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Drug therapy safety in liver cirrhotic patients through implementation of prescription support

Drug therapy safety in liver cirrhotic patients through implementation of prescription support - ALIVe

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033779
Enrollment
414
Registered
2024-12-27
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

K74

Interventions

Group 1: Cohort A: Data collection from patients with liver cirrhosis on wards without ward pharmacists' support (retrospective) Group 2: Cohort B: Data collection as part of the introduction of routi

Sponsors

Uniklinikum Bonn
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients with liver cirrhosis of any origin and severity - Inpatients of the Hufeland ward of the Medical Clinic I of the University Hospital Bonn - Minimum length of stay of 24 hours, as the inpatient admission criterion is then fulfilled - Cohort B and C: At least one screening by the ward pharmacists responsible for the ward

Exclusion criteria

Exclusion criteria: - Patients under 18 years of age - Pregnancy and breastfeeding patients - Patients who were not hospitalised or were hospitalised for < 24 hours

Design outcomes

Primary

MeasureTime frame
Comparison of frequency for drug-related problems in patients with liver cirrhosis vs. without application of the consensus-validated treatment recommendations over the entire case duration

Secondary

MeasureTime frame
1) Comparison of cohort B vs. cohort A (each data collected over the entire case duration): - Comparison of the number and type of drug-related problems in patients with liver cirrhosis - Severity of identified drug-related problems according to NCC MERP - Preventability of the identified drug-related problems (ABPs) - Number and type of (re-)admissions (liver-associated, non-liver-associated, drug-associated) within the observation period - Number of emergency admissions within 30 days (day 0 = discharge day) - Number and type of patient deaths (liver-associated, non-liver-associated, drug-associated) - Correlation of number of ABPs found with: -- Age (geriatric vs. non-geriatric) -- gender -- Severity of liver cirrhosis according to Child-Pugh -- Comorbidity burden CCI = 5 according to Charlston Comorbidity Index (CCI) -- Number of medications taken (< 5, =5, =7, =10) -- Number of emergency admissions 2) Comparison of cohort C vs. cohort B (each data collected over the entire case duration): - Comparison of the number and type of drug-related problems in patients with liver cirrhosis - Severity of identified drug-related problems according to NCC MERP - Preventability of the identified drug-related problems (ABPs) - Number and type of (re-)admissions (liver-associated, non-liver-associated, drug-associated) within the observation period - Number of emergency admissions within 30 days (day 0 = discharge day) - Number and type of patient deaths (liver-associated, non-liver-associated, drug-associated) - Correlation of number of ABPs found with: -- Age (geriatric vs. non-geriatric) -- gender -- Severity of liver cirrhosis according to Child-Pugh -- Comorbidity burden CCI = 5 according to Charlston Comorbidity Index (CCI) -- Number of medications taken (< 5, =5, =7, =10) -- Number of emergency admissions 3) Acceptance rate and rationale for rejection of routine clinical practice recommendations by ward pharmacists and treating physicians

Countries

Germany

Contacts

Public ContactMaria Katharina Karsten Dafonte

Uniklinikum Bonn

Katharina.Karsten_Dafonte@ukbonn.de+49 228 287 14036

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026