the prick will do the trick: protecting our healthcare workers from vaccine-preventable infections

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Healthcare Workers Immunization Update Rontgene M. Solante, MD., FPCP, FPSMID Phillipine Hospital Infection Control Society Annual Convention Crowne Plaza Hotel May 27, 2016

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Healthcare Workers Immunization Update

Rontgene M. Solante, MD., FPCP, FPSMID Phillipine Hospital Infection Control Society Annual Convention Crowne Plaza Hotel May 27, 2016

Rontgene M. Solante, MD

• Phil Society for Microbiology and Infectious Diseases (PSMID), Past President

• Global Steering Committee Member , MEDSCAPE for Pneumococcal Disease Prevention and Education thru vaccination

• Asian Advisory Board , Community Acquired Pneumonia Immunization Trial Adults (CAPiTA) 2015

• Chairman, Fellowship Program Adult Infectious Disease and Tropical Medicine- San Lazaro Hospital

• Medical Specialist III , National Reference Laboratory for HIV/AIDS San Lazaro Hospital

• Infection Control Chair: ManilaMed MCM, San Lazaro Hospital

• Assistant Professor , UERMMMC

• Fellow, Philippine College of Physicians and PSMID

Disclosure

• Pfizer vaccines , Asian and local advisory board member

• MSD vaccines Phil advisory board member

• Sanofi Pasteur Phil advisory board

Objectives

• Discuss the following:

• Why vaccinate healthcare workers?

• What are the currently recommended vaccines?

Definition: Healthcare personnel

Definition: Healthcare personnel

• all paid and unpaid persons working in health-care settings who have the potential for exposure to patients and/or to infectious materials, including body substances, contaminated medical supplies and equipment, contaminated environmental surfaces, or contaminated air.

• include (but are not limited to) the following

– physicians, nurses, nursing assistants, therapists, technicians, emergency medical service personnel, dental personnel, pharmacists, laboratory personnel, autopsy personnel, students and trainees, contractual staff

– clerical, dietary, housekeeping, laundry, security, maintenance, administrative, billing, and volunteers

“risk for exposure to (and possible transmission of) vaccine-preventable diseases”

1.US Department of Health and Human Services. Definition of health- care personnel (HCP). Available at http://www.hhs.gov/ash/programs/ initiatives/vacctoolkit/definition.html. Accessed October 5, 2011

2012 Recommended Immunization for Filipino Healthcare Workers PSMID-PHICS-PFV

Definition: Healthcare worker

Vaccines important for the HCW?

PUBLIC PRIVATE

Informal survey conducted during the HcW annual conventions (AMHOP, PHICS)

Why vaccinate healthcare personnel?

1. Protection against vaccine preventable diseases/infections including its complications

– protection for healthy HCP

– protection of at-risk HCPs (e.g. diabetes, immunocompromised, chronic conditions)

2. Prevent transmission of VPDs to patients and other HCPs

3. Minimize absenteeism and work flow disruption

4. Added cost for contact investigation, source of infection, diagnostics, and antibiotic treatment and prophylaxis

5 key recommended interventions preventing occupational acquisition of infection by HCP

(1) adherence to standard precautions

(2) rapid institution of appropriate isolation precautions

(3) proper use of personal protective equipment

(4) evaluation of personnel with exposure to communicable diseases for receipt of PEP

(5) appropriate immunizations

Vaccines 6th ed. 2013 Chap 66 pp 1290-1308

Healthcare risk of vaccine preventable infections

Infectious Diseases Healthcare risk

Hepatitis B • dependent on the frequency of percutaneous and mucosal exposures to blood or body fluids

• transmission from a needlestick exposure is up to 100 times more likely for exposure to HBeAg positive blood than to HIV-positive blood

• HBV can lead to chronic infection, which can result in cirrhosis of the liver, liver failure, liver cancer, and death

Influenza

• risk of occupationally acquired influenza • transmitting influenza to patients and other HCP • increased risk for severe outcomes from influenza • outbreaks in hospitals and long-term– care

facilities have been associated with low vaccination rates among HCP

SAGE recommendations for

influenza vaccination (2012)

• 5 recommended priority groups for countries using or considering introduction of seasonal influenza vaccination.

• Pregnant women highest priority group.

• Health-care workers

• Children under 5 (particularly 6-23 months)

• Elderly

• Underlying health conditions

Healthcare risk of vaccine preventable infections

Infectious Diseases Healthcare risk

Measles • highly contagious transmitted by respiratory droplets and airborne spread

• severe complications, which might result in death, include pneumonia and encephalitis

• WHO estimated 20 million measles cases occurring worldwide and approximately 164,000 related deaths

• Medical settings played a prominent role in perpetuating outbreaks of measles transmission

(1989-1991 outbreaks ; 2008 outbreaks)

Presumptive evidence of immunity to measles : •written documentation of vaccination with 2 doses of live measles or MMR •laboratory evidence of immunity •laboratory confirmation of disease, or •birth before 1957

MMWR Recommendations and Reports / Vol. 60 / No. 7 November 25, 2011

Healthcare risk of vaccine preventable infections

Infectious Diseases Healthcare risk

Mumps • health-care–associated transmission of mumps is infrequent, it might be underreported

• added economic costs because of furlough or reassignment of staff members from patient-care duties or closure of wards

Pertussis • transmission has occurred from hospital visitors to patients, from HCP to patients, and from patients to HCP

• documented outbreaks were costly and disruptive -diagnostic testing, prophylactic antibiotics, and exclusion from work

MMWR Recommendations and Reports / Vol. 60 / No. 7 November 25, 2011

Healthcare risk of vaccine preventable infections

Infectious Diseases Healthcare risk

Varicella • higher proportion of VZV infections are acquired later in life among 3rd world countries

• nosocomial transmission of VZV is well recognized and can be life-threatening to certain patients

• airborne transmission from patients with either varicella or HZ has resulted in varicella in HCP and patients

• risk for severe varicella disease with complications • pregnant women, premature infants and

immunocompromised pts

Evidence of immunity for HCP

• written documentation of vaccination with 2 doses of • laboratory evidence of immunity • laboratory confirmation of disease, • diagnosis or verification of a history of varicella disease by a

health-care provider • Diagnosis or verification of a history of HZ by a health-

careprovider

MMWR Recommendations and Reports / Vol. 60 / No. 7 November 25, 2011

Healthcare risk of vaccine preventable infections

Infectious Diseases Healthcare risk

Meningococcal Disease • Nosocomial transmission of Neisseria meningitidis is rare

• HCP increased risk after direct contact with respiratory secretions of infected persons (e.g., managing of an airway during resuscitation) and in a laboratory setting

• HCP with known HIV infection are at increased risk for meningococcal disease

Typhoid Fever • transmitted nosocomially via the hands of infected persons

Hepatitis A • HCP not at increased risk for hepatitis A virus infection because of occupational exposure

MMWR Recommendations and Reports / Vol. 60 / No. 7 November 25, 2011

Guidelines and recommendations

• 2011 Advisory Committee Immunization Practices (ACIP) Immunization of Health-Care Personnel

• 2012 PSMID – PHICS – PFV Recommended immunization for healthcare workers

• 2016 ACIP Updated Recommendations

Diseases for Which Vaccination Is Recommended

Hepatitis B

Influenza

Measles Mumps Rubella (MMR)

Pertussis

Varicella

Diseases for Which Vaccination Might Be Indicated in Certain Circumstances

Meningococcal

Typhoid Fever

Pneumococcal

Tetanus and Diphtheria

Human papilloma virus

Zoster

2011 Immunization of Health-Care Personnel Advisory Committee on Immunization Practices (ACIP)

MMWR Recommendations and Reports / Vol. 60 / No. 7 November 25, 2011

Strongly recommended

Hepatitis B

Influenza

Measles Mumps Rubella (MMR)

Tetanus, Diphtheria, acellular Pertussis (Tdap)

Varicella

Recommended

Pneumococcal

Recommended for selected HCW

Hepatitis A

Meningococcal vaccine

Rabies

Typhoid vaccine

2012 Healthcare Workers Vaccination Guide

2012 Recommended immunization for healthcare workers PSMID PHICS and PFV

2012 Healthcare Workers Vaccination Guide

Recommended

Hepatitis B

Influenza

Measles Mumps Rubella (MMR)

Tetanus, Diphtheria, acellular Pertussis (Tdap)

Varicella

HPV * (male thru age 26 years; female thru age 21 years old)

Zoster *

Recommended

Pneumococcal (PCV13; PPV23)

Hepatitis A

Meningococcal vaccine ((MenACWY) /(MPSV4)

Haemophilus influenzae type b (Hib)

2016 ACIP Healthcare personnel Vaccination Guide

Recommended for all persons who meet the age

requirement, lack documentation of vaccination, or lack

evidence of past infection; zoster vaccine is

recommended regardless of past episode of zoster

Recommended for persons with a risk

factor (medical, occupational, lifestyle,

or other indication)

2012 PSMID-PFV-PHICS 2016 ACIP

Routinely Recommended

Hepatitis B Hepatitis B

Influenza Influenza

Measles Mumps Rubella (MMR) Measles Mumps Rubella (MMR)

Tetanus, Diphtheria, acellular Pertussis (Tdap) Tetanus, Diphtheria, acellular Pertussis (Tdap)

Varicella Varicella

Human Papilloma virus

Zoster

Not Routine Recommended but based on Risk

Pneumococcal (PPV23) Pneumococcal (PCV13; PPV23)

Hepatitis A Hepatitis A

Meningococcal Meningococcal

Rabies Hemophilic influenzae type b (Hib)

Typhoid

Recommendations on Immunization of Health Care Personnel with Special Conditions

Pregnancy

HIV infection CD4 <200

Immunocompromising conditions

Chronic liver ,heart and lung dses and alcoholism

Asplenia and complement component deficiencies

Kidney failure, end- stage renal disease, receipt of hemodialysis

Diabetes Men sex with men MSM)

Influenza

Tdap

Varicella

HPV

Rabies

Zoster

MMR

Pneumococcal (PCV13

Pneumococcal (PPV23)

Hepatitis A

Hepatitis B

Meningococcal

R- recommended; UI-use if indicated; C-contraindicated Vaccines 6th ed. 2013 Chap 66 pp 1290-1308

Vaccine with specific indications on selected healthcare personnel

Vaccine Specific indications

Typhoid vaccine • Food handlers, dieticians, cooks, nutritionist • microbiologist

Meningococcal • Clinical and research microbiologists who may be routinely exposed to isolates of Neisseria meningitides

Rabies • Laboratory personnel or researchers who work with rabies virus of potentially infected animals;

• PEP may be required for potential exposure despite primary immunization

• veterinarians and veterinary students, • health care workers directly involved in care of

rabies patients • individuals directly involved in rabies control, field

workers)

Vaccines 6th ed. 2013 Chap 66 pp 1290-1308

Vaccine schedule

HEPATITIS B ROUTINE ADULT VACCINATION

Vaccine type: Target individuals

• Inactivated vaccine • intramuscularly (IM) 3 doses :0,1,6-12 months • Accelerated schedule Days 0, 7, 21-30, and at 12 months • Booster is not routinely recommended

Vaccine efficacy: • >90% after the 3rd dose • 40 y.o., <90% • 60 y.o, 75%

•Those without documented evidence of immunity to

Hepatitis B

•All healthcare workers

•Sexually active persons, MSMs, IV drug users,

•Clients and staff members of institutions for persons

with disabilities

•Travelers to countries with high or intermediate

prevalence of chronic Hepatitis B infection

•Diabetics, Persons with HIV/AIDS

•Chronic liver disease, Hemodialysis patients

•Household contacts of HBV carrier •Recipients of blood products • Immigrants from areas of high HBsAg endemicity

2015 Schedule of Adult Immunization

Philippine Society for Microbiology and Infectious Disease (PSMID) and Philippine Foundation for Vaccination (PFV)

HEPATITIS B and HCPs Pre-exposure Post-exposure

• Pre-vaccination serologic testing is indicated for HCP and is cost-effective in certain high-risk populations regardless of vaccination status

• Post-vaccination serologic testing should be performed for all HCP at high risk for occupational percutaneous or mucosal exposure to blood or body fluids

• Post-vaccination serologic testing is performed 1–2 months after administration of the vaccine series

• Persons determined to have anti-HBs concentrations of ≥10 mIU/mL are considered immune

• If anti-HBs concentrations <10 ,administration a second 3-dose series on an appropriate schedule, followed by anti-HBs testing 1–2 months

• If no response, test for HBsAg and anti-HBc

• Vaccinated HCP with documented immunity

(anti-HBs concentrations of ≥10 mIU/mL)

require no postexposure prophylaxis,

serologic testing, or additional vaccination

• Vaccinated HCP with documented

nonresponse to a 3-dose vaccine series

should receive 1 dose of HBIG and a second

3-dose vaccine series if the source is HBsAg-

positive or known to be at high risk for

carrying hepatitis

• Vaccinated HCP with documented

nonresponse to two 3-dose vaccine series

should receive 2 doses of HBIG, 1 month

apart if the source is HBsAg-positive or

known to be at high risk for carrying

hepatitis

MMWR Recommendations and Reports / Vol. 60 / No. 7 November 25, 2011

Pre-exposure Management for

Healthcare Personnel with a Documented Hepatitis B Vaccine

Series Who Have Not Had Post- vaccination

Serologic Testing

INFLUENZA Vaccine type and schedule WHO 2016 Recommendation

2 types:

•trivalent inactivated

•quadrivalent inactivated

• IM route

• Southern Hemisphere strain

• February to June, but maybe given throughout the year.

Vaccine efficacy: •varies from year to year •age and health status of the person •similarity “match” between the viruses or virus in the vaccine and those in circulation

It is recommended that trivalent vaccines for use in the 2016 influenza season (southern hemisphere ) contain the following:

•an A/California/7/2009 (H1N1)pdm09-like virus;

•an A/Hong Kong/4801/2014 (H3N2)-like virus;

•a B/Brisbane/60/2008-like virus. •It is recommended that quadrivalent vaccines containing two influenza B viruses contain the above three viruses and a B/Brisbane/60/2008-

like virus.

The Rationale For Quadrivalent Influenza Vaccines (QIV)

Why is it important that an

additional B strain be added to

trivalent influenza vaccines?

Circulating Influenza B lineages Philippines 2003-2013 and Vaccine mismatch

Source: Flunet, http://apps.who.int/globalatlas/dataQuery/default.asp, accessed January 2014

Vaccine type/route Schedule

MEASLES, MUMPS, RUBELLA (MMR) •live attenuated, SQ

•2-dose vaccine effectiveness of 99% (Measles) 75-95% (Mumps), 95% (rubella)

2 doses

• 0, 1 month interval

Tetanus, Diphtheria, acellular Pertussis (Tdap) - inactived, IM route

•vaccine effectiveness at 66%- 78%

3 doses (1 Tdap + 2 Td): • 0,1,6-12 months Booster every 10 years with Td

VARICELLA • live attenuated, SQ

• vaccine effectiveness 80%– 85%

2 doses

• 0, 1-2 months

Post-exposure Prophylaxis

• Given within 72 hours of exposure;

Single dose

2015 Schedule of Adult Immunization

Philippine Society for Microbiology and Infectious Disease (PSMID) and Philippine Foundation for Vaccination (PFV)

HUMAN PAPILLOMAVIRUS (HPV)

Vaccine type Target individuals

• Inactivated

1. Bivalent (Types 16,18) • Females only

2. Quadrivalent (Types (6,11,16,18)

• Females and males

Recommended for: • Females: 9-55 years old • Males: 10-26 years old

•May be given as catch up vaccination to 13-21 years old who have not been previously vaccinated or who have not completed the 3-dose series

Schedules

Bivalent – for females only •2 doses: 9 to 13 years old, (0, 6 or 12 months)

•3 doses: >13 years old, (0, 1, 6 months)

Quadrivalent - for males and females •3 doses 0,2,6 months

• Females: 14 to 45 years old • Males: 14 to 26 years old

•2 doses: Female 9-13 years old. 0, 6 or 12 months

2015 Schedule of Adult Immunization

Philippine Society for Microbiology and Infectious Disease (PSMID) and Philippine Foundation for Vaccination (PFV)

Vaccine type Indications and schedule

Pneumococcal vaccine

(inactivated)

•Polysaccharide (PPSV23)

IM or SQ

• Conjugate (PCV13) IM route

•Sequential pneumococcal

vaccination (PCV13-PPV23)

For elderly (>50 yo), immunocompetent

•PCV13 then PPSV23 in 6-12 months

For immunocompromised

•PCV13 then PPSV23 at least 8 weeks

For those previously received 1 or 2 doses PPV23

• Give PCV13 12 months after the most recent dose

of 23vPPV

Revaccination

•Single dose PPV23 after 5 months

Meningococcal Vaccine • Polysaccharide (MPSV): SQ/IM • Conjugate (MCV4) : IM

• For immunocompetent, single dose 0.5 ml’ no revaccination

• For immunocompromised, single dose 0.5 ml, revaccination after 5 years

Hepatitis A

• IM; Single antigen or in

combination with Hepatitis B

For monovalent: 2 doses at 0, 6-12 months In combination with hepatitis B: 0,1,6 months

2015 Schedule of Adult Immunization

Philippine Society for Microbiology and Infectious Disease (PSMID) and Philippine Foundation for Vaccination (PFV)

HERPES ZOSTER

Vaccine type: Target individuals

• Live, attenuated VZV

vaccine • single-dose 0.65 ml SQ

•Prevention of herpes zoster (HZ) •Prevention of postherpetic neuralgia (PHN) •Reduction of acute and chronic HZ-associated pain

•Adults ≥ 60 years old with or without a prior episode of herpes zoster • Persons with history of zoster • Men sex with men (MSMs) •Persons with chronic medical conditions

•chronic renal failure •diabetes mellitus •rheumatoid arthritis •Heart disease, chronic lung and chronic liver disease •healthcare workers •Asplenia

2015 Schedule of Adult Immunization

Philippine Society for Microbiology and Infectious Disease (PSMID) and Philippine Foundation for Vaccination (PFV)

Vaccine type/route Schedule

TYPHOID •IM, •VI capsular polysaccharide

For primary and booster single 0.5 ml M dose on the deltoid

RABIES •IM/Intradermal (HDCV , PVRV, PCECV)

Pre-exposure: 3 injections on days 0, 7 & 21 or 28 Post-exposure :

2015 Schedule of Adult Immunization

Philippine Society for Microbiology and Infectious Disease (PSMID) and Philippine Foundation for Vaccination (PFV)

IMPACT OF VACCINES

Johnson DR, et al. Am J Med 2008;121:S28-S35 JAMA. 2007;298(18):2155-2163

CDC. MMWR January 7, 2011;59(52);1704-1716.

IMPACT OF VACCINES

*? ?JAMA. 2007;298(18):2155-2163 † ?CDC. Active Bacterial Core surveillance Report; S. pneumoniae 2008.

¶ ?2008 Active Bacterial Core surveillance § ?CDC. MMWR. February 6, 2009 / 58(RR02); 1-25

‡ ?New Vaccine Surveillance Network

Barriers for Vaccination

• Both Private and Public HcW views vaccines as expensive increasing barriers for vaccination despite the need.

PUBLIC PRIVATE

BARRIERS

PATIENT AWARENESS/B

ELIEFS

PHYSICIAN RESOURCES / KNOWLEDGE

INFRASTRUCTURE

National Foundation for Infectious Diseases. Call To Action: Adult Vaccination Saves Lives. Bethesda, MD, 2012.

MYTHS

Steps in the process of implementing a vaccination policy for HCWs

H.C. Maltezou, G.A. Poland / Vaccine 32 (2014) 4876–4880

Measures should be taken to ensure healthcare workers are provided convenient access to vaccine.

Employers of healthcare workers need to commit resources toward institutionalizing immunization in the workplace

They need to demonstrate that immunization is an employee and patient safety PRIORITY.

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KEY CHALLENGE

“THE BIGGEST CHALLENGE IS THE CHALLENGE OF CHANGING SOMEONE’S MIND”

-- Paul Sax, MD

http://www.vaccines.gov/basics/protection/

Add perspective: Herd Immunity

http://www.vaccines.gov/basics/protection/

Before you vaccinate adults, consider their “H-A-L-O”!

H-A-L-O checklist of factors that indicate a possible need for adult vaccination

Technical content reviewed by the Centers for Disease Control and Prevention www.immunize.org/catg.d/p3070.pdf

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Thank you