| Component | Amount |
|---|---|
| Sodium glycerophosphate pentahydrate | 4.32 g |
| Phosphate (PO₄³⁻) | 20 mmol |
| Sodium (Na⁺) | 40 mmol |
| pH | ≈ 7.4 |
| Osmolality | ≈ 2,760 mOsm/kg |
| Patient Group | PO₄ Dose | Glycophos |
|---|---|---|
| Adults | 10–20 mmol/day | 10–20 mL/day |
| Children (>1 yr) | 0.5–1.0 mmol/kg/day | 0.5–1.0 mL/kg/day |
| Infants (≤1 yr) | 1.0–2.0 mmol/kg/day | 1.0–2.0 mL/kg/day |
| Severity | Serum PO₄ | IV Dose | Duration |
|---|---|---|---|
| Mild | 0.6–0.8 mmol/L | 0.1–0.15 mmol/kg | 4–6 h |
| Moderate | 0.3–0.6 mmol/L | 0.2–0.25 mmol/kg | 4–6 h |
| Severe | <0.3 mmol/L | 0.4–0.5 mmol/kg | 6–12 h |
- Sodium Chloride 0.9%
- Glucose 5%
- PN admixtures (validated Ca²⁺–PO₄³⁻ ratio)
| Setting | Duration | Max Rate |
|---|---|---|
| PN (maintenance) | 12–24 h | With PN bag |
| Mild–moderate (10–20 mmol) | 4–6 h | ≤ 7.5 mmol/hr |
| Severe (>20 mmol) | 6–12 h |
-
✓Serum PhosphateTherapeutic endpoint; guides repeat dosingBefore → 2–4 h post → Daily
-
✓Serum CalciumInverse homeostatic relationship with PO₄With each PO₄ check
-
✓Serum MagnesiumHypomagnesemia impairs PO₄ repletion; correct if lowBaseline; correct if low
-
✓Renal Function (eGFR / SCr)Risk of phosphate accumulation in renal impairmentBefore & during therapy
-
✓Fluid & Sodium Balance40 mmol Na⁺ per vial — account in sodium-restricted patientsDaily (high-risk patients)
-
✓ECGHypophosphatemia and hypocalcemia can cause arrhythmiasSevere / cardiac risk
-
✓IV Site (Peripheral)Monitor for phlebitis; use well-diluted solutionsEach nursing assessment
-
✓Hemodynamic StatusCorrect dehydration/shock before initiating infusionBefore administration
| Unopened vial | Below 25°C; do not freeze |
| Diluted solution | Use immediately; if prepared in advance, store at 2–8°C and use within 24 hours |
| Visual inspection | Discard if particulate matter or discoloration present |
Initiate phosphate supplementation prophylactically before PN in at-risk patients. Phosphate depletion can be precipitous. Monitor closely for the first 72 hours of nutrition initiation.
If PO₄ fails to correct despite adequate IV replacement, check serum magnesium. Hypomagnesemia impairs intracellular phosphate uptake and is a common reversible cause of refractoriness.
Glycophos (organic phosphate) has significantly superior calcium compatibility in PN admixtures compared to inorganic phosphate salts, reducing precipitation risk at standard PN concentrations.
A 40 mmol replacement dose (2 vials) contributes 80 mmol Na⁺ ≈ 1.86 g sodium. In sodium-restricted, edematous, or hypernatremic patients, always account for this in the daily fluid plan.
Monitoring Ca × PO₄ product (target < 4.4 mmol²/L²) helps prevent metastatic calcification, particularly in patients with renal impairment or prolonged high-dose supplementation.
| Component | Amount |
|---|---|
| Sodium glycerophosphate pentahydrate | 4.32 g |
| Phosphate (PO₄³⁻) | 20 mmol |
| Sodium (Na⁺) | 40 mmol |
| pH | ≈ 7.4 |
| Osmolality | ≈ 2,760 mOsm/kg |
| Patient Group | PO₄ Dose | Glycophos |
|---|---|---|
| Adults | 10–20 mmol/day | 10–20 mL/day |
| Children (>1 yr) | 0.5–1.0 mmol/kg/day | 0.5–1.0 mL/kg/day |
| Infants (≤1 yr) | 1.0–2.0 mmol/kg/day | 1.0–2.0 mL/kg/day |
| Severity | Serum PO₄ | IV Dose | Duration |
|---|---|---|---|
| Mild | 0.6–0.8 mmol/L | 0.1–0.15 mmol/kg | 4–6 h |
| Moderate | 0.3–0.6 mmol/L | 0.2–0.25 mmol/kg | 4–6 h |
| Severe | <0.3 mmol/L | 0.4–0.5 mmol/kg | 6–12 h |
- Sodium Chloride 0.9%
- Glucose 5%
- PN admixtures (validated Ca²⁺–PO₄³⁻ ratio)
| Setting | Duration | Max Rate |
|---|---|---|
| PN (maintenance) | 12–24 h | With PN bag |
| Mild–moderate (10–20 mmol) | 4–6 h | ≤ 7.5 mmol/hr |
| Severe (>20 mmol) | 6–12 h |
-
✓Serum PhosphateTherapeutic endpoint; guides repeat dosingBefore → 2–4 h post → Daily
-
✓Serum CalciumInverse homeostatic relationship with PO₄With each PO₄ check
-
✓Serum MagnesiumHypomagnesemia impairs PO₄ repletion; correct if lowBaseline; correct if low
-
✓Renal Function (eGFR / SCr)Risk of phosphate accumulation in renal impairmentBefore & during therapy
-
✓Fluid & Sodium Balance40 mmol Na⁺ per vial — account in sodium-restricted patientsDaily (high-risk patients)
-
✓ECGHypophosphatemia and hypocalcemia can cause arrhythmiasSevere / cardiac risk
-
✓IV Site (Peripheral)Monitor for phlebitis; use well-diluted solutionsEach nursing assessment
-
✓Hemodynamic StatusCorrect dehydration/shock before initiating infusionBefore administration
| Unopened vial | Below 25°C; do not freeze |
| Diluted solution | Use immediately; if prepared in advance, store at 2–8°C and use within 24 hours |
| Visual inspection | Discard if particulate matter or discoloration present |
Initiate phosphate supplementation prophylactically before PN in at-risk patients. Phosphate depletion can be precipitous. Monitor closely for the first 72 hours of nutrition initiation.
If PO₄ fails to correct despite adequate IV replacement, check serum magnesium. Hypomagnesemia impairs intracellular phosphate uptake and is a common reversible cause of refractoriness.
Glycophos (organic phosphate) has significantly superior calcium compatibility in PN admixtures compared to inorganic phosphate salts, reducing precipitation risk at standard PN concentrations.
A 40 mmol replacement dose (2 vials) contributes 80 mmol Na⁺ ≈ 1.86 g sodium. In sodium-restricted, edematous, or hypernatremic patients, always account for this in the daily fluid plan.
Monitoring Ca × PO₄ product (target < 4.4 mmol²/L²) helps prevent metastatic calcification, particularly in patients with renal impairment or prolonged high-dose supplementation.