Cargando…

Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer

WHAT IS KNOWN AND OBJECTIVE: Immune checkpoint inhibitors can cause immune‐related adverse events (irAEs). Improved monitoring systems for irAEs, which include laboratory tests by a qualified multidisciplinary team, might prevent patients from irAE‐associated events. Kobe City Medical Center General...

Descripción completa

Detalles Bibliográficos
Autores principales: Ikesue, Hiroaki, Kusuda, Kaori, Satsuma, Yukari, Nishiwaki, Fuki, Miura, Rieko, Masuda, Yoshio, Hirabatake, Masaki, Muroi, Nobuyuki, Fujimoto, Daichi, Morimoto, Takeshi, Tomii, Keisuke, Hashida, Tohru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687122/
https://www.ncbi.nlm.nih.gov/pubmed/32519774
http://dx.doi.org/10.1111/jcpt.13207
_version_ 1783613461625831424
author Ikesue, Hiroaki
Kusuda, Kaori
Satsuma, Yukari
Nishiwaki, Fuki
Miura, Rieko
Masuda, Yoshio
Hirabatake, Masaki
Muroi, Nobuyuki
Fujimoto, Daichi
Morimoto, Takeshi
Tomii, Keisuke
Hashida, Tohru
author_facet Ikesue, Hiroaki
Kusuda, Kaori
Satsuma, Yukari
Nishiwaki, Fuki
Miura, Rieko
Masuda, Yoshio
Hirabatake, Masaki
Muroi, Nobuyuki
Fujimoto, Daichi
Morimoto, Takeshi
Tomii, Keisuke
Hashida, Tohru
author_sort Ikesue, Hiroaki
collection PubMed
description WHAT IS KNOWN AND OBJECTIVE: Immune checkpoint inhibitors can cause immune‐related adverse events (irAEs). Improved monitoring systems for irAEs, which include laboratory tests by a qualified multidisciplinary team, might prevent patients from irAE‐associated events. Kobe City Medical Center General Hospital developed protocol‐based pharmacist‐facilitated laboratory tests named protocol‐based pharmacotherapy management (PBPM) to aid the administration of immunotherapy to patients with lung cancer. The protocol defines the laboratory test items and times at which they should be performed. It requires pharmacists to check laboratory orders initiated by physicians and enter additional test items if the orders are incomplete. We evaluated the efficacy of PBPM in irAE monitoring and compared it with those of conventional care systems. METHODS: From January 2016 to March 2018, 114 patients with lung cancer received immunotherapy, which was managed by conventional care (conventional group). From April to September 2018, 62 patients were managed by PBPM (PBPM group), among those 28 patients were transited from conventional group to PBPM group. Data on whether the laboratory tests were conducted or omitted were collected retrospectively for the conventional group and prospectively for the PBPM group. RESULTS: Within the conventional group, 4604 (87.6%) out of the 5253 laboratory test items were ordered by physicians. Of the remaining 649 test items, 224 (4.3%) items were added by physicians based on recommendations by pharmacists. However, of the 1581 (86.6%, from among 1826) test items that were previously ordered by physicians, only 231 (12.7%) test items were added by pharmacists. The execution rate was found to be significantly higher in the PBPM group (99.2% vs 91.9%, P < .001). WHAT IS NEW AND CONCLUSION: PBPM‐based pharmacist‐facilitated laboratory monitoring systems provided higher executing rate of laboratory order to monitor irAEs during immunotherapy.
format Online
Article
Text
id pubmed-7687122
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-76871222020-12-03 Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer Ikesue, Hiroaki Kusuda, Kaori Satsuma, Yukari Nishiwaki, Fuki Miura, Rieko Masuda, Yoshio Hirabatake, Masaki Muroi, Nobuyuki Fujimoto, Daichi Morimoto, Takeshi Tomii, Keisuke Hashida, Tohru J Clin Pharm Ther Original Articles WHAT IS KNOWN AND OBJECTIVE: Immune checkpoint inhibitors can cause immune‐related adverse events (irAEs). Improved monitoring systems for irAEs, which include laboratory tests by a qualified multidisciplinary team, might prevent patients from irAE‐associated events. Kobe City Medical Center General Hospital developed protocol‐based pharmacist‐facilitated laboratory tests named protocol‐based pharmacotherapy management (PBPM) to aid the administration of immunotherapy to patients with lung cancer. The protocol defines the laboratory test items and times at which they should be performed. It requires pharmacists to check laboratory orders initiated by physicians and enter additional test items if the orders are incomplete. We evaluated the efficacy of PBPM in irAE monitoring and compared it with those of conventional care systems. METHODS: From January 2016 to March 2018, 114 patients with lung cancer received immunotherapy, which was managed by conventional care (conventional group). From April to September 2018, 62 patients were managed by PBPM (PBPM group), among those 28 patients were transited from conventional group to PBPM group. Data on whether the laboratory tests were conducted or omitted were collected retrospectively for the conventional group and prospectively for the PBPM group. RESULTS: Within the conventional group, 4604 (87.6%) out of the 5253 laboratory test items were ordered by physicians. Of the remaining 649 test items, 224 (4.3%) items were added by physicians based on recommendations by pharmacists. However, of the 1581 (86.6%, from among 1826) test items that were previously ordered by physicians, only 231 (12.7%) test items were added by pharmacists. The execution rate was found to be significantly higher in the PBPM group (99.2% vs 91.9%, P < .001). WHAT IS NEW AND CONCLUSION: PBPM‐based pharmacist‐facilitated laboratory monitoring systems provided higher executing rate of laboratory order to monitor irAEs during immunotherapy. John Wiley and Sons Inc. 2020-06-10 2020-12 /pmc/articles/PMC7687122/ /pubmed/32519774 http://dx.doi.org/10.1111/jcpt.13207 Text en © 2020 The Authors. Journal of Clinical Pharmacy and Therapeutics published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Ikesue, Hiroaki
Kusuda, Kaori
Satsuma, Yukari
Nishiwaki, Fuki
Miura, Rieko
Masuda, Yoshio
Hirabatake, Masaki
Muroi, Nobuyuki
Fujimoto, Daichi
Morimoto, Takeshi
Tomii, Keisuke
Hashida, Tohru
Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer
title Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer
title_full Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer
title_fullStr Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer
title_full_unstemmed Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer
title_short Evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer
title_sort evaluation of the usefulness of protocol‐based pharmacist‐facilitated laboratory monitoring to ensure the safety of immune checkpoint inhibitors in patients with lung cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687122/
https://www.ncbi.nlm.nih.gov/pubmed/32519774
http://dx.doi.org/10.1111/jcpt.13207
work_keys_str_mv AT ikesuehiroaki evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT kusudakaori evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT satsumayukari evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT nishiwakifuki evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT miurarieko evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT masudayoshio evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT hirabatakemasaki evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT muroinobuyuki evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT fujimotodaichi evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT morimototakeshi evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT tomiikeisuke evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer
AT hashidatohru evaluationoftheusefulnessofprotocolbasedpharmacistfacilitatedlaboratorymonitoringtoensurethesafetyofimmunecheckpointinhibitorsinpatientswithlungcancer