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1.
Advances in Clinical Radiology ; 4(1):189-194, 2022.
Article in English | EMBASE | ID: covidwho-2221491
2.
Open Forum Infect Dis ; 10(1): ofad011, 2023 Jan.
Article in English | MEDLINE | ID: covidwho-2222685

ABSTRACT

Background: Studies of inpatient coronavirus disease 2019 (COVID-19) mortality risk factors have mainly used data from academic medical centers or large multihospital databases and have not examined populations with large proportions of Hispanic/Latino patients. In a retrospective cohort study of 4881 consecutive adult COVID-19 hospitalizations at a single community hospital in Los Angeles County with a majority Hispanic/Latino population, we evaluated factors associated with mortality. Methods: Data on demographic characteristics, comorbidities, laboratory and clinical results, and COVID-19 therapeutics were abstracted from the electronic medical record. Cox proportional hazards regression modeled statistically significant, independently associated predictors of hospital mortality. Results: Age ≥65 years (hazard ratio [HR] = 2.66; 95% confidence interval [CI] = 1.90-3.72), male sex (HR = 1.31; 95% CI = 1.07-1.60), renal disease (HR = 1.52; 95% CI = 1.18-1.95), cardiovascular disease (HR = 1.45; 95% CI = 1.18-1.78), neurological disease (HR = 1.84; 95% CI = 1.41-2.39), D-dimer ≥500 ng/mL (HR = 2.07; 95% CI = 1.43-3.0), and pulse oxygen level <88% (HR = 1.39; 95% CI = 1.13-1.71) were independently associated with increased mortality. Patient household with (1) multiple COVID-19 cases and (2) Asian, Black, or Hispanic compared with White non-Hispanic race/ethnicity were associated with reduced mortality. In hypoxic COVID-19 inpatients, remdesivir, tocilizumab, and convalescent plasma were associated with reduced mortality, and corticosteroid use was associated with increased mortality. Conclusions: We corroborate several previously identified mortality risk factors and find evidence that the combination of factors associated with mortality differ between populations.

3.
Circulation Conference: American Heart Association's ; 146(Supplement 1), 2022.
Article in English | EMBASE | ID: covidwho-2194389
4.
Critical Care Medicine ; 51(1 Supplement):555, 2023.
Article in English | EMBASE | ID: covidwho-2190672
5.
Critical Care Medicine ; 51(1 Supplement):536, 2023.
Article in English | EMBASE | ID: covidwho-2190660
6.
Critical Care Medicine ; 51(1 Supplement):536, 2023.
Article in English | EMBASE | ID: covidwho-2190659
7.
Critical Care Medicine ; 51(1 Supplement):512, 2023.
Article in English | EMBASE | ID: covidwho-2190655
8.
Critical Care Medicine ; 51(1 Supplement):226, 2023.
Article in English | EMBASE | ID: covidwho-2190561
9.
Critical Care Medicine ; 51(1 Supplement):103, 2023.
Article in English | EMBASE | ID: covidwho-2190493
10.
Critical Care Medicine ; 51(1 Supplement):36, 2023.
Article in English | EMBASE | ID: covidwho-2190463
11.
Open Forum Infectious Diseases ; 9(Supplement 2):S814-S815, 2022.
Article in English | EMBASE | ID: covidwho-2189996
12.
Open Forum Infectious Diseases ; 9(Supplement 2):S808, 2022.
Article in English | EMBASE | ID: covidwho-2189992
13.
Open Forum Infectious Diseases ; 9(Supplement 2):S804, 2022.
Article in English | EMBASE | ID: covidwho-2189991
14.
Open Forum Infectious Diseases ; 9(Supplement 2):S803, 2022.
Article in English | EMBASE | ID: covidwho-2189989
15.
Open Forum Infectious Diseases ; 9(Supplement 2):S705, 2022.
Article in English | EMBASE | ID: covidwho-2189877
16.
Open Forum Infectious Diseases ; 9(Supplement 2):S386-S387, 2022.
Article in English | EMBASE | ID: covidwho-2189680
17.
Open Forum Infectious Diseases ; 9(Supplement 2):S385, 2022.
Article in English | EMBASE | ID: covidwho-2189678
18.
Open Forum Infectious Diseases ; 9(Supplement 2):S370, 2022.
Article in English | EMBASE | ID: covidwho-2189671
19.
Open Forum Infectious Diseases ; 9(Supplement 2):S193, 2022.
Article in English | EMBASE | ID: covidwho-2189606
20.
Open Forum Infectious Diseases ; 9(Supplement 2):S186-S187, 2022.
Article in English | EMBASE | ID: covidwho-2189594
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