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LAB INVESTIGATIONS IN OMFS
AND
PRESURGICAL RELEVANCE
PRESENTED BY : BHANU PRIYA U
MODERATED BY :DR. AKSHAY SHETTY
CONTENT
• INTRODUCTION.
• HEMTOLOGICAL INVESTIGATIONS.
• BIOCHEMICAL INVESTIGATIONS.
• MICROBIOLOGICAL INVESTIGATIONS.
• SPECIAL INVESTIGATIONS
• CONCLUSION.
2
INTRODUCTION
• Laboratory tests are an invaluable aid to the practicing oral and
maxillofacial surgeon.
• In conjunction with a thorough history and physical examination,
laboratory tests available can aid in the diagnosis of various diseases
• allow the precise preoperative and postoperative management of patients
with systemic disease.
• In addition, patients without overt disease can be screened before
procedures that carry potentially serious complications, such as general
anesthesia, are begun.
3
HAEMATOLOGICAL
INVESTIGATIONS
1. CBC
2. COGULATION TESTS
3. CALCIUM
4. PHOSPHOROUS
5. GLUCOSE
6. GLYCATED HAEMOGLOBIN.
4
FULL BLOOD COUNT (FBC)/ COMPLETE
BLOOD COUNT (CBC)
1. HB CONCENTRATION.
2. RED CELL COUNT.
3. RED CELL DISTRIBUTION WIDTH (RDW)
4. HAEMATOCRIT (HCT) / PCV.
5. MCV.
6. MCH.
7. MCHC.
8. WHITE CELL COUNT
9. WBC DIFFERENTIAL.
10. PLATELET COUNT.
5
HAEMOGLOBIN CONCENTRATION (HB)
• Defines anaemia (Hb <lower limit of normal adjusted for age and sex).
New born
16.5-19.5 g/dL
Children
11.2-16.5 g/dL
Males
14.0-18.0 g/dl
Females
12.0-16.0 g/dL
6
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Red Blood Cell / Erythrocyte Count
• Children - 4.5-5.1 million/mm3
• Males - 4.6-6.2 million/mm3
• Females - 4.2-5.4 million/mm3
7
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
• Hypoproliferative anaemias, e.g. iron, vitamin B12
and folate deficiencies.
• Aplasia's e.g. idiopathic or drug-induced
• Parvovirus B19 infection-induced red cell aplasia
resulting in transient marked anaemia.
low red
cell count
• PRV.
high red
cell count
8
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
RED CELL DISTRIBUTION WIDTH (RDW)
• Measures the range of red cell size in a sample of blood
• ↓ MCV with normal RDW suggests thalassemia trait.
• ↓ MCV with high RDW suggests iron deficiency. blood
9
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
HAEMATOCRIT OR PCV
Polycythaemia.
High PCV
Anaemia (any cause).
Low PCV
10
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Men: 47% ± 7.0%
Women: 42% ± 5.0%
The ratio of the volume of red blood cells to the total volume of blood.
MEAN CORPUSCULAR VOLUME (MCV)
• Volume of a single RBC in cubic microns.
• MCV =
𝑵𝒐𝒓𝒎𝒂𝒍 𝑷𝑪𝑽 𝒑𝒆𝒓 𝟏𝟎𝟎 𝒎𝒍 𝒃𝒍𝒐𝒐𝒅
𝑹𝑩𝑪 𝒄𝒐𝒖𝒏𝒕 𝒊𝒏 𝒎𝒊𝒍𝒍𝒊𝒐𝒏 /𝒄𝒖𝒎𝒎
𝒙 𝟏𝟎 µ³
• 80- 96 femtoliters /cell.
• normocytes
• Less- microcytes
• More- macrocytes
11
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
12
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
MEAN CORPUSCULAR HEMOGLOBIN
• Average amount of hemoglobin in a single RBC in picogram
• MCH =
hemoglobin in gm%
𝑅𝐵𝐶 𝑐𝑜𝑢𝑛𝑡 𝑖𝑛 𝑚𝑖𝑙𝑙𝑖𝑜𝑛/𝑐𝑢𝑚
x 10 pg.
• 27 - 32 picograms / cell
Macrocytosis.
High Microcytosis,
e.g. iron deficiency
anaemia.
Low
13
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
MEAN CORPUSCULAR HEMOGLOBIN CONCENTRATION
• Hemoglobin Concentration in a single RBC.
• MCHC =
ℎ𝑏 𝑖𝑛 𝑔𝑚 %
𝑃𝐶𝑉 𝑝𝑒𝑟 100 𝑚𝑙 𝑏𝑙𝑜𝑜𝑑
x 100
• Normal range – normochromic ( 32-36 g/dl)
• Less- hypochromic
• More- hyperchromic
14
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
• Severe prolonged
dehydration.
• Hereditary spherocytosis..
High
• Iron deficiency anaemia.
• Thalassaemia.
Low
15
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Total Leukocyte count
• 4–11 × 103 cells/mm3
16
Increased
Acute infections,
uremia, steroids,
hemorrhage,leukemia
Decreased
radiation, aplastic
anemia, infectious
mononucleosis
,septicemia
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
DIFFERENTIAL LEUKOCYTE COUNT
• PMN: 40%–75%
• Lymphocytes: 15%–45%
• Eosinophils: 1%–6%
• Basophils: 0%–2%
• Monocytes: 1%–10%
17
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Neutrophils (PMNs)
• Increased: Infections, granulocytic leukemia, surgery, severe exercise
• Decreased: Viral infections, aplastic anemia, drugs, radiation, dialysis
Eosinophils
• Increased: Allergic disorders, parasitic infection, collagen vascular
diseases, Addison disease,malignancy
• Decreased: Steroids, stress, (ACTH) excess, Cushing syndrome
18
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Basophils
• Increased: Polycythemia, chronic myeloid leukemia
• Decreased: Steroids, stress, acute rheumatic fever, thyrotoxicosis
Lymphocytes
• Increased: Viral infections, tuberculosis, mononucleosis, acute and CLL
• Decreased: Stress, uraemia, steroids
Monocytes
• Increased: Monocytic leukemia, chronic inflammation or infection, collagen disease (RA, SLE ),
SBE, protozoal infections , TB.
• Decreased: Aplasia
19
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
PLATELET COUNT
• Normal: 150,000-400,000/mm3
• Low count – thrombocytopenia
• High count - thrombocytosis
20
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Increased
• Malignancy
• post surgery
• post splenectomy
• rheumatoid arthritis (RA)
• iron deficiency anemia
• trauma
• acute hemorrhage.
Decreased
• Idiopathic
thrombocytopenic purpura
(ITP)
• marrow invasion or aplasia
• Hypersplenism
• DIC
• cirrhosis
• quinidine
• massive transfusions
• viral infections
• Infectious mononucleosis
21
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Recommendations for doing FBC
22
Routine Preoperative Testing In Adults Undergoing Elective Non-cardiothoracic Surgery , Joan Vlayen, Nadia Benahmed, Jo
Robays: KCE Report 280, Belgian health care knowledge centre.
COAGULATION TESTS
1. Bleeding time
2. Clotting time
3. PT
4. PTT
5. INR
23
Clinician’s Handbook of Oral and Maxillofacial Surgery, Daniel M. Laskin
BLEEDING TIME (BT)
• 1 to 6 minutes
• Increased: Thrombocytopenia, von Willibrand disease, aspirin therapy
24
• 6 to 10 minutes.
• Increased: Heparin therapy, clotting factor deficiency
Clotting Time(CT)
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
25
Prothrombin time (PT)
• (12 to 14 seconds)
• Increased: warfarin, vitamin K deficiency, liver disease, DIC, prolonged use of tourniquet
before drawing blood
Partial thromboplastin time (PTT)
• (25 to 45 seconds)
• Increased: Heparin, defects in intrinsic clotting mechanism, hemophilia A and B, prolonged
use of tourniquet before drawing blood
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Interpretation of PT and PTT in patients with bleeding disorders
• Liver disease, decreased vitamin K, decreased or
defective factor VII
PT prolonged, PTT
normal
• Decreased or defective factor VIII, IX, or XI or
anticoagulant present
PT normal, PTT
prolonged
• Decreased or defective factor I, II, V, or X, von
Willebrand disease, liver disease, DIC
PT and PTT
prolonged
• Decreased platelet function, thrombocytopenia,
factor XIII deficiency, mild von Willebrand disease
PT and PTT
normal
26
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
International normalized ratio (INR)
• Ratio of the patient’s PT to a control PT standardized for the potency
of the thromboplastin reagent developed by the World Health
Organization (WHO)
• INR = Patient PT
Control PT
• Normal value <1
27
Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based
Clinical Practice Guidelines
28
• The guidelines of the American college of chest physicians (ACCP)
recommend dental surgery without vitamin k antagonists (VKA)
interruption with use of a pro hemostatic agent.
• The interruption of VKA treatment before dental procedures is not
recommended for interventions that are unlikely to cause bleeding for
low and high bleeding risk procedures if the INR of the patient is≤3.5
24 hours before the planned intervention.
• if the INR ≥3.5, the procedure should be delayed until INR values has
been reduced to ≤ 3.5.
Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based
Clinical Practice Guidelines
Calcium
• (8.5 to 10.5 mg/dL)
• Increased: Hyperparathyroidism, hypervitaminosis D, metastatic bone
tumors, Paget disease, multiple myeloma, sarcoidosis, chronic renal
failure
• Decreased: Hypoparathyroidism, hypoalbuminemia, renal failure,
alkalosis, acute pancreatitis, convulsions, vitamin D deficiency
29
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Phosphorus
• (2.3 to 4.7 mg/dL)
• Increased: Hypoparathyroidism, chronic renal failure, acidosis,
hypervitaminosis D, Addison disease
• Decreased: Hyperparathyroidism, alcoholism, hypokalemia, vitamin D
deficiency, alkalosis, diabetes mellitus
30
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Glucose
• Increased: Diabetes mellitus, stress, hyperthyroidism,
pregnancy, pancreatic disease, steroid therapy, Cushing
syndrome
• Decreased: Reactive hypoglycemia, pancreatic disorders,
starvation, liver disease, hyperinsulinism, hypothyroidism,
hypopituitarism, Addison disease, sepsis
31
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Fasting Plasma Glucose (FPG)
• fasting blood sugar levels.
• not having anything to eat or drink (except water) for at least 8 hours
before the test.
32
Random Plasma Glucose Test
• This test is a blood check at any time of the day
• Diabetes is diagnosed at blood sugar of greater than or equal
to 200 mg/dl
33
GLYCATED HEMOGLOBIN TEST (HBA1C)
• determine how well you are managing your diabetes.
• Glucose enters your red blood cells and links up (or glycates) with molecules
of hemoglobin
• HbA1c reflects average plasma glucose over the previous eight to 12 weeks
34
NICE 2016 GUIDELINES
Offer HbA1c testing to people with diabetes having
surgery if they have not been tested in the last 3
months.
Do not routinely offer HbA1c testing before surgery
to people without diagnosed diabetes.
35
36
Blood
Chemistry
Tests
1. Electrolytes
2. Anion gap
3. Renal Function
4. Liver Function
37
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
1. Electrolytes
Sodium
(135 to 145 mEq/L)
• Increased: Dehydration, glycosuria, diabetes insipidus
• Decreased: Diuretic use, congestive heart failure,
hyperglycemia, renal failure, vomiting, diarrhoea.
38
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Chloride
• (95 to 108 mEq/L)
• Increased: Dehydration, non anion gap metabolic acidosis,
diarrhoea, diabetes insipidus
• Decreased: Vomiting, excess sweating, congestive heart
failure, chronic renal failure, diuretic use, SIADH, diabetes
mellitus with ketoacidosis
39
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Potassium
(3.5 to 5.2 mEq/L)
• Increased: Renal failure, adrenal insufficiency, acidosis,
hemolysis, medications, iatrogenic
• Decreased: Diuretic therapy, alkalosis, vomiting, nasogastric
suctioning, mineralocorticoid excess
40
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Bicarbonate
(24 to 30 mEq/L)
• Increased: Dehydration, respiratory acidosis, emphysema, vomiting,
metabolic alkalosis
• Decreased: Metabolic acidosis, respiratory alkalosis, renal failure,
diarrhoea.
41
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
2.ANION GAP
(8 to 12 mEq)
Difference in mEq between
serum sodium and the sum
of serum chloride and
bicarbonate
• Diarrhoea, renal tubular
acidosis
Normal
• Renal failure, lactic
acidosis, ketoacidosis,
salicylate toxicity
Increased
• Disseminated
intravascular coagulation,
multiple myeloma
Decreased
42
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
3. Renal Function
Blood urea nitrogen (BUN)
(6 to 20 mg/dL)
• Increased: Renal failure of all types, dehydration, gastrointestinal
bleeding, increased protein catabolism
• Decreased: Liver damage, protein deficiency, starvation, overhydration
43
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Creatinine
(0.7 to 1.4 mg/dL)
• Increased: Renal failure, muscle disease, false positives with diabetic
ketoacidosis
• Decreased: Pregnancy; rarely clinically significant
44
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
4. LIVER FUNCTION
45
• bile pigments, bile salts, bromosulphthalein.
Tests based on
excretory function
• transaminases, alkaline phosphatase, 5'nucleotidase y-
glutamyl transpeptidase.
Tests based on serum
enzymes
• Galactose tolerance, antipyrine clearance.
Tests based on
metabolic capacity
• Prothrombin time, serum albumin.
Tests based on
synthetic functions
• Hippuric acid synthesis.
Tests based on
detoxification
Biochemistry , Dr. U Satyanarayana
46
Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan
1. SERUM BILIRUBIN
• Total - 0.2- 1.0 mg/dL
• conjugated bilirubin - 0.2-0.4mg/dl
• Unconjugated bilirubin - 0.2-0.6 mg/dl.
• estimated by van den Bergh reaction.
47
Biochemistry , Dr. U Satyanarayana
48
Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan
2. Urinary Bilirubin & Urobilinogen
• In all cases of jaundice, urine should be examined for the presence of
bile pigments (bilirubin), bile salts and urobilinogen
49
Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan
SERUM ENZYMES
50
• TRANSAMINASES / AMINOTRANSFERASES
Alanine
transaminase-ALT
• 5-4O lU/l
• more sensitive.
• pancreatitis,
biliary obstruction
Aspartate
transaminase - AST
• 5-45 lU/l
• Increased: Liver
disease, acute MI
,pancreatitis,
muscle trauma,
congestive heart
failure, hemolysis
Biochemistry , Dr. U Satyanarayana
Alkaline phosphatase
• Normal -13 KA units/dl
• Increased: Biliary tract obstruction, bone disease (Paget disease), hyperparathyroidism,
osteoblastic bone tumors.
• Decreased: Hypophosphatasia, hypothyroidism, malnutrition
γ - Glutamyl transpeptidase
• normal 5-4O lU/l
• highly elevated in biliary obstruction and alcoholism
51
Biochemistry , Dr. U Satyanarayana
SYNTHETIC FUNCTION
Total protein
(6.0 to 8.5 g/dL)
• Increased: Multiple myeloma, dehydration, sarcoidosis
• Decreased: Liver failure, starvation, inflammatory bowel disease
Albumin
(3.5 to 5.0 g/dL)
• Increased: Dehydration; rarely clinically significant
• Decreased: Liver failure, starvation, hyperthyroidism, leukemia, nephrotic
syndrome
52
Biochemistry , Dr. U Satyanarayana
Microbiology
1. HIV
2. HBsAg
3. VDRL
53
1.HIV
• Enzyme-linked immunosorbent assay (ELISA) (screening test)
• Western blot: Used for confirming presence of HIV antibody
• Positive: AIDS, AIDS-related complex
54
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
2.HBsAg
• hepatitis B virus (HBV).
• A "positive" or "reactive" HBsAg test result means that the
person is infected with hepatitis B.
• can spread the hepatitis B virus to others through blood.
55
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
3. VDRL
• Venereal disease research laboratory test.
• screening test for syphilis.
• If positive , confirm the results with an FTA-ABS test.
56
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
COVID - 19
• Nucleic acid amplification tests (NAAT)
• detection of COVID-19 virus nucleic acid (RNA) by real time RT-PCR assays.
• RNA isolated and purified from upper and lower respiratory specimens is
reverse transcribed to cDNA and subsequently amplified
• The viral genes targeted so far include the N, E, S and RdRP genes.
• E gene as screening, followed by confirmation through the detection of RdRP
gene
57
1.Molecular methods
World Health Organization. (2020). Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases:
interim guidance, 2 March 2020
2.Serological methods
• detection of IgM / IgG antibodies
3. Antigen detection
• During the first days after symptom onset (1 to 5), viral proteins can be detected.
4. Rapid diagnostic tests (RDTs)
So far there are no rapid diagnostic tests have been authorized by competent
regulatory authorities
58
World Health Organization. (2020). Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases:
interim guidance, 2 March 2020
SPECIAL
INVESTIGATIONS
1. CRP
2. BLOOD GASES
59
C-reactive protein (CRP)
• acute phase protein
• Normal value- less than 10mg/l
• sensitive systemic marker of inflammation and tissue damage.
• During infectious or inflammatory disease states, CRP levels rise
rapidly within the first 6 to 8 hours and peak at levels of up to 350–
400 mg/L after 48 hours
• CRP, binds to pathogens and activates the complement to enhance
opsonisation and clearance, even before the production of specific IgM
or IgG
60
61
A. Acute
inflammation
B. Chronic
inflammation
C. Tissue
injury
Higher levels seen in
62
Blood Gases
• Altered ventilatory status:
stroke, asthma, COPD
• Hypoxemia: pneumonia
• Hypocapnia: hyperventilation
• Hypercapnia: COPD
• pH disturbance: ketoacidosis
Indications
for
Measurement
63
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Normal Values—Arterial Blood Sample
• PO2 - 80 to 95 mm Hg
• SaO2 - 93% to 98%
• PCO2 - 36 to 43 mm Hg
• HCO3 : 20 to 30 mEq/L
• Arterial pH: 7.35 to 7.45
64
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Interpretation of Arterial Blood Gas Results
• Arterial pH
• < 7.35 = acidosis
• 7.35 to 7.45 = normal, compensated, or mixed disorder
• > 7.45 = alkalosis
65
Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
Routine preoperative tests for elective
surgery - NICE guideline 2016
66
67
68
69
70
71
Routine Preoperative Testing In Adults Undergoing Elective Non-cardiothoracic Surgery , Joan Vlayen, Nadia Benahmed, Jo
Robays: KCE Report 280
CONCLUSION
• Preoperative laboratory tests should be ordered based on
defined indications such as positive findings on a history and
physical exam.
• A thorough history and physical examination can be used to
identify those medical conditions that might affect
perioperative management and direct further laboratory
testing.
72
REFERENCES
1. Clinician’s Handbook of Oral and Maxillofacial Surgery, Daniel M. Laskin
2. Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
3. Biochemistry , Dr. U Satyanarayana
4. Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan
5. Textbook of physiology ,6th edition, A K Jain
6. Peterson’s Principles Of Oral And Maxillofacial Surgery Second Edition
7. C-reactive protein concentrations as a marker of inflammation or infection for interpreting biomarkers of micronutrient
status –WHO
8. Routine preoperative tests for elective surgery - NICE guideline
9. World Health Organization. (2020). Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human
cases: interim guidance, 2 March 2020
10. Routine Preoperative Testing In Adults Undergoing Elective Non-cardiothoracic Surgery , Joan Vlayen, Nadia Benahmed,
Jo Robays: KCE Report 280
11. NICE guidelines 2016
73
Thank you
74

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lab investigations in OMFS

  • 1. LAB INVESTIGATIONS IN OMFS AND PRESURGICAL RELEVANCE PRESENTED BY : BHANU PRIYA U MODERATED BY :DR. AKSHAY SHETTY
  • 2. CONTENT • INTRODUCTION. • HEMTOLOGICAL INVESTIGATIONS. • BIOCHEMICAL INVESTIGATIONS. • MICROBIOLOGICAL INVESTIGATIONS. • SPECIAL INVESTIGATIONS • CONCLUSION. 2
  • 3. INTRODUCTION • Laboratory tests are an invaluable aid to the practicing oral and maxillofacial surgeon. • In conjunction with a thorough history and physical examination, laboratory tests available can aid in the diagnosis of various diseases • allow the precise preoperative and postoperative management of patients with systemic disease. • In addition, patients without overt disease can be screened before procedures that carry potentially serious complications, such as general anesthesia, are begun. 3
  • 4. HAEMATOLOGICAL INVESTIGATIONS 1. CBC 2. COGULATION TESTS 3. CALCIUM 4. PHOSPHOROUS 5. GLUCOSE 6. GLYCATED HAEMOGLOBIN. 4
  • 5. FULL BLOOD COUNT (FBC)/ COMPLETE BLOOD COUNT (CBC) 1. HB CONCENTRATION. 2. RED CELL COUNT. 3. RED CELL DISTRIBUTION WIDTH (RDW) 4. HAEMATOCRIT (HCT) / PCV. 5. MCV. 6. MCH. 7. MCHC. 8. WHITE CELL COUNT 9. WBC DIFFERENTIAL. 10. PLATELET COUNT. 5
  • 6. HAEMOGLOBIN CONCENTRATION (HB) • Defines anaemia (Hb <lower limit of normal adjusted for age and sex). New born 16.5-19.5 g/dL Children 11.2-16.5 g/dL Males 14.0-18.0 g/dl Females 12.0-16.0 g/dL 6 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 7. Red Blood Cell / Erythrocyte Count • Children - 4.5-5.1 million/mm3 • Males - 4.6-6.2 million/mm3 • Females - 4.2-5.4 million/mm3 7 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 8. • Hypoproliferative anaemias, e.g. iron, vitamin B12 and folate deficiencies. • Aplasia's e.g. idiopathic or drug-induced • Parvovirus B19 infection-induced red cell aplasia resulting in transient marked anaemia. low red cell count • PRV. high red cell count 8 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 9. RED CELL DISTRIBUTION WIDTH (RDW) • Measures the range of red cell size in a sample of blood • ↓ MCV with normal RDW suggests thalassemia trait. • ↓ MCV with high RDW suggests iron deficiency. blood 9 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 10. HAEMATOCRIT OR PCV Polycythaemia. High PCV Anaemia (any cause). Low PCV 10 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz Men: 47% ± 7.0% Women: 42% ± 5.0% The ratio of the volume of red blood cells to the total volume of blood.
  • 11. MEAN CORPUSCULAR VOLUME (MCV) • Volume of a single RBC in cubic microns. • MCV = 𝑵𝒐𝒓𝒎𝒂𝒍 𝑷𝑪𝑽 𝒑𝒆𝒓 𝟏𝟎𝟎 𝒎𝒍 𝒃𝒍𝒐𝒐𝒅 𝑹𝑩𝑪 𝒄𝒐𝒖𝒏𝒕 𝒊𝒏 𝒎𝒊𝒍𝒍𝒊𝒐𝒏 /𝒄𝒖𝒎𝒎 𝒙 𝟏𝟎 µ³ • 80- 96 femtoliters /cell. • normocytes • Less- microcytes • More- macrocytes 11 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 12. 12 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 13. MEAN CORPUSCULAR HEMOGLOBIN • Average amount of hemoglobin in a single RBC in picogram • MCH = hemoglobin in gm% 𝑅𝐵𝐶 𝑐𝑜𝑢𝑛𝑡 𝑖𝑛 𝑚𝑖𝑙𝑙𝑖𝑜𝑛/𝑐𝑢𝑚 x 10 pg. • 27 - 32 picograms / cell Macrocytosis. High Microcytosis, e.g. iron deficiency anaemia. Low 13 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 14. MEAN CORPUSCULAR HEMOGLOBIN CONCENTRATION • Hemoglobin Concentration in a single RBC. • MCHC = ℎ𝑏 𝑖𝑛 𝑔𝑚 % 𝑃𝐶𝑉 𝑝𝑒𝑟 100 𝑚𝑙 𝑏𝑙𝑜𝑜𝑑 x 100 • Normal range – normochromic ( 32-36 g/dl) • Less- hypochromic • More- hyperchromic 14 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 15. • Severe prolonged dehydration. • Hereditary spherocytosis.. High • Iron deficiency anaemia. • Thalassaemia. Low 15 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 16. Total Leukocyte count • 4–11 × 103 cells/mm3 16 Increased Acute infections, uremia, steroids, hemorrhage,leukemia Decreased radiation, aplastic anemia, infectious mononucleosis ,septicemia Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 17. DIFFERENTIAL LEUKOCYTE COUNT • PMN: 40%–75% • Lymphocytes: 15%–45% • Eosinophils: 1%–6% • Basophils: 0%–2% • Monocytes: 1%–10% 17 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 18. Neutrophils (PMNs) • Increased: Infections, granulocytic leukemia, surgery, severe exercise • Decreased: Viral infections, aplastic anemia, drugs, radiation, dialysis Eosinophils • Increased: Allergic disorders, parasitic infection, collagen vascular diseases, Addison disease,malignancy • Decreased: Steroids, stress, (ACTH) excess, Cushing syndrome 18 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 19. Basophils • Increased: Polycythemia, chronic myeloid leukemia • Decreased: Steroids, stress, acute rheumatic fever, thyrotoxicosis Lymphocytes • Increased: Viral infections, tuberculosis, mononucleosis, acute and CLL • Decreased: Stress, uraemia, steroids Monocytes • Increased: Monocytic leukemia, chronic inflammation or infection, collagen disease (RA, SLE ), SBE, protozoal infections , TB. • Decreased: Aplasia 19 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 20. PLATELET COUNT • Normal: 150,000-400,000/mm3 • Low count – thrombocytopenia • High count - thrombocytosis 20 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 21. Increased • Malignancy • post surgery • post splenectomy • rheumatoid arthritis (RA) • iron deficiency anemia • trauma • acute hemorrhage. Decreased • Idiopathic thrombocytopenic purpura (ITP) • marrow invasion or aplasia • Hypersplenism • DIC • cirrhosis • quinidine • massive transfusions • viral infections • Infectious mononucleosis 21 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 22. Recommendations for doing FBC 22 Routine Preoperative Testing In Adults Undergoing Elective Non-cardiothoracic Surgery , Joan Vlayen, Nadia Benahmed, Jo Robays: KCE Report 280, Belgian health care knowledge centre.
  • 23. COAGULATION TESTS 1. Bleeding time 2. Clotting time 3. PT 4. PTT 5. INR 23 Clinician’s Handbook of Oral and Maxillofacial Surgery, Daniel M. Laskin
  • 24. BLEEDING TIME (BT) • 1 to 6 minutes • Increased: Thrombocytopenia, von Willibrand disease, aspirin therapy 24 • 6 to 10 minutes. • Increased: Heparin therapy, clotting factor deficiency Clotting Time(CT) Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 25. 25 Prothrombin time (PT) • (12 to 14 seconds) • Increased: warfarin, vitamin K deficiency, liver disease, DIC, prolonged use of tourniquet before drawing blood Partial thromboplastin time (PTT) • (25 to 45 seconds) • Increased: Heparin, defects in intrinsic clotting mechanism, hemophilia A and B, prolonged use of tourniquet before drawing blood Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 26. Interpretation of PT and PTT in patients with bleeding disorders • Liver disease, decreased vitamin K, decreased or defective factor VII PT prolonged, PTT normal • Decreased or defective factor VIII, IX, or XI or anticoagulant present PT normal, PTT prolonged • Decreased or defective factor I, II, V, or X, von Willebrand disease, liver disease, DIC PT and PTT prolonged • Decreased platelet function, thrombocytopenia, factor XIII deficiency, mild von Willebrand disease PT and PTT normal 26 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 27. International normalized ratio (INR) • Ratio of the patient’s PT to a control PT standardized for the potency of the thromboplastin reagent developed by the World Health Organization (WHO) • INR = Patient PT Control PT • Normal value <1 27 Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines
  • 28. 28 • The guidelines of the American college of chest physicians (ACCP) recommend dental surgery without vitamin k antagonists (VKA) interruption with use of a pro hemostatic agent. • The interruption of VKA treatment before dental procedures is not recommended for interventions that are unlikely to cause bleeding for low and high bleeding risk procedures if the INR of the patient is≤3.5 24 hours before the planned intervention. • if the INR ≥3.5, the procedure should be delayed until INR values has been reduced to ≤ 3.5. Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines
  • 29. Calcium • (8.5 to 10.5 mg/dL) • Increased: Hyperparathyroidism, hypervitaminosis D, metastatic bone tumors, Paget disease, multiple myeloma, sarcoidosis, chronic renal failure • Decreased: Hypoparathyroidism, hypoalbuminemia, renal failure, alkalosis, acute pancreatitis, convulsions, vitamin D deficiency 29 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 30. Phosphorus • (2.3 to 4.7 mg/dL) • Increased: Hypoparathyroidism, chronic renal failure, acidosis, hypervitaminosis D, Addison disease • Decreased: Hyperparathyroidism, alcoholism, hypokalemia, vitamin D deficiency, alkalosis, diabetes mellitus 30 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 31. Glucose • Increased: Diabetes mellitus, stress, hyperthyroidism, pregnancy, pancreatic disease, steroid therapy, Cushing syndrome • Decreased: Reactive hypoglycemia, pancreatic disorders, starvation, liver disease, hyperinsulinism, hypothyroidism, hypopituitarism, Addison disease, sepsis 31 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 32. Fasting Plasma Glucose (FPG) • fasting blood sugar levels. • not having anything to eat or drink (except water) for at least 8 hours before the test. 32
  • 33. Random Plasma Glucose Test • This test is a blood check at any time of the day • Diabetes is diagnosed at blood sugar of greater than or equal to 200 mg/dl 33
  • 34. GLYCATED HEMOGLOBIN TEST (HBA1C) • determine how well you are managing your diabetes. • Glucose enters your red blood cells and links up (or glycates) with molecules of hemoglobin • HbA1c reflects average plasma glucose over the previous eight to 12 weeks 34
  • 35. NICE 2016 GUIDELINES Offer HbA1c testing to people with diabetes having surgery if they have not been tested in the last 3 months. Do not routinely offer HbA1c testing before surgery to people without diagnosed diabetes. 35
  • 36. 36
  • 37. Blood Chemistry Tests 1. Electrolytes 2. Anion gap 3. Renal Function 4. Liver Function 37 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 38. 1. Electrolytes Sodium (135 to 145 mEq/L) • Increased: Dehydration, glycosuria, diabetes insipidus • Decreased: Diuretic use, congestive heart failure, hyperglycemia, renal failure, vomiting, diarrhoea. 38 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 39. Chloride • (95 to 108 mEq/L) • Increased: Dehydration, non anion gap metabolic acidosis, diarrhoea, diabetes insipidus • Decreased: Vomiting, excess sweating, congestive heart failure, chronic renal failure, diuretic use, SIADH, diabetes mellitus with ketoacidosis 39 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 40. Potassium (3.5 to 5.2 mEq/L) • Increased: Renal failure, adrenal insufficiency, acidosis, hemolysis, medications, iatrogenic • Decreased: Diuretic therapy, alkalosis, vomiting, nasogastric suctioning, mineralocorticoid excess 40 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 41. Bicarbonate (24 to 30 mEq/L) • Increased: Dehydration, respiratory acidosis, emphysema, vomiting, metabolic alkalosis • Decreased: Metabolic acidosis, respiratory alkalosis, renal failure, diarrhoea. 41 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 42. 2.ANION GAP (8 to 12 mEq) Difference in mEq between serum sodium and the sum of serum chloride and bicarbonate • Diarrhoea, renal tubular acidosis Normal • Renal failure, lactic acidosis, ketoacidosis, salicylate toxicity Increased • Disseminated intravascular coagulation, multiple myeloma Decreased 42 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 43. 3. Renal Function Blood urea nitrogen (BUN) (6 to 20 mg/dL) • Increased: Renal failure of all types, dehydration, gastrointestinal bleeding, increased protein catabolism • Decreased: Liver damage, protein deficiency, starvation, overhydration 43 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 44. Creatinine (0.7 to 1.4 mg/dL) • Increased: Renal failure, muscle disease, false positives with diabetic ketoacidosis • Decreased: Pregnancy; rarely clinically significant 44 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 45. 4. LIVER FUNCTION 45 • bile pigments, bile salts, bromosulphthalein. Tests based on excretory function • transaminases, alkaline phosphatase, 5'nucleotidase y- glutamyl transpeptidase. Tests based on serum enzymes • Galactose tolerance, antipyrine clearance. Tests based on metabolic capacity • Prothrombin time, serum albumin. Tests based on synthetic functions • Hippuric acid synthesis. Tests based on detoxification Biochemistry , Dr. U Satyanarayana
  • 46. 46 Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan
  • 47. 1. SERUM BILIRUBIN • Total - 0.2- 1.0 mg/dL • conjugated bilirubin - 0.2-0.4mg/dl • Unconjugated bilirubin - 0.2-0.6 mg/dl. • estimated by van den Bergh reaction. 47 Biochemistry , Dr. U Satyanarayana
  • 48. 48 Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan
  • 49. 2. Urinary Bilirubin & Urobilinogen • In all cases of jaundice, urine should be examined for the presence of bile pigments (bilirubin), bile salts and urobilinogen 49 Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan
  • 50. SERUM ENZYMES 50 • TRANSAMINASES / AMINOTRANSFERASES Alanine transaminase-ALT • 5-4O lU/l • more sensitive. • pancreatitis, biliary obstruction Aspartate transaminase - AST • 5-45 lU/l • Increased: Liver disease, acute MI ,pancreatitis, muscle trauma, congestive heart failure, hemolysis Biochemistry , Dr. U Satyanarayana
  • 51. Alkaline phosphatase • Normal -13 KA units/dl • Increased: Biliary tract obstruction, bone disease (Paget disease), hyperparathyroidism, osteoblastic bone tumors. • Decreased: Hypophosphatasia, hypothyroidism, malnutrition γ - Glutamyl transpeptidase • normal 5-4O lU/l • highly elevated in biliary obstruction and alcoholism 51 Biochemistry , Dr. U Satyanarayana
  • 52. SYNTHETIC FUNCTION Total protein (6.0 to 8.5 g/dL) • Increased: Multiple myeloma, dehydration, sarcoidosis • Decreased: Liver failure, starvation, inflammatory bowel disease Albumin (3.5 to 5.0 g/dL) • Increased: Dehydration; rarely clinically significant • Decreased: Liver failure, starvation, hyperthyroidism, leukemia, nephrotic syndrome 52 Biochemistry , Dr. U Satyanarayana
  • 54. 1.HIV • Enzyme-linked immunosorbent assay (ELISA) (screening test) • Western blot: Used for confirming presence of HIV antibody • Positive: AIDS, AIDS-related complex 54 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 55. 2.HBsAg • hepatitis B virus (HBV). • A "positive" or "reactive" HBsAg test result means that the person is infected with hepatitis B. • can spread the hepatitis B virus to others through blood. 55 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 56. 3. VDRL • Venereal disease research laboratory test. • screening test for syphilis. • If positive , confirm the results with an FTA-ABS test. 56 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 57. COVID - 19 • Nucleic acid amplification tests (NAAT) • detection of COVID-19 virus nucleic acid (RNA) by real time RT-PCR assays. • RNA isolated and purified from upper and lower respiratory specimens is reverse transcribed to cDNA and subsequently amplified • The viral genes targeted so far include the N, E, S and RdRP genes. • E gene as screening, followed by confirmation through the detection of RdRP gene 57 1.Molecular methods World Health Organization. (2020). Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases: interim guidance, 2 March 2020
  • 58. 2.Serological methods • detection of IgM / IgG antibodies 3. Antigen detection • During the first days after symptom onset (1 to 5), viral proteins can be detected. 4. Rapid diagnostic tests (RDTs) So far there are no rapid diagnostic tests have been authorized by competent regulatory authorities 58 World Health Organization. (2020). Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases: interim guidance, 2 March 2020
  • 60. C-reactive protein (CRP) • acute phase protein • Normal value- less than 10mg/l • sensitive systemic marker of inflammation and tissue damage. • During infectious or inflammatory disease states, CRP levels rise rapidly within the first 6 to 8 hours and peak at levels of up to 350– 400 mg/L after 48 hours • CRP, binds to pathogens and activates the complement to enhance opsonisation and clearance, even before the production of specific IgM or IgG 60
  • 63. Blood Gases • Altered ventilatory status: stroke, asthma, COPD • Hypoxemia: pneumonia • Hypocapnia: hyperventilation • Hypercapnia: COPD • pH disturbance: ketoacidosis Indications for Measurement 63 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 64. Normal Values—Arterial Blood Sample • PO2 - 80 to 95 mm Hg • SaO2 - 93% to 98% • PCO2 - 36 to 43 mm Hg • HCO3 : 20 to 30 mEq/L • Arterial pH: 7.35 to 7.45 64 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 65. Interpretation of Arterial Blood Gas Results • Arterial pH • < 7.35 = acidosis • 7.35 to 7.45 = normal, compensated, or mixed disorder • > 7.45 = alkalosis 65 Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz
  • 66. Routine preoperative tests for elective surgery - NICE guideline 2016 66
  • 67. 67
  • 68. 68
  • 69. 69
  • 70. 70
  • 71. 71 Routine Preoperative Testing In Adults Undergoing Elective Non-cardiothoracic Surgery , Joan Vlayen, Nadia Benahmed, Jo Robays: KCE Report 280
  • 72. CONCLUSION • Preoperative laboratory tests should be ordered based on defined indications such as positive findings on a history and physical exam. • A thorough history and physical examination can be used to identify those medical conditions that might affect perioperative management and direct further laboratory testing. 72
  • 73. REFERENCES 1. Clinician’s Handbook of Oral and Maxillofacial Surgery, Daniel M. Laskin 2. Oxford Handbook of Clinical and Laboratory Investigation, Drew Provan, Andrew Krentz 3. Biochemistry , Dr. U Satyanarayana 4. Textbook of Biochemistry for Dental Students Third Edition, Dm Vasudevan, Sreekumari S,kannan Vaidyanathan 5. Textbook of physiology ,6th edition, A K Jain 6. Peterson’s Principles Of Oral And Maxillofacial Surgery Second Edition 7. C-reactive protein concentrations as a marker of inflammation or infection for interpreting biomarkers of micronutrient status –WHO 8. Routine preoperative tests for elective surgery - NICE guideline 9. World Health Organization. (2020). Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases: interim guidance, 2 March 2020 10. Routine Preoperative Testing In Adults Undergoing Elective Non-cardiothoracic Surgery , Joan Vlayen, Nadia Benahmed, Jo Robays: KCE Report 280 11. NICE guidelines 2016 73