Edgren Gustaf, Hjalgrim Henrik, Reilly Marie, Tran Trung Nam, Rostgaard Klaus, Shanwell Agneta, Titlestad Kjell, Adami Johanna, Wikman Agneta, Jersild Casper, Gridley Gloria, Wideroff Louise, Nyrén Olof, Melbye Mads
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Lancet. 2007 May 19;369(9574):1724-30. doi: 10.1016/S0140-6736(07)60779-X.
Although mechanisms for detection of short-term complications after blood transfusions are well developed, complications with delayed onset, notably transmission of chronic diseases such as cancer, have been difficult to assess. Our aim was to investigate the possible risk of cancer transmission from blood donors to recipients through blood transfusion.
We did a register-based retrospective cohort study of cancer incidence among patients who received blood from donors deemed to have a subclinical cancer at the time of donation. These precancerous donors were diagnosed with a cancer within 5 years of the donation. Data from all computerised blood bank registers in Sweden and Denmark gathered between 1968 and 2002 were merged into a common database. Demographic and medical data, including mortality and cancer incidence, were ascertained through linkages with nationwide, and essentially complete, population and health-care registers. The risk of cancer in exposed recipients relative to that in recipients who received blood from non-cancerous donors was estimated with multivariate Poisson regression, adjusting for potential confounding factors.
Of the 354 094 transfusion recipients eligible for this analysis, 12,012 (3%) were exposed to blood products from precancerous donors. There was no excess risk of cancer overall (adjusted relative risk 1.00, 95% CI 0.94-1.07) or in crude anatomical subsites among recipients of blood from precancerous donors compared with recipients of blood from non-cancerous donors.
Our data provide no evidence that blood transfusions from precancerous blood donors are associated with increased risk of cancer among recipients compared with transfusions from non-cancerous donors.
尽管检测输血后短期并发症的机制已很完善,但延迟发作的并发症,尤其是诸如癌症等慢性疾病的传播,一直难以评估。我们的目的是调查通过输血将癌症从献血者传播给受血者的潜在风险。
我们对在献血时被认为患有亚临床癌症的献血者所供血的患者进行了一项基于登记的回顾性队列研究。这些癌前献血者在献血后5年内被诊断出患有癌症。将1968年至2002年期间瑞典和丹麦所有电脑化血库登记的数据合并到一个通用数据库中。通过与全国范围且基本完整的人口和医疗保健登记系统相链接,确定人口统计学和医学数据,包括死亡率和癌症发病率。使用多变量泊松回归估计暴露受血者患癌症的风险与接受非癌献血者血液的受血者患癌症风险的比值,并对潜在混杂因素进行调整。
在354094名符合该分析条件的输血受血者中,12012名(3%)接受了癌前献血者的血液制品。与接受非癌献血者血液的受血者相比,癌前献血者血液受血者总体上没有额外的癌症风险(调整后的相对风险为1.00,95%置信区间为0.94 - 1.07),在粗略的解剖部位也是如此。
我们的数据没有提供证据表明,与接受非癌献血者的输血相比,接受癌前献血者的输血会增加受血者患癌症的风险。