Unit Converter
N‑acetylprocainamide (NAPA)

SI UNITS (recommended)

CONVENTIONAL UNITS

Synonym

N acetylprocainamide, N‑acetyl-procainamide, NAPA

Units of measurement

µmol/L, mg/L, mg/dL, mg/100mL, mg%, µg/mL


N-ACETYLOPROCAINAMIDE (NAPA)

(Active Metabolite of Procainamide — Major Therapeutic Drug Monitoring Marker in Cardiac Arrhythmias)

Synonyms

  • N-acetylprocainamide
  • NAPA
  • Acetylprocainamide
  • APA
  • Procainamide metabolite

Units of Measurement

  • µmol/L
  • mg/L
  • mg/dL
  • mg/100 mL
  • mg%
  • µg/mL

Molecular Weight

264.3 g/mol

Key Unit Conversions

Molar ↔ Mass

1 mg/L=3.78 µmol/L1\ \text{mg/L} = 3.78\ \text{µmol/L}1 mg/L=3.78 µmol/L 1 µmol/L=0.264 mg/L1\ \text{µmol/L} = 0.264\ \text{mg/L}1 µmol/L=0.264 mg/L

mg/dL ↔ mg/L

1 mg/dL=10 mg/L1\ \text{mg/dL} = 10\ \text{mg/L}1 mg/dL=10 mg/L

µg/mL

1 µg/mL=1 mg/L1\ \text{µg/mL} = 1\ \text{mg/L}1 µg/mL=1 mg/L

mg%

\text{mg%} = \text{mg/dL}

Description

N-acetylprocainamide (NAPA) is the major active metabolite of the antiarrhythmic drug procainamide.

Produced via hepatic N-acetylation, NAPA has:

  • Class III antiarrhythmic properties
  • Longer half-life than procainamide
  • Important role in overall therapeutic and toxic effects

Therapeutic drug monitoring (TDM) of both procainamide + NAPA is essential because:

  1. Each has independent pharmacologic activity
  2. Total drug effect = procainamide + NAPA
  3. Renal failure causes NAPA accumulation, increasing toxicity risk

Physiological Role

None — NAPA is a pharmacologic compound, not naturally occurring.

Clinical Significance

Therapeutic Uses

NAPA contributes to management of:

  • Ventricular arrhythmias
  • Atrial arrhythmias
  • Supraventricular tachycardia (SVT)
  • Atrial fibrillation conversion in some cases

NAPA is especially important in long-term procainamide therapy.

HIGH NAPA Levels (Toxicity)

Symptoms

  • Hypotension
  • Bradyarrhythmias
  • QRS or QT prolongation
  • Torsades de pointes (most feared complication)
  • Dizziness, syncope
  • CNS effects
  • Seizures (rare)

Major Causes

  • Renal impairment (primary cause)
  • High procainamide dose
  • Slow acetylators vs fast acetylators (pharmacogenetic variability)
  • Drug interactions (cimetidine, amiodarone)
  • Heart failure or shock (reduced clearance)

NAPA increases QT interval more readily than procainamide → higher risk of torsades.

LOW NAPA Levels

Indicate:

  • Subtherapeutic dosing
  • Poor procainamide metabolism
  • Hyperfiltration (rare)
  • Very recent dose (before steady state)
  • Non-adherence

Reference Intervals (Therapeutic Ranges)

(Tietz 8E + Mayo + ARUP + ACCP TDM)

Therapeutic Range

  • 10 – 30 mg/L
    (= 10–30 µg/mL)
    (= 38 – 113 µmol/L)

Toxic Range

  • > 40 mg/L
    (= > 40 µg/mL)
    (= > 150 µmol/L)

Combined Level Interpretation

(Total antiarrhythmic activity = procainamide + NAPA)

  • Combined 10–30 mg/L → desired
  • Combined > 30–40 mg/L → caution
  • Combined > 40 mg/L → high toxicity risk

Units Description

mg/L

Most common clinical reporting unit.

µg/mL

Equivalent to mg/L.

µmol/L

Preferred in pharmacokinetic studies.

mg/dL / mg%

Older units used in older pharmacology literature.

Diagnostic Uses

1. Therapeutic Drug Monitoring (Primary Use)

Used to adjust procainamide therapy.

2. Evaluate Suspected Toxicity

  • QT prolongation
  • Arrhythmias
  • Hypotension
  • Wide QRS complex

3. Monitor Renal Failure Patients

NAPA clearance is almost entirely renal → accumulation is common.

4. Optimize Antiarrhythmic Therapy

Maintaining combined levels within therapeutic range reduces:

  • Recurrence of arrhythmias
  • Drug-induced proarrhythmia
  • Mortality in acute arrhythmia management

Analytical Notes

  • Sample: serum or plasma
  • Trough level preferred (just before next dose)
  • LC–MS/MS or immunoassay used
  • Hemolysis & lipemia interfere with chromatographic assays
  • Levels shift significantly with acute renal changes
  • Measure both procainamide + NAPA simultaneously

Clinical Pearls

  • NAPA is more pro-arrhythmic (QT-prolonging) than procainamide.
  • In renal failure, NAPA accumulates rapidly — monitor closely.
  • Fast/slow acetylators (genetics) alter procainamide → NAPA ratio.
  • Therapeutic effect depends on combined drug levels, not either alone.
  • If QTc > 500 ms → suspect NAPA toxicity.
  • For torsades, discontinue drug + give IV magnesium.

Interesting Fact

NAPA is structurally similar to procainamide but has longer half-life, giving it more stable plasma concentrations — which is why total drug monitoring must include both molecules.

SEO Unit Converter Text

N-acetylprocainamide converter — convert between µmol/L, mg/L, mg/dL, mg%, and µg/mL. Includes therapeutic/toxic ranges, renal adjustment notes, and combined procainamide–NAPA interpretation.

References

  1. Tietz Clinical Chemistry & Molecular Diagnostics, 8th Edition — Therapeutic Drug Monitoring
  2. ACCP Guidelines on Therapeutic Drug Monitoring
  3. Mayo Clinic Laboratories — NAPA
  4. ARUP Consult — Antiarrhythmic Drug TDM
  5. MedlinePlus / NIH — Procainamide & Metabolites

Last updated: December 10, 2025

Reviewed by : Medical Review Board

Other Convertors