The document discusses respiratory care for paramedics, including arterial blood gases (ABGs), continuous positive airway pressure (CPAP), and mechanical ventilation. It covers topics like ventilation vs respiration, respiratory physiology, normal ABG values, abnormalities of respiration, pathophysiology of respiratory disorders, types of respiratory failure, manifestations of respiratory distress, pulse oximetry, and the oxygen saturation curve. The document also discusses topics such as ventilator management, procedures, terminology, fractions of inspired oxygen, airway pressures, inspiratory and expiratory times, compliance, spontaneous vs mechanical breathing, and potential complications of mechanical ventilation.
Pulmonary function tests: A brief Insight- By RxVichuZ! :)RxVichuZ
This is my 51st powerpoint..deals with PULMONARY FUNCTION TESTS..their uses...details on spirometry, lung volumes and capacities & brief insight into other tests.
Happy reading!!!
Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
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
Title: Sense of Taste
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 structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
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.
- 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
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
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.
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
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
11. Types of Failure
u Hypoxemic
– Room air PaO2 ≤ 50 or SpO2 ≤ 85%
u Hypercarbic
– PaCO2 ≥ 50
– pH ≤ 7.32
u Caution with patients that have acute
on chronic failure
– Their normal SpO2 may be ≈ 88%
– Their normal PCO2 may be ≥ 50
1-13 Voitek A. Novakovski RRT, CCEMT-P 11
12. Manifestations of Respiratory Distress
u Altered Mental Status
u Increased Work of Breathing
– Tachypnea -the single most important indicator
of critical illness
– Accessory muscle use, retractions, paradoxical
breathing pattern
u Catecholamine release
– Tachycardia, diaphoresis, hypertension
u Abnormal blood gas values
– Oxyhemaglobin Saturation
1-13 Voitek A. Novakovski RRT, CCEMT-P 12
16. Pathophysiology of Hypoxemia
u Ventilation/Perfusion Mismatch
– Shunt effect
– Increased Dead Space
u Alveolar Hypoventilation
u Decreased Diffusion
– Pulmonary Contusion
– High Altitude
– Pulmonary Edema
1-13 Voitek A. Novakovski RRT, CCEMT-P 16
17. A nasty mosis
Voitek A. Novakovski BSRC, RRT, NREMT-P,
9/11/2011 CCEMT-P, 17
18. Pathophysiology of Hypercapnia
u Bradypnia – decreased f (resp rate)
u Hypopnia – decreased Vt (tidal vol)
a. VT=VA+VD Average VD=150 ml or≈30%
b. Minute Volume = the total amount of
air going in and out of the lungs per
minute
c. Minute Alveolar Ventilation = the total
amount of air going into and out of the
alveoli per minute = f X (VT-VD)
1-13 Voitek A. Novakovski RRT, CCEMT-P 18
20. Pathophysiology of Hypercapnia
A. f=12, VT=400ml
A. ? VA=
B. f=24, VT=250ml
A. ? VA=
1. Which patient will have a higher
CO2?
1-13 Voitek A. Novakovski RRT, CCEMT-P 20
21. Pathophysiology of Hypercapnia
u Hypovolemia
u Low cardiac output
u Pulmonary embolus
u High mean airway pressures
u Short-termcompensation by
increasing tidal volume and/
or respiratory rate
1-13 Voitek A. Novakovski RRT, CCEMT-P 21
22. Capnography
u IR spectroscopy
u CO2 levels at airway entrance
u Alveolar CO2 levels may be
estimated
u Excellent detector of cardiac output
– CPR – Keep ETCO2 ≥ 10
– ROSC – Sudden increase to ≥ 35-40
22
23. Arterial Blood Gas (ABG)
Acid-base balance / respiratory involvement
– pH, PO2, & PCO2 are measured (HCO3 is
calculated)
– Assess pH: acidosis / alkalosis e.g. ± pH 7.40
– Assess pCO2: hyper / hypocapnea ± 40
– Changes in pH from changes in PCO2
u Acute: 10 mmHg change in PCO2 = 0.08
change in pH
u Chronic: 10 mmHg change in PCO2 = 0.03
change in pH
23
24. Arterial Blood Gas (ABG)
– There is no such thing as
complete compensation
u If change in pH not from
PCO2 than there is a
metabolic component
1-13 Voitek A. Novakovski RRT, CCEMT-P 24
25. ABG Sampling
u Radial artery puncture
– Modified Allen Test – needs to
be done
u Indwelling access
– Procedure varies by device
u I-STAT, IRMA etc. portable
blood gas analyzers known as
POC devices. Know the law,
CLIA determines who can
analyze.
25
29. Ventilator Procedures
In case of instability or
mechanical difficulty,
disconnect the ventilator
and use manual
ventilation.
29
30. On-Board O2 Calculation
u To calculate how long an oxygen tank
will last (safety factor ≠! 200 psig)
– Know the tank factors:
u H or K = 3.14
u M = 1.65
u E = 0.28
u D = 0.16
u Tank Life in Minutes =
(tank pressure in psi x factor)
liters per minute
8. You have a Pt on a non-rebreather @ 15 Lpm. You
are using an E cylinder with 1800 psig. How long
will it last before you should change it?
1-13 30
31. Terminology
u Fraction of Inspired u I:E Ratio
Oxygen (FiO2) u Airway Pressure
u Tidal Volume (VT) – Actual
u Deadspace (VD) – Mean
– Peak
u Frequency (f)
u Compliance
u Minute Ventilation (VE)
u Minute Alveolar u PEEP
(Positive End
Ventilation (VA)
Expiratory Pressure)/
u Flow Rate CPAP
u Inspiratory Time
31
32. Fraction of Inspired Oxygen
u Oxygenconcentration, expressed as
fraction in decimal form
– e.g. 50% O2 = FiO2 0.5
– FiO2 of 0.65 = 65% O2
32
33. Airway Pressure
u Actual (Paw)
– Real-time airway pressure
u Mean (MAP)
– Mean pressure over one complete
ventilatory cycle or over a specific
period of time
u Peak (PIP)
– Highest pressure over a single
ventilatory cycle
SM
CCEMT-P 6/98
33
35. Flow Rate
u Inspiratory(I) flow measured in lpm
u Maintain desired I : E ratio
u Flow may affect pressures
u In Time Cycled Ventilation:
flow rate x I time = VT
30 Lpm x 1.5 seconds = 750 ml
60 Lpm x 0.5 seconds = 500 ml
11. 40 Lpm x 0.75 second = ? VT
35
36. I:E Ratio
u Ratio of time for I:E for normal
breathing is 1:2
u Clinical situations may require ratio
to change (ET tubes cause resistance
to exhalation and may require longer
expiratory times and I:E of 1:3 or
longer.
36
37. Compliance
u Measure
of the willingness of the
lungs to expand with a positive
pressure breath
– Increased compliance
u Lungs are more receptive to a mechanical
breath
u Reflected in lower airway pressures
37
39. Spontaneous vs. Mechanical
breathing - supine
u increases ventilation to non-perfused areas
u increases V/Q mismatch
u increases posterior consolidation/atelectasis
u increased diaphragmatic tone decreases
atelectasis
u decreases venous return and cardiac output
9/11/2011 39
Voitek A. Novakovski BSRC, RRT, NREMT-P, CCEMT-P, AE-C
40. Compliance
– Decreased compliance
u Lungs
are less receptive to a mechanical
breath, and airway pressures increase
– Patient may be developing a pneumo or
hemothorax,
– Restrictive lung disease or process such as
pneumonia, or atelecasis
– Developing ARDS or pulmonary edema
u Patients
with COPD usually have high
compliance with increased expiratory
resistance.
1-13 Voitek A. Novakovski RRT, CCEMT-P 40
41. Resistance
u This is reflected when there is a high
PIP but low plateau pressures and a
long exhalation time.
– Common with Asthma or Acute COPD
exacerbation
1-13 Voitek A. Novakovski RRT, CCEMT-P 41
42. Mechanical Ventilation
u Complications
– Bio-mechanical Trauma/Pneumothorax
u Reduced by PEEP
u Avoid overdistention
– Airway trauma
Keep head aligned with
u
torso
– Atelectasis
u Humidify the air (HME)
u Avoid excessive suction
u Vary Pt’s position
– Oxygen toxicity
Use the lowest FIO2 that
u
results in adequate PaO2
– Device dependence
42
47. Principles of Ventilatory Support
u Oxygenation
– PO2
u Affected by controlling FiO2, FRC, and/or
Mean Paw
u Ventilation
– pH
– PCO2
u Affectedby controlling VA (Minute Alveolar
Ventilation)
47
48. Common Mechanical Ventilator
Characteristics (1 of 2)
u Power source: pneumatic or electric
– External
– Internal
u Cycling
– Which variable terminates inspiratory
phase of breath: vol, time, flow, or
pressure
u Breath delivery
– Either positive or negative pressure
49. Common Mechanical Ventilator
Characteristics (2 of 2)
u Parameters
– Mode, tidal volume, respiratory rate,
flow, FiO2, PEEP selected by clinician
u Ventilator circuit
– Reusable or disposable
u Alarms
– Vary in type
– Set for individual patient, never disabled
50. Ventilator Setup Procedures
– FiO2: Always start at 1.0 and adjust by SpO2
– Select mode (if Pt transport try to mimic
settings of ventilator patient is on)
– Set respiratory rate
– Set tidal volume, Insp time, or Pressure
– Set flow rate; if adjustable
– Set PEEP
– Connect ventilator and observe for stability
– Check PIP, Plateau Pressure, and return Vol,
– Set alarms
– Patency of circuitry and all connections
– Check vital signs, SpO2, and ETCO2
50
51. Modes of Ventilation
u Overview
– Control
– Assist/Control
– Synchronized Intermittent Mandatory
Ventilation (SIMV)
– Pressure Control
– Pressure Support
– Continuous Positive Airway Pressure
(CPAP)
51
52. Control
All parameters of the ventilator cycle
(frequency, VT, flow rate) are
controlled by the ventilator
– Patient is “locked out” from triggering a
breath
– Patient has no active role in ventilatory
cycle
– Rarely used
52
53. Assist/Control
u Usually Volume cycled ventilation
– Most popular and easily applied
– Essential parameter to control is volume
delivery, inspiratory flow (time), f (rate),
FiO2, and sensitivity (-2cmH2O)
u Tidal volume (VT) and minute volume
(VE) are predictable, PIP variable
u Anxious patients may create stacking
u Ventilator may be triggered by road
vibrations.
53
55. SIMV or SIMV with PS
u Ventilator
delivers set number of machine
breaths at set FiO2
– Respiratory rate, Insp Flow, and VT are set
– Synchronized with patient’s spontaneous efforts
u Additional
spontaneous breaths possible
through circuit
– Spontaneous breaths may Pressure assisted
– Flow rate and VT are patient controlled
– Keeps respiratory muscles active and
coordinated
u Decreases stacking and need for sedation
55
58. Pressure Control
u Pressure limited-time cycled ventilation
– Inspiration ends at a pre-set time and airway
pressure
– Volume per breath may be variable
– Often used with ARDS to limit applied pressure
– Exhaled volume must be monitored closely
– Not well tolerated by awake patients and
usually requires deep sedation
1-13 Voitek A. Novakovski RRT, CCEMT-P 58
60. Pressure Support
u Pressure limited-flow cycled ventilation
– Inspiration limited by applied pressure, and ends at a
pre-set terminal flow
– Volume per breath may be variable
– Lungs should be relatively free of resistance and
compliant
– Patient sedated or cooperative
– Usually support needed for less than 24 hours or
weaning from long term ventilation
– May be used for long-term chronic support
u Often used with SIMV to enchance spontaneous
breaths and overcome ET tube resistance.
60
62. Dual Modes
u Starts as a Pressure Limited mode which
adjusts the pressure limit on a breath by
breath basis in order to achieve a desired
Tidal Vol (VT) and/or Minute Vol (VE)
u Utilize the advantages of pressure limited
modes which allow flow to more accurately
meet patient demand.
– PRVC: Pressure Regulated Volume Control
– Volume Control Plus
– Volume Support
– Automode
62
63. General Clinical Guidelines
Tidal volume (VT) 6-8 ml/Kg
Respiratory rate (f) 10-14 bpm (ETCO2 35-40)
FiO2 ABG (PO2) or SpO2≥94%
Flowrate 40-60 lpm (I:E ratio)
PIP ≤ 40 cmH2O
Minute volume (VE) ABG(PCO2/pH)ETCO2
Sensitivity -2 cm, adjust as needed
High Pressure Limit 10 cm above PIP
Low Pressure Limit 10 cm below PIP
63
64. Monitors
u Airway Pressure (Paw or PIP)
– Real time manometer or graph
– Range: 0-120 cm H2O (depends on vent)
u Monitor Display
– Breath rate
– Flow
– High pressure alarm
– Low pressure alarm
– PEEP
– I time or I:E
– VT
– VE
64
66. Ventilator Alarms (con’t)
u High pressure limit
– Usually set 10 cm H2O above patient’s average
PIP
– When activated, ventilator terminates breath
u Causes of high pressure alarm violation
– Resistance to gas flow: kinks or water in
tubing, secretions, bronchospasm, patient
coughing, gagging, “fighting the ventilator”
– Decrease in lung compliance, lungs become
“stiffer”: atelectasis, pneumothorax,
pulmonary edema
67. Ventilator Alarms (con’t)
u Low pressure limit
– Primary cause: patient disconnect, or leak in
system
– Inspiratory flow too low and patient gasping
for air (increase flow to meet demand)
u Low exhaled volume or minute ventilation
– Usually set ~10% below set VT and average VE
– Ensures adequate alveolar ventilation is
maintained
– Causes: air leaks, decrease in compliance with
PSV and PCV, high pressure alarm triggered
and breath delivery terminated
– Check for bubbling in chest tubes
68. Ventilator Alarms (con’t)
u High Rate: usually set ≈ 10 over
average rate
– Alarm indicates agitation, hypoxia, or
insufficient VT
– Check vital signs, SpO2, ETCO2, exhaled
VT, or provide sedation
– May be due to “auto-cycling”, check
sensitivity, or check for leaks in circuit
1-13 Voitek A. Novakovski RRT, CCEMT-P 68
70. Ventilator Alarms (con’t)
u Low
Rate: usually set ≈ 10 below
average rate
– For spontaneous breathing modes like
PS or CPAP this alarm is critical and
indicates either patient is fatigued or
over sedated.
u Low
tidal volume: usually ≈ 10%
below average or set VT
– Alarm usually due to leak in the system
– In PS or CPAP pt fatigued or over
sedated
1-13 Voitek A. Novakovski RRT, CCEMT-P 70
71. Ventilator Alarms (cont)
u Apnea
Alarm: this alarm is mostly
used with PS or CPAP:
– Patient has stopped breathing
– May initiate apnea backup ventilation on
some ventilators
u Disconnect:
some ventilators have
this alarm in addition to a low
pressure alarm.
71
72. Ventilator Alarms (cont)
u Apnea
Alarm: this alarm is mostly
used with PS or CPAP:
– Patient has stopped breathing
– May initiate apnea backup ventilation on
some ventilators
u Disconnect:
some ventilators have
this alarm in addition to a low
pressure alarm.
73. Ventilator Alarms (continued)
u Ventilator Inoperative (some vents)
– normal operation ceases
u Breathe room air if spontaneous breathing is present
– recoverable
u Lossof external power or voltage out of range
u Mode switch temporarily set to Off
– non-recoverable
u Software or CPU problem
u External Power Low/Fail
– Ventilators with this alarm switch to internal
battery
73
74. Ventilator Alarms (cont)
u Battery Low/Fail
– Switch to external power
u Low PEEP
– Monitored PEEP value deviates from
manually set value: check for leaks in
system
u Transducer Calibration
– Self test shows baseline pressure +/- 2 cm
H2O from zero
– Calibrate ventilator
74
75. Flow-Restricted, Oxygen-Powered
Ventilation Device (1 of 4)
u Third
potential source for artificial
ventilation
– Manually triggered ventilator or demand
valve
– Used to ventilate apneic patients or to
administer supplemental oxygen to
spontaneously breathing patients
76. Flow-Restricted, Oxygen-Powered
Ventilation Device (2 of 4)
Demand valve triggered by the
negative pressure generated during
inhalation
Valve automatically delivers
100% oxygen and stops
the flow of gas at the
end of inhalation.
Patients find it most
comfortable if they
hold the mask to their
face themselves.
77. Flow-Restricted, Oxygen-Powered
Ventilation Device (3 of 4)
u Apneic patients
– Pushbutton on top of the FROPVD can control
the flow of oxygen.
– When depressed, 100% oxygen flows at a rate
of 40 L/min.
u Requires an oxygen source
– Operator cannot feel whether the patient is
being adequately ventilated with this device.
78. Flow-Restricted, Oxygen-Powered
Ventilation Device (4 of 4)
u Use
– Has been used for several years
– Recent findings suggest that it should not be
used routinely because of the high incidence of
gastric distention and damage to intrathoracic
structures caused by barotraumas.
– Should not be used when ventilating infants or
children or for patients with possible cervical
spine or chest injury
– Cricoid pressure may need to be maintained to
ventilate nonintubated patients.
79. Skill Drill 11-21:
Flow-Restricted, Oxygen-Powered
Ventilation for Apneic Patients (1 of 2)
Step 1
Step 2
Step 3
88. PEEP
u Definition
– Positive End Expiratory Pressure: The
Application of positive pressure to the
airway at end exhalation.
– Used to increase FRC to normal levels.
u Used with other mechanical ventilation modes
such as A/C, SIMV, PS, or PCV
5 cm H2O
PEEP
89. CPAP
u Definition:
PEEP applied to a spontaneously
breathing patient: without mechanical
assist.
– Continuous Positive Airway Pressure: Constant
positive pressure throughout the ventilatory
cycle
– Requires spontaneous respiratory drive
– Rate and VT determined entirely by the patient
10 cm
H2O
PEEP
Time
92. CPAP
u Must set back-up ventilation
parameters if available
u Benefits by normalizing FRC:
– Increases compliance
– Decreases atelectasis
– Reduces pulmonary edema
– Increases PaO2
– Decreases work of breathing (WOB)
– Splints airways in Asthma and COPD
92
93. CPAP
The National Association of EMS Physicians (NAEMSP)
believes that noninvasive positive pressure ventilation
(NIPPV) is an important treatment modality for the
prehospital management of acute dyspnea. This
document is the official position of the NAEMSP.
Read More:
http://informahealthcare.com/doi/abs/
10.3109/10903127.2011.561418
Voitek A. Novakovski BSRC, RRT, NREMT-P,
9/11/2011 CCEMT-P CCEMT-P, AE-C 93
94. 10 Commandments of
Transport Ventilation
1) Maintain set PEEP (bagging)
2) Hold ETT when switching
3) Your vent = their vent
4) Transition to vent early and observe
5) Security of airway. Re-tape if necessary
6) Adequate portable oxygen supply
7) Judicious use of paralytics or sedatives
8) Track plateau versus PIP
9) Maintain EtCO2 and SpO2
10) Minimal to no changes
Voitek A. Novakovski BSRC, RRT, NREMT-P,
9/11/2011 CCEMT-P CCEMT-P, AE-C 94
95. Critical Care Ventilator Transport
u It is important that you set your ventilator to
settings as close as possible to what kept the
patient stable in the hospital. Adjust as needed
u If you are unable to stabilize the patient on your
ventilator, then a respiratory therapist may be
required to accompany you using the hospital
ventilator, or you may have to refuse transport.
u If you take their ventilator, make sure it is
compatible with your power source.
u Do not attempt to transport a patient that is
beyond your capability to maintain.
Voitek A. Novakovski BSRC, RRT, NREMT-P,
9/11/2011 CCEMT-P CCEMT-P, AE-C 95
97. Paul Andrate
Voitek A. Novakovski BSRC, RRT, NREMT-P,
9/11/2011 CCEMT-P CCEMT-P, AE-C 97
98. Quiz
u Pt 32 y/o intubated on vent, VT
450ml, f 14, FiO2 1.0
– ABG pH 7.37, PCO2 42, PO2 64
– What would you change or add?
u Pt 17 y/o Asthmatic on 4L/NC with
bilat insp and exp wheezes.
– ABG pH 7.43, PCO2 36, PO2 92
– What 2 classes of drugs plus other
options might help this young man?
Voitek A. Novakovski BSRC, RRT, NREMT-P,
1-13 CCEMT-P 98
101. Initiation of NPPV
u Set FIO2 at 1.00
u Hypoxemic failure
– Inspiratory pressure (IPAP) 10 cm H2O
– Expiratory pressure (EPAP) 5 cm H2O
– Titrate EPAP in 2 cm H2O increments
u Ventilatory failure
– IPAP 10 and EPAP 2 cm H2O
– Titrate IPAP in 2 cm H2O increments
102. Initiation of NPPV
u Make changes every 15-30 minutes
u Monitor vital signs, appearance,
pulse oximetry and blood gases
u Head of bed at 45° angle
u Consider gastric decompression
u Intubation if patient deteriorates