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Unexpected pulmonary edema and cardiac arrest following wedge resection of spontaneous pneumothorax -A case report
BACKGROUNDReexpansion pulmonary edema is a rare but potentially lethal complication. We report a case of suspected reexpansion pulmonary edema that led to cardiac arrest. CASEA 16-year-old male patient underwent wedge resection due to right pneumothorax. The patient showed pink frothy sputum three h...
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Published in: | Anesthesia and pain medicine 2022, Vol.17 (3), p.298-303 |
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creator | Han, Woong Kim, Gyu Seong Lee, Jong Min Lim, Chang Mook Yang, Hong Seuk Jeong, Chang Yeong Park, Dong Ho |
description | BACKGROUNDReexpansion pulmonary edema is a rare but potentially lethal complication. We report a case of suspected reexpansion pulmonary edema that led to cardiac arrest. CASEA 16-year-old male patient underwent wedge resection due to right pneumothorax. The patient showed pink frothy sputum three hours following surgery, and a chest x-ray showed right unilateral pulmonary edema. Thirteen hours following surgery, the patient continuously showed pink frothy sputum and presented with severe hypoxemia, tachypnea, and tachycardia. After transferring to the intensive care unit (ICU), he developed ventricular tachycardia. Cardiopulmonary resuscitation was performed for 32 min. Chest X-ray showed diffuse bilateral pulmonary edema. Extracorporeal membrane oxygenation was performed. During the 65 days of ICU care, the patient became mentally alert. However, follow-up echocardiography revealed severe heart failure. CONCLUSIONSRexpansion pulmonary edema can rapidly progress to diffuse bilateral pulmonary edema. Therefore, careful observation is required for the patients who show signs of pulmonary edema after reexpansion. |
doi_str_mv | 10.17085/apm.21116 |
format | report |
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We report a case of suspected reexpansion pulmonary edema that led to cardiac arrest. CASEA 16-year-old male patient underwent wedge resection due to right pneumothorax. The patient showed pink frothy sputum three hours following surgery, and a chest x-ray showed right unilateral pulmonary edema. Thirteen hours following surgery, the patient continuously showed pink frothy sputum and presented with severe hypoxemia, tachypnea, and tachycardia. After transferring to the intensive care unit (ICU), he developed ventricular tachycardia. Cardiopulmonary resuscitation was performed for 32 min. Chest X-ray showed diffuse bilateral pulmonary edema. Extracorporeal membrane oxygenation was performed. During the 65 days of ICU care, the patient became mentally alert. However, follow-up echocardiography revealed severe heart failure. CONCLUSIONSRexpansion pulmonary edema can rapidly progress to diffuse bilateral pulmonary edema. Therefore, careful observation is required for the patients who show signs of pulmonary edema after reexpansion.</description><identifier>EISSN: 2383-7977</identifier><identifier>DOI: 10.17085/apm.21116</identifier><language>eng</language><ispartof>Anesthesia and pain medicine, 2022, Vol.17 (3), p.298-303</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,4490,27925</link.rule.ids></links><search><creatorcontrib>Han, Woong</creatorcontrib><creatorcontrib>Kim, Gyu Seong</creatorcontrib><creatorcontrib>Lee, Jong Min</creatorcontrib><creatorcontrib>Lim, Chang Mook</creatorcontrib><creatorcontrib>Yang, Hong Seuk</creatorcontrib><creatorcontrib>Jeong, Chang Yeong</creatorcontrib><creatorcontrib>Park, Dong Ho</creatorcontrib><title>Unexpected pulmonary edema and cardiac arrest following wedge resection of spontaneous pneumothorax -A case report</title><title>Anesthesia and pain medicine</title><description>BACKGROUNDReexpansion pulmonary edema is a rare but potentially lethal complication. We report a case of suspected reexpansion pulmonary edema that led to cardiac arrest. CASEA 16-year-old male patient underwent wedge resection due to right pneumothorax. The patient showed pink frothy sputum three hours following surgery, and a chest x-ray showed right unilateral pulmonary edema. Thirteen hours following surgery, the patient continuously showed pink frothy sputum and presented with severe hypoxemia, tachypnea, and tachycardia. After transferring to the intensive care unit (ICU), he developed ventricular tachycardia. Cardiopulmonary resuscitation was performed for 32 min. Chest X-ray showed diffuse bilateral pulmonary edema. Extracorporeal membrane oxygenation was performed. During the 65 days of ICU care, the patient became mentally alert. However, follow-up echocardiography revealed severe heart failure. CONCLUSIONSRexpansion pulmonary edema can rapidly progress to diffuse bilateral pulmonary edema. 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We report a case of suspected reexpansion pulmonary edema that led to cardiac arrest. CASEA 16-year-old male patient underwent wedge resection due to right pneumothorax. The patient showed pink frothy sputum three hours following surgery, and a chest x-ray showed right unilateral pulmonary edema. Thirteen hours following surgery, the patient continuously showed pink frothy sputum and presented with severe hypoxemia, tachypnea, and tachycardia. After transferring to the intensive care unit (ICU), he developed ventricular tachycardia. Cardiopulmonary resuscitation was performed for 32 min. Chest X-ray showed diffuse bilateral pulmonary edema. Extracorporeal membrane oxygenation was performed. During the 65 days of ICU care, the patient became mentally alert. However, follow-up echocardiography revealed severe heart failure. CONCLUSIONSRexpansion pulmonary edema can rapidly progress to diffuse bilateral pulmonary edema. Therefore, careful observation is required for the patients who show signs of pulmonary edema after reexpansion.</abstract><doi>10.17085/apm.21116</doi></addata></record> |
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source | Open Access: PubMed Central; Alma/SFX Local Collection |
title | Unexpected pulmonary edema and cardiac arrest following wedge resection of spontaneous pneumothorax -A case report |
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