Pleural effusion caused by malignancies has been described as malignant pleural effusion. Etiology,pathogenesis,diagnosis and management of malignant pleural effusion has been descibed in this powerpoint presentation.
Abnormal fluid accumulation in potential space in between parietal and visceral pleurae – there is imbalance between formation and absorption in response to injury, inflammation or both locally and systematically
Pleural effusion caused by malignancies has been described as malignant pleural effusion. Etiology,pathogenesis,diagnosis and management of malignant pleural effusion has been descibed in this powerpoint presentation.
Abnormal fluid accumulation in potential space in between parietal and visceral pleurae – there is imbalance between formation and absorption in response to injury, inflammation or both locally and systematically
Management of parapneumonic effusion and empyemaDileep Benji
Any pleural effusion associated with bacterial pneumonia,lung abscess or bronchiectasis is defined as parapneumonic effusion.Presence of pus in pleural space is called empyema. Pathogenesis,bacteriology,clinical presentation,diagnosis,management has been described in this powerpoint presentation.
Management of parapneumonic effusion and empyemaDileep Benji
Any pleural effusion associated with bacterial pneumonia,lung abscess or bronchiectasis is defined as parapneumonic effusion.Presence of pus in pleural space is called empyema. Pathogenesis,bacteriology,clinical presentation,diagnosis,management has been described in this powerpoint presentation.
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
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
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
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
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.
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.
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
2. DEFINITION:
By detecting exfoliated malignant cells in pleural fluid or demonstrating
these cells in pleural tissues - by percutaneous pleural biopsies,
thoracoscopy, thoracotomy or at autopsy.
22% of all pleural effusions
42% of exudative pleural effusions
3.
4. LUNG MALIGNANCIES:
All type of lung carcinoma
M/C ADENOCARCINOMA
Lung carcinoma - anti-p53 antibodies are more likely
Lung carcinoma + Pleural effusion is M1a , stage IV
Presence of pleural effusion at the time of diagnosis adversely affect
the prognosis.
5. BREAST CARCINOMA:
2nd most common cause of MPE
More common with lymphangitic spread
Determination of steroid receptors in the effusion is useful in
planning the therapy.
6. LYMPHOMAS
Lymphomatous invasion of pleura is an uncommon and late finding in HODGKIN’S
DISEASE but seen with increased frequency in NON HODGKIN’S LYMPHOMA
Responsible for 75% of chylothoraces secondary to malignant diseases
Approximately 40% of the patients with AITL [Angioimmunoblastic T Cell Lymphoma]
have pleural effusion
7. LYMPHOMAS
HODGKIN’S DISEASE
Incidence at presentation - 7 to 21%
Intrathoracic lymph node involvement without
microscopic pleural involvement
HD and pleural effusion have NODULAR
SCLEROSIS type.
NON HODGKIN’S LYMPHOMA
Incidence - 6 to 50%
20 to 70% have evidence of mediastinal
disease.
LARGE CELL LYMPHOMAS are more frequently
associated with pleural effusion than small cell
lymphomas
8. MULTIPLE MYELOMA:
MPE in patients with multiple myeloma - 1%
Develops after an average of 12 months after the diagnosis
Associated pleural or chest wall plasmacytomas
9. MALIGNANT MESOTHELIOMA:
Less common cause of MPE
M/C primary malignant tumor of the pleura
Risk factor- Inhalational exposure to asbestosis
Usually unilateral but in <10% cases it is bilateral.
Epithelial type is associated with large pleural effusion and regional lymh node metastases.
Sarcomatous type is associated with distant metastases but there is no or very little pleural
effusion.
11. CLINICAL MANIFESTATIONS:
* Dyspnoea (> 50% of patients)
* Chest pain ( 34% patients)
* Dry and non productive Cough
* Cachexia and lymphadenopathy (1/3rd patients)
12. Dyspnea:
• Decrease in compliance of chest wall.
• Contralateral shift of mediastinum
• Inversion of ipsilateral diaphragm
• Decrease in ipsilateral lung volume modulated by neurogenic
reflexes from lung and chest wall.
• Post obstructive pneumonia or Atelectasis due to central
bronchial lesion
13. CHEST PAIN:
•Due to involvement of parietal pleura , ribs and chest wall.
•Patients with MPE - dull chest pain
•Patients with benign disease - more intense pleuritic chest pain
•Malignant mesothelioma chest pain is the M/C presenting symptom
•Pleuritic chest pain is referred to abdomen as intercostal nerves are also distributed to
abdomen.
•Pleuritic pain felt simultaneously in lower chest and ipsilateral shoulder is
pathognomonic of diaphragmatic involvement(due to involvement of phrenic
nerve;C3,4,5)
14. DRY & NON PRODUCTIVE COUGH:
•Due to pleural inflammation
•Lung compression by the fluid - bring opposing bronchial walls into contacts
stimulating the cough reflex
18. CT THORAX:
Undiagnosed pleural effusions - CT scan - benign or malignant etiology
Following 4 findings are suggestive of malignancy:
i. Pleural nodularity
ii. Pleural rind (Fibrous swelling of the pleura causing retraction of thoracic wall )
iii. Mediastinal pleural involvement
iv. Pleural thickening greater than 1 cm.
19.
20.
21. Pleural fluid characteristics:
Malignant pleural effusion -exudate following LIGHT’S CRITERIA
• Fluid protein : serum protein > 0.5
• Fluid LDH : serum LDH > 0.6
• Fluid LDH > 2/3rd the upper limit of normal value of serum LDH.
Serous, serosanguineous, or grossly bloody
Limitation: Misidentifies 25% of transudative effusions as exudative effusions
22. Grossly bloody pleural fluid - RBC count >100,000/mm3 >> malignant pleural disease
Either lymphocytes or mononuclear cells (greater than 50% lymphocytes)
WBC count - is variable : 1000 - 10,000/mm3
Low PH (less than 7.3) and glucose (less than 60 mg/dL) - greater burden of tumor
within the pleural space
10% - elevated pleural fluid amylase level
◦ Salivary isoenzyme rather than the pancreatic isoenzyme
◦ Amylase isoenzyme analysis -differentiate pancreatic effusion V/S malignant effusion
Pleural fluid characteristics:
23. Pleural Biopsy
•“closed” biopsy technique
• Minimally invasive, and low-cost method
• Image guided
• Medical thoracoscopy
• Surgical thoracoscopy
• VATS - gold standard for the diagnosis of malignant pleural disease
24. CYTOLOGIC EXAMINATION OF PLEURAL FLUID:
As a definite diagnosis
Important features of malignant cells:
◦ Large cells
◦ Nuclei of malignant cells may exceeds 50µm in diameter in contrast with
mesothelial cell nuclei which rarely exceeds 20µm in diameter.
◦ Malignant cells have high nucleocytoplasmic ratio.
27. PROGNOSIS IN MALIGNANT PLEURAL EFFUSION:
MPE management depends upon prognosis
Certain factors i.e. tumor type, stage and performance status(PS) are accepted prognostic factors in
malignancy, including MPE
Lung cancer carries the worst prognosis
Longer survival - gynaecological tumors d/t underlying sensitivity to treatment
Specific MPE related prognostic factors include:
Effusion size
massive MPE, defined as fluid occupying the entire hemithorax, associated with worse survival in large
prospective study.
Pleural fluid pH ≤7.28 is associated with shorter survival
High serum and pleural fluid VEGF levels -worse outcomes in MPE - effects of inflammation, angiogenesis and
tumor necrosis.
28.
29. Performance status [ecog]:
0 Asymptomatic
1 Symptomatic but ambulatory (able to carry out light work)
2 In bed < 50% of the day (unable to work but able to live at home
with some assistance)
3 In bed >50% of the day (unable to care for the self)
4 Complete bedridden
30.
31. Therapeutic pleural aspiration
High rate of recurrence
Aspiration is not recommended - life expectancy >1 month
Caution should be taken if removing >1.5 litre on a single occasion
32.
33. Pleurodesis
• Small-bore (10-14 F) intercostal catheters - drainage and administration of sclerosing agents
• Large pleural effusions - drained in a controlled fashion - reduce the risk of re-expansion
pulmonary oedema
• Once effusion drainage and lung re-expansion have been radiographically confirmed,
pleurodesis should not be delayed
• Suction to aid pleural drainage before and after pleurodesis is usually unnecessary
• High-volume low-pressure system is recommended
• Partial pleural apposition - chemical pleurodesis may still be attempted - symptomatic relief
• Symptomatic cases - pleural apposition cannot be achieved (‘trapped lung’)- indwelling pleural
catheters
34. • Talc is the most effective sclerosant available for pleurodesis
• Graded talc > ungraded talc - as it reduces the risk of arterial hypoxaemia
• Talc pleurodesis – by slurry or by insufflation
• Bleomycin, Povidone iodine, Tetracycline, Doxycycline
• S/E Pleuritic chest pain and fever
• Patient rotation is not necessary after intrapleural instillation of sclerosant
• The intercostal tube should be clamped for 1 h after sclerosant administration
• In the absence of excessive fluid drainage (>250 ml/ day) - removed within 24 -48 h of
sclerosant administration
35. •Malignant seeding at intercostal tube or port site
•Patients with proven or suspected mesothelioma - prophylactic radiotherapy to the site of
thoracoscopy, surgery or large-bore chest drain insertion
•Not in pleural aspirations or pleural biopsy
36. Intrapleural fibrinolytics
• Relief of distressing dyspnoea due to multiloculated malignant effusion resistant to simple
drainage
• Streptokinase/ Urokinase
• Septations -broken up under direct vision at thoracoscopy(medical/surgical)
• Thoracic surgery -access multiple loculations, especially those positioned on the mediastinum
37. Re-expansion pulmonary oedema
Maximum of 1.5 l on the first occasion
Remaining fluid - drained 1.5 l at a time at 2 h intervals
◦ Stopping if the patient develops chest discomfort, persistent cough or vasovagal symptom
Reperfusion injury of the underlying hypoxic lung
Increased capillary permeability
Local production of neutrophil chemotactic factors such as interleukin-8
38. Indwelling pleural catheter
•PleurX catheter - 15.5 F silicone rubber catheter , 66 cm in
length with fenestrations along the proximal 24 cm.
•Inserted into the pleural space using the Seldinger
technique under local anesthesia
•Catheter is maintained in place with a chest wall tunnel 5
to 8 cm in length.
•It has a special valve on its distal end that prevents fluid or
air from passing in either direction through the catheter
asbestosis(Hydrated magnesium silicate divided into 2 major types serpentines and amphiboles)
Approximately 1/3rd of patients with malignant pleural effusion have a pleural fluid pH below 7.3(due to combination of acid production and block to the movement of CO2 out of pleural space.)
Mean nuclear diameter > 10.5µm or
Mean nuclear diameter > 9.3 µm + Mean nuclear diameter divided by the Cytoplasmic diameter > 0.74 malignant pleural effusion