Clinical risks for development of the acute respiratory distress syndrome
- PMID: 7842182
- DOI: 10.1164/ajrccm.151.2.7842182
Clinical risks for development of the acute respiratory distress syndrome
Abstract
To further understanding of the epidemiology of acute respiratory distress syndrome (ARDS), we prospectively identified 695 patients admitted to our intensive care units from 1983 through 1985 meeting criteria for seven clinical risks, and followed them for development of ARDS and eventual outcome. ARDS occurred in 179 of the 695 patients (26%). The highest incidence of ARDS occurred in patients with sepsis syndrome (75 of 176; 43%) and those with multiple emergency transfusions (> or = 15 units in 24 h) (46 of 115; 40%). Of patients with multiple trauma, 69 of 271 (25%) developed ARDS. If any two clinical risks for trauma were present, the incidence of ARDS was 23 of 57, or 40%. During the study period, we identified 48 patients with ARDS who did not have one of the defined clinical risks, yielding a sensitivity of 79% (179 of 227). Secondary factors associated with increased risk for ARDS in clinical risk subgroups include an elevated Acute Physiologic and Chronic Health Evaluation II (APACHE II) score in patients with sepsis and increased APACHE II and Injury Severity Scores (ISS) in trauma victims. Mortality was threefold higher when ARDS was present (62%) than among patients with clinical risks who did not develop ARDS (19%; p < 0.05). The difference in mortality if ARDS developed was particularly striking in patients with trauma (56% versus 13%), but less in those with sepsis (69% versus 49%). The mortality data should be interpreted with caution, since the fatality rate in ARDS patients appears to have decreased in our institution from the time that these data were collected.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
Risk factors of mortality in road traffic injury patients with acute respiratory distress syndrome.Chin Med J (Engl). 2008 Jun 5;121(11):968-72. Chin Med J (Engl). 2008. PMID: 18706242
-
Improved survival of patients with acute respiratory distress syndrome (ARDS): 1983-1993.JAMA. 1995 Jan 25;273(4):306-9. JAMA. 1995. PMID: 7815658
-
[Scales for evaluation of mortality of patients with trauma and adult respiratory distress syndrome].Salud Publica Mex. 1997 May-Jun;39(3):201-6. Salud Publica Mex. 1997. PMID: 9304223 Spanish.
-
[Current status of spleen-mediated inflammatory response in traumatic acute respiratory distress syndrome].Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2019 May;31(5):654-657. doi: 10.3760/cma.j.issn.2095-4352.2019.05.027. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2019. PMID: 31198159 Review. Chinese.
-
Physiologic, metabolic and mediator responses in posttrauma ARDS and sepsis: is oxygen debt a critical initiating factor?J Physiol Pharmacol. 1997 Dec;48(4):559-85. J Physiol Pharmacol. 1997. PMID: 9444608 Review.
Cited by
-
The rCC16 Protein Protects Against LPS-Induced Cell Apoptosis and Inflammatory Responses in Human Lung Pneumocytes.Front Pharmacol. 2020 Jul 14;11:1060. doi: 10.3389/fphar.2020.01060. eCollection 2020. Front Pharmacol. 2020. PMID: 32760279 Free PMC article.
-
The Epidemiology of Transfusion-related Acute Lung Injury Varies According to the Applied Definition of Lung Injury Onset Time.Ann Am Thorac Soc. 2015 Sep;12(9):1328-35. doi: 10.1513/AnnalsATS.201504-246OC. Ann Am Thorac Soc. 2015. PMID: 26102516 Free PMC article.
-
Frontline Science: D1 dopaminergic receptor signaling activates the AMPK-bioenergetic pathway in macrophages and alveolar epithelial cells and reduces endotoxin-induced ALI.J Leukoc Biol. 2017 Feb;101(2):357-365. doi: 10.1189/jlb.3HI0216-068RR. Epub 2016 Oct 12. J Leukoc Biol. 2017. PMID: 27733575 Free PMC article.
-
A Sequent of Gram-Negative Co-Infectome-Induced Acute Respiratory Distress Syndrome Are Potentially Subtle Aggravators Associated to the SARS-CoV-2 Evolution of Virulence.Diagnostics (Basel). 2024 Jan 4;14(1):120. doi: 10.3390/diagnostics14010120. Diagnostics (Basel). 2024. PMID: 38201429 Free PMC article.
-
Acute respiratory distress syndrome after trauma: development and validation of a predictive model.Crit Care Med. 2012 Aug;40(8):2295-303. doi: 10.1097/CCM.0b013e3182544f6a. Crit Care Med. 2012. PMID: 22809905 Free PMC article.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
