After reading this lesson, you will be able to :



Similar documents
Laboratory No. 3 General Stool Examination (GSE) Collection of samples

Urinalysis and Body Fluids CRg

STAINING OF PBF AND INTERPRETATION OF NORMAL AND ABNORMAL RED CELL MORPHOLOGY

Chapter 14 Urinalysis, Body Fluids and Other Specimens. Objectives:

Preparation of frequently used solutions

Chem 100 Lab Experiment #9 - ACID/BASE INDICATORS

MODIFIED TRICHROME STAIN

Experiment #10: Liquids, Liquid Mixtures and Solutions

Chapter. Guaiac Screening CHAPTER 4: GUAIAC TESTING SCREENING FOR OCCULT BLOOD. Page 1 of 5 Guaiac doc 6/24/2005

1 of 8 5/10/ :47 AM

LABORATORY 3: Microscopic Urinalysis

Chapter 16: Tests for ions and gases

Mixtures and Pure Substances

Comparing Plant and Animal Cells

Cocaine extraction from Coca Leaves

Chemical Processes of Digestion

Organic Chemistry Lab Experiment 4 Preparation and Properties of Soap

Gastrointestinal Bleeding

Cell Biology Prokaryotic and eukaryotic cells

EXTRACTION OF DNA FROM CALF THYMUS CELLS Revised 2/1/96 Introduction

Experiment 12- Classification of Matter Experiment

Diarrhea National Digestive Diseases Information Clearinghouse

4.0 EXPERIMENT ON DETERMINATION OF CHLORIDES

6 Body Fluid Stains and Standards

Crime Scene Unit Presumptive Testing Procedures. Evidence Collection Division

LZV585 (B) The 1-cm path is aligned with the arrow on the adapter

Physical and Chemical Properties and Changes

GIEMSA STAIN PREANALYTICAL CONSIDERATIONS

Methods of sampling and visualisation fingerprints Identification of blood stains

I. ACID-BASE NEUTRALIZATION, TITRATION

RESTRICTION ENZYME ANALYSIS OF DNA

Lab 7 Soil ph and Salinity OBJECTIVE INTRODUCTION Soil ph active

Microscopy and Cellular Morphology

Preparation of Blood Films

OneStep Fecal Occult Blood RapiDip InstaTest. Cat #

Workshop December, 2014

AURAMINE O STAIN. Preanalytical Considerations

Lab Exercise 3: Media, incubation, and aseptic technique

Care and Use of the Compound Microscope

Lynne S. Garcia MS, MT(ASCP), CLS(NCA), BLM(AAB), F(AAM) ti. Diagnostic Medical Parasitology. FAQ s

Cholera Prevention and Control: Introduction and Community Engagement. Module 1

Biology. STANDARD II: Objective 3. Osmosis Inquiry Labs

The most common active ingredient used in deodorants is aluminium chlorohydrate. But not all deodorants contain aluminium chlorohydrate:

The Medical Laboratory Licensing Regulations, 1995

Chapter 48. Nutrients in Food. Carbohydrates, Proteins, and Lipids. Carbohydrates, Proteins, and Lipids, continued

Estimation of Alcohol Content in Wine by Dichromate Oxidation followed by Redox Titration

Absorption and Transport of Nutrients

PREPARATION AND PROPERTIES OF A SOAP

BD Affirm VPIII. Microbial Identification System

CONTROL: An infected appendix, or any tissue containing both negative and positive gram rods.

National Digestive Diseases Information Clearinghouse

6 Characterization of Casein and Bovine Serum Albumin

Titanium Dioxide Raspberry Solar Cell 2012, 2011, 2005 by David A Katz. All rights reserved

Lab #13: Qualitative Analysis of Cations and Anions

TOTAL PROTEIN FIBRINOGEN

Microscope Lab Introduction to the Microscope Lab Activity

Guidance Document Infectious Substances

Factors Affecting Enzyme Activity

Urinalysis and Body Fluids CRg. Chemical Exam of Urine - bilirubin. Chemical Exam of Urine - bilirubin. Unit 3. Chemical Examination of Urine

Use of the Microscope and Cytology

2 MATTER. 2.1 Physical and Chemical Properties and Changes

Luminol Test PROCESS SKILLS SCIENCE TOPICS VOCABULARY

CHAPTER 3 OBSERVING MICROORGANISMS THROUGH A MICROSCOPE. I. UNITS OF MEASUREMENT - See Table 3.1 in text. + Fig. 3.2

A Fishy Tale. Observing the Circulatory System of a Goldfish with a Compound Light Microscope

RBS detergents for laboratories

Petri Dish Electrolysis Electrolysis Reactions

APPENDIX A GUIDANCE DOCUMENT

Chlorine, Total. DPD Method 1 Method to 5.00 mg/l Cl 2 Test 'N Tube Vials. Test preparation. Instrument-specific information

MICROSCOPY OF LIVING MICROBES

RECITATION NOTES FOR EXPERIMENT # 5 A&B THIN LAYER CHROMATOGRAPHY

Making Biodiesel from Virgin Vegetable Oil: Teacher Manual

JUNIOR COLLEGE CHEMISTRY DEPARTMENT EXPERIMENT 21 SECOND YEAR PRACTICAL. Name: Group: Date: THE CHEMISTRY OF COPPER AND IRON

ISOLATION OF CAFFEINE FROM TEA

Stains for Developing TLC Plates

MUCICARMINE STAIN - SOUTHGATE S - MUCIN PURPOSE:

Enteric Unknowns Miramar College Biology 205 Microbiology

Investigating What's In Soil

DNA SPOOLING 1 ISOLATION OF DNA FROM ONION

STEP-BY-STEP INSTRUCTIONS FOR INVESTIGATIONAL USE. Rapid HCV Antibody Test FOR ORAQUICK RAPID HCV ANTIBODY TEST

A little information goes a long way

UltraClean Soil DNA Isolation Kit

PHYSICAL SEPARATION TECHNIQUES. Introduction

Keeping Your Swimming Pool and Spa Healthy Environmental Health Guide

INTRODUCTION. Such chemical substances which are added to food materials to prevent their spoilage are known as chemical preservatives.

Troubleshooting: How to remove unknown stains from nora rubber floorings.

Enzyme Pre-Lab. Using the Enzyme worksheet and Enzyme lab handout answer the Pre-Lab questions the pre-lab must be complete before beginning the lab.

Practical Lesson No 4 TITRATIONS

Vesico-Vaginal Fistula

THE DIGESTIVE SYSTEM

TEACHER ACTIVITY GUIDE

Santa Monica College Chemistry 11

Name Class Date Laboratory Investigation 4B Chapter 4: Cell Structure

Colorectal Cancer: Preventable, Beatable, Treatable. American Cancer Society

Diffusion, Osmosis, and Membrane Transport

ACID-BASE TITRATIONS: DETERMINATION OF CARBONATE BY TITRATION WITH HYDROCHLORIC ACID BACKGROUND

Maintaining Proper Bowel Elimination

COMMON LABORATORY APPARATUS

Discovering cells. The fi rst drawing of cells

CHM 130LL: ph, Buffers, and Indicators

Transcription:

MODULE Stool Examination 50 STOOL EXAMINATION 50.1 INTRODUCTION Stool examination is carried out in laboratories for various diagnostic purposes. It is a specimen which is easily obtained but, they may however be a reluctance on the part of the patient to give the stool specimen due to its offensive nature and foul smell. Mostly a clean container which does not contain any detergent or disinfectant is sufficient for all types of stool examinations including stool culture. OBJECTIVES After reading this lesson, you will be able to : explain physical examination of stool describe microscopic examination of stool explain the chemical examination of stool describe the preservation of stool 50.2 PHYSICAL EXAMINATION OF STOOL The following aspects of stool should be examined (a) Quantity: In intestinal amoebiasis the stools tend to be voluminous. Whereas in bacillary dysentery due to Shigella the stools are scanty in quantity (b) Consistency and form: Normal stools are well formed. In diarrhea and dysentery the stools are semi solid or watery in nature. In malabsorpton 434

Stool Examination states also the stool will be semi solid or watery depending on the severity of the disease. In cases of malabsorption of fats the stools are pale bulky and semi solid. MODULE (c) Colour: Normal stools are light to dark brown in colour due to the presence of stercobilinogen which is a product of bilirubin metabolism. In cases with bleeding into the intestinal tract the stools become dark tarry in nature due to the formation of acid hematin if the bleeding is in the small intestines. In the bleeding in large intestines or rectum the blood may be bright red. In cholera the stools have a rice water appearance as there is no fecal matter and there is presence of flakes of epithelial cells in it. In biliary tract obstruction the stools may be clay coloured due to absence of stercobilinogen. Pateints diet may also lead to alteration in the colour of the stools. For instance if the patient had spinach earlier the stools may be green in colour. In those who had a barium examination the stools may be white in colour. (d) Odour: The fecal odour of stools may become offensive in conditions like intestinal amoebiasis. In cases of bacillary dysentery and cholera the stools are not foul smelling due to the absence of fecal matter. (e) (f) Blood: Blood should be noted in stools if present as it is indicative of ulceration or presence of any other pathology like malignancy. It should also be noted if the blood is bright red or is altered in colour as it may be a clue to the site of pathology in the intestinal tract. Mucus: Mucus is present in certain conditions like amoebic or bacillary dysentery. (g) Parasite: Stools may contain adult helminthes. Nematodes like ascaris are easily visible as their size is large. Hook worms and proglotids of cetodes may also be present. These may be visible to the naked eye. 50.3 MICROSCOPIC EXAMINATION The laboratory diagnosis of most parasitic infections is by the demonstration of ova of the parasite in the stools of the infected person. The stool is collected in a clean container. The stool can be examined by the following techniques. (a) Wet mount examination (b) Iodine preparation 435

MODULE Stool Examination (c) Buffered methylene blue stain: (Nuclear stain in E histolytica) (d) Cellophane tape test:- NIH swab (e) Concentration techniques (a) Saline wet mount examination: The stool is emulsified in normal saline and a large drop is placed on a glass slide and is then covered with a cover slip. This is then examined under a light microscope. It is preferable to keep the condenser down and the intensity of the light low for proper visualization of the ova and cysts. The thickness of the film should be such that one is able to see the printed letters of the newspaper through it. (b) Iodine Preparation: Iodine preparation leads to better visualization of morphological details of ova and cysts as it stains the glycogen in them. It however has the disadvantage that the live trophozoites of Entamoeba histolytica cannot be seen as the iodine kills it. One gram of iodine and two gram of potassium iodide is mixed in 100 ml of distilled water Poassium iodide is mixed in water and then the iodine crystals are added and it is shaken vigorously.. The solution is then filtered into a dark glass bottle and kept away from light. (c) Buffered methylene blue stain: It is used for the Nuclear stain in E histolytica (d) Cellophane tape test: NIH swab (National Institute of Health) is used to pick up the ova of Entrobius vermicularis from the peri -anal area. (e) Concentration methods: Two types of concentration techniques are used for stool examination (i) Sedimentation (ii) Floatation (i) Sedimentation technique Formol ether technique Formol ether SAF Formol ether PVA (ii) Floatation technique Zinc sulfate Saturated salt solution A small amount of stools are emulsified in saturated salt solution in a wide mouth container. When the stool becomes homogenous a few drops of saturated saline 436

Stool Examination are mixed and more saturated saline solution is added. A glass slide is placed across the receptacle in such a way that the slide is in contact with the surface of the saturated solution. If the fluid is not in touch with the slide then more saturated saline should be added till the fluid level touches the slide. The slide is then left in place for fifteen minutes. After this the slide is gently lifted off the container and turned upside down carefully ensuring no fluid from the slide is spilled. A cover slip is placed over the fluid on the slide. And it is examined under a microscope. MODULE Principle of floatation technique: The specific gravity of ova and cysts is less and thus will float to the top of the saturated salt solution where it will stick to the under surface of the glass slide. 50.4 CHEMICAL EXAMINATION OF STOOL (a) ph: This ph of stools is acidic in amoebic dysentery and is alkaline in bacillary dysentery. (b) Occult blood: Occult blood may be present in a number of diseases including malignancy of the gastrointestinal tract. The reagent used is benzidine powder. A pinch of benzidine powder is taken in a test tube and acidified with 1-2 drops of glacial acetic acid and is mixed well in it. To this is added 1ml of hydrogen peroxide which is again mixed well. Then place a clean glass slide and place a small quantity of stool on it. Place 1-2 drops of the benzidine mixture prepared earlier on the stool specimen taken on the glass slide and observe for a change of colour. Development of green to blue colour is indicative of presence of occult blood in the stool specimen. 50.5 PRESERVATION OF STOOL The stool samples containing the ova and cysts of parasites can be preserved by using one of the following methods 10% formol saline Buffered formol saline Merthiolate-iodine formalin Sodium acetate-acetic acid formalin(saf) Polyvinyl alcohol (PVA) Schauddins preservative 437

MODULE Stool Examination Fig. 50.1: Morphology of some common helminthic ova Fig. 50.2: Common helminth ova 438

Stool Examination MODULE INTEXT QUESTION 50.1 1.... stain is used for nuclear stain in E.histolytica 2.... swab is used in cellophane tape test 3. Cellophance test is used to identify... 4. Two concentration techniques for stool examination are... &... WHAT HAVE YOU LEARNT Stool examination is carried out in laboratories for various diagnostic purposes A clean container which does not contain any detergent or disinfectant is sufficient for all types of stool examinations including stool culture Physical Examination of the stool for the following aspects of stool should be examined for its Quantity, Consistency and form, Colour, Odour, Blood, Mucus, Parasite The laboratory diagnosis of most parasitic infections is by the demonstration of ova of the parasite in the stools of the infected person. The stool can be examined by the following techniques namely Wet mount examination, Iodine preparation, Buffered methylene blue stain, Cellophane tape test:- NIH swab and Concentration techniques TERMINAL QUESTIONS 1. Describe the techniques used for examination of stool 2. Describe the concentration method of stool examination ANSWERS TO INTEXT QUESTIONS 50.1 1. Buffered methylene blue 2. NIH 3. Entrobius vermicularis 4. Sedimentation & Floatation 439