approach to pleura leffusion
Transcript of approach to pleura leffusion
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Pleural Effusion
&Approach to the patient
Dr.Muhammad Asim Rana
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Definition
Pleural effusion is the accumulation of fluid in
the pleural space.
The pleural space lies between the lung and
chest wall and normally contains a very thinlayer of fluid, which serves as a coupling
system.
A pleural effusion is present when there is an
excess quantity of fluid in the pleural space.
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Etiology
Normally, fluid enters the pleural space from
the capillaries in the parietal pleura and is
removed via the lymphatics situated in the
parietal pleura. Fluid can also enter the pleural space from
the interstitial spaces of the lung via the
visceral pleura or from the peritoneal cavity
via small holes in the diaphragm.
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Pleural fluid accumulates when pleural fluid formation
exceeds pleural fluid absorption.
The lymphatics have the capacity to absorb ! times
more fluid than is normally formed. Accordingly, a
pleural effusion may develop when there is excess
pleural fluid formation "from the interstitial spaces of
the lung, the parietal pleura, or the peritoneal cavity#
or when there is decreased fluid removal by the
lymphatics.
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Types of pleural effusion
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Transudative pleural effusions
result from alteration of hydrostatic and
oncotic factors that increase the formation or
decrease the absorption of pleural fluid "e.g.,
increased mean capillary pressure $heartfailure% or decreased oncotic pressure
$cirrhosis or nephrotic syndrome%#.
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Exudative pleural effusions
occur when damage or disruption of the
normal pleural membranes or vasculature
"e.g., tumor involvement of the pleural space,
infection, inflammatory conditions, or trauma#leads to increased capillary permeability or
decreased lymphatic drainage.
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Diagnostic Approach
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Clinical Presentation
The underlying cause of the effusion usually
dictates the symptoms, although patients may
be asymptomatic.
Pleural inflammation, abnormal pulmonarymechanics, and worsened alveolar gas
exchange produce symptoms and signs of
disease.
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symptoms and signs
&nflammation of the parietal pleura leads to
pain in local "intercostal# involved areas or
referred "phrenic# distributions "shoulder#.
Dyspnea is frequent and may be presentand out of proportion to the si'e of the
effusion.
Cough can occur.
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Chest examination is notable for
dullness to percussion, decreased or
absent tactile fremitus, and decreased
breath sounds.
Tracheal shift to the contralateral side oran ipsilateral pleural rub may be present.
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The clinical setting is crucial to establishing a proper
diagnosis. A definitive diagnosis based solely upon
pleural fluid analysis is possible in the minority of
pleural effusions.
(istory or physical examination findings suggestive
of congestive heart failure, malignancy, pneumonia,
pulmonary embolism, myocardial infarction, surgery,
cirrhosis, or rheumatologic arthritis provide important
clues to the underlying diagnosis.
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Laboratory and Imaging
Studies
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Chest oentginogram
Pleural effusions are typically detected by
chest radiography as blunting of the
costophrenic angle or opacification of the
base of the hemithorax without loss of volumeof the hemithorax "which would suggest
atelectasis#, and may be accompanied by air
bronchograms "which would suggest an
alveolar filling process such as pneumonia#.
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Prior to invasive diagnostic or therapeutic
procedures, the patient should undergo
imaging to confirm the presence and si'e of
the effusion. Preferred modalities include)
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Decubitus chest radiography
*howing layering fluid will confirm the
presence of pleural effusion and
demonstrates that at least a portion of the
fluid is not loculated.
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Thoracic ultrasonography
&s one of the best modalities to assess for
pleural fluid loculations.
+ltrasonography can also provide realtime
guidance for pleural procedures and canreduce both the complication and failure rate
of thoracentesis.
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Computed tomography of the chest
-ith contrast helps differentiate pleural fluid
from lung masses and atelectatic lung, and
helps define the extent of pleural thicening,
pleural nodularity, and other associatedfindings.
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Pleural fluid analysis
Thoracentesis can be performed safely at thebedside, in the absence of disorders of hemostasis,on effusions that extend /0! mm from the inner chestwall on a lateral decubitus film.
1oculated effusions can be locali'ed withultrasonography or 2T scan.
Proper technique and sonographic guidanceminimi'e the ris of pneumothorax and othercomplications.
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The first step is to determine whether the
effusion is a transudate or an exudate.
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A transudative pleural effusion occurs when
systemic factors that influence the formation
and absorption of pleural fluid are altered.
The leading causes of transudative pleuraleffusions are left ventricular failure and
cirrhosis.
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An exudative pleural effusion occurs when
local factors that influence the formation and
absorption of pleural fluid are altered. The
leading causes of exudative pleural effusionsare bacterial pneumonia, malignancy, viral
infection, and pulmonary embolism.
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The primary reason to mae this
differentiation is that additional diagnostic
procedures are indicated with exudative
effusions to define the cause of the localdisease.
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-hile pleural effusion occurs in a vast arrayof disease states, 3!4 of pleural effusionsare the result of only five diseases.
2ongestive heart failure "564# Pneumonia "4# 7alignancy "084# Pulmonary embolism "004#
9iral disease ":4#
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Chec! pleural fluid for
Appearance,
lactate dehydrogenase "1;(#,
protein,
p(,
glucose and
albumin
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*erum lactate dehydrogenase "1;(#, protein,
p(, glucose and albumin should be
measured within hour of the thoracentesis to
allow appropriate comparison.
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Pleural fluid appearance
7ost transudates are clear, straw colored,
nonviscid, and without odor
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"loody pleural fluid
&f the blood is due to thoracentesis, the
degree of discoloration should clear during
the aspiration.
=loody pleural fluid usually indicates thepresence of malignancy, pulmonary embolism
"P>#, or trauma.
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#emothorax
The presence of gross blood should lead to
the measurement of a pleural fluid
hematocrit.
(emothorax is defined as a pleural fluid toblood hematocrit ratio of /!.?, and chest tube
drainage should be considered.
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>xudative pleural effusions meet at least one
of the 1ight@s criteria , whereas transudative
pleural effusions meet none)
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Light$s criteria
"a# a pleural fluidtoserum protein ratio of
/!.?,
"b# a pleural fluidtoserum 1;( ratio of /!.6,
"c# a pleural fluid 1;( of more than twothirdsof the upper limit of normal for serum 1;(
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The above criteria misidentify ?4 of
transudates as exudates.
&f one or more of the exudative criteria are
met and the patient is clinically thought tohave a condition producing a transudative
effusion, lie in whom clinical suspicion for
heart, liver, or idney disease is high what
should be doneB
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The difference between the protein levels in the
serum and the pleural fluid should be measured.
&f this gradient is greater than 50 gC1 "5.0 gCd1#, the
exudative categori'ation by the above criteria can be
ignored because almost all such patients have atransudative pleural effusion.
&n some texts a gradient of /0. gCd1 suggests that
the pleural fluid is transudate.
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If a patient has an exudati%e pleural
effusion
;escription of the fluid, Dlucose level, ;ifferential cell count, 7icrobiologic studies, 2ytology. 2ultures, Triglycerides, Amylase, and
p(
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"C differential
The -=2 differential is often not diagnostic,
although neutrophilia is suggestive of
infection.
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>osinophilia "/0!4 of total nucleated cellcount# is suggestive of air or blood in the
pleural space. &f air or blood is not present inthe pleural space, consideration should begiven to fungal and parasitic infection, druginduced disease, P>, asbestosrelateddisease, and 2hurg*trauss syndrome.
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1ymphocytosis "/?!4 of the total nucleated
cell count# is suggestive of malignancy or
tuberculosis.
7esothelial cells argues against thediagnosis of tuberculosis.
Plasma cells suggest a diagnosis of multiple
myeloma.
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>xudative effusions with normal protein but
high 1;( are liely to be parapneumonic or
secondary to malignancy.
1;( is an indicator of the degree of pleuralinflammation.
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'lucose concentration
A glucose concentration of E6! mgCd1 isprobably due to
tuberculosis,
malignancy, rheumatoid arthritis, or parapneumonic effusion. For parapneumonic pleural effusions with a
glucose of E6! mgCd1, tube thoracostomyshould be considered.
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Pleural fluid (ith a lo( p#
A p( of E:.5 is seen with
empyema,
tuberculosis,
malignancy, collagen vascular disease, or
esophageal rupture.
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For parapneumonic pleural effusions with a p( of
E:.!, tube thoracostomy should be considered.
Pleural fluid for p( testing should be collected
anaerobically in a heparini'ed syringe and placed on
ice. Pleural fluid with a low p( usually has a low glucose
and a high 1;( otherwise, the low p( may be due to
poor sample collection technique.
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Amylase
An elevation of amylase suggests that the
patient has pancreatic disease, malignancy,
or esophageal rupture.
7alignancy and esophageal rupture havesalivary amylase elevations and not
pancreatic amylase elevations.
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Turbid or mil!y fluid
should be centrifuged.
&f the supernatant clears, the cloudiness is liely due
to cells and debris.
&f the supernatant remains turbid, pleural lipids should
be measured. >levation of triglycerides "/00! mgCd1#
suggests that a chylothorax is present, usually due to
disruption of the thoracic duct from trauma, surgery,
or malignancy "i.e., lymphoma#.
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Cytology
2ytology is positive in approximately 6!4 ofmalignant effusions.
Priming the fluid collection bag with
unfractionated heparin "+F( e.g., 0,!!!&nternational +nits# may increase the yield. The volume of pleural fluid analy'ed does not
impact the yield of cytologic diagnosis.
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Surgical diagnostic
procedures
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Closed pleural biopsy
2losed pleural biopsy adds little to the diagnostic
yield of thoracentesis, except in the diagnosis of
tuberculosis.
For tuberculous effusions, pleural fluid cultures alone
are positive in only !4 to ?4 of cases. (owever,the combination of pleural fluid studies and pleural
biopsy "demonstrating granulomas or organisms# is
3!4 sensitive in establishing tuberculosis as the
etiology of the effusion.
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Diagnostic thoracoscopy
;iagnostic thoracoscopy has largely
replaced closed pleural biopsy. Thoracoscopy
allows directed biopsies that increase the
diagnostic yield for malignancy whilemaintaining the high diagnostic yield of
closed pleural biopsy for T=.
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Indications for diagnostic
thoracoscopy
Pleural effusion of unnown etiology
7esothelioma
1ung cancer
Tuberculosis Gther benign pleural disorders
Pulmonary parenchymal disease
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)ther diagnostic
procedures
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Gther diagnostic procedures that are useful in
establishing the etiology of a pleural effusion
when the aforementioned tests are
nondiagnostic include)
>valuation of liver function
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Differential Diagnoses of
Pleural Effusions
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Transudative Pleural Effusions
0. 2ongestive heart failure
. 2irrhosis
5. Pulmonary emboli'ation
8. Nephrotic syndrome?. Peritoneal dialysis
6. *uperior vena cava obstruction
:. 7yxedemaH. +rinothorax
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Exudative Pleural Effusions
1. Neoplastic diseases
a. 7etastatic disease
b. 7esothelioma
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2. Infectious diseases
a. =acterial infections
b. Tuberculosis
c. Fungal infectionsd. 9iral infections
e. Parasitic infections
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3. Pulmonary emboliation !. "astrointestinal disease
a. >sophageal perforation
b. Pancreatic diseasec. &ntraabdominal abscesses
d. ;iaphragmatic hernia
e. After abdominal surgery
f. >ndoscopic variceal sclerotherapy
g. After liver transplant
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#. Collagen$%ascular diseases
a.
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6. Postcoronary artery bypass surgery
:. Asbestos exposure
H. *arcoidosis
3. +remia 0!. 7eigs@ syndrome
00. Kellow nail syndrome
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12. Drug$induced pleural disease
a. Nitrofurantoin
b. ;antrolene
c. 7ethysergided. =romocriptine
e. Procarba'ine
f. Amiodarone
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05. Trapped lung
08.
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0:. &atrogenic inIury
0H. Gvarian hyperstimulation syndrome
03. Pericardial disease
!. 2hylothorax
*Cl i * d t th t b
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*Classic* exudates that can be
transudates
7alignancy)
;ue to early lymphatic obstruction, obstructive
atelectasis, or concomitant disease "2(F#.
Pulmonary embolism)
5 percent incidence due to atelectasis.
*arcoidosis)
*tage && and &&& disease.
(ypothyroid pleural effusion)From hypothyroid heart disease or hypothyroidism per
se.
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Treatment
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Transudates resolve with treatment of the
underlying heart, idney, or liver disease.
+ncommonly, more aggressive approaches
including pleurodesis and shunts arerequired.
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Parapneumonic effusions and empyema
should be managed with tube drainage when
indicated based on the si'e, gross
appearance, or biochemical analysis of thepleural fluid or the presence of loculations
7ultiple tubes are sometimes required to
adequately drain the pleural space.
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Failure to adequately and quicly drain a
complicated parapneumonic effusion can
lead to organi'ation of the pleural fluid and
formation of a thic pleural adhesions whichmay necessitate surgical removal nown as
decortication.
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Indications for TubeThoracostomy in
Parapneumonic Effusions
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Radiographic criteria
Pleural fluid loculations
>ffusion filling more than half the hemithorax
Air fluid level
Microbiologic criteria
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Microbiologic criteria
Pus in the pleural space
Positive stain for microorganisms
Positive pleural fluid cultures
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Chemical criteria
Pleural fluid p( E:.
Pleural fluid glucose E6! mgCd1
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C)+TAI+DICATI)+S
There are no absolute contraindications totube thoracostomy, particularly if the patient isin respiratory distress.
Anticoagulation or a bleeding diathesis is arelative contraindication in a patientundergoing elective chest tube placement forpleurodesis. =lind insertion of a chest tube isdangerous in a patient with adhesions from
infection, previous pleurodesis, or a lungtransplant guidance by 2T scan withoutcontrast is preferred in these patients.
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Type of tube
*ilasticL tubes are preferred because older
rubber tubes have fewer drainage holes, are
not well visuali'ed on chest radiographs, and
produce more pleural inflammation. *ilasticchest tubes contain a radiopaque strip with a
gap that serves to mar the most proximal
drainage hole.
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Si,e of tube
A chest tube@s internal diameter and lengthare the critical determinants of flow.
*elect the appropriate chest tube si'e to
account for the viscosity and accumulationrate of the pleural material to be drained.
As an example, drainage of viscous fluids
requires a larger bore chest tube than that
required for drainage of a similar volume ofair.
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Malignant effusionM A smallbore catheter "Hto 08 Fr# placed under ultrasound or 2Tguidance is usually adequate to drain amalignant pleural effusion and achieve
pleurodesis. Empyema M For a complicated
parapneumonic effusion or empyema that isamenable to drainage with a single catheter.
Prefer initial imageguided placement ofsmallbore catheters "0! to 08 Fr#, with orwithout intrapleural fibrinolytic agents.
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&t is preferred to use the smaller tube si'e asthis is generally more comfortable for
patients, particularly if more than one tube is
needed. Alternatively, when the fluid appears
viscous, a larger bore tube "068 Fr# may be
used.
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+nsuccessful drainage with a smallborecatheter either indicates the presence ofmultiple loculations or very viscous material.7ultiple smallbore catheters may be used in
multiloculated effusions or large borecatheters in case of very viscous material.Failure to drain with a single smallbore tubeshould also lead to thoracic surgery
consultation to avoid delays in case videoassisted thoracoscopy "9AT*# becomesnecessary.
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Hemothorax M The goals of tubethoracostomy in acute hemothorax are
drainage of fresh blood, quantification of the
rate of bleeding, evacuation of any coexisting
pneumothorax, and tamponade of the
bleeding site. 1arge bore catheters "5 to 8!
Fr# are required to reliably achieve these
goals.
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Gnce a hemothorax is defibrinated in situ,that is after the acute phase, success of
drainage is less dependent on the si'e of the
tube, than on the degree and mode of clot
formation. 1arge amounts of clotted blood
should be evacuated via video assisted
thoracoscopy.
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Gccasionally, a hemothorax may result in asonographically complex septate pattern and
may be treated with smallbore catheters.
Treatment of hemothorax should be
individuali'ed and done in consultation with
thoracic surgery.
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-alignant pleural effusions
Gbservation without invasive interventionsmay be appropriate for some patients with
malignant pleural effusions.
Therapeutic thoracentesis may improvepatient comfort and relieve dyspnea. The
rapid removal of more than 0 1 of pleural fluid
may rarely result in reexpansion pulmonary
edema, especially if the lung is unable to reexpand.
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Chemical pleurodesis
2hemical pleurodesis is an effective therapyfor recurrent effusions. This treatment is
recommended in patients whose symptoms
are relieved with initial drainage but who have
rapid reaccumulation of fluid.
l l d i
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Talc pleurodesis
>ffective and inexpensive.
Fever and hypoxia are common following
instillation of talc into the pleural space, and
respiratory failure has been described onoccasion.
Gverall efficacy is similar for talc slurry
delivered via chest tube versus dry talc
insufflated during thoracoscopy.
D li i li
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Doxycycline or minocycline
;oxycycline or minocycline can also beinstilled into the pleural space via a chest
tube.
Pain is more prevalent and severe followingdoxycycline and minocycline than following
talc.
"l i
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"leomycin
=leomycin appears to be less effective andmore expensive than other drugs.
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*ystemic analgesics and the administration oflidocaine in the sclerosing agent solution help
to decrease the appreciable discomfort
associated with the procedure.
&f the chest tube drainage remains high "/0!!
m1Cd# more than days after the initial
pleurodesis, a second dose of the sclerosing
agent can be administered.
Ch i i d lli l l h
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Chronic ind(elling pleural catheters
Provide good control of effusionrelated
symptoms via intermittent drainage.
The Pleurx catheter is better at controlling
symptoms than doxycycline administered via achest tube. Furthermore, repeated drainage via
a Pleurx catheter leads to pleurodesis in roughly
?!4 of patients, allowing the catheter to be
removed.
Pl t l l b i
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Pleurectomy or pleural abrasion
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C e ot e apy a d ed ast a
radiotherapy
7ay control effusions in responsive tumors, such
as lymphoma or smallcell bronchogenic
carcinoma, although it has poor efficacy inmetastatic carcinoma.
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Than! you %ery much