[Protective effects of high-dose ulinastatin on vital organs in patients receiving total arch replacement for type A

Xian-Yue Wang1, Wen-Peng Dong, Guang Tong

  • 1Department of Cardiovascular Surgery, the Military General Hospital of Guangzhou Command(affiliated hospital of the Second military medical university), Guangzhou, China 510010.

Insights

High-dose ulinastatin may protect pulmonary function and reduce brain injury markers in patients undergoing type A aortic dissection surgery. However, its specific protective effects on the brain require further investigation.

Area of Science:

  • Cardiovascular Surgery
  • Thoracic Surgery
  • Pharmacology

Background:

  • Type A aortic dissection is a life-threatening condition requiring complex surgical repair.
  • Total arch replacement is a critical procedure with potential for organ injury.
  • Ulinastatin is a protease inhibitor with potential organ-protective properties.

Purpose of the Study:

  • To evaluate the efficacy of high-dose ulinastatin in protecting vital organs during total arch replacement for type A aortic dissection.
  • To assess the impact of ulinastatin on postoperative organ function and complications.

Main Methods:

  • A prospective study involving 66 patients with type A aortic dissection undergoing total arch replacement.
  • Patients were divided into two groups: ulinastatin treatment (300,000 U/8h and during cardiopulmonary bypass) and control.
  • Comparison of surgical data, biochemical profiles, and postoperative outcomes including ICU stay, complications, and mortality.

Main Results:

  • Ulinastatin group showed lower lactate, S-100, and neuron-specific enolase levels postoperatively.
  • Patients receiving ulinastatin had a shorter ICU stay and reduced incidence of pulmonary infections and prolonged ventilation.
  • No significant differences were observed in renal or liver function, re-operation rates, or neurological complications.

Conclusions:

  • High-dose ulinastatin demonstrates protective effects on pulmonary function in patients undergoing total arch replacement for type A aortic dissection.
  • Ulinastatin may reduce specific markers of brain injury, but its overall neuroprotective role warrants further study.
  • The treatment did not significantly impact renal function, liver function, or bleeding complications.
Abstract

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