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Influence of a patient transfer network of US inpatient facilities on the incidence of nosocomial infections

Authors :
Jukka-Pekka Onnela
Nicholas A. Christakis
Michael L. Barnett
Víctor M. Eguíluz
Juan Fernández-Gracia
National Institutes of Health (US)
European Commission
Ministerio de Economía y Competitividad (España)
Source :
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017), Digital.CSIC. Repositorio Institucional del CSIC, instname, Scientific Reports
Publication Year :
2017
Publisher :
Springer Science and Business Media LLC, 2017.

Abstract

Antibiotic-resistant bacterial infections are a substantial source of morbidity and mortality and have a common reservoir in inpatient settings. Transferring patients between facilities could be a mechanism for the spread of these infections. We wanted to assess whether a network of hospitals, linked by inpatient transfers, contributes to the spread of nosocomial infections and investigate how network structure may be leveraged to design efficient surveillance systems. We construct a network defined by the transfer of Medicare patients across US inpatient facilities using a 100% sample of inpatient discharge claims from 2006–2007. We show the association between network structure and C. difficile incidence, with a 1% increase in a facility’s C. difficile incidence being associated with a 0.53% increase in C. difficile incidence of neighboring facilities. Finally, we used network science methods to determine the facilities to monitor to maximize surveillance efficiency. An optimal surveillance strategy for selecting “sensor” hospitals, based on their network position, detects 80% of the C. difficile infections using only 2% of hospitals as sensors. Selecting a small fraction of facilities as “sensors” could be a cost-effective mechanism to monitor emerging nosocomial infections.<br />N.A.C. is supported by grant from the NIH (P-01 AG031093), V.M.E. by grant MODASS FIS2011-24785 (Spain and EU FEDER) and M.L.B. by HRSA grant (T32-HP10251). J.P.O. is supported by grants P-01 AG031093 and U54GM088558-06. J.F.-G. is supported by NIH grant U54GM088558-06.

Details

ISSN :
20452322
Volume :
7
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....57906f83ddc1c4d7b43d4edb8f1fd688