Application of peripherally inserted central catheter in immune tolerance induction treatment of children with hemophilia A and accompanying inhibitors in China.

OBJECTIVE To explore the feasibility, safety and cost effectiveness of the use of peripherally inserted central catheter (PICC) in children with hemophilia A and inhibitors who underwent ITI treatment. METHOD This retrospective cohort study evaluated the effect of PICC placement and ITI on bleeding rates, costs, and parents' satisfaction before and within 6 months after PICC placement in children with hemophilia A and inhibitors. RESULTS A total of 20 children with hemophilia A and high-titer inhibitors were included, with a success rate for PICC placement of 100%, at a cost of ¥6730.50. Parents' satisfaction with PICC was 100%, and the total length of catheter indwelling was 6055 days. In terms of curative effect, the success rate of ITI treatment was 75%, and the annualized bleeding rate was decreased from 10.90 ± 12.16 times before placement to 2.10 ± 3.32 times (p < 0.05). The transportation expense for children and their parents to the clinic decreased from ¥20,920 ± 32,274.57 before catheter placement to ¥2915 ± 2195.99 (p < 0.05). Time of children missed school and their parents missed work decreased from 10.85 ± 22.36 days to 1.90 ± 3.58 (p < 0.05) days and 40.33 ± 46.11 days to 3.83 ± 7.11 days (p < 0.05), respectively. CONCLUSION The use of PICC for ITI treatment in children with hemophilia A and accompanying inhibitors in developing countries (e.g. China) can ensure the effect of ITI, reducing expense and improving the quality of life without obvious side effects.

[1]  Wei Li,et al.  Murine cadherin‐6 mediates thrombosis in vivo in a platelet‐independent manner , 2020, Research and practice in thrombosis and haemostasis.

[2]  M. A. Bedoya,et al.  Implantable venous access devices in children with severe hemophilia: a tertiary pediatric institutional experience , 2020, Pediatric Radiology.

[3]  S. Ohga,et al.  The Japanese Immune Tolerance Induction (J‐ITI) study in haemophilia patients with inhibitor: Outcomes and successful predictors of ITI treatment , 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

[4]  J. Gayle,et al.  Burden of illness and costs among paediatric haemophilia patients with and without central venous access devices treated in US hospitals , 2018, Haemophilia : the official journal of the World Federation of Hemophilia.

[5]  K. Khair,et al.  The impact of clinical practice on the outcome of central venous access devices in children with haemophilia , 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

[6]  M. Franchini,et al.  Treatment and Prevention of Bleeds in Haemophilia Patients with Inhibitors to Factor VIII/IX , 2017, Journal of clinical medicine.

[7]  J. Gill,et al.  Complications of haemophilia in babies (first two years of life): a report from the Centers for Disease Control and Prevention Universal Data Collection System , 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

[8]  H. M. van den Berg Different impact of factor VIII products on inhibitor development? , 2016, Thrombosis Journal.

[9]  P. Lähteenmäki,et al.  Complications associated with central venous access device in children with haemophilia: a nationwide multicentre study in Finland , 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

[10]  S. Israels,et al.  Experience with central venous access devices (CVADs) in the Canadian hemophilia primary prophylaxis study (CHPS) , 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

[11]  G. Gorincour,et al.  Introduction of the use of a pediatric PICC line in a French University Hospital: review of the first 91 procedures. , 2014, Diagnostic and interventional imaging.

[12]  E. Santagostino,et al.  Venous access in haemophilic children: choice and management , 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

[13]  V. Rodriguez,et al.  Central venous access devices for paediatric patients with haemophilia: a single‐institution experience , 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

[14]  L. Valentino,et al.  Consensus recommendations for use of central venous access devices in haemophilia , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

[15]  D. Globe,et al.  Utilization of care in haemophilia: a resource‐based method for cost analysis from the Haemophilia Utilization Group Study (HUGS) , 2004, Haemophilia : the official journal of the World Federation of Hemophilia.

[16]  D. DiMichele,et al.  Inhibitors: resolving diagnostic and therapeutic dilemmas , 2002, Haemophilia : the official journal of the World Federation of Hemophilia.

[17]  K. Khair,et al.  The impact of prophylactic treatment on children with severe haemophilia , 1996, British journal of haematology.