Epidemiology and association with outcomes of polypharmacy in patients undergoing surgery: retrospective, population-based cohort study

Author:

Jónsdóttir Freyja12ORCID,Blöndal Anna B13,Guðmundsson Aðalsteinn45,Bates Ian6,Stevenson Jennifer M78,Sigurðsson Martin I59

Affiliation:

1. Pharmaceutical Sciences, University of Iceland , Reykjavik , Iceland

2. Pharmacy Services, Landspitali - The National University Hospital of Iceland , Reykjavik , Iceland

3. Development Centre for Primary Healthcare in Iceland , Primary Health Care of the Capital Area, Reykjavik , Iceland

4. Division of Geriatrics, Landspitali - The National University Hospital of Iceland , Reykjavik , Iceland

5. Faculty of Medicine, University of Iceland , Reykjavik , Iceland

6. School of Pharmacy, University College London , London , UK

7. Institute of Pharmaceutical Science, King's College , London , UK

8. Pharmacy Department, Guy’s and St Thomas’ NHS Foundation Trust , London , UK

9. Division of Anaesthesia and Intensive Care Medicine, Landspitali - The National University Hospital of Iceland , Reykjavik , Iceland

Abstract

Abstract Background The aim of this study was to determine the prevalence of preoperative polypharmacy and the incidence of postoperative polypharmacy/hyper-polypharmacy in surgical patients and their association with adverse outcomes. Methods This was a retrospective, population-based cohort study among patients older than or equal to 18 years undergoing surgery at a university hospital between 2005 and 2018. Patients were categorized based on the number of medications: non-polypharmacy (fewer than 5); polypharmacy (5–9); and hyper-polypharmacy (greater than or equal to 10). The 30-day mortality, prolonged hospitalization (greater than or equal to 10 days), and incidence of readmission were compared between medication-use categories. Results Among 55 997 patients, the prevalence of preoperative polypharmacy was 32.3 per cent (95 per cent c.i. 33.5 to 34.3) and the prevalence of hyper-polypharmacy was 25.5 per cent (95 per cent c.i. 25.2 to 25.9). Thirty-day mortality was higher for patients exposed to preoperative hyper-polypharmacy (2.3 per cent) and preoperative polypharmacy (0.8 per cent) compared with those exposed to non-polypharmacy (0.6 per cent) (P < 0.001). The hazards ratio (HR) of long-term mortality was higher for patients exposed to hyper-polypharmacy (HR 1.32 (95 per cent c.i. 1.25 to 1.40)) and polypharmacy (HR 1.07 (95 per cent c.i. 1.01 to 1.14)) after adjustment for patient and procedural variables. The incidence of longer hospitalization (greater than or equal to 10 days) was higher for hyper-polypharmacy (11.3 per cent) and polypharmacy (6.3 per cent) compared with non-polypharmacy (4.1 per cent) (P < 0.001). The 30-day incidence of readmission was higher for patients exposed to hyper-polypharmacy (10.2 per cent) compared with polypharmacy (6.1 per cent) and non-polypharmacy (4.8 per cent) (P < 0.001). Among patients not exposed to polypharmacy, the incidence of new postoperative polypharmacy/hyper-polypharmacy was 33.4 per cent (95 per cent c.i. 32.8 to 34.1), and, for patients exposed to preoperative polypharmacy, the incidence of postoperative hyper-polypharmacy was 16.3 per cent (95 per cent c.i. 16.0 to 16.7). Conclusion Preoperative polypharmacy and new postoperative polypharmacy/hyper-polypharmacy are common and associated with adverse outcomes. This highlights the need for increased emphasis on optimizing medication usage throughout the perioperative interval. Registration number NCT04805151 (http://clinicaltrials.gov).

Funder

Foundation of St Josef’s Hospital

Icelandic Gerontological Research Centre

National University Hospital of Iceland

Landspitali University Hospital Science Fund

University of Iceland Research Fund

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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