Costanzo-Nordin M R, Swinnen L J, Fisher S G, O'Sullivan E J, Pifarre R, Heroux A L, Mullen G M, Johnson M R
Department of Medicine, Loyola University, Chicago, IL.
J Heart Lung Transplant. 1992 Sep-Oct;11(5):837-46.
To determine the relationship of cytomegalovirus infections (CMVI) to immunosuppression in heart transplants, we retrospectively compared demographic and clinical variables in 154 consecutive heart transplant patients. Forty-one CMVI were compared; of these, 30 (73%) were identified in tissue, and nine (22%) were identified by blood or urine culture. Twenty (49%) of the CMVI were self-limited, and 21 (51%) were progressive, requiring treatment. When comparing patients with and without CMVI, demographic variables, mean preexisting heart disease, cyclosporine level, cumulative corticosteroid dose, and the use of anti-T-cell antibodies were examined. Only the use of OKT3 was significantly associated with the subsequent development of CMVI. Although CMVI subsequently developed in 30 of 79 (38%) patients who had received OKT3, CMVI developed in only 11 of 75 (15%) patients who had not received OKT3 (p = 0.01). Furthermore, the incidence of CMVI increased with increasing total OKT3 dose (none, 11 of 64 [17%]; < or = 75 mg, 23 of 66 [35%]; > 75 mg, 6 of 14 [43%]; p = 0.01). Logistic regression showed that the only two variables predictive of CMVI were the use of OKT3 (p = 0.0023) and ischemic rather than idiopathic heart disease before transplantation (p = 0.0098). Rejection rates, incidence of allograft vasculopathy, and 1-year actuarial survival were not influenced by previous CMVI. Pneumocystis carinii pneumonia occurred more frequently in patients with CMVI than in those without (13 of 41 [32%] patients versus 3/113 [3%] patients; p < 0.001). No correlation existed between CMVI and lymphoproliferative disorder (p = 0.84).(ABSTRACT TRUNCATED AT 250 WORDS)
为确定巨细胞病毒感染(CMVI)与心脏移植受者免疫抑制之间的关系,我们回顾性比较了154例连续心脏移植患者的人口统计学和临床变量。对41例CMVI患者进行了比较;其中,30例(73%)在组织中检测到,9例(22%)通过血液或尿液培养检测到。20例(49%)CMVI为自限性,21例(51%)为进行性,需要治疗。在比较有和没有CMVI的患者时,我们检查了人口统计学变量、既往心脏病平均情况、环孢素水平、累积皮质类固醇剂量以及抗T细胞抗体的使用情况。只有OKT3的使用与随后CMVI的发生显著相关。尽管在接受OKT3的79例患者中有30例(38%)随后发生了CMVI,但在未接受OKT3的75例患者中只有11例(15%)发生了CMVI(p = 0.01)。此外,CMVI的发生率随着OKT3总剂量的增加而增加(无剂量组,64例中的11例[17%];≤75 mg组,66例中的23例[35%];>75 mg组,14例中的6例[43%];p = 0.01)。逻辑回归显示,预测CMVI的仅有的两个变量是OKT3的使用(p = 0.0023)和移植前缺血性而非特发性心脏病(p = 0.0098)。排斥反应发生率、移植血管病变发生率和1年预期生存率不受既往CMVI的影响。卡氏肺孢子虫肺炎在CMVI患者中比在无CMVI患者中更常见(41例患者中的13例[32%]对113例患者中的3例[3%];p < 0.001)。CMVI与淋巴增生性疾病之间无相关性(p = 0.84)。(摘要截短至250字)