This document discusses the laboratory investigation of transfusion reactions. It begins by defining transfusion and transfusion reactions. It then outlines the initial measures taken before investigation, including maintaining IV saline and notifying physicians. The main laboratory investigations include clerical checks to identify errors, visual checks of plasma for hemolysis, and serology checks including ABO testing and direct antiglobulin testing on pre-and post-transfusion samples. If these preliminary tests have positive results, additional tests like grouping, antibody screening and crossmatching are repeated from before transfusion.
I have listed out the LE cells structure and Microscopical examinaton of LE CELLS, Difference between tart cells and le cells, clinical symptoms and diagnostic procedure.
I have listed out the LE cells structure and Microscopical examinaton of LE CELLS, Difference between tart cells and le cells, clinical symptoms and diagnostic procedure.
Describes the mission of laboratory services, the phases of performing laboratory tests, factors affecting laboratory tests and strorage and transport of laboratory samples
Describes the mission of laboratory services, the phases of performing laboratory tests, factors affecting laboratory tests and strorage and transport of laboratory samples
Lab Tests are tools that provide information about the client.
Tests may be used for basic screening as part of a wellness check.
Frequently tests are used to help confirm a diagnosis, monitor an illness, and provide valuable information about the client’s response to treatment.
Lecture By:
Dr Hisham Fakher
Consultant Hematology
Medical Director of Regional Laboratory and Central Blood Bank
Ministry of Health –Almadinah Almonawarah
The Compatibility can be determined by matching the different blood group systems, such as ABO and Rh system, and/or by directly testing for the presence of antibodies against a sample of donor tissues or blood.
The main purpose of this test is to distinguish the appearance of antibodies in the recipient against the red blood cells of the donor. These antibodies can be found on the surface of red blood cells of the donor after transfusion.
Clotting time - Coagulation of whole bloodSHRUTHI VASAN
Coagulation of blood - Clotting Time - Introduction - Methods - Capillary Method - Tube Method - Lee White Method - Procedure - Normal Range - Discussion.
Atherosclerosis - Definition - Risk Factors - Lesser and Non Quantitated risk factors - Arterial wall - The development of Atherosclerosis - Many Features of the injury Hypothesis - The process of Atherogenesis - Pathogenesis in short - Morphology of Atheroma - Components of Atheromatous Plaque (MP) - Complications and clinical significance - Cardiovascular risk and its assessment.
FNAC of breast - definition, history, purpose, preparations, basic equipment, procedure, smear preparation, fixatives, staining solutions, rapid stains - toluidine blue, difference between air dried and wet fixed slides, complications and contraindications, advantages, general criteris for malignancy, nuclear size and pleomorphism, nuclear membrane, irregularity and extranuclear chromatin, nuclear fragility and mitotic figures, types of breast carcinoma.
cytology of urine tract - this slide contains the specimen collection method, preparation of specimen, types of fixatives, other preparation techniques, urinary tract histology, normal urinary tract cytology,
“Microbes matters”. Cooperation among bacteria. Good microbes. Microbes too helps us in various ways. List of uses of microbes. The reason behind tasty foods. Microbes are useful in food production and food industries. “Fermentation may have been greater discovery than fires”. Fermentation – the main job of microbes. Brewing beer, liquors and wine. The need of microbes in agriculture. It helps in encountering of insects. Microorganisms are an important part of wastewater treatment. Contribution to medicine - thousands of antibiotics known to us are made by microorganisms. The best kind of biodegradable plastics are the ones made by bacteria because they can also be broken down by bacteria. It also helps to set up your aquarium. The complex microbial communities on and in the human body can sometimes get out of balance – Maintaining of balance. Microorganisms have evolved as a potential alternate source of energy. Microorganisms are used to produce biofuels like biodiesel, bioalcohol and also microbial fuel cell. We are all here because of an organism that changed the world and also paved the way for complex life on earth – Evolution. Microorganisms help us in researching on diseases, such as in vaccination. We conclude with the a considerations of the consequences of the these complex interactions and we briefly discuss the potential role of social interactions involving multiple traits and multiple environment constraints in the evolution of specialization and division of microbes.
This slide gives you details about
1. embalming
2. museum techniques
3. principles of karyotyping
chemicals used for embalming
instruments used for embalming
embalming procedures
uses of embalming
procedures for museum techniques
procedure for storing specimens
instruments used in specimen storage
different types of jars
karyotyping definition
procedure for karyotyping
This slide gives you details about the following:
Safety precautions.
Rules and regulations to be followed inside laboratory.
Different type of laboratory hazards.
How to deals with laboratory accident incidents.
Diagrammatic representation of dress codes & rules.
bio safety cabinets.
Dress codes for technicians dealing with radioactive materials
sterilization of whole room (Fumigation)
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Cancer cell metabolism: special Reference to Lactate PathwayAADYARAJPANDEY1
Normal Cell Metabolism:
Cellular respiration describes the series of steps that cells use to break down sugar and other chemicals to get the energy we need to function.
Energy is stored in the bonds of glucose and when glucose is broken down, much of that energy is released.
Cell utilize energy in the form of ATP.
The first step of respiration is called glycolysis. In a series of steps, glycolysis breaks glucose into two smaller molecules - a chemical called pyruvate. A small amount of ATP is formed during this process.
Most healthy cells continue the breakdown in a second process, called the Kreb's cycle. The Kreb's cycle allows cells to “burn” the pyruvates made in glycolysis to get more ATP.
The last step in the breakdown of glucose is called oxidative phosphorylation (Ox-Phos).
It takes place in specialized cell structures called mitochondria. This process produces a large amount of ATP. Importantly, cells need oxygen to complete oxidative phosphorylation.
If a cell completes only glycolysis, only 2 molecules of ATP are made per glucose. However, if the cell completes the entire respiration process (glycolysis - Kreb's - oxidative phosphorylation), about 36 molecules of ATP are created, giving it much more energy to use.
IN CANCER CELL:
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
Unlike healthy cells that "burn" the entire molecule of sugar to capture a large amount of energy as ATP, cancer cells are wasteful.
Cancer cells only partially break down sugar molecules. They overuse the first step of respiration, glycolysis. They frequently do not complete the second step, oxidative phosphorylation.
This results in only 2 molecules of ATP per each glucose molecule instead of the 36 or so ATPs healthy cells gain. As a result, cancer cells need to use a lot more sugar molecules to get enough energy to survive.
introduction to WARBERG PHENOMENA:
WARBURG EFFECT Usually, cancer cells are highly glycolytic (glucose addiction) and take up more glucose than do normal cells from outside.
Otto Heinrich Warburg (; 8 October 1883 – 1 August 1970) In 1931 was awarded the Nobel Prize in Physiology for his "discovery of the nature and mode of action of the respiratory enzyme.
WARNBURG EFFECT : cancer cells under aerobic (well-oxygenated) conditions to metabolize glucose to lactate (aerobic glycolysis) is known as the Warburg effect. Warburg made the observation that tumor slices consume glucose and secrete lactate at a higher rate than normal tissues.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
2. TRANSFUSION:
The process of transferring donated blood, blood
products, or other fluids into the circulatory system
of a person or animal.
3. TRANSFUSION REACTION:
Reaction of the body to a transfusion of blood that
is not compatible with its own blood.
It is an adverse reaction that can range from fever
and hives, to renal failure, shock and death.
4. NEED FOR BLOOD TRANSFUSION:
Blood transfusion is needed when if the person is
too much of blood loss, such as the following:
Injury or major surgery
An illness that causes bleeding such as a Bleeding
ulcer.
An illness that destroys blood cells, such as Haemolytic
Anemia or Thrombocytopenia.
If there is an illness in which bone marrow doesn’t make
enough blood, such as Aplastic anemia, you may
needed transfusion.
5. INITIAL MEASURE BEFORE THE INVESTIGATION
TEST:
An intravenous line with normal saline should be maintained.
The patient should be assessed and supported as necessary
while the patient’s physician and the transfusion service are
notified.
A responsible physician will need to evaluated the patient and
determine appropriate clinical care.
The unit and all tubing should be returned to the blood bank
along, along with post-infusion blood and urine sample as
clinically indicated.
The reaction should be documented in the patient’s chart.
6. SAMPLE CRITERIA:
MINIMUM SAMPLE REQUIREMENT:
Verify the patient’s identify using at least two unique
identifiers.
Date and time of sample collection.
Ensure all section in the form are completed in a legible
and detailed manner.
Completed all the information in the ‘specimen
collection’ information.
Ensure both the nursing and facility of blood bank
clerical checks have been completed and this
documented on the form. This will prevent delays in
testing.
7. SAMPLE REJECTION:
Specimen receives unlabeled/improperly labeled or
overloaded with more than one name.
Key identifiers information is missing, incorrect or
discrepant on the sample and / or requisition.
Specimen not received the laboratory within 8 hours of
collection.
Unacceptable tube received.
Specimens which are haemolysed.
Insufficient of sample.
8. LABORATORY INVESTIGATION:
After initial measures, there are three basic
preliminary test are done. They are:
Clerical check
Visual check
Serology check
9. PURPOSE:
To determine the likelihood the occurrence of haemolytic
transfusion reaction.
It is a serious complications that can occur after a blood
transfusion. The reaction occurs when the red blood cells that
were give during the transfusion are destroyed by the persons
immune system.
If there is evidence of haemolysis or if the clinical situation
something severe and unusual, the addition test such as
TRALI and TACO must be performed.
TRALI – Transfusion Belated Acute Lung Injury. it is an acute lung
injury that is temporally related to a blood transfusion, specially it
occurs within the first six hours following a transfusion.
TACO – Transfusion Associated Circulatory Overloaded. It occurs
due to the rapid transfusion of a large volume of blood
11. CLERICAL CHECK:
To identify the possibilities of ABO blood compatibility.
Compare the component bag, label, paper work with
patient sample and look for errors.
If an error is found, the physician must be notified.
Most common errors:
Misidentifications of patient when pre transfusion sample
drawn.
Mix up of sample in the lab.
Not enough incubation time.
12. VISUAL CHECK:
Plasma or serum reaction and compare with pre-transfusion.
This step is done to examine the presence.
This destruction of red cells and releasing haemoglobin will
resulting a pink to red.
The pink colour or red colour serum indicates into haemolysis.
Thus the ABO testing must be repeated of post transfusion
specimen.
An urine examination of a post reaction helps in diagnosis of
acute haemolysis.
The free haemoglobin in the urine indicates the intravascular.
13. SEROLOGY CHECK:
On post transfusion sample redo the ABO test and
perform the direct antiglobulin test (DAT).
The sample post transfusion must be preserved in
a EDTA preservation.
If the DAT is positive on the post transfusion sample
then one should be performed on the pre
transfusion sample.
If the result for the pre transfusion DAT is negative
but the result for post transfusion is positive.
14. If any of these three test above have positive and
suspicious results, REDO test done before blood
transfusion which are:
ABO &Rhesus grouping.
Antibody screening.
Repeat crossmatch.