HYPERCALCEMIA & HYPOCALCEMIA
MODERATOR
DR. RAKESH RANJAN
ASSISTANT PROFESSOR PEDIATRIC
DEPARTMENT
SHRI KRISHNA MEDICAL
COLLEGE,MUZZAFARPUR
PRESENTER
DR. JAIKISHAN
AND
DR. AMANATULLAH
PG-DNB(1
ST
YEAR)
PEDIATRIC DEPARTMENT
SKMC, MUZZAFARPUR
CALCIUM HOMEOSTASIS
It involves interaction of GIT absorption , Bone resorption and Renal excretion .
PTH and Vit D are principle regulators of Calcium Homeostasis.
Normal Serum Calcium level is 9-11 mg /dL.
Calcitonin & PTH-related peptide are important primary regulator in fetus.
PTH is an 84 amino acid chain , but its biologic activity resides in the first 34 residues.
Most (99%) body calcium is stored in the bone and is in constant
equilibrium with serum calcium .
Approx1-2%ofbodycalcium exist in ECF for physiological function
like –
BloodCoagulation
Cellular Communication
Exocytosis and Endocytosis
Muscle contraction
Neuromuscular transmission
Most of the filtered Calcium is Reabsorbed in the
proximal convultedtubule (approx70% ) ,
Ascending Loop of Henle (20%) & the Distal
convultedtubule and Collecting Duct (5-10%) .
Role of Calcium Sensing receptor
Thebodysensescalciumlevelsusingcalciumsensing
receptorspresentinparathyroidglandand kidney.
The Calcium sensing receptor is GPCR
Plasma calciumexistsin 3 different forms –
50 % as biologically active ionized form
45% bounded to plasma protein (mainly albumin)
5% complexed to phosphate
Metabolic acidosis leads to increased ionized calcium
from reduced protein binding
Alkalosis has opposite effect .
Corrected Calciumcanbecalculated by
Corrected Ca = ( 4 –Plasma albumin in g/dL ) x 0.8
+ Measured Serum Calcium
[ for every 1g/dL drop in Serum Albumin below 4g/dL,
measured Sr. calcium decreased by 0.8 mg/dL ]
HYPERCALCEMIA
Defined as Serum Calcium levels > 11mg/dL.
Hypercalcemiaisoftenasymptomaticalthough it can cause
symptoms at levels 12mg/dL
Causes of Hypercalcemia
Hypercalcemia is uncommon in children as compared to Hypocalcemia .
➢1)Neonates
Neonatal primary hyperparathyroidism
Secondary hyperparathyroidism
Excessive supplementation of Calcium
William’s Syndrome
Familial HypocalcemicHypercalcemia
➢Older Children
Hyperparathyroidism –Parathyroid Adenoma
MEN-1
Malignancies -Non Hodgkin or Hodgkin Lymphoma
-Ewing’s Sarcoma
-Neuroblastoma
Granulomatous disease -Sarcoidosis
TB
Wegener disease .
Others -Vit D or Vit A intoxication
-Thiazide diuretic
-Milk-Alkali Syndrome
Symptoms and Signs of Hypercalcemia
Common Symptoms are –
Polyuria
Polydipsia
Poor weight gain
Failure to thrive
Easy Fatigability
Irritability
Confusion
Pain abdomen
Constipation
Severe Hypercalcemia inhibits neuromuscular and myocardial
depolarization causing arrhythmia and neuromuscular weakness.
Severe acute abdominal pain could be a clue to suspect
pancreatitis
Severe Calcium >14 mg/dLmayresultinencephalopathy.
Bone related symptomsareBone pain and Fractures
CVS effect –Prolong PR interval
Short QT interval
Widened QRS complex
Treatment of Hypercalcemia
Treatmentisrequiredforsymptomatichypercalcemiaand
asymptomatichypercalcemiawithserumcalcium> 15 mg/dL .
A)ForincreasingCalciumelimination
Twice maintenance fluid ( IsotonicFluid)
Loop Diuretics –I.V Furosemide 1-2 mg/kg/day
in case of renal or cardiac disease only
Hemodialysis
b) Reducing Bone absorption –Bisphosphonates
Pamidronate (0.5-1 mg/kg)
as an infusion over 4-6 hrs
Calcitonin –4 units /kg IM/S.C
q 12 hourly
c) Reducing calcium absorption –Steroids (1-2 mg/kg/day –
20-40 mg/day )
d) Surgical intervention may be needed in patients with
hyperparathyroidism, particularly with recurrent renal stones .
HYPOCALCEMIA
DEFINITION
Defined as serum calcium level less than
8.5 mg /dL
CausesofHypocalcemia
1) Neonatal
a) Maternal disorder
Diabetes mellitus
Toximiaof pregnancy
Vit D deficiency
Use of anti-convulsants
High intake of alkali or
magnesium sulfate
Hyperparathyroidism
(B) Acquired :
1) Autoimmune polygandularsyndrome type 1 (AIRE Gene mutation)
2) Activating antibodies to the CaSR
3) Hypomagnesemia / Hypermagnesemia
3) VIT D Deficiency
4) Other Causes like –
1) Calcium deficiency due to Nutritional Deprivation , Hypercalcemia
2) Disorders of magnesium Homeostasis
3) Hyperphosphatemia –a) renal failure
b) phosphate administration
ClinicalManifestation
➢The Symptoms of Hypocalcemia are related to disturbance in nerve and muscle conduction as
hypocalcemia causes neuromuscular excitability .
Muscular pain and Cramps ( early manifestations)
➢Numbness, Stiffness and Tingling of hand and feet .
➢Uncommon symptoms –Stridor secondary to laryngeal spasm and apnea in infants .
ChvostekandTrousseausigns can be
elicited in Hypocalcemia
ECGrevealsprolongedQTc interval ( > 0.4 s ) and
QoTc( > 0.2 s )
Investigation
Basic investigation in hypocalcemia
1) Serum Calcium level is low and Phosphorus level is elevated
2) Serum Calcium , Phosphate , Alkaline phosphatase .
3) Serum Vit D , Parathyroid hormone , X ray Wrist or Knee
4) Serum albumin , Serum Creatinine , Serum Magnesium
5) Urine Calcium / Creatinine ratio .
Treatment
Depends on severity of symptoms and underlying etiology of hypocalcemia
-I/V Calcium required in case of Seizure , Laryngospasm , Tetany , Cardiovascular compromise
-10 % Calcium Gluconate ( 1ml contains 9.3 mg of elemental calcium )
-I/V dose –0.5-1 ml/kg (max 2 ml/kg )
Calcium Gluconate diluted with Ns or 5% dextrose ( 1:10 dilution ) over 20 min
-Not more than 5 mg of elemental calcium per minute
-Additionally 1,25 dihydroxycholecalciferol should be given
initial dose –0.25 μg / 24 hr
maintenance dose –0.01 –0.10 μg / kg / 24 hr
maximum dose –1 –2 μg / 24 hr
-I/V calcium should be always infused under cardiac monitoring
-Once the acute symptoms are subsided discontinue I/V Supplementation
-For those children who don’t need urgent correction of serum calcium , oral calcium
supplementation can be administered upto400 mg / kg /day .
-Magnesium deficiencies must be considered In patients with unexplained
hypocalcemia
-Concentration of serum Mg < 1.5 mg/dLareabnormal