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Revision as of 15:26, 12 March 2026
The basic metabolic panel (BMP) is the workhorse lab test in emergency medicine — a panel of 8 blood chemistries that assesses electrolyte balance, renal function, acid-base status, and blood glucose. It is one of the most frequently ordered tests in the ED and provides rapid, actionable data across virtually every acute presentation.[1]
Background
Components and Normal Ranges
| Component | Normal Range | What It Assesses |
|---|---|---|
| Sodium (Na) | 136–145 mEq/L | Fluid balance, osmolality |
| Potassium (K) | 3.5–5.0 mEq/L | Cardiac conduction, neuromuscular function |
| Chloride (Cl) | 98–106 mEq/L | Acid-base balance (with bicarb) |
| Bicarbonate (CO2) | 22–30 mEq/L | Acid-base status |
| BUN | 7–20 mg/dL | Renal function, hydration status |
| Creatinine (Cr) | 0.7–1.3 mg/dL | Renal function (GFR estimation) |
| Glucose | 70–100 mg/dL (fasting) | Metabolic/endocrine status |
| Calcium (Ca) | 8.5–10.5 mg/dL | Neuromuscular, cardiac, bone |
- Reference ranges vary by lab — always use your institution's values
- Most labs also report a calculated anion gap and eGFR with the BMP
- BMP vs. CMP: A comprehensive metabolic panel (CMP) includes all 8 BMP components plus albumin, total protein, total bilirubin, ALP, ALT, and AST. Order a CMP when liver assessment is also needed
Anion Gap
- Anion gap = Na − (Cl + HCO3)
- Normal: 8–12 mEq/L (varies by lab; some use 3–11)
- Always calculate the anion gap when reviewing a BMP — it is the single most important derived value in the ED
- Elevated anion gap with metabolic acidosis → differential includes: MUDPILES (Methanol, Uremia, DKA, Propylene glycol, Isoniazid/Iron, Lactic acidosis, Ethylene glycol, Salicylates)
- Correct the anion gap for albumin if the patient is hypoalbuminemic: Corrected AG = Calculated AG + 2.5 × (4.0 − measured albumin). A "normal" anion gap in a hypoalbuminemic patient may actually be elevated
Clinical Features
The BMP is not ordered based on specific clinical features of the panel itself — it is ordered as a foundational assessment in most acute presentations. The BMP is appropriate in virtually any ED patient being evaluated for:
- Altered mental status, syncope, weakness, seizure
- Nausea, vomiting, diarrhea, dehydration
- Chest pain, dyspnea, cardiac arrest
- DKA, HHS, hypoglycemia
- Acute kidney injury, chronic kidney disease
- Drug overdose/toxicologic emergency
- Sepsis, shock
- Medication monitoring (diuretics, ACEi/ARBs, digoxin, lithium, metformin)
- Trauma (as part of initial laboratory panel)
Differential Diagnosis
The BMP does not generate a single differential — each abnormal component points to its own set of diagnoses. The following are the most ED-relevant abnormalities:
Sodium
- Hyponatremia (<136): Volume depletion, SIADH, heart failure, cirrhosis, psychogenic polydipsia, medications (thiazides, SSRIs), adrenal insufficiency, hypothyroidism, beer potomania
- Hypernatremia (>145): Dehydration, diabetes insipidus, osmotic diuresis, insensible losses, inadequate free water intake (elderly, altered patients)
Potassium
- Hyperkalemia (>5.0): Renal failure, rhabdomyolysis, acidosis, medications (ACEi/ARBs, K-sparing diuretics, TMP-SMX), hemolysis (spurious), adrenal insufficiency, tumor lysis syndrome
- Hypokalemia (<3.5): GI losses (vomiting, diarrhea), diuretics, renal tubular acidosis, hypomagnesemia, DKA treatment, alkalosis
Bicarbonate
- Low HCO3 (<22): Metabolic acidosis — calculate anion gap to differentiate AGMA from non-anion-gap metabolic acidosis (NAGMA)
- High HCO3 (>30): Metabolic alkalosis (vomiting, diuretics, volume contraction), chronic respiratory acidosis compensation
BUN/Creatinine
- Elevated BUN and Cr: Acute kidney injury (prerenal, intrinsic, postrenal), chronic kidney disease, dehydration
- Elevated BUN with normal Cr (high BUN:Cr ratio >20:1): Prerenal azotemia (dehydration, CHF, GI bleed), high-protein diet, catabolic state, upper GI hemorrhage, corticosteroids
- Low BUN: Malnutrition, liver disease, overhydration
Glucose
- Hyperglycemia (>200): DKA, HHS, stress response, steroid use, new-onset diabetes, sepsis
- Hypoglycemia (<70): Insulin/sulfonylurea use, sepsis, liver failure, adrenal insufficiency, alcohol, malnutrition
Calcium
- Hypercalcemia (>10.5): Malignancy, hyperparathyroidism, granulomatous disease, immobilization, thiazides, vitamin D toxicity, milk-alkali syndrome
- Hypocalcemia (<8.5): Hypoparathyroidism, vitamin D deficiency, pancreatitis, rhabdomyolysis, massive transfusion (citrate), chronic kidney disease, hypomagnesemia, sepsis
- Always correct calcium for albumin: Corrected Ca = Measured Ca + 0.8 × (4.0 − albumin)
Evaluation
Workup
- BMP is drawn as a venous blood sample (green-top lithium heparin tube or red/gold-top serum tube depending on institution)
- Results typically available within 30–60 minutes in most ED laboratories
- Point-of-care (POC) devices (e.g., i-STAT) can provide electrolytes, glucose, BUN, and creatinine in minutes from a single drop of blood — particularly useful in resuscitation, cardiac arrest, and critical care settings
- Hemolyzed specimens falsely elevate potassium (K leaks from lysed RBCs) — if potassium is unexpectedly high in a stable patient, repeat with a non-hemolyzed specimen before treating
Diagnosis
- The BMP is a screening and monitoring tool, not a definitive diagnostic test
- Abnormalities should be interpreted in clinical context and often require additional testing (e.g., VBG/ABG for acid-base workup, osmolality for hyponatremia, PTH for calcium disorders, urinalysis for AKI evaluation)
- Serial BMPs are essential for monitoring electrolyte replacement, DKA management, AKI trends, and response to diuretic therapy
Management
Management is directed at the specific abnormality identified. The most time-critical BMP findings in the ED include:
- Hyperkalemia >6.0 mEq/L: ECG immediately → calcium gluconate for membrane stabilization → insulin + glucose, albuterol for intracellular shift → kayexalate/patiromer for elimination → consider emergent dialysis
- Hypoglycemia <70 mg/dL: D50W IV (or oral glucose if alert); identify and treat cause
- Severe hyponatremia <120 mEq/L: Risk of cerebral edema and seizure; hypertonic saline (3% NaCl) if symptomatic; correct slowly (≤8–10 mEq/L in 24 hours) to avoid osmotic demyelination
- Diabetic ketoacidosis: Insulin drip, aggressive IV fluids, potassium replacement, close monitoring with serial BMPs every 1–2 hours
- Anion gap metabolic acidosis: Identify and treat underlying cause (see MUDPILES); consider toxic alcohol workup (osmolar gap, specific levels) if unexplained elevated AG
- Acute kidney injury: Volume resuscitation (if prerenal), identify and treat cause, avoid nephrotoxins, consider emergent dialysis for refractory hyperkalemia, acidosis, or volume overload
Disposition
- Disposition depends on the specific abnormality and clinical context, not the BMP result in isolation
- Admit for: Severe electrolyte derangements requiring IV correction or continuous monitoring, DKA/HHS, AKI with rising creatinine or need for dialysis, symptomatic hyponatremia, hyperkalemia unresponsive to ED treatment
- Discharge with close follow-up for: Mild electrolyte abnormalities that are corrected in the ED, stable chronic kidney disease with known baseline, incidental mild hypo/hyperglycemia with outpatient management plan
- Repeat BMP before discharge when electrolytes have been repleted in the ED (e.g., after potassium or magnesium replacement) to confirm adequate correction
See Also
- Hyperkalemia
- Hyponatremia
- Hypoglycemia
- Diabetic ketoacidosis
- Acute kidney injury
- Metabolic acidosis
- Hypercalcemia
- Rhabdomyolysis
External Links
References
- ↑ Basic Metabolic Panel (BMP). MedlinePlus Lab Tests. Accessed 2025.
