Golper T A
Kidney Disease Program, University of Louisville, Kentucky 40292.
Perit Dial Int. 1992;12(1):37-9.
To determine if the simultaneous initiation of continuous ambulatory peritoneal dialysis (CAPD) and Erythropoietin therapy masks the hematocrit (Hct) rise that frequently follows the initiation of CAPD alone.
Single-center retrospective analysis.
University multidisciplinary dialysis program.
All adult CAPD patients with a Hct less than or equal to 28% whose nephrologist felt they would benefit from Erythropoietin therapy and who did not have technical reasons for exclusion (N = 25).
Eight patients began CAPD and Erythropoietin alfa subcutaneously, at a dose of 128 +/- 9 (X +/- SEM) units/kg/week at the same time. Seventeen patients already on CAPD for 8.7 +/- 1.5 months received Erythropoietin alfa subcutaneously at a dose of 124 +/- 7 units/kg/week. Pre-epoetin Hct's were similar.
Hematocrit changes, status of iron stores, incidence of peritonitis, and dosage of Erythropoietin.
In 1 month, the group initiating both therapies simultaneously demonstrated a mean Hct rise of 7.6 +/- 0.5% while established CAPD patients receiving Erythropoietin increased their Hct by only 4.7 +/- 1.0% (p less than .03). Iron status could not explain this difference. Peritonitis did not appear to dampen the Hct rise following Erythropoietin in either CAPD group. By 2 months after Erythropoietin, the differences were less apparent.
The early rapid increase in Hct is probably the combined effect of CAPD and Erythropoietin and should not be attributed to Erythropoietin alone. When comparing responses to Erythropoietin from patients on different therapies, the timing of dialysis initiation and Erythropoietin initiation must be considered.
确定同时开始持续性非卧床腹膜透析(CAPD)和促红细胞生成素治疗是否会掩盖仅开始CAPD后常见的血细胞比容(Hct)升高。
单中心回顾性分析。
大学多学科透析项目。
所有血细胞比容小于或等于28%的成年CAPD患者,其肾病科医生认为他们将从促红细胞生成素治疗中获益,且无技术上的排除理由(N = 25)。
8名患者同时开始CAPD并皮下注射促红细胞生成素α,剂量为128±9(X±SEM)单位/千克/周。17名已接受CAPD 8.7±1.5个月的患者皮下注射促红细胞生成素α,剂量为124±7单位/千克/周。促红细胞生成素治疗前的血细胞比容相似。
血细胞比容变化、铁储备状态、腹膜炎发生率和促红细胞生成素剂量。
1个月内,同时开始两种治疗的组平均血细胞比容升高7.6±0.5%,而接受促红细胞生成素治疗的已确诊CAPD患者血细胞比容仅升高4.7±1.0%(p <.03)。铁状态无法解释这种差异。在任何一个CAPD组中,腹膜炎似乎都没有抑制促红细胞生成素治疗后血细胞比容的升高。促红细胞生成素治疗2个月后,差异不太明显。
血细胞比容的早期快速升高可能是CAPD和促红细胞生成素的联合作用,不应仅归因于促红细胞生成素。在比较不同治疗患者对促红细胞生成素的反应时,必须考虑透析开始时间和促红细胞生成素开始时间。