What is the Ristocetin (cofactor) test?

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From the Guidelines

The ristocetin cofactor test is no longer considered the gold standard for measuring von Willebrand factor activity due to its poor sensitivity and potential for false diagnoses 1. The test measures the ability of von Willebrand factor (vWF) to interact with platelets in the presence of the antibiotic ristocetin, but it has several disadvantages, including poor sensitivity and a high coefficient of variation, which can lead to false diagnoses in the moderately reduced VWF range 1. Additionally, the test measures two parameters, (i) binding of ristocetin to VWF and (ii) binding of ristocetin-‘activated’ VWF to test platelets, which can be affected by sequence variants, such as p.P1467S and the H-allele of a common polymorphism p.D1472H, in the ristocetin binding region of the A1 domain, leading to spuriously decreased VWF:RCo levels 1. Some key points to consider when interpreting the results of the ristocetin cofactor test include:

  • Normal values typically range from 50-150% of normal control, with values below 30% strongly suggesting vWD 1
  • The test is particularly useful for identifying type 2 vWD, where vWF function is disproportionately reduced compared to vWF antigen levels
  • Blood collection should occur without excessive venous stasis, as this can artificially elevate vWF levels
  • The test should be interpreted alongside other vWF assays, including vWF antigen levels and factor VIII activity, for a comprehensive diagnosis. However, due to the limitations of the ristocetin cofactor test, it is essential to consider alternative assays that can provide more accurate and reliable results, such as the VWF:GPIbM assay, which has been shown to be more sensitive and specific for diagnosing vWD 1.

From the Research

Risticetin Cifactor Test

There is no direct information available on the Risticetin cifactor test in the provided studies.

  • The studies focus on Clostridium difficile infection, its treatment, and prevention, but do not mention the Risticetin cifactor test specifically 2, 3, 4, 5, 6.
  • The studies discuss various diagnostic methods for Clostridium difficile infection, such as direct detection of C. difficile toxins in feces using EIA assay, but do not mention the Risticetin cifactor test 3, 5.
  • The Risticetin cifactor test is not mentioned as a diagnostic tool or a treatment approach for Clostridium difficile infection in any of the provided studies.

Available Diagnostic Methods

  • Direct detection of C. difficile toxins in feces using EIA assay is a common diagnostic method for Clostridium difficile infection 3, 5.
  • Fecal microbiota transplantation is a promising therapy for recurrent Clostridium difficile infection 2, 3, 4, 5.
  • Various antibiotic regimens, such as vancomycin, fidaxomicin, and metronidazole, are used to treat Clostridium difficile infection, but the Risticetin cifactor test is not mentioned as a diagnostic tool or a treatment approach 2, 3, 4, 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Update of treatment algorithms for Clostridium difficile infection.

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2018

Research

Clostridium difficile infection: review.

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2019

Research

Clostridium difficile infection.

Nature reviews. Disease primers, 2016

Research

Fidaxomicin versus metronidazole, vancomycin and their combination for initial episode, first recurrence and severe Clostridioides difficile infection - An observational cohort study.

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2021

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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