key: cord-0846141-wfqxa6g5 authors: Van Biesen, Stefaan; Kwa, David; Bosman, Robert J.; Juffermans, Nicole P. title: Detection of Invasive Pulmonary Aspergillosis in COVID-19 with Nondirected BAL date: 2020-10-15 journal: Am J Respir Crit Care Med DOI: 10.1164/rccm.202005-2018le sha: 0f096b40ffbb8b8f236c7241f3cd65d44cc17db5 doc_id: 846141 cord_uid: wfqxa6g5 nan Invasive pulmonary aspergillosis (IPA) can complicate influenza pneumonia in critically ill patients owing to viral destruction of bronchial mucosa, facilitating invasion of Aspergillus species, and compromised host defenses to Aspergillus (1) . Given the association between IPA and increased mortality in influenza, rapid diagnostic investigations and early (preemptive) treatment of IPA are recommended in critically ill patients with influenza (2) . In ICU patients with coronavirus disease (COVID-19), the same principles may apply as in influenza. A high incidence of IPA in patients with COVID-19 admitted to the ICU has been reported in small cohorts of patients, some of which appeared online (3) (4) (5) (6) (7) . However, in these studies, a bronchoscopy with BAL was not consistently applied, which may hamper estimation of the IPA incidence in COVID-19, as a BAL to obtain material for culture and for galactomannan (GM) measurement is generally recommended for IPA diagnosis in the critically ill. However, owing to risk of aerosolization, only a restricted role for bronchoscopy with BAL is recommended in patients with COVID-19 (8) . We have applied a diagnostic approach by performing a nondirected BAL via a closed-circuit suction catheter, which we describe in this letter. Using this nondirected BAL technique as a standard approach, we aimed to determine the proportion of patients with IPA in a cohort of patients with COVID-19 (PCR confirmed) requiring mechanical ventilation who were consecutively admitted to the ICU of our teaching hospital during a 3-week time frame in April 2020. The institutional review board of the Amsterdam University Medical Center considered the study as not requiring informed consent. The clinical AspICU algorithm can be used to distinguish IPA from colonization in critically ill patients (9) , but as viral infection is not a classified host risk factor in this definition, the host factor was omitted. The IPA definition used in this paper is based on nondirected BAL GM testing with a cutoff of 1 optical density index, for which sensitivity and specificity are 86% and 95%, respectively, combined with worsening clinical symptoms (i.e., increase in C-reactive protein, worsening Pa O 2 /FI O 2 ratio, persistent or rising fever). Nondirected BAL was performed at a median of 2 days (range, 0-8 d) after ICU admission, in nonparalyzed patients, by advancing a 12-F suction catheter with a length of 54 cm via a closed circuit until bronchial wedging (Halyard Turbocleaning closed suction system for adults). Then, 2 3 20 ml of sterile NaCl 0.9% was given via the closed circuit and retrieved via the suction catheter. Samples were sent for GM (by ELISA, Platelia Aspergillus Ag from BIO-RAD) and culture only if it yielded nontransparent fluid. All patients received a 5-day course of hydroxychloroquine and lopinavir/ritonavir, either of which was stopped upon the emergence of side effects. Differences between IPA and non-IPA were tested with Student's t test or Mann-Whitney U or chi-square test/Fisher's exact test depending on data distribution. P value ,0.05 was considered statistically significant. Of 53 included patients, 2 patients died within 24 hours after admission and 9 patients were transferred to another hospital for logistical reasons shortly after admission. The remaining 42 patients underwent a nondirected BAL (patient characteristics in Table 1) . A classical IPA risk factor was present in only one patient, who received immunosuppressive medication in the context of a renal transplant. None of the other patients received corticosteroid treatment before or during ICU admission. Patients with IPA more often had chronic obstructive pulmonary disease or asthma compared with those without IPA (P , 0.05), which may suggest a role for impaired ciliary clearance. Based on clinical symptoms and a positive GM testing on nondirected BAL fluid, the proportion of putative IPA in the tested cohort was 21.4%, with a 95% confidence interval of 9.0-33.8% (Table 2) . Fungal cultures of the nondirected BAL yielded positive results in seven (77.8%) patients with IPA and only one (3%) patient without IPA, who, because of lack of clinical deterioration and lack of increased BAL GM levels, was ruled to be colonized with Aspergillus. At 30-day follow-up after inclusion cessation, ICU mortality in the IPA group was 22.2% and 15.1% in the non-IPA group (P = 0.61). Autopsies were not performed because of a perceived risk of contamination. Mean ICU length of stay was 37 days for patients with IPA versus 19 for those without IPA (P , 0.05). A bronchoscopy with BAL is the preferred diagnostic approach because GM antigen detection and culture have a good sensitivity in influenza-associated IPA. However, given the risk of aerosolization, The American Association for Bronchology and Interventional Pulmonology issued a statement providing a limited role for bronchoscopy in patients with COVID-19, advocating the use of a nonbronchoscopic alveolar lavage (10) . The technique we used in this study minimizes the risk for care providers while providing a diagnostic tool for our patients. However, the nondirected BAL technique is not validated for GM detection. As all patients had consolidations in all regions of the lung, the chances that a nondirected BAL may result in sampling of a lung region that was not affected by IPA may be low, although it is unclear to which extent consolidations are caused by the virus or by the fungus. More importantly, we cannot rule out overdiagnosis, as a nondirected sample may not always reflect microbiology of the lower airways. Therefore, instead of 0.5, a cutoff GM index of 1.0 was applied in this study. Nevertheless, sampling error cannot be ruled out. Of note, however, concordance between GM index .1.0 and positive Aspergillus cultures was high (77.8%). Early detection and treatment of IPA improves outcome compared with delayed diagnosis. Therefore, we opted to treat all nine patients who were deemed to have putative IPA with antifungal therapy (with an empirical regimen consisting of amphotericin B and voriconazole). We noted a longer ICU length of stay for patients who developed IPA, although ICU mortality did not differ between groups. However, whether COVID-19-associated IPA contributes to mortality, or whether IPA therapy improves outcome, cannot be dissected from our study. We conclude that the incidence of putative IPA may be high in patients with COVID-19 and that chronic obstructive pulmonary disease may be a particular risk factor. Implementation of surveillance of mechanically ventilated patients with COVID-19 using the nondirected BAL technique is feasible. As COVID-19-associated IPA appears to resemble influenzaassociated IPA in many ways, and ICU length of stay was longer in those with IPA versus those without, it is our opinion that active surveillance and treatment may be beneficial in patients with COVID-19. n Invasive pulmonary aspergillosis complicating severe influenza: epidemiology, diagnosis and treatment Practice guidelines for the diagnosis and management of aspergillosis: 2016 update by the Infectious Diseases Society of America COVID-19 associated pulmonary aspergillosis COVID-19-associated pulmonary aspergillosis High prevalence of putative invasive pulmonary aspergillosis in critically ill COVID-19 patients. SSRN Electron J [online ahead of print Invasive pulmonary aspergillosis in severe coronavirus disease 2019 pneumonia COVID-19-associated invasive pulmonary aspergillosis Diagnosing COVID-19-associated pulmonary aspergillosis AspICU Study Investigators. A clinical algorithm to diagnose invasive pulmonary aspergillosis in critically ill patients American Association for Bronchology and Interventional Pulmonology (AABIP) statement on the use of bronchoscopy and respiratory specimen collection in patients with suspected or confirmed COVID-19 infection Copyright © 2020 by the American Thoracic Society High Respiratory Drive and Excessive Respiratory Efforts Predict Relapse of Respiratory Failure in Critically Ill Patients with COVID-19 COVID-19) outbreak has rapidly spread This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives Author disclosures are available with the text of this letter at www.atsjournals.org. Author Contributions: P.E., M.C., and C.G. contributed to the study concept and design. P.E., M.C., P.G., E.P'h., and C.G. contributed to the acquisition of data. P.E., S.H., P.G., K.B., and C.G. contributed to the analysis and interpretation of data. P.E., J.B., J.M.-F., E.M., L.P., and C.G. contributed to drafting the manuscript and critically revising the manuscript for important intellectual content. All authors read and approved the final manuscript.This letter has a related editorial.Originally Published in Press as DOI: 10.1164/rccm.202005-1582LE on August 5, 2020