This document discusses fluid therapy in animals. It begins by describing the distribution of water in the body and the composition of intracellular and extracellular fluids. It then discusses three types of fluid disturbances: changes in volume, content, and distribution. The document outlines different types of fluid therapy including replacement, adjunctive, and supportive therapies. It provides details on routes of fluid administration and indications for intravenous fluids. Throughout, it discusses evaluating and monitoring fluid therapy, diagnosing and treating dehydration, and complications of intravenous fluids.
Prevalence of canine leptospirosis has increased in recent years.
As many as 8.2% of dogs are shedding leptospires, some asymptomatically.49
Weather changes, population growth, and habitat encroachment have all increased human and canine exposure to pathogens and their carriers.
Transmission of leptospirosis can occur through direct contact or indirectly through environmental exposure.
Leptospires enter the body through mucous membranes in the mouth, eyes, or nose, or through abraded or water-softened skin.
Leptospires multiply in a host animal's bloodstream.
Leptospires move from the bloodstream to the kidneys and other tissues to continue reproducing.
Leptospires pass from the kidneys into the urine; then are shed back into the environment.
Other dogs, wild animals, or people can become infected through direct or indirect contact.
clinical signs
Fever
Lethargy
Weight loss
Anorexia
Depression
Acute renal failure
Jaundice
Abdominal discomfort
Vomiting and diarrhea
Blood in urine is uncommon, but may occur
Respiratory distress
Dogs at risk
Dogs at risk for developing leptospirosis include those with
Access to ponds, lakes, streams, or standing water
Exposure to urine from other infected animals, including:
Other dogs in shelters or other pet care facilities
Wildlife (e.g. rodents, racoons, opossum, deer), either through direct contact with urine or through contaminated water
Morbidity threats
As leptospirosis progresses, it can result in
Leptospiremia
Leptospires can multiply in the bloodstream and spread to many tissues and organs
Vascular damage/thrombocytopenia
Can lead to kidney failure and interfere with liver function
Contributes to coagulatory abnormalities and hemorrhages
Severe kidney and liver damage
Acute renal failure occurs in dogs with severe clinical signs
Acute hepatic dysfunction or chronic hepatitis have been caused by specific serovars
Prevalence of canine leptospirosis has increased in recent years.
As many as 8.2% of dogs are shedding leptospires, some asymptomatically.49
Weather changes, population growth, and habitat encroachment have all increased human and canine exposure to pathogens and their carriers.
Transmission of leptospirosis can occur through direct contact or indirectly through environmental exposure.
Leptospires enter the body through mucous membranes in the mouth, eyes, or nose, or through abraded or water-softened skin.
Leptospires multiply in a host animal's bloodstream.
Leptospires move from the bloodstream to the kidneys and other tissues to continue reproducing.
Leptospires pass from the kidneys into the urine; then are shed back into the environment.
Other dogs, wild animals, or people can become infected through direct or indirect contact.
clinical signs
Fever
Lethargy
Weight loss
Anorexia
Depression
Acute renal failure
Jaundice
Abdominal discomfort
Vomiting and diarrhea
Blood in urine is uncommon, but may occur
Respiratory distress
Dogs at risk
Dogs at risk for developing leptospirosis include those with
Access to ponds, lakes, streams, or standing water
Exposure to urine from other infected animals, including:
Other dogs in shelters or other pet care facilities
Wildlife (e.g. rodents, racoons, opossum, deer), either through direct contact with urine or through contaminated water
Morbidity threats
As leptospirosis progresses, it can result in
Leptospiremia
Leptospires can multiply in the bloodstream and spread to many tissues and organs
Vascular damage/thrombocytopenia
Can lead to kidney failure and interfere with liver function
Contributes to coagulatory abnormalities and hemorrhages
Severe kidney and liver damage
Acute renal failure occurs in dogs with severe clinical signs
Acute hepatic dysfunction or chronic hepatitis have been caused by specific serovars
This slide share includes definition,indications,dehydration status,types of fluids,when to administer which fluid,how to calculate the fluid to be administered and how to monitor fluid therapy.Hope its helpful.
Common fluids used in anaesthesia and fluid therapyArowojolu Samuel
common fluids used in anaesthesia. fluid therapy in anaesthesia and theatre. emergency fluid replacement. calculation of fluid by anaesthetist. colloids and crystalloids, indication in anaesthesia
Fluid and electrolytes management in post op patientsDr.Sonal Dixit
sonal dixit , mbbs , ms obg
After surgery modification in normal physiology of fluid and electrolytes balance.
- ACUTE STRESS leads to increased sympathetic stimuli- tachycardia, vasoconstriction & stress.
Increased ACTH stimulate adrenal gland which secretes large amount of hydrocortisone to fight acute stress and aldosterone which leads to Na retension and urinary loss of K.
A presentation I gave on Pediatric Fluid Therapy, with the main focus around perioperative fluid therapy in the Pediatric population. This lecture was delivered to my colleagues in the department of Anesthesia, and it was invigilated by consultant Anesthetist, Dr. Anatolly Kravchenko at the Intermediate Hospital Katutura.
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
- 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
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.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
4. Three types of fluid disturbances:
1. Changes in volume (e.g., dehydration, blood loss)
2. Changes in content (e.g., hyperkalemia)
3. Changes in distribution (e.g., pleural effusion)
5. Fluid therapy Types
Replacement therapy:
Therapy in which we infuse same type of fluid
which is lost from body .
Adjunctive Therapy:
One type of fluid is given to remove other type of
fluid e.g. mannitol 25% is given in case of ascites
and edema.
Supportive Therapy:
Fluid is given to animal just to support him to cure
quickly i.e. amino acids, minerals, multivitamins
and carbohydrates etc.
8. Indications for intravenous fluids
Replace extracellular fluid volume
losses
Maintain fluid and electrolyte
balance
Correct existing electrolyte or acid-
base disorders
Provide a source of glucose
9. Reasons for Fluid Therapy
Vasoconstriction
Pale mucous membranes
Prolonged capillary refill time
Peripheral temperature < core temperature
Reduced urine output
Decreased mentation
Tachycardia (cats may present with bradycardia)
Hypotension (poor pulse quality)
Reduced oxygen saturation (low SpO2)
Lactate >2 mmol/L
Metabolic acidosis/Alkalosis
11. Dehydration
Dehydration or the loss of fluid from the interstitial
space in the form of increased fluid loss from
vomiting, diarrhea, or polyuria is one of the main
cause of water reduction in body.
Signs include decreased skin tenting, sunken eyes,
depressed mentation, and tacky/dry mucous
membranes, CRT 2-3 sec in mild cases and >3 sec in
severe cases, Slight depression of eyes into sockets.
12. Determining a patient's degree
of dehydration
5%-6% dehydrated: Subtle loss of skin elasticity
6%-8% dehydrated: Definite delay in return of skin to
normal position (skin turgor), slight increase in capillary
refill time, and eyes may be slightly sunken into orbits
10%-12% dehydrated: Extremely dry mucous
membranes, complete loss of skin turgor, eyes sunken
into orbits, dull eyes, possible signs of shock
(tachycardia, cool extremities, and rapid and weak
pulses), and possible alteration in consciousness
12%-15% dehydrated: Definite signs of shock; death is
imminent if not corrected
13. Assessing for Fluid Therapy
The first step in determining whether a
patient needs fluid therapy is a full
physical examination, including collection
of a complete history.
Check perfusion of tissues
Check for dehydration, and evaluate
losses from any of the fluid
compartments.
Patients that cannot adequately perfuse
their tissues require immediate
intervention with fluid therapy to restore
perfusion and correct shock.
14. IV fluid therapy indicates that
the assessment of patients
should include
Physical examination
Observation of vital signs over
time
Clinical presentation.
15. Diagnosing Dehydration
Physical exam
Weight loss
PCV (HCT) increased
Albumin or total protein
increased
BUN, creatinine
Prerenal azotemia
18. Five ‘Rs’ of intravenous
fluid administration
Resuscitation
Routine maintenance
Replacement
Redistribution
Reassessment
19. Resuscitation
To ascertain the fluid
requirements of patients who
are acutely ill, an accurate
assessment is needed and
should include the ABCDE.
Routine maintenance fluids are
needed in patients who are at
ongoing risk of fluid loss.
20. Replacement
Assessment should focus on:
Ensuring adequate hydration;
Ensuring electrolyte balance;
Checking for any potential fluid overload.
Alterations in potassium – either
hypokalaemia or hyperkalaemia – can
affect patients’ cardiac performance
causing arrhythmias, heart failure and/or
cardiac arrest.
If continued fluid loss is suspected, this
should be checked and losses monitored.
21. Redistribution
Redistribution of fluid can occur in
critical illness. Fluid is lost from the
circulatory volume and moves into
the tissues; this is called ‘third
space loss’.
Monitoring of central venous
pressure, kidney function tests or
high dependency care, may be
required.
22. Reassessment
Regular reassessment of patients’
fluid therapy needs is essential.
Enteral routes reduce the need for
IV access and, in doing so, reduce
the risks of ongoing IV therapy, such
as catheter-related infections
24. Crystalloids
Crystalloid solutions are isotonic plasma
volume expanders that contain
electrolytes.
Isotonic fluids can increase the
circulatory volume without altering the
chemical balance in the vascular spaces.
Crystalloid solutions are mainly used to
increase the intravascular volume when it
is reduced (haemorrhage, dehydration or
loss of fluid during surgery)
25. Colloids
Colloids are gelatinous solutions that
maintain a high osmotic pressure in the
blood.
Colloids are too large to pass semi-
permeable membranes such as capillary
membranes, so colloids stay in the
intravascular spaces longer than
crystalloids.
Examples : albumin, dextran, hetastarch,
Haemaccel and Gelofusin
26. Which fluid to administer?
Crystalloids and colloids are plasma
volume expanders used to increase a
depleted circulating volume.
Both are suitable in fluid resuscitation,
hypovolaemia, trauma, sepsis and burns,
and in the pre-, post- and peri-operative
period.
Colloids carry an increased risk of
anaphylaxis, are more expensive.
30. Clinical characteristic of IV fluids
Ringer lactate is the most physiological iv fluid
Isotonic saline and DNS have maximum sodium Isotonic saline
DNS and ISO-G have maximum chloride
Isolyte – E,P,M directly correct acidosis
Isolyte -G only iv fluid which directly correct metabolic
alkalosis.
Isolyte- M,P,G,E and Ringer lactate are usually avoided in
renal failure.
Isolyte- G and Ringer lactate are avoided in patients with liver
failure.
31. Clinical characteristic of IV
fluids
Isotonic saline and Ringer Lactate do not
contain
glucose so preferred fluid for diabetic
patients.
D5,D10 and D20 are only fluids which do not
contain Na and Cl.
Isolyte -M and P have low Na and Cl.
NS , DNS and dextrose containing fluids do
not
contain potassium and they do not correct
metabolic acidosis and alkalosis directly.
34. Crystalloid classification
Maintenance fluid Replacement
fluid
Special fluid
5% Dextrose Normal Saline 25% Dextose
Dextrose with
0.45%
Normal Saline
DNS Sodium bi
carbonate
Ringers lactate Potasium
Chloride
Isolyte- M, P, G
37. Principles of Rehydration
Correct dehydration, electrolyte, and
acid-base abnormalities prior to surgery.
Do not attempt to replace chronic fluid
losses all at once.
Severe dilution of plasma proteins, blood
cells and electrolytes may result
Aim for 80% rehydration within 24 hours
Monitor pulmonary, renal and cardiac
function closely
38. Example
An adult 18kg cat with 6% dehydration comes into the clinic. It
is estimated that the cat vomited 150 ml of fluid overnight
• Maintenance fluids can be dosed at 50 ml/kg/day in adults and
110 ml/kg/day in young animals
• Calculate maintenance volume
18kg x 50 ml/kg/day = 900ml per day
• Rehydration fluid is based on the estimated percent of
dehydration
% dehydration x weight in kg = deficit in liters
39. Example
Calculate replacement for dehydration 6% = 0.06
0.06 x 18 kg = 1.08 l
1.08 l x 1,000 ml/l = 1080 ml
1080ml x 0.8 (80% of dehydration value replaced
in 24 hours) =840 ml to replace on first day
• Take estimated volume lost in fluid and add to
the other volumes
• Final step: Take all values and add together
900ml + 840 ml + 150 ml = 1890ml
40. Indications of fluid overload
Serous nasal discharge
Increased respiratory rate (Dyspnea)
Crackles or muffled lung sounds on
pulmonary auscultation
Late stage consequence = pulmonary
edema (or pleural effusion in cats)
Decreased PCV
Increased BP