Medication Errors During Treatment with New Oral Anticancer Agents: Consequences for Clinical Practice Based on the AMBORA Study

Clin Pharmacol Ther. 2021 Oct;110(4):1075-1086. doi: 10.1002/cpt.2338. Epub 2021 Jul 18.

Abstract

Patients treated with oral anticancer agents (e.g., kinase inhibitors) are a high-risk population for medication errors due to, for example, polymedication, age, and limited adherence. Systematic evaluations regarding frequencies and causes of medication errors and resulting harm are lacking. Our previously published multicenter randomized AMBORA trial revealed that an intensified support by clinical pharmacologists/pharmacists for patients and the treatment team considerably reduced drug-related problems and improved patient-reported outcomes. Using this database, we performed a comprehensive, additional analysis focusing on medication errors related to the patients' complete medication with consideration of the antitumor agents, concomitantly administered drugs, and herb/food intake. Two hundred two patients starting a new oral anticancer drug regardless of the tumor entity were included. Clinical pharmacologists/pharmacists performed advanced medication reviews for 12 weeks. Medication errors were characterized regarding type, cause, patient harm, and the involved medicines. We detected 1.7 medication errors per patient (335/202). Of the medication errors (216/335), 64.5% occurred within the concomitant medication. Patients caused 28.4% of the medication errors. There were 67.8% detected immediately after the start of the new oral regimen, and 14.9% resulted in temporary harm. Drug-drug or drug-food interactions accounted for 24.8% of the medication errors. Patients and physicians need to be addressed in strategies for systematic reduction of medication errors during treatment with new oral antitumor drugs. Clinical decision support systems focusing on drug-drug interactions capture only a minority of the medication errors. Specialists with expertise in clinical pharmacology/pharmacy should support both the treating physicians as well as the patients for improved patient safety.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Aged, 80 and over
  • Analgesics / therapeutic use
  • Anti-Ulcer Agents / therapeutic use
  • Antihypertensive Agents / therapeutic use
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Agents, Hormonal / therapeutic use
  • Comorbidity
  • Coronary Disease / drug therapy
  • Coronary Disease / epidemiology
  • Decision Support Systems, Clinical
  • Diabetes Mellitus / drug therapy
  • Diabetes Mellitus / epidemiology
  • Drug Interactions*
  • Dyslipidemias / drug therapy
  • Dyslipidemias / epidemiology
  • Female
  • Fibrinolytic Agents / therapeutic use
  • Food-Drug Interactions*
  • Humans
  • Hypertension / drug therapy
  • Hypertension / epidemiology
  • Hypolipidemic Agents / therapeutic use
  • Hypothyroidism / drug therapy
  • Hypothyroidism / epidemiology
  • Male
  • Medication Errors / statistics & numerical data*
  • Middle Aged
  • Neoplasms / drug therapy*
  • Polypharmacy*
  • Protein Kinase Inhibitors / therapeutic use
  • Thyroid Hormones / therapeutic use
  • Vitamins / therapeutic use

Substances

  • Analgesics
  • Anti-Ulcer Agents
  • Antihypertensive Agents
  • Antineoplastic Agents
  • Antineoplastic Agents, Hormonal
  • Fibrinolytic Agents
  • Hypolipidemic Agents
  • Protein Kinase Inhibitors
  • Thyroid Hormones
  • Vitamins