Oxygen therapy provides oxygen at concentrations greater than room air to treat hypoxia. There are several methods of oxygen delivery including nasal cannulas, simple masks, partial and non-rebreathing masks, and high flow devices. The type of delivery system used depends on factors like the needed oxygen concentration, flow rate, patient comfort and cost effectiveness. Proper assessment is important to determine if a patient requires oxygen therapy.
The anaesthetic machine (UK English) or anesthesia machine (US English) or Boyle's machine is used by anaesthesiologists, nurse anaesthetists, and anaesthesiologist assistants to support the administration of anaesthesia. The most common type of anaesthetic machine in use in the developed world is the continuous-flow anaesthetic machine, which is designed to provide an accurate and continuous supply of medical gases (such as oxygen and nitrous oxide), mixed with an accurate concentration of anaesthetic vapour (such as isoflurane), and deliver this to the patient at a safe pressure and flow. Modern machines incorporate a ventilator, suction unit, and patient monitoring devices.
Pre-oxygenation is: safe, simple, cheap, effective, well-tolerated. This article provides a compelling argument in favour of pre-oxygenation prior to all general anaesthesia.
The anaesthetic machine (UK English) or anesthesia machine (US English) or Boyle's machine is used by anaesthesiologists, nurse anaesthetists, and anaesthesiologist assistants to support the administration of anaesthesia. The most common type of anaesthetic machine in use in the developed world is the continuous-flow anaesthetic machine, which is designed to provide an accurate and continuous supply of medical gases (such as oxygen and nitrous oxide), mixed with an accurate concentration of anaesthetic vapour (such as isoflurane), and deliver this to the patient at a safe pressure and flow. Modern machines incorporate a ventilator, suction unit, and patient monitoring devices.
Pre-oxygenation is: safe, simple, cheap, effective, well-tolerated. This article provides a compelling argument in favour of pre-oxygenation prior to all general anaesthesia.
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
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
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
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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.
- 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
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
2. Oxygen:
• Colourless
• Odourless
• Tasteless
• Transparent gas
• Slightly heavier than air
• Constitutes 20-21% of atmospheric air
• Essential for life
3. What is O2 Therapy ?
Oxygen therapy is the administration
of oxygen at concentrations greater
than that in room air to treat or prevent
hypoxia.
4. Oxygen is available to us
• Medical grade oxygen (99% or 99.5% pure) is
manufactured by fractional distillation of liquid air.
• Oxygen can be stored as compressed gas at room
temperature or as liquid when refrigerated.
• Oxygen cylinder
• Delivery system : Hose drops, Gas columns,
Articulating arms
E-cylinder
capacity
H-cylinder
Capacity
Pressure
(psig at 20oC)
Color PIN
index
625-700 liters 6000-8000
liters
1800-2000 Black body with
white shoulder
2, 5
5. Anoxia
No oxygen availability in tissues
Hypoxia
Lack of oxygen availability in
tissues
Hypoxemia
Lack of oxygen in the blood
6. 6
Indications for Oxygen Therapy
• Hypoxemia
– Inadequate amount of oxygen in the blood
– SPO2 < 90%
– PaO2 < 60 mmHg
• Excessive work of breathing
• Excessive myocardial workload
18. Assessment of need
• Presence of clinical indicators
• Measurement of inadequate oxygen saturations
– by invasive or noninvasive methods,
• Arterial blood gas
• Pulse oximetry
Errors in pulse oximetry
• Artificial fingernails
• Dark pigmentation
• Electrical interference
• Intravenous dyes
• Movement
• Nail Polish
• Pulsatile venous system
• Radiated light
19. Types of Oxygen Therapy
• Giving Oxygen more
than 21% at ambient
atm pressure
• Giving Oxygen more
than 21% at high atm
pressure ( >1 atm)
Orthobaric Hyperbaric
20. Three clinical goals of O2 therapy
1. Treat hypoxia
2. Decrease work of breathing
3. Decrease myocardial Work
21. Oxygen therapy
1. Correcting Hypoxemia
• By raising Alveolar & Blood levels of Oxygen
• Easiest objective to measure
2. Decreasing symptoms of Hypoxemia
• Supplemental O2 can help relieve symptoms of
hypoxia
–Lessen dyspnoea/work of breathing
–Improve mental function
22. 3. Minimizing Cardiopulmonary workload
• Cardiopulmonary system will compensate for Hypoxemia
by:
– Increasing ventilation to get more O2 in the lungs & to the Blood
– Increased work of breathing
– Increasing Cardiac Output to get more oxygenated blood to tissues
– Hard on the heart, especially if diseased
• Hypoxia causes Pulmonary vasoconstritcion & Pulmonary
Hypertension
– These cause an increased workload on the right side of heart
– Over time the right heart will become more muscular & then
eventually fail (Cor Pulmonale)
23. • Supplemental o2 can relieve hypoxemia & relieve
pulmonary vasoconstriction & Hypertension,
reducing right ventricular workload!!
• Minimal acceptable saturation for post surgical
patients who are cared for in non critical setup is
92%
24. FACTORS THAT DETERMINE WHICH SYSTEM
TO USE
1. Patient comfort / acceptance
2. The level of FiO2 that is needed
3. The requirement that the FiO2 be controlled
within a certain range
4. The level of humidification and /or
nebulization
5. Minimal resistance to breathing
6. Efficient & economical use of oxygen
30. NASAL CANNULA
HOW TO USE?
disposable.
plastic devise with two protruding
prongs for insertion into the nostrils,
connected to an oxygen source.
31. - The standard nasal cannula delivers an
inspiratory oxygen fraction (FIO2) of 24-44% at
supply flows ranging from 1-6 L·min-1.
- The formula is FIO2 = 20% + (4 × oxygen litre
flow). The FIO2 is influenced by breath rate,
tidal volume and pathophysiology.
- The slower the inspiratory flow the higher the
FIO2.
33. FACTS
ADVANTAGES
Patients are able
to talk and eat with
oxygen in place
Easily used in
home setting
DISADVANTAGES
may cause irritation
to the nasal and
pharyngeal mucosa
if oxygen flow rates
are above 4
liters/minute
Variable FIO2
34.
35. SIMPLE OXYGEN MASK
Simple mask is made of clear, flexible , plastic
or rubber that can be molded to fit the face.
It is held to the head with elastic bands.
Some have a metal clip that can be bent over
the bridge of the nose for a comfortable fit
36. O2 inlet
Exhalation
ports
• Open ports for
exhaled gas
• Air entrained through
ports if O2 flow
through does not
meet peak inspiratory
flow
37. • 5 – 10 liters per minute
• < 5 liters will not flush CO2
from mask
• 40 – 60% FIO2 approximately
depending on the pattern of
breathing.
38. FACTS
ADVANTAGES
• Can provide increased
delivery of oxygen for
short period of time
• The face mask is
indicated in patients
with nasal irritation or
epistaxis.
• It is also useful for
patients who are strictly
mouth breathers.
DISADVANTAGES
-Tight seal required to deliver
higher concentration
- Difficult to keep mask in
position over nose and mouth
-Potential for skin breakdown
due(pressure, moisture)
- Uncomfortable for pt while
eating or talking.
- Obtrusive, uncomfortable
and confining.
- It muffles communication,
obstructs coughing.
39.
40. PARTIAL REBREATHING MASK
• Mask is a simple mask with a reservoir bag.
• Same as the Non re-breathing bag
but..without a one way valve.
• Low flow, medium concentration
• 50 – 70%
• 8 – 12 liters per minute
• Bag should remain at least 1/3 full during
inspiration
• Allow the mixture or oxygen and carbon
dioxide in the mask.
41. Partial Rebreather mask
Exhalation
ports
O2
Reservoir
• O2 directed into
reservoir
• Insp: draw gas from bag
& room air
• Exp: first 1/3 of exhaled
gas goes into bag (dead
space)
• Dead space gas mixes
with ‘new’ O2 going into
bag
• Deliver ~60% O2
42. FACTS
ADVANTAGES
- Can inhale room
air through
openings in mask if
oxygen supply is
briefly interrupted.
- Not as drying to
mucous
membranes
DISADVANTAGES
- Requires tight
seal
- Eating and
talking difficult,
uncomfortable
-
43.
44. NON REBREATHING MASK
the one-way valve closes and all of the expired air is
deposited into the atmosphere, not the reservoir
bag.
This mask provides the highest concentration of oxygen
(95-100%) at a flow rate 8-15 L/min.
It is similar to the partial rebreather mask except
two one-way valves prevent conservation of
exhaled air.
45. Non-Rebreathing Mask
• Valve prevents exhaled
gas flow into reservoir
bag
• Valve over exhalation
ports prevents air
entrainment
• Delivers ~100% O2, if
bag does not
completely collapse
during inhalation
O2
Reservoir
One-way valves
47. FACTS
ADVANTAGES
Delivers the highest
possible oxygen
concentration
Suitable for pt breathing
spontaneous with sever
hypoxemia
DISADVANTAGES
- Impractical for long term
Therapy
- Malfunction can cause
CO2 buildup
-- suffocation
Expensive
Feeling of suffocation
Uncomfortable
50. AIR ENTRAINMENT DEVICES
• High flow device (o2 concentration)
• Entrains air through side ports to achieve
high flows
• Variable entrainment ports and/or jets
adjust FIO2
• Air Entrainment or Venti Masks
• Manufacturer recommends liter flows for
each FIO2
51. The Venturi System
Room air dilutes the oxygen entering
the tubing to a certain concentration
The amount of air drawn in is
determined by the size of the orifice
(jet adapter).
Applying the Bernoulli principle
55. Oxygen from 24 - 50%
At liters flow of 4 to 15 L/min.
The mask is so constructed that there is a
constant flow of room air blended with a fixed
concentration of oxygen
Is designed with wide- bore tubing and
various color - coded jet adapters.
Each color code corresponds to a precise
It is high flow concentration of oxygen.
Oxygen concentration and a specific liter flow.
56.
57. Color FiO2 O2 Flow
Blue 24% 2 L/min
White 28% 4 L/min
Orange 31% 6 L/min
Yellow 35% 8 L/min
Red 40% 10 L/min
Green 60% 15 L/min
Venturi valve
59. TRACHEOSTOMY COLLAR
Directed into trachea
Is indicated for chronic o2 therapy need
O2 flow rate 8 to 10L
Provides accurate FIO2
Provides good humidity.
Comfortable ,more efficient
Less expensive
60.
61.
62. FACTS
ADVANTAGES
• Delivers high
concentrations of oxygen
directly to the lungs.
• Stable and not moved
when the patient is moved
or cleaned.
• Maintains saturation
levels.
DISADVANTAGES
• Viscosity of secretions
• Clinical status
• Systemic hydration
• Patient compliance
• Method of humidification in use
• if any of the above list remain a
problem the current method of
humidification may be
inadequate
63. Additional devices for high flow
• T-PIECE ADOPTOR
Used on end of ET tube
Prove when weaning from
ventilator
is accurate FIO2
Provides good humidity
65. Airway Adjuncts
• Oropharyngeal Airway (OP)
– Helps prevent tongue from obstructing posterior
pharynx
– Potential use in unconscious patient
– Cannot use in patients with intact gag reflex
– SIZING: measure from corner of mouth to angle of
jaw
– PLACEMENT: direct method vs rotation method.
66. Airway Adjuncts
• Nasopharyngeal Airway (NP)
– Unconscious or depressed mental status
– SIZING: Measure from the tip of the nares to the
tragus of ear
– CONTRAINDICATIONS: basilar skull fracture,
midface fractures, bleeding disorders
– Relative contraindication: children < 1 year old
69. Bag-Mask Ventilation
• Key—ventilation volume: “enough to produce
obvious chest rise”
1-Person:
difficult, less effective
2-Person:
easier, more effective
OXYGENATION AND VENTILATION
70. Successful bag-mask ventilation
depends on three things:
• Patent airway :Airway patency can be
established using basic airway maneuvers
• Adequate mask seal :In order to secure a
good seal, the mask must be placed and held
correctly
• Proper ventilation (ie, proper volume, rate )
71. LMA
• Dr. Archie Brain developed LMA in 1982 as a
modification of Goldman dental mask.
• Standard of airway management , filling the
niche between facemask and tracheal tubes.
• They sit outside the trachea and provide a
handsfree means of gas tight airway.
• The first Supraglottic airway device was LMA-
Classic(1989)
72. Indications Contraindications
Alternative Airway during GA Risk of aspiration
Essential part of difficult airway trolley Local pathology in pharynx , larynx or
upper airway.
Cardiopulmonary resuscitaion :
to secure airway
Trismus, facial or upper airway trauma
Relative indication in professional singers:
To avoid trauma to vocal cords
Morbid obese, > 14 week pregnant,
prior opiods medication, delayed gastric
empting
Reduced lung compliance/increase work
of breathing
75. • Endotracheal tubes are curved tubes used for
intubation
• Tubes were previously made up of latex (indian
rubber) and those still available , currently plastic
tubes (PVC) are preferred because of following
advantages :
Disposable (less chances of infection)
Hypoallergenic ( since latex allergy is fairly
common)
Transparent (easy visualization of blockage ETT
due to blood , pus , secretions
76. • THE ET TUBE HAS THE FOLLOWING
COMPONENTS :
PROXIMAL END – 15mm adapter (connector)
which fits to ventilator or AMBU bag
CENTRAL PORTION –
1. A vocal cord guide (black line ) which should be
placed at the level of the opening of the vocal
cords so that the tip of the ET tube is
positioned above the bifurcation if the trachea.
2. A radio-opaque marker which is essential for
accurate visualization of the position of the ET
tube within the trachea by means of an X-ray
77. 3. The distance indicator (marked in
centimeters) which facilitates placement of
ET tube.
4. A cuff- incase of cuff ET tube
DISTAL END – has Murphy’s eye (opening in
the lateral wall ) which prevents complete
blockage of ET tube incase the distal end is
impacted with secretion , blood , etc.
78. TYPES
• ET tubes can be :
- cuffed
- uncuffed
• Cuffed ET tubes are used in children > 8 years
• The cuff when inflated maintains the ET tube in proper
position and prevents aspiration of contents from GI
tract into respiratory tract
• In children < 8 uncuffed ET tubes are used because the
narrow subglottic area performs the function of a cuff
and prevents the ET tube from slipping.
83. USES
For Mechanical Ventilation
For Intermittent Positive Pressure Ventilation
(IPPV)
During resuscitation
Direct suctioning of trachea in meconium
aspiration
In Epiglottits & life threatening croup
In tetanus (however for long term bases,
tracheostomy is preferable)
In angioneurotic edema
84. COMPLICATIONS
Mechanical trauma to tongue, teeth , palate ,
pharynx & larynx during intubation procedure
Stimulation of posterior of posterior pharyngeal
wall leading to coughing , vomiting or vasovagal
episode with resultant hypoxia , bradycardia.
Prolonged intubation may cause pressure
necrosis of laryngeal structures leading to
persistant hoarseness ( hence tracheostomy) is
indicated in patients requiring long-term
mechanical ventilation)
Pneumothorax,Pneumonia
86. OXYGEN TENT
Consists of a canopy placed
over the head and shoulders
or over the entire body of
a patient
FiO2 – 40-50% @12-15L/minO2
Variable performance device
Provides concurrent aerosol
therapy
Disadvantage
Expensive
Cumbersome
Difficult to clean
Constant leakage
Limits patient mobility
87. OXYGEN HOOD
• An oxygen hood covers only the
head of the infant
• O2 is delivered to hood through
either a heated entrainment
nebulizer or a blending system
• Fixed performance device
• Fio2 – 21-100%
• Minimum Flow > 7/min to
prevent CO2 accumulation
88. INCUBATOR
• Incubators are polymethyl
methacrylate enclosures that
combine servo-controlled
convection heating with
supplemental O2
• Provides temperature control
• FiO2 – 40-50% @ flow of 8-15
L/min
• Variable performance device
89. Evaluation:
Breathing pattern - regular and at normal rate.
Color - nail beds, lips, conjunctiva of eyes -
pink
No confusion, disorientation, difficulty with
cognition.
Arterial oxygen concentration or hemoglobin
within normal
Oxygen saturation within normal limits.
90. Will be explained in other class
ECMO (Extracorporeal
Membrane Oxygenation )
92. DEFINITION
• A mode of medical treatment wherein
the patient breathes 100% oxygen at a
pressure greater than one Atmosphere
Absolute (1 ATA)
• 1 ATA is equal to 760 mm Hg at sea level
93. Physiological effects of HBO
• Bubble reduction ( boyle’s law)
• Hyperoxia of blood
• Enhanced host immune function
• Neovascularization
• Vasoconstriction
98. Long Term Oxygen Therapy
• To provide prolong and improve quality of
life in hypoxic pt with COPD
• Indicated For
–Pt with PaO2< 55mmHg or less
–Pt with PaO2< 59mmHg or less plus
peripheral edema, hematocrit of >55% or
P-pulmonale on ECG
Should be reassessed at one
month
99. Complications of Oxygen therapy
1. Oxygen toxicity
2. Depression of ventilation
3. Retinopathy of Prematurity
4. Absorption atelectasis
5. Fire hazard
100. 1. O2 Toxicity
• Primarily affects lung and CNS.
• 2 factors: PaO2 & exposure time
• CNS O2 toxicity (Paul Bert effect)
– occurs on breathing O2 at pressure > 1 atm
– tremors, twitching, convulsions
102. Pulmonary O2 Toxicity (Lorrain-Smith
effect)
Mechanism: High pO2 for a prolonged period of time
↓
intracellular generation of free radicals e.g.:
superoxide,H2O2 , singlet oxygen
↓
react with cellular DNA, sulphydryl proteins &lipids
↓
cytotoxicity
↓
damages capillary endothelium,
↓
105. 2. Depression of Ventilation
• Seen in COPD patients with chronic hypercapnia
• Mechanism
↑PaO2
suppresses peripheral V/Q mismatch
chemoreceptors
depresses ventilatory drive ↑ dead space/tidal volume ratio
↑PaCO2
106. 3. Retinopathy of prematurity (ROP)
• Premature or low-birth-weight infants who receive
supplemental O2
• Mechanism
↑PaO2
↓
retinal vasoconstriction
↓
necrosis of blood vessels
↓
new vessels formation
↓
Hemorrhage → retinal detachment and blindness
To minimize the risk of ROP - PaO2 below 80 mmHg
107. 4. Absorption atelectasis
100% O2
oxygen
nitrogen
PO2 =673
PCO2 = 40
PH2O = 47
A B
A – UNDERVENTILATED
B – NORMAL VENTILATED
114. Take home message!!
• Oxygen is a drug, prescribe it as other drugs, i.e,
amount, device and time should be specified.
• If patient’s SpO2 is not good with nasal cannula,
consider changing the device instead of
increasing flow rate.
• Over jealous use of oxygen is often without
justification & consideration of toxic effects of
oxygen therapy. So think before such
unaccounted for use of oxygen.