|
|
||||||||
Guest Access | Sign In via User Name/Password |
|||||||||
* From the Department of Medicine, National Cheng Kung University, College of Medicine, Tainan, Taiwan.
| Abstract |
|---|
|
|
|---|
Design and settings: Retrospective chart review over a 55-month period at a tertiary referred medical center.
Patients and measurements: The medical charts of patients with empyema or CPE were reviewed. Data including age, gender, clinical symptoms, important underlying diseases, leukocyte count, duration of preadmission symptoms, interval from first procedure to second procedure, the time from first procedure to discharge (recovery time), the amount of effusion drained, administration of intrapleural streptokinase, chest tube size and position, loculation of pleural effusion, and characteristics and culture results of pleural effusion were recorded and compared between groups of patients with successful and failed outcome of tube thoracostomy drainage.
Results: One
hundred twenty-one patients were selected for study. One hundred of
these patients had received tube thoracostomy drainage with 53
successful outcomes and 47 failed outcomes of chest tube drainage.
Nineteen patients received decortication directly, and the other two
received antibiotics alone. Univariate analysis showed that pleural
effusion leukocyte count, effusion amount, and loculation of pleural
effusion were significantly related to the outcome of chest tube
drainage. Multiple logistic regression analysis demonstrated that
loculation and pleural effusion leukocyte count
6,400/µL were
the only independent predicting factors related to failure of tube
thoracostomy drainage.
Conclusions: Loculation
and pleural effusion leukocyte count
6,400/µL were independent
predicting factors of poor outcome of tube thoracostomy drainage. These
results suggest that if the initial attempt at chest tube drainage
fails, early surgical intervention should be considered in good
surgical candidates with loculated empyema or pleural effusion with
leukocyte count
6,400/µL.
Key Words: complicated parapneumonic effusion empyema predicting factors tube thoracostomy
| Introduction |
|---|
|
|
|---|
tube thoracostomy drainage, and the organizational stage virtually always requires more aggressive surgical drainage. The evolution of pleural infection is not sharply defined, but rather represents a continuous spectrum of events. The decision for surgical intervention after failure of first tube thoracostomy is always empiric. Very few studies have focused on the predicting factors for outcome of tube thoracostomy drainage. LeMense et al3 reported no significant difference in procedure success rate or hospital stay between multiloculated and uniloculated empyemas, parapneumonic and nonparapneumonic empyemas, and culture proved and biochemically proved empyemas. Other studies4 ,5 suggest that failures of tube thoracostomy drainage were usually due to improper tube positioning, loculated or inaccessible collections, kinking of the thoracostomy tubes, or the presence of highly viscous fluid. None of these previous studies, however, had control groups, and their patient numbers were small. In this study, we reviewed our experience with thoracic empyema and CPE over a 55-month period at our hospital, a tertiary referred medical center, with special focus on the factors influencing the outcome of tube thoracostomy drainage.
| Materials and Methods |
|---|
|
|
|---|
Data Collection
The following data were collected for each patient: age, gender,
clinical symptoms, important underlying diseases, leukocyte count,
duration of preadmission symptoms, the size and loculations of pleural
effusions, interval from first procedure to second procedure (second
chest tube or decortication), and time from first procedure to hospital
discharge (recovery time). The characteristics of pleural effusion,
including gross appearance, cell count, pH, glucose, protein, LDH,
Gram's stain, acid-fast stain, and culture findings, were also
recorded. Data related to tube thoracostomy were also recorded,
including the volume of effusion drained from the chest tube within the
first 24 h (D24), chest tube size and position, and intrapleural
streptokinase administration.
In our hospital, we used water-seal drainage after chest tube insertion and applied low-pressure suction (-20 cm H2O) if the drainage was not satisfactory. Good chest tube position was defined as chest radiograph or CT scan evidence of tube tip placement within the dependent part of the effusions. Large-amount effusion was defined as a height of the meniscus or size of the effusion reaching more than one third of the chest height or volume. Loculations were defined as the presence of one or more of the following criteria: (1) failure of the effusion to layer on decubitus x-ray films; (2) fixed fluid in an abnormal location; (3) septations seen on ultrasound or CT scan; or (4) irregular scalloped appearance of the effusion contour. Chest tube drainage success was defined as either complete drainage of pleural effusion or incomplete drainage of pleural effusion but concomitant improvement in fever and leukocytosis with almost complete resolution of pleural effusion on chest radiograph 1 to 6 months later. Chest tube drainage failure was defined as incomplete drainage of pleural effusion concomitant with persistent fever, leukocytosis, or fatal outcome. The sizes of the chest tubes inserted were 24F, 28F, or 32F.
Statistical Analysis
The primary end point of the present study was the success or
failure of tube thoracostomy for the treatment of empyema or CPE.
Possible predicting factors for the success or failure of therapy were
assessed against this end point. For comparison of means, the Wilcoxon
rank-sum test was used for continuous variables when they departed from
a normal distribution; otherwise, Student's t test was
used; and the
2 (Fisher's Exact Test when needed) test
was used for discrete data. Moreover, the area under the receiver
operating characteristic curve (AROC) and its 95% confidence interval
(CI) were calculated for the continuous variables.7
Continuous variables with an AROC significantly different from 0.5 were
categorized with the cutoff values from the receiver operating
characteristic curve analysis and selected for multivariate analysis.
For the multivariate analysis, multiple logistic regression analysis
was applied to adjust for confounding variables in order to assess the
possible predicting factors. Data were reported as mean ± SEM. All
reported p values are two tailed, and a p value < 0.05 was
considered to be statistically significant. A software program (JMP;
SAS Institute Inc; Cary, NC) was used for the analysis.
| Results |
|---|
|
|
|---|
|
|
|
|
6,400/µL was established. Table 5
shows the results of multiple logistic regression analysis of all the
variables tested for possible association with the outcome of chest
tube drainage. Multiple logistic regression analysis demonstrated that
loculation (odds ratio, 10.29; 95% CI, 2.18 to 79.65; p = 0.008) and
pleural fluid WBC count
6,400/µL (odds ratio, 5.53; 95% CI,
1.37 to 28.05; p = 0.02) were the only two independent predicting
factors related to failure of chest tube drainage.
|
|
| Discussion |
|---|
|
|
|---|
In the present study, K pneumoniae was the most common pathogen isolated in empyemas or CPE. This is contrast to recent studies in the West,3 ,15 ,16 in which Streptococcus pneumoniae and Staphylococcus aureus were usually the predominant organisms. In our study, 10 of the 20 patients with K pneumoniae isolated from pleural fluid had diabetes mellitus. This result is similar to other reports17 ,18 ,19 from Taiwan, in which K pneumoniae is the major pathogen of diabetics. The predilection of K pneumoniae infection for diabetics remains unexplained.
Very few studies have focused on the predicting factors for outcome of tube thoracostomy drainage. The review of Moran20 suggests that the duration of the pleural infection, the characteristics of the pleural fluid, the presence or absence of loculations, and the overall condition of the patient are the four critical important factors to be considered in the selection of a pleural drainage method. It is reasonable to think that these four factors also influence the tube thoracostomy drainage outcome. The duration of the pleural infection may be difficult to determine because of the indolent nature of many infections and the potential for rapid progression of empyemas. In the study of LeMense et al,3 no difference in procedure success rates or hospital stay was observed between multiloculated and uniloculated empyemas, parapneumonic and nonparapneumonic empyemas, and culture proved and biochemically proved empyemas. Their success rate of tube thoracostomy drainage was only 11%, because all patients had loculated pleural fluid at presentation. Other studies4 ,5 have suggested that improper tube positioning, loculated or inaccessible collections, kinking of the thoracostomy tubes, or the presence of highly viscous fluid were possible causes of tube thoracostomy drainage failure. However, none of these previous studies was controlled and their patient numbers were small.
In the present study, multivariate analysis revealed that
loculation of pleural effusion and pleural fluid WBC
count
6,400/µL were both independent predicting factors for poor
outcome of tube thoracostomy drainage. The success rates of tube
drainage in loculated and nonloculated empyema were 40% and 76%,
respectively; and in empyema with pleural fluid WBC
count
6,400/µL and > 6,400/µL, rates were 52% and 85%,
respectively. The finding that pleural fluid WBC count
6,400/µL
was a predictor of poor outcome of tube thoracostomy drainage
contrasted with the general concept that the degree of leukocytosis is
related to the disease severity. The reason for this apparent
discrepancy is not clear, but one possible explanation may be related
to the release of tumor necrosis factor (TNF) during pleural infection.
Interleukin-8 and TNF are the major chemoattractants in the pleural
liquid of patients with empyema.21
Polymorphonuclear
leukocytes (PMNs) stimulated with TNF adhere and form zones of close
apposition to fibrin, so PMN migration through fibrin gels is
inhibited.22
In addition, fibrin formation is the
predominant biological activity of TNF for survival of experimental
septic peritonitis.23
Idell et al24
also
reported that TNF increases plasminogen activator inhibitors 1 and 2
expression or release from human pleural mesothelial cells in
vitro. Our hypothesis is that if a large amount of TNF surges into
the pleural fluid of patients early in the course of empyema or CPE,
fibrin will form rapidly and PMNs will adhere firmly to fibrin over the
pleural surface. This model can explain why in our study pleural fluid
WBC count
6,400/µL was a predictor of poor outcome of tube
drainage.
To our knowledge, no previous study has compared the effect of different chest tube sizes on drainage outcome. In our study, the concern that a small-size chest tube may become plugged more easily than larger sizes was not a major factor in drainage outcome, although only chest tube sizes of 24F, 28F, and 32F were used in the study. Tube malposition was also reported as a cause of tube drainage failure.5 However, in that study, the major causes of tube malposition occurred in tubes exiting from infected pleural space, such as in major fissures, anterior or posterior to the empyema. Today, the use of echo-guided chest tube insertion can avoid these events. However, Duponselle25 reported that hemothoraces in ambulatory patients seemed to drain adequately regardless of the site of tube insertion. The result of our study was similar to that report, with nondependent tube position not being a major determinant of tube drainage failure.
Many studies26 ,27 ,28 ,29 ,30 ,31 ,32 have reported on the safety and efficacy of intrapleural thrombolysis in the treatment of thoracic empyema, with success rates ranging from about 44 to 100%. The strategies used by these studies appeared to be more aggressive with placement of several tubes in most patients27 and the use of CT scan guidance during placement.27 ,28 Some studies included only early-stage (stage I and II) empyema29 or empyema related to pneumonia.30 ,31 ,32 ,33 In the present study, although the success rate was only 50% (9/18), our results were similar to those of Chin and Lim30 in that intrapleural streptokinase did not influence the need for further surgical intervention.
Pothula and Krellenstein34
reported that prolonged
unsuccessful tube drainage is associated with increased morbidity and
mortality. The present study showed the recovery time of tube drainage
failure patients (27.6 ± 4.2 days) was significantly longer than
that of direct decortication patients (16.4 ± 2.9 days;
p = 0.002). The interval from first procedure to second procedure was
significantly longer in patients with tube drainage failure than that
of patients with successful tube drainage. The mortality was also
significantly higher in patients with tube drainage failure than in
those with successful tube drainage or direct decortication. Early
thoracotomy also has the additional advantage that if decortication is
accomplished within 2 weeks of pleural infection, the visceral pleural
rind usually is easily extricated from the lung.35
Several
recent studies36
,37
have reported that video-assisted
thoracoscopic surgery has the same rate of success as formal
thoracotomy but offers substantial advantages over formal
thoracotomy in terms of hospital stay and cosmetics in the treatment of
loculated or tube thoracostomy-resistant empyemas. Although
video-assisted thoracoscopic surgery may fail in cases of extensive
pleural adhesions or late-stage empyema,38
it may be a
safe and effective alternative in the treatment of empyema with
loculations or pleural fluid WBC count
6,400/µL.
In conclusion, our results showed that loculation of pleural
effusion and pleural fluid WBC count
6,400/µL were independent
predicting factors for poor outcome of tube thoracostomy in this
series. These results suggest that surgical intervention should be
considered early after failure of first chest tube drainage in good
surgical candidates with loculated empyema or pleural fluid with WBC
count
6,400/µL to minimize the mortality and morbidity
associated with thoracic empyema or CPE.
| Footnotes |
|---|
Abbreviations: AROC = area under the receiver operating characteristic curve; CI = confidence interval; CPE = complicated parapneumonic effusion; D24 = the volume of pleural effusion drained from the chest tube within the first 24 h; LDH = lactate dehydrogenase; PMN = polymorphonuclear leukocyte; TNF = tumor necrosis factor
Received for publication July 28, 1998. Accepted for publication October 28, 1998.
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
G. F. Tassi, R. J. O. Davies, and M. Noppen Advanced techniques in medical thoracoscopy. Eur. Respir. J., November 1, 2006; 28(5): 1051 - 1059. [Abstract] [Full Text] [PDF] |
||||
![]() |
H.-B. Ris and T. Krueger Video-assisted thoracoscopic surgery and open decortication for pleural empyema MMCTS, January 9, 2006; 2006(0109): 273. [Abstract] [Full Text] [PDF] |
||||
![]() |
A Medford and N Maskell Pleural effusion Postgrad. Med. J., November 1, 2005; 81(961): 702 - 710. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Misthos, E. Sepsas, M. Konstantinou, K. Athanassiadi, I. Skottis, and A. Lioulias Early use of intrapleural fibrinolytics in the management of postpneumonic empyema. A prospective study Eur. J. Cardiothorac. Surg., October 1, 2005; 28(4): 599 - 603. [Abstract] [Full Text] [PDF] |
||||
![]() |
C.-L. Chung, C.-H. Chen, J.-R. Sheu, Y.-C. Chen, and S.-C. Chang Proinflammatory Cytokines, Transforming Growth Factor-{beta}1, and Fibrinolytic Enzymes in Loculated and Free-Flowing Pleural Exudates Chest, August 1, 2005; 128(2): 690 - 697. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Mennander, J. Laurikka, P. Kuukasjarvi, and M. Tarkka Continuous pleural lavage may decrease postoperative morbidity in patients undergoing thoracotomy for stage 2 thoracic empyema Eur. J. Cardiothorac. Surg., January 1, 2005; 27(1): 32 - 34. [Abstract] [Full Text] [PDF] |
||||
![]() |
C W H Davies, F V Gleeson, and R J O Davies BTS guidelines for the management of pleural infection Thorax, May 1, 2003; 58(90002): ii18 - 28. [Full Text] |
||||
![]() |
C. W. H. DAVIES, S. E. KEARNEY, F. V. GLEESON, and R. J. O. DAVIES Predictors of Outcome and Long-term Survival in Patients with Pleural Infection Am. J. Respir. Crit. Care Med., November 1, 1999; 160(5): 1682 - 1687. [Abstract] [Full Text] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |