PMID- 30462237 OWN - NLM STAT- MEDLINE DCOM- 20200603 LR - 20210109 IS - 1460-2091 (Electronic) IS - 0305-7453 (Print) IS - 0305-7453 (Linking) VI - 74 IP - 3 DP - 2019 Mar 1 TI - Intravenous catheter-related adverse events exceed drug-related adverse events in outpatient parenteral antimicrobial therapy. PG - 787-790 LID - 10.1093/jac/dky474 [doi] AB - BACKGROUND: Drug-related adverse events (AEs) are reported to be common amongst patients receiving outpatient parenteral antimicrobial therapy (OPAT). However, comparative data regarding intravenous (iv) catheter-related AEs are lacking. OBJECTIVES: To compare drug- and iv catheter-related AEs from a large UK OPAT centre. PATIENTS AND METHODS: We reviewed 544 OPAT episodes [median (IQR) age: 57 (39-71) years, 60% male, 13% with diabetes] with a median (IQR) duration of 7 (2-18) days. Clinically significant drug- and iv catheter-related AEs were calculated as a percentage of OPAT episodes with an AE and also as AEs per 1000 iv drug/catheter days. RESULTS: Drug-related AEs complicated 13 (2.4%) OPAT episodes at 1.7 (95% CI 0.9-2.9) per 1000 drug days. Catheter-related AEs occurred more frequently, complicating 32 (5.9%) episodes at 5.7 (95% CI 4.2-7.9) per 1000 iv catheter days (chi2 test for difference in AE rate: P < 0.001). Non-radiologically guided midline catheters were associated with the most frequent AEs (n = 23) at 15.6 (95% CI 10.3-23.4) per 1000 iv catheter days compared with other types of iv catheters (HR 8.4, 95% CI 2.4-51.9, P < 0.004), and self-administration was associated with a higher rate of catheter-related AEs at 12.0 (95% CI 6.0-23.9) per 1000 iv catheter days (HR 4.15, 95% CI 1.7-9.1, P = 0.007). CONCLUSIONS: Clinically significant iv catheter-related AEs occurred more frequently than drug-related AEs, especially when using non-radiologically guided midline catheters. Regular review of the need for iv therapy and switching to oral antimicrobials when appropriate is likely to minimize OPAT-related AEs. CI - (c) The Author(s) 2018. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. FAU - Underwood, Jonathan AU - Underwood J AD - The Hospital for Tropical Diseases, Division of Infection, University College London Hospitals NHS Foundation Trust, London, UK. FAU - Marks, Michael AU - Marks M AD - The Hospital for Tropical Diseases, Division of Infection, University College London Hospitals NHS Foundation Trust, London, UK. AD - Clinical Research Department, London School of Hygiene and Tropical Medicine, London, UK. FAU - Collins, Steve AU - Collins S AD - The Hospital for Tropical Diseases, Division of Infection, University College London Hospitals NHS Foundation Trust, London, UK. FAU - Logan, Sarah AU - Logan S AD - The Hospital for Tropical Diseases, Division of Infection, University College London Hospitals NHS Foundation Trust, London, UK. FAU - Pollara, Gabriele AU - Pollara G AD - The Hospital for Tropical Diseases, Division of Infection, University College London Hospitals NHS Foundation Trust, London, UK. AD - Division of Infection & Immunity, University College London, London, UK. LA - eng GR - WT_/Wellcome Trust/United Kingdom GR - WT102807/WT_/Wellcome Trust/United Kingdom GR - WT101766/WT_/Wellcome Trust/United Kingdom PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - J Antimicrob Chemother JT - The Journal of antimicrobial chemotherapy JID - 7513617 RN - 0 (Anti-Infective Agents) SB - IM MH - Administration, Intravenous/adverse effects MH - Adult MH - Aged MH - Anti-Infective Agents/administration & dosage/*adverse effects MH - Catheters/*adverse effects/*statistics & numerical data MH - Drug-Related Side Effects and Adverse Reactions/*epidemiology/etiology MH - Female MH - Health Care Surveys MH - Humans MH - Infusions, Intravenous/adverse effects MH - Infusions, Parenteral/*adverse effects/methods/*statistics & numerical data MH - Kaplan-Meier Estimate MH - Male MH - Middle Aged MH - *Outpatients MH - Vascular Access Devices/adverse effects/statistics & numerical data PMC - PMC6376853 EDAT- 2018/11/22 06:00 MHDA- 2020/06/04 06:00 PMCR- 2018/11/20 CRDT- 2018/11/22 06:00 PHST- 2018/08/04 00:00 [received] PHST- 2018/10/09 00:00 [revised] PHST- 2018/10/16 00:00 [accepted] PHST- 2018/11/22 06:00 [pubmed] PHST- 2020/06/04 06:00 [medline] PHST- 2018/11/22 06:00 [entrez] PHST- 2018/11/20 00:00 [pmc-release] AID - 5193697 [pii] AID - dky474 [pii] AID - 10.1093/jac/dky474 [doi] PST - ppublish SO - J Antimicrob Chemother. 2019 Mar 1;74(3):787-790. doi: 10.1093/jac/dky474.