Skip to main content
Log in

Potential drug-drug interactions and admissions due to drug-drug interactions in patients treated in medical departments

Potentielle Medikamenteninteraktionen und stationäre Aufnahmen wegen Medikamenteninteraktionen bei Patienten auf inneren Abteilungen

  • Original Article
  • Published:
Wiener klinische Wochenschrift Aims and scope Submit manuscript

Zusammenfassung

ZIEL DER STUDIE: Unerwünschte Nebenwirkungen als Folge von Medikamenteninteraktionen spielen eine wichtige Rolle bei der Sicherheit von Medikamenten. Ziel dieser Studie war es, mögliche Medikamenteninteraktionen bei der Spitalsaufnahme und -entlassung zu erfassen, bzw. die Aufnahmen infolge solcher Interaktionen auf internen Abteilungen eines primären Stadtspitals und tertiären Referenzspitals zu evaluieren. METHODEN: Bei 520 zufällig ausgesuchten Patienten des medizinischen Zentrums der Universität Ljubljana wurden Alter, Geschlecht, Nieren- und Leberfunktion, Medikamente, Diagnosen sowie Dringlichkeit und Grund der Zuweisung retrospektiv erhoben. Bei den Patienten, bei denen Information über die bei Aufnahme und Entlassung eingenommenen Medikamente vorlag, wurde auf Medikamenteninteraktionen mittels des Interaktions-Screening Programms "Drug-Reax" geprüft. Basierend auf den erhobenen Daten wurde der Anteil an Aufnahmen, deren Grund eine Medikamenteninteraktion war, geschätzt. ERGEBNISSE: Bei 14,6% (76/520) Patienten war die Information über die Medikamentennamen bei Aufnahme nicht vollständig. Nach der Behandlung wurden 416 Patienten nach Hause entlassen, bei 52 von diesen (12,5%) war die Information über die Medikamentennamen im Entlassungsbrief ebenfalls unvollständig. Die restlichen 323 Patienten mit kompletter Information wurden in die Studie inkludiert. Mindestens eine Nebenwirkung wegen potentieller Medikamenteninteraktion hatten 51% (166/323) der Patienten bei Aufnahme und 63% (204/323) bei Entlassung (p = 0,001). Schwere potentiell interaktionsbedingte Nebenwirkungen hatten 13% (41/323) der Patienten bei Aufnahme und 18% (59/323) bei Entlassung (p = 0,001). Die gleichzeitige Gabe von ACE-Hemmern mit Spironolacton war die häufigste Interaktion. (20% der Interaktionen bei Aufnahme bzw. 25,6% bei Entlassung). Nur 2,4% (4/166) der Patienten mit potentiell interaktionsbedingter Nebenwirkungen wurden unter dieser Diagnose zugewiesen. 1,2% (2/323) aller Patienten wurden wegen Medikamenteninteraktion aufgenommen. SCHLUSSFOLGERUNGEN: Die Information über die Medikation der Patienten bei Spitals-Aufnahme und -entlassung ist nicht vollständig. Bei Aufnahme hatte die Hälfte und bei Entlassung zwei Drittel der Patienten potentiell interaktionsbedingte Nebenwirkungen. Unerwünschte durch Interaktionen von Medikamenten bedingte Nebenwirkungen machten 1,2% der Zuweisungen zur Aufnahme auf internen Abteilungen eines primären Stadtspitals und tertiären Referenzzentrums aus.

Summary

PURPOSE: Adverse drug reactions due to drug-drug interactions (DDIs) are important in drug safety. The aim of this study was to check potential DDIs (pDDIs) on hospital admission and discharge and to evaluate admissions due to DDIs in medical departments of a primary city and tertiary referral hospital. METHODS: Age, sex, presence of renal and liver failure, drug information, diagnosis, and urgency and reason for admission were retrospectively recorded in 520 randomly selected patients in medical departments of the University Medical Center Ljubljana. The screening program Drug-Reax was used to check for pDDIs in patients with drug information on both admission and discharge home, and the proportion of patients admitted as the consequence of a DDI was estimated. RESULTS: Overall, 14.6% (76/520) of patients had incomplete information on drug names in their medical documentation on admission; at the end of treatment 12.5% (52/416) of patients were discharged home with incomplete information on drug names in their discharge letters. A total of 323 patients had complete information on drug names on both admission and discharge and were included in the analysis of pDDIs: 51% (166/323) of patients on admission and 63% (204/323) on discharge had at least one pDDI (P = 0.001). Major pDDIs were found in 13% (41/323) of patients on admission and 18% (59/323) on discharge (P = 0.001). An ACE inhibitor combined with spironolactone was the most common major pDDI, representing 20.0% of all pDDIs on admission and 25.6% on discharge. Among patients with pDDI on admission, 2.4% (4/166) of were admitted because of an ADR caused by a DDI. Overall, 1.2% (4/323) of patients were admitted as the consequence of a DDI. CONCLUSIONS: The information on patient medication on hospital admission and discharge is incomplete. Half of patients on admission and almost two-thirds on discharge had pDDIs. ADRs due to DDIs caused 1.2% of admissions to medical departments in Ljubljana's primary city and tertiary referral hospital.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  • Camargo AL, Cardoso Ferreira MB, Heineck I (2006) Adverse drug reactions: a cohort study in internal medicine units at a university hospital. Eur J Clin Pharmacol 62: 143–149

    Article  PubMed  Google Scholar 

  • Patel KJ, Kedia MS, Bajpai D, Mehta SS, Kshirsagar NA, Gogtay NJ (2007) Evaluation of the prevalence and economic burden of adverse drug reactions presenting to the medical emergency department of a tertiary referral centre: a prospective study. BMC Clin Pharmacol 7: 8

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Schuler J, Dückelmann C, Beindl W, Prinz E, Michalski T, Pichler M (2008) Polypharmacy and inappropriate prescribing in elderly internal-medicine patients in Austria. Wien Klin Wochenschr 120: 733–741

    Article  PubMed  Google Scholar 

  • Müller M (2008) Polypharmacy, inappropriate prescribing and adverse drug reactions in Austria. Wien Klin Wochenschr 120: 713–714

    Article  PubMed  Google Scholar 

  • Pirmohamed M, James S, Meakin S, Green C, Scott AK, Walley TJ, et al (2004) Adverse drug reactions as cause of admission to hospital: prospective analysis of 18,820 patients. BMJ 329: 15–19

    Article  PubMed  PubMed Central  Google Scholar 

  • Turnheim K (2005) Drug interactions with antiepileptic agents. Wien Klin Wochenschr 116: 112–118

    Article  Google Scholar 

  • Lütgendorf C, Rojanawatsirivet C, Wernsdorfer G, Sirichaisinthop J, Kollaritsch H, Wernsdorfer WH (2006) Pharmacodynamic interaction between atovaquone and other antimalarial compounds against Plasmodium falciparum in vitro. Wien Klin Wochenschr 118: 70–76

    Article  PubMed  Google Scholar 

  • Egger SS, Drewe J, Schlienger RG (2003) Potential drug-drug interactions in the medication of medical patients at hospital discharge. Eur J Clin Pharmacol 58: 773–778

    PubMed  Google Scholar 

  • Gosney M, Tallis R (1984) Prescription of contraindicated and interacting drugs in elderly patients admitted to hospital. Lancet 2: 564–567

    Article  CAS  PubMed  Google Scholar 

  • Schneider JK, Mion LC, Frengley JD (1992) Adverse drug reactions in an elderly outpatient population. Am J Hosp Pharm 49: 90–96

    CAS  PubMed  Google Scholar 

  • Costa AJ (1991) Potential drug interactions in an ambulatory geriatric population. Fam Pract 8: 234–236

    Article  CAS  PubMed  Google Scholar 

  • Shinn AF, Shrewsbury RP, Anderson KW (1983) Development of a computerized drug interaction database (MED-ICOM) for use in a patient specific environment. Drug Inf J 17: 205–210

    CAS  PubMed  Google Scholar 

  • Bonetti PO, Hartmann K, Kuhn M, Reinhart WH, Wieland T (2000) Potential drug interactions and number of prescription drugs with special instructions at hospital discharge. Praxis (Bern 1994) 89: 182–189

    CAS  Google Scholar 

  • Di Castri A, Jacquot JM, Hemmi P, Moati L, Rouy JM, Compan B, et al (1995) Drug interactions: study of 409 prescriptions at the time of discharge from geriatric hospitalization. Therapie 50: 259–264

    CAS  PubMed  Google Scholar 

  • Köhler GI, Bode-Böger SM, Busse R, Hoopmann M, Welte T, Böger RH (2000) Drug-drug interactions in medical patients: effects of in-hospital treatment and relation to multiple drug use. Int J Clin Pharmacol Ther 38: 504–513

    Article  PubMed  Google Scholar 

  • Kruse W, Köhler J, Oster P, Schlierf G (1988) Potential drug interactions in the treatment of elderly patients with multiple morbidity. Z Gerontol 21: 164–168

    CAS  PubMed  Google Scholar 

  • Becker ML, Kallewaard M, Caspers PW, Visser LE, Leufkens HG, Stricker BH (2007) Hospitalisations and emergency department visits due to drug-drug interactions: a literature review. Pharmacoepidemiol Drug Saf 16: 641–651

    Article  PubMed  Google Scholar 

  • Malone DC, Abarca J, Hansten PD, Grizzle AJ, Armstrong EP, Van Bergen RC, et al (2004) Identification of serious drug-drug interactions: results of the partnership to prevent drug-drug interactions. J Am Pharm Assoc 44: 142–151

    Article  Google Scholar 

  • World Health Organization (2002) Safety of medicine: a guide to detecting and reporting adverse drug reaction. Geneva

  • Edwards IR, Biriell C (1994) Harmonisation in pharmacovigilance. Drug Safety 10: 93–102

    Article  CAS  PubMed  Google Scholar 

  • Brvar M, Fokter N, Bunc M, Mozina M (2009) The frequency of adverse drug reaction related admissions according to method of detection, admission urgency and medical department specialty. BMC Clin Pharmacol 9: 8

    Article  PubMed  PubMed Central  Google Scholar 

  • Lau HS, Florax C, Porsius AJ, De Boer A (2000) The completeness of medication histories in hospital medical records of patients admitted to general internal medicine wards. Br J Clin Pharmacol 49: 597–603

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Reeder TA, Mutnick A (2008) Pharmacist versus physician-obtained medication histories. Am J Health Syst Pharm 65: 857–860

    Article  PubMed  Google Scholar 

  • Fitzgerald RJ (2009) Medication errors: the importance of an accurate drug history. Br J Clin Pharmacol 67: 671–675

    Article  PubMed  PubMed Central  Google Scholar 

  • Peral Aguirregoitia J, Lertxundi Etxebarria U, Martínez Bengoechea MJ, Mora Atorrasagasti O, Franco Lamela E, Gabilondo Zelaia I (2007) Prospective assessment of drug interactions in hospitalized patients using a computer programme. Farm Hosp 31: 93–100

    Article  CAS  PubMed  Google Scholar 

  • Bjerrum L, Søgaard J, Hallas J, Kragstrup J (1998) Polypharmacy: correlations with sex, age and drug regimen. A prescription database study. Eur J Clin Pharmacol 54: 197–202

    Article  CAS  PubMed  Google Scholar 

  • Halkin H, Katzir I, Kurman I, Jan J, Malkin BB (2001) Preventing drug interactions by online prescription screening in community pharmacies and medical practices. Clin Pharmacol Ther 69: 260–265

    Article  CAS  PubMed  Google Scholar 

  • Egger T, Dormann H, Ahne G, Runge U, Neubert A, Criegee-Rieck M, et al (2003) Identification of adverse drug reactions in geriatric inpatients using a computerised drug database. Drugs Aging 20: 769–776

    Article  CAS  PubMed  Google Scholar 

  • Nobili A, Pasina L, Tettamanti M, Lucca U, Riva E, Marzona I, et al (2009) Potentially severe drug interactions in elderly outpatients: results of an observational study of an administrative prescription database. Clin Pharm Ther 34: 377–386

    Article  CAS  Google Scholar 

  • Haefeli WE, Martin-Facklam M (2002) Kombinationstherapien und Arzneimittel-wechselwirkungen. In: Arzneimittel-Kombinationstherapie. Heidelberg: Abt. Innere Medizin VI, Klinische Pharmakologie und Pharmakoepidemiologie, Universitätsklinikum Heidelberg

  • Weingart SN, Toth M, Sands DZ, Aronson MD, Davis RB, Phillips RS (2003) Physicians' decisions to override computerized drug alerts in primary care. Arch Intern Med 163: 2625–2631

    Article  PubMed  Google Scholar 

  • Payne TH, Nichol WP, Hoey P, Savarino J (2002) Characteristics and override rates of order checks in a practitioner order entry system. Proc AMIA Symp: 602–606

  • van der Sijs H, Mulder A, van Gelder T, Aarts J, Berg M, Vulto A (2009) Drug safety alert generation and overriding in a large Dutch university medical centre. Pharmacoepidemiol Drug Saf (In press)

  • Shah NR, Seger AC, Seger DL, Fiskio JM, Kuperman GJ, Blumenfeld B, et al (2005) Improving override rates for computerized prescribing alerts in ambulatory care. AMIA Annu Symp Proc: 1110

  • Davies EC, Green CF, Taylor S, Williamson PR, Mottram DR, Pirmohamed M (2009) Adverse drug reactions in hospital in-patients: a prospective analysis of 3695 patient-episodes. PLoS One 4: e4439

    Article  PubMed  PubMed Central  Google Scholar 

  • Mannheimer B, Ulfvarson J, Eklöf S, Bergqvist M, Andersén-Karlsson E, Pettersson H, et al (2006) Drug-related problems and pharmacotherapeutic advisory intervention at a medicine clinic. Eur J Clin Pharmacol 62: 1075–1081

    Article  PubMed  Google Scholar 

  • Krähenbühl-Melcher A, Schlienger R, Lampert M, Haschke M, Drewe J, Krähenbühl S (2007) Drug-related problems in hospitals: a review of the recent literature. Drug Saf 30: 379–407

    Article  PubMed  Google Scholar 

  • Omar MA, Wilson JP (2002) FDA adverse event reports on statin-associated rhabdomyolysis. Ann Pharmacother 36: 288–295

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Miran Brvar.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fokter, N., Možina, M. & Brvar, M. Potential drug-drug interactions and admissions due to drug-drug interactions in patients treated in medical departments. Wien Klin Wochenschr 122, 81–88 (2010). https://doi.org/10.1007/s00508-009-1251-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00508-009-1251-2

Keywords

Navigation