The document provides guidelines for analyzing stool samples in a laboratory setting. Key steps include collecting the sample in a clean cup, examining a thin smear of the stool under the microscope using 10x and 40x lenses, and noting any observations of mucus, pus, blood cells, parasites, or other abnormal findings. The results are interpreted to help diagnose common gastrointestinal issues or parasites present in the stool. Multiple samples over several days may be needed to rule out the presence of parasites if not seen on initial examination.
Stool Examination Abridged What A Medical Graduate Should KnowDr. Varughese George
The document provides information on stool examination for medical graduates. It discusses the advantages of stool examination in investigating gastrointestinal diseases such as detecting parasites, evaluating chronic diarrhea, dysentery, and identifying causative bacteria. It describes the collection and macroscopic examination of stool samples and preparation of slides for microscopic examination. The microscopic examination may reveal leukocytes, red blood cells, fat, meat fibers, and ova/cysts/trophozoites of parasites. Concentration techniques like sedimentation and floatation are used if parasites are present in low numbers. Common parasites like Entamoeba histolytica and Giardia intestinalis are also described.
Fecal or stool tests examine human feces to check for various indicators of health conditions. Feces should be collected in a clean, dry container without contamination from urine or other substances. Macroscopic examination of feces considers characteristics like color, odor, blood, mucus, and consistency. Tests on feces can check for blood, which may indicate issues in the upper intestinal tract, and fats, to detect malabsorption. Parasite examination looks for worms or their eggs. Liver function tests evaluate enzymes and proteins that provide information about hepatic function by examining levels in urine and stool. Radioiodine uptake tests also use stool samples to check thyroid function.
Stool/feces is the end product of digestive system of the body. Following digestion and absorption of the essential food ingredients in the stomach and intestine, the undigested food and unabsorbed secretions of stomach, liver, pancreas and intestine appear in stool.
This document provides an overview of stool analysis procedures, including:
- Specimen collection guidelines such as using leak-proof containers and avoiding refrigeration.
- Macroscopic examination of stool color, consistency, and presence of blood or mucus.
- Wet preparation techniques like saline and lugol's iodine slides.
- Concentration methods like formol-ether and flotation that recover parasites.
- Microscopic examination of samples for parasites, eggs, cysts, and trophozoites using 10x and 40x objectives.
I am working as a pathologist at the department of clinical pathology, Mandalay General Hospital, Mandalay Division, Myanmar.
Dr San Yu Maung (M.B.B.S.) (M.Med.Sc.) (Pathology)
A basic and worth information for diagnostic is urine microscopy. ideally it should be by the physician at his clinic to add and correlate diagnosis promptly. this will make physician confident in dealing with patients. it also help in follow up the consequences in some important glomerulopathies.
Stool analysis is a series of tests on a stool sample that can diagnose diseases of the digestive system such as infections, poor nutrient absorption, or cancer. It involves microscopic examination of the stool sample to check for things like blood, parasites, meat fibers, and leukocytes. There are also techniques like sedimentation and flotation to concentrate any parasites in the sample. In addition to microscopic examination, gross visual inspection of the stool and certain chemical analyses can provide diagnostic information. Stool analysis is useful for identifying digestive infections, pancreas and liver disorders, and screening for conditions like colon cancer.
Stool Examination Abridged What A Medical Graduate Should KnowDr. Varughese George
The document provides information on stool examination for medical graduates. It discusses the advantages of stool examination in investigating gastrointestinal diseases such as detecting parasites, evaluating chronic diarrhea, dysentery, and identifying causative bacteria. It describes the collection and macroscopic examination of stool samples and preparation of slides for microscopic examination. The microscopic examination may reveal leukocytes, red blood cells, fat, meat fibers, and ova/cysts/trophozoites of parasites. Concentration techniques like sedimentation and floatation are used if parasites are present in low numbers. Common parasites like Entamoeba histolytica and Giardia intestinalis are also described.
Fecal or stool tests examine human feces to check for various indicators of health conditions. Feces should be collected in a clean, dry container without contamination from urine or other substances. Macroscopic examination of feces considers characteristics like color, odor, blood, mucus, and consistency. Tests on feces can check for blood, which may indicate issues in the upper intestinal tract, and fats, to detect malabsorption. Parasite examination looks for worms or their eggs. Liver function tests evaluate enzymes and proteins that provide information about hepatic function by examining levels in urine and stool. Radioiodine uptake tests also use stool samples to check thyroid function.
Stool/feces is the end product of digestive system of the body. Following digestion and absorption of the essential food ingredients in the stomach and intestine, the undigested food and unabsorbed secretions of stomach, liver, pancreas and intestine appear in stool.
This document provides an overview of stool analysis procedures, including:
- Specimen collection guidelines such as using leak-proof containers and avoiding refrigeration.
- Macroscopic examination of stool color, consistency, and presence of blood or mucus.
- Wet preparation techniques like saline and lugol's iodine slides.
- Concentration methods like formol-ether and flotation that recover parasites.
- Microscopic examination of samples for parasites, eggs, cysts, and trophozoites using 10x and 40x objectives.
I am working as a pathologist at the department of clinical pathology, Mandalay General Hospital, Mandalay Division, Myanmar.
Dr San Yu Maung (M.B.B.S.) (M.Med.Sc.) (Pathology)
A basic and worth information for diagnostic is urine microscopy. ideally it should be by the physician at his clinic to add and correlate diagnosis promptly. this will make physician confident in dealing with patients. it also help in follow up the consequences in some important glomerulopathies.
Stool analysis is a series of tests on a stool sample that can diagnose diseases of the digestive system such as infections, poor nutrient absorption, or cancer. It involves microscopic examination of the stool sample to check for things like blood, parasites, meat fibers, and leukocytes. There are also techniques like sedimentation and flotation to concentrate any parasites in the sample. In addition to microscopic examination, gross visual inspection of the stool and certain chemical analyses can provide diagnostic information. Stool analysis is useful for identifying digestive infections, pancreas and liver disorders, and screening for conditions like colon cancer.
This document discusses cytology of the urinary tract. It describes three methods for collecting urine specimens: voided urine, catheter specimens, and bladder washings. Voided urine is the simplest but cells may degrade over time. Catheter specimens avoid contamination but can damage cells. Bladder washings provide high cellularity and preservation through saline irrigation. Specimens can be prepared via several methods including cytocentrifugation and direct smears. Normal urinary tract cytology shows a range of superficial and deep urothelial cell morphologies depending on collection method and location in the tract.
Urine analysis involves physical and chemical tests performed on urine to evaluate health and diagnose diseases. Key aspects of urine analysis include examining the urine's volume, color, odor, pH, specific gravity, and testing for proteins, glucose, ketones, blood, and other substances. Abnormal results can indicate issues with the kidneys, urinary tract, or other systemic diseases like diabetes. Common tests include those for glucose, proteins, ketones, and specific gravity which provide important health information.
This document provides information about evaluating semen quality through various tests and examinations. It describes how to collect and transport semen samples, the normal characteristics of semen, and different abnormalities that can be detected through physical, microscopic, biochemical and other analyses of semen samples. The goal of semen analysis is to assess male fertility and detect any issues that may be causing infertility.
This document discusses the process of decalcification, which is the removal of calcium salts from bones and calcified tissues. There are four main methods: 1) using simple dilute mineral acids like nitric acid or formic acid; 2) ion exchange resins with acid fluids; 3) electrolytic decalcification using electrodes; and 4) chelating agents like EDTA that bind calcium ions. The document provides details on procedures and advantages/disadvantages of each method.
Semen is a “ thick, viscous, creamy, slightly yellowish or grayish” substance made up of spermatozoa — commonly known as sperm — and a fluid called seminal plasma, secret from the male reproductive organs.
The function of seminal plasma are:
To provide motility to sperm
To provide nutrition to spermatozoa
The document provides information on cerebrospinal fluid (CSF) examination including indications, collection, analysis, and findings in different conditions like meningitis. It discusses three clinical cases. For case 1, the diagnosis is bacterial meningitis based on cloudy CSF, low glucose, and high neutrophil count. Further tests would include cultures and sensitivity. For case 2, the diagnosis is viral meningitis (measles) based on clear CSF, normal glucose, and lymphocytic pleocytosis; complications include encephalitis. For case 3, the diagnosis is tuberculous meningitis based on low glucose, low chloride, and lymphocytic pleocytosis; confirmation requires microbiological tests.
This document summarizes the key equipment and processes used in histotechnology laboratories. It describes the main steps of processing tissue samples, which include preparation, processing, sectioning, staining, and mounting. The major laboratory equipment are then outlined, such as tissue processors, embedding centers, microtomes, slide warmers, coverslippers, and microscopes. Key safety procedures are also reviewed, such as proper handling of hazardous chemicals and sharp instruments, use of personal protective equipment, and emergency equipment.
This document provides details on microscopic examination of urine sediment. Key points include:
- Urine sample collection and preparation for examination under microscope by centrifuging and examining the sediment.
- Classification of findings as organised or unorganised substances, and types of cells, casts, crystals and other formed elements that may be observed.
- Significance of various normal and abnormal findings in identifying renal and other diseases. Detailed morphology of different cell types, casts, crystals and other structures are described.
This document summarizes guidelines for examining various body fluids, including cerebrospinal fluid, pleural fluid, peritoneal fluid, and semen. For cerebrospinal fluid, normal volumes and cell counts are provided. Guidelines are given for collection into tubes and microscopic examination, including normal cell differentials. Similar information is provided for examining pleural fluid, peritoneal fluid, and semen, including gross appearance, cell counts, differentials, and factors that affect analysis.
Basics of laboratory internal quality control, Ola Elgaddar, 2012Ola Elgaddar
Total Quality Management (TQM) is a continuous approach to improve quality and performance. It requires integrating quality functions throughout an organization with involvement from management, employees, suppliers, and customers. For medical laboratories, quality control has three main stages - pre-analytical, analytical, and post-analytical. Analytical quality control involves internal quality control (IQC) using control materials and external quality assessment (EQA) to monitor quality and compare results between laboratories. IQC follows procedures like plotting daily control results on Levey-Jennings charts and evaluating them using Westgard rules to detect errors.
This document provides information on staining blood films and smears. It discusses the different types of stains used including Romanowsky stains like Leishman stain, Giemsa stain, Wright stain, and Field stain. Specimens should be collected in EDTA and smears prepared within an hour then fixed in methanol or ethanol to preserve cell morphology before staining. Romanowsky stains use methylene blue and eosin dyes to reveal subtle differences in cell structures and components.
Enterobacteriacea ii biochemical reaction 2بكتريا عملي في رحاب الله
This document provides information on biochemical reactions of the Enterobacteriaceae family of bacteria. It discusses that members of Enterobacteriaceae are gram-negative rods that ferment glucose with acid production and reduce nitrates. It describes several selective media used to isolate and distinguish lactose fermenters from non-fermenters, including MacConkey agar which produces pink colonies for fermenters and colorless for non-fermenters. Biochemical tests like TSI, lysine iron agar, and oxidase are also summarized to differentiate bacterial species within the Enterobacteriaceae family.
diagnostic Cytology introduction , Body fluids cytologyAayra
This document discusses diagnostic cytopathology. It covers:
1. Cytopathology examines cells from body cavities, mucosal surfaces, and organs/masses obtained via needle aspiration to determine the cause of disease microscopically.
2. The history of cytopathology including the contributions of Papanicolaou and Koss.
3. The advantages of cytopathology include rapid diagnosis, low cost, ability to sample without tissue injury, and ability to repeatedly sample. Disadvantages include inability to always determine tumor type or distinguish pre-invasive from invasive changes.
4. Types of cytopathology include exfoliative from spontaneously shed cells, abrasive which dislodges
This document provides an overview of stool examination. It defines stool and describes its normal composition as 3/4 water and 1/4 solid matter. It outlines precautions for stool collection such as avoiding certain foods/medications prior. Collection details like using a clean container and preserving samples are provided. The types of examination covered are physical, chemical, and microscopic. Physical examines properties like color, consistency, and contents. Chemical analyzes pH, fats, nitrogen, and occult blood. Microscopic looks for parasites, bacteria, epithelial cells, and other components under stained and unstained preparations with concentration techniques.
This document discusses procedures for semen analysis, which is the first test performed to investigate male infertility. It describes how semen is examined physically, microscopically, chemically, and through immunological and microbiological assays. Tests evaluate semen volume, pH, motility, count, morphology, and the presence of fructose or acid phosphatase. Additional sperm function tests and cryopreservation are discussed. Semen donation is also summarized as a procedure to help individuals conceive.
Routine stool examination provides important information about gastrointestinal health and disease. A stool sample is examined macroscopically for characteristics like color, consistency, and presence of blood or mucus. Microscopic examination looks for items like white blood cells, red blood cells, parasites, fat, and bacteria. Chemical tests can detect occult blood, excess fat, sugars, and other markers. Proper collection and preservation of stool samples is important for accurate examination and detection of parasites. Both wet mount microscopy and concentration techniques may be used depending on the suspected condition. Stool examination aids in diagnosis of gastrointestinal infections, inflammation, malignancy, and malabsorption disorders.
This document summarizes serum iron estimation and total iron binding capacity (TIBC) tests. Serum iron measures the amount of iron in the blood serum, revealing low or high iron levels which can cause health issues. TIBC gauges how much iron is in the bloodstream, indicating deficiencies or excesses. Both tests help diagnose anemias and other iron-related conditions by checking iron and iron-carrying protein levels compared to normal ranges. Abnormal results can be caused by liver or blood disorders, genetic conditions, medications, or frequent transfusions.
This document discusses stool examination, including the composition of stool, collection and examination of stool samples, and various macroscopic, chemical, and microscopic tests that can be performed on stool samples. It provides details on normal findings and what various abnormalities may indicate. The tests described allow examination of stool volume, color, consistency, odor, presence of blood or mucus, pH, fat, nitrogen, and occult blood levels. Microscopic evaluation includes wet mount preparations, staining, and concentration methods to detect parasites, eggs, cysts, trophozoites, and other elements.
Intrauterine insemination (IUI) is a fertility treatment that involves placing sperm inside a woman’s uterus to facilitate fertilisation. The goal of IUI is to increase the number of sperm that reach the fallopian tubes and subsequently increase the chance of fertilisation.
This document provides information about performing a semen analysis, including definitions of key terms, procedures, and normal ranges. It discusses:
1. The components and normal appearance of semen after liquefaction.
2. Procedures for assessing semen volume, viscosity, pH, sperm motility, morphology, concentration, and vitality under a microscope.
3. Factors that can affect the results, such as abstinence time, sample handling, and medical conditions.
The document is intended as a reference for medical professionals performing semen analyses to evaluate male fertility and identify potential issues.
This document discusses cytology of the urinary tract. It describes three methods for collecting urine specimens: voided urine, catheter specimens, and bladder washings. Voided urine is the simplest but cells may degrade over time. Catheter specimens avoid contamination but can damage cells. Bladder washings provide high cellularity and preservation through saline irrigation. Specimens can be prepared via several methods including cytocentrifugation and direct smears. Normal urinary tract cytology shows a range of superficial and deep urothelial cell morphologies depending on collection method and location in the tract.
Urine analysis involves physical and chemical tests performed on urine to evaluate health and diagnose diseases. Key aspects of urine analysis include examining the urine's volume, color, odor, pH, specific gravity, and testing for proteins, glucose, ketones, blood, and other substances. Abnormal results can indicate issues with the kidneys, urinary tract, or other systemic diseases like diabetes. Common tests include those for glucose, proteins, ketones, and specific gravity which provide important health information.
This document provides information about evaluating semen quality through various tests and examinations. It describes how to collect and transport semen samples, the normal characteristics of semen, and different abnormalities that can be detected through physical, microscopic, biochemical and other analyses of semen samples. The goal of semen analysis is to assess male fertility and detect any issues that may be causing infertility.
This document discusses the process of decalcification, which is the removal of calcium salts from bones and calcified tissues. There are four main methods: 1) using simple dilute mineral acids like nitric acid or formic acid; 2) ion exchange resins with acid fluids; 3) electrolytic decalcification using electrodes; and 4) chelating agents like EDTA that bind calcium ions. The document provides details on procedures and advantages/disadvantages of each method.
Semen is a “ thick, viscous, creamy, slightly yellowish or grayish” substance made up of spermatozoa — commonly known as sperm — and a fluid called seminal plasma, secret from the male reproductive organs.
The function of seminal plasma are:
To provide motility to sperm
To provide nutrition to spermatozoa
The document provides information on cerebrospinal fluid (CSF) examination including indications, collection, analysis, and findings in different conditions like meningitis. It discusses three clinical cases. For case 1, the diagnosis is bacterial meningitis based on cloudy CSF, low glucose, and high neutrophil count. Further tests would include cultures and sensitivity. For case 2, the diagnosis is viral meningitis (measles) based on clear CSF, normal glucose, and lymphocytic pleocytosis; complications include encephalitis. For case 3, the diagnosis is tuberculous meningitis based on low glucose, low chloride, and lymphocytic pleocytosis; confirmation requires microbiological tests.
This document summarizes the key equipment and processes used in histotechnology laboratories. It describes the main steps of processing tissue samples, which include preparation, processing, sectioning, staining, and mounting. The major laboratory equipment are then outlined, such as tissue processors, embedding centers, microtomes, slide warmers, coverslippers, and microscopes. Key safety procedures are also reviewed, such as proper handling of hazardous chemicals and sharp instruments, use of personal protective equipment, and emergency equipment.
This document provides details on microscopic examination of urine sediment. Key points include:
- Urine sample collection and preparation for examination under microscope by centrifuging and examining the sediment.
- Classification of findings as organised or unorganised substances, and types of cells, casts, crystals and other formed elements that may be observed.
- Significance of various normal and abnormal findings in identifying renal and other diseases. Detailed morphology of different cell types, casts, crystals and other structures are described.
This document summarizes guidelines for examining various body fluids, including cerebrospinal fluid, pleural fluid, peritoneal fluid, and semen. For cerebrospinal fluid, normal volumes and cell counts are provided. Guidelines are given for collection into tubes and microscopic examination, including normal cell differentials. Similar information is provided for examining pleural fluid, peritoneal fluid, and semen, including gross appearance, cell counts, differentials, and factors that affect analysis.
Basics of laboratory internal quality control, Ola Elgaddar, 2012Ola Elgaddar
Total Quality Management (TQM) is a continuous approach to improve quality and performance. It requires integrating quality functions throughout an organization with involvement from management, employees, suppliers, and customers. For medical laboratories, quality control has three main stages - pre-analytical, analytical, and post-analytical. Analytical quality control involves internal quality control (IQC) using control materials and external quality assessment (EQA) to monitor quality and compare results between laboratories. IQC follows procedures like plotting daily control results on Levey-Jennings charts and evaluating them using Westgard rules to detect errors.
This document provides information on staining blood films and smears. It discusses the different types of stains used including Romanowsky stains like Leishman stain, Giemsa stain, Wright stain, and Field stain. Specimens should be collected in EDTA and smears prepared within an hour then fixed in methanol or ethanol to preserve cell morphology before staining. Romanowsky stains use methylene blue and eosin dyes to reveal subtle differences in cell structures and components.
Enterobacteriacea ii biochemical reaction 2بكتريا عملي في رحاب الله
This document provides information on biochemical reactions of the Enterobacteriaceae family of bacteria. It discusses that members of Enterobacteriaceae are gram-negative rods that ferment glucose with acid production and reduce nitrates. It describes several selective media used to isolate and distinguish lactose fermenters from non-fermenters, including MacConkey agar which produces pink colonies for fermenters and colorless for non-fermenters. Biochemical tests like TSI, lysine iron agar, and oxidase are also summarized to differentiate bacterial species within the Enterobacteriaceae family.
diagnostic Cytology introduction , Body fluids cytologyAayra
This document discusses diagnostic cytopathology. It covers:
1. Cytopathology examines cells from body cavities, mucosal surfaces, and organs/masses obtained via needle aspiration to determine the cause of disease microscopically.
2. The history of cytopathology including the contributions of Papanicolaou and Koss.
3. The advantages of cytopathology include rapid diagnosis, low cost, ability to sample without tissue injury, and ability to repeatedly sample. Disadvantages include inability to always determine tumor type or distinguish pre-invasive from invasive changes.
4. Types of cytopathology include exfoliative from spontaneously shed cells, abrasive which dislodges
This document provides an overview of stool examination. It defines stool and describes its normal composition as 3/4 water and 1/4 solid matter. It outlines precautions for stool collection such as avoiding certain foods/medications prior. Collection details like using a clean container and preserving samples are provided. The types of examination covered are physical, chemical, and microscopic. Physical examines properties like color, consistency, and contents. Chemical analyzes pH, fats, nitrogen, and occult blood. Microscopic looks for parasites, bacteria, epithelial cells, and other components under stained and unstained preparations with concentration techniques.
This document discusses procedures for semen analysis, which is the first test performed to investigate male infertility. It describes how semen is examined physically, microscopically, chemically, and through immunological and microbiological assays. Tests evaluate semen volume, pH, motility, count, morphology, and the presence of fructose or acid phosphatase. Additional sperm function tests and cryopreservation are discussed. Semen donation is also summarized as a procedure to help individuals conceive.
Routine stool examination provides important information about gastrointestinal health and disease. A stool sample is examined macroscopically for characteristics like color, consistency, and presence of blood or mucus. Microscopic examination looks for items like white blood cells, red blood cells, parasites, fat, and bacteria. Chemical tests can detect occult blood, excess fat, sugars, and other markers. Proper collection and preservation of stool samples is important for accurate examination and detection of parasites. Both wet mount microscopy and concentration techniques may be used depending on the suspected condition. Stool examination aids in diagnosis of gastrointestinal infections, inflammation, malignancy, and malabsorption disorders.
This document summarizes serum iron estimation and total iron binding capacity (TIBC) tests. Serum iron measures the amount of iron in the blood serum, revealing low or high iron levels which can cause health issues. TIBC gauges how much iron is in the bloodstream, indicating deficiencies or excesses. Both tests help diagnose anemias and other iron-related conditions by checking iron and iron-carrying protein levels compared to normal ranges. Abnormal results can be caused by liver or blood disorders, genetic conditions, medications, or frequent transfusions.
This document discusses stool examination, including the composition of stool, collection and examination of stool samples, and various macroscopic, chemical, and microscopic tests that can be performed on stool samples. It provides details on normal findings and what various abnormalities may indicate. The tests described allow examination of stool volume, color, consistency, odor, presence of blood or mucus, pH, fat, nitrogen, and occult blood levels. Microscopic evaluation includes wet mount preparations, staining, and concentration methods to detect parasites, eggs, cysts, trophozoites, and other elements.
Intrauterine insemination (IUI) is a fertility treatment that involves placing sperm inside a woman’s uterus to facilitate fertilisation. The goal of IUI is to increase the number of sperm that reach the fallopian tubes and subsequently increase the chance of fertilisation.
This document provides information about performing a semen analysis, including definitions of key terms, procedures, and normal ranges. It discusses:
1. The components and normal appearance of semen after liquefaction.
2. Procedures for assessing semen volume, viscosity, pH, sperm motility, morphology, concentration, and vitality under a microscope.
3. Factors that can affect the results, such as abstinence time, sample handling, and medical conditions.
The document is intended as a reference for medical professionals performing semen analyses to evaluate male fertility and identify potential issues.
Tolerance to tissue and cell antigens can be
induced by injection of hemopoietic (stem)
cells in neonatal or severely
immunocompromised (by lethal irradiation
or drug treatment) animals.
Also, grafting of allogeneic bone marrow or
thymus in early life results in tolerance to
the donor type cells and tissues. Such
animals are known as chimeras. These
findings are of significant practical
application in bone marrow grafting
sperm assessment- traditional and novel approaches.pptxDeepekaTS
The latest WHO recommendations,2010 are based on semen parameters from approximately 2000 fertile men, from eight countries and three continents, whose partners achieved pregnancy within 12 months of unprotected sexual intercourse.
Pitfalls- huge shift in the lower reference values, one sided criteria.
Reference limits shouldn’t be over-interpreted
Interpret along with clinical history and physical examination.
This document describes procedures for examining fecal samples to detect parasite eggs under a microscope. Several methods are discussed, including direct smear, McMaster technique, simple floatation, and sedimentation. Using these methods on samples from sheep, cattle, and dogs, several parasite eggs were observed, including Ancylostoma caninum, Toxocara canis, Fasciola eggs, Trichuris eggs, and Dipylidium caninum eggs enclosed in a capsule. The document concludes that multiple examination methods are needed to thoroughly detect parasites at different infection levels in fecal samples.
This document describes culture methods for cultivating various protozoan parasites. It discusses the purposes of culturing parasites, including for diagnostic, research, and teaching purposes. It provides examples of parasite species that can be cultured, such as Entamoeba histolytica, Giardia lamblia, and Plasmodium spp. The document outlines different types of culture media, including xenic, polyxenic, monoxenic, and axenic cultures. It also describes specific culture media and methods used for cultivating intestinal protozoa like amoebae, as well as haematozoan parasites including Leishmania and trypanosomes.
This document provides information about performing a semen analysis. It discusses the structures involved in semen production, contributions to semen volume, indications for a semen analysis, how to collect a semen sample, and the various tests that can be done on a semen sample including physical examination, microscopic examination of sperm count, motility, viability and morphology, immunologic analysis for antisperm antibodies, biochemical analysis of fructose, and sperm function tests. A normal semen analysis provides important information for investigating male factor infertility while abnormal results can help identify potential causes of reduced fertility.
The document provides guidance on proper specimen collection and transport procedures. It discusses appropriate containers, labeling, storage, and handling of spillages. Specimen containers must be sealed securely and labeled with patient details. Storage should be in a refrigerator if delivery to the lab is delayed. Only clinically-indicated specimens should be collected to avoid inappropriate antibiotic prescribing. Proper collection methods are outlined for various sample types like urine, sputum, and feces.
This document discusses urine specimen collection and processing for microbiological examination. Urine is collected to detect disorders like urinary tract infections. Common microorganisms found in urine include E. coli, Proteus, and Candida species. Mid-stream clean-catch urine is the preferred specimen type. Urine is cultured on agar plates like CLED, blood, and MacConkey to isolate pathogens and test for lactose fermentation. Bacterial colonies are counted and used to interpret urine culture results. Isolated organisms are identified using biochemical tests and antibiotic sensitivity testing.
This document summarizes histological and cytological specimens. It describes tissue samples obtained from biopsies or autopsies that can be either histological (muscular) or cytological (liquid). Cytological specimens include bodily fluids like urine, cerebrospinal fluid, joint fluid, endoscopy samples, sputum, and other fluids. The procedures for processing and staining samples of each fluid type are provided. Semen is also discussed as a cytological specimen, including normal parameters for analysis and staining techniques.
Examination of feces is commonly used to diagnose parasitic infections as many parasites live in the intestinal tract. When collecting stool specimens, wide-mouthed leak-proof containers should be used and handled carefully to avoid infection. Multiple specimens collected on alternate days within 10 days are examined microscopically, looking for parasites like Entamoeba histolytica trophozoites and cysts, Giardia lamblia cysts, and eggs of worms such as Ascaris lumbricoides and Trichuris trichura under saline and iodine mounts. The morphology and features of common intestinal parasites can be observed with these microscopic examination techniques.
The document discusses investigations for male infertility. It lists various tests that may be conducted to evaluate male fertility including semen analysis, hormone levels, imaging tests, and genetic testing. Semen analysis is described as the primary test, examining parameters like volume, pH, sperm concentration, motility, morphology, and vitality. Abnormal results on semen analysis may indicate issues like low sperm count, poor motility, or abnormal morphology which could require further testing and treatment.
A semen analysis measures the amount and quality of semen and sperm. It is one of the first tests done to evaluate male fertility issues. It determines semen volume, sperm concentration, motility, morphology, pH, and presence of white blood cells or other abnormalities. The sample is collected through masturbation and analyzed under a microscope to measure these parameters. Normal ranges are defined by the WHO for factors like sperm concentration, motility, and morphology. Abnormal results can indicate issues that reduce fertility. The analysis provides important information about male reproductive health and ability to conceive.
A semen analysis measures the amount and quality of semen and sperm. It is one of the first tests done to evaluate male fertility issues. It determines semen volume, sperm concentration, motility, morphology, pH and presence of white blood cells or other abnormalities. The sample is collected through masturbation and analyzed under a microscope to measure these parameters. Normal ranges have been established by the WHO. Abnormal results could indicate issues that reduce fertility. The analysis provides important information about male reproductive health and ability to conceive.
The document provides information about andrology laboratory services for male infertility evaluation and treatment. It discusses:
- Tests offered including semen analysis, specialized tests of sperm function and morphology, sperm processing for infertility treatments, and cryopreservation.
- Procedures for semen sample collection, transport, and analysis following WHO standards, including macroscopic examination of volume, pH, and microscopic examination of motility, concentration, vitality, and morphology.
- Uses of semen analysis to diagnose infertility issues, identify treatment options, and assess effectiveness of treatments like vasectomy reversal. Computer-assisted semen analysis is also discussed.
This document discusses calf diarrhea, a major cause of economic loss in the cattle industry. It notes that infectious agents like viruses (rotavirus, coronavirus), bacteria (E. coli, Salmonella species, Clostridium perfringens), and protozoa (Eimeria, Cryptosporidium) are leading causes of neonatal calf diarrhea. Clinical signs can include anorexia, fever, depression, watery to bloody diarrhea. Diagnosis involves isolating and identifying the causal bacteria or virus through culturing fecal samples and performing biochemical tests. Management practices like ensuring adequate colostrum intake and hygiene can help prevent calf diarrhea.
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...Donc Test
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Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Promoting Wellbeing - Applied Social Psychology - Psychology SuperNotesPsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
5.
مثل الروتينى البراز تحليل فى تشخيصها يتم ال الهضمى الجهاز مشاكل معظم
:
o
العصبى القولون
o
القولون تقرحات
o
االنتفاخات
o
المعدة جرثومة
o
الهضم عسر
o
الطعام حساسية
o
المعوية النزالت
o
والبروسيلال التيفود
o
الجهاز سرطان
الهضمى
o
الدرقية الغدة امراض
o
المزمن االمساك
للمريض البراز نتيجة تفسير على مالحظات
73. Cells in stool mistaken for Giardia lamblia
Giardia lamblia cyst Yeast cells
Fungal spore
Iodine-stained cyst 40X
74. Blastocystis hominis
Size: 6-40 µm
no parasites are present
Kingdom:
Chromista
Clinical picture : asymptomatic or symptomatic
Written in the following condition:
Stool sample shows watery diarrhoea
many Blastocystis hominis are seen
75. Artifacts in stool mistaken for Ascaris Eggs
Ascaris egg 10X
Pollen grains 40X
Plant cell 10X
78. Air-born fungus
Plant parasites
attached to plant roots
Artifacts in stool mistaken for human parasites
Diatoms in
stool
Pollen grain
Plant parasite
(Heterodera)
79. Strongyloides larva
250 µ
Hairs of variable length
Iodine stained Unstained
Artifacts in stool mistaken for Strongyloides larva
84. Giardia lamblia cyst
E.histolytica
/ dispar cyst
Entamoeba histolytica
seen within mucus
Protozoa in stool seen by the High Power
E.coli cyst
Endolimax
nana cyst
12X7µ
15X8µ 25µ
12µ 15µ
30µ
iodine stained
E.histolytica/dispar
pre-cyst
Giardia lamblia trophozoites
89. 1- Direct smear:
1. Prepare slides for each sample and numbering them.
2. Put one drop of normal saline on the slide.
3. Take small amount of stool by using stick & mix well with
normal saline.
4. Cover the sample by “cover slip”.
5. Examine it under the microscopic power (5,10,40).
Procedure:
90. A- Sedimentation:
• Add 3 ml of normal saline in test tube & add on it small a mount of stool (2-3)g. Mix
well.
• Filter the mixture in other test tube by using funnel & gouse.
• Add 6 ml of (10% formalin) solution in test tube that contains the filtrate sample for 5
min so as fix the sample.
• Add 3ml of “ether” to dissolve the fat in the sample , then lock the tube with cover &
shake well to mix ether with the sample.
• Put the test tube in centrifuge (1000 u / m) for 1 min , then take the test tube from the
instrument.
“Note:” If 4 layer are formed in test tube your procedure is correct. Otherwise you must
repeat the same steps.
• After that gets red from all contents in tube by pouring the contents in special box.
• Take one drop from the sediment & examine it under the microscopic power(5,10,40)
Procedure:
2- concentration methods
91. B- Floatation:
• Take (2-3)g of stool sample & dissolve it in 8 ml of normal saline. Mix
well.
• Filter the contents by using funnel & gouse.
• Place the tube in centrifuge (1000 u / m) for 1 min.
• Gets red the decetate & add 7 ml of “ ZnSO4 ”.
• Put the tube in centrifuge for 1 min.
• Take one drop from the decetate & examine it under the microscopic
power (5,10,40).
2- concentration methods
Procedure:
92. Occult blood test:
1. Take small amount from stool sample.
2. Prepare thin smear of stool on filter paper.
3. Add 2 drops from dereloping solution (stabilized solution of hydrogen
peroxide & alcohol ) on filter paper.
4. Read the result (1-2) min.
5. If the color change to blue, the result is positive & if it's not change the
result is negative.
Introduction:
It's A test use to examine occult blood in stool in colon & rectum disease.
Procedure:
97. Routine stool analysis
Test Principle:
1- Naked eye examination of stool sample.
2- Microscopic examination of stool sample.
Clinical Significance:
Detection of parasitic infection.
98. Before Analysis
Stool sample is better provided in the lab.
Stool samples must be examined
within 1 hour.
Parasites as
Stool sample contaminated with urine is refused
Giardia lamblia trophozoites
Entamoeba histolytica trophozoites
rapidly disintegrate at room temperature
Trichomonas hominis trophozoites
commonly mistaken
99. Inspect by the naked eye for :
Steps of analysis
1- Colour of stool sample:
Brown
Greenish
Reddish
normal
Much green vegetables eaten
Giardia infection
Bleeding or due to some drugs
Light brown Undigested fat
Black Occult blood or due to some drugs
100. Steps of analysis (continued)
Undigested food (Nil, +, ++, +++)
Mucus especially when mucus is tinged with blood
Worms (Enterobius, Ascaris, Taenia segments)
Blood (may be due to piles or anal fissure)
3- Inspect for the presence of:
2- Assess the pH of diarrhoeic stool specimen using
litmus paper. Normally it is alkaline.
It turns acidic e.g. in Entamoeba histolytica infection.
101. Worms Recovered In Stool
Ascaris lumbricoides
Cylindrical worm
about 20 cm long
Taenia worm
Ribbon-like
several meters long
Enterobius
vermicularis
cylindrical worm
about 10 mm long
Single segments
creep out of anus
102. Artifacts in stool mistaken for worms
Citrus particles
Tomato skin
Earthworm
Bean sprouts
Aquatic larvae
of arthropods
Mucus casts
103. Loose or watery stool samples & mucoid samples
should be examined by direct smear method
e.g. Entamoeba trophozoite
Drop of
iodine
- Iodine stained (10% in distilled water)
Formed, semi-formed, soft stool samples should be
examined after concentration by sedimentation method
Steps of analysis (continued)
104. Concentration of Faecal Samples by Sedimentation
10%
formal
saline
Stool
sample
Wooden
rod
Ethyl acetate
Stool
sediment
Supernatant
Fat
10% iodine
Centrifugation for 10 min at 3000 RPM
Slide
105. Microscopic examination
• Digestion:
Vegetable cells
Starch
Muscle fibres
Fat
• Cytology:
• Pus cells / H.P.F.
• RBCs / H.P.F.
• Epithelial cells.
• Yeast cells
• Parasites:
• Helminths (eggs, larvae)
• Protozoa (trophozoite, cyst)
Screening by
Low Power
Different shapes of
vegetable cells
Fat droplets
Don’t write many bacteria in stool
analysis report
Muscle fibres
Starch
106. After Analysis
If pus cells (more than 10 / H.P.F. or with clumps) and no
parasite is seen during examination:
- Recommend for stool culture
For watery stool samples showing no parasites:
- Recommend test for Cryptosporidium in stool
- Recommend test for Rota virus in stool
For samples provided to the lab write the following comment:
The sample was provided to the lab
The person who performed the analysis must write his
name at the end of the report.
Done samples are kept for 24 hours before discarding.
In children
between 2-5
years
- Recommend test for Cryptosporidium only
in stool
In adults
113. Artifacts in stool mistaken for Enterobius eggs
Morel Mushroom
spore Enterobius eggs
unstained
Iodine
stained
114. Air-born fungus
Plant parasites
attached to plant roots
Artifacts in stool mistaken for human parasites
Diatoms in
stool
Pollen grain
Plant parasite
(Heterodera)
115. Strongyloides larva
250 µ
Hairs of variable length
Iodine stained Unstained
Artifacts in stool mistaken for Strongyloides larva
116. Giardia lamblia cyst
E.histolytica
/ dispar cyst
Entamoeba histolytica
seen within mucus
Protozoa in stool seen by the High Power
E.coli cyst
Endolimax
nana cyst
12X7µ
15X8µ 25µ
12µ 15µ
30µ
iodine stained
E.histolytica/dispar
pre-cyst
Giardia lamblia trophozoites
117. Cells in stool mistaken for Giardia lamblia
Giardia lamblia cyst Yeast cells
Fungal spore
Iodine-stained cyst 40X
118. Blastocystis hominis
Size: 6-40 µm
no parasites are present
Kingdom:
Chromista
Clinical picture : asymptomatic or symptomatic
Written in the following condition:
Stool sample shows watery diarrhoea
many Blastocystis hominis are seen