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Pulmonary Hemorrhage in Pediatric Hematopoietic Stem Cell Transplant Recipients: A Single-Center Retrospective Study.
Chopra, Yogi; Alsabahi, Amal; Schechter, Tal; Mtaweh, Haifa; Sweezey, Neil; Balit, Corinne; Ali, Muhammad; Chiang, Kuang-Yueh; Gassas, Adam; Krueger, Joerg.
Afiliação
  • Chopra Y; Department of Hematology, Oncology, Blood and Marrow Transplant and Cellular Therapy, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Alsabahi A; Department of Paediatric Haemato-Oncology, Royal Hospital, Muscat, Oman.
  • Schechter T; Department of Hematology, Oncology, Blood and Marrow Transplant and Cellular Therapy, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Mtaweh H; Department of Pediatric Intensive Care Medicine, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Sweezey N; Department of Respiratory Medicine, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Balit C; Department of Paediatric Intensive Care Medicine, The Children's Hospital Westmead, NSW, Australia.
  • Ali M; Department of Hematology, Oncology, Blood and Marrow Transplant and Cellular Therapy, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Chiang KY; Department of Hematology, Oncology, Blood and Marrow Transplant and Cellular Therapy, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
  • Gassas A; Department of Bone Marrow Transplantation, Royal Hospital for Children, Bristol, United Kingdom.
  • Krueger J; Department of Hematology, Oncology, Blood and Marrow Transplant and Cellular Therapy, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Pediatr Crit Care Med ; 25(1): e47-e51, 2024 Jan 01.
Article em En | MEDLINE | ID: mdl-37539962
OBJECTIVES: Pulmonary hemorrhage (PH) is a serious complication posthematopoietic stem cell transplant (HSCT). In view of limited available pediatric data, we performed a retrospective study to describe epidemiology, management, and outcomes of PH post-HSCT in children in our national center. DESIGN: Retrospective study. SETTING: Academic children's hospital (2000-2015). SUBJECTS: Children (< 18 yr) with PH and requiring PICU care post-HSCT. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: The historical prevalence of PH in our center was 2.7% (31/1,148). Twenty patients had a concomitant infection, 15 had bacterial infection, 8 had viral infection, and 3 patients had a fungal infection. With a median follow-up time of 60 months, 7 of 31 patients were alive. Early PH (< 40 d post-HSCT) was associated with improved survival (6/15 vs 1/16, p = 0.035). Patients who received high-dose pulsed corticosteroid had improved survival when compared with those who did not (7/22 vs 0/9, p = 0.0012); this also applied to the subgroup of patients with a concomitant infection (5/15 vs 0, p = 0.001). None of the patients who survived had measurable respiratory sequelae. CONCLUSIONS: PH is a rare but serious complication after HSCT. Corticosteroids were associated with improved survival even in patients with a concomitant infection.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Pediatr Crit Care Med Assunto da revista: PEDIATRIA / TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Pediatr Crit Care Med Assunto da revista: PEDIATRIA / TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá