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Diffuse alveolar haemorrhage in children hospitalised in a tertiary‑level hospital: A retrospective descriptive study
1Department of Paediatrics and Child Health, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Insights
Diffuse alveolar haemorrhage (DAH) is rare in children. This study in South Africa found most children with DAH responded well to oral prednisone treatment, showing positive outcomes despite resource limitations.
Area of Science:
- Pediatric Pulmonology
- Rare Diseases
- Hematology
Background:
- Diffuse alveolar haemorrhage (DAH) is a rare pediatric condition with no established management guidelines in low-resource settings.
- This report details clinical characteristics, management, and outcomes of pediatric DAH at a South African tertiary hospital.
Purpose of the Study:
- To describe the clinical features, treatment approaches, and outcomes of children diagnosed with diffuse alveolar haemorrhage (DAH).
- To provide data on DAH management in a resource-limited African setting.
Main Methods:
- A case series of 15 children treated for DAH at Chris Hani Baragwanath Academic Hospital.
- Analysis of clinical presentation, bronchoalveolar lavage findings, lung biopsies, treatment regimens, and long-term hemoglobin levels.
Main Results:
- 11 out of 15 children (73.3%) presented with severe microcytic anemia.
- Bronchoalveolar lavage revealed haemosiderin-laden macrophages in 81.8% of cases; lung biopsies showed capillaritis in 60% of cases.
- 9 out of 15 children (60%) achieved normal hemoglobin levels one year post-treatment with oral prednisone and complementary therapies.
Conclusions:
- Diffuse alveolar haemorrhage is uncommon in children, consistent with previous reports.
- A significant majority of pediatric DAH patients in this series responded well to oral prednisone treatment, even with resource constraints.
- Further national audits are recommended to establish incidence and inform management strategies for DAH in South Africa.
Background:
Diffuse alveolar haemorrhage (DAH) is considered a rare condition in children. There is no consensus on the management of DAH syndromes in Africa or other low- and middle-income countries. In this brief report, the clinical characteristics, management and outcomes of children treated for DAH in the Chris Hani Baragwanath Academic Hospital paediatric pulmonology unit in Johannesburg, South Africa are described. Fifteen children were included in this case series, of whom 11 (73.3%) presented with severe microcytic anaemia. Of the 11 children who had bronchoalveolar lavage, 9 (81.8%; 60.0% of the total) had haemosiderin-laden macrophages on microscopy. Only 5 children had a lung biopsy, of whom 3 (60.0%) had capillaritis. All the children were started on oral prednisone at presentation, and 11 (73.3%) received additional complementary treatment. Nine children (60.0%) had normal haemoglobin levels 1 year after initiation of treatment. Our series supports previous reports that DAH is uncommon in children. A large proportion of our patients responded well to treatment despite some resource limitations.
What The Study Adds:
The study provides additional data on children presenting with diffuse alveolar haemorrhage in a South African tertiary hospital.
What Are The Implications Of The Findings:
There is a need for South African pulmonologists to come together and conduct a national audit of these patients in different hospitals to determine the incidence in our country, as well as to inform a management plan in the presence or absence of specialised tests.
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