Specialist Referral for Primary Hyperparathyroidism
Patients with confirmed primary hyperparathyroidism (PHPT) should be referred to both an endocrinologist for medical management and a high-volume parathyroid surgeon for surgical evaluation. 1, 2, 3
Initial Referral to Endocrinology
The endocrinologist plays a critical role in confirming the diagnosis, excluding secondary causes, and determining surgical candidacy. 1, 2
Key responsibilities of the endocrinologist include:
- Confirming PHPT by measuring serum calcium (corrected for albumin) and intact PTH simultaneously, ensuring PTH is elevated or inappropriately normal in the setting of hypercalcemia 1, 2, 3
- Excluding vitamin D deficiency (target 25-OH vitamin D >20 ng/mL or 50 nmol/L) before finalizing the diagnosis, as deficiency causes secondary hyperparathyroidism that mimics PHPT biochemically 4, 2, 3
- Assessing dietary calcium intake through detailed history, as calcium deprivation can produce similar biochemical findings 4
- Evaluating for surgical indications including: corrected calcium >1 mg/dL (0.25 mmol/L) above upper limit of normal, age <50 years, impaired kidney function (GFR <60 mL/min/1.73 m²), osteoporosis (T-score ≤-2.5), history of nephrolithiasis or nephrocalcinosis, or hypercalciuria (>300 mg/24hr) 1, 2, 3
Important caveat: PTH assays vary significantly between laboratories—measurements can differ by up to 47% between different assay generations—so always use assay-specific reference values when interpreting results. 1, 3 PTH is more stable in EDTA plasma than serum and should be measured at least 12 hours after any previous dose if the patient is on treatment. 1, 3
Referral to High-Volume Parathyroid Surgeon
All patients meeting surgical criteria should be referred to an experienced, high-volume parathyroid surgeon (not just any general surgeon), as outcomes are significantly better with specialized expertise. 1, 5
The surgical referral is appropriate when:
- Any of the surgical indications listed above are met 1, 2, 3
- The patient has symptomatic disease (renal symptoms, bone disease, gastrointestinal complaints, psychiatric symptoms, or fatigue), even if biochemical values are only mildly elevated 6, 5, 7
- Hypercalcemia persists despite medical optimization 3
Critical pitfall to avoid: Do not delay surgical referral for years while attempting medical management in patients who meet surgical criteria. Studies show 24% of patients experience delays exceeding 2 years between diagnosis and surgery, during which time they develop severe complications including renal disease, osteoporosis, and psychiatric symptoms. 6 Even patients with "asymptomatic" PHPT often have vague nonspecific complaints that improve dramatically after parathyroidectomy. 5
Special Consideration: Normal or Low-Normal PTH
Patients with hypercalcemia and PTH in the normal range (even as low as 40 pg/mL) can still have PHPT—the PTH is "inappropriately normal" for the degree of hypercalcemia. 1, 7, 8 These patients are typically younger, more symptomatic, and have higher rates of multiglandular disease (59% vs 32%). 8 They should still be referred to endocrinology and surgery, as cure rates are similar (97%) to those with elevated PTH. 7, 8
Medical Management for Non-Surgical Candidates
If parathyroidectomy is contraindicated or the patient refuses surgery, the endocrinologist manages with:
- Cinacalcet (calcimimetic) starting at 30 mg twice daily, titrated to normalize serum calcium 9
- Maintaining normal calcium intake (1000-1200 mg/day, not exceeding 2000 mg/day total) 3
- Ensuring adequate vitamin D (>20 ng/mL) with supplementation if needed 2, 3
- Monitoring serum calcium monthly initially, then every 2 months once stable 9
Important limitation: Cinacalcet is FDA-approved for hypercalcemia in primary HPT only when parathyroidectomy would be indicated based on serum calcium levels but the patient is unable to undergo surgery. 9 It is not a substitute for appropriate surgical referral in surgical candidates.
Coordination Between Specialists
The endocrinologist and surgeon should work collaboratively, with the endocrinologist optimizing vitamin D status and calcium levels preoperatively, and the surgeon performing preoperative localization imaging (ultrasound and/or 99mTc-sestamibi SPECT/CT) only after biochemical diagnosis is confirmed. 2, 3 Never order parathyroid imaging before confirming the biochemical diagnosis—imaging is for surgical planning, not diagnosis. 3
For patients with suspected hereditary syndromes (MEN 2A, MEN 2B, or hyperparathyroid-jaw tumor syndrome), genetic counseling and germline testing should be considered, with management coordinated between endocrinology, surgery, and genetics. 1