What is the recommended level of intact parathyroid hormone (iPTH) among dialysis patients?

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Recommended iPTH Level for Dialysis Patients

The target intact PTH (iPTH) level for dialysis patients should be maintained between 150-300 pg/mL (16.5-33.0 pmol/L), with treatment initiated when iPTH exceeds 300 pg/mL. 1

Target Range and Treatment Thresholds

For hemodialysis and peritoneal dialysis patients:

  • Target range: 150-300 pg/mL (16.5-33.0 pmol/L) 1
  • Treatment threshold: iPTH >300 pg/mL (33.0 pmol/L) requires active vitamin D sterol therapy 1
  • Lower safety limit: iPTH <100 pg/mL (11.0 pmol/L) indicates adynamic bone disease risk 1, 2

The K/DOQI guidelines explicitly state that patients with iPTH >300 pg/mL should receive active vitamin D sterols (calcitriol, alfacalcidol, paricalcitol, or doxercalciferol) to reduce PTH to the 150-300 pg/mL target range. 1

Rationale for This Range

The 150-300 pg/mL target represents 2-4 times the upper limit of normal to account for PTH resistance in uremic patients. 3 This range balances two critical risks:

  • iPTH <150 pg/mL: Associated with low-turnover/adynamic bone disease, which impairs the skeleton's ability to buffer calcium and phosphorus loads, leading to vascular calcification 1, 2
  • iPTH >300 pg/mL: Associated with high-turnover bone disease (osteitis fibrosa) and progressive secondary hyperparathyroidism 1

Cardiovascular Disease Prevention

For cardiovascular disease prevention specifically, the target PTH should be 150-300 pg/mL. 1 This recommendation integrates bone disease management with cardiovascular risk reduction, as both excessively low and high PTH levels are associated with increased mortality and major adverse cardiac events. 4

Important Caveats and Clinical Nuances

The K/DOQI Target May Be Too Low

Critical limitation: Research demonstrates that 88% of patients achieving the K/DOQI target range (150-300 pg/mL) had low-turnover bone disease on biopsy. 5 This suggests the recommended range may be associated with oversuppression and adynamic bone disease in clinical practice. 5

Low PTH carries significant mortality risk: Patients with time-averaged iPTH <65 pg/mL have a 2-fold increased risk of overall mortality (HR=2.06) and 1.8-fold increased risk of major adverse cardiac and cerebrovascular events (HR=1.82) compared to those with iPTH 65-300 pg/mL. 4

Severity-Based Considerations

Disease severity affects treatment response: 6

  • Mild disease (iPTH 300-500 pg/mL): 60% achieve target with treatment 7
  • Moderate disease (iPTH 500-800 pg/mL): 41% achieve target 7
  • Severe disease (iPTH >800 pg/mL): Only 11% achieve target; may require parathyroidectomy if iPTH persistently >800 pg/mL with refractory hypercalcemia/hyperphosphatemia 1, 7

Monitoring Protocol

When initiating or adjusting vitamin D therapy: 1, 2

  • Calcium and phosphorus: Every 2 weeks for 1 month, then monthly 1, 2
  • iPTH: Monthly for at least 3 months, then every 3 months once target achieved 1, 2, 8

Treatment must be held if: 2, 8

  • Corrected calcium >9.5 mg/dL 2, 8
  • Phosphorus >4.6 mg/dL 2, 8
  • iPTH falls below 150 pg/mL (resume at 50% dose when iPTH rises above target) 2, 8

Practical Algorithm for PTH Management

Step 1 - Assess iPTH level:

  • <100 pg/mL: Hold/reduce vitamin D and calcium-based binders; allow PTH to rise 1, 2
  • 100-150 pg/mL: Monitor closely; consider reducing vitamin D dose 2
  • 150-300 pg/mL: Target range; maintain current therapy 1
  • 300-800 pg/mL: Initiate/increase vitamin D sterols 1
  • >800 pg/mL: Consider parathyroidectomy if refractory to medical therapy 1

Step 2 - Verify calcium and phosphorus are controlled before treating elevated PTH:

  • Calcium must be <9.5 mg/dL 2, 8
  • Phosphorus must be <4.6 mg/dL 2, 8

Step 3 - Select appropriate vitamin D sterol:

  • Hemodialysis: Intravenous calcitriol preferred (more effective than oral) 1
  • Peritoneal dialysis: Oral calcitriol 0.5-1.0 μg or doxercalciferol 2.5-5.0 μg, 2-3 times weekly 1, 8
  • If hypercalcemia/hyperphosphatemia present: Consider paricalcitol or doxercalciferol (less calcemic) 1

Common Pitfalls to Avoid

Oversuppression is more dangerous than previously recognized. The evidence shows that achieving the lower end of the K/DOQI target range frequently results in adynamic bone disease. 5 In clinical practice, aim for the middle-to-upper portion of the 150-300 pg/mL range rather than aggressively targeting the lower end. 5, 4

Do not treat elevated PTH when calcium or phosphorus are uncontrolled. This leads to dangerous calcium-phosphorus product elevation and vascular calcification. 2, 8 Always optimize phosphate binders and dietary restriction first. 1

Recognize that iPTH alone may not accurately reflect bone turnover status. Bone biopsy remains the gold standard, though impractical for routine use. 1, 5 When iPTH is in the target range but clinical suspicion exists for adynamic bone (low alkaline phosphatase, hypercalcemia), consider holding vitamin D therapy. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Mineral Bone Disease in Hemodialysis Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Relationship between intact 1-84 parathyroid hormone and bone histomorphometric parameters in dialysis patients without aluminum toxicity.

American journal of kidney diseases : the official journal of the National Kidney Foundation, 1995

Research

Low serum intact parathyroid hormone level is an independent risk factor for overall mortality and major adverse cardiac and cerebrovascular events in incident dialysis patients.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2016

Guideline

Vitamin D Treatment in End-Stage Kidney Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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