Using a treatment diary to improve the medication adherence in patients with chronic myeloid leukaemia

J Oncol Pharm Pract. 2019 Jul;25(5):1035-1041. doi: 10.1177/1078155218759184. Epub 2018 Feb 20.

Abstract

Purpose: The aim of this study was to verify whether the distribution of a treatment diary by a pharmacist could influence the adherence to oral treatment with imatinib, nilotinib, and dasatinib in patients with chronic myeloid leukaemia.

Methods: The level of adherence was calculated using the received daily dose/prescribed daily dose ratio and compared between patients who used a diary and those who did not.

Results: Forty-four (35.8%) of 123 patients with chronic myeloid leukaemia completed the diary: 20 (45.4%) receiving imatinib, 17 (38.6%) receiving nilotinib, and seven (15.9%) receiving dasatinib. Treatment adherence with the diary calculated using received daily dose/prescribed daily dose method was 93.6% (imatinib 94.9%, nilotinib 91.1%, and dasatinib 95.8%). Adherence during the period without a diary was 86.5% (84.9, 87.4, and 90%). Adherence was significantly greater with than without a diary (p < 0.0001).

Conclusions: The findings of this study that, in the case of chronic diseases, direct pharmacist-patient contact is important in order to maintain high levels of adherence, and a treatment diary is a valid means of doing this. According to these data, it is necessary to support similar patient-oriented programmes in order to ensure high levels of adherence and optimize drug management.

Keywords: Medication adherence; chronic myeloid leukaemia; dasatinib; imatinib; nilotinib.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / administration & dosage*
  • Dasatinib / therapeutic use
  • Female
  • Humans
  • Imatinib Mesylate / therapeutic use
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
  • Male
  • Medication Adherence*
  • Middle Aged
  • Prospective Studies
  • Pyrimidines / administration & dosage
  • Young Adult

Substances

  • Antineoplastic Agents
  • Pyrimidines
  • Imatinib Mesylate
  • nilotinib
  • Dasatinib