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1.
目的 观察低钙(1.25 mmol/L)透析液加大剂量碳酸钙口服对血液透析患者高磷血症、高钙血症及低甲状旁腺素(PTH)的作用.方法 选择长期使用1.50 mmol/L浓度钙透析液,同时伴血磷、血钙水平升高,血PTH水平降低的患者27例,观察其在改用1.25 mmol/L浓度钙透析液后血钙、血磷、钙磷乘积及血PTH水平的变化.结果 使用1.25 mmol/L浓度钙透析液2周后血钙水平较使用前即有明显下降(P<0.01),6周后(加用大剂量碳酸钙口服4周后),血钙水平有所回升(P<0.05),血磷水平显著下降(P<0.01),钙磷乘积下降(P<0.05),血PTH水平显著升高(P<0.01).结论 低钙透析液可显著降低血液透析患者血钙水平,升高PTH水平,同时口服大剂量碳酸钙可改善高磷血症,降低钙磷乘积,可能起到防止低转运骨病的作用.  相似文献   

2.
目的 研究低钙透析联合1、25(OH)2D3及碳酸钙治疗维持性血液透析患者继发性甲状旁腺功能亢进的有效性和安全性。方法选择维持性血透患者共30例,合并继发性甲状旁腺功能亢进。透析采用浓度为1.25mmol/L的碳酸低钙透析液,口服碳酸钙每次1500mg,1次/d,口服活性维生素D每次0.75~1.0μg,每周2~3次,观察透析前后血钙、血磷、钙磷乘积和PTH。结果3个月后血钙维持正常水平,无显著性差异,血磷明显下降,有显著性差异(P〈0.01),钙磷乘积明显下降,有显著性差异(P〈0.01),IPTH明显下降,有显著性差异(P〈0.01)。结论维持性血透合并继发性甲状旁腺功能亢进的患者,在口服碳酸钙骨化三醇(罗盖全)治疗过程中,应用低钙透析液进行透析,可以有效避免高钙血症及转移性钙化的出现,同时有效降低血磷、钙磷乘积,血清甲状旁腺激素水平。  相似文献   

3.
目的 动态监测使用不同钙浓度腹膜透析液行持续性不卧床腹膜透析(CAPD)对尿毒症患者钙磷代谢的影响。方法将加例初行CAPD的尿毒症患者随机分为标准钙组和低钙组,每组各20例,行正规CAPD治疗并配合碳酸钙口服,观察12个月。结果两组患者初行CAPD时,血清钙、磷、钙磷乘积及免疫反应性甲状旁腺素(iPTH)浓度比较差异均无统计学意义,普遍存在高磷血症及低iPTH血症。经过6个月的治疗,标准钙组患者的高钙、高磷血症进一步加重,而低钙组患者的血清钙[(2.29±0.27)mmol/L]、血清磷[(1.50±0.25)mmol/L]及钙磷乘积[(41.62±19.55)mg^2/dl^2]较治疗前显著降低,且均低于治疗后的同期标准钙组患者(P〈0.01),iPTH则显著上升(P〈0.01)。在随后的6个月中,低钙组患者血清钙、钙磷乘积保持稳定并维持在正常范围,血清磷进一步降至正常范围(0.8~1.5mmol/L),iPTH则维持在150ng/L左右,与标准钙组比较有显著改善(P〈0.01)。结论低钙浓度腹膜透析液有助于减轻尿毒症CAPD患者的钙磷代谢紊乱,延缓并发症的发生。  相似文献   

4.
目的研究低钙透析联合1、25(OH)2D3及碳酸钙治疗维持性血液透析患者继发性甲状旁腺功能亢进的有效性和安全性。方法选择维持性血透患者共30例,合并继发性甲状旁腺功能亢进。透析采用浓度为1.25 mmol/L的碳酸低钙透析液,口服碳酸钙每次1 500 mg,1次/d,口服活性维生素D每次0.75~1.0μg,每周2~3次,观察透析前后血钙、血磷、钙磷乘积和PTH。结果3个月后血钙维持正常水平,无显著性差异,血磷明显下降,有显著性差异(P<0.01),钙磷乘积明显下降,有显著性差异(P<0.01),IPTH明显下降,有显著性差异(P<0.01)。结论维持性血透合并继发性甲状旁腺功能亢进的患者,在口服碳酸钙骨化三醇(罗盖全)治疗过程中,应用低钙透析液进行透析,可以有效避免高钙血症及转移性钙化的出现,同时有效降低血磷、钙磷乘积,血清甲状旁腺激素水平。  相似文献   

5.
目的探讨低钙透析液对血液透析患者难治性高血压的影响。方法选取合并难治性高血压的维持性血液透析患者26例,采取自身对照的方法,先后应用钙浓度为1.75mmol/L(DCa2+1.75)及1.25mmol/L(DCa2+1.25)的透析液各连续进行20次透析,观察每次开始透析后0h、1h、2h、3h及透析结束时的血压,并分别与20次透析前后观察一般临床指标及血清总钙(Ca2+)、磷(P3+)、钙磷乘积及全段甲状旁腺激素(iPTH)的变化。结果与常规采用DCa2+1.75比较,采用低钙透析液(DCa2+1.25)进行透析,患者的血压降低,尤其在第3小时及透析结束后.差异有统计学意义(P〈0.05);血钙、钙磷乘积降低(P〈0.05),其他临床指标差异无统计学意义(P〉0.05)。结论低钙透析液对维持性血液透析患者难治性高血压的控制有利。  相似文献   

6.
目的观察生理性钙浓度透析液联合碳酸钙、骨化三醇治疗在维持性血液透析患者血清钙、磷的变化。方法29例维持性血液透析患者使用1.75mmol/L浓度钙离子透析液12月以上后改为1.25mmol/L浓度钙离子透析液(生理性钙透析液),联合碳酸钙和小剂量骨化三醇口服,3个月后观察血清总钙、磷、钙磷乘积以及全段甲状旁腺激素(iPTH)的变化。结果经3个月生理性钙透析液治疗后,患者血清总钙、iPTH未见明显变化,而血清磷以及钙磷乘积均明显下降。结论长期维持性血液透析患者应用生理性钙透析加碳酸钙有助于降低血磷,提高了对活性维生素取和含钙磷结合剂治疗的耐受性,避免加重高钙血症和转移性钙化的出现。  相似文献   

7.
目的观察不同钙离子浓度的透析液对血液透析患者血清钙离子水平及血压变化的影响,为肾功能衰竭血液透析患者高血压的防治提供依据。方法采用自身对照法将维持性血液透析中的难治性高血压患者的透析液钙离子浓度由原来一直使用的1.5mmol/L换成低钙1.25mmol/L,比较患者换液前后血压及血钙、iPTH浓度的变化。结果换用钙离子浓度1.25mmol/L透析液后,患者血钙在首次透析后及治疗4周后均有下降,差异有统计学意义(P〈0.05),iPTH有所升高,无统计学意义。而患者换用1.25mmol/L透析液首次透析后及治疗4周后收缩压均明显下降,差异均有统计学意义(P〈0.01)。结论低钙透析液透析有助于维持性血液透析患者高血压的控制,但会导致透前血钙在正常范围内或偏低的患者透后血钙降低,应调整钙剂及活性维生素D的用量。  相似文献   

8.
目的:观察碳酸镧(lanthanum carbonate)在慢性肾衰竭持续非卧床腹膜透析(CAPD)患者应用骨化三醇治疗继发性甲状旁腺功能亢进(SHPT)时对血钙、血磷的影响。方法:将40例血清全段甲状旁腺激素(iPTH)300—500pg/ml、血钙磷乘积〈4.52(mmol/L)2的CAPD患者随机分为2组,每组20例。碳酸镧组给予口服碳酸钢500mg,3次/天,同时口服骨化三醇1.0μg,2次/周冲击治疗;碳酸钙组给予口服碳酸钙750mg,2次/天,同时口服骨化三醇1.0μg,2次/周。结果:碳酸镧组12周后血磷及iPTH较治疗前明显下降,碳酸镧组血钙、血磷明显低于碳酸钙组,差异有统计学意义(P〈0.05)。结论:碳酸镧能有效预防CAPD患者应用骨化三醇冲击治疗SHPT时的高钙血症及高磷血症。  相似文献   

9.
目的探讨骨化三醇联合长时血液透析对维持性血液透析继发性甲状旁腺功能亢进患者血甲状旁腺激素(PTH)、钙、磷水平的影响。方法将22例维持性血液透析继发性甲状旁腺功能亢进患者进行长时血液透析治疗,3次/周,每次6h。同时口服骨化三醇1I,zg/次,3次/周,共治疗3个月。分别于治疗前和治疗后检测血PTH、钙及磷水平。结果患者治疗后血PTH和血磷较治疗前明显下降[(484.21±230.18)nmol/L比(750.53±327.41)nmol/L、(1.49±0.27)mmol/L比(2.37±0.76)mmol/L],血钙较治疗前明显上升[(2.35±0.32)mmol/L比(1.81±0.53)mmol/L],差异均有统计学意义(P〈0.05)。结论骨化三醇联合长时血液透析可以降低维持性血液透析继发性甲状旁腺功能亢进患者血磷及血PTH,升高血钙,对治疗维持性血液透析继发性甲状旁腺功能亢进有一定的疗效。  相似文献   

10.
目的观察非卧床连续性腹膜透析(CAPD)患者长期使用低钙透析液(LCD)的安全性。方法在规律性随访的患者中选择28名CAPD患者,在使用标准钙透析液(SCD)3个月后改为使用LCD3年,以SCD为对照组,分别在使用LCD后的第1、3、6、12个月和第2、3年每年两次检测血清钙、血磷、全段甲状旁腺素(iPTH)和血白蛋白水平;计算发生瘙痒的人数和发生腹膜透析感染并发症的人数。结果使用LCD治疗第1个月开始血清钙上升,至第12个月显著升高(P〈0.05),iPTH值在治疗第12个月显著降低(P〈0.05),平均值〉300pg/ml。整个治疗过程中,瘙痒人数明显增加(P〈0.05),发生感染的并发症无明显增加(P〉0.05)。结论长期使用低钙透析液应严密检测血钙、磷和iPTH水平,同时注意钙的补充。  相似文献   

11.
目的:探讨低钙透析液联合鲑鱼降钙素对维持血透(Maintenance hemodialysis, MHD)患者高磷血症的影响。方法选取我院近期维持性血液透析患者中高磷血症患者40例,采用随机数字表法分为对照组21例,给予常规钙透析液+活性维生素D3治疗;试验组19例,给予低钙透析液联合鲑鱼降钙素注射液治疗。观察两组患者治疗后第3、6个月时血清钙磷代谢等指标有无差别。结果对照组治疗后血清钙较治疗前无明显变化(P>0.05),但血磷和甲状旁腺激素(iPTH)较透析前明显增加(P〈0.05);试验组治疗后血清钙、iPTH无明显变化(P>0.05),血磷显著降低(P〈0.05)。结论鲑鱼降钙素联合低钙透析液治疗MHD能有效降低患者血磷水平且不致影响iPTH。  相似文献   

12.
The object of the present study was to follow prospectively the serum levels of intact parathormone (PTH) of hemodialysis patients and the subsequent changes following the oral administration of 1.25(OH)D3 and calcium. METHODS: We studied 30 chronic renal failure hemodialysis patients--16 men and 14 women, aged 20-70 years. Twenty-one of them were on hemodialysis with duration of up to 5 years (Group 1) and nine--up to 10 years (Group 2). All patients received oral supplementation therapy with 1.0 elemental calcium and Rocaltrol (Roche) 0.25 microgram/day. We measured the serum calcium, ionized calcium, serum phosphorus, alkaline phosphatase and the intact serum PTH levels in intervals of 12 months. RESULTS: Patients with duration of dialysis of up to 5 years had a significantly lower baseline PTH level of 392.5 +/- 94.7 pg/ml versus 896.4 +/- 160.7 pg/ml for those from the second group (P < 0.01). The intact PTH levels showed a tendency towards decrease--at the end of the study they were as follows: 372.02 +/- 76.9 for group 1 versus a significant increase for those from group 2--serum PTH levels of 1793.65 +/- 290.3 (P < 0.02). The differences in alkaline phosphatase and serum phosphorus levels at the end of the study period failed to reach statistical significance. Serum calcium levels were increased in both groups following the initiation of treatment but the difference was statistically significant only for group 2. A significant positive correlation was observed between the duration of hemodialysis treatment and the intact serum PTH levels. CONCLUSIONS: 1. Long-term low-dose conventional calcitriol therapy in combination with calcium supplementation could slow the progression of secondary hyperparathyroidism in some hemodialysis patients. 2. Low-dose therapy with active vitamin D-metabolites is effective only in hemodialysis patients with baseline serum PTH levels below 500 pg/ml and without pronounced hyperphosphatemia.  相似文献   

13.
超微颗粒钙在大鼠体内的吸收和利用   总被引:15,自引:0,他引:15  
方法:用超微颗粒(80%<1μm)钙、碳酸钙、脱脂乳粉配制的饲料及基础的低钙饲料分别喂养4组断乳Wistar大鼠4周,并做3天钙代谢实验。结果:超微颗粒钙组大鼠体重增长率为80.4%;钙吸收率、储留率及利用率分别为71.1%、91.4%和61.4%;股骨指数为5.88;股骨钙存留率为4.97%,与碳酸钙组比较差异显著(P<0.05或P<0.01)。血清钙为2.39mmol/L;血清磷为2.31mmol/L,均在正常范围以内。与脱脂乳粉组比较,超微颗粒钙的利用率达到脱脂乳粉组的73%以上。结论:超微颗粒钙可以作为机体良好的钙源,广泛用于食品添加剂和药物。  相似文献   

14.
目的 改进对血液透析患者钙磷代谢异常的治疗,观察患者生活质量的改善.方法按照美国肾脏基金会(NKF)制定的"慢性肾脏病,透析病人生存质量指南(K/DOQI)"改进对血液透析患者钙磷代谢异常的治疗,观察1年后患者的血清钙、磷、钙磷乘积、全段甲状旁腺素(iPTH)等水平及治疗达标率的变化.应用肾脏病调查表(KDQ)评估患者生活质量的改善.结果改进治疗后患者的血清钙、磷、钙磷乘积及iPTH水平均较改进治疗前有明显下降(P<0.01或<0.05).改进治疗后治疗达标率分别为:血清钙74.42%(32/43)、血清磷62.79%(27/43)、钙磷乘积55.81%(24/43)、iPTH 60.47%(26/43)、四项达标25.58%(11/43),均较改进治疗前有明显上升(P<0.01或<0.05).改进治疗后KDQ评分的总分及各方面得分均较改进治疗前有明显增加(P<0.01).结论改进治疗后患者钙磷代谢情况较改进治疗前改善,生活质量提高.  相似文献   

15.
目的:观察不同制剂密钙息联合骨化三醇对血液透析导致肾性骨病患者的治疗效果。方法:选择血液透析导致肾性骨病伴高甲状旁腺素(PTH)、高磷血症同时伴有临床症状的患者106例,按照前瞻随机和对照的研究方法分为治疗组与对照组,每组各53例,对所有患者除治疗基础疾病、透析(血液或腹膜透析)、补充钙剂外,治疗组给予密钙息鼻喷剂联合骨化三醇:密盖息鼻喷剂200 IU,前2周每天1次,后隔天1次。3个月为一疗程;对照组给予密钙息肌注联合骨化三醇:密盖息注射液50 IU,肌肉注射,前2周每天1次,第3、4周隔日1次,后每周2次。3个月后观察各组治疗前后肾性骨病症状及血磷、血钙、PTH改变。结果:治疗后,两组肾性骨病相关症状明显好转,血磷、血PTH明显下降,血钙升高;治疗组治疗前血清钙、血清磷和PTH分别为(2.04±0.27)、(2.78±0.31)、(858.50±119.98),治疗后分别为(2.36±0.19)、(2.18±0.21)、(719.79±120.14);对照组治疗前血钙、血磷水平、PTH分别为(2.11±0.39)、(2.87±0.23)、(891.45±124.73),治疗后分别为(2.39±0.34)、(2.19±0.13)、(721.69±117.56)。两组上述指标治疗前后比较差异有统计学意义(P〈0.05),但两组间比较差异无统计学意义(P〉0.05);两组骨痛症状均改善明显,但治疗组在缓解时间上优于对照组,差异有统计学意义(P〈0.05);且治疗组副作用较少。结论:密钙息对肾性骨病治疗鼻喷剂副作用少,更为简便、实用、耐受性好,并可以迅速缓解骨痛。  相似文献   

16.
血液透析对游离肉碱的清除及影响因素的研究   总被引:2,自引:0,他引:2  
目的 研究维持性血液透析 (MHD)患者血浆游离肉碱 (FC)水平以及透析对FC清除的影响。方法 应用酶法检测MHD组血浆和透析液中FC水平及对照组尿中FC水平。结果 MHD患者透前血浆FC水平明显低于正常人 (P <0 .0 1)。透析后 ,血浆FC水平较透析前下降 70 %。每周MHD患者透析所致的FC丢失量远远超过对照组尿液排出量 (P <0 .0 1)。透析过程中 ,FC在第 1小时清除最多。透析中FC的清除量与血浆FC浓度呈正相关 (R =0 .5 1,P =0 .0 1)。应用不同透析器及其复用对FC的清除无显著差异。结论 透析中丢失是MHD患者肉碱缺乏的重要原因。应用不同透析器及其复用对FC清除无明显影响。  相似文献   

17.
The purpose of this study was to assess whether there are any differences in postprandial physiological responses to skim milk powder enriched with milk calcium (SMP + milk calcium) and skim milk powder enriched with calcium carbonate (SMP + CaCO3), with each of the milks providing 1200 mg calcium. This was a randomised, controlled, crossover study involving 16 men and 29 women over 55 years of age. Measurements of calcium and bone metabolism were taken after an overnight fast before each drink, and postprandially every hour for 8 h. The impact of time and drink on the responses was analysed by repeated measures of analysis of variance. Serum calcium was significantly higher between 2 and 8 h after consumption of SMP + CaCO3 compared with SMP + milk calcium (P < 0.0001). Serum phosphate was significantly higher between 2 and 5 h after drinking the SMP + milk calcium compared with SMP + CaCO3 (P < 0.0001). The level of parathyroid hormone (PTH) was virtually unchanged after consumption of SMP + milk calcium, but decreased between 1 and 4 h after SMP + CaCO3 (P = 0.02). The serum C-telopeptide level, a marker of bone resorption, was significantly lower after SMP + CaCO3, compared with SMP + milk calcium, between 4 and 8 h after drinking the milk (P < 0.05). We conclude that serum calcium levels have a higher increase after SMP + CaCO3 consumption than after SMP + milk calcium consumption, and that this is associated with lower serum PTH concentrations and a more prolonged postprandial decrease in bone resorption.  相似文献   

18.
BACKGROUND: Increased dietary calcium is associated with changes in body composition. One proposed mechanism is that dietary calcium increases fat oxidation, potentially via regulation of serum parathyroid hormone (PTH) concentrations. OBJECTIVES: The objectives of the study were to determine whether acute or chronic increased dairy calcium intakes alter postprandial whole-body fat oxidation and whether the increased intake is related to changes in PTH concentrations. DESIGN: Normal-weight women aged 18-30 y were randomly assigned to a low (<800 mg/d, control; n = 10) or high (1000-1400 mg/d; n = 9) dietary calcium intake group for 1 y. Whole-body fat oxidation was assessed by measuring respiratory gas exchange after each subject consumed 2 isocaloric liquid meals containing 100 or 500 mg Ca at baseline and 1 y. Fasting serum PTH was measured at baseline and 1 y. RESULTS: The mean 1-y change in fat oxidation was higher in the high-calcium group than in the low-calcium control group after a low-calcium meal (0.10 +/- 0.05 compared with 0.005 +/- 0.04 g/min; P < 0.001) and a high-calcium meal (0.06 +/- 0.05 compared with 0.03 +/- 0.04 g/min; P < 0.05). The 1-y change in serum log PTH was negatively associated with the 1-y change in postprandial fat oxidation after a high-calcium meal (partial r = -0.46, P < 0.04) when controlled for the1-y change in total body fat mass. CONCLUSIONS: The results suggest that a chronic diet high in dairy calcium increases whole-body fat oxidation from a meal, and increases in fasting serum PTH relate to decreases in postprandial whole-body fat oxidation.  相似文献   

19.
目的 了解青春期儿童维生素D(VD)水平状况及其影响因素,分析导致VD不足的原因,为后续研究和防治提供科学依据。方法 2015-2016年随机抽取哈尔滨市某城区某中学603名6~8年级11~17岁青春期儿童进行体格检查、问卷调查及实验室检测血清25(OH)D、甲状旁腺素(PTH)、钙(Ca)、磷(P)和碱性磷酸酶(ALP)的水平。结果 603名青春期儿童血清25(OH)D的中位数和四分间距位数为14.16 (10.68, 18.46)ng/ml,VD不足和缺乏占81.1%。血清PTH、Ca、P、ALP水平分别为42.7(31.90, 60.70)pg/ml、(2.47±0.13) mmol/L、(1.57±0.21) mmol/L、(275.23±127.60) U/L。血清25(OH)D与PTH水平和ALP水平之间呈负相关(r=-0.039、-0.141,P<0.001),与Ca呈正相关(r=0.312,P<0.001),与P无明显相关性。PTH和25(OH)D为对数关系,当PTH达到最大抑制状态时无25(OH)D拐点值。户外活动时间、补充VD制剂与血清25(OH)D水平呈正相关(P趋势<0.001),户外活动时间、VD制剂的补充是青春期儿童VD水平的重要影响因素。结论 11~17岁青春期儿童VD缺乏情况普遍存在。血清PTH、ALP和Ca,这些指标的测定有助于评价青春期儿童VD水平状况,建议通过鼓励青春期儿童增加户外活动,补充VD制剂等手段,可以提高血清25(OH)D水平。  相似文献   

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