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Year : 2009  |  Volume : 4  |  Issue : 2  |  Page : 75-87
Reading chest radiographs in the critically ill (Part I): Normal chest radiographic appearance, instrumentation and complications from instrumentation

Department of Medicine and Medical Imaging, King Saud University for Health Science, King Abdulaziz Medical City, King Fahad National Guard Hospital, Riyadh, Saudi Arabia

Date of Submission11-Nov-2008
Date of Acceptance14-Dec-2008

Correspondence Address:
Ali Nawaz Khan
Chairman of Medical Imaging Department, King Abdulaziz Medical City, King Fahad National Guard Hospital, P.O. Box 22490, Riyadh - 11426
Saudi Arabia
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/1817-1737.49416

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How to cite this article:
Khan AN, Al-Jahdali H, Al-Ghanem S, Gouda A. Reading chest radiographs in the critically ill (Part I): Normal chest radiographic appearance, instrumentation and complications from instrumentation. Ann Thorac Med 2009;4:75-87

How to cite this URL:
Khan AN, Al-Jahdali H, Al-Ghanem S, Gouda A. Reading chest radiographs in the critically ill (Part I): Normal chest radiographic appearance, instrumentation and complications from instrumentation. Ann Thorac Med [serial online] 2009 [cited 2023 Apr 1];4:75-87. Available from:

Interpreting chest radiographs of the critically ill patients who are in intensive care units (ICUs) poses a challenge not only for the intensive care physicians but also for the radiologist. These challenges arise because of several factors: [1] ICU patients are prone to several cardiopulmonary disorders which when superimposed on the underlying pathology that prompted admission create a complex radiological appearance, which may be difficult to interpret on the basis of imaging findings alone. [2] The standard posteroanterior (PA) radiograph is replaced by the suboptimal anteroposterior (AP) radiograph in the ICU patient. [3] Instrumentation, mechanical ventilation, cardiac and other vital sign monitoring and feeding tubes, etc., detract from other findings on the ICU chest radiograph. [4] Radiologists/Intensive care physicians are under pressure for rapid interpretation of chest x-rays when treating critically ill patients, often with inadequate clinical information, partly due to the fact that things can change rapidly in the critically ill. [5] Radiological interpretation is hampered by the bewildering array of line placements in the ICU patient, where incorrect placement is not uncommon, which may not be obvious to the observer without clinical input. [6] Air space shadowing in the ICU patient may have identical appearances in a variety of cardiopulmonary pathologies. Although the imaging modality of choice in the ICU patient remains that of chest radiography, computed tomography is often performed as computed tomographic pulmonary angiography (CTPA) with suspected pulmonary embolism. Ultrasound is used to confirm pleural and pericardial effusions and when pleural intervention is planned.

The aim of this paper is [1] to discuss the radiographic findings of cardiopulmonary disorders common in the ICU patient and suggest guidelines for interpretation based not only on the chest radiograph but also on the pathophysiology and clinical grounds. [2] In addition, to describe the normal position of monitoring devices and other line placements, and prompt recognition when they are misplaced or when other complications occur.

This is a 2-part series [1] : Part I: Normal chest radiographic appearances in the ICU patient, correct and incorrect placement of various intra-thoracic tubes and lines and complications from instrumentation.

Part II: Radiography of lung pathologies common in the ICU patient.

   The Normal Chest X-ray Top

The standard PA chest radiograph is rarely taken in the ICU patient and is replaced by an anteroposterior (AP) radiograph. These radiographs are ideally obtained in the AP projection with a patient-to-x-ray plate distance of 72 inches with the patient in the upright position at maximum inspiration; but more often, a distance of 40 inches is used in the supine or sitting position due to the impaired mobility of ICU patients [Figure 1]. A radiograph obtained in this way magnifies the mediastinum and heart due to gravitational and geometrical effects. Moreover, supine position alters the physiology of the pulmonary vasculature, diverting the blood to lung apices - an appearance that is regarded as normal on AP supine radiograph but considered abnormal on a PA radiograph. Supine radiographs have further limitations, including problems of differentiating pleural effusions from air space shadowing and detecting a pneumothorax. Exposing a radiograph in full inspiration in an ICU patient poses further challenges as these patients are often uncooperative or are suffering from postoperative pain [Figure 2]. A more-than-perfect inspiratory effort creates artifacts, making the diagnosis of basilar atelectasis and pulmonary edema difficult, besides causing changes in the apparent size of the heart and mediastinum. [1],[2],[3],[4]

The sensitivity and specificity of the ICU chest radiograph are low, but its common use stems from studies that have shown that as much as 65% of ICU chest radiographs reveal a significant pathology that results in a change in patient management. Current recommendations from the American College of Radiology suggest that daily chest radiographs be obtained on patients with acute cardiopulmonary problems and those receiving mechanical ventilation. The college further recommends that only an initial chest radiograph is needed for the placement or change of indwelling devices. [5]

In patients that have undergone thoracotomy for whatever reason, the initial postoperative radiographs after return from operating theatre will show the lines and tubes placed perioperatively, such as an endotracheal tube, thoracostomy tubes, mediastinal drains and central venous catheters. These devices need to be identified and their positions checked for incorrect placement. Immediately following and a few days after CABG, lower lobe atelectasis is common, usually more pronounced on the left, generally resolving within a few days without complications. There is slight widening of the mediastinum, but significant increase in diameter might indicate complications such as a mediastinal bleeding. A small left pleural effusion is invariable following CABG, but a larger pleural effusion or a subsequent increase in size may need intervention so as not to cause respiratory compromise [Figure 3]. Therefore, comparison with previous radiographs is essential to assess a change in size of a pleural effusion.

   Identifying Lines and Tubes and Other Devices Top

Tubes, lines and drainage catheters play a vital role in monitoring and treating critically ill patients. Accurate placement of these devices and monitoring malfunction are crucial. The initial portable chest radiograph plays an essential role in recognizing correct placement and complications. All placed devices should be identified on the preliminary radiograph as a priority in these patients before looking for cardiopulmonary disorders [Figure 4] and [Figure 5]. [Table 1] summarizes the correct positioning of various lines and tubes.

The endotracheal tube

Endotracheal or tracheostomy tubes (ETs) maintain an airway access and allow mechanical ventilation of patients with respiratory failure. These tubes are cuffed and placed in the trachea, either via the oropharynx or introduced surgically through a tracheostomy. If it is anticipated that the patient needs intubation for a period longer than a week or has upper airway obstruction, a tracheostomy is usually preferred. A chest radiograph is essential to correctly locate the tip of endotracheal tubes. Misplaced ET may cause serious compromise of respiratory function and has been reported in 10% of the patients. Thus, daily chest radiographs are recommended in these patients as these devices may migrate. A correctly placed endotracheal tube lies at the level of the mid-trachea, about 5 cm from the carina. Placing the tip at this level allows for flexion or extension of the head. The minimal safe distance from the carina is 2 cm. Poor chest x-ray exposure may sometimes not allow recognition of the carina. A previous radiograph, if available, may be used to estimate the position of the carina. Alternatively, the position of the tip of the ET can be assessed by looking at the upper dorsal spine. As the carina normally lies at the T4-T5 interspace, the tip of the endotracheal tube lying at this level is regarded as correct placement [Figure 6] and [Figure 7]. The Dee method has been devised for approximating the position of the carina. This involves identifying the aortic arch and then drawing a line inferomedially through the middle of the arch at a 45-degree angle to the midline. The intersection of the midline and the diagonal line is the most likely position of the carina. This is a cumbersome method for the busy ICU physician/radiologist and is seldom used.

ETs are misplaced in approximately 10% of the patients. A comparatively common misplacement is when the tube enters the right main stem bronchus, due to its more vertical orientation. This position impairs the left lung ventilation, leading to collapse of the left lung; similarly, if the endotracheal tube enters the bronchus intermedius, the right upper lobe may collapse. ET that has been placed at a higher level may slip into the pharynx or the esophagus, causing gastric air distension with the potential danger of reflux of gastric contents and aspiration. More serious complications of ETs include tracheal stenosis, tracheal rupture, cord paralysis, cervical and mediastinal emphysema, hematoma and abscess formation.

When upper airway injury is suspected, a lateral radiograph may be useful. The soft tissue space between the trachea and cervical spine is increased in diameter to over the width of one vertebral body in the presence of a hematoma or infection.

Severe injury such as tracheal rupture should be suspected in patients with pneumothorax, pneumomediastinum, subcutaneous emphysema in the neck or precipitous respiratory failure following intubation [Figure 8]. Most tracheal ruptures are placed posteriorly. [6],[7],[8],[9]

The thoracostomy tube

Thoracostomy tubes are often placed into the pleural space to treat a pneumothorax or drain pleural fluid [Figure 9]. Chest radiographs are often obtained following placement of thoracostomy tubes to identify their position. It is important to recognize that on a supine AP radiograph, air accumulates anteriorly and fluid gravitates posteriorly. This fact is taken into account when placing thoracostomy tubes relevant to the pathology in hand. Determining whether a tube is anterior or posterior is often difficult with a single AP chest radiograph. Thoracostomy tubes placed within pleural fissures often cease to drain when the lung surfaces become apposed. Correct placement of thoracostomy tube fenestrations within the thoracic cavity is important to proper functioning of these tubes. The last side-hole in a thoracostomy tube can be identified by an interruption in the radiopaque line. This interruption in the radiopaque line should lie within the thoracic cavity, if not and or with evidence of subcutaneous air, a misplaced tube should be suspected. Incorrectly placed tubes for empyemas may delay drainage and result in loculation of the purulent fluid. [10]

The feeding tube

Nasogastric tubes (NGs) are used to feed patients or for gastric aspiration in appropriate clinical circumstances. Radiographs are seldom required for accurate placement of NG tubes and are not used except when the patient is unconscious and there is risk of placement of the tube into the bronchial tree. There are other exceptions where a chest radiograph is useful and may prevent serious consequences, which include instances where small-bore feeding tubes are inserted and in status-post esophagectomy [Figure 10],[Figure 11],[Figure 12]. The lower tip of the NG is generally placed in the upper small bowel, which may be confirmed with an abdominal radiograph. [11],[12],[13],[14]

Monitoring central venous pressures

Central venous pressures (CVPs) are monitored by central vein catheters placed either through the subclavian or the internal jugular vein; or occasionally via the femoral vein, particularly in babies where access via jugular or subclavian vein is unavailable. These catheters are also used for safe delivery of large volumes of fluids over long periods with minimal chances of venous thrombosis. Correct placement of the tip of the CVP line is important for accurate measurement of central venous pressure. The ideal location of the tip of the CVP line is between the most proximal venous valves of the subclavian or jugular veins and the right atrium. Misplacing CVP lines is not uncommon when lines are placed within the internal jugular vein, right atrium and right ventricle. Placing the CVP catheter distal to the superior vena cava may cause arrhythmias or may risk cardiac a perforation [Figure 13],[Figure 14],[Figure 15],[Figure 16],[Figure 17]. Other complications of CVP line placement are a pneumothorax; and intimal injury to veins, causing perforation or thrombosis. These complications can be avoided by using ultrasound guidance for CVP catheter placement, and jugular vein placement is preferred because of lower complication rates. [15],[16],[17]

Monitoring pulmonary capillary wedge pressure

Pulmonary capillary wedge pressure monitors are introduced via the venous system to help accurate assessment of the patient's volume status and can help differentiate between cardiac and noncardiac pulmonary edema.  Swan-Ganz catheter More Detailss are generally used as pulmonary capillary wedge pressure monitors. These catheters are introduced percutaneously via the right heart and into the pulmonary artery. This allows pulmonary wedge pressure to be calculated by inflating a balloon located at the tip of the catheter. The tip is advanced into a distal pulmonary artery and wedged there. The balloon is deflated once the pressure is taken, and the tip is pulled back to the main pulmonary artery. The tip of the catheter located within the mediastinal shadow indicates correct placement. The catheter tip should ideally be placed proximal to an interlobar pulmonary artery [Figure 18],[Figure 19],[Figure 20]. Malpositioning of Swan-Ganz catheters may occur in a quarter of the patients, resulting in false pulmonary capillary wedge pressure readings, risk for pulmonary infarction, pulmonary artery perforation, cardiac arrhythmias and endocarditis. [18],[19],[20],[21],[22],[23]

The intra-aortic counterpulsation balloon pump

The intra-aortic counterpulsation balloon pump (IACB) is used to decrease afterload and increase cardiac perfusion in patients with cardiogenic shock. The device is synchronized with either the aortic pressures or the patient's EKG, to inflate during diastole and deflate during systole [Figure 21]. The device is introduced via the right femoral artery to be positioned above the celiac axis in the region of the aortic isthmus or left main bronchus. During systole, the lucent air-filled balloon appears as fusiform. [24],[25],[26]

Cardiac pacing devices

ICU patients with cardiac arrhythmias or a heart block may require temporary cardiac pacemakers. The pacing wires of these devices are introduced via the cephalic or subclavian vein into the apex of the right ventricle. AP and lateral chest radiographs are usually required to evaluate accurate pacemaker placement. The tip of the cardiac pacemaker should be at the apex of the heart, and there should be no sharp angulations along the length of the pacemaker wires. The lateral radiograph should show the tip imbedded within the cardiac trabeculae. For correct placement to have occurred, the tip should appear 3 to 4 mm beneath the epicardial fat pad [Figure 22],[Figure 23],[Figure 24]. A tip that appears to be placed beyond the epicardial fat stripe may have perforated the myocardium. Cardiac pacers placed within the coronary sinus appear to be directed posteriorly on the lateral chest radiographs. [27],[28],[29],[30]

Pneumothorax and other intrathoracic air collections

Extra-alveolar thoracic air collections in the ICU patients are not uncommon - often the result of intubation, other thoracic interventional procedures and barotrauma from positive end-expiratory pressure ventilation. This extra-alveolar air can collect as pulmonary interstitial emphysema, pneumothorax, pneumomediastinum, pneumopericardium or subcutaneous air.

Subcutaneous emphysema is not uncommon and often follows percutaneous intrathoracic placement of drains and other devices. Air dissects through the fascial planes, which usually has no clinical consequences [Figure 25]. Subcutaneous emphysema may be associated with a pneumomediastinum; however, in the presence of isolated cervical subcutaneous emphysema, the patient needs to be examined for upper airway injury, particularly relevant following a difficult intubation or the placement of a new nasogastric tube. The chest x-ray findings of subcutaneous emphysema may be striking; and the air dissecting the fascial planes, particularly between muscle bundles in the pectoralis region, is well seen obscuring underlying lung parenchymal changes. In the presence of subcutaneous emphysema, the detection of a pneumothorax also can become difficult.


A pneumothorax represents accumulation of air in the pleural space and it may occur spontaneously, or secondary to trauma, it may or may not be associated with lung parenchymal disease. Air rises to the nondependent position, and the radiographic appearance depends upon how the radiograph has been exposed. In the erect patient, air rises to apicolateral surface of the lung and appears as a thin, white pleural line with no lung markings beyond [Figure 26],[Figure 27],[Figure 28]; however, the presence of lung markings beyond the pleural line does not exclude a pneumothorax. The diagnosis of a pneumothorax may be particularly difficult in the presence of parenchymal disease, which may alter the compliance or affect the compliance of the lung, making collapse more difficult. A skin fold may mimic a pneumothorax. A skin fold line when followed continues outside of the chest [Figure 29].

In an ICU patient, diagnosis of pneumothorax is often made on a supine radiograph. In a supine patient air rises anteromedially. An apical air collection in a supine patient is a sign of a large pneumothorax. Air can sometimes be trapped in a subpulmonic location between the lung and the diaphragm. Anterolateral extension of air into the costophrenic sulcus may increase the radiolucency at the costophrenic sulcus. This is called the deep sulcus sign. Other features of a subpulmonic pneumothorax include visualization of the superior surface of the diaphragm and the superior part of the inferior vena cava.

A tension pneumothorax is accumulation of air within the pleural space due to free ingress of air with limited egress of air. The intrapleural pressure exceeds atmospheric pressure in the lung during expiration (ball-valve mechanism). The diagnosis of tension pneumothorax is a clinical one based on respiratory and cardiac compromise. Diagnosis of a tension pneumothorax in a critically ill patient can be extremely challenging, partly due to the fact that lung pathology such as ARDS may reduce lung compliance, preventing total lung collapse as occurs in a tension pneumothorax. Similarly, a mediastinal shift, a hallmark of tension pneumothorax, may not occur with the use of PEEP. Signs of a tension pneumothorax include depression of a hemidiaphragm, a shift of the heart border, the superior vena cava and the inferior vena cava. [31],[32]


A pneumomediastinum represents air in the mediastinum and may be related to pulmonary interstitial air dissecting centripetally in the intubated patient [Figure 30] and [Figure 31]. Mediastinal air may also represent a leak from a major airway injury or air dissecting through fascial planes from the retroperitoneum. Unlike a pneumopericardium, air from a pneumomediastinum often dissects up into the neck. Moreover, a pneumopericardium can extend inferior to the heart. A pneumomediastinum usually remains asymptomatic. However, occasionally a retrosternal crunch may be heard on auscultation. Radiographic features of a pneumomediastinum include air around the great vessels, the medial border of the superior vena cava, and the azygos vein seen as surrounding lucencies. Air may also be seen outlining the aortic knuckle, descending aorta and the pulmonary arteries. A posteromedial pneumomediastinum is usually the result of esophageal rupture, where air dissects into the paraspinal costophrenic angle and beneath the parietal pleura of the left diaphragm. The result is a V-shaped lucency called the V-sign of Naclerio. [33]


A pneumopericardium refers to an accumulation of gas/air between the myocardium and pericardium [Figure 32],[Figure 33],[Figure 34]. Pneumopericardium can be an occasional complication of pneumothorax but is more often found in the postoperative cardiac patient. The chest x-ray findings are those of a lucent line around the heart, extending up to the main pulmonary arteries. Air may accumulate inferior to the cardiac shadow, which crosses the midline above the diaphragm, which is said to be diagnostic for pneumopericardium, the so-called continuous diaphragm sign. [34]

Pleural effusions

Pleural effusions are accumulations of fluid within the pleural space [Figure 35],[Figure 36],[Figure 37],[Figure 38],[Figure 39],[Figure 40],[Figure 41]. Pleural effusions occur frequently in the ICU patients, which may be secondary to heart failure, fluid overload, hypoproteinemia, infection, pulmonary embolism, thoracic and upper abdominal surgery, neoplastic disease, subphrenic inflammatory processes, trauma and ascites. The fluid could be blood, chyme, pus, transudates or exudates. The radiographic appearance of a pleural effusion is dependent on the position of the patient. Pleural fluid accumulates in the dependent areas of the chest. A pleural effusion is easier to identify in the erect patient as fluid collects at the base of the lung, causing costophrenic angle blunting and decreased visibility of the lower lobe vessels. In the supine position, identification of a pleural effusion is more challenging. In the supine position, pleural fluid accumulates in the posterior basilar space, which appears as homogenous density that increases in intensity towards the lung base. The normal bronchovascular markings are retained in this veil-like density. With increasing amount of pleural fluid, the diaphragm loses its contour and costophrenic angle may be obliterated. However, it should be remembered that the pleural space may accommodate up to a liter of fluid above the diaphragm without blunting of the costophrenic angle. With larger pleural effusions, the fluid may appear as pleural cap at the lung apex, making it easier to identify on a supine radiograph. The fluid may sometimes accumulate on the medial side of the lung, appearing as a widened mediastinum. Often, smaller pleural effusions are missed on supine chest radiographs despite meticulous technique. When effusions are not readily apparent on a supine chest radiograph but clinically suspected, a lateral decubitus film is indicated. The film should be taken with the side of the patient suspected to have an effusion in the dependent position. The lateral decubitus film would not only confirm smaller pleural effusions but can also differentiate between loculated and free effusions. The latter information is important when pleural drainage is planned, as loculated effusions may need more than one drain. A pleural effusion at the lung base is termed a subpulmonic effusion and is a common occurrence in the ICU patient. On the chest radiograph, a subpulmonic pleural effusion appears as a raised hemidiaphragm with flattening and lateral displacement of the dome. A lateral decubitus film can usually resolve this.

Loculated pleural effusions may pose a diagnostic challenge, especially when fluid is retained within the fissures; and in particular, when the fissures are incomplete. A loculated effusion in the minor fissure and right middle lobe atelectasis may be difficult to differentiate on a supine chest radiograph. Interlobar effusion appears as a homogenous density with biconvex edges and preservation of the minor fissure, while atelectasis appears as an inhomogeneous density with concave margins and obliteration of both the right heart border and minor fissure. CT or an erect lateral radiograph, if possible, may resolve the issue. [35],[36],[37],[38],[39]

Pericardial effusions

Pericardial effusions are accumulations of fluid between the visceral and parietal pericardium [Figure 42],[Figure 43],[Figure 44]. They usually cannot be seen on plain chest radiographs, and smaller effusions are difficult to differentiate from cardiomegaly. A variety of pathologies may cause pericardial effusions, including lymphatic or venous obstruction by tumors, changes in osmotic pressures, or inflammation of the pericardium causing increased permeability. Generally, pericardial effusions only become symptomatic when the intrapericardial pressure rises by 3 or 4 mm Hg. A hemopericardium may follow cardiac surgery or trauma. The rapidity at which the pericardial effusion accumulates dictates hemodynamic consequences. Radiographically, a pericardial effusion appears as cardiomegaly with a change in cardiac silhouette, resulting in a featureless, globular or "water bottle" shape. The best and quickest way to determine the presence of a pericardial effusion is by echocardiography. [40],[41],[42],[43]

   References Top

1.Brainsky A, Fletcher RH, Glick HA, Lanken PN, Williams SV, Kundel HL. Routine portable chest radiographs in the medical intensive care unit: Effects and costs. Crit Care Med 1997;25:801-5.   Back to cited text no. 1    
2.Chahine-Malus N, Stewart T, Lapinsky SE, Marras T, Dancey D, Leung R, et al . Utility of routine chest radiographs in a medical-surgical intensive care unit: A quality assurance survey. Crit Care 2001;5:271-5.   Back to cited text no. 2    
3.Graat ME, Krφner A, Spronk PE, Korevaar JC, Stoker J, Vroom MB, et al . Elimination of daily routine chest radiographs in a mixed medical-surgical intensive care unit. Intensive Care Med 2007;33:639-44.   Back to cited text no. 3    
4.Bhagwanjee S. Muckart DJ. Routine daily chest radiography is not indicated for ventilated patients in a surgical ICU. Intensive Care Med 1996;22:1335-8.   Back to cited text no. 4    
5.Henschke CI, Yankelevitz DF, Wand A, Davis SD, Shiau M. Accuracy and efficacy of chest radiography in the intensive care unit. Radiol Clin North Am 1996;34:21-31.   Back to cited text no. 5    
6.Chander S, Feldman E. Correct placement of endotracheal tubes. N Y State J Med 1979;79:1843-4.   Back to cited text no. 6    
7.Roberts JR, Spadafora M, Cone DC. Proper depth placement of oral endotracheal tubes in adults prior to radiographic confirmation. Acad Emerg Med 1995;2:20-4.   Back to cited text no. 7    
8.Dennie CJ, Coblentz CL. The trachea: Pathologic conditions and trauma. Can Assoc Radiol J 1993;44:157-67.   Back to cited text no. 8    
9.Datta D, Onyirimba F, McNamee MJ. The utility of chest radiographs following percutaneous dilatational tracheostomy. Chest 2003;123:1603-6.   Back to cited text no. 9    
10.Biffi R, Pozzi S, Cenciarelli S, Zambelli M, Andreoni B. Treatment of pneumothorax as a complication of long-term central venous port placement in oncology patients: An observational study. J Vasc Access 2001;2:129-36.   Back to cited text no. 10    
11.Ghahremani GG, Turner MA. Port RB. Iatrogenic intubation injuries of the upper gastrointestinal tract in adults. Gastrointest Radiol. 1980;5:1-10.   Back to cited text no. 11    
12.Libman RH. Correct positioning of the endotracheal tube. IMJ Ill Med J 1977;151:384.   Back to cited text no. 12    
13.May S. Testing nasogastric tube positioning in the critically ill: Exploring the evidence. Br J Nurs 2007;16:414-8.   Back to cited text no. 13    
14.Metheny NA, Meert KL. Monitoring feeding tube placement. Nutr Clin Pract 2004;19:487-95.  Back to cited text no. 14    
15.Pikwer A, Bεεth L, Davidson B, Perstoft I, Akeson J. The incidence and risk of central venous catheter malpositioning: A prospective cohort study in 1619 patients. Anaesth Intensive Care 2008;36:30-7.   Back to cited text no. 15    
16.Biffi R, Pozzi S, Cenciarelli S, Zambelli M, Andreoni B. Treatment of pneumothorax as a complication of long-term central venous port placement in oncology patients: An observational study. J Vasc Access 2001;2:129-36.   Back to cited text no. 16    
17.Hayashi Y, Maruyama K, Takaki O, Yamauchi J, Ohnishi Y, Kuro M. Optimal placement of CVP catheter in paediatric cardiac patients. Can J Anaesth 1995;42:479-82.   Back to cited text no. 17    
18.Sharma S, Eagle KA. Monitoring pulmonary artery wedge pressure in medical patients. Am Fam Physician 1996;54:1039-49. Review. Erratum in: Am Fam Physician 1996 Dec;54:2377.   Back to cited text no. 18    
19.Sharkey SW. Beyond the wedge: Clinical physiology and the Swan-Ganz catheter. Am J Med 1987;83:111-22.   Back to cited text no. 19    
20.Raper R, Sibbald WJ. Misled by the wedge? The Swan-Ganz catheter and left ventricular preload. Chest 1986;89:427-34.   Back to cited text no. 20    
21.Wiedemann HP, Matthay MA, Matthay RA. Cardiovascular-pulmonary monitoring in the intensive care unit. Chest 1984;85:537-49.   Back to cited text no. 21    
22.Pierson DJ, Hudson LD. Monitoring hemodynamics in the critically ill. Med Clin North Am 1983;67:1343-60.   Back to cited text no. 22    
23.Kaye W. Invasive monitoring techniques: Arterial cannulation, bedside pulmonary artery catheterization, and arterial puncture. Heart Lung 1983;12:395-427.   Back to cited text no. 23    
24.Sheldon CA, Leonard AS. Hemodynamic monitoring. Urol Clin North Am 1983;10:19-34.   Back to cited text no. 24    
25.Baskett RJ, Ghali WA, Maitland A, Hirsch GM. The intraaortic balloon pump in cardiac surgery. Ann Thorac Surg 2002;74:1276-87.   Back to cited text no. 25    
26.Scheidt S, Collins M, Goldstein J, Fisher J. Mechanical circulatory assistance with the intraaortic balloon pump and other counterpulsation devices. Prog Cardiovasc Dis 1982;25:55-76.   Back to cited text no. 26    
27.Higgins SL, Yong P, Sheck D, McDaniel M, Bollinger F, Vadecha M, et al . Biventricular pacing diminishes the need for implantable cardioverter defibrillator therapy: Ventak CHF Investigators. J Am Coll Cardiol 2000;36:824-7.   Back to cited text no. 27    
28.Coman JA, Trohman RG. Incidence and electrocardiographic localization of safe right bundle branch block configurations during permanent ventricular pacing. Am J Cardiol 1995;76:781-4.   Back to cited text no. 28    
29.Littleford PO, Curry RC Jr, Schwartz KM, Pepine CJ. Clinical evaluation of a new temporary atrial pacing catheter: Results in 100 patients. Am Heart J 1984;107:237-40.   Back to cited text no. 29    
30.Brown CG, Gurley HT, Hutchins GM, MacKenzie EJ, White JD. Injuries associated with percutaneous placement of transthoracic pacemakers. Ann Emerg Med 1985;14:223-8.   Back to cited text no. 30    
31.Sahn SA. State of the art: The pleura. Am Rev Respir Dis 1988;138:184-234.   Back to cited text no. 31    
32.Müller NL. Imaging of the pleura. Radiology 1993;186:297-309.   Back to cited text no. 32    
33.Bejvan SM, Godwin JD. Pneumomediastinum: old signs and new signs. AJR Am J Roentgenol 1996;166:1041-8.   Back to cited text no. 33    
34.Brander L, Ramsay D, Dreier D, Peter M, Graeni R. Continuous left hemidiaphragm sign revisited: A case of spontaneous pneumopericardium and literature review. Heart 2002;88:e5.   Back to cited text no. 34    
35.Neagley SR, Zwillich CW. The effect of positional changes on oxygenation in patients with pleural effusions. Chest 1985;88:714-7.   Back to cited text no. 35    
36.Chinnan NK, Rathore A, Shabaan AI, Al Samman W. The "forbidden" chest x-ray: Tension pyopneumothorax. Am J Emerg Med 2007;25:200-1.   Back to cited text no. 36    
37.Mφller A. Pleural effusion: Use of the semi-supine position for radiographic detection. Radiology 1984;150:245-9.   Back to cited text no. 37    
38.Henschke CI, Davis SD, Romano PM, Yankelevitz DF. The pathogenesis, radiologic evaluation, and therapy of pleural effusions. Radiol Clin North Am 1989;27:1241-55.   Back to cited text no. 38    
39.Johnson JL. Pleural effusions in cardiovascular disease: Pearls for correlating the evidence with the cause. Postgrad Med 2000;107:95-101; quiz 257.   Back to cited text no. 39    
40.Miller SW. Imaging pericardial disease. Radiol Clin North Am 1989;27:1113-25.   Back to cited text no. 40    
41.Nowlen TT, Rosenthal GL, Johnson GL, Tom DJ, Vargo TA. Pericardial effusion and tamponade in infants with central catheters. Pediatrics 2002;110:137-42.   Back to cited text no. 41    
42.Roy CL, Minor MA, Brookhart MA, Choudhry NK. Does this patient with a pericardial effusion have cardiac tamponade? JAMA 2007;297:1810-8.   Back to cited text no. 42    
43.Kirkland LL, Taylor RW. Pericardiocentesis. Crit Care Clin 1992;8:699-712.  Back to cited text no. 43    


  [Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6], [Figure 7], [Figure 8], [Figure 9], [Figure 10], [Figure 11], [Figure 12], [Figure 13], [Figure 14], [Figure 15], [Figure 16], [Figure 17], [Figure 18], [Figure 19], [Figure 20], [Figure 21], [Figure 22], [Figure 23], [Figure 24], [Figure 25], [Figure 26], [Figure 27], [Figure 28], [Figure 29], [Figure 30], [Figure 31], [Figure 32], [Figure 33], [Figure 34], [Figure 35], [Figure 36], [Figure 37], [Figure 38], [Figure 39], [Figure 40], [Figure 41], [Figure 42], [Figure 43], [Figure 44]

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