Hattori M, Ito K, Konomoto T, Kawaguchi H, Yoshioka T, Khono M
Department of Pediatric Nephrology, Tokyo Women's Medical University, School of Medicine, Japan.
Am J Kidney Dis. 1999 Mar;33(3):427-33. doi: 10.1016/s0272-6386(99)70178-2.
To clarify the therapeutic role of plasmapheresis (PP) for patients with Henoch-Schönlein purpura (HSP) nephritis, the clinical courses of nine children with a rapidly progressive type of HSP nephritis, who were treated with PP as the sole therapy, were retrospectively evaluated. All patients had nephrotic-range proteinuria (4.9 +/- 2.5 g/m2/d, mean +/- SD) and decreased glomerular filtration rate (GFR) (46.5 +/- 9.5 mL/min/1.73 m2) at the time of the initiation of PP. Biopsy specimens taken before PP showed large crescents involving more than 50% of the glomerular circumference in 56.8 +/- 6.9% of the glomeruli examined. The mean interval between disease onset and initiation of PP was 39.1 +/- 22.1 days. The PP regimen consisted of thrice-weekly treatment for 2 weeks, then weekly treatment for 6 weeks. No patients received any steroids or cytotoxic drugs, except for the use of steroids to manage severe abdominal pain. All patients responded promptly to PP with improvement in renal function, reduction of proteinuria, and subsidence of purpuric rash and abdominal pain. Six of nine patients showed further improvements without any other treatments; four had complete recovery, and two had only microscopic hematuria at the latest observation (follow-up period, 9.6 +/- 4.3 years). The remaining three patients showed a rebound increase of proteinuria after completion of PP; two of whom progressed to end-stage renal failure at 14.1 years and 1.8 years after disease onset. Because all patients had the most severe forms of nephritis, reported to carry a grave prognosis, this study suggests that PP as the sole therapy is effective in improving the prognosis of patients with rapidly progressive HSP nephritis, particularly if instituted early in the course of the disease. The role of PP in treating HSP nephritis deserves to be assessed further in larger randomized controlled trials.
为阐明血浆置换(PP)对过敏性紫癜(HSP)肾炎患者的治疗作用,我们回顾性评估了9例快速进展型HSP肾炎患儿的临床病程,这些患儿仅接受PP治疗。所有患者在开始PP治疗时均有肾病范围蛋白尿(4.9±2.5g/m²/d,均值±标准差)和肾小球滤过率(GFR)下降(46.5±9.5mL/min/1.73m²)。PP治疗前获取的活检标本显示,在所检查的肾小球中,56.8±6.9%有大新月体,累及超过50%的肾小球圆周。疾病发作至开始PP治疗的平均间隔时间为39.1±22.1天。PP方案包括每周3次治疗,共2周,然后每周治疗6周。除了使用类固醇治疗严重腹痛外,没有患者接受任何类固醇或细胞毒性药物治疗。所有患者对PP治疗反应迅速,肾功能改善,蛋白尿减少,紫癜皮疹和腹痛消退。9例患者中有6例未经任何其他治疗进一步好转;4例完全康复,2例在最近一次观察(随访期9.6±4.3年)时仅存在镜下血尿。其余3例患者在PP治疗完成后蛋白尿出现反弹增加;其中2例在疾病发作后14.1年和1.8年进展为终末期肾衰竭。由于所有患者均患有最严重的肾炎形式,据报道预后严重,本研究表明,PP作为唯一治疗方法可有效改善快速进展型HSP肾炎患者的预后,特别是在疾病病程早期实施时。PP在治疗HSP肾炎中的作用值得在更大规模的随机对照试验中进一步评估。