Simplified apparatus for ultrafiltration by centrifugation.

Abstract

<h3>ABSTRACT</h3> <h3>Objective</h3> To identify sex-specific effects of risk factors for in-hospital mortality among COVID-19 patients admitted to a hospital system in New York City. <h3>Design</h3> Prospective observational cohort study with in-hospital mortality as the primary outcome. <h3>Setting</h3> Five acute care hospitals within a single academic medical system in New York City. <h3>Participants</h3> 3,086 hospital inpatients with COVID-19 admitted on or before April 13, 2020 and followed through June 2, 2020. Follow-up till discharge or death was complete for 99.3% of the cohort. <h3>Results</h3> The majority of the cohort was male (59.6%). Men were younger (median 64 vs. 70, p&lt;0.001) and less likely to have comorbidities such as hypertension (32.5% vs. 39.9%, p&lt;0.001), diabetes (22.6% vs. 26%, p=0.03), and obesity (6.9% vs. 9.8%, p=0.004) compared to women. Women had lower median values of laboratory markers associated with inflammation compared to men: white blood cells (5.95 vs. 6.8 K/uL, p&lt;0.001), procalcitonin (0.14 vs 0.21 ng/mL, p&lt;0.001), lactate dehydrogenase (375 vs. 428 U/L, p&lt;0.001), C-reactive protein (87.7 vs. 123.2 mg/L, p&lt;0.001). Unadjusted mortality was similar between men and women (28.8% vs. 28.5%, p=0.84), but more men required intensive care than women (25.2% vs. 19%, p&lt;0.001). Male sex was an independent risk factor for mortality (OR 1.26, 95% 1.04-1.51) after adjustment for demographics, comorbidities, and baseline hypoxia. There were significant interactions between sex and coronary artery disease (p=0.038), obesity (p=0.01), baseline hypoxia (p&lt;0.001), ferritin (p=0.002), lactate dehydrogenase (p=0.003), and procalcitonin (p=0.03). Except for procalcitonin, which had the opposite association, each of these factors was associated with disproportionately higher mortality among women. <h3>Conclusions</h3> Male sex was an independent predictor of mortality, consistent with prior studies. Notably, there were significant sex-specific interactions which indicated a disproportionate increase in mortality among women with coronary artery disease, obesity, and hypoxia. These new findings highlight patient subgroups for further study and help explain the recognized sex differences in COVID-19 outcomes.