2021
DOI: 10.1513/annalsats.202008-996oc
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Relationship of Viral Detection with Duration of Ventilation in Critically Ill Infants with Lower Respiratory Tract Infection

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Cited by 5 publications
(15 citation statements)
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“…Twenty-seven studies [ 13–39 ] provided descriptive data on the clinical decisions to test for RSV in various settings: 16 provided data for IP [ 13–16 , 18–29 ], 1 for IP and for ED [ 17 ], 9 for ED [ 30–38 ], and 1 for OP [ 39 ] ( Supplementary Table 3 A and 3 B ). Thirteen studies describing laboratory testing practice for combined settings (ie, IP with other settings, ED with other settings, or OP with other settings) are listed in Supplementary Table 3 C .…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Twenty-seven studies [ 13–39 ] provided descriptive data on the clinical decisions to test for RSV in various settings: 16 provided data for IP [ 13–16 , 18–29 ], 1 for IP and for ED [ 17 ], 9 for ED [ 30–38 ], and 1 for OP [ 39 ] ( Supplementary Table 3 A and 3 B ). Thirteen studies describing laboratory testing practice for combined settings (ie, IP with other settings, ED with other settings, or OP with other settings) are listed in Supplementary Table 3 C .…”
Section: Resultsmentioning
confidence: 99%
“…One study reported data for LRTI and upper respiratory illness populations separately [ 56 ]. One study combined data for LRTI with other respiratory distress [ 13 ], 6 studies grouped data by acute respiratory infections (ARI) or symptomatic (eg, fever) populations [ 40 , 57–61 ], 1 study included healthy infants [ 62 ], and 4 studies provided information among populations of unknown respiratory conditions [ 24 , 63–65 ]. Higher RSV testing incidence proportions among studies with LRTI populations were not consistently observed in the IP setting compared with studies among ARI, symptomatic, healthy, or unknown respiratory condition populations, likely due to differences in study designs, time periods, test types, locations, and other population characteristics ( Table 2 ).…”
Section: Resultsmentioning
confidence: 99%
“…First, VPS does not collect/ report all pertinent variables. Exact patient age was unavailable and likely would have been included in the models if available, but patient weight was likely a sufficient surrogate and is preferred by some authors (34). Gestational age and other granular details of comorbid conditions were not available, so we conservatively grouped all comorbidities into a single "yes/no" variable rather than risk misclassifying some as minor or major.…”
Section: Discussionmentioning
confidence: 99%
“…Thirty-six were retrospective cohort studies [ 13–48 ], 3 were surveillance studies [ 1 , 2 , 49 ], 2 were case-control studies [ 50 , 51 ], and 1 was a prospective cohort study [ 52 ]. Study locations were varied: 20 were located within a single state [ 14 , 16 , 18 , 22 , 23 , 28 , 30 , 31 , 34 , 35 , 38–42 , 44 , 45 , 47 , 48 , 50 , 51 ], 8 used nationally representative databases [ 17 , 19–21 , 29 , 33 , 36 , 53 ], and 4 used nationwide death certificate data [ 25–27 , 37 ]. Six other studies [ 1 , 2 , 32 , 46 , 49 , 52 ] were conducted in multiple states and 3 used large datasets that were not location specific (eg, MarketScan, Vizient [ 15 , 24 , 28 ]).…”
Section: Resultsmentioning
confidence: 99%
“…While 22 studies did not restrict the study eligibility to specific groups by wGA, race, or comorbidities [ 1 , 2 , 13 , 19–29 , 33 , 35–37 , 39–42 ], 4 studies were restricted to only premature (<37 wGA) infants and 2 to full-term infants [ 43 , 51 ]. Insurance status was reported in 2 studies [ 1 , 24 ] and ICU admission status in 10 [ 1 , 13 , 16 , 18 , 24 , 30 , 31 , 45 , 46 , 51 ]. Two studies were conducted in late-preterm (35–36 wGA) or full-term otherwise healthy infants [ 43 , 51 ].…”
Section: Resultsmentioning
confidence: 99%