Table 2. Questions left unanswered with regard to Active Bacterial Core surveillance*.
Organism or disease |
Questions |
Streptococcus pneumoniae
|
Should PCV13 be recommended for adults? |
What proportion of invasive pneumococcal disease is preventable with vaccine? | |
What other strategies are available to prevent non–vaccine type disease? | |
Neisseria meningitidis
|
Should serogroup B vaccines be recommended for routine use in the United States? |
Haemophilus influenzae
|
Are control strategies (e.g., chemoprophylaxis, vaccines) needed for non-Hib disease? |
Group B Streptococcus |
Will antimicrobial drug resistance reduce the effectiveness of intrapartum prophylaxis? |
What will be the projected effect of vaccines on infant disease? | |
Are there interventions to reduce infant late-onset disease? | |
Group A Streptococcus |
What age groups should be targeted for vaccines according to potential effect on invasive disease? |
MRSA |
Can modifiable risk factors for HACO MRSA be identified? |
What are effective strategies for preventing infections outside acute-care settings? | |
Pertussis |
Does the acellular vaccine given during pregnancy effectively prevent pertussis in infants? |
What is the effect of newly emerging Bordatella pertussis strain changes on disease epidemiology, clinical presentation, and vaccine effectiveness? | |
Legionellosis | Why are rates higher among black than white persons and higher among men than women? |
Why do rates differ by geographic area? |
*PCV13, 13-valent pneumococcal conjugate vaccine; Hib, H. influenzae type b; HACO, health care–associated community onset; MRSA, methicillin-resistant Staphylococcus aureus.