Calcium
Hypercalcemia
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Hypercalcemia
, High Serum Calcium, Serum Calcium Elevation, Hypercalcemic Crisis
See Also
Serum Calcium
Hyperparathyroidism
Familial Benign Hypocalciuric Hypercalcemia
Hypercalcemia of Malignancy
Calcium Homeostasis
Causes
Gene
ral
Most common causes of Hypercalcemia
Malignancy
Primary Hyperparathyroidism
Malignancy
See
Hypercalcemia of Malignancy
(mediated by PTH-Related peptide)
Presents with rapid onset, low PTH Levels and weight loss,
Night Sweats
Breast Cancer
with bone metastases
Squamous Cell Lung Cancer
Head and Neck squamous cell cancer
Renal Cell Cancer
Esophageal Cancer
Skin Cancer
Hematologic
Multiple Myeloma
Hodgkin's Lymphoma
Paget's Disease of Bone
Medications
Thiazide Diuretic
s
Lithium
Vitamin A Toxicity
Vitamin D Toxicity
(e.g. 25-Hydroxyvitamin D2)
Milk Alkali Syndrome
Theophylline
Synthetic PTH (
Teriparatide
,
Abaloparatide
)
Hyperparathyroidism
(PTH Dependent
Hyperparathyroidism
)
Primary Hyperparathyroidism
(most common cause)
Multiple Endocrine Neoplasia
(type 1 or 2A)
Familial Hypocalciuric Hypercalcemia
Lithium
treatment
Chronic Kidney Disease
(
Renal Osteodystrophy
)
Hyperparathyroidism
- Jaw Tumor Syndrome
Endocrine
Vitamin D Deficiency
(Secondary
Hyperparathyroidism
)
Adrenal Insufficiency
Thyrotoxicosis
(
Hyperthyroidism
)
Pheochromocytoma
Acromegaly
Other causes
Familial Hypocalciuric Hypercalcemia
Prolonged immobilization
Granuloma
tous disease (
Sarcoidosis
,
Tuberculosis
,
Histoplasmosis
,
Coccidioidomycosis
)
Williams Syndrome
Jansen Disease (metaphyseal chondrodysplasia)
Findings
Symptoms and Signs
Often asymptomatic
Symptoms and Signs are related to
Serum Calcium
Levels
Calcium
> 11.5 mg/dl (2.9 mmol/L)
Symptom onset
Calcium
> 13 mg/dl (3.2 mmol/L)
Nephrocalcinosis
Acute Renal Failure
Calcium
>14 mg/dl (3.5 mmol/L)
Severe Hypercalcemia (or
Parathyroid
crisis)
Cardiovascular
Chest Pain
Dyspnea
Palpitation
s
Syncope
Hypertension
Bradycardia
Gastrointestinal
Anorexia
Constipation
Epigastric Pain
or other
Abdominal Pain
Dyspepsia
Nausea
Vomiting
Pancreatitis
Renal
Polydipsia
Polyuria
Renal Colic
or
Flank Pain
Renal Failure
Neurologic
Anxiety
Confusion,
Delirium
Decreased Concentration
Memory Loss
Headache
Fatigue
Lethargy
Weakness
Psychiatric
Anxiety
Depressed Mood
Emotional lability
Musculoskeletal
Bone pain
Arthralgia
s
Myalgias
Pathologic
Fracture
s
Skin
Pruritus
(Metastatic calcification of skin)
Complications
Stones, Bones, Moans, Psychic Groans
Renal ("Stones")
Nephrolithiasis
(
Calcium
Oxalate)
Nephrocalcinosis
Metastatic calcification renal tubules
Polyuria
from loss of urine concentrating function
Musculoskeletal ("Bones")
Osteitis fibrosa cystica (Late finding)
Bone cysts from subperiosteal bone resorption
"Brown tumor" in jaw
Pseudogout
Calcium
pyrophosphate - Positively birefringent
Osteoporosis
Gastrointestinal ("Abdominal Moans")
Peptic Ulcer Disease
Calcium
stimulates
Gastrin
release
Acute Pancreatitis
Calcium
activates phospholipases
Constipation
Most common gastrointestinal symptom
Neuropsychiatric ("Psychic groans")
Altered Level of Consciousness
or
Delirium
Decreased concentration and memory
Personality change
Psychosis
Major Depression
Eye
Band Keratopathy (
Cornea
l calcification)
Metastatic calcification in eye limbus
Cardiovascular
Cardiac Arrhythmia
Diastolic Dysfunction
Hypertension
Hypercalcemia
Vasocon
stricts vessels
Imaging
Calcified soft tissues
Labs
Serum Calcium
Total
Serum Calcium
increased
Hypercalcemia: Total
Serum Calcium
> 10.5 mg/dl
Severe Hypercalcemia (Hypercalcemic Crisis):
Serum Calcium
>14 mg/dl (>3.50 mmol/L)
Confirmatory
Ionized Calcium
>5.6 mg/dl or
Corrected Serum Calcium
increased (corrected for
Serum Albumin
)
Labs
Hypercalcemia Evaluation
First-line
Parathyroid Hormone
25-Hydroxyvitamin D
Serum Magnesium
Serum Creatinine
Second-line: PTH level normal or high (PTH-dependent Hypercalcemia)
Urine Calcium to Creatinine Ratio
Decreased <0.01 in
Familial Hypocalciuric Hypercalcemia
Increased >0.01 in
Primary Hyperparathyroidism
, Hypercalcemia or Malignancy,
MEN I
Second-line: PTH level <20 pg/ml (PTH-independent Hypercalcemia)
Parathyroid Hormone
-related Peptide (PTHrp) increased
Hypercalcemia of Malignancy
Consider broad evaluation for malignancy
Complete Blood Count
Liver Function Test
s
Chest XRay
Chest
CT and
Abdominal CT
Protein
electrophoresis (
SPEP
and UPEP)
Bone Scan
Mammogram
1,25 Dihydroxyvitamin D increased
Lymphoma
Granuloma
(e.g.
Sarcoidosis
)
25-Hydroxyvitamin D (Calcitriol) increased
Vitamin D Toxicity
Diagnostics
Electrocardiogram
Short
QT Interval
Prolonged PR Interval
Wide
QRS Complex
Bradycardia
Evaluation
Gene
ral
Primary Hyperparathyroidism
and
Hypercalcemia of Malignancy
: 90% of cases
Step 1: Confirm Hypercalcemia present (see labs above)
Confirm Hypercalcemia with
Ionized Calcium
>5.6 mg/dl or
Corrected Serum Calcium
>10.5 mg/dl
Immediate management for symptomatic or severe Hypercalcemia (
Serum Calcium
>14 mg/dl)
See protocol below
Step 2: Obtain history for potential causes
See causes above
Perform history (including diet, medications) and exam
Consider
Renal Osteodystrophy
Eliminate potential causative medications (
Thiazide Diuretic
s,
Lithium
)
Step 3: Obtain intact
Parathyroid Hormone
(PTH) Level
PTH low: Go to Step 4
PTH normal or high (PTH-Dependent Hypercalcemia)
Labs
Urine Calcium to Creatinine Ratio
(
24 hour Urine Calcium
and
Urine Creatinine
)
Serum Creatinine
Bone Mineral Density
25-Hydroxyvitamin D
Urine Calcium to Creatinine Ratio
<0.01
Familial Benign Hypocalciuric Hypercalcemia
(
FBHH
)
Urine Calcium to Creatinine Ratio
normal or high
Causes
Primary Hyperparathyroidism
Recovery from
Acute Tubular Necrosis
Lithium
Multiple Endocrine Neoplasia Type I
(
MEN I
)
Parathyroid
carcinoma (severe Hypercalcemia and very high PTH)
Approach
Consult Endocrinology
Exclude
Multiple Endocrine Neoplasia Type I
(
MEN I
)
Manage
Primary Hyperparathyroidism
Medical management of
Primary Hyperparathyroidism
Parathyroid
ectomy if symptomatic, age <50, complications (e.g. renal)
Step 4: PTH-Independent Hypercalcemia
Assess for malignancy and endocrinopathy
Careful history and examination for tumor
Initial Labs
Parathyroid Hormone
-related Peptide (PTHrp)
Increased in solid tumors (see
Hypercalcemia of Malignancy
)
Consider broad evaluation for malignancy
Complete Blood Count
Liver Function Test
s
Chest XRay
Chest
CT and
Abdominal CT
Protein
electrophoresis (
SPEP
and UPEP)
Bone Scan
Mammogram
1,25-dihydroxyvitamin D (Calcitriol) increased
Obtain chest imaging (
Chest XRay
or
Chest
CT)
Causes
Lymphoma
Granuloma
tous Disease (
Sarcoidosis
,
Tuberculosis
,
Histoplasmosis
,
Coccidioidomycosis
)
25-Hydroxyvitamin D Level increased
Vitamin D Toxicity
Other Labs to consider
Alkaline Phosphatase
: Increased with bone lysis
Consider bone scan
Protein
electrophoresis (
SPEP
and UPEP)
Monoclonal peak in
Multiple Myeloma
Endocrine Labs
Thyroid Stimulating Hormone
(
Hyperthyroidism
)
Corticotropin Stimulation Test
(
Addison's Disease
)
Insulin
-like Growth Factor 1 (
Acromegaly
)
Reconsider medication causes of low PTH
Thiazide Diuretic
s
Vitamin D Toxicity
Vitamin A Toxicity
Milk-Alkali Syndrome
Aluminum
Intoxication
Management
Identify and treat underlying cause
Mild Hypercalcemia (
Serum Calcium
<12 mg/dl)
Adequate Hydration (>2 Liters per day)
Maximize mobility
Diuretic
s if symptomatic
Furosemide
(
Lasix
) 40-160 mg/day
Severe Hypercalcemia or Hypercalcemic Crisis (
Serum Calcium
>14 mg/dl, >3.50 mmol/L)
Consider also in moderate symptomatic Hypercalcemia
Normal Saline
2 to 4 Liters/day for 1-3 days
Adjust to obtain 200 ml
Urine Output
per hour
Exercise
caution in
Congestive Heart Failure
Anticipate 1-3 mg/dl drop in
Serum Calcium
Additional measures if refractory after hydration
Furosemide
(
Lasix
) 10-20 mg every 1-2 hours as needed
Most effective agent in
Calcium
elimination
Calcitonin
4-8 IU/kg IM or SQ every 6 hours for 24 hours (up to 48 hours)
Rapid onset, but weakest of the agents (do not use as monotherapy)
Agents with specific indications
Malignancy:
Bisphosphonates
Zoledronic acid (Zometa) 4 mg IV over 15 minutes
Pamidronate
(
Aredia
) 60-90 mg IV over 4 hours
Vitamin D Toxicity
,
Lymphoma
,
Myeloma
or
Granuloma
Hydrocortisone
200 mg IV qd for 3 days
Other measures
Oral Phosphate (Neutra-Phos) 250 mg PO q6 hours
Denosumab
Hu (2014) J Clin Endocrinol Metab 99(9):3144-52 +PMID: 24915117 [PubMed]
Eremkina (2020) Endocr Connect 9(10):1019-27 +PMID: 33112830 [PubMed]
Third line agents due to toxicity (avoid if possible)
Plicamycin 10-25 mcg/kg/day IV over 6 hours x3 dose
Cumulative liver,
Kidney
and
Platelet
toxicity
Bisphosphonates
are preferred over Plicamycin
Gallium Nitrate (Ganite)
Dose: 100-200 mg/m2 IV over 24 hours for 5 days
Significant renal and
Bone Marrow
toxicity
Refractory Cases
Hemodialysis
Loh (2014) Case Rep Crit Care +PMID: 24829837 [PubMed]
Prognosis
Hypercalcemia of Malignancy
suggests terminal stages
Implies
Life Expectancy
of days to weeks
References
Gibbs in Marx (2002) Rosen's Emergency Med, p. 1734-6
Spiegel in Goldman (2000) Cecil Medicine, p. 1400-2
Carroll (2003) Am Fam Physician 67(9):1959-66 [PubMed]
Michels (2013) in Am Fam Physician 88(4): 249-57 [PubMed]
Minisola (2015) BMJ 350: h2723 [PubMed]
Sell (2022) Am Fam Physician 105(3): 289-98 [PubMed]
Suliburk (2007) Oncologist 12(6): 644-53 [PubMed]
Ziegler (2001) J Am Soc Nephrol 12 Suppl 17:S3-9 [PubMed]
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