Abstract
Objectives Examine differences in the detection of influenza by specimen and test type using paired nasal and nasopharyngeal swabs.
Design Prospective study
Setting Enrollment took place between January and March of 2007 in a central Wisconsin population.
Participants Adult patients were screened and enrolled by trained research coordinators following medical encounters for acute respiratory illnesses of <10 days duration.
Methods Paired nasal and NP swabs were collected from consenting patients and tested by both real time reverse transcriptase polymerase chain reaction (rRT-PCR) and viral culture. A composite measure of positivity was used as the gold standard; cases included any positive result by rRT-PCR or viral culture from either specimen type.
Results Paired samples were collected from 240 adults; 33 (14%) individuals tested positive for influenza by rRT-PCR. Using rRT-PCR, the sensitivity of the nasal swab was 89% (95% CI 78 – 99%) and the sensitivity of the nasopharyngeal swab was 94% (95% CI 87 – 100%), compared to a composite gold standard.
Conclusion Test sensitivity did not vary significantly by swab type when using a highly sensitive molecular diagnostic test, but power was limited to detect modest differences.
- Received February 23, 2012.
- Revision received May 1, 2012.
- Accepted May 9, 2012.
