This document discusses the principles and types of neuromuscular monitoring. It describes the goals of neuromuscular monitoring including quantitative assessment of blockade. It outlines the types of nerve stimulation including electrical and magnetic, and discusses commonly used nerve-muscle units like the ulnar nerve-adductor pollicis. Patterns of nerve stimulation are covered like train-of-four, double burst, and post-tetanic count. Objective monitoring techniques like acceleromyography and mechanomyography are also summarized. Finally, the document evaluates recorded evoked responses with depolarizing and non-depolarizing neuromuscular blocking agents.
anaesthesia Breathing circuits and its classification and functional analysisprateek gupta
anaesthesia breathing circuits. mapleson circuits. classification of circuits. functional analysia of circuits. draw over circuit. advantages and disadvantages of different circuits.
anaesthesia Breathing circuits and its classification and functional analysisprateek gupta
anaesthesia breathing circuits. mapleson circuits. classification of circuits. functional analysia of circuits. draw over circuit. advantages and disadvantages of different circuits.
Neuromuscular monitoring, also known as train of four monitoring, is a technique used during recovery from the application of general anesthesia to objectively determine how well a patient's muscles are able to function. It involves the application of electrical stimulation to nerves and recording of muscle response using, for example, an acceleromyograph. Neuromuscular monitoring is typically used when neuromuscular-blocking drugs have been part of the general anesthesia and the doctor wishes to avoid postoperative residual curarization (PORC) in the patient, that is, the residual paralysis of muscles stemming from these drugs.
Neuromuscular monitoring, also known as train of four monitoring, is a technique used during recovery from the application of general anesthesia to objectively determine how well a patient's muscles are able to function. It involves the application of electrical stimulation to nerves and recording of muscle response using, for example, an acceleromyograph. Neuromuscular monitoring is typically used when neuromuscular-blocking drugs have been part of the general anesthesia and the doctor wishes to avoid postoperative residual curarization (PORC) in the patient, that is, the residual paralysis of muscles stemming from these drugs.
neuromuscular monitoring. different types of stimulation. patterns in both non- depolarizing and depolarizing blocking agents.various tools to assess the degree of block
A motor point is a specific skin area where the targeted muscle is best stimulated with the smallest amount of current amplitude and the shortest pulse duration
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
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solar wind sources and understand what drives the complexity seen in the
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Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
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2. Goals
Principles
Types of neuromuscular monitoring
Definitions
Sites of nerve stimulation and responses
Patterns
Clinical practice
3. PRINCIPLES
Supra-maximal stimulation: the electrical stimulus required to block all the
muscle fibers of a muscle which are supplied by a single nerve,is the maximum
stimulus. Supra-maximal stimulus is 15 to 20 percent greater than the maximal
stimulus.
Calibration: It adjusts the gain f the device to ensure that the observed response is
within the measurement window of the device and is closest to 100% of control
response.
Impedance: is the resistance offered by the skin to the passage of current. Value =
5 kilo ohms.
Safety margins: neuromuscular block is evident only once 70% of the receptors
are blocked. So, this should be kept in mind 70 % of the receptors may still be
blocked and not detectable on the nerve stimulator.
4. Types of peripheral nerve stimulation
Electrical
Commonly used in clinical practice
Easy to use
painful
Magnetic
Not used clinically
Bulky apparatus
Not painful
5. Site of nerve stimulation selection
The site should be easily accessible.
Allow quantitative monitoring.
Direct muscle stimulation should be avoided.
Happens when electrodes are directly placed on the muscle being tested.
To prevent this, the nerve-muscle unit should be chosen so that the site of nerve and site
of responding muscle are anatomically distinct.
6. Nerve-Muscle Units
Ulnar nerve--adductor pollicis muscle.
Easily accessible
When arms are abducted and patient is supine.
Nerve and muscle are topographically distinct.
Adduction of the thumb.
Facial Nerve--orbicularis oculi; Facial Nerve—Corrugator supercilli
When arms are tucked under drapes.
Risk of direct muscle stimulation is significant.
Can be elicited with lower current i.e 23 to 30 mA.
winking of eye and wrinkling of the brow respectively.
7. Nerve-Muscle Units
Posterior Tibial Nerve—Flexor halluces brevis
Easily accessible
When hands are inaccessible.
Nerve and muscle are topographically distinct.
Flexion of big toe.
8. Electrodes and assembly
Two types of electrodes are used:
needle
surface
Surface electrode:
pre-gelled silver or silver chloride
Conduction area should be 7 to 11 mm
Negative terminal is placed on nerve
Positive terminal is placed proximally
Space between the centre of two electrodes should be 3 to 6cm.
9. Electrodes and assembly contt.
Needle electrodes
Used when skin electrodes cannot be applied
When the selected current cannot be delivered with surface electrodes
Specially coated needles or ordinary injection needles can be used
Sterile technique is mendatory
Needle is placed subcutaneously to avoid direct injury to the nerve.
10. Patterns of Nerve Stimulation
Single Twitch
Train Of Four
Train Of Four Ratio
Double Burst
Tetanic Stimulation
Post-tetanic Count Stimulation
11. Single Twitch Stimulation
Stimulation Pattern
Single electrical stimulus is applied to the peripheral motor nerve.
Frequency 1hz (once every sec) to 0.1Hz (one every 10 seconds).
Clinical application
Only pattern used to assess the neuromuscular block with depolarizing NMBA
succinylcholine.
As a component of PTC stimulation.
As 0.1 Hz single twitch stimulation, sometimes used in the clinical trials to see the onset
of neuromuscular blockade.
13. Train Of Four Stimulation
Stimulation Pattern
Consists of four supra-maximal stimuli given every 0.5sec (2Hz); and each stimulus in TOF
causes the muscle to contract.
The response evaluation is based upon either of two:
TOF Count: No. of discernible responses after TOF simulation i.e TOF Count.
TOF Ratio: Fade in TOF responses i.e dividing the amplitude of fourth response to that of 1st
response.
1. Without NMBA: all four responses are same---TOF ratio is 1.
2. With Non-dep NMBA:TOF ratio decrease---fade occurs.
3. With Dep NMBA:No Fade occurs---TOF Ratio is 1. Phase 1 block.
4. Fade with dep NMBA: phase II block has occurred.
15. Train Of Four Stimulation
Clinical Application
TOF count:
Onset of neuromuscular blockade
Moderate block
TOF Ratio
Onset
Surgical relaxation (maintenance).
Recovery.
Reversal.
Extubation.
Post-op residual neuromuscular blockade.
16. Train Of Four Stimulation
Advantages:
Most frequently used.
Less painful than DBS and PTC.
Reliable for all phases of anesthesia(onset of neuromuscular blockade till recovery).
Limitations:
Subjective assessment overestimates the neuromuscular recovery i,.e. TOF ratio 0.4 to 0.9 fade
cannot be detected either visually or tactically.
TOF ratio does not allow the clinician to quantify intense and deep levelsof neuromuscular
blockade.
Does not allow monitoring of depolarizing neuromuscular blockade.
17. Double-Burst Stimulation
Stimulation Pattern:
Two short burst of 50 Hz of tetanic stimulation separated by 750ms, with a 0.2 ms
duration of each square wave impulse in the burst.
Modes of DBS: depend upon the no. of impulses in each burst.
DBS 3,3 Mode: three impulses in each burst
DBS3,2 Mode: 1st burst has 3impulses and second burst has 2 impulses.
Each impulse is of 0.2 second regardless ofDBS mode.
19. Double-Burst Stimulation
Response:
The individual twitches in each burst are blended and felt to be single amplified muscle
contraction.
The response is two short muscle contractions and fade in second burst compared to the
first burst is the basis for evaluation.
20. Double-Burst Stimulation
Clinical application
Manual (tactile or visual) detection of block.
Recovery
Post-op residual block.
Advantages vs disadvantages:
Better visal assessment cpmpared to TOF count.
Objective monitoring is superior to DBS.
DBS is painful as compared to TOF.
21. Tetanic Stimulation
Stimulation Pattern
High frequency delivery of electrical stimuli i.e. 50 Hz for 5 seconds or 100 Hz to 200 Hz
given for 1second.
Response
Without any NMBD: fade does not occur.
With non-dep NMBD: fade occurs.
With Dep NMBD: no fade.
Fade with Dep NMBD: phase II block.
24. Post Tetanic Count Stimulation
Stimulation Pattern
A composite stimulation pattern consisting of tetanic stimulation of 50 Hz for 5 seconds
followed by 10 t 15 single twitches given at 1 Hz starting at 3 seconds past the tetanic
stimulation.
Clinical application
When dense neuromuscular paralysis is required.
Onset (deep paralysis—less than 3 post tetanic count.
Surgical paralysis
Recovery( although painful but ideal).
26. Subjective monitor
Peripheral nerve stimulator: only allows the stimulation of the target nerve;
subsequent muscular response is evaluated subjectively (tactilely or visually).
27. Objective Monitors
Mechanomyography:
Evoked mechanical response of the muscle.
gold standard technique.
Electromyography:
Evoked electrical response of the muscle
Oldest method
Acceleromyography:
Acceleration of musv;le response
Based on newton’s second law i.e. Force= Mass X acceleration.
Kinemyography:
Evoked electrical response in a flexible piezoelectric film sensor attatched to the muscle.
Cuff pressure modality:
Measurement of pressure changes in BP Cuff after contaction of upper arm muscles.
Compressomyography:
measurement of a spherical balloon after hand contraction
32. Evaluation Of Recorded Evoked Responses with Non-
Depolarizing NMBA
Intense Block
Onset: within 3 to 6 minutes of intubating dose.
Also called ‘period of no response’.
Can only be antagonized by sugammadex high dose 16mg/kg.
Deep block
Intense block is followed by deep block.
Absence of response to TOF but with 1 PTC.
Assured by PTC less than and equal to 3 in laparoscopic surgeries.
Can only be reversed by sugammadex moderate dose 4mg/kg.
33. Evaluation Of Recorded Evoked Responses with
Non-Depolarizing NMBA
Moderate block
Begins with first response to TOF and gradual return of four stiuli of TOF.
When Ist TOF response reappears, degree of block is 90 to 95 %
When fouryth response to TOF reappears, degree of block is 60 to 85%.
Reversed with sugammadex low dose 2mg/kg.
Or by neostigmine if TOF ratio 0.7 or above.
Recovery from block
Return of fourth response to TOF
TOF ratio should be 0.9 with MMG or EMG and 1.0 with AMG to exclude residual blockade.
34. Evaluation Of Recorded Evoked Responses
with Depolarizing NMBA
Phase I block
Occurs in patients given succinylcholine once or with normal plasma pseudocholinesterase levels and
genetics.
No fade
No post tetanic facilitation
TOF ratio 1.0
TOF count is either 4 or 0.
Phase II block
Occures with repeated doses or continuous infusion of succinylcholinein patients with normal
pseudocholinesterase levels and normal genetics or patients with abormal plama pseudocholinesterase
levels or abnormal genetics.
Fade occurs
TOF ratio is utilized to differentiate the phase I and phase II blockade.