
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Hypoparathyroidism medical therapy
Introduction
Overview
Overview
Pharmacologic medical therapies for hypoparathyroidism include calcium and Vitamin D3 supplementation. Severe hypocalcemia, a potentially life-threatening condition, is treated as soon as possible with intravenous calcium (e.g. as calcium gluconate). Generally, a central venous catheter is recommended, as the calcium can irritate peripheral veins and cause phlebitis. Natpara (rhPTH) is a synthetic recombinant human parathyroid hormone approved by U.S. FDA in 2015 for treatment of hypoparathyroidism.
Medical Therapy
Medical Therapy
- Pharmacologic medical therapies for hypoparathyroidism include calcium and Vitamin D3 supplementation.[1]
- Severe hypocalcemia, a potentially life-threatening condition, is treated as soon as possible with intravenous calcium (e.g. as calcium gluconate).
- Generally, a central venous catheter is recommended, as the calcium can irritate peripheral veins and cause phlebitis.
Hypoparathyroidism
Management guidelines for hypoparathyroidism are as follows:
- 1 Management of Acute hypocalcemia
- Note(1): IV calcium used for marked hypocalcemia (<7.0 mg/dL), hypocalcemia associated with signs and symptoms, and if patients unable to take or absorb oral calcium supplements.
- 1.1 Intravenous calcium supplementation
- Preferred regimen (1): Calcium gluconate 1 to 2 g in 50 mL of 5% dextrose over 10-20 minutes initially followed by maintenance by 50 – 100 mg/hour.
- Note(1): 10% calcium gluconate is used which contains 90 mg of elemental calcium per 10 mL.
- Note(2): 1 mg/mL solution of elemental calcium is prepared as follows: Add 11 g of calcium gluconate (110 mL ) to 890 mL normal saline or 5% dextrose water making a final volume of 1000 mL. 11 g of calcium gluconate contains 990 mg of elemental calcium.
- Note(3): Rapid infusion of calcium gluconate should not be used as it carries serious risk of cardiac dysfunction, including systolic arrest.
- 1.2 Parenteral vitamin D therapy
- Preferred regimen (1): Calcitriol 0.25 to 0.5 μg q12h
- 1.3 Intravenous Magnesium supplementation (in case of hypomagnesia)
- Preferred regimen (1): Magnesium sulfate 2g (16mEq) as 10% solution, infused over 10 -20 minutes initially, followed by 1g (8 mEq) in 100 mL infused over an hour.
- 2 Conventional therapy for hypoparathyroidism
- 2.1 Oral calcium
- Preferred regimen (1): Calcium carbonate (40% elemental calcium) (better absorption with meals)
- Alternative regimen (1): Calcium citrate (21% elemental calcium) (more effective in patients with achlorhydria and proton pump inhibitors use, worsening constipation)
- 2.2 Vitamin D supplementation
- Preferred regimen (1): Calcitriol 0.25 to 2 μg q24h (>.75 μg administered in divided doses)
- Preferred regimen (2): Cholecalciferol (parent vitamin D3)
- Preferred regimen (3): Ergocalciferol (parent vitamin D2)
- Alternative regimen (1): 1α-Hydroxyvitamin D (alfacalcidol) (used outside the United States)
- Alternative regimen (2): Dihydrotachysterol (used outside the United States)
- Note(1): Serum calcium (corrected for albumin), phosphorus, and creatinine concentrations should be measured weekly to monthly during dose adjustments, and twice annually once a stable regimen has been reached.
- Note(2): 24 Hour urinary calcium and creatinine should be considered during dose adjustments and should be measured twice annually on a stable regimen to evaluate for renal toxicity.
- 2.1 Oral calcium
- 3 Adjunctive Treatments
- 3.1 Diuretics
- 3.1.1 Thiazides
- Preferred regimen (1): Hydrochlorothiazide 25–50 mg q12h (minimum 25 mg to maximum 100 mg)
- Alternative regimen (1): Chlorthalidone
- Note(1): Thiazide diuretics are not advised in congenital hypoparathyroidism due to autoimmune polyendocrine syndrome type 1 in patients who have concurrent Addison’s disease or in autosomal dominant hypocalcemia.
- 3.1.2 Potassium sparing diuretics
- Alternative regimen (1): Amiloride 2.5 to 5 mg q12h
- 3.1.1 Thiazides
- 3.2 Treatment of hyperphoshatemia
- Preferred regimen (1): Low phosphate diet
- Preferred regimen (2): Phosphate binders
- 3.3 PTH replacement
- 3.1 Diuretics
References
References
- ↑ Bilezikian JP, Brandi ML, Cusano NE, Mannstadt M, Rejnmark L, Rizzoli R, Rubin MR, Winer KK, Liberman UA, Potts JT (2016). “Management of Hypoparathyroidism: Present and Future”. J. Clin. Endocrinol. Metab. 101 (6): 2313–24. doi:10.1210/jc.2015-3910. PMC 5393596. PMID 26938200.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Anmol Pitliya, M.B.B.S. M.D.[2]
