Clostridium difficile infection laboratory findings: Difference between revisions

Jump to navigation Jump to search
Line 3: Line 3:
{{CMG}}
{{CMG}}


==Laboratory Findings==
== Overview ==
===Cytotoxicity assay===
Testing is generally not necessarily for patients with formed stools (no diarrhea). Among patients with diarrhea,''C. difficil''e infection is diagnosed either by [[enzyme immunoassay]] ([[ELISA]]) for toxins A and/or B in stools or by [[DNA-based test]]<nowiki/>s that detect bacterial toxin genes in stools. Although both ELISA and DNA-based tests may be performed sequentially, only one positive test is sufficient to diagnose ''C. difficile'' infection. Both ELISA and DNA-based tests also have a high [[negative predictive value]] > 95% among average-risk patients, and generally negative results warrants the search for alternative diagnoses. The advantage of DNA-based tests over ELISA is that it may detect the presence of [[BI/NAP1/027]] strain, which alters the management plan. However, DNA-based tests may also detect clinically irrelevant findings that may delay the diagnosis. Stool culture requires [[anaerobic]] culture and may not be available. Although not diagnostic, additional blood testing may be necessary to monitor for possible development of complications or the success/failure of antimicrobial therapy.
''C. difficile'' toxin detection as cytopathic effect in cell culture, and neutralized with specific anti-sera is the practical gold standard for studies investigating new CDAD diagnostic techniques. Toxigenic culture, in which organisms are cultured on selective medium and tested for toxin production remains the [[Gold standard (test)|gold standard]] and is the most sensitive and specific test, although it is slow and labour-intensive.<ref name=Murray_1993>{{cite book | author = Murray PR, Baron EJ, Pfaller EA, Tenover F, Yolken RH (editors) |title = Manual of Clinical Microbiology | edition = 8th ed | publisher=ASM Press | location = Washington DC | date = 2003 | isbn = 1-55581-255-3}}</ref>


===Enzyme-linked immunoabsorbant assay (ELISA) for toxin===
== Laboratory Findings ==
Assessment of the A and B toxins by [[ELISA|enzyme-linked immunoabsorbant assay]] (ELISA) for toxin A or B (or both) has:
Testing is generally not necessarily for patients with formed stools (no diarrhea). Among patients with diarrhea, ''C. difficile'' infection is diagnosed either by enzyme immunoassay (ELISA) for toxins A and/or B in stools or by DNA-based tests that detect bacterial toxin genes in stools. Although not diagnostic, additional blood testing may be necessary to monitor for possible development of complications or the success/failure of antimicrobial therapy.
* [[sensitivity (tests)|Sensitivity]] 63-99%
 
* [[specificity (tests)|Specificity]] 93-100%
== Blood Work-Up ==
 
=== Complete blood count with differential ===
* [[Leukocytosis]] with left shift
* [[Leucopenia]] is occasionally reported
 
=== Electrolytes ===
* [[Hypokalemia]]
* [[Hyponatremia]]
* [[Metabolic acidosis]] (low [[bicarbonate]])
 
=== Inflammatory markers ===
Inflammatory markers, such as [[CRP]] or [[ESR]] may be helpful for follow-up of patients with ''C. difficile'' infection or a non-specific means to monitor the success of antimicrobial therapy.
 
=== Coagulation profile ===
* [[Coagulation profile]], such as [[PTT]], [[PT]], and [[INR]] should be ready because surgery may be required among patients with complicated disease.
 
=== Albumin ===
* [[Hypoalbuminemia]]
 
== Stool Work-Up ==


At a prevalence of 15%, this leads to:
=== Stool analysis ===
* [[Positive predictive value]] 73%
* [[Leukocytosis]]
* [[Negative predictive value]] 96%
* Blood in stools


Experts recommend sending as many as three samples to rule-out disease if initial tests are negative.  ''C. difficile'' toxin should clear from the stool of previously infected patients if treatment is effective.
===Enzyme-linked immunoabsorbant assay (ELISA) for toxin===
* Assessment of the A and B toxins by [[ELISA|enzyme-linked immunoabsorbant assay]] (ELISA) for toxin A or B (or both) is generally sensitive and specific:
** [[sensitivity (tests)|Sensitivity]] 63-99%
** [[specificity (tests)|Specificity]] 93-100%


Unfortunately, many hospitals only test for the prevalent toxin A. Strains that express only the B toxin are now present in many hospitals and ordering both toxins should occur. Not testing for both may contribute to a delay in obtaining laboratory results, which is often the cause of prolonged illness and poor outcomes.
* [[Negative predictive value]] > 95% for patients with average risk (generally if ELISA negative, search for alternative diagnoses warranted)
* Following successful antimicrobial therapy, patients may remain positive for many weeks/months. No additional treatment recommended.
* ELISA and DNA-based tests (below) may be used sequentially, but one positive result is sufficient for diagnosis.


===Other Stool Tests===
=== DNA-based tests ===
Stool [[leukocyte]] measurements and stool [[lactoferrin]] levels have also been proposed as diagnostic tests, but may have limited diagnostic accuracy.<ref name=Vaishnavi_2000>{{cite journal |author=Vaishnavi C, Bhasin D, Kochhar R, Singh K |title=Clostridium difficile toxin and faecal lactoferrin assays in adult patients |journal=Microbes Infect |volume=2 |issue=15 |pages=1827-30 |year=2000 |pmid=11165926}}</ref>
* Higher sensitivity and specificity than ELISA
* Negative predictive value > 95% for patients with average risk (generally if DNA-based tests negative, search for alternative diagnoses warranted)
* Identify microbial toxin genes and toxicogenic strains in unformed stools
* Detects presence of BI/NAP1/027 strain
* May detect clinically irrelevant findings.
* Following successful antimicrobial therapy, patients may remain positive for many weeks/months. No additional treatment recommended.
* DNA-based tests and ELISA (above) may be used sequentially, but one positive result is sufficient for diagnosis.


===Routine Laboratory Findings===
=== Stool culture ===
* [[Leukocytosis]] up to 40,000 mm3
* [[Anaerobic]] culture needed.
* [[Metabolic acidosis]]
* Not widely available.


==References==
==References==

Revision as of 14:02, 24 April 2015

Clostridium difficile Microchapters

Home

Patient Information

Overview

Historical Perspective

Pathophysiology

Causes

Differentiating Clostridium difficile from other Diseases

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Abdominal X Ray

CT

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Clostridium difficile infection laboratory findings On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Clostridium difficile infection laboratory findings

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Clostridium difficile infection laboratory findings

CDC on Clostridium difficile infection laboratory findings

Clostridium difficile infection laboratory findings in the news

Blogs on Clostridium difficile infection laboratory findings

Directions to Hospitals Treating Clostridium difficile

Risk calculators and risk factors for Clostridium difficile infection laboratory findings

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Testing is generally not necessarily for patients with formed stools (no diarrhea). Among patients with diarrhea,C. difficile infection is diagnosed either by enzyme immunoassay (ELISA) for toxins A and/or B in stools or by DNA-based tests that detect bacterial toxin genes in stools. Although both ELISA and DNA-based tests may be performed sequentially, only one positive test is sufficient to diagnose C. difficile infection. Both ELISA and DNA-based tests also have a high negative predictive value > 95% among average-risk patients, and generally negative results warrants the search for alternative diagnoses. The advantage of DNA-based tests over ELISA is that it may detect the presence of BI/NAP1/027 strain, which alters the management plan. However, DNA-based tests may also detect clinically irrelevant findings that may delay the diagnosis. Stool culture requires anaerobic culture and may not be available. Although not diagnostic, additional blood testing may be necessary to monitor for possible development of complications or the success/failure of antimicrobial therapy.

Laboratory Findings

Testing is generally not necessarily for patients with formed stools (no diarrhea). Among patients with diarrhea, C. difficile infection is diagnosed either by enzyme immunoassay (ELISA) for toxins A and/or B in stools or by DNA-based tests that detect bacterial toxin genes in stools. Although not diagnostic, additional blood testing may be necessary to monitor for possible development of complications or the success/failure of antimicrobial therapy.

Blood Work-Up

Complete blood count with differential

Electrolytes

Inflammatory markers

Inflammatory markers, such as CRP or ESR may be helpful for follow-up of patients with C. difficile infection or a non-specific means to monitor the success of antimicrobial therapy.

Coagulation profile

Albumin

Stool Work-Up

Stool analysis

Enzyme-linked immunoabsorbant assay (ELISA) for toxin

  • Negative predictive value > 95% for patients with average risk (generally if ELISA negative, search for alternative diagnoses warranted)
  • Following successful antimicrobial therapy, patients may remain positive for many weeks/months. No additional treatment recommended.
  • ELISA and DNA-based tests (below) may be used sequentially, but one positive result is sufficient for diagnosis.

DNA-based tests

  • Higher sensitivity and specificity than ELISA
  • Negative predictive value > 95% for patients with average risk (generally if DNA-based tests negative, search for alternative diagnoses warranted)
  • Identify microbial toxin genes and toxicogenic strains in unformed stools
  • Detects presence of BI/NAP1/027 strain
  • May detect clinically irrelevant findings.
  • Following successful antimicrobial therapy, patients may remain positive for many weeks/months. No additional treatment recommended.
  • DNA-based tests and ELISA (above) may be used sequentially, but one positive result is sufficient for diagnosis.

Stool culture

  • Anaerobic culture needed.
  • Not widely available.

References

Template:WH Template:WS