Anti inflammatory drugs
Non steroidal anti inflammatory drugs
steroids
mechanism of action of anti inflammatory drugs
adverse effects of drugs
contraindications of anti inflammatory agents
uses of anti inflammatory drugs
dose rates of anti inflammatory agents
list of anti inflammatory drugs
This document discusses drugs that act on the autonomic nervous system. It focuses on the parasympathetic nervous system neurotransmitter acetylcholine and drugs that interact with acetylcholine receptors. Acetylcholine is the major neurotransmitter of the parasympathetic nervous system and activates muscarinic and nicotinic receptors. Drugs that mimic acetylcholine, called cholinergic drugs, directly activate muscarinic receptors or indirectly increase acetylcholine levels by inhibiting the acetylcholinesterase enzyme. Examples include pilocarpine, neostigmine, and organophosphate pesticides. Anticholinergic drugs such as atropine competitively block muscarinic receptors, producing effects like tachy
The document discusses various antipyretic drugs, including their mechanisms of action, pharmacological effects, clinical uses, and side effects. It provides details on common antipyretic drugs like paracetamol, aspirin, meloxicam, and piroxicam. The drugs are used to reduce fever and inflammation, and help relieve pain, with their effects stemming from inhibition of prostaglandin synthesis.
A brief Presentation of Pharmacology on the Drug " Physostigmine " . Includes origin ,Indication, uses, treatment, trade name pharmacodynamics, side effects,
References -https://en.wikipedia.org/wiki/Physostigmine
The document provides information on analgesics used in dentistry, including classifications, mechanisms of action, uses, and side effects. It discusses both opioid analgesics like morphine and codeine as well as non-opioid analgesics/NSAIDs like aspirin, ibuprofen, indomethacin, piroxicam, and paracetamol. It notes that NSAIDs work by inhibiting prostaglandin synthesis and describes considerations for patients taking common analgesics like aspirin.
Codeine is a commonly used antitussive (cough suppressant) that works by raising the stimulus threshold of the cough center in the brain. It is effective at reducing coughs by 40-60% compared to placebos. Codeine is also a mild opioid analgesic. Other antitussives include dextromethorphan (non-opioid), expectorants like guaifenesin to loosen mucus, and mucolytics like acetylcysteine that work to liquefy mucus in the respiratory tract.
This document discusses cholinergic agonists, which are drugs that act on receptors activated by acetylcholine in the autonomic nervous system. It describes the synthesis and mechanisms of acetylcholine as a neurotransmitter. It then discusses various direct-acting cholinergic agonists like bethanechol, carbachol, and pilocarpine and their actions and uses. Pilocarpine is used topically to treat glaucoma by contracting the iris and ciliary muscles. The document also covers indirect agonists known as anticholinesterases, which inhibit the enzyme acetylcholinesterase and thereby increase acetylcholine levels. Physostigmine is an example of a reversible anticholinesterase
The document discusses antiseptics and disinfectants used to kill or inhibit microorganisms. It describes different categories of antiseptics including phenols, alcohols, aldehydes, acids, metallic salts, dyes, and ectoparasiticides. It provides examples of common antiseptics such as iodine, chlorhexidine, and hydrogen peroxide. It also outlines the mechanisms of action, uses, and properties of various antiseptics and disinfectants.
This document discusses drugs that act on the autonomic nervous system, specifically cholinergic and anticholinergic drugs. It begins by explaining that cholinergic drugs act on acetylcholine receptors, while anticholinergic drugs block these receptors. Acetylcholine is described as the neurotransmitter of the cholinergic system. Examples of direct and indirect acting cholinergic drugs are provided. Clinical uses and effects of specific cholinergic drugs like Bethanechol and Pilocarpine are summarized. Common anticholinergic drugs such as Atropine are also discussed in detail, outlining their mechanisms and therapeutic uses in conditions like peptic ulcer disease and asthma. Side effects of anticholinergic over
This document discusses drugs that act on the autonomic nervous system. It focuses on the parasympathetic nervous system neurotransmitter acetylcholine and drugs that interact with acetylcholine receptors. Acetylcholine is the major neurotransmitter of the parasympathetic nervous system and activates muscarinic and nicotinic receptors. Drugs that mimic acetylcholine, called cholinergic drugs, directly activate muscarinic receptors or indirectly increase acetylcholine levels by inhibiting the acetylcholinesterase enzyme. Examples include pilocarpine, neostigmine, and organophosphate pesticides. Anticholinergic drugs such as atropine competitively block muscarinic receptors, producing effects like tachy
The document discusses various antipyretic drugs, including their mechanisms of action, pharmacological effects, clinical uses, and side effects. It provides details on common antipyretic drugs like paracetamol, aspirin, meloxicam, and piroxicam. The drugs are used to reduce fever and inflammation, and help relieve pain, with their effects stemming from inhibition of prostaglandin synthesis.
A brief Presentation of Pharmacology on the Drug " Physostigmine " . Includes origin ,Indication, uses, treatment, trade name pharmacodynamics, side effects,
References -https://en.wikipedia.org/wiki/Physostigmine
The document provides information on analgesics used in dentistry, including classifications, mechanisms of action, uses, and side effects. It discusses both opioid analgesics like morphine and codeine as well as non-opioid analgesics/NSAIDs like aspirin, ibuprofen, indomethacin, piroxicam, and paracetamol. It notes that NSAIDs work by inhibiting prostaglandin synthesis and describes considerations for patients taking common analgesics like aspirin.
Codeine is a commonly used antitussive (cough suppressant) that works by raising the stimulus threshold of the cough center in the brain. It is effective at reducing coughs by 40-60% compared to placebos. Codeine is also a mild opioid analgesic. Other antitussives include dextromethorphan (non-opioid), expectorants like guaifenesin to loosen mucus, and mucolytics like acetylcysteine that work to liquefy mucus in the respiratory tract.
This document discusses cholinergic agonists, which are drugs that act on receptors activated by acetylcholine in the autonomic nervous system. It describes the synthesis and mechanisms of acetylcholine as a neurotransmitter. It then discusses various direct-acting cholinergic agonists like bethanechol, carbachol, and pilocarpine and their actions and uses. Pilocarpine is used topically to treat glaucoma by contracting the iris and ciliary muscles. The document also covers indirect agonists known as anticholinesterases, which inhibit the enzyme acetylcholinesterase and thereby increase acetylcholine levels. Physostigmine is an example of a reversible anticholinesterase
The document discusses antiseptics and disinfectants used to kill or inhibit microorganisms. It describes different categories of antiseptics including phenols, alcohols, aldehydes, acids, metallic salts, dyes, and ectoparasiticides. It provides examples of common antiseptics such as iodine, chlorhexidine, and hydrogen peroxide. It also outlines the mechanisms of action, uses, and properties of various antiseptics and disinfectants.
This document discusses drugs that act on the autonomic nervous system, specifically cholinergic and anticholinergic drugs. It begins by explaining that cholinergic drugs act on acetylcholine receptors, while anticholinergic drugs block these receptors. Acetylcholine is described as the neurotransmitter of the cholinergic system. Examples of direct and indirect acting cholinergic drugs are provided. Clinical uses and effects of specific cholinergic drugs like Bethanechol and Pilocarpine are summarized. Common anticholinergic drugs such as Atropine are also discussed in detail, outlining their mechanisms and therapeutic uses in conditions like peptic ulcer disease and asthma. Side effects of anticholinergic over
Pharmacodynamics is the study of how drugs act on the body and their mechanisms of action. It involves drug-receptor interactions and explains the relation between drug effects. Pharmacodynamics provides a basis for rational drug use and design. Drugs can act through stimulation, depression, irritation, replacement or cytotoxic effects on cells. Their main targets are receptors, ion channels, enzymes, and transporter proteins. Understanding drug-receptor interactions is important for explaining drug effects and determining their potency and efficacy. Drug interactions can enhance or reduce the effects of drugs and should be considered when administering multiple medications.
This document discusses the autonomic nervous system and cholinergic transmission. It describes how drugs can have parasympathomimetic or parasympatholytic effects by stimulating or opposing muscarinic receptors. There are three main types of muscarinic receptors (M1, M2, M3) located throughout the body. Drugs that stimulate muscarinic receptors can be direct acting parasympathomimetics or indirect acting via inhibiting acetylcholinesterase. Common cholinergic drugs and their effects/indications are also outlined.
This document discusses sedative, hypnotic, and anxiolytic drugs. It describes barbiturates and benzodiazepines, which are commonly used as sedative-hypnotics. Barbiturates act by potentiating the inhibitory neurotransmitter GABA, while benzodiazepines facilitate GABA effects by binding to GABAA receptors. The document outlines the mechanisms, effects on sleep, and adverse effects of these drug classes. It also discusses newer nonbenzodiazepine hypnotics and the benzodiazepine antagonist flumazenil.
Drugs acting on the GI system include:
- Antiemetics which prevent nausea and vomiting like ondansetron and metoclopramide.
- Laxatives and purgatives like lactulose, bisacodyl, and docusate which are used to treat constipation.
- Antacids such as aluminum hydroxide, magnesium hydroxide, and calcium carbonate which neutralize stomach acid.
- Cholinergic drugs which increase GI motility and secretions. Anticholinergic drugs block acetylcholine and decrease motility and secretions.
Diabetes mellitus is a metabolic disorder characterized by hyperglycemia. There are two major types: insulin-dependent diabetes mellitus (IDDM) and non-insulin dependent diabetes mellitus (NIDDM). Insulin is secreted by pancreatic beta cells and helps regulate blood sugar levels. It is essential for treating IDDM and sometimes needed for NIDDM. Oral hypoglycemic drugs like sulfonylureas and thiazolidinediones are also used to treat NIDDM by stimulating insulin secretion or improving insulin sensitivity. Both insulin and oral hypoglycemic drugs can cause hypoglycemia as an adverse reaction if not used properly.
This document discusses histamine and antihistamines. It begins by introducing histamine, describing its discovery and roles in allergic reactions and as a neurotransmitter. It then covers histamine's chemistry, distribution in the body, synthesis, storage, and metabolism. The document discusses the four types of histamine receptors (H1-H4) and histamine's pharmacological effects. It also provides details on antihistamines, including their pharmacokinetics, mechanisms of action, side effects, and classifications of first versus second generation antihistamines. The document concludes by mentioning clinical uses of histamine and antihistamines for conditions like allergies and gastric hypersecretions.
Salbutamol is a short-acting bronchodilator used to treat conditions such as asthma and COPD. It works by stimulating beta-2 receptors in the lungs, relaxing the airways. Common side effects include palpitations, tremors, and anxiety. It is administered via inhaler or orally and works within a few minutes to rapidly improve breathing.
This document summarizes inflammation and anti-inflammatory drugs. It describes the phases of inflammation, signs of inflammation, and mediators of the inflammatory response such as histamine, bradykinin, prostaglandins, and leukotrienes. It then discusses nonsteroidal anti-inflammatory drugs (NSAIDs) and their mechanisms of action by inhibiting cyclooxygenase enzymes and decreasing prostaglandin synthesis. Common NSAIDs are described including their pharmacological properties, mechanisms of action, therapeutic uses, and potential adverse effects such as gastrointestinal issues and bleeding risks.
Anticholinergic drugs work by blocking the effects of the neurotransmitter acetylcholine at muscarinic receptors in the central and peripheral nervous systems. The main anticholinergic drugs discussed are atropine, glycopyrrolate, and scopolamine. Atropine is a naturally occurring tertiary amine that can cross the blood-brain barrier and exert central effects. Glycopyrrolate is a synthetic quaternary ammonium compound that does not cross the blood-brain barrier and lacks central effects. Scopolamine is similar to atropine but is more potent and lipid soluble, allowing it to more easily cross the blood-brain barrier and exert greater central antimuscarinic effects than atrop
coagulants in detail with all drugs, mechanism of action, advantages, adverse effect, contraindication with example and pictures.
in simplified manner , easy to understand
cholinergic receptors definetion and classifcation to 1-nicotinic and 2-muscarinic ...and their subtybes ..... then the sites and the mechanism ... and last the drugs effect
Chlorpheniramine is a mild sedative antihistamine that works by blocking the H1 receptor and preventing histamine from causing allergic symptoms. It is used to treat allergic conditions like hay fever and rhinitis. Common side effects include drowsiness, dry mouth, and dizziness. Nurses should monitor patients for signs of central nervous system depression and educate patients to avoid driving or other hazardous activities until their response to the drug is known.
This document defines local anesthetics and describes their properties and mechanisms of action. It discusses various local anesthetics including lidocaine, prilocaine, bupivacaine, ropivacaine, dibucaine, benzocaine, butamben, and oxethazaine. It covers their uses for surface anesthesia, infiltration, nerve blocks, epidurals, and other techniques. Complications are also summarized.
Pharmacokinetics is the study of the movement of drug molecules in the body. It includes absorption, distribution, metabolism, and excretion of drugs. Pharmacokinetics is the study of what happens to drugs once they enter the body (the movement of the drugs into, within, and out of the body). For a drug to produce its specific response, it should be present in adequate concentrations at the site of action. This depends on various factors apart from the dose.
Four pharmacokinetic properties determine the onset, intensity, and the duration of drug action (Figure 1.6.1):
• Absorption: First, absorption from the site of administration permits entry of the drug (either directly or indirectly) into plasma.
• Distribution: Second, the drug may then reversibly leave the bloodstream and distribute it into the interstitial and intracellular fluids.
• Metabolism: Third, the drug may be biotransformed by metabolism by the liver or other tissues.
• Elimination: Finally, the drug and its metabolites are eliminated from the body in urine, bile, or feces.
In short, pharmacokinetics means what the body does to the drug.
The document summarizes key aspects of the nervous system, including the central nervous system (brain and spinal cord), peripheral nervous system, and autonomic nervous system. It describes the sympathetic and parasympathetic divisions of the autonomic nervous system which provide involuntary control of organs. It also outlines the basic structure and function of neurons, neurotransmission, and the roles of key neurotransmitters like acetylcholine and norepinephrine.
This document provides information on nonsteroidal anti-inflammatory drugs (NSAIDs) and antipyretic-analgesics. It discusses the classes of NSAIDs including mechanisms of action, therapeutic uses, examples of drugs, and side effects. NSAIDs work by inhibiting cyclooxygenase enzymes and thereby reducing production of prostaglandins involved in inflammation, pain, and fever. The document also reviews antirheumatic drugs for conditions like rheumatoid arthritis, as well as drugs for treating gout such as allopurinol, probenecid, and corticosteroids.
Just the type of presentation a top presenter would look for.
The topic is well introduced, the designs of the slides are simple yet the explanation is very powerful.
Oral hypoglycemic drugs are used only in the treatment of type 2 diabetes which is a disorder involving resistance to secreted insulin. Type 1 diabetes involves a lack of insulin and requires insulin for treatment. There are now four classes of hypoglycemic drugs:
This document discusses nonsteroidal anti-inflammatory drugs (NSAIDs), including their classification, mechanisms of action, examples of different drug classes, and pharmacological effects. It focuses on aspirin as the prototype NSAID, describing its absorption, metabolism, uses, adverse effects, and interactions. Selective COX-2 inhibitors like celecoxib and rofecoxib are also introduced as NSAIDs with reduced gastric irritation.
anti inflammatory drugs and inflammation.pptxadesholakhaliid
Inflammation is the body's response to injury and involves vascularized tissue. NSAIDs can relieve pain and inflammation without the adverse effects of corticosteroids but have their own risks. NSAIDs work by inhibiting cyclooxygenase and reducing prostaglandin biosynthesis. Common NSAIDs include flunixin, ketoprofen, naproxen, and meloxicam. Flunixin is used to treat pain and inflammation in various species but its use is contraindicated in some cases due to risks of adverse effects like gastrointestinal distress.
- Gout is caused by elevated uric acid levels in the blood (hyperuricemia) which can lead to the deposition of urate crystals in the joints, causing inflammation and pain.
- There are different treatments for the acute attacks and long-term management. For acute attacks, NSAIDs or corticosteroids can be used to reduce pain and inflammation. Colchicine may also be used.
- For long-term management and prevention of recurrent attacks, allopurinol is commonly prescribed to lower uric acid levels by inhibiting its production. Probenecid or other uricosuric
Pharmacodynamics is the study of how drugs act on the body and their mechanisms of action. It involves drug-receptor interactions and explains the relation between drug effects. Pharmacodynamics provides a basis for rational drug use and design. Drugs can act through stimulation, depression, irritation, replacement or cytotoxic effects on cells. Their main targets are receptors, ion channels, enzymes, and transporter proteins. Understanding drug-receptor interactions is important for explaining drug effects and determining their potency and efficacy. Drug interactions can enhance or reduce the effects of drugs and should be considered when administering multiple medications.
This document discusses the autonomic nervous system and cholinergic transmission. It describes how drugs can have parasympathomimetic or parasympatholytic effects by stimulating or opposing muscarinic receptors. There are three main types of muscarinic receptors (M1, M2, M3) located throughout the body. Drugs that stimulate muscarinic receptors can be direct acting parasympathomimetics or indirect acting via inhibiting acetylcholinesterase. Common cholinergic drugs and their effects/indications are also outlined.
This document discusses sedative, hypnotic, and anxiolytic drugs. It describes barbiturates and benzodiazepines, which are commonly used as sedative-hypnotics. Barbiturates act by potentiating the inhibitory neurotransmitter GABA, while benzodiazepines facilitate GABA effects by binding to GABAA receptors. The document outlines the mechanisms, effects on sleep, and adverse effects of these drug classes. It also discusses newer nonbenzodiazepine hypnotics and the benzodiazepine antagonist flumazenil.
Drugs acting on the GI system include:
- Antiemetics which prevent nausea and vomiting like ondansetron and metoclopramide.
- Laxatives and purgatives like lactulose, bisacodyl, and docusate which are used to treat constipation.
- Antacids such as aluminum hydroxide, magnesium hydroxide, and calcium carbonate which neutralize stomach acid.
- Cholinergic drugs which increase GI motility and secretions. Anticholinergic drugs block acetylcholine and decrease motility and secretions.
Diabetes mellitus is a metabolic disorder characterized by hyperglycemia. There are two major types: insulin-dependent diabetes mellitus (IDDM) and non-insulin dependent diabetes mellitus (NIDDM). Insulin is secreted by pancreatic beta cells and helps regulate blood sugar levels. It is essential for treating IDDM and sometimes needed for NIDDM. Oral hypoglycemic drugs like sulfonylureas and thiazolidinediones are also used to treat NIDDM by stimulating insulin secretion or improving insulin sensitivity. Both insulin and oral hypoglycemic drugs can cause hypoglycemia as an adverse reaction if not used properly.
This document discusses histamine and antihistamines. It begins by introducing histamine, describing its discovery and roles in allergic reactions and as a neurotransmitter. It then covers histamine's chemistry, distribution in the body, synthesis, storage, and metabolism. The document discusses the four types of histamine receptors (H1-H4) and histamine's pharmacological effects. It also provides details on antihistamines, including their pharmacokinetics, mechanisms of action, side effects, and classifications of first versus second generation antihistamines. The document concludes by mentioning clinical uses of histamine and antihistamines for conditions like allergies and gastric hypersecretions.
Salbutamol is a short-acting bronchodilator used to treat conditions such as asthma and COPD. It works by stimulating beta-2 receptors in the lungs, relaxing the airways. Common side effects include palpitations, tremors, and anxiety. It is administered via inhaler or orally and works within a few minutes to rapidly improve breathing.
This document summarizes inflammation and anti-inflammatory drugs. It describes the phases of inflammation, signs of inflammation, and mediators of the inflammatory response such as histamine, bradykinin, prostaglandins, and leukotrienes. It then discusses nonsteroidal anti-inflammatory drugs (NSAIDs) and their mechanisms of action by inhibiting cyclooxygenase enzymes and decreasing prostaglandin synthesis. Common NSAIDs are described including their pharmacological properties, mechanisms of action, therapeutic uses, and potential adverse effects such as gastrointestinal issues and bleeding risks.
Anticholinergic drugs work by blocking the effects of the neurotransmitter acetylcholine at muscarinic receptors in the central and peripheral nervous systems. The main anticholinergic drugs discussed are atropine, glycopyrrolate, and scopolamine. Atropine is a naturally occurring tertiary amine that can cross the blood-brain barrier and exert central effects. Glycopyrrolate is a synthetic quaternary ammonium compound that does not cross the blood-brain barrier and lacks central effects. Scopolamine is similar to atropine but is more potent and lipid soluble, allowing it to more easily cross the blood-brain barrier and exert greater central antimuscarinic effects than atrop
coagulants in detail with all drugs, mechanism of action, advantages, adverse effect, contraindication with example and pictures.
in simplified manner , easy to understand
cholinergic receptors definetion and classifcation to 1-nicotinic and 2-muscarinic ...and their subtybes ..... then the sites and the mechanism ... and last the drugs effect
Chlorpheniramine is a mild sedative antihistamine that works by blocking the H1 receptor and preventing histamine from causing allergic symptoms. It is used to treat allergic conditions like hay fever and rhinitis. Common side effects include drowsiness, dry mouth, and dizziness. Nurses should monitor patients for signs of central nervous system depression and educate patients to avoid driving or other hazardous activities until their response to the drug is known.
This document defines local anesthetics and describes their properties and mechanisms of action. It discusses various local anesthetics including lidocaine, prilocaine, bupivacaine, ropivacaine, dibucaine, benzocaine, butamben, and oxethazaine. It covers their uses for surface anesthesia, infiltration, nerve blocks, epidurals, and other techniques. Complications are also summarized.
Pharmacokinetics is the study of the movement of drug molecules in the body. It includes absorption, distribution, metabolism, and excretion of drugs. Pharmacokinetics is the study of what happens to drugs once they enter the body (the movement of the drugs into, within, and out of the body). For a drug to produce its specific response, it should be present in adequate concentrations at the site of action. This depends on various factors apart from the dose.
Four pharmacokinetic properties determine the onset, intensity, and the duration of drug action (Figure 1.6.1):
• Absorption: First, absorption from the site of administration permits entry of the drug (either directly or indirectly) into plasma.
• Distribution: Second, the drug may then reversibly leave the bloodstream and distribute it into the interstitial and intracellular fluids.
• Metabolism: Third, the drug may be biotransformed by metabolism by the liver or other tissues.
• Elimination: Finally, the drug and its metabolites are eliminated from the body in urine, bile, or feces.
In short, pharmacokinetics means what the body does to the drug.
The document summarizes key aspects of the nervous system, including the central nervous system (brain and spinal cord), peripheral nervous system, and autonomic nervous system. It describes the sympathetic and parasympathetic divisions of the autonomic nervous system which provide involuntary control of organs. It also outlines the basic structure and function of neurons, neurotransmission, and the roles of key neurotransmitters like acetylcholine and norepinephrine.
This document provides information on nonsteroidal anti-inflammatory drugs (NSAIDs) and antipyretic-analgesics. It discusses the classes of NSAIDs including mechanisms of action, therapeutic uses, examples of drugs, and side effects. NSAIDs work by inhibiting cyclooxygenase enzymes and thereby reducing production of prostaglandins involved in inflammation, pain, and fever. The document also reviews antirheumatic drugs for conditions like rheumatoid arthritis, as well as drugs for treating gout such as allopurinol, probenecid, and corticosteroids.
Just the type of presentation a top presenter would look for.
The topic is well introduced, the designs of the slides are simple yet the explanation is very powerful.
Oral hypoglycemic drugs are used only in the treatment of type 2 diabetes which is a disorder involving resistance to secreted insulin. Type 1 diabetes involves a lack of insulin and requires insulin for treatment. There are now four classes of hypoglycemic drugs:
This document discusses nonsteroidal anti-inflammatory drugs (NSAIDs), including their classification, mechanisms of action, examples of different drug classes, and pharmacological effects. It focuses on aspirin as the prototype NSAID, describing its absorption, metabolism, uses, adverse effects, and interactions. Selective COX-2 inhibitors like celecoxib and rofecoxib are also introduced as NSAIDs with reduced gastric irritation.
anti inflammatory drugs and inflammation.pptxadesholakhaliid
Inflammation is the body's response to injury and involves vascularized tissue. NSAIDs can relieve pain and inflammation without the adverse effects of corticosteroids but have their own risks. NSAIDs work by inhibiting cyclooxygenase and reducing prostaglandin biosynthesis. Common NSAIDs include flunixin, ketoprofen, naproxen, and meloxicam. Flunixin is used to treat pain and inflammation in various species but its use is contraindicated in some cases due to risks of adverse effects like gastrointestinal distress.
- Gout is caused by elevated uric acid levels in the blood (hyperuricemia) which can lead to the deposition of urate crystals in the joints, causing inflammation and pain.
- There are different treatments for the acute attacks and long-term management. For acute attacks, NSAIDs or corticosteroids can be used to reduce pain and inflammation. Colchicine may also be used.
- For long-term management and prevention of recurrent attacks, allopurinol is commonly prescribed to lower uric acid levels by inhibiting its production. Probenecid or other uricosuric
This document discusses the pathophysiology, treatment, and pharmacology of gout. It covers the following key points:
1) Gout is caused by the buildup of uric acid crystals in the joints due to high levels of uric acid in the blood. It discusses the biochemical pathway involved in uric acid production.
2) Treatment involves managing acute gout attacks with NSAIDs or colchicine, and lowering uric acid levels long-term with xanthine oxidase inhibitors like allopurinol and febuxostat, or uricosuric drugs like probenecid.
3) Colchicine provides rapid relief of gout attacks but has gastrointestinal side
There are over 127 types of arthritis. This document discusses gout, which is caused by uric acid crystals forming in the joints due to abnormally high levels of uric acid in the blood (hyperuricemia). Gout can cause acute attacks of severe pain and inflammation. Treatment involves drugs to terminate attacks, prevent complications, and manage chronic gout through reducing uric acid production or increasing excretion. Key drugs discussed are colchicine, NSAIDs, corticosteroids for acute gout and allopurinol, probenecid, sulfinpyrazone for chronic management and uric acid control.
The patient is experiencing recurrent acute attacks of severe joint pain characteristic of gout. For the acute attacks, the GP should prescribe a potent non-steroidal anti-inflammatory drug (NSAID) or corticosteroid to reduce pain and inflammation. The rheumatologist can test the patient's blood and joint fluid for uric acid crystals to confirm a diagnosis of gout. Gout is caused by elevated uric acid levels leading to urate crystal deposition in joints. NSAIDs, colchicine, or corticosteroids can treat acute gout attacks, while allopurinol or probenecid given long-term can prevent recurrent attacks by lowering uric acid levels.
drugs used in hormonal disorders supplementation.pptxJayesh Patidar
This document discusses several classes of drugs used to treat hormonal disorders and for contraception and abortion. It provides details on mechanisms of action, examples of drugs and their doses, indications for use, adverse effects, contraindications, drug interactions, and nursing responsibilities for:
- Insulin and oral hypoglycemics for diabetes mellitus
- Thyroid supplements and suppressants for hypothyroidism and hyperthyroidism
- Anabolic steroids to promote tissue building
- Oral contraceptives and other estrogens/progestins for contraception
- Corticotrophins, gonadotrophins, and other hormones
Drugs used in hormonal disorders & supplementation etcMr. Dipti sorte
This document discusses drugs used for hormonal disorders and supplementation, contraception, and medical termination of pregnancy. It covers several categories of drugs including:
- Insulin and oral hypoglycemics used to treat diabetes by lowering blood glucose.
- Thyroid supplements and suppressants that control metabolic rate by increasing or decreasing thyroid hormone levels.
- Uterine stimulants and relaxants that respectively increase or decrease uterine contractions, used for labor induction/augmentation or to prevent preterm labor.
- Oral contraceptives, anabolic steroids, and abortifacients (drugs that induce abortion) are also mentioned.
The document discusses gout, including its causes, symptoms, diagnosis and treatment. It is a metabolic disorder caused by elevated uric acid levels (hyperuricemia) which can be due to overproduction or underexcretion of uric acid. Gout causes sudden, severe attacks of pain and inflammation in joints due to urate crystals depositing in the joints. Treatment involves drugs to relieve acute attacks like NSAIDs or colchicine, and long term drugs like allopurinol or probenecid to lower uric acid levels and prevent future attacks.
Gastrointestinal medications are used to treat various GI conditions. They include stimulants, anticholinergics, antidiarrheals, laxatives, antacids, and protective agents. Nursing considerations include monitoring for side effects, ensuring proper administration, and educating clients. The goal is to relieve GI symptoms while preventing complications related to medication effects or interactions.
Drugs used in hormonal disorders supplementation etc.Abhay Rajpoot
The endocrine system is a chemical messenger system comprising feedback loops of the hormones released by internal glands of an organism directly into the circulatory system, regulating distant target organs.
Bronchodilators work by dilating the airways and relaxing smooth muscle. They are used to treat conditions like asthma, COPD, and bronchospasm. Common side effects include palpitations, tachycardia, headaches, and dry mouth. When administering bronchodilators, nurses monitor for cardiac issues and assess lung and breathing sounds. Patients are instructed on proper use and monitoring of their medications and symptoms.
Spondylitis is a form of arthritis that affects the spine. It causes inflammation of the spinal joints that can lead to pain, discomfort, and in advanced cases, fusion of spinal sections. Spondylitis affects men more often than women. Common types include Ankylosing Spondylitis, Pott's Disease, and Spondylodiscitis. Treatment depends on the type but may include medications like NSAIDs, biologics, DMARDs, and in some cases surgery. Exercise and physical therapy can help manage symptoms.
This document discusses the pathophysiology, clinical presentation, and management of common minor ailments including nausea/vomiting, dyspepsia, diarrhea, and constipation. It describes the causes and symptoms of each condition. For management, it recommends lifestyle modifications and discusses various pharmacological treatments including antacids, H2 receptor antagonists, proton pump inhibitors, loperamide, and lactobacillus preparations. The goal is to prevent dehydration and electrolyte loss through oral rehydration and replacement of fluids and minerals.
This document summarizes various intoxication emergencies, including ivermectin, amitraz, chocolate, and acetaminophen toxicity. Ivermectin toxicity occurs in certain dog breeds due to a genetic mutation affecting the blood-brain barrier. Signs include neurologic deficits. Treatment focuses on decontamination and supportive care. Amitraz poisoning results from topical or ingestion exposure and causes neurological and cardiovascular effects by agonizing alpha-2 receptors. Chocolate toxicity is due to methylxanthine alkaloids like theobromine and caffeine, which can cause gastrointestinal, neurological and cardiac abnormalities in dogs. Decontamination and intravenous fluid diuresis are used to treat chocolate poisoning.
This document discusses inflammatory bowel disease (IBD), including ulcerative colitis and Crohn's disease. It covers the etiology, pathogenesis, clinical features, and pharmacotherapy of IBD. Regarding treatment, it describes the use of 5-aminosalicylic acids, corticosteroids, immunomodulators, antibiotics/probiotics, biological therapies targeting TNF-α, and newer non-TNF-α inhibitors to induce and maintain remission of IBD. Adverse effects of the different drug classes are also outlined.
This document discusses antidiarrheal agents including opioid agonists like loperamide, bile salt-binding resins like cholestyramine, and octreotide. Opioid agonists increase colonic transit time through inhibition of nerves in the colon wall. Bile salt-binding resins bind excess bile salts in the colon that cause diarrhea. Octreotide is a synthetic somatostatin analogue that reduces intestinal secretion and slows motility, making it effective for treating diarrhea from various causes like short bowel syndrome or dumping syndrome. Potential side effects include changes in pancreatic function, gallbladder sludge, and alterations in blood sugar.
This document discusses autacoids and drugs used for the treatment of inflammatory disorders. It defines autacoids as biological factors that act like local hormones near their site of synthesis. Various classifications of autacoids are described, including biogenic amines, peptides, proteins, and membrane-derived lipids. Histamine is discussed in detail as an example autacoid. The document then covers antihistamines, their classifications, mechanisms of action, and examples of first and second generation agents. Finally, the document discusses eicosanoids and nonsteroidal anti-inflammatory drugs used for treating inflammation.
This document discusses autacoids and drugs used for the treatment of inflammatory disorders. It defines autacoids as biological factors that act like local hormones near their site of synthesis. Various classifications of autacoids are described, including biogenic amines, peptides, proteins, and membrane-derived lipids. Histamine is discussed in detail as an example autacoid. The document then covers antihistamines, their classifications, mechanisms of action, and examples of first and second generation agents. Finally, the document discusses eicosanoids and nonsteroidal anti-inflammatory drugs used for treating inflammation.
Blood transfusion in animals. How to cure hypovolemia.
blood matching. blood groups in animals. formula to transfuse blood. anemia. blood typing. indications of blood transfusion . blood collection.
Entropion is a condition where the lower eyelid turns inward, causing the eyelashes to rub against the eyeball. It can be congenital or acquired due to trauma, scarring, dehydration or other conditions. Signs include ocular discomfort, keratitis, conjunctivitis, and corneal ulcers. Diagnosis involves tests like intraocular pressure and tear tests. Treatment options include lubricating eye drops, antibiotics, temporary everting sutures, or permanent surgical procedures like modified Hotz-Celsus to correct the entropion.
This document discusses x-rays and the process of radiography. It describes the interactions of x-ray photons with matter, including Compton scattering and the photoelectric effect. It explains how differential absorption of x-rays during radiography creates an image, noting that denser tissues absorb more x-rays. Filters are used to remove low-energy x-rays, while collimators shape the beam, grids reduce scatter, and film blackness depends on factors like mAs and FFD. Intensifying screens and smaller focal spots can improve detail in radiographs.
The role of human in poultry diseases outbreakMutahirRehman
Human movement between poultry farms is the primary cause of disease outbreaks in the industry. Over 90% of disease transmission occurs due to human activity like farm visits. Strict biosecurity protocols must be followed by all people, including managers, to prevent spread. High-risk groups are work crews who visit multiple farms and backyard poultry owners who can unintentionally transmit pathogens. Preventive measures include limiting visits, thorough cleaning of vehicles and clothing, handwashing, and medical monitoring of employees. Strict employee education and adherence to biosecurity is essential to control disease spread.
Pigeons are stout, seed-eating birds with short legs and grey/white plumage. Domestic pigeons were derived from rock doves, which were among the first birds domesticated by humans as early as 10,000 years ago. Pigeons occupy a wide variety of habitats globally and have contributed importantly to humanity through their use as military messengers. They are social birds that require gentle handling and live in flocks for protection. Common health issues for pigeons include various parasites, bacteria, and viruses.
Papillomatosis, also known as warts, are caused by infection with papillomavirus. The virus infects and replicates in epithelial cells, causing excessive growth and formation of warts. Warts can occur on many species of animals. Transmission occurs through direct contact with infected animals or fomites. While usually a minor problem, warts can sometimes cause significant issues. Diagnosis involves clinical appearance and histological examination. Most cases resolve spontaneously, but cryosurgery or vaccines may aid treatment. Control relies on disinfection of environments and equipment to prevent transmission.
Newcastle disease is a contagious viral disease of birds caused by avian paramyxovirus-1. It is transmitted through contact with infected birds or their feces/secretions. Clinical signs include respiratory, neurological and intestinal symptoms with high mortality in some strains. Diagnosis involves virus isolation from samples and serological tests. Control relies on vaccination, biosecurity, and culling infected flocks.
different sites for taking pulse and respiration in sheepMutahirRehman
This document discusses how to take the temperature, pulse, and respiration of sheep and goats. It provides information on locating pulse sites like the saphenous artery and radial artery. For temperature, the thermometer should be lubricated and inserted rectally. Normal parameters are listed for goats and sheep, including a temperature range of 101.3-103.5 F, pulse of 70-80, and respiration of 14-22 for goats. Physiological factors like pregnancy and the estrus cycle can impact temperature readings.
Hippopotamus are large semi-aquatic herbivorous mammals native to sub-Saharan Africa. They are classified as artiodactyls and are the third largest type of land mammal. Hippos inhabit rivers, lakes, and mangrove swamps, congregating in groups in water during the day and dispersing at night to graze on land. They face threats from habitat loss and hunting. Proper care of captive hippos requires large enclosures with both land and water areas and a diet high in fiber. Common health issues include obesity, dental problems, and infections.
The document discusses hiatal hernia, which occurs when part of the stomach bulges through an opening in the diaphragm. It outlines the causes, symptoms, diagnosis through imaging and endoscopy, differential diagnosis, and treatment options including medication, surgery to repair the diaphragm and prevent reflux, and post-operative care. The prognosis is generally good if the hernia is repaired and complications like aspiration pneumonia are managed.
Hematopoiesis refers to the production and development of blood cells. In the early stages of embryonic development and gestation, red blood cells are produced in the yolk sac, liver, spleen and lymph nodes. After birth, red blood cell production occurs exclusively in the bone marrow. The bone marrow contains pluripotential hematopoietic stem cells that differentiate into committed stem cells and then mature blood cells through growth and differentiation inducers like erythropoietin. Erythropoietin is a hormone that stimulates red blood cell production in response to low oxygen states.
This document provides an overview of gerbil care, including their physical characteristics, habitat, diet, handling, common clinical problems, and behavior. Gerbils are small rodents native to arid regions that live in underground burrows. As pets, they require social housing, bedding to burrow in, and a diet of commercial rodent food supplemented with fruits and vegetables. Common health issues include teeth problems, trauma, tumors, and infectious diseases. Gerbils can be used in medical research due to their size and susceptibility to certain diseases.
Fish come in a wide variety of shapes and sizes and live in many different habitats around the world. They range from primitive jawless fish to sharks and rays to the over 30,000 species of bony fish. Fish are cold-blooded aquatic vertebrates that breathe through gills and have fins and scales. They can be carnivorous, herbivorous, or omnivorous depending on the species. Proper aquarium management is needed to care for fish and prevent health issues. Some diseases can potentially spread from fish to humans.
This document provides information on various first aid procedures for animals. It begins with definitions of first aid and its goals of preserving life, preventing conditions from worsening, and promoting recovery. It then covers assessing medical versus trauma cases and the priorities of airway, breathing and circulation. Specific conditions and injuries discussed include abscesses, bee stings, bandaging, bloat, burns, dehydration, difficult birth, chemical injuries, electrocution, choking, poisoning, fainting, near drowning, nosebleeds, paralysis, snake bites, and more. For each issue, it describes what to look for and provides steps for appropriate first aid treatment as well as things to avoid doing.
How to Manage Your Lost Opportunities in Odoo 17 CRMCeline George
Odoo 17 CRM allows us to track why we lose sales opportunities with "Lost Reasons." This helps analyze our sales process and identify areas for improvement. Here's how to configure lost reasons in Odoo 17 CRM
This presentation includes basic of PCOS their pathology and treatment and also Ayurveda correlation of PCOS and Ayurvedic line of treatment mentioned in classics.
A review of the growth of the Israel Genealogy Research Association Database Collection for the last 12 months. Our collection is now passed the 3 million mark and still growing. See which archives have contributed the most. See the different types of records we have, and which years have had records added. You can also see what we have for the future.
Introduction to AI for Nonprofits with Tapp NetworkTechSoup
Dive into the world of AI! Experts Jon Hill and Tareq Monaur will guide you through AI's role in enhancing nonprofit websites and basic marketing strategies, making it easy to understand and apply.
How to Build a Module in Odoo 17 Using the Scaffold MethodCeline George
Odoo provides an option for creating a module by using a single line command. By using this command the user can make a whole structure of a module. It is very easy for a beginner to make a module. There is no need to make each file manually. This slide will show how to create a module using the scaffold method.
Thinking of getting a dog? Be aware that breeds like Pit Bulls, Rottweilers, and German Shepherds can be loyal and dangerous. Proper training and socialization are crucial to preventing aggressive behaviors. Ensure safety by understanding their needs and always supervising interactions. Stay safe, and enjoy your furry friends!
Assessment and Planning in Educational technology.pptxKavitha Krishnan
In an education system, it is understood that assessment is only for the students, but on the other hand, the Assessment of teachers is also an important aspect of the education system that ensures teachers are providing high-quality instruction to students. The assessment process can be used to provide feedback and support for professional development, to inform decisions about teacher retention or promotion, or to evaluate teacher effectiveness for accountability purposes.
A workshop hosted by the South African Journal of Science aimed at postgraduate students and early career researchers with little or no experience in writing and publishing journal articles.
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This is part 1 of my Java Learning Journey. This Contains Custom methods, classes, constructors, packages, multithreading , try- catch block, finally block and more.
2. References
Theresa Welch Fossum ( 151-152)
Complications in small animal surgery ( 92 , 97-105)
Merck veterinary manual (2707-2721)
Clinical vet guide ( 1-8)
Plumb’s veterinary drug handbook
3. Inflammation
•Inflammation is the complex pathophysiological response of
vascularized tissue to injury
•The injury may result from various stimuli, including thermal,
chemical, or physical damage; ischemia; infectious agents and
antigen-antibody interactions
4.
5.
6.
7. NSAIDS
•NSAIDs have the potential to relieve pain and inflammation
without the potential metabolic, hemodynamic, and
immunosuppressive adverse effects associated with corticosteroids
•However, all NSAIDs have the potential for other adverse effects
that should be considered
8. Mode of action
•NSAIDs act primarily to reduce the biosynthesis of prostaglandins
by inhibiting Cyclooxygenase (COX)
•ln general, NSAIDs do not inhibit the formation of 5-lipoxygenase
(5-LOX) and hence leukotriene, or the formation of other
inflammatory mediators
•The novel NSAID tepoxalin is an exception in that it inhibits both
COX and 5-LOX
9. Pharmacologic effects
•All NSAlDs, except for acetaminophen ( also named paracetamol),
are antipyretic, analgesic, and anti-inflammatory
•They are routinely used for the relief of pain and inflammation
associated with osteoarthritis in dogs and horses and for colic,
navicular disease, and laminitis in horses
•As analgesics, they are generally less effective than opioids
11. Flunixin
Uses/Indications:
Alleviation of inflammation and pain associated with
musculoskeletal disorders and alleviation of visceral pain
associated with colic
In cattle for the control of pyrexia associated with BRD and
endotoxemia, and control of inflammation in endotoxemia
In ruminants, flunixin is a better analgesic for visceral pain rather
than musculoskeletal pain
May improve hemodynamics in animals with septic shock
12. Contraindications
•Flunixin should be used cautiously in animals with renal, hepatic,
or hematologic diseases
•When using to treat colic, flunixin may mask the behavioral and
cardiopulmonary signs associated with endotoxemia or intestinal
devitalization
•In horses with known or suspected EGUS, use should be
avoided; repeated doses can exacerbate gastric ulcers
•Flunixin is usually considered contraindicated in cats
13. Adverse effects
•In horses following IM injection, reports of localized swelling,
induration, stiffness, and sweating have been reported
•Do not inject intra-arterially as it may cause CNS stimulation
(hysteria), ataxia, hyperventilation, and muscle weakness
•Flunixin appears to be a relatively safe agent for use in the horse, but
the potential exists for GI intolerance, hypoproteinemia, and
hematologic abnormalities to occur
14. •IM injections may rarely be associated with clostridial myonecrosis
•Hematochezia and hematuria have been reported in cattle treated
for longer than the 3-day recommendation.
•In dogs, GI distress is the most likely adverse reaction
•Clinical signs may include, vomiting, diarrhea, and ulceration
•In birds, flunixin has been shown to cause significant renal ischemia
and nephrotoxicity
17. Ketoprofen
Uses/Indications:
•Ketoprofen is used in horses for the alleviation of inflammation and
pain associated with musculoskeletal disorders
NSAID of choice for short-term analgesia in cats
•Indicated for use in dogs and cats for the alleviation of inflammation,
lameness and pain due to osteoarthritis, hip dysplasia, disc disease,
spondylosis, panosteitis
•For the management of post-surgical pain
19. Adverse Effects
•Ketoprofen appears to have low toxicity in horses
•Potentially, gastric mucosal damage and GI ulceration, renal crest
necrosis, and mild hepatitis may occur
•Do not administer intra-arterially and avoid SC injections
•In dogs or cats, ketoprofen may cause vomiting, anorexia, and GI
ulcers
20.
21.
22.
23.
24. Meloxicam
Uses/Indications:
•Meloxicam is principally used for the symptomatic treatment of
osteoarthritis in dogs
•In for cats for the control of postoperative pain and inflammation
associated with orthopedic surgery, ovariohysterectomy and
castration pre-operatively
•In calves to treat painful procedures such as castration or
dehorning
25. Contraindications/Precautions
•It should be used with caution in patients with impaired hepatic,
cardiac or renal function and hemorrhagic disorders
•Due to its long half-life in dogs, a 5–7 day washout period after
stopping meloxicam has been recommended before starting a new
NSAID
•Use extreme caution in dehydrated, hypovolemic, or hypotensive
animals as there is a potential increased risk of renal toxicity
26. Adverse Effects
•GI distress is the most commonly reported adverse effect
•Elevation of liver enzymes, pruritis, elevated creatinine, and renal
failure
•Repeated use of meloxicam in cats is associated with renal failure and
death
27.
28.
29.
30.
31.
32. Piroxicam
Uses/Indications:
•In dogs, piroxicam may be beneficial in reducing the pain and
inflammation associated with degenerative joint disease
•Its primary use is in dogs as adjunctive treatment of bladder
transitional cell carcinoma
•It may also be of benefit in squamous cell carcinomas, mammary
adenocarcinoma, and transmissible venereal tumor (TVT)
33. Contraindications/Precautions
• Because peripheral edema has been noted in some human
patients, it should be used with caution in patients with severely
compromised cardiac function
•Piroxicam has not been evaluated for use in cats
34. Adverse Effects
•Doses as low as 1 mg/kg given daily have caused significant GI
ulceration, renal papillary necrosis, and peritonitis
• In dogs include: CNS effects (headache, dizziness), otic effects
(tinnitus), pruritis and rash, and peripheral edema
•In cats, GI effects (vomiting, anorexia, diarrhea) may be seen
•There are reports of piroxicam decreasing hematocrits in cats
when dosed daily for 7- 14 days
35.
36.
37. Phenylbutazone
Uses/Indications:
•“For the relief of inflammatory conditions associated with the
musculoskeletal system in dogs and horses”
• It has been used primarily for the treatment of lameness in
horses
38. Contraindications/Precautions
•Cautious use is recommended because of increased incidences of
hypoproteinemia and GI ulceration
•Phenylbutazone may cause decreased renal blood flow and sodium
and water retention, and should be used cautiously in animals with
preexisting renal disease or CHF
•Do not administer injectable preparation IM or SC as it is very irritating
(swelling, to necrosis and sloughing)
39. Adverse Effects
•Toxic effects in horses include oral and GI erosions and ulcers,
hypoalbuminemia, diarrhea, anorexia, and renal effects
•Phenylbutazone-induced blood dyscrasias and hepatotoxicity have
also been reported in dogs
•Bone marrow effects (aplastic anemia), renal and cardiovascular effects
(fluid retention to acute renal failure), and GI effects (dyspepsia to
perforated ulcers)
•The use of H2 blockers (cimetidine, ranitidine) have been suggested
for use in treating the GI effects
41. Acetaminophen
Uses/Indications:
•Acetaminophen is occasionally used as an oral analgesic in dogs
•It may be particularly beneficial in dogs with renal dysfunction for
the treatment of chronic pain conditions
•In situations where moderate pain occurs, it may be used in
combination with tramadol
42. Contraindications/Precautions
•Acetaminophen is contraindicated in cats at any dosage
•Severe methemoglobinemia, hematuria, and icterus can be seen
•While dogs are not as sensitive to acetaminophen as cats, they may
also be susceptible to methemoglobinemia when given high dosages
•In dogs, it is generally not recommended during the immediate post-
operative phase due to an increased risk of hepatotoxicity
44. Ketorolac
Uses/Indications:
•Ketorolac is used primarily for its analgesic effects for short-
term treatment of mild to moderate pain in dogs and rodents
•The duration of analgesic effect in dogs is about 8–12 hours
45. Contraindications/Precautions
•Ketorolac is relatively contraindicated in patients with a history of,
or preexisting, hematologic, renal or hepatic disease
•It should be used cautiously in patients with a history of GI ulcers,
or heart failure (may cause fluid retention), and in geriatric patients
•Because Ketorolac has a tendency to cause gastric erosion and
ulcers in dogs, long-term use (>3 days) is not recommended
46. Adverse Effects
•The primary issue in dogs is its GI toxicity
•GI ulceration can be common if the drug is used chronically
•Like other NSAIDS, platelet inhibition, renal, and hepatic
toxicity are also possible with this drug
47.
48.
49. Aspirin
Uses/Indications:
•Aspirin is used in all species for its analgesic and antipyretic effects
•Aspirin is used therapeutically for its effects on platelet aggregation in
the treatment of DIC and pulmonary artery disease secondary to
heartworm infestation in dogs
•It is also used in cats with cardiomyopathy
•Aspirin (at low doses) may be of benefit in the adjunctive treatment of
glomerular disease
50. Contraindications/Precautions
• It is relatively contraindicated in patients with hemorrhagic
disorders, asthma, or renal insufficiency
•Because aspirin is highly protein bound to plasma albumin, patients
with hypoalbuminemia may require lower dosages to prevent clinical
signs of toxicity
•Because of its effects on platelets, aspirin therapy should be halted,
if possible, one week prior to surgical procedures
51. Adverse Effects
•The most common adverse effect at therapeutic doses is gastric
(nausea, anorexia, vomiting) or intestinal irritation with varying
degrees of occult GI blood loss occurring
•The resultant irritation may result in vomiting and/or anorexia
•Severe blood loss may result in a secondary anemia or
hypoproteinemia
•Cats may develop acidosis from aspirin therapy
52.
53.
54.
55. CORTICOSTEROIDS
Two classes of steroid hormones, mineralocorticoids and glucocorticoids,
are naturally synthesized in the adrenal cortex from cholesterol
Mineralocorticoids ( aldosterone) are so named because they are important
in maintaining electrolyte homeostasis
Glucocorticoids suppress virtually every component of the inflammatory
process; they inhibit PLA2, decrease synthesis of interleukins and
numerous other inflammatory cytokines, suppress cell-mediated immunity
and decrease production and activity of leukocytes
56.
57. Dexamethasone
Uses/Indications:
Glucocorticoids have been used in an attempt to treat practically every
malady that afflicts animal, but there are three broad uses:
1) Replacement of glucocorticoid activity in patients with adrenal
insufficiency
2) As an antiinflammatory agent
3) As an immunosuppressive
58. Contraindications/Precautions
•Because dexamethasone has negligible mineralocorticoid effect, it
should generally not be used alone in the treatment of adrenal
insufficiency
•Do not administer the injectable rapidly intravenously ;
hypotension, collapse, and hemolytic anemia can occur
•There is a high incidence of gastrointestinal bleeding and colonic
perforation in canine neurosurgical patients treated with
dexamethasone
59. •Systemic use of Glucocorticoids is generally considered
contraindicated in systemic fungal infections
•Animals that have received glucocorticoids systemically should be
tapered off the drugs
•Animals, particularly cats, at risk for diabetes mellitus or with
concurrent cardiovascular disease should receive glucocorticoids
with caution due to these agents’ potent hyperglycemic effect
60. Adverse Effects
•Glucocorticoids can retard growth in young animals
•In dogs, polydipsia , polyphagia and polyuria , may all be seen
•Very high doses in dogs with spinal cord injuries have caused fatal
colon perforations
•Adverse effects associated with immunosuppressive doses are more
common
•Administration of dexamethasone may play a role in the development
of
laminitis in horses
61.
62.
63. Prednislone
Uses/Indications:
•There are there are four primary uses and dose ranges:
1) replacement or supplementation
2) as an antiinflammatory
3) as an immunosuppressive
4) as an antineoplastic agent