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Respiratory and systemic infections in children with severe aplastic anemia on immunosuppressive therapy
Katarzyna Pawelec1, Malgorzata Salamonowicz, Anna Panasiuk
1Department of Pediatric Hematology and Oncology, Medical University of Warsaw, 24 Marszalkowska St., 00-576, Warsaw, Poland, katpawelec@poczta.onet.p.
Insights
Severe acquired aplastic anemia (SAA) patients on immunosuppressive therapy (IST) face high infection risks, particularly pneumonia and sepsis. Granulocyte colony-stimulating factors (G-CSF) significantly reduced infectious complications in this vulnerable pediatric cohort.
Area of Science:
- Pediatric Hematology
- Infectious Diseases
- Immunosuppression Therapy
Background:
- Severe acquired aplastic anemia (SAA) is a rare but serious condition requiring immunosuppressive therapy (IST).
- Patients undergoing IST are at increased risk for systemic and respiratory infections.
- Identifying infection risks is crucial for improving outcomes in pediatric SAA patients.
Purpose of the Study:
- To investigate the incidence and types of infections in children with SAA receiving IST.
- To evaluate the impact of different immunosuppressive agents and G-CSF on infection rates.
- To identify key risk factors and causes of mortality in this patient population.
Main Methods:
- Retrospective analysis of a cohort of 123 children with SAA on IST.
- Recording and categorizing infection episodes, including pneumonia and sepsis.
- Comparing infection rates between patients treated with horse vs. rabbit antithymocyte globulin (h-ATG vs. r-ATG) and with or without G-CSF.
Main Results:
- 62.6% of patients experienced 101 infection episodes; pneumonia occurred in 16.8%.
- Mortality was 18.7% (23/123), with sepsis and pneumonia complications being leading causes.
- G-CSF treatment was associated with a 36% relative risk reduction in infectious complications (RR 0.64; p < 0.0001).
Conclusions:
- Respiratory and disseminated infections pose a significant threat and are primary causes of death in pediatric SAA patients.
- Active surveillance for opportunistic infections is essential.
- G-CSF may be a valuable adjunct therapy for reducing infection risk in SAA patients on IST.
Abstract:
In the present study we investigated the occurrence of systemic and respiratory infections in a cohort of 123 children with severe acquired aplastic anemia (SAA) on immunosuppressive therapy (IST). We recorded 101 episodes of infection in 77 patients (62.6 %). Pneumonia was among the most frequently observed clinical forms of infection (17 cases - 16.8 %). In the entire group, 23 children died, mostly in the course of fatal sepsis (15/23) and in 3 cases because of pneumonia complications. All patients were treated with horse (h-ATG) or rabbit antithymocyte globulin (r-ATG) supplemented with cyclosporine and corticosteroids. The crude incidence rate for serious infections in h-ATG group and r-ATG group was comparable. The relative risk of infectious complications was lower in patients treated with granulocyte colony stimulating factors (G-CSF) by 36 % (RR 0.64; p < 0.0001). The analysis confirmed that respiratory tract and disseminated infections comprise a very serious clinical problem and are the leading cause of death of SAA children. Active surveillance and the analysis of associated risk factors are required to detect opportunistic infections in this group of patients.
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