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VENIPUNCTURE EQUIPMENTS

MULTISAMPLE NEEDLES
PHLEBOTOMY EQUIPMENT  A double ended needle. One tip of the needle
 Are collection equipment which includes the penetrates the patient’s skin, and the second
needles and tubes that allow to collect patient’s pierces the rubber cap of an evacuated collection
blood, plus materials to ensure that a vein can be tube.
located, the puncture site is sterile, and the
samples is labelled and transported correctly. SAFETY SYRINGES AND NEEDLES
 Proper handling of phlebotomy equipment is of  Is used for patients with fragile or small veins,
the utmost importance for the safety of both the when the vacuum of the collection tube is likely
phlebotomist and the patient. to collapsed the vein.

ORGANIZATION OF EQUIPMENTS WINGED INFUSION SET OR BUTTERFLY


 An important key to successful blood collection  Is used for venepuncture on small veins, such as
is making sure that all the required equipment is those in the hand, elderly, pediatric patient.
conveniently present in the collection area.  Has plastic wings attached to the needle and
includes two types of systems.
LOCATING THE VEIN
NEEDLE SAFETY
TOURNIQUET  Is used to reduce the number of sharp injuries.
 Prevents venous blood flow out of the arm,
causing the vein to bulge. NEEDLE ADAPTERS
 Most frequently used:  Is used to ensure a firm, stable connection
o Flat Latex or Vinyl Strips between the multi-sample needle and the
o Snap evacuated tube.
o Blood Pressure Cuffs
LANCETS
CLEANING THE PUNCTURE SITE  Are small cutting instruments designed to
control the depth of the dermal puncture.
ANTISEPTICS
 Agent used to clean living tissues EVACUATED COLLECTION TUBES
 Contain a premeasured vacuum and are most
DISINFECTANTS widely used system in blood collection
 Agent used to clean a surface other than living  These tubes are sterile and contain additives.
tissues  Variety of sizes and colors and are made of glass
or plastics.
 70% Isopropyl Alcohol – most commonly used
antiseptic TUBE ADDITIVES
 Benzalkonium Chloride, Chlorhexidine  Additives include anticoagulants to
Gluconate and Povidone-Iodine – alternative o prevent clotting,
disinfectants if the patient is allergic to isopropyl o clot activator to promote it
alcohol o thixotropic gel to separate components
o preservatives and inhibitors of cellular
PROTECTING THE PUNCTURE SITE reactions to maintain the integrity of
the specimen.
GAUZE PAD  Many tubes are coated inside with silicone, to
 A loosely woven cotton fabric used to cover a prevent blood from adhering to the wall of the
puncture site when applying pressure tube and to slow down the cooling process.
immediately upon completion of the procedure.
 ANTICOAGULANT
NEEDLES o Prevent blood from clotting.
 Inserted into a vein that allows blood to flow out  EDTA
into an evacuated tube or syringe. (Ethylenediaminetetraacetic
 Composed of a hub, the shaft, and the bevel. acid),
 SPS(sodium polyanethol ROUTINE VENIPUNCTURE
sulfonate),
 Sodium citrate, REQUISITIONS
 sodium oxalate,  The form the phlebotomist used to determine
 heparin what type of sample to collect from the patient.
o Patient Demographic (Age, Sex, etc.)
o Physician’s name
 CLOT ACTIVATOR
o Test name
o Promote coagulation. Thrombin directly
o Test status
increase clotting.
o Hospital ID number, room and bed
o inert substances are glass or silica,
number.
siliceous earth, clay, and celite.
BASIC BLOOD COLLECTION
 THIXOTROPIC GEL
1. Greet and properly identify the patient
o An inert, synthetic substance whose
2. Select and assemble the appropriate equipment
density is in between that of cells and
3. Use aseptic technique and Standard precaution
that of blood serum plasma.
during venepuncture and specimen collection
o Thixo “Related to touch” and refers to
4. Provide post-puncture patient care
gel’s ability to liquefy when shaken.
5. Adhere to specimen labelling equipment
TUBES ADDITIVE/COLOR CODED TOPS
GREETING THE PATIENT
 A phlebotomist’s demeanor instills confidence
and trust in the patient, which can effectively
ease patient apprehension about the
procedure.

ASSEMBLING THE VENIPUNCTURE EQUIPMENT


 Line up the venepuncture equipment needed
for the procedure near the patient by having
the phlebotomy cart or tray placed next to the
patient’s bed.

 The needle must not touch anything to


NEEDLE DISPOSAL CONTAINER prevent contamination, otherwise, raw
 A used needle is considered biohazard waste needle must be use.
and must be treated as such.
 Dispose the needle and activate the needle PATIENT POSITIONING
safety device.  The patient’s position is another critical factor
 needles must be placed in a clearly marked for a successful venipuncture. When
puncture-resistant biohazard container. identification is completed, the patient must be
positioned conveniently and safely for the
procedure.

APPLYING THE TOURNIQUET


 When tourniquet is applied, the flow of venous
blood is slowed, which increases pressure in the
veins, making them more visible and palpable.
 Applied to the arm 3 to 4 inches above the
puncture site

SELECTING THE PUNCTURE SITE


 The most common area to perform a
venipuncture is the antecubital area of the arm.
 Patients generally have prominent veins on the DERMAL PUNCTURE
dominant arm.
 Palpate the vein using the tip of the index DERMAL/CAPILLARY PUNCTURE
finger. Select a vein that is large.  The preferred blood collection technique for
infants (heel) and very small children (finger)
SELECTING THE PUNCTURE SITE o Infants/Children
(Don’ts in selecting a puncture site) o Geriatric Patients (elderly)
1. Do not pump the fist because this can cause o Oncology patients (cancer patients)
hemaconcentration – increased concentration o Severely burned patients
of cells and solids in the blood usually resulting o Obese patients
from loss of fluid to the tissues . o At risk venous thrombosis
2. DO NOT select a vein that moves easily or roll o IV therapy
from side to side. o Capillary specimen only
3. AVOID a vein that exhibits sclerosis, or feels  The blood specimen obtained during dermal
hard and cordlike. puncture is a mixture of capillary blood, venous
4. Avoid paralyzed limbs and sites with shunts.
blood, arterial blood, and interstitial fluid.
5. Do not use the anterior side of the wrist
Example:
6. Ankle veins are not used for venipuncture
o Capillary (glucose, haemoglobin)
7. Never select an arm that is edematous – An
accumulation of an excessive amount of watery o Venous (potassium, calcium, total
fluid in cells, tissues, or body cavities. protein)
8. Do not perform venipuncture above IV site DISADVANTAGE
(contamination)  Hematoma
9. Avoid the arm on the side of mastectomy –  Contamination
removal of the whole breast.  Micro clot formation
a. Lymphostasis – Obstruction of the
normal flow of lymph. DERMAL PUNCTURE PREPARATION
1. Acquire and examine the requisition slip
CLEANSING THE VENIPUNCTURE SITE 2. Greet and identify the patient
 Prevents microbial contamination of the 3. Explain the procedure
specimen and the patient’s venepuncture site. 4. Verify and dietary restriction
 70% alcohol – recommended antiseptic 5. Wash your hands
 Cleanse the site using concentric circles. 6. Put on gloves

PERFORMING THE VENIPUNCTURE SELECTING THE SITE FOR DERMAL PUNCTURE


VERIFY THE PUNCTURE SITE  The skin should be warm, pink, free from scars,
 Inserting the needle into the skin at 15- to 30 cuts, rashes, or bruises.
degree angle.  SITES TO CONSIDER:
 collecting the specimen. It is important to hold o Regions of middle finger and ring finger
the puncture assembly steady during the entire in adults and children
tube filling method. o Medial or lateral regions of the plantar
 Removing the needle. Remove the tourniquet surface of the heel of the infant.
prior.
 Remove the last tube from the holder. Gently SELECTING THE SITE FOR DERMAL PUNCTURE
place the – directly in the site (DON’T’S)
 Apply gentle pressure to the site 1. Do not use the thumb, pinkie or pointer finger
 3 – 8 mins or until bleeding stops. they are poor choices because the area is often
too thick and calloused.
AFTER VENIPUNCTURE 2. Do not use the end or tip of the finger
3. Never perform on an infant who has begun to
 DISPOSING THE EQUIPMENT walk because of the potential for pain at the
 LABELLING THE SPECIMEN site.
 APPLY THE BANDAGE
4. Do not use the arch of the foot, the back of the WINGED INFUSION SET (BUTTERFLY
heel, or the plantar area of the foot. METHOD)
5. Do not puncture from the area of the calcaneus
or heel bone; it can cause osteochondritis or  When suitable vein cannot be found in the
osteomyelitis. antecubital fossa
o Hand, foot, leg
PERFORMING A DERMAL PUNCTURE  Collection from the leg and foot usually requires
 Clean the finger with an alcohol pad and allow the physician’s permission
to dry.  Veins at the back of the hand is recommended.
 The finger should be heel in such a way that the
skin is stretched tightly VEINS AT THE BACK OF THE HAND
 For finger puncture, the cut is made across the  Small and fragile
fingerprint lines  Use smaller gauge needle and tube or syringe is
 The puncture depth could be 1.5 to 2.00 mm. advised
 Premature babies is 0.65 to 0.85 mm o Basillic vein, cephalic vein, dorsal
metacarpal vein.
COLLECTING THE CAPILLARY SPECIMEN
 Wipe away the first drop of blood WINGED INFUSION SET (BUTTERFLIES)
 The second drop is collected by touching the
open end of the micro collection container to  Used for the infusion of IV fluids and for
the drop of blood. The container will fill by performing venipuncture from very small or
gravity or capillary action. fragile veins of children and geriatrics
 Capillary tubes are typically collected population.
horizontally using a capillary action and require  Needles are usually 21 or 23 guage with
very little blood lengths of ½ ti ¾ inch.
 Gently squeeze and release the site periodically,  Plastic attachments to the needle that resemble
allowing for capillary refill. butterfly wings are used for holding the needle
 Gently tap the container on a hard surface to during insertion
mix the blood.  The flexible needle can be attached to an IV set
up, syringe, and evacuated tube holder.
COLLECTING THE CAPILLARY SPECIMEN (DON’TS)
 Do not “milk” the finger. It will contaminate the PROCEDURE
specimen with interstitial fluid.
 Do not scrape the collection container against 1. Support the hand on the bed or drawing chair
the skin because it will cause the blood to armrest and have the patient make a fist.
hemolyze or clot 2. Apply the tourniquet 3-4 inches above the wrist
 Do not underfill or overfill the container bone.
3. Palpate the top of the hand or wrist. Select a
AFTER THE DERMAL PUNCTURE vein that is large and straight and that can be
 Mix the specimen easily anchored.
 Dispose of the contaminated safety lancet in the 4. Release the tourniquet, have the patient relax
sharps container the fist, and clean the site with 70% isopropyl
 Label the micro containers and observe any alcohol in concentric circles and allow it to dry.
specimen handling instruction 5. Anchor the vein by placing the thumb of the
 Check the site of puncture and apply a bandage. non-dominant hand below the knuckles and
pulling the skin taut.
o Having the patient make a fist may be
helpful.
o Grasp the needle between the thumb
and index finger by holding the back of
the needle or by folding the wings
together.
6. Pull back on the plunger of the syringe slowly VENIPUNCTURE COMPLICATIONS
and smoothly with the non-dominant hand to
collect blood. Do not pull back on the syringe IDENTIFICATION
plunger if blood does not appear.  You can’t access the patient without any
o When using an evacuated tube holder, identification
o TEMPORARY IDENTIFICATION
insert the tubes in the correct order of
 Requisition form
draw.
 Location
7. Cover the puncture site with gauze, remove the
 Identification of the patient
needle smoothly or activate the safety device
on needles designated to be retracted while the COMMUNICATION BARRIER
needle is in the vein.  Language
8. Remove the winged blood collection set form  When the patient is still sleeping or unconscious
the syringe and discard it in the sharps
container. SITE SELECTION
9. Label the tubes and confirm identification with  Veins that are small
the patient. o Massage. Bending of arm, etc.
10. Examine the puncture site and apply a bandage. o Proceed to alternative sites
11. Remove gloves and wash hands.  Hematoma, Scars, Bruise

SITE CLEANING
 Allergic reaction to alcohol
o Povidone-iodine (betadine)
 Blood culture collection and arterial puncture
(Contamination)
 Blood Alcohol Testing – test that alcohol should
not be used for cleaning the puncture site.
Note: Only doctor, nurses, and medical
technologists are allowed to do the procedure.

TOURNIQUET APPLICATION
 HEMOCONCENTRATION – increases ammonia,
bilirubin, calcium, enzymes, iron, lactic acid,
lipids, potassium, proteins, red blood cells.
o Fluid goes to the tissues
o Hemoglobin increases – 3%
o Pumping
 Petechiae – are small, non-raised red spots.
 Tourniquet applied too tightly – the patient
complains of pinching or numbing of the arm.
 Latex allergy
 Ischemia – anoxia; lack of oxygen supply
 Nerve Injury/Neuropaxia – loss of nerve
function
 Rhabdomyolysis – destruction of muscles.

DURING COLLECTION
 CHANGES IN PATIENT’S STATUS
o Nausea and vomiting
o Syncope – fainting
o Seizure
o Pain
 HEMATOMA – leakage of blood within tissues
- old blood.
 LACK OF BLOOD FLOW TESTS AFFECTED BY PATIENT POSITION
o Defective evacuated tubes Cells counts Haemoglobin or
o Improperly positioned needle haematocrit
 Bevel is stuck to the vein wall Protein Albumin
 Needle is not advanced far Bilirubin Calcium
enough into the vein Enzymes Triglycerides
 Needle has passed through Cholesterol
both sides of the vein
 Vein was missed completely
o Blown out vein – for the term bbq 4. ANTICOAGULANT REFLUX
o Probing – cross stitch
o Reposition – push and pull LONG TERM COMPLICATIONS ASSOCIATED WITH
VENIPUNCTURE
COMPLETING THE PROCEDURE  ANEMIA – Iatrogenic anemia
 Collapsed vein o Decrease of RBC
 Inadvertent puncture of the artery o Cause of treatment
 Failure to collect on the first.  HEMATOMA
o Do it only twice, asap. o Failure to remove tourniquet
 Patient’s request – let him/her sign the request o Applying inadequate pressure
 Prolonged bleeding o Bending the arm
o Excessing probing
FACTORS THAT AFFECT SAMPLE INTEGRITY o Failure to insert the needle enough into
1. HEMOLYSIS the vein
 Using too small needle in respect to vein o Inserting the needle through the vein
size o Selecting a needle too large
 Using a needle smaller than 23 gauge o Using veins that are small
 Using a needle with large vacuum tube o Puncturing brachial artery
 Too much agitation of blood
 Vigorously mixing or shaking tubes  COMPARTMENT SYNDROME
 Blood frothing, from a needle improperly
 NERVE DAMAGE
attached to a syringe
 INFECTION
 Failing to allow blood to run down the side
of the tube
REMEDIES TO MAKE VEIN PROMINENT
 Forcing blood from a syringe into vacuum
 Massage the puncture site
 Blood flow is slow
 Warm wash cloth <42 degree Celsius
 NOT ACCEPTED
 Light exercise
 Tapping the puncture site
TEST AFFECTED BY HEMOLYSIS
 Cleansing it with an alcohol
Seriously Moderately Slightly
 Twisting the wrist
affected affected affected
Potassium CBC Phosphorus
INFORMATIONS
LD Serum iron Total protein  Patient’s full name
AST ALT Albumin  Age
Thyroxine Magnesium  Gender
Calcium  Date and time
ACP  Phlebotomist’s initial
 Test name
2. BLOOD DRAWN FROM HEMATOMA – OLD o FBS – Fasting Blood Sugar
BLOOD o CREA - Creatinine
o SUA - Serum Uric Acid
3. PATIENT POSITION o TRI - Triglyceride
o CHOL – Cholesterol
o BUN – Blood Urea Nitrogen
ARTERIAL PUNCTURE
DELIVERING SAMPLES AT A TIMELY MANNER
 Stability of analysis CLSI – Clinical and Laboratory Standards Institute
 Accurate results
 Immediate diagnosis and treatment 5 PURPOSES OF TRAINING
 1. Supervision
ETS VS. SYRINGE 2. To correct puncture procedure
EVACUATED TUBE SYRINGE 3. Precaution/ensure safety procedure
SYSTEM 4. Complications
Multiple collection Back flow 5. Sample handling
Faster way of collecting Controlled pressure
COMPOSITION OF ARTERIAL BLOOD
Closed system – reduce Cheaper
 Rich in oxygen and electrolytes
the risk of exposure of
 Uniform in composition throughout the body
blood
 Ideal for managing oxygen, electrolytes, and
Prevent exposure of Less painful
acid-base balance
Ammonia and Carbon
 Often used for testing Arterial Blood Gas (ABG),
Dioxide
ammonia, and lactic acid.
Reduce hemolysis (no Change the needle
transferring of blood will gauge for smaller and
DISEASES THAT RECOMMENDS AP
happen) thinner vein
 COPD (Chronic obstructive pulmonary
Calibrated tubes Can be maneuvered
disorder)
(additives)
 Lung cancer
Simpler and safer (safety Recommended for
 Diabetic coma
device) children and geriatrics
 Schoch
Storage efficient
 Respiratory distress in fetus
 Respiratory diseases

ARTERIAL BLOOD GASES


 Determines the concentrations of oxygen and
carbon dioxide in the blood and measures the
pH
 Measures the gas exchange ability of the lungs
and the buffering capacity of the blood.

EQUIPMENT FOR ARTERIAL PUNCTURE


- GAS IMPERMEABLE PLASTIC SYRINGE

 HEPARINIZED SYRINGED AND NEEDLE


o Pre-treated with heparin to prevent
coagulation
o Glass or gas impermeable plastic
 Plastic is safer
o 1-5 mL
o 21 or 22 gauge, 1 to ½ inch long
o Brachial and radial arteries, 1inch.
o Femoral arteries 1 ½ inches

 ANTISEPTIC
o Both alcohol and povidone-iodine or
chlorhexidine
 Stringent cleansing
 ANTESTHETIC o Poor collateral circulation – MOD Allen’s
o 0.5 mL of lidocaine, a local anaesthetic test
is injected. o Difficult site to keep aseptic
o Near the groin
 SAFETY EQUIPMENT
o Need fluid resistant gown, face ALTERNATIVE SITES IN ADULT
protection, gloves  Dorsalis Pedis Artery
 LUER TIP  Umbilical artery (babies)
o Plastic tip that covers the syringe top  Scalp artery (babies)
after removing needle.
 Prevents alteration of the ARTERIAL PUNCTURE COMPLICATIONS
sample
Arteriospasm The spontaneous
 OTHER EQUIPMENT constriction of an
o Transport container artery in response to
o Crushed ice pain
o Ice and water Nerve damage Cause by an
 If there is a delay. To prevent inadvertent contact
any other metabolism or with the nerve
oxygen Hematoma Resulting from
o Gauze pads inadequate pressure on
o Pressure bandages the site. This is more
o Thermometer likely in elderly patients
whose artery walls are
SITE SELECTION not as elastic.
 Large enough to accept 25 gauge needle Hematoma – near the
 Located near the skin surface so that deep basillic vein
puncture is not required Thrombosis Clot formation within
 In an area where injury to surrounding tissues the artery (bleeding
will not be critical disorders)
 Located in an area where other arteries are Haemorrhage More likely in patients
present to supply blood in case the puncture who have coagulation
artery is damaged disorders or receiving
anticoagulant therapy.
 RADIAL ARTERY (ideal site) (delay in healing)
o Supplying the hand, the artery of choice Infection From skin contaminant
o Smaller than brachial and femoral Vasovagal reaction Result in sudden loss of
artery, good collateral circulation, and consciousness.
accessible
o Ulnar artery provides collateral SAMPLING ERROR
circulation to the hand  Using too much heparin
o ADVANTAGE – SMALL SIZE  Using too little heparin
 BRACHIAL ARTERY  Insufficient mixing
 More dangerous because it has  Allowing air bubbles to enter the syringe
lots of tissues on the area  Using improper plastic syringe
o Very large, it is easy to palpate and  Using improper anticoagulant
puncture o O.05 mL = 1mL of blood
o It is very deep and is close to median o Alteration
nerve  Puncturing of vein instead of artery
o Lies in soft tissue and is more difficult to o Artery = bright red
compress.  Exposing the specimen to the atmosphere after
 FEMORAL ARTERY collection
o Largest artery used, useful when cardiac
output is low
EFFECTS OF ERRORS ON ABG RESULT BLOOD COLLECTION IN SPECIAL
TECHNICAL ERROR EFFECT POPULATION
AIR BUBBLES PRESENT Atmospheric oxygen enters
the sample, and CO2 from PEDIATRIC PATIENTS
the sample enters the air
bubbles  PHYSIOLOGIC DISORDERS
TOO MUCH HEPARIN pH is lowered  Children have a lower total blood
TOO LITTLE The presence of clots that volume
HEPARIN/INADEQUATE will interfere with the  Removal of more than 10% of total
MIXING analyser
blood volume can cause cardiac arrest
DELAYED ANALYSIS WBC and platelets in the
sample continue their
 Repeated withdrawal of even smaller
metabolism, utilizing oxygen amounts can cause anemia
and producing CO2  Removal of 3% or less is the preferred
Venous rather than the Falsely decreased PO2 and maximum
arterial sample increased PCO2 (p = partial)
 Dermal puncture is the most common
pediatric collection procedure
SPECIMEN REJECTION  Children differ in their levels of
 Inadequate volume understanding, ability to cooperate, and
 Clotting anxiety about medical condition
 Improper label  Needles represent pain, and their fear
 Wrong syringe of pain often makes collection
 Air bubbles challenging
 Delayed delivery to the lab  Prolonged crying effects WBC and the
 Failure to ice the specimen pH level of blood.

 Pressure applied must be EXTRA MINIMIZE CHILD’S ANXIETY


 30-45 DEGREE ANGLE 1. Prepare the materials ahead of time
2. If possible, perform the procedure in a
room that is not the child’s hospital
room
3. Be friendly, cheerful, and empathetic.
Use of soothing tone voice.
4. Explain what will you do appropriate for
the child’s age
5. Do not say that it will not hurt
6. Give the child choices whenever
possible
7. Use the shortest possible needle for the
procedure
8. Distract the child just before the actual
stick
9. Tell the child how much longer it will be
10. Afterward, praise the child, offer him a
small reward

 INVOLVEMENT OF PARENTS AND SIBLINGS

 IDENTIFICATION OF NEWBORNS
 Identification bracelet, hospital ID
number

 SUPPLIES
 Use shorter needles, smaller guage.
Butterfly needles and pediatric tube
 Rewards such as stickers or small toys
 ANAESTHETICS  Minimize the damage by frequently rotating the
 Topical anaesthetic cream sites form which you draw
 IMMOBILIZATION OF INFANTS  Use alternative sites; forearm, underside of the
 this ensure their safety during the draw. arm, wrist or fingers.
Wrapping new born in a receiving
blanket is usually sufficient SPECIAL EQUIPMENTS USED IN THE INTENSIVE CARE
 patient either seated on the lap or lying UNIT (ICU) AND EMERGENCY ROOM (ER)
down
 the assistant may support the arm from  VASCULAR ACCESS DEVICES
behind, at the bend in the elbow o Peripherally Inserted Central Catheter
(PICC)
GERIATRICS PATIENTS o Arterial Line
 collection from geriatric patients presents o Heparin or saline lock
both physical and physiologic challenges o External AV shunt
 they feel less in control pf their medical o Arteriovenous shunt
situations and some may feel apprehensive
of the procedure  DRAWING FROM VAD
 a little extra TLC goes a long way to this o Never use a syringe larger than 20ml
population o VADs are often periodically flushed with
heparin to keep the line open.
 PHYSICAL CHANGES Therefore, discard at least the 5ml. for
o Aging often results in gradual hearing coagulation, discard the first 10ml
loss o Order of draw should be blood cultures,
o Failing eyesight anticoagulated tubes, and then clotted
o Sense of taste, smell, and feeling are tubes
also affected
o Muscles weakness unable to make fist  WORKING WITH INTRAVENOUSE LINES (IV)
o Memory loss, inability to remember o Have the nurse turn off the IV drip for
when he or she last eaten less than 2 minutes before the draw
o Apply tourniquet distal to the IV
 BLOOD COLLECTION CONSIDERATIONS insertion site
o Identifying the patient o Select a vein distal to the IV insertion
o Limiting blood loss and bruising site, and in different vein
o Applying the tourniquet o Discard the first 5ml blood because it
o Locating the vein will contaminate with the IV fluid
o Performing venepuncture

 DISEASE STATE
o A patient with Alzheimer’s disease may
be confused or combative
o Stroke patient may have paralysis
o Patient in coma
o Arthritic patients may be in pain, unable
to strengthened arm
o Older patients may have tremors

PATIENT’S REQUIRING BLOOD DRAWS FOR EXTENDED


PERIODS OF TIME
 Frequent blood drawing often caused the most
commonly sites to become damaged
 Veins become hardened and difficult to
penetrate with the needle, the skin develop scar
tissue
SPECIAL COLLECTIONS  Is used to test for DM. it compares the
fasting glucose level with level 2 hours
Sweeping schedule – warding after consuming glucose.
 ORAL GLUCOSE TOLERANCE
COLLECTION PRIORITIES  Is used to diagnose DM and gestation
 ROUTINE SAMPLE diabetes (for pregnant women)
 Are collected early in the morning or  4 times extraction
throughout the day  EPINEPHRINE TOLERANCE TEST
 ASAP SAMPLE  Determine patient ability to mobilize
 The response time for the collection of glycogen from the liver
the test sample
 STAT SAMPLE  LACTOSE TOLERANCE TEST
 Sample is collected, analysed, and  Determine whether the lactose-
results reported immediately digesting enzyme lactase is present in
FACTORS the gut
 Age
 Altitude – Different normal values DIURNAL VARIATION
because of the place  Refers to the normal daily fluctuations in body
 Dehydration chemistry related to hormonal cycles, sleep-
 Environment wakes cycles and other regular patterns of
 Gender change
 Pregnancy o HORMONES
 Stress  The time is very important
 Diet  Cortisol
 Diurnal variation  Testosterone
 Drugs  Estradiol
 Exercise  Progesterone
 Body position  Serum iron
 Smoking  Glucose
 White blood cells
FASTING SPECIMEN AND THE BASAL STATE
Nothing per orem (NPO) SPECIAL HANDLING PROCEDURES
- Patients (surgery)  COLD AGGLUTININS (False (+))
- Hours of fasting depends on the doctor  Are antibodies often formed in
- Collapsed vein response to infection cause by
Mycoplasma pneumoniae
 FASTING SPECIMEN  The antibodies react with rbc
 Patient must refrain from eating and temperature below body temperature
drinking (except water) for 12 hours.  Prewarm a plain red-topped tube in a
 BASAL STATE 37◦C for 3o minutes. Keep the specimen
 Patient must refrain from eating, warm heel warmer pack or in an
drinking (except water) and exercise for incubator. Deliver soon in the
12 hours. laboratory
 Cyrofibrinogen and cryoglobulin are
TIMED SPECIMEN two proteins that precipitate when cold.
 Are taken to determine changes in the level of  CHILLED SPECIMEN
some substance of interest over time.  Chilling is used to prevent chemical
 Medication levels changes that could alter results
 Changes in the patient condition  The sample is placed in crushed ice or in
 Normal diurnal variation of blood levels an ice water mixture
at different times of the day  The temperature should be 1◦C to 5◦C
 2 HOUR POSTPRANDIAL TEST  Sample should be transported to the lab
for testing within 5 minutes of
collection.
 TESTS SPECIAL HANDLING
 Arterial blood gas (if indicated)
 Ammonia “ACCURATE RESULTS”
 Lactic acid “ACCURATE DIAGNOSIS”
 Pyruvate
 Glucagon GENERAL GUIDELINES FOR SPECIMEN TRANSPORT
 Gastrin  Tubes with additives should be inverted gently
 Adrenocorticotropic hormone and completely 5 to 10 times
 Parathyroid hormone o Right tubes
o Mix properly
 LIGHT SENSITIVE SPECIMEN  Specimen must be correctly labelled
 Exposure to light can break down or  Use leak-resistant bag for transport
alter certain blood constituents  Use of crush-resistant containers with
 Wrap the tube in aluminium foil absorbent material
immediately after collection. An  Tubes should remain upright during transport
amber colored microtube can be
used. TIME CONSTRAINTS
 BLOOD CONSTITUENTS THAT ARE QUALITY CREED – doing right things right, all the
LIGHT SENSITIVE time, every time
 BILIRUBIN
 BETA-CAROTENE  Quality test results depends on the time
 VITAMIN A between collection and analysis
 VITAMIN B6  Delayed processing may lead to glycolysis
 PORPHYRINS o Glucose
 TIME-SENSITIVE SPECIMENS  Gray top – anticoagulant
 Unstable and volatile analytes agent
 Test be performed rapidly after the  24 hours at room
sample taken temperature
 BLOOD CONSTITUENTS THAT ARE  48 hours at 2-8◦C
TIME SENSITIVE o Phosphorus
 Ammonia o Aldosterone
 Lactate o Enzyme
 Platelet aggregation  Samples should be delivered in the lab
 Brain natriuretic peptide within 45 minutes of being drawn
 Prostatic acid phosphatase  No more that 2 hours should pass between
 ACTH collection and separation of cells from
 Aldolase serum
o EDTA (CBC)
 LEGAL AND FORENSIC SPECIMENS  24 hours distortion of cells
 Evidence in legal proceedings,  Make a blood smear within
including alcohol and drug testing, an hour
DNA analysis, or paternity testing  Preserved the # of
 Such samples must be handled with cell but not the
special procedures designed to morphology
prevent tampering misidentification
or interference with the test result TEMPERATURE CONSIDERATIONS
 Chain of custody  Temperature can cause hemolysis
 Trace the sample  Keeping specimen warm at 37◦C during
transport and handling are cold agglutinins
 Keeping specimen cool during transport
handling are blood gases and lactic acid
PROTECTING SPECIMENS FROM LIGHT  Plasma specimens, can be centrifuged
 Light exposure can breakdown light immediately
sensitive analytes  Complete clotting may take 30 to 45
 Samples are collected in amber colored minutes at room temperature
microtubes, wrapped in aluminium foil, or  Patients on anticoagulants have longer
placed in a brown envelope, or heavy paper clotting time
bag.
 Samples with clot activators clot more
o Blood constituents that are light
rapidly at 15 minutes
sensitive
 Bilirubin  CENTRIFUGING
 Byproduct of rbc  Spins the sample at a very high speed,
 Beta-carotene separating components based on
 Vitamin a density
 Vitamin B6  The stopper should remain on the
 Porphyrins sample to prevent contamination
 Principle of centrifugation involves
TRANSPORTING SAMPLES IN LABORATORY samples must be balanced by another
 Samples are carried by phlebotomist or another of equal weight
lab member  The lid of the centrifuge must be closed
 Samples may be dropped off at designated
and secured during operation, and it
areas
must be closed until the rotor stops.
 Use of logbook at the drop off and pick up area.
 Patient’s name
 Specimen type  REMOVING THE STOPPER
 Date and time of delivery  Major risk of stopper removal is
 Name of the person depositing it formation of aerosol
 Careful stopper removal reduces the
 Pneumatic tube system, in which samples are risk of aerosol stopper
carried in sealed container within a network of  Place a 4- by 4-inch of gauze over the
tubes. top, and pull the stopper straight up
 Hemogard top, is aplastic top that fits
PROCESSING over the stopper to reduce aerosol
Chyle / chylomicros – fats, serum, mucoid. White thing formation and splattering
that sometimes appear at the tubes
 PREPARING ALIQUOTS
 SAFETY
 Tubes into which aliquots are placed
 OHSHA requires PPE during sample
should be labelled before filling and
processing
capped before delivery.
 Aliquot is removed with the use of
 CENTRAL PROCESSING
disposable pipetting system.
 An area devoted to cataloguing and
 Aliquots – FOR SEPARATION
sorting sample
 Sample are logged with date and time SPECIMEN REJECTION
of arrival, and accession number (a  Improper of inadequate identification
unique identifying number)  Hemolysis
 Samples are also labelled with bar codes  Incorrect tube for the test ordered
that are read by electronic reader and  Tubes used past their expiration date
stores in the computer system.  Inadequate ratio of blood to additive
 CLOTTING  Insufficient volume of testing
 Specimen at a wrong time
 Specimen must be clotted before
 Improper handling
centrifugation
 Contaminated specimen
 Incompletely clotted samples continue
to clot after serum separation
SPECIAL NONBLOOD COLLECTION
PROCEDURE  COLLECTION PROCEDURE
 Patient is provided a container and
 Provides valuable information about patient’s instruct to defecate on it
health or diseases state  Container must be tightly sealed
 It requires strict adherence to protocol as it is  Specimen must be at room temperature
for blood collection or refrigerated (most common) until
 It includes urine, feces, semen, and body fluids delivery at the lab
 Special handling procedure are needed to  If delayed, transfer to vials containing
maintain sterility, preserve specimen integrity preservative
and chain of custody.  Pea sized
 Formalin – most common preservative
URINE SPECIMEN  Routine – drop of Saline solution
 TYPES OF URINE SPECIMEN
 Random specimen SEMEN SPECIMENS
 First morning specimen  Fertility test
 Ideal for urinalysis  Sperm count
 Concentrated specimen  Forensic studies
 Best for pregnancy test  Evaluate post vasectomy procedures
 Timed specimen  Spermatozoa (testis) 5%
 It is good when you want to do  Acid – 20-30% - Seminal fluid, fructose
a quantitative analysis on the  Bulbourethral gland 5% - neutralization of
specimen or certain substances semen.
( e.g. creatinine, urea, etc.)
 COLLECTION PROCEDURE
 COLLECTION PROCEDURE  Avoid ejaculation for 3 days before
 Midstream clean catch collection
 Middle of urinating  Immotile sperm
 Pediatric collection  increase
 Cellophane-like with adhesive  Time collection is recorded
 Catheter collection  Volume of semen is IMPORTANT
 Sterile urine  Sample must be kept close to body
 Invasive procedure temperature and delivered to the lab
 Suprapubic aspiration within 30 mins.
 Inject directly to the bladder  Polyurethane condom is used in
collection
 Urea detects infection and abnormalities  Sterile glass container/beaker
 Volume affects fertility
FECAL SPECIMEN
 Determine the presence of ava / parasite CEREBROSPINAL FLUID SPECIMEN
 Screen colorectal cancer  CNS Disorders
 Fats, fibers  Lumbar top L1-L%

 TYPES OF FECAL SPECIMEN  COLLECTION PROCEDURE


 Random specimen  CSF collection is done only by a
 Occult blood specimen physician
 “hidden blood”  Three tubes are collected
 Seventy-two hours stool specimen  Culture / microbiology
 Steatorrhea - the excretion of  Chemistry
abnormal quantities of fat with  hematology
the feces owing to reduced  Must be handled in STAT collections
absorption of fat by the
intestine. (Malabsorption of
fats)
NASOPHARYNGAL SPECIMEN
 Respiratory infection

 COLLECTION PROCEDURE
 Specimen is collected using a cotton or
Dacron tipped sterile wire
 The swab is passed carefully through
the nostril to reach the back of the
nasopharynx
 The swab is placed in either transport
media or growth media

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