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Published on: September 6, 2017
Pulmonary dysfunction in pediatric hematopoietic stem cell transplant patients: overview, diagnostic considerations,
J Michael Collaco1, W Adam Gower, Peter J Mogayzel
1Eudowood Division of Pediatric Respiratory Sciences, The Johns Hopkins Medical Institutions, Baltimore, Maryland.
Insights
Pulmonary complications are common after pediatric hematopoietic stem cell transplantation (HSCT). This review covers diagnostic tools like bronchoscopy and biopsy, and infectious complications in HSCT patients.
Area of Science:
- Pediatric Hematology
- Pulmonology
- Transplantation Medicine
Background:
- Pulmonary complications are frequent and severe sequelae in hematopoietic stem cell transplantation (HSCT) recipients.
- Pediatric HSCT patients face significant risks of lung issues post-transplant.
Purpose of the Study:
- To review diagnostic modalities for pulmonary complications in pediatric HSCT patients.
- To discuss infectious pulmonary complications in pediatric HSCT recipients based on post-transplant phases.
Main Methods:
- Review of available data on diagnostic modalities, including flexible bronchoscopy with bronchoalveolar lavage (BAL) and open lung biopsy (OLB).
- Categorization of infectious pulmonary complications by chronologic phases: neutropenic (0-30 days), early (30-100 days), and late (>100 days) post-HSCT.
Main Results:
- Diagnostic tools like bronchoscopy and biopsy are crucial for evaluating lung issues in pediatric HSCT.
- Infectious pulmonary complications vary significantly across the neutropenic, early, and late phases post-transplant.
Conclusions:
- Accurate diagnosis and timely management of pulmonary complications are vital for pediatric HSCT outcomes.
- Understanding the temporal patterns of infectious pulmonary complications aids in clinical decision-making for HSCT patients.
Abstract:
Pulmonary complications are among the most common and serious sequelae seen in hematopoietic stem cell transplantation (HSCT) recipients. This two-part review addresses the incidence and impact of pulmonary complications in pediatric HSCT patients. In this first part we review the available data for the use of diagnostic modalities in this population, including flexible bronchoscopy with bronchoalveolar lavage (BAL) and open lung biopsy (OLB). We also review the many infectious pulmonary complications that may occur in pediatric HSCT recipients, utilizing the traditional chronologic divisions of neutropenic phase (0-30 days following HSCT), early phase (30-100 days), and late phase (>100 days).
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