A Regional Observational Study on COVID-19-Associated Pulmonary Aspergillosis (CAPA) within Intensive Care Unit: Trying to Break the Mold.
Tommaso LupiaGiorgia MontrucchioAlberto GaviraghiGaia MussoMattia PuppoCesare BollaNour ShbakloBarbara RizzelloAndrea Della SelvaErika ConcialdiFrancesca RumboloAnna Maria BarbuiLuca BrazziFrancesco Giuseppe De RosaSilvia CorcionePublished in: Journal of fungi (Basel, Switzerland) (2022)
The reported incidence of COVID-19-associated pulmonary aspergillosis (CAPA) ranges between 2.4% and 35% in intensive care unit (ICU) patients, and awareness in the medical community is rising. We performed a regional retrospective observational study including patients diagnosed with CAPA defined according to the Modified AspICU Dutch/Belgian Mycosis Study Group and CAPA-EECMM, from five different ICUs, admitted between March, 2020 and September, 2021. Forty-five patients were included. The median age was 64 (IQR 60-72), mostly (73%) males. At ICU admission, the median Charlson comorbidity index was 3 (2-5), and the simplified acute physiology score (SAPS)-II score was 42 (31-56). The main underlying diseases were hypertension (46%), diabetes (36%) and pulmonary diseases (15%). CAPA was diagnosed within a median of 17 days (IQR 10-21.75) after symptoms onset and 9 days (IQR 3-11) after ICU admission. The overall 28-day mortality rate was 58%, and at univariate analysis, it was significantly associated with older age ( p = 0.009) and SAPS-II score at admission ( p = 0.032). The use of immunomodulatory agents, p = 0.061; broad-spectrum antibiotics, p = 0.091; positive culture for Aspergillus on BAL, p = 0.065; and hypertension, p = 0.083, were near reaching statistical significance. None of them were confirmed in multivariate analysis. In critically ill COVID-19 patients, CAPA acquired clinical relevance in terms of incidence and reported mortality. However, the risk between underdiagnosis-in the absence of specific invasive investigations, and with a consequent possible increase in mortality-and over-diagnosis (case identification with galactomannan on broncho-alveolar fluid alone) might be considered. Realistic incidence rates, based on local, real-life epidemiological data, might be helpful in guiding clinicians.
Keyphrases
- intensive care unit
- end stage renal disease
- ejection fraction
- risk factors
- sars cov
- emergency department
- blood pressure
- coronavirus disease
- mechanical ventilation
- prognostic factors
- healthcare
- type diabetes
- cardiovascular disease
- cardiovascular events
- mental health
- peritoneal dialysis
- skeletal muscle
- coronary artery disease
- metabolic syndrome
- adipose tissue
- palliative care
- cross sectional
- electronic health record
- hepatitis b virus
- insulin resistance