A patient with pacemaker presents a complex challenge to the attending anaesthesiologist. The mode of management will be according to the type of pacemaker implanted. This presentation discusses in brief the peri-operative consideration in a patient with pacemaker.
Intro to Hypoxic pulmonary vasoconstriction Arun Shetty
Hypoxic pulmonary vasoconstriction, a seldom heard phenomenon but very effective physiologic property which helps lungs utilise ventilation to the maximum
Intro to Hypoxic pulmonary vasoconstriction Arun Shetty
Hypoxic pulmonary vasoconstriction, a seldom heard phenomenon but very effective physiologic property which helps lungs utilise ventilation to the maximum
Electrical cardiac pacing for the management of bradyarrhythmias
was first described in 1952, and permanent transvenous pacing
devices were introduced into clinical practice in the early 1960s.
Artificial Cardiac pacemaker |medical device that generates electrical impulses NEHA MALIK
A pacemaker is a device that sends small electrical impulses to the heart muscle to maintain a suitable heart rate or to stimulate the lower chambers of the heart (ventricles). A pacemaker may also be used to treat fainting spells (syncope), congestive heart failure and hypertrophic cardiomyopathy.
A basic note on pacemaker that will be usefull to undergraduate students to attain a brief and basic knowledge on pacemaker. when the natural pacemaker of the heart becomes unrelyable , an artificial pacemaker needs to be implanted in the which will cause contraction of the myocardium by initiating electrical activity of the heart.
this is dealt about the pacemaker temporary and permanent its aim and basic indication for pacemaker breif history of pacemaker development its design and detailed indication of both temporary and permanent pacemaker then method of pacing which should be based on the patient ECG its parts and procedure and complication
Pacemakers are the electrode devices that can be used to initiate the heartbeat .
when the hearts intrinsic electrical system cannot effectively generate a rate adequate to support cardiac output.
It consists of a pulse generator, lead and appropriate electrodes.
In the past few years electronic pacemaker systems have become extremely important in saving and sustaining the lives of cardiac patients whose normal pacing function of the heart have been impaired.
Pacemaker powerpoint presentation med surgNehaNupur8
pacemaker - artificial pump to the heart, this contained definition, components,working, types, indication, methods of pacaing, temporary and permanent pacemaker, signs of failure of pacemaker , medical and nursing management of patient with pacemaker.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
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
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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
3. WHAT IS A PACEMAKER?
• A PACEMAKER (OR ARTIFICIAL
PACEMAKER) IS A MEDICAL DEVICE
WHICH GENERATES ELECTRICAL
IMPULSES AND DELIVERS BY ELECTRODES
CONTRACTING THE HEART MUSCLES, TO
REGULATE THE BEATING OF THE HEART.
4. PARTS OF PACEMAKER
1. Pulse Generator: power source or battery.
(Zinc,Lithium Iodide)
2. Leads Or Wire: deliver electrical impulse.
3. Cathode: (-) electrode.
4. Anode: (+) electrode.
6. TEMPORARY PACEMAKERS
• External, battery-powered, pulse generators
with exteriorized electrodes produce electrical
cardiac stimulation to treat a bradyarrhythmia
or tachyarrhythmia until it resolves or until
long-term therapy can be initiated.
• Used for less than three days.
11. PERMANENT PACEMAKER
INDICATIONS:-
1. Symptomatic diseases of impulse formation (SA
Node Disease).
2. Symptomatic diseases of impulse conduction (AV
Node Disease).
3. Hypertrophic Obstructive Cardiomyopathy
(HOCM).
4. Dilated Cardiomyopathy (DCM).
5. Long QTSyndrome. Bryce et al, Ann Intern Med. 2001; 134:1130-41.
12. GENERIC CODE FOR PACEMAKER
NASPE/BPEG (North American Society Of
Pacing And Electrophysiology/ British Pacing
And Electrophysiology Group) Alliance
14. 1. Pacing:-regular output of electrical current,
for the purpose of depolarizing the cardiac
tissue in the immediate vicinity of the lead,
with resulting propagation of a wave of
depolarization throughout that chamber.
2. Sensing:- response of a pacemaker to
intrinsic heartbeats.
15. 3. Pacing Threshold:-The threshold is the
minimum amount of energy the pacemaker
sends down the lead to initiate a heart beat.
4. Capture:- Cardiac depolarization and
resultant contraction (atrial or ventricular) -
Caused by pacemaker stimulus.
5. Rate response:- it have various sensors that
will active while patient during activities and
adjust the rate .
16. 6. Triggered pacing:- Dual chamber
pacemakers can be programmed to sense
activity in one chamber (usually the atrium)
and deliver a pacing stimulus in the other
chamber (usually the ventricle) after a certain
time delay.
7. Inhibition of Output:-pacemaker can be
programmed to inhibit pacing if it senses
intrinsic activity, or it can be programmed to
ignore intrinsic activity and deliver a pacing
stimulus anyway.
17. MODES OF PACING
1. Asynchronous Pacing.( eg. AOO,VOO,DOO)
2. Single Chamber Demand Pacing.
(eg. AAI,VVI)
3. Dual Chamber AV Sequential Demand
Pacing.(eg. DDD 70 with AV interval 200msec)
18. PROGRAMMABLE PACEMAKER
• Recent generation pacemakers provide flexibility
to device to patients changing metabolic needs.
• Capacity to noninvasively alter one of several
aspects of the function of a pacer.
• Sensors capable of detecting body movements,
changes in ventricular repolarisation, central
venous temprature, respiratory rate and depth
and right ventricular contractibility.
20. BIVENTRICULAR PACEMAKER/CRS
(CARDIAC RESYNCHRONISATION THERAPY)
• A pacemaker that paces both the septal and
lateral wall of left ventricle simultaneously.
• This resynchronizes a heart to contract in full
synchrony.
• Leads in right and left ventricle and right
atrium.
21. INDICATION:-
1. patients with dilated cardiomyopathy with
LVEF <35%
2. NYHA III/IV despite maximal medical
therapy(CHF)
22. Preoperative Evaluation
• Evaluation Of The Patient:-
• Underlying cardiovascular disease
responsible for pacemaker implantation.
• Any other associated illness e.g CAD, HTN,
DM etc.
• Severity of the cardiac disease.
• Current functional status.
• Medication status of the patient.
23. • PACEMAKER EVALUATION:-
• Type of pacemaker (fixed rate or demand rate).
• Conduct a focused physical examination (check for
scars and palpate for device).
• Half-life of the pacemaker battery.
• Effect of the Magnet Application on Pacemaker
Function.
• Time since implantation.
• Pacemaker rate at the time of
implantation.
25. PREOPERATIVE PREPARATION
• Determine whether EMI is likely to occur
during the planned procedure.
• If interference is likely, reprogram CRMD and
suspend anti tachyarrhythmia function.
• Determine pacemaker baseline rate and
rhythm.
• Correct any underlying electrolyte abnormality
( if present)
26. CHOICE OFANAESTHESIA
• Technique may not influence directly but
physiological changes (acid-base, electrolytes)
& hemodynamic shifts (heart rate, rhythm,
hypertension, coronary ischemia) can change
CIED function & adversely effect patient
outcome.
27. ANAESTHETIC TECHNIQUE
• Narcotic and inhalational techniques can be
used successfully.
• In a patient with newly implanted pacemaker,
nitrous oxide is avoided – expansion of gas in
pacemaker pocket.
• Etomidate and ketamine should be avoided as
these cause myoclonic movements.
• Pacemaker function should be verified before
and after initiating mechanical ventilation as
Positive Pressure Ventilation can dislodge
pacemaker leads.
28. • Skeletal myopotentials, electroconvulsive
therapy, succinylcholine fasciculation,
myoclonic movements, or direct muscle
stimulation can inappropriately inhibit or
trigger stimulation, depending on the
programmed pacing modes.
• Care should be taken during insertion of guide
wire or central venous catheter as they are
arrhythmogenic and can dislodge pacemaker
leads.
29. MONITORING
• Based on the patient’s underlying disease and the
type of surgery.
• Continuous ECG monitoring (artifact filter
disabled).
• NIBP, ETCO2 and peripheral temperature
monitoring.
• Both electrical and mechanical evidence of the
heart function should be monitored by manual
palpation of the pulse, pulse oximetry, precordial
stethoscope and arterial line.
31. EFFECT OF EMI (Electromagnetic
Interference) ON PACEMAKER
1. Inhibition of pacing.
2. Asynchronous pacing.
3. Reset to back up mode.
4. Myocardial burn.(rare)
5. Ventricular fibrillation.(rare)
32. Measures To Decrease Possibility Of
Adverse Effects Due To EMI
• Bipolar cautery or ultrasonic (harmonic) scalpel
in place of a monopolar cautery, if possible.
• Unipolar cautery (grounding plate should be
placed close to the operative site and as far away as
possible from the site of pacemaker)
• Electrocautery should not be used within 15cm of
pacemaker.
• Pacemaker may be programmed to asynchronous
mode by a magnet or by a programmer.
33. • Provision of alternate temporary pacing.
• Drugs (isoproterenol and atropine) should
be available.
• Careful monitoring of pulse, pulse oximetry
and arterial pressure is necessary during
electrocautery, as ECG monitoring can also be
affected by interference.
• The device should always be rechecked after
operation.
34. MAGNET APPLICATION ON PACEMAKER
FUNCTION
• The magnet is placed over the pulse generator
to trigger the reed switch present in the pulse
generator resulting in a non-sensing
asynchronous mode with a fixed pacing rate
(magnet rate).
• It shuts down the demand function so that the
pacemaker stimulates asynchronous pacing.
Thus, it protects the pacemaker dependent
patient during EMI, such as diathermy or
electrocautery.
35. • The response varies with the model and the
manufacturer so advisable to consult the
manufacturer to know the magnet response
before use.
• Demonstrates remaining battery life and
sometimes pacing thresholds.
• Complications- ventricular asynchrony, altered
programming.
36. EMERGENCY DEFIBRILLATION OR
CARDIOVERSION
• In a patient with ICD and magnet-disabled
therapies, Before attempting emergency
defibrillation or cardioversion:-
-All sources of EMI should be terminated.
-Remove the magnet to reenable antitachycardia
therapies.
• Patient with ICD and antiarrhythmic therapies that
have been disabled by programming, consider re
enabling therapies through programming.
• If it fail to restore ICD function, proceed with
emergency external defibrillation or cardioversion.
37. • Follow ACLS guidelines for energy level and for
paddle placement.
• If possible, attempt to minimize the current flowing
through the pulse generator and lead system by
positioning the pads or paddles:-
-as far as possible from the pulse generator.
-perpendicular to the major axis of the CIED pulse
generator and leads to the extent possible by
placing them in an anterior-posterior location.
38. Specific Perioperative Considerations
Transuretheral Resection of Prostate (TURP)
and Uterine Hysteroscopy.
Electroconvulsive Therapy.
Radiation.
Nerve Stimulator Testing or Transcutaneous
Electronic Nerve Stimulator Unit. (TENS)
Lithotripsy.
Magnetic Resonance Imaging (MRI).
39. Postoperative Care
• Cardiac rate, rhythm monitoring continuously.
• Shivering and fasciculation should be avoided.
• Back-up pacing capability and cardioversion
defibrillation equipment should be immediately
available at all time.
• Interrogate CIED; consultation with a cardiologist
or pacemaker-ICD service may be necessary.
• Restore all antitachyarrhythmic therapies in ICDs
• Assure that all other settings of the CIED are
appropriate.
40. SUMMARY
• Adopting a multidisciplinary approach that
involves the surgeon, anesthetist, cardiologist and
industry employed allied health professional is
ideal for safe peri-operative CIED management .
• Decision-making process should be tailored to
individual patients and their needs, with the aim
of preventing haemodynamic embarrassment
consequent to CIED malfunction.
• Anaesthetic management should be planned
preoperatively according to patient’s medical
status.
41. • Monitoring and anesthesia technique with due
considerations to patients CVS status.
• Initiate invasive arterial pressure monitoring in
addition to standard monitoring.
• Avoid electrocautery use, If necessary consider
use of bipolar or harmonic scalpel.
• Be ready for alternate mode of pacemaker and
defibrillator if necessity arises.
• Rate responsive pacemakers should have rate
responsive mode disabled before surgery.
• Pacemaker should be rechecked after the
procedure.