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DIAGNOSTI
C TESTING
Unit -VI
THAMARAI SELVI P M
NURSING TUTOR
Preparing a client for diagnostic
testing
Phases of diagnostic testing
 Pre test
 Intra test
 Post test
Pre test
 Identity band
 Medical record for herbal supplements , allergies or
prior reactions to dyes , contrast media, if so mention
it in the file
 Consent
 Any physical or communication restriction
 Vital signs
 Orders – NPO, any premedications, dosage etc
 Physical and Psychological preparation
 Explanation of procedure
 If any IV access required, establish it
 In case of pediatrics, accompany the attender
Intra test
 Invasive diagnosis- protective barrier to be worn
 Positioning and draping
 In dye administration, skin allergy test to be conducted
 Relax the client during procedure
 Keep resuscitation supplies in hand
 Labelling of specimens
 Storage if necessary (ABG)
 Report any problems to the health care professional
 Safe client transportation out of the diagnostic area
Post test
 Clients on NPO, if awake and able to swallow, provide
water
 Allow the client to express
 Clarify doubts to the patient and family
 Describe what to expect throughout the initial stages
of recovery
 Documentation – in patient file…what specimen, dye,
anaesthesia, who performed, when, how, why, if any
complications arised, vital signs, transportation of
patient……
Common investigations and clinical
implications
 CBC
 Serum electrolytes
 LFT
 Lipid protein profile
 Serum – glucose – fasting, post prandial, HbA1c
 Capillary blood glucose, GRBS
 Urine – Albumin, Acetone, pH, Specific gravity, Culture
, routine, timed urine specimen
 Sputum culture
 Overview of radiological and endoscopic procedures
COMPLETE
BLOOD
COUNT
CBC- Complete Blood Count
 It is a composite report of a number of peripheral
blood tests
 It includes – their number, proportion, variety,
concentrations and quality.
 Hematocrit, hemoglobin, RBC indices (MCV-mean
corpuscular volume ,MCH -(Mean corpuscular
hemoglobin, MCHC – Mean corpuscular volume
concentration), WBC count, platelet count, and
differential white blood cell count (neutrophils,
eosinophils, basophils, lymphocytes and monocyte )
CBC- Complete Blood Count
 Equipment – alcohol swab, a purple topped tube, a
needle and syringe or vacutainer
 Techniques – label the test tube, identify the client,
collect 1ml -5ml sample of blood depending on the
test, gently shake the tube
 Deliver the tube to the lab
RBC
million/mm3
Men- 4.7-6.1
Women – 4.2-5.4
Infants and children - 3.8-5.5
New-borns 4.8-7.1
Erythropnoea
Polycythemia or
erythrocytosis
Hemoglobin
g/dl
Men – 14-18
Women - 12-16,
in pregnancy - >11
Children - 11-16
Newborns – 14-24
Aneamia
WBC
Cells /mm3
4500 -11000 Leucopenia
Leucocytosis/
Leukemia
Platelets
Cells /mm3
1,50,000 -4,00,000 Thrombocytopenia
thrombocytosis
CBC- Normal range
Serum
Electrolyte
s
It is a blood test
that measures the
levels of the body's
mean electrolytes.
Tests Normal
range
Functions Additional information
sodium 136-145
mEq/L
Maintains Extra cellular
volume, acid base balance,
transmits nerve impulse
Hyper/hypo natraemia
Potassium 3.5-5.2
mEq/L
Nerve conduction,
muscular function, acid
base balance
Hyper/hypokalaemia
Magnesium 1.6-3.0
mEq/L
Protein synthesis, muscle
contraction, glucose
metabolism
Hyper/hypomagnesemia
Chloride 90-110
mEq/L
Regulates flow of water
and acid base balance
-Ecclampsia, Cushing’s
-Dehydration, burns
Bicarbonate 22-26
mEq/L
Maintains blood pH Acidosis and
Alkalosis
Phosphate 2.7-4.5
mg/dl
Bone and teeth
formation,metabolism
Hyper/
hypophosphatemia
Calcium 9-10.5
Mg/dl
Bones, cardiac and
skeletal muscle
Hyper /hypo calcemia
LIVER
FUNCTION
TEST
Helps to monitor
liver diseases or
liver damages
Tests Normal range Additional information
ALT- Alanine
transaminase (SGPT)
7-55U/L Elevation indicates hepatic damage
AST- Aspartate
transaminase ( SGOT)
8-48 U/L Increased levels indicates liver damage,
muscle injury
ALP- Alkaline
phosphatase
40-129 U/L Increased in liver pathology
Albumin
Total protein
3.5- 5 g/dl
6.3-7.9g/dl
Maintains oncotic pressure , reduced in
nephrotic syndrome
C- Reactive protein <10mg/L Elevated in inflammation
Prothrombin time- PT 9.4-12.5 sec Measurement of blood coagulation
Elevated in vitamin-K deficiency
Bilirubin 0.1- 1.2mg/dl Jaundice is a sign of liver diseases
GGT- Gamma
glutamyltransferase
8-61 U/L Enzyme in blood. Increased in liver
damage
LDH- Lactate
dehydrogenase
122-222 U/L Liver enzyme. Elevated in liver disease
RENAL
FUNCTION
TEST
These tests check how
good the kidney clear
the waste from the
body
Tests Reference range Additional information
Blood urea
nitrogen - BUN
5-25 mg/dl Product of protein metabolism. Elevated in
dehydration and if persists after correction
indicates renal disorders
Serum
creatinine
0.5- 1.5mg/dl Elevated creatinine indicates renal damage
It is not affected by dehydration, hence an
important test in detecting kidney functions
Serum uric acid 3.5 -8.0 mg/dl
2.6-6.8mg/dl
Increased levels indicates renal disorders
eGFR 90 or higher – RFT
is normal
60 or higher – mild
loss of renal
function
45-59 – moderate
damage
Glomerular filtration rate…calculates how much
blood the glomeruli filters every minute..
LIPID
PROFILE
Lipid profile
 It is a blood test that evaluates the risk of
cardiovascular disorders such as heart
diseases, heart attack and stroke by
measuring the level of specific fat molecules
known as lipids in the blood
Tests Reference range Additional information
Total cholesterol
mg/dl
Normal - <200mg/dl
Borderline high – 200-239
High - >240mg/dl
Total amount of cholesterol
in the blood
LDL - Low density
lipoprotein
mg/dl
Optimal -<100mg/dl
Near optimal – 100-129
Borderline high- 130-159
High – 160-189
Very high - 190
“Bad cholesterol” – causes
atherosclerosis
HDL – High density
lipoprotein
mg/dl
>40 mg/dl
>60mg/dl will protect against
heart disease
“Good cholesterol” –it
removes LDL cholesterol,
keeps arteries open, allows
greater blood flow
VLDL- Very low density
lipoprotein
mg/dl
Normal - 2-30 mg/dl VLDL carries triglycerides,
bad cholesterol which
causes plaque deposits on
the artery walls.
Triglycerides
mg/dl
Normal < 150mg/dl
Borderline high -150-199
High – 200-499 mg/dl
Very high - >500 mg/dl
Excess calories are stored
as triglycerides
Blood glucose
 The breakdown of carbohydrates produces glucose, a
simple sugar that the body uses as fuel for its cells
 Glucose must be transported into the cells via insulin
 A blood glucose test is a method to determine how
much sugar, is in the blood.
 This is prescribed to identify diabetes as well to
control diabetes in people with type 1 and type 2
diabetes.
Blood glucose tests
 FBS- Fasting blood sugar:
Monitors blood glucose after at least 8
hours without eating. Used as an initial test to
identify pre diabetes and diabetes
 RBS- Random blood sugar:
It is without consideration when the
patient last had a meal
 2 hour post prandial blood sugar:
Examines blood sugar exactly 2 hours
after the patient finish eating
Blood glucose tests
 HbA1C- Hemoglobin A1C:
It is used to calculate the average blood sugar
during the previous 2 to 3 months.
Glucose sticks to hemoglobin for as long as the red
blood cells are alive. Red blood cells live about 3 months
 (OGTT) - Oral glucose tolerance test :
It is frequently used to identify pregnancy related
diabetes.
Lancet device
Test Normal range Additional information
FBS <100mg/dl
100-125mg/dl- Pre
diabetes
>125mg/dl – Diabetes (on
2 occasions)
8-12 hours fasting needed
PPBS <140mg/dl 2 hours after the meal
RBS < or = to 200mg/dl Anytime , or no consideration with food
HbA1C Normal -< 5.7%
Pre diabetes– 5.7-6.4%
Diabetes- >6.4%
97% -98% of normal adult Hb is made of
Hb A.
HbA1c is a subgroup which has
undergone some changes due to the
addition of glucose molecule.
This is called as glycoselated hemoglobin
Stool
examination
 The digestive system excrete feces, a waste product
of digestion, through the GI tract
 Studies of feces can help diagnose GI problems
 Eg. Bacterial infections, GI bleeding, obstruction,
inflammatory bowel diseases, malabsorption, parasite
disease, and colon cancer
 An adult excretes 100-300 grams of feces every day
 Normal feces contains water, undigested matter,
intestinal secretions, a lot of bacteria, bile, epithelial
cells, white blood cells, gastric secretions, pancreatic
juices, and inorganic substances like calcium and
phosphorus.
Techniques of collecting the sample
 Within an hour it should be sent to lab or else
refrigerated
 Drugs like antibiotics and antacids can hinder bacterial
development
 Stool sample gathered in a bedpan or plastic hat
container placed in the toilet
 It should not contain any water or urine
 Using gloves, 2 clean tongue blades used to take
sample from the centre of the feces , put into the
container.
 If any blood, pus, microbes sample should contain the
same
Techniques of collecting the sample
 Formed feces- sample should be of walnut size,
unformed feces – 15 to 20ml.
 Physical and chemical,
Biological , microscopic
analysis will be done
Toilet hat
Physical analysis
 Analysis of the quantity, colour, consistency,
odour and shape of the stool, also parasites if
found
Physical analysis of stool
Characteristic variation Condition
Colour Black Upper GI bleeding, Iron or coal ingestion
Dark brown Hemolytic anemia and high meat
Gray, silvery Steatorrhea, pancreatic diseaseses
Pasty and gray-
white
Bile duct obstruction
Red Hemorrhoids , lower GI bleed
Consistency Mucoid, watery, no
blood
Irritable bowel syndrome
Mucoid and bloody Inflammatory bowel disease, ulcerative
colitis (UC)
Loose, purulent
with necrotic
Diverticulitis, UC, parasitic infection and
bacillary dysentry
Chemical analysis
 To detect the presence of:
 Occult blood- GI bleeding, malignancy, ulcerative
colitis and hemorrhoids
 Test for carbohydrates – metabolic or intestinal
abnormalities. Negative is normal
 Test for bile – hemolytic anemia or rapid passage of
feces in GI tract. Negative is normal
 Test for trypsin – pancreatic disorders .
 Negative is normal in adults and children over age 2..
 Positive is normal in children younger than 2
Microscopic examination of stools
 Leucocytes, lipids and parasites are detected in feces
via microscopic examination
Test Normal Abnormal
Leukocytes Stool does not
contain leucocytes
Bacterial diarrhoea, ulcerative colitis
Fats <60- normal sized
droplets
Triglycerides 1-5%
Fatty acids – 5-15%
Increased triglycerides- pancreatic enzyme
insufficiency
Increased fatty acids with normal triglyceride –
malabsorption syndrome
Parasites No parasite present Protozoa – dysentry, peritonitis, perforation
Hookworms – anaemia
Pinworm – irritation and itching around anus
Tapeworms – diarrhoea, epigastric pain, weight
loss
URINE
EXAMINATION
Urine analysis
 Urine is an ultrafiltrate of plasma that contains
a variety of chemicals carried by blood
 Urine samples are simple to collect and give
the practitioner data to assess the client’s
health
Urine routine analysis
 Macroscopic analysis and microscopic analysis are
2 main parts of a routine urinalysis
 Macroscopic analysis comprises colour,
appearance, odour, specific gravity, pH, protein,
glucose, ketones, blood, bilirubin and urobilinogen,
nitrite and leukocyte esterase.
 Microscopic analysis includes RBC’s ,WBC’s,
epithelial cells, casts and crystals and others such
as bacteria, yeast, mucus, spermatazoa and
parasites
Urine – Macroscopic analysis
Characteristics Normal findings
Colour Pale yellow to amber
Appearance Clear to slightly cloudy
Odour Mildly aromatic
Specific gravity 1.001-1.035
pH 4.5- 8.0
Protein Negative
Glucose Negative
Other sugars Negative
Ketones Negative
Blood Negative
Bilirubin Negative
Urine – Microscopic analysis
Test Normal findings
Red bllod cells 0-3 per high – power field (HPF)
White blood cells 0-4 per HPF
Epithelial cells Few
Casts Occasional (hyaline or granular)
Crystals Occasional (uric acid, urate,
phosphate, or calcium oxalate)
Routine urinalysis - Volume
 The amount of urine excreted in a 24 hour period
can be a useful tool clinical diagnosis
 Average 24 hour urine volume is 1200-1500ml
 Normal range can be 600-1700ml
 Diuresis – increase in urine volume
 Anuria –no urine output or <100ml/day
 Oliguria –low urine output < 400ml/day
 Polyuria – excessive urine output >3000ml/day
Routine urinalysis - Colour
 The pigment urochrome, which is produced by
endogenous metabolic process, is the primary cause
of colour of urine.
 Colour includes– light yellow, straw, yellow, dark
yellow and amber
 Examining the sample in bright light on a white
background will help in determining the urine colour.
Routine urinalysis - Appearance
 Typically, urine appearance is clear or slightly cloudy
 Caused by presence of WBC, RBC, bacteria, and
epithelial cells. These indicate infection or
inflammation of the vaginal and urinary systems
 Mucus, sperm, prostatic fluid , menstrual and vaginal
discharges , fecal debris, and external compounds
like talcum powder, antiseptics can also cause cloudy
urine
Routine urinalysis- Odour
 A fresh urine specimen has a light aromatic odour.
 As urine stands, the odour of ammonia predominates
because of the breakdown of urea.
 Urine acquires distinct smells after ingesting particular
foods and medicines
 Fruity smelling urine – starvation or uncontrolled DM
related ketonuria
 Fishy smell – bacterial infection
Routine urinalysis-
Specific gravity
The ability of kidney to reabsorb water and
compounds from the glomerular filtrate is
indicated by specific gravity of urine
Normal range is 1.001 – 1.035
Patients with over hydration – low specific
gravity
Dehydration , nephrosis – high specific gravity
Routine urinalysis- pH
 The ability of kidneys to maintain the body’s acid-base
balance can be seen in the pH of the urine.
 Respiratory and metabolic acidosis- acidic urine expelled
ie.. Low pH
 Respiratory and metabolic alkalosis – alkaline urine I
expelled ie.. High pH
 Urinary pH is alos impacted by many meals and
medications
 Normal pH varies from 4.6- 8.0
Routine urinalysis-Protein
Only a small quantity of protein is typically
present in urine. The proximal convoluted
tubule reabsorb most of these filtered proteins.
PROTEINURIA can occur in people after
physical exertion or when dehydrated
If persistent – then it is a sign of renal disease,
systemic illness (CHF, Fever)
Routine urinalysis-Glucose
 Most cases, urine contains no glucose
 Majority of the glucose is reabsorbed by PCT. Only
when plasma glucose levels are extremely high that
the carrier mechanisms are exhausted, glucose will
show up in the urine
 Uncontrolled diabetes mellitus is the most common
cause of GLYCSOURIA
 Sample for urine to be collected before meals
 Glycosuria can be caused by food as well medication
Routine urinalysis-Ketones
 Ketones are not typically found in urine in quantifiable
concentrations.
 It may be found in cases of excessive fat metabolism
 Ketones are found in diabetes mellitus where there is
defective carbohydrate metabolism, or also by
excessive carbohydrate loss such as diarrhoea and
vomiting, dieting
 Ketonuria is a sign of systemic acidosis.
URINE
TESTING
Urine testing (pH,Albumin, Specific
gravity, Acetone)
Urine pH
 A procedure to assess a solution’s alkalinity,
neutrality or acidity .
 pH 7 is considered neutral
 Acidity is indicated by a pH below 7
 Alkalinity by pH above 7
 Normal pH of urine varies between 4.6-8
Urine pH- Procedure
Different methods
 Litmus paper
 Nitrazine paper
 Dipstick method etc..
Litmus paper test
Nitrazine paper test
Dipstick method
Urine specific gravity- Urinometer
Urine - Acetone
Principle:
A purple colour complex or ring appear when acetone or
acetoacelate due to reaction with alkaline sodium
nitroprusside.
Tests done are:
 Rothera’s test
 Lang’s test
 Acetest tablet testing
 Acetone powder test
 Ketostix , reagent strip test method
Rothera ‘s test
Acetest tablet testing
Urine – Protein
Principle:
Protein is precipitated out of the urine samples using a
chemical, such as a strong acid , or it is heated until it
coagulates out of solution.
Tests done are:
 The Robert’s test
 The Heller test
 The sulphosalycylic acid test
 Acetic acid and heat test
Acetic acid and heat test
Collection of
urine specimen
COLLECTION OF URINE
SPECIMEN
 The specimen must be carefully procured, handled and
maintained before analysis
 The technique for collection, the timing and the handling
all affect the clinical information that can be gathered
from a urine sample
 The specimen should be kept at 4 degree celsius as
soon as feasible after collection, if urine testing cannot
be done within 2 hours
 Specimens can be kept in the refrigerator for 6 to 8
hours without any significant changes to their constituent
elements
METHODS OF URINE COLLECTION
 Random specimen collection- collected at any time.
 First morning sample – the first urine passed in the
morning. This specimen has relatively high
concentrations of biological components and analytes
like protein and glucose
 Clean catch midstream urine – it is the preferable
form of specimen for culture and sensitivity testing due
to the decreased frequency of cellular and
microbiological contamination
 Timed or 24 hour specimen – it is used in the
metabolic evaluation of urinary stone disease, the
assessment of proteinuria, the estimation of renal
function via creatinine clearance.
METHODS OF URINE COLLECTION
 Specimen obtained using catheter- when a patient is
confined to bed or is unable to urinate on their own
 Supra pubic aspiration specimens – it is used when a
bedridden patient cannot be catheterized or a sterile
specimen is required. The sample is obtained by
inserting a needle through the abdominal wall into the
bladder
General instructions in urine specimen
collection
 Prevent contamination of specimen – instruct clearly
not to touch the inner part of the container
 A fresh specimen to be obtained in a clean and dry
container
 The concentrated first morning sample is the most
suitable one to
 Ideal specimen for testing urine sugar is on that has
been voided 2-3 hours after eating
 For mid stream clean catch urine- patients must first
clean their urethra before voiding first part of their urine
stream into the toilet
SPUTU
M
CULTUR
E
SPUTUM CULTURE
 A sputum culture is a test that checks for bacteria or
another type of organism that may be causing an infection
in the lungs or the airways leading to the lungs.
 Sputum, also known as phlegm, is a thick type of mucus
made in the lungs.
 Sputum is not the same as spit or saliva. Sputum contains
cells from the immune system that help fight the
bacteria, fungi, or other foreign substances in the lungs or
airways.
 The thickness of sputum helps trap the foreign material.
The cilia (tiny hairs) in the airways push it through the
mouth and be coughed out.
SPUTUM CULTURE
 Normal respiratory flora include Neisseria catarrhalis,
Candida albicans, diphtheroids, alpha-hemolytic
streptococci, and some staphylococci
INDICATIONS
Detects the etiology of respiratory infection
Confirmatory diagnosis of tuberculosis
Monitoring the response to therapy for respiratory
infections
Identification of antibiotics who which the cultured
organism is sensitive.
SPUTUM CULTURE
 INTERFERING FACTORS
 Inadequate specimen collection
 Delay in shipping specimen to the laboratory
 C&S to be performed prior to antimicrobial therapy to
assess the efficacy of therapy
Pre- procedure
 Specimen to be collected in the morning after secretion
have accumulated overnight
 Saliva or post nasal drainage should not be used
 Specimen to be taken by coughing or tracheal
suctioning and deep from the respiratory tract
 Increase fluid intake at night helps to liquefy secretions
 Quantity to be kept in mind
Preparation for the procedure
 Assist in suppling extra fluids and proper
humidification , unless contraindicated
 If the patient is prescribed nebulizer treatments, it is
helpful to administer this treatment prior to the
procedure to help mobilize secretions
 Assist with oral hygiene
 Keep sputum collecting containers available
 Oxygenation is needed for 20 -30 minutes before the
procedure, if sample is to be taken via tracheal
suctioning
 100% O2 hyperventilation to be done both before and
after the procedure
Preparation for the procedure
 It is also important to assess if the patient is
experiencing pain related to coughing. For example,
pain following chest or abdominal surgery can inhibit
the patient from taking deep breaths and
expectorating. In this case, pain medication should be
provided prior to performing the procedure.
 Patients can also be encouraged to support surgical
wounds with a pillow while coughing to provide
additional support and comfort.
Procedure
 Nurse should wear gloves, a facemask, and
potentially glasses or goggles
 Client should sit up straight, with support if necessary
 Client should take deep breaths twice or thrice and
cough vigorously
 Any raised sputum needs to be immediately
expectorated into a sterile container without touching
the inside or rim of the container.
 The specimen should be at least 5 mL .Ask the
patient to continue producing and expectorating
sputum until this amount is achieved.
Procedure
 Assess the sputum specimen to ensure it is sputum and
not saliva. Sputum appears thick and opaque, whereas
saliva appears thin, clear, and watery.
 If a patient is unable to expectorate a sputum sample,
other interventions may be required to mobilize
secretions.
 It is often helpful to collaborate with a respiratory
therapist for assistance in this situation.
 Interventions may include nebulizers, hydration, deep-
breathing exercises, chest percussion, and postural
drainage. If these interventions are not successful, a
sputum sample may be obtained via oropharyngeal or
endotracheal suctioning.[1],[2]
Overview of
radiologic and
endoscopic
procedures
Radiologic studies
 It is frequently the first diagnostic tool or
screening device used to uncover anomalies
in the structure of the body’s soft and bone
components
 It is based on the variations in body structure
density.
 It is hazardous too. Which can be reduced
with right protective measures
Radiologic studies
Without
contrast
 X rays
 Mammogr- -
aphy
 KUB studies
 Obstruction
series
 With contrast
 Angiography
 Biliary and gall bladder systems
radiography- eg: cholecystography
 Radiography of digestive system-
barium meal , barium enema
 Radiography of urinary system -IVP
 Radiographic examintion of
encapsulated joint- myelography,
hysterosalpingography
 CT scan, MRI scan
 Radio nucleide tests
Endoscopic studies
 It includes a variety of diagnostic techniques that
involve inserting an endoscope through a natural or
surgical incision into body cavities or organs
 Majority are flexible fibre optic scopes that may be put
into smaller body cavities and organs, however rigid
also are used.
 Eg:
 Bronchoscopy- visualize bronchial tree and lungs
 Cystoscopy- bladder
 Laparascope – abdominal cavity
 Colposcopy- vaginal and cervix
 Arthroscopy – joints etc,…
Thank you

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Diagnostic testing unit 6

  • 1. DIAGNOSTI C TESTING Unit -VI THAMARAI SELVI P M NURSING TUTOR
  • 2. Preparing a client for diagnostic testing Phases of diagnostic testing  Pre test  Intra test  Post test
  • 3. Pre test  Identity band  Medical record for herbal supplements , allergies or prior reactions to dyes , contrast media, if so mention it in the file  Consent  Any physical or communication restriction  Vital signs  Orders – NPO, any premedications, dosage etc  Physical and Psychological preparation  Explanation of procedure  If any IV access required, establish it  In case of pediatrics, accompany the attender
  • 4. Intra test  Invasive diagnosis- protective barrier to be worn  Positioning and draping  In dye administration, skin allergy test to be conducted  Relax the client during procedure  Keep resuscitation supplies in hand  Labelling of specimens  Storage if necessary (ABG)  Report any problems to the health care professional  Safe client transportation out of the diagnostic area
  • 5. Post test  Clients on NPO, if awake and able to swallow, provide water  Allow the client to express  Clarify doubts to the patient and family  Describe what to expect throughout the initial stages of recovery  Documentation – in patient file…what specimen, dye, anaesthesia, who performed, when, how, why, if any complications arised, vital signs, transportation of patient……
  • 6. Common investigations and clinical implications  CBC  Serum electrolytes  LFT  Lipid protein profile  Serum – glucose – fasting, post prandial, HbA1c  Capillary blood glucose, GRBS  Urine – Albumin, Acetone, pH, Specific gravity, Culture , routine, timed urine specimen  Sputum culture  Overview of radiological and endoscopic procedures
  • 8. CBC- Complete Blood Count  It is a composite report of a number of peripheral blood tests  It includes – their number, proportion, variety, concentrations and quality.  Hematocrit, hemoglobin, RBC indices (MCV-mean corpuscular volume ,MCH -(Mean corpuscular hemoglobin, MCHC – Mean corpuscular volume concentration), WBC count, platelet count, and differential white blood cell count (neutrophils, eosinophils, basophils, lymphocytes and monocyte )
  • 9. CBC- Complete Blood Count  Equipment – alcohol swab, a purple topped tube, a needle and syringe or vacutainer  Techniques – label the test tube, identify the client, collect 1ml -5ml sample of blood depending on the test, gently shake the tube  Deliver the tube to the lab
  • 10. RBC million/mm3 Men- 4.7-6.1 Women – 4.2-5.4 Infants and children - 3.8-5.5 New-borns 4.8-7.1 Erythropnoea Polycythemia or erythrocytosis Hemoglobin g/dl Men – 14-18 Women - 12-16, in pregnancy - >11 Children - 11-16 Newborns – 14-24 Aneamia WBC Cells /mm3 4500 -11000 Leucopenia Leucocytosis/ Leukemia Platelets Cells /mm3 1,50,000 -4,00,000 Thrombocytopenia thrombocytosis CBC- Normal range
  • 11. Serum Electrolyte s It is a blood test that measures the levels of the body's mean electrolytes.
  • 12. Tests Normal range Functions Additional information sodium 136-145 mEq/L Maintains Extra cellular volume, acid base balance, transmits nerve impulse Hyper/hypo natraemia Potassium 3.5-5.2 mEq/L Nerve conduction, muscular function, acid base balance Hyper/hypokalaemia Magnesium 1.6-3.0 mEq/L Protein synthesis, muscle contraction, glucose metabolism Hyper/hypomagnesemia Chloride 90-110 mEq/L Regulates flow of water and acid base balance -Ecclampsia, Cushing’s -Dehydration, burns Bicarbonate 22-26 mEq/L Maintains blood pH Acidosis and Alkalosis Phosphate 2.7-4.5 mg/dl Bone and teeth formation,metabolism Hyper/ hypophosphatemia Calcium 9-10.5 Mg/dl Bones, cardiac and skeletal muscle Hyper /hypo calcemia
  • 13. LIVER FUNCTION TEST Helps to monitor liver diseases or liver damages
  • 14. Tests Normal range Additional information ALT- Alanine transaminase (SGPT) 7-55U/L Elevation indicates hepatic damage AST- Aspartate transaminase ( SGOT) 8-48 U/L Increased levels indicates liver damage, muscle injury ALP- Alkaline phosphatase 40-129 U/L Increased in liver pathology Albumin Total protein 3.5- 5 g/dl 6.3-7.9g/dl Maintains oncotic pressure , reduced in nephrotic syndrome C- Reactive protein <10mg/L Elevated in inflammation Prothrombin time- PT 9.4-12.5 sec Measurement of blood coagulation Elevated in vitamin-K deficiency Bilirubin 0.1- 1.2mg/dl Jaundice is a sign of liver diseases GGT- Gamma glutamyltransferase 8-61 U/L Enzyme in blood. Increased in liver damage LDH- Lactate dehydrogenase 122-222 U/L Liver enzyme. Elevated in liver disease
  • 15. RENAL FUNCTION TEST These tests check how good the kidney clear the waste from the body
  • 16. Tests Reference range Additional information Blood urea nitrogen - BUN 5-25 mg/dl Product of protein metabolism. Elevated in dehydration and if persists after correction indicates renal disorders Serum creatinine 0.5- 1.5mg/dl Elevated creatinine indicates renal damage It is not affected by dehydration, hence an important test in detecting kidney functions Serum uric acid 3.5 -8.0 mg/dl 2.6-6.8mg/dl Increased levels indicates renal disorders eGFR 90 or higher – RFT is normal 60 or higher – mild loss of renal function 45-59 – moderate damage Glomerular filtration rate…calculates how much blood the glomeruli filters every minute..
  • 18. Lipid profile  It is a blood test that evaluates the risk of cardiovascular disorders such as heart diseases, heart attack and stroke by measuring the level of specific fat molecules known as lipids in the blood
  • 19. Tests Reference range Additional information Total cholesterol mg/dl Normal - <200mg/dl Borderline high – 200-239 High - >240mg/dl Total amount of cholesterol in the blood LDL - Low density lipoprotein mg/dl Optimal -<100mg/dl Near optimal – 100-129 Borderline high- 130-159 High – 160-189 Very high - 190 “Bad cholesterol” – causes atherosclerosis HDL – High density lipoprotein mg/dl >40 mg/dl >60mg/dl will protect against heart disease “Good cholesterol” –it removes LDL cholesterol, keeps arteries open, allows greater blood flow VLDL- Very low density lipoprotein mg/dl Normal - 2-30 mg/dl VLDL carries triglycerides, bad cholesterol which causes plaque deposits on the artery walls. Triglycerides mg/dl Normal < 150mg/dl Borderline high -150-199 High – 200-499 mg/dl Very high - >500 mg/dl Excess calories are stored as triglycerides
  • 21.  The breakdown of carbohydrates produces glucose, a simple sugar that the body uses as fuel for its cells  Glucose must be transported into the cells via insulin  A blood glucose test is a method to determine how much sugar, is in the blood.  This is prescribed to identify diabetes as well to control diabetes in people with type 1 and type 2 diabetes.
  • 22. Blood glucose tests  FBS- Fasting blood sugar: Monitors blood glucose after at least 8 hours without eating. Used as an initial test to identify pre diabetes and diabetes  RBS- Random blood sugar: It is without consideration when the patient last had a meal  2 hour post prandial blood sugar: Examines blood sugar exactly 2 hours after the patient finish eating
  • 23. Blood glucose tests  HbA1C- Hemoglobin A1C: It is used to calculate the average blood sugar during the previous 2 to 3 months. Glucose sticks to hemoglobin for as long as the red blood cells are alive. Red blood cells live about 3 months  (OGTT) - Oral glucose tolerance test : It is frequently used to identify pregnancy related diabetes.
  • 24.
  • 25.
  • 27. Test Normal range Additional information FBS <100mg/dl 100-125mg/dl- Pre diabetes >125mg/dl – Diabetes (on 2 occasions) 8-12 hours fasting needed PPBS <140mg/dl 2 hours after the meal RBS < or = to 200mg/dl Anytime , or no consideration with food HbA1C Normal -< 5.7% Pre diabetes– 5.7-6.4% Diabetes- >6.4% 97% -98% of normal adult Hb is made of Hb A. HbA1c is a subgroup which has undergone some changes due to the addition of glucose molecule. This is called as glycoselated hemoglobin
  • 29.  The digestive system excrete feces, a waste product of digestion, through the GI tract  Studies of feces can help diagnose GI problems  Eg. Bacterial infections, GI bleeding, obstruction, inflammatory bowel diseases, malabsorption, parasite disease, and colon cancer  An adult excretes 100-300 grams of feces every day  Normal feces contains water, undigested matter, intestinal secretions, a lot of bacteria, bile, epithelial cells, white blood cells, gastric secretions, pancreatic juices, and inorganic substances like calcium and phosphorus.
  • 30. Techniques of collecting the sample  Within an hour it should be sent to lab or else refrigerated  Drugs like antibiotics and antacids can hinder bacterial development  Stool sample gathered in a bedpan or plastic hat container placed in the toilet  It should not contain any water or urine  Using gloves, 2 clean tongue blades used to take sample from the centre of the feces , put into the container.  If any blood, pus, microbes sample should contain the same
  • 31. Techniques of collecting the sample  Formed feces- sample should be of walnut size, unformed feces – 15 to 20ml.  Physical and chemical, Biological , microscopic analysis will be done
  • 33. Physical analysis  Analysis of the quantity, colour, consistency, odour and shape of the stool, also parasites if found
  • 34. Physical analysis of stool Characteristic variation Condition Colour Black Upper GI bleeding, Iron or coal ingestion Dark brown Hemolytic anemia and high meat Gray, silvery Steatorrhea, pancreatic diseaseses Pasty and gray- white Bile duct obstruction Red Hemorrhoids , lower GI bleed Consistency Mucoid, watery, no blood Irritable bowel syndrome Mucoid and bloody Inflammatory bowel disease, ulcerative colitis (UC) Loose, purulent with necrotic Diverticulitis, UC, parasitic infection and bacillary dysentry
  • 35. Chemical analysis  To detect the presence of:  Occult blood- GI bleeding, malignancy, ulcerative colitis and hemorrhoids  Test for carbohydrates – metabolic or intestinal abnormalities. Negative is normal  Test for bile – hemolytic anemia or rapid passage of feces in GI tract. Negative is normal  Test for trypsin – pancreatic disorders .  Negative is normal in adults and children over age 2..  Positive is normal in children younger than 2
  • 36. Microscopic examination of stools  Leucocytes, lipids and parasites are detected in feces via microscopic examination Test Normal Abnormal Leukocytes Stool does not contain leucocytes Bacterial diarrhoea, ulcerative colitis Fats <60- normal sized droplets Triglycerides 1-5% Fatty acids – 5-15% Increased triglycerides- pancreatic enzyme insufficiency Increased fatty acids with normal triglyceride – malabsorption syndrome Parasites No parasite present Protozoa – dysentry, peritonitis, perforation Hookworms – anaemia Pinworm – irritation and itching around anus Tapeworms – diarrhoea, epigastric pain, weight loss
  • 38. Urine analysis  Urine is an ultrafiltrate of plasma that contains a variety of chemicals carried by blood  Urine samples are simple to collect and give the practitioner data to assess the client’s health
  • 39. Urine routine analysis  Macroscopic analysis and microscopic analysis are 2 main parts of a routine urinalysis  Macroscopic analysis comprises colour, appearance, odour, specific gravity, pH, protein, glucose, ketones, blood, bilirubin and urobilinogen, nitrite and leukocyte esterase.  Microscopic analysis includes RBC’s ,WBC’s, epithelial cells, casts and crystals and others such as bacteria, yeast, mucus, spermatazoa and parasites
  • 40. Urine – Macroscopic analysis Characteristics Normal findings Colour Pale yellow to amber Appearance Clear to slightly cloudy Odour Mildly aromatic Specific gravity 1.001-1.035 pH 4.5- 8.0 Protein Negative Glucose Negative Other sugars Negative Ketones Negative Blood Negative Bilirubin Negative
  • 41. Urine – Microscopic analysis Test Normal findings Red bllod cells 0-3 per high – power field (HPF) White blood cells 0-4 per HPF Epithelial cells Few Casts Occasional (hyaline or granular) Crystals Occasional (uric acid, urate, phosphate, or calcium oxalate)
  • 42. Routine urinalysis - Volume  The amount of urine excreted in a 24 hour period can be a useful tool clinical diagnosis  Average 24 hour urine volume is 1200-1500ml  Normal range can be 600-1700ml  Diuresis – increase in urine volume  Anuria –no urine output or <100ml/day  Oliguria –low urine output < 400ml/day  Polyuria – excessive urine output >3000ml/day
  • 43. Routine urinalysis - Colour  The pigment urochrome, which is produced by endogenous metabolic process, is the primary cause of colour of urine.  Colour includes– light yellow, straw, yellow, dark yellow and amber  Examining the sample in bright light on a white background will help in determining the urine colour.
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  • 46. Routine urinalysis - Appearance  Typically, urine appearance is clear or slightly cloudy  Caused by presence of WBC, RBC, bacteria, and epithelial cells. These indicate infection or inflammation of the vaginal and urinary systems  Mucus, sperm, prostatic fluid , menstrual and vaginal discharges , fecal debris, and external compounds like talcum powder, antiseptics can also cause cloudy urine
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  • 50. Routine urinalysis- Odour  A fresh urine specimen has a light aromatic odour.  As urine stands, the odour of ammonia predominates because of the breakdown of urea.  Urine acquires distinct smells after ingesting particular foods and medicines  Fruity smelling urine – starvation or uncontrolled DM related ketonuria  Fishy smell – bacterial infection
  • 51. Routine urinalysis- Specific gravity The ability of kidney to reabsorb water and compounds from the glomerular filtrate is indicated by specific gravity of urine Normal range is 1.001 – 1.035 Patients with over hydration – low specific gravity Dehydration , nephrosis – high specific gravity
  • 52. Routine urinalysis- pH  The ability of kidneys to maintain the body’s acid-base balance can be seen in the pH of the urine.  Respiratory and metabolic acidosis- acidic urine expelled ie.. Low pH  Respiratory and metabolic alkalosis – alkaline urine I expelled ie.. High pH  Urinary pH is alos impacted by many meals and medications  Normal pH varies from 4.6- 8.0
  • 53. Routine urinalysis-Protein Only a small quantity of protein is typically present in urine. The proximal convoluted tubule reabsorb most of these filtered proteins. PROTEINURIA can occur in people after physical exertion or when dehydrated If persistent – then it is a sign of renal disease, systemic illness (CHF, Fever)
  • 54. Routine urinalysis-Glucose  Most cases, urine contains no glucose  Majority of the glucose is reabsorbed by PCT. Only when plasma glucose levels are extremely high that the carrier mechanisms are exhausted, glucose will show up in the urine  Uncontrolled diabetes mellitus is the most common cause of GLYCSOURIA  Sample for urine to be collected before meals  Glycosuria can be caused by food as well medication
  • 55. Routine urinalysis-Ketones  Ketones are not typically found in urine in quantifiable concentrations.  It may be found in cases of excessive fat metabolism  Ketones are found in diabetes mellitus where there is defective carbohydrate metabolism, or also by excessive carbohydrate loss such as diarrhoea and vomiting, dieting  Ketonuria is a sign of systemic acidosis.
  • 57. Urine testing (pH,Albumin, Specific gravity, Acetone) Urine pH  A procedure to assess a solution’s alkalinity, neutrality or acidity .  pH 7 is considered neutral  Acidity is indicated by a pH below 7  Alkalinity by pH above 7  Normal pH of urine varies between 4.6-8
  • 58. Urine pH- Procedure Different methods  Litmus paper  Nitrazine paper  Dipstick method etc..
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  • 64. Urine - Acetone Principle: A purple colour complex or ring appear when acetone or acetoacelate due to reaction with alkaline sodium nitroprusside. Tests done are:  Rothera’s test  Lang’s test  Acetest tablet testing  Acetone powder test  Ketostix , reagent strip test method
  • 67. Urine – Protein Principle: Protein is precipitated out of the urine samples using a chemical, such as a strong acid , or it is heated until it coagulates out of solution. Tests done are:  The Robert’s test  The Heller test  The sulphosalycylic acid test  Acetic acid and heat test
  • 68. Acetic acid and heat test
  • 70. COLLECTION OF URINE SPECIMEN  The specimen must be carefully procured, handled and maintained before analysis  The technique for collection, the timing and the handling all affect the clinical information that can be gathered from a urine sample  The specimen should be kept at 4 degree celsius as soon as feasible after collection, if urine testing cannot be done within 2 hours  Specimens can be kept in the refrigerator for 6 to 8 hours without any significant changes to their constituent elements
  • 71. METHODS OF URINE COLLECTION  Random specimen collection- collected at any time.  First morning sample – the first urine passed in the morning. This specimen has relatively high concentrations of biological components and analytes like protein and glucose  Clean catch midstream urine – it is the preferable form of specimen for culture and sensitivity testing due to the decreased frequency of cellular and microbiological contamination  Timed or 24 hour specimen – it is used in the metabolic evaluation of urinary stone disease, the assessment of proteinuria, the estimation of renal function via creatinine clearance.
  • 72. METHODS OF URINE COLLECTION  Specimen obtained using catheter- when a patient is confined to bed or is unable to urinate on their own  Supra pubic aspiration specimens – it is used when a bedridden patient cannot be catheterized or a sterile specimen is required. The sample is obtained by inserting a needle through the abdominal wall into the bladder
  • 73. General instructions in urine specimen collection  Prevent contamination of specimen – instruct clearly not to touch the inner part of the container  A fresh specimen to be obtained in a clean and dry container  The concentrated first morning sample is the most suitable one to  Ideal specimen for testing urine sugar is on that has been voided 2-3 hours after eating  For mid stream clean catch urine- patients must first clean their urethra before voiding first part of their urine stream into the toilet
  • 75. SPUTUM CULTURE  A sputum culture is a test that checks for bacteria or another type of organism that may be causing an infection in the lungs or the airways leading to the lungs.  Sputum, also known as phlegm, is a thick type of mucus made in the lungs.  Sputum is not the same as spit or saliva. Sputum contains cells from the immune system that help fight the bacteria, fungi, or other foreign substances in the lungs or airways.  The thickness of sputum helps trap the foreign material. The cilia (tiny hairs) in the airways push it through the mouth and be coughed out.
  • 76. SPUTUM CULTURE  Normal respiratory flora include Neisseria catarrhalis, Candida albicans, diphtheroids, alpha-hemolytic streptococci, and some staphylococci INDICATIONS Detects the etiology of respiratory infection Confirmatory diagnosis of tuberculosis Monitoring the response to therapy for respiratory infections Identification of antibiotics who which the cultured organism is sensitive.
  • 77. SPUTUM CULTURE  INTERFERING FACTORS  Inadequate specimen collection  Delay in shipping specimen to the laboratory  C&S to be performed prior to antimicrobial therapy to assess the efficacy of therapy
  • 78. Pre- procedure  Specimen to be collected in the morning after secretion have accumulated overnight  Saliva or post nasal drainage should not be used  Specimen to be taken by coughing or tracheal suctioning and deep from the respiratory tract  Increase fluid intake at night helps to liquefy secretions  Quantity to be kept in mind
  • 79. Preparation for the procedure  Assist in suppling extra fluids and proper humidification , unless contraindicated  If the patient is prescribed nebulizer treatments, it is helpful to administer this treatment prior to the procedure to help mobilize secretions  Assist with oral hygiene  Keep sputum collecting containers available  Oxygenation is needed for 20 -30 minutes before the procedure, if sample is to be taken via tracheal suctioning  100% O2 hyperventilation to be done both before and after the procedure
  • 80. Preparation for the procedure  It is also important to assess if the patient is experiencing pain related to coughing. For example, pain following chest or abdominal surgery can inhibit the patient from taking deep breaths and expectorating. In this case, pain medication should be provided prior to performing the procedure.  Patients can also be encouraged to support surgical wounds with a pillow while coughing to provide additional support and comfort.
  • 81. Procedure  Nurse should wear gloves, a facemask, and potentially glasses or goggles  Client should sit up straight, with support if necessary  Client should take deep breaths twice or thrice and cough vigorously  Any raised sputum needs to be immediately expectorated into a sterile container without touching the inside or rim of the container.  The specimen should be at least 5 mL .Ask the patient to continue producing and expectorating sputum until this amount is achieved.
  • 82. Procedure  Assess the sputum specimen to ensure it is sputum and not saliva. Sputum appears thick and opaque, whereas saliva appears thin, clear, and watery.  If a patient is unable to expectorate a sputum sample, other interventions may be required to mobilize secretions.  It is often helpful to collaborate with a respiratory therapist for assistance in this situation.  Interventions may include nebulizers, hydration, deep- breathing exercises, chest percussion, and postural drainage. If these interventions are not successful, a sputum sample may be obtained via oropharyngeal or endotracheal suctioning.[1],[2]
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  • 87. Radiologic studies  It is frequently the first diagnostic tool or screening device used to uncover anomalies in the structure of the body’s soft and bone components  It is based on the variations in body structure density.  It is hazardous too. Which can be reduced with right protective measures
  • 88. Radiologic studies Without contrast  X rays  Mammogr- - aphy  KUB studies  Obstruction series  With contrast  Angiography  Biliary and gall bladder systems radiography- eg: cholecystography  Radiography of digestive system- barium meal , barium enema  Radiography of urinary system -IVP  Radiographic examintion of encapsulated joint- myelography, hysterosalpingography  CT scan, MRI scan  Radio nucleide tests
  • 89. Endoscopic studies  It includes a variety of diagnostic techniques that involve inserting an endoscope through a natural or surgical incision into body cavities or organs  Majority are flexible fibre optic scopes that may be put into smaller body cavities and organs, however rigid also are used.  Eg:  Bronchoscopy- visualize bronchial tree and lungs  Cystoscopy- bladder  Laparascope – abdominal cavity  Colposcopy- vaginal and cervix  Arthroscopy – joints etc,…