simulate_phenytoin_mc_optloading_ncmin_24h: Phenytoin » Optimal loading dose » Cmin

In rx-stud-io/R-client: Client to Rx Studio

Description

Phenytoin » Optimal loading dose simulation » Post-dose concentration after 24 hrs

Usage

simulate_phenytoin_mc_optloading_ncmin_24h(
  PATID,
  AGE,
  HEIGHT,
  WEIGHT,
  GENDER,
  PHENYTOINFORM,
  MODEL,
  ALBUMIN,
  RENALFUNCTIONSTATUS,
  VALPROICACID,
  CPOSTDOSE24H
)

Arguments

PATID	Patient Identifier. User-provided free text (such as patient id, name or alias) to identify related simulations. Must be provided as string.
AGE	Age. Age of the patient in years. Must be provided as numeric (min. 18, max. 120 year).
HEIGHT	Height. Height of the patient. Must be provided as numeric (min. 100, max. 250 cm).
WEIGHT	Weight. Actual body weight of the patient. Must be provided as numeric (min. 20, max. 500 kg).
GENDER	Sex. Patient's sex for clinical decision-making. Must be provided as string ('Male' or 'Female').
PHENYTOINFORM	Phenytoin form. Form of phenytoin to be used during simulations. Must be provided as string ('Phenytoin sodium IV' or 'Fosphenytoin sodium IV').
MODEL	Model for population of interest. Pharmacokinetic model to be used for specific patient type during simulations. Must be provided as string ('Muñoz et al. (2019) - ICU').
ALBUMIN	Albumin. Serum albumin. Must be provided as numeric (min. 0.01, max. 15 g/dL).
RENALFUNCTIONSTATUS	Renal function status. Renal function status of the patient. Must be provided as string ('Patients without renal impairment' or 'Dialysis or End-Stage Renal Disease').
VALPROICACID	Valproic acid blood level (leave empty if none). Total valproic acid concentration, leave empty or set to zero if no concurrent administration. Must be provided as numeric (min. 0, max. 500 mg/L).
CPOSTDOSE24H	Post-dose plasma concentration after 24 hrs target. The PK/PD target can be provided as post-dose blood plasma concentration after 24 hrs (Cmin). Must be provided as numeric (min. 0.1, max. 200 mg/L).

Details

Drug: Phenytoin

Method: Calculate optimal loading dose and simulate concentrations for the first 24 hours.

PK/PD target: Post-dose blood plasma concentration after 24 hrs (mg/L).

References

• Muñoz-Pichuante, Daniel et al. (2019): Dosage of phenytoin in neurocritical patients using Bayesian algorithms: a pilot study. In. Drug Metabolism and Personalized Therapy. https://pubmed.ncbi.nlm.nih.gov/31981450

Examples

## Not run: 
structure(list("Anonymous", 
    45, 175, 75, "Male", 
    "Fosphenytoin sodium IV", 
    "Muñoz et al. (2019) - ICU", 
    3, "Dialysis or End-Stage Renal Disease", 
    NULL, 10), .Names = c("PATID", 
"AGE", "HEIGHT", "WEIGHT", 
"GENDER", "PHENYTOINFORM", 
"MODEL", "ALBUMIN", "RENALFUNCTIONSTATUS", 
NA, "CPOSTDOSE24H"))

## End(Not run)

rx-stud-io/R-client documentation built on Dec. 22, 2021, 8:16 p.m.