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Clinical Pharmacist Anticoagulant Stewardship

Clinical Pharmacist Led Hospital-Wide Direct Oral Anticoagulant Stewardship Program

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03527615
Enrollment
4000
Registered
2018-05-17
Start date
2017-01-01
Completion date
2020-01-01
Last updated
2018-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anticoagulant Toxicity, Safety Issues

Brief summary

Initiative to improve direct anticoagulant utilization involving programmatic review by clinical pharmacists in collaboration with multidisciplinary team.

Detailed description

The Hadassah Hebrew University Medical Centers' Clinical Pharmacy team initiated a hospital-wide program, in collaboration with the institutions' coagulation specialists, including two hematologists and a clinical pharmacologist, for monitoring and promoting safe and effective prescription of direct oral anticoagulants (DOAC) during hospitalization. Electronic medical records throughout the hospital are screened for DOAC orders. All DOAC orders are assessed by a clinical pharmacist for potentially-inappropriate prescribing. When potentially-inappropriate prescribing or a drug-related problem is identified, the clinical pharmacist provided consultation on management options. In specific cases, additional guidance is provided by coagulation specialists. Consultations are recorded in the electronic medical record. Performance measures are collected and summarized.

Interventions

OTHERClinical Pharmacist Medication Review

Programmatic review of physician orders for direct anticoagulants by clinical pharmacists.

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Patients hospitalized in Hadassah Medical Center with a physician's order for direct oral anticoagulants (apixaban, rivaroxaban, or dabigatran).

Exclusion criteria

Patients hospitalized in departments without computerized physician order entry.

Design outcomes

Primary

MeasureTime frameDescription
Percent of clinical pharmacist consultations accepted by attending physician.At forty-eight monthsCalculated by dividing the number of clinical pharmacist consultations accepted, by the number of clinical pharmacist consultations given, during the period. Data for consultation counts will be obtained from patient electronic medical record.

Secondary

MeasureTime frameDescription
Percent of clinical pharmacist consultations accepted by attending physician.At six monthsCalculated by dividing the number of clinical pharmacist consultations accepted, by the number of clinical pharmacist consultations given, during the period. Data for consultation counts will be obtained from patient electronic medical record.

Countries

Israel

Contacts

Primary ContactAmichai Perlman, Pharmd
amichaip@hadassah.org.il972505172768

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026