Willmore and Shearman1 first described the fecal leukocyte stain in 1918 followed by its clinical use for diagnosis of bacterial diarrhea in 1972 by Harris et al 2. Today fecal leukocyte testing (FLT) is widely used to screen for inflammatory diarrhea including C. difficile diarrhea, which account for more than 25 % of all antibiotic associated diarrhea. Laboratory diagnosis of C. difficile associated diarrhea (CDAD) is based on the detection of C. difficile toxins in stool samples by a cell culture cytotoxicity assay or enzyme immunoassay. We evaluated FLT within an inpatient cohort, defining the test's sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) for patients with CDAD.

After obtaining approval from the institutional review board at Louisiana State University Health Sciences Center, Shreveport, a retrospective review of laboratory data was done on 263 inpatients whose stool samples were simultaneously submitted for FLT and C. difficile toxin assay (CDTA). Specimens were submitted between January 2001 and June 2004.

FLT was performed on fresh stool specimens. Samples are obtained in a clean dry container. Stool specimens are applied as a thin smear on a slide using a cotton swab. After the slides are air dried, they are smeared with Wright stain and examined under the microscope for white blood cells (WBC). Criteria for positive FLT are > 1 WBC/high power field. The cost of obtaining a FLT is about $30. Time of availability of the test is approximately one hour after submission of the stool specimen. Specimens were processed in the same laboratory, but likely by different technicians.

CDTA was done using Premier™ Toxins A&B (PT A&B). PT A&B is an EIA for the direct detection of C.difficile toxin A and toxin B. CDAD was defined as diarrhea with a positive CDTA. The cost of obtaining CDTA is about $30. Time of availability is approximately 45 minutes after submission of the specimen.

Of the 263 stool samples tested at the same time for FLT and CDTA, 68 were positive for FLT and 30 were positive for CDTA (Table 1). The sensitivity and specificity of FLT as compared to CDTA was 30 % and 74.9 % respectively. The PPV and NPV of FLT was 13.2 % and 89.3 % respectively for CDTA. 70% of all stool specimens positive for CDTA had a negative FLT. Prevalence of a positive CDTA was 11.4%.

Clostridium difficile (C.difficile) is the commonest cause of nosocomial diarrhea associated with significant morbidity and health care costs.34. Despite being perceived as a common cause of antibiotic associated diarrhea, C.difficile associated diarrhea (CDAD) is often difficult to diagnose.3 Enzyme immunoassay (EIA) against C.difficile toxin A and/or toxin B in stool specimens is currently the acceptable method of diagnosing C.difficile diarrhea. 567 Since C.difficile is considered to be a type of invasive diarrhea, fecal leukocyte test (FLT), that has been proposed by Harris et al 2 as a rapid test to differentiate invasive versus non-invasive diarrhea 28 might be useful as a predictor of C.difficile diarrhea.

There is conflicting evidence regarding the use of FLT as a screening test for CDAD. While the studies done by Savola et al 9, Mark et al 10, Manabe et al 11 and Shanholtzer et al 12 concluded FLT as a poor predictor of CDAD; studies done by Bartlett et al 13 and Fekety et al 14 proposed that FLT might be a useful predictor in CDAD. The results of our study reinforce the fact that FLT is a poor predictor of CDAD; because 70% of stool specimens positive for C. difficile toxin are negative for fecal leukocyte. There is no significant time or cost savings by obtaining a FLT, as opposed to CDTA in patients with suspected CDAD.

Poor predictability of CDAD with a FLT can partially be explained by inter-observer variability in interpreting fecal leukocytes under microscopy. False negative results could also be due to degeneration of fecal leukocytes secondary to delay in processing stool specimens. This is reinforced by the fact that objective tests to detect fecal leukocytes like the fecal lactoferrin 15161718 or the fecal leukocyte esterase test 19 are better indicators of fecal leukocytes than the FLT. Low PPV can also be explained by the fact that EIA for toxin detection is less sensitive compared to the neutralizing tissue culture cytotoxicity assay for CDAD.

Considering the poor sensitivity and comparable cost and promptness with C.difficile toxins assay in our institution, we conclude that FLT is not a good screening test for CDAD in inpatients.

None

The author(s) declare that they have no competing interests.

SR conceived of the study and participated in its design and data collection. AR participated in data collection, analysis and drafting of manuscript. DB participated in design and coordination of the study. All authors read and approved the final version of the manuscript