Kim Y J, Kim M G, Jeon H J, Ro H, Park H C, Jeong J C, Oh K H, Ha J, Yang J, Ahn C
Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Transplant Proc. 2012 Apr;44(3):651-6. doi: 10.1016/j.transproceed.2011.12.050.
Abnormalities of calcium and phosphorus metabolism in end-stage renal disease patients can persist after transplantation. We investigated their natural courses after transplantation, their risk factors for posttransplantation hypercalcemia and hypophosphatemia, and their impacts on allograft outcomes.
We retrospectively analyzed a total of 490 adult patients who underwent kidney transplantations between 2000 and 2009.
The serum calcium continued to increase, and reaching a plateau at around 3 months after transplantation. Thereafter it decreased, reaching a stable level by 2 years. Forty-four patients (9.0%) displayed hypercalcemia within 1 year; it persisted longer than that in 23 subjects (4.7%). Both longer dialysis duration (odds ratio [OR] 1.423; 95% confidence interval [CI], 1.192-1.699) and high intact serum parathyroid hormone (iPTH) level before transplantation (OR 1.002; 95% CI, 1.000-1.003) increased the risk for posttransplantation hypercalcemia. After a significant decrease during the first week, the serum phosphorus level increased, becoming stable between 1 and 6 months after transplantation. Hypophsphatemia occurred in 379 patients (77.3%) with 336 patients displaying hypophosphatemia without hypercalcemia. However, neither hypercalcemia nor hypophosphatemia influenced graft outcomes. Eight patients underwent pretransplantation parathyroidectomy, whereas 4 patients underwent posttransplantation parathyroidectomy. Neither group of patients experienced posttransplantation hypercalcemia.
Both hypercalcemia and hypophosphatemia are common after renal transplantation, especially among patients with a long history of dialysis before transplantation. Strict control of hyperparathyroidism including parathyroidectomy before transplantation may be the appropriate approach to these abnormalities.
终末期肾病患者钙磷代谢异常在移植后可能持续存在。我们研究了移植后它们的自然病程、移植后高钙血症和低磷血症的危险因素及其对移植肾结局的影响。
我们回顾性分析了2000年至2009年间接受肾移植的490例成年患者。
血清钙持续升高,在移植后约3个月达到平台期。此后下降,到2年时达到稳定水平。44例患者(9.0%)在1年内出现高钙血症;23例患者(4%)持续时间更长。移植前透析时间较长(比值比[OR]1.423;95%置信区间[CI],1.192 - 1.699)和移植前血清甲状旁腺激素(iPTH)水平较高(OR 1.002;95% CI,1.000 - 1.003)均增加了移植后高钙血症的风险。血清磷水平在术后第一周显著下降后升高,在移植后1至6个月之间趋于稳定。379例患者(77.3%)发生低磷血症,其中336例患者出现单纯低磷血症而无高钙血症。然而,高钙血症和低磷血症均未影响移植肾结局。8例患者在移植前接受了甲状旁腺切除术,4例患者在移植后接受了甲状旁腺切除术。两组患者均未出现移植后高钙血症。
肾移植后高钙血症和低磷血症均很常见,尤其是在移植前透析病史较长的患者中。严格控制甲状旁腺功能亢进,包括移植前甲状旁腺切除术,可能是处理这些异常情况的合适方法。