Occupational Health & Infection Control Dr Faisal Al Haddad Consultant of Family Medicine & Occupational Health PSMMC
May 16, 2015
Occupational Health &
Infection Control
Dr Faisal Al Haddad
Consultant of Family Medicine & Occupational Health
PSMMC
Outlines
Occupational Health (OH)
Role of OH in Infection Control
Prevention of Blood-borne virus infections in Healthcare setting
What is occupational health?
The promotion and maintenance of the highest degree of physical, mental and social wellbeing of workers in all occupations.
(ILO/WHO, 1950)
Why Occupational Health?
To prevent occurrence of occupational injury or illness
and their costs on workers and employers
Costs on workers
Pain and suffering of the injury or illness
Possible loss of income
Possible loss of a job
Health-care costs
Costs on employers
Payment for work not performed
Medical and compensation payments
Possible reduction in the quality of work Replacement of the injured/ill worker
Time
Concern of fellow workers
Poor public relations
Occupational Health Services
Risk assessment and risk control
Pre-employment assessments
Periodic medical examinations including HS
Post-sickness absence review
Immunization
Occupational Health Services
Health education and counseling
Treatment of occupational injury or illness
Advice on compensation
Advice on environmental issues
Role of OH in Infection Control
Microbial Risk Assessment
Microbial Risk Control
Education of Health Care Workers (HCWs)
Microbial Risk Assessment
Steps:
Identification of microbiological hazards in workplace
Assessment of the risk of exposure to the microbiological hazards
Information:
Workplace surveillance (walk-through visit)
Pre-employment assessment (history, testing)
Ongoing interactions between OH and the HCW
Microbial Risk Control
Microbial Risk control is the eradication or minimization of the risk
of exposure to microbiological hazards .
Includes:
Risk control measures to prevent HCW exposure to or infection with disease
Risk control measures to manage HCWs exposed to or infected with disease
Control measures to prevent exposure to or infection with disease
1) Engineering Controls
2) Administrative Controls
3) OH Work Practices
4) Personal Protective Equipment (PPE)
OH Work Practices
Regular workplace microbial risk assessment
Pre-employment and periodic screening
Vaccination and post-exposure prophylaxis
Managing HCWs (infected, immunocompromised, dermatitis)
*OH should establish and maintain communication with appropriatedepartments (Admin, IC, Lab, Operation and Maintenance, Safety..)
Routine vaccination for HCWs
HBV: 3 doses given at 0, 1, and 6 months
DTP: primary series of 3 doses and booster doses of Td/10 y
MMR: 2 doses one month apart
Varicella: 2 doses on month apart
BCG: one dose
Meningococcal: one dose /3 y
Influenza: one dose annually
Control measures to manage HCWs exposed to or infected with disease
1. Assessment of the incident: The method of transmission Type of exposure Use of PPE Compliance with precautions
2. Assessment of the source of exposure: Communicability Diagnosis of infection
3. Assessment of the HCW exposed to or infected with disease: Determining immune status of HCW Diagnosis of infection
Management of HCWs exposed to or infected with disease
Post-exposure prophylaxis
Treatment of infected HCW
Counseling
Work restriction/reassignment/return to work Tracing close contacts
Assessing worker for fitness to work
Education of HCWs
Prevention and management of exposure to and infection with disease
Universal and additional precautions
Action recommended following potential exposure
The consequences of non-compliance
Outlines
BBV-specific exposure definition
Occupations at increased risk of exposure
Risk of transmission
Prevention of exposure/transmission
Employment implications
HIV, HBV, HCV - Vaccination - Post-exposure prophylaxis - Fitness for work
Occupational infections in Healthcare
1. Airborne Transmission: Adenovirus Diphtheria Influenza Measles Meningococcus Mumps Mycoplasma infection Parvorvirus Pertussis Rubella SARS Tuberculosis Varicella
2. Bloodborne Transmission AIDS Hepatitis B Hepatitis C Cytomegalovirus Hepatitis D virus Human parvovirus Human T-cell lymphotropic virus
3. Oral-Fecal Transmission Hepatitis A Typhoid fever
4. Direct-contact Herpes simplex Scabies and pediculosis
Exposure definition (CCDR)
A percutaneous injury from equipment contaminated with blood or body fluids, or mucous membrane or non-intact skin contact with blood or body fluids. Blood on intact skin is not an exposure.
The types of body fluids capable of transmitting BBVs: Blood, serum, plasma, and all biologic fluids visibly contaminated with
blood. Lab specimens, samples or cultures that contain concentrated BBVs. Organ and tissue transplants. Pleural, amniotic, pericardial, peritoneal, synovial, and CS fluids. Uterine/vaginal secretions or semen (HCV unlikely) Saliva for HBV only, unless contaminated with blood.
Occupations at risk of exposure to BBVs
Healthcare workers
Laboratory staff
Staff of residential for those with learning difficulties
Those handling human remains
Prison service staff in regular contact with inmates
Emergency frontline responders
The risk of transmission after exposure
After parenteral exposure to infected blood:
HIV 0.3%
Hepatitis C 3%-10% Hepatitis B 30%
Transmission is more likely where the worker has been exposed to infected blood through NSI injury than through exposure of MM.
Prevention of exposure to BBVs
Reduction in the number of blood samples taken from a patient
Safer-needle devices
Needleless drug administration
Reduce work duration and night work
Advice on bloodborne pathogen precautions and action recommended following potential exposure to blood
Bloodborne pathogen precautions
Wear gloves
Wash hands
Cover existing wounds and skin lesions
Avoid sharps
Safe handling and disposal of contaminated waste
Contd;
Avoid wearing open footwear
Clean up spillage of blood and disinfect surfaces
Protect mucus membrane of eyes with protective eyewear
Never resheath needles and never put hands in a used sharps box.
Action recommended following potential exposure to blood
Encourage bleeding
Wash the site of bleeding
Cover the bleeding site
If splashed in eye, nose or mouth wash immediately
Note the name and location of the patient concerned
Contact occupational health department
Report the accident and complete an incident-report form
Employment implications
Restriction from EEP Sickness absence
Discrimination
Loss of skilled workers
Staff shortage
Hepatitis B virus
Vaccination Strongly recommended before employment. Hepatitis B vaccines are not 100% effective in all workers.
The normal course of vaccination comprises 3 doses of vaccine over a 6month period.
HCWs with postvaccinal anti-HBs levels, one to two months after vaccine completion, ≥10 mIU/ml are considered as responders and immune against HBV infection.
In responders, booster doses of vaccine or periodic antibody concentration testing are not recommended
Non- responders can be given another course of vaccines followed by retesting. If the HCW fail to respond they need to be informed of the implications of this.
Non-responding HCWs involved in a high risk incident should be offered PEP with IG.
Hepatitis B virus
Post-exposure management
Hepatitis B vaccine + hepatitis IG within 24 hours of exposure.
HBsAg status of the source (HBsAg-positive)
Immune status of exposed person (non-immune)
Hepatitis B virus
Fitness of HBsAg-positive HCWs for work
HBeAg-positive HCWs Not allowed to carry out exposure-prone procedures (EPP) Undergoing antiviral treatment have to show that their viral load
has been reduced to <1000 GEq/ml 1 year after finishing their therapy.
HBeAg-negative HCWs Viral load >1000 GEq/ml are restricted from performing EPP Viral load <1000 GEq/ml need not have their working practices
restricted
Exposure-Prone Procedures (EPP)
Insertion of hands or fingers inside the body cavity
Hands or fingers may disappear from view
Hands or fingers may come into contact with a sharp instrument or tissue
The operator may bleed into the patient
Hepatitis C virus
Vaccination
No vaccine available
Post-exposure management
IG and antiviral agents are not recommended for PEP after exposure to HCV-positive blood.
HCWs exposed should be tested for HCV-Ab at baseline and after 6 months.
Hepatitis C virus
Fitness to work
HCV RNA-positive HCWs should not be allowed to perform EPP
HCV RNA-positive HCWs who have responded successfully to
treatment with antiviral therapy should be allowed to resume EPP
Successful response is defined as remaining HCV RNA negative six months after cessation of treatment.
HIV
VaccinationNo vaccine available
Post exposure management
Prophylaxis 300mg zidovudine + 150mg lamivudine (one Combivir tab) 28 days 200mg lopinavir + 50mg ritonavir (two Kaletra tab) 28 days HIV testing at baseline at 6-8 weeks at least 6 months post exposure
HIV (indications of PEP)
1. Type of injury: Percutaneous injury (recommended) Exposure of mucus membrane or non-intact skin (considered) Exposure of intact skin (discouraged)
2. Type of source material: Blood, body fluid containing visible blood, CSF, concentrated virus in a lab
setting (recommended) Semen, vaginal secretions, synovial, pleural, peritoneal, amniotic fluids and
tissues (considered) Urine, vomit, saliva, tears, faeces, sweats, sputum (discouraged)
3. Source patient: Known to be HIV-positive (recommended) HIV status unknown, consent refused or unavailable (considered) HIV-negative (discouraged)
HIV-positive HCWs
HIV-positive HCWs must not undertake EPP and they must receive appropriate guidance from an occupational physician.
There is little evidence of HCWs passing HIV to their patients
through normal medical procedures.
Efficient and confidential reporting channels are required to ensure that HCWs who know or suspect that they could be HIV-positive can report to the OH department.
Testing source patients
It is considered unethical to test a source patient for BBV infection without their fully informed consent.
The clinician who has received the needlestick injury should never seek the consent from the source patient.
Source patients should be counseled on the implications of the test and results including possible need to discuss any positive test with his/her sexual partner.
It is unacceptable to seek preoperative consent for source-patient testing in order to guard against an exposure incident occurring during surgery.
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