Dear Editor,

Coronavirus disease 2019 (COVID-19)-associated pulmonary aspergillosis (CAPA) has emerged as an important complication among patients with acute respiratory failure caused by SARS-CoV-2 [1,2,3]. A cornerstone in CAPA diagnosis is microbiology, including culture from lower respiratory tract samples, and bronchoalveolar lavage fluid (BALF) galactomannan (GM) [4, 5].

We performed a multinational cohort study including 20 centers in 9 countries with the aim to evaluate diagnostic approaches and treatment of CAPA as well as CAPA prevalence. All participating centers were invited to provide data on diagnostic work-up, treatment and outcome on prospective cohorts of consecutive COVID-19 ICU patients (inclusion criteria: SARS-CoV-2-positive polymerase chain reaction, admission to intensive care unit (ICU) due to respiratory failure) with and without CAPA via an online case report form between 03/2020 and 05/2021. Cases were then classified according to the 2020 ECMM/ISHAM consensus criteria [4]. The study protocol was approved by the Medical University of Graz (EC #32–296 ex 19/20) and the other participating centers.

A total of 592 cases were entered (98.5% from Europe; for demographics see Supplementary Table 1) of whom 11 (1.9%) had proven CAPA, 80 (13.5%) probable CAPA and 18 (3%) possible CAPA. Table 1 displays diagnostic characteristics of those with CAPA. Median BALF-GM optical density index (ODI) in 83 CAPA patients was 2.74 (IQR 1.70–5.78). BALF-GM ODI > 1.0 was also reported in 4/170 (2.4%) patients without CAPA. BALF culture growing Aspergillus was detected exclusively among CAPA patients (0/184 non-CAPA patients). Serum GM was positive (> 0.5 ODI) in 1/192 patients without CAPA (0.5%). Antifungal treatment details are depicted in Table 1. Among those receiving systemic antifungal treatment, 52% were alive at ICU discharge.

Table 1 Diagnostic and treatment characteristics among CAPA patients
Full size table

During a median observation time of 32 days, 261 ICU deaths were observed. This corresponded to an − 30, − 60 and − 90 day ICU mortality of 36% (95% CI 33–40), 46% (95% CI 42–51) and 49% (95% CI 44–53). By applying a Fine-Gray competing risk model the 109 diagnosed CAPA cases (i.e., possible, probable or proven) on ICU corresponded to an − 1, − 15- and − 90 day ICU CAPA rate of 1% (95% CI 1–3), 16% (95% CI 13–20) and 20% (95% CI 16–32) (Supplementary Fig. 1).

Overall CAPA prevalence in our cohort was 15.4% and, therefore, within the range that has been previously reported in the literature [5], although prevalence varied widely between centers. Several factors such as awareness, diagnostic algorithms, local epidemiology and socioeconomic factors may explain these differences. Our results confirm that diagnosis of CAPA remains a challenge with limited sensitivity of serum GM (19%) for CAPA and the need for a lower respiratory sample or tracheal/bronchial/lung biopsy to confirm diagnosis. Early diagnosis is considered a cornerstone in successful CAPA management, as ICU mortality rate is high in CAPA patients (52% versus 39% in non-CAPA COVID-19 patients on ICU; p = 0.027). Voriconazole and isavuconazole were most frequently used for antifungal monotherapy, following current treatment recommendations for CAPA [4]. Even though > 90% of CAPA patients received antifungal treatment, there was also one CAPA case not receiving antifungal therapy among the survivors, indicating that not all patients who are diagnosed with CAPA based on consensus definitions may in fact have invasive fungal disease.