This document provides guidelines and recommendations from the ATS for the diagnosis and treatment of community-acquired pneumonia (CAP) in adult patients. It addresses questions such as when to obtain cultures, perform testing, and initiate antibiotics and corticosteroids. It recommends obtaining cultures for severe CAP or if treating for specific drug-resistant pathogens. It suggests testing for influenza when circulating and provides guidance on antibiotic selection and duration based on severity and location of treatment. The recommendations are meant to guide clinicians in diagnosing and managing CAP.
Pulmonary medicine- Scope and Future by Dr. Jebin Abraham, MD.Jebin Abraham
Pulmonary Medicine is a branch of medicine that deals with respiratory diseases, chest wall diseases, sleep disorders, allergy and much more. This presentation describes this specialty branch in detail with scope and current perspectives being emphasized. It will help in PG aspirant medicos, academicians and undergraduate students to know about Pulmonary Medicine in detail.
Pulmonary medicine- Scope and Future by Dr. Jebin Abraham, MD.Jebin Abraham
Pulmonary Medicine is a branch of medicine that deals with respiratory diseases, chest wall diseases, sleep disorders, allergy and much more. This presentation describes this specialty branch in detail with scope and current perspectives being emphasized. It will help in PG aspirant medicos, academicians and undergraduate students to know about Pulmonary Medicine in detail.
Antifungal Strategies in the Intensive Care UnitsYazan Kherallah
Discuss the different anti-fungal treatment strategies for suspected systemic candidiasis in the intensive care units: prophylaxis, preemptive, empiric and definitive.
Hello members...this is my 39th powerpoint...
It deals with LABA & SABA...The brochodilators used in the treatment of Pulmonary diseases like Asthma & COPD.
It gives a short insight into the drugs used, their indications with dosages, ADRs, interactions, etc.
Worthwhile for a precise information on the same!!
Happy reading!!!
:) :)
Endobronchial Ultrasound Guidance of TBNA. Current Approach To Lung Cancer St...Bassel Ericsoussi, MD
EBUS-TBNA, EUS-FNA or their combination have finally gained acceptance as the tests of first choice in mediastinal staging. In suspected non-small cell lung cancer, endobronchial ultrasound may be preferred in the histologic sampling of paratracheal and subcarinal mediastinal adenopathy because the diagnostic yield can surpass mediastinoscopy
Antifungal Strategies in the Intensive Care UnitsYazan Kherallah
Discuss the different anti-fungal treatment strategies for suspected systemic candidiasis in the intensive care units: prophylaxis, preemptive, empiric and definitive.
Hello members...this is my 39th powerpoint...
It deals with LABA & SABA...The brochodilators used in the treatment of Pulmonary diseases like Asthma & COPD.
It gives a short insight into the drugs used, their indications with dosages, ADRs, interactions, etc.
Worthwhile for a precise information on the same!!
Happy reading!!!
:) :)
Endobronchial Ultrasound Guidance of TBNA. Current Approach To Lung Cancer St...Bassel Ericsoussi, MD
EBUS-TBNA, EUS-FNA or their combination have finally gained acceptance as the tests of first choice in mediastinal staging. In suspected non-small cell lung cancer, endobronchial ultrasound may be preferred in the histologic sampling of paratracheal and subcarinal mediastinal adenopathy because the diagnostic yield can surpass mediastinoscopy
Approach to the therapy of cap , vap and hapazza mokhtar
Many od us as clinician facing an issue regarding appropiate choosing of antibiotics especially in ICU setting . This presentation view outlines of antibiotics therapy based on resistance and patient risks.
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.
263778731218 Abortion Clinic /Pills In Harare ,sisternakatoto
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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
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
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
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
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.
5. We recommend obtaining pretreatment Gram stain and culture of respiratory
secretions in adults with CAP managed in the hospital setting who:
● 1. are classified as severe CAP , especially if they are intubated (strong
recommendation, very low quality of evidence); or
● 2.
○ a. are being empirically treated for MRSA or P. aeruginosa (strong
recommendation, very low quality of evidence); or
○ b. were previously infected with MRSA or P. aeruginosa, especially those
with prior respiratory tract infection (conditional recommendation, very
low quality of evidence); or
○ c. were hospitalized and received parenteral antibiotics, whether during
the hospitalization event or not, in the last 90 days (conditional
recommendation, very low quality of evidence).
6. In Adults with CAP, Should Blood
Cultures Be Obtained at the Time of
Diagnosis?
8. 1. We recommend not obtaining blood cultures in adults with
CAP managed in the outpatient setting (strong
recommendation, very low quality of evidence).
1. We suggest not routinely obtaining blood cultures in
adults with CAP managed in the hospital setting
(conditional recommendation, very low quality of
evidence).
9. We recommend obtaining pretreatment blood cultures in adults with CAP managed in the hospital setting
who:
● 1. are classified as severe CAP (strong recommendation, very low quality of evidence); or
● 2.
○ a. are being empirically treated for MRSA or P. aeruginosa (strong recommendation, very low
quality of evidence); or
○ b. were previously infected with MRSA or P. aeruginosa, especially those with prior respiratory
tract infection (conditional recommendation, very low quality of evidence); or
○ c. were hospitalized and received parenteral antibiotics, whether during the hospitalization
event or not, in the last 90 days (conditional recommendation, very low quality of evidence).
10. In Adults with CAP, Should Legionella and
Pneumococcal Urinary Antigen Testing Be Performed at
the Time of Diagnosis?
12. We suggest not routinely testing urine for pneumococcal antigen in adults with
CAP (conditional recommendation, low quality of evidence), except in adults with
severe CAP (conditional recommendation, low quality of evidence).
We suggest not routinely testing urine for Legionella antigen in adults with CAP
(conditional recommendation, low quality of evidence), except
● 1. in cases where indicated by epidemiological factors, such as association
with a Legionella outbreak or recent travel (conditional recommendation, low
quality of evidence); or
● 2. in adults with severe CAP .(conditional recommendation, low quality of
evidence).
13. In Adults with CAP, Should a
Respiratory Sample Be Tested for
Influenza Virus at the Time of
Diagnosis?
15. When influenza viruses are circulating in the community, we
recommend testing for influenza with a rapid influenza
molecular assay (i.e., influenza nucleic acid amplification
test), which is preferred over a rapid influenza diagnostic test
(i.e., antigen test) (strong recommendation, moderate quality
of evidence).
(https://www.cdc.gov/flu/professionals/diagnosis/index.htm).
16. In Adults with CAP, Should Serum Procalcitonin plus
Clinical Judgment versus Clinical Judgment Alone Be
Used to Withhold Initiation of Antibiotic Treatment?
18. We recommend that empiric antibiotic therapy
should be initiated in adults with clinically
suspected and radiographically confirmed CAP
regardless of initial serum procalcitonin level
(strong recommendation, moderate quality of
evidence).
19. Should a Clinical Prediction Rule for
Prognosis plus Clinical Judgment versus
Clinical Judgment Alone Be Used to
Determine Inpatient versus Outpatient
Treatment Location for Adults with CAP?
21. In addition to clinical judgement, we recommend that
clinicians use a validated clinical prediction rule for prognosis,
preferentially the Pneumonia Severity Index (PSI) (strong
recommendation, moderate quality of evidence) over the
CURB-65 (tool based on confusion, urea level, respiratory
rate, blood pressure, and age ≥65) (conditional
recommendation, low quality of evidence), to determine the
need for hospitalization in adults diagnosed with CAP.
22.
23. Should a Clinical Prediction Rule for Prognosis plus
Clinical Judgment versus Clinical Judgment Alone Be
Used to Determine Inpatient General Medical versus
Higher Levels of Inpatient Treatment Intensity (ICU, Step-
Down, or Telemetry Unit) for Adults with CAP?
25. We recommend direct admission to an ICU for patients with
hypotension requiring vasopressors or respiratory failure
requiring mechanical ventilation (strong recommendation, low
quality of evidence).
For patients not requiring vasopressors or mechanical
ventilator support, we suggest using the IDSA/ATS 2007
minor severity criteria together with clinical judgment to guide
the need for higher levels of treatment intensity (conditional
recommendation, low quality of evidence).
26. In the Outpatient Setting, Which Antibiotics
Are Recommended for Empiric Treatment of
CAP in Adults?
28. 1. For healthy outpatient adults without comorbidities listed below or risk
factors for antibiotic resistant pathogens, we recommend :
○ • amoxicillin 1 g three times daily (strong recommendation, moderate
quality of evidence), or
○ • doxycycline 100 mg twice daily (conditional recommendation, low
quality of evidence), or
○ • a macrolide (azithromycin 500 mg on first day then 250 mg daily or
clarithromycin 500 mg twice daily or clarithromycin extended release
1,000 mg daily) only in areas with pneumococcal resistance to
macrolides <25% (conditional recommendation, moderate quality of
evidence).
29.
30. 2. For outpatient adults with comorbidities such as chronic heart, lung, liver, or renal disease;
diabetes mellitus; alcoholism; malignancy; or asplenia we recommend (in no particular order of
preference)::
○ • Combination therapy:
■ ∘ amoxicillin/clavulanate 500 mg/125 mg three times daily, or amoxicillin/clavulanate 875
mg/125 mg twice daily, or 2,000 mg/125 mg twice daily, or a cephalosporin
(cefpodoxime 200 mg twice daily or cefuroxime 500 mg twice daily); AND
■ ∘ macrolide (azithromycin 500 mg on first day then 250 mg daily, clarithromycin [500 mg
twice daily or extended release 1,000 mg once daily]) (strong recommendation,
moderate quality of evidence for combination therapy), or doxycycline 100 mg twice daily
(conditional recommendation, low quality of evidence for combination therapy); OR
○ • Monotherapy:
■ ∘ respiratory fluoroquinolone (levofloxacin 750 mg daily, moxifloxacin 400 mg daily, or
gemifloxacin 320 mg daily) (strong recommendation, moderate quality of evidence).
31. In the Inpatient Setting, Which Antibiotic
Regimens Are Recommended for Empiric
Treatment of CAP in Adults without Risk
Factors for MRSA and P. aeruginosa?
34. In the Inpatient Setting, Should Patients with
Suspected Aspiration Pneumonia Receive
Additional Anaerobic Coverage beyond
Standard Empiric Treatment for CAP?
36. We suggest not routinely adding anaerobic
coverage for suspected aspiration pneumonia
unless lung abscess or empyema is suspected
(conditional recommendation, very low quality of
evidence).
37. In the Inpatient Setting, Should Adults with
CAP and Risk Factors for MRSA or P.
aeruginosa Be Treated with Extended-
Spectrum Antibiotic Therapy Instead of
Standard CAP Regimens?
39. We recommend abandoning use of the prior
categorization of healthcare-associated
pneumonia (HCAP) to guide selection of
extended antibiotic coverage in adults with CAP
(strong recommendation, moderate quality of
evidence).
40. We recommend clinicians only cover empirically for MRSA or
P. aeruginosa in adults with CAP if locally validated risk
factors for either pathogen are present (strong
recommendation, moderate quality of evidence).
41. If clinicians are currently covering empirically for MRSA or P.
aeruginosa in adults with CAP on the basis of published risk
factors but do not have local etiological data, we recommend
continuing empiric coverage while obtaining culture data to
establish if these pathogens are present to justify continued
treatment for these pathogens after the first few days of
empiric treatment (strong recommendation, low quality of
evidence).
42. In the Inpatient Setting, Should
Adults with CAP Be Treated with
Corticosteroids?
44. We recommend not routinely using corticosteroids in adults with nonsevere CAP
(strong recommendation, high quality of evidence).
We suggest not routinely using corticosteroids in adults with severe CAP
(conditional recommendation, moderate quality of evidence).
We suggest not routinely using corticosteroids in adults with severe influenza
pneumonia (conditional recommendation, low quality of evidence).
We endorse the Surviving Sepsis Campaign recommendations on the use of
corticosteroids in patients with CAP and refractory septic shock
45. In Adults with CAP Who Test Positive for
Influenza, Should the Treatment Regimen
Include Antiviral Therapy?
47. We recommend that antiinfluenza treatment, such as oseltamivir, be prescribed
for adults with CAP who test positive for influenza in the inpatient setting,
independent of duration of illness before diagnosis (strong recommendation,
moderate quality of evidence).
We suggest that antiinfluenza treatment be prescribed for adults with CAP who
test positive for influenza in the outpatient setting, independent of duration of
illness before diagnosis (conditional recommendation, low quality of evidence).
48. In Adults with CAP Who Test Positive for Influenza,
Should the Treatment Regimen Include Antibacterial
Therapy?
50. We recommend that standard antibacterial treatment be
initially prescribed for adults with clinical and radiographic
evidence of CAP who test positive for influenza in the
inpatient and outpatient settings (strong recommendation, low
quality of evidence).
51. In Outpatient and Inpatient Adults with CAP Who Are
Improving, What Is the Appropriate Duration of Antibiotic
Treatment?
52. We recommend that the duration of antibiotic therapy should be guided by a
validated measure of clinical stability (resolution of vital sign abnormalities [heart
rate, respiratory rate, blood pressure, oxygen saturation, and temperature], ability
to eat, and normal mentation), and antibiotic therapy should be continued until the
patient achieves stability and for no less than a total of 5 days (strong
recommendation, moderate quality of evidence).
53. In Adults with CAP Who Are Improving,
Should Follow-up Chest Imaging Be
Obtained?
54. In adults with CAP whose symptoms have resolved within 5
to 7 days, we suggest not routinely obtaining follow-up chest
imaging (conditional recommendation, low quality of
evidence).