National guidelines for community-acquired pneumonia in the works

  • October 3, 2010

SAN FRANCISCO — Community-acquired pneumonia remains a significant concern for pediatricians, yet no national recommendations exist for diagnosis, treatment and prevention of the disease. Forthcoming guidelines that will address these issues, however, are in development and publication is expected in 2011.

Carrie L. Byington, MD, HA and Edna Bennington Presidential Professor of Pediatrics at the University of Utah in Salt Lake City and vice chair of the AAP’s Committee on Infectious Diseases, discussed the diagnosis, treatment and prevention of pediatric community-acquired pneumonia as well as the process of developing guidelines during a presentation here at the 2010 American Academy of Pediatrics National Conference and Exhibition.

Diagnosis

For children who appear well enough for outpatient treatment, Byington suggested that pediatricians focus more on the physical exam instead of outside diagnostic procedures, although obtaining chest radiographs and X-rays would be appropriate for:

  • Children whom a physician intends to admit to a hospital..
  • Children with hypoxia or significant respiratory distress.
  • Children who are unresponsive to antimicrobial therapy.
  • Children suspected of having pleural effusion empyema.

Pediatricians may suspect empyema in patients who have a fever that persists for 4 or 5 days or a fever that reappears after apparent resolution. Chest and abdominal pain are also potential indicators of the condition, according to Byington, as are use of ibuprofen, azythromycin or single-dose IM ceftriaxone without improvement.

Recent history of varicella or influenza is also associated with complications of community-acquired pneumonia, highlighting the importance of vaccination, she said.

Diagnostic testing

Other modes of diagnostic testing, such as obtaining a complete blood count, are not necessary in the outpatient setting, although they are indicated for children with hypoxia or those children that are likely to be admitted to the hospital.

Additionally, C-reactive protein testing is unreliable in distinguishing between bacterial and viral disease, and therefore may not be helpful in diagnosing community-acquired pneumonia. Procalcitonin is more predictive of bacteremic pneumonia, but these tests are less available and considerably more expensive.

Nontoxic, immunized patients who will receive outpatient treatment also do not warrant blood cultures because of the high likelihood for false positives, according to Byington, but inpatients with evidence of empyema may benefit from these tests.

Byington also noted high false positive rates of urinary antigen testing for Streptococcus pneumoniae in children. Antigen testing of pleural fluid, however, may help identify pathogens in cases of complicated pneumonia.

Viral testing also has merit, Byington said, such as rapid diagnosis of influenza and respiratory syncytial virus. These tests can easily be performed in inpatient and outpatient settings, and the results allow for early antiviral treatment; decreases in the use of antibiotics; the identification of children at high risk for hospital admission; and cohorting of patients who are admitted to inpatient facilities.

Treatment

Byington recommended amoxicillin as an appropriate antibiotic treatment for preschool- and school-aged children with community-acquired pneumonia in outpatient settings. She also identified clindamycin as an alternative for penicillin-allergic children. Usual treatment courses last for approximately 10 days, with dosing depending on the susceptibility of S. pneumoniae.

Drug treatment for complicated cases is the same, according to Byington, although a longer course, lasting approximately 2 to 4 weeks, with ampicillin is preferred for penicillin-susceptible S. pneumoniae.

Drainage of pleural fluid in cases of community-acquired pneumonia is appropriate for all effusions that are classified as moderate or large, with the choice of drainage technique depending on local expertise, said Byington.

Prevention

In accordance with AAP guidelines, palivizumab should be administered to high-risk infants, said Byington. Immunization with the influenza vaccine, the Haemophilus influenzae type B vaccine and the 13-valent pneumococcal conjugate vaccine are also important in preventing community-acquired pneumonia.

Byington said the Infectious Disease Society of America and the Pediatric Infectious Disease Society are currently collaborating to create evidence-based recommendations for the national guidelines. - by Melissa Foster

For more information:

Byington CL. F1044. Presented at: 2010 AAP National Conference and Exhibition; Oct. 2-5, 2010; San Francisco

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