Clinical practice update of antifungal prophylaxis in immunocompromised children
JOSÉ TOMÁS RAMOS, CONCEPCIÓN ALBA ROMERO, SYLVIA BELDA, FRANCISCO JAVIER CANDEL, BEGOÑA CARAZO GALLEGO, AURORA FERNÁNDEZ-POLO, LAURA FERRERAS ANTOLÍN, CARMEN GARRIDO COLINO, MARÍA LUISA NAVARRO, OLAF NETH, PETER OLBRICH, ELENA RINCÓN-LÓPEZ, JESÚS RUIZ CONTRERAS, PERE SOLER-PALACÍN, ON BEHALF OF THE FUNGAL INFECTION STUDY GROUP OF SPANISH SOCIETY OF PAEDIATRIC INFECTIOUS DISEASE (SEIP); TRASLATIONAL RESEARCH NETWORK IN PEDIATRIC INFECTIOUS DISEASES (RITIP)
Due to the rise in the number and types of immunosuppressed patients, invasive fungal infections (IFI) are an increasing and major cause of morbidity and mortality in immunocompromised adults and children. There is a broad group of pediatric patients at risk for IFI in whom primary and/or secondary antifungal prophylaxis (AFP) should be considered despite scant evidence. Pediatric groups at risk for IFI includes extremely premature infants in some settings, while in high-risk children with cancer receiving chemotherapy or undergoing haematopoietic stem cell transplantation (HCT), AFP against yeast and moulds is usually recommended. For solid organ transplanted, children, prophylaxis depends on the type of transplant and associated risk factors. In children with primary or acquired immunodeficiency such as HIV or long-term immunosuppressive treatment, AFP depends on the type of immunodeficiency and the degree of immunosuppression. Chronic granulomatous disease is associated with a particular high-risk of IFI and anti-mould prophylaxis is always indicated. In contrast, AFP is not generally recommended in children with long stay in intensive care units. The choice of AFP is limited by the approval of antifungal agents in different age groups and by their pharmacokinetics characteristics. This document aims to review current available information on AFP in children and to provide a comprehensive proposal for each type of patient.
Rev Esp Quimioter 2019; September 11 [Full-text PDF]