Analysis and Interpretation of Automated Blood Count in the Treatment of Chronic Paracoccidioidomycosis.
Eliana da Costa Alvarenga de BritoAdriana de Oliveira FrançaIgor Valadares SiqueiraVinícius Lopes Teodoro FélixAmanda Alves RezendeBárbara Casella AmorimSuzane Eberhart Ribeiro da SilvaRinaldo Pôncio MendesSimone Schneider WeberAnamaria Mello Miranda PaniagoPublished in: Journal of fungi (Basel, Switzerland) (2024)
Blood count is crucial for assessing bone marrow's cell production and differentiation during infections, gaging disease severity, and monitoring therapeutic responses. The profile of blood count in chronic forms of paracoccidioidomycosis (PCM) has been insufficiently explored. To better understand the changes in hematological cells in different stages of the PCM chronic form, we evaluated the blood count, including immature blood cells in automated equipment, before and during the treatment follow-up of 62 chronic PCM patients. Predominantly male (96.8%) with an average age of 54.3 (standard deviation SD 6.9) years, participants exhibited pre-treatment conditions such as anemia (45.2%), monocytosis (38.7%), and leukocytosis (17.7%), which became less frequent after clinical cure. Anemia was more prevalent in severe cases. Notably, hemoglobin and reticulocyte hemoglobin content increased, while leukocytes, monocytes, neutrophils, immature granulocytes, and platelets decreased. Chronic PCM induced manageable hematological abnormalities, mainly in the red blood series. Monocytosis, indicating monocytes' role in PCM's immune response, was frequent. Post-treatment, especially after achieving clinical cure, significant improvements were observed in various hematological indices, including immature granulocytes and reticulocyte hemoglobin content, underscoring the impact of infection on these parameters.
Keyphrases
- immune response
- bone marrow
- peripheral blood
- induced apoptosis
- chronic kidney disease
- end stage renal disease
- machine learning
- high throughput
- early onset
- cell proliferation
- ejection fraction
- combination therapy
- red blood cell
- toll like receptor
- replacement therapy
- endothelial cells
- high glucose
- cell death
- stress induced