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Effect of blood purification combined with antibiotics on CC-16 and SP-D levels and prognosis in patients with severe acute pancreatitis complicated by acute respiratory distress syndrome.

American journal of translational research2025-02-17PubMed
Total: 68.5Innovation: 7Impact: 7Rigor: 7Citation: 6

Summary

In 128 SAP-ARDS patients, adding continuous blood purification to standard care plus antibiotics yielded shorter edema resolution and ventilator weaning times, reduced hospital stay, improved respiratory mechanics and oxygenation, and lower 28-day mortality. CC-16 and SP-D levels decreased more in the CBP group, aligning with attenuated lung injury.

Key Findings

  • CBP plus antibiotics reduced pancreatic edema resolution time, ventilator weaning time, and hospital stay versus routine care (all P<0.05).
  • 28-day mortality was significantly lower in the CBP group compared to control (P<0.05).
  • Greater post-treatment improvements in CC-16, SP-D, respiratory mechanics (Peak, Plat, rate), and arterial oxygenation were observed in the CBP group.

Clinical Implications

Consider CBP as an adjunct in selected SAP-ARDS patients alongside timely antibiotics, with CC-16/SP-D as monitoring biomarkers; randomized trials are needed before routine adoption.

Why It Matters

Suggests a feasible extracorporeal adjunct that improves clinical outcomes and lung injury biomarkers in a high-mortality ARDS phenotype (pancreatitis-associated).

Limitations

  • Non-randomized single-center design with potential selection and confounding biases; allocation method not described.
  • The combined intervention (CBP plus antibiotics) limits attribution of effects to CBP alone; CBP protocol details not fully specified.

Future Directions

Conduct multicenter randomized trials to validate efficacy, define optimal CBP timing/dose, and isolate CBP-specific effects; evaluate cost-effectiveness and patient selection criteria.

Study Information

Study Type
Cohort
Research Domain
Treatment
Evidence Level
III - Non-randomized comparative cohort study with concurrent controls
Study Design
OTHER