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5PSQ-164 Drug-drug interactions in patients with cardiovascular diseases
  1. G Lo Surdo1,
  2. E Volpi1,
  3. M Zizevskikh1,
  4. S Tonazzini1,
  5. S Alduini1,
  6. S Maffei2,
  7. M Baroni3,
  8. S Biagini1
  1. 1Fondazione Toscana Gabriele Monasterio, Hospital Pharmacy, Massa, Italy
  2. 2Fondazione Toscana Gabriele Monasterio, Division of Clinical And Surgical Heart Diseases, Massa, Italy
  3. 3Fondazione Toscana Gabriele Monasterio, Clinical Risk Manager, Massa, Italy


Background Medication reconciliation (MedRec) is the process of comparing a patient’s medication orders to all of the medications that the patient has been taking. This reconciliation is done to avoid medication errors such as drug interactions. The World Health Organization has recognized MedRec as a recommended standard of quality in health assistance.

Purpose The aim of this analysis was to estimate the prevalence of patients exposed to potentially relevant drug-drug interaction (DDI) at hospital discharge.

Material and methods This was an observational retrospective study involving patients with cardiovascular diseases discharged from our hospital between December 2016 and May 2017.

A total of 1033 patients were included in this study and 8005 drug prescriptions at discharge were analysed (7.75 per patient). DDIs were classified as moderate (pharmacological effects must be controlled by individual dose adjustment or on the basis of drug plasma concentration) or severe (drug combination should be avoided in clinical practice).

Results Among 1033 patients included, 271 (26.2%) were exposed to at least one potential DDI. In particular, 173 patients were discharged with one interaction (16.7%), 54 patients with two interactions (5.2%), 23 patients with three interactions (2.2%) and 21 were exposed to four or more DDIs (2%). A total of 445 DDIs were recorded, 75.1% were classified as moderate and 24.9% as severe interactions. The median number of DDIs per patients with interactions was 1.6 (range 1–7). The most frequent severe interaction was the combination of some selective serotonin reuptake inhibitors (Paroxetine, Sertraline and Citalopram) and Furosemide (n=46;1%). This combination is known to be associated with an increased risk of cardiotoxicity (QT prolongation and cardiac arrest).

Conclusion From this first analysis, it emerged that one-third of our patients were discharged with at least one potential DDI and a remarkable portion of these combinations was severe. The next step will be to investigate whether adverse clinical events, readmission or death after discharge could be associated with a potentially severe DDI. The final target will be the involvement of a clinical pharmacist within a multidisciplinary team to highlight potential DDIs at discharge and minimise the occurrence of the related risks.

References and/or acknowledgements No conflict of interest.

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