Presentation on theme: "Specimen Collection &Processing MLCC-203"— Presentation transcript:
1Specimen Collection &Processing MLCC-203 Eman El-AttarMsc, MD, CPHQ
2ILOs To recognize the different types of human specimens To understand the different types of blood samplingTo understand the different types of urine samplesTo know the guidelines & techniques to collect blood samplesTo recognize the different types of urine samplesTo understand different methods of sample preservation
3Types of Specimens blood urine faeces spinal fluid synovial fluid amniotic fluidpleural, pericardial, and ascitic fluidssalivasolid tissue
5General precautionsasks the pt for his/her name (check with the name on the wrist band)specimen containers should be labeled with:patient namehospital or identification numberlocation in the hospitaldate & time of collectionuse of disposable latex rubber gloves, especially before collection of any blood specimen.if the pt has an infectious disease, the phlebotomist should observe universal precautions (wearing of a face mask, glasses or goggles, gloves and gown).
6Blood Sites for obtaining blood: veins, arteries or capillaries. Venous blood: (specimen of choice) obtained by venipunctureCapillary blood: (in young children) obtained by skin punctureArterial blood: (for blood gas analysis) obtained by arterial puncture.Means for obtaining blood:SyringeEvacuated blood tube (less expensive, more convenient, easier to use, less contamination)lancet (for skin puncture)
7Precautions for venipuncture pt should be fasting.pt should be comfortably seated (or in supine position for at least 20 min before sampling)pt arm should be extended (straight line from shoulder to the wrist)The arm chosen for sampling (many pt do not prefer the arm with which they write).In severely ill pt or multiple IV inj (eg: chemotherapy), keep the good veins for treatment-Avoid the use of an arm with :inserted IV line.cannula or IV fistula (without physician consent).extensive scarring or hematoma at the intended site of venipuncture.In females who had a mastectomy operation, do not use the arm veins on that side
8If IV fluid infusion is running, close for 3 minute If IV fluid infusion is running, close for 3 minute. Take sample from below the infusion site in the same arm or from the opposite arm. A suitable note should be made in the lab report form . This type of specimen is usually suitable for most analytes except those contained in the infused solneg: glucose or electrolytes.Avoid prolonged tourniquet application (max for 1 min ) or fist pumping as well as stress . Fist pumping increases K , phosphate, lactate and Ca++Check for the suitable time of specimen collection (diurnal variation of the analyteeg: iron, cortisol – and monitoring of drug therapy eg: digoxin level, prothrombin time).Estimate the volume of blood needed and select the appropriate number & types of tubes for the plasma or serum tests requested.An appropriate needle must be selected (the larger the gauge size the smaller the bore-the most commonly used gauge sizes are 19 – 22 & the usual size for an adult with normal veins is size 20. if veins are small & tend to collapse use size 21). All needles must be sterile.
9Sites of venipuncture : median cubital vein : the preferred site in adults, where the vein is both large & close to the skin surface.Veins on the back of the hand or at the ankle : less preferred & should be avoided in persons with poor circulation (eg : DM).
10Technique of venipuncture : Selection of the area for venipuncture : by palpation.Clean the area around the venipuncture :By a prepackaged alcohol swab, or a gauze pad saturated with 70% isopropanol, in a circular motion and from the site outward.By benzalkonium chloride soln (alcohol free): for alcohol determination.NEVER by povidone-iodine ( betadine) because of possible interference with several chemistry proceduresAllow the skin to dry in the air (alcohol traces may cause haemolysis and invalid test results).Never touch the skin until venipuncture is completed.Tourniquet application (max for 1 min): cm above the intended puncture site, to obtain the return of venous blood to the heart, and to distend the veins. The pt should not pump fist while tourniquet is in place
11Blood collection with syringe : needle is placed firmly over the nozzle of the syringe and the needle cover is removed the syringe & needle are aligned with the vein to be entered and the needle is pushed into the vein with a 15º angle to the skin. When the initial resistance of the vessel wall during needle piercing is overcome, forward pressure on the syringe is eased and the blood is is withdrawn by gently pulling back the plunger of the syring. After needle removal from the syringe, transfer the drawn blood by gentle ejection into the appropriate tubes. The tubes containing anticoagulants (or additives) are capped & gently mixed (5-10 inversions).Blood collection with evacuated blood tubes :Before use, the tube should be gently tapped to move any anticoagulant from the stopper before the needle is inserted into a vein (to preventanticoagulant from entering into the vein).The needle is screwed into the collection tube holder, and the tube is inserted into this holder.Technique :After skin cleaning, the needle is guided gently into the vein.Once needle is inside the vein, tube is pressed forward into the holder (to puncture the the stopper and release the vacuum)As blood begins flowing in the tube, tourniquet is released.The tube is filled until the vacuum is exhausted, and the tube can be moved from the holder and replaced by another if more blood is needed (this requires a shut off valve, consisting of a rubber tubing that slides over the needle opening inside the tube, to prevent blood spilling during tube exchange)
14AssignmentTypes, colors and order of vacutainers
15Order of Draw Order of Draw Sterile Specimens Coagulation Tubes Serum Blood Culture TubesCoagulationTubesLight BlueSSTGold or Red/BlackSerumGreenLight GreenLavenderGrayRed
16Adv of blood tubes over syringes: Easy to use – low risk of contamination.Disadv of blood tubes:1-collection procedu-Vacuum tends to decrease by time . (check the expiry date before use)2-You have to draw the amount of blood indicated on tubes with anticoagulants. (check for volume of draw before use).
17Properties of blood tubes : 1-Two tyoesof evacuated blood tubes: those with serum separators (SST) – those without separators. In the SST, the disk between the packed cells and the supernatant.2-Various additives (anticoagulants – preservatives) may be present, indicated by stopper colour.3-They are also siliconizedto activate the clotting mechanism, reduce adhesion of clots to walls or stoppers & to decrease hemolysis risk.
18Skin puncture:Done when small blood volume is needed (blood glucose estimation by glucocheck- BT & CT)Sites of skin puncture in:- Adults & grown children: finger tips – ear lobes- Neonates (up to 1 yr of age): lateral or medial plantar surface of the heel of the foot
19Tech of skin puncture :1- skin cleaning : a gauze pad sat with 70% isopropanol.2- leave the alcohol to dry (to avoid hemolysis) and use the lancet to quickly puncture the skin.3- the finger is held in a way that allows gravity to assist in blood collection4- avoid finger massage after pricking (to avoid outflow of skin cells and tissue fluid5- 1st blood drop is wiped away then blood drops are transferred to the collection tubes quickly (to avoid clotting) and without bubbles or froths (to minimize hemolysis) by placing the tube in contact at only a slight angle to the skin surface.NB : a 3 min warm up of the finger prior to puncture (to improve the circulation) is done by a warm wet wash cloth.
20Arterial puncture:It requires considerable skill (performed by physicians or trained technicians or nurses)Preferred sites: radial artery (at the wrist) – brachial artery (at the elbow) – femoral artery (in the groin)Identify the artery by: its thick wall – pulsations
211-clean the skin around the puncture site (as in venipuncture) 2-no tourniquet is required for arterial puncture3-use 18 or 20 gauge needle for large arteries (eg;femoral) and smaller ones (23-25 gauge) for smaller arteries4-heparinized syringe (for adequate anticoagulation )5-never use evacuated blood tubes for collection of ABG specimens because they contain air.7-after arterial puncture is done, pressure of the puncture site for a 5 min. period is done to avoid bleeding.8-The syringe nozzle is sealed (after blood is collected) and the syringe is placed in ice for immediate transport to the lab (analysis within a 15 min. period from blood collection).Remarks:In neonates, an catheter in the umbilical artery is used for ABG purposes.In older children or adults where arterial puncture is impossible (eg : obesity): capillary puncture can be done to obtain arterialized capillary blood. This gives acceptable values for pH & PCO2, but not for PO2.The preferred sites for capillary puncture in :-adults and older children : is the ear lobe-younger children or infants : is the heel
22Blood collection from intravenous (IV) lines IV fluid is shut from the CVP ( central venous pressure) catheter and 10 ml whole blood is aspirated and discarded before the specimen for analysis is drawn.Blood may be collected from the veins of an arm below an IV linewithout interference from the infused fluid, since the infused fluid must first circulate through the heart and return to the tissues before it reaches the sample site.
23Anticoagulants and preservatives for blood: Whole blood: for analysis of : Blood gases-ammonia-some trace elements- others(glucose- glycatedHb)Serum: for analysis of most of the analytes, particularly the serological tests (that depend on Ag- Ab reaction)Plasma obtained with the appropriate anticoagulant: is equally effective as serumAdvantage of plasma over serum:Rapid in emergencies; serum requires a min period for clottingVolume of plasma is always greater than that of the serum.Disadvantage of plasma:Fibrin clot or fragment formation upon plasma storage and risk of clogging sample probes of automated analyzers.Interference of fibrinogen with electrophoretic mobility resulting in confused interpretation of the electrophoretic pattern
24Types of anticoagulants Heparin:Most widely used for clinical chemical analysisAvailable in the salt form (Na, K, Mg, Li, NH4): Avoid the Na and K heparinate analyzed Na & K (use Li heparinate).EDTA (Ethylene Diamine Tetra Acetic Acid):Uses: hematology as it preserves the cellular composition of bloodEDTA salts available are: Disodium, Dipotassium, and TripotassiumSodium Fluoride:Uses: preservative for blood glucoseNB: without an antiglycolytic agent, blood glucose decreases by 10mg/dL/hr at 25ºC, and the rate is faster in newborns and leukemic pt dt higher WBCs .Sodium Citrate:Uses: erythrocyte sedimentation rate (ESR) – Prothrombin time (PT) & activity – Partial thromboplastin time (PTT) & activity.Ratio of sodium citrate to blood: (both must be well mixed together)-1:10 for PT and PTT (0.2 mL Na citrate mL whole blood)-1:5 for ESR (0.4 mL Na citrate mL whole blood)Oxalates, Iodoacetate
25Changes that occur to exposed blood sample All tests should be done on a fresh blood sample, (less than 1/2 hr at R.T). A preservative could be used to decrease these changes
26Changes that occur to exposed blood sample Physically: clotting of blood (if no anticoagulant is used)Chemically:Evaporation of water content of blood→ increase concentrationDecrease blood glucose used up by cells: prevented by rapid separation & use of NaF.Increased ammonia production: blood contamination with bacteria that break down urea into ammona(prevented by keeping the blood sterile as well as rapid analysis)CO2 loss: avoided by collection of blood under paraffin, and rapid separation & analysispH changes : usually towards the acidic side (N. pH : 7.35 – 7.45)Destruction of blood cells and platelets with the release of their contents into the plasma e.g K
27HemolysisBreakdown of RBCs with release of their Hb content. Serum shows visual evidence of haemolysis when Hbconc exceeds 20 mg/dlSevere haemolysis causes1-marked increase of analytesthat are present in RBCs at a high conc.or activity (eg: potassium, magnesium, inorganic phosphates, LDH, AST)2-interference with some analytes in plasma (eg: Total CK & CK-MB activities)Precautions to avoid haemolysis:1-use of wide bore needles2-use the appropriate amounts of anticoagulants (excess heparin causes hemolysis)3-apply minimum amount of constriction to the arm4-allow smooth slow blood flow to the syringe to prevent froths6-allow blood flow easily and slowly on the walls of the tube7-gentle mixing of the blood with the anticoagulant8-centrifugation of the blood at a medium speed in order to obtain serum or plasma
28URINETypes of urine specimens to be collected from adults: (depending on the tests to be done)I-Untimed (Random) specimenUses : qualitative purposes or semiquantitative purposesTime of the specimen : clean (midstream), early morning, fasting specimen is preferred because :Constant urine composition.Most concentrated form (useful for microscopic examination & detection of abnormal amounts of urinary constituents eg: proteins, or of unusual compounds eg:HCG).Midstream urine is preferred as the first stream is used for washing the urethra.
29II-Timed urine sample : urine collected over a period of time Uses : for quantitative determination of analytes that pass in urine.Proper collection of a timed urine specimen :The collection period should be long enough to decrease biological variations.The pt should follow the instructions (better to give oral as well as in written notes).Lab gives the patient collection bottles containing suitable urine preservativesCollection bottle : (better to collect in one bottle for good mixing and avoid possible loss of containers during transport to the lab).For 2 hr collection : a 1L bottle .For 12 hr collection : a 2 L bottle .For 24 hrs collection: a 3-4 L bottleThe bladder should be emptied at the beginning of the collection time.After that, ALL urine is collected until the end of the scheduled time, and at the end of the collection time the pt should collect all urine even if there is no desire to.The large container should be stored at 4ºC in the refrigerator in between void.Avoid faecalcontamination.It is better to pass the urine into a small container at each voiding, then empty it into big container. This protects the patient from splashing himself with the urine preservative in the large container, particularly acids.The whole sample should be mixed together and total volume recorded. Then aliquots for microscopic examination and analysis are prepared.
30Urine collection from children : - It is very difficult to collect urine-Cleaning of the scrotal or perineal area, and remove skin oils.-For untimed (random) specimens ; a urine bag is placed around the infant genitalia
31Urine Preservatives Function of preservatives : reduce bacterial action.reduce chemical decomposition.solubilize constituents that might precipitate.decrease oxidation or evaporationTypes of preservation :1-physicalRefrigeration (2-8ºC):Freezing (-20ºC) : done for small aliquots of timed urine specimens if quantitative analysis is going to be delayed.2-chemical :Acidification of urine : (below pH of 3) used for 24 hrs urinary calcium, Example : HCl 6 mol/L : 10 mL/24hrs urine, sulfamic acid : 10 gm/L, boric acid : 5 mg/30 mLUrinary preservative tablets : They can be used for chemical & microscopic examination, but not for Na & K analysis.Others : Formalin, Thymol and chloroform , Toluene, S odium bicarbonate (mild basic salt) or NaOH (small amount)
32Changes that occur to urine on keeping : It is better to examine a freshly voided urine as soon as possible:I- Physical :colour changes : dt breakdown of the pigmentsodour changes : as a result of bacterial growth and decompositionaspect changes (turbidity) : as a result of bacterial multiplication or crystal formationpH changes : low pH : as a result of increased pus cellsHigh pH: as a result of bacteria → ammonia productionII- Chemical :glucose : decrease consumption by bacteriketone bodies : decrease due to breakdown and highly volatile.bilirubin&urobilinogen ; decrease due todestruction by light.nitrites :False +ve: as a result of nitrite producing bacteria.False –ve: as a result of nitrite conversion to nitrogen gas.III- Microscopic :1-cells and casts : decompose2-crystals formation : especially in cold weather and in acidic pH (eg : urates, oxalates).