TY - JOUR
T1 - Pulmonary histopathologic abnormalities and predictor variables in autopsies of burned pediatric patients
AU - Sousse, Linda
AU - Herndon, David
AU - Andersen, Clark R.
AU - Zovath, Andrew
AU - Finnerty, Celeste C.
AU - Mlcak, Ronald P.
AU - Cox, Robert
AU - Traber, Daniel L.
AU - Hawkins, Hal
N1 - Funding Information:
There are no conflicts of interests or financial disclosures from any authors of this original work. This study was supported by Grants: 84060 , 84080 , 71008 , 71009 , 71935 from the Shriners Hospitals for Children (SHC) , and Grants P50-GM60338, R01-GM056687, T32-GM8256 from the National Institutes of Health . Additionally, Dr. Celeste Finnerty is an Institute for Translational Science (ITS) Scholar (NIH Grants No. KL2RR029875 , UL1RR029876 ).
Publisher Copyright:
© 2014 Elsevier Ltd and ISBI.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Pulmonary abnormalities occur in 30-80% of fatalities after burn. The objective of our study is to investigate lung pathology in autopsy tissues of pediatric burn patients. Methods Three scientists with pathology training in pediatric burn care reviewed masked autopsy slides of burned children who died after admission to a burn center from 2002 to 2012 (n = 43). Autopsy lung tissue was assigned scores for histologic abnormalities in 9 categories, including alveolar and interstitial fibrosis, hyaline membranes, and type II epithelial cell proliferation. Scores were then tested for correlation with age, TBSA burn, number of days between burn and death, time between burn and admission, and the presence of inhalation injury using analyses with linear models. Results Type II epithelial cell proliferation was significantly more common in cases with a longer time between burn and admission (p < 0.02). Interstitial fibrosis was significantly more severe in cases with longer survival after burn (p < 0.01). The scores for protein were significantly higher in cases with longer survival after burn (p < 0.03). Enlarged air spaces were significantly more prominent in cases with longer survival after burn (p < 0.01), and in cases with the presence of inhalation injury (p < 0.01). Conclusions Histological findings associated with diffuse alveolar damage (DAD), which is the pathological correlate of the acute respiratory distress syndrome (ARDS), were seen in approximately 42% of autopsies studied. Protein-rich alveolar edema, which is the abnormality that leads to ARDS, may occur from multiple causes, including inhalation injury.
AB - Pulmonary abnormalities occur in 30-80% of fatalities after burn. The objective of our study is to investigate lung pathology in autopsy tissues of pediatric burn patients. Methods Three scientists with pathology training in pediatric burn care reviewed masked autopsy slides of burned children who died after admission to a burn center from 2002 to 2012 (n = 43). Autopsy lung tissue was assigned scores for histologic abnormalities in 9 categories, including alveolar and interstitial fibrosis, hyaline membranes, and type II epithelial cell proliferation. Scores were then tested for correlation with age, TBSA burn, number of days between burn and death, time between burn and admission, and the presence of inhalation injury using analyses with linear models. Results Type II epithelial cell proliferation was significantly more common in cases with a longer time between burn and admission (p < 0.02). Interstitial fibrosis was significantly more severe in cases with longer survival after burn (p < 0.01). The scores for protein were significantly higher in cases with longer survival after burn (p < 0.03). Enlarged air spaces were significantly more prominent in cases with longer survival after burn (p < 0.01), and in cases with the presence of inhalation injury (p < 0.01). Conclusions Histological findings associated with diffuse alveolar damage (DAD), which is the pathological correlate of the acute respiratory distress syndrome (ARDS), were seen in approximately 42% of autopsies studied. Protein-rich alveolar edema, which is the abnormality that leads to ARDS, may occur from multiple causes, including inhalation injury.
KW - Adult respiratory distress syndrome
KW - Diffuse alveolar damage
KW - Histology
KW - Pediatric patients
KW - Predictor variables
KW - Scoring
KW - Survivability
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U2 - 10.1016/j.burns.2014.09.014
DO - 10.1016/j.burns.2014.09.014
M3 - Article
C2 - 25445004
AN - SCOPUS:84925667518
SN - 0305-4179
VL - 41
SP - 519
EP - 527
JO - Burns
JF - Burns
IS - 3
ER -