Table 5.
IDSA Recommendation | Study cohort | Assessment | Strategy to improve antibiotic and health care resource utilization |
---|---|---|---|
Use severity of illness score (e.g., CURB-65) to assist in decision to admit | 66% had CURB-65 score of 0 or 1; 27% had score of 0 or 1 and absence of hypoxemia | Frequent hospitalization of low-risk patients | Emergency department provider education and implementation of CURB- 65 score as adjunct in site of care decision |
Perform sputum gram stain and culture only if good-quality specimen can be obtained and processed appropriately; obtain prior to antibiotic therapy | When ordered, adequate sputum sample obtained in 45% of cases and yield of pathogen in 16% Median time to sputum collection 11 hours after antibiotic initiation | Low-yield test due to inadequate samples and time delay | Target use to ICU cases and those with risk of multi-drug resistant pathogen. Engage nursing, respiratory therapy, and microbiology laboratory to improve sample collection, processing, and timing. |
Obtain pretreatment blood cultures in selected cases | Blood cultures obtained in 81% of non-ICU cases; 12 of 21 (57%) positive results were false-positive | Blood cultures obtained routinely rather than selectively in non-ICU cases with a high proportion of false-positive results | Limit blood cultures in non-ICU to those with risk for multi-drug resistant pathogens. Engage nursing and phlebotomy to reduce blood culture contamination rate. |
Empirically treat with a respiratory fluoroquinolone or a β-lactam plus macrolide in non-ICU cases | >90% of non-ICU cases treated with guideline-recommended therapy | Excellent adherence to empiric antibiotic selection guidance | Promote ongoing adherence to guideline- concordant empiric therapy |
For CA-MRSA infection, add vancomycin or linezolid | MRSA cultured from respiratory specimens in 3 cases; 53 (25%) treated with vancomycin | Empiric therapy against MRSA common | Educate providers regarding local incidence of CA-MRSA pneumonia and provide specific guidance on when to consider empiric MRSA therapy |
When switching to oral antibiotics, either the same agent as the intravenous antibiotic or the same drug class should be used* | 66% of patients initially treated with ceftriaxone and azithromycin discharged on a new drug class, most often a fluoroquinolone | Unnecessary exposure to a third drug class and contribution to fluoroquinolone overuse | Provide institution-specific recommendations for oral step-down therapy consistent with IDSA/ATS guidance |
Treat until afebrile and clinically stable (5 days minimum). Most patients become clinically stable in 3–7 days, so longer durations rarely necessary | Duration of therapy ≥10 days in 56% of cases | Prolonged treatment durations the norm in both non-ICU and ICU cases | Promote short-course therapy (5–7 days) in uncomplicated, clinically responding cases. |
macrolide alone suggested for those treated with intravenous β-lactam plus macrolide combination