MindMap Gallery Overview and staining of clinical blood examination
An overview of clinical blood examination and staining knowledge for medical examinations, including blood composition, blood properties, blood collection methods, cell staining and production, etc.
Edited at 2022-11-16 10:13:21This is a mind map about bacteria, and its main contents include: overview, morphology, types, structure, reproduction, distribution, application, and expansion. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about plant asexual reproduction, and its main contents include: concept, spore reproduction, vegetative reproduction, tissue culture, and buds. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about the reproductive development of animals, and its main contents include: insects, frogs, birds, sexual reproduction, and asexual reproduction. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about bacteria, and its main contents include: overview, morphology, types, structure, reproduction, distribution, application, and expansion. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about plant asexual reproduction, and its main contents include: concept, spore reproduction, vegetative reproduction, tissue culture, and buds. The summary is comprehensive and meticulous, suitable as review materials.
This is a mind map about the reproductive development of animals, and its main contents include: insects, frogs, birds, sexual reproduction, and asexual reproduction. The summary is comprehensive and meticulous, suitable as review materials.
blood
Blood Overview
blood composition
Blood cells 45%
Plasma 55%
No Ca ions
The difference from serum: serum does not contain coagulation factors L, II, V, VIII
properties of blood
HP
Adult 4~5L, 6%~8%
Arterial blood - bright red Venous blood-dark red C0 poisoning or cyanide poisoning - cherry red Patients with severe anemia-the red color becomes lighter
PH value 7.35~7.45
Arterial blood 7.40 Venous blood 7.35
Plasma penetration: 290~310mOsm/(kg·H2O)
Physiological function
Transport function
coordination function
defense function
Maintain the stability of the internal environment of the body
Blood collection method
phlebotomy
elbow vein
dorsal hand vein
medial malleolus vein
femoral vein
External jugular vein can be harvested in children
Skin blood collection method
WHO recommendation: Inner tip of the ring finger of the left hand
Infants and young children: the inner and outer edges of the big toe or heel
Severe burn patients: intact skin
Vacuum blood collection method
Blood collection device
Simplified form
scalp vein type
Blood collection sequence
Blood culture→sodium citrate anticoagulant tube→serum tube with or without anticoagulant or separation gel→heparin tube with or without separation gel→EDTA anticoagulant tube→sodium fluoride gray tube
Blood collection tube
red
Chemistry, Serology, Blood Bank
Purple
EDTA combines with calcium ions to form a chelate EDTA-2k>EDTA-2Na
Suitable for complete blood count (CBC) and glycosylated hemoglobin determination
ICSH recommendation: EDTA-K2·2H2O, 1.5-2.2mg/mL blood
Not suitable for coagulation tests and platelet function tests
light blue
Sodium citrate 1:9 combines with calcium ions to form a chelate
Coagulation tests (PT, APTT, coagulation factors, D-D, FDP, thromboelastography)
Blood Transfusion Maintenance Solution (CPDA)
C citrate
P phosphate
D glucose
A Adenine
green
Heparin strengthens the effect of anticoagulase (ATⅢ) on inactivating serine protease and prevents the formation of thrombin. And prevent platelet aggregation and other effects, thereby preventing blood coagulation
Used for emergency biochemistry, blood gas analysis, and chemical examination of serosal effusion
Ideal anticoagulant for erythrocyte osmotic fragility
Not applicable: CBC, cell morphology examination, PCR detection
When measuring electrolytes using ion selective electrode method, you should choose: lithium heparin
grey
Sodium fluoride, potassium oxalate, fluoride ions combined with calcium, used for glucose, glucose tolerance, ethanol concentration detection (fluoride ions can inhibit enolase in glycolysis and prevent the occurrence of glycolysis)
yellow
Sodium polyanetole sulfonate (SPS) blood culture
Golden
Separating gel/clot activator chemical, not suitable for blood banks to be used in biochemistry, hormones, tumors and other projects
light green
Separating gel/lithium heparin potassium determination
black
Sodium citrate 1:4 combines with calcium ions to form a chelate
ESR
Wei's method
Influencing factors:
rise
Cholesterol (swing)
Globulin (Autumn)
Fibrinogen (thousands)
reduce
Albumin (white)
Lecithin (cobblestone road)
Oxalates (no longer used)
Double oxalate: ammonium oxalate + potassium oxalate (6:4)
Potassium oxalate alone shrinks RBCs Ammonium oxalate alone distends RBCs (ammonium oxalate alone enables PLT counting):
Suitable for hematocrit, CBC, reticulocyte counting
Not suitable for: coagulation tests (very poor protection of factor V), PLT counts, WBC differential counts
arterial blood collection
Radial artery
femoral artery
brachial artery
QC
patient
Age, gender, drugs, mental state, activities, etc.
Hemolysis
Strong shaking, unclean containers, irregular operations, etc. can cause hemolysis and lead to false increases in LD, K+, etc.
Sample processing
Send for inspection as soon as possible after collection. Improper storage can directly affect the test results.
Cell staining and preparation
Blood smear preparation
clean
New glass slides with free alkali should be soaked in 1moI/L HCLHCL for 24 hours.
Slides Slides should be clean, dry, neutral, and non-greasy
Features
Appropriate thickness, clear head, body and tail, evenly distributed cells, The edges of the blood film are neat and leave a certain gap. The blood film occupies about 2/3 of the length of the slide.
preparation
The larger the blood drop, the greater the angle, and the faster the speed, the thicker the blood film; The smaller the blood drop, the smaller the angle, and the slower the speed, the thinner the blood film.
When HCT is increased and blood viscosity is high, small blood droplets, small angle, and slow push When HCT is reduced and blood viscosity is thin, large blood droplets, large angles, and fast push
Plasmodium and microfilariae using thick blood film smear method
blood cell staining
Wright's stain
A composite dye composed of the acidic dye eosin and the basic dye methylene blue is dissolved in methanol. The effects of methanol: 1. Dissolve dye; 2. Fix cell morphology.
Dyeing principle: It has both physical adsorption and chemical affinity.
Influence of pH value: Acidic environment tends to be reddish; alkaline environment tends to be blue. The pH value of the buffer should be between 6.4 and 6.8 PH<PI increases the positive charge and combines with acid eosin. (acidic) red blood cells and eosinophils stain red, and white blood cell nuclei appear light blue or not stained. PH>PI increases the negative charge and combines with alkaline methylene blue (alkaline). All cells are stained grey-blue, and the granules are dark brown; eosinophilic granules are dark brown or even black or blue, and neutral granules are thicker. Purple black.
Precautions
Rinse with running water, do not pour out the dye solution
When there are dye particles deposited on the blood smear, methanol can be added dropwise and then rinsed immediately with running water.
If the dyeing is too deep, it can be washed or soaked in running water, or methanol can be used to decolorize.
When staining the smear, do not remove the staining solution or rinse the smear directly to prevent the dye from adhering to the smear. The rinse time should not be too long to avoid discoloration.
Evaluation: It is the most classic and commonly used dyeing method. Good staining of cytoplasm, poor staining of nuclei
Giemsa stain
Composed of azure and eosin
The principle is basically the same as Wright's staining
For cell nuclei, parasites (such as Plasmodium) are better stained and have clearer structures, but have poor ability to stain cytoplasmic components.
Wright-Giemsa compound stain
Cytoplasm and nucleus staining effect is good
Freshly prepared dyes tend to be alkaline and must be stored at room temperature or 37°C for a period of time until methylene blue changes to azure B. The longer it is stored, the better the dyeing effect will be. It must be plugged during storage to prevent methanol from evaporating and oxidizing into formic acid. Methanol must be AR grade.