hypercalcemia
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HypercalcemiaAhmed ElshebinyAhmed Elshebiny
University of MenoufyiaUniversity of Menoufyia
Case : History A 41-year-old woman was brought by her
husband to the emergency department with a history of 72 hours of epigastric pain, nausea, repeated vomiting, and altered mental status. Her blood calcium was found to be 18.9 mg per deciliter (4.7 mmol per liter).
Alcoholic, peptic ulcer, analgesics for back pain
Examination On physical examination, the blood pressure was 160/90 mm Hg, the heart rate 100 beats per minute, and the temperature 37.4°C. The patient was disoriented and intermittently writhing in pain. Her skin turgor was poor, and her oral mucosa was dry. The cardiac examination was significant only for tachycardia, and the pulmonary examination was normal. There was epigastric tenderness on palpation but no rebound
tenderness. The patient was responsive to simple commands and was not
tremulous. There were no other significant neurologic findings.
Investigations
Specific investigations Intact parathyroid= undetectable 25 hydroxy vitamin D = normal PTH related protein= normal Calcium fall with hydration only
Computed tomography (CT) of the neck revealed no parathyroid masses. CT of the chest was normal. Abdominal CT showed an edematous pancreas with surrounding infiltration of the mesenteric fat, a finding consistent with acute pancreatitis. No bone lesions were noted on the chest or abdominal CT scans.
Diagnosis In response to further questioning, the patient
reported that during the days before admission she had consumed the contents of entire containers of Tums and a preparation containing sodium bicarbonate (Alka-Seltzer, Bayer) because of the severe abdominal pain. She did not consume any other medications or supplements.
This history, together with the laboratory-test results, establishes the "milk alkali syndrome" as the primary diagnosis
Milk Alkali Syndrome The pathogenesis of the milk alkali syndrome involves a reduction in the
ability of the kidney to excrete excess calcium. This reduction is secondary to a decrease in the glomerular filtration rate
(due to renal vasoconstriction and hypovolemia) and to a significant increase in tubular reabsorption of calcium (secondary to metabolic alkalosis).
The plasma PTH level decreases with the rise in the serum calcium level. Thus, the constellation of excess oral intake of calcium and milk, plus
impaired renal function, may result in PTH suppression, hypercalcemia, and hyperphosphatemia.
In cases of chronic ingestion of excessive alkaline calcium preparations and milk, metastatic calcifications and occasionally nephrocalcinosis may occur,7 whereas such complications are not expected with acute milk alkali syndrome, as in the present case.
Calcium Plays a role inside (intracellular) and outside (extarcellular) cells Functions of calcium
Muscle contraction Nerve conduction Coagulation Enzyme and electrolyte regulation Hormone release and exocytosis Cell division
Calcium enters extra-cellular fluid from intestine and bone Calcium is excreted through kidneys Calcium is tightly controlled by hormones (PTH, Calcitriol, calcitonin) Human body contains 1100 g calcium
Hypercalcemia For hypercalcemia to develop, the normal calcium regulation
system must be overwhelmed by an excess of PTH, Calcitriol, some other serum factor that can mimic these hormones, or a huge calcium load.
Between 20 and 40% of patients with cancer develop hypercalcemia at some point in their disease
the most common serious electrolyte presenting in adults with malignancies
primary hyperparathyroidism is considerably higher in women.
Hyperparathyroidism and malignancy increases with age Breast cancer is one of the most common malignancies
responsible for hypercalcemia.
PTH dependent hypercalcemia Primary hyperpara( adenoma commonly) Tertiary hyperparathyroidism FHH MEN syndromes Lithium therapy
PTH independent hypercalcemia Malignancy related Vitamin D related( Granulomas, infections,
toxcicity, williams syndrome) Other endocrine( hyperthyroidism,
pheochromocytoma, adrenal insufficiency, islet cell tumor)
Miscellaneous( immobilization, milk alkali, other medications)
Hypercalcemia of Hyperparathyroid Primary: Usually adenoma Secondary tertiary Hypophosphatemia and elevated urine
calcium Surgery Complications of surgery
PTH and calcium measurment PTH assay PTH related protein Total calcium Ionized calcium
FHH Autosomal dominant, usually mild elevation Shift of the set point Urine calcim is low Previous history of normal calcium rules out
FHH
Hypercalcemia of Malignancy Secretion of PTH related peptide Osteoclastic activation Secretion of vitamin D Unknown mechanisms Common with( Breast cancer with bone
metastasis, lung cancer, multiple myeloma, Hodgikins, pancreatic islet tumors, cholangiocarcinoma and adenocarcinomas)
Symptoms Depends on the underlying disease and rate of
increase in serum calcium Mild elevations in calcium levels usually have few
or no symptoms Manifestations include
Nausea, vomiting, abd pain, stones, constipation, pancreatitis, ulcer Polyuria, polydepsia, nocturia Weakness and vague muscle and Joint aches Altered mental state, lethargy, depression, Headache , confusion Coma
Hypercalcemia of malignancy Hypercalcemia of Hyperparathroid
Examination Mental state Pulse and blood pressure Abdomen Reflexes and muscle power Hydration Malignancy Other specific disease Band keratopathy
ECG Short Q-T Prolonged P-R At high levels …. Wide QRS Flat or inverted T Variable degrees of Heart block N.B. Digoxin effects are amplified
Phosphate and Chloride Serum phosphate levels tend to be low or normal
in primary hyperparathyroidism and hypercalcemia of malignancy.
Phospate levels are elevated in hypercalcemia secondary to vitamin D–related disorders or thyrotoxicosis.
Serum chloride levels usually are higher than 102 mEq/L in hyperparathyroidism and less than this value in other forms of hypercalcemia.
Investigations and DD
Vitamin D metabolism
Treatment1. Hydration
2. Loop diuretics (avoid thiazide)
3. Biphosphonates and other medications
4. Dialysis
5. Surgery
6. Chemo or radiotherapy for malignancy
Medications used to treat Hypercalcemia
Medications used to treat Hypercalcemia
Bisphosphonates Calcitonin Gallium nitrate(Ganite) Plicamycin Glucocorticoids Phosphate Cinacalcite
Pamidronate Zolidronic acid Etidronate
Acute management Rehdrate + or - lasix Bisphosphonate Other Medicate Calcitonin May be phosphate
Chronic management Indications of surgery in hyperparathyroidism Biphosphonates Cortisone in myeloma Cortisone in granulomas and /or hydroxy
chloroquine or ketokonazole Cinacalcet
Take home points Majority of hypercalcemias are caused by
hyperparathyroid or malignancy but others other sought when the diagnosis is not clear
Symptoms are usually subtle Severer hypercalcemia(stones , bones, moans and
groans) History + PTH levels are the essentials for diagnosis Acute management focuses on hydration the other
medications Chroni management focuses on the underlying
aetiology
References Washington subspecialty consult:
Endocrinology 2009 Kumar and Klark’s Medicine 2009 E-medicine online text book – emergency
medicine/ and Nephrology Nejm CASES, 2008
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