Venipuncture
In medicine, venipuncture or venepuncture is the process of obtaining intravenous access for the purpose of venous blood sampling (also called phlebotomy) or intravenous therapy. In healthcare, this procedure is performed by medical laboratory scientists, medical practitioners, some EMTs, paramedics, phlebotomists, dialysis technicians, and other nursing staff.[1] In veterinary medicine, the procedure is performed by veterinarians and veterinary technicians.
It is essential to follow a standard procedure for the collection of blood specimens to get accurate laboratory results. Any error in collecting the blood or filling the test tubes may lead to erroneous laboratory results.[2]
Venipuncture is one of the most routinely performed invasive procedures and is carried out for any of five reasons:
- to obtain blood for diagnostic purposes;
- to monitor levels of blood components;[3]
- to administer therapeutic treatments including medications, nutrition, or chemotherapy;
- to remove blood due to excess levels of iron or erythrocytes (red blood cells); or
- to collect blood for later uses, mainly transfusion either in the donor or in another person.
Blood analysis is an important diagnostic tool available to clinicians within healthcare.
Blood is most commonly obtained from the superficial veins of the upper limb.[1] The median cubital vein, which lies within the cubital fossa anterior to the elbow, is close to the surface of the skin without many large nerves positioned nearby. Other veins that can be used in the cubital fossa for venipuncture include the cephalic, basilic, and median antebrachial veins.[4]
Minute quantities of blood may be taken by fingerstick sampling and collected from infants by means of a heelprick or from scalp veins with a winged infusion needle.
Phlebotomy (incision into a vein) is also the treatment of certain diseases such as hemochromatosis and primary and secondary polycythemia.
Complications
A 1996 study of blood donors (a larger needle is used in blood donation than in routine venipuncture) found that 1 in 6,300 donors suffered a nerve injury.[5]
Equipment
There are many ways in which blood can be drawn from a vein, and the method used depends on the person's age, the equipment available, and the type of tests required.
Most blood collection in the US, UK, Canada and Hong Kong is done with an evacuated tube system, (two common systems are Vacutainer (Becton, Dickinson and company) and Vacuette (Greiner Bio-One). The equipment consists of a plastic adapter, also known as a tube or needle holder/ hub, a hypodermic needle and a vacuum tube. Under certain circumstances, a syringe may be used, often with a butterfly needle, which is a plastic catheter attached to a short needle. In the developing world, the evacuated tube system is the preferred method of drawing blood
With evacuated or vacuum tubes
Greiner Bio-One manufactured the first ever plastic evacuated blood collection tube in 1985 under the VACUETTE brand name. Today, many companies sell vacuum tubes as the patent for this device is now in the public domain. These tubes are manufactured with a specific volume of gas removed from the sealed tube. When a needle from a hub or transfer device is inserted into the stopper, the tube's vacuum automatically pulls in the required volume of blood.
The basic Evacuated Tube System (ETS) consists of a needle, a tube holder, and the evacuated tubes. The needle is attached to the tube holder by the phlebotomist prior to collection, or may come from the manufacturer as one unit. The needle protrudes through the end of the tube holder, and has a needle on each end. After first cleaning the venipuncture site and applying a tourniquet, the phlebotomist uncaps the needle attached to the tube holder, inserts the needle into the vein, then slides evacuated tubes into the tube holder, where the tube's stopper is pierced by the back end of the needle. The vacuum in the tube then automatically draws the needed blood directly from the vein. Multiple vacuum tubes can be attached to and removed in turn from a single needle, allowing multiple samples to be obtained from a single procedure. This is possible due to the multiple sample sleeve, which is a flexible rubber fitting over the posterior end of the needle cannula which seals the needle until it is pushed out of the way. This keeps blood from freely draining out of the back of the needle inserted in the vein, as each test tube is removed and the next impaled. OSHA safety regulations require that needles or tube holders come equipped with a safety device to cover the needle after the procedure to prevent accidental needle stick injury.[6]
Fittings and adapters used to fill evacuated tubes from butterfly needle kits and syringes are also available.
There are several needle gauges for a phlebotomist to choose from. The most commonly used are as follows: a 21g (green top) needle, a 22g (black top) needle, a 21g (green label) butterfly needle, a 23g (light blue label) butterfly needle, and a 25g (orange or dark blue label) butterfly needle (however this needle is only used in pediatrics or extreme cases as it is so small that it can often result in hemolyzing the blood sample). There are also a variety of tube and bottle sizes and volumes for different test requirements.[7]
Additives and order of draw
The test tubes in which blood is collected may contain one or more of several additives. In general, tests requiring whole blood call for blood samples collected in test tubes containing some form of the anticoagulant EDTA. EDTA chelates calcium to prevent clotting. EDTA is preferred for hematology tests because it does minimum damage to cell morphology. Sodium Citrate is the anticoagulant used in specimens collected for coagulation tests. The majority of chemistry and immunology tests are performed on serum, which is produced by clotting and then separating the blood specimen via centrifuge. These specimens are collected in either a non-additive tube or one containing a clotting activator. This clotting activator can interfere with some assays, and so a plain tube is recommended in these cases, but will delay testing. Tubes containing lithium heparin or sodium heparin are also commonly used for a variety of chemistry tests, as they do not require clotting and can be centrifuged immediately after collection. A combination of sodium fluoride and potassium oxalate is used for glucose tests, as these additives both prevent clotting and stop glycolosis, so that blood glucose levels are preserved after collection.[8] Another specialty tube is an opaque amber colored tube used to collect blood for light sensitive analytes, such as bilirubin.
Test tubes are labeled with the additive they contain, but the stopper on each tube is color coded according to additive as well. While colors vary between manufacturers, stopper colors generally are associated with each additive as listed below. Because the additives from each tube can be left on the needle used to fill the tubes, they must be drawn in a specific order to ensure that cross contamination will not negatively affect testing of the samples if multiple tubes are to be drawn at once. The "order of draw" varies by collection method. Below in the order of draw generally required for the Evacuated Tube System (ETS) collection method are the most common tubes, listing additive and color:[9][10]
| Tube cap color or type in order of draw | Additive | Usage and comments |
|---|---|---|
| Blood culture bottle | Sodium polyanethol sulfonate (anticoagulant) and growth media for microorganisms | Usually drawn first for minimal risk of contamination.[11] Two bottles are typically collected in one blood draw; one for aerobic organisms and one for anaerobic organisms.[12] |
| Blue
("light blue") |
Sodium citrate
(weak calcium chelator/anticoagulant) |
Coagulation tests such as prothrombin time (PT) and partial thromboplastin time (PTT) and thrombin time (TT). Tube must be filled 100%. |
| Plain red | No additive | Serum: Total complement activity, cryoglobulins |
| Gold (sometimes red and grey "tiger top"[13]) | Clot activator and serum separating gel[14] | Serum-separating tube (SST): Tube inversions promote clotting. Most chemistry, endocrine and serology tests, including hepatitis and HIV. |
| Orange | Clot activator and serum separating gel[15] | Rapid serum-separating tube (RST). |
| Dark green | Sodium heparin (anticoagulant) | Chromosome testing, HLA typing, ammonia, lactate |
| Light green | Lithium heparin (anticoagulant)
Plasma separator gel |
Plasma. Tube inversions prevent clotting |
| Lavender ("purple") | EDTA (chelator / anticoagulant) | Whole blood: CBC, ESR, Coombs test, platelet antibodies, flow cytometry, blood levels of tacrolimus and cyclosporin |
| Pink | K2 EDTA (chelator / anticoagulant) | Blood typing and cross-matching, direct Coombs test, HIV viral load |
| Royal blue
("navy") |
EDTA (chelator / anticoagulant) | Trace elements, heavy metals, most drug levels, toxicology |
| Tan | Sodium EDTA (chelator / anticoagulant) | Lead |
| Gray |
Fluoride Oxalate
|
Glucose, lactate,[16] toxicology[17] |
| Yellow | Acid-citrate-dextrose A (anticoagulant) | Tissue typing, DNA studies, HIV cultures |
| Pearlescent ("white") | Separating gel and (K2)EDTA | PCR for adenovirus, toxoplasma and HHV-6 |
| Black | Sodium Citrate | Paediatric ESR |
| QuantiFERON
Grey, Green, Yellow, Purple |
QuantiFERON
1. Grey (nil) tube 2. Green (TB1 antigen) tube 3. Yellow (TB2 antigen) tube 4. Purple (mitogen) tube |
Tuberculosis |
In children
Use of lidocaine iontophoresis is effective for reducing pain and alleviating distress during venipuncture in children.[18] A needle-free powder lignocaine delivery system has been shown to decrease the pain of venipuncture in children.[19][20] Rapid dermal anesthesia can be achieved by local anesthetic infiltration, but it may evoke anxiety in children frightened by needles or distort the skin, making vascular access more difficult and increasing the risk of needle exposure to health care workers. Dermal anesthesia can also be achieved without needles by the topical application of local anesthetics or by lidocaine iontophoresis. By contrast, noninvasive dermal anesthesia can be established in 5–15 min without distorting underlying tissues by lidocaine iontophoresis, where a direct electric current facilitates dermal penetration of positively charged lidocaine molecules when placed under the positive electrode.
One study concluded that the iontophoretic administration of lidocaine was safe and effective in providing dermal anesthesia for venipuncture in children 6–17 years old. This technique may not be applicable to all children. Future studies may provide information on the minimum effective iontophoretic dose for dermal anesthesia in children and the comparison of the anesthetic efficacy and satisfaction of lidocaine iontophoresis with topical anesthetic creams and subcutaneous infiltration.[18]
Non-pharmacological treatments for pain associated with venipuncture in children includes hypnosis and distraction. These treatments reduced self reported pain and when combined with cognitive-behavioural therapy (CBT) the reduction of pain was even greater. Other interventions have not been found to be effective and these are suggestion, blowing out air, and distraction with parent coaching did not differ from control for pain and distress.[21]
With needle and syringe
Some health care workers prefer to use a syringe-needle technique for venipuncture. Sarstedt manufactures a blood-drawing system (S-Monovette) that uses this principle.[22] This method can be preferred on the elderly, those with cancer, severe burns, obesity, or where the veins are unreliable or fragile. Because syringes are manually operated, the amount of suction applied may be easily controlled. This is particularly helpful when veins are small which may collapse under the suction of an evacuated tube. In children or other circumstances where the quantity of blood gained may be limited it can be helpful to know how much blood can be obtained before distributing it amongst the various additives that the laboratory will require. Another alternative is drawing blood from indwelling cannulae. [23]
Blood cultures
There are times when a blood culture collection is required. The culture will determine if there are pathogens in the blood. Normally blood is sterile. When drawing blood from cultures use a sterile solution such as Betadine rather than alcohol. This is done using sterile gloves, while not wiping away the surgical solution, touching the puncture site, or in any way compromising the sterile process. It is vital that the procedure is performed in as sterile a manner as possible as the persistent presence of skin commensals in blood cultures could indicate endocarditis but they are most often found as contaminants. It is encouraged to use an abrasive method of skin preparation. This removes the upper layers of dead skin cells along with their contaminating bacteria.[24] Povidone-iodine has traditionally been used but in the UK a 2% chlorhexidine in 70% ethanol or isopropyl alcohol solution is preferred and time must be allowed for it to dry. The tops of any containers used when drawing a blood culture should also be disinfected using a similar solution. Some labs will actively discourage iodine use where iodine is thought to degrade the rubber stopper through which blood enters the bottle, thus allowing contaminates to enter the container.
The blood is collected into special transport bottles, which are like vacuum tubes but shaped differently. The blood culture bottle contains transport media to preserve any microorganisms present while they are being transported to the laboratory for cultures. Because it is unknown whether the pathogens are anaerobic (living without oxygen) or aerobic (living with oxygen), blood is collected to test for both. The aerobic bottle is filled first, and then the anaerobic bottle is filled. However, if the collection is performed using a syringe, the anaerobic bottle is filled first. If a butterfly collection kit is used, the aerobic bottle is filled first, so that any air in the tubing is released into the oxygen-containing bottle.
Specially designed blood culture collection bottles eliminate the need for either the syringe or butterfly collection method. These specially designed bottles have long necks that fit into the evacuated tubes holders that are use for regular venipuncture collection. These bottles also allow for collection of other blood specimens via evacuated tubes, to be collected without additional venipuncture.
The amount of blood that is collected is critical for the optimal recovery of microorganisms. Up to 10mL of blood is typical, but can vary according to the recommends of the manufacturer of the collection bottle. Collection from infants and children are 1 to 5 mL. If too little blood is collected, the ratio of blood-to-nutrient broth will inhibit the growth of microorganisms. If too much blood is collected, there is the risk of a hospital-induced anemia and the ratio of blood-to-nutrient broth will tilt in the opposite direction, which also is not conductive to optimal growth.
The bottles are then incubated in specialized units for 24 hours before a lab technician studies and/or tests it. This step allows the very small numbers of bacteria (potentially 1 or 2 organisms) to multiply to a level which is sufficient for identification +/-antibiotic resistance testing. Modern blood culture bottles have an indicator in the base which changes color in the presence of bacterial growth and can be read automatically by machine. (For this reason the barcoded stickers found on these bottles should not be removed as they are used by the laboratory's automated systems.)
Taking blood samples from animals
Blood samples from living laboratory animals may be collected using following methods:[25][26]
- Blood collection not requiring anesthesia:
- Saphenous vein (rat, mice, guinea pig)
- Dorsal pedal vein (rat, mice)
- Blood collection requiring anesthesia (local/general anesthesia):
- Tail vein (rat, mice)
- Tail snip (mice)
- Orbital sinus (rat, mice)[27]
- Jugular vein (rat, mice)
- Temporary cannula (rat, mice)
- Blood vessel cannulation (guinea pig, ferret)
- Tarsal vein (guinea pig)
- Marginal ear vein or artery (rabbit)
- Terminal procedure:
- Cardiac puncture (rat, mice, guinea pig, rabbit, ferret)
- Orbital sinus (rat, mice)
- Posterior vena cava (rat, mice)
The volume of the blood sample collection is very important in experimental animals. All nonterminal blood collection without replacement of fluids is limited up to 10% of total circulating blood volume in healthy, normal, adult animals on a single occasion and collection may be repeated after three to four weeks. In case repeated blood samples are required at short intervals, a maximum of 0.6 ml/kg/day or 1.0% of an animal's total blood volume can be removed every 24 hours. The estimated blood volume in adult animals is 55 to 70 ml/kg body weight. Care should be taken for older and obese animals. If blood collection volume exceeds more than 10% of total blood volume, fluid replacement may be required. Lactated Ringer's solution (LRS) is recommended as the best fluid replacement by National Institutes of Health (NIH). If the volume of blood collection exceeds more than 30% of the total circulatory blood volume, adequate care should be taken so that the animal does not suffer from hypovolemia.[26]
Blood alcohol tests
It is generally not advisable to use isopropyl alcohol to cleanse the venipuncture site when obtaining a specimen for a blood alcohol test. This has been related largely to the potential legal implications associated with use of alcohol based cleaners that could theoretically impact analysis. Numerous police alcohol collection kits have been marketed that incorporate a sodium fluoride/potassium oxalate preservative and non-alcohol based cleansing agents to ensure proper collection. Using soap and hot water or a povidone-iodine swab are advisable alternatives to isopropyl alcohol in this case.
See also
- Arterial blood is taken from an artery instead of a vein
References
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- ^ Dg, Dayyal. "PROCEDURES FOR THE COLLECTION OF BLOOD FOR HEMOTOLOGICAL INVESTIGATIONS". BioScience Pakistan. BioScience Pakistan. ISSN 2521-5760.
- ^ Lavery, I; Ingram, P (August 2005). "Venepuncture: Best Practice". Nurs Stand. 19 (49): 55–65. doi:10.7748/ns2005.08.19.49.55.c3936. PMID 16134421.
- ^ Ialongo, Cristiano; Bernardini, Sergio (2016-02-15). "Phlebotomy, a bridge between laboratory and patient". Biochemia Medica. 26 (1): 17–33. doi:10.11613/BM.2016.002. ISSN 1330-0962. PMC 4783087. PMID 26981016.
- ^ "'A Little Sting' Can Become a Debilitating Injury". Retrieved 25 March 2020.
- ^ McCall, Ruth (2020). Phlebotomy Essentials (7th ed.). Wolters Kluwer. p. 193. ISBN 9781496387073.
- ^ Perry, Sally (2007). "Ask the Lab: Hemolyze blood specimens". Nursing.advanceweb.com. Retrieved 2013-12-29.
- ^ a b Castellini MA, Castellini JM, Kirby VL (1992). "Effects of standard anticoagulants and storage procedures on plasma glucose values in seals". J Am Vet Med Assoc. 201 (1): 145–8. PMID 1644639.
- ^ "Collection". www.osfhealthcare.org. Retrieved 2019-12-08.
- ^ Christopher Parker (2019-01-31). "Phlebotomy Services". University of North Carolina School of Medicine.
- ^ Pagana, KD; Pagana, TJ; Pagana, TN (19 September 2014). Mosby's Diagnostic and Laboratory Test Reference - E-Book. Elsevier Health Sciences. p. xiii. ISBN 978-0-323-22592-2.
- ^ "Chapter 3.4.1: Blood cultures; general detection and interpretation". Clinical Microbiology Procedures Handbook. Wiley. 6 August 2020. ISBN 978-1-55581-881-4.
- ^ "Test Tube Guide and Order of Draw" (PDF). Guthrie Laboratory Services. June 2019.
- ^ "Specimen requirements/containers". Pathology & Laboratory Medicine, UCI School of Medicine. Retrieved 2020-09-10.
- ^ "Proper Order of Draw" (PDF). Memorial Lab Services. Retrieved 2023-06-15.
- ^ Amitava Dasgupta; Jorge L. Sepulveda (20 July 2019). Accurate Results in the Clinical Laboratory: A Guide to Error Detection and Correction. Elsevier Science. p. 131. ISBN 978-0-12-813777-2.
- ^ "What types of samples will the Toxicology Lab analyze?". Oklahoma State Bureau of Investigation. Retrieved 2024-01-24.
- ^ a b Rose, John B.; Galinkin, Jeffrey L.; Jantzen, Ellen C.; Chiavacci, Rosetta M. (2002). "A Study of Lidocaine Iontophoresis for Pediatric Venipuncture". Anesthesia & Analgesia. 94 (4): 867–71, table of contents. doi:10.1097/00000539-200204000-00017. PMID 11916787.
- ^ Lacroix, Helene (October 2008). "A needle-free powder lignocaine delivery system reduced the pain of venipuncture in children". Evidence-Based Nursing. 11 (4): 106. doi:10.1136/ebn.11.4.106. PMID 18815318.
- ^ Robertson, J (January 2006). "Liposomal lidocaine improved intravenous cannulation success rates in children". Evid Based Nurs. 9 (1): 10. doi:10.1136/ebn.9.1.10. PMID 16437788.
- ^ Robertson, J (July 2007). "Review: Distraction, Hypnosis, and Combined Cognitive-Behavioural Interventions Reduce Needle Related Pain and Distress in Children and Adolescents". Evid Based Nurs. 10 (3): 75. doi:10.1136/ebn.10.3.75. PMID 17596380.
- ^ "Blood collection with the S-Monovette" (PDF). Retrieved 27 May 2020.
- ^ Lesser, Finnian D; Lanham, David A; Davis, Daniel (6 May 2020). "Blood sampled from existing peripheral IV cannulae yields results equivalent to venepuncture: a systematic review". JRSM Open. 11 (5). doi:10.1177/2054270419894817.
- ^ Garcia, RA; Spitzer, ED; Beaudry, J; Beck, C; Diblasi, R; Gilleeny-Blabac, M; Haugaard, C; Heuschneider, S; Kranz, BP; McLean, K; Morales, KL; Owens, S; Paciella, ME; Torregrosa, E (November 2015). "Multidisciplinary Team Review of Best Practices for Collection and Handling of Blood Cultures to Determine Effective Interventions for Increasing the Yield of True-positive Bacteremias, Reducing Contamination, and Eliminating False-positive Central Line-associated Bloodstream Infections". Am J Infect Control. 43 (11): 1222–37. doi:10.1016/j.ajic.2015.06.030. PMID 26298636.
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{{cite journal}}: CS1 maint: unflagged free DOI (link) - ^ Parasuraman, Subramani; Zhen, Khor Ming; Raveendran, Ramasamy (22 May 2015). "Retro-orbital Blood Sample Collection in Rats-a Video Article". Pharmacology, Toxicology and Biomedical Reports. 1 (2): 37–40. doi:10.5530/PTB.1.2.1.