Other regiments are available for known HIV-

source patients with specific drug resistance but these cases are rare.

Hepatitis B

• Universal; HCP with potential blood exposure (OSHA required or HCP may decline)» No need to routinely obtain Hep B titers if an

employee has documented vaccine series and a positive titer

» In practice, we usually titer and give a booster if titer is < 10

» For known non-responders, they should get Hepatitis B Immune Globulin (HBIG) within 24 hours (up to 7 days after exposure)

Hepatitis C

• No post-exposure prophylaxis

Follow-up testing

• Hepatitis B» Not required if employee has immunity

• HIV» Dependent on source patient and available

testing• Hepatitis C

» Dependent on source patient, test for HCV antibodies and HCV RNA

Americans with Disability Act

ADA

• Modifications» making existing facilities accessible;» job restructuring;» part-time or modified work schedules;» acquiring or modifying equipment;» changing tests, training materials, or

policies;» providing qualified readers or interpreters;» reassignment to a vacant position

ADA• Reasonable modifications

• Modifications or adjustments to a job application process that enable a qualified applicant with a disability to be considered for the position such qualified applicant desires; or

• Modifications or adjustments to the work environment, or to the manner or circumstances under which the position held or desired is customarily performed, that enable a qualified individual with a disability to perform the essential functions of that position;

• Modifications or adjustments that enable a covered entity's employee with a disability to enjoy equal benefits and privileges of employment as are enjoyed by its other similarly situated employees without disabilities.

ADA

• The employer does not have to» Eliminate an essential function of the job» Adopt a lower production standard» Provide personal use items for use on or off

the job (may provide job-related items) » Provide personal use amenities (unless they

are provided to employees without disabilities)

ADA

• Undue hardship» No change or modification is required if

significant difficulty or expense will be incurred and focuses on the resources and circumstances of the particular employer in relationship to the cost or difficulty of providing a specific accommodation.

» Undue hardship refers not only to financial difficulty, but to reasonable accommodations that are unduly extensive, substantial, or disruptive, or those that would fundamentally alter the nature or operation of the business.

» This is decided on a case-by-case basis

Take your son to work day

Questions and (hopefully) Answers?

Contact Information

[email protected]

Thanks!