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Haematology in critical care · Anticoagulation in acute chest syndrome

TASC randomised trial

Prophylactic versus Therapeutic Anticoagulation for Acute Chest Syndrome in Sickle Cell Disease

TASC trial design and results
Design Double-blind randomised controlled trial
Treatment Therapeutic-dose anticoagulation
Control Prophylactic-dose anticoagulation
Population 172 adults with sickle cell disease hospitalised for acute chest syndrome across 12 French hospitals, with no initial thrombosis on CT pulmonary angiogram
Follow-up 15 days or discharge
Primary endpoint Time to resolution of acute chest syndrome
Result Time to resolution of acute chest syndrome was shorter with therapeutic anticoagulation (hazard ratio 0.71, 95% CI 0.51 to 0.99, p=0.044). Restricted mean time to resolution over a 15-day horizon or to discharge was 4.8±0.4 versus 6.1±0.5 days. Major bleeding, the primary safety outcome, occurred in neither group. Cumulative parenteral opioid use was lower with therapeutic dosing — median 124 mg (IQR 80 to 272) versus 219 mg (IQR 65 to 378) morphine equivalent, difference -96 mg (95% CI -202 to -46, p=0.02).
Secondary endpoints Opioid consumption, oxygen requirement, length of stay, major bleeding

In adult patients with ACS, a therapeutic anticoagulation shortened ACS duration and reduced opioid consumption compared with prophylactic doses, without increasing bleeding risk.

The trial authors, in the published abstract

How it has aged

Acute chest syndrome sits between thrombosis and infection, and this is the first randomised support for treating the thrombotic component directly. The opioid reduction is the finding patients would actually notice. With 172 patients and no major bleeding in either arm, the trial cannot exclude a bleeding risk that a larger study would detect, and the primary hazard ratio reaches significance only marginally.

Publications

Comparison of Prophylactic and Therapeutic Doses of Anticoagulation for Acute Chest Syndrome in Sickle Cell Disease: The TASC Double-Blind Controlled Randomized Clinical Trial

Mekontso Dessap A, Habibi A, Arlet JB, et al. Comparison of Prophylactic and Therapeutic Doses of Anticoagulation for Acute Chest Syndrome in Sickle Cell Disease: The TASC Double-Blind Controlled Randomized Clinical Trial. Am J Respir Crit Care Med 2025 May;211(5):832-841.

  • Time to resolution shortened from 6.1 to 4.8 days
  • Cumulative parenteral opioid requirement nearly halved
  • No major bleeding in either group
  • 172 patients, and no major bleeding in either arm, so a bleeding risk cannot be excluded