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用甲氨蝶呤治疗顽固性心脏移植排斥反应。心脏移植团队。

Treatment of recalcitrant cardiac allograft rejection with methotrexate. Cardiac Transplant Team.

作者信息

Chan G L, Weinstein S S, Vijayanagar R R

机构信息

Department of Pharmacotherapy and Research, Tampa General Hospital, FL 33606, USA.

出版信息

Clin Transplant. 1995 Apr;9(2):106-14.

PMID:7599398
Abstract

Acute rejection continues to be a major cause of mortality and morbidity among cardiac allograft recipients. In this retrospective analysis, we evaluated the efficacy and safety of methorexate in the treatment of recalcitrant rejection in 16 heart transplant patients. Methotrexate was initiated in these patients for rejection refractory to conventional therapy or for multiple, recurrent rejection episodes. Before methotrexate therapy, these patients had experienced 3.2 +/- 1.1 (mean +/- SD) episodes of allograft rejection. Methotrexate was administered at 5.9 +/- 5.3 months postransplant, at a starting oral dose of 7.8 +/- 2.7 mg/week. The methotrexate dose was increased as tolerated by white blood cell counts to 10-25 mg/week. These patients had been followed for 26 +/- 12 months after initiation of methotrexate. All ongoing rejection episodes were reversed with methotrexate. Rejection resolution was typically delayed and was observed at 19 +/- 15 days after methotrexate initiation. Compared to the 6 months before methotrexate therapy, there was significant reduction in the linearized rejection rate (0.44 +/- 0.14 vs 0.06 +/- 0.09 episodes/patient/month), and the time spent in rejection (29.8 +/- 14.0 vs 5.8 +/- 8.7 days) in the 6 months after methotrexate initiation. Nadir white blood cell counts were observed at 4.0 +/- 1.8 weeks after methotrexate initiation, but were above 2000/mm3 in all patients. Multiple infections occurred in 2 patients who received repeat courses of methotrexate and the highest cumulative doses of methotrexate. These findings suggest that methotrexate may be effective in the management of recalcitrant cardiac allograft rejection. Methotrexate therapy appears to be well tolerated by most patients.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

急性排斥反应仍是心脏移植受者死亡和发病的主要原因。在这项回顾性分析中,我们评估了甲氨蝶呤对16例心脏移植患者顽固性排斥反应的治疗效果和安全性。这些患者因常规治疗难治性排斥反应或多次反复发生排斥反应而开始使用甲氨蝶呤。在甲氨蝶呤治疗前,这些患者经历了3.2±1.1(均值±标准差)次移植排斥反应。甲氨蝶呤在移植后5.9±5.3个月开始使用,起始口服剂量为7.8±2.7毫克/周。根据白细胞计数耐受情况,甲氨蝶呤剂量增加至10 - 25毫克/周。这些患者在开始使用甲氨蝶呤后随访了26±12个月。所有正在进行的排斥反应均被甲氨蝶呤逆转。排斥反应的缓解通常延迟,在开始使用甲氨蝶呤后19±15天观察到。与甲氨蝶呤治疗前的6个月相比,开始使用甲氨蝶呤后的6个月内,线性化排斥率显著降低(0.44±0.14 vs 0.06±0.09次/患者/月),且处于排斥反应的时间减少(29.8±14.0 vs 5.8±8.7天)。甲氨蝶呤开始使用后4.0±1.8周观察到白细胞计数最低点,但所有患者的白细胞计数均高于2000/mm³。2例接受甲氨蝶呤重复疗程和最高累积剂量的患者发生了多次感染。这些发现表明,甲氨蝶呤可能对顽固性心脏移植排斥反应的治疗有效。大多数患者对甲氨蝶呤治疗的耐受性似乎良好。(摘要截选至250字)

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