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Hyper-oncotic Albumin Reduces Mortality in ARDS Compared to Crystalloid
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Hyper-oncotic Albumin Reduces Mortality in ARDS Compared to Crystalloid

Key Takeaway
Consider hyper-oncotic albumin for ARDS as it may reduce mortality compared to crystalloids.

A systematic review and meta-analysis evaluated the impact of albumin administration on mortality in adult patients with acute respiratory distress syndrome (ARDS), comparing it to crystalloid solutions. The analysis included five studies: three randomized controlled trials (RCTs) and two non-randomized studies (NRSs). The primary endpoint was 28-day mortality, with secondary outcomes including oxygenation changes and lengths of ICU and hospital stay. Overall, mortality was lower in the albumin group (33.2%, 97/292) compared to the crystalloid group (44.9%, 133/296), with an odds ratio (OR) of 0.61 (95% CI 0.43-0.85, p=0.004). While RCTs (n=204) showed no mortality benefit (OR=0.83, p=0.54), NRSs (n=384) demonstrated reduced mortality with albumin (OR=0.52, p=0.002). Specifically, hyper-oncotic albumin was associated with lower mortality in NRSs (OR=0.40, p=0.02) but not in RCTs (OR=0.74, p=0.57). Iso-oncotic albumin showed no mortality benefit (OR=0.88, p=0.72). Significant improvements in oxygenation were noted on the first (p=0.05) and second days (p<0.0001) post-administration. The trial sequential analysis highlighted the need for more high-quality RCTs to confirm these findings and clarify the clinical role of hyper-oncotic albumin in ARDS management.

AI Accuracy Review: 8/10 · Auto-published
View Original Abstract ↓
BACKGROUND: To evaluate the association between albumin administration as volume replacement and mortality in adult ARDS patients, we performed this meta-analysis and trial sequential analysis (TSA). METHODS: We searched databases including PubMed, Science Direct, Scopus, Web of Science databases and Cochrane Central Register of Controlled Trials up to 12 December 2024. We screened trials that included adult ARDS patients and compared albumin with crystalloid. The 28-day mortality served as the primary endpoint, while the oxygenation change, the length of ICU stay and the length of hospital stay were designated as secondary outcomes. To clarify the differing concentrations of albumin, we formed two distinct subgroups: the hyper-oncotic albumin subgroup (≥20%) and the iso-oncotic albumin subgroup (4%∼5%). Statistical synthesis was performed with Cochrane Review Manager 5.4.1, employing random-effects models. To mitigate random errors, TSA was implemented with α = 0.05 and β = 0.20 parameters. RESULTS: The analysis incorporated 5 publications: 3 randomized controlled trials (RCTs) and 2 non-randomized studies (NRSs). Overall mortality was lower in the albumin group (33.2%, 97/292) than in the crystalloid group (44.9%, 133/296) (OR = 0.61, 95%CI 0.43-0.85,  = 0.004). RCTs ( = 204) showed no benefit (OR = 0.83,  = 0.54), but NRSs ( = 384) demonstrated reduced mortality (OR = 0.52,  = 0.002). Hyper-oncotic albumin was associated with lower mortality in NRSs (OR = 0.40,  = 0.02) but not in RCTs (OR = 0.74,  = 0.57). Iso-oncotic albumin showed no benefit (OR = 0.88,  = 0.72). Regarding the impact of albumin on oxygenation, significant improvements in oxygenation were observed only on the first ( = 0.05) and second days ( < 0.0001). The TSA indicated a continued need for high-quality RCTs. CONCLUSIONS: Our analysis suggests that hyper-oncotic albumin may reduce mortality and improve early oxygenation in ARDS patients compared to crystalloids. Larger RCTs are urgently needed to validate these findings and define their potential role in clinical management.