A: Diagnostic testing for C. difficile should be performed only in patients with clinically significant diarrhea (patients with 3 or more loose stools in ≤24 hours) who have risk factors for CDI such as recent exposure to antibiotics, older age, and/or duration of stay at a hospital or nursing facility.1 Acceptable samples should be unformed stool specimens that take the shape of the container.
Webinaire et questions fréquentes sur C. difficile
Q: Who should be tested for C. difficile?
Q: Do molecular or Nucleic Acid Amplification Tests (NAAT) “overdiagnose” C. difficile?
A: Molecular tests/NAATs are designed to detect DNA from Clostridium difficile organisms capable of producing toxin (also referred to as toxigenic C. difficile) found in stool. PCR is one type of NAAT. The sensitivity of detection of toxigenic C. difficile organism by GeneXpert has been reported to be 94–99%2-4 and correlated well with a clinical diagnosis of C. difficile infection (CDI).2 Commercially available molecular assays are not designed to assess host response or to determine if the patient requires treatment, although they do provide valuable information to the physician when used in the context of other clinical features. In addition, 80–90% of samples tested for C. difficile are negative. Because they are very sensitive, molecular tests can be used to “rule out” C. difficile in the majority of patients more confidently than with immunologic methods. Thus, a rapid and sensitive molecular test can help to avoid unnecessary empiric therapy that is often administered to patients during the time clinicians are waiting for lab results (as described below).
Q: How do clinicians determine if a patient has C. difficile infection?
A: The first step is to determine if the patient’s sample contains toxigenic C. difficile. Patients positive for toxigenic C. difficile constitute an infection control risk, and can transmit disease to other patients.5,6 Once a patient with toxigenic C. difficile has been identified and appropriate infection control measures have been implemented, the next step is to determine if the patient has CDI and requires treatment. A number of features can be used to determine the presence of infection including the clinical picture (antibiotic history, frequency/severity of diarrhea) as well as other indicators of disease severity (for example, WBC count, creatinine level, albumin level, fever etc). Free toxin has also been evaluated as an indicator of infection.6,7 Guidelines advise that since enzyme immunoassay (EIA) tests for toxin A and B are less sensitive than other methods, such as PCR, they are not recommended for standalone use.1,8 A recent study by Polage et al. showed that the toxin assay failed to detect toxin in 30% of PCR-positive samples, as detected by cell cytotoxin assay repeat testing.6 In fact, among stool samples initially positive by PCR and negative for toxin that were sent for retesting (likely because the physician still suspected CDI), 21% of the toxin assays were positive upon retest. In lieu of definitive measure of disease, clinicians must take into account the complete clinical picture. As a recent editorial stated, “Regardless of which assay is used, it is best to remember to treat the patient, not the test.”9
Q: Do all patients with CDI require treatment?
A: Yes, all patients with CDI, including mild CDI, should be treated in accordance with SHEA and IDSA recommendations.1 Treatment strategies should be based on disease severity, history of prior CDI, and the individual patient's risk of recurrence.10
Q: Are molecular or PCR-based tests too sensitive?
A: PCR-based assays are used to determine if the patient sample contains toxigenic C. difficile and, consequently, whether that patient constitutes an infection control risk; in this case, a sensitive test is needed. In fact, a recent health economic analysis concluded that sensitive, on-demand PCR testing is more cost-effective than other testing approaches because it reduces the likelihood of infection transmission and associated infection-related outcomes.11 A positive result from a PCR assay should not be the sole basis for determining if the patient requires treatment. The decision to administer antibiotic therapy should be based on disease severity, history of prior CDI, and the individual patient's risk of recurrence.10
Q: Should toxin immunoassays be used to determine if a patient requires treatment?
A: Some published studies have shown that patients with toxin-positive stool samples had worse outcomes than patients with samples negative for toxin.6,7 However, another study showed that among PCR-positive samples, the outcomes of patients with toxin-positive stools and toxin-negative stools were similar.12 Thus, the decision as to whether to use a toxin assay to decide on therapy will be institution specific. It is important to note that not all toxin assays perform the same and the performance of more commonly used rapid lateral-flow EIA toxin tests was not evaluated in the larger, published studies noted in the previous paragraph. Although toxin ELISA assays are more sensitive than their lateral-flow counterparts, they are very manual, require technical expertise and contain multiple incubation and wash steps. They are best suited for batch testing, which is likely to delay the time to result. Antigenic variation in the toxin proteins can affect performance of toxin immunoassays compared to molecular methods; the latter are generally unaffected by toxin variation because they are designed to detect conserved regions of the toxin genes. It should be noted that studies performed at a single medical center may not include enough strain variation to see these effects. Finally, C. difficile toxins break down in stool over time,13 so time spent in specimen transport and in waiting for batch analysis can affect performance. For these and other reasons, toxin immunoassays are not recommended for standalone use in the diagnosis of CDI.
Q: Should all patients with a positive PCR-based C. difficile test be treated?
A: No, not all patients testing positive for C. difficile with PCR-based assays should be treated. Only patients who meet the clinical criteria for CDI should be treated; patients who test positive by PCR who do not meet those criteria may be colonized. The decision to administer antibiotic therapy should be based on disease severity, history of prior CDI, and the individual patient's risk of recurrence.10
Q: Is the use of molecular assays associated with overtreatment?
A: A recent study6 and accompanying editorial9 suggested that the use of molecular tests for the diagnosis of CDI was likely to result in overtreatment. The same study showed that 32% of patients with stool samples negative for C. difficile by both PCR and toxin testing received treatment. The fact that a third of patients negative for both tests received antibiotics speaks to the pervasive use of empiric therapy, regardless of the test results. In addition, the chance that a patient receives empiric therapy is likely to increase the longer it takes to obtain a test result. This underscores the need for a rapid test, like a PCR-based test, which can provide an accurate result in less than an hour. Having a negative test result by a more sensitive test should give treating physicians more confidence in making a decision to avoid unnecessary empiric therapy, especially in the absence of other risk factors.
Q: Will using a more-sensitive molecular C. difficile assay result in higher lab event reporting and associated penalties?
A: An initial increase in positive results is expected, but this should subsequently decline as improved case detection reduces rates of transmission. Since PCR-based assays are more sensitive, institutions will likely see an initial increase in reported rates of C. difficile after implementation that may fall below the historic rates over time with proper adherence to infection control procedures.14 From a reporting perspective, the Centers for Disease and Prevention (CDC) performs calculations on National Healthcare Safety Network (NHSN)-reported data before submitting to the Centers for Medicare & Medicaid Services (CMS). The calculations for the “expected” rates of C. difficile, specific for each hospital, include a risk adjustment to control for the test type (NAAT, EIA, other), bed size, and medical school affiliation.15 They also take into consideration the prevalence of C. difficile in the community. The expected rates are then compared to observed rates that the hospital reports. When observed rates are much higher than expected, the penalty can be assigned. (Note: CMS will include hospital-onset C. difficile infections in its Value-Based Purchasing and Hospital-Acquired Conditions Reduction Programs beginning FY2017.) Because institutions using PCR are given an adjustment that takes into account the greater sensitivity of the test, these institutions will NOT be penalized for using a more-sensitive assay simply because of their choice in test method. It is the difference between the reported rates and the expected rate based on the test method they chose that matters, not the absolute number of events reported.
References: 1. Cohen SH, Gerding DN, Johnson S, et al. Clinical practice guidelines for Clostridium difficile infection in adults: 2010 update by the society for healthcare epidemiology of America (SHEA) and the infectious diseases society of America (IDSA). Infect Control Hosp Epidemiol. 2010;31: 431-55.
2. Berry N, Sewell B, Jafri S, et al. Real-time polymerase chain reaction correlates well with clinical diagnosis of Clostridium difficile infection. J Hosp Infect. 2014;87:109-14.
3. Novak-Weekley SM, Marlowe EM, Miller JM, et al. Clostridium difficile testing in the clinical laboratory by use of multiple testing algorithms. J Clin Microbiol. 2010;48:889-93.
4. Tenover FC, Novak-Weekley S, Woods CW, et al. Impact of strain type on detection of toxigenic Clostridium difficile: comparison of molecular diagnostic and enzyme immunoassay approaches. J Clin Microbiol. 2010;48:3719-24.
5. Curry SR, Muto CA, Schlackman JL, et al. Use of multilocus variable number of tandem repeats analysis genotyping to determine the role of asymptomatic carriers in Clostridium difficile transmission. Clin Infect Dis. 2013;57:1094–102.
6. Polage CR, Gyorke CE, Kennedy MA et al. Overdiagnosis of Clostridium difficile Infection in the Molecular Test Era. JAMA Intern Med. 2015:1-10. Published online 8 septembre, 2015.
7. Planche TD, Davies KA, Coen PG, et al. Differences in outcome according to Clostridium difficile testing method: a prospective multicentre diagnostic validation study of C difficile infection. Lancet Infect Dis. 2013;13:936-45.
8. Surawicz CM, Brandt LJ, Binion DG, et al. Guidelines for diagnosis, treatment, and prevention of Clostridium difficile infections. Am J Gastroenterol. 2013;108:478-98.
9. Dubberke ER, Burnham CD. Diagnosis of Clostridium difficile Infection: Treat the Patient, Not the Test. JAMA Intern Med. 2015:1-10. Published online 8 septembre, 2015.
10. Bagdasarian N, Rao K, Malani PN. Diagnosis and treatment of Clostridium difficile in adults: a systematic review. JAMA. 2015;313(4):398-408.
11. Schroeder LF, Robilotti E, Peterson LR, et al. Economic evaluation of laboratory testing strategies for hospital-associated Clostridium difficile infection. J Clin Microbiol. 2014;52:489-96.
12. Guerrero DM, Chou C, Jury LA, et al. Clinical and infection control implications of Clostridium difficile infection with negative enzyme immunoassay for toxin. Clin Infect Dis. 2011;53:287-90.
13. Centers for Disease Control and Prevention. Frequently Asked Questions about Clostridium difficile for Healthcare Providers. Joignable au : http://www.cdc.gov/HAI/organisms/cdiff/Cdiff_faqs_HCP.html.
14. Mermel LA, Jefferson J, Blanchard K, et al. Reducing Clostridium difficile incidence, colectomies, and mortality in the hospital setting: a successful multidisciplinary approach. Jt Comm J Qual Patient Saf. 2013;39:298-305.
15. Dudeck MA, Weiner LM, Malpiedi PJ, et al. Risk Adjustment for Healthcare Facility-Onset C. difficile and MRSA Bacteremia Laboratory-identified Event Reporting in NHSN. Published 12 mars, 2013. Joignable au : http://www.cdc.gov/nhsn/pdfs/mrsa-cdi/RiskAdjustment-MRSA-CDI.pdf.