Interventional radiology treatment of empyema and lung abscesses

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1 PAEDIATRIC RESPIRATORY REVIEWS (2008) 9, CME ARTICLE Interventional radiology treatment of empyema and lung abscesses Mark J. Hogan* and Brian D. Coley Nationwide Children s Hospital and The Ohio State University, Columbus, Ohio, USA EDUCATIONAL AIMS To discuss the known complications of pneumonia in children. To list the treatments for empyema in children. To discuss novel treatments for empyema in children. To show the role of imaging in children with complicated pneumonias. To list the indications for image guided drainage of lung abscesses in children. KEYWORDS paediatrics; child; empyema; pneumonia; lung abscess; radiology; interventional Summary Pneumonias in children can be complicated by pleural effusions, empyema and abscesses. The incidence of these complications is increasing, correlated to an increased virulence of the pneumococcal bacterium. These complications may prolong morbidity and lead to decreased pulmonary function. Traditionally, patients were treated medically with antibiotics, and refractory complications were treated surgically with large bore chest tube placement and thoracotomy. Improvements included instilling fibrinolytics into the chest tubes and video-assisted thoracoscopic surgery, which expedited recovery and improved outcomes. Image guided techniques from interventional radiology have been developed as an alternative to treat these patients with minimal invasiveness. These therapies have achieved high success and low complication rates, and are the preferred first-line procedures when available. ß 2008 Elsevier Ltd. All rights reserved. INTRODUCTION Pneumonia in children is quite common and usually responds either to oral or intravenous antibiotics. However, in a subset of patients, the pneumonia can be complicated by pleural * Corresponding author. Section of Vascular and Interventional Radiology, Nationwide Children s Hospital, Department of Radiology, 700 Children s Drive, Columbus, OH 43205, USA. Tel.: ; Fax: address: mark.hogan@nationwidechildrens.org (M.J. Hogan). effusion, empyema or necrotization progressing to pneumatoceles or abscesses. These children often require additional interventional therapies to resolve their primary illness, with a secondary goal of preserving lung function. 1 These complications are most likely related to the virulence of the pathogen, with Streptococcus pneumoniae being the most common bacterium. 2 5 The incidence of complicated pneumonia due to pneumoccocal disease is increasing. 2,3 It is well established that appropriate treatment of empyema will help control sepsis, restore pulmonary function and prevent lung entrapment from the fibrous peel. 2,6, /$ see front matter ß 2008 Elsevier Ltd. All rights reserved. doi: /j.prrv

2 78 M. J. HOGAN AND B. D. COLEY Traditionally, pleural collections were treated with large bore catheters inserted by a surgeon. If this failed to completely drain the pleural space, surgical intervention with a decortication was performed. Later developments included instilling a fibrinolytic into the chest tube in an attempt to break up loculations and video-assisted thoracoscopic surgery (VATS). 1,8 11 Interventional radiologists originally had a limited role in the management of these patients, with image guided procedures indicated if residual loculated collections remained after surgical therapy. However, after successful treatment of these post-surgical patients, image guided interventional techniques were adapted for primary treatment of patients with pleural collections, as they were better tolerated than surgery, avoided general anaesthesia, had a high clinical success and were without significant complications. Abscess and pneumatocele complications from pneumonia occur less often than does pleural infection, and while most commonly due to pneumococcal disease, polymicrobial infection or other pathogens have a higher incidence than with empyema. In addition, congenital malformations such as sequestration or congenital cystic adenomatoid malformation may present as pulmonary abscesses. 12 In the majority of patients, the abscess spontaneously drains via the airways and prolonged antibiotic therapy is sufficient. Spontaneous drainage is less common is patients younger than 7 years old, with up to 21% failing medical treatment. 13 Similar to pleural disease, this problem was traditionally managed surgically and usually required a partial or complete lobectomy, with the potential of reducing later pulmonary function. Interventional radiology is the preferred treatment modality for abscesses in most other areas of the body. These same techniques have been adapted to treating intrapulmonary collections, with a high degree of success. The purpose of the article is to describe image guided techniques for treating complicated pneumonias and to evaluate the role of these techniques in the care of paediatric patients. INTERVENTIONAL RADIOLOGY TECHNIQUES Empyema Imaging Chest radiographs are usually the first imaging to be done in a patient with pneumonia (Fig. 1a). Advanced imaging may not be needed, but is often helpful. The amount of pleural fluid is often not apparent on the chest film as an opaque hemithorax may have little fluid or the entire lung may be collapsed by a large empyema. 14 A CT scan will show all areas of pleural disease and can direct tube placement; however, CT is poor at distinguishing the character of the fluid (transudate versus exudate) or the presence of loculations 2,14 16 (Fig. 1b). Ultrasound imaging can verify or exclude the presence of fluid. It also grades the fluid, depending on the identification of loculations. 2 Stage I is anechoic fluid, Stage II has loculations and Stage III is identified to be a solid peel. 17 However, ultrasound is a directed study and distant sites of disease may be missed 14 (Fig. 1c). Procedure Almost all patients will require some form of sedation or anaesthesia. Standard sedation protocols are followed. We typically use a combination of pentobarbital and fentanyl intravenously in children younger than 12 years old, with midazolam substituting for pentobarbital in older patients. General anaesthesia or other medications may be used as well, when available. While some advocate serial thoracentesis for thin effusions, 7 we only perform thoracentesis for diagnosis of the pathogen. If a patient has fever or oxygen requirement, we always place a tube. This eliminates the need for multiple sedations and it is easier to remove the tube than to perform the procedure again. The patient is placed supine or with the affected side slightly elevated. The arm is either raised over the head or placed across the anterior chest. Pre-procedural ultrasound scanning is performed to determine the best site for access, the most appropriate transducer and the character of the fluid. Typically, we use an 8 MHz curvilinear transducer with a small footprint as it easily fits into the small imaging window between the ribs. A standard sterile prep and drape are performed. The goal is to place the tube in a posterior location as the fluid is dependent. The mid-axillary line is usually chosen as it allows for posterior tube placement without the patient having to lie on the tube. For isolated collections, the most appropriate access to the empyema is chosen based on imaging findings. Local anaesthesia is provided, and with direct ultrasonographic guidance, a sheathed needle is directed posteriorly and over the rib to avoid the intercostal vessels. A small sample of fluid is taken and sent to the laboratory. The remainder of the procedure is performed with fluoroscopic guidance. A guidewire with a floppy tip is advanced and directed posteriorly. Over the wire, the tract is dilated and a pigtail catheter placed. We generally use 12- French catheters, although the size may be decreased in smaller children or increased if the ultrasound characteristics suggest thick fluid. Alternatively, other catheters may be used. The wire or catheter can be manipulated through the pleural space to try and break up adhesions; however, this may lead to wire or catheter kinking and does not usually result is a large amount of additional drainage compared to the use of fibrinolytics. The catheter is secured to the patient and is attached to a standard chest drain with 20 cmh 2 O suction.

3 INTERVENTIONAL RADIOLOGY TREATMENT OF EMPYEMA AND LUNG ABSCESSES 79 Figure 1 This patient presented with a right upper lobe pneumonia (*) and a pleural effusion (arrow) seen in (a). The chest CT (b) shows the effusion (*) which appears to be free flowing as it is dependent. An ultrasound in (c) shows multiple septations in the pleural fluid (arrows). (d) shows the radiograph after image guided insertion of a small bore chest tube and fibrinolytic therapy. The empyema is nearly resolved, with persistent pneumonia (*) causing persistent fevers. After removal of the chest tube and completion of antibiotics, (e) shows minimal residual pleural thickening (arrow). Fibrinolytics Originally, we reserved the use of fibrinolytics for when ultrasound showed multiple loculations, or when tube output dropped and imaging showed significant residual fluid; however, we believe this lead to some failures. Now, unless the fluid appears serous and is purely anechoic without loculations (rare), every patient is started on a fibrinolytic. We currently use tissue plasminogen activator (tpa) 2 mg for all patients, mixed in 20 ml of saline. The tpa

4 80 M. J. HOGAN AND B. D. COLEY is injected into the tube, the tube is clamped for 1 h and then the tube is returned to suction. This is repeated every 12 h until fluid output decreases to <25 ml in a 12-h period. Follow-up Tube output, fever and oxygen requirement are followed, and a chest radiograph is obtained daily (Fig. 1d). At h, if the patient has not improved, and residual fluid is suspected from tube output less than expected (from initial imaging) or there is a worsening chest radiograph, repeat imaging is performed. If significant pleural disease is present, then tube drainage with fibrinolytics is considered a failure and the patient is referred for surgical intervention. Otherwise, tpa is continued and the tube is removed when output falls and one of the two following criteria is met: 1. The patient is afebrile and off supplemental oxygen, or 2. Imaging has demonstrated no significant pleural disease. We do not routinely obtain follow-up CT or ultrasound imaging if these criteria are met (Fig. 1e). Results The results of image guided small bore catheter drainage with adjuvant fibrinolytics have been reported in a number of series and these are summarized in Table Abscesses Indications for drainage include persistent symptoms despite appropriate medical treatment, and failure of resolution on imaging after a course of antibiotics. In addition, there is an operative risk of spillage from the abscess into the normal lung via the airways when the patient in placed in the decubitis position for thoracotomy. Pre-operative drainage is thus often requested. Imaging Intrapulmonary infected collections require cross-sectional imaging. CT can identify the abscess, determine the number of collections, identify its position relative to the visceral pleura, vasculature and airways, determine if a BPF is present and evaluate the pleural space for concomitant empyema (Fig. 2a). Ultrasound is of limited use in preprocedural planning as interposed air makes identification of the abscess difficult. Procedure The technique for image guided abscess drainage is similar to that for empyema, with some key differences. The site of access and path for tube placement are more critical. Tube placement across normal lung or an interlobar fissures is avoided if possible. While ultrasound guidance is used Complications Theoretical complications from image guided drainage include bleeding, vascular injury, bronchopleural fistula (BPF), anaesthesia or sedation complications, and death. However, these are rare. There is only one published report of a death from haemorrhage. 2 There have been some reports of BPF development after drainage and fibrinolytics. However, distinguishing an iatrogenic BPF from a pre-existing or developing air leak from lung necrotization is difficult. Table 1 Results of image guided small bore catheter drainage with adjuvant fibrinolytics for empyema Study Success rate LOS (days) Gates et al /29 (89%) 9.3 Wells & Havens 19 70/71 (99%) 11.2 Yao et al /20 (90%) 16.6 Ekingen et al /32 (81%) 19.9 Sonnappa et al /30 (83%) 6.0 Cochran et al /19 (74%) 13.0 Khalil et al /17 (82%) 11.0 Feola et al /58 (93%) 9.1 LOS, length of stay. Figure 2 (a) Shows a cavitary lesion in the left lower lobe (*) with an air fluid level representing an abscess. After insertion of a chest drain with image guidance (b), a follow up CT shows a markedly smaller abscess (arrow) with the drain in the middle.

5 INTERVENTIONAL RADIOLOGY TREATMENT OF EMPYEMA AND LUNG ABSCESSES 81 Table 2 Results of image guided small bore catheter drainage with adjuvant fibrinolytics for pulmonary abscesses 12,26 30 Study Success rate Kosloske et al. 26 3/4 (75%) Zuhdi et al. 27 6/6 (100%) Hoffer et al. 28 4/5 (90%) Patradoon-Ho & Fitzgerald 12 19/19 (100%) Imamoglu et al. 29 5/7 (71%) Ball et al. 30 8/8 (100%) whenever possible, CT or fluoroscopy may need to be used instead if the sonographic window is poor (Fig. 2b). Fibrinolytics Fibrinolytics are not usually indicated for pulmonary abscesses although, if the collection is loculated, they may be used in an attempt to get complete drainage via a single catheter. Follow-up Follow-up for abscesses is also similar to that for empyema. In our experience, the duration of drainage is about the same, unless a BPF occurs. With a BPF, longer drainage with a higher suction pressure may be required. The catheter is removed when drainage slows, symptoms improve and the abscess decreases in size based on a chest radiograph. As with empyema, we discourage additional CT imaging in a patient with clinical improvement for radiation protection reasons. Results The results of image guided small bore catheter drainage with adjuvant fibrinolytics have been reported in a number of series, as summarized in Table 2. 12,26 30 Complications Potential complications are the same for empyema drainage, with the incidence of BPF ranging from 0 to 75% However, many abscesses already communicate with the airway and BPFs should be expected. The overall complication rate is low, with no reported deaths. DISCUSSION Multiple reports have cited the incidence of pleural effusion with pneumonia to be 36 57%, with 15 20% progressing to empyema, defined as pus within the pleural space. 2,4,6,7,15,21,31 Empyema is classically divided into three separate stages: 5,6,16, Early-exudative: lasts from 24 to 48 h; fluid forms due to pleural inflammation. 2. Fibrinopurulent: lasts from 7 to 10 d; characterized by thickened exudates, fibrin deposition, white cell infiltration and formation of loculations. 3. Organized: starts 2 4 weeks from effusion onset. There is fibroblast formation and creation of a thick peel. Grading of pleural disease based on laboratory criteria has also been described, with ph, glucose and lactose dehydrogenase (LDH) levels, Gram stain and cultures all being performed. 2,7,21 However, laboratory evaluation does not define how the patient should be treated, with the exception of antibiotic coverage for the appropriate pathogen. 12 Several factors have prognostic value in determining if interventional therapy will be required. These include duration of symptoms, co-existing medical conditions and ultrasonographic stage. 5,1,10,36 Early intervention can improve symptoms, decrease the length of morbidity and reduce complications. Serial thoracentesis has been proposed; however, this requires multiple invasive procedures in a child who might require sedation. 2,31 Alternatively, early tube drainage while the fluid is simple can be effective. VATS has been recommended as a first-line approach in patients with empyema. 1,5,8 11 This has been shown to be successful with high curative rates and a low complication rate. The primary measured outcome is length of stay (LOS) with improvement compared to traditional therapies. However, VATS is still an operative procedure requiring general anaesthesia. While this therapy may be necessary in some patients, many of these children could be successfully treated with a less aggressive approach. Therefore, alternative treatments have been explored. Image guided small bore tube placement with adjuvant fibrinolytic therapy also has high success rates and low complications rates At institutions with interventional radiology facilities to perform image guided small tube placement and fibrinolytic therapy, success rates are 74 99% The LOS in multiple studies is similar to VATS. Imaging of patients with pneumonia can help determine if complications such as empyema, abscess or BPF are present, or if interventional therapy is needed, and can also direct therapy. When empyema is present, CT is the most efficient way to identify every area of involvement and can guide where a catheter needs to be placed. In our experience, CT is most valuable in evaluating the parenchymal disease. Necrotization is readily identified and the full extent of the pneumonia is seen. This provides prognostic information about the duration of medical therapy and possible need for future interventions such as abscess drainage. In addition, in many cases where patients have remained ill despite interventional radiology empyema drainage, CT has shown that the problem was progressive necrotizing pneumonia instead of failure of pleural infection therapy. While a CT scan prior to empyema treatment

6 82 M. J. HOGAN AND B. D. COLEY gives valuable prognostic information (primarily about the necrotizing pneumonia), it can be deferred due to radiation concerns. However, a CT scan is mandatory before declaring interventional radiology pleural drainage a failure, and sending a patient to the operating room for VATS or thoracotomy. Ultrasound is valuable in these patients. Ultrasound grading of the empyema is prognostic, with Grades II and III requiring a greater level of intervention. 36 While Grade I fluid is thin and easily removed by thoracentesis, tube placement may be in the patient s best interest to avoid multiple procedures with sedation. Due to loculations, the higher grades will not completely drain via simple tube placement; therefore, fibrinolytics are indicated for these patients. In addition, empyema is a dynamic process 2 and a Grade I pleural collection may change character over time as the visceral pleura continues to secrete fluid as a response to the pneumonia. In our early experience, 18 some failures of tube drainage occurred when Grade I fluid treated without fibrinolytics became loculated over time, or when we stopped fibrinolytic therapy early, with later peel formation. In our practice, for Grade I empyemas, we start fibrinolytic therapy immediately if the tube output is below expected (as predicted by imaging), or within 12 h if the chest radiograph is not completely clear of pleural disease. Fibrinolytics are always given if there are loculations on ultrasound (Grades II and III). Grade III empyemas have a greater failure rate with interventional techniques, although others find no difference in these patients compared to surgery. Therefore, if ultrasound shows what appears to be a fibrous peel, we consult surgery. Some of these patients will respond to interventional techniques, and they can be attempted with the knowledge that surgery will not be delayed if the patient does not improve expediently. The limit of ultrasound is that it is a focused study; not all areas of the pleura can be evaluated. Therefore, the risk is that some areas of loculated empyema could be missed if a CT scan is not performed. This may not make a difference, as the fibrinolytics break up these loculations; however, this reiterates why a CT scan is important in the follow-up of a patient who remains ill despite therapy. Fibrinolytics significantly increase the amount of pleural fluid amenable to drain out of small tubes. The primary benefit of this is the access gained to collections that are walled off by septations. Contrary to some perceptions, the fluid in loculated empyemas usually remains thin. It can easily be drained by a tube if not isolated by the loculations. The type of fibrinolytic used has not been shown to make a significant difference. Urokinase was most commonly used, but conversion to streptokinase or tpa was required in the USA when the Food and Drug Administration (FDA) removed urokinase from the market. Most institutions have stopped using streptokinase due to concerns over possible immunological reactions. There are both weight-based (0.1 mg/kg, up to 3 mg) and set doses (2 mg) for tpa; however, the efficacy of each appears similar, and no pleural bleeding requiring transfusion has been identified. 18,19,25 The dose of urokinase is typically U. All of these medications are mixed with normal saline to an appropriate volume, injected into the tube and left in the pleural space for approximately 1 h before resuming drainage. While image guided small bore tube drainage with fibrinolytics has a similar success rate to VATS, the results are not absolute. Some patients will fail this less aggressive treatment. Even with VATS, some patients are converted to thoracotomy based on the operative findings. Since the LOS for the patient has been proposed as an appropriate outcome indicator for results, treatment algorithms should be tailored to the goal of providing the least aggressive therapy to improve symptoms as quickly as possible. Several studies comparing VATS to tube drainage (with or without fibrinolytics) have concluded that VATS is better due to a reduced LOS. However, a problem with these papers is that in some patients the tube drainage was continued for long periods of time, despite having not succeeded in reducing symptoms in a timely manner. In our practice, if the patient is not improving within h, we consult with surgery to determine if VATS or a thoracotomy is indicated. This decision is based on clinical parameters such as fever and oxygen requirement. Imaging is also obtained to determine if there is significant residual pleural disease, as surgery is not indicated if it is absent. In most patients with continued symptoms, significant pulmonary disease remains, often with necrotization. This approach of attempting to identify pleural peel (Grade III) with ultrasound, early fibrinolytic treatment and reassessment at h has improved our success rate to >95% (unpublished). In addition, tube drainage and surgery are not mutually exclusive. 22,23 Many patients requiring VATS have had a trial of drainage via a surgically placed tube, and patients receiving VATS are referred for interventional radiology drainage or open thoracotomy if they do not improve. Infected lung collections can be primary from a necrotizing pneumonia, or secondary in a patient with a predisposing condition such as a congenital lung lesion. The incidence of abscesses, like empyema, is increasing due primarily to the increased virulence of pneumoccocal disease. Historically, these cases were treated with a prolonged course of antibiotics. There are several case series, dating back to the 1980s, of image guided drainage of these abscesses, performed when antibiotics failed or to ameliorate the symptoms expediently. The experience in adults is greater, but similar techniques and success rates have been found in children. As an alternative to thoracotomy and lobectomy, interventional radiology can treat these patients if the clinical symptoms warrant. In addition, pre-operative drainage of infected congenital lesions decreases the risks of pulmonary failure and overwhelming sepsis which can occur due to bronchial spillage during surgery.

7 INTERVENTIONAL RADIOLOGY TREATMENT OF EMPYEMA AND LUNG ABSCESSES 83 The incidence of complications from interventional radiology drainage of pleural disease and intrapulmonary collections is low, with BPFs being the most common. BPFs are also identified after VATS. The development of a BPF is most likely a result of the necrotizing pneumonia causing pleural disruption, as it is rarely seen without concomitant lung necrosis. Theoretically, pleural damage can occur with tube placement, or the fibrinolytic could break up a loculation that is sealing a pre-existing contained air leak. Regardless of the cause of the BPF, treatment is indicated for patient s symptoms, they occur despite the therapy provided, and they can usually be treated with a course of prolonged drainage. PRACTICE POINTS Complications such as empyema and abscess formation from pneumonia are increasing in incidence in children. Interventional radiology image guided therapies are successful in treating these complications. Ultrasound grading has prognostic importance. Computed tomography is indicated if patients remain symptomatic despite therapy. Algorithms can be developed to expedite patient care. RESEARCH DIRECTIONS Dose and timing of fibrinolytic therapy. Algorithm development. Role of ultrasound in prognosis. Importance of empyema on future lung function. Cost analysis of treatment. CONCLUSION Interventional radiological techniques can successfully treat empyemas and abscesses complicating pneumonia in children. These therapies are less invasive, have a similar LOS and have similar success and complication rates as compared to operative techniques such as VATS or thoracotomy. Treatment algorithms can be developed to expedite patient care. Less aggressive techniques should be employed first, with rapid referral to surgery if the patient does not improve. With this approach, most patients can be treated with image guided techniques, with the occasional failure being referred to the operating room expediently, and the LOS kept within acceptable parameters. REFERENCES 1. Kalfa N, Allal H, Lopez M et al. Thoracoscopy in pediatric pleural empyema: a prospective study of prognostic factors. J Pediatr Surg 2006; 41: Jaffe A, Balfour-Lynn IM. Management of empyema in children. Pediatr Pulmonol 2005; 40: Margenthaler JA, Weber TR, Keller MS. Predictors of surgical outcome for complicated pneumonia in children: impact of bacterial virulence. World J Surg 2004; 28: Jamal M, Reebye SC, Zamakhshary M, Skarsgard ED, Blair GK. Can we predict the failure of thoracostomy tube drainage in the treatment of pediatric parapneumonic collections? J Pediatr Surg 2005; 40: Gates RL, Caniano DA, Hayes JR, Arca MJ. Does VATS provide optimal treatment of empyema in children? J Pediatr Surg 2004; 39: Russell-Taylor M. Bacterial pneumonias: management and complication. Paediatr Respir Rev 2000; 1: Ozcelik C, Ulku R, Onat S, Ozcelik Z, Inci I, Satici O. Management of postpneumonic empyemas in children. Eur J Cardiothorac Surg 2004; 25: Kurt BA, Winterhalter KM, Connors RH, Betz BW, Winters JW. Therapy of parapneumonic effusions in children: video-assisted thoracoscopic surgery versus conventional thoracostomy drainage. Pediatrics 2006; 118: e547 e Doski JJ, Lou D, Hicks BA et al. Management of parapneumonic collections in infants and children. J Pediatr Surg 2000; 35: Kalfa N, Allal H, Montes-Tapia F et al. Ideal timing of thoracoscopic decortication and drainage for empyema in children. Surg Endosc 2004; 18: Dzielicki J, Korlacki W. The role of thoracoscopy in the treatment of pleural empyema in children. Surg Endosc 2006; 20: Patradoon-Ho P, Fitzgerald DA. Lung abscess in children. Paediatr Respir Rev 2007; 8: Erasmus JJ, McAdams HP, Rossi S, Kelley MJ. Percutaneous management of intrapulmonary air and fluid collections. Radiol Clin North Am 2000; 38: Cleveland RH, Foglia RP. CT in the evaluation of pleural versus pulmonary disease in children. Pediatr Radiol 1998; 18: Lewis RA, Feigin RD. Current issues in the diagnosis and management of pediatric empyema. Semin Pediatr Infect Dis 2002; 13: Chang YT, Dai ZK, Kao EL, Chou SH, Huang MF. Thoracosocopic decortication: First-line therapy for pediatric empyema. Eur Surg Res 2005; 37: Ramnath RR, Heller RM, Ben-Ami T et al. Implications of early sonographic evaluation of parapneumonic effusions in children with pneumonia. Pediatrics 1998; 101(1 Pt 1): Gates RL, Hogan M, Weinstein S, Arca MJ. Drainage, fibrinolytics, or surgery: a comparison of treatment options in pediatric empyema. J Pediatr Surg 2004; 39: Wells RG, Havens PL. Intrapleural fibrinolysis for parapneumonic effusion and empyema in children. Radiology 2003; 228: Yao CT, Wu JM, Liu CC, Wu MH, Chuang HY, Wang JN. Treatment of complicated parapneumonic pleural effusion with intrapleural streptokinase in children. Chest 2004; 125: Ekingen G, Guvenc B, Sozubir S, Tuzlaci A, Senel U. Fibrinolytic treatment of complicated pediatric thoracic empyemas with intrapleural streptokinase. Eur J Cardiothorac Surg 2004; 26: Sonnappa S, Cohen G, Owens CM et al. Comparison of urokinase and video-assisted thoracoscopic surgery for treatment of childhood empyema. Am J Respir Crit Care Med 2006; 174: Cochran JB, Tecklenburg FW, Turner RB. Intrapleural instillation of fibrinolytic agents for treatment of pleural empyema. Pediatr Crit Care Med 2003; 4: Khalil BA, Corbett PA, Jones MO et al. Less is best? The impact of urokinase as the first line management of empyema thoracis. Pediatr Surg Int 2007; 23:

8 84 M. J. HOGAN AND B. D. COLEY 25. Feola GP, Shaw CA, Coburn L. Management of complicated parapneumonic effusions in children. Tech Vasc Interv Radiol 2003; 6: Kosloske AM, Ball WS Jr, Butler C, Musemeche CA. Drainage of pediatric lung abscess by cough, catheter, or complete resection. J Pediatr Surg 1986; 21: Zuhdi MK, Spear RM, Worthen HM, Peterson BM. Percutaneous catheter drainage of tension pneumatocele, secondarily infected pneumatocele, and lung abscess in children. Crit Care Med 1996; 24: Hoffer FA, Bloom DA, Colin AA, Fishman SJ. Lung abscess versus necrotizing pneumonia: implications for interventional therapy. Pediatr Radiol 1999; 29: Imamoglu M, Cay A, Kosucu P et al. Pneumatoceles in postpneumonic empyema: an algorithmic approach. J Pediatr Surg 2005; 40: Ball WS Jr, Bisset GS 3rd, Towbin RB. Percutaneous drainage of chest abscesses in children. Radiology 1989; 171: Coote N, Kay E. Surgical versus non-surgical management of pleural empyema. Cochrane Database Syst Rev 2005; 19: CD Campbell PW 3rd. New developments in pediatric pneumonia and empyema. Curr Opin Pediatr 1995; 7: Misthos P, Sepsas E, Konstantinou M, Athanassiadi K, Skottis I, Lioulias A. Early use of intrapleural fibrinolytics in the management of postpneumonic empyema. A prospective study. Eur J Cardiothorac Surg 2005; 28: Mattei P, Allen JL. Treatment of empyema in children. Am J Respir Crit Care Med 2006; 174: Barnes NP, Hull J, Thomson AH. Medical management of parapneumonic pleural disease. Pediatr Pulmonol 2005; 39: Park CS, Chung WM, Lim MK, Cho CH, Suh CH, Chung WK. Transcatheter instillation of urokinase into loculated pleural effusion: analysis of treatment effect. AJR Am J Roentgenol 1996; 167: CME SECTION This article has been accredited for CME learning by the European Board for Accreditation in Pneumology (EBAP). You can receive 1 CME credit by successfully answering these questions online. (A) Visit the journal CME site at com. (B) Complete the answers online, and receive your final score upon completion of the test. (C) Should you successfully complete the test, you may download your accreditation certificate (subject to an administrative charge). Educational questions Answer true or false. 1. Traditional treatment of complicated pneumonias in children include all except: a. Antibiotics. b. Large bore chest tubes. c. Thoracotomy with decortication. d. Bronchial stenting. e. Lobectomy. 2. The roles of ultrasound in complicated pneumonias include: a. Identifying if pleural fluid is present. b. Guiding tube placement. c. Grading empyemas. d. Visualizing pulmonary abscesses adjacent to the visceral pleura. e. All of the above. 3. With regard to empyema in children: a. Thoracotomy should be done on all children to improve outcomes. b. No treatment is indicated as it might hurt the child. c. Image guided procedures are highly successful. d. They are almost always due to aspiration. e. The fluid is too thick to come out of a tube. 4. Reasons for image guided drainage of a pulmonary abscess include: a. Persistent fever and oxygen requirement despite appropriate antibiotics. b. A CT scan that shows an abscess. c. Pre-operative drainage to reduce complications. d. A foreign body is seen. e. a and c. 5. With regard to fibrinolytics: a. Only tpa has been shown to work with empyema. b. There are many variations of dosing and techniques. c. It breaks up the thick fluid so that it can be drained. d. It can only be used once. e. Systemic bleeding is a major problem with pleural doses.

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