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Books on the topic 'Effusion'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 March 2023

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1

Pleural effusion. Mount Kisco, N.Y: Futura Pub. Co., 1986.

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2

Mercè, Jordà, and Krishan Awtar, eds. Effusion cytology. New York, NY: Demos Medical Pub., 2011.

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3

United States. Otitis Media Guideline Panel, ed. Otitis media with effusion in children. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1995.

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4

1925-, Stool Sylvan E., and Otitis Media Guideline Panel and Consortium., eds. Otitis media with effusion in children. Rockville, Maryland: U.S. Department of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1994.

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5

1925-, Stool Sylvan E., and Otitis Media Guideline Panel, eds. Otitis media with effusion in young children. Rockville, Md: U.S. Dept. of Health and Human Services, 1994.

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6

United States. Otitis Media Guideline Panel. Otitis media with effusion in young children. Rockville, Md: Agency for Health Care Policy and Research, Public Health Service, US Department of Health and Human Services, 1994.

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7

D, Meyerson Mark, Thiery Daniel, and Falk Oren 1969-, eds. A great effusion of blood?: Interpreting medieval violence. Toronto: University of Toronto Press, 2004.

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8

Yuichi, Majima, and Hamaguchi Yukiyoshi, eds. Rheological and biochemical properties of middle ear effusion. St. Louis, Mo: Annals Pub. Co., 1986.

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9

Yoshihiro, Ohashi, and Nakai Yoshiaki 1934-, eds. Experimental evidence of the usefulness of clinical application of pharmacological ciliostimulatory agents in middle ear and paranasal sinus diseases. Stockholm, Sweden: Scandinavian University Press, 1997.

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10

1935-, Lim David J., Ohio State University. Dept. of Otolaryngology., Ohio State University. Center for Continuing Medical Education., and Deafness Research Foundation (U.S.), eds. Recent advances in otitis media: Proceedings of the fourth international symposium, June 1-4, 1987, Bal Harbour, Florida. Toronto: B.C. Decker, 1988.

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11

Markus, T., and Nathan S. Jacobson. Proceedings of the Workshop on Knudsen Effusion Mass Spectrometry. Pennington, NJ: The Electrochemical Society, 2013.

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12

David, Chalmers, and University of Otago. Dept. of Paediatrics and Child Health. Dunedin Multidisciplinary Health and Development Research Unit., eds. Otitis media with effusion in children: The Dunedin study. London: Mac Keith, 1989.

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13

David, Chalmers, and Dunedin Study, eds. Otitis media with effusion in children: The Dunedin Study. Oxford: MacKeith Press ; Philadelphia : Lippincott, 1989.

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14

International Conference on Acute and Secretory Otitis Media. Acute and secretory otitis media: Proceedings of the International Conference on Acute and Secretory Otitis Media, part I, Jerusalem, Israel, 17-22 November 1985. Amsterdam: Kugler Publications, 1986.

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15

Glenn, Takata, Chan Linda S, Mangione-Smith Rita, United States. Agency for Healthcare Research and Quality., and Southern California Evidence-Based Practice Center/RAND., eds. Diagnosis, natural history, and late effects of otitis media with effusion. Rockville, MD: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Healthcare Research and Quality, 2003.

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16

Glue ear in childhood: A prospective study of otitis media with effusion. London: Mac Keith, 1995.

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17

Maw, A. Richard. Glue ear in childhood: A prospective study of otitis media with effusion. [London]: MacKeith Press, 1995.

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18

S, Jacobson Nathan, and NASA Glenn Research Center, eds. Measuring thermodynamic properties of metals and alloys with Knudsen effusion mass spectrometry. Cleveland, Ohio: National Aeronautics and Space Administration, Glenn Research Center, 2010.

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19

International, Academic Otological Conference (2nd 1984 Lövångers Kyrkstad Sweden). Middle ear with special reference to connective tissue and middle ear effusion: Proceedings of the 2nd International Academic Otological Conference, Lövångers Kyrkstad, August 22-24, 1984. Umea: Universitets Tryckeri, 1987.

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20

J, Soler Soler, Permanyer G, and Sagristà-Sauleda J. 1946-, eds. Pericardial disease: New insights and old dilemmas. Dordrecht: Kluwer Academic, 1990.

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21

Felding, Jens Ulrik. Middle ear gas: Its composition in the normal and in the tubulated ear : a methodological and clinical study. Oslo: Scandinavian University Press, 1998.

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22

Effusion et tourment, le récit des corps: Histoire du peuple au XVIIIe siècle. Paris: O. Jacob, 2007.

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23

Farge, Arlette. Effusion et tourment, le récit des corps: Histoire du peuple au XVIIIe siècle. Paris: O. Jacob, 2007.

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24

Button, Jeremy Stuart. An examination into deposition uniformity across substrates due to evaporation from Knudsen effusion sources. Salford: University of Salford, 1990.

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25

United States. Agency for Health Care Policy and Research., ed. Cuando se acumula líquido en el oído medio de su niño: Guía para los padres. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1995.

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26

Jerusalem), International Conference on Acute and Secretory Otitis Media (1985. The Eustachian tube: Proceedings of the International Conference on Acute and Secretory Otitis Media, part II, Jerusalem, Israel, 17-22 November 1985. Amsterdam: Kugler Publications, 1987.

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27

National Institute on Deafness and Other Communication Disorders (U.S.), ed. Otitis media: Facts for parents. [Bethesda, Md.?]: National Institutes of Health, National Institute on Deafness and Other Communication Disorders, 2000.

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28

Mathur, Praveen N. Interventional pulmonology. Philadelphia: Saunders, 1995.

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29

T, Brown David, ed. Drugs affecting clearance of middle ear secretions: A perspective for the management of otitis media with effusion. St. Louis, Mo: Annals Publishing Co., 1985.

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30

Eustachian tube and middle ear diseases. Tokyo: Springer-Verlag, 1988.

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31

United States. Agency for Health Care Policy and Research, ed. Cuando se acumula líquido en el oído medio de su niño: Guía para los padres. Rockville, Md: U.S. Dept. of Health and Human Services, Public Health Service, Agency for Health Care Policy and Research, 1995.

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32

Sauzet, Jean-Paul. Renouveau charismatique: Les catholiques du New age ? : effusion de l'Esprit, prophéties, guérisons : fonctions anthropologique et théologique de l'expérience charismatique. Villeurbanne: Golias, 1994.

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33

Essence de l'onomastique dans la civilisation negro-africaine d'hier et d'aujourd'hui: Panacée de règlement des conflits sans effusion de sang. Yaoundé, Cameroun: Éditions Maranatha Polygraphique, 2005.

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34

Demosthenes, Bouros, ed. Pleural disease. New York: Marcel Dekker, Inc., 2004.

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35

Kiselevsky, Mikhail V., ed. Malignant Effusions. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4783-8.

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36

Davidson, Ben, Pinar Firat, and Claire W. Michael, eds. Serous Effusions. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-76478-8.

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37

Davidson, Ben, Pinar Firat, and Claire W. Michael, eds. Serous Effusions. London: Springer London, 2012. http://dx.doi.org/10.1007/978-0-85729-697-9.

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38

Poetical effusions. Oxford: Woodstock Books, 1994.

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39

Llewellyn, Liam. Effusion. Independently Published, 2017.

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40

ya, Del. Effusion. Independently Published, 2019.

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41

Grundy, Seamus. Pleural effusion. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0019.

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Pleural effusion is a common clinical problem which can present both to primary and secondary care. The process by which fluid accumulates can be divided into transudative or exudative. Transudative effusions occur in the presence of normal pleura and are caused by increased oncotic or hydrostatic pressures. Exudative effusions are associated with abnormal pleura and are caused either by increased pleural fluid production due to local inflammation or infiltration or by decreased fluid removal which is caused by obstruction of the lymphatic drainage system. Patients may be entirely asymptomatic or they may present with breathlessness, particularly if the effusion is large. Other symptoms include a cough and systemic symptoms such as weight loss, anorexia, and fever. Chest pain is suggestive of inflammation/infiltration of the parietal pleura and points towards malignancy or empyema. This chapter describes the assessment and diagnosis of the patient with pleural effusion.

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42

Chiumello, Davide, and Silvia Coppola. Management of pleural effusion and haemothorax. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0125.

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The main goal of management of pleural effusion is to provide symptomatic relief removing fluid from the pleural space. The options depend on type, stage, and underlying disease. The first diagnostic instrument is the chest radiography, while ultrasound can be very useful to guide thoracentesis. Pleural effusion can be a transudate or an exudate. Generally, a transudate is uncomplicated effusion treated by medical therapy, while an exudative effusion is considered complicated effusion and should be managed by drainage. Refractory non-malignant effusions can be transudative (congestive heart failure, cirrhosis, nephrosis) or exudative (pancreatitis, connective tissue disease, endocrine dysfunction), and the management options include repeated therapeutic thoracentesis, in-dwelling pleural catheter for intermittent external drainage, pleuroperitoneal shunts for internal drainage, or surgical pleurectomy. Parapneumonic pleural effusions can be classified as complicated when there is persistent bacterial invasion of the pleural space, uncomplicated and empyema with specific indications for pleural fluid drainage. Malignancy is the most common cause of exudative pleural effusions in patients aged >60 years and the decision to treat depends upon the presence of symptoms and the underlying tumour type. Options include in-dwelling pleural catheter drainage, pleurodesis, pleurectomy, and pleuroperitoneal shunt. Haemothorax needs to be differentiated from a haemorrhagic pleural effusion and, when suspected, the essential management is intercostal drainage. It achieves two objectives to drain the pleural space allowing expansion of the lung and to allow assessment of rates of blood loss to evaluate the need for emergency or urgent thoracotomy.

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43

Walsh, Jack. Effusion of Poems. Independently Published, 2018.

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44

White, Jack. Messages of Effusion. Lulu Press, Inc., 2010.

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45

Little, Paul. Otitis media with effusion. Edited by John Phillips and Sally Erskine. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198834281.003.0072.

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46

Katritsis, Demosthenes G., Bernard J. Gersh, and A. John Camm. Pericardial effusion and cardiac tamponade. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199685288.003.1029_update_002.

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47

Meyerson, Mark D., Daniel Thiery, and Oren Falk, eds. 'A Great Effusion of Blood'? University of Toronto Press, 2003. http://dx.doi.org/10.3138/9781442670334.

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48

Chalmers, David. Otitis Media Effusion in Children. MacKeith Press, 1989.

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49

Blasi, Francesco, and Paolo Tarsia. Pathophysiology and causes of haemoptysis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0126.

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The main goal of management of pleural effusion is to provide symptomatic relief removing fluid from pleural space and the options depend on type, stage and underlying disease. The first diagnostic instrument is the chest radiography while ultrasound can be very useful to guide thoracentesis. Pleural effusion can be a transudate or an exudate. Generally a transudate is uncomplicated effusion treated by medical therapy, while an exudative effusion is considered complicated effusion and should be managed by drainage. Refractory non-malignant effusions can be transudative (congestive heart failure, cirrhosis, nephrosis) or exudative (pancreatitis, connective tissue disease, endocrine dysfunction), and the management options include repeated therapeutic thoracentesis, indwelling pleural catheter for intermittent external drainage, pleuroperitoneal shunts for internal drainage, or surgical pleurectomy. Parapneumonic pleural effusions can be divided in complicated when there is persistent bacterial invasion of the pleural space, uncomplicated and empyema with specific indications for pleural fluid drainage. Malignancy is the most common cause of exudative pleural effusions in patients aged >60 years and the decision to treat depends upon the presence of symptoms and the underlying tumour type. Options include indwelling pleural catheter drainage, pleurodesis, pleurectomy and pleuroperitoneal shunt. Hemothorax needs to be differentiated from a haemorrhagic pleural effusion and when is suspected the essential management is the intercostal drainage. It achieves two objectives to drain the pleural space allowing expansion of the lung and to allow assessment of rates of blood loss to evaluate the need for emergency or urgent thoracotomy.

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50

Grundy, Seamus. Pleural infection and malignancy. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0143.

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Pleural infection transitions from simple parapneumonic effusion, to complex parapneumonic effusion, to empyema. Primary empyema occurs without an underlying pneumonic process. Pleural infection commonly presents identically to pneumonia with dyspnoea, purulent sputum, and fevers. It may be associated with pleuritic chest pain. Empyema can cause systemic sepsis, leading to cardiovascular instability and multi-organ failure. A malignant pleural effusion arises when malignant cells infiltrate the pleura, resulting in increased production and decreased lymphatic drainage of pleural fluid. Malignant pleural effusions are either metastatic or primary mesothelioma. This chapter discusses pleural infection, malignant pleural effusion, and mesothelioma, focusing on etiology, symptoms, demographics, diagnosis, prognosis, and treatment.

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