This document summarizes drugs that affect blood and their uses. It discusses haematinics like iron, vitamin B12, and folic acid, which are used to treat anaemias caused by deficiencies in red blood cell production. It also covers coagulants and anticoagulants. Coagulants like vitamin K and fibrinogen promote coagulation, while anticoagulants like heparin, low molecular weight heparins, fondaparinux, and oral anticoagulants reduce coagulability of blood and are used to prevent thrombosis. Local haemostatics are used to stop bleeding from accessible sites. Care must be taken with patients on medications or with conditions that can affect haemostasis
This lecture is about what is the neostigmine and what are its medical uses, mechanism of action and side effects.
Neostigmine is a cholinesterase inhibitor used in the symptomatic treatment of myasthenia gravis by improving muscle tone.
Neostigmine is in the cholinergic family of medications. It works by blocking the action of acetylcholinesterase and therefore increases the levels of acetylcholine.
Neostigmine: Cholinesterase inhibitor = ↑ ACh
Neostigmine is an anticholinesterase inhibitor and inhibits the hydrolysis of acetylcholine by competing with acetylcholine for binding to acetylcholinesterase at the site of cholinergic transmission. By reducing the hydrolysis of acetylcholine, the transmission of nerve impulses is facilitated.
At the end of surgery, neostigmine has been given for the reversal of neuromuscular blocking agents with several adverse effects such as bradycardia and profuse secretion.
Atropine has been used to prevent those side effects of neostigmine.
Side effects titles as review:
.
Nausea, headache, insomnia, dry mouth, dizziness, vomiting, allergic reactions, skin rash, hot flashes, joint pain, stroke, weakness, muscle cramps, frequent urination
Neostigmine is rapidly absorbed after intramuscular injection (IM). Neostigmine binding to human serum albumin is approximately 15 to 25%.
Neostigmine is metabolized in the liver by microsomal enzymes. The apparent excretory half-life of neostigmine is between 24 and 113 minutes.
Presented by: Mohammadsaleh Moallem
This lecture is about what is the neostigmine and what are its medical uses, mechanism of action and side effects.
Neostigmine is a cholinesterase inhibitor used in the symptomatic treatment of myasthenia gravis by improving muscle tone.
Neostigmine is in the cholinergic family of medications. It works by blocking the action of acetylcholinesterase and therefore increases the levels of acetylcholine.
Neostigmine: Cholinesterase inhibitor = ↑ ACh
Neostigmine is an anticholinesterase inhibitor and inhibits the hydrolysis of acetylcholine by competing with acetylcholine for binding to acetylcholinesterase at the site of cholinergic transmission. By reducing the hydrolysis of acetylcholine, the transmission of nerve impulses is facilitated.
At the end of surgery, neostigmine has been given for the reversal of neuromuscular blocking agents with several adverse effects such as bradycardia and profuse secretion.
Atropine has been used to prevent those side effects of neostigmine.
Side effects titles as review:
.
Nausea, headache, insomnia, dry mouth, dizziness, vomiting, allergic reactions, skin rash, hot flashes, joint pain, stroke, weakness, muscle cramps, frequent urination
Neostigmine is rapidly absorbed after intramuscular injection (IM). Neostigmine binding to human serum albumin is approximately 15 to 25%.
Neostigmine is metabolized in the liver by microsomal enzymes. The apparent excretory half-life of neostigmine is between 24 and 113 minutes.
Presented by: Mohammadsaleh Moallem
This presentation was given by me during my M.pharm.
It contains description, classification, mechanism of actions and therapeutic uses of Neuromuscular blockers.
5-Hydroxytryptamine & it’s Antagonist is a Topic in Pharmacology which will defiantly Help You in pharmacy field All information is related to pharmacology drug acting and it's effect on body. it is collage project given by our department i would like to share with you.
Diuretics
Pharmacology
Katzung
Abnormalities in fluid volume and electrolyte composition are common and important clinical disorders. Drugs that block specific transport functions of the renal tubules are valuable clinical tools in the treatment of these disorders. Although various agents that increase urine volume (diuretics) have been described since antiquity, it was not until 1937 that carbonic anhydrase inhibitors were first described and not until 1957 that a much more useful and powerful diuretic agent (chlorothiazide) became available. Technically, a “diuretic” is an agent that increases urine volume, whereas a “natriuretic” causes an increase in renal sodium excretion and an “aquaretic” increases excretion of solute-free water. Because natriuretics almost always also increase water excretion, they are usually called diuretics. Osmotic diuretics and antidiuretic hormone antagonists (see Agents That Alter Water Excretion) are aquaretics that are not directly natriuretic.
Lecture slides for undergraduates medical (MBBS) Students. Source material for this presentation is Essentials of Pharmacology, KD Tripathi, Katzung and Goodman and Gillman. It deals with Local anaesthetics with their mechanism of action, pharmacokinetics , adverse effects and therapeutic uses.
Histamine is a biogenic amine present in many animal and plant tissues that function as neurotransmitters and are also found in non-neural tissues, have complex physiologic and pathologic effects through multiple receptor subtypes, and are often released locally.
It is also present in venoms and stinging secretions. It is synthesized by decarboxylation of the amino acid, histidine. Histamine is mainly present in storage granules of mast cells in tissues like skin, lungs, liver, gastric mucosa, placenta, etc. It is one of the mediators involved in inflammatory and hypersensitivity reactions.
Hemostasis
Seminar Prepared by :-
Mohammed Saadi
Mohammed Musa
Hussein Jassam
Mahmoud Ahmed
Internal Medicine
College of Medicine - University of Kirkuk
This presentation was given by me during my M.pharm.
It contains description, classification, mechanism of actions and therapeutic uses of Neuromuscular blockers.
5-Hydroxytryptamine & it’s Antagonist is a Topic in Pharmacology which will defiantly Help You in pharmacy field All information is related to pharmacology drug acting and it's effect on body. it is collage project given by our department i would like to share with you.
Diuretics
Pharmacology
Katzung
Abnormalities in fluid volume and electrolyte composition are common and important clinical disorders. Drugs that block specific transport functions of the renal tubules are valuable clinical tools in the treatment of these disorders. Although various agents that increase urine volume (diuretics) have been described since antiquity, it was not until 1937 that carbonic anhydrase inhibitors were first described and not until 1957 that a much more useful and powerful diuretic agent (chlorothiazide) became available. Technically, a “diuretic” is an agent that increases urine volume, whereas a “natriuretic” causes an increase in renal sodium excretion and an “aquaretic” increases excretion of solute-free water. Because natriuretics almost always also increase water excretion, they are usually called diuretics. Osmotic diuretics and antidiuretic hormone antagonists (see Agents That Alter Water Excretion) are aquaretics that are not directly natriuretic.
Lecture slides for undergraduates medical (MBBS) Students. Source material for this presentation is Essentials of Pharmacology, KD Tripathi, Katzung and Goodman and Gillman. It deals with Local anaesthetics with their mechanism of action, pharmacokinetics , adverse effects and therapeutic uses.
Histamine is a biogenic amine present in many animal and plant tissues that function as neurotransmitters and are also found in non-neural tissues, have complex physiologic and pathologic effects through multiple receptor subtypes, and are often released locally.
It is also present in venoms and stinging secretions. It is synthesized by decarboxylation of the amino acid, histidine. Histamine is mainly present in storage granules of mast cells in tissues like skin, lungs, liver, gastric mucosa, placenta, etc. It is one of the mediators involved in inflammatory and hypersensitivity reactions.
Hemostasis
Seminar Prepared by :-
Mohammed Saadi
Mohammed Musa
Hussein Jassam
Mahmoud Ahmed
Internal Medicine
College of Medicine - University of Kirkuk
In this Slide we will talk about coagulation Disorders in periodontics in detail
Also discuss about anticoagulant,antiplatelet
And Thrombocytopenic purpura treatment and laboratory tests etc.
The Indian Dental Academy is the Leader in continuing dental education , training dentists in all aspects of dentistry and
offering a wide range of dental certified courses in different formats.for more details please visit
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The hemophilia are disorders of hemostasis resulting from a deficiency of a procoagulant. Hemophilia is an inherited bleeding disorder affecting approximately 1 in 7500 males.
Hello friends. In this PPT I am talking about drugs used in the treatment of type 2 diabetes mellitus. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
AMA General considerations 12.6.23.pptxKarun Kumar
Hello friends. In this PPT I am talking about Antimicrobial drugs-General Considerations. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about general anaesthetics and skeletal muscle relaxants. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Drugs & Aids with specific applications in dentalKarun Kumar
Hello friends. In this PPT I am talking about drugs & aids with specific applications in dental disorders. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about diuretics. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about Cardiovascular system drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about CNS drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about CNS drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about Autacoids. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about Anti-viral drugs drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about Anti-TB & anti leprosy drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about antiseptics, disinfectants. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about antiprotozoal drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about anti-fungal drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about anti-cancer drugs. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about autonomic nervous system. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about autonomic nervous system. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Hello friends. In this PPT I am talking about autonomic nervous system. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
AETCOM (Attitude, Ethics and Communication module)Karun Kumar
Hello friends. In this PPT I am talking about AETCOM (Attitude, Ethics and Communication module) of Pharmacology. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way
Hello friends. In this PPT I am talking about adverse drug effects. If you like it, please do let me know in the comments section. A single word of appreciation from you will encourage me to make more of such videos. Thanks. Enjoy and welcome to the beautiful world of pharmacology where pharmacology comes to life. This video is intended for MBBS, BDS, paramedical and any person who wishes to have a basic understanding of the subject in the simplest way.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
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
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
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
2. Haematinics
• Substances required in the formation of blood
• Used for treatment of anaemias
• Anaemia occurs when the balance between
production and destruction of RBCs is disturbed
3. • The disturbance can be caused by :-
1. Blood loss (acute or chronic)
2. Impaired red cell formation due to:
1. Deficiency of essential factors, i.e. iron, vitamin B12, folic
acid.
2. Bone marrow depression (hypoplastic anaemia),
erythropoietin deficiency.
3. Increased destruction of RBCs (haemolytic anaemia)
5. Oral iron preparations
1. Ferrous sulfate (hydrated salt 20% iron, dried salt
32% iron) is cheapest
Leaves metallic taste in mouth
2. Ferrous gluconate (12% iron)
3. Ferrous fumarate (33% iron); less water soluble
than ferrous sulfate and tasteless
4. Colloidal ferric hydroxide (50% iron)
6. Adverse effects of oral iron
1. Epigastric pain
2. Heart burn
3. Nausea & vomiting
4. Bloating
5. Staining of teeth
6. Metallic taste
7. Constipation
7. Parenteral iron
• Indicated only when:
1. Oral iron is not tolerated (bowel upset too much)
2. Failure to absorb oral iron
3. Non-compliance to oral iron
4. Severe deficiency with chronic bleeding
5. Along with erythropoietin to meet the accelerated
demand
8. • Parenteral iron therapy needs calculation of the total
iron requirement of the patient
• Iron requirement (mg) = 4.4 × body weight (kg) × Hb
deficit (g/dl)
• Parenteral iron preparations :-
1. Iron-dextran
2. Iron isomaltoside-100
3. Ferrous-sucrose
4. Ferric carboxymaltose
9. Use
• Prophylaxis & t/t of iron deficiency anaemia
• Prophylactic administration of supplemental iron is
routinely advised during later part of pregnancy and
to infants
• Also needed in menorrhagic women and during
chronic illnesses
• Iron is given in megaloblastic anaemia along with vit.
B12 /folic acid
• Ferric chloride used in throat paint as astringent
10. Vitamin B12 deficiency
• Due to absence of intrinsic factor secretion by
stomach
– Pernicious anaemia (autoimmune gastric mucosal damage)
– Chronic gastritis
– Gastric carcinoma
– Malabsorption
– ↑ demand or nutritional deficiency
11. • Manifestations of deficiency are:
1. Megaloblastic anaemia (neutrophils with
hypersegmented nuclei, giant platelets)
2. Glossitis, g.i. disturbances Damage to epithelial
structures
3. Neurological Subacute combined degeneration
of spinal cord; peripheral neuritis, paresthesias,
depressed stretch reflexes; mental changes—poor
memory, mood changes, hallucinations, etc.
12. Uses
1. Prevention & t/t of B12 deficiency Confirmed B12
deficiency should be treated by i.m./s.c injection of
cyanocobalamin/ hydroxocobalamin
2. Methylcobalamine, an active coenzyme form of vit
B12 has been especially advocated for neurological
defects in diabetic and other forms of neuropathy
15. Uses
1. Megaloblastic anaemia due to
1. Nutritional folate deficiency
2. ↑ folate demand
3. Malabsorption
4. Antiepileptic therapy
2. Prophylaxis of folate deficiency (during pregnancy
to reduce the risk of neural tube defects in the
newborn)
3. Methotrexate toxicity Folinic acid (Leucovorin,
citrovorum factor, 5-formyl-THFA) is used
16. • Folic acid should never be given alone to patients
with megaloblastic anaemia because:-
1. Folic acid t/t will improve symptoms of anemia
without affecting neurological defect of vitamin B12;
defects can progress & may become irreversible
2. There is diversion of meagre amount of B12 present
in body to haematopoiesis. It can result in
worsening of neurological defects.
18. Coagulants
• Substances which promote coagulation
• Indicated in haemorrhagic states
• Haemostasis Vasoconstriction + Primary
hemostasis + Secondary hemostasis
• Primary haemostasis Platelets adhere to the
damaged walls of the blood vessel, and also to each
other, to form a platelet plug
19. • Secondary haemostasis Meshwork of cross-linked
fibrin forms around the platelet plug to stabilize it
• Thrombosis Primary haemostasis + Secondary
haemostasis
• Coagulation Secondary haemostasis
• Deficiency of any clotting factor Fresh whole
blood or plasma; immediate action
22. Intrinsic pathway
• Activated by surface contact with foreign body
(Contact pathway) or extravascular tissue
• All factors and activators are contained within
(intrinsic to) the blood
• Responsible for clotting when blood is kept in a glass
tube (in vitro)
23. Extrinsic pathway
• Activated by thromboplastin (tissue factor)
• As a consequence of trauma, a tissue protein (tissue
factor) leaks into the blood from cells outside
(extrinsic to) blood vessels
• Pathways converge with the activation of factor X,
(rate-limiting step in coagulation cascade)
• Activation of factor XIIa(fibrinogen to fibrin)
26. Vitamin K uses
1. Prophylaxis & t/t of bleeding due to deficiency of
clotting factors
2. Vit. K 1 mg i.m. soon after birth has been
recommended routinely
3. Reverse the effect of overdose of oral
anticoagulants: Phytonadione (K1) is prep. of choice
27. Fibrinogen
• Fibrinogen fraction of human plasma is employed to
control bleeding in
1. Haemophilia
2. Antihaemophilic globulin (AHG) deficiency
3. Acute afibrinogenemic states
• 0.5 g is infused i.v.
28. Antihaemophilic factor
• Concentrated human AHG prepared from pooled
human plasma
• Indications (along with human fibrinogen)
1. Haemophilia
2. AHG deficiency
• Effective in controlling bleeding episodes
• Short lasting action (1 to 2 days)
29. Desmopressin
• V2 receptor agonist analogue of Vasopressin
• Releases factor VIII and von Willebrand’s factor from
vascular endothelium
• Checks bleeding in
1. Haemophilia
2. von Willebrand’s disease
30. Ethamsylate
• Reduces capillary bleeding when platelets are
adequate
• Corrects abnormalities of platelet adhesion, but does
not stabilize fibrin (not an antifibrinolytic)
• Used in prev. & t/t of capillary bleeding in
menorrhagia, after abortion, PPH, epistaxis, malena,
hematuria and after tooth extraction
• S/E nausea, rash, headache, and fall in BP
31. Haemostasis in dentistry
• Post extraction bleeding from the tooth socket is
usually arrested by a cotton gauze pressure pack held
for 20 to 30 min
• Suturing may be required if bleeding is due to tear
around the socket
• Control of bleeding may need to be aided by the use
of local haemostatics
32. Local haemostatics (Styptics)
• Substances used to stop bleeding from a local and
approachable site
• Effective on oozing surfaces, e.g. tooth socket
• Absorbable materials like
– Fibrin (prepared from human plasma and dried as sheet or
foam)
– Gelatin foam
– Oxidized cellulose (as strips which can be cut and placed in
the wound)
• Provide a meshwork which activates the clotting
mechanism and checks bleeding
33. • Left in situ these materials are abs. in 1–4 weeks
• Cause no foreign body reaction
• Thrombin Applied as dry powder or freshly
prepared solution to the bleeding surface in
haemophiliacs
• Vasoconstrictors (0.1% Adr solution) Soaked in
sterile cotton gauze & packed in bleeding tooth
socket to check bleeding when spontaneous
vasoconstriction is inadequate
• Astringents [Tannic acid or metallic salts (Alum, Ferric
chloride)] Applied for bleeding gums
34. • Many diseases and drugs can affect the vascular
response to injury, platelet function or coagulation to
create haemostatic problems
• When dental surgery is contemplated, careful
planning and consultation with their physician are
needed
1. Vitamin C deficiency
2. Deficient platelet function
3. Haemophilia
4. Anticoagulant medication
35. Vitamin C deficiency
1. Scurvy should be corrected before elective dental
surgery
2. In emergency surgery, careful packing and pressure
can stop the bleed
3. Long term corticosteroid therapy can also
compromise haemostasis by impairing vessel
retraction as well as by reducing platelet count
36. Deficient platelet function
1. Transfusion of platelet rich plasma is indicated
before dental surgery
2. Corticosteroid therapy helps to restore platelet
count in idiopathic thrombocytopenic purpura
3. Aspirin and other NSAIDs are the most important
drugs that inhibit platelet aggregation. A large
number of older individuals now receive long term
low dose aspirin prophylaxis for Ischaemic heart
disease or stroke
37. • Many others receive long term Clopidogrel for a
variety of thromboembolic disorders
• Several patients of arthritis regularly take NSAIDs
• Discontinuation of aspirin for 5 days before dental
surgery should be considered
• In case not possible, proper packing & use of local
haemostatics is needed to prevent excess bleeding
38. Haemophilia
• Minor dental procedures (like scaling) put the
haemophiliac patient at great risk of bleeding
• Patient should be covered before and after the
procedure with i.v. infusion of AHG or factor VIII
along with fibrinogen
• Tranexaemic acid has adjuvant value
• Desmopressin injected i.v. also helps in checking
dental bleeding in haemophiliacs & vW disease
39. Anticoagulant medication
• Any oral surgery in patients on anticoagulant
medication requires due care to avoid excessive
bleeding
• Since the action of i.v. heparin lasts for only 4–6
hours, the extraction can be scheduled at a time
when anticoagulation is minimal
• Low dose s.c. heparin and LMWH therapy does not
↑ dental surgery associated bleeding
• Heparin antagonist Protamine
41. Actions of heparin
1. Anticoagulant Heparin is a powerful and
instantaneously acting anticoagulant, effective both in
vivo and in vitro
• It acts indirectly by activating plasma antithrombin III
(AT III, a serine proteinase inhibitor)
• Heparin-AT III complex then binds to clotting factors
of the intrinsic and common pathways (Xa, IIa, IXa,
XIa, XIIa and XIIIa) and inactivates them but not
factor VIIa operative in the extrinsic pathway
42. • At low concentrations of heparin, factor Xa mediated
conversion of prothrombin to thrombin is selectively
affected
• The anticoagulant action is exerted mainly by
inhibition of factor Xa as well as thrombin (IIa)
mediated conversion of fibrinogen to fibrin
43. • Low concentrations of heparin prolong aPTT without
significantly prolonging PT
• High concentrations prolong both
• Low concentrations interfere selectively with the
intrinsic pathway, affecting amplification and
continuation of clotting, while high concentrations
affect the common pathway as well
44.
45.
46. 2. Antiplatelet Heparin in higher doses inhibits
platelet aggregation and prolongs bleeding time
3. Lipaemia clearing Injection of heparin clears
turbid post-prandial lipaemic plasma by releasing a
lipoprotein lipase from the vessel wall and tissues,
which hydrolyses triglycerides of chylomicra and very
low density lipoproteins to free fatty acids
• These then pass into tissues and the plasma looks
clear
47. Adverse effects
1. Bleeding due to overdose is the most serious
complication of heparin therapy
• Aspirin, other NSAIDs & antiplatelet drugs enhance
heparin induced bleeding
2. Thrombocytopenia is another common problem
• Low molecular weight (LMW) heparins are not safe
in such patients.
48.
49. Advantages of LMWH
1. Better s.c. bioavailability
2. Effects are longer & consistent (once daily s.c. adm.)
3. Dose is given in mg (not in units) can be easily
calculated on body weight basis
4. Chance of haemorrhage is less
5. Lesser antiplatelet action—less interference with
haemostasis
6. Thrombocytopenia is less frequent
7. aPTT/clotting times are not prolonged
Laboratory monitoring is not needed
50. Indications of LMWH
1. Prophylaxis of deep vein thrombosis and pulmonary
embolism in high-risk patients undergoing surgery;
stroke or other immobilized patients
2. Treatment of established deep vein thrombosis
3. Unstable angina and MI
4. To maintain patency of cannulae and shunts in
dialysis patients, and in extracorporeal circulation
52. Fondaparinux
• Synthetically produced pentasaccharide segment
present in heparin molecules which binds to AT III
with high affinity to selectively inactivate factor Xa
without binding to thrombin (factor IIa)
• 100% bioavailable on s.c. injection
• Longer acting
• Less likely to cause thrombocytopenia
• Does not require laboratory monitoring
• Uses Prophylaxis & t/t of DVT, PE, ACS
53.
54. Protamine sulfate
• It is a strongly basic, low molecular weight protein
obtained from the sperm of certain fish
• I.v. Neutralises heparin weight for weight, i.e. 1
mg is needed for every 100 U of heparin
• Used when heparin action needs to be terminated
rapidly
1. After cardiac surgery
2. After vascular surgery
3. Heparin induced bleeding
55. Direct thrombin inhibitors
• Bivalirudin Congener of hirudin (polypeptide
anticoagulant secreted by salivary glands of leech)
• Binds to thrombin & inhibits it directly
• Quick onset & short duration (t1/2 25 mins.)
• Not antagonized by Protamine
• Uses PCI, UA, MI, HIT
• Argatroban I.v. produces rapid & short-lasting
antithrombin action
56. Oral anticoagulants
• Warfarin and its congeners act as anticoagulants only
in vivo, not in vitro (WEPT)
• Act indirectly by interfering with synthesis of vit. K
dependent clotting factors (II, VII, IX, X, prot. C & S)
• Inhibits vit K epoxide reductase (VKOR) & interferes
with regeneration of the active hydroquinone form
of vit K which acts as a cofactor for the enzyme γ-
glutamyl carboxylase that carries out the final step of
γ carboxylating glutamate residues of prothrombin
and factors VII, IX and X
57.
58. Adverse effects
• Bleeding as a result of extension of the desired
pharmacological action is the most important
problem causing ecchymosis, epistaxis, hematuria,
bleeding in the g.i.t. , Intracranial or other internal
haemorrhages may even be fatal
59. Treatment of bleeding due to oral
anticoagulants
1. Withhold the anticoagulant.
2. Fresh blood transfusion (supplies clotting factors
and replenishes lost blood)
3. Fresh frozen plasma may be used as a source of
clotting factors
4. Vit. K1 (specific antidote); takes 6–24 hours for the
clotting factors to be resynthesized and released in
blood after vit K administration
60. Dose regulation
• Dose must be individualised by repeated
measurement of prothrombin time
• Aim Achieve a therapeutic effect without unduly
increasing the chances of bleeding
• A INR of 2-4.5 is considered therapeutic for different
indications
62. Drug interactions
A. Enhanced anticoagulant action
1. Broad-spectrum antibiotics Inhibit gut flora and
reduce vit K production
2. Newer cephalosporins (ceftriaxone, cefoperazone)
cause hypoprothrombinaemia by the same
mechanism as warfarin —additive action
3. Aspirin Inhibits platelet aggregation and causes
GI bleeding—this may be hazardous in
anticoagulated patients
63. 4. Sulfonamides, indomethacin, phenytoin and
probenecid: displace warfarin from plasma protein
binding
5. Chloramphenicol, erythromycin, celecoxib,
cimetidine, allopurinol, amiodarone and
metronidazole: inhibit warfarin metabolism
B. Reduced anticoagulant action
1. Barbiturates, carbamazepine, rifampin and
griseofulvin induce the metabolism of oral
anticoagulants.
2. Oral contraceptives: increase blood levels of clotting
factors
64. Direct factor Xa inhibitor
• Rivaroxaban Inactivates factor Xa
• Acts rapidly (within 3-4 hrs.) without a lag period,
and has a shorter duration of action (~24 hours)
• No laboratory monitoring required
• Uses
1. Prophylaxis of DVT & PE following knee/hip
replacement surgery
2. Preventing stroke in patients with AF
3. T/t of DVT & PE
65. Apixaban
• Approved for
1. Prev. of VTE following knee/hip replacement
2. Preventing stroke in patients with AF
3. T/t of DVT & PE
66. Oral direct thrombin inhibitor
• Dabigatran Reversibly blocks the catalytic site of
thrombin and produces a rapid (within 2 hours)
anticoagulant action
• No laboratory monitoring required
• Uses
1. Prevention of post knee replacement venous
thromboembolism
2. Stroke due to atrial fibrillation
67. Uses of anticoagulants
1. Prophyl. of DVT & PE
1. Following knee/hip replacement surgery
2. High-risk bed ridden
3. Elderly
4. Postoperative
5. Postpartum
6. Poststroke
7. Leg fracture patients
2. T/t of DVT & PE
68. 3. Prophyl. of stroke & systemic embolism in pts. of
nonvalvular AF
4. To cover PCI in pts. of MI & high-risk UA
5. Adjuvant to antiplatelet drugs to prev. reoccl. of cor.
art. following fibrinolytic therapy of MI
6. Combined with antiplatelet drugs in pts. with
prosthetic heart valves, in those undergoing vasc. surg.
or haemodialysis
7. To maintain patency of intravasc. cannulae/catheters
8. To preserve clotting factors in defibrination syndr.
69. Heparin Warfarin
Route of admin. I.v., S.c. Oral
Onset of action Immediate Delayed
Activity In vitro & in vivo In vivo only
Mechanism Activ. Of AT-III ↓ activ. Of c.f.
2,7,9,10
Antagonist Protamine sulphate Vitamin K
Lab control aPTT PT
Drug interact. Few Many
Placental barrier Does not cross Fetal warf. syndrome
Use To initiate therapy For maintenance
70. Fibrinolytic drugs (SURAT)
• Drugs used to lyse thrombi/clot to recanalize
occluded blood vessels (mainly coronary artery)
• Work by activating the natural fibrinolytic system
1. Streptokinase
2. Urokinase
3. Reteplase
4. Alteplase
5. Tenecteplase
74. Anti fibrinolytic drugs
• Drugs which inhibit plasminogen activation &
dissolution of clot, and are used to check bleeding
due to fibrinolysis
1. Epsilon Aminocaproic acid Blocks plasminogen
activation. Antidote for fibrinolytic agents.
2. Tranexamic acid 7 times more potent.
75. Tranexamic acid
• Preferred for prev./control of exc. Bleeding due to
1. Fibrinolytic drugs.
2. Cardio-pulmonary bypass surgery.
3. Tonsillectomy, prostatic surgery, tooth extraction in
haemophiliacs.
4. Menorrhagia, especially due to IUCD.
5. Recurrent epistaxis, ocular trauma
76. • Main side effects are nausea and diarrhoea.
• Thromboembolic events, disturbed colour vision and
allergic reactions are infrequent
• Headache, giddiness and thrombophlebitis of
injected vein can occur
77. Antiplatelet drugs
(Antithrombotic drugs)
• Drugs which interfere with platelet function and are
useful in the prophylaxis of thromboembolic
disorders
• All of them are likely to accentuate dental surgery
related bleeding
79. Antiplatelet Drugs
Platelets adhere to damaged vasc. Endoth. Via
GP Ia + collagen & GP Ib + vWF (similar to clotting
factor VIII)
↓
Synth. & rel. (degranulation) of TXA2,ADP,5-HT
↓
↑ expression of GP IIb/IIIa rec.
↓
Bind to fibrinogen & cause platelet aggregation
80.
81. 1. NSAIDs inhibit the synthesis of thromboxane A2 by
blocking cyclooxygenase (COX).
2. Clopidogrel, prasugrel, ticagrelor, and others block
the target of ADP, the purine 2Y12 receptor (P2Y12).
3. Epifibatide, tirofiban, abciximab, and other agents
bind to GP-2b/GP3a proteins and prevent
fibrinogen crosslinking of platelets.
4. Dipyridamole inhibits PDE ↑ cAMP ↑ PGI2
decreasing platelet aggregation.
83. Aspirin
• It acetylates and inhibits the enzyme COX-1
irreversibly
• TXA2 is the major arachidonic acid product generated
by platelets
• Platelets are exposed to aspirin in the portal
circulation before it is deacetylated during first pass
in the liver, and because platelets cannot synthesize
fresh enzyme (have no nuclei), TXA2 formation is
suppressed at very low doses and till fresh platelets
are formed
84. • Aspirin induced prolongation of bleeding time lasts
for 5–7 days.
• Doses as low as 40 mg/day have an effect on platelet
aggregation
• Maximal inhibition of platelet function occurs at 75–
150 mg aspirin per day.
• Aspirin also ↓ PGI2 synthesis as well. However, since
intimal cells can synthesize fresh enzyme, activity
returns rapidly.
85. • At low doses (75–150 mg/day or 300 mg twice
weekly), TXA2 formation by platelets is selectively
suppressed, whereas higher doses (> 900 mg/day)
may decrease both TXA2 and PGI2 production
• Aspirin inhibits the release of ADP from platelets and
their sticking to each other, but has no effect on
platelet survival time and their adhesion to damaged
vessel wall
86.
87. Ticlopidine
• Alters surface receptors on platelets and inhibits ADP
as well as fibrinogen-induced platelet aggregation
• Blocks P2Y12 type of purinergic receptors through
which ADP mediates adenylyl cyclase inhibition in
platelets
• Activation of platelets is interfered
• Fibrinogen binding to platelets is prevented without
modification of GPIIb/IIIa receptor
88. • No effect on platelet TXA2, but bleeding time is
prolonged
• Synergistic effect on platelets with aspirin
• Superseded by Clopidogrel due to side effects
89. Clopidogrel
• Safer and better tolerated
• Used for TIAs, UA, prev. of stroke and recurrence of
MI
• Aspirin is synergistic in preventing ischaemic
episodes, and is utilized for checking restenosis of
stented coronaries
• Side effects Diarrhoea, epigastric pain and rashes
• Has replaced Ticlopidine
91. • Along with warfarin ↓ thromboembolism in patients
with prosthetic heart valves
• Enhances antiplatelet action of aspirin
• Risk of stroke in patients with transient ischaemic
attacks (TIAs) may ↓ when combined with Aspirin
92. Prasugrel
• Most potent and faster acting P2Y12 purinergic
receptor blocker, that is being increasingly used in
acute coronary syndromes (ACS) and to cover
coronary angioplasty
• Bleeding complications are also more frequent and
more serious
• C/I Patients with history of ischaemic stroke and
TIAs (greater risk of intracranial haemorrhage)
93. Ticagrelor
• Reversible P2Y12 blocker
• Faster onset & quicker offset of action
• Requires twice daily dosing
• Prophylactic Ticagrelor is recommended in all high
risk ACS patients
• S/E Shortness of breath, tightness in chest,
nausea, dizziness
94. Glycoprotein (GP) IIb/IIIa receptor
antagonists
• Block GPIIb/IIIa [adhesive receptor (integrin)] on
platelet surface for fibrinogen and vWF through
which agonists like collagen, thrombin, TXA2, ADP,
etc. induce platelet aggregation
• Eptifibatide Inhibits platelet aggregation; Used as
alternative to Abciximab in ACS & Coronary
angioplasty
• Tirofiban Used in ACS & Coronary angioplasty
• Antiplatelet action similar to Eptifibatide
95. Abciximab
• Fab fragment of a chimeric monoclonal antibody
against GP IIb/IIIa, which is given along with aspirin +
heparin during coronary angioplasty
• Indications MI & UA
96.
97. Uses of antiplatelet drugs
1. Coronary artery disease Low dose aspirin 75–150
mg/day; Aspirin/clopidogrel prophylaxis in post-MI
patients clearly prevents reinfarction and ↓ mortality
2. Acute coronary syndromes (ACSs) Asp. + LMWH.
Clopidogrel can be used. Prasugrel or Ticagrelor +
Asp. pref. to cover coronary angioplasty
3. Cerebrovascular disease Aspirin ↓ incidence of
TIAs, stroke in patients with TIAs or pts. with
persistent AF, H/O of stroke in the past.
98. • Clopidogrel also ↓ TIAs & stroke
4. Prosthetic heart valves and arteriovenous shunts
Antiplatelet drugs, used with warfarin ↓ formation of
microthrombi on artificial heart valves & incidence of
embolism. Also prolong the patency of chronic
arteriovenous shunts.
5. Peripheral vascular disease Aspirin/clopidogrel
may produce some improvement in intermittent
claudication & ↓ incidence of thromboembolism
99. Hypolipidaemic drugs
• Drugs which lower the levels of lipids and
lipoproteins in blood
• ↑ LDL-CH Atherogenic
• ↑ HDL-CH Protective
• ↑ TG Risk of CAD & stroke irrespective of
cholesterol level
103. HMG-CoA Reductase inhibitors
(Statins)
• Most efficacious & best tolerated
• Competitively inhibit conversion of 3-Hydroxy-3-
methyl glutaryl coenzyme A (HMG-CoA) to
mevalonate (rate limiting step in CH synthesis) by the
enzyme HMG-CoA reductase
• Compensatory ↑ LDL rec. expr. on liver cells → ↑
rec. mediated uptake and catabolism of IDL and LDL
• Dose dependent lowering of LDL-CH levels
106. Use
• 1st choice drugs for lowering ↑ LDL and total CH
levels, with or without raised TG levels
• Efficacy of statins in ↓ LDL-CH associated mortality
and morbidity well established
• Venous thromboembolism following knee
replacement is ↓ by Rosuvastatin
• Additional mechanisms Improvement in
endothelial function, ↓ LDL oxidation & an anti
inflammatory effect
107. Bile acid sequestrants (Resins)
• Ion exchange resins
• Neither digested nor absorbed in the gut
Bind bile acids in the intestine
↓
Interrupting enterohepatic circulation
↓
Fecal excretion of bile salts & CH
(absorbed with the help of bile salts) ↑
↓
108. ↑ hepatic metabolism of CH to bile acids
↓
↑ LDL receptors expressed on liver cells
↓
Clearance of IDL, LDL & VLDL ↑
109.
110. Lipoprotein-lipase activators
(Fibrates)
• Fibrates activate LPL (enzyme causing degradation of
VLDL resulting in lowering of circulating TGs)
• Effect is exerted through PPARα which enhances
lipoprotein lipase synthesis and fatty acid oxidation
• PPARα may also ↑ LDL receptor expression in liver
• Fibrates ↓ hepatic TG synthesis as well
• S/E G.i. upset, rashes, body ache, myopathy
• DOC in pts. with ↑ TG levels ± CH levels ↑
111. Nicotinic Acid (Niacin)
• B group vitamin ↓ plasma lipids (2-4 g/day)
• TGs & VLDL ↓; followed by ↓ LDL-CH & total CH
• Most effective drug to raise HDL-CH
• Nicotinic acid reduces production of VLDL in liver by
inhibiting TG synthesis.
• Inhibits lipolysis in adipose tissue & ↑ activity of
lipoprotein lipase that clears TGs
112. Inhibits lipolysis in adipose
tissue
↓
↓ hepatic VLDL synthesis &
production of LDLs in the
plasma
113. Adverse effects
• Large doses poorly tolerated
• Marked flushing, heat and itching (especially in the
blush area) occur after every dose [PGD2 in the skin]
• Aspirin is taken before niacin
• Laropiprant (prostanoid rec. inh.) also ↓ flushing
• Dyspepsia, vomiting & diarrhea; Peptic ulcer
• Long-term effects Liver dysfunction & diabetes
• Risk of myopathy due to statins ↑
114. Use
1. Used to lower VLDL & TGs and raise HDL levels
2. Adjunctive drug to statins/fibrates
3. Pancreatitis associated with severe
hypertriglyceridaemia
• Due to marked s/e, use restricted to high risk cases
only
115. Ezetimibe
• Interferes with a specific CH transport protein
NPC1L1 in the intestinal mucosa and reduces
absorption of both dietary and biliary CH
• Ezetimibe + low dose statin As effective in
lowering LDL-CH as high dose of statin alone
• Well tolerated
In aplastic anemia, the bone marrow is described in medical terms as aplastic or hypoplastic — meaning that it's empty (aplastic) or contains very few blood cells (hypoplastic).
Hypoplasia is the incomplete development or underdevelopment of an organ or tissue. Hence, organs or tissue affected by hypoplasia have a below average number of cells.
Ingested iron is absorbed from the intestinal mucosa into the circulation, where it is bound to transferrin. Iron is distributed to tissues for incorporation into hemoglobin, myoglobin, and enzymes, or it is stored as ferritin. After about 120 days, erythrocytes are degraded by reticuloendothelial cells, and the iron is returned to the plasma or stored. Reticuloendothelial System (RES) consists of cells descending from the monocytes which are able to perform phagocytosis of foreign materials and particles. 90% of the RES are located in the liver
a swollen state caused by retention of fluid or gas
Erythropoietin (EPO) is a hormone produced primarily by the kidneys. It plays a key role in the production of red blood cells (RBCs), which carry oxygen from the lungs to the rest of the body.
Ppt. proteins & toughen the surface
Megaloblastic anemia is a condition in which the bone marrow produces unusually large, structurally abnormal, immature red blood cells (megaloblasts).
Folinic acid (Leucovorin, citrovorum factor, 5formylTHFA) which is an active coenzyme form, is used in this condition.
Hematopoiesis is the production of all of the cellular components of blood and blood plasma. It occurs within the hematopoietic system, which includes organs and tissues such as the bone marrow, liver, and spleen.
. A, Dietary folate is reduced by
folate reductase to tetrahydrofolate (H4-folate). Single-carbon units are added to H4-folate to form active folate,
which donates single-carbon units in the synthesis of pyrimidine and purine bases and amino acids. B, The two
active forms of vitamin B12 are methylcobalamin and deoxyadenosylcobalamin. These forms are cofactors for
methylation reactions, including the conversion of homocysteine to methionine and the conversion of methylmalonyl-CoA to succinyl-CoA. Methyl H4-folate donates a methyl group to cobalamin to form
methylcobalamin.
Megaloblastic anemia is a condition in which the bone marrow produces unusually large, structurally abnormal, immature red blood cells (megaloblasts).
Hemostasis is a collective word for several processes that causes bleeding to stop. Briefly, there are three major processes that will help bleeding to stop when a blood vessel has been damaged. First, the blood vessel will compress and become narrower (vasoconstriction). Second, platelets (thrombocytes) adhere to the damaged walls of the blood vessel, and also to each other, to form a platelet plug (primary hemostasis). Third, though the process called coagulation, fibrinogen is converted to fibrin. A meshwork of cross-linked fibrin forms around the platelet plug to stabilize it (secondary hemostasis); a blood clot has formed. Hemostasis most often has a positive connotation, as this is the process that helps bleeding to stop. Thrombosis (blood clotting), on the other hand, is most often used when there is a problem. This is the process in which a thrombus (blood clot) forms inside a blood vessel, without the rupture of any blood vessel. For instance, when a blood clot has formed that obstructs the blood flow in a vessel such as in the condition Deep Vein Thrombosis (DVT).
So, the absolutely simplest way to define the three words is the following:
hemostasis = vasoconstriction + primary hemostasis + secondary hemostasis
thrombosis = primary hemostasis + secondary hemostasis
coagulation = secondary hemostasis
. (1) When a small blood vessel is injured, vasospasm reduces blood flow and facilitates platelet aggregation and coagulation. (2) The platelets, which adhere to extravascular collagen, are activated to release mediators that cause platelet aggregation and the formation of a platelet plug to arrest bleeding. (3) Exposure of the blood to tissue factors also activates coagulation and leads to the formation of a fibrin clot, which arrests bleeding until the vessel is repaired. (4) After the vessel is repaired, the clot is removed by the process of fibrinolysis.
Factor I - fibrinogen
Factor II - prothrombin
Factor III - tissue thromboplastin (tissue factor)
Factor IV - ionized calcium ( Ca++ )
Factor V - labile factor or proaccelerin
Factor VI - unassigned
Factor VII - stable factor or proconvertin
Factor VIII - antihemophilic factor
Factor IX - plasma thromboplastin component, Christmas factor
Factor X - Stuart-Prower factor
Factor XI - plasma thromboplastin antecedent
Factor XII - Hageman factor
Factor XIII - fibrin-stabilizing factor
Haemophilia is an inherited bleeding disorder where the blood doesn't clot properly.
Pooled Human Plasma from Innovative Research is apheresis derived. The plasma is collected from donors in an FDA-approved collection center. The plasma is collected via apheresis, aliquoted to customer specifications, and frozen. Apheresis is a medical procedure that involves removing whole blood from a donor or patient and separating the blood into individual components so that one particular component can be removed. The remaining blood components then are re-introduced back into the bloodstream of the patient or donor. a portion of a larger whole, especially a sample taken for chemical analysis or other treatment
situated or occurring outside the body
Dialysate, also called dialysis fluid, dialysis solution or bath, is a solution of pure water, electrolytes and salts, such as bicarbonate and sodium. The purpose of dialysate is to pull toxins from the blood into the dialysate. The way this works is through a process called diffusion.
digestion or depolymerization of longer chains of heparin into shorter chains by chemical or enzymatic means. Interaction of heparin and related anticoagulants with antithrombin III (AT-III). (1, 2) Heparin and related drugs bind to the pentasaccharide-binding site on AT-III. (3) Anticoagulant–AT-III complexes inactivate factor Xa (active Stuart factor). (4) Unfractionated heparin–AT-III also inactivates thrombin, whereas low-molecular-weight heparin–AT-III and fondaparinux–AT-III produce little or no inactivation of thrombin, respectively.
Antithrombin III is a protein in the blood that blocks abnormal blood clots from forming
a discoloration of the skin resulting from bleeding underneath, typically caused by bruising
In healthy people an INR of 1.1 or below is considered normal. An INR range of 2.0 to 3.0 is generally an effective therapeutic range for people taking warfarin for disorders such as atrial fibrillation or a blood clot in the leg or lung
INR is advised to monitor the thinning drug’s medication like warfarin therapy. international standard for the PT
(A) Excess platelet and less fibrin, thus called white clot Less platelet and more fibrin, thus termed red clot (V) Example MI, Stroke, Peripheral artery diseases Deep vein thrombosis
Defibrination syndrome or ‘disseminated intravascular coagulation’ occurs in abruptio placentae and other obstetric conditions, certain malignancies and infections. The coagulation factors get consumed for the formation of intravascular microclots and blood is incoagulable. Abruptio placentae is defined as the premature separation of the placenta from the uterus.
A clot that adheres to a vessel wall is called a “thrombus,” whereas an intravascular clot that floats in the blood is termed an “embolus.” Thus, a detached thrombus becomes an embolus.
(protease-activated receptor, PAR-1) antagonist
A transient ischemic attack (TIA) is a brief episode of neurological dysfunction caused by loss of blood flow (ischemia) in the brain, spinal cord, or retina, without tissue death (infarction)
cramping pain in the leg
Sequester: 1. In medicine, to set apart, detach or separate a small portion of tissue from the rest.
Dec. CH Activation of SREBP2 (transc. Factor) Upregul. Of genes encoding for LDL R; liver cells
resin is a solid or highly viscous substance of plant or synthetic origin that is typically convertible into polymers; isolate
Lipoprotein lipase (LPL) is an extracellular enzyme on the vascular endothelial surface that degrades circulating triglycerides in the bloodstream. These triglycerides are embedded in very low-density lipoproteins (VLDL) and in chylomicrons that travel through the bloodstream. PPAR-alpha activity also increases the oxidation of fatty acids in the liver, which leads to decreased levels of very low-density lipoprotein. Ultimately, this leads to decreased serum triglyceride levels, as they increase hydrolysis of VLDL and chylomicron triglycerides via lipoprotein lipase.
VLDL and LDL contain TGs; Niacin inhibits lipolysis in adipose tissue, resulting in decreased hepatic VLDL synthesis and production of LDLs in the plasma
Niacin inhibits lipolysis in adipose
tissue, resulting in decreased hepatic
VLDL synthesis and production of
LDLs in the plasma
Dyspepsia, also known as indigestion, refers to discomfort or pain that occurs in the upper abdomen, often after eating or drinking.
Ezetimibe inhibits the absorption of dietary
and biliary cholesterol from the intestines. The HMG-CoA reductase inhibitors block the rate-limiting step in
cholesterol biosynthesis. The bile acid–binding resins inhibit the reabsorption of bile acids from the gut. Niacin
inhibits the secretion of very-low-density lipoproteins (VLDLs) from the liver, and fibrates such as gemfibrozil
stimulate lipoprotein lipase to increase the hydrolysis of VLDL triglycerides and the delivery of fatty acids to
adipose and other tissues. IDL, Intermediate-density lipoprotein; LL, lipoprotein lipase.