TY - JOUR
T1 - Massive Bleeding in Children With Cancer or Hematopoietic Cell Transplant
T2 - International, Multicenter Retrospective Study, 2017–2021
AU - on behalf of the Massive Transfusion In Children (MATIC)Cancer Investigators, and in collaboration with the Pediatric Critical Care Blood Research Network (BloodNet) subgroup and the Hematopoietic Cell Transplant subgroup of the Pediatric Acute Lung Injur
AU - Nellis, Marianne E.
AU - Steiner, Marie E.
AU - Bhar, Saleh
AU - McArthur, Jennifer
AU - McMichael, Ali
AU - Rahrig, April L.
AU - Leeper, Christine
AU - Perdichizzi, Salvatore
AU - Chiusolo, Fabrizio
AU - Shamash, Jacob
AU - Bruns, Nora
AU - Schreiber, Hilary
AU - Sharron, Matthew P.
AU - Butragueño-Laiseca, Laura
AU - Killinger, James S.
AU - Pringle, Charlene P.
AU - Koenig, Samantha M.
AU - Josephson, Cassandra
AU - Crawford, David
AU - Scott, Briana L.
AU - Remy, Kenneth E.
AU - Puthawala, Christine
AU - Spinella, Philip C.
AU - Navaei, Amir
AU - DiNardo, Matteo
AU - Giudici, Luigi Dei
AU - Rowan, Courtney M.
AU - Barukcic, Katarina
AU - Schündeln, Michael
AU - Jeyapalan, Asumthia
AU - Guedes, Maria
AU - Avent, Yvonne
AU - Frett, Michael
AU - Ghafoor, Saad
AU - Lassiter, Rebekah
AU - Zheng, Yan
AU - Russell, Robert T.
AU - Juluri, Nikhila
AU - Rasal, Rajashri
AU - Karam, Oliver
AU - Kreml, Erin
AU - DeSimone, Robert
N1 - Publisher Copyright:
Copyright © 2025 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.
PY - 2025/7/1
Y1 - 2025/7/1
N2 - OBJECTIVES: To characterize the epidemiology and management of massive bleeding events in children with cancer and/or hematopoietic cell transplant (HCT). DESIGN: Multicenter, retrospective cohort study. SETTING: Nineteen pediatric hospitals in Europe and United States. SUBJECTS: Children ages 0–21 years old with malignancy and/or HCT and massive bleeding admitted from January 1, 2017, to December 31, 2021. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Demographics, oncologic history, laboratory values, interventions, and PICU outcomes were collected. One hundred fifty-two bleeding episodes from 135 patients were analyzed. The median (interquartile range [IQR]) age was 7 years (2–14 yr). Forty-three percent (58/135) were female sex. Nineteen percent of children (26/135) had death attributable to hemorrhage. Forty percent had solid tumors and one-third had undergone at least one HCT. The majority of bleeding events occurred in the PICU (81/152, 53%). The median (IQR) platelet count at time of bleeding was 52 × 109/L (24–115 × 109/L), prothrombin time 18.5 seconds (15.2–24.8 s), activated partial thromboplastin time 42.2 seconds (33.2–56.0 s), and international normalized ratio 1.51 (1.21–2.11). To treat these bleeding events, 99% (148/152) of the time children received RBC transfusions, 84% (126/152) of the time plasma transfusions, 88% (132/152) of the time platelet transfusions, and less than one-fifth hemostatic medications. Half (77/152, 52%) of the time the children received high plasma ratios and half (73/152, 49%) received high platelet ratios. Pulmonary bleeding, oral/nasal bleeding, and receipt of prothrombin complex concentrate were each associated with greater odds of death attributed to hemorrhage: odds ratio (95% CI), respectively: 5.44 (2.250–13.171; p < 0.001); 3.30 (1.20–9.09; p = 0.021); and 3.24 (1.18–8.93; p = 0.023). CONCLUSIONS: Children with malignancy and/or HCT have a high mortality rate from hemorrhage despite being hospitalized at the time of their bleeding event. The majority of children received balanced resuscitation. Definitive trials are needed to determine optimal hemostatic resuscitation practice in this population.
AB - OBJECTIVES: To characterize the epidemiology and management of massive bleeding events in children with cancer and/or hematopoietic cell transplant (HCT). DESIGN: Multicenter, retrospective cohort study. SETTING: Nineteen pediatric hospitals in Europe and United States. SUBJECTS: Children ages 0–21 years old with malignancy and/or HCT and massive bleeding admitted from January 1, 2017, to December 31, 2021. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Demographics, oncologic history, laboratory values, interventions, and PICU outcomes were collected. One hundred fifty-two bleeding episodes from 135 patients were analyzed. The median (interquartile range [IQR]) age was 7 years (2–14 yr). Forty-three percent (58/135) were female sex. Nineteen percent of children (26/135) had death attributable to hemorrhage. Forty percent had solid tumors and one-third had undergone at least one HCT. The majority of bleeding events occurred in the PICU (81/152, 53%). The median (IQR) platelet count at time of bleeding was 52 × 109/L (24–115 × 109/L), prothrombin time 18.5 seconds (15.2–24.8 s), activated partial thromboplastin time 42.2 seconds (33.2–56.0 s), and international normalized ratio 1.51 (1.21–2.11). To treat these bleeding events, 99% (148/152) of the time children received RBC transfusions, 84% (126/152) of the time plasma transfusions, 88% (132/152) of the time platelet transfusions, and less than one-fifth hemostatic medications. Half (77/152, 52%) of the time the children received high plasma ratios and half (73/152, 49%) received high platelet ratios. Pulmonary bleeding, oral/nasal bleeding, and receipt of prothrombin complex concentrate were each associated with greater odds of death attributed to hemorrhage: odds ratio (95% CI), respectively: 5.44 (2.250–13.171; p < 0.001); 3.30 (1.20–9.09; p = 0.021); and 3.24 (1.18–8.93; p = 0.023). CONCLUSIONS: Children with malignancy and/or HCT have a high mortality rate from hemorrhage despite being hospitalized at the time of their bleeding event. The majority of children received balanced resuscitation. Definitive trials are needed to determine optimal hemostatic resuscitation practice in this population.
KW - bleeding
KW - cancer
KW - children
KW - critical illness
KW - hematopoietic cell transplant
KW - hemorrhage
UR - https://www.scopus.com/pages/publications/105004317510
UR - https://www.scopus.com/pages/publications/105004317510#tab=citedBy
U2 - 10.1097/PCC.0000000000003751
DO - 10.1097/PCC.0000000000003751
M3 - Article
C2 - 40277427
AN - SCOPUS:105004317510
SN - 1529-7535
VL - 26
SP - e889-e899
JO - Pediatric Critical Care Medicine
JF - Pediatric Critical Care Medicine
IS - 7
ER -