Fresh frozen plasma prepared with amotosalen HCl (S-59) photochemical pathogen inactivation: transfusion of patients with congenital coagulation factor deficiencies

被引:56
作者
de Alarcon, P
Benjamin, R
Dugdale, M
Kessler, C
Shopnick, R
Smith, P
Abshire, T
Hambleton, J
Matthew, P
Ortiz, I
Cohen, A
Konkle, BA
Streiff, M
Lee, M
Wages, D
Corash, L
机构
[1] Univ Virginia, Dept Pediat Hematol, Charlottesville, VA 22903 USA
[2] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[3] Univ Tennessee, Oncol & Hematol Ctr, Memphis, TN USA
[4] Georgetown Univ, Med Ctr, Washington, DC 20007 USA
[5] Hemophilia & Thrombosis Ctr Nevada, Las Vegas, NV USA
[6] Rhode Isl Hosp, Dept Pediat, Providence, RI USA
[7] Emory Univ, Dept Pediat, Atlanta, GA 30322 USA
[8] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[9] Univ New Mexico, Dept Pediat, Albuquerque, NM 87131 USA
[10] Univ Puerto Rico, Ctr Invest Clin, Rio Piedras, PR 00931 USA
[11] Univ Penn, Philadelphia, PA 19104 USA
[12] Newark Beth Israel Med Ctr, Newark, NJ USA
[13] Johns Hopkins Univ, Dept Med, Baltimore, MD 21218 USA
[14] Univ Calif Los Angeles, Dept Biostat, Los Angeles, CA 90024 USA
[15] Cerus Corp, Concord, CA 94520 USA
关键词
D O I
10.1111/j.1537-2995.2005.00216.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Photochemical treatment (PCT) with amotosalen HCl (S-59) was developed to inactivate pathogens and white blood cells in plasma (PCT-FFP) used for transfusion support. STUDY DESIGN AND METHODS: An open-label, multicenter trial was conducted in patients with congenital coagulation factor deficiencies (factors [F]I, FII, FV, FVII, FX, FXI, and FXIII and protein C) to measure the kinetics of specific coagulation factors, hemostatic efficacy, and safety of PCT-FFP. Posttransfusion prothrombin time (PT), partial thromboplastin time (PTT), and clinical hemostasis were evaluated before and after PCT-FFP transfusions. RESULTS: Thirty-four patients received 107 transfusions of PCT-FFP for kinetic studies or therapeutic indications (mean dose, 12.8 +/- 8.5 mL/kg). Incremental factor recoveries ranged from 0.9 to 2.4 IU per dL per IU per kg (FII, FV, FVII, FX, FXI, and protein C). Mean pretransfusion PT (20.7 +/- 22.2 sec) corrected after PCT-FFP (13.8 +/- 2.4 sec, p < 0.001). Mean pretransfusion PTT (51.2 +/- 29.3 sec) corrected after PCT-FFP (32.0 +/- 5.1 sec, p < 0.001). Thirteen patients required 77 transfusions for therapeutic indications. PCT-FFP provided effective hemostasis and was well tolerated. CONCLUSIONS: Replacement coagulation factors in PCT-FFP exhibited kinetics and therapeutic efficacy consistent with conventional FFP.
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收藏
页码:1362 / 1372
页数:11
相关论文
共 47 条
[1]  
Alfonso R., 1996, Blood, V88, p526A
[2]  
ALVING B, 2003, BLOOD BANKING TRANSF, P307
[3]  
[Anonymous], 1994, JAMA, V271, P777
[4]   Transfusing methylene blue-photoinactivated plasma instead of FFP is associated with an increased demand for plasma and cryoprecipitate [J].
Atance, R ;
Pereira, A ;
Ramírez, B .
TRANSFUSION, 2001, 41 (12) :1548-1552
[5]   In vitro characterization of solvent/detergent-treated human plasma and of quarantine fresh frozen plasma [J].
Beeck, H ;
Hellstern, P .
VOX SANGUINIS, 1998, 74 :219-223
[6]   Vitamin K-dependent coagulation factors and fibrinogen levels in FFP remain stable upon repeated freezing and thawing [J].
Ben-Tal, O ;
Zwang, E ;
Eichel, R ;
Badalbev, T ;
Hareuveni, M .
TRANSFUSION, 2003, 43 (07) :873-877
[7]   Estimated risk of transmission of the West Nile virus through blood transfusion in the US, 2002 [J].
Biggerstaff, BJ ;
Petersen, LR .
TRANSFUSION, 2003, 43 (08) :1007-1017
[8]   The Medical Dictionary for Regulatory Activities (MedDRA) [J].
Brown, EG ;
Wood, L ;
Wood, S .
DRUG SAFETY, 1999, 20 (02) :109-117
[9]   Protein composition and activation markers in plasma collected by three apheresis procedures [J].
Burnouf, T ;
Kappelsberger, C ;
Frank, K ;
Burkhardt, T .
TRANSFUSION, 2003, 43 (09) :1223-1229
[10]   Preclinical safety profile of plasma prepared using the INTERCEPT Blood System [J].
Ciaravino, V ;
McCullough, T ;
Cimino, G ;
Sullivan, T .
VOX SANGUINIS, 2003, 85 (03) :171-182