Ong Lay Ping, Sachdeva Ashwin, Ramesh Bandigowdanapalya Channaiah, Muse Hazel, Wallace Kirstie, Parry Gareth, Clark Stephen C
Department of Cardiothoracic Surgery, Freeman Hospital, Newcastle Upon Tyne, United Kingdom.
Department of Urology, Freeman Hospital, Newcastle Upon Tyne, United Kingdom.
Ann Thorac Surg. 2016 Feb;101(2):512-9. doi: 10.1016/j.athoracsur.2015.07.048. Epub 2015 Oct 9.
Allogeneic blood transfusion has been associated with immune modulation in other solid organ transplants. Within cardiothoracic surgery, allogeneic blood transfusion is associated with greater postoperative morbidity and mortality. We investigated the impact of allogeneic blood transfusion on rejection, function, and late mortality within lung transplantation.
A retrospective review was made of 311 adult patients who underwent bilateral lung transplantation with cardiopulmonary bypass from 2003 to 2013. Patients were stratified based on the amount of blood products transfused within 24 hours of transplantation. Kaplan-Meier methods and multivariate Cox proportional hazards models were used for time to first rejection/death and all-cause mortality analyses.
In all, 174 men and 137 women (mean age 41.4 ± 14.0 years) utilized a median number of 3 units (range, 0 to 40) of red blood cells (RBC), 2 units (range, 0 to 26) of fresh frozen plasma (FFP), and 1 unit (range, 0 to 7) of platelets within the first 24 hours of transplantation. Time to first treated rejection/death was not statistically different whether patients were transfused with more or less than the median number of units of RBC (unadjusted p = 0.233, adjusted hazard ratio [HR] 1.02, 95% confidence interval [CI]: 0.75 to 1.40, p = 0.177), FFP (unadjusted p = 0.146, adjusted HR 1.29, 95% CI: 0.95 to 1.76, p = 0.108), or platelets (unadjusted p = 0.701, adjusted HR 0.74, 95% CI: 0.47 to 1.15, p = 0.177). Rate of rejection and number of rejection episodes per patient at 1 year after transplant were not statistically different. Forced expiratory volume in 1 second expressed as percentage of forced vital capacity at 3 and 6 months was similar for all groups. Unadjusted early all-cause mortality was not influenced by RBC (p = 0.162) or FFP (p = 0.298) but was significantly different with more platelets (p = 0.032). Adjusted 10-year mortality showed no significant differences for RBC (HR 1.12, 95% CI: 0.70 to 1.79, p = 0.645), FFP (HR 1.24, 95% CI: 0.78 to 1.97, p = 0.356), or platelets (HR 1.49, 95% CI: 0.84 to 2.64, p = 0.172.).
All blood products administration regardless of amount transfused did not appear to affect early rejection outcomes or forced expiratory volume in 1 second expressed as percentage of forced vital capacity at 3 and 6 months. Use of RBC and FFP had no effect on survival. However, greater platelet usage appeared to adversely affect early but not late mortality.
同种异体输血与其他实体器官移植中的免疫调节有关。在心胸外科手术中,同种异体输血与更高的术后发病率和死亡率相关。我们研究了同种异体输血对肺移植中排斥反应、功能及晚期死亡率的影响。
对2003年至2013年期间接受体外循环下双侧肺移植的311例成年患者进行回顾性研究。根据移植后24小时内输注的血液制品量对患者进行分层。采用Kaplan-Meier方法和多变量Cox比例风险模型进行首次排斥反应/死亡时间及全因死亡率分析。
共有174例男性和137例女性(平均年龄41.4±14.0岁)在移植后的头24小时内输注了中位数为3单位(范围为0至40)的红细胞(RBC)、2单位(范围为0至26)的新鲜冰冻血浆(FFP)和1单位(范围为0至7)的血小板。无论患者输注的RBC单位数高于还是低于中位数,首次治疗性排斥反应/死亡时间在统计学上均无差异(未调整p = 0.233,调整后风险比[HR]为1.02,95%置信区间[CI]:0.75至1.40,p = 0.177),FFP(未调整p = 0.146,调整后HR为1.29,95% CI:0.95至1.76,p = 0.108)或血小板(未调整p = 0.701,调整后HR为0.74,95% CI:0.47至1.15,p = 0.177)。移植后1年时的排斥反应发生率及每位患者的排斥反应次数在统计学上无差异。所有组在3个月和6个月时以用力肺活量百分比表示的第1秒用力呼气量相似。未调整的早期全因死亡率不受RBC(p = 0.162)或FFP(p = 0.298)影响,但血小板输注量较多时差异显著(p = 0.032)。调整后的10年死亡率在RBC(HR为1.12,95% CI:0.70至1.79,p = 0.645)、FFP(HR为1.24,95% CI:0.78至1.97,p = 0.356)或血小板(HR为1.49,95% CI:0.84至2.64,p = 0.172)方面均无显著差异。
无论输注量多少,所有血液制品的输注似乎均不影响早期排斥反应结局或3个月和6个月时以用力肺活量百分比表示的第1秒用力呼气量。RBC和FFP的使用对生存率无影响。然而,更多的血小板使用似乎对早期死亡率有不利影响,但对晚期死亡率无影响。