Pulmonary Medicine

Pleural Space Infections/Empyema

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What every physician needs to know:

Pleural space infection/empyema is usually seen in association with pneumonia, although primary empyema is occasionally seen (~4%) with no radiographic evidence of pneumonia or other obvious cause.

Reactive vs. infected pleural effusions

Up to 57 percent of patients with pneumonia have an associated pleural effusion, which varies in size from a tiny sub-centimeter effusion not visible on chest X-ray to a large effusion that causes ventilatory compromise. The priority for physicians is to distinguish non-infected reactive effusions ("simple" parapneumonic effusions) from pleural infection ("complicated" parapneumonic effusions/empyema) since this distinction is essential in determining appropriate treatment. Simple parapneumonic effusions usually resolve with standard pneumonia antibiotic therapy, whereas an infected pleural space requires prompt chest tube drainage and prolonged broad-spectrum antibiotic therapy.

When to consider pleural infection

Pleural infection should be suspected in any patient who presents with pneumonia and is found to have a pleural effusion. Pleural infection should also be suspected in those with a non-resolving pneumonia despite appropriate antibiotic therapy (i.e., ongoing fevers, poorly resolving C-reactive protein, or high white cell count).

Diagnostic strategies

The gold standard for diagnosis of pleural space infection is a microbiological culture of pathogens in pleural fluid. However, cultures are typically slow, often taking 24-72 hours, and they also frequently produce by false negatives, particularly in patients who have received prior antibiotic therapy. Therefore, biochemical surrogates of infection (low pH, low glucose, and high lactate dehydrogenase, or LDH) are used to identify patients who require chest tube drainage.

Other considerations

Tuberculosis is a common cause of pleural effusion worldwide, but it is usually associated with a low mycobacterial load in the pleural cavity, and it normally develops as a type IV hypersensitivity reaction. Unlike standard bacterial pleural infection, acute presentation with TB pleuritis is uncommon, and symptoms with dyspnea and constitutional features develop insidiously. Chest tube drainage is rarely required, and the effusion usually responds to antituberculous therapy. Parasitic infections, such as amebiasis, echinococcosis, and paragonimiasis, may cause pleural infections in endemic regions.


Pleural effusions found in association with pneumonia are classified as simple parapneumonic effusions, complicated parapneumonic effusions, and empyema.

Simple parapneumonic effusions comprise the majority of pneumonia-associated pleural effusions (~60%). These are reactive non-infected effusions that usually resolve with standard pneumonia treatment.

Complicated parapneumonic effusions are infected parapneumonic effusions that may be clear or turbid in appearance. About 25 percent of these effusions are culture-positive. Bacterial and host cell metabolism in the pleural space causes a characteristic biochemical pattern with low pH, low glucose, and high LDH, and these criteria are used to define infection when the culture is negative.

Empyema is defined by frank pus in the pleural space. A culture is positive in about 70 percent of cases.

Pleural infection may also be defined as community-acquired or healthcare-associated infection. This distinction is useful given the distinct microbiological profiles associated with each category (which inform antibiotic selection strategies) and the higher mortality found in healthcare-associated infection.

Other sources of pleural infection include esophageal rupture and intra-abdominal sources of infection (e.g., subphrenic abscess), traumatic pleural infection secondary to penetrating or blunt chest trauma, and Iatrogenic pleural infection secondary to thoracic surgery or pleural procedures, such as thoracentesis or chest tube insertion.

Pleural infections can also be classified on the basis of the infecting pathogen:

Gram-positive aerobic bacteria are the commonest cause of pleural infection. However, causative bacteria vary, particularly dependent on whether the infection is community-acquired or healthcare-associated.

Community-acquired pleural infection

Streptococci, including Streptococcus pneumoniae(~20%) and the Streptococcus "milleri"/anginosus (constellatus-intermedius-anginosus) group (~25%), are the commonest causes of community-acquired infection. Gram-negative organisms, including Haemophilus influenzae, Escherichia coli, Pseudomonas spp., and Klebsiella spp., occur in about 10 percent of cases, particularly among patients with comorbidities, such as diabetes.

Estimates of the incidence of anaerobic organisms are usually that they occur in 10-35 percent of cases, although some studies suggest a much higher incidence. Therefore, empiric antibiotic therapy should include anaerobic cover. Polymicrobial infection is comparatively common, often involving anaerobes and gram-negative organisms, especially in the elderly and in those with comorbidities.

Healthcare-associated pleural infection

Similar to healthcare-associated pneumonia, resistant pathogens, such as gram-negative organisms and MRSA, are more common in healthcare-associated pleural infection than in community-acquired pleural infection. In patients who have positive pleural fluid culture results, Staphylococcus aureus(frequently MRSA) is isolated in about half of cases. Gram-negatives, including Pseudomonas spp., Enterobacter spp., and E. coli, are common and are associated with patients who require intensive care. Fungal pleural infection (particularly with Candida spp.), although rare, carries a high mortality rate (>70%) and is usually associated with immunosuppression.

Are you sure your patient has pleural infection? What should you expect to find?

Patients typically present with an acute illness associated with fevers/sweats, dyspnea, cough, pleuritic chest pain, malaise, and decreased appetite. Some cases of pleural infection have a more insidious history, dominated by weight loss, decreased appetite, and malaise. (These symptoms are also compatible with myriad other conditions, including pleural malignancy.) The average time between symptom onset and hospital presentation is more than two weeks.

Clinical examination usually reveals signs of a pleural effusion--that is, stony, dull percussion note in association with decreased breath sounds and reduced tactile vocal fremitus. Fever, tachycardia, tachypnea, hypotension, and reduced oxygen saturations are frequently seen.

Beware: there are other diseases that can mimic pleural infection:

Pleural malignancy

One of the most common mimics of pleural infection is malignant pleural disease. Patients with pleural malignancy often present with a low-grade fever in association with modestly elevated inflammatory markers and a pleural effusion. Biochemical analysis of such effusions may be indistinguishable from pleural infection, particularly in aggressive malignancy with a poor prognosis.

Pleural inflammation

Patients with other inflammatory conditions, such as rheumatoid arthritis, may present with a unilateral pleural effusion and elevated blood inflammatory markers in association with dyspnea, cough, chest pain, and constitutional symptoms. Pleural fluid pH and glucose is characteristically low, although there are often other indications of a significant rheumatoid arthritis flare.

Chylothorax and pseudochylothorax

These conditions give milky-appearing pleural fluid, which may be mistaken for the pus of empyema. Usually, the clinical condition of the patient suggests that pleural infection is unlikely, but diagnostic doubt could be resolved by centrifugation of pleural fluid, after which chyle and pseudochyle remains cloudy, while pus sediments.

How and/or why did the patient develop pleural infection?

Development of a non-infected effusion

A simple (non-infected) parapneumonic effusion is thought to develop secondary to the ingress of pneumonia associated leucocytes into the pleural space, which ingress causes an increase in intrapleural inflammatory cytokines (e.g., interleukin-8 and tumor necrosis factor-α), resulting in increased vascular permeability and development of a sterile exudative pleural effusion.

Progression to pleural infection

Conventional wisdom is that a complicated parapneumonic effusion develops when bacteria migrate across the visceral pleura. Bacteria create an intrapleural procoagulant state with increased levels of plasminogen activator inhibitor (PAI) and decreased tissue-type plasminogen activator (tPA). This procoagulant milieu stimulates fibrin deposition and septation development (also known as the "fibrinopurulent" stage of pleural infection).

Which individuals are at greatest risk of developing pleural infection?


Pleural infection is more common in children and the elderly than in other cohorts. Several cohort studies have suggested that overall incidence is increasing, particularly in children. For example, one study demonstrated incidence rates increasing by 12 percent across all age ranges between 1995 and 2003.

In children, Streptococcus pneumoniae is the commonest cause of pleural infection. Since the licensing of the seven-valent pneumococcal conjugate vaccine (PCV7) in 2000, which are active against serotypes 4, 6B, 9V, 14, 18C, 19F and 23F, there is evidence that the non-vaccine serotype 1 is causing increasing numbers of cases of empyema and other invasive pneumococcal disease.

Recent novel genetic studies suggest that a variant of the protein tyrosine phosphatase (PTPN22 Trp620) is associated with susceptibility to invasive pneumococcal disease and gram-positive empyema.

There are four primary risk factors for pleural infection: diabetes, immunosuppression, alcohol misuse, and intravenous drug abuse. Anerobic pleural infection is particularly found in association with aspiration and poor oral hygiene.

A prospective study found several factors predictive of the development of pleural infection in patients with pneumonia;

  • Serum albumin less than 30 g/L

  • C-reactive protein greater than 100 mg/L

  • Platelet count greater than 400x109/L

  • Serum sodium less than 130 mmol/L

  • Intravenous drug use

  • Alcohol misuse

What laboratory studies should you order to help make the diagnosis, and how should you interpret the results?

Laboratory blood tests

Patients should have standard hematological and biochemical blood tests, including C-reactive protein (CRP), total protein (TP), and lactate dehydrogenase (LDH). All patients should have peripheral blood cultures drawn, which are positive in about 15 percent of patients with pleural infection.

Laboratory pleural fluid tests

A pleural aspiration (thoracentesis) facilitates the analysis of pleural fluid. Various tests are routinely performed on pleural fluid: (Table 1)

Location Request Comment
Microbiology Gram stain, culture and sensitivity analysis Culture is positive in 40-60 percent of patients with pleural infection. Physicians should have a low threshold for requested specialized mycobacterial culture.
Culture of pleural fluid in "blood culture bottles" Bedside inoculation of pleural fluid into aerobic and anaerobic blood culture bottles increases microbiological yield by about 20 percent compared with standard culture techniques.
Bedside pH measurement pH should be measured using an anticoagulated blood gas syringe and a point-of-care blood gas analysis machine. Intrapleural bacterial metabolism and host cell phagocytic activity utilizes glucose and produces lactic acid, producing the characteristic biochemical profile of pleural infection: low pleural fluid pH less than 7.2* and glucose with elevated lactate dehydrogenase (LDH). Care should be taken to expel excess heparin and to avoid contamination with lidocaine, both of which may give spuriously acidic pH values. Free air in the syringe may increase pH readings.
Biochemistry Total protein (TP) When paired with serum values, pleural fluid TP and LDH allow transudates and exudates to be distinguished using Light's criteria (see below). Pleural infection is associated with exudative pleural effusions that characteristically have LDH greater than 1000U/L.
Glucose According to the 2010 British Thoracic Society guidelines, pleural fluid glucose less than 40 mg/dL (<2.2 mmol/L) is associated with pleural infection, while the 2000 American College of Chest Physicians guidelines suggests less than 60 mg/dL (<3.3 mmol/L).
Cytology Cytological examination Given that some cases of pleural malignancy may mimic pleural infection (with low pH and glucose), cytological assessment of pleural fluid is advocated.

Light's criteria for distinguishing between transudates and exudates

An exudate is defined if pleural fluid serum TP is greater than 0.5, pleural fluid serum LDH is greater than 0.6, or pleural fluid LDH is greater than 0.67 of the serum LDH upper limit of normal.

Summary of parapneumonic effusion categorization based on laboratory tests

See Table 2.

Table 2

Simple parapneumonic effusions Complicated parapneumonic effusions Empyema
Appearance Clear or slightly turbid Usually cloudy Pus
pH ≥7.20 <7.20 Not usually measured
Glucose ≥40 mg/dL (2.2 mmol/L) <40 mg/dL (2.2 mmol/L) Not usually measured
LDH ≤1000U/L >1000U/L Not usually measured
Microbiological positivity No ~25% ~70%

What imaging studies will be helpful in making or excluding the diagnosis of pleural infection?

Chest X-ray

Parapneumonic effusions are usually detectable on chest x-rays, often with accompanying consolidation. Complicated parapneumonic effusions/empyema are often loculated, sometimes with air-fluid levels. Given an infective presentation, the finding of a new encapsulated effusion in a non-dependent position is suggestive of pleural infection (Figure 1).

Figure 1.

Thoracic ultrasound demonstrating a small (~1cm depth) anechoic parapneumonic effusion and underlying consolidated lung

Thoracic ultrasound

Pleural ultrasonography can detect low volumes of pleural fluid with greater sensitivity than chest x-ray can. Pleural ultrasonography facilitates accurate pleural fluid localization, which is particularly important given that infected effusions are often loculated. Recent guidelines from the British Thoracic Society Pleural Diseases group, among others, suggest that ultrasound guidance is strongly recommended in sampling pleural fluid. Such guidance reduces the risk of organ perforation and iatrogenic pneumothorax and improves rates of fluid recovery (Figure 2).

Figure 2.

Heavily echogenic fluid on ultrasound. Features demonstrate an exudate and are suggestive of pus (or blood).

The characteristics of sonographic pleural fluid further inform physicians about the nature of the effusion: Echogenic pleural fluid is exudative, and densely echogenic fluid suggests frank pus or intrapleural hemorrhage (Figure 3). Septations, which also predict an exudate, are usually seen in association with low pleural fluid pH glucose and high pleural fluid LDH. Studies have suggested a correlation between significant septations evident on ultrasound and drainage success, although septated effusions may still drain well (Figure 4).

Figure 3.

Moderately septated parapneumonic effusion on ultrasound with underlying consolidation

Figure 4.

A loculated pleural effusion typical of pleural infection, with a chest tube in situ. Underlying consolidation is sometimes difficult to discern.

Thoracic computed tomography

Pleural-phase contrast-enhanced thoracic CT is helpful in patients with ambiguous chest x-ray or sonographic appearance. The CT often shows that fluid is lenticular in shape with compression of surrounding lung parenchyma, and pleural thickening occurs in 56-100 percent of cases. In addition, increased attenuation is often seen in the extrapleural subcostal fat.

CT is useful in distinguishing between a peripheral pulmonary abscess and pleural infection. The "split pleura" sign found in pleural infection describes visceral and parietal pleural enhancement around infected pleural fluid that is not present in pulmonary abscess. However, unlike ultrasonography, CT is relatively insensitive at detecting pleural septations.

Practice point

While various pleural fluid imaging features may suggest pleural infection, the absence of such findings does not rule out infection, and most clinicians would advocate performing a thoracentesis on pleural fluid with depth greater than 1 cm.

What non-invasive pulmonary diagnostic studies will be helpful in making or excluding the diagnosis of pleural infection?

Chest ultrasonography is the diagnostic study with the most sensitivity in identifying a pleural effusion in association with pneumonia.

What diagnostic procedures will be helpful in making or excluding the diagnosis of pleural infection?

Thoracentesis with pleural fluid analysis is the most important test in detecting pleural space infection.

What pathology/cytology/genetic studies will be helpful in making or excluding the diagnosis of pleural infection?

Pleural fluid analysis with fluid culture and gram stain is the most direct way of establishing pleural infections. Frank plural pus also establishes the presence of infection. Other pleural fluid tests, such as low pleural fluid pH, low glucose, and high LDH, provide presumptive evidence of infection.

If you decide the patient has pleural infection, how should the patient be managed?

Having diagnosed pleural infection, physicians should address several treatment goals;

  • Initiation of prolonged broad-spectrum antibiotic therapy

  • Prompt pleural fluid drainage

  • Early surgical referral when required

  • Nutritional support

  • Prophylaxis against venothromboembolism

Antibiotic therapy

Patients should be initially treated with empiric broad-spectrum antibiotic therapy, particularly given that culture techniques may be negative and take several days to yield a result. The duration of antibiotic treatment has not been the subject of formal randomized trials, but it is commonplace to give a total of at least three weeks of antibiotics for pleural infection.

Initial therapy is usually with intravenous antibiotics for about one week, guided by clinical course and laboratory indices (e.g., white cell count and C-reactive protein). Empirical antibiotic therapy should be determined by considering whether the infection is community-acquired or healthcare-associated, the local prevalence of bacteria, and their resistance patterns.

Community-acquired pathogens are often covered by a beta-lactam antibiotic in conjunction with the beta-lactamase inhibitor, such as amoxicillin and clavulinic acid or piperacillin-tazobactam. Metronidazole is often given to increase anerobic coverage. Healthcare-associated pleural infection is often associated with resistant bacteria, including gram-negative enteric bacteria and MRSA. A reasonable choice of antibiotic is a carbapenem combined with vancomycin. Given the excellent pleural penetration of most intravenous and oral antibiotics, intrapleural antibiotic administration is not used.

Prompt pleural fluid drainage

Pleural infection (complicated parapneumonic effusions or empyema) requires prompt tube drainage to prevent increased morbidity. Uninfected simple parapneumonic effusions do not usually require drainage. Traditionally, large-bore chest tubes were used to drain empyema pus, but recent evidence and clinician practice suggest that small-bore tubes (<15 F) have a similar efficacy, and they are associated with less pain.

Chest tubes should be inserted with image guidance (usually ultrasound) because that infected pleural spaces are often loculated. Clinical examination alone predicts the pleural fluid location poorly and causes organ perforation in about 10 percent of cases. Ultrasound-inserted chest drains are associated with fewer complications, particularly iatrogenic pneumothorax. A chest tube flush regime (such as 20mL 0.9% sodium chloride solution every six hours) is often used with a small-bore chest tube and thoracic suction using a dedicated thoracic suction unit should be considered.

Adjunctive intrapleural medication

Recent research has examined the potential role of intrapleural fibrinolytics in improving the drainage of poorly resolving pleural infection, particularly those that are heavily septated. Small studies have suggested that streptokinase, a bacterially derived fibrinolytic, may improve pleural fluid drainage when instilled into the pleural space. However, a large randomized trial, MIST-1 (the first multicenter intrapleural sepsis trial), showed that streptokinase did not improve mortality, surgical requirement, hospital stay, lung function, or radiologic outcome.

Preliminary reports from MIST-2, a randomized controlled trial of intrapleural tPA (tissue plasminogen activator, a fibrinolytic) and DNase (deoxyribonuclease, an enzyme that disrupts DNA), suggest that tPA and DNase in combination improve pleural fluid drainage, but other studies are required to define a treatment effect. The combination of tPA/DNase may be particularly useful in patients with ventilatory compromise who are too unwell to undergo surgical evacuation of the pleural space.

Early surgical referral when required

Thirty percent of patients have ongoing sepsis and poorly resolving pleural fluid despite optimal medical management. These patients should be considered for an early surgical opinion. There is no evidence concerning the timing or clinical criteria for such referrals, although the patient's failure to improve clinically and radiologically after seven days of treatment is often used. Conversely, patients who have some residual pleural fluid but are otherwise well and have improving clinical and laboratory parameters normally see gradual resolution of their pleural fluid over time.

Video-assisted thoracoscopic surgery (VATS) enables decortication of pleural thickening, septation division, and pleural fluid removal, thereby allowing lung re-expansion. VATS is usually performed under general anesthesia with single lung ventilation, although some centers prefer regional anesthesia (epidural or paravertebral blocks). Thoracotomy has slightly higher success rates than VATS, although it is more invasive and associated with greater morbidity and mortality, particularly in older patients.

Some patients who are unfit for general anesthesia may be considered for local anesthetic rib resection, allowing chronic open surgical drainage and gradual withdrawal of chest tubes over several months. This strategy is associated with considerable risk, including ventilatory failure (worsened by chronic pneumothorax) and secondary infection. Several trials have examined the role of primary VATS versus chest tube drainage on initial presentation of pleural infection. Methodological limitations mean that definitive evidence is lacking, although there may be a reduction in length of hospital stay associated with primary VATS.

Nutritional support

Weight loss and low serum albumin concentration, the latter of which is associated with a poorer outcome, are commonplace in pleural infection. While specific nutritional therapy has not been subjected to formal trials in this setting, nutritional support, including nasogastric feeding in selected cases, is likely to be important in counteracting the catabolic state associated with parapneumonic effusion.

Prophylaxis against venothromboembolism

Given the sepsis and relative immobility associated with pleural infection, inpatients should receive regular thromboprophylaxis with a low molecular weight heparin unless contraindicated.

What is the prognosis for patients managed in the recommended ways?

Hospital stay

Median duration of inpatient care is fifteen days, with 20 percent of cases requiring inpatient stays longer than one month.

Morbidity and mortality

Pleural infection is associated with significant morbidity and mortality, as about 20 percent of patients die, and about 15 percent of patients require surgery to treat their pleural infection. Healthcare-associated infection has poorer outcomes than community-acquired infection does. Even so, provided that patients survive to one year, long-term outcomes are favorable. Radiographic pleural abnormalities often take many months to resolve, but they are usually not associated with symptomatic impairment. About 10 percent of patients develop variable degrees of pleural thickening, which are usually of no functional significance. The development of significant pleural fibrosis sufficient to cause activity restriction is rare.

What other considerations exist for patients with pleural infection?

Patients with compromised lung function, as occurs with severe pneumonia, lung cancer, or COPD, require general support to prevent respiratory compromise.

What’s the evidence?

Barnes, TW, Morgenthaler, TI, Olson, EJ, Hesley, GK, Decker, PA, Ryu, JH. "Sonographically guided thoracentesis and rate of pneumothorax". J Clin Ultrasound. vol. 33. 2005. pp. 442-6.

This and the following study are observational studies suggesting that ultrasound-guided thoracentesis is more closely associated with a lower rate of iatrogenic pneumothorax than unguided thoracentesis (pneumothorax rate decreasing from 10.3% to 4.9% in Barnes’ study (n=450); and 18% to 3% in Raptopoulos’ study (n=342)).

Raptopoulos, V, Davis, LM, Lee, G, Umali, C, Lew, R, Irwin, RS. "Factors affecting the development of pneumothorax associated with thoracentesis". AJR Am J Roentgenol. vol. 156. 1991. pp. 917-20.

Bilgin, M, Akcali, Y, Oguzkaya, F. "Benefits of early aggressive management of empyema thoracis". ANZ J Surg. vol. 76. 2006. pp. 120-2.

Small, randomized study (n=70) comparing primary VATS with chest tube insertion in adults. Suggests a decreased hospital stay associated with VATS (8.3 days vs. 12.8 days). However, the primary outcome measure was not specified, and indications for further surgery were subjective.

Chalmers, JD, Singanayagam, A, Murray, MP, Scally, C, Fawzi, A, Hill, AT. "Risk factors for complicated parapneumonic effusion and empyema on presentation to hospital with community-acquired pneumonia". Thorax. vol. 64. 2009. pp. 592-7.

Observational study of factors that predict complicated parapneumonic effusion development in 1269 patients admitted with community-acquired pneumonia. Albumin less than 30 g/l, sodium less than 130 mmol/l, platelet count greater than 400 x 109/l, C-reactive protein greater than 100 mg/l, and a history of alcohol abuse or intravenous drug use were independently associated with development of pleural infection, while COPD was associated with decreased risk.

Chapman, SJ, Khor, CC, Vannberg, FO, Maskell, NA, Davies, CWH, Hedley, EL. "PTPN22 and invasive bacterial disease.". Nat Genet. vol. 38. 2006. pp. 499-500.

Genetic study suggesting that a variant of the protein tyrosine phosphatase (PTPN22 Trp620), which downregulates T cell responses and is associated with susceptibility to multiple autoimmune diseases, is also associated with susceptibility to invasive pneumococcal disease and gram-positive empyema.

Davies, HE, Davies, RJ, Davies, CW. "Management of pleural infection in adults: British Thoracic Society Pleural Disease Guideline 2010.". Thorax. vol. 65. 2010. pp. ii41-53.

Latest evidence-based guidelines for investigation and management of pleural infection.

Diacon, AH, Brutsche, MH, Soler, M. "Accuracy of pleural puncture sites: a prospective comparison of clinical examination with ultrasound". Chest. vol. 123. 2003. pp. 436-41.

Study comparing chest ultrasonography and clinical examination in proposing sites for thoracentesis in sixty-seven patients seen by thirty physicians. Physicians were unable to propose a thoracentesis site using clinical examination alone in 33 percent of cases (of which 54% had sites subsequently successfully identified by ultrasound). Clinically proposed sites could have caused organ puncture in 10 percent of all cases.

Duncan, DR, Morgenthaler, TI, Ryu, JH, Daniels, CE. "Reducing iatrogenic risk in thoracentesis: establishing best practice via experiential training in a zero-risk environment". Chest. vol. 135. 2009. pp. 1315-20.

Mayo Clinic study showing a dramatic reduction (from 8% to 1%) of thoracentesis-related complications since the initiation of a pleural safety program that included pleural ultrasound training and mandated its use before thoracentesis.

Finley, C, Clifton, J, Fitzgerald, JM, Yee, J. "Empyema: an increasing concern in Canada". Can Respir J. vol. 15. 2008. pp. 85-9.

This study examines the Canadian empyema incidence between 1995 and 2003 and demonstrates significant increases, with an overall incidence rate ratio (IRR) of 1.30 and more dramatic increases in patients under age nineteen, with IRR 2.20.

Heffner, JE, Brown, LK, Barbieri, C, DeLeo, JM. "Pleural fluid chemical analysis in parapneumonic effusions. a meta-analysis". Am J Respir Crit Care Med. vol. 151. 1995. pp. 1700-8.

Meta-analysis that assesses the relative merits of pleural fluid pH, LDH, and glucose in defining pleural infection using receiver-operating characteristic techniques. Pleural fluid pH was the best predictor of complicated effusions, with the exact cut-off value determined by the pre-test probability of infection (varying between 7.21 and 7.29). Pleural fluid glucose and LDH did not improve diagnostic reliability.

Maskell, NA, Batt, S, Hedley, EL, Davies, CW, Gillespie, SH, Davies, RJ. "The bacteriology of pleural infection by genetic and standard methods and its mortality significance". Am J Respir Crit Care Med. vol. 174. 2006. pp. 817-23.

Study defining the microbiology of the MIST1 cohort based on culture techniques and 16S ribosomal RNA gene sequencing (genetic DNA testing to identify bacteria).

Maskell, NA, Davies, CW, Nunn, AJ, Hedley, EL, Gleeson, FV, Miller, R. "U.K. Controlled trial of intrapleural streptokinase for pleural infection.". N Engl J Med. vol. 352. 2005. pp. 865-74.

The first multicenter intrapleural sepsis trial (MIST1), which was a randomized trial of intrapleural streptokinase for pleural infection (n=454). The trial failed to demonstrate a benefit on mortality, need for surgery, or duration of hospital stay associated with streptokinase.

Menzies, SM, Rahman, NM, Wrightson, JM, Davies, HE, Shorten, R, Gillespie, SH. "Blood culture bottle culture of pleural fluid in pleural infection.". Thorax. 2011.

The authors compared two culture techniques for pathogen identification in pleural infection (n=62): standard culture vs. culture of pleural fluid inoculated into aerobic and anerobic “blood culture bottles” (BCB) at the bedside. The addition of pleural fluid culture in BCB significantly increased microbiological positivity, from 37.7 percent to 58.5 percent. BCB should be used in addition to, rather than in place of, standard culture, given that some cases were positive only on standard culture.

Porcel, JM, Vives, M, Cao, G, Bielsa, S, Ruiz-Gonzalez, A, Martinez-Irribarren, A. "Biomarkers of infection for the differential diagnosis of pleural effusions.". Euro Resp J. vol. 34. 2009. pp. 1383-9.

A study of 308 patients confirmed that pleural fluid pH (or glucose) were superior to other biomarkers tested (pleural fluid procalcitonin, C-reactive protein, lipopolysaccharide-binding protein, and triggering receptor expressed on myeloid cells (sTREM-1)) in distinguishing between simple and complicated parapneumonic effusions.

Rahman, NM, Maskell, N, Davies, CWH, West, A, Teoh, R, Arnold, A. "Primary result of the second multicentre intrapleural sepsis (MIST2) Trial; randomised trial of intrapleural tPA and DNase in pleural infection.". Thorax. vol. 64. 2009. pp. A1-A.

Preliminary results of the MIST2 trial, a randomized 2x2 factorial trial of intrapleural tPA and DNase in 210 patients with pleural infection. This trial showed significantly improved drainage when a combination of tPA and DNase was used, while monoagent therapy with tPA or DNase was ineffective (and DNase alone was associated with increased adverse events). Additional trials to define treatment effects are required.

Rahman, NM, Maskell, NA, Davies, CW, Hedley, EL, Nunn, AJ, Gleeson, FV. "The relationship between chest tube size and clinical outcome in pleural infection.". Chest. vol. 137. 2010. pp. 536-43.

Study suggesting that the use of small-bore chest tubes in pleural infection was associated with less pain than was the use of large-bore tubes without increasing requirements for thoracic surgery or death rates.

Sonnappa, S, Cohen, G, Owens, CM, van Doorn, C, Cairns, J, Stanojevic, S. "Comparison of urokinase and video-assisted thoracoscopic surgery for treatment of childhood empyema.". Am J Respir Crit Care Med. vol. 174. 2006. pp. 221-7.

Pediatric study comparing primary VATS with chest tube insertion together with intrapleural urokinase (a fibrinolytic) in sixty children finds no benefit to VATS in terms of outcomes of hospital stay, failure rate, and six-month radiology.
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