| Literature DB >> 32435109 |
Parvaiz A Koul1, Subramanium Swaminathan2, Thirumalai Rajgopal3, V Ramsubramanian4, Bobby Joseph5, Shrinivas Shanbhag6, Ashish Mishra7, Sidram K Raut8.
Abstract
There is an increasing focus on instituting wellness programs at the workplace among organizations in India. Such programs are aimed at improving employee health, which in turn, helps in reducing absenteeism, as well as in increasing work productivity and improving employee engagement. Of note, adult vaccination plays a significant role in ensuring the well-being of employees, as well as in keeping an organization profitable. The burden of vaccine-preventable diseases (VPDs) in adults is increasing in India, causing significant morbidity and disability. Moreover, adult immunization is an underpublicized concept in India. There is an urgent need to create awareness about adult immunization in India, particularly in occupational health settings-both at the employee and employer levels. In view of this, an expert meeting was held under the aegis of the Indian Association of Occupational Health (IAOH) to discuss key issues pertaining to the burden of VPDs in the working population in India and to formulate guidelines on adult vaccination in occupational health settings. This consensus guideline document may act as a guide for organizations across India to create awareness about adult vaccination and also to design workplace vaccination programs to promote better health among employees. Copyright:Entities:
Keywords: Adult vaccination; occupational health; recommendations; vaccine-preventable disease; wellness programs
Year: 2020 PMID: 32435109 PMCID: PMC7227733 DOI: 10.4103/ijoem.IJOEM_50_20
Source DB: PubMed Journal: Indian J Occup Environ Med ISSN: 0973-2284
Prevalence/incidence of vaccine-preventable diseases (VPDs) in India[914]
| Disease | Incidence/Prevalence |
|---|---|
| Influenza | Between 2015 and 2019, 126,906 H1N1 cases and 7865 deaths were reported.[ |
| Pneumococcal disease | As per a recent study, out of 374 adult invasive pneumococcal disease (IPD) cases: |
| Hepatitis | In a study, among 599,605 cases tested for hepatitis A, 44,663 cases were found to be positive.[ |
| Measles and rubella | 55,399 cases of measles and 1066 cases of rubella (all age groups)[ |
| Typhoid | 120/100,000 population-years in adults older than 15 years[ |
VPDs: Vaccine-preventable diseases
Characteristics for pneumococcal vaccines[505961]
| Characteristics | PPSV23 | PCV13 |
|---|---|---|
| Type of vaccine | Unconjugated capsular polysaccharide antigens | Capsular polysaccharides conjugated with a protein carrier |
| Contains antigens from 23 common serotypes (1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F, and 33F) | Contains antigens from 13 common serotypes (1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F) | |
| Immune response | T-cell-independent immune response (IgM antibody produced, response declines in 3-5 years, and no anamnestic response at revaccination) | T-cell-dependent immune response (larger duration and boosting effect at revaccination) |
| Efficacy | Considerable efficacy proven against IPD (50-70%) in immunocompetent elderly individuals | High efficacy (80%-90%) against vaccine-type IPD proven in children |
| Unclear (null to small) efficacy against nonbacteremic pneumococcal pneumonia | At present, relatively small serotype coverage for IPD in the elderly (30-40%) | |
| No efficacy demonstrated in reducing nasopharyngeal carriage | Potential efficacy in reducing nasopharyngeal carriage | |
| No impact proved in reducing overall pneumococcal disease burden | Future reduction of vaccination impact in adults/elderly (because of indirect effects from pediatric use of PCV13) |
IPD: invasive pneumococcal disease; IgM: immunoglobulin M; PPSV23: 23-valent pneumococcal polysaccharide vaccine; PCV13: 13-valent pneumococcal conjugate vaccine
Chronological evolution of pneumococcal vaccine recommendations[6566]
| Advocacy group/body | Recommendation/s |
|---|---|
| Global Initiative for Chronic Obstructive Lung Disease (GOLD, 2019)[ | PCV13 and PPSV23 recommended for all patients ≥65 years of age. |
| Advisory Committee on Immunization Practices (ACIP, 2019)[ | ACIP recommends administration of PCV13 based on shared clinical decision-making for adults aged ≥65 years (who do not have an immunocompromising condition [e.g., CSF leak, or cochlear implant] and who have not previously received PCV13). |
COPD: chronic obstructive lung disease; PPSV23: 23-valent pneumococcal polysaccharide vaccine; PCV13: 13-valent pneumococcal conjugate vaccine; CSF: cerebrospinal fluid
Figure 1Number of reported cases and deaths due to influenza.[10]
Concomitant use of pneumococcal and influenza vaccines[6970]
| Study authors | Patients | Outcome of co-administration of pneumococcal and influenza vaccines |
|---|---|---|
| Sumitani | A total of 98 adults with chronic respiratory disease underwent the additive inoculation of influenza vaccine (I-V) and 23-valent pneumococcal vaccine (P-V) to prevent lower respiratory tract infections. | Significant reduction in: |
| Christenson | 100,242 participants aged ≥65 years; 76% of the participants received both vaccines. | The incidence of hospital treatment was lower in the vaccinated group vs non-vaccinated group. |
IPD: Invasive pneumococcal disease
Vaccination schedule for healthcare workers[5386]
| Vaccine | Dose/s | Schedule |
|---|---|---|
| Hepatitis B | 3 | 0-1-6 months |
| Hepatitis A | 2/1 | 0-6 months or single dose (live vaccine) |
| Tdap | 1 | 1 dose every 10 years |
| Varicella (Chickenpox) | 2* | 2 doses at 4-8 weeks interval |
| Polio (IPV) | 1 or 2 | If previously unimmunized, 2 doses (0, 4-8 weeks) |
| Influenza | 1 | 1 dose every year |
| Pneumococcal | 12 | >50 years 1 single dose |
| Typhoid | 1 | Single dose. If unconjugated vaccine, give 3 yearly. |
| MMR | 2 | 2 doses at 4-8 weeks interval |
| Meningococcal (ACWY) | 1 | 1 dose is enough; repeat dose after 3-5 years if still at risk |
| Rabies | 3 | Pre-exposure prophylaxis 0, 7, and 28 days (especially veterinarians) |
IPV: inactivated polio vaccine, Tdap: tetanus diphtheria (acellular) pertussis; MMR: measles, mumps, and rubella. *Single dose for live vaccine
Vaccination schedule during preconception and pregnancy[53]
| Vaccine | Dose/s | Schedule | Remarks |
|---|---|---|---|
| Preconception | |||
| Hepatitis B | 3 | 0-1-6 month | Avoid conception for at least 4 weeks after MMR or varicella vaccine |
| Varicella (Chickenpox) | 2 | 2 doses at 4-8 weeks | |
| MMR | 2 | 2 doses at 4-8 weeks | |
| HPV | 3 | 0-1 month (HPV2) or 2-6 months (HPV4) | |
| Influenza | 1 | 1 dose every year | |
| During pregnancy | |||
| TT/Td | 2 | 1 dose early in pregnancy and 2nd dose 4 weeks after 1st dose | |
| Tdap | 1 | 3rd trimester | |
| Influenza | 1 | 1 at any stage of gestation | |
| During lactation | |||
| All vaccines except typhoid and yellow fever can be given as catch-up immunization. | |||
TT: tetanus toxoid; Td: tetanus and adult diphtheria; HPV: human papillomavirus; MMR: measles, mumps, and rubella
Vaccine recommendations for Hajj pilgrims and Kumbh Mela attendees[5387]
| Vaccine recommendations | Comments |
|---|---|
| Hajj pilgrims[ | |
| Meningococcal | Mandatory |
| Influenza | Recommended |
| Polio (IPV) | <15 years, endemic countries |
| Yellow fever | Endemic countries |
| Pneumococcal | PCV13: 4 weeks before traveling for HajjPPSV23: Post-return from Hajj (depends upon risk status) |
| Hepatitis A | Recommended |
| Hepatitis B | Recommended |
| Kumbh Mela attendees[ | |
| Typhoid | Strong recommendation |
| Hepatitis A | Strong recommendation |
| Hepatitis B | For prolonged stay |
| Japanese encephalitis | If stay is over 1 month |
| Influenza | Strong recommendation |
| Yellow fever | Travelers coming from endemic countries |
| Diphtheria, pertussis, tetanus | Should be up to date |
| Measles, mumps, rubella | Should be up to date |
| Rabies | Pre-exposure prophylaxis |
| Polio (IPV) | 1 booster (IPV) |
IPV: inactivated polio vaccine; PCV 13: pneumococcal conjugate vaccine 13; PPSV23: 23-valent pneumococcal polysaccharide vaccine
Figure 2Hosting vaccination program in company[33]
Vaccination recommended by IAOH for working adults
| Vaccine | 19-21 years | 22-26 years | 27-49 years | 50-64 years | ≥65 years | |
|---|---|---|---|---|---|---|
| Influenza vaccine (quadrivalent) | 1 dose annually | |||||
| Pneumococcal conjugate (PCV13) | Special situationS | 1 dose* | ||||
| Pneumococcal polysaccharide (PPSV23) | 1 dose | |||||
| Tetanus, diphtheria, pertussis (Tdap or Td) | 1 dose Tdap, then Td booster every 10 years | |||||
| Measles, mumps, rubella (MMR) | 2 doses (4-8 weeks interval) | |||||
| Varicella | 2 doses (4-8 weeks interval)δ | |||||
| Zoster live | 1 dose | |||||
| Human papillomavirus (HPV) | 3 doses schedule (0, 1-2 months, 6 months)∞ | |||||
| Hepatitis A (Hep A) | 2 doses (Single-antigen vaccine; 0 and 6-12 months) or 3 doses (Combined Hep A and Hep B; 0, 1, and 6 months)@ | |||||
| Hepatitis B (Hep B) | 3 doses (0, 1, 6 months)! | |||||
| Meningococcal A, C, W, Y | 1 or 2 doses depending on indication, then booster every 5 years if risk remains | |||||
| Haemophilus influenzae type b (Hib) | 1 or 3 doses depending on indication | |||||
| Special vaccine recommendation | ||||||
| Rabies$ | Total 3-4 doses | |||||
| Typhoid | Compulsory for food-handlers | |||||
Recommended vaccination for adults who meet age requirement, lack documentation of vaccination, or lack evidence of past infection. No recommendation Recommended vaccination for adults with an additional risk factor. SPCV13 is recommended in series with PPSV23 for adults aged ≥19 years with an immunocompromising condition, CSF leak, or cochlear implant. For PPSV23 dosing instruction, please refer to the respective guideline for special situations. *Administer 1 dose PCV13 followed by 1 dose PPSV23 at least 1 year after PCV13. PCV13 is recommended based on shared clinical decision making for adults who do not have an immunocompromising condition, cerebrospinal fluid (CSF) leak, or cochlear implant, and who have not previously received PCV13. Immunocompromising conditions include chronic renal failure, nephrotic syndrome, immunodeficiency, iatrogenic immunosuppression, generalized malignancy, human immunodeficiency virus, Hodgkin disease, leukemia, lymphoma, multiple myeloma, solid organ transplants, congenital or acquired asplenia, sickle cell disease, or other hemoglobinopathies. δ2-dose series VAR 4–8 weeks apart if previously did not receive the varicella-containing vaccine (VAR or MMRV [measles mumps-rubella-varicella vaccine] for children); if previously received 1 dose varicella-containing vaccine: 1 dose VAR at least 4 weeks after first dose. ∞A three-dose schedule (at 0, 1–2 months, and 6 months) is recommended for individuals above 15 to 45 years. @Not at risk but want protection from hepatitis A: Single-antigen vaccine formulations: Administer in a 2-dose schedule at 0 and 6–12 months. Combined hepatitis A and hepatitis B vaccine: Administer 3 doses at 0, 1, and 6 months. !Not at risk but want protection from hepatitis B: 3 doses. The second dose. should be administered one month after the first dose; the third dose should be administered at least 6 months after the first dose $Pre-exposure prophylaxis, as well as post-exposure vaccine, is recommended for risk groups such as medical and paramedical personnel treating rabies patients, veterinarians, laboratory personnel working with rabies virus; others, such as zookeepers, dog catchers, forest staff; postmen, policemen, courier boys, etc.
| Vaccines for influenza in adults: Recommendations |
|---|
| One dose every year is recommended. |
| Vaccines for hepatitis A and B in adults: Recommendations |
|---|
| Single-antigen vaccine formulations should be administered in a two-dose schedule at 0 and 6-12 months.[ |
| Hepatitis A immunization is recommended for the following groups of adults:[ |
| Live HBV is administered subcutaneously at a dose of 0.5 mL. |
| Vaccines for MMR in adults: Recommendations |
|---|
| For MMR, live, attenuated vaccine is available. |
| Vaccines for DPT in adults: Recommendations |
|---|
| The two types of DPT vaccine are whole-cell pertussis vaccine and acellular pertussis vaccine.[ |
DPT: Diphtheria, pertussis, and tetanus toxoids; Tdap: Tetanus, diphtheria, and pertussis; Td: Tetanus and diphtheria
| Vaccines for varicella in adults: Recommendations |
|---|
| Varicella vaccine is available as a live, attenuated vaccine.[ |
| Vaccines for typhoid in adults: Recommendations |
|---|
| The Vi vaccine is given as a single intramuscular dose of 0.5 mL. |
| Vaccines for rabies in adults: Recommendations |
|---|
| The rabies vaccine is available as a concentrated, purified cell culture, and as an embryonated egg-based vaccine. |
| Vaccines for HPV in adults: Recommendations |
|---|
| Vaccine for HPV is available as a recombinant protein capsid liquid vaccine. |
| Vaccine recommendation for healthcare workers | |
|---|---|
| Recommended vaccines | Hepatitis A and B |
| Vaccination during preconception and pregnancy | |
| Preconception | Hepatitis B |
| During pregnancy | TT/Td |
| Lactation | All vaccines except typhoid and yellow fever can be given as catch-up immunization. |
| Vaccines recommended for mass gathering | |
| Kumbh Mela attendees | Typhoid—Strong recommendation |
| Hajj pilgrims | Meningococcal (mandatory)—Mandatory |
^At any stage of pregnancy. Note: No QIV in India has labeled indication for pregnancy.ªStrong recommendation. Meningococcal ACWY special situations:
Anatomical or functional asplenia (including sickle cell disease), HIV infection, persistent complement component deficiency, eculizumab use: 2-dose series MenACWY (Menactra, Menveo) at least 8 weeks apart and revaccinate every 5 years if risk remains.
Travel in countries with hyperendemic or epidemic meningococcal disease, microbiologists routinely exposed to Neisseria meningitidis: 1 dose MenACWY and revaccinate every 5 years if risk remains.
First-year college students who live in residential housing (if not previously vaccinated at age 16 years or older) and military recruits: 1 dose MenACWY.
Hepatitis A special situations:
At risk for HAV infection (2-dose series Hep A or 3-dose series Hep A-Hep B; as mentioned above.)
Chronic liver disease
Clotting factor disorders
Men who have sex with men
Injection or non-injection drug use
Homelessness
Work with HAV in research laboratory or nonhuman primates with HAV infection
Travel in countries with high or intermediate endemic hepatitis AClose personal contact with international adoptee
Hepatitis B special situations:
At risk for HBV infection (3-dose series, as mentioned above)
Hepatitis C virus infection
Chronic liver diseaseSexual exposure risk
HIV infection
Current or recent injection drug use
Percutaneous or mucosal risk for exposure to blood
Incarcerated persons
Travel in countries with high or intermediate endemic hepatitis B
Haemophilus influenzae type b vaccination special situations:
Anatomical or functional asplenia (including sickle cell disease): 1 dose Hib if previously did not receive Hib; if elective splenectomy, 1 dose Hib, preferably at least 14 days before splenectomy
Hematopoietic stem cell transplant (HSCT): 3-dose series Hib 4 weeks apart starting 6–12 months after successful transplant, regardless of Hib vaccination history
IPV: inactivated polio vaccine, Tdap: tetanus diphtheria (acellular) pertussis; TT: tetanus toxoid; Td: tetanus and adult diphtheria; HPV: human papillomavirus; MMR: measles, mumps, and rubella