Covid-19肺炎和侵袭性肺曲霉病

H. Desai, J. Selickman, K. Pendleton
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引用次数: 1

摘要

侵袭性肺曲霉病(Invasive pulmonary aspergillosis, IPA)是一种罕见、严重的真菌感染,预后差,死亡率高。IPA主要发生在免疫抑制状态、血液恶性肿瘤和干细胞移植患者。诊断具有挑战性,需要高度怀疑。目前文献支持对covid-19重症肺炎患者进行长时间大剂量地塞米松治疗,可能引起明显的免疫抑制。在这里,我们报告了一例covid-19肺炎患者在地塞米松和托珠单抗治疗后出现IPA。病例报告:患者为75岁男性,因covid-19肺炎继发的严重低氧性呼吸衰竭入住内科ICU,在被送到急诊室后立即需要机械通气。患者于2018年有继发于肺结核的空腔性肺病病史,已完成4药治疗。住院期间,有3份痰液抗酸杆菌呈阴性。患者开始接受地塞米松治疗,每日6mg,持续10天,并接受单剂量托珠单抗。患者最初有所改善,但在第9天开始再次恶化,需要增加呼吸支持和旋前治疗。他的痰培养培养出了黄曲霉。胸部CT显示既往空洞性肺病周围实质浸润增加。血清半乳甘露聚糖曲霉抗原阳性。病人开始静脉注射伏立康唑。在最初改善后,患者出现咯血和氧合恶化。根据家属的意愿,病人被转移到舒适护理,并在同情拔管后去世。讨论:使用大剂量地塞米松治疗COVID-19肺炎可能会无意中引起免疫抑制状态。同时使用托珠单抗可能会进一步加重这些免疫抑制作用。相对免疫抑制加上病毒感染可能造成的上皮损伤可能是IPA发生的机制。来自法国的病例系列报告了27例COVID-19 ICU患者中有9例(33.3%)可能出现IPA,观察到的死亡率预期很高。结论:临床医生应对COVID-19患者中未恢复或初步好转后恶化的其他感染保持高度怀疑,并进行早期调查。既往患有结构性肺部疾病的患者也应谨慎使用类固醇,因为他们可能由于先前存在的曲霉定植而处于发生IPA的高风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Covid-19 Pneumonia and Invasive Pulmonary Aspergillosis
Introduction: Invasive pulmonary aspergillosis (IPA) is a rare, severe fungal infection with a poor prognosis and high mortality rate. IPA is mainly noted in patients with immunosuppressed status, hematological malignancies and stem cell transplants. Diagnosis is challenging and requires a high index of suspicion. Current literature supports treating patients with severe covid-19 pneumonia with high dose dexamethasone therapy for a prolonged period of time which may cause significant immune suppression. Here, we present a case of a patient with covid-19 pneumonia who developed IPA after dexamethasone and tocilizumab therapy. Case report: Patient is a 75-year-old male who was admitted to the medical ICU with severe hypoxemic respiratory failure secondary to covid-19 pneumonia requiring mechanical ventilation immediately on presentation to the emergency room. The patient had a past history of cavitary lung disease secondary to tuberculosis in 2018 and had completed treatment with 4-drug therapy. During this hospitalization, three sputum samples were negative for acid fast bacillus. He was started on dexamethasone therapy of 6mg daily for 10 days and received a single dose of tocilizumab. The patient initially improved but started to worsen again on the ninth day requiring increased ventilatory support and pronation therapy. His sputum culture grew Aspergillus FLavus. CT chest showed increased parenchymal infiltrates around prior cavitary lung disease. Serum aspergillus galactomannan antigen returned positive. Patient was started on intravenous Voriconazole. After initial improvement, the patient developed hemoptysis and worsening oxygenation. As per the family's wishes, patient was transitioned to comfort care and he passed away after compassionate extubation. Discussion:Treatment of COVID-19 pneumonia with high dose dexamethasone therapy may inadvertently cause an immunosuppressed state. These immunosuppressive effects may be further compounded by concurrent use of tocilizumab. Relative immunosuppression combined with possible epithelial damage due to viral infection may be a mechanism for development of IPA. A case series from France reported possible IPA in 9 of 27 (33.3%) ICU patients with COVID-19 with an expectedly high observed mortality rate. Conclusion: Clinicians should carry a high index of suspicion and pursue early investigations for other infections in COVID-19 patients who are not recovering or have worsened after initial improvement. Careful use of steroids in patients with prior structural lung disease is also warranted as they may be at high risk of developing IPA due to pre-existing aspergillus colonization.
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