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240 oracic ultrasound
194. Lensing AW, Prandoni P, Prins MH et al. Deep vein thrombosis. Lancet 1999; 353: 479-485.
195. Birdwell RG, Raskob GE, Whitsett TL et al. e clinical validity of normal compression ultrasonography in outpatients suspected of having deep vein thrombosis. Ann Intern Med 1998; 128: 1-7.
196. Farahmand S, Farnia M, Shahriaran S, Khashayar P. e accuracy of limited B-Mode compression technique in diagnosing deep venous thrombosis in lower extremities. Am J Emerg Med 2011; 29: 687-690.
197. Lensing AWA, Prandoni P, Brandjes D et al. Detection of deep vein thrombosis by real time B-Mode ultrasonography. N Engl J Med 1989; 320: 342-345.
198. Bernardi E, Camporese G, Büller HR et al.; Erasmus Study Group. Serial 2-point ultrasonography plus D-dimer vs whole-leg color-coded Doppler ultrasonography for diagnosing suspected symptomatic deep vein thrombosis: a randomized controlled trial. JAMA 2008; 300(14): 1653-1659.
199. Fraser JD, Anderson DR. Deep venous thrombosis: recent advances and optimal invetigation with US. Radiology 1999; 21: 9-24.
200. Kearon C, Julian JA, Newman TE et al. Noninvasive diagnosis of deep venous thrombosis. Ann Intern Med 1998; 128: 663-677.
Updated bibliography
Reissig A, Gramegna A, Aliberti S. e role of lung ultrasound in the diagnosis and follow-up of community acquired pneumonia. Eur J Intern Med 2012;23:391-397. Reissig A, Copetti R, Mathis G, Mempel C, Schuler A, Zechner P, Aliberti S, Neumann R, Kroegel C, Hoyer H. Lung ultrasound in the diagnosis and follow-up of community acquired pneumonia: a prospective, multicenter, diagnostic accuracy study. Chest 2012;142:965-972. Bourcier JE, Paquet J, Seinger M, Gallard E, Redonnet JP, Cheddadi F, Garnier D, Bourgeois JM, Geeraerts T. Performance comparison of lung ultrasound and chest x-ray for the diagnosis of pneumonia in the ED. Am J Emerg Med 2014;32:115-118.
ese studies exhort to promote thoracic ultrasound in the first line diagnosis of community acquired pneumonia and Emergency Department pneumonia. oracic ultrasound shows sensitivity and specificity values over 95%. Chest radiograph is less accurate. About 8% of pneumonic lesions are not detectable by ultrasound.
Hu QJ, Shen YC, Jia LQ, Guo SJ, Pang CS, Yang T, Wen FQ. Diagnostic performance of lung ultrasound in the diagnosis of pneumonia: a bivariate meta-analysis. Int J Clin Exp Med 2014;7:115-121.
Meta-analysis including nine studies and 1080 subjects. It demonstrates sensitivity and specificity values for lung ultrasound of 0.97 and 0.94 respectively for detecting pneumonia. e area under the receiver operating charac­teristic curve is 0.99.
Busti C, Agnelli G, Duranti M, Orlandi C, Marcucci M, Paciaroni M. Lung ultrasound in the diagnosis of stroke associated pneumonia. Intern Emerg Med 2014;9:173-178.
is study demonstrates the utility of ultrasound to rule out pneumonia in patients with stroke.
Lichtenstein D, Karakitsos D. Integrating lung ultrasound in the hemodynamic evaluation of acute circulatory failure (the fluid administration limited by lung sonography protocol). J Crit Care. 2012;Epub 2012, Apr 18.
A contribution for the use of chest ultrasound as a guide for treatment in circulatory failure and for hemodynamic evaluation.
Kajimoto K, Madeen K, Nakayama T, Tsudo H, Kuroda T, Abe T. Rapid evaluation by lung-cardiac-inferior vena cava (LCI) integrated ultrasound for differentiating heart failure from pulmonary disease as the cause of acute dyspnea. Cardiovascular Ultrasound 2012;10:49.
is study highlights the role of integrated ultrasound (lung, heart, inferior vena cava) for differentiating cardiac and pulmonary causes of dyspnea.
Parenchymal lung patology 241
Martindale JL, Noble VE, Liteplo A. Diagnosing pulmonary edema: lung ultrasound versus chest radiography. Eur J Emerg Med 2013;20:356-360.
In this study, residents were able to more accurately identify pulmonary edema with lung ultrasound than with chest radiography.
Miglioranza MH, Gargani L, Sant’anna RT, Rover MM, Martins VM, Mantovani A, Weber VM, Moraes MA, Feldman CJ, Kalil RA, Sicari R, Picano E, Leiria TL. Lung ultrasound for the evaluation of pulmonary congestion in outpatients: a comparison with clinical assessment, natriuretic peptides and echocardiography. JACC Cardiovasc Imaging 2013;6:1141-1151.
A confirmation of the role of B-Lines for diagnosing heart decompensation (systolic heart failure) in outpatients.
Panuccio V, Enia G, Tripepi R, Torino C, Garozzo M, Battaglia GC, Marcantoni C, Infantone L, Giordano G, De Giorgi M, Lupia M, Bruzzese V, Zoccali C. Chest ultrasound and hidden lung congestion in peritoneal dialysis patients. Nephrol Dial Transplant 2012;27:3601-3605.
Contribution for understanding the role of B-Lines for estimating extravascular lung water in peritoneal dialysis patients.
Baldi G, Gargani L, Abramo A, D’Errico L, Caramella D, Picano E, Giunta F, Forfori F. Lung water assessment by lung ultrasonography in intensive care: a pilot study. Intensive Care Med 2013:39:74-84.
Lung ultrasound B-Lines are correlated with lung weight and density determined by CT. is is a clinical con­firmation of the hypothesis expressed in this book on the role of interstitial syndrome in interpreting subpleural density and geometry.
Gardelli G, Feletti F, Nanni A, Mughetti M, Piraccini A, Zompatori M. Chest ultrasonography in ICU. Respir Care 2012;57:773-781. Via G, Storti E, Gulati G, Neri L, Mojoli F, Braschi A. Lung ultrasound in the ICU. from diagnostic instru­ment to respiratory monitoring tool. Minerva Anestesiol 2012;78:1282-1296. Piette E, Daoust R, Denault A. Basic concepts in the use of thoracic and lung ultrasound. Curr Opin Anaesthesiol 2013;26:20-30. Bilotta F, Giudici LD, Zeppa IO, Guerra C, Stazi E, Rosa G. Ultrasound imaging and use of B-Lines for functional lung evaluation in neurocritical care: a prospective observational study. Eur J Anaestesiol 2013;30:464-468. Silva S, Biendel C, Ruiz J, Olivier M, Bataille B, Geeraerts T, Mari A, Riu B, Fourcade O, Genestal M. Usefulness of cardiothoracic chest utrasound in the management of acute respiratory failure in critical care practice. Chest 2013;144:859-865. Ashton Cleary DT. Is thoracic ultrasound a viable alternative to conventional imaging in critical care setting? Br J Anaesth 2013;111:152-160.
Recent advances on the role of chest ultrasound in Intensive Care and Anesthesiology.
Nazerian P, Vanni S, Volpicelli G, Gigli C, Zanobetti M, Bartolucci M, Ciavattone A, Lamorte A, Veltri A, Fabbri A, Grifoni S. Accuracy of point of care multiorgan ultrasonography for the diagnosis of pulmonary embolism. Chest 2013;13:1087.
Multiorgan sonography (lung, heart and leg veins ultrasonography) is more sensitive (90%) than single-organ sonography for detecting pulmonary embolism. It may safely reduce the CT angiography burden.
Tardella M, Gutierrez M, Salaffi F, Carotti M, Ariani A, Bertolazzi C, Filippucci E, Grassi W. Ultrasound in the assessment of pulmonary fibrosis in connective tissue disorders: correlation with high resolution computed tomography. J Reumatol 2012; 39:1641-1647. Moazedi Fuerst FC, Zechner PM, Tripolt NJ, Kielhauser SM, Brickman K, Scheidl S, Lufti A, Graninger WG. Pulmonary echography In systemic sclerosis. Clin Rheumatol 2012;31:1621-1625. Barskova T, Gargani L, Guiducci S, Randone SB, Bruni C, Carnesecchi G, Conforti ML, Porta F, Pignone A, CAramella D, Picano E, Cerinic MM. Ann Rheum Dis 2013;72:390-395.
ese studies demonstrate the utility of lung ultrasound for assessing lung involvement in patients with pulmonary fibrosis in connective tissue disorders.
242 oracic ultrasound
Hasan A, Makhlouf HA. B-Lines: Transthoracic chest ultrasound signs useful in assessment of Interstitial lung diseases. Ann orac Med 2014;9:99-103. Pinal Fernandez I, Pallisa Nunez E, Selva O’Callaghan A, Castella Fierro E, Martinez Gomez X, Vilardell Tarres M. Correlation of ultrasound B-Lines with high resolution computed tomography in antisynthetase syndrome. Clin Exp Rheumatol 2014 Apr 28 [Epub ahead of print]. Cogliati C, Antivalle M, Torzillo D, Birocchi S, Norsa A, Bianco R, Costantino G, Ditto MC, Battellino M, Sarzi Puttini PC, Montano N. Standard and pocket size lung ultrasound devices can detect interstitial lung disease in rheumatoid artrhritis patients. Rheumatology (Oxford) 2014 Mar 31[Epub ahead of print]. Moazedi Fuerst F, Kielhauser SM, Scheidl S, Tripolt NJ, Yazdani Biuki B, Dejaco C, Graninger WB. Ultrasound screening for interstitial lung disease In rheumatoid arthritis. Clin Exp Rheumatol 2014;32:199-2013. Aghdashi M, Broofeh B, Mohammadi A. Diagnostic performances of high resolution trans-thoracic lung ulrasonography in pulmonary alveoli-Interstitial involvement in rheumatoid lung disease. Int J Clin Exp Med 2013;6:562-566.
Transthoracic lung ultrasound is an inexpensive and safe tool to screen patients with lung involvement in rheu­matoid arthritis. Moreover, its utility is demonstrated in subjects with interstitial lung diseases. A good correlation between dense B-lines (3 mm apart) and high resolution computed tomography ground glass opacities was observed.
Zieleskiewicz L, Contargyris C, Brun C, Touret M, Vllin A, Antonini F, Muller L, Bretelle F, Martin C, Leone M. Lung ultrasound predicts interstitial syndrome and hemodynamic profile in parturients with severe preeclampsia. Anestesiology 2014;120:906-914.
In parturients with severe preeclampsia, lung ultrasound detects both pulmonary edema and increased left ven­tricular end diastolic pressure.
An official American oracic Society/European Respiratory Society statement: Update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med. 2013 Sep 15;188(6):733-48.
e ARDS Definition Task Force. Acute respiratory distress syndrome: the Berlin definition. JAMA 2012; 307(23):2526-2533. New ARDS definition.
8
Pathology of the diaphragm
Diaphragmatic pathology is complex and concerns congenital and ac­quired diseases with variable gravity ultrasound features of the diaphragm are discussed in chapter 4. In these pages we will consider its diseases and dysfunctions from the ultrasound perspective, highlighting their anatomic, artifactual and dynamic aspects (Table 1).
Physiologically, the diaphragm is the most important respiratory muscle, its vertical move­ment is 1 to 2 cm during quiet breathing and 6 to 7 cm during deep breathing. Each cm of vertical movement mobilizes 300 to 400 ml of air during normal breathing
Table 2 summarizes some dynamic aspects of the muscle useful for the ultrasound diagnosis in diaphragm pathology.
e assessment of diaphragmatic excursion has some limitations when the probe is in inter­costal or subcostal position (Fig. 1) by measuring the shift in M-Mode
1
. Anatomy, function and normal
2,3
.
4,5
:
Figure 1 – Ultrasound scans. A: Subcostal. B: Intercostal. C: With linear probe for the apposition zone. D: Orthostatic subcostal.
243
244 oracic ultrasound
• On the left, the colic angle and the poor acoustic window of the spleen prevent the meas-
urement many times.
• On the right, the lung curtain can obscure the vision of the diaphragmatic dome in its
maximum displacement, if the scans are carried out with the probe in intercostals posi­tion (Fig. 2).
Figure 2 – On the left: The M Mode track is partially obscured by the inspiratory lung curtain. On the right: inspiratory curtain in B Mode.
• ere is uncertainty related to the angle of incidence of the ultrasound on the diaphragm
that can make measurements not repeatable (Fig. 3).
• Consequently, when measuring diaphragmatic excursion, the exploring beam should be
as perpendicular as possible to the excursion line of the muscle.
e measurement with linear probe of the length and dynamics of the area of apposition of the diaphragm, and of the inspiratory thickening of the diaphragm
Figure 3 – Sometimes it is not easy to keep the line of sight of M Mode perfectly orthogonal to the line of the diaphragm (arrow).
6,7
is much more reproducible
Pathology of the diaphragm 245
and can be performed either on the right or left (Fig. 4). However, the thickness and thicken­ing of the muscle are small (an average of 3-4 mm vital capacity and 30-60% during forced inspiration), and then the measurements must be accurate (Fig. 5).
Figure 4 – Diaphragm in the apposition zone. A: B Mode visualization. Pleural and peritoneal fluid contrasts the muscle. B: The diaphragm against the chest wall is made evident by the presence of ascites. C: The lung curtain during inspiration shortens the muscle affixed to the wall. D: During maximum inspiration the apposition zone of the diaphragm is greatly reduced and the muscle is thickened (4.4 mm).
Figure 5 – Thickening of the diaphragm at the apposition zone during inspiration. In this case the fraction of thickening is 39%.
246 oracic ultrasound
Table 1 – Diaphragm diseases
Pathology Characteristics
Congenital hernias (CH)
• Bochdalek hernia
• Morgagni hernia
Acquired hernias
• Hiatal hernias
• Traumatic hernias
Tumors Benign
Eventration Diaphragmatic dysfunction (monolateral/bilateral)
• Paralysis
• Weakness
Mimics
• Increased intraabdominal pressure
• Lung volume loss
• Subpulmonic pleural effusion
• Pleural tethering of the diaphragm
CH with antenatal diagnosis CH associated with pulmonary hypoplasia CH diagnosed shortly after birth in patients with respiratory distress CH with postnatal diagnosis (symptomatic and asymptomatic congenital hernias of the adult). Type 1,2,3,4
Malignant
Neurogenic
• Multiple sclerosis
• Stroke
• Arnold-Chiari malformation
• Quadriplegia
• Amyotrophic lateral sclerosis
• Poliomyelitis
• Spinal muscular atrophy
• Syringomyelia
• Guillain-Barrè syndrome
• Tumor compression
• Neuralgic neuropathy
Myogenic or neuro-myogenic
• Myastenia gravis
• Lambert Eaton syndrome
• Muscular dystrophies
• Myositis
• Acid maltase deficiency
Toxic or drug related
• Organophosphates
• Glucocorticoids
• Paralyzing agents
• Botulism
Pneumogenic
• Hyperinflation (COPD, Asthma) Critical illness polyneuropathy Chronic inflammatory demyelinating polyneuropathy Idiopatic Disuse atrophy (ventilator dependency) Obesity, ascites, hepatomegaly, splenomegaly, subphrenic abscesses Atelectasis, pulmonary fibrosis, lung resection
Pathology of the diaphragm 247
Table 2 – Sonographic measures concerning the diaphragm
Diaphragmatic excursion in echography (M-Mode, hemicoronal)
Diaphragmatic excursion in echography (M-Mode, intercostal)
Diaphragmatic excursion (M-Mode, subcostal) quiet breathing
Diaphragmatic excursion (M-Mode, subcostal) deep breathing
Diaphragmatic excursion (M-Mode, subcostal) voluntary sniffing
Thickness of the diaphragmatic zone of apposition
Length of diaphragmatic zone of apposition to mid-axillary line
Maximum inspiratory lowering of 4.9 cm to the right and 5 cm to the left
1.8 +/- 0.76 to 7.9 +/- 1.3 cm, forced inspiration
1.8 +/- 0.3 (males), 1.6 +/- 0.3 (females)
7+/- 0.6 (males), 5.7 +/- 0.1 (females)
2.9 +/- 0.6 (males), 2.6 +/- 0.5 (females)
3.2 +/- 0.8 to over 4 mm
0.7 +/- 0.6 cm at Total Lung Capacity, 7.1 +/-
0.9 cm at RFC, 11 +/- 1.2 cm at Residual Volume
Diaphragmatic thickness measurements during spontaneous breathing are influenced by lung volume in a non linear relationship. ickness of the diaphragm changes according to lung volumes, increasing slightly from residual volume to functional residual capacity (FRC), and sharply from FRC to total lung capacity.
In diaphragmatic ultrasound some principles have general validity.
• Diaphragmatic dysfunction is an underdiagnosed cause of dyspnea and should always be
considered in the differential diagnosis of unexplained dyspnea8.
• Diaphragmatic anatomy and function are affected by disorders of contiguous structures
(free and loculated pleural effusion, atelectasis, pulmonary fibrosis, pulmonary hyperin­flation, supradiaphragmatic pneumonia, subdiaphragmatic abscess, ascites, peritonitis, pyelonephritis, pleural adhesions, tumors, etc…). Before attributing a dysfunction to a primitive neuromuscular disease, these diagnoses must be excluded9.
• A state of lung hyperinflation10 or, on the contrary, pleuropulmonary restriction respec-
tively show a decrease or an increase of the area of apposition of the diaphragm (Fig. 6).
• e bronchial obstructive pathology alters the movement of the diaphragm but also the
duration of the expiratory movement (Fig. 7).
• e diaphragmatic hernia involves occupation of the pleural cavity by omental tissue or
abdominal organs, resulting in pulmonary compression (or hypoplasia).
• An elevation of the diaphragm on chest X-ray11 always requires an echographic evaluation
of lung, pleura and of the subdiaphragmatic peritoneum.
• Elevation caused by paralysis or weakness involves an entire hemidiaphragm, whereas eleva-
tion secondary to eventration involves only a portion of hemidiaphragm, most commonly the anteromedial portion of the right hemidiaphragm.
• In diaphragmatic weakness the impaired hemidiaphragm may be thinned by atrophy of
the muscle12; in diaphragmatic paralysis that lasts few days the involved hemidiaphragm is thinned.
248 oracic ultrasound
Figure 6 – Air trapping in a patient with CPOD. A: Standard chest X-ray. B: Specular pattern of the lung (hypermirror). C: the opening of the costophrenic angle during maximum inspiration is minimal and the length of the apposition zone of the diaphragm is minimal. D: Muscle hypertrophy with marked thickening at the end of inspiration.
Figure 7 – Assessement of diaphragmatic mobility in M Mode. A: Quiet breathing. B: Maximum inspiration. C: Maximum exhalation from inspiratory reserve volume. D: The normal subject, in 1 second exhales over 80% of vital capacity.
Pathology of the diaphragm 249
• Unilateral diaphragmatic involvement is often asymptomatic and discovered incidentally.
Bilateral diaphragmatic dysfunction is usually symptomatic and may lead to ventilator failure13.
• Functional imaging allows further evaluation after diaphragmatic elevation is recognized.
Diaphragmatic ultrasound may be used as an alternative to fluoroscopic tests.
Clinical features
Patients with diaphragmatic pathology may be asymptomatic, may have dyspnea on exertion and limited ability to exercise, or may be critically ill with severe respiratory distress. Often these patients show signs and symptoms related to the causal pathology (pain, fever, neuro­logic disturbances) and a progressive and/or evocative history (recurrent respiratory failure and infections, mediastinal mass, chest surgery, trauma, spinal and neuromuscular disease, mechanical ventilation)
e distinction between monolateral and bilateral diaphragmatic dysfunction represents the first evaluative step.
In the case of unilateral diaphragmatic paralysis, motility and inspiratory thickening of the involved hemidiaphragm are abolished, while motility and thickening of the opposite hemidiaphragm remain preserved. e concerned hemidiaphragm is raised and there is a paradoxical (cephalad) movement of this muscle during a short, sharp inspiratory effort through the nostrils (sniff test).
Unilateral muscle weakness involves a reduced movement and thickening. Sonographic features of hypoventilation or atelectasis appear in the lower lobe in a patient with diaphragmatic dysfunction or paralysis (Fig. 8). Table 3 illustrates the clinical and sonographic features distinguishing between mono- and bilateral paralysis of the diaphragm
14,15
.
1,8,14,16
.
Figure 8 – Atelectasis of the right inferior lobe in case of right diaphragmatic paralysis.