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Pharmaceutical management of elderly patients in the perioperative setting

Pharmaceutical management of elderly patients in the perioperative setting - PHAROS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014621
Enrollment
140
Registered
2018-06-21
Start date
2018-10-17
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Polymedication of elderly risk patients

Interventions

Group 1: Control group: a Status Quo Survey will be conducted (time of inclusion about 9 months) Group 2: Intervention group: clinical pharmacist will perform an additional medication anamnesis with t
entering of the medication into the electronic prescription software (in communication with the ward physician)
in case of DRP and PIM contact with the general practitioner and written recommendations on how to possibly optimise the medication
use of the national medication plan ("Bundeseinheitlicher Medikationsplan") (time of inclusion about 9 months, duration of the study for each patient about 4 months, control and intervention phase wil

Sponsors

Klinik und Poliklinik für Anästhesiologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: - patients of the University Medical Centre Hamburg-Eppendorf - age > 65 years - planned surgery in not less than 21 days - POSPOM-Score >20 (risk patients) - long-term medication >/= 5 drugs

Exclusion criteria

Exclusion criteria: - refusal of confession - emergency surgery - surgery with planned postoperative intensive medical care - cerebral and ophtalmological surgery as well as surgerys with planned inpatient care less than one day - drug abuse (intravenous, in medical history or current) - psychosis - chronically abuse of benzodiazepines - Parkinson's disease - illiteracy - blindness/deafness - poor knowledge of the German language - preexisting mental disorder

Design outcomes

Primary

MeasureTime frame
Medication Appropriatness Index (MAI) - at T1 (patients’ initial visit), T3 (after admission to hospital), T4 (immediately after discharge from hospital) and T5 (three months after discharge)

Secondary

MeasureTime frame
- Occurrence of postoperative complications - Correct recording of the medication at the interfaces (Medication Reconciliation) - satisfaction with medical care (outpatient: ZAPA/ inpatient: ZUF-8) - occurrence and frequency of DRP and PIM - health-related quality of life (SF-12) - treatment adherence (MARS-D)

Countries

Germany

Contacts

Public ContactCynthia Olotu

Universitätsklinikum Hamburg Eppendorf, Klinik und Poliklinik für Anästhesiologie

c.olotu@uke.de+49 7410 53480

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 17, 2026