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Critical Care

Open Access

Attributable cost of methicillin resistance: an issue that is difficult to evaluate

Critical Care200610:157

https://doi.org/10.1186/cc4994

Published: 11 August 2006

Abstract

Estimating the consequences and the cost of methicillin resistance is a difficult challenge. Patients who develop methicillin-resistant ventilator-associated pneumonia (VAP) are very different from those who develop methicillin-sensitive VAP, and biased estimates are frequent. We reviewed some important confounding factors of which the reader should be aware.

In the previous issue of Critical Care, Shorr and coworkers [1] provided new data on the morbidity and cost burden attributable to methicillin-resistant Staphylococcus aureus (MRSA)-associated early-onset pneumonia (EOP). Based on the data recorded by 42 US hospitals, those investigators found methicillin resistance to be associated with a significant 4- to 6-day excess in mechanical ventilation, and intensive care unit (ICU) and in-hospital days. It was associated with a nonsignificant increase of about US$8000 in total costs, after controlling for case mix and severity. The authors made particular effort to select monomicrobial pneumonias and to adjust the calculations based on underlying illness, and on the severity and duration of ICU stay before EOP. However, this estimated increase in costs should be regarded with caution because of a number of potential biases associated with this type of analysis.

First, the observed incidence of EOP was very low. The overall risk for ventilator-associated pneumonia (VAP) is between 9.7% and 22.8% [2]. EOP represents at least one-third of cases. Consequently, the rate of EOP should be higher than 3.2% [3]. Because Shorr and coworkers found that only 499 episodes were recorded in 42 hospitals over 2 years, this suggests that the incidence was unusually low or that EOP was largely under-reported. This could have introduced bias because unrecognized episodes might be different (probably less severe) than reported ones. Any under-recognition of EOP might have resulted from the known lack of reproducibility of ICD-9 (International Classification of Diseases, ninth edition) [4]. Moreover, MRSA VAP has been reported to occur mainly late in the ICU stay [58]; MRSA represents fewer than 5% of micro-organisms encountered in EOP episodes [9]. The factors that impact on outcomes of EOP may be different from those in late-onset pneumonia [9, 10]. For example, EOP is associated a shorter ICU stay, with significantly fewer days of mechanical ventilation, of central vein catheterization and of use of ICU resources [9]. This fact probably largely explained why the ICU length of stay (4 days) was considerably lower in the report by Shorr and coworkers than in the recent report by Combes and coworkers (i.e. 11 days) [5].

Second, MRSA and methicillin-sensitive Staphylococcus aureus (MSSA) EOP were not matched for the same hospital, and therefore variability in charges between hospitals could account for some of the observed differences. Surprisingly, the authors found that the ICU resources and extra costs related to MRSA EOP were higher only for survivors, as opposed to MSSA EOP. On the contrary, deaths occurred earlier in fatal MRSA EOP, leading to lower hospital costs for nonsurvivors. Because MRSA VAP has not been associated with higher rates of organ dysfunction than MSSA VAP [5], the potential causes of this finding are speculative (e.g. differences in the rate of do-not-resuscitate orders, differences in case mix, differences in the adequacy of antimicrobial treatment, or chance) and might have had a confounding impact on the final result.

Despite these limitations, economic studies such as that conducted by Shorr and coworkers [1] provided further evidence of the cost of MRSA infections and provide new arguments for funding the fight against MRSA spread in the ICU.

Abbreviations

EOP: 

early-onset pneumonia

ICU: 

intensive care unit

MRSA: 

methicillin-resistant Staphylococcus aureus

MSSA: 

methicillin-sensitive Staphylococcus aureus

VAP: 

ventilator-associated pneumonia.

Declarations

Authors’ Affiliations

(1)
Groupe d'épidémiologie des cancers et des affections graves INSERM U 578, Service de réanimation médicale, University Hospital Albert Michallon, Grenoble Cedex, France

References

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Copyright

© BioMed Central Ltd 2006

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