Ana Flávia Garcia Silva, Lívia Maria Garcia Melro, Bruno Adler Maccagnan Pinheiro Besen, Pedro Vitale Mendes, Marcelo Park
{"title":"Sulfonamide-induced acute eosinophilic pneumonia requiring extracorporeal membrane oxygenation support: a case report.","authors":"Ana Flávia Garcia Silva, Lívia Maria Garcia Melro, Bruno Adler Maccagnan Pinheiro Besen, Pedro Vitale Mendes, Marcelo Park","doi":"10.5935/2965-2774.20230404-en","DOIUrl":null,"url":null,"abstract":"Acute eosinophilic pneumonia (AEP) is a rare cause of acute respiratory failure that affects people aged 20-40 years old.(1) Patients with AEP present with rapid onset of cough, dyspnea, tachypnea and fever of usually less than 7 days of duration. Hypoxemia is present in all cases, and most patients do not have peripheral blood eosinophilia. In contrast, an increase in eosinophils in bronchoalveolar lavage fluid (BALF) is a marker of the disease, exceeding 20% of the BALF cell count in most patients. Radiographs show mixed reticular and alveolar infiltrates, which then can progress to be densely alveolar as the condition worsens.(2,3) Acute and organizing diffuse alveolar damage is common and is usually responsive to corticosteroids.(1) The major causes of pulmonary eosinophilia include inhalation of antigens, such as demolition dust, cigarette smoke, electronic cigarettes, cannabis, crack cocaine; parasitic and fungal infections; HIV infection; previous irradiation of the chest; and recent use of drugs associated with pulmonary eosinophilia, such as ranitidine, venlafaxine, infliximab, phenytoin, nitrofurantoin, beta-lactam antibiotics, sulfazalazine-mesalazine, among others. Differential diagnosis includes acute interstitial pneumonia, cryptogenic organizing pneumonia, diffuse alveolar hemorrhage and granulomatosis with polyangiitis. These conditions have similar clinical presentations but without pulmonary eosinophilia. Sulfonamide-induced AEP is described as the cause of severe acute respiratory distress syndrome (ARDS).(4-6) Right ventricle failure (RVF) due to acute pulmonary hypertension may occur in up to 25% of severe ARDS patients.(7) Nitric oxide and veno-venous extracorporeal membrane oxygenation (VV-ECMO) support are therapeutic options, but little has been discussed about further options in refractory cases.(4-6) Here, we describe the use of balloon atrial septostomy(8) – a procedure currently indicated in venoarterial ECMO (VA-ECMO) for left ventricle decompression – as a possible rescue therapy for RVF.","PeriodicalId":72721,"journal":{"name":"Critical care science","volume":"35 2","pages":"239-242"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406408/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Critical care science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5935/2965-2774.20230404-en","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Acute eosinophilic pneumonia (AEP) is a rare cause of acute respiratory failure that affects people aged 20-40 years old.(1) Patients with AEP present with rapid onset of cough, dyspnea, tachypnea and fever of usually less than 7 days of duration. Hypoxemia is present in all cases, and most patients do not have peripheral blood eosinophilia. In contrast, an increase in eosinophils in bronchoalveolar lavage fluid (BALF) is a marker of the disease, exceeding 20% of the BALF cell count in most patients. Radiographs show mixed reticular and alveolar infiltrates, which then can progress to be densely alveolar as the condition worsens.(2,3) Acute and organizing diffuse alveolar damage is common and is usually responsive to corticosteroids.(1) The major causes of pulmonary eosinophilia include inhalation of antigens, such as demolition dust, cigarette smoke, electronic cigarettes, cannabis, crack cocaine; parasitic and fungal infections; HIV infection; previous irradiation of the chest; and recent use of drugs associated with pulmonary eosinophilia, such as ranitidine, venlafaxine, infliximab, phenytoin, nitrofurantoin, beta-lactam antibiotics, sulfazalazine-mesalazine, among others. Differential diagnosis includes acute interstitial pneumonia, cryptogenic organizing pneumonia, diffuse alveolar hemorrhage and granulomatosis with polyangiitis. These conditions have similar clinical presentations but without pulmonary eosinophilia. Sulfonamide-induced AEP is described as the cause of severe acute respiratory distress syndrome (ARDS).(4-6) Right ventricle failure (RVF) due to acute pulmonary hypertension may occur in up to 25% of severe ARDS patients.(7) Nitric oxide and veno-venous extracorporeal membrane oxygenation (VV-ECMO) support are therapeutic options, but little has been discussed about further options in refractory cases.(4-6) Here, we describe the use of balloon atrial septostomy(8) – a procedure currently indicated in venoarterial ECMO (VA-ECMO) for left ventricle decompression – as a possible rescue therapy for RVF.