Therapeutic efficacy and safety of platelets treated with a photochemical process for pathogen inactivation: the SPRINT Trial

被引:329
作者
McCullough, J
Vesole, DH
Benjamin, RJ
Slichter, SJ
Pineda, A
Snyder, E
Stadtmauer, EA
Lopez-Plaza, I
Coutre, S
Strauss, RG
Goodnough, LT
Fridey, JL
Raife, T
Cable, R
Murphy, S
Howard, F
Davis, K
Lin, JS
Metzel, P
Corash, L
Koutsoukos, A
Lin, L
Buchholz, DH
Conlan, MG
机构
[1] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[2] Med Coll Wisconsin, Blood & Marrow Transplant Program, Milwaukee, WI 53226 USA
[3] Brigham & Womens Hosp, Joint Program Transfus Med, Boston, MA 02115 USA
[4] Puget Sound Blood Ctr, Seattle, WA 98104 USA
[5] Mayo Clin, Dept Lab Med, Rochester, MN USA
[6] Yale Univ, Sch Med, Yale New Haven Hosp, New Haven, CT USA
[7] Univ Penn, Med Ctr, Philadelphia, PA 19104 USA
[8] Inst Transfus Med, Pittsburgh, PA USA
[9] Stanford Med Ctr, Palo Alto, CA USA
[10] Univ Iowa, DeGowin Blood Ctr, Iowa City, IA USA
[11] Washington Univ, Sch Med, St Louis, MO USA
[12] Blood Bank San Bernadino Cty, San Bernardino, CA USA
[13] Blood Ctr SE Wisconsin Inc, Milwaukee, WI USA
[14] Amer Red Cross, Blood Serv, Farmington, CT USA
[15] Amer Red Cross, Blood Serv, Philadelphia, PA USA
[16] Loma Linda Univ, Inst Canc, Loma Linda, CA 92350 USA
[17] Univ Washington, Seattle, WA 98195 USA
[18] Cerus Corp, Concord, CA USA
[19] Quintiles Inc, Rockville, MD USA
[20] Baxter Healthcare Corp, Round Lake, IL USA
关键词
D O I
10.1182/blood-2003-12-4443
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a transfusion trial of platelets photochemically treated for pathogen inactivation using the synthetic psoralen amotosalen HCI. Patients with thrombocytopenia were randomly assigned to receive either photochemically treated (PCT) or conventional (control) platelets for up to 28 days. The primary end point was the proportion of patients with World Health Organization (WHO) grade 2 bleeding during the period of platelet support. A total of 645 patients (318 PCT and 327 control) were evaluated. The primary end point, the incidence of grade 2 bleeding (58.5% PCT versus 57.5% control), and the secondary end point, the incidence of grade 3 or 4 bleeding (4.1% PCT versus 6.1% control), were equivalent between the 2 groups (P = .001 by noninferiority). The mean 1-hour posttransfusion platelet corrected count increment (CCI) (11.1 X 10(3) PCT versus 16.0 x 10(3) control), average number of days to next platelet transfusion (1.9 PCT versus 2.4 control), and number of platelet transfusions (8.4 PCT versus 6.2 control) were different (P < .001). Transfusion reactions were fewer following PCT platelets (3.0% PCT versus 4.4% control; P = .02). The incidence of grade 2 bleeding was equivalent for PCT and conventional platelets, although posttransfusion platelet count increments and days to next transfusion were decreased for PCT compared with conventional platelets. (C) 2004 by The American Society of Hematology.
引用
收藏
页码:1534 / 1541
页数:8
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