{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T06:30:46Z","timestamp":1787725846989,"version":"build-2784847793"},"reference-count":24,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T00:00:00Z","timestamp":1787702400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Med."],"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Sepsis is a condition that can lead to severe complications and is estimated to affect 300 million people annually. Patients requiring mechanical ventilation represent a particularly critical subgroup with high mortality. While hematocrit (HCT) has been identified as a prognostic marker in general sepsis populations, its specific role in mechanically ventilated patients remains unexplored. The objective of this study is to examine the relationship between HCT levels and 28-day mortality in this vulnerable patient cohort.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>In this prospective observational study, an exploratory candidate cutoff for HCT was empirically derived by maximizing the Youden index from the ROC curve to predict 28-day mortality. The cohort was then stratified into low-HCT and high-HCT groups, utilizing the aforementioned candidate threshold. To assess the stability of this data-driven cutoff, an internal bootstrap validation procedure was performed. Subsequently, the association between HCT stratification and 28-day mortality was evaluated using a Cox proportional hazards regression model, adjusting for prespecified covariates.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Among the 233 patients included in the study, 40 (17.2%) died within 28\u202fdays. Patients were stratified into two groups, low HCT (&amp;lt;26.65%) and high HCT (\u226526.65%), based on the exploratory HCT cutoff of 26.65%. In the multivariable Cox proportional hazards model, patients in the low HCT group exhibited a significantly elevated risk of 28-day mortality compared to those in the high HCT group (adjusted hazard ratio [HR]\u202f=\u202f2.16, 95% CI: 1.04\u20134.52;\n                      <jats:italic>p<\/jats:italic>\n                      \u202f&amp;lt;\u202f0.05).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>In this multicenter study, an exploratory HCT cutoff of 26.65% was identified, and it was observed that low HCT was associated with a 2.16-fold increased risk of 28-day mortality in mechanically ventilated sepsis patients. However, the discriminative ability of HCT was modest (AUC\u202f\u2248\u202f0.537), suggesting limited predictive utility as a standalone test. Given its low cost and routine availability, HCT may still hold value as an adjunctive variable in risk stratification. However, further investigation is necessary to validate its incremental prognostic value and determine its optimal integration with other established predictors in larger, well-powered cohorts.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.3389\/fmed.2026.1890758","type":"journal-article","created":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T06:04:53Z","timestamp":1787724293000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["Hematocrit and 28-day mortality in mechanically ventilated septic patients: a prospective observational study"],"prefix":"10.3389","volume":"13","author":[{"given":"Lianghai","family":"Cao","sequence":"first","affiliation":[{"name":"Chengdu Integrated TCM and Western Medicine Hospital","place":["Chengdu, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Youlian","family":"Zhou","sequence":"additional","affiliation":[{"name":"Chengdu Integrated TCM and Western Medicine Hospital","place":["Chengdu, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pengcheng","family":"Shen","sequence":"additional","affiliation":[{"name":"The First People\u2019s Hospital of Yibin","place":["Yibin, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hui","family":"Cui","sequence":"additional","affiliation":[{"name":"Chengdu Integrated TCM and Western Medicine Hospital","place":["Chengdu, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jin","family":"Tang","sequence":"additional","affiliation":[{"name":"West China Hospital, Sichuan University, Sichuan University West China Hospital Guang'an Hospital, Guang\u2019an People\u2019s Hospital","place":["Guangan, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Min","family":"Xiao","sequence":"additional","affiliation":[{"name":"Affiliated Hospital of North Sichuan Medical College","place":["Nanchong, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ping","family":"Fang","sequence":"additional","affiliation":[{"name":"The Second People\u2019s Hospital of Neijiang","place":["Neijiang, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guilan","family":"Ding","sequence":"additional","affiliation":[{"name":"Dazhou Central Hospital","place":["Dazhou, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jun","family":"Qiu","sequence":"additional","affiliation":[{"name":"Chengdu Integrated TCM and Western Medicine Hospital","place":["Chengdu, Sichuan, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2026,8,26]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","first-page":"2003","DOI":"10.1001\/jama.2019.5791","article-title":"Derivation, validation, and potential treatment implications of novel 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