AI Article Synopsis

  • * In a study comparing two groups of MDRO patients, those receiving early pharmacist consultation (PEAC) experienced a 70% reduction in 30-day mortality and better clinical improvement than those who did not receive this consultation.
  • * Despite the positive effects on mortality and clinical outcomes, there were no notable differences in hospital stay length, antibiotic usage, or costs between the two patient groups.

Article Abstract

Infectious disease (ID) consultation can improve multidrug-resistant organism (MDRO) treatment outcomes. However, the impact of clinical pharmacists' ID consultation on MDRO therapy, especially early initiation, has not been reported. In this study, we try to explore the impact of the pharmacist early active consultation (PEAC) on MDRO patient management. We conducted a prospective historical controlled study based on PEAC in MDRO patients. The retrospective control group was patients hospitalized 18 months before the PEAC initiation, and the prospective PEAC group was patients hospitalized 18 months after the PEAC initiation. Primary endpoint was 30-day all-cause mortality. Secondary outcomes were MDRO clinical outcome, duration of antibiotic use, length of stay, antibiotic consumption and antibiotic costs. Further subgroup analysis of secondary outcomes was performed by the condition at admission, MDRO pathogenicity and MDRO clinical outcome. 188 MDRO patients were included. After adjusting for potential predictors, PEAC reduced the 30-day all-cause mortality by 70% (HR 0.30, 95% CI 0.09-0.96, = 0.042). PEAC group had clinical improvement than control group (89.47% vs. 65.59%, < 0.001), especially in patients with non-severe clinical conditions at admission (98.41% vs. 70.18%, < 0.001). However, no significant differences were found between groups in length of stay, antibiotics consumption, and antibiotics costs. Early active pharmacy ID consultation can reduce 30-day all-cause mortality and improve clinical outcomes in MDRO patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017476PMC
http://dx.doi.org/10.3389/fphar.2023.1128219DOI Listing

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