This document discusses different methods of blood doping used by athletes to boost oxygen carrying capacity and endurance. It describes how blood doping involves increasing red blood cells through blood transfusions, EPO injections, or blood substitutes. Blood transfusions involve extracting and later reinfusing a person's own red blood cells or receiving another person's blood. EPO injections stimulate the body to produce more red blood cells. Detection methods try to identify abnormal increases in hemoglobin levels that would indicate blood doping. While blood doping can enhance exercise performance, it also carries health risks like heart or lung problems.
Shock is a life threatening situation due to poor tissue perfusion with impaired cellular metabolism, manifested in turn by serious pathophysiology abnormalities.
What is BLOOD? What are the differents components and their functions in the ...D.R. Chandravanshi
Blood is a body fluid in humans and other animals that delivers necessary substances such as nutrients and oxygen to the cells and transports metabolic waste products away from those same cells.[1]
In vertebrates, it is composed of blood cells suspended in blood plasma. Plasma, which constitutes 55% of blood fluid, is mostly water (92% by volume),[2] and contains proteins, glucose, mineral ions, hormones, carbon dioxide (plasma being the main medium for excretory product transportation), and blood cells themselves. Albumin is the main protein in plasma, and it functions to regulate the colloidal osmotic pressure of blood. The blood cells are mainly red blood cells (also called RBCs or erythrocytes), white blood cells (also called WBCs or leukocytes) and platelets (also called thrombocytes). The most abundant cells in vertebrate blood are red blood cells. These contain hemoglobin, an iron-containing protein, which facilitates oxygen transport by reversibly binding to this respiratory gas and greatly increasing its solubility in blood. In contrast, carbon dioxide is mostly transported extracellularly as bicarbonate ion transported in plasma.
Shock is a life threatening situation due to poor tissue perfusion with impaired cellular metabolism, manifested in turn by serious pathophysiology abnormalities.
What is BLOOD? What are the differents components and their functions in the ...D.R. Chandravanshi
Blood is a body fluid in humans and other animals that delivers necessary substances such as nutrients and oxygen to the cells and transports metabolic waste products away from those same cells.[1]
In vertebrates, it is composed of blood cells suspended in blood plasma. Plasma, which constitutes 55% of blood fluid, is mostly water (92% by volume),[2] and contains proteins, glucose, mineral ions, hormones, carbon dioxide (plasma being the main medium for excretory product transportation), and blood cells themselves. Albumin is the main protein in plasma, and it functions to regulate the colloidal osmotic pressure of blood. The blood cells are mainly red blood cells (also called RBCs or erythrocytes), white blood cells (also called WBCs or leukocytes) and platelets (also called thrombocytes). The most abundant cells in vertebrate blood are red blood cells. These contain hemoglobin, an iron-containing protein, which facilitates oxygen transport by reversibly binding to this respiratory gas and greatly increasing its solubility in blood. In contrast, carbon dioxide is mostly transported extracellularly as bicarbonate ion transported in plasma.
En el marco del evento académico "Los Olímpicos pasan al Tablero" de la Facultad de Ciencias Económicas de la Universidad de Antioquia, el médico David Londoño habló sobre los avances tecnológicos en la evaluación y control del uso de sustancias para mejorar el desempeño deportivo.
Más info.:
Facultad de Ciencias Económicas
Universidad de Antioquia
http://economicas.udea.edu.co/
comunicacioneseconomicas@udea.edu.co
Fijo: (57 4 ) 219 88 05-219 58 00
Medellín
Networks must be able to transfer data from one device to another with acceptable
accuracy. For most applications, a system must guarantee that the data received are
identical to the data transmitted. Any time data are transmitted from one node to the
next, they can become corrupted in passage. Many factors can alter one or more bits of
a message. Some applications require a mechanism for detecting and correcting errors.
Some applications can tolerate a small level of error. For example, random errors
in audio or video transmissions may be tolerable, but when we transfer text, we expect
a very high level of accuracy.
At the data-link layer, if a frame is corrupted between the two nodes, it needs to be
corrected before it continues its journey to other nodes. However, most link-layer protocols
simply discard the frame and let the upper-layer protocols handle the retransmission
of the frame. Some multimedia applications, however, try to correct the corrupted frame.
This chapter is divided into five sections.
❑ The first section introduces types of errors, the concept of redundancy, and distinguishes
between error detection and correction.
❑ The second section discusses block coding. It shows how error can be detected
using block coding and also introduces the concept of Hamming distance.
❑ The third section discusses cyclic codes. It discusses a subset of cyclic code, CRC,
that is very common in the data-link layer. The section shows how CRC can be
easily implemented in hardware and represented by polynomials.
❑ The fourth section discusses checksums. It shows how a checksum is calculated for
a set of data words. It also gives some other approaches to traditional checksum.
❑ The fifth section discusses forward error correction. It shows how Hamming distance
can also be used for this purpose. The section also describes cheaper methods
to achieve the same goal, such as XORing of packets, interleaving chunks, or
compounding high and low resolutions packets.
Artificial blood is an innovative concept of transfusion medicine where specifically designed compounds perform the task of transport and delivery of oxygen in the body to replace this function of allogenic human blood transfusion.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
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Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of 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 leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
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. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
12. Blood Substitutes
• Synthetic oxygen carriers
human blood unavailable
blood infection
there isn't enough time to match of blood type
• Example
HBOCs
PFCs
13. HBOCs
• Resistance to dissociate when dissolved in media
• greater benefits than hemoglobin
• highly effective O2 donors in terms of tissue oxygenation
14. PFCs
• dissolve 100 times more
oxygen than plasma.
• Small size = flow in tiny
capillaries.
15. EPO Injections
• Hormone, produced by kidney.
• Regulates production of RBCs by
acting on bone marrow.
• EPO injections are given to
stimulate the production of RBCs
to treat patients with anemia.
16. Athletes using EPO to produce higher
than normal amounts of red blood
cells
18. Detection for Homologous Blood Doping
• Fluorescent-activated cell sorting
• Examining markers on the surface
of rbcs
• Determine whether blood from
more than one person is present
19. Detection for Autologous Blood doping
• CO rebreathing technique
• To measure the nonphysiologic
increases in hb mass
• O2-CO gas mixture inhalation for
about 10-15mins
• By measuring the difference in
carboxyhemoglobin concentration
(hbco) before and after
rebreathing total hb mass can be
calculated.
20. Pros Of Blood Doping
• Affects the brain of the athlete,
• Athlete’s exercise endurance level
• Improve the health of athletes
• Benefits the athlete's long exercise
• No oxygen depletion and lactic acid formation.
21. Cons of blood doping
• Increased viscosity of the
blood
• Risk of heart diseases
• Cerebral or pulmonary
embolisms
• Weakened immune system,
increases the risk of
autoimmune diseases.
22. • Blood clots
• Deterioration of the Mind
• Negative mental effects
• EPO addicting drug
The injury-prone Pakistani fast bowlers, Shoaib Akhtar and Mohammad Asif both failed tests for nandrolone in 2006 and were handed bans which were later overturned on appeal. Asif claimed his was due to a faulty nutritional supplement. He later failed a test in the IPL for steroids in 2008 and also was detained at Dubai airport that same year for possessing illegal substances – all apparently linked to injury recovery.
Nandrolone (19-nortestosterone) is an anabolic steroid. The positive effects of the drug include muscle growth, appetite stimulation and increasedred blood cell production and bone density.
Doping is generally the practice of adding impurities to something.
Doping in sport, a term for the use of performance-enhancing drugs in sport often to improve athletic performance
Blood doping, another means of improving athletic performance
Blood doping is the practice of boosting the number of red blood cells in the bloodstream in order to enhance athletic performance. Because such blood cells carry oxygen from the lungs to the muscles, a higher concentration in the blood can improve an athlete’saerobic capacity (VO2 max) and endurance.
VO2 max (also maximal oxygen consumption, maximal oxygen uptake, peak oxygen uptake or maximal aerobic capacity) is the maximum rate of oxygen consumption as measured during incremental exercise, most typically on a motorized treadmill.
The body undergoes aerobic respiration in order to provide sufficient delivery of O2 to the exercising skeletal muscles and the main determining factors is shown in figure 1. The rate maximum O2 uptake (O2max) depends on cardiac output, O2 extraction and hemoglobin mass. The cardiac output of an athlete is difficult to manipulate during a competitions and the distributions of cardiac output is at the maximum rate (i.e. 80%) during competitions. In addition, the O2 extraction is approximately 90% at maximal exercise.[2] Therefore, the only method to enhance the physical performance left to increase the O2 content in the artery is by enhancing the hemoglobin mass. In other words, hemoglobin concentration and blood volume contributes to hemoglobin mass.
Hemoglobin is an oxygen-carrying protein in the blood. So increasing hemoglobin allows higher amounts of oxygen to reach and fuel an athlete's muscles. This can improve stamina and performance, particularly in long-distance events, such as running and cycling.
Blood transfusion begins by the withdrawal of 1 to 4 units of blood (1 unit = 450 ml of blood) several weeks before competition. The blood is centrifuged, the plasma components are immediately reinfused, and the corpuscular elements, principally red blood cells (RBCs), are stored refrigerated at 4◦C or frozen at −80◦C.[3] As blood stored by refrigeration displays a steady decline in the number of RBCs, a substantial percentage, up to 40%, of the stored RBCs may not be viable.[4] The freezing process, conversely, limits the aging of the cells, allowing the storage of the blood for up to 10 years with a 10% to 15% loss of RBCs.[5] Stored RBCs are then reinfused, usually 1 to 7 days before a high-endurance event. As a significant amount of iron is removed by each autologous transfusion, an adequate time for recovery of not less than 3 days from the last donation, and appropriate iron supplements, are usually required for patients undergoing autologous donations.
. This involves a transfusion of the athlete's own blood, which is drawn and then stored for future use.
. In this type of transfusion, athletes use the blood of someone else with the same blood type.
Synthetic oxygen carriers. These are chemicals that have the ability to carry oxygen. Two examples are:
HBOCs (hemoglobin-based oxygen carriers)
PFCs (perfluorocarbons)
Synthetic oxygen carriers have a legitimate medical use as emergency therapy. It is Athletes use synthetic oxygen carriers to achieve the same performance-enhancing effects of other types of blood doping: increased oxygen in the blood that helps fuel muscles.
A common feature of all HBOCs is their, which contrasts hemoglobin of natural dissociation under non-physiological conditions. HBOCs may hypothetically supply greater benefits to athletes than those provided by the equivalent hemoglobin in traditional RBC infusion. Recent developments have shown that HBOCs are not only simple RBC substitutes, but highly effective O2 donors in terms of tissue oxygenation.
Some of these molecules can dissolve 100 times more oxygen than plasma.
Due to their small size, PFCs are able to permeate circulation where erythrocytes may not flow. In tiny capillaries, PFCs produce the greatest benefit,
EPO injections. EPO is a hormone produced by the kidney. It regulates the body's production of red blood cells.
In medical practice, EPO injections are given to stimulate the production of red blood cells. For example, a synthetic EPO can be used to treat patients with anemia related to chronic or end-stage kidney disease.
Athletes using EPO do so to encourage their bodies to produce higher than normal amounts of red blood cells to enhance performance.
EPO is already present in the human body. The kidneys release this peptide hormone and it stimulates the production of red blood cells by acting on the bone marrow. This may help in increasing the buffering of lactic acid. It is also known to increase how much oxygen is sent to the muscles by increasing red blood cell counts.
The test method is based on a technique known as fluorescent-activated cell sorting. By examining markers on the surface of blood cells, the method can determine whether blood from more than one person is present in an athlete’s circulation. The test utilizes 12 antisera directed against the blood group antigens, obtained from donor plasma. The antigens are labeled with secondary antibodies, which are conjugated with fluorescein to label IgG-coated RBCs and enhance the detection by flow cytometry
Autologous blood doping detection is done indirectly via CO rebreathing technique to measure the nonphysiologic increases in Hb mass. The principle of CO rebreathing method used currently requires an O2-CO gas mixture inhalation for about 10-15mins.[21] By measuring the difference in carboxyhemoglobin concentration (HbCO) before and after rebreathing, the volume of CO and the binding capacity of Hb for CO ( 1.39ml g-1), total Hb mass can be calculated.
Blood doping affects the brain of the athlete. It can cause an increase in motivation level. The way that this is done is by the brain sends signals to the nerves, which in turn sends signals to the body, to secrete the hormones and enzymes that play a role in how the person is feeling
increase the athlete’s exercise endurance levelEndurance refers to the power or capability of doing a certain activity for long periods without getting tired. Such a trait is important for any athlete or individual in body building workouts. Blood doping is said to enhance endurance levels by about 5%
improve the health of athletes that have low haematocrit for genetic or dietary reason
blood doping also benefits the athlete's long exercise; people who take part in long exercises such as marathon running and cross country skating and skiing, can increase their effectivenessand helps the athlete avoid oxygen depletion. During exercises of high intensity, such as weight training, oxygen usually becomes depleted. The body therefore cannot get sufficient amounts of oxygen for it to optimally perform. This state is known as oxygen debt, which may lead to formation of lactic acid. Blood doping prevents both oxygen depletion and also lactic acid formation.
Increased Viscosity of the Blood: Since the usage of EPO increases the red blood cell production, it increases the viscosity of the blood (World ant-doping agency, 2011). This means that the blood of the user is thicker than non-users, and this inevitably makes it harder for the blood to circulate throughout the body. Medical issues arise when a person does not have proper blood circulation. It leads to a higher risk of heart diseases and the possibility of having a stroke. In addition, it leads to a high risk of having cerebral or pulmonary embolisms which are the blood clotting in the user’s brain or lungs. hyperviscosity syndrome which is characterized by increased blood viscosity and decreased cardiac output and blood flow velocity which results in the reduction of peripheral oxygen delivery.
Weakened Immune System: Blood doping weakens the immune system, and increases the risk of autoimmune diseases. Autoimmune diseases are a large group of diseases that cause the immune system in the body to produce antibodies against the user’s own tissues. The body attacks itself when a person has an autoimmune disease. The immune system in the body is what is supposed to keep the person alive and healthy.
Blood clots are also a serious effect from having a weakened immune system.
Deterioration of the Mind: Not only does blood doping have negative physical effects on the body, it also has negative mental effects. After multiple uses of EPO, the athlete becomes reliant on it as if EPO were any other type of addicting drug. The athlete goes through withdrawal as would an addict on any other type of drug when it is removed from the body. Blood doping deteriorates the mind and causes the user to believe that they need EPO in order to survive, which is certainly not
Blood contamination during preparation or storage is another issue. Contamination was seen in 1 in every 500,000 transfusions of red blood cells in 2002.[41] Blood contamination can lead to septicemia or an infection that affects the whole body.
kidney damage from allergic reactions and transmission of infectious diseases like HIV.
rash, fever and shock due to an allergic reaction, metabolic shock, acute hemolytic reactions with kidney damage if incorrectly typed blood is used, delayed transfusion reactions resulting in fever and jaundice (potentially life-threatening) andtransmission of infectious diseases (viral hepatitis and AIDS