Tg. Emori et al., ACCURACY OF REPORTING NOSOCOMIAL INFECTIONS IN INTENSIVE-CARE-UNIT PATIENTS TO THE NATIONAL-NOSOCOMIAL-INFECTIONS-SURVEILLANCE-SYSTEM - A PILOT-STUDY, Infection control and hospital epidemiology, 19(5), 1998, pp. 308-316
OBJECTIVE: To assess the accuracy of nosocomial infections data report
ed on patients in the intensive-care unit by nine hospitals participat
ing in the National Nosocomial Infections Surveillance (NNIS) System.
DESIGN: A pilot study was done in two phases to review the charts of s
elected intensive-care-unit patients who had nosocomial infections rep
orted to the NNIS System. The charts of selected high-and low-risk pat
ients in the same cohort who had no infections reported to the NNIS Sy
stem also were included. In phase I, trained data collectors reviewed
a sample of charts for nosocomial infections. Retrospectively detected
infections that matched with previously reported infections were deem
ed to be true infections. In phase II, two Centers for Disease Control
and Prevention (CDC) epidemiologists reexamined a sample of charts fo
r which a discrepancy existed. Each sampled infection either was confi
rmed or disallowed by the epidemiologists. Confirmed infections also w
ere deemed to be true infections. True infections hom both phases were
used to estimate the accuracy of reported NNIS data by calculating th
e predictive value positive, sensitivity, and specificity at each majo
r infection site and the ''other sites,'' RESULTS: The data collectors
examined a total of 1,136 patients' charts in phase I. Among these ch
arts were 611 infections that the study hospitals had reported to the
CDC. The data collectors retrospectively matched 474 (78%) of the pros
pectively identified infections, but also detected 790 infections that
were not reported prospectively. Phase II focused on the discrepant i
nfections: the 137 infections that were identified prospectively and r
eported but not detected retrospectively, and the 790 infections that
were detected retrospectively but not reported previously. The CDC epi
demiologists examined a sample of 113 of the discrepant reported infec
tions and 369 of the discrepant detected infections, and estimated tha
t 37% of all discrepant reported infections and 43% of all discrepant
detected infections were true infections. The predictive value positiv
e for reported bloodstream infections, pneumonia, surgical-site infect
ion, urinary tract infection, and other sites was 87%, 89%, 72%, 92%,
and 80%, respectively; the sensitivity was 85%, 68%, 67%, 59%, and 30%
, respectively; and the specificity was 98.3%, 97.8%, 97.7%, 98.7%, an
d 98.6%, respectively.CONCLUSIONS: When the NNIS hospitals in the stud
y reported a nosocomial infection, the infection most likely was a tru
e infection, and they infrequently reported conditions that were not i
nfections. The hospitals also identified and reported most of the noso
comial infections that occurred in the patients they monitored, but ac
curacy varied by infection site. Primary bloodstream infection was the
most accurately identified and reported site. Measures that will be t
aken to improve the quality of the infection data reported to the NNIS
System include reviewing the criteria for definitions of infections a
nd other data fields, enhancing communication between the CDC and NNIS
hospitals, and improving the training of surveillance personnel in NN
IS hospitals (Infect Control Hosp Epidemiol 1998;19:308-316).