Blood Transfusion
Blood transfusion is the process of transferring blood or blood based products from one person into the circulatory system of another. Safe blood transfusion should be safe to both the donor and the recipient. Blood transfusions can be life saving in some situations such as -Massive blood loss due to trauma or can be used to replace blood lost during surgery.BT may also be used to treat a severe anemia orThrombocytopenia caused by a blood disease.People suffering from hemophilia or sickle disease may require frequent transfusion.
Blood transfusion is the process through which blood and blood products are transferred to circulation intravenously. Early transfusions used whole blood but modern medical practice commonly used components of blood.It helps to replace blood lost during injury or surgery. It is a life saving procedure. before transfusion of blood it is necessary to know your blood group type. As blood group o is considered as universal donor and blood group AB considered as universal accepter.
Blood transfusion are relatively safe but can be fatal if incorrectly administered. Donated blood can be processed into components such as PCV, FFP, Platelets, Cryoprecipitate. Doctors and nurses plays a major role in blood transfusion. They should follows all safety precautions throughout all steps of administrating procedure.
A PowerPoint presentation outlining the physiology of blood transfusion, and clinical precautions to take in preventing and managing blood transfusion reactions.
how to select a healthy donor & care of donor .A healthy donor is one of the most vital part of transfusion medicine for safe transfusion of blood & blood product
Blood transfusion is the process through which blood and blood products are transferred to circulation intravenously. Early transfusions used whole blood but modern medical practice commonly used components of blood.It helps to replace blood lost during injury or surgery. It is a life saving procedure. before transfusion of blood it is necessary to know your blood group type. As blood group o is considered as universal donor and blood group AB considered as universal accepter.
Blood transfusion are relatively safe but can be fatal if incorrectly administered. Donated blood can be processed into components such as PCV, FFP, Platelets, Cryoprecipitate. Doctors and nurses plays a major role in blood transfusion. They should follows all safety precautions throughout all steps of administrating procedure.
A PowerPoint presentation outlining the physiology of blood transfusion, and clinical precautions to take in preventing and managing blood transfusion reactions.
how to select a healthy donor & care of donor .A healthy donor is one of the most vital part of transfusion medicine for safe transfusion of blood & blood product
Rh typing and its technique , BLOOD TYPING , Rhesus (Rh) typing , procedures of rh typing, process of Rh typing, Test limitations, Sources of Error in Rh Antigen Typing, False positive reactions' reason, False negative reactions' reasons
This PPT is basically based on the topic - Blood transfusion in Bailey & Love and mainly very useful for Final MBBS students.during their course as well as their in clinical practice.
blood transfusion is a life saving procedure. so role of nurse here while transfused the blood in the ward is important. in this slide role of nurse is given here. if you like kindly give your comment and share it to others. follow my account to know more.
Rh typing and its technique , BLOOD TYPING , Rhesus (Rh) typing , procedures of rh typing, process of Rh typing, Test limitations, Sources of Error in Rh Antigen Typing, False positive reactions' reason, False negative reactions' reasons
This PPT is basically based on the topic - Blood transfusion in Bailey & Love and mainly very useful for Final MBBS students.during their course as well as their in clinical practice.
blood transfusion is a life saving procedure. so role of nurse here while transfused the blood in the ward is important. in this slide role of nurse is given here. if you like kindly give your comment and share it to others. follow my account to know more.
dr m laban
Tanta fever hospital scientific activity
sunday
12-8-2018
Blood transfusion
Aims of Transfusion Center
To care for the donor - ensure act of donation does not harm donor.
Provision of Blood of the best possible quality and safety for the patient receiving it.
Safe blood transfusion means:
Compatible and without transmission of infection
The Safest blood transfusion is No
transfusion
Blood donation
Careful donor selection with donor interview.
Age: not less than 17 years.
Pulse: between 50-100 beat / minute without irregularities.
Blood pressure: systole<180mmHg, diastolic <100mmHg.
Temperature: <37.5C
Hemoglobin:>12g/dl, Hct>38%
Site of vein puncture must be free of lesions and infections.
ABO grouping.
Rh typing.
Cross matching
Laboratory screening test for:-
HBsAg.
HCV Ab.
HIV.
HTLV1.
HTLV2.
Blood grouping means:-
the determination of the antigens of a specific group on the red cells
and the antibodies relevant to this group in the normal serum.
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.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
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.
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.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
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.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
(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.
2. Introduction:
Blood transfusion is the process of transferring blood or
blood based products from one person into the circulatory system
of another. Safe blood transfusion should be safe to both the donor
and the recipient. Blood transfusions can be life saving in some
situations such as –
i. Massive blood loss due to trauma or can be used to replace
blood lost during surgery.
ii. BT may also be used to treat a severe anemia or
iii. Thrombocytopenia caused by a blood disease.
3. iv. People suffering from hemophilia or sickle disease may require
frequent transfusion.
• Blood transfusion usually done as a lifesaving maneuver to
replace blood cells or blood products lost through severe
bleeding
5. History
» Human blood replacement therapy was accepted in the late 19th
century
» This was followed by introduction of blood grouping by
Landsteiner who identified the major A,B & O groups in 1900,
resulting in widespread use of blood products in world war 1.
» Levine & Stetson in 1939 followed with the concept of Rh
grouping.
» Whole blood was considered the standard in transfusion in late
1970s when component therapy began to take prominence.
6. GENERAL INDICATIONS OF BLOOD TRANSFUSION
1. External bleeding
2. Internal bleeding (i) non-traumatic
(ii) traumatic
3. RBC lysis : e.g. malaria, HIV
4. Anemia
5. Bleeding disorders
6. Burns
7. Anticipated need for blood
10. For safe blood transfusions to prevent immediate reaction the
following steps mustbe taken.
1. Age: not less than 17 years.
2. Pulse: between 50-100 beat /minute without irregularities.
3. Blood pressure: systole<180mmHg, diastolic <100mmHg.
4. Temperature: <37.5C
5. Hemoglobin:>12g/dl, Hct>38%
6. Site of vein puncture must be free of lesions and infections.
7. ABO grouping.
8. Rh typing.
9. Cross matching
10. Laboratory screening test for:- HBsAg, HCV Ab, HIV, HTLV1, HTLV2.
11. BLOODGROUPING
Because blood types are responsible for the interactions between
cells such as red blood cells and the immune system, it is
important that the blood types of the donor and the recipient of
red blood cells match. If the donor and recipient's blood types are
not matched, the recipient's immune system will destroy the
donor's cells.
Blood grouping means:-
• the determination of the antigens of a
specific group on the red cells
• and the antibodies relevant to this
group in the normal serum.
14. RHESUS(Rh) BLOOD GROUP
The Rh system, which includes the D, C, c, E, and e
antigens, differs from the ABO system in several ways
It is second only to the ABO system in importance in
transfusion medicine.
The Rh antigens are highly immunogenic, especially the D
antigen since these antigens are membrane-spanning proteins,
in contrast to polysaccharide moieties.
In the Rh system the antibodies are of IgG type and antigen
–antibody reaction occurs best at body temperature .[warm
antibodies]
In Rh negative individuals , anti – D antibodies are not
naturally present in the plasma
15.
16. CROSS MATCHING
Blood matching between a patient and a donor is a direct
compatibility test
RBCs and plasma are crossmatched through major and minor
crossmatching process
A compatible donor blood
is chosen. As a final
check, a blood bank
technologist will mix a
small sample of your blood
with a small sample of the
donor blood to confirm
they are compatible.
21. 1. Use of Sterile Apparatus.
2. Blood bag should be checked
3. Temperature of blood to be
transfused must be same as body
temperature.
4. Transfusion rate must be slow in
order to prevent increase load on
heart.
5. Care full watch on the recipients
condition for 10 mins
PRECAUTIONS TO BE TAKEN DURING BLOOD TRANSFUSION
22. The interval b/w 2 donations : at least 12 weeks.
At least 48 hours must elapse after
plasmapheresis or cytapheresis before whole
blood is collected from a donor.
Apheresisshould be done only after 90 days
of whole blood collection or in an event
when red cells are not returned at the
end of apheresis
DONATIONINTERVAL