| Literature DB >> 30478489 |
Roos Wijnakker1, Loes E Visser2, Emile F Schippers3,4, Leo G Visser3, Nathalie D van Burgel5, Cees van Nieuwkoop4.
Abstract
Background There is increasing interest in outpatient parenteral antimicrobial treatment. Objective To evaluate the added value of consultation of an infectious diseases expert team (consisting of two internist-infectious diseases specialists and a microbiologist) for advice regarding type, administration route and duration of antibiotic treatment. Setting A retrospective case series was performed at the Haga Teaching Hospital, a 700-bed regional teaching hospital in The Hague, The Netherlands. Methods Complication rate and mortality was evaluated during 60 days of follow-up. Therapeutic rationality regarding outpatient parenteral antimicrobial treatment was determined by presenting randomly selected paper cases from the database to two independent infectious diseases specialists who were blinded to patient's treatment and outcomes. The concordance between the two advices were analysed using Cohen's kappa. For those with discordance, an infectious diseases expert team meeting was organized to reach consensus. The final recommendation was compared to the actual given antibiotic treatment. Main outcome measure Discrepancy between the infectious disease expert team recommendations upon type, administration route and duration of antibiotics and the real outpatient parenteral antimicrobial treatment practice. Results Out of 89 included cases, 50 were randomly selected for review by the infectious diseases specialists. The kappa statistic regarding antimicrobial policy was 0.581 (P < 0.001). In 78% (39/50 cases), they had complete agreement upon all aspects of antibiotic treatment. The remaining 11 cases were reviewed by the expert team. Comparing the consensus of 50 cases to actual practice, in 14(28%) cases there was a discrepancy suggesting potential room for improvement. Comparing the cases in whom an individual infectious diseases specialist was involved in real practice to those cases without, there was 18% versus 42% discrepancy with the recommendations of the expert team (OR 3.4; 95% CI: 0.9-12.5, P = 0.06). Complication rate was 19% including unplanned readmissions and side effects of antimicrobial agent or administration route. Conclusion Though outpatient parenteral antimicrobial treatment policies in the Netherlands appear to be safe, consultation of an ID expert team, rather than an individual ID specialist, has the potential to optimize antimicrobial treatment in patients considered suitable for outpatient parenteral antimicrobial treatment.Entities:
Keywords: Antimicrobial stewardship; Expert Consultation; Home treatment; Infectious diseases; OPAT; Outpatients; The Netherlands
Mesh:
Substances:
Year: 2018 PMID: 30478489 PMCID: PMC6394504 DOI: 10.1007/s11096-018-0751-4
Source DB: PubMed Journal: Int J Clin Pharm
Fig. 1Flow chart of patient selection
Baseline patient characteristics
| Variable | Total population (n = 89) |
|---|---|
| Male sex (n, %) | 57 (64) |
| Age (median + range) | 66 (20–87) |
| Department ( | |
| Internal Medicine | 42 (47.2) |
| Urology | 14 (15.7) |
| Orthopedics | 12 (13.5) |
| Clinical diagnoses ( | |
| Bone and Joint Infections | 35 (38.1) |
| Septic Arthritis | 13 (14.6) |
| Spondylodiscitis | 10 (11.2) |
| Prothetic joint infections | 8 (8.9) |
| Osteomyelitis | 4 (4.5) |
| Urinary tract infections | 25 (28.1) |
| Pyelonefritis | 9 (10.1) |
| Prostatitis | 5 (5.6) |
| Urosepsis | 11 (12.3) |
| Community acquired | 10 (11.2) |
| Abscess | 5 (5.6) |
| Endocarditis | 4 (3.3) |
| Other (bacteremia, meningitis, neuroborreliosis, neurosyphilis) | 10 (11.2) |
| Antimicrobial diagnoses ( | |
| None | 10 (11.2) |
| | 24 (26.9) |
| | 21 (23.6) |
| | 3 (3,4) |
| | 3 (3.4) |
| | 5 (5.6) |
| Other ( | 16 (17.9) |
|
| 8 (8.9) |
| Multiresistant pathogen (%) | 19 (21.3) |
| Formal ID consult ( | 35 (39.3) |
| Type of antimicrobial used (%) | |
| Flucloxacillin | 26 (29.2) |
| Carbapenems | 15 (16.9) |
| Ceftriaxon | 15 (16.9) |
| Benzylpenicillin | 12 (13.5) |
| Cefuroxim | 10 (11.2) |
| Vancomycin | 7 (7.9) |
| Ceftazidim | 2 (2.2) |
| Cefalozin and others | 2 (2.2) |
| Duration OPAT treatment (median +IQR) | 28 days (14–47) |
Fig. 2Potential room for improvement of OPAT by multidisciplinary ID expert team