These lecture notes were prepared by Dr. Hamdi Turkey- Pulmonologist- Department of internal medicine - Taiz university
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Pleural effusion may be defined figuratively as the juice, oozing from the leaky lingerie of the lung. However the text book definition is the abnormal accumulation of fluid in the pleural space due to disturbances in the forces that keep the pleural fluid economy in equilibrium...
PATHOGENESIS OF BRONCHIECTASIS BY DR BASHIR AHMED DAR ASSOCIATE PROFESSOR MED...Prof Dr Bashir Ahmed Dar
Dr Bashir Ahmed Dar associate professor medicine chinkipora sopore kashmir presently working in malaysia speaks about bronchiectasis.Bronchiectasis which is defined as the irreversible dilatation of the cartilage-containing airways bronchi or bronchioles.
These lecture notes were prepared by Dr. Hamdi Turkey- Pulmonologist- Department of internal medicine - Taiz university
Do Not Forget To Visit Our Pages On Facebook on the following Links:
https://www.facebook.com/groups/569435236444761/
AND
https://www.facebook.com/groups/690331650977113/
Pleural effusion may be defined figuratively as the juice, oozing from the leaky lingerie of the lung. However the text book definition is the abnormal accumulation of fluid in the pleural space due to disturbances in the forces that keep the pleural fluid economy in equilibrium...
PATHOGENESIS OF BRONCHIECTASIS BY DR BASHIR AHMED DAR ASSOCIATE PROFESSOR MED...Prof Dr Bashir Ahmed Dar
Dr Bashir Ahmed Dar associate professor medicine chinkipora sopore kashmir presently working in malaysia speaks about bronchiectasis.Bronchiectasis which is defined as the irreversible dilatation of the cartilage-containing airways bronchi or bronchioles.
Empyema is a collection of pus in the cavity between the lung and the membrane that surrounds it (pleural space). Caused by an infection that spreads from the lung and leads to an accumulation of pus in the pleural space, the infected fluid can build up to a quantity of a pint or more, which puts pressure on the lungs, causing shortness of breath and pain. Risk factors include recent lung conditions like bacterial pneumonia, lung abscess, thoracic surgery, trauma or injury to the chest.
Help for medical students about topic Suppurative lung diseases - Abscess and gangrene of the lungs, Pneumothorax, Hematorax, Purulent pleurisy. And useful material as required by students. Everything is inserted as per outlines of topics.
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
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Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
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
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
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.
2. HISTORY
460 BC hippocratic physicians recommended
treating empyema with open drainage.
Napolean’s surgeon dupuytren, whose name is
linked to the palmar fascia contractures of liver
disease, died of empyema in 1835 after
declaring he would “rather die at hands of God
than of surgeons”
Sir William Osler who thought “empyema
needs a surgeon and 3in. Of cold steel , instead
of a fool of a physician” provided a compelling
description of his own empyema before
succumbing to disease.
3. THE WORD: EMPYEMA
Em=within
Pyema=accumulation of pus
Empyema is known to be the formation and collection of pus
within a naturally present cavity inside the body primarily the
pleural cavity
Light’s : “I prefer to reserve the term empyema for those
pleural effusions with thick, purulent appearing pleural fluid”.
4. Other descriptions
Weese et al. defined an empyema as pleural fluid with
a sp. Gravity >1.018,
a WBC count >500 cells/mm3 or
a protein level >2.5g/dl.
Vianna defined an empyema as pleural fluid on which
the bacterial cultures are positive or
the WBC count is > 15,000/mm3 and
the protein level is >3.0g/dl.
5. •abscess
Empyema is different
from an abscess
because the latter is
the formation And
collection of pus in a
newly formed cavity
inside the body.
Parapneumonic effusion:
Any pleural effusion associated with bacterial
pneumonia , lung abscess or bronchiectasis is
a parapneumonic effusion.
Many complicated parapneumonic effusions
are empyemas.
Some patients with empyema have no
associated pneumonic process.
6. Introduction of infection
Non-traumatic Traumatic
Direct extension from an
adjacent site : lung infection
Aspiration pneumonia
Post-obstructive pneumonia
Bronchiectasis, lung abscess
Instrumentation and rupture of esophagus
Leakage of an esophageal anastomosis after
resection
Development of a bronchopleural fistula following
pneumonectomy
Pleual aspiration/ tube drainage
Abdominal sepsis: subphrenic abscess , liver
abscess
Sepsis in the pharynx, thoracic spine or chest wall
may extend into the pleura via tissue planes or
mediastinum
Non- surgical trauma:
Gun shot wounds, blast injuries and stab wounds.
7. Pathology
(1) Exudative STAGE
Once infected by pathogenic organisms, the connective tissue
layers within the pleural memberanes become oedematous and
produce an exudation of sterile proteinaceous fluid that starts to
fill the pleural cavity.
The deepest layers of the pleural membranes are relatively
impervious so that infection tends to be contained within the
pleural cavity itself and spread beyond it is unusual.
At this stage, the pleural fluid is thin with a relatively low white
cell count and the visceral pleura and underlying lung remain
mobile.
Fluid at this stage is having a low WBC count, low LDH level and
a normal glucose level and ph.
8. (2) Fibrinopurulent STAGE
If the infection proceeds unchecked by antimicrobial agents, the
inflammatory process continues so that newly formed layers of fibrin become
laid down on the epithelial surface within the pleural cavity, particularly on
the pleural cavity.
The empyma fluid now becomes more thicker and more turbid, containing, a
higher white cell count.
Such empyemas may become loculated into smaller collections by the
development of fibrinous bands which prevent the extension of empyema but
making the work of percutaneous aspiration difficult or impossible.
With the deposition of fibrin on both pleural surfaces, lung movements in
this stage may become increasingly restricted.
The pleural fluid ph and glucose levels becomes progressively lower and
LDH level becomes progressively higher.
9. (3) ORGANIZATIONAL STAGE
Depending upon the nature of the infecting organism and whether
or not antibiotics and drainage procedures have been employed,
these thickened fibrinous layers organize as collagen and become
vascularized by an ingrowth of capillaries.
This stage may begin within two weeks but usually takes 4-6
weeks to develop to a point at which the empyema cavity becomes
surrounded by a cortex, peel or rind that may be more than 2 cm
thick.
This inelastic pleural peel encases the lung and renders it virtually
functionless.
By this time the empyema contains frank pus, which may be
viscid.
10. Ultimately, an inadequately treated empyema cavity may
become obliterated and its rind may calcify, producing a so-
called firothorax, particularly in case of old tuberculous pleural
infection.
The inner layers of the thickened empyema cortex continue to
show a considerable inflammatory cell infiltrate and the fibrous
outermost layers exert an increasingly restrictive effect, both
compressing the underlying lung( the so called “trapped lung”
effect) and also tending to draw the overlying ribs together,
ultimately producing a chest deformity with a dorsal scoliosis
that is concave towards the affected side.
11. Dry “sicca” pleuritis stage, the inflammatory process of the
pulmonary parenchyma extends to the visceral pleura, causing
a local pleuritic reaction.
This leads to a pleural rub and a characteristic pleuritic chest
pain which originates from the sensitive innervations of the
adjacent parietal pleura.
12. Clinical stages
• Acute stage :
within the first 2 weeks of the onset.
• Chronic Stage :
after 2 weeks or with the formation of the thick peel and
loculations.
13. Causes for chronicity
Inadequate Tube Drainage.
Chronic pulmonary Disease( T.B. or Fungal Infection)
Immunosupressed patients.
Presence of Foreign body within the pleural space.
14. bacteriologic features
Influence of pre-disposing factors:
CAP: pneumococcal
HAP: MRSA
Aspiration or lung abscess: anaerobes
Infection from below the diaphragm: gram negative enteric bacilli
External trauma/haemothorax: staph. Aureus
Tuberculous empyema – same mechanism as TB pl. effusion with
spillage of large amount of mycobacterium into pleural space
purulent effusion that requires surgical intervention and can result in
pleural fibrosis and restrictive lung disease
15. BACTERIOLOGIC FEATURES CONT..
Influence of age:
Anaerobes in elderly
S. pneumoniae in young ambulatory patients
Children: h. influenzae
Uncommon microbial causes: fungal(cryptococcus neoformans,
blastomyces,coccidioides,histoplasmosis) , actinomyces,
nocardia, clostridia, echinococcus spp. , protozoa( trichomonas,
entamoeba)
16. Clinical presentation
Aerobic bacterial infections: acute febrile illness
Anaerobic bacterial infections:
Subacute illness.
Median symptom duration 10 days
Predisposing factors present : h/o alcoholism, an
episode of unconsciousness , poor oral hygeine
17. Symptoms Signs
Generalized malaise Oral cavity: decaying teeth
Fever Finger clubbing: in chronic empyema
Pleural pain Chest examn: similar to that of pleural
effusion
Warm, tender and bulging ICS
Cough:
If BPF patent, variable quantities of
purulent sputum, can be foul smelling and
associated with postural variation.
Empyema necessitans: the suppuration
process if undrained and uncontrolled by
AB, may extend beyond the pleural cavity,
with pointing occurring in an ICS close to
the sternum where chest wall is thinnest.
Dyspnoea: a. compression of underlying
lung by empyema
b. Primary disease involving lung itself
Discharging sinus: EN will then rupture
through the chest wall to s/o tissues,
ultimately reaching the skin surface
leading to discharging sinus.
19. Chest x-ray
Decubitus view: suspect side down – fluid b/w chest wall and inferior part of lung
Suspect side up : parenchymal infiltrate.
In early stages: identical to those of uncomplicated pl. eff.
As the time passes by, fibrosis develops around the empyema cavity so that fluid is
contained in one location irrespective of patient’s position.
“D shaped shadow” may be visible along with obliteration of CP angle.
Parenchymal lesion may be visible : consolidation, lung abscess
Air fluid level: pneumothorax : spontaneous or iatrogenic
broncho-pleural fistula
presence of gas forming organisms such as clostridia
20. ultrasound
May show septa when there is loculation
Also helpful in targeting an empyema for needle or tube drainage.
Portable
Helpful in distinguishing b/w
Loculated pyopneumothorax
And
Peripheral lung abscess
21. Computed tomography
Able to detect underlying abnormalities such as oesophageal perforation ,
bronchial carcinoma and associated lymphadenopathy .
It also aids in the differentiation between empyema and lung abscess.
Empyemas are usually lenticular in shape, compress the lung, and create
obtuse angles as they follow the contour of the chest wall.
There is usually an indistinct border between lung parenchyma and a lung
abscess, which forms an acute angle where contact with the chest wall is
made.
The ‘split pleura’ sign, where both parietal and visceral pleura enhances
showing their separation, can be present in an empyema.
Computed tomography (CT) is not as accurate as ultrasound in
detecting septations and requires transferring the patient.
22.
23. Empyema fluid :
GROSS EXAMN : COLOUR, TURBIDITY AND ODOR
Can be distinguished from pleural fluid that is turbid due to chyle i.e.
chylothorax by use of centrifugation in which case a whitish layer of
chylomicrons is found on surface of pleural fluid.
appearance: E. histolytica: anchovy sauce
actinomyces: sulfur granules
Smell: putrid (FECULENT) smell in anaerobic infection.
24. Microbiology :
ZN
Gram’s
culture: aerobic as well as anaerobic, mycobacterial and
fungal
PCR
Cytology : total and differential WBC counts
Ph : should not be done as it will plug up the blood gas
machines.
25. Biochemistry of empyema fluid
Low p H
Low glucose
Raised LDH
Decreased pH and glucose occur as a result of leucocyte and bacterial
anaerobic metabolism of glucose and process that produce lactic acid.
Exception The one situation in which pleural fluid ph is not reduced is when
the offending organism is of the proteus sp.. These organisms produce
ammonia by their urea splitting ability which leads to and elevated pleural
fluid ph.
26.
27.
28. Non significant PE
N NAUGHTY
Typical parapneumonic PE
T TINY
Borderline complicated PE
B BUTTERFLIES
Simple complicated
PE
S SUCK
Complex complicated PE
C COMPLETE
Simple empyema
S SQUASH
Complex empyema
C CONTAINER
29.
30. complications
Rupture into the lung: Dissection into lung
parenchyma
BronchoPleural fistula and
pyopneumothorax
Spread to the subcutaneous
tissue: Dissection through chest wall
Empyema Necessitans
Dissection into abdominal
cavity.
Septicaemia & septic shock.
31. Management
Principles of management:
Control of the Infection process.
Drainage of pus form the pleura.
Obliteration of the space & complete Re-expansion of
the Lung.
MANAGEMENT OPTIONS:
General
Medical
Surgery
32. general
Supportive
Bed rest
Analgesia
Oxygen
Fluids
Identify the cause
Malnutrition
TB
HIV
33. antibiotic selection
If the fluid’s gram stain and culture reports are available, it should guide the choice
of AB.
The initial antibiotic selection : some do not penetrate pleura.
Metronidazole> penicillin>clindamycin>vancomycin>ceftriaxone>gentamicin
Quinolones and clarithromycin also penetrate well
1.Severe CAP : fluoroquinolones(levofloxacin, moxifloxacin, gatifloxacin or
gemifloxacin)
Advanced macrolide(azithromycin or clindamycin) plus b-lactam(cefotaxime,
ceftriaxone)
2. If pseudomonas suspected: piperacilin-tazobactam, imipenem, meropenem
3. Anaerobic: clindamycin or metronidazole.
4. MRSA: vancomycin until culture results are available.
34. Surgical management
“those diseases that medicines do not cure are cured by the knife”
TECHNIQUE DEPENDS UPON THE STAGE OF EMPYEMA
CLOSED: INTERMITTENT (REPEATED ASPIRATION OR THORACOCENTESIS)
CONTINUOUS (INERCOASTAL DRAINAGE )
OPEN: RIB RESECTION
ELOESSER FLAP
35. CLOSED
These methods are more likely to appertain in the exudative
stage but may be continued into the fibrino-purulent stage in
some cases.
THORACOCENTESIS : frequency with which thoracentesis is
repeated depends upon the rate at which pus reaccumulates,
which in turn is judged by clinical and radiographic appearance.
Such treatment along with antibiotics is appropriate for many
individuals with pleural empyema and these patients may have a
shorter and less complicated stay than those by tube drainage.
36.
37. Closed tube drainage
Tube is placed under local anaesthesia into most dependent part of empyema
determined by USG/CT guidance and is connected to an underwater-seal drainage
system.
The relatively large (28 to 36F ) tubes have been recommended because of the belief
that smaller tubes would become obstructed with the thick fluid.
The advantage of the smaller tube is that it is easier to insert and is less painful to the
patient.
Patency is maintained with irrigation and fibrinolytic therapy
If the patient has not demonstrated significant improvement within 24hrs of initiating
tube thoracostomy, either the pleural drainage is unsatisfactory(tube placed in wrong
position, loculations) or the patient is receiving the wrong antibiotic.
Advantages: successful when infected material is too viscid to remove by manual
aspiration.
Disadvantages: greater discomfort and immobility for the patient
introduction of new infection at drainage site
tube blocked by fibrin clot
38.
39. Indications for removal of tube:
Volume of the pleural drainage is less than 50ml for 24 hrs and
until the draining fluid becomes clear yellow.
The amount of sediment (representing WBCs and debris) in the
collection system should not be more than 5ml.
Tube ceases to work
Because it serves no useful purpose rather it as a conduit for
pleural super-infection.
40. Closed drainage
Successful:
Empyema is small
Is started In acute exudative or early fibrinopurulent stagees of infection
In this case, the wall of the empyema cavity gradually becomes absorbed
allowing re-expansion of the underlying lung and obliteration of space.
It may fail:
If the pus is too thick to drain by thoracentesis or tube
BPF has developed
Pockets of pus become loculated and inaccessible.
If drainage is inadequate, ultrasonography or CT should be performed to
delineate which factor is responsible.
Then, more invasive surgical procedures are required.
41. Intrapleural streptokinase
The pleural fluid loculations are produced by fibrin membranes that prevent
the spread of the infected pleural fluid throughout the body, but which make
drainage of the pleural space difficult.
Intrapleural fibrinolytics will destroy the fibrin membranes and facilitate
drainage of the pleural fluid.
Indications
Acute or fibrino purulent stage
Presence of loculations.
Incomplete drainage after tube insertion
Contraindications:
Chronic stage
Post-operative empyema
Empyema with BPF.
42. fibrinolytics
Streptokinase: 15 000U/kg in 20-50ml saline once daily for 3
days (vial 750 000U R1400, 1 million units R2700)
Urokinase: 40 000u in 40ml saline (> 1 year) or 10 000 in 10
ml BD for 3 days(< 1 year)
tPA 0.1mg/kg in 10-30ml saline dwell time 1 hour (50mg vial
R3100)
43. vats
Advantages:
the loculi can be disrupted
pleural space can be completely drained
Chest tube can be optimally placed.
In addition, if lung is trapped(not expanded), the VATS
incision can be enlarged so that decortication can be
completed with a full thoracotomy.
44. Pulmonary decortication
In a non-medical aspect, decortication is the removal of the bark, husk, or
outer layer, or peel of an object.
It is a surgical procedure that involves the removal of a dysfunctional layer
covering the lungs and evacuation of all pus and debris from the pleural
space.
The primary aim of performing lung decortication is to be able to promote
lung expansion and chest wall compliance.
IF AFTER 6MONTHS, PLEURA REMAINS THICKENED AND THE
PATIENT’S PFTS IS SIGNIFICANTLY REDUCED TO LIMIT
ACTIVITIES, DECORTICATION SHOULD BE CONSIDERED
45. Open drainage
Rib resection: resecting segments of one to three ribs overlying the lower part of
empyma cavity and inserting large bore tubes into the empyema cavity.
Following this, tubes are irrigated daily with a mild antiseptic solution and daily
redressed.
Successful open drainage results in gradual obliteration of empyema space.
Open window thoracostomy (eloesser flap) :
involves the removal of sections of two or more ribs in order to fashion a larger
stoma, which is kept open by suturing the skin to the parietal pleura/cortex
thereby creating a pleurocutaneous flap, stoma closed if the underlying lung re-
expands or may occasionally be left permanently open with daily dressings.
46. Empyema associated with bpf
Adequate pleural drainage is crucial: an emergency
Pleural fluid if not drained exteriorly with chest tubes is likely to drained
interiorly into the lung
The bacteria then spread throughout the broncho-pulmonary tree and an
overwhelming pneumonia can result.
Drainage should be instituted immediately to prevent the possibility of
contaminating the entire respiratory system by the infected pleural fluid.
How to suspect: a patient with pleural fluid collection:
Raises more sputum than would be expected
With postural variation
On x-ray(upright position): presence of an air fluid level in the pleural space
Need USG and CT chest to differentiate from a peripheral lung abscess.
47. Empyema distal to an obstructed bronchus
• Contraindication for chest tube placement
• If chest tubes placed: bronchial obstruction will prevent the
expansion of underlying lung.
• What should be done: appropriate AB should be
administered along with therapy for obstructed
bronchus: radiotherapy, endo-bronchial stent or laser
therapy. Once obstruction relieved, ICT to be done.
48. Post traumatic empyema
Factors leading to development of empyema:
Retained hemothorax
Pulmonary contusion
Multiple chest tube placement
Management : similar to that of other para-pneumonic effusions.
49. Post pneumonectomy empyema
how to suspect : 2nd day to 7yrs (4wks)
A febrile illness with signs of systemic toxicity
Expectoration of large amounts of pleural fluid
An air-fluid level in the pneumonectomy space
Drainage of purulent material from surgical incision
Mediastinal shift towards contralateral side
Organism responsible: staph aureus
Diagnosis and treatment : all aptients: AB + chest tube placement
51. prognosis
Favourable in patients started on appropriate antibiotic
Early chest tube drainage is beneficial.
Decortication or open drainage has decreased
mortality and morbidity
Mortality 6-12%