2012
DOI: 10.1007/s11606-012-2011-y
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Guideline-Based Antibiotics and Mortality in Healthcare-Associated Pneumonia

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Cited by 23 publications
(20 citation statements)
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References 25 publications
(30 reference statements)
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“…By limiting our cohort to ICU patients, we expected that restrictions on care would have a smaller role, and that GC-HCAP antibiotics might be more likely to be beneficial. Despite this approach, the effects of GC-HCAP therapy remained consistent with prior studies, where GC-HCAP therapy given to patients in the medical ward or mixed ward/ICU patients either increased mortality or had no effect on mortality [5,1315]. Data using a less strict combination of guideline-similar antibiotics (e.g., one anti-MRSA antibiotic and only one antipseudomonal antibiotic) in mixed ward/ICU cohorts have also demonstrated similar results to our study [15,16].…”
Section: Discussionsupporting
confidence: 65%
“…By limiting our cohort to ICU patients, we expected that restrictions on care would have a smaller role, and that GC-HCAP antibiotics might be more likely to be beneficial. Despite this approach, the effects of GC-HCAP therapy remained consistent with prior studies, where GC-HCAP therapy given to patients in the medical ward or mixed ward/ICU patients either increased mortality or had no effect on mortality [5,1315]. Data using a less strict combination of guideline-similar antibiotics (e.g., one anti-MRSA antibiotic and only one antipseudomonal antibiotic) in mixed ward/ICU cohorts have also demonstrated similar results to our study [15,16].…”
Section: Discussionsupporting
confidence: 65%
“…Some authors have found higher mortality rates with the use of guideline-concordant empirical therapy, with a trend toward higher mortality rates even in the subset with MRSA (741,742). A more nuanced view emerged from Madaras-Kelly et al, in which receipt of "guideline-similar therapy" increased the 30-day mortality rate overall but appeared to improve mortality in the subset of patients with an a priori increased risk of resistance to ceftriaxone or moxifloxacin (743).…”
Section: Managementmentioning
confidence: 99%
“…[2][3][4][21][22][23][24] It is also not well defined whether HCAP treatment should align with CAP or HAP therapy. [38][39][40][41][42][43][44][45][46] The classification of HCAP was introduced in the 2005 American Thoracic Society/Infectious Diseases Society of America (ATS/IDSA) guidelines, 3 which suggested that patients who develop pneumonia in the community and have specific risk factors should be treated similarly to those with HAP, including coverage for MDR pathogens ( Table 2). The frequency of MDR pathogens and whether all MDR risk factors are relevant in all practice settings is unclear and complicate determination of antibiotic recommendations using local data.…”
Section: Pre-intervention Chart Auditmentioning
confidence: 99%
“…The frequency of MDR pathogens and whether all MDR risk factors are relevant in all practice settings is unclear and complicate determination of antibiotic recommendations using local data. [38][39][40][41][42][43][44][45][46] Given limited identification of MDR pathogens in the authors' health region and to prevent the unnecessary use of broad-spectrum antibiotics, the algorithms did not incorporate all MDR risk factors identified by the ATS/IDSA guidelines ( Table 2). The most common MDR pathogens identified in the health region were Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus (MRSA) ( Table 3).…”
Section: Pre-intervention Chart Auditmentioning
confidence: 99%