Patient Scenario: Hypoparathyroidism, desired phosphate and hypercalcemia
Assessing the Clinical and Laboratory Parameters
Was there a prior parathyroidectomy. Low or undetectable PTH levels are an expected finding. Are parathyroids intact (or partially resected/reimplanted during prior PT surgery)?
- PTH secretion is suppressed secondary to hypercalcemia and/or use of vitamin D analogues;
- PT gland may remain sensitive to ambient ionized calcium, i.e. is not autonomous
Less than 1% of all patients are in this category.
- Dialysis Prescription
- Phosphate and Calcium Management
- PTH Management
- Other Options of Controversies in Management
- Suggested References
Lowering dialysis calcium from 1.25 to 1.0 mmol/L may temporarily alleviate the hypercalcemia, and restore PTH secretion.
Phosphate and Calcium Management
Phosphate and Calcium Management
Dietary phosphate control, and adherence to prescribed dose of binder is successful.
Therapeutic avenues include:
- Lower dose of calcium-based phosphate binder
- Switch to non-calcium based phosphate binder
However, if taking calcium based binder, the dose may be excessive.
a) lower dose of calcium-based binder (may adversely affect Pi control)
b) switch to non-calcium based phosphate binder, either aluminum in the short term, or sevelamer/lanthanum in the long term
c) if taking aluminum-based binders, discontinue and check serum aluminum levels – aluminum intoxication includes hypercalcemia and toxic effects on PTH secretion
Suggested Guidelines include
5. Give priority to phosphate and calcium targets over the management of PTH. (Grade D, opinion)
7. Vitamin D sterols can be used in the treatment of secondary hyperparathyroidism, but should be discontinued when PTH levels decrease below target levels, or if calcium or phosphate levels increase above target levels. (Grade C)
4.1.5 In patients with CKD stages 3–5D and hyperphosphatemia, we recommend restricting the dose of calcium-based phosphate binders and/or the dose of calcitriol or vitamin D analog in the presence of persistent or recurrent hypercalcemia (1B). In patients with CKD stages 3–5D and hyperphosphatemia, we suggest restricting the dose of calcium based phosphate binders in the presence of arterial calcification (2C) and/or adynamic bone disease (2C) and/or if serum PTH levels are persistently low (2C).
4.1.6 In patients with CKD stages 3–5D, we recommend avoiding the long-term use of aluminum-containing phosphate binders and, in patients with CKD stage 5D, avoiding dialysate aluminum contamination to prevent aluminum intoxication (1C).
Vitamin D Sterols
Lower dose of vitamin D analogue; Active 1-hydroxylated vitamin D sterols (calcitriol, 1-alpha) cause direct suppression of PTH. In the absence of severe parathyroid bone disease (usually indicated by very high PTH levels and high serum (bone) alkaline phosphatase), hypercalcemia results from excessive calcium absorption from diet and calcium supplements.
- Therapeutic avenues are based on lowering the effective dose;
- Switch from daily to alternate day, (night-time) oral dosing.
- Switch to intravenous dosing on dialysis 3- or 2- times weekly
- Switch to an analogue with potentially less calcemic action (doxercalciferol, 10-30 µg p.o. 2-3 times weekly)
Lower dose of calcimimetic; over suppression of parathyroid glands with a calcimimetic is possible; hypercalcemia with normal Pi control is less consistent with this diagnosis
- Modify calcium-based phosphate binder, and vitamin D dose first.
- Reduce the dose of calcimimetic to maintain serum intact PTH levels between 10-50 pmol/ L
Other Options of Controversies in Management
Other Options of Controversies in Management
There is a clear epidemiologic association and biological plausibility between hyperphosphatemia, net calcium intake and important negative health consequences (including progressive vascular calcification and cardiovascular morbidity) for patients with CKD. However, randomized controlled trials and meta-analyses performed to date do not conclusively support the use of one type of phosphate binder in preference to another for important patient outcomes.
Specifically, controversy exists as to the efficacy of non-calcium based phosphate binders (i.e. sevelamer and lanthanum) on relevant clinical outcomes (cardiovascular events, mortality and hospitalization). The evidence to date was summarized in detail by the KDIGO working group. Given some significant methodological limitations and therefore concerns over study validity for the largest trials of non-calcium phosphate binders, the impact of non-calcium based binders on clinically relevant outcomes is uncertain.
Non-calcium based phosphate binders are more than twenty-fold more expensive than calcium carbonate. The recommendation by KDIGO to limit the use of calcium-based binders in the scenarios outlined (and presumably use noncalcium based binders) has generated significant controversy among Canadian nephrologists and there is no clear consensus. On the one hand the lack of conclusive evidence of benefit, the lack of randomized trials which have assessed morbidity and mortality among patients with vascular calcification, and the expense of sevelamer and lanthanum, use of these agents may not be justified until further evidence of clinical benefit can be established in valid randomized trials. On the other hand, others feel that the use of noncalcium-based binders in the situations recommended or suggested by KDIGO is justified on theoretical grounds, that the existing RCTs were underpowered to show statistically significant benefit, and that recent meta-analyses suggest clinical benefit. Moreover, calcium-based phosphate binders are likely to cause positive calcium balance in late stages of CKD, and have never been proven to be safe.
The use of aluminum-containing phosphate binders has been extensively evaluated in the KDOQI Bone and Mineral Metabolism Guidelines. The major toxicities are neurotoxicity and impairment of bone mineralization, both of which can be prevented by minimizing aluminum exposure. The KDIGO Work Group acknowledged that the literature, as detailed in the KDOQI guidelines, supports that the most severe cases of aluminum toxicity occurred in patients whose dialysate was contaminated with aluminum, and that aluminum-based binders only play a secondary role. The quantity of aluminum-based phosphate binders that is safe is unknown. Moreover, several conditions may favor intestinal aluminum absorption, such as diabetes mellitus, secondary HPT, vitamin D status, and a high citrate intake. The Work Group was unanimous in recommending against the use of aluminum-based binders on the grounds that there is no ability to predict a safe aluminum dose, and numerous alternative phosphate binders have become available. However, Canadian nephrologists may still feel that short-term (several months) use of these agents is still justified when financial constraints make it impractical to use other non-calcium-based binders.
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