Pediatric acute respiratory distress syndrome associated with human metapneumovirus and respiratory syncytial virus

被引:14
|
作者
Ravindranath, Thyyar M. [1 ]
Gomez, Amanda [1 ]
Harwayne-Gidansky, Ilana [2 ]
Connors, Thomas J. [1 ]
Neill, Nathan [3 ]
Levin, Bruce [3 ]
Howell, Joy D. [2 ]
Saiman, Lisa [1 ,4 ]
Baird, John S. [1 ]
机构
[1] Columbia Univ, Dept Pediat, NewYork Presbyterian Hosp, Med Ctr, 3959 Broadway,CHN 10-24, New York, NY 10032 USA
[2] NewYork Presbyterian Hosp, Weill Cornell Med Ctr, Dept Pediat, New York, NY USA
[3] Columbia Univ, Dept Biostat, Mailman Sch Publ Hlth, New York, NY USA
[4] NewYork Presbyterian Hosp, Dept Infect Prevent & Control, New York, NY USA
关键词
human metapneumovirus; pediatric acute respiratory distress syndrome; pediatric intensive care unit; respiratory syncytial virus; EXTRACORPOREAL MEMBRANE-OXYGENATION; INTENSIVE-CARE-UNIT; YOUNG-CHILDREN; TRACT INFECTION; LUNG INJURY; INFLUENZA; INFANTS; DISEASE; SEVERITY; PATHOGEN;
D O I
10.1002/ppul.24044
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
ObjectivesTo study the incidence, risk factors, clinical course, and outcome of ARDS in children with HMP and RSV. Working HypothesisWe hypothesized that ARDS in children with HMP was similar in incidence, risk factors, clinical course, and outcomes to ARDS in children with RSV. Study DesignRetrospective, observational study over 2 years. Patient-Subject SelectionPatients included were <18 years old with HMP or RSV detected from nasopharyngeal specimens by commercial reverse transcriptase polymerase chain reaction assay admitted to a study site. MethodologyWe described the incidence of ARDS within 1 week following the detection of HMP or RSV using recently developed Pediatric ARDS (PARDS) criteria. We also assessed risk factors, clinical course, and outcomes of children in the PICU with HMP or RSV and PARDS or non-PARDS. ResultsWe identified 57 patients with HMP and 161 patients with RSV: the proportions of patients with either virus who developed PARDS (HMP: 23%, RSV: 20%) and severe PARDS (HMP: 9%, RSV: 7%) were similar, as were the proportions of patients with acute (or acute-on-chronic) respiratory failure who developed PARDS (HMP: 41%, RSV: 31%). In a logistic regression model, risk factors associated with PARDS included neurologic comorbidity and PIM 3 probability of mortality, but not virus type. The risk factors, clinical course, and outcomes were similar for patients with PARDS associated with HMP and RSV. ConclusionsAbout 1/3 of children with HMP or RSV and acute (or acute-on-chronic) respiratory failure developed PARDS. Children with either virus and a neurologic comorbidity or an increased PIM 3 probability of mortality were at increased risk for PARDS.
引用
收藏
页码:929 / 935
页数:7
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