Pneumococcal Vaccination: PCV13 vs PPSV23
For adults ≥65 years without immunocompromising conditions, PPSV23 is the only routinely recommended vaccine as of 2019, with PCV13 reserved for shared clinical decision-making in select high-risk exposure scenarios. For immunocompromised patients, children, and high-risk adults, both vaccines are required in sequence, with PCV13 given first. 1
Current Recommendations by Population
Healthy Adults ≥65 Years
- All adults ≥65 years should receive PPSV23 as the standard recommendation. 1, 2
- PCV13 is no longer routinely recommended for this population since 2019, when ACIP removed the universal recommendation due to successful indirect protection from pediatric PCV13 vaccination programs. 1
- PCV13 may be considered through shared clinical decision-making for adults ≥65 years in specific high-exposure scenarios: nursing home residents, those in areas with low pediatric PCV13 uptake, or travelers to regions without pediatric PCV13 programs. 1
- If PCV13 is given, it must be administered at least 1 year before PPSV23. 1
Important caveat: The 2019 guideline change reflects the dramatic success of pediatric PCV13 vaccination in reducing adult disease through herd immunity—PCV13-type disease burden dropped substantially, making routine adult vaccination less cost-effective at the population level. 1 However, individual patients may still benefit, particularly those with chronic conditions (heart disease, lung disease, diabetes, smoking history) who have higher residual disease rates. 1
Immunocompromised Adults and High-Risk Groups
- Both PCV13 and PPSV23 are required in sequence for adults ≥19 years with immunocompromising conditions, CSF leaks, or cochlear implants. 1, 2
- Give PCV13 first, followed by PPSV23 at least 8 weeks later (not 1 year) for immunocompromised patients. 3, 2
- Immunocompromising conditions include: chronic renal failure, nephrotic syndrome, HIV infection, malignancies, immunosuppressive therapy, functional or anatomic asplenia, sickle cell disease, transplant recipients, and complement deficiencies. 3, 2
- A second dose of PPSV23 is recommended 5 years after the first PPSV23 dose for immunocompromised adults. 3
Critical distinction: The shorter 8-week interval (versus 1 year for immunocompetent adults) reflects the urgent need for protection in patients at dramatically higher risk—for example, children with hematologic malignancies have 822 times the risk of PCV13-type invasive disease compared to healthy children. 1
Children and Adolescents
- PCV13 is the primary vaccine for all children aged 2-59 months as part of the routine immunization schedule (doses at 2,4,6, and 12-15 months). 1, 4
- For children aged 6-18 years with immunocompromising conditions, functional/anatomic asplenia, CSF leaks, or cochlear implants: give PCV13 first, then PPSV23 at least 8 weeks after completing all PCV13 doses. 1
- Among immunocompromised children aged 6-18 years, 49% of invasive disease is caused by PCV13 serotypes and an additional 23% by PPSV23-only serotypes, demonstrating the need for both vaccines. 1
Key Differences Between PCV13 and PPSV23
Immunologic Mechanisms
- PCV13 is a conjugate vaccine that stimulates T-cell dependent immunity, creates immunologic memory, and provides mucosal immunity that reduces nasopharyngeal carriage and transmission. 5
- PPSV23 is a polysaccharide vaccine that provides T-cell independent immunity without immunologic memory and has limited efficacy in immunocompromised individuals. 5
- PCV13 demonstrated 75% efficacy against PCV13-type invasive disease and 45% efficacy against noninvasive PCV13-type pneumonia in the landmark CAPiTA trial. 1, 6
Serotype Coverage
- PCV13 covers 13 serotypes with superior immunogenicity and herd protection effects. 6
- PPSV23 covers 23 serotypes, including 12 in common with PCV13 plus 11 additional serotypes that account for 32-37% of invasive disease in adults ≥65 years. 1, 2
- This explains why both vaccines are needed for high-risk patients—PCV13 provides better immunity to its 13 serotypes, while PPSV23 adds coverage for 11 additional serotypes. 2
Practical Implementation Algorithm
For Previously Unvaccinated Adults ≥65 Years Without High-Risk Conditions:
- Give PPSV23 as a single dose (standard recommendation). 1
- Consider PCV13 through shared decision-making only if: nursing home resident, low pediatric vaccination area, or frequent travel to areas without pediatric PCV13 programs. 1
- If PCV13 is given, administer it first, then PPSV23 at least 1 year later. 1
For Adults ≥19 Years With Immunocompromising Conditions:
- Give PCV13 first. 2
- Give PPSV23 at least 8 weeks after PCV13. 3, 2
- Give a second PPSV23 dose 5 years after the first PPSV23. 3
- If elective splenectomy or immunosuppressive therapy is planned, complete vaccination at least 2 weeks before the procedure. 3
For Adults Who Received PPSV23 Before Age 65:
- Give one additional dose of PPSV23 at age ≥65 years, at least 5 years after the previous dose. 1, 2
- No further PPSV23 doses are needed after the dose given at age ≥65 years. 3
Common Pitfalls to Avoid
- Do not co-administer PCV13 and PPSV23 on the same day—they must be given separately with appropriate intervals. 1, 7, 2
- Do not give PPSV23 before PCV13 in vaccine-naive patients requiring both vaccines—PCV13 must come first for optimal immune priming. 1, 2
- Do not use the 1-year interval for immunocompromised patients—they require the shorter 8-week interval between PCV13 and PPSV23. 3, 2
- Do not give multiple PPSV23 boosters beyond recommendations—there is insufficient evidence for safety with three or more doses. 3
- Do not delay vaccination waiting for complete medical records—use verbal history and proceed with indicated vaccination. 3
Safety Considerations
- Both vaccines have similar safety profiles with comparable rates of severe adverse events. 1
- Common PCV13 reactions include injection site pain, redness, swelling, arm movement limitation, fatigue, headache, chills, decreased appetite, muscle pain, and joint pain. 1
- Influenza and pneumococcal vaccines can be safely co-administered at the same visit in different anatomic sites (e.g., one in each deltoid). 7