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镰状细胞病或镰状细胞性状患者肾移植自然史的全国性研究。

National study on natural history of renal allografts in sickle cell disease or trait.

作者信息

Chatterjee S N

出版信息

Nephron. 1980;25(4):199-201. doi: 10.1159/000181781.

Abstract

The natural history of renal allograft in recipients who have sickle cell disease or trait has not been widely studied. This survey attempted to collect all the case histories known at present and to assess the relationship of sickle cell disease or trait to the natural history of renal allograft. A questionnaire was sent to 120 transplant centers in North America. 106 centers responded to the study, compliance rate being 88%. 88 centers reported not having any experience with such a case, whereas 18 centers transplanted 34 kidneys in 30 patients with this disease or trait. 9 of these had sickle cell disease and 21 had the trait. Graft survival at 1 year was 23 of 34, i.e., 67%. Mortality was 4 of 30, i.e., 13% in the first year. Sickle cell crisis was noted in 8 patients during the first year, 7 of whom had sickle cell disease. Thus, sickle cell crisis is very common in sickle cell transplant patients. From the points of view of patient survival and graft survival, recipients of kidneys who have the disease or the trait do just as well after transplant as the remaining patient population.

摘要

镰状细胞病或镰状细胞性状受者的肾移植自然史尚未得到广泛研究。本次调查试图收集目前已知的所有病例史,并评估镰状细胞病或镰状细胞性状与肾移植自然史之间的关系。向北美120个移植中心发送了调查问卷。106个中心回复了该研究,回复率为88%。88个中心报告没有此类病例的经验,而18个中心为30例患有这种疾病或性状的患者移植了34个肾脏。其中9例患有镰状细胞病,21例具有镰状细胞性状。34个移植肾1年时的移植肾存活率为23个,即67%。30例患者中第一年的死亡率为4例,即13%。第一年有8例患者出现镰状细胞危象,其中7例患有镰状细胞病。因此,镰状细胞危象在镰状细胞移植患者中非常常见。从患者存活和移植肾存活的角度来看,患有这种疾病或性状的肾移植受者在移植后的情况与其他患者群体一样好。

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