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Immature platelet fraction levels predict the development of prolonged thrombocytopenia after haematopoietic stem cell transplantation.
Cao, Jun; Qiu, Jun; Jin, Jieyu; Zhang, Sheng; Qu, Jiahui; Wang, Mingyue; Qiao, Longwei; Liang, Yuting.
Afiliación
  • Cao J; Center for Clinical Laboratory, The First Affiliated Hospital of Soochow University, Suzhou, China.
  • Qiu J; Center for Clinical Laboratory, The First Affiliated Hospital of Soochow University, Suzhou, China.
  • Jin J; Center for Clinical Laboratory, The First Affiliated Hospital of Soochow University, Suzhou, China.
  • Zhang S; Center for Clinical Laboratory, The First Affiliated Hospital of Soochow University, Suzhou, China.
  • Qu J; Department of Laboratory Medicine, Hongci Blood Disease Hospital, Suzhou, China.
  • Wang M; Department of Ultrasonography, The First Affiliated Hospital of Soochow University, Suzhou, China.
  • Qiao L; School of Gusu, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Nanjing Medical University, Suzhou, China. Electronic address: qiaolongwei1@126.com.
  • Liang Y; Center for Clinical Laboratory, The First Affiliated Hospital of Soochow University, Suzhou, China. Electronic address: liangyuting666@126.com.
Pathology ; 2024 Jul 14.
Article en En | MEDLINE | ID: mdl-39143000
ABSTRACT
Prolonged thrombocytopenia (PT) is a serious complication after haematopoietic stem cell transplantation (HSCT). PT has been suggested to be associated with an increased platelet transfusion requirement and poor outcomes after transplantation. Due to the complex mechanism of PT development, it is difficult to diagnose in the early post-transplant period. Our study aimed to identify an early predictive marker for PT after HSCT. Previous studies showed that the clinical utility of immature platelet fraction (IPF) predicts platelet recovery after chemotherapy and successful engraftment. However, the relationship between IPF and PT after HSCT remains unclear. Fifty-two patients with malignant haematological diseases who underwent HSCT were included in the study. We observed the kinetics of recovery of haematological parameters after transplantation and performed receiver operating characteristics (ROC) curve analysis using data from the 52 HSCT patients. The days to rise and peak of IPF, absolute IPF count (A-IPF) and highly fluorescent IPF (H-IPF) were almost synchronised in all patients, at day 10 and day 15, respectively. The begin to rise levels of IPF, H-IPF and A-IPF were all significantly lower in the PT group than in the good engraftment (GE) group (p=0.0016, p=0.0094, p=0.0086, respectively). The peak levels of IPF were significantly lower in the PT group than the GE group (p=0.0036). However, the peaks of H-IPF and A-IPF were not statistically significant between the two groups (p=0.3383, p=0.0887, respectively). The area under the ROC curve (AUC) of IPF rise was 0.739 (95% CI 0.583-0.896; p<0.05) and the cut-off value was 3.5%, while the AUC of IPF peak was 0.800 (95% CI 0.637-0.962; p<0.01) and the cut-off value was 8.0%. In conclusion, early low levels of IPF predict the development of PT after HSCT. These findings may help improve the management and treatment strategies for PT after HSCT.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pathology Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pathology Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido