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Text Content

Press Alt+1 for screen-reader mode, Alt+0 to cancelAccessibility Screen-Reader
Guide, Feedback, and Issue Reporting
 * The Problem
   * False Positives
   * The 3% Standard
   * Sources of Contamination
   * Costs of False Positives
 * The Kurin Solution
   * Kurin Lock Sets
   * Kurin Jet
   * Kurin IFU
 * Clinical Resources
   * Evidence
   * Clinical Guidelines
   * Videos
   * Blood Culture Collection FAQs
   * Fast Facts
 * About
   * About Kurin
   * News
   * Events
   * Careers
   * Patents
   * 510(k)
 * Order
 * Portal
 * 
 * Menu Menu



 * CDC & AHVAP Top Priorities:
   Optimize blood culture orders
   Prevent blood culture contamination
   Ensure appropriate blood volume
   
   
   Learn more

 * Introducing Kurin Jet™
   The fastest way to sideline
   blood culture contaminants.
   
   Learn more

PreviousNext
News
 * Kurin Works with The Ohio State University Wexner Medical Center on Patient
   Safety and Increased Access to High Quality Healthcare
 * Final Judgment Entered in Kurin’s Favor over Magnolia Medical
 * Kurin Announces Appointment of Chief Commercial Officer
 * Court Determines that Kurin Does Not Infringe Magnolia Medical Patent
 * Kurin, Inc. Reports Record Revenue for Q1 2024
 * Kurin, Inc. Files False Advertising Lawsuit Against ICU Medical and Vascular
   Integrity
 * USPTO Examiner Affirms Rejection of Claims Asserted by Magnolia Medical, Inc.
   against Kurin, Inc.
 * USPTO Issues Final Rejection of Magnolia Medical’s ‘483 Patent at Issue in
   Litigation
 * Kurin, Inc. Reports Record Revenue for Q3 2023
 * Kurin, Inc. Named 2023 Diverse Supplier of the Year by Vizient


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KURIN BLOOD CULTURE COLLECTION SETS


CLINICALLY PROVEN AND FDA INDICATED FOR REDUCING BLOOD CULTURE CONTAMINATION.*


Click here to view 510(k) clearances for all Kurin product codes.

Kurin Lock® blood culture collection sets passively sideline the initial 0.15ml
of blood, which may contain contaminants from the patient’s own skin, ensuring
that the best possible blood specimen reaches the collection bottles.

Studies show compliance with best practice combined with Kurin technology to
sideline the initial flash of blood can reduce contaminated cultures by more
than 80%, improving the clinical value of blood culture testing for safer, more
effective, and lower cost treatment of patients.

Learn more


BATTLING FALSE-POSITIVE BLOOD CULTURES

Bloodstream infection diagnosis is critical to the wellbeing of patients and the
financial health of hospitals.

Each year, millions of blood culture tests occur, though the majority will find
no infection.1 Of the cultures that test positive, almost 33% are FALSE-positive
results caused by contamination.

Roughly 20% of the skin microbes reside deep in the dermis layer and may be
drawn into blood samples.2 Unavoidable until now, hospitals have accepted the
consequences of high rates of false positive results.

Learn more



Just like the boy who cried wolf, high numbers of false positive results lead to
inappropriate treatment and cause physicians to question the test. Hear experts
explain the consequences of blood culture contamination.
Watch video


CENTERS FOR DISEASE CONTROL AND PREVENTION

In offering guidance, the CDC references a study by Doern et al which identifies
ways to address blood culture contamination. Among the preventive actions, the
CDC authors call for the use of diversion devices saying, “There are devices
that are commercially available that have shown promise in further reducing
blood culture contamination rates. These devices initially divert a small amount
of potentially contaminated blood and then collect blood for the blood culture.”

Read the full guidance: Blood Culture Contamination: An Overview for Infection
Control and Antibiotic Stewardship Programs Working with the Clinical Laboratory


RESOURCES TO LEARN MORE



Kurin in Action

Best Practices

BetterBlood
Cultures.com




Kurin Studies

Clinical Evidence

Clinical Guidelines


 
PreviousNext


*The Kurin Blood Collection System is for use as a blood collection system and
its Kurin Lock allows the specimen of blood from the patient to be sidelined
prior to the collection of the test sample to reduce the frequency of blood
culture contamination when contaminates are present in the initial blood sample
compared to blood cultures drawn using standard practice without the Kurin Lock.
[FDA 510(k) Indication Number K220677]

REFERENCES:
1 Zwang O, Albert RK. J Hosp Med. 2006 Sep;1(5):272-6.
2 Garcia RA, Spitzer ED, Beaudry J, et al. Am J Infect Control. 2015 Nov
1;43(11):1222-37.

ML-008 Rev I

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