Perioperative Management for Port Catheter Procedures in Pediatric Patients with Severe Hemophilia and Inhibitors

被引:0
作者
Woestemeier, Anna [1 ]
Horneff, Silvia [2 ]
Lueder, Vincent Marlon [1 ]
Nadal, Jennifer [3 ]
Koscielny, Arne [4 ]
Kalff, Jorg C. [1 ]
Oldenburg, Johannes [2 ]
Goldmann, Georg [2 ]
Lingohr, Philipp [1 ]
机构
[1] Univ Hosp Bonn, Dept Gen Visceral Thorac & Vasc Surg, Bonn, Germany
[2] Univ Hosp Bonn, Inst Expt Haematol & Transfus Med, Bonn, Germany
[3] Univ Hosp Bonn, Inst Med Biometr Informat & Epidemiol, Bonn, Germany
[4] St Elisabeth Hosp Leipzig, Dept Gen & Visceral Surg, Leipzig, Germany
来源
HAMOSTASEOLOGIE | 2024年
关键词
hemophilia A; hemophilia B; port catheter; inhibitors; antibodies; rFVIIa; VON-WILLEBRAND DISEASE; VENOUS ACCESS DEVICES; LONG-TERM; SURGERY; CHILDREN; PROPHYLAXIS; STRATEGIES;
D O I
10.1055/a-2337-3687
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The objective of this systematic study was to assess the perioperative management and outcome of surgery in pediatric patients with hemophilia A/B and inhibitors compared to nonhemophilic pediatric patients. Methods The surgical outcome of 69 port catheter operations in patients with hemophilia who developed inhibitory antibodies against the administered factor was compared to 51 procedures in the control group. In the patients with hemophilia and inhibitors, a standardized protocol for recombinant activated factor VII was used to prevent perioperative bleeding. Results Hemophilic pediatric patients with inhibitors showed no significant differences in perioperative management (blood transfusion: p = 0.067, duration of surgery: p = 0.69; p = 0.824) in comparison to patients without hemophilia . The length of hospital stay was significantly longer in pediatric patients with hemophilia and inhibitors (20 days vs. 4 days for insertion; 12 days vs. 1 day for explantation). Moreover, no statistically significant difference was found for secondary bleeding (three patients with hemophilia vs. none in the control group; p = 0.11) or surgical complications (five hemophilia patients vs. none with grade I complication; one hemophilia patient vs. none with grade II complications; p = 0.067). Conclusion This study has demonstrated that port catheter insertion and removal is safe in these patients. Moreover, it shows the importance of a coordinated approach with a multidisciplinary team.
引用
收藏
页数:5
相关论文
共 50 条
  • [21] Pharmacokinetic variability of factor VIII concentrates in Chinese pediatric patients with moderate or severe hemophilia A
    Chen, Zhenping
    Huang, Kun
    Li, Gang
    Zhen, Yingzi
    Wu, Xinyi
    Ai, Di
    Liu, Guoqing
    Li, Zekun
    Alfonso, Iorio
    Wu, Runhui
    PEDIATRIC INVESTIGATION, 2021, 5 (01) : 38 - 45
  • [22] IgG subclasses of FVIII inhibitors in an argentine cohort of severe hemophilia A patients: Analysis by flow cytometry
    Irigoyen, M. B.
    Primiani, L.
    Felippo, M.
    Candela, M.
    de Bracco, M. M. E.
    Galassi, N. V.
    INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2017, 39 (06) : 569 - 576
  • [23] Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A
    Castaman, Giancarlo
    Linari, Silvia
    THERAPEUTICS AND CLINICAL RISK MANAGEMENT, 2016, 12 : 1029 - 1037
  • [24] Perioperative Management and Outcomes of Pediatric Craniosynostosis Patients Undergoing Cranioplasty: A Retrospective Analysis
    Battistelli, Elisa Zoe
    Calabria, Orlando
    Giani, Marco
    Moretto, Alessandra
    Cattaneo, Federico
    Alberio, Giovanni
    Trezza, Andrea
    Ventura, Maria Luisa
    Mazzoleni, Fabio
    Biondi, Andrea
    Citerio, Giuseppe
    Giussani, Carlo
    Foti, Giuseppe
    JOURNAL OF CRANIOFACIAL SURGERY, 2025, 36 (01) : 215 - 218
  • [25] Kinetics of factor VIII: C inhibitors and treatment response in severe hemophilia A patients
    Luna-Zaizar, H.
    Esparza-Flores, M. A.
    Lopez-Guido, B.
    Aguilar-Lopez, L. B.
    Cortes Alvarez, C. R.
    Jaloma-Cruz, A. R.
    INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2009, 31 (06) : 673 - 682
  • [26] The Development of FVIII Inhibitors in Relation to IL10 Gene Polymorphism in Hemophilia A Egyptian Pediatric Patients
    Sadek, Hoda
    Youssry, Ilham
    Ibrahim, Nihal Salah Eldeen
    Abou-Elalla, Amany Ahmed
    Atef, Gehad
    Mousa, Somaia Mohammed
    FETAL AND PEDIATRIC PATHOLOGY, 2017, 36 (03) : 184 - 189
  • [27] Diagnostic procedures and management of fever in pediatric cancer patients
    Laws, HJ
    Ammann, RA
    Lehrnbecher, T
    KLINISCHE PADIATRIE, 2005, 217 : S9 - S16
  • [28] Validation of a perioperative population factor VIII pharmacokinetic model with a large cohort of pediatric hemophilia a patients
    Preijers, Tim
    Liesner, Ri
    Hazendonk, Hendrika C. A. M.
    Chowdary, Pratima
    Driessens, Mariette H. E.
    Hart, Dan P.
    Laros-van Gorkom, Britta A. P.
    van der Meer, Felix J. M.
    Meijer, Karina
    Fijnvandraat, Karin
    Leebeek, Frank W. G.
    Mathot, Ron A. A.
    Cnossen, Marjon H.
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2021, 87 (11) : 4408 - 4420
  • [29] Impact of pharmacokinetics to reduce bleeding in a cohort of patients with severe hemophilia A in a personalized comprehensive management program
    Sarmiento Doncel, Samuel
    Diaz Mosquera, Gina Alejandra
    Mauricio Cortes, Javier
    Ramirez Plazas, Nelson
    Javier Meza, Francisco
    Agudelo Rico, Carol
    HEMATOLOGY REPORTS, 2021, 13 (04)
  • [30] Management of Severe Atopic Dermatitis in Pediatric Patients
    Mancuso, Jennifer B.
    Lee, Stephanie S.
    Paller, Amy S.
    Ohya, Yukihiro
    Eichenfield, Lawrence F.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2021, 9 (04) : 1462 - 1471