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Performance and safety of femoral central venous catheters in pediatric autologous peripheral blood stem cell collection.
Cooling, Laura; Hoffmann, Sandra; Webb, Dawn; Yamada, Chisa; Davenport, Robertson; Choi, Sung Won.
Afiliação
  • Cooling L; Department of Pathology, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, Michigan.
  • Hoffmann S; Department of Pathology, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, Michigan.
  • Webb D; Department of Pathology, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, Michigan.
  • Yamada C; Department of Pathology, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, Michigan.
  • Davenport R; Department of Pathology, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, Michigan.
  • Choi SW; Department of Pediatric, Blood and Marrow Transplantation Program, University of Michigan, Ann Arbor, Michigan.
J Clin Apher ; 32(6): 501-516, 2017 Dec.
Article em En | MEDLINE | ID: mdl-28485045
ABSTRACT

INTRODUCTION:

Autologous peripheral blood hematopoietic progenitor cell collection (A-HPCC) in children typically requires placement of a central venous catheter (CVC) for venous access. There is scant published data regarding the performance and safety of femoral CVCs in pediatric A-HPCC.

METHODS:

Seven-year, retrospective study of A-HPCC in pediatric patients collected between 2009 and January 2017. Inclusion criteria were an age ≤ 21 years and A-HPCC using a femoral CVC for venous access. Femoral CVC performance was examined by CD34 collection rate, inlet rate, collection efficiency (MNC-FE, CD34-FE), bleeding, flow-related adverse events (AE), CVC removal, and product sterility testing. Statistical analysis and graphing were performed with commercial software.

RESULTS:

A total of 75/119 (63%) pediatric patients (median age 3 years) met study criteria. Only 16% of children required a CVC for ≥ 3 days. The CD34 collect rate and CD34-FE was stable over time whereas MNC-FE decreased after day 4 in 80% of patients. CD34-FE and MNC-FE showed inter- and intra-patient variability over time and appeared sensitive to plerixafor administration. Femoral CVC showed fewer flow-related AE compared to thoracic CVC, especially in pediatric patients (6.7% vs. 37%, P = 0.0005; OR = 0.12 (95%CI 0.03-0.45). CVC removal was uneventful in 73/75 (97%) patients with hemostasis achieved after 20-30 min of pressure. In a 10-year period, there were no instances of product contamination associated with femoral CVC colonization.

CONCLUSION:

Femoral CVC are safe and effective for A-HPCC in young pediatric patients. Femoral CVC performance was maintained over several days with few flow-related alarms when compared to thoracic CVCs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Veia Femoral / Cateteres Venosos Centrais / Células-Tronco de Sangue Periférico Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Veia Femoral / Cateteres Venosos Centrais / Células-Tronco de Sangue Periférico Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2017 Tipo de documento: Article