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Empyema Thoracis: Definition and Treatment

This document discusses empyema thoracis, or pus in the chest cavity. It defines empyema and notes that it usually develops secondary to bacterial pneumonia. The stages of empyema are described from exudative to organizing. Diagnosis involves imaging like chest X-ray and CT scan. Treatment involves drainage of pus, lung expansion, and infection elimination through antibiotics, intrapleural fibrinolytics, and surgery. Video-assisted thoracoscopic surgery (VATS) is recommended as the first approach for stage II empyema due to benefits like shorter recovery time compared to open thoracotomy.

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Arrol Iswahyudi
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100% found this document useful (1 vote)
181 views19 pages

Empyema Thoracis: Definition and Treatment

This document discusses empyema thoracis, or pus in the chest cavity. It defines empyema and notes that it usually develops secondary to bacterial pneumonia. The stages of empyema are described from exudative to organizing. Diagnosis involves imaging like chest X-ray and CT scan. Treatment involves drainage of pus, lung expansion, and infection elimination through antibiotics, intrapleural fibrinolytics, and surgery. Video-assisted thoracoscopic surgery (VATS) is recommended as the first approach for stage II empyema due to benefits like shorter recovery time compared to open thoracotomy.

Uploaded by

Arrol Iswahyudi
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PPT, PDF, TXT or read online on Scribd

EMPYEMA THORACIS

the role of VATS


Empyema Thoracis
 Defined as “pus in the
chest”
 Ancient disease
 Hippocrates credited with
first description of natural
history and treatment
 Most common precursor
is bacterial pneumonia
and subsequent
parapneumonic effusion

Hippocrates of Kos 460-370 B.C.


Empyema
 Aetiology
 Empyema is always secondary to infection in a neighboring
structure, usually the lung;
 1-Bacterial pneumonia &tuberculosis.
 2-Over 40% of patients with community-acquired pneumonia
develop an associated pleural effusion
 And 15% of them develop secondary bacterial infection and
empyema.
 3-Infection of haemothorax,& rapture of subphrenic abscess.
 4-Delay in the diagnosis and instigation of appropriate therapy.
The Stages of Empyema
 Stage I - “Exudative”
 sterile pleural fluid develops secondary to inflammation
without fusion of the pleura
 Stage II - “Fibrinopurulent”
 a fibrinous peel develops on both pleural surfaces
limiting lung expansion
 Stage III - “Organizing”
 in-growth of capillaries & fibroblasts into the fibrinous
peel
Clinical features
Systemic features ;
1-Pyrexia,usually high and remittent
2-Rigors,sweating,malaise and weight loss
3-Polymorphonuclear leucocytosis, high (C-Reactive Protein)
CRP.
 Local feature ;
 1-Pleural pain; breathlessness; cough and sputum usually
because of underlying lung disease; copious purulent sputum if
empyema rupture into a bronchus (bronchopleural fistula)
 2-Clinical signs of fluid in the pleural space
Differential diagnosis
 Pleural involvement occurs in up to 5% of patients with
rheumatoid arthritis.
 Pleural malignancy
 Chylothorax and pseudochylous effusion
 Pulmonary embolism
 Esophageal rupture
Bacteriology
 Aerobic organisms are the most frequent organisms
identified from infected pleural fluid.
 These are most commonly Gram-positive organisms
from Streptococcal species, followed by Staphylococcus
aureus.
 Gram-negative empyema is more frequent in patients
with underlying diseases, especially those with diabetes
and alcoholism.
 Staphylococcus aureus and Gram-negative enteric
bacteria such as Klebsiella pneumonia have a particular
propensity to cause pleural infection.
Bacteriological data.
 Streptococcus pneumoniae: 15-20%
Increased resistance

 Staphylococcus:15-30%
 Streptococcus spp
 Gram Negative: 20-50%
Klebsiella, Enterobacter, Pseudomonas, Hemophilus,
[Link]
 Anaerobes:
Fusobacterium, Bacteroides fragilis
Diagnostic
 X-ray
 Pleura USG
 Fast, safe&effective in confirming the presence of pleural fluid
and estimating its volume, can differentiate between pleural
fluid and thickening ,guiding thoracosintesis (dx and therapy)
 CT Scan
 should be obtained when pleural space infection is
suspected
 Bronchoscopy
 particularly recommended where there is a mass or volume
loss on imaging
Goal of Treatment
 Evacuation of Pus
 Expansion of Lung
 Eliminate of ongoing infection
Non Surgery Therapy
 Antibiotics
 Intrapleural fibrinolytics
Intrapleural fibrinolytics
 1949 Tillet and Sherry: partial purified streptococcal fibrinolysin
 Highly purified streptokinase: 250000IU
 Urokinase: 100000IU
 It form a complex with plasminogen that converts additional circulating
plasminogen to plasmin. Plasmin lyses fresh fibrin clot and digests
prothrobin and fibrinogen.
 Improvement in the chest radiograph and greater volume pleural
drainage, not outcome of mortality, surgical frequency, or hospital stay.
 Tube drainage with streptokinase and early surgical intervention showed
reduced length of hospitalization
 Potential side effect: hemorrhage, pleuritic pain and fever
What Surgery can do ?
 The goals of surgery for empyema are:
 to debride the pleural cavity and
 to achieve lung re-expansion
 Debridement of the pleural cavity comprises drainage of
all fluid, breaking of all loculations and removal of all the
pleural exudate.
 Decortication entails thorough removal of the restrictive
cortex of fibrous and infected tissue overlying the visceral
pleura to allow the lung to re-expand
Surgical management of empyema
(AATS)
Best surgical approach to manage stage
II empyema?
 Class IIa:VATS should be the first line approach in all patients
with stage II acute empyema (LOE B)
Surgical management of empyema
(EACTS)
VATS benefit
 Benefits of a minimally invasive approach including:
 reduction in operative time
 postoperative pain,
 duration of chest tube
 length of hospital stay
 Greater satisfaction with postoperative wound appearance
 an earlier return to work

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