LOW-DOSE INTRAVENOUS CALCITRIOL TREATMENT OF SECONDARY HYPERPARATHYROIDISM IN HEMODIALYSIS-PATIENTS

被引:105
作者
GALLIENI, M
BRANCACCIO, D
PADOVESE, P
ROLLA, D
BEDANI, P
COLANTONIO, G
BRONZIERI, C
BAGNI, B
TAROLO, G
机构
[1] OSPED SAN PAOLO,DEPT NEPHROL & DIALYSIS,RENAL UNIT,VIA A DI RUKINI 8,I-20142 MILAN,ITALY
[2] OSPED S ANNA COMO,RENAL UNIT,COMO,ITALY
[3] OSPED SAN MARTINO GENOVA,RENAL UNIT,GENOA,ITALY
[4] ARCISPEDALE ST ANNA,RENAL UNIT,FERRARA,ITALY
[5] OSPED PREDABISSI,RENAL UNIT,MELEGNANO,ITALY
[6] OSPED SAN PAOLO,DEPT NUCL MED,MILAN,ITALY
[7] ARCISPEDALE ST ANNA,DEPT NUCL MED,FERRARA,ITALY
关键词
D O I
10.1038/ki.1992.404
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Intravenous calcitriol is known to directly suppress PTH secretion and release. We evaluated the effect of four months of treatment with low-dose intravenous calcitriol on PTH levels in 83 hemodialysis patients. The criteria for including patients in the study were a serum PTH levels at least four times the normal limit, a serum total calcium less than 10 mg/dl and good control of the serum phosphorus level. All patients underwent standard bicarbonate or acetate dialysis; dialysate calcium level was maintained at the usual 3.5 mEq/liter concentration. Initial calcitriol dose was 0.87 +/- 0.02 (SEM) mug (0.015 mug body wt) thrice weekly at the end of dialysis, and it was reduced in case of hypercalcemia or elevated calcium-phosphate product. Seven out of 83 patients dropped out during treatment. Among the 76 patients who completed the study, 58 (76%) showed a highly significant decrease of intact PTH levels (average reduction 48%) and of alkaline phosphatase levels after four months of therapy. Total serum calcium increased slightly but significantly in the responder group but remained unchanged in the non-responders. No significant changes in ionized calcium levels could be detected, even in responders. Treatment was well tolerated by patients, but 60% of them had transient episodes of hyperphosphatemia, Mean serum phosphate was 4.95 mg/dl at the beginning of the study. It increased significantly after four months of treatment in patients who showed a decrease of PTH levels, although it remained within acceptable limits, below 5.5 mg/dl. Twenty-eight of 76 patients (37%) reduced the dose of calcitriol because their calcium-phosphate products exceeded 60. Low-dose intravenous calcitriol therapy for secondary hyperparathyroidism in dialysis patients is safe and may be highly effective in reducing serum PTH and alkaline phosphatase levels without significant increases of ionized calcium concentrations. However, the frequent occurrence of asymptomatic hyperphosphatemia indicates that similar precautions are needed for intravenous and oral calcitriol administration.
引用
收藏
页码:1191 / 1198
页数:8
相关论文
共 36 条
  • [21] DISAPPEARANCE OF ALUMINIC BONE-DISEASE IN A LONG-TERM ASYMPTOMATIC DIALYSIS POPULATION RESTRICTING AL(OH)3 INTAKE - EMERGENCE OF AN IDIOPATHIC ADYNAMIC BONE-DISEASE NOT RELATED TO ALUMINUM
    MORINIERE, P
    COHENSOLAL, M
    BELBRIK, S
    BOUDAILLIEZ, B
    MARIE, A
    WESTEEL, PF
    RENAUD, H
    FIEVET, P
    LALAU, JD
    SEBERT, JL
    FOURNIER, A
    [J]. NEPHRON, 1989, 53 (02) : 93 - 101
  • [22] TREATMENT OF REFRACTORY HYPERPARATHYROIDISM IN PATIENTS ON HEMODIALYSIS BY INTERMITTENT ORAL-ADMINISTRATION OF 1,25(OH)2 VITAMIN-D3
    MURAMOTO, H
    HARUKI, K
    YOSHIMURA, A
    MIMO, N
    ODA, K
    TOFUKU, Y
    [J]. NEPHRON, 1991, 58 (03): : 288 - 294
  • [23] NAPOLI JL, 1983, J BIOL CHEM, V258, P2100
  • [24] NORRIS KC, 1986, J BONE MINER RES S1, V1, P374
  • [25] NUSSBAUM SR, 1987, CLIN CHEM, V33, P1364
  • [26] ORAL CALCITRIOL AND CALCIUM - EFFICIENT THERAPY FOR UREMIC HYPERPARATHYROIDISM
    QUARLES, LD
    DAVIDAI, GA
    SCHWAB, SJ
    BARTHOLOMAY, DW
    LOBAUGH, B
    [J]. KIDNEY INTERNATIONAL, 1988, 34 (06) : 840 - 844
  • [27] RODRIGUEZ M, 1991, J AM SOC NEPHROL, V2, P1014
  • [28] SUPPRESSION BY 1,25(OH)2D3 OF TRANSCRIPTION OF THE PRE-PROPARATHYROID HORMONE GENE
    RUSSELL, J
    LETTIERI, D
    SHERWOOD, LM
    [J]. ENDOCRINOLOGY, 1986, 119 (06) : 2864 - 2866
  • [29] SALUSKY IB, 1988, VITAMIN D MOL CELLUL, P783
  • [30] REGULATION BY VITAMIN-D METABOLITES OF PARATHYROID-HORMONE GENE-TRANSCRIPTION INVIVO IN THE RAT
    SILVER, J
    NAVEHMANY, T
    MAYER, H
    SCHMELZER, HJ
    POPOVTZER, MM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1986, 78 (05) : 1296 - 1301