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New-onset atrial fibrillation, thrombocytopenia, and short-term outcomes in patients with cancer requiring intensive care: a retrospective ICU cohort study
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Abstract
Background
Cancer and atrial fibrillation frequently coexist. Intensive care adds hemodynamic stress, organ failure, and competing bleeding risk. The interaction between new-onset atrial fibrillation and thrombocytopenia in patients with cancer requiring intensive care remains insufficiently defined.
Methods
We performed a retrospective ICU cohort study using de-identified critical care data. Adult ICU stays with solid or hematologic malignancy were included. The main exposure was new-onset atrial fibrillation surrogate. Early thrombocytopenia was defined from the minimum platelet count within 48 hours and categorized as > = 150, 100–149, 50–99, and < 50 x10^9/L. The primary outcome was in-hospital death. Secondary outcomes were 28-day death, major bleeding identified by ICD coding, and ischemic stroke identified by ICD coding. Multivariable logistic regression tested interaction between new-onset atrial fibrillation and platelet category.
Results
Among 9,640 cancer ICU stays, 1,788 (18.5%) met criteria for new-onset atrial fibrillation surrogate. In-hospital death occurred in 1,724 (17.9%) stays, 28-day death in 2,394 (24.8%), major bleeding ICD in 1,001 (10.4%), and ischemic stroke ICD in 410 (4.3%). In complete-case interaction models (n = 9,505), the association between new-onset atrial fibrillation and in-hospital death differed by platelet category (P for interaction = 0.069). Severe thrombocytopenia (< 50 x10^9/L) showed the strongest mortality signal (adjusted OR 1.607, 95% CI 1.090–2.370). For major bleeding, platelet category significantly modified the association (P for interaction = 0.040). In the platelet 50–99 x10^9/L stratum, new-onset atrial fibrillation was associated with lower odds of major bleeding (adjusted OR 0.534, 95% CI 0.306–0.933). In the platelet > = 150 x10^9/L stratum, new-onset atrial fibrillation was associated with higher odds of ischemic stroke (adjusted OR 1.663, 95% CI 1.231–2.248).
Conclusions
New-onset atrial fibrillation identified a clinically distinct short-term risk phenotype in patients with cancer requiring intensive care. Platelet strata differentiated mortality and bleeding patterns. Severe thrombocytopenia marked the subgroup with the strongest mortality signal.
Springer Science and Business Media LLC
Title: New-onset atrial fibrillation, thrombocytopenia, and short-term outcomes in patients with cancer requiring intensive care: a retrospective ICU cohort study
Description:
Abstract
Background
Cancer and atrial fibrillation frequently coexist.
Intensive care adds hemodynamic stress, organ failure, and competing bleeding risk.
The interaction between new-onset atrial fibrillation and thrombocytopenia in patients with cancer requiring intensive care remains insufficiently defined.
Methods
We performed a retrospective ICU cohort study using de-identified critical care data.
Adult ICU stays with solid or hematologic malignancy were included.
The main exposure was new-onset atrial fibrillation surrogate.
Early thrombocytopenia was defined from the minimum platelet count within 48 hours and categorized as > = 150, 100–149, 50–99, and < 50 x10^9/L.
The primary outcome was in-hospital death.
Secondary outcomes were 28-day death, major bleeding identified by ICD coding, and ischemic stroke identified by ICD coding.
Multivariable logistic regression tested interaction between new-onset atrial fibrillation and platelet category.
Results
Among 9,640 cancer ICU stays, 1,788 (18.
5%) met criteria for new-onset atrial fibrillation surrogate.
In-hospital death occurred in 1,724 (17.
9%) stays, 28-day death in 2,394 (24.
8%), major bleeding ICD in 1,001 (10.
4%), and ischemic stroke ICD in 410 (4.
3%).
In complete-case interaction models (n = 9,505), the association between new-onset atrial fibrillation and in-hospital death differed by platelet category (P for interaction = 0.
069).
Severe thrombocytopenia (< 50 x10^9/L) showed the strongest mortality signal (adjusted OR 1.
607, 95% CI 1.
090–2.
370).
For major bleeding, platelet category significantly modified the association (P for interaction = 0.
040).
In the platelet 50–99 x10^9/L stratum, new-onset atrial fibrillation was associated with lower odds of major bleeding (adjusted OR 0.
534, 95% CI 0.
306–0.
933).
In the platelet > = 150 x10^9/L stratum, new-onset atrial fibrillation was associated with higher odds of ischemic stroke (adjusted OR 1.
663, 95% CI 1.
231–2.
248).
Conclusions
New-onset atrial fibrillation identified a clinically distinct short-term risk phenotype in patients with cancer requiring intensive care.
Platelet strata differentiated mortality and bleeding patterns.
Severe thrombocytopenia marked the subgroup with the strongest mortality signal.
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