Mechanical Ventilation of Patient with COPD Exacerbation lecture presented by Dr Andres Esteban at the Egyptian Critical care Summit 2015 held at Cairo, egypt.
The Egyptian Critical Care Summit is the leading medical event and exhibition for Intensive Care Medicine in Egypt.
Ventilatory management in obstructive airway diseasesVitrag Shah
Presentation on ventilatory management in COPD & Asthma
Updated information till 26/5/16
For powerpoint format, contact dr.vitrag@gmail.com
http://www.medicalgeek.com/presentation/36441-ventilatory-management-obstructive-airway-diseases-presentation.html
Ventilatory management in obstructive airway diseasesVitrag Shah
Presentation on ventilatory management in COPD & Asthma
Updated information till 26/5/16
For powerpoint format, contact dr.vitrag@gmail.com
http://www.medicalgeek.com/presentation/36441-ventilatory-management-obstructive-airway-diseases-presentation.html
Basic information on the Graphics displayed on the Ventilators. Prepared to educate about the graphics to train the professionals who work with Ventilators.
Mechanical Ventilation in COPD Lecture presented by Dr Lluis Blanch at Venti Cairo Mechanical Ventilation Course held on 14-15 November at Cairo, Egypt.
Basic information on the Graphics displayed on the Ventilators. Prepared to educate about the graphics to train the professionals who work with Ventilators.
Mechanical Ventilation in COPD Lecture presented by Dr Lluis Blanch at Venti Cairo Mechanical Ventilation Course held on 14-15 November at Cairo, Egypt.
Presented by D.Niall Ferguson at 9th Pulmonary Medicine Update Course held at Cairo, Egypt.
This course is the leading Pulmonary Critical Care event in Egypt. The course is organized by Scribe (www.scribeofegypt.com)
Evolution of mechanical ventilation in the last 20 yearsDr.Mahmoud Abbas
Evolution of mechanical ventilation in the last 20 years lecture presented by Dr Andres Esteban at the Egyptian Critical care Summit 2015 held at Cairo, Egypt. The Summit is the leading medical event and exhibition for critical care medicine in Egypt
Presentation of Dr. Lluis Blanch at 10th Pulmonary Medicine Update Course, Cairo, Egypt. Pulmonary Medicine Update Course is organized by Scribe : www.scribeofegypt.com
The Changing Role of the Coronary Care Cardiologist & The Emerging Role of Ca...Dr.Mahmoud Abbas
The Changing Role of the Coronary Care Cardiologist
&
The Emerging Role of Cardiac Intensive Care Specialists lecture presented by Dr Sherif Mokhtar, President ECCCP at the Egyptian Spanish Critical care Symposium held at Cairo, Egypt on 11 May 2023
Drug induced Kidney Injury in the ICU. Presentation by Dr Sandra Kane Gill , President Society of Critical Care Medicine (SCCM) , USA at the Egyptian Critical care Summit 2022 conference , organized by the Egyptian College of Critical care Physicians (ECCCP) , Egypt
Using Novel Kidney Biomarkers to Guide Drug Therapy.pdfDr.Mahmoud Abbas
Using Novel Kidney Biomarkers to Guide Drug Therapy: Presentation by Dr Sandra Gill , President SCCM at the Egyptian Critical Care Summit 2022 held at Cairo, Egypt and organized by the Egyptian College of Critical care Physicians (ECCCP)
Presentation by Dr Marwa Atef , National Research Center, Cairo, Egypt . Presented at Cairo Textile Week 2021 , the leading textiles conference in Egypt
Cairo Textile Week 2021 Conference -Egypt Textiles & Home Textiles Export Cou...Dr.Mahmoud Abbas
Egyptian Textiles Export
Opportunities & Requirements
Presentation by Engineer Hany Salam, CEO Salam Textiles, Board member Egypt Textiles & Home Textiles
Export Council (THTEC)
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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
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
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
3. COPD is the 5th leading cause
of death
Chronic bronchitis accounts for
approximately 85% of COPD
4. Rennard S Eur Respir J. 2002.
1.616 cases / 100.000 inhabitans/year
13,8% of patients admited at the hospital in the last
year
Seneff. JAMA 1995
Moran. Crit Care Med 1998
Groenewegen. Chest 2003
Gunen. Eur Respir J. 2005
11% a 74% need admission in the UCI
6. Have more complications
Use more resources
Have more difficulty weaning from
mechanical ventilation
Have a higher mortality
THE PATIENTS WITH COPD
EXACERBATED
CANDIDATES TO RECIVE MECH.
VENTILATION
7. Have more complications
Use more resources
Have more difficulty weaning
from
mechanical ventilation
Have a higher mortality
THE PATIENTS WITH COPD
EXACERBATED
CANDIDATES TO RECIVE MECH.
VENTILATION
9. COPD 507 10.1 % 15 9.7 %
Pneumonia 691 13.7 % 30 19.5 %
ARDS 216 4.3 % 15 9.7 %
Aspiration 123 2.4 % 6 3.9 %
Trauma 393 7.8 % 14 9.1 %
Neuromuscular disease 89 1.8 % 5 3.2 %
Asthma 74 1.5 % 5 3.2 %
Chronic interstitial lung
disease
54 1.1 % 6 3.9 %
PATIENTS
WITHOUT
BAROTRAUMA
PATIENTES
WITH
BAROTRAUMA
n = 5029 n = 154
A. Anzueto, F. Frutos, A. Esteban, et al
Intensive Care Med 2004;30
10. Have more complications
Use more resources
Have more difficulty weaning from
mechanical ventilation
Have a higher mortality
THE PATIENTS WITH COPD
EXACERBATED
CANDIDATES TO RECIVE MECH.
VENTILATION
11. Days with mechanical ventilation
(Esteban A, et al. 2º ISMV. AJRCCM 2008
Mean (SD)
COPD: 6,0 days (6,5)
No COPD: 6,2 days (7,0)
p = 0,72
Median (P25, P75)
COPD: 4 days (2,7)
No COPD: 4 days (2, 8)
p = 0,73
17
16
15
14
13
12
11
10
9
8
7
6
5
4
3
2
1
0
COPD No COPD
12. Days of stay
(Esteban A, Frutos F, et al. 2º ISMV. AJRCCM 2008
ICU
Mean (SD)
COPD: 11 days (11)
No COPD: 12 days (13)
p = 0,34
Median (P25, P75)
COPD: 8 days (5, 13)
No COPD: 8 days (4, 15)
p = 0,70
Hospital
Mean (SD)
COPD: 20 days (18)
No COPD: 25 days (28)
p = 0,007
Median (P25, P75)
COPD: 17 days (10 , 26)
No COPD: 17 days (9, 31)
p = 0,12
13. Long time mechanical ventilation
Mechanical ventilation > 14 days
COPD
Acute lung
failure
Neurologic
Esteban et al.
JAMA 2002
3,4% 8,6% 7,1%
Esteban et al.
AJRCCM 2008
7,9% 9,4% 5,7%
16. Have more complications
Use more resources
Have more difficulty weaning from
mechanical ventilation
Have a higher mortality
THE PATIENTS WITH COPD
EXACERBATED
CANDIDATES TO RECIVE MECH.
VENTILATION
17. Days of weaning
(Esteban A, et al. 2º ISMV. AJRCCM 2008
Mean (SD)
COPD: 2,5 days (2.3)
No COPD: 2,3 days (2.7)
p = 0,51
Median (P25, P75)
COPD: 2 days (1 , 3)
No COPD: 1 days (1 , 2)
p = 0,10
10
9
8
7
6
5
4
3
2
1
0
COPD No COPD
19. Have more complications
Use more resources
Have more difficulty weaning
from
mechanical ventilation
Have a higher mortality
THE PATIENTS WITH COPD
EXACERBATED
CANDIDATES TO RECIVE MECH.
VENTILATION
20. 0
0,1
0,2
0,3
0,4
0,5
0,6
0,7
0,8
0,9
1
1 3 5 7 9 11 13 15 17 19 21 23 25 27
COPD
Asthma
ARDS
ARF non
ARDS
Probability
of survival
Days from the start of
mechanical ventilation
A.Esteban, A. Anzueto, F. Frutos, I. Alía et
JAMA 2002;287:345-355
22. Mortality is 4% in hospitalized with mild
to moderate disease
Mushlin AI, et al. JAMA 1991;226:80-83
24 % mortality in patients admitted to an ICU
with respiratory failure (COPD exacerbated)
Connors AF, et al (Support) AJRCCM
1996;154:959-967
23. Mortality Associated With Severe
AECOPD
Connors et al. Am J Respir Crit Care Med 1996;154:959.
MortalityRate(%)
Mortality Following Hospitalization
for Severe AECOPD
24. DEAD 116 / 522
(22.2%)
COPD Ventilated >12 h.
NO
DEAD
80/466 (17%)
< 18
DEAD
64/437 (14.7%)
> 18
DEAD
16/29 (55%)
YES
DEAD
36/56 (64%)
NO
DEAD
50/402 (12.5%)
YES
DEAD
14/35 (40%)
RENAL
FAILURE
DAYS OF
MECH. VENT.
SHOCK
25. 1 Renal failure 56 64 % 12.7 6.8 - 23.6
2
Not renal failure
Days of M.V. >18
29 55 % 8.7 3.9 - 19.1
3
Not renal failure
Days of M.V. <18
Shock
35 40 % 4.7 2.2 - 9.8
4
Not renal failure
Days of M.V. <18
No shock
402 12.5% 1.0 ---
nº Exitus OR CI 95%
COPD (n=522)
28. Have more complications
Use more resources
Have more difficulty weaning
from mechanical ventilation
Have a higher mortality
THE PATIENTS WITH COPD EXACERBATED
CANDIDATES TO RECIVE MECH. VENTILATION
NOT
NOT
NOT
NOT
29. Treatment of the exacerbation
1. Oxigen if hypoxemia
2. Broncodilators
• Beta-agonists
• Anticolinérgyc
3. Non-Invasive Mechánical Vent.
4. Steroids
5. Antibiótics
6. Metilxantins
30. Canadian Thoracic Society recomendations
for management of chronic obstructive
pulmonary disease -2008 update – highlights
for primary care.
ACUTE EXACERBATIONS
“Oral or parenteral corticosteroids (dosage of
25 mg to 50 mg of prednisone equivalent per
day for between sever and 14 days) are
recomended in most patients with moderate
to severe AECOPD”.
D.E. O’Donnell, et al.
Can Resp J 2008;15:1A-8A
31. CHRONIC OBSTRUCTIVE PULMONARY DISEASE
National clinical guideline on management of chronic obstructive
pulmonary disease in adults in primery and secondary care
The guideline will include recommendations in the following areas.
Management of stable patients, management of exacerbations and
prevention of progression of the disease, to include:
smoking cessation, including pharmacological and non-
pharmacological approaches as they relate specifically to COPD
bronchodilator management including methods of delivery &
methods of assessing effcacy inhaled and oral corticosteroid
therapy
non-pharmacological interventions, including pulmonary
rehabilitacion, lifestyle advice and self-management techniques
oxygen therapy
non-invasive ventilation
indications for surgery
criteria for admission and/or management at home, and the
problems of respiratory failure
Thorax 2004;59:1-232
32. ORIGINAL INVESTIGATION
Efficacy of Corticosteroid Therapy in Patients With an Acute
Exacerbation of Chronic Obstructive Pulmonary Disease
Receiving
Ventilatory Support
Inmaculada Alıa, MD; Miguel A. de la Cal, MD; Andres Esteban, MD, PhD; Ana Abella, MD;
Ricard Ferrer, MD; Francisco J. Molina, MD; Antoni Torres, MD, PhD; Federico Gordo, MD;
Jose. Elizalde, MD; Raul de Pablo, MD; Alejandro Huete, MD; Antonio Anzueto, MD, PhD
Arch Intern Med. 2011;171(21):1939-1946
COPD exacerbation with IMV and NIMV
40With Placebo
38With Corticoids
Primary outcome: Duration of MV; length of stay in ICU;
Intubation
in patients with NIV
Secundary outcome: Mortality ; Length of stay in Hospital
33. Characteristic Placebo
Group
(n = 40)
Corticostero,
Group
(n = 43)
p value
Reason for acute
exacerbation of COPD
Respiratory infection
Cardiac failure
Sepsis
Postoperative
Unidentified cause
Others
28 (70%)
9 (22%)
1 (2%)
1 (2%)
0 (0%)
2 (5%)
30 (70%)
8 (19%)
1 (2%)
0 (0%)
4 (9%)
3 (7%)
0,72
Initial ventilatory support
Non-invasive
Conventional
19 (47%)
21 (52%)
18 (42%)
25 (58%)
0,60
Baseline characteristics of the 83 patients
according to treatment assignment
I Alia,M A de la Cal,A Esteban,et al.
Arch Internal Med 2011;171:1939
34. Characteristic Placebo
Group
(n = 40)
Corticosteroid
Group
(n = 43)
p
value
Blood gases
PaO2/FIO2 (mm Hg)
PaCO2 (mm Hg)
pH
191,5 ±75,9
68,7 ± 18,5
7,31 ± 0,10
197,8 ± 83,7
69,9 ± 19,7
7,27 ± 0,11
0,72
0,78
0,12
Blood glucose (mg/dl) 158,7 ± 65,7 193,3 ± 60,6 0,016
White-cell count (per mm3)
10.515 ±
3.645
12.166 ±
5.268
0,10
Baseline characteristics of the 83 patients
according to treatment assignment
I Alia,M A de la Cal,A Esteban,et al.
Arch Internal Med 2011;171:1939
35. Event Placebo
Group
(n = 40)
Corticosteroid
s Group
(n = 43)
p
value
Superinfection 6 (15%) 5 (12%) 0,65
Gastrointestinal
bleeding
2 (5%) 2 (5%) 0,60
Arterial hypertension 4 (10%) 2 (5%) 0,42
Hyperglycemia 10 (25%) 20 (46%) 0,04
Ventilator-associated
pneumonia
3 (7%) 4 (9%) 0,77
Delirium 3 (7%) 1 (2%) 0,35
ICU-acquired paresis 0 0
Frecuency of adverse events
I Alia,M A de la Cal,A Esteban,et al.
Arch Internal Med 2011;171:1939
38. Outcomes Placebo
Group
(n = 40)
Corticostero
ids Group
(n = 43)
p
value
Duration of mechanical
ventilation (days)
Non-invasive ventilation
Conventional ventilation
4 (3-7)
4 (2-5)
7 (4-11)
3 (2-6)
2 (2-3)
5 (3-7)
0,036
0,008
0,09
Length of ICU stay (days)
Non-invasive ventilation
Conventional ventilation
7,5 (5-12)
5 (4-9)
10 (7-18)
6 (4-10)
4 (3-5)
9 (6-12)
0,09
0,042
0,18
Length of hospital stay (days)
Non-invasive ventilation
Conventional ventilation
15 (11-21)
15 (9-20)
17 (12-31)
13 (8-21)
14 (8-19)
13 (8-22)
0,30
0,99
0,07
Outcome measures
I Alia,M A de la Cal,A Esteban,et al.
Arch Internal Med 2011;171:1939
39. Outcomes Placebo
Group
(n = 40)
Corticosteroi
ds Group
(n = 43)
p value
In-ICU mortality
Non-invasive ventilation
Conventional ventilation
4 (10%)
1/19 (5%)
3/21 (14%)
5 (12%)
0/18 (0%)
5/25 (20%)
0,81
0.04
0,17
Failure of non-invasive
ventilation
7/19 (37%) 0/18 (0%) 0,004
Reintubation within 48
hours*
5/26 (19%) 3/22 (14%) 0,71
Outcome measures
I Alia,M A de la Cal,A Esteban,et al.
Arch Internal Med 2011;171:1939
40. The treatment with corticosteroids of patients with
COPD exacerbations requiring mechanical ventilation
(invasive and non-invasive)
Was not associated with and increased risk of
gastrointestinal bleeding, superinfections,
psychiatric disorders, or adquired neuromuscular
weakness.
Is associated with a significantly increase in the
success of NIV.
Is associated with a reduction in the duration of
invasive mechanical ventilation.
SUMMARY