Table of Contents
Introduction
Aetiology
transient intracellular shifts
increased urinary losses
decreased intestinal absorption
increased cellular use
Mx of low phosphate
hypophosphataemia
see also:
phosphate
Introduction
hypophosphatemia is usually asymptomatic even if severe, however, levels below 0.32mmol/L may cause symptoms such as
seizures
, muscle weakness, and even
coma
Aetiology
transient intracellular shifts
acute respiratory alkalosis
(eg. hyperventilation)
perhaps the most common cause in hospital settings
increased urinary losses
primary or secondary
hyperparathyroidism
vitamin D deficiency or resistance
primary renal wasting - rare hereditary forms - no hypocalcaemia though
Fanconi syndrome
osmotic diuresis
some other diuretics - acetazolamide, some thiazides
some chemotherapy agents
some iron infusions
renal dialysis
hereditary hypophosphatasia (HHP)
:
a molecular defect in the gene encoding tissue non-specific alkaline phosphatase (TNSALP)
low alkaline phosphate levels, increased pyrophosphate and decreased phosphylation of vitamin B6 and thus reduced entry of B6 into cells
severe hypophosphatasia is estimated to be 1:100,000 in a population of largely Anglo-Saxon origin;
higher prevalence in Spanish
1)
and in Mennonites in Canada
perinatal form: most fatal form; profound hypomineralization; stillbirth or neonatal death rates are high;
infantile form: poor feeding and inadequate weight gain; rickets; rib fractures; hypercalcaemia;
childhood form: delayed walking; premature loss of deciduous teeth or fusing of cranial sutures; rickets; myopathy; growth retardation;
adult form: may have features of childhood form; early loss of adult dentation; pseudogout / pyrophosphate arthropathy; stress fractures;
decreased intestinal absorption
poor intake is rarely a cause
medications that bind phosphate eg. aluminium, magnesium
steatorrhoea or chronic diarrhoea
increased cellular use
acute glycolysis
causes increased phosphorylation within cells causing reduction in extracellular phosphate
fall more likely to be severe if underlying phosphate depletion
eg. insulin, glucagon, adrenaline, DKA
acute post-parathyroidectomy / hungry bone syndrome
Mx of low phosphate
see
phosphate
for phosphate replacement Rx
if high PTH:
if low calcium then:
exclude pancreatitis, hypomagnesaemia, over-hydration
otherwise likely to be vitamin D deficiency Rx with vitamin D
if high calcium then either primary or tertiary hyperparathyroidism
:
phosphate replacement
consider cinacalcet as a temporary measure to lower calcium levels and potentially improve phosphate levels before definitive surgery
surgical excision of parathyroid gland causing the hyper PTH
1)
https://www.news-medical.net/news/20191115/Study-15000-cases-of-hypophosphatasia-potentially-undetected-in-Spanish-population.aspx