Idiopathic pneumonia syndrome after hematopoietic cell transplantation: evidence of occult infectious etiologies.
Sachiko SeoChristian RenaudJane M KuypersCharles Y ChiuMeei-Li HuangErik SamayoaHu XieGuixia YuCynthia E FisherTed A GooleySteven MillerRobert C HackmanDavid MyersonRuth H SedlakYae-Jean KimTakahiro FukudaDavid N FredricksDavid K MadtesKeith R JeromeMichael J BoeckhPublished in: Blood (2015)
Newer diagnostic methods may link more idiopathic pneumonia syndrome (IPS) cases to an infectious agent. Bronchoalveolar lavage (BAL) samples from 69 hematopoietic cell transplant (HCT) recipients with IPS diagnosed between 1992 and 2006 were tested for 28 pathogens (3 bacteria and 25 viruses) by quantitative polymerase chain reaction and for Aspergillus by galactomannan assay. Research BALs from 21 asymptomatic HCT patients served as controls. Among 69 HCT patients with IPS, 39 (56.5%) had a pathogen detected. The most frequent pathogens were human herpesvirus-6 (HHV-6) (N = 20 [29%]) followed by human rhinovirus (HRV), cytomegalovirus (CMV), and Aspergillus (N = 8 [12%] in each). HHV-6 and HRV were rarely detected in controls, whereas CMV and Aspergillus were occasionally detected with low pathogen load. Patients with pathogens had worse day-100 survival than those without (hazard ratio, 1.88; P = .03). Mortality in patients with only pathogens of "uncertain" significance in lung was similar to that in patients with pathogens of "established" significance. Metagenomic next-generation sequencing did not reveal additional significant pathogens. Our study demonstrated that approximately half of patients with IPS had pathogens detected in BAL, and pathogen detection was associated with increased mortality. Thus, an expanded infection detection panel can significantly increase the diagnostic precision for idiopathic pneumonia.
Keyphrases
- gram negative
- antimicrobial resistance
- endothelial cells
- multidrug resistant
- end stage renal disease
- chronic kidney disease
- risk factors
- bone marrow
- high throughput
- stem cells
- ejection fraction
- coronary artery disease
- mesenchymal stem cells
- induced pluripotent stem cells
- cell cycle arrest
- case report
- cell therapy
- cell death
- real time pcr
- genome wide
- type diabetes
- patient reported outcomes
- dna methylation
- acute respiratory distress syndrome
- mass spectrometry
- circulating tumor