Barnhart G R, Hastillo A, Goldman M H, Szentpetery S, Wolfgang T C, Mohanakumar T, Katz M R, Rider S, Hanrahan J, Lower R R
Circulation. 1985 Sep;72(3 Pt 2):II227-30.
Cyclosporine has gained acceptance as the immunosuppressive agent of choice in cardiac transplantation, but the validity of this assumption has yet to be established. Since January 1983, 25 patients have been randomly assigned to receive either conventional immunosuppression (azathioprine/antithymocyte globulin/prednisone) and pretransplant transfusion (PAAP, n = 11) or cyclosporine immunosuppression (cyclosporine and prednisone [CyA], n = 14). There was no difference in the age distribution (41 +/- 9 vs 38 +/- 11 years), indications for transplantation, preoperative serum creatinine level (1.2 +/- 0.2 vs 1.4 +/- 0.3 mg/dl), or postoperative follow-up time (13.5 +/- 5.4 vs 13.5 +/- 5.2 months). Mortality was not different (PAAP = 2, CyA = 3) and there was no difference in rejection episodes per patient (PAAP = 1.8, CyA = 1.9). Patients in the PAAP group had more serious infections (PAAP = 8, CyA = 3; P less than .02), but those in the CyA group developed a greater incidence of systemic hypertension (PAAP = 1, CyA = 10; p less than .02), pericardial effusion (PAAP = 0, CyA = 6; p = .05), and impaired renal function (creatinine 1.5 mg/dl, PAAP = 2, CyA = 11; p less than .02). Thus it appears that in this small series, cyclosporine is not associated with a significant increase in early survival. It does appear that patients on PAAP immunosuppression develop a greater number of serious infections, but the incidence of rejection episodes appears to be the same. Renal dysfunction and hypertension in patients receiving cyclosporine continue to be long-term concerns and may add to the morbidity and mortality of patients treated with this immunosuppressive regimen.
环孢素已成为心脏移植中首选的免疫抑制剂,但这一假设的有效性尚未得到证实。自1983年1月以来,25例患者被随机分配接受传统免疫抑制治疗(硫唑嘌呤/抗胸腺细胞球蛋白/泼尼松)和移植前输血(PAAP组,n = 11)或环孢素免疫抑制治疗(环孢素和泼尼松[CyA]组,n = 14)。两组患者在年龄分布(41±9岁 vs 38±11岁)、移植指征、术前血清肌酐水平(1.2±0.2 vs 1.4±0.3 mg/dl)或术后随访时间(13.5±5.4 vs 13.5±5.2个月)方面没有差异。死亡率无差异(PAAP组 = 2例,CyA组 = 3例),每位患者的排斥反应次数也无差异(PAAP组 = 1.8次,CyA组 = 1.9次)。PAAP组患者发生更严重感染的情况更多(PAAP组 = 8例,CyA组 = 3例;P < 0.02),但CyA组患者发生系统性高血压的发生率更高(PAAP组 = 1例,CyA组 = 10例;p < 0.02)、心包积液更多(PAAP组 = 0例,CyA组 = 6例;p = 0.05)以及肾功能受损(肌酐>1.5 mg/dl,PAAP组 = 2例,CyA组 = 11例;p < 0.02)。因此,在这个小样本系列中,环孢素似乎并未使早期生存率显著提高。确实,接受PAAP免疫抑制治疗的患者发生严重感染的次数更多,但排斥反应的发生率似乎相同。接受环孢素治疗的患者出现的肾功能障碍和高血压仍是长期问题,可能会增加接受这种免疫抑制方案治疗患者的发病率和死亡率。