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TechTalk Hemolysis

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1K views

TechTalk Hemolysis

BD

Uploaded by

ARIF AHAMMED P
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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TechTalk

Volume 8, No. 1 January 2010


Author: Lena Arzoumanian
The BD Technical Services Department receives
many questions about our products. To address
these questions, we have developed a news bulletin
called Tech Talk to be sent out periodically.

What Is Hemolysis?
Hemolysis is the breakage of the red blood cells (RBCs) membrane, causing the release of the hemoglobin and other
internal components into the surrounding fluid. Hemolysis is visually detected by showing a pink to red tinge in serum
or plasma.1 Hemolysis is a common occurrence seen in serum samples and may compromise the laboratorys test
parameters. Hemolysis can occur from two sources:
I n-vivo hemolysis may be due to pathological conditions, such as autoimmune hemolytic anemia or
transfusion reaction.1
In-vitro hemolysis may be due to improper specimen collection, specimen processing, or specimen transport.

What Are The Causes?


Specimen Collection:
Evacuated Tubes
An improper choice in the venipuncture site, such as drawing from a distal site to the antecubital region of the arm
rather than drawing from an antecubital site, has been shown to result in more hemolysis.2
Prolonged tourniquet time causes the interstitial fluid to leak into the tissue and cause hemolysis.2
Cleansing the venipuncture site with alcohol and not allowing the site to dry may cause hemolysis.3
An improper venipuncture, indicated by a slow blood flow, may indicate occlusion due to the lumen of the needle being
too close to the inner wall of the vein, causing hemolysis.4
The use of a small-bore needle, resulting in a large vacuum force applied to the blood, may cause shear stress on the red
blood cells, causing them to rupture.1,5,6
The use of a large bore needle may result in a much faster and more forceful flow of blood through the needle, resulting
in hemolysis.1,7
Syringe Draws
Pulling the plunger of a syringe back too far while using a large bore needle, may cause enough pressure for hemolysis
to result during collection. The pressure may be greater than a standardized evacuated tube.
Transferring into a tube by pushing down on the syringe plunger in order to force blood into a tube may cause hemolysis,
as well as create a positive pressure in the tube which may cause the stopper to come off.
IV Catheters
Several studies have noted that when blood is drawn from a peripheral IV catheter, a higher incidence of hemolysis
occurs due to frothing of the blood from a loose connection of the blood collection assemblies.1,8
Specimen Processing:
Vigorous mixing or shaking of a specimen may cause hemolysis.
Not allowing the serum specimen to clot for the recommended amount of time can result in fibrin formation in the
serum. The use of applicator sticks to dislodge the fibrin may cause rupture of RBCs, resulting in hemolysis.1,5
Prolonged contact of serum or plasma with cells may result in hemolysis.9
Exposure to excessive heat or cold can cause RBC rupture and hemolysis.10
Specimen Transport:
Mechanical trauma during transport may occur with the use of a pneumatic tube system, resulting in hemolysis.
Variable factors associated with the system are related to system differences such as length, speed, and number of times
the specimen is transported, as well as the number of angles or turns the system uses.2

continued on reverse side


What Are The Effects Of Hemolysis?
Test results from all laboratory disciplines can be affected by hemolysis, especially in chemistry. Hemolysis may cause
certain analytes to be increased due to leakage of red cell constituents (e.g., lactate dehydrogenase and potassium),
or may cause interference in the test method (e.g., spectrophotometric methods). The amount of interference will
depend on the degree of hemolysis and on the specific test method being used. Hemolysis is a common cause of specimen
rejection in laboratories, which requires the specimen to be redrawn.5,10,11,12,13

Corrective Actions
Redraw the specimen.
T
 he most common sites to draw from are the median cubital, basilic, and cephalic veins from the antecubital
region of the arm.
T
 he choice of the needle gauge size is dependent on the patients physical characteristics and the amount of
blood to be drawn. Avoid using a needle that is too small or too large.
The tourniquet should be released after no more than one minute, and excessive fist clenching should be avoided.
Without touching, allow the venipuncture site to air dry.
Avoid drawing the syringe plunger back too forcefully when collecting blood with a needle and syringe.
A
 void pushing the plunger too forcefully when transferring to a tube. Use a blood transfer device when transferring
from a syringe to a tube without pushing the plunger.
E
 nsure all blood collection assemblies are fitted securely, to avoid frothing. Utilize a luer-locking device with
infusion equipment to ensure a secure fit.14
G
 ently invert the blood collection tube and mix additive specimens thoroughly according to manufacturers
recommendations.
- I nvert specimen with a clot activator 5 times to ensure the distribution of the clot activator within the sample,
and allow the specimen to clot for a full 30 minutes in a vertical position.
- Non-gel serum tubes should be allowed to clot for 60 minutes in a vertical position.
- Sodium citrate tubes for coagulation testing should be inverted 3-4 times.
- All other anticoagulant tubes should be inverted 8-10 times.3
References:
1. Lemery L. Oh, No! Its Hemolyzed! What, Why, Who, How? Advance for Medical Laboratory Professionals, Feb. 15, 1998: 24-25.
2. Burns ER, Yoshikawa N. Hemolysis in serum samples drawn by emergency department personnel versus laboratory phlebotomists.
Lab Med. 2002; 33: 378 380.
3. CLSI Document H3-A6. Procedures for the collection of diagnostic blood specimens by venipuncture; approved standard 6th ed.
Wayne, PA: National Committee for Clinical Laboratory Standards; 1998.
4. Garza D and Becan-McBride K. Phlebotomy Handbook, 5th Ed. Stamford, CT: Appleton & Lange; 1999.
5. Laessig RH, Hassemer DJ, Paskey TA., Schwartz TH, The effects of 0.1 % and 1.0 % erythrocytes and hemolysis on serum chemistry values.
Am J Clin. Pathol. 1976; 66: 639-44.
6. Sharp MK, Mohammad SF. Scaling of hemolysis in needles and catheters. Ann Biochem Engineer. 1998; 26: 788-797.
7. Savory J. Bill JG. Hemolysis of specimens drawn in the ER [Q&A]. Lab Med. 1996; 27: 802.
8. Kennedy C, Angemuller S, King R, et al. A comparison of hemolysis rates using intravenous catheters versus venipuncture tubes for obtaining
blood samples. J Emer Nurs 1996; 22: 566-9.
9. Boyanton BL. Jr. Blick KE., Stability studies of twenty-four analytes in human plasma and serum. Clin. Chem. 2002; 48: 2242-7.
10. Kroll MH, Elin RJ. Interference with clinical laboratory analyses (review). Clin. Chem. 1994; 40: 1996-2005.
11. Sonntag O. Haemolysis as an interference factor in clinical chemistry. J Clin Chem Clin Biochem. 1986; 24: 127-39.
12. Frank JJ, Bermes EW, Bickel MJ, Watkins BF. Effect of in vitro hemolysis on chemical values for serum. Clin Chem. 1978; 24: 1966-70.
13. Carraro P, Servidio G, Plebani M. Hemolyzed specimens: a reason for rejection or a clinical challenge? Clin Chem. 2000; 46: 306-7.
14. Journal of Infusion Nursing, Infusion Nursing Standards of Practice, Jan/Feb 2006; Vol. 29, No. 1S.

Please call BD Technical Services for clinical support material.

BD Technical Services: 1.800.631.0174


BD Customer Service: 1.888.237.2762 1 Becton Drive
Franklin Lakes, NJ 07417
www.bd.com/vacutainer
BD, BD Logo and Vacutainer are trademarks of Becton, Dickinson and Company. 2010 BD
Printed in USA 1/10 VS 7167-1

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