Or. Admin. Code § 855-115-0315 - Collaborative Drug Therapy Management
(1) As used in this rule "Collaborative Drug
Therapy Management" (CDTM) means the participation by a practitioner and a
pharmacist in the management of drug therapy pursuant to a written agreement
that includes information on the dosage, frequency, duration and route of
administration of the drug, authorized by a practitioner and initiated upon a
prescription order for an individual patient and:
(a) Is agreed to by one practitioner and one
pharmacist; or
(b) Is agreed to by
one or more practitioners in a single organized medical group, such as a
hospital medical staff, clinic or group practice, including but not limited to
organized medical groups using a pharmacy and therapeutics committee, and one
or more pharmacists.
(2)
A pharmacist shall engage in collaborative drug therapy management with a
practitioner only under a written arrangement that includes:
(a) The identification, either by name or by
description, of each of the participating pharmacists;
(b) The identification, by name or
description, of each of the participating practitioners or group of
practitioners;
(c) The name of the
principal pharmacist and practitioner who are responsible for development,
training, administration, and quality assurance of the arrangement;
(d) The types of decisions that the
pharmacist is allowed to make, which may include:
(A) A detailed description of the types of
diseases, drugs, or drug categories involved, and the activities allowed in
each case;
(B) A detailed
description of the methods, procedures, decision criteria, and plan the
pharmacist is to follow when conducting allowed activities;
(C) A detailed description of the activities
the pharmacist is to follow including documentation of decisions made and a
plan or appropriate mechanism for communication, feedback, and reporting to the
practitioner concerning specific decisions made. In addition to the agreement,
documentation shall occur on the prescription record, patient profile, a
separate log book, or in some other appropriate system;
(D) Circumstances which will cause the
pharmacist to initiate communication with the practitioner, including but not
limited to the need for a new prescription order and a report of a patient's
therapeutic response or any adverse effect.
(e) Training requirement for pharmacist
participation and ongoing assessment of competency, if necessary;
(f) Quality assurance and periodic review by
a panel of the participating pharmacists and practitioners;
(g) Authorization by the practitioner for the
pharmacist to participate in collaborative drug therapy; and
(h) A requirement for the collaborative drug
therapy arrangement to be reviewed and updated, or discontinued at least every
two years.
(3) The
collaborative drug therapy arrangement and associated records must be kept on
file in the pharmacy and made available to any appropriate health licensing
board upon request.
(4) Nothing in
this rule shall be construed to allow therapeutic substitution outside of the
CDTM agreement.
Notes
Statutory/Other Authority: ORS 689.205
Statutes/Other Implemented: ORS 689.151 & ORS 689.155
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.